PubMed Mentions

The links below are to publications on PubMed referring to PLINK. This list is gathered weekly from PubMed automatically.

Publication/References
Application of genome-wide single nucleotide polymorphism typing: simple association and beyond. Description: Gibbs, J Raphael, et al. Application of genome-wide single nucleotide polymorphism typing: simple association and beyond. ''PLoS Genet''. 2006 Oct 6; '''2''' (10):e150
IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease. Description: Tremelling, Mark, et al. IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease. ''Gastroenterology''. 2007 May; '''132''' (5):1657-64
Identification of two independent risk factors for lupus within the MHC in United Kingdom families. Description: Fernando, Michelle M A, et al. Identification of two independent risk factors for lupus within the MHC in United Kingdom families. ''PLoS Genet''. 2007 Nov; '''3''' (11):e192
Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese. Description: Gong, Wei Fen, et al. Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese. ''Mol Vis''. 2008; '''14''': 2381-9
Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma. Description: Fan, Bao Jian, et al. Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma. ''Mol Vis''. 2008; '''14''': 2484-91
Contributions of MYOC and CYP1B1 mutations to JOAG. Description: Bayat, Behnaz, et al. Contributions of MYOC and CYP1B1 mutations to JOAG. ''Mol Vis''. 2008 Mar 13; '''14''': 508-17
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. Description: Liu, Ying, et al. A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. ''PLoS Genet''. 2008 Mar 28; '''4''' (3):e1000041
Analysis of genomic admixture in Uyghur and its implication in mapping strategy. Description: Xu, Shuhua, et al. Analysis of genomic admixture in Uyghur and its implication in mapping strategy. ''Am J Hum Genet''. 2008 Apr; '''82''' (4):883-94
Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus. Description: Taylor, Kimberly E, et al. Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus. ''PLoS Genet''. 2008 May 30; '''4''' (5):e1000084
Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle. Description: Tallila, Jonna, et al. Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle. ''Am J Hum Genet''. 2008 Jun; '''82''' (6):1361-7
Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations. Description: Kristjansdottir, G, et al. Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations. ''J Med Genet''. 2008 Jun; '''45''' (6):362-9
Common variation in the fat mass and obesity-associated (FTO) gene confers risk of obesity and modulates BMI in the Chinese population. Description: Chang, Yi-Cheng, et al. Common variation in the fat mass and obesity-associated (FTO) gene confers risk of obesity and modulates BMI in the Chinese population. ''Diabetes''. 2008 Aug; '''57''' (8):2245-52
Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians. Description: Ng, Maggie C Y, et al. Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians. ''Diabetes''. 2008 Aug; '''57''' (8):2226-33
Polymorphisms within the adenosine receptor 2a gene are associated with adverse events in RA patients treated with MTX. Description: Hider, S L, et al. Polymorphisms within the adenosine receptor 2a gene are associated with adverse events in RA patients treated with MTX. ''Rheumatology (Oxford)''. 2008 Aug; '''47''' (8):1156-9
WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. Description: Lee, Jenny C, et al. WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. ''Am J Hum Genet''. 2008 Aug; '''83''' (2):180-92
Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations. Description: Fawcett, Katherine A, et al. Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations. ''Diabetes''. 2008 Sep; '''57''' (9):2527-33
The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research. Description: Nelson, Matthew R, et al. The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research. ''Am J Hum Genet''. 2008 Sep; '''83''' (3):347-58
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. Description: Abraham, Richard, et al. A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. ''BMC Med Genomics''. 2008 Sep 29; '''1''': 44
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series. Description: Webb, T E F, et al. Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series. ''Brain''. 2008 Oct; '''131''' (Pt 10):2632-46
Tissue-specific genetic control of splicing: implications for the study of complex traits. Description: Heinzen, Erin L, et al. Tissue-specific genetic control of splicing: implications for the study of complex traits. ''PLoS Biol''. 2008 Dec 23; '''6''' (12):e1
Association of genetic variants at 3q22 with nephropathy in patients with type 1 diabetes mellitus. Description: He, Bing, et al. Association of genetic variants at 3q22 with nephropathy in patients with type 1 diabetes mellitus. ''Am J Hum Genet''. 2009 Jan; '''84''' (1):5-13
Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry. Description: Grant, Struan Fa, et al. Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry. ''Appl Clin Genet''. 2009; '''2''': 1-5
Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12. Description: Schache, Maria, et al. Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12. ''Mol Vis''. 2009; '''15''': 722-30
Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies. Description: Aldinger, Kimberly A, et al. Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies. ''PLoS One''. 2009; '''4''' (3):e4729
Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis. Description: Hinks, Anne, et al. Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis. ''Arthritis Rheum''. 2009 Jan; '''60''' (1):258-63
Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. Description: Liu, Yang, et al. Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. ''J Biomed Biotechnol''. 2009; '''2009''': 536918
HECTD2 is associated with susceptibility to mouse and human prion disease. Description: Lloyd, Sarah E, et al. HECTD2 is associated with susceptibility to mouse and human prion disease. ''PLoS Genet''. 2009 Feb; '''5''' (2):e1000383
Positive association of common variants in CD36 with neovascular age-related macular degeneration. Description: Kondo, Naoshi, et al. Positive association of common variants in CD36 with neovascular age-related macular degeneration. ''Aging (Albany NY)''. 2009 Feb 12; '''1''' (2):266-74
A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose. Description: Takeuchi, Fumihiko, et al. A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose. ''PLoS Genet''. 2009 Mar; '''5''' (3):e1000433
Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche. Description: Liu, Yao-Zhong, et al. Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche. ''PLoS Genet''. 2009 Mar; '''5''' (3):e1000420
Multi-criteria decision making approaches for quality control of genome-wide association studies. Description: Malovini, Alberto, et al. Multi-criteria decision making approaches for quality control of genome-wide association studies. ''Summit Transl Bioinform''. 2009 Mar 1; '''2009''': 74-8
Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease. Description: Gu, YuanYuan, et al. Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease. ''Nature''. 2009 Apr 23; '''458''' (7241):1039-42
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. Description: Himes, Blanca E, et al. Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. ''Am J Hum Genet''. 2009 May; '''84''' (5):581-93
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder. Description: Schulze, T G, et al. Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder. ''Mol Psychiatry''. 2009 May; '''14''' (5):487-91
ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai. Description: Yang, Wanling, et al. ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai. ''Hum Mol Genet''. 2009 Jun 1; '''18''' (11):2063-70
Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis. Description: Zinovieva, Elena, et al. Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis. ''PLoS Genet''. 2009 Jun; '''5''' (6):e1000528
Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Description: He, Chunyan, et al. Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. ''Nat Genet''. 2009 Jun; '''41''' (6):724-8
Postural changes in blood pressure associated with interactions between candidate genes for chronic respiratory diseases and exposure to particulate matter. Description: Wilker, Elissa, et al. Postural changes in blood pressure associated with interactions between candidate genes for chronic respiratory diseases and exposure to particulate matter. ''Environ Health Perspect''. 2009 Jun; '''117''' (6):935-40
Reduced-function SLC22A1 polymorphisms encoding organic cation transporter 1 and glycemic response to metformin: a GoDARTS study. Description: Zhou, Kaixin, et al. Reduced-function SLC22A1 polymorphisms encoding organic cation transporter 1 and glycemic response to metformin: a GoDARTS study. ''Diabetes''. 2009 Jun; '''58''' (6):1434-9
Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk. Description: Drenos, Fotios, et al. Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk. ''Hum Mol Genet''. 2009 Jun 15; '''18''' (12):2305-16
Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array. Description: Sober, Siim, et al. Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array. ''PLoS One''. 2009 Jun 29; '''4''' (6):e6034
A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta. Description: Drogemuller, Cord, et al. A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta. ''PLoS Genet''. 2009 Jul; '''5''' (7):e1000579
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. Description: Takeuchi, Fumihiko, et al. Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. ''Diabetes''. 2009 Jul; '''58''' (7):1690-9
Current software for genotype imputation. Description: Ellinghaus, David, et al. Current software for genotype imputation. ''Hum Genomics''. 2009 Jul; '''3''' (4):371-80
Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy. Description: Kaunisto, Mari A, et al. Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy. ''Diabetes''. 2009 Jul; '''58''' (7):1710-4
Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE. Description: Morris, D L, et al. Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE. ''Genes Immun''. 2009 Jul; '''10''' (5):404-13
Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI. Description: Kalnina, Ineta, et al. Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI. ''BMC Med Genet''. 2009 Jul 14; '''10''': 63
A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory disease. Description: Ko, Dennis C, et al. A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory disease. ''Am J Hum Genet''. 2009 Aug; '''85''' (2):214-27
CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Description: Newbury, Dianne F, et al. CMIP and ATP2C2 modulate phonological short-term memory in language impairment. ''Am J Hum Genet''. 2009 Aug; '''85''' (2):264-72
Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. Description: Hancock, Dana B, et al. Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. ''PLoS Genet''. 2009 Aug; '''5''' (8):e1000623
Identification of the UBP1 locus as a critical blood pressure determinant using a combination of mouse and human genetics. Description: Koutnikova, Hana, et al. Identification of the UBP1 locus as a critical blood pressure determinant using a combination of mouse and human genetics. ''PLoS Genet''. 2009 Aug; '''5''' (8):e1000591
A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene. Description: Nakano, Motoi, et al. A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene. ''BMC Genet''. 2009 Aug 4; '''10''': 42
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. Description: Potkin, Steven G, et al. Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. ''PLoS One''. 2009 Aug 7; '''4''' (8):e6501
Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions. Description: Casselbrant, Margaretha L, et al. Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions. ''BMC Med Genet''. 2009 Sep 3; '''10''': 85
Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation. Description: Hesselson, Stephanie E, et al. Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation. ''PLoS One''. 2009 Sep 9; '''4''' (9):e6942
HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q. Description: Lloyd, Sarah E, et al. HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q. ''BMC Med Genet''. 2009 Sep 15; '''10''': 90
Association between KCNJ6 (GIRK2) gene polymorphisms and postoperative analgesic requirements after major abdominal surgery. Description: Nishizawa, Daisuke, et al. Association between KCNJ6 (GIRK2) gene polymorphisms and postoperative analgesic requirements after major abdominal surgery. ''PLoS One''. 2009 Sep 16; '''4''' (9):e7060
Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy. Description: Al-Chalabi, Ammar, et al. Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy. ''PLoS One''. 2009 Sep 22; '''4''' (9):e7114
Genomewide association study for onset age in Parkinson disease. Description: Latourelle, Jeanne C, et al. Genomewide association study for onset age in Parkinson disease. ''BMC Med Genet''. 2009 Sep 22; '''10''': 98
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Description: Harold, Denise, et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. ''Nat Genet''. 2009 Oct; '''41''' (10):1088-93
Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population. Description: Simon-Sanchez, Javier, et al. Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population. ''PLoS One''. 2009 Oct 22; '''4''' (10):e7494
Evidence for genetic association of RORB with bipolar disorder. Description: McGrath, Casey L, et al. Evidence for genetic association of RORB with bipolar disorder. ''BMC Psychiatry''. 2009 Nov 12; '''9''': 70
Genetic variation and recent positive selection in worldwide human populations: evidence from nearly 1 million SNPs. Description: Lopez Herraez, David, et al. Genetic variation and recent positive selection in worldwide human populations: evidence from nearly 1 million SNPs. ''PLoS One''. 2009 Nov 18; '''4''' (11):e7888
Genomic dissection of population substructure of Han Chinese and its implication in association studies. Description: Xu, Shuhua, et al. Genomic dissection of population substructure of Han Chinese and its implication in association studies. ''Am J Hum Genet''. 2009 Dec; '''85''' (6):762-74
Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans. Description: Dong, C, et al. Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans. ''Mol Psychiatry''. 2009 Dec; '''14''' (12):1105-18
The common FTO variant rs9939609 is not associated with BMI in a longitudinal study on a cohort of Swedish men born 1920-1924. Description: Jacobsson, Josefin A, et al. The common FTO variant rs9939609 is not associated with BMI in a longitudinal study on a cohort of Swedish men born 1920-1924. ''BMC Med Genet''. 2009 Dec 9; '''10''': 131
Application of Bayesian classification with singular value decomposition method in genome-wide association studies. Description: Kwon, Soonil, et al. Application of Bayesian classification with singular value decomposition method in genome-wide association studies. ''BMC Proc''. 2009 Dec 15; '''3 Suppl 7''': S9
Classification tree for detection of single-nucleotide polymorphism (SNP)-by-SNP interactions related to heart disease: Framingham Heart Study. Description: Yao, Li, et al. Classification tree for detection of single-nucleotide polymorphism (SNP)-by-SNP interactions related to heart disease: Framingham Heart Study. ''BMC Proc''. 2009 Dec 15; '''3 Suppl 7''': S83
Transferability and fine-mapping of genome-wide associated loci for adult height across human populations. Description: Shriner, Daniel, et al. Transferability and fine-mapping of genome-wide associated loci for adult height across human populations. ''PLoS One''. 2009 Dec 22; '''4''' (12):e8398
Promoter variant of PIK3C3 is associated with autoimmunity against Ro and Sm epitopes in African-American lupus patients. Description: Kariuki, Silvia N, et al. Promoter variant of PIK3C3 is associated with autoimmunity against Ro and Sm epitopes in African-American lupus patients. ''J Biomed Biotechnol''. 2010; '''2010''': 826434
The role of genetic variation near interferon-kappa in systemic lupus erythematosus. Description: Harley, Isaac T W, et al. The role of genetic variation near interferon-kappa in systemic lupus erythematosus. ''J Biomed Biotechnol''. 2010; '''2010''':
A sequence polymorphism in MSTN predicts sprinting ability and racing stamina in thoroughbred horses. Description: Hill, Emmeline W, et al. A sequence polymorphism in MSTN predicts sprinting ability and racing stamina in thoroughbred horses. ''PLoS One''. 2010 Jan 20; '''5''' (1):e8645
CLOCK is suggested to associate with comorbid alcohol use and depressive disorders. Description: Sjoholm, Louise K, et al. CLOCK is suggested to associate with comorbid alcohol use and depressive disorders. ''J Circadian Rhythms''. 2010 Jan 21; '''8''': 1
Gene expression profiling in monocytes and SNP association suggest the importance of the STAT1 gene for osteoporosis in both Chinese and Caucasians. Description: Chen, Xiang-Ding, et al. Gene expression profiling in monocytes and SNP association suggest the importance of the STAT1 gene for osteoporosis in both Chinese and Caucasians. ''J Bone Miner Res''. 2010 Feb; '''25''' (2):339-55
Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth. Description: Ryckman, Kelli K, et al. Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth. ''PLoS One''. 2010 Feb 3; '''5''' (2):e9040
Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. Description: Kung, Annie W C, et al. Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. ''Am J Hum Genet''. 2010 Feb 12; '''86''' (2):229-39
Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability. Description: Ruano, Dina, et al. Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability. ''Am J Hum Genet''. 2010 Feb 12; '''86''' (2):113-25
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. Description: Jakkula, Eveliina, et al. Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. ''Am J Hum Genet''. 2010 Feb 12; '''86''' (2):285-91
Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance. Description: Utge, Siddheshwar J, et al. Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance. ''PLoS One''. 2010 Feb 18; '''5''' (2):e9259
Evaluation of DOK5 as a susceptibility gene for type 2 diabetes and obesity in North Indian population. Description: Tabassum, Rubina, et al. Evaluation of DOK5 as a susceptibility gene for type 2 diabetes and obesity in North Indian population. ''BMC Med Genet''. 2010 Feb 27; '''11''': 35
Genetic variation in the hypothalamic-pituitary-adrenal stress axis influences susceptibility to musculoskeletal pain: results from the EPIFUND study. Description: Holliday, Kate L, et al. Genetic variation in the hypothalamic-pituitary-adrenal stress axis influences susceptibility to musculoskeletal pain: results from the EPIFUND study. ''Ann Rheum Dis''. 2010 Mar; '''69''' (3):556-60
Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs. Description: Mu, Jianbing, et al. Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs. ''Nat Genet''. 2010 Mar; '''42''' (3):268-71
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. Description: Pattaro, Cristian, et al. A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. ''BMC Med Genet''. 2010 Mar 11; '''11''': 41
Systems genetics analysis of gene-by-environment interactions in human cells. Description: Romanoski, Casey E, et al. Systems genetics analysis of gene-by-environment interactions in human cells. ''Am J Hum Genet''. 2010 Mar 12; '''86''' (3):399-410
ARNTL (BMAL1) and NPAS2 gene variants contribute to fertility and seasonality. Description: Kovanen, Leena, et al. ARNTL (BMAL1) and NPAS2 gene variants contribute to fertility and seasonality. ''PLoS One''. 2010 Apr 2; '''5''' (4):e10007
Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time. Description: Houlihan, Lorna M, et al. Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time. ''Am J Hum Genet''. 2010 Apr 9; '''86''' (4):626-31
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset. Description: Glas, Jurgen, et al. Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset. ''PLoS One''. 2010 Apr 29; '''5''' (4):e10373
Interpretation of association signals and identification of causal variants from genome-wide association studies. Description: Wang, Kai, et al. Interpretation of association signals and identification of causal variants from genome-wide association studies. ''Am J Hum Genet''. 2010 May 14; '''86''' (5):730-42
Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population. Description: Han, Xueyao, et al. Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population. ''BMC Med Genet''. 2010 May 28; '''11''': 81
Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment. Description: Tan, Rachael J L, et al. Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment. ''Ann Rheum Dis''. 2010 Jun; '''69''' (6):1029-35
Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain. Description: Swaminathan, Bhairavi, et al. Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain. ''J Neuroimmunol''. 2010 Jun; '''223''' (1-2):100-3
Pooled association tests for rare variants in exon-resequencing studies. Description: Price, Alkes L, et al. Pooled association tests for rare variants in exon-resequencing studies. ''Am J Hum Genet''. 2010 Jun 11; '''86''' (6):832-8
Principal-component analysis for assessment of population stratification in mitochondrial medical genetics. Description: Biffi, Alessandro, et al. Principal-component analysis for assessment of population stratification in mitochondrial medical genetics. ''Am J Hum Genet''. 2010 Jun 11; '''86''' (6):904-17
Transforming growth factor beta 2 and heme oxygenase 1 genes are risk factors for the cerebral malaria syndrome in Angolan children. Description: Sambo, Maria Rosario, et al. Transforming growth factor beta 2 and heme oxygenase 1 genes are risk factors for the cerebral malaria syndrome in Angolan children. ''PLoS One''. 2010 Jun 16; '''5''' (6):e11141
Haplotypes that include the integrin alpha 11 gene are associated with tick burden in cattle. Description: Porto Neto, Laercio R, et al. Haplotypes that include the integrin alpha 11 gene are associated with tick burden in cattle. ''BMC Genet''. 2010 Jun 21; '''11''': 55
Pathway-based genome-wide association analysis identified the importance of regulation-of-autophagy pathway for ultradistal radius BMD. Description: Zhang, Lishu, et al. Pathway-based genome-wide association analysis identified the importance of regulation-of-autophagy pathway for ultradistal radius BMD. ''J Bone Miner Res''. 2010 Jul; '''25''' (7):1572-80
Quantitative trait analysis suggests human DAZL may be involved in regulating sperm counts and motility. Description: Hsu, Chao-Chin, et al. Quantitative trait analysis suggests human DAZL may be involved in regulating sperm counts and motility. ''Reprod Biomed Online''. 2010 Jul; '''21''' (1):77-83
Visualizing chromosome mosaicism and detecting ethnic outliers by the method of "rare" heterozygotes and homozygotes (RHH). Description: McGinnis, Ralph E, et al. Visualizing chromosome mosaicism and detecting ethnic outliers by the method of "rare" heterozygotes and homozygotes (RHH). ''Hum Mol Genet''. 2010 Jul 1; '''19''' (13):2539-53
Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot". Description: Johnatty, Sharon E, et al. Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot". ''PLoS Genet''. 2010 Jul 8; '''6''' (7):e1001016
A versatile gene-based test for genome-wide association studies. Description: Liu, Jimmy Z, et al. A versatile gene-based test for genome-wide association studies. ''Am J Hum Genet''. 2010 Jul 9; '''87''' (1):139-45
Genome-wide association study of pancreatic cancer in Japanese population. Description: Low, Siew-Kee, et al. Genome-wide association study of pancreatic cancer in Japanese population. ''PLoS One''. 2010 Jul 29; '''5''' (7):e11824
Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer. Description: Wang, Xuting, et al. Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer. ''PLoS One''. 2010 Aug 3; '''5''' (8):e11934
The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia. Description: Hsiung, Chao Agnes, et al. The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia. ''PLoS Genet''. 2010 Aug 5; '''6''' (8):
Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene. Description: Pointon, J J, et al. Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene. ''Genes Immun''. 2010 Sep; '''11''' (6):490-6
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. Description: Raychaudhuri, Soumya, et al. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. ''PLoS Genet''. 2010 Sep 9; '''6''' (9):e1001097
A novel statistic for genome-wide interaction analysis. Description: Wu, Xuesen, et al. A novel statistic for genome-wide interaction analysis. ''PLoS Genet''. 2010 Sep 23; '''6''' (9):e1001131
Association of the CCR5 gene with juvenile idiopathic arthritis. Description: Hinks, A, et al. Association of the CCR5 gene with juvenile idiopathic arthritis. ''Genes Immun''. 2010 Oct; '''11''' (7):584-9
High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. Description: Strom, S P, et al. High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. ''Mol Psychiatry''. 2010 Oct; '''15''' (10):996-1005
Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population. Description: Zhao, Fuxin, et al. Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population. ''Mol Vis''. 2010 Oct 2; '''16''': 1920-7
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. Description: Stark, Klaus, et al. Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. ''PLoS Genet''. 2010 Oct 21; '''6''' (10):e1001167
Genome-wide effects of long-term divergent selection. Description: Johansson, Anna M, et al. Genome-wide effects of long-term divergent selection. ''PLoS Genet''. 2010 Nov 4; '''6''' (11):e1001188
Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma. Description: Burdon, Kathryn P, et al. Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma. ''Mol Vis''. 2010 Nov 4; '''16''': 2286-93
Interaction of Crohn's disease susceptibility genes in an Australian paediatric cohort. Description: Wagner, Josef, et al. Interaction of Crohn's disease susceptibility genes in an Australian paediatric cohort. ''PLoS One''. 2010 Nov 8; '''5''' (11):e15376
Unifying candidate gene and GWAS Approaches in Asthma. Description: Michel, Sven, et al. Unifying candidate gene and GWAS Approaches in Asthma. ''PLoS One''. 2010 Nov 12; '''5''' (11):e13894
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Description: Sotoodehnia, Nona, et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. ''Nat Genet''. 2010 Dec; '''42''' (12):1068-76
Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. Description: Kopplin, L J, et al. Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. ''Genes Immun''. 2010 Dec; '''11''' (8):609-21
Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study. Description: Ryu, Euijung, et al. Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study. ''Mol Vis''. 2010 Dec 17; '''16''': 2811-21
Genes involved in the metabolism of poly-unsaturated fatty-acids (PUFA) and risk for Crohn's disease in children & young adults. Description: Costea, Irina, et al. Genes involved in the metabolism of poly-unsaturated fatty-acids (PUFA) and risk for Crohn's disease in children & young adults. ''PLoS One''. 2010 Dec 20; '''5''' (12):e15672
The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants. Description: Glas, Jurgen, et al. The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants. ''PLoS One''. 2010 Dec 30; '''5''' (12):e14466
A common CNR1 (cannabinoid receptor 1) haplotype attenuates the decrease in HDL cholesterol that typically accompanies weight gain. Description: Feng, Qiping, et al. A common CNR1 (cannabinoid receptor 1) haplotype attenuates the decrease in HDL cholesterol that typically accompanies weight gain. ''PLoS One''. 2010 Dec 31; '''5''' (12):e15779
Accelerating haplotype-based genome-wide association study using perfect phylogeny and phase-known reference data. Description: He, Yungang, et al. Accelerating haplotype-based genome-wide association study using perfect phylogeny and phase-known reference data. ''PLoS One''. 2011; '''6''' (7):e22097
A common complement C3 variant is associated with protection against wet age-related macular degeneration in a Japanese population. Description: Yanagisawa, Suiho, et al. A common complement C3 variant is associated with protection against wet age-related macular degeneration in a Japanese population. ''PLoS One''. 2011; '''6''' (12):e28847
A comparison of approaches to estimate the inbreeding coefficient and pairwise relatedness using genomic and pedigree data in a sheep population. Description: Li, Meng-Hua, et al. A comparison of approaches to estimate the inbreeding coefficient and pairwise relatedness using genomic and pedigree data in a sheep population. ''PLoS One''. 2011; '''6''' (11):e26256
A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations. Description: Downs, Louise M, et al. A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations. ''PLoS One''. 2011; '''6''' (6):e21452
A genome-wide SNP scan reveals novel loci for egg production and quality traits in white leghorn and brown-egg dwarf layers. Description: Liu, Wenbo, et al. A genome-wide SNP scan reveals novel loci for egg production and quality traits in white leghorn and brown-egg dwarf layers. ''PLoS One''. 2011; '''6''' (12):e28600
A latent model for prioritization of SNPs for functional studies. Description: Fridley, Brooke L, et al. A latent model for prioritization of SNPs for functional studies. ''PLoS One''. 2011; '''6''' (6):e20764
Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations. Description: Fahim, Abigail T, et al. Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations. ''PLoS One''. 2011; '''6''' (8):e23021
A methodology for multivariate phenotype-based genome-wide association studies to mine pleiotropic genes. Description: Park, Sung Hee, et al. A methodology for multivariate phenotype-based genome-wide association studies to mine pleiotropic genes. ''BMC Syst Biol''. 2011; '''5 Suppl 2''': S13
A network-based approach to prioritize results from genome-wide association studies. Description: Akula, Nirmala, et al. A network-based approach to prioritize results from genome-wide association studies. ''PLoS One''. 2011; '''6''' (9):e24220
A novel, functional and replicable risk gene region for alcohol dependence identified by genome-wide association study. Description: Zuo, Lingjun, et al. A novel, functional and replicable risk gene region for alcohol dependence identified by genome-wide association study. ''PLoS One''. 2011; '''6''' (11):e26726
An SNP selection strategy identified IL-22 associating with susceptibility to tuberculosis in Chinese. Description: Zhang, Guoliang, et al. An SNP selection strategy identified IL-22 associating with susceptibility to tuberculosis in Chinese. ''Sci Rep''. 2011; '''1''': 20
A pilot study of the association of tumor necrosis factor alpha polymorphisms with psoriatic arthritis in the Romanian population. Description: Popa, Olivia M, et al. A pilot study of the association of tumor necrosis factor alpha polymorphisms with psoriatic arthritis in the Romanian population. ''Int J Mol Sci''. 2011; '''12''' (8):5052-9
Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population. Description: Kiliszek, Marek, et al. Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population. ''PLoS One''. 2011; '''6''' (7):e21790
Association of MDR1 gene SNPs and haplotypes with the tacrolimus dose requirements in Han Chinese liver transplant recipients. Description: Yu, Xiaobo, et al. Association of MDR1 gene SNPs and haplotypes with the tacrolimus dose requirements in Han Chinese liver transplant recipients. ''PLoS One''. 2011; '''6''' (11):e25933
Association of the adiponectin gene variations with risk of ischemic stroke in a Korean population. Description: Cheong, My-Young, et al. Association of the adiponectin gene variations with risk of ischemic stroke in a Korean population. ''Yonsei Med J''. 2011 Jan; '''52''' (1):20-5
Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier. Description: Taylor, A E, et al. Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier. ''J Obes''. 2011; '''2011''': 307542
A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis. Description: Nakaoka, Hirofumi, et al. A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis. ''PLoS One''. 2011; '''6''' (9):e25389
A targeted association study of immunity genes and networks suggests novel associations with placental malaria infection. Description: Sikora, Martin, et al. A targeted association study of immunity genes and networks suggests novel associations with placental malaria infection. ''PLoS One''. 2011; '''6''' (9):e24996
BDNF contributes to the genetic variance of milk fat yield in german holstein cattle. Description: Zielke, Lea G, et al. BDNF contributes to the genetic variance of milk fat yield in german holstein cattle. ''Front Genet''. 2011; '''2''': 16
Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass. Description: Sun, Lu, et al. Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass. ''PLoS One''. 2011; '''6''' (11):e27325
Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans. Description: Signorello, Lisa B, et al. Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans. ''PLoS One''. 2011; '''6''' (12):e28623
Comparison of strategies to detect epistasis from eQTL data. Description: Kapur, Karen, et al. Comparison of strategies to detect epistasis from eQTL data. ''PLoS One''. 2011; '''6''' (12):e28415
Contributions of dopamine-related genes and environmental factors to highly sensitive personality: a multi-step neuronal system-level approach. Description: Chen, Chunhui, et al. Contributions of dopamine-related genes and environmental factors to highly sensitive personality: a multi-step neuronal system-level approach. ''PLoS One''. 2011; '''6''' (7):e21636
Convergence of miRNA expression profiling, alpha-synuclein interacton and GWAS in Parkinson's disease. Description: Martins, Madalena, et al. Convergence of miRNA expression profiling, alpha-synuclein interacton and GWAS in Parkinson's disease. ''PLoS One''. 2011; '''6''' (10):e25443
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk. Description: Salyakina, Daria, et al. Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk. ''PLoS One''. 2011; '''6''' (10):e26049
Copy number variation across European populations. Description: Chen, Wanting, et al. Copy number variation across European populations. ''PLoS One''. 2011; '''6''' (8):e23087
Copy number variation in CNP267 region may be associated with hip bone size. Description: Liu, Shan-Lin, et al. Copy number variation in CNP267 region may be associated with hip bone size. ''PLoS One''. 2011; '''6''' (7):e22035
Copy number variation in familial Parkinson disease. Description: Pankratz, Nathan, et al. Copy number variation in familial Parkinson disease. ''PLoS One''. 2011; '''6''' (8):e20988
Cost-effective prediction of gender-labeling errors and estimation of gender-labeling error rates in candidate-gene association studies. Description: Qu, Conghui, et al. Cost-effective prediction of gender-labeling errors and estimation of gender-labeling error rates in candidate-gene association studies. ''Front Genet''. 2011; '''2''': 31
CYBA Gene Polymorphisms and Adverse Outcomes in Acute Kidney Injury: A Prospective Cohort Study. Description: Perianayagam, Mary C, et al. CYBA Gene Polymorphisms and Adverse Outcomes in Acute Kidney Injury: A Prospective Cohort Study. ''Nephron Extra''. 2011 Jan; '''1''' (1):112-23
Detailed analysis of variants in FTO in association with body composition in a cohort of 70-year-olds suggests a weakened effect among elderly. Description: Jacobsson, Josefin A, et al. Detailed analysis of variants in FTO in association with body composition in a cohort of 70-year-olds suggests a weakened effect among elderly. ''PLoS One''. 2011; '''6''' (5):e20158
Determination of the loss of function complement C4 exon 29 CT insertion using a novel paralog-specific assay in healthy UK and Spanish populations. Description: Boteva, Lora, et al. Determination of the loss of function complement C4 exon 29 CT insertion using a novel paralog-specific assay in healthy UK and Spanish populations. ''PLoS One''. 2011; '''6''' (8):e22128
Dissecting cis regulation of gene expression in human metabolic tissues. Description: Dobrin, Radu, et al. Dissecting cis regulation of gene expression in human metabolic tissues. ''PLoS One''. 2011; '''6''' (8):e23480
EphB2 SNPs and sporadic prostate cancer risk in African American men. Description: Robbins, Christiane M, et al. EphB2 SNPs and sporadic prostate cancer risk in African American men. ''PLoS One''. 2011; '''6''' (5):e19494
Fine Mapping of Loci on BTA2 and BTA26 Associated with Bovine Viral Diarrhea Persistent Infection and Linked with Bovine Respiratory Disease in Cattle. Description: Zanella, Ricardo, et al. Fine Mapping of Loci on BTA2 and BTA26 Associated with Bovine Viral Diarrhea Persistent Infection and Linked with Bovine Respiratory Disease in Cattle. ''Front Genet''. 2011; '''2''': 82
From SNPs to genes: disease association at the gene level. Description: Lehne, Benjamin, et al. From SNPs to genes: disease association at the gene level. ''PLoS One''. 2011; '''6''' (6):e20133
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. Description: Paraboschi, Elvezia Maria, et al. Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. ''Int J Mol Sci''. 2011; '''12''' (12):8695-712
Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and Caucasians. Description: Kupfer, Sonia S, et al. Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and Caucasians. ''PLoS One''. 2011; '''6''' (10):e26123
Genetic association study of common mitochondrial variants on body fat mass. Description: Yang, Tie-Lin, et al. Genetic association study of common mitochondrial variants on body fat mass. ''PLoS One''. 2011; '''6''' (6):e21595
Genetic Modulation of Training and Transfer in Older Adults: BDNF ValMet Polymorphism is Associated with Wider Useful Field of View. Description: Colzato, Lorenza S, et al. Genetic Modulation of Training and Transfer in Older Adults: BDNF ValMet Polymorphism is Associated with Wider Useful Field of View. ''Front Psychol''. 2011; '''2''': 199
Genetics of sputum gene expression in chronic obstructive pulmonary disease. Description: Qiu, Weiliang, et al. Genetics of sputum gene expression in chronic obstructive pulmonary disease. ''PLoS One''. 2011; '''6''' (9):e24395
Genetic variation of VKORC1 and CYP4F2 genes related to warfarin maintenance dose in patients with myocardial infarction. Description: Kringen, Marianne K, et al. Genetic variation of VKORC1 and CYP4F2 genes related to warfarin maintenance dose in patients with myocardial infarction. ''J Biomed Biotechnol''. 2011; '''2011''': 739751
Genome-wide association study for atopy and allergic rhinitis in a Singapore Chinese population. Description: Andiappan, Anand Kumar, et al. Genome-wide association study for atopy and allergic rhinitis in a Singapore Chinese population. ''PLoS One''. 2011; '''6''' (5):e19719
Genome-wide association study of body weight in chicken F2 resource population. Description: Gu, Xiaorong, et al. Genome-wide association study of body weight in chicken F2 resource population. ''PLoS One''. 2011; '''6''' (7):e21872
Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection. Description: Chan, Kelvin Yuen-Kwong, et al. Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection. ''PLoS One''. 2011; '''6''' (12):e28798
Genome-wide scan identifies loci associated with classical BSE occurrence. Description: Murdoch, Brenda M, et al. Genome-wide scan identifies loci associated with classical BSE occurrence. ''PLoS One''. 2011; '''6''' (11):e26819
Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. Description: Swaminathan, Shanker, et al. Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. ''Int J Alzheimers Dis''. 2011; '''2011''': 729478
Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. Description: Johnson, Catherine, et al. Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. ''PLoS One''. 2011; '''6''' (7):e19210
Host genetic risk factors for West Nile virus infection and disease progression. Description: Bigham, Abigail W, et al. Host genetic risk factors for West Nile virus infection and disease progression. ''PLoS One''. 2011; '''6''' (9):e24745
hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets. Description: Johnson, Todd A, et al. hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets. ''Genome Biol''. 2011; '''12''' (3):R21
Identification of close relatives in the HUGO Pan-Asian SNP database. Description: Yang, Xiong, et al. Identification of close relatives in the HUGO Pan-Asian SNP database. ''PLoS One''. 2011; '''6''' (12):e29502
Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences. Description: Kovacic, Melinda Butsch, et al. Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences. ''PLoS One''. 2011; '''6''' (8):e23714
Identifying host genetic risk factors in the context of public health surveillance for invasive pneumococcal disease. Description: Lingappa, Jairam R, et al. Identifying host genetic risk factors in the context of public health surveillance for invasive pneumococcal disease. ''PLoS One''. 2011; '''6''' (8):e23413
Impact of genetic variation in SORCS1 on memory retention. Description: Reitz, Christiane, et al. Impact of genetic variation in SORCS1 on memory retention. ''PLoS One''. 2011; '''6''' (10):e24588
Investigating the pathogenic role of PADI4 in oesophageal cancer. Description: Chang, Xiaotian, et al. Investigating the pathogenic role of PADI4 in oesophageal cancer. ''Int J Biol Sci''. 2011; '''7''' (6):769-81
Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping. Description: Siemiatkowska, Anna M, et al. Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping. ''Mol Vis''. 2011; '''17''': 3013-24
Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5AC. Description: Guo, Xueliang, et al. Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5AC. ''PLoS One''. 2011; '''6''' (10):e25452
Multifactor dimensionality reduction as a filter-based approach for genome wide association studies. Description: Oki, Noffisat O, et al. Multifactor dimensionality reduction as a filter-based approach for genome wide association studies. ''Front Genet''. 2011; '''2''': 80
Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses. Description: Terao, Chikashi, et al. Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses. ''PLoS One''. 2011; '''6''' (6):e20457
Oncogenic CagA promotes gastric cancer risk via activating ERK signaling pathways: a nested case-control study. Description: Yang, Jae Jeong, et al. Oncogenic CagA promotes gastric cancer risk via activating ERK signaling pathways: a nested case-control study. ''PLoS One''. 2011; '''6''' (6):e21155
Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression. Description: Schoof, Nils, et al. Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression. ''PLoS One''. 2011; '''6''' (12):e29451
Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population. Description: Xie, Fang, et al. Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population. ''PLoS One''. 2011; '''6''' (6):e20833
Runs of homozygosity do not influence survival to old age. Description: Kuningas, Maris, et al. Runs of homozygosity do not influence survival to old age. ''PLoS One''. 2011; '''6''' (7):e22580
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. Description: Moens, Lotte N, et al. Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. ''PLoS One''. 2011; '''6''' (8):e23450
Statistical epistasis and functional brain imaging support a role of voltage-gated potassium channels in human memory. Description: Heck, Angela, et al. Statistical epistasis and functional brain imaging support a role of voltage-gated potassium channels in human memory. ''PLoS One''. 2011; '''6''' (12):e29337
Strategies for selection of subjects for sequencing after detection of a linkage peak. Description: Allen-Brady, Kristina, et al. Strategies for selection of subjects for sequencing after detection of a linkage peak. ''BMC Proc''. 2011; '''5 Suppl 9''': S77
Survey of SSC12 Regions Affecting Fatty Acid Composition of Intramuscular Fat Using High-Density SNP Data. Description: Munoz, Maria, et al. Survey of SSC12 Regions Affecting Fatty Acid Composition of Intramuscular Fat Using High-Density SNP Data. ''Front Genet''. 2011; '''2''': 101
The fat mass and obesity associated gene, FTO, is also associated with osteoporosis phenotypes. Description: Guo, Yan, et al. The fat mass and obesity associated gene, FTO, is also associated with osteoporosis phenotypes. ''PLoS One''. 2011; '''6''' (11):e27312
The genetic structure of the Swedish population. Description: Humphreys, Keith, et al. The genetic structure of the Swedish population. ''PLoS One''. 2011; '''6''' (8):e22547
The role of osteopontin (OPN/SPP1) haplotypes in the susceptibility to Crohn's disease. Description: Glas, Jurgen, et al. The role of osteopontin (OPN/SPP1) haplotypes in the susceptibility to Crohn's disease. ''PLoS One''. 2011; '''6''' (12):e29309
The role of toll-like receptor variants in acute anterior uveitis. Description: Pratap, Divya S, et al. The role of toll-like receptor variants in acute anterior uveitis. ''Mol Vis''. 2011; '''17''': 2970-7
GCTA: a tool for genome-wide complex trait analysis. Description: Yang, Jian, et al. GCTA: a tool for genome-wide complex trait analysis. ''Am J Hum Genet''. 2011 Jan 7; '''88''' (1):76-82
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. Description: Lanktree, Matthew B, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. ''Am J Hum Genet''. 2011 Jan 7; '''88''' (1):6-18
Characterization of novel and uncharacterized p53 SNPs in the Chinese population--intron 2 SNP co-segregates with the common codon 72 polymorphism. Description: Phang, Beng Hooi, et al. Characterization of novel and uncharacterized p53 SNPs in the Chinese population--intron 2 SNP co-segregates with the common codon 72 polymorphism. ''PLoS One''. 2011 Jan 10; '''6''' (1):e15320
LINGO1 variants in the French-Canadian population. Description: Bourassa, Cynthia V, et al. LINGO1 variants in the French-Canadian population. ''PLoS One''. 2011 Jan 11; '''6''' (1):e16254
Accuracy of CNV Detection from GWAS Data. Description: Zhang, Dandan, et al. Accuracy of CNV Detection from GWAS Data. ''PLoS One''. 2011 Jan 13; '''6''' (1):e14511
Global analysis of the impact of environmental perturbation on cis-regulation of gene expression. Description: Grundberg, Elin, et al. Global analysis of the impact of environmental perturbation on cis-regulation of gene expression. ''PLoS Genet''. 2011 Jan 20; '''7''' (1):e1001279
Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in southern Chinese. Description: Li, Yan, et al. Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in southern Chinese. ''PLoS One''. 2011 Jan 20; '''6''' (1):e14562
Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. Description: Been, Latonya F, et al. Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. ''BMC Med Genet''. 2011 Jan 24; '''12''': 18
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles. Description: Chen, Pei-Lung, et al. Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles. ''PLoS One''. 2011 Jan 28; '''6''' (1):e16635
Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey. Description: Dumitrescu, Logan, et al. Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey. ''PLoS One''. 2011 Jan 28; '''6''' (1):e16604
An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians. Description: Juyal, Garima, et al. An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians. ''PLoS One''. 2011 Jan 31; '''6''' (1):e16565
Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia. Description: Hill, Lori D, et al. Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia. ''PLoS One''. 2011 Jan 31; '''6''' (1):e16681
Pharmacogenetics of telatinib, a VEGFR-2 and VEGFR-3 tyrosine kinase inhibitor, used in patients with solid tumors. Description: Steeghs, Neeltje, et al. Pharmacogenetics of telatinib, a VEGFR-2 and VEGFR-3 tyrosine kinase inhibitor, used in patients with solid tumors. ''Invest New Drugs''. 2011 Feb; '''29''' (1):137-43
The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population. Description: Cheng, Xiang, et al. The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population. ''Diabetes''. 2011 Feb; '''60''' (2):680-4
Neuronal genes for subcutaneous fat thickness in human and pig are identified by local genomic sequencing and combined SNP association study. Description: Lee, Kyung-Tai, et al. Neuronal genes for subcutaneous fat thickness in human and pig are identified by local genomic sequencing and combined SNP association study. ''PLoS One''. 2011 Feb 2; '''6''' (2):e16356
Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. Description: Haataja, Ritva, et al. Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. ''PLoS Genet''. 2011 Feb 3; '''7''' (2):e1001293
A genome-wide association study of serum uric acid in African Americans. Description: Charles, Bashira A, et al. A genome-wide association study of serum uric acid in African Americans. ''BMC Med Genomics''. 2011 Feb 4; '''4''': 17
Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study. Description: Tsai, Fuu-Jen, et al. Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study. ''PLoS One''. 2011 Feb 4; '''6''' (2):e16853
Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility. Description: Ma, Gerry Z M, et al. Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility. ''PLoS One''. 2011 Feb 8; '''6''' (2):e16964
Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease. Description: Kauwe, John S K, et al. Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease. ''PLoS One''. 2011 Feb 9; '''6''' (2):e15918
Swedish population substructure revealed by genome-wide single nucleotide polymorphism data. Description: Salmela, Elina, et al. Swedish population substructure revealed by genome-wide single nucleotide polymorphism data. ''PLoS One''. 2011 Feb 9; '''6''' (2):e16747
Genome-wide association studies of the PR interval in African Americans. Description: Smith, J Gustav, et al. Genome-wide association studies of the PR interval in African Americans. ''PLoS Genet''. 2011 Feb 10; '''7''' (2):e1001304
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Description: Lettre, Guillaume, et al. Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. ''PLoS Genet''. 2011 Feb 10; '''7''' (2):e1001300
Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans. Description: Bonilla, Carolina, et al. Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans. ''PLoS One''. 2011 Feb 16; '''6''' (2):e16044
Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. Description: Hu, Xiaolan, et al. Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. ''PLoS One''. 2011 Feb 24; '''6''' (2):e16616
On the origin of Tibetans and their genetic basis in adapting high-altitude environments. Description: Wang, Binbin, et al. On the origin of Tibetans and their genetic basis in adapting high-altitude environments. ''PLoS One''. 2011 Feb 28; '''6''' (2):e17002
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. Description: McKay, James D, et al. A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. ''PLoS Genet''. 2011 Mar; '''7''' (3):e1001333
An autoimmune-associated variant in PTPN2 reveals an impairment of IL-2R signaling in CD4(+) T cells. Description: Long, S A, et al. An autoimmune-associated variant in PTPN2 reveals an impairment of IL-2R signaling in CD4(+) T cells. ''Genes Immun''. 2011 Mar; '''12''' (2):116-25
A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogs. Description: Olsson, Mia, et al. A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogs. ''PLoS Genet''. 2011 Mar; '''7''' (3):e1001332
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. Description: Chung, Sharon A, et al. Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. ''PLoS Genet''. 2011 Mar; '''7''' (3):e1001323
Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. Description: Speliotes, Elizabeth K, et al. Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. ''PLoS Genet''. 2011 Mar; '''7''' (3):e1001324
Genome-wide association scan of korean autism spectrum disorders with language delay: a preliminary study. Description: Cho, Soo-Churl, et al. Genome-wide association scan of korean autism spectrum disorders with language delay: a preliminary study. ''Psychiatry Investig''. 2011 Mar; '''8''' (1):61-6
Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci. Description: Plant, Darren, et al. Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci. ''Arthritis Rheum''. 2011 Mar; '''63''' (3):645-53
Study of the common genetic background for rheumatoid arthritis and systemic lupus erythematosus. Description: Orozco, Gisela, et al. Study of the common genetic background for rheumatoid arthritis and systemic lupus erythematosus. ''Ann Rheum Dis''. 2011 Mar; '''70''' (3):463-8
The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. Description: Rizzi, Thais S, et al. The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. ''Am J Med Genet B Neuropsychiatr Genet''. 2011 Mar; '''156''' (2):145-57
The impact of childhood abuse and recent stress on serum brain-derived neurotrophic factor and the moderating role of BDNF Val66Met. Description: Elzinga, Bernet M, et al. The impact of childhood abuse and recent stress on serum brain-derived neurotrophic factor and the moderating role of BDNF Val66Met. ''Psychopharmacology (Berl)''. 2011 Mar; '''214''' (1):319-28
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort. Description: van der Zee, Julie, et al. TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort. ''Brain''. 2011 Mar; '''134''' (Pt 3):808-15
GATES: a rapid and powerful gene-based association test using extended Simes procedure. Description: Li, Miao-Xin, et al. GATES: a rapid and powerful gene-based association test using extended Simes procedure. ''Am J Hum Genet''. 2011 Mar 11; '''88''' (3):283-93
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Description: Cichon, Sven, et al. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. ''Am J Hum Genet''. 2011 Mar 11; '''88''' (3):372-81
Assessing matched normal and tumor pairs in next-generation sequencing studies. Description: Goh, Liang, et al. Assessing matched normal and tumor pairs in next-generation sequencing studies. ''PLoS One''. 2011 Mar 18; '''6''' (3):e17810
Leukocyte DNA methylation signature differentiates pancreatic cancer patients from healthy controls. Description: Pedersen, Katrina S, et al. Leukocyte DNA methylation signature differentiates pancreatic cancer patients from healthy controls. ''PLoS One''. 2011 Mar 24; '''6''' (3):e18223
A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE. Description: Sandling, Johanna K, et al. A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE. ''Eur J Hum Genet''. 2011 Apr; '''19''' (4):479-84
An evolutionary genomic approach to identify genes involved in human birth timing. Description: Plunkett, Jevon, et al. An evolutionary genomic approach to identify genes involved in human birth timing. ''PLoS Genet''. 2011 Apr; '''7''' (4):e1001365
Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. Description: Pare, Guillaume, et al. Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. ''PLoS Genet''. 2011 Apr; '''7''' (4):e1001374
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. Description: Duncan, Emma L, et al. Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. ''PLoS Genet''. 2011 Apr; '''7''' (4):e1001372
Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum. Description: Van Tyne, Daria, et al. Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum. ''PLoS Genet''. 2011 Apr; '''7''' (4):e1001383
Polygenic dissection of the bipolar phenotype. Description: Hamshere, M L, et al. Polygenic dissection of the bipolar phenotype. ''Br J Psychiatry''. 2011 Apr; '''198''' (4):284-8
NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells. Description: Savas, Sevtap, et al. NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells. ''PLoS One''. 2011 Apr 4; '''6''' (4):e18306
Genetic and metabolic characterization of insomnia. Description: Ban, Hyo-Jeong, et al. Genetic and metabolic characterization of insomnia. ''PLoS One''. 2011 Apr 6; '''6''' (4):e18455
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle. Description: Drogemuller, Cord, et al. An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle. ''PLoS One''. 2011 Apr 15; '''6''' (4):e18931
SNP-based pathway enrichment analysis for genome-wide association studies. Description: Weng, Lingjie, et al. SNP-based pathway enrichment analysis for genome-wide association studies. ''BMC Bioinformatics''. 2011 Apr 15; '''12''': 99
Complement factor B polymorphism 32W protects against age-related macular degeneration. Description: Hughes, Anne E, et al. Complement factor B polymorphism 32W protects against age-related macular degeneration. ''Mol Vis''. 2011 Apr 20; '''17''': 983-8
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. Description: Li, Yi-Ju, et al. Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. ''PLoS One''. 2011 Apr 20; '''6''' (4):e18044
The distal end of porcine chromosome 6p is involved in the regulation of skatole levels in boars. Description: Ramos, Antonio M, et al. The distal end of porcine chromosome 6p is involved in the regulation of skatole levels in boars. ''BMC Genet''. 2011 Apr 20; '''12''': 35
Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS data. Description: Hu, Valerie W, et al. Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS data. ''PLoS One''. 2011 Apr 27; '''6''' (4):e19067
Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis. Description: Knight, Jo, et al. Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis. ''PLoS One''. 2011 Apr 27; '''6''' (4):e14808
A genome-wide association study on obesity and obesity-related traits. Description: Wang, Kai, et al. A genome-wide association study on obesity and obesity-related traits. ''PLoS One''. 2011 Apr 28; '''6''' (4):e18939
The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: a multicenter case-control study. Description: The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: a multicenter case-control study. ''PLoS One''. 2011 Apr 28; '''6''' (4):e18813
A genetic risk score combining ten psoriasis risk loci improves disease prediction. Description: Chen, Haoyan, et al. A genetic risk score combining ten psoriasis risk loci improves disease prediction. ''PLoS One''. 2011 Apr 29; '''6''' (4):e19454
Analysis of an extended chromosome locus 2p14-21 for replication of the 2p16.3 association with glaucoma susceptibility. Description: Kim, Kyunglan, et al. Analysis of an extended chromosome locus 2p14-21 for replication of the 2p16.3 association with glaucoma susceptibility. ''Mol Vis''. 2011 Apr 29; '''17''': 1136-43
Association analysis of urotensin II gene (UTS2) and flanking regions with biochemical parameters related to insulin resistance. Description: Saez, Maria E, et al. Association analysis of urotensin II gene (UTS2) and flanking regions with biochemical parameters related to insulin resistance. ''PLoS One''. 2011 Apr 29; '''6''' (4):e19327
CEACAM6 gene variants in inflammatory bowel disease. Description: Glas, Jurgen, et al. CEACAM6 gene variants in inflammatory bowel disease. ''PLoS One''. 2011 Apr 29; '''6''' (4):e19319
A -436C>A polymorphism in the human FAS gene promoter associated with severe childhood malaria. Description: Schuldt, Kathrin, et al. A -436C>A polymorphism in the human FAS gene promoter associated with severe childhood malaria. ''PLoS Genet''. 2011 May; '''7''' (5):e1002066
Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. Description: Zhao, Jian, et al. Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. ''PLoS Genet''. 2011 May; '''7''' (5):e1002079
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Description: Naj, Adam C, et al. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. ''Nat Genet''. 2011 May; '''43''' (5):436-41
Fractalkine is a novel human adipochemokine associated with type 2 diabetes. Description: Shah, Rachana, et al. Fractalkine is a novel human adipochemokine associated with type 2 diabetes. ''Diabetes''. 2011 May; '''60''' (5):1512-8
Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue. Description: Innocenti, Federico, et al. Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue. ''PLoS Genet''. 2011 May; '''7''' (5):e1002078
A frameshift mutation within LAMC2 is responsible for Herlitz type junctional epidermolysis bullosa (HJEB) in black headed mutton sheep. Description: Momke, Stefanie, et al. A frameshift mutation within LAMC2 is responsible for Herlitz type junctional epidermolysis bullosa (HJEB) in black headed mutton sheep. ''PLoS One''. 2011 May 4; '''6''' (5):e18943
Genetic background of patients from a university medical center in Manhattan: implications for personalized medicine. Description: Tayo, Bamidele O, et al. Genetic background of patients from a university medical center in Manhattan: implications for personalized medicine. ''PLoS One''. 2011 May 4; '''6''' (5):e19166
Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension. Description: Citterio, Lorena, et al. Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension. ''PLoS One''. 2011 May 9; '''6''' (5):e19620
Genome-wide association study of relative telomere length. Description: Prescott, Jennifer, et al. Genome-wide association study of relative telomere length. ''PLoS One''. 2011 May 10; '''6''' (5):e19635
Fetal ERAP2 variation is associated with preeclampsia in African Americans in a case-control study. Description: Hill, Lori D, et al. Fetal ERAP2 variation is associated with preeclampsia in African Americans in a case-control study. ''BMC Med Genet''. 2011 May 11; '''12''': 64
Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks. Description: Turner, Stephen D, et al. Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks. ''PLoS One''. 2011 May 11; '''6''' (5):e19586
A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort. Description: Yu, Jindan, et al. A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort. ''Behav Brain Funct''. 2011 May 14; '''7''': 13
Rheumatoid arthritis-associated polymorphisms are not protective against Alzheimer's disease. Description: Simmons, Christopher R, et al. Rheumatoid arthritis-associated polymorphisms are not protective against Alzheimer's disease. ''Mol Neurodegener''. 2011 May 19; '''6''': 33
The impact of FADS genetic variants on omega6 polyunsaturated fatty acid metabolism in African Americans. Description: Mathias, Rasika A, et al. The impact of FADS genetic variants on omega6 polyunsaturated fatty acid metabolism in African Americans. ''BMC Genet''. 2011 May 20; '''12''': 50
A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders. Description: Kim, Soo-Jeong, et al. A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders. ''Mol Autism''. 2011 May 24; '''2''' (1):8
GENIE: a software package for gene-gene interaction analysis in genetic association studies using multiple GPU or CPU cores. Description: Chikkagoudar, Satish, et al. GENIE: a software package for gene-gene interaction analysis in genetic association studies using multiple GPU or CPU cores. ''BMC Res Notes''. 2011 May 26; '''4''': 158
A functional variant in microRNA-146a promoter modulates its expression and confers disease risk for systemic lupus erythematosus. Description: Luo, Xiaobing, et al. A functional variant in microRNA-146a promoter modulates its expression and confers disease risk for systemic lupus erythematosus. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002128
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Description: Fox, Ervin R, et al. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. ''Hum Mol Genet''. 2011 Jun 1; '''20''' (11):2273-84
A two-stage meta-analysis identifies several new loci for Parkinson's disease. Description: A two-stage meta-analysis identifies several new loci for Parkinson's disease. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002142
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population. Description: Cui, R, et al. Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population. ''Gut''. 2011 Jun; '''60''' (6):799-805
Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans. Description: Freedman, Barry I, et al. Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002150
Fine Mapping of a QTL for Fertility on BTA7 and Its Association With a CNV in the Israeli Holsteins. Description: Glick, Giora, et al. Fine Mapping of a QTL for Fertility on BTA7 and Its Association With a CNV in the Israeli Holsteins. ''G3 (Bethesda)''. 2011 Jun; '''1''' (1):65-74
Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels. Description: Parikh, Hemang, et al. Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels. ''Hum Genet''. 2011 Jun; '''129''' (6):675-85
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. Description: Wright, Fred A, et al. Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. ''Nat Genet''. 2011 Jun; '''43''' (6):539-46
Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. Description: Smith, Erin N, et al. Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002134
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). Description: Reiner, Alexander P, et al. Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002108
Glutathione pathway gene variation and risk of autism spectrum disorders. Description: Bowers, Katherine, et al. Glutathione pathway gene variation and risk of autism spectrum disorders. ''J Neurodev Disord''. 2011 Jun; '''3''' (2):132-43
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. Description: Arking, Dan E, et al. Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002158
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. Description: Okada, Yukinori, et al. Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002067
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. Description: Tomlinson, Ian P M, et al. Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002105
Sex-specific role for adenylyl cyclase type 7 in alcohol dependence. Description: Desrivieres, Sylvane, et al. Sex-specific role for adenylyl cyclase type 7 in alcohol dependence. ''Biol Psychiatry''. 2011 Jun 1; '''69''' (11):1100-8
A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. Description: Pereira, Tiago V, et al. A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. ''BMC Res Notes''. 2011 Jun 6; '''4''': 172
DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. Description: Gusev, Alexander, et al. DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. ''Am J Hum Genet''. 2011 Jun 10; '''88''' (6):706-717
Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus. Description: Kim, Jason Y, et al. Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus. ''BMC Med Genet''. 2011 Jun 10; '''12''': 82
Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. Description: Hibar, Derrek P, et al. Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. ''Neuroimage''. 2011 Jun 15; '''56''' (4):1875-91
Comparison of buccal and blood-derived canine DNA, either native or whole genome amplified, for array-based genome-wide association studies. Description: Rincon, Gonzalo, et al. Comparison of buccal and blood-derived canine DNA, either native or whole genome amplified, for array-based genome-wide association studies. ''BMC Res Notes''. 2011 Jun 30; '''4''': 226
Genome Wide Association Study to predict severe asthma exacerbations in children using random forests classifiers. Description: Xu, Mousheng, et al. Genome Wide Association Study to predict severe asthma exacerbations in children using random forests classifiers. ''BMC Med Genet''. 2011 Jun 30; '''12''': 90
A selective sweep of >8 Mb on chromosome 26 in the Boxer genome. Description: Quilez, Javier, et al. A selective sweep of >8 Mb on chromosome 26 in the Boxer genome. ''BMC Genomics''. 2011 Jul 1; '''12''': 339
A worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing DEFB103 gene copy in East Asia. Description: Hardwick, Robert J, et al. A worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing DEFB103 gene copy in East Asia. ''Hum Mutat''. 2011 Jul; '''32''' (7):743-50
Gene-based tests of association. Description: Huang, Hailiang, et al. Gene-based tests of association. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002177
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. Description: Winkelmann, Juliane, et al. Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002171
Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. Description: Allanore, Yannick, et al. Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002091
Glucocorticoid receptor (NR3C1) gene polymorphisms and onset of alcohol abuse in adolescents. Description: Desrivieres, Sylvane, et al. Glucocorticoid receptor (NR3C1) gene polymorphisms and onset of alcohol abuse in adolescents. ''Addict Biol''. 2011 Jul; '''16''' (3):510-3
Identification of a mutation associated with fatal Foal Immunodeficiency Syndrome in the Fell and Dales pony. Description: Fox-Clipsham, Laura Y, et al. Identification of a mutation associated with fatal Foal Immunodeficiency Syndrome in the Fell and Dales pony. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002133
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. Description: Gorlova, Olga, et al. Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002178
Interactions between glucocorticoid treatment and cis-regulatory polymorphisms contribute to cellular response phenotypes. Description: Maranville, Joseph C, et al. Interactions between glucocorticoid treatment and cis-regulatory polymorphisms contribute to cellular response phenotypes. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002162
LGI2 truncation causes a remitting focal epilepsy in dogs. Description: Seppala, Eija H, et al. LGI2 truncation causes a remitting focal epilepsy in dogs. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002194
Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans. Description: Putku, Margus, et al. Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans. ''Hum Mutat''. 2011 Jul; '''32''' (7):806-14
Reconstruction of genealogical relationships with applications to Phase III of HapMap. Description: Kyriazopoulou-Panagiotopoulou, Sofia, et al. Reconstruction of genealogical relationships with applications to Phase III of HapMap. ''Bioinformatics''. 2011 Jul 1; '''27''' (13):i333-41
SNPsyn: detection and exploration of SNP-SNP interactions. Description: Curk, Tomaz, et al. SNPsyn: detection and exploration of SNP-SNP interactions. ''Nucleic Acids Res''. 2011 Jul; '''39''' (Web Server issue):W444-9
Recent admixture in an Indian population of African ancestry. Description: Narang, Ankita, et al. Recent admixture in an Indian population of African ancestry. ''Am J Hum Genet''. 2011 Jul 15; '''89''' (1):111-20
Association of VSNL1 with schizophrenia, frontal cortical function, and biological significance for its gene product as a modulator of cAMP levels and neuronal morphology. Description: Braunewell, K H, et al. Association of VSNL1 with schizophrenia, frontal cortical function, and biological significance for its gene product as a modulator of cAMP levels and neuronal morphology. ''Transl Psychiatry''. 2011 Jul 19; '''1''': e22
Genetic regulation of Nrxn1 [corrected] expression: an integrative cross-species analysis of schizophrenia candidate genes. Description: Mozhui, K, et al. Genetic regulation of Nrxn1 [corrected] expression: an integrative cross-species analysis of schizophrenia candidate genes. ''Transl Psychiatry''. 2011 Jul 26; '''1''': e25
Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays. Description: Gross, Arnd, et al. Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays. ''BMC Genet''. 2011 Jul 28; '''12''': 67
Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study. Description: Carrasquillo, Minerva M, et al. Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study. ''Mol Neurodegener''. 2011 Jul 28; '''6''' (1):54
Association of the 5-aminoimidazole-4-carboxamide ribonucleotide transformylase gene with response to methotrexate in juvenile idiopathic arthritis. Description: Hinks, Anne, et al. Association of the 5-aminoimidazole-4-carboxamide ribonucleotide transformylase gene with response to methotrexate in juvenile idiopathic arthritis. ''Ann Rheum Dis''. 2011 Aug; '''70''' (8):1395-400
Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited. Description: Deelen, Joris, et al. Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited. ''Aging Cell''. 2011 Aug; '''10''' (4):686-98
Novel locus FER is associated with serum HMW adiponectin levels. Description: Qi, Lu, et al. Novel locus FER is associated with serum HMW adiponectin levels. ''Diabetes''. 2011 Aug; '''60''' (8):2197-201
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. Description: Antoni, Guillemette, et al. Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. ''BMC Med Genet''. 2011 Aug 2; '''12''': 102
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. Description: Liu, Xinmin, et al. Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. ''BMC Med Genet''. 2011 Aug 3; '''12''': 104
Polymorphisms in melatonin synthesis pathways: possible influences on depression. Description: Kripke, Daniel F, et al. Polymorphisms in melatonin synthesis pathways: possible influences on depression. ''J Circadian Rhythms''. 2011 Aug 9; '''9''': 8
Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa. Description: Ozgul, Riza Koksal, et al. Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa. ''Am J Hum Genet''. 2011 Aug 12; '''89''' (2):253-64
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. Description: Larsson, Mats, et al. GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. ''Am J Hum Genet''. 2011 Aug 12; '''89''' (2):334-43
No association of TNFRSF1B variants with type 2 diabetes in Indians of Indo-European origin. Description: Tabassum, Rubina, et al. No association of TNFRSF1B variants with type 2 diabetes in Indians of Indo-European origin. ''BMC Med Genet''. 2011 Aug 17; '''12''': 110
Parkinson's disease induced pluripotent stem cells with triplication of the alpha-synuclein locus. Description: Devine, Michael J, et al. Parkinson's disease induced pluripotent stem cells with triplication of the alpha-synuclein locus. ''Nat Commun''. 2011 Aug 23; '''2''': 440
Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk. Description: Simmons, Christopher R, et al. Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk. ''Mol Neurodegener''. 2011 Aug 25; '''6''': 62
Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort. Description: Nyman, Emma S, et al. Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort. ''BMJ Open''. 2011 Aug 27; '''1''' (1):e000087
A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. Description: Bradfield, Jonathan P, et al. A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. ''PLoS Genet''. 2011 Sep; '''7''' (9):e1002293
Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Description: Stein, J L, et al. Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. ''Mol Psychiatry''. 2011 Sep; '''16''' (9):927-37, 881
Genetically determined dosage of follicle-stimulating hormone (FSH) affects male reproductive parameters. Description: Grigorova, Marina, et al. Genetically determined dosage of follicle-stimulating hormone (FSH) affects male reproductive parameters. ''J Clin Endocrinol Metab''. 2011 Sep; '''96''' (9):E1534-41
Genetic association for renal traits among participants of African ancestry reveals new loci for renal function. Description: Liu, Ching-Ti, et al. Genetic association for renal traits among participants of African ancestry reveals new loci for renal function. ''PLoS Genet''. 2011 Sep; '''7''' (9):e1002264
Genome-wide association study identifies four loci associated with eruption of permanent teeth. Description: Geller, Frank, et al. Genome-wide association study identifies four loci associated with eruption of permanent teeth. ''PLoS Genet''. 2011 Sep; '''7''' (9):e1002275
Large-scale gene-centric analysis identifies novel variants for coronary artery disease. Description: Large-scale gene-centric analysis identifies novel variants for coronary artery disease. ''PLoS Genet''. 2011 Sep; '''7''' (9):e1002260
Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data. Description: Keller, Matthew C, et al. Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data. ''Genetics''. 2011 Sep; '''189''' (1):237-49
Robust association tests under different genetic models, allowing for binary or quantitative traits and covariates. Description: So, Hon-Cheong, et al. Robust association tests under different genetic models, allowing for binary or quantitative traits and covariates. ''Behav Genet''. 2011 Sep; '''41''' (5):768-75
A global view of porcine transcriptome in three tissues from a full-sib pair with extreme phenotypes in growth and fat deposition by paired-end RNA sequencing. Description: Chen, Congying, et al. A global view of porcine transcriptome in three tissues from a full-sib pair with extreme phenotypes in growth and fat deposition by paired-end RNA sequencing. ''BMC Genomics''. 2011 Sep 10; '''12''': 448
Genome-wide association mapping reveals a rich genetic architecture of complex traits in Oryza sativa. Description: Zhao, Keyan, et al. Genome-wide association mapping reveals a rich genetic architecture of complex traits in Oryza sativa. ''Nat Commun''. 2011 Sep 13; '''2''': 467
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. Description: Yu, Yi, et al. Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. ''Hum Mol Genet''. 2011 Sep 15; '''20''' (18):3699-709
Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia. Description: Takata, Atsushi, et al. Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia. ''Genome Biol''. 2011 Sep 28; '''12''' (9):R92
A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. Description: Wohlke, Anne, et al. A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. ''PLoS Genet''. 2011 Oct; '''7''' (10):e1002304
Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus. Description: Cunninghame Graham, Deborah S, et al. Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus. ''PLoS Genet''. 2011 Oct; '''7''' (10):e1002341
Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping. Description: Vaysse, Amaury, et al. Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping. ''PLoS Genet''. 2011 Oct; '''7''' (10):e1002316
Identification of QTL genes for BMD variation using both linkage and gene-based association approaches. Description: Li, Gloria Hoi-Yee, et al. Identification of QTL genes for BMD variation using both linkage and gene-based association approaches. ''Hum Genet''. 2011 Oct; '''130''' (4):539-46
Influence of pharmacogenetic variability on the pharmacokinetics and toxicity of the aurora kinase inhibitor danusertib. Description: Steeghs, Neeltje, et al. Influence of pharmacogenetic variability on the pharmacokinetics and toxicity of the aurora kinase inhibitor danusertib. ''Invest New Drugs''. 2011 Oct; '''29''' (5):953-62
Population genomics of wild and laboratory zebrafish (Danio rerio). Description: Whiteley, Andrew R, et al. Population genomics of wild and laboratory zebrafish (Danio rerio). ''Mol Ecol''. 2011 Oct; '''20''' (20):4259-76
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association. Description: Wood, Andrew R, et al. Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association. ''Hum Mol Genet''. 2011 Oct 15; '''20''' (20):4082-92
Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1. Description: Khor, Chiea Chuen, et al. Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1. ''Nat Genet''. 2011 Oct 16; '''43''' (11):1139-41
Cumulative Effect of Common Genetic Variants Predicts Incident Type 2 Diabetes: A Study of 21,183 Subjects from Three Large Prospective Cohorts. Description: Yang, Jingyun, et al. Cumulative Effect of Common Genetic Variants Predicts Incident Type 2 Diabetes: A Study of 21,183 Subjects from Three Large Prospective Cohorts. ''Epidemiology (Sunnyvale)''. 2011 Nov 1; '''1''' (3):108
Genetic examination of SETD7 and SUV39H1/H2 methyltransferases and the risk of diabetes complications in patients with type 1 diabetes. Description: Syreeni, Anna, et al. Genetic examination of SETD7 and SUV39H1/H2 methyltransferases and the risk of diabetes complications in patients with type 1 diabetes. ''Diabetes''. 2011 Nov; '''60''' (11):3073-80
Genetic variation in APOE cluster region and Alzheimer's disease risk. Description: Cervantes, Sebastian, et al. Genetic variation in APOE cluster region and Alzheimer's disease risk. ''Neurobiol Aging''. 2011 Nov; '''32''' (11):2107.e7-17
Genome-wide association analysis of ischemic stroke in young adults. Description: Cheng, Yu-Ching, et al. Genome-wide association analysis of ischemic stroke in young adults. ''G3 (Bethesda)''. 2011 Nov; '''1''' (6):505-14
Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment. Description: Hu, X, et al. Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment. ''Transl Psychiatry''. 2011 Nov 15; '''1''': e54
A LASSO-based approach to analyzing rare variants in genetic association studies. Description: Brennan, Jennifer S, et al. A LASSO-based approach to analyzing rare variants in genetic association studies. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S100
A pathway-based association analysis model using common and rare variants. Description: Cheng, Lu, et al. A pathway-based association analysis model using common and rare variants. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S85
Application of Bayesian network structure learning to identify causal variant SNPs from resequencing data. Description: Schlosberg, Christopher E, et al. Application of Bayesian network structure learning to identify causal variant SNPs from resequencing data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S109
Application of Bayesian regression with singular value decomposition method in association studies for sequence data. Description: Kwon, Soonil, et al. Application of Bayesian regression with singular value decomposition method in association studies for sequence data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S57
Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data. Description: Saad, Mohamad, et al. Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S33
Comparison of collapsing methods for the statistical analysis of rare variants. Description: Dering, Carmen, et al. Comparison of collapsing methods for the statistical analysis of rare variants. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S115
Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression. Description: Sung, Heejong, et al. Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S15
Evaluating aggregate effects of rare and common variants in the 1000 Genomes Project exon sequencing data using latent variable structural equation modeling. Description: Nock, Nl, et al. Evaluating aggregate effects of rare and common variants in the 1000 Genomes Project exon sequencing data using latent variable structural equation modeling. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S47
Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection. Description: Pungpapong, Vitara, et al. Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S5
Genome-wide case-control study in GAW17 using coalesced rare variants. Description: Wang, Libo, et al. Genome-wide case-control study in GAW17 using coalesced rare variants. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S110
Identification of multiple rare variants associated with a disease. Description: Jung, Jeesun, et al. Identification of multiple rare variants associated with a disease. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S103
Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives. Description: Akula, Nirmala, et al. Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S76
Mutational load analysis of unrelated individuals. Description: Howrigan, Daniel P, et al. Mutational load analysis of unrelated individuals. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S55
Novel tree-based method to generate markers from rare variant data. Description: Jiang, Yuan, et al. Novel tree-based method to generate markers from rare variant data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S102
Pathway analysis following association study. Description: Ngwa, Julius S, et al. Pathway analysis following association study. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S18
Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data. Description: Ayers, Kristin L, et al. Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S92
Performance of random forests and logic regression methods using mini-exome sequence data. Description: Kim, Yoonhee, et al. Performance of random forests and logic regression methods using mini-exome sequence data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S104
Principal components ancestry adjustment for Genetic Analysis Workshop 17 data. Description: Jin, Jing, et al. Principal components ancestry adjustment for Genetic Analysis Workshop 17 data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S66
Rare variant collapsing in conjunction with mean log p-value and gradient boosting approaches applied to Genetic Analysis Workshop 17 data. Description: Cherkas, Yauheniya, et al. Rare variant collapsing in conjunction with mean log p-value and gradient boosting approaches applied to Genetic Analysis Workshop 17 data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S94
Region-based and pathway-based QTL mapping using a p-value combination method. Description: Yang, Hsin-Chou, et al. Region-based and pathway-based QTL mapping using a p-value combination method. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S43
Using LASSO regression to detect predictive aggregate effects in genetic studies. Description: Fontanarosa, Joel B, et al. Using LASSO regression to detect predictive aggregate effects in genetic studies. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S69
Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study. Description: Kramer, Patricia L, et al. Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study. ''Neurobiol Aging''. 2011 Dec; '''32''' (12):2113-22
Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. Description: Lefeber, Dirk J, et al. Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. ''PLoS Genet''. 2011 Dec; '''7''' (12):e1002427
Genetic variation in base excision repair pathway genes, pesticide exposure, and prostate cancer risk. Description: Barry, Kathryn Hughes, et al. Genetic variation in base excision repair pathway genes, pesticide exposure, and prostate cancer risk. ''Environ Health Perspect''. 2011 Dec; '''119''' (12):1726-32
Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism. Description: Fan, Qiao, et al. Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism. ''PLoS Genet''. 2011 Dec; '''7''' (12):e1002402
Influence of polymorphisms in the RANKL/RANK/OPG signaling pathway on volumetric bone mineral density and bone geometry at the forearm in men. Description: Roshandel, Delnaz, et al. Influence of polymorphisms in the RANKL/RANK/OPG signaling pathway on volumetric bone mineral density and bone geometry at the forearm in men. ''Calcif Tissue Int''. 2011 Dec; '''89''' (6):446-55
Rapid testing of gene-gene interactions in genome-wide association studies of binary and quantitative phenotypes. Description: Bhattacharya, Kanishka, et al. Rapid testing of gene-gene interactions in genome-wide association studies of binary and quantitative phenotypes. ''Genet Epidemiol''. 2011 Dec; '''35''' (8):800-8
The relationship between fertility and lifespan in humans. Description: Kuningas, Maris, et al. The relationship between fertility and lifespan in humans. ''Age (Dordr)''. 2011 Dec; '''33''' (4):615-22
An exonic insertion within Tex14 gene causes spermatogenic arrest in pigs. Description: Sironen, Anu, et al. An exonic insertion within Tex14 gene causes spermatogenic arrest in pigs. ''BMC Genomics''. 2011 Dec 2; '''12''': 591
Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. Description: Dauber, Andrew, et al. Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. ''Am J Hum Genet''. 2011 Dec 9; '''89''' (6):751-9
Identification of autoimmune gene signatures in autism. Description: Jung, J-Y, et al. Identification of autoimmune gene signatures in autism. ''Transl Psychiatry''. 2011 Dec 13; '''1''': e63
Risk variants in BMP4 promoters for nonsyndromic cleft lip/palate in a Chilean population. Description: Suazo, Jose, et al. Risk variants in BMP4 promoters for nonsyndromic cleft lip/palate in a Chilean population. ''BMC Med Genet''. 2011 Dec 19; '''12''': 163
High frequencies of de novo CNVs in bipolar disorder and schizophrenia. Description: Malhotra, Dheeraj, et al. High frequencies of de novo CNVs in bipolar disorder and schizophrenia. ''Neuron''. 2011 Dec 22; '''72''' (6):951-63
Candidate gene analysis of spontaneous preterm delivery: new insights from re-analysis of a case-control study using case-parent triads and control-mother dyads. Description: Myking, Solveig, et al. Candidate gene analysis of spontaneous preterm delivery: new insights from re-analysis of a case-control study using case-parent triads and control-mother dyads. ''BMC Med Genet''. 2011 Dec 30; '''12''': 174
A canine BCAN microdeletion associated with episodic falling syndrome. Description: Gill, Jennifer L, et al. A canine BCAN microdeletion associated with episodic falling syndrome. ''Neurobiol Dis''. 2012 Jan; '''45''' (1):130-6
A COL7A1 mutation causes dystrophic epidermolysis bullosa in Rotes Hohenvieh cattle. Description: Menoud, Annie, et al. A COL7A1 mutation causes dystrophic epidermolysis bullosa in Rotes Hohenvieh cattle. ''PLoS One''. 2012; '''7''' (6):e38823
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder. Description: Verbeek, Eva C, et al. A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder. ''PLoS One''. 2012; '''7''' (5):e37384
A functional variant in ERAP1 predisposes to multiple sclerosis. Description: Guerini, Franca Rosa, et al. A functional variant in ERAP1 predisposes to multiple sclerosis. ''PLoS One''. 2012; '''7''' (1):e29931
Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. Description: Chow, Maggie L, et al. Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. ''PLoS Genet''. 2012; '''8''' (3):e1002592
A gene co-expression network in whole blood of schizophrenia patients is independent of antipsychotic-use and enriched for brain-expressed genes. Description: de Jong, Simone, et al. A gene co-expression network in whole blood of schizophrenia patients is independent of antipsychotic-use and enriched for brain-expressed genes. ''PLoS One''. 2012; '''7''' (6):e39498
A genome-wide association search for type 2 diabetes genes in African Americans. Description: Palmer, Nicholette D, et al. A genome-wide association search for type 2 diabetes genes in African Americans. ''PLoS One''. 2012; '''7''' (1):e29202
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese. Description: Okada, Yukinori, et al. A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002455
A genome-wide association study of circulating galectin-3. Description: de Boer, Rudolf A, et al. A genome-wide association study of circulating galectin-3. ''PLoS One''. 2012; '''7''' (10):e47385
A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1. Description: Urabe, Yuji, et al. A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1. ''PLoS Genet''. 2012; '''8''' (3):e1002541
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. Description: Milton, Jacqueline N, et al. A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. ''PLoS One''. 2012; '''7''' (4):e34741
A genome-wide association study reveals loci influencing height and other conformation traits in horses. Description: Signer-Hasler, Heidi, et al. A genome-wide association study reveals loci influencing height and other conformation traits in horses. ''PLoS One''. 2012; '''7''' (5):e37282
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. Description: Kenny, Eimear E, et al. A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. ''PLoS Genet''. 2012; '''8''' (3):e1002559
A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. Description: McCue, Molly E, et al. A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002451
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. Description: Qayyum, Rehan, et al. A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. ''PLoS Genet''. 2012; '''8''' (3):e1002491
Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Description: Swaminathan, Shanker, et al. Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. ''PLoS One''. 2012; '''7''' (12):e50640
Analysis of IL12B gene variants in inflammatory bowel disease. Description: Glas, Jurgen, et al. Analysis of IL12B gene variants in inflammatory bowel disease. ''PLoS One''. 2012; '''7''' (3):e34349
Analysis of IL28B variants in an Egyptian population defines the 20 kilobases minimal region involved in spontaneous clearance of hepatitis C virus. Description: Pedergnana, Vincent, et al. Analysis of IL28B variants in an Egyptian population defines the 20 kilobases minimal region involved in spontaneous clearance of hepatitis C virus. ''PLoS One''. 2012; '''7''' (6):e38578
Analysis of polymorphisms and haplotype structure of the human thymidylate synthase genetic region: a tool for pharmacogenetic studies. Description: Ghosh, Soma, et al. Analysis of polymorphisms and haplotype structure of the human thymidylate synthase genetic region: a tool for pharmacogenetic studies. ''PLoS One''. 2012; '''7''' (4):e34426
An ICA with reference approach in identification of genetic variation and associated brain networks. Description: Liu, Jingyu, et al. An ICA with reference approach in identification of genetic variation and associated brain networks. ''Front Hum Neurosci''. 2012; '''6''': 21
A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VII. Description: Hytonen, Marjo K, et al. A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VII. ''PLoS One''. 2012; '''7''' (7):e40281
An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. Description: Maher, Bridget H, et al. An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. ''PLoS One''. 2012; '''7''' (5):e37903
A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers. Description: Karjalainen, Minna K, et al. A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers. ''PLoS One''. 2012; '''7''' (12):e51378
A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. Description: Braun, Timothy R, et al. A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. ''PLoS One''. 2012; '''7''' (5):e37056
A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery. Description: Kyostila, Kaisa, et al. A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery. ''PLoS Genet''. 2012; '''8''' (6):e1002759
Assessment of genotype imputation performance using 1000 Genomes in African American studies. Description: Hancock, Dana B, et al. Assessment of genotype imputation performance using 1000 Genomes in African American studies. ''PLoS One''. 2012; '''7''' (11):e50610
Assessment of the association of matrix metalloproteinases with myopia, refractive error and ocular biometric measures in an Australian cohort. Description: Schache, Maria, et al. Assessment of the association of matrix metalloproteinases with myopia, refractive error and ocular biometric measures in an Australian cohort. ''PLoS One''. 2012; '''7''' (10):e47181
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes. Description: Greenwood, Tiffany A, et al. Association analysis of 94 candidate genes and schizophrenia-related endophenotypes. ''PLoS One''. 2012; '''7''' (1):e29630
Association analysis of single nucleotide polymorphisms at five loci: comparison between atopic dermatitis and asthma in the Chinese Han population. Description: Tang, Hua-Yang, et al. Association analysis of single nucleotide polymorphisms at five loci: comparison between atopic dermatitis and asthma in the Chinese Han population. ''PLoS One''. 2012; '''7''' (4):e35334
Association analysis of the extended MHC region in celiac disease implicates multiple independent susceptibility loci. Description: Ahn, Richard, et al. Association analysis of the extended MHC region in celiac disease implicates multiple independent susceptibility loci. ''PLoS One''. 2012; '''7''' (5):e36926
Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. Description: Osman, Wael, et al. Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. ''PLoS One''. 2012; '''7''' (4):e32683
Association of OX40L polymorphisms with sporadic breast cancer in northeast Chinese Han population. Description: Weiguang, Yuan, et al. Association of OX40L polymorphisms with sporadic breast cancer in northeast Chinese Han population. ''PLoS One''. 2012; '''7''' (8):e41277
Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population. Description: Zhang, Yuping, et al. Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population. ''PLoS One''. 2012; '''7''' (9):e42969
Association of the type 2 diabetes mellitus susceptibility gene, TCF7L2, with schizophrenia in an Arab-Israeli family sample. Description: Alkelai, Anna, et al. Association of the type 2 diabetes mellitus susceptibility gene, TCF7L2, with schizophrenia in an Arab-Israeli family sample. ''PLoS One''. 2012; '''7''' (1):e29228
ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population. Description: Lahut, Suna, et al. ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population. ''PLoS One''. 2012; '''7''' (8):e42956
A variant in the ABO gene explains the variation in soluble E-selectin levels-results from dense genotyping in two independent populations. Description: Karakas, Mahir, et al. A variant in the ABO gene explains the variation in soluble E-selectin levels-results from dense genotyping in two independent populations. ''PLoS One''. 2012; '''7''' (12):e51441
AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study. Description: Morley, Andrew P, et al. AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study. ''PLoS One''. 2012; '''7''' (2):e31763
BMP4 was associated with NSCL/P in an Asian population. Description: Chen, Qianqian, et al. BMP4 was associated with NSCL/P in an Asian population. ''PLoS One''. 2012; '''7''' (4):e35347
CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy. Description: Barbier, Mathieu, et al. CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy. ''PLoS One''. 2012; '''7''' (1):e29872
Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide. Description: Maurer, Marie, et al. Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide. ''PLoS One''. 2012; '''7''' (10):e46408
Chapter 7: Pharmacogenomics. Description: Karczewski, Konrad J, et al. Chapter 7: Pharmacogenomics. ''PLoS Comput Biol''. 2012; '''8''' (12):e1002817
Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk. Description: Papp, Audrey C, et al. Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk. ''PLoS One''. 2012; '''7''' (3):e31930
Chromosome 9 ALS and FTD locus is probably derived from a single founder. Description: Mok, Kin, et al. Chromosome 9 ALS and FTD locus is probably derived from a single founder. ''Neurobiol Aging''. 2012 Jan; '''33''' (1):209.e3-8
CNR1 genotype influences HDL-cholesterol response to change in dietary fat intake. Description: Silver, Heidi J, et al. CNR1 genotype influences HDL-cholesterol response to change in dietary fat intake. ''PLoS One''. 2012; '''7''' (5):e36166
Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. Description: Ermini, Luca, et al. Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. ''Mol Immunol''. 2012 Jan; '''49''' (4):640-8
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. Description: Wiggs, Janey L, et al. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. ''PLoS Genet''. 2012; '''8''' (4):e1002654
Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese. Description: Nakano, Masakazu, et al. Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese. ''PLoS One''. 2012; '''7''' (3):e33389
Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients. Description: Koide, Takayoshi, et al. Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients. ''PLoS One''. 2012; '''7''' (5):e36836
Common variants of FTO are associated with childhood obesity in a cross-sectional study of 3,126 urban Indian children. Description: Dwivedi, Om Prakash, et al. Common variants of FTO are associated with childhood obesity in a cross-sectional study of 3,126 urban Indian children. ''PLoS One''. 2012; '''7''' (10):e47772
Common variants of homocysteine metabolism pathway genes and risk of type 2 diabetes and related traits in Indians. Description: Chauhan, Ganesh, et al. Common variants of homocysteine metabolism pathway genes and risk of type 2 diabetes and related traits in Indians. ''Exp Diabetes Res''. 2012; '''2012''': 960318
Common variants of the liver fatty acid binding protein gene influence the risk of type 2 diabetes and insulin resistance in Spanish population. Description: Mansego, Maria Luisa, et al. Common variants of the liver fatty acid binding protein gene influence the risk of type 2 diabetes and insulin resistance in Spanish population. ''PLoS One''. 2012; '''7''' (3):e31853
Common variants on chromosome 9p21 are associated with normal tension glaucoma. Description: Takamoto, Mitsuko, et al. Common variants on chromosome 9p21 are associated with normal tension glaucoma. ''PLoS One''. 2012; '''7''' (7):e40107
Comparison of pathway analysis approaches using lung cancer GWAS data sets. Description: Fehringer, Gordon, et al. Comparison of pathway analysis approaches using lung cancer GWAS data sets. ''PLoS One''. 2012; '''7''' (2):e31816
Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration. Description: Cantsilieris, Stuart, et al. Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration. ''PLoS One''. 2012; '''7''' (4):e35255
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. Description: Simon-Sanchez, Javier, et al. Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. ''PLoS One''. 2012; '''7''' (3):e28787
CUBN as a novel locus for end-stage renal disease: insights from renal transplantation. Description: Reznichenko, Anna, et al. CUBN as a novel locus for end-stage renal disease: insights from renal transplantation. ''PLoS One''. 2012; '''7''' (5):e36512
Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with and without Oncogenic KRAS Mutations. Description: Kalari, Krishna R, et al. Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with and without Oncogenic KRAS Mutations. ''Front Oncol''. 2012; '''2''': 12
Deletion of CDKAL1 affects high-fat diet-induced fat accumulation and glucose-stimulated insulin secretion in mice, indicating relevance to diabetes. Description: Okamura, Tadashi, et al. Deletion of CDKAL1 affects high-fat diet-induced fat accumulation and glucose-stimulated insulin secretion in mice, indicating relevance to diabetes. ''PLoS One''. 2012; '''7''' (11):e49055
delta-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer-related structural and functional brain changes. Description: Jun, Gyungah, et al. delta-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer-related structural and functional brain changes. ''PLoS One''. 2012; '''7''' (9):e43728
Environmental stress affects DNA methylation of a CpG rich promoter region of serotonin transporter gene in a nurse cohort. Description: Alasaari, Jukka S, et al. Environmental stress affects DNA methylation of a CpG rich promoter region of serotonin transporter gene in a nurse cohort. ''PLoS One''. 2012; '''7''' (9):e45813
Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs. Description: Watson, Corey T, et al. Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs. ''Sci Rep''. 2012; '''2''': 770
Evaluation of Parkinson disease risk variants as expression-QTLs. Description: Latourelle, Jeanne C, et al. Evaluation of Parkinson disease risk variants as expression-QTLs. ''PLoS One''. 2012; '''7''' (10):e46199
Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. Description: Buyske, Steven, et al. Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. ''PLoS One''. 2012; '''7''' (4):e35651
Evidence for two independent associations with type 1 diabetes at the 12q13 locus. Description: Keene, K L, et al. Evidence for two independent associations with type 1 diabetes at the 12q13 locus. ''Genes Immun''. 2012 Jan; '''13''' (1):66-70
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled. Description: Attar, Homa, et al. Extensive natural variation for cellular hydrogen peroxide release is genetically controlled. ''PLoS One''. 2012; '''7''' (8):e43566
Fine-mapping and initial characterization of QT interval loci in African Americans. Description: Avery, Christy L, et al. Fine-mapping and initial characterization of QT interval loci in African Americans. ''PLoS Genet''. 2012; '''8''' (8):e1002870
First WNK4-hypokalemia animal model identified by genome-wide association in Burmese cats. Description: Gandolfi, Barbara, et al. First WNK4-hypokalemia animal model identified by genome-wide association in Burmese cats. ''PLoS One''. 2012; '''7''' (12):e53173
Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients. Description: Spellicy, Catherine J, et al. Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients. ''PLoS One''. 2012; '''7''' (12):e51330
Functional variant in the autophagy-related 5 gene promotor is associated with childhood asthma. Description: Martin, Lisa J, et al. Functional variant in the autophagy-related 5 gene promotor is associated with childhood asthma. ''PLoS One''. 2012; '''7''' (4):e33454
Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. Description: Ersland, Kari M, et al. Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. ''PLoS One''. 2012; '''7''' (2):e31687
Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. Description: van Eerde, Albertien M, et al. Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. ''PLoS One''. 2012; '''7''' (4):e31327
Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese. Description: Kawaguchi, Takahisa, et al. Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese. ''PLoS One''. 2012; '''7''' (6):e38322
Genetic susceptibility factors on genes involved in the steroid hormone biosynthesis pathway and progesterone receptor for gastric cancer risk. Description: Cho, Lisa Y, et al. Genetic susceptibility factors on genes involved in the steroid hormone biosynthesis pathway and progesterone receptor for gastric cancer risk. ''PLoS One''. 2012; '''7''' (10):e47603
Genetic susceptibility on CagA-interacting molecules and gene-environment interaction with phytoestrogens: a putative risk factor for gastric cancer. Description: Yang, Jae Jeong, et al. Genetic susceptibility on CagA-interacting molecules and gene-environment interaction with phytoestrogens: a putative risk factor for gastric cancer. ''PLoS One''. 2012; '''7''' (2):e31020
Genetic variant of AMD1 is associated with obesity in urban Indian children. Description: Tabassum, Rubina, et al. Genetic variant of AMD1 is associated with obesity in urban Indian children. ''PLoS One''. 2012; '''7''' (4):e33162
Genetic variants in ER cofactor genes and endometrial cancer risk. Description: Li, Yuqing, et al. Genetic variants in ER cofactor genes and endometrial cancer risk. ''PLoS One''. 2012; '''7''' (8):e42445
Genetic variants in the Fat and Obesity Associated (FTO) gene and risk of Alzheimer's disease. Description: Reitz, Christiane, et al. Genetic variants in the Fat and Obesity Associated (FTO) gene and risk of Alzheimer's disease. ''PLoS One''. 2012; '''7''' (12):e50354
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. Description: Fan, Qiao, et al. Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. ''PLoS Genet''. 2012; '''8''' (6):e1002753
Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression. Description: McIntosh, Andrew M, et al. Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression. ''Front Genet''. 2012; '''3''': 116
Genetic variation in the EGFR gene and the risk of glioma in a Chinese Han population. Description: Hou, Wu-Gang, et al. Genetic variation in the EGFR gene and the risk of glioma in a Chinese Han population. ''PLoS One''. 2012; '''7''' (5):e37531
Genetic variation in TLR genes in Ugandan and South African populations and comparison with HapMap data. Description: Baker, Allison R, et al. Genetic variation in TLR genes in Ugandan and South African populations and comparison with HapMap data. ''PLoS One''. 2012; '''7''' (10):e47597
Gene-wide characterization of common quantitative trait loci for ABCB1 mRNA expression in normal liver tissues in the Chinese population. Description: Shou, Weihua, et al. Gene-wide characterization of common quantitative trait loci for ABCB1 mRNA expression in normal liver tissues in the Chinese population. ''PLoS One''. 2012; '''7''' (9):e46295
Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment. Description: Izutsu, Minako, et al. Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment. ''PLoS One''. 2012; '''7''' (3):e33288
Genome-wide analysis in Brazilian Xavante Indians reveals low degree of admixture. Description: Kuhn, Patricia C, et al. Genome-wide analysis in Brazilian Xavante Indians reveals low degree of admixture. ''PLoS One''. 2012; '''7''' (8):e42702
Genome wide assessment of young onset Parkinson's disease from Finland. Description: Hernandez, Dena G, et al. Genome wide assessment of young onset Parkinson's disease from Finland. ''PLoS One''. 2012; '''7''' (7):e41859
Genome-wide association and functional follow-up reveals new loci for kidney function. Description: Pattaro, Cristian, et al. Genome-wide association and functional follow-up reveals new loci for kidney function. ''PLoS Genet''. 2012; '''8''' (3):e1002584
Genome-wide association identifies multiple genomic regions associated with susceptibility to and control of ovine lentivirus. Description: White, Stephen N, et al. Genome-wide association identifies multiple genomic regions associated with susceptibility to and control of ovine lentivirus. ''PLoS One''. 2012; '''7''' (10):e47829
Genome-wide association mapping and identification of candidate genes for the rumpless and ear-tufted traits of the Araucana chicken. Description: Noorai, Rooksana E, et al. Genome-wide association mapping and identification of candidate genes for the rumpless and ear-tufted traits of the Araucana chicken. ''PLoS One''. 2012; '''7''' (7):e40974
Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. Description: Johnson, Matthew P, et al. Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. ''PLoS One''. 2012; '''7''' (3):e33666
Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. Description: Candille, Sophie I, et al. Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. ''PLoS One''. 2012; '''7''' (10):e48294
Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh. Description: Pierce, Brandon L, et al. Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh. ''PLoS Genet''. 2012; '''8''' (2):e1002522
Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer. Description: Long, Jirong, et al. Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer. ''PLoS Genet''. 2012; '''8''' (2):e1002532
Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. Description: Adrianto, Indra, et al. Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. ''PLoS One''. 2012; '''7''' (8):e43907
Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. Description: Boraska, Vesna, et al. Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. ''PLoS One''. 2012; '''7''' (3):e31369
Genome-wide linkage and association analysis identifies major gene loci for guttural pouch tympany in Arabian and German warmblood horses. Description: Metzger, Julia, et al. Genome-wide linkage and association analysis identifies major gene loci for guttural pouch tympany in Arabian and German warmblood horses. ''PLoS One''. 2012; '''7''' (7):e41640
Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population. Description: Yang, Ming, et al. Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population. ''PLoS One''. 2012; '''7''' (10):e47990
Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy. Description: Shiffman, Dov, et al. Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy. ''PLoS One''. 2012; '''7''' (5):e38240
Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics. Description: Ghani, Mahdi, et al. Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics. ''G3 (Bethesda)''. 2012 Jan; '''2''' (1):71-8
Genomic ancestry of North Africans supports back-to-Africa migrations. Description: Henn, Brenna M, et al. Genomic ancestry of North Africans supports back-to-Africa migrations. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002397
Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels. Description: Gao, Xiaoyi, et al. Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels. ''Front Genet''. 2012; '''3''': 117
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis. Description: Kiryluk, Krzysztof, et al. Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis. ''PLoS Genet''. 2012; '''8''' (6):e1002765
Glucocorticoid receptor 1B and 1C mRNA transcript alterations in schizophrenia and bipolar disorder, and their possible regulation by GR gene variants. Description: Sinclair, Duncan, et al. Glucocorticoid receptor 1B and 1C mRNA transcript alterations in schizophrenia and bipolar disorder, and their possible regulation by GR gene variants. ''PLoS One''. 2012; '''7''' (3):e31720
GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers. Description: Li, Shengping, et al. GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers. ''PLoS Genet''. 2012; '''8''' (7):e1002791
Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits. Description: Vattikuti, Shashaank, et al. Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits. ''PLoS Genet''. 2012; '''8''' (3):e1002637
Heterogeneity in genetic admixture across different regions of Argentina. Description: Avena, Sergio, et al. Heterogeneity in genetic admixture across different regions of Argentina. ''PLoS One''. 2012; '''7''' (4):e34695
High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency. Description: Ferreira, Ricardo C, et al. High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002476
HLA associations in classical Hodgkin lymphoma: EBV status matters. Description: Huang, Xin, et al. HLA associations in classical Hodgkin lymphoma: EBV status matters. ''PLoS One''. 2012; '''7''' (7):e39986
Identification of a novel idiopathic epilepsy locus in Belgian Shepherd dogs. Description: Seppala, Eija H, et al. Identification of a novel idiopathic epilepsy locus in Belgian Shepherd dogs. ''PLoS One''. 2012; '''7''' (3):e33549
Identification of a potential susceptibility locus for macular telangiectasia type 2. Description: Parmalee, Nancy L, et al. Identification of a potential susceptibility locus for macular telangiectasia type 2. ''PLoS One''. 2012; '''7''' (8):e24268
Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. Description: Yang, Hsin-Chou, et al. Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. ''PLoS One''. 2012; '''7''' (3):e32907
Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26. Description: McAuley, Erica Z, et al. Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26. ''PLoS One''. 2012; '''7''' (5):e38172
IL12RB2 gene is associated with the age of type 1 diabetes onset in Croatian family Trios. Description: Pehlic, Marina, et al. IL12RB2 gene is associated with the age of type 1 diabetes onset in Croatian family Trios. ''PLoS One''. 2012; '''7''' (11):e49133
IL28B genetic variation is associated with spontaneous clearance of hepatitis C virus, treatment response, serum IL-28B levels in Chinese population. Description: Shi, Xiaodong, et al. IL28B genetic variation is associated with spontaneous clearance of hepatitis C virus, treatment response, serum IL-28B levels in Chinese population. ''PLoS One''. 2012; '''7''' (5):e37054
Incorporating Information of microRNAs into Pathway Analysis in a Genome-Wide Association Study of Bipolar Disorder. Description: Shih, Wei-Liang, et al. Incorporating Information of microRNAs into Pathway Analysis in a Genome-Wide Association Study of Bipolar Disorder. ''Front Genet''. 2012; '''3''': 293
Innate immunity and non-Hodgkin's lymphoma (NHL) related genes in a nested case-control study for gastric cancer risk. Description: Park, Sue K, et al. Innate immunity and non-Hodgkin's lymphoma (NHL) related genes in a nested case-control study for gastric cancer risk. ''PLoS One''. 2012; '''7''' (9):e45274
Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis. Description: Ronninger, Marcus, et al. Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis. ''PLoS One''. 2012; '''7''' (3):e32861
Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure. Description: Gaal, Emilia Ilona, et al. Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure. ''PLoS Genet''. 2012; '''8''' (3):e1002563
Investigation of CD28 gene polymorphisms in patients with sporadic breast cancer in a Chinese Han population in Northeast China. Description: Chen, Shuang, et al. Investigation of CD28 gene polymorphisms in patients with sporadic breast cancer in a Chinese Han population in Northeast China. ''PLoS One''. 2012; '''7''' (10):e48031
Investigation of homocysteine-pathway-related variants in essential hypertension. Description: Fowdar, Javed Y, et al. Investigation of homocysteine-pathway-related variants in essential hypertension. ''Int J Hypertens''. 2012; '''2012''': 190923
Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis. Description: Derks, Eske M, et al. Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis. ''PLoS One''. 2012; '''7''' (6):e37852
KDM2B is implicated in bovine lethal multi-organic developmental dysplasia. Description: Testoni, Stefania, et al. KDM2B is implicated in bovine lethal multi-organic developmental dysplasia. ''PLoS One''. 2012; '''7''' (9):e45634
Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations. Description: Ma, Li, et al. Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations. ''PLoS Genet''. 2012; '''8''' (5):e1002714
Lactase persistence and lipid pathway selection in the Maasai. Description: Wagh, Kshitij, et al. Lactase persistence and lipid pathway selection in the Maasai. ''PLoS One''. 2012; '''7''' (9):e44751
Large scale association analysis for drug addiction: results from SNP to gene. Description: Guo, Xiaobo, et al. Large scale association analysis for drug addiction: results from SNP to gene. ''ScientificWorldJournal''. 2012; '''2012''': 939584
Limitations of the human reference genome for personalized genomics. Description: Rosenfeld, Jeffrey A, et al. Limitations of the human reference genome for personalized genomics. ''PLoS One''. 2012; '''7''' (7):e40294
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. Description: Diekstra, Frank P, et al. Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. ''PLoS One''. 2012; '''7''' (4):e35333
Mass homozygotes accumulation in the NCI-60 cancer cell lines as compared to HapMap Trios, and relation to fragile site location. Description: Ruan, Xiaoyang, et al. Mass homozygotes accumulation in the NCI-60 cancer cell lines as compared to HapMap Trios, and relation to fragile site location. ''PLoS One''. 2012; '''7''' (2):e31628
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. Description: Velez Edwards, Digna R, et al. MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. ''PLoS One''. 2012; '''7''' (2):e32275
Mitochondrial mutations and polymorphisms in psychiatric disorders. Description: Sequeira, Adolfo, et al. Mitochondrial mutations and polymorphisms in psychiatric disorders. ''Front Genet''. 2012; '''3''': 103
*Multiple sclerosis risk variant HLA-DRB11501 associates with high expression of DRB1 gene in different human populations.** Description: Alcina, Antonio, et al. Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations. ''PLoS One''. 2012; '''7''' (1):e29819
Multi-species data integration and gene ranking enrich significant results in an alcoholism genome-wide association study. Description: Zhao, Zhongming, et al. Multi-species data integration and gene ranking enrich significant results in an alcoholism genome-wide association study. ''BMC Genomics''. 2012; '''13 Suppl 8''': S16
Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses. Description: Hauswirth, Regula, et al. Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses. ''PLoS Genet''. 2012; '''8''' (4):e1002653
NetView: a high-definition network-visualization approach to detect fine-scale population structures from genome-wide patterns of variation. Description: Neuditschko, Markus, et al. NetView: a high-definition network-visualization approach to detect fine-scale population structures from genome-wide patterns of variation. ''PLoS One''. 2012; '''7''' (10):e48375
Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. Description: Jia, Peilin, et al. Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. ''PLoS Comput Biol''. 2012; '''8''' (7):e1002587
Networks of neuronal genes affected by common and rare variants in autism spectrum disorders. Description: Ben-David, Eyal, et al. Networks of neuronal genes affected by common and rare variants in autism spectrum disorders. ''PLoS Genet''. 2012; '''8''' (3):e1002556
Neurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humans. Description: Olszewski, Pawel K, et al. Neurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humans. ''PLoS Genet''. 2012; '''8''' (3):e1002568
Nicotine reward and affective nicotine withdrawal signs are attenuated in calcium/calmodulin-dependent protein kinase IV knockout mice. Description: Jackson, Kia J, et al. Nicotine reward and affective nicotine withdrawal signs are attenuated in calcium/calmodulin-dependent protein kinase IV knockout mice. ''PLoS One''. 2012; '''7''' (11):e51154
No association of a set of candidate genes on haloperidol side effects. Description: Drago, Antonio, et al. No association of a set of candidate genes on haloperidol side effects. ''PLoS One''. 2012; '''7''' (10):e44853
Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. Description: Inouye, Michael, et al. Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. ''PLoS Genet''. 2012; '''8''' (8):e1002907
Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed. Description: Forman, Oliver P, et al. Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002462
Parameters in dynamic models of complex traits are containers of missing heritability. Description: Wang, Yunpeng, et al. Parameters in dynamic models of complex traits are containers of missing heritability. ''PLoS Comput Biol''. 2012; '''8''' (4):e1002459
Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breed. Description: Neff, Mark W, et al. Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breed. ''PLoS One''. 2012; '''7''' (12):e51917
Patterns of ancestry, signatures of natural selection, and genetic association with stature in Western African pygmies. Description: Jarvis, Joseph P, et al. Patterns of ancestry, signatures of natural selection, and genetic association with stature in Western African pygmies. ''PLoS Genet''. 2012; '''8''' (4):e1002641
PLXNC1 and RDH13 associated with bilateral convergent strabismus with exophthalmus in German Brown cattle. Description: Fink, Steffen, et al. PLXNC1 and RDH13 associated with bilateral convergent strabismus with exophthalmus in German Brown cattle. ''Mol Vis''. 2012; '''18''': 2229-40
Polymorphisms in HSD17B1: Early Onset and Increased Risk of Alzheimer's Disease in Women with Down Syndrome. Description: Lee, Joseph H, et al. Polymorphisms in HSD17B1: Early Onset and Increased Risk of Alzheimer's Disease in Women with Down Syndrome. ''Curr Gerontol Geriatr Res''. 2012; '''2012''': 361218
Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population. Description: Gaj, Pawel, et al. Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population. ''PLoS One''. 2012; '''7''' (4):e35307
Population genetic structure and origins of Native Hawaiians in the multiethnic cohort study. Description: Kim, Sung K, et al. Population genetic structure and origins of Native Hawaiians in the multiethnic cohort study. ''PLoS One''. 2012; '''7''' (11):e47881
Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis. Description: Manichaikul, Ani, et al. Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis. ''PLoS Genet''. 2012; '''8''' (4):e1002640
Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation. Description: Chang, Diana, et al. Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation. ''PLoS Comput Biol''. 2012; '''8''' (7):e1002600
PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-kappaB and XBP1 binding sites. Description: Glas, Jurgen, et al. PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-kappaB and XBP1 binding sites. ''PLoS One''. 2012; '''7''' (12):e52873
PTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease background. Description: Glas, Jurgen, et al. PTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease background. ''PLoS One''. 2012; '''7''' (3):e33682
Rare and low frequency variant stratification in the UK population: description and impact on association tests. Description: Babron, Marie-Claude, et al. Rare and low frequency variant stratification in the UK population: description and impact on association tests. ''PLoS One''. 2012; '''7''' (10):e46519
Recessive mutations in SPTBN2 implicate beta-III spectrin in both cognitive and motor development. Description: Lise, Stefano, et al. Recessive mutations in SPTBN2 implicate beta-III spectrin in both cognitive and motor development. ''PLoS Genet''. 2012; '''8''' (12):e1003074
Reduced lentivirus susceptibility in sheep with TMEM154 mutations. Description: Heaton, Michael P, et al. Reduced lentivirus susceptibility in sheep with TMEM154 mutations. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002467
Regions of homozygosity in the porcine genome: consequence of demography and the recombination landscape. Description: Bosse, Mirte, et al. Regions of homozygosity in the porcine genome: consequence of demography and the recombination landscape. ''PLoS Genet''. 2012; '''8''' (11):e1003100
Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. Description: Keller, Matthew C, et al. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. ''PLoS Genet''. 2012; '''8''' (4):e1002656
Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples. Description: Gladwin, Thomas E, et al. Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples. ''PLoS One''. 2012; '''7''' (6):e38828
Significant association of estrogen receptor binding site variation with bipolar disorder in females. Description: Graae, Lisette, et al. Significant association of estrogen receptor binding site variation with bipolar disorder in females. ''PLoS One''. 2012; '''7''' (2):e32304
SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma. Description: Chen, Li Jia, et al. SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma. ''Mol Vis''. 2012; '''18''': 1629-39
The aromatase gene (CYP19A1) variants and circulating hepatocyte growth factor in postmenopausal women. Description: Lin, Jennifer H, et al. The aromatase gene (CYP19A1) variants and circulating hepatocyte growth factor in postmenopausal women. ''PLoS One''. 2012; '''7''' (7):e42079
The diamine oxidase gene is associated with hypersensitivity response to non-steroidal anti-inflammatory drugs. Description: Agundez, Jose A G, et al. The diamine oxidase gene is associated with hypersensitivity response to non-steroidal anti-inflammatory drugs. ''PLoS One''. 2012; '''7''' (11):e47571
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. Description: Scerri, Thomas S, et al. The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. ''PLoS One''. 2012; '''7''' (11):e50321
The Interaction between Pesticide Use and Genetic Variants Involved in Lipid Metabolism on Prostate Cancer Risk. Description: Andreotti, Gabriella, et al. The Interaction between Pesticide Use and Genetic Variants Involved in Lipid Metabolism on Prostate Cancer Risk. ''J Cancer Epidemiol''. 2012; '''2012''': 358076
The interactive effect of SIRT1 promoter region polymorphism on type 2 diabetes susceptibility in the North Indian population. Description: Rai, Ekta, et al. The interactive effect of SIRT1 promoter region polymorphism on type 2 diabetes susceptibility in the North Indian population. ''PLoS One''. 2012; '''7''' (11):e48621
The interleukin 3 gene (IL3) contributes to human brain volume variation by regulating proliferation and survival of neural progenitors. Description: Luo, Xiong-jian, et al. The interleukin 3 gene (IL3) contributes to human brain volume variation by regulating proliferation and survival of neural progenitors. ''PLoS One''. 2012; '''7''' (11):e50375
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. Description: Voight, Benjamin F, et al. The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. ''PLoS Genet''. 2012; '''8''' (8):e1002793
The principal genetic determinants for nasopharyngeal carcinoma in China involve the HLA class I antigen recognition groove. Description: Tang, Minzhong, et al. The principal genetic determinants for nasopharyngeal carcinoma in China involve the HLA class I antigen recognition groove. ''PLoS Genet''. 2012; '''8''' (11):e1003103
Tracking the emergence of a new breed using 49,034 SNP in sheep. Description: Kijas, James W, et al. Tracking the emergence of a new breed using 49,034 SNP in sheep. ''PLoS One''. 2012; '''7''' (7):e41508
Unexpected relationships and inbreeding in HapMap phase III populations. Description: Stevens, Eric L, et al. Unexpected relationships and inbreeding in HapMap phase III populations. ''PLoS One''. 2012; '''7''' (11):e49575
Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression. Description: Fu, Jingyuan, et al. Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002431
Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays. Description: Smith, Andrew J P, et al. Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays. ''PLoS Genet''. 2012; '''8''' (8):e1002908
Variation of BMP3 contributes to dog breed skull diversity. Description: Schoenebeck, Jeffrey J, et al. Variation of BMP3 contributes to dog breed skull diversity. ''PLoS Genet''. 2012; '''8''' (8):e1002849
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. Description: Chahrour, Maria H, et al. Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. ''PLoS Genet''. 2012; '''8''' (4):e1002635
Widespread site-dependent buffering of human regulatory polymorphism. Description: Maurano, Matthew T, et al. Widespread site-dependent buffering of human regulatory polymorphism. ''PLoS Genet''. 2012; '''8''' (3):e1002599
Further evidence for a male-selective genetic association of synapse-associated protein 97 (SAP97) gene with schizophrenia. Description: Uezato, Akihito, et al. Further evidence for a male-selective genetic association of synapse-associated protein 97 (SAP97) gene with schizophrenia. ''Behav Brain Funct''. 2012 Jan 6; '''8''': 2
Genome-wide association scan and phased haplotype construction for quantitative trait loci affecting boar taint in three pig breeds. Description: Gregersen, Vivi R, et al. Genome-wide association scan and phased haplotype construction for quantitative trait loci affecting boar taint in three pig breeds. ''BMC Genomics''. 2012 Jan 13; '''13''': 22
Genetic adaptation to high altitude in the Ethiopian highlands. Description: Scheinfeldt, Laura B, et al. Genetic adaptation to high altitude in the Ethiopian highlands. ''Genome Biol''. 2012 Jan 20; '''13''' (1):R1
TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data. Description: Londono, Douglas, et al. TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data. ''BMC Bioinformatics''. 2012 Jan 20; '''13''': 13
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population. Description: Guha, Saurav, et al. Implications for health and disease in the genetic signature of the Ashkenazi Jewish population. ''Genome Biol''. 2012 Jan 25; '''13''' (1):R2
Combining evidence of selection with association analysis increases power to detect regions influencing complex traits in dairy cattle. Description: Schwarzenbacher, Hermann, et al. Combining evidence of selection with association analysis increases power to detect regions influencing complex traits in dairy cattle. ''BMC Genomics''. 2012 Jan 30; '''13''': 48
BDNF val66met affects hippocampal volume and emotion-related hippocampal memory activity. Description: Molendijk, M L, et al. BDNF val66met affects hippocampal volume and emotion-related hippocampal memory activity. ''Transl Psychiatry''. 2012 Jan 31; '''2''': e74
A genome-wide association study of gestational diabetes mellitus in Korean women. Description: Kwak, Soo Heon, et al. A genome-wide association study of gestational diabetes mellitus in Korean women. ''Diabetes''. 2012 Feb; '''61''' (2):531-41
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. Description: Williams, Nigel M, et al. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. ''Am J Psychiatry''. 2012 Feb; '''169''' (2):195-204
Genome-wide analysis of the world's sheep breeds reveals high levels of historic mixture and strong recent selection. Description: Kijas, James W, et al. Genome-wide analysis of the world's sheep breeds reveals high levels of historic mixture and strong recent selection. ''PLoS Biol''. 2012 Feb; '''10''' (2):e1001258
Mixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancer. Description: Im, Hae Kyung, et al. Mixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancer. ''PLoS Genet''. 2012 Feb; '''8''' (2):e1002525
Modeling the functional genomics of autism using human neurons. Description: Konopka, G, et al. Modeling the functional genomics of autism using human neurons. ''Mol Psychiatry''. 2012 Feb; '''17''' (2):202-14
Psoriasis patients are enriched for genetic variants that protect against HIV-1 disease. Description: Chen, Haoyan, et al. Psoriasis patients are enriched for genetic variants that protect against HIV-1 disease. ''PLoS Genet''. 2012 Feb; '''8''' (2):e1002514
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. Description: Spain, Sarah L, et al. Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. ''Hum Mol Genet''. 2012 Feb 15; '''21''' (4):934-46
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes. Description: Lotta, Luca A, et al. Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes. ''BMC Med Genomics''. 2012 Feb 21; '''5''': 7
Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms. Description: Lu, James T, et al. Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms. ''Genome Biol''. 2012 Feb 29; '''13''' (2):R15
Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. Description: Swaminathan, Shanker, et al. Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. ''Brain Imaging Behav''. 2012 Mar; '''6''' (1):1-15
Common variants of IL6, LEPR, and PBEF1 are associated with obesity in Indian children. Description: Tabassum, Rubina, et al. Common variants of IL6, LEPR, and PBEF1 are associated with obesity in Indian children. ''Diabetes''. 2012 Mar; '''61''' (3):626-31
Genetic variants in interferon regulatory factor 2 (IRF2) are associated with atopic dermatitis and eczema herpeticum. Description: Gao, Pei-Song, et al. Genetic variants in interferon regulatory factor 2 (IRF2) are associated with atopic dermatitis and eczema herpeticum. ''J Invest Dermatol''. 2012 Mar; '''132''' (3 Pt 1):650-7
Replication of association of the PTPRC gene with response to anti-tumor necrosis factor therapy in a large UK cohort. Description: Plant, Darren, et al. Replication of association of the PTPRC gene with response to anti-tumor necrosis factor therapy in a large UK cohort. ''Arthritis Rheum''. 2012 Mar; '''64''' (3):665-70
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population. Description: Trotta, Luca, et al. SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population. ''Parkinsonism Relat Disord''. 2012 Mar; '''18''' (3):257-62
The same ELA class II risk factors confer equine insect bite hypersensitivity in two distinct populations. Description: Andersson, Lisa S, et al. The same ELA class II risk factors confer equine insect bite hypersensitivity in two distinct populations. ''Immunogenetics''. 2012 Mar; '''64''' (3):201-8
Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24. Description: Jones, Angela M, et al. Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24. ''J Med Genet''. 2012 Mar; '''49''' (3):158-63
TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis. Description: Tejasvi, Trilokraj, et al. TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis. ''J Invest Dermatol''. 2012 Mar; '''132''' (3 Pt 1):593-600
Polymorphisms in Toll-like receptor genes influence antibody responses to cytomegalovirus glycoprotein B vaccine. Description: Arav-Boger, Ravit, et al. Polymorphisms in Toll-like receptor genes influence antibody responses to cytomegalovirus glycoprotein B vaccine. ''BMC Res Notes''. 2012 Mar 13; '''5''': 140
TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humans. Description: Ollila, H M, et al. TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humans. ''Transl Psychiatry''. 2012 Mar 20; '''2''': e97
IFITM3 restricts the morbidity and mortality associated with influenza. Description: Everitt, Aaron R, et al. IFITM3 restricts the morbidity and mortality associated with influenza. ''Nature''. 2012 Mar 25; '''484''' (7395):519-23
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases. Description: Li, Miao-Xin, et al. A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases. ''Nucleic Acids Res''. 2012 Apr; '''40''' (7):e53
Amino acid position 11 of HLA-DRbeta1 is a major determinant of chromosome 6p association with ulcerative colitis. Description: Achkar, J-P, et al. Amino acid position 11 of HLA-DRbeta1 is a major determinant of chromosome 6p association with ulcerative colitis. ''Genes Immun''. 2012 Apr; '''13''' (3):245-52
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Description: Casey, Jillian P, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. ''Hum Genet''. 2012 Apr; '''131''' (4):565-79
Distribution of functional polymorphic variants of inflammation-related genes RANTES and CCR5 in long-lived individuals. Description: Laplana, Marina, et al. Distribution of functional polymorphic variants of inflammation-related genes RANTES and CCR5 in long-lived individuals. ''Cytokine''. 2012 Apr; '''58''' (1):10-3
Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL. Description: Ellinghaus, Eva, et al. Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL. ''J Invest Dermatol''. 2012 Apr; '''132''' (4):1133-40
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls. Description: Soemedi, Rachel, et al. Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls. ''Hum Mol Genet''. 2012 Apr 1; '''21''' (7):1513-20
Tau acts as an independent genetic risk factor in pathologically proven PD. Description: Charlesworth, Gavin, et al. Tau acts as an independent genetic risk factor in pathologically proven PD. ''Neurobiol Aging''. 2012 Apr; '''33''' (4):838.e7-11
UGT1A1 is a major locus influencing bilirubin levels in African Americans. Description: Chen, Guanjie, et al. UGT1A1 is a major locus influencing bilirubin levels in African Americans. ''Eur J Hum Genet''. 2012 Apr; '''20''' (4):463-8
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. Description: Ellinghaus, David, et al. Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. ''Am J Hum Genet''. 2012 Apr 6; '''90''' (4):636-47
Linkage-disequilibrium-based binning affects the interpretation of GWASs. Description: Christoforou, Andrea, et al. Linkage-disequilibrium-based binning affects the interpretation of GWASs. ''Am J Hum Genet''. 2012 Apr 6; '''90''' (4):727-33
Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study. Description: Hammer, C, et al. Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study. ''Transl Psychiatry''. 2012 Apr 17; '''2''': e103
The renal urate transporter SLC17A1 locus: confirmation of association with gout. Description: Hollis-Moffatt, Jade E, et al. The renal urate transporter SLC17A1 locus: confirmation of association with gout. ''Arthritis Res Ther''. 2012 Apr 27; '''14''' (2):R92
A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer. Description: Wheless, Lee, et al. A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer. ''J Invest Dermatol''. 2012 May; '''132''' (5):1354-62
Evaluating the evidence for transmission distortion in human pedigrees. Description: Meyer, Wynn K, et al. Evaluating the evidence for transmission distortion in human pedigrees. ''Genetics''. 2012 May; '''191''' (1):215-32
Footprints of genetic susceptibility to pulmonary tuberculosis: cytokine gene variants in north Indians. Description: Bose, Mridula, et al. Footprints of genetic susceptibility to pulmonary tuberculosis: cytokine gene variants in north Indians. ''Indian J Med Res''. 2012 May; '''135''' (5):763-70
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. Description: Ellinghaus, E, et al. Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. ''Leukemia''. 2012 May; '''26''' (5):902-9
Quantitative genetics in the genomics era. Description: Hill, William G. Quantitative genetics in the genomics era. ''Curr Genomics''. 2012 May; '''13''' (3):196-206
Ultrahigh-dimensional variable selection method for whole-genome gene-gene interaction analysis. Description: Ueki, Masao, et al. Ultrahigh-dimensional variable selection method for whole-genome gene-gene interaction analysis. ''BMC Bioinformatics''. 2012 May 3; '''13''': 72
Association between SNPs and gene expression in multiple regions of the human brain. Description: Kim, S, et al. Association between SNPs and gene expression in multiple regions of the human brain. ''Transl Psychiatry''. 2012 May 8; '''2''': e113
Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterol. Description: Guthrie, Philip A I, et al. Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterol. ''Gene''. 2012 May 10; '''499''' (1):8-13
SparSNP: fast and memory-efficient analysis of all SNPs for phenotype prediction. Description: Abraham, Gad, et al. SparSNP: fast and memory-efficient analysis of all SNPs for phenotype prediction. ''BMC Bioinformatics''. 2012 May 10; '''13''': 88
Genome-wide association study of Alzheimer's disease. Description: Kamboh, M I, et al. Genome-wide association study of Alzheimer's disease. ''Transl Psychiatry''. 2012 May 15; '''2''': e117
Variation in regulator of G-protein signaling 17 gene (RGS17) is associated with multiple substance dependence diagnoses. Description: Zhang, Huiping, et al. Variation in regulator of G-protein signaling 17 gene (RGS17) is associated with multiple substance dependence diagnoses. ''Behav Brain Funct''. 2012 May 16; '''8''': 23
The MAP2K5-linked SNP rs2241423 is associated with BMI and obesity in two cohorts of Swedish and Greek children. Description: Rask-Andersen, Mathias, et al. The MAP2K5-linked SNP rs2241423 is associated with BMI and obesity in two cohorts of Swedish and Greek children. ''BMC Med Genet''. 2012 May 17; '''13''': 36
Genome-wide linkage analysis of QTL for growth and body composition employing the PorcineSNP60 BeadChip. Description: Fernandez, Ana I, et al. Genome-wide linkage analysis of QTL for growth and body composition employing the PorcineSNP60 BeadChip. ''BMC Genet''. 2012 May 20; '''13''': 41
Discovery of regulatory elements in human ATP-binding cassette transporters through expression quantitative trait mapping. Description: Matsson, P, et al. Discovery of regulatory elements in human ATP-binding cassette transporters through expression quantitative trait mapping. ''Pharmacogenomics J''. 2012 Jun; '''12''' (3):214-26
Effect of genetic predisposition on blood lipid traits using cumulative risk assessment in the korean population. Description: Go, Min Jin, et al. Effect of genetic predisposition on blood lipid traits using cumulative risk assessment in the korean population. ''Genomics Inform''. 2012 Jun; '''10''' (2):99-105
Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. Description: Dumitriu, Alexandra, et al. Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. ''PLoS Genet''. 2012 Jun; '''8''' (6):e1002794
Genetic mapping of habitual substance use, obesity-related traits, responses to mental and physical stress, and heart rate and blood pressure measurements reveals shared genes that are overrepresented in the neural synapse. Description: Nikpay, Majid, et al. Genetic mapping of habitual substance use, obesity-related traits, responses to mental and physical stress, and heart rate and blood pressure measurements reveals shared genes that are overrepresented in the neural synapse. ''Hypertens Res''. 2012 Jun; '''35''' (6):585-91
Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study. Description: Pyun, Jung-A, et al. Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study. ''Genomics Inform''. 2012 Jun; '''10''' (2):88-98
Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors. Description: Wong, M-L, et al. Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors. ''Mol Psychiatry''. 2012 Jun; '''17''' (6):624-33
P-selectin genotype is associated with the development of cancer cachexia. Description: Tan, Benjamin H L, et al. P-selectin genotype is associated with the development of cancer cachexia. ''EMBO Mol Med''. 2012 Jun; '''4''' (6):462-71
Replication of the Association of the 6q22.31c Locus near GJA1 with Pulse Rate in the Korean Population. Description: Kim, Nam Hee, et al. Replication of the Association of the 6q22.31c Locus near GJA1 with Pulse Rate in the Korean Population. ''Genomics Inform''. 2012 Jun; '''10''' (2):106-9
Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets. Description: Ionita-Laza, Iuliana, et al. Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets. ''Am J Hum Genet''. 2012 Jun 8; '''90''' (6):1002-13
A defect in dystrophin causes a novel porcine stress syndrome. Description: Nonneman, Dan J, et al. A defect in dystrophin causes a novel porcine stress syndrome. ''BMC Genomics''. 2012 Jun 12; '''13''': 233
Leveraging input and output structures for joint mapping of epistatic and marginal eQTLs. Description: Lee, Seunghak, et al. Leveraging input and output structures for joint mapping of epistatic and marginal eQTLs. ''Bioinformatics''. 2012 Jun 15; '''28''' (12):i137-46
No association for Chinese HBV-related hepatocellular carcinoma susceptibility SNP in other East Asian populations. Description: Sawai, Hiromi, et al. No association for Chinese HBV-related hepatocellular carcinoma susceptibility SNP in other East Asian populations. ''BMC Med Genet''. 2012 Jun 19; '''13''': 47
Inferring genome-wide patterns of admixture in Qataris using fifty-five ancestral populations. Description: Omberg, Larsson, et al. Inferring genome-wide patterns of admixture in Qataris using fifty-five ancestral populations. ''BMC Genet''. 2012 Jun 26; '''13''': 49
Genetic variation in glutathione S-transferase omega-1, arsenic methyltransferase and methylene-tetrahydrofolate reductase, arsenic exposure and bladder cancer: a case-control study. Description: Beebe-Dimmer, Jennifer L, et al. Genetic variation in glutathione S-transferase omega-1, arsenic methyltransferase and methylene-tetrahydrofolate reductase, arsenic exposure and bladder cancer: a case-control study. ''Environ Health''. 2012 Jun 29; '''11''': 43
Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene. Description: Himes, Blanca E, et al. Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene. ''PLoS Genet''. 2012 Jul; '''8''' (7):e1002824
Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Description: Badner, J A, et al. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. ''Mol Psychiatry''. 2012 Jul; '''17''' (8):818-26
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain. Description: Hernandez, Dena G, et al. Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain. ''Neurobiol Dis''. 2012 Jul; '''47''' (1):20-8
Protective effect of human endogenous retrovirus K dUTPase variants on psoriasis susceptibility. Description: Lai, Olivia Y, et al. Protective effect of human endogenous retrovirus K dUTPase variants on psoriasis susceptibility. ''J Invest Dermatol''. 2012 Jul; '''132''' (7):1833-40
Reprioritizing genetic associations in hit regions using LASSO-based resample model averaging. Description: Valdar, William, et al. Reprioritizing genetic associations in hit regions using LASSO-based resample model averaging. ''Genet Epidemiol''. 2012 Jul; '''36''' (5):451-62
*Genome-wide pharmacogenomic study of citalopram-induced side effects in STARD.** Description: Adkins, D E, et al. Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D. ''Transl Psychiatry''. 2012 Jul 3; '''2''': e129
A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. Description: Kim, Jong Wook, et al. A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. ''Am J Hum Genet''. 2012 Jul 13; '''91''' (1):180-4
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. Description: Pagani, Luca, et al. Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. ''Am J Hum Genet''. 2012 Jul 13; '''91''' (1):83-96
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. Description: Tang, Weihong, et al. Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. ''Am J Hum Genet''. 2012 Jul 13; '''91''' (1):152-62
Multifaceted genomic risk for brain function in schizophrenia. Description: Chen, Jiayu, et al. Multifaceted genomic risk for brain function in schizophrenia. ''Neuroimage''. 2012 Jul 16; '''61''' (4):866-75
Glucocorticoid receptor mRNA and protein isoform alterations in the orbitofrontal cortex in schizophrenia and bipolar disorder. Description: Sinclair, Duncan, et al. Glucocorticoid receptor mRNA and protein isoform alterations in the orbitofrontal cortex in schizophrenia and bipolar disorder. ''BMC Psychiatry''. 2012 Jul 20; '''12''': 84
Association study of genes associated to asthma in a specific environment, in an asthma familial collection located in a rural area influenced by different industries. Description: Morin, Andreanne, et al. Association study of genes associated to asthma in a specific environment, in an asthma familial collection located in a rural area influenced by different industries. ''Int J Environ Res Public Health''. 2012 Aug; '''9''' (8):2620-35
Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy. Description: Williams, Winfred W, et al. Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy. ''Diabetes''. 2012 Aug; '''61''' (8):2187-94
Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. Description: Hamilton, Gillian, et al. Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. ''Neurobiol Aging''. 2012 Aug; '''33''' (8):1848.e1-13
High-throughput analysis of epistasis in genome-wide association studies with BiForce. Description: Gyenesei, Attila, et al. High-throughput analysis of epistasis in genome-wide association studies with BiForce. ''Bioinformatics''. 2012 Aug 1; '''28''' (15):1957-64
Runs of homozygosity and population history in cattle. Description: Purfield, Deirdre C, et al. Runs of homozygosity and population history in cattle. ''BMC Genet''. 2012 Aug 14; '''13''': 70
Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction. Description: Ayalew, M, et al. Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction. ''Mol Psychiatry''. 2012 Sep; '''17''' (9):887-905
Functional variants in NFKBIE and RTKN2 involved in activation of the NF-kappaB pathway are associated with rheumatoid arthritis in Japanese. Description: Myouzen, Keiko, et al. Functional variants in NFKBIE and RTKN2 involved in activation of the NF-kappaB pathway are associated with rheumatoid arthritis in Japanese. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002949
Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. Description: Yang, Xiaobo, et al. Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002916
New susceptibility loci associated with kidney disease in type 1 diabetes. Description: Sandholm, Niina, et al. New susceptibility loci associated with kidney disease in type 1 diabetes. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002921
Polymorphisms in AKR1C4 and HSD3B2 and differences in serum DHEAS and progesterone are associated with paranoid ideation during mania or hypomania in bipolar disorder. Description: Johansson, Anette G M, et al. Polymorphisms in AKR1C4 and HSD3B2 and differences in serum DHEAS and progesterone are associated with paranoid ideation during mania or hypomania in bipolar disorder. ''Eur Neuropsychopharmacol''. 2012 Sep; '''22''' (9):632-40
Prediction of Colorectal Cancer Risk Using a Genetic Risk Score: The Korean Cancer Prevention Study-II (KCPS-II). Description: Jo, Jaeseong, et al. Prediction of Colorectal Cancer Risk Using a Genetic Risk Score: The Korean Cancer Prevention Study-II (KCPS-II). ''Genomics Inform''. 2012 Sep; '''10''' (3):175-83
Rare copy number variants contribute to congenital left-sided heart disease. Description: Hitz, Marc-Phillip, et al. Rare copy number variants contribute to congenital left-sided heart disease. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002903
Variation in genes related to cochlear biology is strongly associated with adult-onset deafness in border collies. Description: Yokoyama, Jennifer S, et al. Variation in genes related to cochlear biology is strongly associated with adult-onset deafness in border collies. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002898
Replication and meta-analysis of TMEM132D gene variants in panic disorder. Description: Erhardt, A, et al. Replication and meta-analysis of TMEM132D gene variants in panic disorder. ''Transl Psychiatry''. 2012 Sep 4; '''2''': e156
UMOD as a susceptibility gene for end-stage renal disease. Description: Reznichenko, Anna, et al. UMOD as a susceptibility gene for end-stage renal disease. ''BMC Med Genet''. 2012 Sep 5; '''13''': 78
Association between the ABO locus and hematological traits in Korean. Description: Hong, Kyung-Won, et al. Association between the ABO locus and hematological traits in Korean. ''BMC Genet''. 2012 Sep 10; '''13''': 78
Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent. Description: Al-Eitan, Laith N, et al. Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent. ''BMC Res Notes''. 2012 Sep 10; '''5''': 497
The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility. Description: Holliday, Kate L, et al. The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility. ''Mol Pain''. 2012 Sep 24; '''8''': 72
Fine-mapping in African-American women confirms the importance of the 10p12 locus to sarcoidosis. Description: Cozier, Y C, et al. Fine-mapping in African-American women confirms the importance of the 10p12 locus to sarcoidosis. ''Genes Immun''. 2012 Oct; '''13''' (7):573-8
Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Description: Lips, E S, et al. Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. ''Mol Psychiatry''. 2012 Oct; '''17''' (10):996-1006
Polymorphisms in the myeloperoxidase gene locus are associated with acute kidney injury-related outcomes. Description: Perianayagam, Mary C, et al. Polymorphisms in the myeloperoxidase gene locus are associated with acute kidney injury-related outcomes. ''Kidney Int''. 2012 Oct; '''82''' (8):909-19
A genome-wide association study using international breeding-evaluation data identifies major loci affecting production traits and stature in the Brown Swiss cattle breed. Description: Guo, Jiazhong, et al. A genome-wide association study using international breeding-evaluation data identifies major loci affecting production traits and stature in the Brown Swiss cattle breed. ''BMC Genet''. 2012 Oct 2; '''13''': 82
Genetic association of cyclic AMP signaling genes with bipolar disorder. Description: McDonald, M L, et al. Genetic association of cyclic AMP signaling genes with bipolar disorder. ''Transl Psychiatry''. 2012 Oct 2; '''2''': e169
Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study. Description: Lv, Xiaofei, et al. Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study. ''Lipids Health Dis''. 2012 Oct 4; '''11''': 128
Fine mapping of complex traits in non-model species: using next generation sequencing and advanced intercross lines in Japanese quail. Description: Fresard, Laure, et al. Fine mapping of complex traits in non-model species: using next generation sequencing and advanced intercross lines in Japanese quail. ''BMC Genomics''. 2012 Oct 15; '''13''': 551
Convergent animal and human evidence suggests the activin/inhibin pathway to be involved in antidepressant response. Description: Ganea, K, et al. Convergent animal and human evidence suggests the activin/inhibin pathway to be involved in antidepressant response. ''Transl Psychiatry''. 2012 Oct 23; '''2''': e177
Genome-wide association of mood-incongruent psychotic bipolar disorder. Description: Goes, F S, et al. Genome-wide association of mood-incongruent psychotic bipolar disorder. ''Transl Psychiatry''. 2012 Oct 23; '''2''': e180
Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans. Description: Walsh, Kyle M, et al. Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans. ''Oncotarget''. 2012 Nov; '''3''' (11):1428-38
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Description: Amin, N, et al. Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. ''Mol Psychiatry''. 2012 Nov; '''17''' (11):1116-29
Genome-wide meta-analysis of common variant differences between men and women. Description: Boraska, Vesna, et al. Genome-wide meta-analysis of common variant differences between men and women. ''Hum Mol Genet''. 2012 Nov 1; '''21''' (21):4805-15
Individual common variants exert weak effects on the risk for autism spectrum disorders. Description: Anney, Richard, et al. Individual common variants exert weak effects on the risk for autism spectrum disorders. ''Hum Mol Genet''. 2012 Nov 1; '''21''' (21):4781-92
A novel analytical method, Birth Date Selection Mapping, detects response of the Angus (Bos taurus) genome to selection on complex traits. Description: Decker, Jared E, et al. A novel analytical method, Birth Date Selection Mapping, detects response of the Angus (Bos taurus) genome to selection on complex traits. ''BMC Genomics''. 2012 Nov 9; '''13''': 606
From expression pattern to genetic association in asthma and asthma-related phenotypes. Description: Vaillancourt, Vanessa T, et al. From expression pattern to genetic association in asthma and asthma-related phenotypes. ''BMC Res Notes''. 2012 Nov 13; '''5''': 630
Meta-analysis of genome-wide association studies for panic disorder in the Japanese population. Description: Otowa, T, et al. Meta-analysis of genome-wide association studies for panic disorder in the Japanese population. ''Transl Psychiatry''. 2012 Nov 13; '''2''': e186
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. Description: Timofeeva, Maria N, et al. Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. ''Hum Mol Genet''. 2012 Nov 15; '''21''' (22):4980-95
Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects. Description: van Eijk, Kristel R, et al. Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects. ''BMC Genomics''. 2012 Nov 17; '''13''': 636
Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans. Description: Brambilla, Paola, et al. Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans. ''Neurosci Lett''. 2012 Nov 21; '''530''' (2):155-60
A discovery resource of rare copy number variations in individuals with autism spectrum disorder. Description: Prasad, Aparna, et al. A discovery resource of rare copy number variations in individuals with autism spectrum disorder. ''G3 (Bethesda)''. 2012 Dec; '''2''' (12):1665-85
Association analysis of reactive oxygen species-hypertension genes discovered by literature mining. Description: Lim, Ji Eun, et al. Association analysis of reactive oxygen species-hypertension genes discovered by literature mining. ''Genomics Inform''. 2012 Dec; '''10''' (4):244-8
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Description: Eyre, Steve, et al. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. ''Nat Genet''. 2012 Dec; '''44''' (12):1336-40
Network graph analysis of gene-gene interactions in genome-wide association study data. Description: Lee, Sungyoung, et al. Network graph analysis of gene-gene interactions in genome-wide association study data. ''Genomics Inform''. 2012 Dec; '''10''' (4):256-62
No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis. Description: Luong, Hien T T, et al. No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis. ''Hum Reprod''. 2012 Dec; '''27''' (12):3616-21
Population stratification may bias analysis of PGC-1alpha as a modifier of age at Huntington disease motor onset. Description: Ramos, Eliana Marisa, et al. Population stratification may bias analysis of PGC-1alpha as a modifier of age at Huntington disease motor onset. ''Hum Genet''. 2012 Dec; '''131''' (12):1833-40
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. Description: Mangino, Massimo, et al. Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. ''Hum Mol Genet''. 2012 Dec 15; '''21''' (24):5385-94
Genome-wide association scan of dental caries in the permanent dentition. Description: Wang, Xiaojing, et al. Genome-wide association scan of dental caries in the permanent dentition. ''BMC Oral Health''. 2012 Dec 21; '''12''': 57
Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease. Description: Fernandez, Raquel Ma, et al. Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease. ''Orphanet J Rare Dis''. 2012 Dec 28; '''7''': 103
1,25-dihydroxyvitamin D and the vitamin D receptor gene polymorphism Apa1 influence bone mineral density in primary hyperparathyroidism. Description: Christensen, Monika H E, et al. 1,25-dihydroxyvitamin D and the vitamin D receptor gene polymorphism Apa1 influence bone mineral density in primary hyperparathyroidism. ''PLoS One''. 2013; '''8''' (2):e56019
Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses. Description: Haase, Bianca, et al. Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses. ''PLoS One''. 2013; '''8''' (9):e75071
A CNGB1 frameshift mutation in Papillon and Phalene dogs with progressive retinal atrophy. Description: Ahonen, Saija J, et al. A CNGB1 frameshift mutation in Papillon and Phalene dogs with progressive retinal atrophy. ''PLoS One''. 2013; '''8''' (8):e72122
A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism. Description: Frischknecht, Mirjam, et al. A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism. ''PLoS One''. 2013; '''8''' (3):e60149
A common functional promoter variant links CNR1 gene expression to HDL cholesterol level. Description: Feng, Q, et al. A common functional promoter variant links CNR1 gene expression to HDL cholesterol level. ''Nat Commun''. 2013; '''4''': 1973
Adaptation of maize to temperate climates: mid-density genome-wide association genetics and diversity patterns reveal key genomic regions, with a major contribution of the Vgt2 (ZCN8) locus. Description: Bouchet, Sophie, et al. Adaptation of maize to temperate climates: mid-density genome-wide association genetics and diversity patterns reveal key genomic regions, with a major contribution of the Vgt2 (ZCN8) locus. ''PLoS One''. 2013; '''8''' (8):e71377
A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor. Description: Lubieniecka, Joanna M, et al. A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor. ''Front Genet''. 2013; '''4''': 231
Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production. Description: Molineros, Julio E, et al. Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production. ''PLoS Genet''. 2013; '''9''' (2):e1003222
A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Grasbeck syndrome (selective cobalamin malabsorption). Description: Owczarek-Lipska, Marta, et al. A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Grasbeck syndrome (selective cobalamin malabsorption). ''PLoS One''. 2013; '''8''' (4):e61144
A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. Description: Fernandes, Carla P D, et al. A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. ''PLoS One''. 2013; '''8''' (12):e81052
A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe. Description: Khrunin, Andrey V, et al. A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe. ''PLoS One''. 2013; '''8''' (3):e58552
A genome-wide association study for somatic cell score using the Illumina high-density bovine beadchip identifies several novel QTL potentially related to mastitis susceptibility. Description: Meredith, Brian K, et al. A genome-wide association study for somatic cell score using the Illumina high-density bovine beadchip identifies several novel QTL potentially related to mastitis susceptibility. ''Front Genet''. 2013; '''4''': 229
A genome wide association study identifies common variants associated with lipid levels in the Chinese population. Description: Zhou, Li, et al. A genome wide association study identifies common variants associated with lipid levels in the Chinese population. ''PLoS One''. 2013; '''8''' (12):e82420
A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. Description: Li, Huaixing, et al. A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. ''Diabetes''. 2013 Jan; '''62''' (1):291-8
A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses. Description: Kulbrock, Maike, et al. A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses. ''PLoS One''. 2013; '''8''' (8):e71619
A genome-wide association study points out the causal implication of SOX9 in the sex-reversal phenotype in XX pigs. Description: Rousseau, Sarah, et al. A genome-wide association study points out the causal implication of SOX9 in the sex-reversal phenotype in XX pigs. ''PLoS One''. 2013; '''8''' (11):e79882
A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. Description: Hass, Johanna, et al. A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. ''PLoS One''. 2013; '''8''' (6):e64872
A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation. Description: Bendjilali, Nasrine, et al. A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation. ''PLoS One''. 2013; '''8''' (10):e71434
A genome-wide survey of transgenerational genetic effects in autism. Description: Tsang, Kathryn M, et al. A genome-wide survey of transgenerational genetic effects in autism. ''PLoS One''. 2013; '''8''' (10):e76978
Alzheimer's disease: analyzing the missing heritability. Description: Ridge, Perry G, et al. Alzheimer's disease: analyzing the missing heritability. ''PLoS One''. 2013; '''8''' (11):e79771
AMD-associated genes encoding stress-activated MAPK pathway constituents are identified by interval-based enrichment analysis. Description: SanGiovanni, John Paul, et al. AMD-associated genes encoding stress-activated MAPK pathway constituents are identified by interval-based enrichment analysis. ''PLoS One''. 2013; '''8''' (8):e71239
A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation. Description: Jagannathan, Vidhya, et al. A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation. ''PLoS Genet''. 2013; '''9''' (10):e1003848
An empirical workflow for genome-wide single nucleotide polymorphism-based predictive modeling. Description: Floudas, Charalampos S, et al. An empirical workflow for genome-wide single nucleotide polymorphism-based predictive modeling. ''AMIA Jt Summits Transl Sci Proc''. 2013; '''2013''': 53-7
A next-generation sequencing method for genotyping-by-sequencing of highly heterozygous autotetraploid potato. Description: Uitdewilligen, Jan G A M L, et al. A next-generation sequencing method for genotyping-by-sequencing of highly heterozygous autotetraploid potato. ''PLoS One''. 2013; '''8''' (5):e62355
An in-depth characterization of the major psoriasis susceptibility locus identifies candidate susceptibility alleles within an HLA-C enhancer element. Description: Clop, Alex, et al. An in-depth characterization of the major psoriasis susceptibility locus identifies candidate susceptibility alleles within an HLA-C enhancer element. ''PLoS One''. 2013; '''8''' (8):e71690
A panel of ancestry informative markers for the complex five-way admixed South African coloured population. Description: Daya, Michelle, et al. A panel of ancestry informative markers for the complex five-way admixed South African coloured population. ''PLoS One''. 2013; '''8''' (12):e82224
A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. Description: Ostensson, Malin, et al. A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. ''PLoS One''. 2013; '''8''' (8):e70174
Apparent variation in Neanderthal admixture among African populations is consistent with gene flow from Non-African populations. Description: Wang, Shuoguo, et al. Apparent variation in Neanderthal admixture among African populations is consistent with gene flow from Non-African populations. ''Genome Biol Evol''. 2013; '''5''' (11):2075-81
A refined study of FCRL genes from a genome-wide association study for Graves' disease. Description: Zhao, Shuang-Xia, et al. A refined study of FCRL genes from a genome-wide association study for Graves' disease. ''PLoS One''. 2013; '''8''' (3):e57758
ARLTS1 and prostate cancer risk--analysis of expression and regulation. Description: Siltanen, Sanna, et al. ARLTS1 and prostate cancer risk--analysis of expression and regulation. ''PLoS One''. 2013; '''8''' (8):e72040
A SNP profiling panel for sample tracking in whole-exome sequencing studies. Description: Pengelly, Reuben J, et al. A SNP profiling panel for sample tracking in whole-exome sequencing studies. ''Genome Med''. 2013; '''5''' (9):89
A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats. Description: Gandolfi, Barbara, et al. A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats. ''Sci Rep''. 2013; '''3''': 2000
Association analysis of genetic variants in the myosin IXB gene in acute pancreatitis. Description: Nijmeijer, Rian M, et al. Association analysis of genetic variants in the myosin IXB gene in acute pancreatitis. ''PLoS One''. 2013; '''8''' (12):e85870
Association analysis of the SLC22A11 (organic anion transporter 4) and SLC22A12 (urate transporter 1) urate transporter locus with gout in New Zealand case-control sample sets reveals multiple ancestral-specific effects. Description: Flynn, Tanya J, et al. Association analysis of the SLC22A11 (organic anion transporter 4) and SLC22A12 (urate transporter 1) urate transporter locus with gout in New Zealand case-control sample sets reveals multiple ancestral-specific effects. ''Arthritis Res Ther''. 2013; '''15''' (6):R220
Association between a multi-locus genetic risk score and inflammatory bowel disease. Description: Hu, Pingzhao, et al. Association between a multi-locus genetic risk score and inflammatory bowel disease. ''Bioinform Biol Insights''. 2013; '''7''': 143-52
Association between IL28B polymorphisms and spontaneous clearance of hepatitis B virus infection. Description: Kim, Seung Up, et al. Association between IL28B polymorphisms and spontaneous clearance of hepatitis B virus infection. ''PLoS One''. 2013; '''8''' (7):e69166
Association between the SPRY1 gene polymorphism and obesity-related traits and osteoporosis in Korean women. Description: Jin, Hyun-Seok, et al. Association between the SPRY1 gene polymorphism and obesity-related traits and osteoporosis in Korean women. ''Mol Genet Metab''. 2013 Jan; '''108''' (1):95-101
Association of a common variant at 10q26 and benign prostatic hyperplasia aggressiveness in han chinese descent. Description: Gu, Xin, et al. Association of a common variant at 10q26 and benign prostatic hyperplasia aggressiveness in han chinese descent. ''Biochem Res Int''. 2013; '''2013''': 820849
Association of CD247 polymorphisms with rheumatoid arthritis: a replication study and a meta-analysis. Description: Teruel, Maria, et al. Association of CD247 polymorphisms with rheumatoid arthritis: a replication study and a meta-analysis. ''PLoS One''. 2013; '''8''' (7):e68295
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. Description: Leone, Maurizio A, et al. Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. ''PLoS One''. 2013; '''8''' (6):e64408
Association of STAT4 polymorphism with severe renal insufficiency in lupus nephritis. Description: Bolin, Karin, et al. Association of STAT4 polymorphism with severe renal insufficiency in lupus nephritis. ''PLoS One''. 2013; '''8''' (12):e84450
Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degeneration. Description: Kaur, Inderjeet, et al. Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degeneration. ''Mol Vis''. 2013; '''19''': 822-8
Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population. Description: Wang, Erli, et al. Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population. ''PLoS One''. 2013; '''8''' (9):e72423
Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies. Description: Wang, Quan, et al. Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies. ''PLoS One''. 2013; '''8''' (8):e72653
Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. Description: Eicher, John D, et al. Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. ''PLoS One''. 2013; '''8''' (5):e63762
Association study confirmed susceptibility loci with keloid in the Chinese Han population. Description: Zhu, Fei, et al. Association study confirmed susceptibility loci with keloid in the Chinese Han population. ''PLoS One''. 2013; '''8''' (5):e62377
Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis. Description: Zhao, Zhongming, et al. Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis. ''PLoS One''. 2013; '''8''' (7):e67776
Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs. Description: Gupta, Vipin, et al. Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs. ''PLoS One''. 2013; '''8''' (1):e53944
Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls. Description: McLaren, Paul J, et al. Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls. ''PLoS Pathog''. 2013; '''9''' (7):e1003515
Association study of fibroblast growth factor 10 (FGF10) polymorphisms with susceptibility to extreme myopia in a Japanese population. Description: Yoshida, Masao, et al. Association study of fibroblast growth factor 10 (FGF10) polymorphisms with susceptibility to extreme myopia in a Japanese population. ''Mol Vis''. 2013; '''19''': 2321-9
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. Description: Peters, Ulrike, et al. A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. ''PLoS Genet''. 2013; '''9''' (1):e1003171
Atenolol induced HDL-C change in the pharmacogenomic evaluation of antihypertensive responses (PEAR) study. Description: McDonough, Caitrin W, et al. Atenolol induced HDL-C change in the pharmacogenomic evaluation of antihypertensive responses (PEAR) study. ''PLoS One''. 2013; '''8''' (10):e76984
Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation. Description: Alsalem, Ahmed B, et al. Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation. ''PLoS Genet''. 2013; '''9''' (12):e1004030
Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. Description: Grove, Megan L, et al. Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. ''PLoS One''. 2013; '''8''' (7):e68095
Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche. Description: Ran, Shu, et al. Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche. ''PLoS One''. 2013; '''8''' (4):e60362
Bivariate genome-wide association analysis of the growth and intake components of feed efficiency. Description: Serao, Nick V L, et al. Bivariate genome-wide association analysis of the growth and intake components of feed efficiency. ''PLoS One''. 2013; '''8''' (10):e78530
CACNA1C risk variant and amygdala activity in bipolar disorder, schizophrenia and healthy controls. Description: Tesli, Martin, et al. CACNA1C risk variant and amygdala activity in bipolar disorder, schizophrenia and healthy controls. ''PLoS One''. 2013; '''8''' (2):e56970
Canine chondrodysplasia caused by a truncating mutation in collagen-binding integrin alpha subunit 10. Description: Kyostila, Kaisa, et al. Canine chondrodysplasia caused by a truncating mutation in collagen-binding integrin alpha subunit 10. ''PLoS One''. 2013; '''8''' (9):e75621
cgaTOH: extended approach for identifying tracts of homozygosity. Description: Zhang, Li, et al. cgaTOH: extended approach for identifying tracts of homozygosity. ''PLoS One''. 2013; '''8''' (3):e57772
Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry. Description: Wang, Jen-Chyong, et al. Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry. ''PLoS One''. 2013; '''8''' (11):e80204
Cognitive manic symptoms in bipolar disorder associated with polymorphisms in the DAOA and COMT genes. Description: Hukic, Dzana Sudic, et al. Cognitive manic symptoms in bipolar disorder associated with polymorphisms in the DAOA and COMT genes. ''PLoS One''. 2013; '''8''' (7):e67450
Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome. Description: Li, Tao, et al. Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome. ''PLoS One''. 2013; '''8''' (7):e66250
Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples. Description: Jiang, Lei, et al. Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples. ''G3 (Bethesda)''. 2013 Jan; '''3''' (1):23-9
Complex variation in measures of general intelligence and cognitive change. Description: Rowe, Suzanne J, et al. Complex variation in measures of general intelligence and cognitive change. ''PLoS One''. 2013; '''8''' (12):e81189
Comprehensive SNP scan of DNA repair and DNA damage response genes reveal multiple susceptibility loci conferring risk to tobacco associated leukoplakia and oral cancer. Description: Mondal, Pinaki, et al. Comprehensive SNP scan of DNA repair and DNA damage response genes reveal multiple susceptibility loci conferring risk to tobacco associated leukoplakia and oral cancer. ''PLoS One''. 2013; '''8''' (2):e56952
Contribution of 32 GWAS-identified common variants to severe obesity in European adults referred for bariatric surgery. Description: Magi, Reedik, et al. Contribution of 32 GWAS-identified common variants to severe obesity in European adults referred for bariatric surgery. ''PLoS One''. 2013; '''8''' (8):e70735
Contribution of common PCSK1 genetic variants to obesity in 8,359 subjects from multi-ethnic American population. Description: Choquet, Helene, et al. Contribution of common PCSK1 genetic variants to obesity in 8,359 subjects from multi-ethnic American population. ''PLoS One''. 2013; '''8''' (2):e57857
Copy number variants in German patients with schizophrenia. Description: Priebe, Lutz, et al. Copy number variants in German patients with schizophrenia. ''PLoS One''. 2013; '''8''' (7):e64035
Copy number variations in alternative splicing gene networks impact lifespan. Description: Glessner, Joseph T, et al. Copy number variations in alternative splicing gene networks impact lifespan. ''PLoS One''. 2013; '''8''' (1):e53846
CpG methylation changes within the IL2RA promoter in type 1 diabetes of childhood onset. Description: Belot, Marie-Pierre, et al. CpG methylation changes within the IL2RA promoter in type 1 diabetes of childhood onset. ''PLoS One''. 2013; '''8''' (7):e68093
CRY2 genetic variants associate with dysthymia. Description: Kovanen, Leena, et al. CRY2 genetic variants associate with dysthymia. ''PLoS One''. 2013; '''8''' (8):e71450
Defining the contribution of CNTNAP2 to autism susceptibility. Description: Sampath, Srirangan, et al. Defining the contribution of CNTNAP2 to autism susceptibility. ''PLoS One''. 2013; '''8''' (10):e77906
Determining ancestry proportions in complex admixture scenarios in South Africa using a novel proxy ancestry selection method. Description: Chimusa, Emile R, et al. Determining ancestry proportions in complex admixture scenarios in South Africa using a novel proxy ancestry selection method. ''PLoS One''. 2013; '''8''' (9):e73971
Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia. Description: Agim, Zeynep Sena, et al. Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia. ''PLoS One''. 2013; '''8''' (1):e53042
Disease-related growth factor and embryonic signaling pathways modulate an enhancer of TCF21 expression at the 6q23.2 coronary heart disease locus. Description: Miller, Clint L, et al. Disease-related growth factor and embryonic signaling pathways modulate an enhancer of TCF21 expression at the 6q23.2 coronary heart disease locus. ''PLoS Genet''. 2013; '''9''' (7):e1003652
DNA sequence variants in PPARGC1A, a gene encoding a coactivator of the omega-3 LCPUFA sensing PPAR-RXR transcription complex, are associated with NV AMD and AMD-associated loci in genes of complement and VEGF signaling pathways. Description: SanGiovanni, John Paul, et al. DNA sequence variants in PPARGC1A, a gene encoding a coactivator of the omega-3 LCPUFA sensing PPAR-RXR transcription complex, are associated with NV AMD and AMD-associated loci in genes of complement and VEGF signaling pathways. ''PLoS One''. 2013; '''8''' (1):e53155
Dogs and humans share a common susceptibility gene SRBD1 for glaucoma risk. Description: Kanemaki, Nobuyuki, et al. Dogs and humans share a common susceptibility gene SRBD1 for glaucoma risk. ''PLoS One''. 2013; '''8''' (9):e74372
Effects of fertility on gene expression and function of the bovine endometrium. Description: Minten, Megan A, et al. Effects of fertility on gene expression and function of the bovine endometrium. ''PLoS One''. 2013; '''8''' (8):e69444
EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. Description: Namjou, Bahram, et al. EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. ''Front Genet''. 2013; '''4''': 268
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. Description: McDavid, Andrew, et al. Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. ''PLoS One''. 2013; '''8''' (6):e63481
Epistatic genetic effects among Alzheimer's candidate genes. Description: Hohman, Timothy J, et al. Epistatic genetic effects among Alzheimer's candidate genes. ''PLoS One''. 2013; '''8''' (11):e80839
Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese population. Description: Xu, Miaofei, et al. Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese population. ''PLoS One''. 2013; '''8''' (11):e80374
Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene. Description: Diaz-Gallo, Lina-Marcela, et al. Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene. ''PLoS One''. 2013; '''8''' (4):e60646
Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes. Description: Pasquale, Louis R, et al. Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes. ''Front Genet''. 2013; '''4''': 7
Expression levels of LCORL are associated with body size in horses. Description: Metzger, Julia, et al. Expression levels of LCORL are associated with body size in horses. ''PLoS One''. 2013; '''8''' (2):e56497
Finding type 2 diabetes causal single nucleotide polymorphism combinations and functional modules from genome-wide association data. Description: Kang, Chiyong, et al. Finding type 2 diabetes causal single nucleotide polymorphism combinations and functional modules from genome-wide association data. ''BMC Med Inform Decis Mak''. 2013; '''13 Suppl 1''': S3
Fine mapping and functional analysis of the multiple sclerosis risk gene CD6. Description: Swaminathan, Bhairavi, et al. Fine mapping and functional analysis of the multiple sclerosis risk gene CD6. ''PLoS One''. 2013; '''8''' (4):e62376
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus. Description: Trabzuni, Daniah, et al. Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus. ''PLoS One''. 2013; '''8''' (8):e70724
Functional coding variants in SLC6A15, a possible risk gene for major depression. Description: Quast, Carina, et al. Functional coding variants in SLC6A15, a possible risk gene for major depression. ''PLoS One''. 2013; '''8''' (7):e68645
Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans. Description: Smeekens, Sanne P, et al. Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans. ''Nat Commun''. 2013; '''4''': 1342
Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients. Description: Mavroconstanti, Thegna, et al. Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients. ''PLoS One''. 2013; '''8''' (8):e71445
Gene-based testing of interactions in association studies of quantitative traits. Description: Ma, Li, et al. Gene-based testing of interactions in association studies of quantitative traits. ''PLoS Genet''. 2013; '''9''' (2):e1003321
Gene network analysis in a pediatric cohort identifies novel lung function genes. Description: Ong, Bruce A, et al. Gene network analysis in a pediatric cohort identifies novel lung function genes. ''PLoS One''. 2013; '''8''' (9):e72899
Gene polymorphisms in African buffalo associated with susceptibility to bovine tuberculosis infection. Description: le Roex, Nikki, et al. Gene polymorphisms in African buffalo associated with susceptibility to bovine tuberculosis infection. ''PLoS One''. 2013; '''8''' (5):e64494
Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity. Description: Knoll, Nadja, et al. Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity. ''PLoS One''. 2013; '''8''' (2):e55884
Genetic analysis of a rat model of aerobic capacity and metabolic fitness. Description: Ren, Yu-Yu, et al. Genetic analysis of a rat model of aerobic capacity and metabolic fitness. ''PLoS One''. 2013; '''8''' (10):e77588
Genetic Association of Peptidoglycan Recognition Protein Variants with Inflammatory Bowel Disease. Description: Zulfiqar, Fareeha, et al. Genetic Association of Peptidoglycan Recognition Protein Variants with Inflammatory Bowel Disease. ''PLoS One''. 2013; '''8''' (6):e67393
Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations. Description: Lam, Vincent Kwok Lim, et al. Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations. ''PLoS One''. 2013; '''8''' (6):e62378
Genetic diversity in the modern horse illustrated from genome-wide SNP data. Description: Petersen, Jessica L, et al. Genetic diversity in the modern horse illustrated from genome-wide SNP data. ''PLoS One''. 2013; '''8''' (1):e54997
Genetic diversity, linkage disequilibrium and selection signatures in chinese and Western pigs revealed by genome-wide SNP markers. Description: Ai, Huashui, et al. Genetic diversity, linkage disequilibrium and selection signatures in chinese and Western pigs revealed by genome-wide SNP markers. ''PLoS One''. 2013; '''8''' (2):e56001
Genetic heterogeneity of susceptibility gene in different ethnic populations: refining association study of PTPN22 for Graves' disease in a Chinese Han population. Description: Xue, Liqiong, et al. Genetic heterogeneity of susceptibility gene in different ethnic populations: refining association study of PTPN22 for Graves' disease in a Chinese Han population. ''PLoS One''. 2013; '''8''' (12):e84514
Genetic modification of the association between peripubertal dioxin exposure and pubertal onset in a cohort of Russian boys. Description: Humblet, Olivier, et al. Genetic modification of the association between peripubertal dioxin exposure and pubertal onset in a cohort of Russian boys. ''Environ Health Perspect''. 2013 Jan; '''121''' (1):111-7
Genetic structure of Tibeto-Burman populations of Bangladesh: evaluating the gene flow along the sides of Bay-of-Bengal. Description: Gazi, Nurun Nahar, et al. Genetic structure of Tibeto-Burman populations of Bangladesh: evaluating the gene flow along the sides of Bay-of-Bengal. ''PLoS One''. 2013; '''8''' (10):e75064
Genetic substructure of Kuwaiti population reveals migration history. Description: Alsmadi, Osama, et al. Genetic substructure of Kuwaiti population reveals migration history. ''PLoS One''. 2013; '''8''' (9):e74913
Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese. Description: Yiu, Wai Chi, et al. Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese. ''PLoS One''. 2013; '''8''' (4):e61805
Genetic variation of ITGB3 is associated with asthma in Chinese Han children. Description: Zhang, Yan, et al. Genetic variation of ITGB3 is associated with asthma in Chinese Han children. ''PLoS One''. 2013; '''8''' (2):e56914
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes. Description: Behr, Elijah R, et al. Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes. ''PLoS One''. 2013; '''8''' (11):e78511
Genome-wide analysis reveals selection for important traits in domestic horse breeds. Description: Petersen, Jessica L, et al. Genome-wide analysis reveals selection for important traits in domestic horse breeds. ''PLoS Genet''. 2013; '''9''' (1):e1003211
Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. Description: Vernau, Karen M, et al. Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. ''PLoS One''. 2013; '''8''' (3):e57195
Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naive patients with schizophrenia. Description: Wang, Qiang, et al. Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naive patients with schizophrenia. ''PLoS One''. 2013; '''8''' (9):e75083
Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study. Description: Lee, Joseph H, et al. Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study. ''Front Genet''. 2013; '''4''': 310
Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans. Description: Safra, Noa, et al. Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans. ''PLoS Genet''. 2013; '''9''' (7):e1003646
Genome-wide association studies for growth and meat production traits in sheep. Description: Zhang, Li, et al. Genome-wide association studies for growth and meat production traits in sheep. ''PLoS One''. 2013; '''8''' (6):e66569
Genome-wide association study for levels of total serum IgE identifies HLA-C in a Japanese population. Description: Yatagai, Yohei, et al. Genome-wide association study for levels of total serum IgE identifies HLA-C in a Japanese population. ''PLoS One''. 2013; '''8''' (12):e80941
Genome-wide association study identifies a novel canine glaucoma locus. Description: Ahonen, Saija J, et al. Genome-wide association study identifies a novel canine glaucoma locus. ''PLoS One''. 2013; '''8''' (8):e70903
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese. Description: Dong, Jing, et al. Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese. ''PLoS Genet''. 2013; '''9''' (1):e1003190
Genome-wide association study identifies Loci and candidate genes for body composition and meat quality traits in Beijing-You chickens. Description: Liu, Ranran, et al. Genome-wide association study identifies Loci and candidate genes for body composition and meat quality traits in Beijing-You chickens. ''PLoS One''. 2013; '''8''' (4):e61172
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Description: Lencz, Todd, et al. Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. ''Nat Commun''. 2013; '''4''': 2739
Genome-wide association study link novel loci to endometriosis. Description: Albertsen, Hans M, et al. Genome-wide association study link novel loci to endometriosis. ''PLoS One''. 2013; '''8''' (3):e58257
Genome wide association study of age at menarche in the Japanese population. Description: Tanikawa, Chizu, et al. Genome wide association study of age at menarche in the Japanese population. ''PLoS One''. 2013; '''8''' (5):e63821
Genome-wide association study of antiphospholipid antibodies. Description: Kamboh, M Ilyas, et al. Genome-wide association study of antiphospholipid antibodies. ''Autoimmune Dis''. 2013; '''2013''': 761046
Genome-wide association study of breast cancer in the Japanese population. Description: Low, Siew-Kee, et al. Genome-wide association study of breast cancer in the Japanese population. ''PLoS One''. 2013; '''8''' (10):e76463
*Genome-wide association study of HLA-DQB106:02 negative essential hypersomnia.** Description: Khor, Seik-Soon, et al. Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia. ''PeerJ''. 2013; '''1''': e66
Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder. Description: Greenwood, Tiffany A, et al. Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder. ''PLoS One''. 2013; '''8''' (1):e53804
Genome-wide association study of meat quality traits in a White DurocxErhualian F2 intercross and Chinese Sutai pigs. Description: Ma, Junwu, et al. Genome-wide association study of meat quality traits in a White DurocxErhualian F2 intercross and Chinese Sutai pigs. ''PLoS One''. 2013; '''8''' (5):e64047
Genome-wide association study on the development of cross-reactive neutralizing antibodies in HIV-1 infected individuals. Description: Euler, Zelda, et al. Genome-wide association study on the development of cross-reactive neutralizing antibodies in HIV-1 infected individuals. ''PLoS One''. 2013; '''8''' (1):e54684
Genome-wide association study reveals genetic architecture of eating behavior in pigs and its implications for humans obesity by comparative mapping. Description: Do, Duy Ngoc, et al. Genome-wide association study reveals genetic architecture of eating behavior in pigs and its implications for humans obesity by comparative mapping. ''PLoS One''. 2013; '''8''' (8):e71509
Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music. Description: Ukkola-Vuoti, Liisa, et al. Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music. ''PLoS One''. 2013; '''8''' (2):e56356
Genome-wide diversity in the levant reveals recent structuring by culture. Description: Haber, Marc, et al. Genome-wide diversity in the levant reveals recent structuring by culture. ''PLoS Genet''. 2013; '''9''' (2):e1003316
Genome-wide genetic diversity and differentially selected regions among Suffolk, Rambouillet, Columbia, Polypay, and Targhee sheep. Description: Zhang, Lifan, et al. Genome-wide genetic diversity and differentially selected regions among Suffolk, Rambouillet, Columbia, Polypay, and Targhee sheep. ''PLoS One''. 2013; '''8''' (6):e65942
Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family. Description: Nolan, Daniel, et al. Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family. ''PLoS One''. 2013; '''8''' (8):e71779
Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease. Description: Bhatnagar, Pallav, et al. Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease. ''PLoS One''. 2013; '''8''' (9):e74193
Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines. Description: Duan, Jubao, et al. Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines. ''Sci Rep''. 2013; '''3''': 1318
Genomic analysis of natural selection and phenotypic variation in high-altitude mongolians. Description: Xing, Jinchuan, et al. Genomic analysis of natural selection and phenotypic variation in high-altitude mongolians. ''PLoS Genet''. 2013; '''9''' (7):e1003634
Genomic risk models improve prediction of longitudinal lipid levels in children and young adults. Description: Wineinger, Nathan E, et al. Genomic risk models improve prediction of longitudinal lipid levels in children and young adults. ''Front Genet''. 2013; '''4''': 86
Genomics assisted ancestry deconvolution in grape. Description: Sawler, Jason, et al. Genomics assisted ancestry deconvolution in grape. ''PLoS One''. 2013; '''8''' (11):e80791
Global patterns of diversity and selection in human tyrosinase gene. Description: Hudjashov, Georgi, et al. Global patterns of diversity and selection in human tyrosinase gene. ''PLoS One''. 2013; '''8''' (9):e74307
Heritable influence of DBH on adrenergic and renal function: twin and disease studies. Description: Pasha, Dalal N, et al. Heritable influence of DBH on adrenergic and renal function: twin and disease studies. ''PLoS One''. 2013; '''8''' (12):e82956
*HLA-DQB103 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study.** Description: Miki, Daiki, et al. HLA-DQB1*03 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study. ''PLoS One''. 2013; '''8''' (12):e84226
How genome-wide SNP-SNP interactions relate to nasopharyngeal carcinoma susceptibility. Description: Su, Wen-Hui, et al. How genome-wide SNP-SNP interactions relate to nasopharyngeal carcinoma susceptibility. ''PLoS One''. 2013; '''8''' (12):e83034
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Description: Xu, Jianfeng, et al. HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). ''Hum Genet''. 2013 Jan; '''132''' (1):5-14
Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). Description: Sang, Qing, et al. Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). ''PLoS One''. 2013; '''8''' (1):e55178
Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma. Description: Raffler, Johannes, et al. Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma. ''Genome Med''. 2013; '''5''' (2):13
Identification of a 31-bp deletion in the RELN gene causing lissencephaly with cerebellar hypoplasia in sheep. Description: Suarez-Vega, Aroa, et al. Identification of a 31-bp deletion in the RELN gene causing lissencephaly with cerebellar hypoplasia in sheep. ''PLoS One''. 2013; '''8''' (11):e81072
Identification of a breast cancer susceptibility locus at 4q31.22 using a genome-wide association study paradigm. Description: Sapkota, Yadav, et al. Identification of a breast cancer susceptibility locus at 4q31.22 using a genome-wide association study paradigm. ''PLoS One''. 2013; '''8''' (5):e62550
Identification of a KEAP1 germline mutation in a family with multinodular goitre. Description: Teshiba, Risa, et al. Identification of a KEAP1 germline mutation in a family with multinodular goitre. ''PLoS One''. 2013; '''8''' (5):e65141
Identification of single nucleotide polymorphisms regulating peripheral blood mRNA expression with genome-wide significance: an eQTL study in the Japanese population. Description: Sasayama, Daimei, et al. Identification of single nucleotide polymorphisms regulating peripheral blood mRNA expression with genome-wide significance: an eQTL study in the Japanese population. ''PLoS One''. 2013; '''8''' (1):e54967
Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study. Description: Liu, Yang, et al. Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study. ''Sci Rep''. 2013; '''3''': 2147
Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis. Description: Lin, Rui, et al. Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis. ''PLoS One''. 2013; '''8''' (3):e56379
ImmunoChip study implicates antigen presentation to T cells in narcolepsy. Description: Faraco, Juliette, et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. ''PLoS Genet''. 2013; '''9''' (2):e1003270
Impact of PSCA variation on gastric ulcer susceptibility. Description: Tanikawa, Chizu, et al. Impact of PSCA variation on gastric ulcer susceptibility. ''PLoS One''. 2013; '''8''' (5):e63698
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Description: Wood, Andrew R, et al. Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. ''PLoS One''. 2013; '''8''' (5):e64343
Indian signatures in the westernmost edge of the European Romani diaspora: new insight from mitogenomes. Description: Gomez-Carballa, Alberto, et al. Indian signatures in the westernmost edge of the European Romani diaspora: new insight from mitogenomes. ''PLoS One''. 2013; '''8''' (10):e75397
Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel. Description: Kim, Sungeun, et al. Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel. ''PLoS One''. 2013; '''8''' (7):e70269
Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure. Description: Wangkumhang, Pongsakorn, et al. Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure. ''PLoS One''. 2013; '''8''' (11):e79522
Insulin-like growth factor 1 is not associated with high myopia in a large Japanese cohort. Description: Miyake, Masahiro, et al. Insulin-like growth factor 1 is not associated with high myopia in a large Japanese cohort. ''Mol Vis''. 2013; '''19''': 1074-81
Integrative analysis of mRNA expression and half-life data reveals trans-acting genetic variants associated with increased expression of stable transcripts. Description: Nguyen, Thong T, et al. Integrative analysis of mRNA expression and half-life data reveals trans-acting genetic variants associated with increased expression of stable transcripts. ''PLoS One''. 2013; '''8''' (11):e79627
Interactions between genetic variants in AMH and AMHR2 may modify age at natural menopause. Description: Braem, Marieke G M, et al. Interactions between genetic variants in AMH and AMHR2 may modify age at natural menopause. ''PLoS One''. 2013; '''8''' (3):e59819
Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2. Description: Diegelmann, Julia, et al. Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2. ''PLoS One''. 2013; '''8''' (11):e77773
Involvement of the neutral amino acid transporter SLC6A15 and leucine in obesity-related phenotypes. Description: Drgonova, Jana, et al. Involvement of the neutral amino acid transporter SLC6A15 and leucine in obesity-related phenotypes. ''PLoS One''. 2013; '''8''' (9):e68245
IRGM variants and susceptibility to inflammatory bowel disease in the German population. Description: Glas, Jurgen, et al. IRGM variants and susceptibility to inflammatory bowel disease in the German population. ''PLoS One''. 2013; '''8''' (1):e54338
Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology. Description: Zou, Fanggeng, et al. Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology. ''PLoS One''. 2013; '''8''' (5):e64802
Low frequency variants, collapsed based on biological knowledge, uncover complexity of population stratification in 1000 genomes project data. Description: Moore, Carrie B, et al. Low frequency variants, collapsed based on biological knowledge, uncover complexity of population stratification in 1000 genomes project data. ''PLoS Genet''. 2013; '''9''' (12):e1003959
Mapping of PARK2 and PACRG overlapping regulatory region reveals LD structure and functional variants in association with leprosy in unrelated indian population groups. Description: Chopra, Rupali, et al. Mapping of PARK2 and PACRG overlapping regulatory region reveals LD structure and functional variants in association with leprosy in unrelated indian population groups. ''PLoS Genet''. 2013; '''9''' (7):e1003578
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. Description: Mosley, Jonathan D, et al. Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. ''PLoS One''. 2013; '''8''' (12):e81503
MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus. Description: Deng, Yun, et al. MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus. ''PLoS Genet''. 2013; '''9''' (2):e1003336
Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed. Description: Forman, Oliver P, et al. Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed. ''PLoS One''. 2013; '''8''' (5):e64627
Multiple autoimmune-associated variants confer decreased IL-2R signaling in CD4+ CD25(hi) T cells of type 1 diabetic and multiple sclerosis patients. Description: Cerosaletti, Karen, et al. Multiple autoimmune-associated variants confer decreased IL-2R signaling in CD4+ CD25(hi) T cells of type 1 diabetic and multiple sclerosis patients. ''PLoS One''. 2013; '''8''' (12):e83811
Multi-population classical HLA type imputation. Description: Dilthey, Alexander, et al. Multi-population classical HLA type imputation. ''PLoS Comput Biol''. 2013; '''9''' (2):e1002877
Native American admixture in the Quebec founder population. Description: Moreau, Claudia, et al. Native American admixture in the Quebec founder population. ''PLoS One''. 2013; '''8''' (6):e65507
New insights into the genetic mechanism of IQ in autism spectrum disorders. Description: Wang, Harold Z, et al. New insights into the genetic mechanism of IQ in autism spectrum disorders. ''Front Genet''. 2013; '''4''': 195
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Description: Horikoshi, Momoko, et al. New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. ''Nat Genet''. 2013 Jan; '''45''' (1):76-82
No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort. Description: Bagshaw, Andrew T M, et al. No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort. ''PLoS One''. 2013; '''8''' (1):e55208
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls. Description: Hudson, Gavin, et al. No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls. ''Ann Rheum Dis''. 2013 Jan; '''72''' (1):136-9
No evidence of association between common autoimmunity STAT4 and IL23R risk polymorphisms and non-anterior uveitis. Description: Cenit, Maria Carmen, et al. No evidence of association between common autoimmunity STAT4 and IL23R risk polymorphisms and non-anterior uveitis. ''PLoS One''. 2013; '''8''' (11):e72892
North-South differentiation and a region of high diversity in European wolves (Canis lupus). Description: Stronen, Astrid V, et al. North-South differentiation and a region of high diversity in European wolves (Canis lupus). ''PLoS One''. 2013; '''8''' (10):e76454
Novel SACS mutations identified by whole exome sequencing in a norwegian family with autosomal recessive spastic ataxia of Charlevoix-Saguenay. Description: Tzoulis, Charalampos, et al. Novel SACS mutations identified by whole exome sequencing in a norwegian family with autosomal recessive spastic ataxia of Charlevoix-Saguenay. ''PLoS One''. 2013; '''8''' (6):e66145
Novel single nucleotide polymorphisms in interleukin 6 affect tacrolimus metabolism in liver transplant patients. Description: Chen, Dawei, et al. Novel single nucleotide polymorphisms in interleukin 6 affect tacrolimus metabolism in liver transplant patients. ''PLoS One''. 2013; '''8''' (8):e73405
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. Description: Mero, Inger-Lise, et al. Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. ''PLoS One''. 2013; '''8''' (3):e58352
Ovine HSP90AA1 expression rate is affected by several SNPs at the promoter under both basal and heat stress conditions. Description: Salces-Ortiz, Judit, et al. Ovine HSP90AA1 expression rate is affected by several SNPs at the promoter under both basal and heat stress conditions. ''PLoS One''. 2013; '''8''' (6):e66641
PADI2 is significantly associated with rheumatoid arthritis. Description: Chang, Xiaotian, et al. PADI2 is significantly associated with rheumatoid arthritis. ''PLoS One''. 2013; '''8''' (12):e81259
Pathway analysis using information from allele-specific gene methylation in genome-wide association studies for bipolar disorder. Description: Chuang, Li-Chung, et al. Pathway analysis using information from allele-specific gene methylation in genome-wide association studies for bipolar disorder. ''PLoS One''. 2013; '''8''' (1):e53092
Pharmacometabolomics reveals racial differences in response to atenolol treatment. Description: Wikoff, William R, et al. Pharmacometabolomics reveals racial differences in response to atenolol treatment. ''PLoS One''. 2013; '''8''' (3):e57639
Plasma level of adrenomedullin is influenced by a single nucleotide polymorphism in the adiponectin gene. Description: Wong, Hoi Kin, et al. Plasma level of adrenomedullin is influenced by a single nucleotide polymorphism in the adiponectin gene. ''PLoS One''. 2013; '''8''' (8):e70335
Polymorphism in serotonin receptor 3B is associated with pain catastrophizing. Description: Horjales-Araujo, Emilia, et al. Polymorphism in serotonin receptor 3B is associated with pain catastrophizing. ''PLoS One''. 2013; '''8''' (11):e78889
Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium. Description: Shah, Tina, et al. Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium. ''PLoS One''. 2013; '''8''' (8):e71345
Power analysis of C-TDT for small sample size genome-wide association studies by the joint use of case-parent trios and pairs. Description: Rajabli, Farid, et al. Power analysis of C-TDT for small sample size genome-wide association studies by the joint use of case-parent trios and pairs. ''Comput Math Methods Med''. 2013; '''2013''': 235825
Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression. Description: Sakurai, Daisuke, et al. Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression. ''PLoS Genet''. 2013; '''9''' (10):e1003870
PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes. Description: Namjou, Bahram, et al. PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes. ''PLoS One''. 2013; '''8''' (8):e69404
PUMA: a unified framework for penalized multiple regression analysis of GWAS data. Description: Hoffman, Gabriel E, et al. PUMA: a unified framework for penalized multiple regression analysis of GWAS data. ''PLoS Comput Biol''. 2013; '''9''' (6):e1003101
Rare copy number variants are a common cause of short stature. Description: Zahnleiter, Diana, et al. Rare copy number variants are a common cause of short stature. ''PLoS Genet''. 2013; '''9''' (3):e1003365
Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways. Description: Kerner, Berit, et al. Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways. ''Front Psychiatry''. 2013; '''4''': 154
Rare variants in PLXNA4 and Parkinson's disease. Description: Schulte, Eva C, et al. Rare variants in PLXNA4 and Parkinson's disease. ''PLoS One''. 2013; '''8''' (11):e79145
Reconstructing Roma history from genome-wide data. Description: Moorjani, Priya, et al. Reconstructing Roma history from genome-wide data. ''PLoS One''. 2013; '''8''' (3):e58633
Refining susceptibility loci of chronic obstructive pulmonary disease with lung eqtls. Description: Lamontagne, Maxime, et al. Refining susceptibility loci of chronic obstructive pulmonary disease with lung eqtls. ''PLoS One''. 2013; '''8''' (7):e70220
Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility. Description: Chang, Chia-Jung, et al. Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility. ''PLoS One''. 2013; '''8''' (8):e72037
Replication of association between schizophrenia and chromosome 6p21-6p22.1 polymorphisms in Chinese Han population. Description: Zhang, Yang, et al. Replication of association between schizophrenia and chromosome 6p21-6p22.1 polymorphisms in Chinese Han population. ''PLoS One''. 2013; '''8''' (2):e56732
Replication of genome wide association studies of alcohol dependence: support for association with variation in ADH1C. Description: Biernacka, Joanna M, et al. Replication of genome wide association studies of alcohol dependence: support for association with variation in ADH1C. ''PLoS One''. 2013; '''8''' (3):e58798
Replication of type 2 diabetes candidate genes variations in three geographically unrelated Indian population groups. Description: Ali, Shafat, et al. Replication of type 2 diabetes candidate genes variations in three geographically unrelated Indian population groups. ''PLoS One''. 2013; '''8''' (3):e58881
Replication study confirms link between TSPAN18 mutation and schizophrenia in Han Chinese. Description: Yuan, Jianmin, et al. Replication study confirms link between TSPAN18 mutation and schizophrenia in Han Chinese. ''PLoS One''. 2013; '''8''' (3):e58785
Resequencing three candidate genes for major depressive disorder in a Dutch cohort. Description: Verbeek, Eva C, et al. Resequencing three candidate genes for major depressive disorder in a Dutch cohort. ''PLoS One''. 2013; '''8''' (11):e79921
Role of HLA-DP polymorphisms on chronicity and disease activity of hepatitis B infection in Southern Chinese. Description: Wong, Danny Ka-Ho, et al. Role of HLA-DP polymorphisms on chronicity and disease activity of hepatitis B infection in Southern Chinese. ''PLoS One''. 2013; '''8''' (6):e66920
RPS19 and TYMS SNPs and Prevalent High Risk Human Papilloma Virus Infection in Nigerian Women. Description: Famooto, Ayo, et al. RPS19 and TYMS SNPs and Prevalent High Risk Human Papilloma Virus Infection in Nigerian Women. ''PLoS One''. 2013; '''8''' (6):e66930
Rs4074134 near BDNF gene is associated with type 2 diabetes mellitus in Chinese Han population independently of body mass index. Description: Han, Xueyao, et al. Rs4074134 near BDNF gene is associated with type 2 diabetes mellitus in Chinese Han population independently of body mass index. ''PLoS One''. 2013; '''8''' (2):e56898
RTK/ERK pathway under natural selection associated with prostate cancer. Description: Chen, Yang, et al. RTK/ERK pathway under natural selection associated with prostate cancer. ''PLoS One''. 2013; '''8''' (11):e78254
SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children. Description: Urayama, Kevin Y, et al. SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children. ''PLoS One''. 2013; '''8''' (8):e72557
SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays. Description: Weissensteiner, Hansi, et al. SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays. ''PLoS One''. 2013; '''8''' (3):e59508
Soluble guanylate cyclase alpha1-deficient mice: a novel murine model for primary open angle glaucoma. Description: Buys, Emmanuel S, et al. Soluble guanylate cyclase alpha1-deficient mice: a novel murine model for primary open angle glaucoma. ''PLoS One''. 2013; '''8''' (3):e60156
SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians. Description: Miyashita, Akinori, et al. SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians. ''PLoS One''. 2013; '''8''' (4):e58618
Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates. Description: Markunas, Christina A, et al. Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates. ''PLoS One''. 2013; '''8''' (4):e61521
Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. Description: Vijai, Joseph, et al. Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. ''PLoS Genet''. 2013; '''9''' (1):e1003220
TATES: efficient multivariate genotype-phenotype analysis for genome-wide association studies. Description: van der Sluis, Sophie, et al. TATES: efficient multivariate genotype-phenotype analysis for genome-wide association studies. ''PLoS Genet''. 2013; '''9''' (1):e1003235
The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population. Description: Radovica, Ilze, et al. The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population. ''PLoS One''. 2013; '''8''' (5):e64191
The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population. Description: Alobeidy, Barrak F, et al. The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population. ''PLoS One''. 2013; '''8''' (6):e66976
The geography of recent genetic ancestry across Europe. Description: Ralph, Peter, et al. The geography of recent genetic ancestry across Europe. ''PLoS Biol''. 2013; '''11''' (5):e1001555
The impact of genome-wide supported schizophrenia risk variants in the neurogranin gene on brain structure and function. Description: Walton, Esther, et al. The impact of genome-wide supported schizophrenia risk variants in the neurogranin gene on brain structure and function. ''PLoS One''. 2013; '''8''' (10):e76815
The impact of phenotypic and genetic heterogeneity on results of genome wide association studies of complex diseases. Description: Manchia, Mirko, et al. The impact of phenotypic and genetic heterogeneity on results of genome wide association studies of complex diseases. ''PLoS One''. 2013; '''8''' (10):e76295
The missing link of Jewish European ancestry: contrasting the Rhineland and the Khazarian hypotheses. Description: Elhaik, Eran. The missing link of Jewish European ancestry: contrasting the Rhineland and the Khazarian hypotheses. ''Genome Biol Evol''. 2013; '''5''' (1):61-74
The molecular genetic architecture of self-employment. Description: van der Loos, Matthijs J H M, et al. The molecular genetic architecture of self-employment. ''PLoS One''. 2013; '''8''' (4):e60542
The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits. Description: Uemoto, Yoshinobu, et al. The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits. ''Front Genet''. 2013; '''4''': 232
The presence of methylation quantitative trait loci indicates a direct genetic influence on the level of DNA methylation in adipose tissue. Description: Drong, Alexander W, et al. The presence of methylation quantitative trait loci indicates a direct genetic influence on the level of DNA methylation in adipose tissue. ''PLoS One''. 2013; '''8''' (2):e55923
The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-epsilon4 carriers. Description: Benitez, Bruno A, et al. The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-epsilon4 carriers. ''PLoS Genet''. 2013; '''9''' (8):e1003685
The role of SNP-loop diuretic interactions in hypertension across ethnic groups in HyperGEN. Description: de Las Fuentes, Lisa, et al. The role of SNP-loop diuretic interactions in hypertension across ethnic groups in HyperGEN. ''Front Genet''. 2013; '''4''': 304
The rs1142345 in TPMT Affects the Therapeutic Effect of Traditional Hypoglycemic Herbs in Prediabetes. Description: Li, Xi, et al. The rs1142345 in TPMT Affects the Therapeutic Effect of Traditional Hypoglycemic Herbs in Prediabetes. ''Evid Based Complement Alternat Med''. 2013; '''2013''': 327629
The STK33-linked SNP rs4929949 is associated with obesity and BMI in two independent cohorts of Swedish and Greek children. Description: Rask-Andersen, Mathias, et al. The STK33-linked SNP rs4929949 is associated with obesity and BMI in two independent cohorts of Swedish and Greek children. ''PLoS One''. 2013; '''8''' (8):e71353
The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis. Description: Carmona, F David, et al. The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis. ''PLoS One''. 2013; '''8''' (1):e54419
Thorough investigation of a canine autoinflammatory disease (AID) confirms one main risk locus and suggests a modifier locus for amyloidosis. Description: Olsson, Mia, et al. Thorough investigation of a canine autoinflammatory disease (AID) confirms one main risk locus and suggests a modifier locus for amyloidosis. ''PLoS One''. 2013; '''8''' (10):e75242
To the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat Breed. Description: Gandolfi, Barbara, et al. To the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat Breed. ''PLoS One''. 2013; '''8''' (6):e67105
Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4. Description: Manku, Harinder, et al. Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4. ''PLoS Genet''. 2013; '''9''' (7):e1003554
Two functional variants of IRF5 influence the development of macular edema in patients with non-anterior uveitis. Description: Marquez, Ana, et al. Two functional variants of IRF5 influence the development of macular edema in patients with non-anterior uveitis. ''PLoS One''. 2013; '''8''' (10):e76777
Ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in Koreans. Description: Yang, Jian, et al. Ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in Koreans. ''PLoS Genet''. 2013; '''9''' (3):e1003355
Use of net reclassification improvement (NRI) method confirms the utility of combined genetic risk score to predict type 2 diabetes. Description: Tam, Claudia H T, et al. Use of net reclassification improvement (NRI) method confirms the utility of combined genetic risk score to predict type 2 diabetes. ''PLoS One''. 2013; '''8''' (12):e83093
Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma. Description: Li, Lin, et al. Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma. ''Front Genet''. 2013; '''4''': 103
Utilizing twins as controls for non-twin case-materials in genome wide association studies. Description: Ganna, Andrea, et al. Utilizing twins as controls for non-twin case-materials in genome wide association studies. ''PLoS One''. 2013; '''8''' (12):e83101
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. Description: Frampton, Matthew, et al. Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. ''Nat Commun''. 2013; '''4''': 2549
Vitis phylogenomics: hybridization intensities from a SNP array outperform genotype calls. Description: Miller, Allison J, et al. Vitis phylogenomics: hybridization intensities from a SNP array outperform genotype calls. ''PLoS One''. 2013; '''8''' (11):e78680
Weighted SNP set analysis in genome-wide association study. Description: Dai, Hui, et al. Weighted SNP set analysis in genome-wide association study. ''PLoS One''. 2013; '''8''' (9):e75897
Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles. Description: Gracia-Aznarez, Francisco Javier, et al. Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles. ''PLoS One''. 2013; '''8''' (2):e55681
Whole Genome Association Studies of Residual Feed Intake and Related Traits in the Pig. Description: Onteru, Suneel K, et al. Whole Genome Association Studies of Residual Feed Intake and Related Traits in the Pig. ''PLoS One''. 2013; '''8''' (6):e61756
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism. Description: Proverbio, Maria Carla, et al. Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism. ''PLoS One''. 2013; '''8''' (7):e68740
Softwares and methods for estimating genetic ancestry in human populations. Description: Liu, Yushi, et al. Softwares and methods for estimating genetic ancestry in human populations. ''Hum Genomics''. 2013 Jan 5; '''7''': 1
From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software. Description: Forster, Michael, et al. From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software. ''Nucleic Acids Res''. 2013 Jan 7; '''41''' (1):e16
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12. Description: Fernandez-Rozadilla, Ceres, et al. A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12. ''BMC Genomics''. 2013 Jan 26; '''14''': 55
Association between paraoxonase gene and stroke in the Han Chinese population. Description: Zhang, Guojun, et al. Association between paraoxonase gene and stroke in the Han Chinese population. ''BMC Med Genet''. 2013 Jan 28; '''14''': 16
A gene-centric study of common carotid artery remodelling. Description: Harrison, Seamus C, et al. A gene-centric study of common carotid artery remodelling. ''Atherosclerosis''. 2013 Feb; '''226''' (2):440-6
CYP4A11 variant is associated with high-density lipoprotein cholesterol in women. Description: White, C C, et al. CYP4A11 variant is associated with high-density lipoprotein cholesterol in women. ''Pharmacogenomics J''. 2013 Feb; '''13''' (1):44-51
Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis. Description: Liu, Yun, et al. Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis. ''Nat Biotechnol''. 2013 Feb; '''31''' (2):142-7
Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways. Description: Deelen, Joris, et al. Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways. ''Age (Dordr)''. 2013 Feb; '''35''' (1):235-49
*Genetic association with ERAP1 in psoriasis is confined to disease onset after puberty and not dependent on HLA-C06.** Description: Lysell, Josefin, et al. Genetic association with ERAP1 in psoriasis is confined to disease onset after puberty and not dependent on HLA-C*06. ''J Invest Dermatol''. 2013 Feb; '''133''' (2):411-7
Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. Description: Jia, Wei-Hua, et al. Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. ''Nat Genet''. 2013 Feb; '''45''' (2):191-6
Genome-wide association analysis of copy number variation in recurrent depressive disorder. Description: Rucker, J J H, et al. Genome-wide association analysis of copy number variation in recurrent depressive disorder. ''Mol Psychiatry''. 2013 Feb; '''18''' (2):183-9
Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations. Description: Wheeler, H E, et al. Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations. ''Pharmacogenomics J''. 2013 Feb; '''13''' (1):35-43
The catechol-O-methyltransferase gene (COMT) and cognitive function from childhood through adolescence. Description: Gaysina, Darya, et al. The catechol-O-methyltransferase gene (COMT) and cognitive function from childhood through adolescence. ''Biol Psychol''. 2013 Feb; '''92''' (2):359-64
CrypticIBDcheck: an R package for checking cryptic relatedness in nominally unrelated individuals. Description: Nembot-Simo, Annick, et al. CrypticIBDcheck: an R package for checking cryptic relatedness in nominally unrelated individuals. ''Source Code Biol Med''. 2013 Feb 6; '''8''' (1):5
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Description: Chapman, Jade, et al. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. ''Hum Mol Genet''. 2013 Feb 15; '''22''' (4):816-24
High-density SNP-based genetic map development and linkage disequilibrium assessment in Brassica napus L. Description: Delourme, Regine, et al. High-density SNP-based genetic map development and linkage disequilibrium assessment in Brassica napus L. ''BMC Genomics''. 2013 Feb 22; '''14''': 120
A copy number variant at the KITLG locus likely confers risk for canine squamous cell carcinoma of the digit. Description: Karyadi, Danielle M, et al. A copy number variant at the KITLG locus likely confers risk for canine squamous cell carcinoma of the digit. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003409
Association between Interferon-Inducible Protein 6 (IFI6) Polymorphisms and Hepatitis B Virus Clearance. Description: Park, Geun-Hee, et al. Association between Interferon-Inducible Protein 6 (IFI6) Polymorphisms and Hepatitis B Virus Clearance. ''Genomics Inform''. 2013 Mar; '''11''' (1):15-23
Combined genome-wide linkage and association analyses of fasting glucose level in healthy twins and families of Korea. Description: Suh, Young Ju, et al. Combined genome-wide linkage and association analyses of fasting glucose level in healthy twins and families of Korea. ''J Korean Med Sci''. 2013 Mar; '''28''' (3):415-23
Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. Description: Gamazon, E R, et al. Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. ''Mol Psychiatry''. 2013 Mar; '''18''' (3):340-6
Genetic architecture of skin and eye color in an African-European admixed population. Description: Beleza, Sandra, et al. Genetic architecture of skin and eye color in an African-European admixed population. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003372
Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. Description: Cui, Jing, et al. Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003394
Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. Description: Tabassum, Rubina, et al. Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. ''Diabetes''. 2013 Mar; '''62''' (3):977-86
Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. Description: Peters, Marjolein J, et al. Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. ''Ann Rheum Dis''. 2013 Mar; '''72''' (3):427-36
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. Description: Lopes, Alexandra M, et al. Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003349
Maize chromosomal knobs are located in gene-dense areas and suppress local recombination. Description: Ghaffari, Rashin, et al. Maize chromosomal knobs are located in gene-dense areas and suppress local recombination. ''Chromosoma''. 2013 Mar; '''122''' (1-2):67-75
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Description: Kirby, Andrew, et al. Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. ''Nat Genet''. 2013 Mar; '''45''' (3):299-303
Study in 1790 Baltic men: FSHR Asn680Ser polymorphism affects total testes volume. Description: Grigorova, M, et al. Study in 1790 Baltic men: FSHR Asn680Ser polymorphism affects total testes volume. ''Andrology''. 2013 Mar; '''1''' (2):293-300
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. Description: Wu, Ying, et al. Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003379
Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. Description: Ng, Maggie C Y, et al. Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. ''Diabetes''. 2013 Mar; '''62''' (3):965-76
A candidate gene based approach validates Md-PG1 as the main responsible for a QTL impacting fruit texture in apple (Malus x domestica Borkh). Description: Longhi, Sara, et al. A candidate gene based approach validates Md-PG1 as the main responsible for a QTL impacting fruit texture in apple (Malus x domestica Borkh). ''BMC Plant Biol''. 2013 Mar 4; '''13''': 37
Multigenic nature of the mouse pulmonary adenoma progression 1 locus. Description: Dassano, Alice, et al. Multigenic nature of the mouse pulmonary adenoma progression 1 locus. ''BMC Genomics''. 2013 Mar 6; '''14''': 152
Schizophrenia susceptibility and NMDA-receptor mediated signalling: an association study involving 32 tagSNPs of DAO, DAOA, PPP3CC, and DTNBP1 genes. Description: Sacchetti, Emilio, et al. Schizophrenia susceptibility and NMDA-receptor mediated signalling: an association study involving 32 tagSNPs of DAO, DAOA, PPP3CC, and DTNBP1 genes. ''BMC Med Genet''. 2013 Mar 9; '''14''': 33
Patterns of population epigenomic diversity. Description: Schmitz, Robert J, et al. Patterns of population epigenomic diversity. ''Nature''. 2013 Mar 14; '''495''' (7440):193-8
A genome-wide association study of early menopause and the combined impact of identified variants. Description: Perry, John R B, et al. A genome-wide association study of early menopause and the combined impact of identified variants. ''Hum Mol Genet''. 2013 Apr 1; '''22''' (7):1465-72
All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. Description: Schork, Andrew J, et al. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. ''PLoS Genet''. 2013 Apr; '''9''' (4):e1003449
A polymorphism in the thyroid hormone receptor gene is associated with bronchodilator response in asthmatics. Description: Duan, Q L, et al. A polymorphism in the thyroid hormone receptor gene is associated with bronchodilator response in asthmatics. ''Pharmacogenomics J''. 2013 Apr; '''13''' (2):130-6
Genetic associations with neonatal thyroid-stimulating hormone levels. Description: Alul, Farah Y, et al. Genetic associations with neonatal thyroid-stimulating hormone levels. ''Pediatr Res''. 2013 Apr; '''73''' (4 Pt 1):484-91
Genetic diversity and phylogenetic analysis of native mountain ponies of Britain and Ireland reveals a novel rare population. Description: Winton, Clare L, et al. Genetic diversity and phylogenetic analysis of native mountain ponies of Britain and Ireland reveals a novel rare population. ''Ecol Evol''. 2013 Apr; '''3''' (4):934-47
Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep. Description: Demars, Julie, et al. Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep. ''PLoS Genet''. 2013 Apr; '''9''' (4):e1003482
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. Description: Cordell, Heather J, et al. Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. ''Hum Mol Genet''. 2013 Apr 1; '''22''' (7):1473-81
LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis. Description: Garcia-Martin, Elena, et al. LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis. ''BMC Neurol''. 2013 Apr 10; '''13''': 34
The ESR1 gene is associated with risk for canine mammary tumours. Description: Borge, Kaja Sverdrup, et al. The ESR1 gene is associated with risk for canine mammary tumours. ''BMC Vet Res''. 2013 Apr 10; '''9''': 69
LILRA3 is associated with benign prostatic hyperplasia risk in a Chinese Population. Description: Jiao, Yang, et al. LILRA3 is associated with benign prostatic hyperplasia risk in a Chinese Population. ''Int J Mol Sci''. 2013 Apr 24; '''14''' (5):8832-40
Centenarians as super-controls to assess the biological relevance of genetic risk factors for common age-related diseases: a proof of principle on type 2 diabetes. Description: Garagnani, Paolo, et al. Centenarians as super-controls to assess the biological relevance of genetic risk factors for common age-related diseases: a proof of principle on type 2 diabetes. ''Aging (Albany NY)''. 2013 May; '''5''' (5):373-85
Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. Description: Powell, Joseph E, et al. Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. ''PLoS Genet''. 2013 May; '''9''' (5):e1003502
Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. Description: Schmidts, Miriam, et al. Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. ''J Med Genet''. 2013 May; '''50''' (5):309-23
Genes encoding heterotrimeric G-proteins are associated with gray matter volume variations in the medial frontal cortex. Description: Chavarria-Siles, Ivan, et al. Genes encoding heterotrimeric G-proteins are associated with gray matter volume variations in the medial frontal cortex. ''Cereb Cortex''. 2013 May; '''23''' (5):1025-30
Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis. Description: Tengvall, Katarina, et al. Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis. ''PLoS Genet''. 2013 May; '''9''' (5):e1003475
Genome-wide analysis of runs of homozygosity identifies new susceptibility regions of lung cancer in Han Chinese. Description: Wang, Cheng, et al. Genome-wide analysis of runs of homozygosity identifies new susceptibility regions of lung cancer in Han Chinese. ''J Biomed Res''. 2013 May; '''27''' (3):208-14
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. Description: Saxena, Richa, et al. Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. ''Diabetes''. 2013 May; '''62''' (5):1746-55
Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway. Description: Li, Gang, et al. Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway. ''PLoS Genet''. 2013 May; '''9''' (5):e1003487
Replication of established common genetic variants for adult BMI and childhood obesity in Greek adolescents: the TEENAGE study. Description: Ntalla, Ioanna, et al. Replication of established common genetic variants for adult BMI and childhood obesity in Greek adolescents: the TEENAGE study. ''Ann Hum Genet''. 2013 May; '''77''' (3):268-74
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Description: Weinhold, Niels, et al. The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. ''Nat Genet''. 2013 May; '''45''' (5):522-525
The confounding effect of cryptic relatedness for environmental risks of systolic blood pressure on cohort studies. Description: Shibata, Kyoko, et al. The confounding effect of cryptic relatedness for environmental risks of systolic blood pressure on cohort studies. ''Mol Genet Genomic Med''. 2013 May; '''1''' (1):45-53
The impact of polymorphisms in STAT6 on treatment outcome in HCV infected Taiwanese Chinese. Description: Lim, Yun-Ping, et al. The impact of polymorphisms in STAT6 on treatment outcome in HCV infected Taiwanese Chinese. ''BMC Immunol''. 2013 May 8; '''14''': 21
Genome-wide association study of antibody response to Newcastle disease virus in chicken. Description: Luo, Chenglong, et al. Genome-wide association study of antibody response to Newcastle disease virus in chicken. ''BMC Genet''. 2013 May 10; '''14''': 42
Variants in the 3' UTR of general Transcription factor IIF, polypeptide 2 affect female calving efficiency in Japanese Black cattle. Description: Sasaki, Shinji, et al. Variants in the 3' UTR of general Transcription factor IIF, polypeptide 2 affect female calving efficiency in Japanese Black cattle. ''BMC Genet''. 2013 May 10; '''14''': 41
Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Description: Reitz, C, et al. Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). ''Transl Psychiatry''. 2013 May 14; '''3''': e256
Evaluation of the IL2/IL21, IL2RA and IL2RB genetic variants influence on the endogenous non-anterior uveitis genetic predisposition. Description: Cenit, Maria Carmen, et al. Evaluation of the IL2/IL21, IL2RA and IL2RB genetic variants influence on the endogenous non-anterior uveitis genetic predisposition. ''BMC Med Genet''. 2013 May 15; '''14''': 52
RTEL1 tagging SNPs and haplotypes were associated with glioma development. Description: Li, Gang, et al. RTEL1 tagging SNPs and haplotypes were associated with glioma development. ''Diagn Pathol''. 2013 May 17; '''8''': 83
Alzheimer's disease risk gene CD33 inhibits microglial uptake of amyloid beta. Description: Griciuc, Ana, et al. Alzheimer's disease risk gene CD33 inhibits microglial uptake of amyloid beta. ''Neuron''. 2013 May 22; '''78''' (4):631-43
A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage. Description: Rull, Kristiina, et al. A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage. ''Fertil Steril''. 2013 Jun; '''99''' (7):1930-6.e6
Association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression. Description: Duarte, J D, et al. Association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression. ''Pharmacogenomics J''. 2013 Jun; '''13''' (3):257-63
Common genetic variants associated with disease from genome-wide association studies are mutually exclusive in prostate cancer and rheumatoid arthritis. Description: Orozco, Gisela, et al. Common genetic variants associated with disease from genome-wide association studies are mutually exclusive in prostate cancer and rheumatoid arthritis. ''BJU Int''. 2013 Jun; '''111''' (7):1148-55
Definition of high-risk type 1 diabetes HLA-DR and HLA-DQ types using only three single nucleotide polymorphisms. Description: Nguyen, Cao, et al. Definition of high-risk type 1 diabetes HLA-DR and HLA-DQ types using only three single nucleotide polymorphisms. ''Diabetes''. 2013 Jun; '''62''' (6):2135-40
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. Description: Hinks, Anne, et al. Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. ''Nat Genet''. 2013 Jun; '''45''' (6):664-9
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Description: Liu, Jimmy Z, et al. Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. ''Nat Genet''. 2013 Jun; '''45''' (6):670-5
Exploring the genetic basis of chronic periodontitis: a genome-wide association study. Description: Divaris, Kimon, et al. Exploring the genetic basis of chronic periodontitis: a genome-wide association study. ''Hum Mol Genet''. 2013 Jun 1; '''22''' (11):2312-24
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. Description: Grarup, Niels, et al. Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. ''PLoS Genet''. 2013 Jun; '''9''' (6):e1003530
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. Description: Esko, Tonu, et al. Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. ''Eur J Hum Genet''. 2013 Jun; '''21''' (6):659-65
Genetic polymorphisms in key methotrexate pathway genes are associated with response to treatment in rheumatoid arthritis patients. Description: Owen, S A, et al. Genetic polymorphisms in key methotrexate pathway genes are associated with response to treatment in rheumatoid arthritis patients. ''Pharmacogenomics J''. 2013 Jun; '''13''' (3):227-34
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. Description: Ma, R C W, et al. Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. ''Diabetologia''. 2013 Jun; '''56''' (6):1291-305
Genome-wide association study of lung cancer in Korean non-smoking women. Description: Kim, Jin Hee, et al. Genome-wide association study of lung cancer in Korean non-smoking women. ''J Korean Med Sci''. 2013 Jun; '''28''' (6):840-7
Genome-wide association study of Tourette's syndrome. Description: Scharf, J M, et al. Genome-wide association study of Tourette's syndrome. ''Mol Psychiatry''. 2013 Jun; '''18''' (6):721-8
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14. Description: Ruark, Elise, et al. Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14. ''Nat Genet''. 2013 Jun; '''45''' (6):686-9
Link between GIP and osteopontin in adipose tissue and insulin resistance. Description: Ahlqvist, Emma, et al. Link between GIP and osteopontin in adipose tissue and insulin resistance. ''Diabetes''. 2013 Jun; '''62''' (6):2088-94
Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia. Description: Miotto, Olivo, et al. Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia. ''Nat Genet''. 2013 Jun; '''45''' (6):648-55
Peeling back the evolutionary layers of molecular mechanisms responsive to exercise-stress in the skeletal muscle of the racing horse. Description: Kim, Hyeongmin, et al. Peeling back the evolutionary layers of molecular mechanisms responsive to exercise-stress in the skeletal muscle of the racing horse. ''DNA Res''. 2013 Jun; '''20''' (3):287-98
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. Description: Randall, Joshua C, et al. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. ''PLoS Genet''. 2013 Jun; '''9''' (6):e1003500
Association study of NRXN3 polymorphisms with schizophrenia and risperidone-induced bodyweight gain in Chinese Han population. Description: Hu, Xiaofeng, et al. Association study of NRXN3 polymorphisms with schizophrenia and risperidone-induced bodyweight gain in Chinese Han population. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2013 Jun 3; '''43''': 197-202
Passive and active DNA methylation and the interplay with genetic variation in gene regulation. Description: Gutierrez-Arcelus, Maria, et al. Passive and active DNA methylation and the interplay with genetic variation in gene regulation. ''Elife''. 2013 Jun 4; '''2''': e00523
Comprehensive genotyping of the USA national maize inbred seed bank. Description: Romay, Maria C, et al. Comprehensive genotyping of the USA national maize inbred seed bank. ''Genome Biol''. 2013 Jun 11; '''14''' (6):R55
Novel genomic approaches unravel genetic architecture of complex traits in apple. Description: Kumar, Satish, et al. Novel genomic approaches unravel genetic architecture of complex traits in apple. ''BMC Genomics''. 2013 Jun 12; '''14''': 393
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression. Description: Kote-Jarai, Zsofia, et al. Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression. ''Hum Mol Genet''. 2013 Jun 15; '''22''' (12):2520-8
Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia. Description: Fedorova, Sardana A, et al. Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia. ''BMC Evol Biol''. 2013 Jun 19; '''13''': 127
A DPYD variant (Y186C) in individuals of african ancestry is associated with reduced DPD enzyme activity. Description: Offer, S M, et al. A DPYD variant (Y186C) in individuals of african ancestry is associated with reduced DPD enzyme activity. ''Clin Pharmacol Ther''. 2013 Jul; '''94''' (1):158-66
A Novel ERAP2 Haplotype Structure in a Chilean Population: Implications for ERAP2 Protein Expression and Preeclampsia Risk. Description: Vanhille, Derek L, et al. A Novel ERAP2 Haplotype Structure in a Chilean Population: Implications for ERAP2 Protein Expression and Preeclampsia Risk. ''Mol Genet Genomic Med''. 2013 Jul 1; '''1''' (2):98-107
An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease. Description: Chu, Xun, et al. An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease. ''J Med Genet''. 2013 Jul; '''50''' (7):479-85
CD33 Alzheimer's disease locus: altered monocyte function and amyloid biology. Description: Bradshaw, Elizabeth M, et al. CD33 Alzheimer's disease locus: altered monocyte function and amyloid biology. ''Nat Neurosci''. 2013 Jul; '''16''' (7):848-50
Further evidence for association of polymorphisms in the CNR1 gene with cocaine addiction: confirmation in an independent sample and meta-analysis. Description: Clarke, Toni-Kim, et al. Further evidence for association of polymorphisms in the CNR1 gene with cocaine addiction: confirmation in an independent sample and meta-analysis. ''Addict Biol''. 2013 Jul; '''18''' (4):702-8
Identification of the NF-kappaB activating protein-like locus as a risk locus for rheumatoid arthritis. Description: Xie, Gang, et al. Identification of the NF-kappaB activating protein-like locus as a risk locus for rheumatoid arthritis. ''Ann Rheum Dis''. 2013 Jul; '''72''' (7):1249-54
Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel. Description: Nievergelt, Caroline M, et al. Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel. ''Investig Genet''. 2013 Jul 1; '''4''' (1):13
Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects. Description: Williams, Frances M K, et al. Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects. ''Ann Rheum Dis''. 2013 Jul; '''72''' (7):1141-8
Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels. Description: Kloiber, Stefan, et al. Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels. ''Eur Neuropsychopharmacol''. 2013 Jul; '''23''' (7):653-62
Variation in tau isoform expression in different brain regions and disease states. Description: Majounie, Elisa, et al. Variation in tau isoform expression in different brain regions and disease states. ''Neurobiol Aging''. 2013 Jul; '''34''' (7):1922.e7-1922.e12
Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study. Description: Ding, Keyue, et al. Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study. ''G3 (Bethesda)''. 2013 Jul 8; '''3''' (7):1061-8
The identification of 14 new genes for meat quality traits in chicken using a genome-wide association study. Description: Sun, Yanfa, et al. The identification of 14 new genes for meat quality traits in chicken using a genome-wide association study. ''BMC Genomics''. 2013 Jul 8; '''14''': 458
Using genome-wide association analysis to characterize environmental sensitivity of milk traits in dairy cattle. Description: Streit, Melanie, et al. Using genome-wide association analysis to characterize environmental sensitivity of milk traits in dairy cattle. ''G3 (Bethesda)''. 2013 Jul 8; '''3''' (7):1085-93
SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. Description: Chudasama, Kishan Kumar, et al. SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. ''Am J Hum Genet''. 2013 Jul 11; '''93''' (1):150-7
Integrative genomic analysis of the human immune response to influenza vaccination. Description: Franco, Luis M, et al. Integrative genomic analysis of the human immune response to influenza vaccination. ''Elife''. 2013 Jul 16; '''2''': e00299
Analysis of copy number variants by three detection algorithms and their association with body size in horses. Description: Metzger, Julia, et al. Analysis of copy number variants by three detection algorithms and their association with body size in horses. ''BMC Genomics''. 2013 Jul 18; '''14''': 487
Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis. Description: Parry, Helen M, et al. Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis. ''Cardiovasc Diabetol''. 2013 Jul 23; '''12''': 109
Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults. Description: Teraishi, Toshiya, et al. Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults. ''Behav Brain Funct''. 2013 Jul 30; '''9''': 30
A genome-wide association study of post-traumatic stress disorder identifies the retinoid-related orphan receptor alpha (RORA) gene as a significant risk locus. Description: Logue, M W, et al. A genome-wide association study of post-traumatic stress disorder identifies the retinoid-related orphan receptor alpha (RORA) gene as a significant risk locus. ''Mol Psychiatry''. 2013 Aug; '''18''' (8):937-42
Effects of common genetic variants associated with type 2 diabetes and glycemic traits on alpha- and beta-cell function and insulin action in humans. Description: Jonsson, Anna, et al. Effects of common genetic variants associated with type 2 diabetes and glycemic traits on alpha- and beta-cell function and insulin action in humans. ''Diabetes''. 2013 Aug; '''62''' (8):2978-83
EvoSNP-DB: A database of genetic diversity in East Asian populations. Description: Kim, Young Uk, et al. EvoSNP-DB: A database of genetic diversity in East Asian populations. ''BMB Rep''. 2013 Aug; '''46''' (8):416-21
Polygenic risk and white matter integrity in individuals at high risk of mood disorder. Description: Whalley, Heather C, et al. Polygenic risk and white matter integrity in individuals at high risk of mood disorder. ''Biol Psychiatry''. 2013 Aug 15; '''74''' (4):280-6
QTL mapping of egg albumen quality in egg layers. Description: Honkatukia, Mervi, et al. QTL mapping of egg albumen quality in egg layers. ''Genet Sel Evol''. 2013 Aug 16; '''45''': 31
Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome. Description: Campbell, Nicholas G, et al. Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome. ''Mol Autism''. 2013 Aug 16; '''4''' (1):28
Generalization of adiposity genetic loci to US Hispanic women. Description: Graff, M, et al. Generalization of adiposity genetic loci to US Hispanic women. ''Nutr Diabetes''. 2013 Aug 26; '''3''': e85
Molecular footprints of domestication and improvement in soybean revealed by whole genome re-sequencing. Description: Li, Ying-hui, et al. Molecular footprints of domestication and improvement in soybean revealed by whole genome re-sequencing. ''BMC Genomics''. 2013 Aug 28; '''14''': 579
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. Description: Clayton, P, et al. A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. ''Eur J Endocrinol''. 2013 Sep; '''169''' (3):277-89
Association of matrix metalloproteinase 8 genetic polymorphisms with bronchial asthma in a Japanese population. Description: Shimoda, Terufumi, et al. Association of matrix metalloproteinase 8 genetic polymorphisms with bronchial asthma in a Japanese population. ''Allergy Rhinol (Providence)''. 2013 Fall; '''4''' (3):e132-9
Gene set analyses of genome-wide association studies on 49 quantitative traits measured in a single genetic epidemiology dataset. Description: Kim, Jihye, et al. Gene set analyses of genome-wide association studies on 49 quantitative traits measured in a single genetic epidemiology dataset. ''Genomics Inform''. 2013 Sep; '''11''' (3):135-41
Genome-wide association study of liver enzymes in korean children. Description: Park, Tae-Joon, et al. Genome-wide association study of liver enzymes in korean children. ''Genomics Inform''. 2013 Sep; '''11''' (3):149-54
Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations. Description: Hong, Kyung-Won, et al. Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations. ''Genomics Inform''. 2013 Sep; '''11''' (3):129-34
Identification of grouped rare and common variants via penalized logistic regression. Description: Ayers, Kristin L, et al. Identification of grouped rare and common variants via penalized logistic regression. ''Genet Epidemiol''. 2013 Sep; '''37''' (6):592-602
Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi Jews. Description: Liu, X, et al. Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi Jews. ''Mol Genet Genomic Med''. 2013 Sep; '''1''' (3):142-154
mu-Opioid receptor gene (OPRM1) polymorphism A118G: lack of association in Finnish populations with alcohol dependence or alcohol consumption. Description: Rouvinen-Lagerstrom, Noora, et al. mu-Opioid receptor gene (OPRM1) polymorphism A118G: lack of association in Finnish populations with alcohol dependence or alcohol consumption. ''Alcohol Alcohol''. 2013 Sep-Oct; '''48''' (5):519-25
Replication study of RAD54B and GREB1 polymorphisms and risk of PCOS in Han Chinese. Description: Wang, Zhenyan, et al. Replication study of RAD54B and GREB1 polymorphisms and risk of PCOS in Han Chinese. ''Reprod Biomed Online''. 2013 Sep; '''27''' (3):316-21
Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. Description: Jones, Ashley R, et al. Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. ''Neurobiol Aging''. 2013 Sep; '''34''' (9):2234.e1-7
A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. Description: Martin, P-M, et al. A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. ''Transl Psychiatry''. 2013 Sep 3; '''3''': e301
Signatures of selection identify loci associated with milk yield in sheep. Description: Moioli, Bianca, et al. Signatures of selection identify loci associated with milk yield in sheep. ''BMC Genet''. 2013 Sep 3; '''14''': 76
Association between rs10118757(A/G) in methylthioadenosine phosphorylase gene and coronary artery disease in Chinese Hans. Description: Lv, Xiaofei, et al. Association between rs10118757(A/G) in methylthioadenosine phosphorylase gene and coronary artery disease in Chinese Hans. ''Gene''. 2013 Sep 10; '''526''' (2):344-6
Genome-wide association analyses for carcass quality in crossbred beef cattle. Description: Lu, Duc, et al. Genome-wide association analyses for carcass quality in crossbred beef cattle. ''BMC Genet''. 2013 Sep 11; '''14''': 80
Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease. Description: Bishop, Matthew T, et al. Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease. ''BMC Med Genet''. 2013 Sep 12; '''14''': 91
Genetic diversity in black South Africans from Soweto. Description: May, Andrew, et al. Genetic diversity in black South Africans from Soweto. ''BMC Genomics''. 2013 Sep 23; '''14''': 644
Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease. Description: Gao, Kai, et al. Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease. ''BMC Neurol''. 2013 Sep 25; '''13''': 125
Improved estimation of inbreeding and kinship in pigs using optimized SNP panels. Description: Lopes, Marcos S, et al. Improved estimation of inbreeding and kinship in pigs using optimized SNP panels. ''BMC Genet''. 2013 Sep 25; '''14''': 92
Single nucleotide polymorphisms and haplotypes associated with feed efficiency in beef cattle. Description: Serao, Nick Vl, et al. Single nucleotide polymorphisms and haplotypes associated with feed efficiency in beef cattle. ''BMC Genet''. 2013 Sep 25; '''14''': 94
Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway. Description: Lee, James C, et al. Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway. ''Cell''. 2013 Sep 26; '''155''' (1):57-69
Associations between single-nucleotide polymorphism in the FNDC3A and autism spectrum disorder in a Korean population. Description: Ro, Myungja, et al. Associations between single-nucleotide polymorphism in the FNDC3A and autism spectrum disorder in a Korean population. ''Psychiatry Res''. 2013 Sep 30; '''209''' (2):246-8
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Description: Chubb, Daniel, et al. Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. ''Nat Genet''. 2013 Oct; '''45''' (10):1221-1225
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Description: Kasperaviciute, Dalia, et al. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. ''Brain''. 2013 Oct; '''136''' (Pt 10):3140-50
Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome. Description: Jones, Emma L, et al. Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome. ''Neurobiol Aging''. 2013 Oct; '''34''' (10):2441.e1-5
Genetic modifiers of cystic fibrosis-related diabetes. Description: Blackman, Scott M, et al. Genetic modifiers of cystic fibrosis-related diabetes. ''Diabetes''. 2013 Oct; '''62''' (10):3627-35
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. Description: Han, Fang, et al. Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. ''PLoS Genet''. 2013 Oct; '''9''' (10):e1003880
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Description: Ripke, Stephan, et al. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. ''Nat Genet''. 2013 Oct; '''45''' (10):1150-9
Mining the human phenome using allelic scores that index biological intermediates. Description: Evans, David M, et al. Mining the human phenome using allelic scores that index biological intermediates. ''PLoS Genet''. 2013 Oct; '''9''' (10):e1003919
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Description: Davis, Lea K, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. ''PLoS Genet''. 2013 Oct; '''9''' (10):e1003864
Genome-wide association study on serum alkaline phosphatase levels in a Chinese population. Description: Li, Jun, et al. Genome-wide association study on serum alkaline phosphatase levels in a Chinese population. ''BMC Genomics''. 2013 Oct 5; '''14''': 684
A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral control. Description: Bartha, Istvan, et al. A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral control. ''Elife''. 2013 Oct 29; '''2''': e01123
Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects. Description: Henry, N L, et al. Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects. ''Br J Cancer''. 2013 Oct 29; '''109''' (9):2331-9
An association study of TOLL and CARD with leprosy susceptibility in Chinese population. Description: Liu, Hong, et al. An association study of TOLL and CARD with leprosy susceptibility in Chinese population. ''Hum Mol Genet''. 2013 Nov 1; '''22''' (21):4430-7
Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation. Description: Bonnycastle, Lori L, et al. Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation. ''Diabetes''. 2013 Nov; '''62''' (11):3943-50
Developmental programming of growth: genetic variant in GH2 gene encoding placental growth hormone contributes to adult height determination. Description: Timasheva, Y, et al. Developmental programming of growth: genetic variant in GH2 gene encoding placental growth hormone contributes to adult height determination. ''Placenta''. 2013 Nov; '''34''' (11):995-1001
Discovery and refinement of loci associated with lipid levels. Description: Willer, Cristen J, et al. Discovery and refinement of loci associated with lipid levels. ''Nat Genet''. 2013 Nov; '''45''' (11):1274-1283
Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects. Description: Patsopoulos, Nikolaos A, et al. Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects. ''PLoS Genet''. 2013 Nov; '''9''' (11):e1003926
Genetic susceptibility to obesity and diet intakes: association and interaction analyses in the Malmo Diet and Cancer Study. Description: Rukh, Gull, et al. Genetic susceptibility to obesity and diet intakes: association and interaction analyses in the Malmo Diet and Cancer Study. ''Genes Nutr''. 2013 Nov; '''8''' (6):535-47
Genome-wide Association Study of Chicken Plumage Pigmentation. Description: Park, Mi Na, et al. Genome-wide Association Study of Chicken Plumage Pigmentation. ''Asian-Australas J Anim Sci''. 2013 Nov; '''26''' (11):1523-8
Reconstructing the population genetic history of the Caribbean. Description: Moreno-Estrada, Andres, et al. Reconstructing the population genetic history of the Caribbean. ''PLoS Genet''. 2013 Nov; '''9''' (11):e1003925
Ridge regression in prediction problems: automatic choice of the ridge parameter. Description: Cule, Erika, et al. Ridge regression in prediction problems: automatic choice of the ridge parameter. ''Genet Epidemiol''. 2013 Nov; '''37''' (7):704-14
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjogren's syndrome. Description: Lessard, Christopher J, et al. Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjogren's syndrome. ''Nat Genet''. 2013 Nov; '''45''' (11):1284-92
Variation in psychosis gene ZNF804A is associated with a refined schizotypy phenotype but not neurocognitive performance in a large young male population. Description: Stefanis, Nicholas C, et al. Variation in psychosis gene ZNF804A is associated with a refined schizotypy phenotype but not neurocognitive performance in a large young male population. ''Schizophr Bull''. 2013 Nov; '''39''' (6):1252-60
Association of Parkinson disease with structural and regulatory variants in the HLA region. Description: Wissemann, William T, et al. Association of Parkinson disease with structural and regulatory variants in the HLA region. ''Am J Hum Genet''. 2013 Nov 7; '''93''' (5):984-93
The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies. Description: Steinberg, Julia, et al. The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies. ''Am J Hum Genet''. 2013 Nov 7; '''93''' (5):825-39
Body mass index, but not FTO genotype or major depressive disorder, influences brain structure. Description: Cole, J H, et al. Body mass index, but not FTO genotype or major depressive disorder, influences brain structure. ''Neuroscience''. 2013 Nov 12; '''252''': 109-17
Emerging paradigms in genomics-based crop improvement. Description: Bohra, Abhishek. Emerging paradigms in genomics-based crop improvement. ''ScientificWorldJournal''. 2013 Nov 17; '''2013''': 585467
A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease. Description: Hill-Burns, E M, et al. A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease. ''Pharmacogenomics J''. 2013 Dec; '''13''' (6):530-7
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Description: Weidinger, Stephan, et al. A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. ''Hum Mol Genet''. 2013 Dec 1; '''22''' (23):4841-56
Gene-environment interaction effects on lung function- a genome-wide association study within the Framingham heart study. Description: Liao, Shu-Yi, et al. Gene-environment interaction effects on lung function- a genome-wide association study within the Framingham heart study. ''Environ Health''. 2013 Dec 1; '''12''': 101
Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference. Description: Chen, Jiayu, et al. Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference. ''Neuroimage''. 2013 Dec; '''83''': 384-96
RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families. Description: Domarkiene, I, et al. RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families. ''Balkan J Med Genet''. 2013 Dec; '''16''' (2):17-22
Pathways systematically associated to Hirschsprung's disease. Description: Fernandez, Raquel M, et al. Pathways systematically associated to Hirschsprung's disease. ''Orphanet J Rare Dis''. 2013 Dec 2; '''8''': 187
Discovering epistasis in large scale genetic association studies by exploiting graphics cards. Description: Chen, Gary K, et al. Discovering epistasis in large scale genetic association studies by exploiting graphics cards. ''Front Genet''. 2013 Dec 3; '''4''': 266
Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism. Description: Warrier, Varun, et al. Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism. ''Mol Autism''. 2013 Dec 9; '''4''' (1):48
Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B. Description: Karlsson, Elinor K, et al. Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B. ''Genome Biol''. 2013 Dec 12; '''14''' (12):R132
Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease). Description: Xie, Zhihui, et al. Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease). ''Rare Dis''. 2013 Dec 12; '''1''' (1):
Genomic divergence of zebu and taurine cattle identified through high-density SNP genotyping. Description: Porto-Neto, Laercio R, et al. Genomic divergence of zebu and taurine cattle identified through high-density SNP genotyping. ''BMC Genomics''. 2013 Dec 13; '''14''': 876
A genome wide study of genetic adaptation to high altitude in feral Andean Horses of the paramo. Description: Hendrickson, Sher L. A genome wide study of genetic adaptation to high altitude in feral Andean Horses of the paramo. ''BMC Evol Biol''. 2013 Dec 17; '''13''': 273
RNA-Seq optimization with eQTL gold standards. Description: Ellis, Shannon E, et al. RNA-Seq optimization with eQTL gold standards. ''BMC Genomics''. 2013 Dec 17; '''14''': 892
Dysregulation of glucocorticoid receptor co-factors FKBP5, BAG1 and PTGES3 in prefrontal cortex in psychotic illness. Description: Sinclair, Duncan, et al. Dysregulation of glucocorticoid receptor co-factors FKBP5, BAG1 and PTGES3 in prefrontal cortex in psychotic illness. ''Sci Rep''. 2013 Dec 18; '''3''': 3539
Genome wide association studies in presence of misclassified binary responses. Description: Smith, Shannon, et al. Genome wide association studies in presence of misclassified binary responses. ''BMC Genet''. 2013 Dec 26; '''14''': 124
A 3'UTR polymorphism of IL-6R is associated with Chinese pediatric tuberculosis. Description: Shen, Chen, et al. A 3'UTR polymorphism of IL-6R is associated with Chinese pediatric tuberculosis. ''Biomed Res Int''. 2014; '''2014''': 483759
A candidate gene approach identifies an IL33 genetic variant as a novel genetic risk factor for GCA. Description: Marquez, Ana, et al. A candidate gene approach identifies an IL33 genetic variant as a novel genetic risk factor for GCA. ''PLoS One''. 2014; '''9''' (11):e113476
A CARD9 polymorphism is associated with decreased likelihood of persistent conjugated hyperbilirubinemia in intestinal failure. Description: Burghardt, Karolina Maria, et al. A CARD9 polymorphism is associated with decreased likelihood of persistent conjugated hyperbilirubinemia in intestinal failure. ''PLoS One''. 2014; '''9''' (1):e85915
Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases. Description: Chang, Diana, et al. Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases. ''PLoS One''. 2014; '''9''' (12):e113684
Accounting for relatedness in family-based association studies: application to Genetic Analysis Workshop 18 data. Description: Eu-Ahsunthornwattana, Jakris, et al. Accounting for relatedness in family-based association studies: application to Genetic Analysis Workshop 18 data. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S79
Accurate and robust prediction of genetic relationship from whole-genome sequences. Description: Li, Hong, et al. Accurate and robust prediction of genetic relationship from whole-genome sequences. ''PLoS One''. 2014; '''9''' (2):e85437
A chromosomal region on ECA13 is associated with maxillary prognathism in horses. Description: Signer-Hasler, Heidi, et al. A chromosomal region on ECA13 is associated with maxillary prognathism in horses. ''PLoS One''. 2014; '''9''' (1):e86607
A co-association network analysis of the genetic determination of pig conformation, growth and fatness. Description: Puig-Oliveras, Anna, et al. A co-association network analysis of the genetic determination of pig conformation, growth and fatness. ''PLoS One''. 2014; '''9''' (12):e114862
A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. Description: Real, Luis M, et al. A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. ''PLoS One''. 2014; '''9''' (6):e101178
A COLQ missense mutation in Labrador Retrievers having congenital myasthenic syndrome. Description: Rinz, Caitlin J, et al. A COLQ missense mutation in Labrador Retrievers having congenital myasthenic syndrome. ''PLoS One''. 2014; '''9''' (8):e106425
A comparison of multivariate genome-wide association methods. Description: Galesloot, Tessel E, et al. A comparison of multivariate genome-wide association methods. ''PLoS One''. 2014; '''9''' (4):e95923
A comparison of whole genome sequencing with exome sequencing for family-based association studies. Description: Lacey, Sean, et al. A comparison of whole genome sequencing with exome sequencing for family-based association studies. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S38
Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans. Description: Jeff, Janina M, et al. Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans. ''PLoS One''. 2014; '''9''' (3):e86931
A genetic variant in 12q13, a possible risk factor for bipolar disorder, is associated with depressive state, accounting for stressful life events. Description: Shimasaki, Ayu, et al. A genetic variant in 12q13, a possible risk factor for bipolar disorder, is associated with depressive state, accounting for stressful life events. ''PLoS One''. 2014; '''9''' (12):e115135
A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA. Description: Awata, Takuya, et al. A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA. ''PLoS One''. 2014; '''9''' (11):e111715
A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese. Description: Liu, Yun, et al. A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese. ''PLoS One''. 2014; '''9''' (1):e85043
A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study. Description: Baron-Cohen, Simon, et al. A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study. ''PLoS One''. 2014; '''9''' (5):e96374
A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. Description: Chang, Su-Wei, et al. A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. ''PLoS One''. 2014; '''9''' (6):e99724
A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis. Description: Rafiq, Sajjad, et al. A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis. ''PLoS One''. 2014; '''9''' (12):e101488
A genome-wide "pleiotropy scan" does not identify new susceptibility loci for estrogen receptor negative breast cancer. Description: Campa, Daniele, et al. A genome-wide "pleiotropy scan" does not identify new susceptibility loci for estrogen receptor negative breast cancer. ''PLoS One''. 2014; '''9''' (2):e85955
Allele-specific methylation occurs at genetic variants associated with complex disease. Description: Hutchinson, John N, et al. Allele-specific methylation occurs at genetic variants associated with complex disease. ''PLoS One''. 2014; '''9''' (6):e98464
Allelic variant in the anti-Mullerian hormone gene leads to autosomal and temperature-dependent sex reversal in a selected Nile tilapia line. Description: Wessels, Stephan, et al. Allelic variant in the anti-Mullerian hormone gene leads to autosomal and temperature-dependent sex reversal in a selected Nile tilapia line. ''PLoS One''. 2014; '''9''' (8):e104795
A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH). Description: Drogemuller, Michaela, et al. A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH). ''PLoS Genet''. 2014; '''10''' (5):e1004370
An adaptive permutation approach for genome-wide association study: evaluation and recommendations for use. Description: Che, Ronglin, et al. An adaptive permutation approach for genome-wide association study: evaluation and recommendations for use. ''BioData Min''. 2014; '''7''': 9
Analysis of ancestral and functionally relevant CD5 variants in systemic lupus erythematosus patients. Description: Cenit, Maria Carmen, et al. Analysis of ancestral and functionally relevant CD5 variants in systemic lupus erythematosus patients. ''PLoS One''. 2014; '''9''' (11):e113090
Analysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels. Description: Ma, Li, et al. Analysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels. ''PLoS One''. 2014; '''9''' (3):e92469
Analysis of nuclear export sequence regions of FUS-Related RNA-binding proteins in essential tremor. Description: Lorenzo-Betancor, Oswaldo, et al. Analysis of nuclear export sequence regions of FUS-Related RNA-binding proteins in essential tremor. ''PLoS One''. 2014; '''9''' (11):e111989
A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development. Description: Darlow, J M, et al. A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development. ''Mol Genet Genomic Med''. 2014 Jan; '''2''' (1):7-29
An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers. Description: Downs, Louise M, et al. An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers. ''PLoS One''. 2014; '''9''' (4):e93990
A novel missense mutation in ADAMTS10 in Norwegian Elkhound primary glaucoma. Description: Ahonen, Saija J, et al. A novel missense mutation in ADAMTS10 in Norwegian Elkhound primary glaucoma. ''PLoS One''. 2014; '''9''' (11):e111941
A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever. Description: Downs, Louise M, et al. A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever. ''Canine Genet Epidemiol''. 2014; '''1''': 4
A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias. Description: Siddiqi, Saima, et al. A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias. ''PLoS One''. 2014; '''9''' (12):e113258
Applying compressed sensing to genome-wide association studies. Description: Vattikuti, Shashaank, et al. Applying compressed sensing to genome-wide association studies. ''Gigascience''. 2014; '''3''': 10
Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence? Description: Sieradzka, Dominika, et al. Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence? ''PLoS One''. 2014; '''9''' (4):e94398
A regulatory polymorphism in HAVCR2 modulates susceptibility to HIV-1 infection. Description: Sironi, Manuela, et al. A regulatory polymorphism in HAVCR2 modulates susceptibility to HIV-1 infection. ''PLoS One''. 2014; '''9''' (9):e106442
A review of multivariate analyses in imaging genetics. Description: Liu, Jingyu, et al. A review of multivariate analyses in imaging genetics. ''Front Neuroinform''. 2014; '''8''': 29
Assessing SNP-SNP interactions among DNA repair, modification and metabolism related pathway genes in breast cancer susceptibility. Description: Sapkota, Yadav, et al. Assessing SNP-SNP interactions among DNA repair, modification and metabolism related pathway genes in breast cancer susceptibility. ''PLoS One''. 2014; '''8''' (6):e64896
Assessing the effects of common variation in the FOXP2 gene on human brain structure. Description: Hoogman, Martine, et al. Assessing the effects of common variation in the FOXP2 gene on human brain structure. ''Front Hum Neurosci''. 2014; '''8''': 473
Association between Expression Quantitative Trait Loci and Metabolic Traits in Two Korean Populations. Description: Hong, Kyung-Won, et al. Association between Expression Quantitative Trait Loci and Metabolic Traits in Two Korean Populations. ''PLoS One''. 2014; '''9''' (12):e114128
Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhauser syndrome and central corneal thickness. Description: Davidson, Alice E, et al. Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhauser syndrome and central corneal thickness. ''PLoS One''. 2014; '''9''' (8):e104163
Association of COMT and COMT-DRD2 interaction with creative potential. Description: Zhang, Shun, et al. Association of COMT and COMT-DRD2 interaction with creative potential. ''Front Hum Neurosci''. 2014; '''8''': 216
Association of genetic ancestry with breast cancer in ethnically diverse women from Chicago. Description: Al-Alem, Umaima, et al. Association of genetic ancestry with breast cancer in ethnically diverse women from Chicago. ''PLoS One''. 2014; '''9''' (11):e112916
Association of IRGM gene mutations with inflammatory bowel disease in the Indian population. Description: Baskaran, Kirankumar, et al. Association of IRGM gene mutations with inflammatory bowel disease in the Indian population. ''PLoS One''. 2014; '''9''' (9):e106863
Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico. Description: Ballester, Veroushka, et al. Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico. ''PLoS One''. 2014; '''9''' (9):e108204
Association of the hepatocyte growth factor gene with keratoconus in an Australian population. Description: Sahebjada, Srujana, et al. Association of the hepatocyte growth factor gene with keratoconus in an Australian population. ''PLoS One''. 2014; '''9''' (1):e84067
Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon. Description: Wonkam, Ambroise, et al. Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon. ''PLoS One''. 2014; '''9''' (3):e92506
ATP-Binding Cassette Genes Genotype and Expression: A Potential Association with Pancreatic Cancer Development and Chemoresistance? Description: Pang, Li, et al. ATP-Binding Cassette Genes Genotype and Expression: A Potential Association with Pancreatic Cancer Development and Chemoresistance? ''Gastroenterol Res Pract''. 2014; '''2014''': 414931
A two-stage association study suggests BRAP as a susceptibility gene for schizophrenia. Description: Zhang, Fuquan, et al. A two-stage association study suggests BRAP as a susceptibility gene for schizophrenia. ''PLoS One''. 2014; '''9''' (1):e86037
A variant of IL6R is associated with the recurrence of atrial fibrillation after catheter ablation in a Chinese Han population. Description: Wu, Gang, et al. A variant of IL6R is associated with the recurrence of atrial fibrillation after catheter ablation in a Chinese Han population. ''PLoS One''. 2014; '''9''' (6):e99623
A web-portal for interactive data exploration, visualization, and hypothesis testing. Description: Bartsch, Hauke, et al. A web-portal for interactive data exploration, visualization, and hypothesis testing. ''Front Neuroinform''. 2014; '''8''': 25
BAIAP2 is related to emotional modulation of human memory strength. Description: Luksys, Gediminas, et al. BAIAP2 is related to emotional modulation of human memory strength. ''PLoS One''. 2014; '''9''' (1):e83707
Bivariate linear mixed model analysis to test joint associations of genetic variants on systolic and diastolic blood pressure. Description: Neupane, Binod, et al. Bivariate linear mixed model analysis to test joint associations of genetic variants on systolic and diastolic blood pressure. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S75
Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. Description: Schulte, Eva C, et al. Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. ''PLoS One''. 2014; '''9''' (5):e98092
CARAT-GxG: CUDA-Accelerated Regression Analysis Toolkit for Large-Scale Gene-Gene Interaction with GPU Computing System. Description: Lee, Sungyoung, et al. CARAT-GxG: CUDA-Accelerated Regression Analysis Toolkit for Large-Scale Gene-Gene Interaction with GPU Computing System. ''Cancer Inform''. 2014; '''13''' (Suppl 7):27-33
Catechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responses. Description: Wendt, Laura, et al. Catechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responses. ''PLoS One''. 2014; '''9''' (9):e107665
CDKAL1-related single nucleotide polymorphisms are associated with insulin resistance in a cross-sectional cohort of Greek children. Description: Rask-Andersen, Mathias, et al. CDKAL1-related single nucleotide polymorphisms are associated with insulin resistance in a cross-sectional cohort of Greek children. ''PLoS One''. 2014; '''9''' (4):e93193
Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder. Description: Shaw, Alex D, et al. Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder. ''PLoS One''. 2014; '''9''' (3):e92556
Characterization of genome-methylome interactions in 22 nuclear pedigrees. Description: Plongthongkum, Nongluk, et al. Characterization of genome-methylome interactions in 22 nuclear pedigrees. ''PLoS One''. 2014; '''9''' (7):e99313
Combined analysis with copy number variation identifies risk loci in lung cancer. Description: Li, Xinlei, et al. Combined analysis with copy number variation identifies risk loci in lung cancer. ''Biomed Res Int''. 2014; '''2014''': 469103
Combined linkage and association studies show that HLA class II variants control levels of antibodies against Epstein-Barr virus antigens. Description: Pedergnana, Vincent, et al. Combined linkage and association studies show that HLA class II variants control levels of antibodies against Epstein-Barr virus antigens. ''PLoS One''. 2014; '''9''' (7):e102501
Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease. Description: Sabater-Lleal, Maria, et al. Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease. ''PLoS One''. 2014; '''9''' (8):e104082
Comparison of two methods for analysis of gene-environment interactions in longitudinal family data: the Framingham heart study. Description: Sung, Yun Ju, et al. Comparison of two methods for analysis of gene-environment interactions in longitudinal family data: the Framingham heart study. ''Front Genet''. 2014; '''5''': 9
Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women. Description: Zhou, Qiu-Hong, et al. Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women. ''PLoS One''. 2014; '''9''' (11):e112358
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures. Description: Evans, Tiffany-Jane, et al. Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures. ''PLoS One''. 2014; '''9''' (10):e110255
Congenital cataracts: de novo gene conversion event in CRYBB2. Description: Garnai, Sarah J, et al. Congenital cataracts: de novo gene conversion event in CRYBB2. ''Mol Vis''. 2014; '''20''': 1579-93
Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene. Description: Drogemuller, Michaela, et al. Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene. ''PLoS One''. 2014; '''9''' (10):e110125
Copy number variation in Thai population. Description: Suktitipat, Bhoom, et al. Copy number variation in Thai population. ''PLoS One''. 2014; '''9''' (8):e104355
Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins. Description: Wei, Wei-Qi, et al. Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins. ''AMIA Jt Summits Transl Sci Proc''. 2014; '''2014''': 112-9
Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle. Description: Murgiano, Leonardo, et al. Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle. ''PLoS One''. 2014; '''9''' (4):e94861
Dense genotyping of immune-related loci identifies variants associated with clearance of HPV among HIV-positive women in the HIV epidemiology research study (HERS). Description: Sudenga, Staci L, et al. Dense genotyping of immune-related loci identifies variants associated with clearance of HPV among HIV-positive women in the HIV epidemiology research study (HERS). ''PLoS One''. 2014; '''9''' (6):e99109
Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. Description: Carnes, Megan Ulmer, et al. Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. ''PLoS Genet''. 2014; '''10''' (5):e1004372
DNA methylation changes in the postmortem dorsolateral prefrontal cortex of patients with schizophrenia. Description: Numata, Shusuke, et al. DNA methylation changes in the postmortem dorsolateral prefrontal cortex of patients with schizophrenia. ''Front Genet''. 2014; '''5''': 280
Endometriosis is associated with rare copy number variants. Description: Chettier, Rakesh, et al. Endometriosis is associated with rare copy number variants. ''PLoS One''. 2014; '''9''' (8):e103968
Endothelial protein C receptor gene variants not associated with severe malaria in ghanaian children. Description: Schuldt, Kathrin, et al. Endothelial protein C receptor gene variants not associated with severe malaria in ghanaian children. ''PLoS One''. 2014; '''9''' (12):e115770
Environmental and genetic contributors to salivary testosterone levels in infants. Description: Xia, Kai, et al. Environmental and genetic contributors to salivary testosterone levels in infants. ''Front Endocrinol (Lausanne)''. 2014; '''5''': 187
Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing. Description: Thornton, Timothy, et al. Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing. ''BMC Proc''. 2014; '''8''' (Suppl 1):S5
Evaluating the coverage and potential of imputing the exome microarray with next-generation imputation using the 1000 Genomes Project. Description: Tantoso, Erwin, et al. Evaluating the coverage and potential of imputing the exome microarray with next-generation imputation using the 1000 Genomes Project. ''PLoS One''. 2014; '''9''' (9):e106681
Evaluation of SLE Susceptibility Genes in Malaysians. Description: Molineros, Julio E, et al. Evaluation of SLE Susceptibility Genes in Malaysians. ''Autoimmune Dis''. 2014; '''2014''': 305436
False-positive rates in two-point parametric linkage analysis. Description: Szymczak, Silke, et al. False-positive rates in two-point parametric linkage analysis. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S110
Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese. Description: Ma, Ronald Ching Wan, et al. Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese. ''PLoS One''. 2014; '''9''' (1):e84770
Fast principal component analysis of large-scale genome-wide data. Description: Abraham, Gad, et al. Fast principal component analysis of large-scale genome-wide data. ''PLoS One''. 2014; '''9''' (4):e93766
First regional evaluation of nuclear genetic diversity and population structure in northeastern coyotes ( Canis latrans). Description: Monzon, Javier. First regional evaluation of nuclear genetic diversity and population structure in northeastern coyotes ( Canis latrans). ''F1000Res''. 2014; '''3''': 66
Footprints of directional selection in wild Atlantic salmon populations: evidence for parasite-driven evolution? Description: Zueva, Ksenia J, et al. Footprints of directional selection in wild Atlantic salmon populations: evidence for parasite-driven evolution? ''PLoS One''. 2014; '''9''' (3):e91672
Functional annotation of putative regulatory elements at cancer susceptibility Loci. Description: Rosse, Stephanie A, et al. Functional annotation of putative regulatory elements at cancer susceptibility Loci. ''Cancer Inform''. 2014; '''13''' (Suppl 2):5-17
Gender specific association of RAS gene polymorphism with essential hypertension: a case-control study. Description: Dhanachandra Singh, Kh, et al. Gender specific association of RAS gene polymorphism with essential hypertension: a case-control study. ''Biomed Res Int''. 2014; '''2014''': 538053
Gene polymorphisms of micrornas in Helicobacter pylori-induced high risk atrophic gastritis and gastric cancer. Description: Kupcinskas, Juozas, et al. Gene polymorphisms of micrornas in Helicobacter pylori-induced high risk atrophic gastritis and gastric cancer. ''PLoS One''. 2014; '''9''' (1):e87467
Genetic association analysis for common variants in the Genetic Analysis Workshop 18 data: a Dirichlet regression approach. Description: Espin-Garcia, Osvaldo, et al. Genetic association analysis for common variants in the Genetic Analysis Workshop 18 data: a Dirichlet regression approach. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S70
Genetic association analysis of paratuberculosis forms in holstein-friesian cattle. Description: Vazquez, Patricia, et al. Genetic association analysis of paratuberculosis forms in holstein-friesian cattle. ''Vet Med Int''. 2014; '''2014''': 321327
Genetic association analysis using weighted false discovery rate approach on Genetic Analysis Workshop 18 data. Description: Qiu, Xin, et al. Genetic association analysis using weighted false discovery rate approach on Genetic Analysis Workshop 18 data. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S76
Genetic basis of delay discounting in frequent gamblers: examination of a priori candidates and exploration of a panel of dopamine-related loci. Description: Gray, Joshua C, et al. Genetic basis of delay discounting in frequent gamblers: examination of a priori candidates and exploration of a panel of dopamine-related loci. ''Brain Behav''. 2014; '''4''' (6):812-21
Genetic determinants of chronic obstructive pulmonary disease in South Indian male smokers. Description: Arja, Cholendra, et al. Genetic determinants of chronic obstructive pulmonary disease in South Indian male smokers. ''PLoS One''. 2014; '''9''' (2):e89957
Genetic diversity and population structure among six cattle breeds in South Africa using a whole genome SNP panel. Description: Makina, Sithembile O, et al. Genetic diversity and population structure among six cattle breeds in South Africa using a whole genome SNP panel. ''Front Genet''. 2014; '''5''': 333
Genetic factors regulating lung vasculature and immune cell functions associate with resistance to pneumococcal infection. Description: Jonczyk, Magda S, et al. Genetic factors regulating lung vasculature and immune cell functions associate with resistance to pneumococcal infection. ''PLoS One''. 2014; '''9''' (3):e89831
Genetic risk score of NOS gene variants associated with myocardial infarction correlates with coronary incidence across Europe. Description: Carreras-Torres, Robert, et al. Genetic risk score of NOS gene variants associated with myocardial infarction correlates with coronary incidence across Europe. ''PLoS One''. 2014; '''9''' (5):e96504
Genetic variability of the grey wolf Canis lupus in the Caucasus in comparison with Europe and the Middle East: distinct or intermediary population? Description: Pilot, Malgorzata, et al. Genetic variability of the grey wolf Canis lupus in the Caucasus in comparison with Europe and the Middle East: distinct or intermediary population? ''PLoS One''. 2014; '''9''' (4):e93828
Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network. Description: Malinowski, Jennifer R, et al. Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network. ''PLoS One''. 2014; '''9''' (12):e111301
Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma. Description: Rendleman, Justin, et al. Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma. ''PLoS One''. 2014; '''9''' (7):e101685
Genetic variation modifies risk for neurodegeneration based on biomarker status. Description: Hohman, Timothy J, et al. Genetic variation modifies risk for neurodegeneration based on biomarker status. ''Front Aging Neurosci''. 2014; '''6''': 183
Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients. Description: Kaur, Harpreet, et al. Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients. ''PLoS One''. 2014; '''9''' (7):e102556
Genome wide analysis indicates genes for basement membrane and cartilage matrix proteins as candidates for hip dysplasia in Labrador Retrievers. Description: Lavrijsen, Ineke C M, et al. Genome wide analysis indicates genes for basement membrane and cartilage matrix proteins as candidates for hip dysplasia in Labrador Retrievers. ''PLoS One''. 2014; '''9''' (1):e87735
Genome-wide analysis of cold adaptation in indigenous Siberian populations. Description: Cardona, Alexia, et al. Genome-wide analysis of cold adaptation in indigenous Siberian populations. ''PLoS One''. 2014; '''9''' (5):e98076
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Description: Jarick, I, et al. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. ''Mol Psychiatry''. 2014 Jan; '''19''' (1):115-21
Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk. Description: Willis, Jason A, et al. Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk. ''Front Genet''. 2014; '''5''': 29
Genome-wide association scan for variants associated with early-onset prostate cancer. Description: Lange, Ethan M, et al. Genome-wide association scan for variants associated with early-onset prostate cancer. ''PLoS One''. 2014; '''9''' (4):e93436
Genome-wide association studies using haplotypes and individual SNPs in Simmental cattle. Description: Wu, Yang, et al. Genome-wide association studies using haplotypes and individual SNPs in Simmental cattle. ''PLoS One''. 2014; '''9''' (10):e109330
Genome-wide association study and ancestral origins of the slick-hair coat in tropically adapted cattle. Description: Huson, Heather J, et al. Genome-wide association study and ancestral origins of the slick-hair coat in tropically adapted cattle. ''Front Genet''. 2014; '''5''': 101
Genome wide association study identifies 20 novel promising genes associated with milk fatty acid traits in Chinese Holstein. Description: Li, Cong, et al. Genome wide association study identifies 20 novel promising genes associated with milk fatty acid traits in Chinese Holstein. ''PLoS One''. 2014; '''9''' (5):e96186
Genome-wide association study identifies a potent locus associated with human opioid sensitivity. Description: Nishizawa, D, et al. Genome-wide association study identifies a potent locus associated with human opioid sensitivity. ''Mol Psychiatry''. 2014 Jan; '''19''' (1):55-62
Genome-wide association study identifies phospholipase C zeta 1 (PLCz1) as a stallion fertility locus in Hanoverian warmblood horses. Description: Schrimpf, Rahel, et al. Genome-wide association study identifies phospholipase C zeta 1 (PLCz1) as a stallion fertility locus in Hanoverian warmblood horses. ''PLoS One''. 2014; '''9''' (10):e109675
Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population. Description: Liao, Ming, et al. Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population. ''PLoS One''. 2014; '''9''' (8):e105844
Genome-wide association study of maternal and inherited loci for conotruncal heart defects. Description: Agopian, A J, et al. Genome-wide association study of maternal and inherited loci for conotruncal heart defects. ''PLoS One''. 2014; '''9''' (5):e96057
Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections. Description: Ye, Zhan, et al. Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections. ''Front Genet''. 2014; '''5''': 125
Genome-wide association study of susceptibility to infection by Mycobacterium avium subspecies paratuberculosis in Holstein cattle. Description: Alpay, Fazli, et al. Genome-wide association study of susceptibility to infection by Mycobacterium avium subspecies paratuberculosis in Holstein cattle. ''PLoS One''. 2014; '''9''' (12):e111704
Genome-wide association study reveals a polymorphism in the podocyte receptor RANK for the decline of renal function in coronary patients. Description: Leiherer, Andreas, et al. Genome-wide association study reveals a polymorphism in the podocyte receptor RANK for the decline of renal function in coronary patients. ''PLoS One''. 2014; '''9''' (12):e114240
Genome-wide linkage study suggests a susceptibility locus for isolated bilateral microtia on 4p15.32-4p16.2. Description: Li, Xin, et al. Genome-wide linkage study suggests a susceptibility locus for isolated bilateral microtia on 4p15.32-4p16.2. ''PLoS One''. 2014; '''9''' (7):e101152
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. Description: Simpson, Claire L, et al. Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. ''PLoS One''. 2014; '''9''' (9):e107110
Genome wide screening of candidate genes for improving piglet birth weight using high and low estimated breeding value populations. Description: Zhang, Lifan, et al. Genome wide screening of candidate genes for improving piglet birth weight using high and low estimated breeding value populations. ''Int J Biol Sci''. 2014; '''10''' (3):236-44
Genomic and metabolomic profile associated to microalbuminuria. Description: Marrachelli, Vannina G, et al. Genomic and metabolomic profile associated to microalbuminuria. ''PLoS One''. 2014; '''9''' (2):e98227
Genomic architecture of sickle cell disease in West African children. Description: Quinlan, Jacklyn, et al. Genomic architecture of sickle cell disease in West African children. ''Front Genet''. 2014; '''5''': 26
Genomic assortative mating in marriages in the United States. Description: Guo, Guang, et al. Genomic assortative mating in marriages in the United States. ''PLoS One''. 2014; '''9''' (11):e112322
Genomic scan reveals loci under altitude adaptation in Tibetan and Dahe pigs. Description: Dong, Kunzhe, et al. Genomic scan reveals loci under altitude adaptation in Tibetan and Dahe pigs. ''PLoS One''. 2014; '''9''' (10):e110520
Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. Description: Bodian, Dale L, et al. Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. ''PLoS One''. 2014; '''9''' (4):e94554
Haplotype approach for association analysis on hypertension. Description: Shen, Xiaowei, et al. Haplotype approach for association analysis on hypertension. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S57
Host genetic variants and gene expression patterns associated with Epstein-Barr virus copy number in lymphoblastoid cell lines. Description: Houldcroft, Charlotte J, et al. Host genetic variants and gene expression patterns associated with Epstein-Barr virus copy number in lymphoblastoid cell lines. ''PLoS One''. 2014; '''9''' (10):e108384
Hybrid origin of European commercial pigs examined by an in-depth haplotype analysis on chromosome 1. Description: Bosse, Mirte, et al. Hybrid origin of European commercial pigs examined by an in-depth haplotype analysis on chromosome 1. ''Front Genet''. 2014; '''5''': 442
Identification of genetic loci associated with primary angle-closure glaucoma in the basset hound. Description: Ahram, Dina F, et al. Identification of genetic loci associated with primary angle-closure glaucoma in the basset hound. ''Mol Vis''. 2014; '''20''': 497-510
Identification of genomic loci associated with Rhodococcus equi susceptibility in foals. Description: McQueen, Cole M, et al. Identification of genomic loci associated with Rhodococcus equi susceptibility in foals. ''PLoS One''. 2014; '''9''' (6):e98710
Identification of novel genetic risk loci in Maltese dogs with necrotizing meningoencephalitis and evidence of a shared genetic risk across toy dog breeds. Description: Schrauwen, Isabelle, et al. Identification of novel genetic risk loci in Maltese dogs with necrotizing meningoencephalitis and evidence of a shared genetic risk across toy dog breeds. ''PLoS One''. 2014; '''9''' (11):e112755
Identification of rare variants for hypertension with incorporation of linkage information. Description: Chiu, Yen-Feng, et al. Identification of rare variants for hypertension with incorporation of linkage information. ''BMC Proc''. 2014; '''8''' (Suppl 1):S109
Identifying genetic interactions associated with late-onset Alzheimer's disease. Description: Floudas, Charalampos S, et al. Identifying genetic interactions associated with late-onset Alzheimer's disease. ''BioData Min''. 2014; '''7''' (1):35
Identifying rare variants associated with hypertension using the C-alpha test. Description: Faino, Anna, et al. Identifying rare variants associated with hypertension using the C-alpha test. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S56
Immunization associated with erectile dysfunction based on cross-sectional and genetic analyses. Description: Chen, Yang, et al. Immunization associated with erectile dysfunction based on cross-sectional and genetic analyses. ''PLoS One''. 2014; '''9''' (10):e111269
Impact of measurement error on testing genetic association with quantitative traits. Description: Liao, Jiemin, et al. Impact of measurement error on testing genetic association with quantitative traits. ''PLoS One''. 2014; '''9''' (1):e87044
Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes. Description: Almoguera, Berta, et al. Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes. ''Front Genet''. 2014; '''5''': 96
Increased expression of MERTK is associated with a unique form of canine retinopathy. Description: Ahonen, Saija J, et al. Increased expression of MERTK is associated with a unique form of canine retinopathy. ''PLoS One''. 2014; '''9''' (12):e114552
Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts. Description: Hagleitner, Melanie M, et al. Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts. ''PLoS One''. 2014; '''9''' (12):e115869
Integrated analysis of germline and somatic variants in ovarian cancer. Description: Kanchi, Krishna L, et al. Integrated analysis of germline and somatic variants in ovarian cancer. ''Nat Commun''. 2014; '''5''': 3156
Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations. Description: Mosley, Jonathan D, et al. Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations. ''PLoS One''. 2014; '''9''' (6):e100322
Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene. Description: Okada, Yukinori, et al. Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene. ''PLoS One''. 2014; '''9''' (2):e87645
Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease. Description: Cabrera, Sonia, et al. Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease. ''PLoS One''. 2014; '''9''' (11):e112171
Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies. Description: Mitchell, Sabrina L, et al. Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies. ''BioData Min''. 2014; '''7''': 6
Investigating the Role of Gene-Gene Interactions in TB Susceptibility. Description: Daya, Michelle, et al. Investigating the Role of Gene-Gene Interactions in TB Susceptibility. ''PLoS One''. 2014; '''10''' (4):e0123970
Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy. Description: Moreira, Danielle P, et al. Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy. ''PLoS One''. 2014; '''9''' (9):e107705
Lack of association of the caspase-12 long allele with community-acquired pneumonia in people of African descent. Description: Chen, Jiwang, et al. Lack of association of the caspase-12 long allele with community-acquired pneumonia in people of African descent. ''PLoS One''. 2014; '''9''' (2):e89194
Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants. Description: Narahara, Maiko, et al. Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants. ''PLoS One''. 2014; '''9''' (6):e100924
Linkage disequilibrium and haplotype block structure in a composite beef cattle breed. Description: Mokry, Fabiana Barichello, et al. Linkage disequilibrium and haplotype block structure in a composite beef cattle breed. ''BMC Genomics''. 2014; '''15 Suppl 7''': S6
Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattle. Description: Murgiano, Leonardo, et al. Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattle. ''PLoS One''. 2014; '''9''' (10):e110628
Lupus risk variants in the PXK locus alter B-cell receptor internalization. Description: Vaughn, Samuel E, et al. Lupus risk variants in the PXK locus alter B-cell receptor internalization. ''Front Genet''. 2014; '''5''': 450
MAPKAP1 rs10118570 polymorphism is associated with anti-infection and anti-hepatic fibrogenesis in schistosomiasis japonica. Description: Zhu, Xiao, et al. MAPKAP1 rs10118570 polymorphism is associated with anti-infection and anti-hepatic fibrogenesis in schistosomiasis japonica. ''PLoS One''. 2014; '''9''' (8):e105995
Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities. Description: Musolf, Anthony, et al. Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S81
Mapping the genetic architecture of gene regulation in whole blood. Description: Schramm, Katharina, et al. Mapping the genetic architecture of gene regulation in whole blood. ''PLoS One''. 2014; '''9''' (4):e93844
Matrix metalloproteinase-1 (MMP-1) Promoter polymorphisms are well linked with lower stomach tumor formation in eastern Indian population. Description: Dey, Sanjib, et al. Matrix metalloproteinase-1 (MMP-1) Promoter polymorphisms are well linked with lower stomach tumor formation in eastern Indian population. ''PLoS One''. 2014; '''9''' (2):e88040
Multivariate dimensionality reduction approaches to identify gene-gene and gene-environment interactions underlying multiple complex traits. Description: Xu, Hai-Ming, et al. Multivariate dimensionality reduction approaches to identify gene-gene and gene-environment interactions underlying multiple complex traits. ''PLoS One''. 2014; '''9''' (9):e108103
NAT2 genetic variations among South Indian populations. Description: Lakkakula, Saikrishna, et al. NAT2 genetic variations among South Indian populations. ''Hum Genome Var''. 2014; '''1''': 14014
New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. Description: Vinayagamoorthy, Nadimuthu, et al. New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. ''PLoS One''. 2014; '''9''' (4):e95866
Novel host genetic variations associated with spontaneous clearance of a single-source outbreak of HCV1b infections. Description: You, Hong, et al. Novel host genetic variations associated with spontaneous clearance of a single-source outbreak of HCV1b infections. ''BMJ Open Gastroenterol''. 2014; '''1''' (1):e000010
Novel insights into the regulatory architecture of CD4+ T cells in rheumatoid arthritis. Description: Aterido, Adria, et al. Novel insights into the regulatory architecture of CD4+ T cells in rheumatoid arthritis. ''PLoS One''. 2014; '''9''' (6):e100690
OTX2 duplication is implicated in hemifacial microsomia. Description: Zielinski, Dina, et al. OTX2 duplication is implicated in hemifacial microsomia. ''PLoS One''. 2014; '''9''' (5):e96788
Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies. Description: Perez-Palma, Eduardo, et al. Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies. ''PLoS One''. 2014; '''9''' (4):e95413
Pharmacogenetic associations with long-term response to anti-vascular endothelial growth factor treatment in neovascular AMD patients. Description: Park, Un Chul, et al. Pharmacogenetic associations with long-term response to anti-vascular endothelial growth factor treatment in neovascular AMD patients. ''Mol Vis''. 2014; '''20''': 1680-94
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. Description: Cronin, Robert M, et al. Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. ''Front Genet''. 2014; '''5''': 250
Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis. Description: Namjou, Bahram, et al. Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis. ''Front Genet''. 2014; '''5''': 401
Phenotype refinement strengthens the association of AHR and CYP1A1 genotype with caffeine consumption. Description: McMahon, George, et al. Phenotype refinement strengthens the association of AHR and CYP1A1 genotype with caffeine consumption. ''PLoS One''. 2014; '''9''' (7):e103448
Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruption. Description: Denis, Marie, et al. Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruption. ''PLoS One''. 2014; '''9''' (12):e116346
Pleiotropic effect of common variants at ABO Glycosyltranferase locus in 9q32 on plasma levels of pancreatic lipase and angiotensin converting enzyme. Description: Pleiotropic effect of common variants at ABO Glycosyltranferase locus in 9q32 on plasma levels of pancreatic lipase and angiotensin converting enzyme. ''PLoS One''. 2014; '''9''' (2):e55903
Population genomic analyses based on 1 million SNPs in commercial egg layers. Description: Gholami, Mahmood, et al. Population genomic analyses based on 1 million SNPs in commercial egg layers. ''PLoS One''. 2014; '''9''' (4):e94509
Potentially functional SNPs (pfSNPs) as novel genomic predictors of 5-FU response in metastatic colorectal cancer patients. Description: Wang, Jingbo, et al. Potentially functional SNPs (pfSNPs) as novel genomic predictors of 5-FU response in metastatic colorectal cancer patients. ''PLoS One''. 2014; '''9''' (11):e111694
Practical issues in screening and variable selection in genome-wide association analysis. Description: Hong, Sungyeon, et al. Practical issues in screening and variable selection in genome-wide association analysis. ''Cancer Inform''. 2014; '''13''' (Suppl 7):55-65
Prediction of genetic contributions to complex traits using whole genome sequencing data. Description: Yao, Chen, et al. Prediction of genetic contributions to complex traits using whole genome sequencing data. ''BMC Proc''. 2014; '''8''' (Suppl 1):S68
PREST-plus identifies pedigree errors and cryptic relatedness in the GAW18 sample using genome-wide SNP data. Description: Sun, Lei, et al. PREST-plus identifies pedigree errors and cryptic relatedness in the GAW18 sample using genome-wide SNP data. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S23
Protective association of tumor necrosis factor superfamily 15 (TNFSF15) polymorphic haplotype with Ulcerative Colitis and Crohn's disease in an Indian population. Description: Baskaran, Kirankumar, et al. Protective association of tumor necrosis factor superfamily 15 (TNFSF15) polymorphic haplotype with Ulcerative Colitis and Crohn's disease in an Indian population. ''PLoS One''. 2014; '''9''' (12):e114665
Quantitative trait loci (QTL) study identifies novel genomic regions associated to Chiari-like malformation in Griffon Bruxellois dogs. Description: Lemay, Philippe, et al. Quantitative trait loci (QTL) study identifies novel genomic regions associated to Chiari-like malformation in Griffon Bruxellois dogs. ''PLoS One''. 2014; '''9''' (4):e89816
Rare variant analysis of blood pressure phenotypes in the Genetic Analysis Workshop 18 whole genome sequencing data using sequence kernel association test. Description: Mallaney, Cates, et al. Rare variant analysis of blood pressure phenotypes in the Genetic Analysis Workshop 18 whole genome sequencing data using sequence kernel association test. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S10
Refined candidate region for F4ab/ac enterotoxigenic Escherichia coli susceptibility situated proximal to MUC13 in pigs. Description: Goetstouwers, Tiphanie, et al. Refined candidate region for F4ab/ac enterotoxigenic Escherichia coli susceptibility situated proximal to MUC13 in pigs. ''PLoS One''. 2014; '''9''' (8):e105013
Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population. Description: Naess, Sigrid, et al. Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population. ''PLoS One''. 2014; '''9''' (12):e114486
Replication of 6 obesity genes in a meta-analysis of genome-wide association studies from diverse ancestries. Description: Tan, Li-Jun, et al. Replication of 6 obesity genes in a meta-analysis of genome-wide association studies from diverse ancestries. ''PLoS One''. 2014; '''9''' (5):e96149
Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations. Description: Zhao, Bijun, et al. Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations. ''PLoS One''. 2014; '''9''' (9):e107411
Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T. Description: Grigorova, Marina, et al. Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T. ''PLoS One''. 2014; '''9''' (4):e94244
Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci. Description: Service, Susan K, et al. Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci. ''PLoS Genet''. 2014 Jan; '''10''' (1):e1004147
RNA-Seq transcriptome profiling identifies CRISPLD2 as a glucocorticoid responsive gene that modulates cytokine function in airway smooth muscle cells. Description: Himes, Blanca E, et al. RNA-Seq transcriptome profiling identifies CRISPLD2 as a glucocorticoid responsive gene that modulates cytokine function in airway smooth muscle cells. ''PLoS One''. 2014; '''9''' (6):e99625
Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder. Description: Korhonen, Tellervo, et al. Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder. ''PLoS One''. 2014; '''9''' (6):e98199
Rs7206790 and rs11644943 in FTO gene are associated with risk of obesity in Chinese school-age population. Description: Xu, Yuyang, et al. Rs7206790 and rs11644943 in FTO gene are associated with risk of obesity in Chinese school-age population. ''PLoS One''. 2014; '''9''' (9):e108050
Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection. Description: Di Gaetano, Cornelia, et al. Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection. ''PLoS One''. 2014; '''9''' (3):e91237
Searching for "monogenic diabetes" in dogs using a candidate gene approach. Description: Short, Andrea D, et al. Searching for "monogenic diabetes" in dogs using a candidate gene approach. ''Canine Genet Epidemiol''. 2014; '''1''': 8
Shared and unique signals of high-altitude adaptation in geographically distinct Tibetan populations. Description: Wuren, Tana, et al. Shared and unique signals of high-altitude adaptation in geographically distinct Tibetan populations. ''PLoS One''. 2014; '''9''' (3):e88252
Single-marker and multi-marker mixed models for polygenic score analysis in family-based data. Description: Bohossian, Nora, et al. Single-marker and multi-marker mixed models for polygenic score analysis in family-based data. ''BMC Proc''. 2014; '''8''' (Suppl 1):S63
Smoking quit success genotype score predicts quit success and distinct patterns of developmental involvement with common addictive substances. Description: Uhl, G R, et al. Smoking quit success genotype score predicts quit success and distinct patterns of developmental involvement with common addictive substances. ''Mol Psychiatry''. 2014 Jan; '''19''' (1):50-4
SNP identification by transcriptome sequencing and candidate gene-based association analysis for heat tolerance in the bay scallop Argopecten irradians. Description: Du, Xuedi, et al. SNP identification by transcriptome sequencing and candidate gene-based association analysis for heat tolerance in the bay scallop Argopecten irradians. ''PLoS One''. 2014; '''9''' (8):e104960
Standing at the gateway to Europe--the genetic structure of Western balkan populations based on autosomal and haploid markers. Description: Kovacevic, Lejla, et al. Standing at the gateway to Europe--the genetic structure of Western balkan populations based on autosomal and haploid markers. ''PLoS One''. 2014; '''9''' (8):e105090
Study of a Functional Polymorphism in the PER3 Gene and Diurnal Preference in a Colombian Sample. Description: Perea, Claudia S, et al. Study of a Functional Polymorphism in the PER3 Gene and Diurnal Preference in a Colombian Sample. ''Open Neurol J''. 2014; '''8''': 7-10
Systematic fine-mapping of association with BMI and type 2 diabetes at the FTO locus by integrating results from multiple ethnic groups. Description: Akiyama, Koichi, et al. Systematic fine-mapping of association with BMI and type 2 diabetes at the FTO locus by integrating results from multiple ethnic groups. ''PLoS One''. 2014; '''9''' (6):e101329
Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome. Description: Woltmann, Andrea, et al. Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome. ''PLoS One''. 2014; '''9''' (6):e98229
Testing for associations between systolic blood pressure and single-nucleotide polymorphism profiles obtained from sparse principal component analysis. Description: Bonner, Ashley, et al. Testing for associations between systolic blood pressure and single-nucleotide polymorphism profiles obtained from sparse principal component analysis. ''BMC Proc''. 2014; '''8''' (Suppl 1):S95
Testing optimally weighted combination of variants for hypertension. Description: Zhao, Xingwang, et al. Testing optimally weighted combination of variants for hypertension. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S59
The Andean adaptive toolkit to counteract high altitude maladaptation: genome-wide and phenotypic analysis of the Collas. Description: Eichstaedt, Christina A, et al. The Andean adaptive toolkit to counteract high altitude maladaptation: genome-wide and phenotypic analysis of the Collas. ''PLoS One''. 2014; '''9''' (3):e93314
The association of genotype-based inbreeding coefficient with a range of physical and psychological human traits. Description: Verweij, Karin J H, et al. The association of genotype-based inbreeding coefficient with a range of physical and psychological human traits. ''PLoS One''. 2014; '''9''' (7):e103102
The association of transporter genes polymorphisms and lung cancer chemotherapy response. Description: Wang, Ying, et al. The association of transporter genes polymorphisms and lung cancer chemotherapy response. ''PLoS One''. 2014; '''9''' (3):e91967
The associations between immunity-related genes and breast cancer prognosis in Korean women. Description: Choi, Jaesung, et al. The associations between immunity-related genes and breast cancer prognosis in Korean women. ''PLoS One''. 2014; '''9''' (7):e103593
The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study. Description: Kullo, Iftikhar J, et al. The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study. ''Front Genet''. 2014; '''5''': 166
The effect of inversion at 8p23 on BLK association with lupus in Caucasian population. Description: Namjou, Bahram, et al. The effect of inversion at 8p23 on BLK association with lupus in Caucasian population. ''PLoS One''. 2014; '''9''' (12):e115614
The effects of socioeconomic status, clinical factors, and genetic ancestry on pulmonary tuberculosis disease in northeastern Mexico. Description: Young, Bonnie N, et al. The effects of socioeconomic status, clinical factors, and genetic ancestry on pulmonary tuberculosis disease in northeastern Mexico. ''PLoS One''. 2014; '''9''' (4):e94303
The episode of genetic drift defining the migration of humans out of Africa is derived from a large east African population size. Description: Elhassan, Nuha, et al. The episode of genetic drift defining the migration of humans out of Africa is derived from a large east African population size. ''PLoS One''. 2014; '''9''' (5):e97674
The gene-gene interaction of INSIG-SCAP-SREBP pathway on the risk of obesity in Chinese children. Description: Liu, Fang-Hong, et al. The gene-gene interaction of INSIG-SCAP-SREBP pathway on the risk of obesity in Chinese children. ''Biomed Res Int''. 2014; '''2014''': 538564
The genetic architecture of climatic adaptation of tropical cattle. Description: Porto-Neto, Laercio R, et al. The genetic architecture of climatic adaptation of tropical cattle. ''PLoS One''. 2014; '''9''' (11):e113284
The interplay between natural selection and susceptibility to melanoma on allele 374F of SLC45A2 gene in a South European population. Description: Lopez, Saioa, et al. The interplay between natural selection and susceptibility to melanoma on allele 374F of SLC45A2 gene in a South European population. ''PLoS One''. 2014; '''9''' (8):e104367
The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals. Description: Abuli, Anna, et al. The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals. ''PLoS One''. 2014; '''9''' (4):e95022
The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067. Description: Schnitzler, Fabian, et al. The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067. ''PLoS One''. 2014; '''9''' (11):e108503
The peculiar epidemiology of dracunculiasis in Chad. Description: Eberhard, Mark L, et al. The peculiar epidemiology of dracunculiasis in Chad. ''Am J Trop Med Hyg''. 2014 Jan; '''90''' (1):61-70
The SNP rs3128965 of HLA-DPB1 as a genetic marker of the AERD phenotype. Description: Kim, Seung-Hyun, et al. The SNP rs3128965 of HLA-DPB1 as a genetic marker of the AERD phenotype. ''PLoS One''. 2014; '''9''' (12):e111220
Transcriptome profiling of human ulcerative colitis mucosa reveals altered expression of pathways enriched in genetic susceptibility loci. Description: Cardinale, Christopher J, et al. Transcriptome profiling of human ulcerative colitis mucosa reveals altered expression of pathways enriched in genetic susceptibility loci. ''PLoS One''. 2014; '''9''' (5):e96153
tranSMART: An Open Source Knowledge Management and High Content Data Analytics Platform. Description: Scheufele, Elisabeth, et al. tranSMART: An Open Source Knowledge Management and High Content Data Analytics Platform. ''AMIA Jt Summits Transl Sci Proc''. 2014; '''2014''': 96-101
Trps1 differentially modulates the bone mineral density between male and female mice and its polymorphism associates with BMD differently between women and men. Description: Wang, Lishi, et al. Trps1 differentially modulates the bone mineral density between male and female mice and its polymorphism associates with BMD differently between women and men. ''PLoS One''. 2014; '''9''' (1):e84485
Using Mendelian inheritance errors as quality control criteria in whole genome sequencing data set. Description: Pilipenko, Valentina V, et al. Using Mendelian inheritance errors as quality control criteria in whole genome sequencing data set. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S21
Variation in genes involved in epigenetic processes offers insights into tropically adapted cattle diversity. Description: Porto-Neto, Laercio R, et al. Variation in genes involved in epigenetic processes offers insights into tropically adapted cattle diversity. ''Front Genet''. 2014; '''5''': 89
ViVar: a comprehensive platform for the analysis and visualization of structural genomic variation. Description: Sante, Tom, et al. ViVar: a comprehensive platform for the analysis and visualization of structural genomic variation. ''PLoS One''. 2014; '''9''' (12):e113800
Whole brain expression of bipolar disorder associated genes: structural and genetic analyses. Description: McCarthy, Michael J, et al. Whole brain expression of bipolar disorder associated genes: structural and genetic analyses. ''PLoS One''. 2014; '''9''' (6):e100204
Whole-exome sequencing for the identification of susceptibility genes of Kashin-Beck disease. Description: Yang, Zhenxing, et al. Whole-exome sequencing for the identification of susceptibility genes of Kashin-Beck disease. ''PLoS One''. 2014; '''9''' (4):e92298
Whole genome sequence and analysis of the Marwari horse breed and its genetic origin. Description: Jun, JeHoon, et al. Whole genome sequence and analysis of the Marwari horse breed and its genetic origin. ''BMC Genomics''. 2014; '''15 Suppl 9''': S4
Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. Description: Mayes, Maureen D, et al. Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. ''Am J Hum Genet''. 2014 Jan 2; '''94''' (1):47-61
Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals. Description: Yang, Shengjie, et al. Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals. ''BMC Genomics''. 2014 Jan 9; '''15''': 13
Association between JY-1 gene polymorphisms and reproductive traits in beef cattle. Description: de Camargo, Gregorio Miguel Ferreira, et al. Association between JY-1 gene polymorphisms and reproductive traits in beef cattle. ''Gene''. 2014 Jan 10; '''533''' (2):477-80
Diversity, differentiation, and linkage disequilibrium: prospects for association mapping in the malaria vector Anopheles arabiensis. Description: Marsden, Clare Diana, et al. Diversity, differentiation, and linkage disequilibrium: prospects for association mapping in the malaria vector Anopheles arabiensis. ''G3 (Bethesda)''. 2014 Jan 10; '''4''' (1):121-31
Analysis of schizophrenia-related genes and electrophysiological measures reveals ZNF804A association with amplitude of P300b elicited by novel sounds. Description: Del Re, E C, et al. Analysis of schizophrenia-related genes and electrophysiological measures reveals ZNF804A association with amplitude of P300b elicited by novel sounds. ''Transl Psychiatry''. 2014 Jan 14; '''4''': e346
Association of the RYR3 gene polymorphisms with atherosclerosis in elderly Japanese population. Description: Zhao, Chenxi, et al. Association of the RYR3 gene polymorphisms with atherosclerosis in elderly Japanese population. ''BMC Cardiovasc Disord''. 2014 Jan 14; '''14''': 6
A genome-wide scan for signatures of selection in Chinese indigenous and commercial pig breeds. Description: Yang, Songbai, et al. A genome-wide scan for signatures of selection in Chinese indigenous and commercial pig breeds. ''BMC Genet''. 2014 Jan 15; '''15''': 7
Identification of a major locus interacting with MC1R and modifying black coat color in an F(2) Nellore-Angus population. Description: Hanna, Lauren L Hulsman, et al. Identification of a major locus interacting with MC1R and modifying black coat color in an F(2) Nellore-Angus population. ''Genet Sel Evol''. 2014 Jan 24; '''46''': 4
The PARK2 gene is involved in the maintenance of pancreatic beta-cell functions related to insulin production and secretion. Description: Jin, Hyun-Seok, et al. The PARK2 gene is involved in the maintenance of pancreatic beta-cell functions related to insulin production and secretion. ''Mol Cell Endocrinol''. 2014 Jan 25; '''382''' (1):178-189
Critical role for mast cell Stat5 activity in skin inflammation. Description: Ando, Tomoaki, et al. Critical role for mast cell Stat5 activity in skin inflammation. ''Cell Rep''. 2014 Jan 30; '''6''' (2):366-76
Analysis of copy number variations at 15 schizophrenia-associated loci. Description: Rees, Elliott, et al. Analysis of copy number variations at 15 schizophrenia-associated loci. ''Br J Psychiatry''. 2014 Feb; '''204''' (2):108-14
Association of four insulin resistance genes with type 2 diabetes mellitus and hypertension in the Chinese Han population. Description: Jiang, Bo, et al. Association of four insulin resistance genes with type 2 diabetes mellitus and hypertension in the Chinese Han population. ''Mol Biol Rep''. 2014 Feb; '''41''' (2):925-33
Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24. Description: Agler, Caryline, et al. Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24. ''PLoS Genet''. 2014 Feb; '''10''' (2):e1003991
Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. Description: Avery, C L, et al. Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. ''Pharmacogenomics J''. 2014 Feb; '''14''' (1):6-13
Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin. Description: He, Bin Z, et al. Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin. ''Genetics''. 2014 Feb; '''196''' (2):557-67
Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer. Description: Saunders, Edward J, et al. Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer. ''PLoS Genet''. 2014 Feb; '''10''' (2):e1004129
Genetic variants associated with methotrexate efficacy and toxicity in early rheumatoid arthritis: results from the treatment of early aggressive rheumatoid arthritis trial. Description: Aslibekyan, S, et al. Genetic variants associated with methotrexate efficacy and toxicity in early rheumatoid arthritis: results from the treatment of early aggressive rheumatoid arthritis trial. ''Pharmacogenomics J''. 2014 Feb; '''14''' (1):48-53
Genome-wide association study of endometrial cancer in E2C2. Description: De Vivo, Immaculata, et al. Genome-wide association study of endometrial cancer in E2C2. ''Hum Genet''. 2014 Feb; '''133''' (2):211-24
Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links. Description: Rueedi, Rico, et al. Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links. ''PLoS Genet''. 2014 Feb; '''10''' (2):e1004132
Genome-wide protein QTL mapping identifies human plasma kallikrein as a post-translational regulator of serum uPAR levels. Description: Portelli, Michael A, et al. Genome-wide protein QTL mapping identifies human plasma kallikrein as a post-translational regulator of serum uPAR levels. ''FASEB J''. 2014 Feb; '''28''' (2):923-34
Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene. Description: Ruiz, A, et al. Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene. ''Transl Psychiatry''. 2014 Feb 4; '''4''': e358
The utility of low-density genotyping for imputation in the Thoroughbred horse. Description: Corbin, Laura J, et al. The utility of low-density genotyping for imputation in the Thoroughbred horse. ''Genet Sel Evol''. 2014 Feb 4; '''46''': 9
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population. Description: Yang, Binyao, et al. A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population. ''BMC Med Genomics''. 2014 Feb 11; '''7''': 10
A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting. Description: Nelson, Charlotte L, et al. A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting. ''BMC Infect Dis''. 2014 Feb 13; '''14''': 83
Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder. Description: Werling, Donna M, et al. Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder. ''Mol Autism''. 2014 Feb 17; '''5''' (1):13
STX1A and Asperger syndrome: a replication study. Description: Durdiakova, Jaroslava, et al. STX1A and Asperger syndrome: a replication study. ''Mol Autism''. 2014 Feb 18; '''5''' (1):14
Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years. Description: Shaffer, John R, et al. Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years. ''G3 (Bethesda)''. 2014 Feb 19; '''4''' (2):307-14
Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes. Description: Udpa, Nitin, et al. Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes. ''Genome Biol''. 2014 Feb 20; '''15''' (2):R36
Methylation quantitative trait loci (meQTLs) are consistently detected across ancestry, developmental stage, and tissue type. Description: Smith, Alicia K, et al. Methylation quantitative trait loci (meQTLs) are consistently detected across ancestry, developmental stage, and tissue type. ''BMC Genomics''. 2014 Feb 21; '''15''': 145
Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue. Description: Shi, Jianxin, et al. Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue. ''Nat Commun''. 2014 Feb 27; '''5''': 3365
Linkage maps of the Atlantic salmon (Salmo salar) genome derived from RAD sequencing. Description: Gonen, Serap, et al. Linkage maps of the Atlantic salmon (Salmo salar) genome derived from RAD sequencing. ''BMC Genomics''. 2014 Feb 27; '''15''': 166
Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations. Description: Yang, Tian, et al. Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations. ''Mol Genet Genomic Med''. 2014 Mar; '''2''' (2):138-51
An evolutionary analysis of antigen processing and presentation across different timescales reveals pervasive selection. Description: Forni, Diego, et al. An evolutionary analysis of antigen processing and presentation across different timescales reveals pervasive selection. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004189
APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study. Description: Ramanan, V K, et al. APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study. ''Mol Psychiatry''. 2014 Mar; '''19''' (3):351-7
Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African Americans. Description: Bentley, Amy R, et al. Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African Americans. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004190
Genome-wide association studies and prediction of 17 traits related to phenology, biomass and cell wall composition in the energy grass Miscanthus sinensis. Description: Slavov, Gancho T, et al. Genome-wide association studies and prediction of 17 traits related to phenology, biomass and cell wall composition in the energy grass Miscanthus sinensis. ''New Phytol''. 2014 Mar; '''201''' (4):1227-39
Genome-Wide Association Study of Human Immunodeficiency Virus (HIV)-1 Coreceptor Usage in Treatment-Naive Patients from An AIDS Clinical Trials Group Study. Description: Henrich, Timothy J, et al. Genome-Wide Association Study of Human Immunodeficiency Virus (HIV)-1 Coreceptor Usage in Treatment-Naive Patients from An AIDS Clinical Trials Group Study. ''Open Forum Infect Dis''. 2014 Mar; '''1''' (1):ofu018
Genome-wide Association Study of Integrated Meat Quality-related Traits of the Duroc Pig Breed. Description: Lee, Taeheon, et al. Genome-wide Association Study of Integrated Meat Quality-related Traits of the Duroc Pig Breed. ''Asian-Australas J Anim Sci''. 2014 Mar; '''27''' (3):303-9
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke. Description: Williams, Stephen R, et al. Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004214
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. Description: Borglum, A D, et al. Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. ''Mol Psychiatry''. 2014 Mar; '''19''' (3):325-33
Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate. Description: Georgi, Benjamin, et al. Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004229
Global footprints of purifying selection on Toll-like receptor genes primarily associated with response to bacterial infections in humans. Description: Mukherjee, Souvik, et al. Global footprints of purifying selection on Toll-like receptor genes primarily associated with response to bacterial infections in humans. ''Genome Biol Evol''. 2014 Mar; '''6''' (3):551-8
Identification of genes promoting skin youthfulness by genome-wide association study. Description: Chang, Anne L S, et al. Identification of genes promoting skin youthfulness by genome-wide association study. ''J Invest Dermatol''. 2014 Mar; '''134''' (3):651-657
Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants. Description: Romanos, Jihane, et al. Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants. ''Gut''. 2014 Mar; '''63''' (3):415-22
Rare variants in LRRK1 and Parkinson's disease. Description: Schulte, Eva C, et al. Rare variants in LRRK1 and Parkinson's disease. ''Neurogenetics''. 2014 Mar; '''15''' (1):49-57
The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of age. Description: MacArthur, Jacqueline A L, et al. The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of age. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004195
Worldwide patterns of ancestry, divergence, and admixture in domesticated cattle. Description: Decker, Jared E, et al. Worldwide patterns of ancestry, divergence, and admixture in domesticated cattle. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004254
ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease. Description: Medway, Christopher W, et al. ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease. ''Mol Neurodegener''. 2014 Mar 10; '''9''': 11
Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder. Description: Tang, Ruqi, et al. Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder. ''Genome Biol''. 2014 Mar 14; '''15''' (3):R25
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Description: Rees, Elliott, et al. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. ''Hum Mol Genet''. 2014 Mar 15; '''23''' (6):1669-76
Composite selection signals can localize the trait specific genomic regions in multi-breed populations of cattle and sheep. Description: Randhawa, Imtiaz Ahmed Sajid, et al. Composite selection signals can localize the trait specific genomic regions in multi-breed populations of cattle and sheep. ''BMC Genet''. 2014 Mar 17; '''15''': 34
The extent of linkage disequilibrium in beef cattle breeds using high-density SNP genotypes. Description: Porto-Neto, Laercio R, et al. The extent of linkage disequilibrium in beef cattle breeds using high-density SNP genotypes. ''Genet Sel Evol''. 2014 Mar 24; '''46''': 22
Genome-wide association studies for hematological traits in Chinese Sutai pigs. Description: Zhang, Feng, et al. Genome-wide association studies for hematological traits in Chinese Sutai pigs. ''BMC Genet''. 2014 Mar 27; '''15''': 41
Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy. Description: Sadler, Brooke, et al. Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy. ''Sci Rep''. 2014 Mar 28; '''4''': 4497
Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome. Description: Durdiakova, Jaroslava, et al. Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome. ''Mol Autism''. 2014 Mar 31; '''5''' (1):25
A central role for GRB10 in regulation of islet function in man. Description: Prokopenko, Inga, et al. A central role for GRB10 in regulation of islet function in man. ''PLoS Genet''. 2014 Apr; '''10''' (4):e1004235
A high-definition view of functional genetic variation from natural yeast genomes. Description: Bergstrom, Anders, et al. A high-definition view of functional genetic variation from natural yeast genomes. ''Mol Biol Evol''. 2014 Apr; '''31''' (4):872-88
A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence. Description: Wolf, Zena T, et al. A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence. ''PLoS Genet''. 2014 Apr; '''10''' (4):e1004257
Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adults. Description: Coon, Hilary, et al. Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adults. ''Alcohol Clin Exp Res''. 2014 Apr; '''38''' (4):930-7
Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain. Description: Viana, Joana, et al. Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain. ''Epigenetics''. 2014 Apr; '''9''' (4):587-99
Genetic predisposition to in situ and invasive lobular carcinoma of the breast. Description: Sawyer, Elinor, et al. Genetic predisposition to in situ and invasive lobular carcinoma of the breast. ''PLoS Genet''. 2014 Apr; '''10''' (4):e1004285
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Description: Nudel, R, et al. Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. ''Genes Brain Behav''. 2014 Apr; '''13''' (4):418-29
Imputation without doing imputation: a new method for the detection of non-genotyped causal variants. Description: Howey, Richard, et al. Imputation without doing imputation: a new method for the detection of non-genotyped causal variants. ''Genet Epidemiol''. 2014 Apr; '''38''' (3):173-90
One in four individuals of African-American ancestry harbors a 5.5kb deletion at chromosome 11q13.1. Description: Zainabadi, Kayvan, et al. One in four individuals of African-American ancestry harbors a 5.5kb deletion at chromosome 11q13.1. ''Genomics''. 2014 Apr; '''103''' (4):276-87
The 8p23 inversion polymorphism determines local recombination heterogeneity across human populations. Description: Alves, Joao M, et al. The 8p23 inversion polymorphism determines local recombination heterogeneity across human populations. ''Genome Biol Evol''. 2014 Apr; '''6''' (4):921-30
Genomic analysis establishes correlation between growth and laryngeal neuropathy in Thoroughbreds. Description: Boyko, Adam R, et al. Genomic analysis establishes correlation between growth and laryngeal neuropathy in Thoroughbreds. ''BMC Genomics''. 2014 Apr 3; '''15''': 259
mtDNA haplogroup and single nucleotide polymorphisms structure human microbiome communities. Description: Ma, Jun, et al. mtDNA haplogroup and single nucleotide polymorphisms structure human microbiome communities. ''BMC Genomics''. 2014 Apr 3; '''15''': 257
Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study. Description: Adams, Jeremy N, et al. Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study. ''Cardiovasc Diabetol''. 2014 Apr 12; '''13''': 77
Genome-wide linkage analysis and association study identifies loci for polydactyly in chickens. Description: Sun, Yanfa, et al. Genome-wide linkage analysis and association study identifies loci for polydactyly in chickens. ''G3 (Bethesda)''. 2014 Apr 21; '''4''' (6):1167-72
The total burden of rare, non-synonymous exome genetic variants is not associated with childhood or late-life cognitive ability. Description: Marioni, Riccardo E, et al. The total burden of rare, non-synonymous exome genetic variants is not associated with childhood or late-life cognitive ability. ''Proc Biol Sci''. 2014 Apr 22; '''281''' (1781):20140117
New insight into the SSC8 genetic determination of fatty acid composition in pigs. Description: Revilla, Manuel, et al. New insight into the SSC8 genetic determination of fatty acid composition in pigs. ''Genet Sel Evol''. 2014 Apr 23; '''46''': 28
Development and evaluation of the first high-throughput SNP array for common carp (Cyprinus carpio). Description: Xu, Jian, et al. Development and evaluation of the first high-throughput SNP array for common carp (Cyprinus carpio). ''BMC Genomics''. 2014 Apr 24; '''15''': 307
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). Description: Glover, Mark, et al. Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). ''Clin Sci (Lond)''. 2014 May; '''126''' (10):721-6
Dose-dependent incidence of hepatic tumors in adult mice following perinatal exposure to bisphenol A. Description: Weinhouse, Caren, et al. Dose-dependent incidence of hepatic tumors in adult mice following perinatal exposure to bisphenol A. ''Environ Health Perspect''. 2014 May; '''122''' (5):485-91
Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant. Description: Almeida, Rodrigo, et al. Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant. ''Hum Mol Genet''. 2014 May 1; '''23''' (9):2481-9
Genetic variation in vitamin D-related genes and risk of colorectal cancer in African Americans. Description: Pibiri, Fabio, et al. Genetic variation in vitamin D-related genes and risk of colorectal cancer in African Americans. ''Cancer Causes Control''. 2014 May; '''25''' (5):561-70
Genome-wide association study identifies novel loci associated with resistance to bovine tuberculosis. Description: Bermingham, M L, et al. Genome-wide association study identifies novel loci associated with resistance to bovine tuberculosis. ''Heredity (Edinb)''. 2014 May; '''112''' (5):543-51
Mild expression differences of MECP2 influencing aggressive social behavior. Description: Tantra, Martesa, et al. Mild expression differences of MECP2 influencing aggressive social behavior. ''EMBO Mol Med''. 2014 May; '''6''' (5):662-84
On detecting incomplete soft or hard selective sweeps using haplotype structure. Description: Ferrer-Admetlla, Anna, et al. On detecting incomplete soft or hard selective sweeps using haplotype structure. ''Mol Biol Evol''. 2014 May; '''31''' (5):1275-91
POT1 loss-of-function variants predispose to familial melanoma. Description: Robles-Espinoza, Carla Daniela, et al. POT1 loss-of-function variants predispose to familial melanoma. ''Nat Genet''. 2014 May; '''46''' (5):478-481
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma. Description: Shi, Jianxin, et al. Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma. ''Nat Genet''. 2014 May; '''46''' (5):482-6
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases. Description: Hudson, Gavin, et al. Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases. ''PLoS Genet''. 2014 May; '''10''' (5):e1004369
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland. Description: Wang, Sophie R, et al. Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland. ''Am J Hum Genet''. 2014 May 1; '''94''' (5):710-20
The impairment of MAGMAS function in human is responsible for a severe skeletal dysplasia. Description: Mehawej, Cybel, et al. The impairment of MAGMAS function in human is responsible for a severe skeletal dysplasia. ''PLoS Genet''. 2014 May; '''10''' (5):e1004311
TLR4 single nucleotide polymorphisms (SNPs) associated with Salmonella shedding in pigs. Description: Kich, Jalusa Deon, et al. TLR4 single nucleotide polymorphisms (SNPs) associated with Salmonella shedding in pigs. ''J Appl Genet''. 2014 May; '''55''' (2):267-71
Association of serine racemase gene variants with type 2 diabetes in the Chinese Han population. Description: Zhang, Simin, et al. Association of serine racemase gene variants with type 2 diabetes in the Chinese Han population. ''J Diabetes Investig''. 2014 May 4; '''5''' (3):286-9
Epidermal growth factor receptor (EGFR) pathway genes and interstitial lung disease: an association study. Description: Li, Chong, et al. Epidermal growth factor receptor (EGFR) pathway genes and interstitial lung disease: an association study. ''Sci Rep''. 2014 May 13; '''4''': 4893
Deciphering the genetic blueprint behind Holstein milk proteins and production. Description: Lee, Hyun-Jeong, et al. Deciphering the genetic blueprint behind Holstein milk proteins and production. ''Genome Biol Evol''. 2014 May 14; '''6''' (6):1366-74
Association between risk of oral precancer and genetic variations in microRNA and related processing genes. Description: Roy, Roshni, et al. Association between risk of oral precancer and genetic variations in microRNA and related processing genes. ''J Biomed Sci''. 2014 May 17; '''21''': 48
Genome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in Flat-Coated Retrievers. Description: Lavrijsen, Ineke C M, et al. Genome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in Flat-Coated Retrievers. ''BMC Genet''. 2014 May 28; '''15''': 64
Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population. Description: Vishal, Mansi, et al. Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population. ''Sci Rep''. 2014 May 30; '''4''': 5115
Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder. Description: Kandaswamy, Radhika, et al. Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder. ''Am J Med Genet B Neuropsychiatr Genet''. 2014 Jun; '''165B''' (4):365-72
ATP5H/KCTD2 locus is associated with Alzheimer's disease risk. Description: Boada, M, et al. ATP5H/KCTD2 locus is associated with Alzheimer's disease risk. ''Mol Psychiatry''. 2014 Jun; '''19''' (6):682-7
Early back-to-Africa migration into the Horn of Africa. Description: Hodgson, Jason A, et al. Early back-to-Africa migration into the Horn of Africa. ''PLoS Genet''. 2014 Jun; '''10''' (6):e1004393
Gene-set based genome-wide association analysis for the speed of sound in two skeletal sites of Korean women. Description: Kwon, Ji-Sun, et al. Gene-set based genome-wide association analysis for the speed of sound in two skeletal sites of Korean women. ''BMB Rep''. 2014 Jun; '''47''' (6):348-53
Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study. Description: Varga, Tibor V, et al. Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study. ''PLoS Genet''. 2014 Jun; '''10''' (6):e1004388
Genetic variation in OPRD1 and the response to treatment for opioid dependence with buprenorphine in European-American females. Description: Clarke, T-K, et al. Genetic variation in OPRD1 and the response to treatment for opioid dependence with buprenorphine in European-American females. ''Pharmacogenomics J''. 2014 Jun; '''14''' (3):303-8
Germline genetic variants in ABCB1, ABCC1 and ALDH1A1, and risk of hematological and gastrointestinal toxicities in a SWOG Phase III trial S0221 for breast cancer. Description: Yao, S, et al. Germline genetic variants in ABCB1, ABCC1 and ALDH1A1, and risk of hematological and gastrointestinal toxicities in a SWOG Phase III trial S0221 for breast cancer. ''Pharmacogenomics J''. 2014 Jun; '''14''' (3):241-7
Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. Description: Juraeva, Dilafruz, et al. Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. ''PLoS Genet''. 2014 Jun; '''10''' (6):e1004345
Introgression from domestic goat generated variation at the major histocompatibility complex of Alpine ibex. Description: Grossen, Christine, et al. Introgression from domestic goat generated variation at the major histocompatibility complex of Alpine ibex. ''PLoS Genet''. 2014 Jun; '''10''' (6):e1004438
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. Description: Zhang, Ben, et al. Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. ''Nat Genet''. 2014 Jun; '''46''' (6):533-42
Missense variant in TREML2 protects against Alzheimer's disease. Description: Benitez, Bruno A, et al. Missense variant in TREML2 protects against Alzheimer's disease. ''Neurobiol Aging''. 2014 Jun; '''35''' (6):1510.e19-26
Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome. Description: Mok, Kin Y, et al. Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome. ''Neurobiol Aging''. 2014 Jun; '''35''' (6):1513.e1-5
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. Description: Auer, Paul L, et al. Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. ''Nat Genet''. 2014 Jun; '''46''' (6):629-34
Variants in host viral replication cycle genes are associated with heterosexual HIV-1 acquisition in Africans. Description: Bigham, Abigail W, et al. Variants in host viral replication cycle genes are associated with heterosexual HIV-1 acquisition in Africans. ''J Acquir Immune Defic Syndr''. 2014 Jun 1; '''66''' (2):127-34
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. Description: Ko, Arthur, et al. Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. ''Nat Commun''. 2014 Jun 2; '''5''': 3983
Functional analysis of the TRIB1 associated locus linked to plasma triglycerides and coronary artery disease. Description: Douvris, Adrianna, et al. Functional analysis of the TRIB1 associated locus linked to plasma triglycerides and coronary artery disease. ''J Am Heart Assoc''. 2014 Jun 3; '''3''' (3):e000884
Genetic architecture of rind penetrometer resistance in two maize recombinant inbred line populations. Description: Li, Kun, et al. Genetic architecture of rind penetrometer resistance in two maize recombinant inbred line populations. ''BMC Plant Biol''. 2014 Jun 3; '''14''': 152
Single nucleotide polymorphism and haplotype effects associated with somatic cell score in German Holstein cattle. Description: Abdel-Shafy, Hamdy, et al. Single nucleotide polymorphism and haplotype effects associated with somatic cell score in German Holstein cattle. ''Genet Sel Evol''. 2014 Jun 4; '''46''': 35
Association mapping of germination traits in Arabidopsis thaliana under light and nutrient treatments: searching for GxE effects. Description: Morrison, Ginnie D, et al. Association mapping of germination traits in Arabidopsis thaliana under light and nutrient treatments: searching for GxE effects. ''G3 (Bethesda)''. 2014 Jun 5; '''4''' (8):1465-78
Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance. Description: Choudhury, Ananyo, et al. Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance. ''BMC Genomics''. 2014 Jun 6; '''15''': 437
Regulatory and coding genome regions are enriched for trait associated variants in dairy and beef cattle. Description: Koufariotis, Lambros, et al. Regulatory and coding genome regions are enriched for trait associated variants in dairy and beef cattle. ''BMC Genomics''. 2014 Jun 6; '''15''': 436
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism. Description: Hadley, Dexter, et al. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism. ''Nat Commun''. 2014 Jun 13; '''5''': 4074
Weighted risk score-based multifactor dimensionality reduction to detect gene-gene interactions in nasopharyngeal carcinoma. Description: Li, Chao-Feng, et al. Weighted risk score-based multifactor dimensionality reduction to detect gene-gene interactions in nasopharyngeal carcinoma. ''Int J Mol Sci''. 2014 Jun 13; '''15''' (6):10724-37
Performance of HLA allele prediction methods in African Americans for class II genes HLA-DRB1, -DQB1, and -DPB1. Description: Levin, Albert M, et al. Performance of HLA allele prediction methods in African Americans for class II genes HLA-DRB1, -DQB1, and -DPB1. ''BMC Genet''. 2014 Jun 16; '''15''': 72
Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. Description: Nakano, Masakazu, et al. Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. ''Sci Rep''. 2014 Jun 18; '''4''': 5340
Homoeologous duplicated regions are involved in quantitative resistance of Brassica napus to stem canker. Description: Fopa Fomeju, Berline, et al. Homoeologous duplicated regions are involved in quantitative resistance of Brassica napus to stem canker. ''BMC Genomics''. 2014 Jun 19; '''15''': 498
The role of FKBP5 genotype in moderating long-term effectiveness of exposure-based psychotherapy for posttraumatic stress disorder. Description: Wilker, S, et al. The role of FKBP5 genotype in moderating long-term effectiveness of exposure-based psychotherapy for posttraumatic stress disorder. ''Transl Psychiatry''. 2014 Jun 24; '''4''': e403
A linkage map of transcribed single nucleotide polymorphisms in rohu (Labeo rohita) and QTL associated with resistance to Aeromonas hydrophila. Description: Robinson, Nicholas, et al. A linkage map of transcribed single nucleotide polymorphisms in rohu (Labeo rohita) and QTL associated with resistance to Aeromonas hydrophila. ''BMC Genomics''. 2014 Jun 30; '''15''': 541
Evaluating the accuracy of AIM panels at quantifying genome ancestry. Description: Pardo-Seco, Jacobo, et al. Evaluating the accuracy of AIM panels at quantifying genome ancestry. ''BMC Genomics''. 2014 Jun 30; '''15''': 543
TM6SF2 rs58542926 influences hepatic fibrosis progression in patients with non-alcoholic fatty liver disease. Description: Liu, Yang-Lin, et al. TM6SF2 rs58542926 influences hepatic fibrosis progression in patients with non-alcoholic fatty liver disease. ''Nat Commun''. 2014 Jun 30; '''5''': 4309
A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach. Description: Traylor, Matthew, et al. A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach. ''PLoS Genet''. 2014 Jul; '''10''' (7):e1004469
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. Description: Eicher, John D, et al. Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. ''Hum Genet''. 2014 Jul; '''133''' (7):869-81
CYP1A1 Ile462Val polymorphism and colorectal cancer risk in Polish patients. Description: Gil, Justyna, et al. CYP1A1 Ile462Val polymorphism and colorectal cancer risk in Polish patients. ''Med Oncol''. 2014 Jul; '''31''' (7):72
Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. Description: Mullins, Niamh, et al. Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. ''Am J Med Genet B Neuropsychiatr Genet''. 2014 Jul; '''165B''' (5):428-37
Microsatellite interruptions stabilize primate genomes and exist as population-specific single nucleotide polymorphisms within individual human genomes. Description: Ananda, Guruprasad, et al. Microsatellite interruptions stabilize primate genomes and exist as population-specific single nucleotide polymorphisms within individual human genomes. ''PLoS Genet''. 2014 Jul; '''10''' (7):e1004498
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. Description: Wang, Yufei, et al. Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. ''Nat Genet''. 2014 Jul; '''46''' (7):736-41
Sorafenib dose escalation is not uniformly associated with blood pressure elevations in normotensive patients with advanced malignancies. Description: Karovic, S, et al. Sorafenib dose escalation is not uniformly associated with blood pressure elevations in normotensive patients with advanced malignancies. ''Clin Pharmacol Ther''. 2014 Jul; '''96''' (1):27-35
Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease. Description: Petersen, Britt-Sabina, et al. Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease. ''BMC Genomics''. 2014 Jul 5; '''15''': 564
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission. Description: Karayannis, T, et al. Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission. ''Nature''. 2014 Jul 10; '''511''' (7508):236-40
Joint identification of genetic variants for physical activity in Korean population. Description: Kim, Jayoun, et al. Joint identification of genetic variants for physical activity in Korean population. ''Int J Mol Sci''. 2014 Jul 14; '''15''' (7):12407-21
Insight into genetic determinants of resting heart rate. Description: Mezzavilla, Massimo, et al. Insight into genetic determinants of resting heart rate. ''Gene''. 2014 Jul 15; '''545''' (1):170-4
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay. Description: Weber, Megan L, et al. Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay. ''BMC Med Genet''. 2014 Jul 15; '''15''': 81
Fast and cost-effective genetic mapping in apple using next-generation sequencing. Description: Gardner, Kyle M, et al. Fast and cost-effective genetic mapping in apple using next-generation sequencing. ''G3 (Bethesda)''. 2014 Jul 16; '''4''' (9):1681-7
Whole-genome sequence analysis reveals differences in population management and selection of European low-input pig breeds. Description: Herrero-Medrano, Juan Manuel, et al. Whole-genome sequence analysis reveals differences in population management and selection of European low-input pig breeds. ''BMC Genomics''. 2014 Jul 16; '''15''': 601
Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis. Description: Backes, Christina, et al. Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis. ''BMC Genomics''. 2014 Jul 22; '''15''': 622
Validation and assessment of variant calling pipelines for next-generation sequencing. Description: Pirooznia, Mehdi, et al. Validation and assessment of variant calling pipelines for next-generation sequencing. ''Hum Genomics''. 2014 Jul 30; '''8''': 14
A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain. Description: Gershon, E S, et al. A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain. ''Mol Psychiatry''. 2014 Aug; '''19''' (8):890-4
Comprehensive identification of single nucleotide polymorphisms associated with beta-lactam resistance within pneumococcal mosaic genes. Description: Chewapreecha, Claire, et al. Comprehensive identification of single nucleotide polymorphisms associated with beta-lactam resistance within pneumococcal mosaic genes. ''PLoS Genet''. 2014 Aug; '''10''' (8):e1004547
Genetic variation of oxidative phosphorylation genes in stroke and Alzheimer's disease. Description: Biffi, Alessandro, et al. Genetic variation of oxidative phosphorylation genes in stroke and Alzheimer's disease. ''Neurobiol Aging''. 2014 Aug; '''35''' (8):1956.e1-8
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1. Description: Cai, Qiuyin, et al. Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1. ''Nat Genet''. 2014 Aug; '''46''' (8):886-90
Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats. Description: Alhaddad, Hasan, et al. Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats. ''Mamm Genome''. 2014 Aug; '''25''' (7-8):354-62
Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases. Description: Cobb, J, et al. Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases. ''Pharmacogenomics J''. 2014 Aug; '''14''' (4):356-64
Global genetic variations predict brain response to faces. Description: Dickie, Erin W, et al. Global genetic variations predict brain response to faces. ''PLoS Genet''. 2014 Aug; '''10''' (8):e1004523
Heritability and genetic association analysis of cognition in the Diabetes Heart Study. Description: Cox, Amanda J, et al. Heritability and genetic association analysis of cognition in the Diabetes Heart Study. ''Neurobiol Aging''. 2014 Aug; '''35''' (8):1958.e3-1958.e12
MODMatcher: multi-omics data matcher for integrative genomic analysis. Description: Yoo, Seungyeul, et al. MODMatcher: multi-omics data matcher for integrative genomic analysis. ''PLoS Comput Biol''. 2014 Aug; '''10''' (8):e1003790
Patterns of admixture and population structure in native populations of Northwest North America. Description: Verdu, Paul, et al. Patterns of admixture and population structure in native populations of Northwest North America. ''PLoS Genet''. 2014 Aug; '''10''' (8):e1004530
Genetic evidence of African slavery at the beginning of the trans-Atlantic slave trade. Description: Martiniano, Rui, et al. Genetic evidence of African slavery at the beginning of the trans-Atlantic slave trade. ''Sci Rep''. 2014 Aug 8; '''4''': 5994
Lack of association between miR-27a, miR-146a, miR-196a-2, miR-492 and miR-608 gene polymorphisms and colorectal cancer. Description: Kupcinskas, Juozas, et al. Lack of association between miR-27a, miR-146a, miR-196a-2, miR-492 and miR-608 gene polymorphisms and colorectal cancer. ''Sci Rep''. 2014 Aug 8; '''4''': 5993
Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. Description: Wang, Hansong, et al. Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. ''Nat Commun''. 2014 Aug 8; '''5''': 4613
Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population. Description: Motoike, Ikuko N, et al. Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population. ''BMC Genomics''. 2014 Aug 10; '''15''': 673
Impact of pre-imputation SNP-filtering on genotype imputation results. Description: Roshyara, Nab Raj, et al. Impact of pre-imputation SNP-filtering on genotype imputation results. ''BMC Genet''. 2014 Aug 12; '''15''': 88
Association study of genes controlling IL-12-dependent IFN-gamma immunity: STAT4 alleles increase risk of pulmonary tuberculosis in Morocco. Description: Sabri, Ayoub, et al. Association study of genes controlling IL-12-dependent IFN-gamma immunity: STAT4 alleles increase risk of pulmonary tuberculosis in Morocco. ''J Infect Dis''. 2014 Aug 15; '''210''' (4):611-8
Impact of a functional polymorphism in the PAR-1 gene promoter in COPD and COPD exacerbations. Description: Plate, Manuela, et al. Impact of a functional polymorphism in the PAR-1 gene promoter in COPD and COPD exacerbations. ''Am J Physiol Lung Cell Mol Physiol''. 2014 Aug 15; '''307''' (4):L311-6
Top associated SNPs in prostate cancer are significantly enriched in cis-expression quantitative trait loci and at transcription factor binding sites. Description: Jiang, Junfeng, et al. Top associated SNPs in prostate cancer are significantly enriched in cis-expression quantitative trait loci and at transcription factor binding sites. ''Oncotarget''. 2014 Aug 15; '''5''' (15):6168-77
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. Description: Enroth, Stefan, et al. Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. ''Nat Commun''. 2014 Aug 22; '''5''': 4684
MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD. Description: Nieratschker, V, et al. MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD. ''Transl Psychiatry''. 2014 Aug 26; '''4''': e429
QTL for white spot syndrome virus resistance and the sex-determining locus in the Indian black tiger shrimp (Penaeus monodon). Description: Robinson, Nicholas A, et al. QTL for white spot syndrome virus resistance and the sex-determining locus in the Indian black tiger shrimp (Penaeus monodon). ''BMC Genomics''. 2014 Aug 28; '''15''': 731
An intronic PICALM polymorphism, rs588076, is associated with allelic expression of a PICALM isoform. Description: Parikh, Ishita, et al. An intronic PICALM polymorphism, rs588076, is associated with allelic expression of a PICALM isoform. ''Mol Neurodegener''. 2014 Aug 29; '''9''': 32
A Follow-up Association Study of Genetic Variants for Bone Mineral Density in a Korean Population. Description: Ham, Seokjin, et al. A Follow-up Association Study of Genetic Variants for Bone Mineral Density in a Korean Population. ''Genomics Inform''. 2014 Sep; '''12''' (3):114-20
A single codon insertion in PICALM is associated with development of familial subvalvular aortic stenosis in Newfoundland dogs. Description: Stern, Joshua A, et al. A single codon insertion in PICALM is associated with development of familial subvalvular aortic stenosis in Newfoundland dogs. ''Hum Genet''. 2014 Sep; '''133''' (9):1139-48
A whole genome association study on meat palatability in hanwoo. Description: Hyeong, K-E, et al. A whole genome association study on meat palatability in hanwoo. ''Asian-Australas J Anim Sci''. 2014 Sep; '''27''' (9):1219-27
Co-regulated transcripts associated to cooperating eSNPs define Bi-fan motifs in human gene networks. Description: Kreimer, Anat, et al. Co-regulated transcripts associated to cooperating eSNPs define Bi-fan motifs in human gene networks. ''PLoS Genet''. 2014 Sep; '''10''' (9):e1004587
Epidemiological and genome-wide association study of gastritis or gastric ulcer in korean populations. Description: Oh, Sumin, et al. Epidemiological and genome-wide association study of gastritis or gastric ulcer in korean populations. ''Genomics Inform''. 2014 Sep; '''12''' (3):127-33
Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Description: Beecham, Gary W, et al. Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. ''PLoS Genet''. 2014 Sep; '''10''' (9):e1004606
Genome-wide association study of medication adherence in chronic diseases in the korean population. Description: Seo, Incheol, et al. Genome-wide association study of medication adherence in chronic diseases in the korean population. ''Genomics Inform''. 2014 Sep; '''12''' (3):121-6
Genome-wide screening for DNA variants associated with reading and language traits. Description: Gialluisi, A, et al. Genome-wide screening for DNA variants associated with reading and language traits. ''Genes Brain Behav''. 2014 Sep; '''13''' (7):686-701
GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Description: Christoforou, A, et al. GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. ''Genes Brain Behav''. 2014 Sep; '''13''' (7):663-74
Inferring population structure and relationship using minimal independent evolutionary markers in Y-chromosome: a hybrid approach of recursive feature selection for hierarchical clustering. Description: Srivastava, Amit Kumar, et al. Inferring population structure and relationship using minimal independent evolutionary markers in Y-chromosome: a hybrid approach of recursive feature selection for hierarchical clustering. ''Nucleic Acids Res''. 2014 Sep; '''42''' (15):e122
Principal component analysis characterizes shared pathogenetics from genome-wide association studies. Description: Chang, Diana, et al. Principal component analysis characterizes shared pathogenetics from genome-wide association studies. ''PLoS Comput Biol''. 2014 Sep; '''10''' (9):e1003820
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles. Description: Goldstein, Jacqueline I, et al. Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles. ''Nat Commun''. 2014 Sep 4; '''5''': 4757
EYA4 is inactivated biallelically at a high frequency in sporadic lung cancer and is associated with familial lung cancer risk. Description: Wilson, I M, et al. EYA4 is inactivated biallelically at a high frequency in sporadic lung cancer and is associated with familial lung cancer risk. ''Oncogene''. 2014 Sep 4; '''33''' (36):4464-73
Genetic polymorphisms and asthma: findings from a case-control study in the Madeira island population. Description: Berenguer, Anabela Goncalves, et al. Genetic polymorphisms and asthma: findings from a case-control study in the Madeira island population. ''Biol Res''. 2014 Sep 4; '''47''': 40
Genetic variation in taste receptor pseudogenes provides evidence for a dynamic role in human evolution. Description: Risso, Davide, et al. Genetic variation in taste receptor pseudogenes provides evidence for a dynamic role in human evolution. ''BMC Evol Biol''. 2014 Sep 13; '''14''': 198
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. Description: Timpson, Nicholas J, et al. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. ''Nat Commun''. 2014 Sep 16; '''5''': 4871
Common variation near ROBO2 is associated with expressive vocabulary in infancy. Description: St Pourcain, Beate, et al. Common variation near ROBO2 is associated with expressive vocabulary in infancy. ''Nat Commun''. 2014 Sep 16; '''5''': 4831
Ancient human genomes suggest three ancestral populations for present-day Europeans. Description: Lazaridis, Iosif, et al. Ancient human genomes suggest three ancestral populations for present-day Europeans. ''Nature''. 2014 Sep 18; '''513''' (7518):409-13
A powerful tool for genome analysis in maize: development and evaluation of the high density 600 k SNP genotyping array. Description: Unterseer, Sandra, et al. A powerful tool for genome analysis in maize: development and evaluation of the high density 600 k SNP genotyping array. ''BMC Genomics''. 2014 Sep 29; '''15''': 823
Genetic association of impulsivity in young adults: a multivariate study. Description: Khadka, S, et al. Genetic association of impulsivity in young adults: a multivariate study. ''Transl Psychiatry''. 2014 Sep 30; '''4''': e451
Genomic evidence for a globally distributed, bimodal population in the ovine footrot pathogen Dichelobacter nodosus. Description: Kennan, Ruth M, et al. Genomic evidence for a globally distributed, bimodal population in the ovine footrot pathogen Dichelobacter nodosus. ''MBio''. 2014 Sep 30; '''5''' (5):e01821-14
A Genome Wide Association Study on Age at First Calving Using High Density Single Nucleotide Polymorphism Chips in Hanwoo (Bos taurus coreanae). Description: Hyeong, K-E, et al. A Genome Wide Association Study on Age at First Calving Using High Density Single Nucleotide Polymorphism Chips in Hanwoo (Bos taurus coreanae). ''Asian-Australas J Anim Sci''. 2014 Oct; '''27''' (10):1406-10
An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. Description: Ekenstedt, Kari J, et al. An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004635
A splice mutation in the PHKG1 gene causes high glycogen content and low meat quality in pig skeletal muscle. Description: Ma, Junwu, et al. A splice mutation in the PHKG1 gene causes high glycogen content and low meat quality in pig skeletal muscle. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004710
Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles. Description: Kripke, Daniel F, et al. Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles. ''Psychiatry Investig''. 2014 Oct; '''11''' (4):345-62
Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation. Description: Kauwe, John S K, et al. Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004758
Genome-wide discovery of drug-dependent human liver regulatory elements. Description: Smith, Robin P, et al. Genome-wide discovery of drug-dependent human liver regulatory elements. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004648
Genomic prediction based on data from three layer lines: a comparison between linear methods. Description: Calus, Mario Pl, et al. Genomic prediction based on data from three layer lines: a comparison between linear methods. ''Genet Sel Evol''. 2014 Oct 1; '''46''': 57
Germline mutations in MAP3K6 are associated with familial gastric cancer. Description: Gaston, Daniel, et al. Germline mutations in MAP3K6 are associated with familial gastric cancer. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004669
Imputation of sequence level genotypes in the Franches-Montagnes horse breed. Description: Frischknecht, Mirjam, et al. Imputation of sequence level genotypes in the Franches-Montagnes horse breed. ''Genet Sel Evol''. 2014 Oct 1; '''46''': 63
Pathway-based analysis tools for complex diseases: a review. Description: Jin, Lv, et al. Pathway-based analysis tools for complex diseases: a review. ''Genomics Proteomics Bioinformatics''. 2014 Oct; '''12''' (5):210-20
Population history and genomic signatures for high-altitude adaptation in Tibetan pigs. Description: Ai, Huashui, et al. Population history and genomic signatures for high-altitude adaptation in Tibetan pigs. ''BMC Genomics''. 2014 Oct 1; '''15''': 834
Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers. Description: Sanchez-Molano, Enrique, et al. Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers. ''BMC Genomics''. 2014 Oct 1; '''15''': 833
Study of five novel non-synonymous polymorphisms in human brain-expressed genes in a Colombian sample. Description: Ojeda, Diego A, et al. Study of five novel non-synonymous polymorphisms in human brain-expressed genes in a Colombian sample. ''Ann Neurosci''. 2014 Oct; '''21''' (4):138-43
Using ancestry-informative markers to identify fine structure across 15 populations of European origin. Description: Huckins, Laura M, et al. Using ancestry-informative markers to identify fine structure across 15 populations of European origin. ''Eur J Hum Genet''. 2014 Oct; '''22''' (10):1190-200
Comparative genomics reveals multiple genetic backgrounds of human pathogenicity in the Trypanosoma brucei complex. Description: Sistrom, Mark, et al. Comparative genomics reveals multiple genetic backgrounds of human pathogenicity in the Trypanosoma brucei complex. ''Genome Biol Evol''. 2014 Oct 5; '''6''' (10):2811-9
alphaCaMKII controls the establishment of cocaine's reinforcing effects in mice and humans. Description: Easton, A C, et al. alphaCaMKII controls the establishment of cocaine's reinforcing effects in mice and humans. ''Transl Psychiatry''. 2014 Oct 7; '''4''': e457
A meta-analysis of gene expression quantitative trait loci in brain. Description: Kim, Y, et al. A meta-analysis of gene expression quantitative trait loci in brain. ''Transl Psychiatry''. 2014 Oct 7; '''4''': e459
A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival. Description: Baecklund, Fredrik, et al. A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival. ''BMC Med Genet''. 2014 Oct 8; '''15''': 113
Genome wide linkage disequilibrium and genetic structure in Sicilian dairy sheep breeds. Description: Mastrangelo, Salvatore, et al. Genome wide linkage disequilibrium and genetic structure in Sicilian dairy sheep breeds. ''BMC Genet''. 2014 Oct 10; '''15''': 108
The genetics of monarch butterfly migration and warning colouration. Description: Zhan, Shuai, et al. The genetics of monarch butterfly migration and warning colouration. ''Nature''. 2014 Oct 16; '''514''' (7522):317-21
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. Description: Fejerman, Laura, et al. Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. ''Nat Commun''. 2014 Oct 20; '''5''': 5260
An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. Description: Zochling, Jane, et al. An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. ''Arthritis Res Ther''. 2014 Oct 21; '''16''' (5):438
Common variants at 1p36 are associated with superior frontal gyrus volume. Description: Hashimoto, R, et al. Common variants at 1p36 are associated with superior frontal gyrus volume. ''Transl Psychiatry''. 2014 Oct 21; '''4''': e472
Genome flux and stasis in a five millennium transect of European prehistory. Description: Gamba, Cristina, et al. Genome flux and stasis in a five millennium transect of European prehistory. ''Nat Commun''. 2014 Oct 21; '''5''': 5257
Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma. Description: Darlington, T M, et al. Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma. ''Transl Psychiatry''. 2014 Oct 21; '''4''': e471
Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population. Description: Liao, Li-Na, et al. Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population. ''BMC Genet''. 2014 Oct 31; '''15''': 113
Adiposity significantly modifies genetic risk for dyslipidemia. Description: Cole, Christopher B, et al. Adiposity significantly modifies genetic risk for dyslipidemia. ''J Lipid Res''. 2014 Nov; '''55''' (11):2416-22
Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2). Description: Karaderi, T, et al. Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2). ''Ann Rheum Dis''. 2014 Nov; '''73''' (11):2054-8
A population-based study of genetic variation and psychotic experiences in adolescents. Description: Zammit, Stanley, et al. A population-based study of genetic variation and psychotic experiences in adolescents. ''Schizophr Bull''. 2014 Nov; '''40''' (6):1254-62
A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia. Description: Huusko, Johanna M, et al. A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia. ''BMC Med Genet''. 2014 Nov 1; '''15''': 120
BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT. Description: Piras, Ignazio Stefano, et al. BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT. ''Bone Marrow Transplant''. 2014 Nov; '''49''' (11):1400-1404
Common vitamin D pathway gene variants reveal contrasting effects on serum vitamin D levels in African Americans and European Americans. Description: Batai, Ken, et al. Common vitamin D pathway gene variants reveal contrasting effects on serum vitamin D levels in African Americans and European Americans. ''Hum Genet''. 2014 Nov; '''133''' (11):1395-405
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. Description: Kiryluk, Krzysztof, et al. Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. ''Nat Genet''. 2014 Nov; '''46''' (11):1187-96
Evaluation of genome based estimated breeding values for meat quality in a berkshire population using high density single nucleotide polymorphism chips. Description: Baby, S, et al. Evaluation of genome based estimated breeding values for meat quality in a berkshire population using high density single nucleotide polymorphism chips. ''Asian-Australas J Anim Sci''. 2014 Nov; '''27''' (11):1540-7
Evaluation of variant identification methods for whole genome sequencing data in dairy cattle. Description: Baes, Christine F, et al. Evaluation of variant identification methods for whole genome sequencing data in dairy cattle. ''BMC Genomics''. 2014 Nov 1; '''15''': 948
Genetic determinants in the development of sensitization to environmental allergens in early childhood. Description: Tripathi, Priya, et al. Genetic determinants in the development of sensitization to environmental allergens in early childhood. ''Immun Inflamm Dis''. 2014 Nov; '''2''' (3):193-204
Genetic variations in protocadherin 15 and their interactions with noise exposure associated with noise-induced hearing loss in Chinese population. Description: Zhang, Xuhui, et al. Genetic variations in protocadherin 15 and their interactions with noise exposure associated with noise-induced hearing loss in Chinese population. ''Environ Res''. 2014 Nov; '''135''': 247-52
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. Description: Deelen, Patrick, et al. Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. ''Eur J Hum Genet''. 2014 Nov; '''22''' (11):1321-6
No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure. Description: Cousijn, Helena, et al. No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure. ''Schizophr Res''. 2014 Nov; '''159''' (2-3):329-32
Unusual Stuve-Wiedemann syndrome with complete maternal chromosome 5 isodisomy. Description: Melone, Mariarosa A B, et al. Unusual Stuve-Wiedemann syndrome with complete maternal chromosome 5 isodisomy. ''Ann Clin Transl Neurol''. 2014 Nov; '''1''' (11):926-32
Genetic variants in ADAM33 are associated with airway inflammation and lung function in COPD. Description: Wang, Xinyan, et al. Genetic variants in ADAM33 are associated with airway inflammation and lung function in COPD. ''BMC Pulm Med''. 2014 Nov 4; '''14''': 173
The genome of a Mongolian individual reveals the genetic imprints of Mongolians on modern human populations. Description: Bai, Haihua, et al. The genome of a Mongolian individual reveals the genetic imprints of Mongolians on modern human populations. ''Genome Biol Evol''. 2014 Nov 5; '''6''' (12):3122-36
Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants. Description: Panoutsopoulou, Kalliope, et al. Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants. ''Nat Commun''. 2014 Nov 6; '''5''': 5345
Sexually dimorphic genetic architecture of complex traits in a large-scale F2 cross in pigs. Description: Cui, Leilei, et al. Sexually dimorphic genetic architecture of complex traits in a large-scale F2 cross in pigs. ''Genet Sel Evol''. 2014 Nov 6; '''46''': 76
Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa. Description: Alkan, Can, et al. Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa. ''BMC Genomics''. 2014 Nov 7; '''15''': 963
Large-scale gene-centric analysis identifies polymorphisms for resistant hypertension. Description: Fontana, Vanessa, et al. Large-scale gene-centric analysis identifies polymorphisms for resistant hypertension. ''J Am Heart Assoc''. 2014 Nov 10; '''3''' (6):e001398
Gender specific association of a complement component 3 polymorphism with polypoidal choroidal vasculopathy. Description: Liu, Ke, et al. Gender specific association of a complement component 3 polymorphism with polypoidal choroidal vasculopathy. ''Sci Rep''. 2014 Nov 12; '''4''': 7018
WISP1 polymorphisms contribute to platinum-based chemotherapy toxicity in lung cancer patients. Description: Chen, Juan, et al. WISP1 polymorphisms contribute to platinum-based chemotherapy toxicity in lung cancer patients. ''Int J Mol Sci''. 2014 Nov 14; '''15''' (11):21011-27
Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs. Description: Cao, Hongbao, et al. Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs. ''Neuroimage''. 2014 Nov 15; '''102 Pt 1''': 220-8
Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity. Description: Willmann, Katharina L, et al. Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity. ''Nat Commun''. 2014 Nov 19; '''5''': 5360
Association of rs6982567 near GDF6 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a Han Chinese cohort. Description: Ji, Yuying, et al. Association of rs6982567 near GDF6 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a Han Chinese cohort. ''BMC Ophthalmol''. 2014 Nov 22; '''14''': 140
Effect of diversity and missing data on genetic assignment with RAD-Seq markers. Description: Chattopadhyay, Balaji, et al. Effect of diversity and missing data on genetic assignment with RAD-Seq markers. ''BMC Res Notes''. 2014 Nov 25; '''7''': 841
Using multi-way admixture mapping to elucidate TB susceptibility in the South African Coloured population. Description: Daya, Michelle, et al. Using multi-way admixture mapping to elucidate TB susceptibility in the South African Coloured population. ''BMC Genomics''. 2014 Nov 25; '''15''': 1021
Endophenotypes for Age-Related Macular Degeneration: Extending Our Reach into the Preclinical Stages of Disease. Description: Gorin, Michael B, et al. Endophenotypes for Age-Related Macular Degeneration: Extending Our Reach into the Preclinical Stages of Disease. ''J Clin Med''. 2014 Nov 28; '''3''' (4):1335-56
Adaptations to climate-mediated selective pressures in sheep. Description: Lv, Feng-Hua, et al. Adaptations to climate-mediated selective pressures in sheep. ''Mol Biol Evol''. 2014 Dec; '''31''' (12):3324-43
A genome-wide association study identifies a LEPR gene as a novel predisposing factor for childhood fasting plasma glucose. Description: Go, Min Jin, et al. A genome-wide association study identifies a LEPR gene as a novel predisposing factor for childhood fasting plasma glucose. ''Genomics''. 2014 Dec; '''104''' (6 Pt B):594-8
Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder. Description: Witt, Stephanie H, et al. Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder. ''Psychiatr Genet''. 2014 Dec; '''24''' (6):262-5
Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population. Description: Radovica, I, et al. Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population. ''Meta Gene''. 2014 Dec; '''2''': 565-78
Association of Toll-like receptor polymorphisms with HIV status in North Americans. Description: Willie, B, et al. Association of Toll-like receptor polymorphisms with HIV status in North Americans. ''Genes Immun''. 2014 Dec; '''15''' (8):569-77
Drosophila suzukii: the genetic footprint of a recent, worldwide invasion. Description: Adrion, Jeffrey R, et al. Drosophila suzukii: the genetic footprint of a recent, worldwide invasion. ''Mol Biol Evol''. 2014 Dec; '''31''' (12):3148-63
Establishment of CYP2D6 reference samples by multiple validated genotyping platforms. Description: Fang, H, et al. Establishment of CYP2D6 reference samples by multiple validated genotyping platforms. ''Pharmacogenomics J''. 2014 Dec; '''14''' (6):564-72
Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13. Description: Tomlinson, M Joseph 4th, et al. Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13. ''Diabetes''. 2014 Dec; '''63''' (12):4360-8
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Description: Bras, Jose, et al. Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. ''Hum Mol Genet''. 2014 Dec 1; '''23''' (23):6139-46
Genetic analysis of axial length genes in high grade myopia from Indian population. Description: Sharmila, Ferdinamarie, et al. Genetic analysis of axial length genes in high grade myopia from Indian population. ''Meta Gene''. 2014 Dec; '''2''': 164-75
Genome-wide association study identifies candidate Loci associated with platelet count in koreans. Description: Oh, Ji Hee, et al. Genome-wide association study identifies candidate Loci associated with platelet count in koreans. ''Genomics Inform''. 2014 Dec; '''12''' (4):225-30
Genome-wide association study of hepatitis in korean populations. Description: Hong, Youngbok, et al. Genome-wide association study of hepatitis in korean populations. ''Genomics Inform''. 2014 Dec; '''12''' (4):203-7
Genome-wide association study of metabolic syndrome in koreans. Description: Jeong, Seok Won, et al. Genome-wide association study of metabolic syndrome in koreans. ''Genomics Inform''. 2014 Dec; '''12''' (4):187-94
High-density genotyping of immune loci in Kawasaki disease and IVIG treatment response in European-American case-parent trio study. Description: Shendre, A, et al. High-density genotyping of immune loci in Kawasaki disease and IVIG treatment response in European-American case-parent trio study. ''Genes Immun''. 2014 Dec; '''15''' (8):534-42
Joint GWAS Analysis: Comparing similar GWAS at different genomic resolutions identifies novel pathway associations with six complex diseases. Description: McGeachie, Michael J, et al. Joint GWAS Analysis: Comparing similar GWAS at different genomic resolutions identifies novel pathway associations with six complex diseases. ''Genom Data''. 2014 Dec 1; '''2''': 202-211
Large-scale metabolomic profiling identifies novel biomarkers for incident coronary heart disease. Description: Ganna, Andrea, et al. Large-scale metabolomic profiling identifies novel biomarkers for incident coronary heart disease. ''PLoS Genet''. 2014 Dec; '''10''' (12):e1004801
Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts. Description: Shim, Unjin, et al. Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts. ''Genomics Inform''. 2014 Dec; '''12''' (4):195-202
Profile of differential promoter activity by nucleotide substitution at GWAS signals for multiple sclerosis. Description: Ryu, Jihye, et al. Profile of differential promoter activity by nucleotide substitution at GWAS signals for multiple sclerosis. ''Medicine (Baltimore)''. 2014 Dec; '''93''' (28):e281
Relevance Epistasis Network of Gastritis for Intra-chromosomes in the Korea Associated Resource (KARE) Cohort Study. Description: Jeong, Hyun-Hwan, et al. Relevance Epistasis Network of Gastritis for Intra-chromosomes in the Korea Associated Resource (KARE) Cohort Study. ''Genomics Inform''. 2014 Dec; '''12''' (4):216-24
Replication of Interactions between Genome-Wide Genetic Variants and Body Mass Index in Fasting Glucose and Insulin Levels. Description: Hong, Kyung-Won, et al. Replication of Interactions between Genome-Wide Genetic Variants and Body Mass Index in Fasting Glucose and Insulin Levels. ''Genomics Inform''. 2014 Dec; '''12''' (4):236-9
Short reads phasing to construct haplotypes in genomic regions that are associated with body mass index in korean individuals. Description: Lee, Kichan, et al. Short reads phasing to construct haplotypes in genomic regions that are associated with body mass index in korean individuals. ''Genomics Inform''. 2014 Dec; '''12''' (4):165-70
The ABCG2 Polymorphism rs2725220 Is Associated with Hyperuricemia in the Korean Population. Description: Sull, Jae Woong, et al. The ABCG2 Polymorphism rs2725220 Is Associated with Hyperuricemia in the Korean Population. ''Genomics Inform''. 2014 Dec; '''12''' (4):231-5
The Usage of an SNP-SNP Relationship Matrix for Best Linear Unbiased Prediction (BLUP) Analysis Using a Community-Based Cohort Study. Description: Lee, Young-Sup, et al. The Usage of an SNP-SNP Relationship Matrix for Best Linear Unbiased Prediction (BLUP) Analysis Using a Community-Based Cohort Study. ''Genomics Inform''. 2014 Dec; '''12''' (4):254-60
Characterization of the porcine nutrient and taste receptor gene repertoire in domestic and wild populations across the globe. Description: da Silva, Elizabete C, et al. Characterization of the porcine nutrient and taste receptor gene repertoire in domestic and wild populations across the globe. ''BMC Genomics''. 2014 Dec 3; '''15''': 1057
Khoisan hunter-gatherers have been the largest population throughout most of modern-human demographic history. Description: Kim, Hie Lim, et al. Khoisan hunter-gatherers have been the largest population throughout most of modern-human demographic history. ''Nat Commun''. 2014 Dec 4; '''5''': 5692
Genetic landscape of populations along the Silk Road: admixture and migration patterns. Description: Mezzavilla, Massimo, et al. Genetic landscape of populations along the Silk Road: admixture and migration patterns. ''BMC Genet''. 2014 Dec 5; '''15''': 131
Genome-wide mapping in a house mouse hybrid zone reveals hybrid sterility loci and Dobzhansky-Muller interactions. Description: Turner, Leslie M, et al. Genome-wide mapping in a house mouse hybrid zone reveals hybrid sterility loci and Dobzhansky-Muller interactions. ''Elife''. 2014 Dec 9; '''3''':
A hereditary disposition for bovine peripheral nerve sheath tumors in Danish Holstein cattle. Description: Grossi, Anette B, et al. A hereditary disposition for bovine peripheral nerve sheath tumors in Danish Holstein cattle. ''Acta Vet Scand''. 2014 Dec 10; '''56''': 85
An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins. Description: Yuan, Wei, et al. An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins. ''Nat Commun''. 2014 Dec 12; '''5''': 5719
Identification of single nucleotide polymorphisms in Toll-like receptor candidate genes associated with tuberculosis infection in water buffalo (Bubalus bubalis). Description: Alfano, Flora, et al. Identification of single nucleotide polymorphisms in Toll-like receptor candidate genes associated with tuberculosis infection in water buffalo (Bubalus bubalis). ''BMC Genet''. 2014 Dec 14; '''15''': 139
De novo CNVs in bipolar affective disorder and schizophrenia. Description: Georgieva, Lyudmila, et al. De novo CNVs in bipolar affective disorder and schizophrenia. ''Hum Mol Genet''. 2014 Dec 15; '''23''' (24):6677-83
Functionally reciprocal mutations of the prolactin signalling pathway define hairy and slick cattle. Description: Littlejohn, Mathew D, et al. Functionally reciprocal mutations of the prolactin signalling pathway define hairy and slick cattle. ''Nat Commun''. 2014 Dec 18; '''5''': 5861
ESR1 and ESR2 gene polymorphisms are associated with human reproduction outcomes in Brazilian women. Description: de Mattos, Clarissa Santiago, et al. ESR1 and ESR2 gene polymorphisms are associated with human reproduction outcomes in Brazilian women. ''J Ovarian Res''. 2014 Dec 20; '''7''': 114
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. Description: Haraksingh, Rajini R, et al. Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. ''BMC Genomics''. 2014 Dec 20; '''15''': 1155
Genetic association between germline JAK2 polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case-control study. Description: Koh, Su Pin, et al. Genetic association between germline JAK2 polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case-control study. ''BMC Genet''. 2014 Dec 20; '''15''': 147
Protective variant associated with alcohol dependence in a Mexican American cohort. Description: Norden-Krichmar, Trina M, et al. Protective variant associated with alcohol dependence in a Mexican American cohort. ''BMC Med Genet''. 2014 Dec 21; '''15''': 136
A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS. Description: Rosmarin, Dan, et al. A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS. ''Gut''. 2015 Jan; '''64''' (1):111-20
Accounting for genetic architecture improves sequence based genomic prediction for a Drosophila fitness trait. Description: Ober, Ulrike, et al. Accounting for genetic architecture improves sequence based genomic prediction for a Drosophila fitness trait. ''PLoS One''. 2015; '''10''' (5):e0126880
A Common Variant of NGEF Is Associated with Abdominal Visceral Fat in Korean Men. Description: Kim, Hyun-Jin, et al. A Common Variant of NGEF Is Associated with Abdominal Visceral Fat in Korean Men. ''PLoS One''. 2015; '''10''' (9):e0137564
A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM). Description: Gerber, Martina, et al. A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM). ''PLoS One''. 2015; '''10''' (2):e0108917
Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes. Description: Niranjan, Tejasvi S, et al. Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes. ''PLoS One''. 2015; '''10''' (2):e0116454
A genetic predictive model for canine hip dysplasia: integration of Genome Wide Association Study (GWAS) and candidate gene approaches. Description: Bartolome, Nerea, et al. A genetic predictive model for canine hip dysplasia: integration of Genome Wide Association Study (GWAS) and candidate gene approaches. ''PLoS One''. 2015; '''10''' (4):e0122558
A Genome-Wide Association Analysis Reveals Epistatic Cancellation of Additive Genetic Variance for Root Length in Arabidopsis thaliana. Description: Lachowiec, Jennifer, et al. A Genome-Wide Association Analysis Reveals Epistatic Cancellation of Additive Genetic Variance for Root Length in Arabidopsis thaliana. ''PLoS Genet''. 2015; '''11''' (9):e1005541
A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. Description: Xu, Wei, et al. A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. ''Biomark Res''. 2015; '''3''': 6
A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans. Description: Cha, Seongwon, et al. A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans. ''PLoS One''. 2015; '''10''' (12):e0145220
A Genome-wide Combinatorial Strategy Dissects Complex Genetic Architecture of Seed Coat Color in Chickpea. Description: Bajaj, Deepak, et al. A Genome-wide Combinatorial Strategy Dissects Complex Genetic Architecture of Seed Coat Color in Chickpea. ''Front Plant Sci''. 2015; '''6''': 979
A genome-wide copy number variant study of suicidal behavior. Description: Gross, Jeffrey A, et al. A genome-wide copy number variant study of suicidal behavior. ''PLoS One''. 2015; '''10''' (5):e0128369
A GWAS Study on Liver Function Test Using eMERGE Network Participants. Description: Namjou, Bahram, et al. A GWAS Study on Liver Function Test Using eMERGE Network Participants. ''PLoS One''. 2015; '''10''' (9):e0138677
Altered Brain Activation during Emotional Face Processing in Relation to Both Diagnosis and Polygenic Risk of Bipolar Disorder. Description: Tesli, Martin, et al. Altered Brain Activation during Emotional Face Processing in Relation to Both Diagnosis and Polygenic Risk of Bipolar Disorder. ''PLoS One''. 2015; '''10''' (7):e0134202
Altered CSMD1 Expression Alters Cocaine-Conditioned Place Preference: Mutual Support for a Complex Locus from Human and Mouse Models. Description: Drgonova, Jana, et al. Altered CSMD1 Expression Alters Cocaine-Conditioned Place Preference: Mutual Support for a Complex Locus from Human and Mouse Models. ''PLoS One''. 2015; '''10''' (7):e0120908
A Multi-Marker Genetic Association Test Based on the Rasch Model Applied to Alzheimer's Disease. Description: Wang, Wenjia, et al. A Multi-Marker Genetic Association Test Based on the Rasch Model Applied to Alzheimer's Disease. ''PLoS One''. 2015; '''10''' (9):e0138223
Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease. Description: Musameh, Muntaser D, et al. Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease. ''PLoS One''. 2015; '''10''' (2):e0117684
Analysis of Genetic and Environmental Risk Factors and Their Interactions in Korean Patients with Age-Related Macular Degeneration. Description: Woo, Se Joon, et al. Analysis of Genetic and Environmental Risk Factors and Their Interactions in Korean Patients with Age-Related Macular Degeneration. ''PLoS One''. 2015; '''10''' (7):e0132771
Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world. Description: Morrison, Margaux A, et al. Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world. ''Front Genet''. 2015; '''6''': 238
An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer's disease in the Han Chinese population. Description: Zhang, Feng, et al. An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer's disease in the Han Chinese population. ''Neuropsychiatr Dis Treat''. 2015; '''11''': 1443-8
An IL-13 promoter polymorphism associated with liver fibrosis in patients with Schistosoma japonicum. Description: Long, Xin, et al. An IL-13 promoter polymorphism associated with liver fibrosis in patients with Schistosoma japonicum. ''PLoS One''. 2015; '''10''' (8):e0135360
A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17. Description: Forman, Oliver P, et al. A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17. ''PLoS One''. 2015; '''10''' (12):e0143546
A Pooled Genome-Wide Association Study of Asperger Syndrome. Description: Warrier, Varun, et al. A Pooled Genome-Wide Association Study of Asperger Syndrome. ''PLoS One''. 2015; '''10''' (7):e0131202
Application of LogitBoost Classifier for Traceability Using SNP Chip Data. Description: Kim, Kwondo, et al. Application of LogitBoost Classifier for Traceability Using SNP Chip Data. ''PLoS One''. 2015; '''10''' (10):e0139685
Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries. Description: Anjomshoaa, Ida, et al. Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries. ''PLoS One''. 2015; '''10''' (12):e0143068
A rare co-segregation-mutation in the insulin receptor substrate 1 gene in one Chinese family with ankylosing spondylitis. Description: Rong, Ju, et al. A rare co-segregation-mutation in the insulin receptor substrate 1 gene in one Chinese family with ankylosing spondylitis. ''PLoS One''. 2015; '''10''' (5):e0126348
A re-formulation of generalized linear mixed models to fit family data in genetic association studies. Description: Wang, Tao, et al. A re-formulation of generalized linear mixed models to fit family data in genetic association studies. ''Front Genet''. 2015; '''6''': 120
A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis. Description: Lekman, Magnus, et al. A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis. ''BioData Min''. 2015; '''8''': 42
Association between Genetic Variation in the Oxytocin Receptor Gene and Emotional Withdrawal, but not between Oxytocin Pathway Genes and Diagnosis in Psychotic Disorders. Description: Haram, Marit, et al. Association between Genetic Variation in the Oxytocin Receptor Gene and Emotional Withdrawal, but not between Oxytocin Pathway Genes and Diagnosis in Psychotic Disorders. ''Front Hum Neurosci''. 2015; '''9''': 9
Association between the European GWAS-identified susceptibility locus at chromosome 4p16 and the risk of atrial septal defect: a case-control study in Southwest China and a meta-analysis. Description: Zhao, Li, et al. Association between the European GWAS-identified susceptibility locus at chromosome 4p16 and the risk of atrial septal defect: a case-control study in Southwest China and a meta-analysis. ''PLoS One''. 2015; '''10''' (4):e0123959
Association between the Interaction of Key Genes Involved in Effector T-Cell Pathways and Susceptibility to Develop allergic Rhinitis: A Population-Based Case-Control Association Study. Description: Zhang, Yuan, et al. Association between the Interaction of Key Genes Involved in Effector T-Cell Pathways and Susceptibility to Develop allergic Rhinitis: A Population-Based Case-Control Association Study. ''PLoS One''. 2015; '''10''' (7):e0131248
Association between Variants in Atopy-Related Immunologic Candidate Genes and Pancreatic Cancer Risk. Description: Cotterchio, Michelle, et al. Association between Variants in Atopy-Related Immunologic Candidate Genes and Pancreatic Cancer Risk. ''PLoS One''. 2015; '''10''' (5):e0125273
Association Mapping of Total Carotenoids in Diverse Soybean Genotypes Based on Leaf Extracts and High-Throughput Canopy Spectral Reflectance Measurements. Description: Dhanapal, Arun Prabhu, et al. Association Mapping of Total Carotenoids in Diverse Soybean Genotypes Based on Leaf Extracts and High-Throughput Canopy Spectral Reflectance Measurements. ''PLoS One''. 2015; '''10''' (9):e0137213
Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort. Description: Li, Yuqing, et al. Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort. ''PLoS One''. 2015; '''10''' (9):e0136796
Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components. Description: Martinez-Hernandez, Angelica, et al. Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components. ''PLoS One''. 2015; '''10''' (5):e0123313
Association of interleukin 7 receptor (rs1494555 and rs6897932) gene polymorphisms with asthma in a north Indian population. Description: Sinha, Shweta, et al. Association of interleukin 7 receptor (rs1494555 and rs6897932) gene polymorphisms with asthma in a north Indian population. ''Allergy Rhinol (Providence)''. 2015 Jan; '''6''' (3):168-76
Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population. Description: Wang, Pengyun, et al. Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population. ''PLoS One''. 2015; '''10''' (5):e0125926
Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk. Description: Huentelman, Matthew J, et al. Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk. ''PLoS One''. 2015; '''10''' (10):e0135076
Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women. Description: Jin, Hyun-Seok, et al. Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women. ''PLoS One''. 2015; '''10''' (8):e0135285
Association of the NOTCH4 Gene Polymorphism rs204993 with Schizophrenia in the Chinese Han Population. Description: Zhang, Bao, et al. Association of the NOTCH4 Gene Polymorphism rs204993 with Schizophrenia in the Chinese Han Population. ''Biomed Res Int''. 2015; '''2015''': 408096
Assumption-free estimation of the genetic contribution to refractive error across childhood. Description: Guggenheim, Jeremy A, et al. Assumption-free estimation of the genetic contribution to refractive error across childhood. ''Mol Vis''. 2015; '''21''': 621-32
A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer. Description: Savas, Sevtap, et al. A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer. ''Biomed Res Int''. 2015; '''2015''': 968743
Attenuated monocyte apoptosis, a new mechanism for osteoporosis suggested by a transcriptome-wide expression study of monocytes. Description: Liu, Yao-Zhong, et al. Attenuated monocyte apoptosis, a new mechanism for osteoporosis suggested by a transcriptome-wide expression study of monocytes. ''PLoS One''. 2015; '''10''' (2):e0116792
Breast cancer risk and genetic ancestry: a case-control study in Uruguay. Description: Bonilla, Carolina, et al. Breast cancer risk and genetic ancestry: a case-control study in Uruguay. ''BMC Womens Health''. 2015; '''15''': 11
Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels. Description: Deelen, Patrick, et al. Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels. ''Genome Med''. 2015; '''7''' (1):30
Candidate gene analysis supports a role for polymorphisms at TCF7L2 as risk factors for type 2 diabetes in Sudan. Description: Ibrahim, Amir T, et al. Candidate gene analysis supports a role for polymorphisms at TCF7L2 as risk factors for type 2 diabetes in Sudan. ''J Diabetes Metab Disord''. 2015; '''15''': 4
Candidate Gene Association Analysis of Neuroblastoma in Chinese Children Strengthens the Role of LMO1. Description: Lu, Jie, et al. Candidate Gene Association Analysis of Neuroblastoma in Chinese Children Strengthens the Role of LMO1. ''PLoS One''. 2015; '''10''' (6):e0127856
Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs. Description: Willet, Cali E, et al. Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs. ''PLoS One''. 2015; '''10''' (2):e0117055
Case-control study of ADARB1 and ADARB2 gene variants in migraine. Description: Gasparini, Claudia F, et al. Case-control study of ADARB1 and ADARB2 gene variants in migraine. ''J Headache Pain''. 2015; '''16''': 511
Characterization of genetic diversity and gene mapping in two Swedish local chicken breeds. Description: Johansson, Anna M, et al. Characterization of genetic diversity and gene mapping in two Swedish local chicken breeds. ''Front Genet''. 2015; '''6''': 44
Characterizing neutral genomic diversity and selection signatures in indigenous populations of Moroccan goats (Capra hircus) using WGS data. Description: Benjelloun, Badr, et al. Characterizing neutral genomic diversity and selection signatures in indigenous populations of Moroccan goats (Capra hircus) using WGS data. ''Front Genet''. 2015; '''6''': 107
Combining GWAS and RNA-Seq Approaches for Detection of the Causal Mutation for Hereditary Junctional Epidermolysis Bullosa in Sheep. Description: Suarez-Vega, Aroa, et al. Combining GWAS and RNA-Seq Approaches for Detection of the Causal Mutation for Hereditary Junctional Epidermolysis Bullosa in Sheep. ''PLoS One''. 2015; '''10''' (5):e0126416
Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk. Description: Chornokur, Ganna, et al. Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk. ''PLoS One''. 2015; '''10''' (6):e0128106
Common variants related to serum uric acid concentrations are associated with glucose metabolism and insulin secretion in a Chinese population. Description: Sun, Xue, et al. Common variants related to serum uric acid concentrations are associated with glucose metabolism and insulin secretion in a Chinese population. ''PLoS One''. 2015; '''10''' (1):e0116714
Comparison of DNA methylation profiles in human fetal and adult red blood cell progenitors. Description: Lessard, Samuel, et al. Comparison of DNA methylation profiles in human fetal and adult red blood cell progenitors. ''Genome Med''. 2015; '''7''' (1):1
Comparison of linkage disequilibrium levels in Iranian indigenous cattle using whole genome SNPs data. Description: Karimi, Karim, et al. Comparison of linkage disequilibrium levels in Iranian indigenous cattle using whole genome SNPs data. ''J Anim Sci Technol''. 2015; '''57''': 47
Comprehensive assessment of genetic sequence variants in the antioxidant 'master regulator' NRF2 in idiopathic Parkinson's disease. Description: Todorovic, Michael, et al. Comprehensive assessment of genetic sequence variants in the antioxidant 'master regulator' NRF2 in idiopathic Parkinson's disease. ''PLoS One''. 2015; '''10''' (5):e0128030
COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study. Description: Sampaio, Aline Santos, et al. COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study. ''PLoS One''. 2015; '''10''' (3):e0119592
Cryptic relatedness in epidemiologic collections accessed for genetic association studies: experiences from the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study and the National Health and Nutrition Examination Surveys (NHANES). Description: Malinowski, Jennifer, et al. Cryptic relatedness in epidemiologic collections accessed for genetic association studies: experiences from the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study and the National Health and Nutrition Examination Surveys (NHANES). ''Front Genet''. 2015; '''6''': 317
Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study. Description: Qian, Yun, et al. Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study. ''PLoS One''. 2015; '''10''' (1):e0116537
dcVar: a method for identifying common variants that modulate differential correlation structures in gene expression data. Description: Lareau, Caleb A, et al. dcVar: a method for identifying common variants that modulate differential correlation structures in gene expression data. ''Front Genet''. 2015; '''6''': 312
Detection and analysis of disease-associated single nucleotide polymorphism influencing post-translational modification. Description: Kim, Yul, et al. Detection and analysis of disease-associated single nucleotide polymorphism influencing post-translational modification. ''BMC Med Genomics''. 2015; '''8 Suppl 2''': S7
Detection of convergent genome-wide signals of adaptation to tropical forests in humans. Description: Amorim, Carlos Eduardo G, et al. Detection of convergent genome-wide signals of adaptation to tropical forests in humans. ''PLoS One''. 2015; '''10''' (4):e0121557
Differences in the ovine HSP90AA1 gene expression rates caused by two linked polymorphisms at its promoter affect rams sperm DNA fragmentation under environmental heat stress conditions. Description: Salces-Ortiz, Judit, et al. Differences in the ovine HSP90AA1 gene expression rates caused by two linked polymorphisms at its promoter affect rams sperm DNA fragmentation under environmental heat stress conditions. ''PLoS One''. 2015; '''10''' (2):e0116360
Differential Evolution approach to detect recent admixture. Description: Kozlov, Konstantin, et al. Differential Evolution approach to detect recent admixture. ''BMC Genomics''. 2015; '''16 Suppl 8''': S9
Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC). Description: Salfati, Elias, et al. Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC). ''PLoS One''. 2015; '''10''' (7):e0133031
Discovering Alzheimer Genetic Biomarkers Using Bayesian Networks. Description: Sherif, Fayroz F, et al. Discovering Alzheimer Genetic Biomarkers Using Bayesian Networks. ''Adv Bioinformatics''. 2015; '''2015''': 639367
Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. Description: Cutler, David J, et al. Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. ''PLoS One''. 2015; '''10''' (6):e0128074
Do variants associated with susceptibility to pancreatic cancer and type 2 diabetes reciprocally affect risk? Description: Wu, Lang, et al. Do variants associated with susceptibility to pancreatic cancer and type 2 diabetes reciprocally affect risk? ''PLoS One''. 2015; '''10''' (2):e0117230
Early modern human dispersal from Africa: genomic evidence for multiple waves of migration. Description: Tassi, Francesca, et al. Early modern human dispersal from Africa: genomic evidence for multiple waves of migration. ''Investig Genet''. 2015; '''6''': 13
Educational attainment influences levels of homozygosity through migration and assortative mating. Description: Abdellaoui, Abdel, et al. Educational attainment influences levels of homozygosity through migration and assortative mating. ''PLoS One''. 2015; '''10''' (3):e0118935
Effective population size, extended linkage disequilibrium and signatures of selection in the rare dog breed lundehund. Description: Pfahler, Sophia, et al. Effective population size, extended linkage disequilibrium and signatures of selection in the rare dog breed lundehund. ''PLoS One''. 2015; '''10''' (4):e0122680
Employing genome-wide SNP discovery and genotyping strategy to extrapolate the natural allelic diversity and domestication patterns in chickpea. Description: Kujur, Alice, et al. Employing genome-wide SNP discovery and genotyping strategy to extrapolate the natural allelic diversity and domestication patterns in chickpea. ''Front Plant Sci''. 2015; '''6''': 162
Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease. Description: Zhu, Zuobin, et al. Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease. ''PLoS One''. 2015; '''10''' (7):e0133421
Epidemiological support for genetic variability at hypothalamic-pituitary-adrenal axis and serotonergic system as risk factors for major depression. Description: Ching-Lopez, Ana, et al. Epidemiological support for genetic variability at hypothalamic-pituitary-adrenal axis and serotonergic system as risk factors for major depression. ''Neuropsychiatr Dis Treat''. 2015; '''11''': 2743-54
Evidence for Association of Cell Adhesion Molecules Pathway and NLGN1 Polymorphisms with Schizophrenia in Chinese Han Population. Description: Zhang, Zhengrong, et al. Evidence for Association of Cell Adhesion Molecules Pathway and NLGN1 Polymorphisms with Schizophrenia in Chinese Han Population. ''PLoS One''. 2015; '''10''' (12):e0144719
Evolutionary Trade-Offs Underlie the Multi-faceted Virulence of Staphylococcus aureus. Description: Laabei, Maisem, et al. Evolutionary Trade-Offs Underlie the Multi-faceted Virulence of Staphylococcus aureus. ''PLoS Biol''. 2015; '''13''' (9):e1002229
Examination of candidate exonic variants for association to Alzheimer disease in the Amish. Description: D'Aoust, Laura N, et al. Examination of candidate exonic variants for association to Alzheimer disease in the Amish. ''PLoS One''. 2015; '''10''' (2):e0118043
Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes. Description: Shigemizu, Daichi, et al. Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes. ''PLoS One''. 2015; '''10''' (7):e0130329
Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow up. Description: Mistry, Vanisha, et al. Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow up. ''PLoS One''. 2015; '''10''' (1):e0116845
Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus. Description: Labbe, Catherine, et al. Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus. ''PLoS One''. 2015; '''10''' (6):e0128586
Exploring the genetic signature of body size in Yucatan miniature pig. Description: Kim, Hyeongmin, et al. Exploring the genetic signature of body size in Yucatan miniature pig. ''PLoS One''. 2015; '''10''' (4):e0121732
Expression-associated polymorphisms of CAV1-CAV2 affect intraocular pressure and high-tension glaucoma risk. Description: Kim, Sewon, et al. Expression-associated polymorphisms of CAV1-CAV2 affect intraocular pressure and high-tension glaucoma risk. ''Mol Vis''. 2015; '''21''': 548-54
Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation. Description: Croteau-Chonka, Damien C, et al. Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation. ''PLoS One''. 2015; '''10''' (10):e0140758
Extent of Linkage Disequilibrium and Effective Population Size in Four South African Sanga Cattle Breeds. Description: Makina, Sithembile O, et al. Extent of Linkage Disequilibrium and Effective Population Size in Four South African Sanga Cattle Breeds. ''Front Genet''. 2015; '''6''': 337
Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2. Description: Volckmar, Anna-Lena, et al. Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2. ''PLoS One''. 2015; '''10''' (5):e0125660
Gene interactions and structural brain change in early-onset Alzheimer's disease subjects using the pipeline environment. Description: Moon, Seok Woo, et al. Gene interactions and structural brain change in early-onset Alzheimer's disease subjects using the pipeline environment. ''Psychiatry Investig''. 2015 Jan; '''12''' (1):125-35
Genes Regulated by Vitamin D in Bone Cells Are Positively Selected in East Asians. Description: Arciero, Elena, et al. Genes Regulated by Vitamin D in Bone Cells Are Positively Selected in East Asians. ''PLoS One''. 2015; '''10''' (12):e0146072
Genetic Affinity of the Bhil, Kol and Gond Mentioned in Epic Ramayana. Description: Chaubey, Gyaneshwer, et al. Genetic Affinity of the Bhil, Kol and Gond Mentioned in Epic Ramayana. ''PLoS One''. 2015; '''10''' (6):e0127655
Genetic analysis identifies DDR2 as a novel gene affecting bone mineral density and osteoporotic fractures in Chinese population. Description: Guo, Yan, et al. Genetic analysis identifies DDR2 as a novel gene affecting bone mineral density and osteoporotic fractures in Chinese population. ''PLoS One''. 2015; '''10''' (2):e0117102
Genetic analysis of membrane cofactor protein (CD46) of the complement system in women with and without preeclamptic pregnancies. Description: Lokki, A Inkeri, et al. Genetic analysis of membrane cofactor protein (CD46) of the complement system in women with and without preeclamptic pregnancies. ''PLoS One''. 2015; '''10''' (2):e0117840
Genetic analysis of Thai cattle reveals a Southeast Asian indicine ancestry. Description: Wangkumhang, Pongsakorn, et al. Genetic analysis of Thai cattle reveals a Southeast Asian indicine ancestry. ''PeerJ''. 2015; '''3''': e1318
Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women. Description: Huerta-Chagoya, Alicia, et al. Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women. ''PLoS One''. 2015; '''10''' (5):e0126408
Genetic Determinants of Metabolism and Benign Prostate Enlargement: Associations with Prostate Volume. Description: Giri, Ayush, et al. Genetic Determinants of Metabolism and Benign Prostate Enlargement: Associations with Prostate Volume. ''PLoS One''. 2015; '''10''' (7):e0132028
Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative. Description: Giri, Ayush, et al. Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative. ''PLoS One''. 2015; '''10''' (11):e0141647
Genetic Effects on Longitudinal Changes from Healthy to Adverse Weight and Metabolic Status - The HUNT Study. Description: Kvaloy, Kirsti, et al. Genetic Effects on Longitudinal Changes from Healthy to Adverse Weight and Metabolic Status - The HUNT Study. ''PLoS One''. 2015; '''10''' (10):e0139632
Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study. Description: Diaz-Lacava, A N, et al. Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study. ''Int J Genomics''. 2015; '''2015''': 693193
Genetic Heterogeneity in Algerian Human Populations. Description: Bekada, Asmahan, et al. Genetic Heterogeneity in Algerian Human Populations. ''PLoS One''. 2015; '''10''' (9):e0138453
Genetic Interactions Explain Variance in Cingulate Amyloid Burden: An AV-45 PET Genome-Wide Association and Interaction Study in the ADNI Cohort. Description: Li, Jin, et al. Genetic Interactions Explain Variance in Cingulate Amyloid Burden: An AV-45 PET Genome-Wide Association and Interaction Study in the ADNI Cohort. ''Biomed Res Int''. 2015; '''2015''': 647389
Genetic Loci Associated with Allergic Sensitization in Lithuanians. Description: Sauliene, Ingrida, et al. Genetic Loci Associated with Allergic Sensitization in Lithuanians. ''PLoS One''. 2015; '''10''' (7):e0134188
Genetic markers of white matter integrity in schizophrenia revealed by parallel ICA. Description: Gupta, Cota Navin, et al. Genetic markers of white matter integrity in schizophrenia revealed by parallel ICA. ''Front Hum Neurosci''. 2015; '''9''': 100
Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise. Description: Grondin, Yohann, et al. Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise. ''PLoS One''. 2015; '''10''' (6):e0130827
Genetic stratigraphy of key demographic events in Arabia. Description: Fernandes, Veronica, et al. Genetic stratigraphy of key demographic events in Arabia. ''PLoS One''. 2015; '''10''' (3):e0118625
Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome. Description: Di Napoli, Agnese, et al. Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome. ''Mol Autism''. 2015; '''6''': 9
Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes. Description: Kong, Xiaomu, et al. Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes. ''PLoS One''. 2015; '''10''' (8):e0135145
Genetic variants modulating CRIPTO serum levels identified by genome-wide association study in Cilento isolates. Description: Ruggiero, Daniela, et al. Genetic variants modulating CRIPTO serum levels identified by genome-wide association study in Cilento isolates. ''PLoS Genet''. 2015 Jan; '''11''' (1):e1004976
Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population. Description: Salo, Perttu P, et al. Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population. ''PLoS One''. 2015; '''10''' (10):e0140576
Genetic variation at the human connexin 43 locus but not at the connexin 40 locus is associated with left bundle branch block. Description: Ladenvall, Per, et al. Genetic variation at the human connexin 43 locus but not at the connexin 40 locus is associated with left bundle branch block. ''Open Heart''. 2015; '''2''' (1):e000187
Genetic variations in the serotonergic system contribute to amygdala volume in humans. Description: Li, Jin, et al. Genetic variations in the serotonergic system contribute to amygdala volume in humans. ''Front Neuroanat''. 2015; '''9''': 129
Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy body disease. Description: Clark, Lorraine N, et al. Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy body disease. ''PLoS One''. 2015; '''10''' (5):e0125204
Genome Scan for Selection in Structured Layer Chicken Populations Exploiting Linkage Disequilibrium Information. Description: Gholami, Mahmood, et al. Genome Scan for Selection in Structured Layer Chicken Populations Exploiting Linkage Disequilibrium Information. ''PLoS One''. 2015; '''10''' (7):e0130497
Genome-wide analysis of attention deficit hyperactivity disorder in Norway. Description: Zayats, Tetyana, et al. Genome-wide analysis of attention deficit hyperactivity disorder in Norway. ''PLoS One''. 2015; '''10''' (4):e0122501
Genome-Wide Assessment of Differential DNA Methylation Associated with Autoantibody Production in Systemic Lupus Erythematosus. Description: Chung, Sharon A, et al. Genome-Wide Assessment of Differential DNA Methylation Associated with Autoantibody Production in Systemic Lupus Erythematosus. ''PLoS One''. 2015; '''10''' (7):e0129813
Genome-Wide Association Analysis for Blood Lipid Traits Measured in Three Pig Populations Reveals a Substantial Level of Genetic Heterogeneity. Description: Yang, Hui, et al. Genome-Wide Association Analysis for Blood Lipid Traits Measured in Three Pig Populations Reveals a Substantial Level of Genetic Heterogeneity. ''PLoS One''. 2015; '''10''' (6):e0131667
Genome Wide Association Analysis Reveals New Production Trait Genes in a Male Duroc Population. Description: Wang, Kejun, et al. Genome Wide Association Analysis Reveals New Production Trait Genes in a Male Duroc Population. ''PLoS One''. 2015; '''10''' (9):e0139207
Genome-Wide Association Identifies SLC2A9 and NLN Gene Regions as Associated with Entropion in Domestic Sheep. Description: Mousel, Michelle R, et al. Genome-Wide Association Identifies SLC2A9 and NLN Gene Regions as Associated with Entropion in Domestic Sheep. ''PLoS One''. 2015; '''10''' (6):e0128909
Genome-wide association mapping for yield and other agronomic traits in an elite breeding population of tropical rice (Oryza sativa). Description: Begum, Hasina, et al. Genome-wide association mapping for yield and other agronomic traits in an elite breeding population of tropical rice (Oryza sativa). ''PLoS One''. 2015; '''10''' (3):e0119873
Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians. Description: Hwang, Joo-Yeon, et al. Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians. ''Diabetes''. 2015 Jan; '''64''' (1):291-8
Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population. Description: Kuo, Po-Hsiu, et al. Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population. ''PLoS One''. 2015; '''10''' (9):e0138695
Genome-Wide Association Study Identifies Novel Pharmacogenomic Loci For Therapeutic Response to Montelukast in Asthma. Description: Dahlin, Amber, et al. Genome-Wide Association Study Identifies Novel Pharmacogenomic Loci For Therapeutic Response to Montelukast in Asthma. ''PLoS One''. 2015; '''10''' (6):e0129385
Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behcet disease. Description: Kappen, Jasper H, et al. Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behcet disease. ''PLoS One''. 2015; '''10''' (3):e0119085
Genome-wide association study of parity in Bangladeshi women. Description: Aschebrook-Kilfoy, Briseis, et al. Genome-wide association study of parity in Bangladeshi women. ''PLoS One''. 2015; '''10''' (3):e0118488
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population. Description: Matsukura, Mitsuru, et al. Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population. ''PLoS One''. 2015; '''10''' (10):e0139262
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy. Description: Van Driest, Sara L, et al. Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy. ''PLoS One''. 2015; '''10''' (6):e0127791
Genome-wide association study of serum minerals levels in children of different ethnic background. Description: Chang, Xiao, et al. Genome-wide association study of serum minerals levels in children of different ethnic background. ''PLoS One''. 2015; '''10''' (4):e0123499
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas. Description: Brown, Eric L, et al. Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas. ''PLoS One''. 2015; '''10''' (11):e0142130
Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics. Description: Wang, Leyao, et al. Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics. ''PLoS One''. 2015; '''10''' (12):e0144114
Genomic analysis for managing small and endangered populations: a case study in Tyrol Grey cattle. Description: Meszaros, Gabor, et al. Genomic analysis for managing small and endangered populations: a case study in Tyrol Grey cattle. ''Front Genet''. 2015; '''6''': 173
Genomic data as the "hitchhiker's guide" to cattle adaptation: tracking the milestones of past selection in the bovine genome. Description: Utsunomiya, Yuri T, et al. Genomic data as the "hitchhiker's guide" to cattle adaptation: tracking the milestones of past selection in the bovine genome. ''Front Genet''. 2015; '''6''': 36
Genomic prediction of traits related to canine hip dysplasia. Description: Sanchez-Molano, Enrique, et al. Genomic prediction of traits related to canine hip dysplasia. ''Front Genet''. 2015; '''6''': 97
Genotypic and allelic variability in CYP19A1 among populations of African and European ancestry. Description: Starlard-Davenport, Athena, et al. Genotypic and allelic variability in CYP19A1 among populations of African and European ancestry. ''PLoS One''. 2015; '''10''' (2):e0117347
Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome. Description: Ajjemami, Maria, et al. Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome. ''J Diabetes Metab Disord''. 2015; '''14''': 29
Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis. Description: Chettier, Rakesh, et al. Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis. ''PLoS One''. 2015; '''10''' (2):e0117708
Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease. Description: Yan, Jingwen, et al. Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease. ''Front Genet''. 2015; '''6''': 117
Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs. Description: Akkad, Denis A, et al. Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs. ''Canine Genet Epidemiol''. 2015; '''2''': 5
Human Genetic Ancestral Composition Correlates with the Origin of Mycobacterium leprae Strains in a Leprosy Endemic Population. Description: Cardona-Castro, Nora, et al. Human Genetic Ancestral Composition Correlates with the Origin of Mycobacterium leprae Strains in a Leprosy Endemic Population. ''PLoS Negl Trop Dis''. 2015; '''9''' (9):e0004045
Identification of an interaction between VWF rs7965413 and platelet count as a novel risk marker for metabolic syndrome: an extensive search of candidate polymorphisms in a case-control study. Description: Nakatochi, Masahiro, et al. Identification of an interaction between VWF rs7965413 and platelet count as a novel risk marker for metabolic syndrome: an extensive search of candidate polymorphisms in a case-control study. ''PLoS One''. 2015; '''10''' (2):e0117591
Identification of Genetic Variation between Obligate Plant Pathogens Pseudoperonospora cubensis and P. humuli Using RNA Sequencing and Genotyping-By-Sequencing. Description: Summers, Carly F, et al. Identification of Genetic Variation between Obligate Plant Pathogens Pseudoperonospora cubensis and P. humuli Using RNA Sequencing and Genotyping-By-Sequencing. ''PLoS One''. 2015; '''10''' (11):e0143665
Identification of novel loci associated with gastrointestinal parasite resistance in a Red Maasai x Dorper backcross population. Description: Benavides, Magda Vieira, et al. Identification of novel loci associated with gastrointestinal parasite resistance in a Red Maasai x Dorper backcross population. ''PLoS One''. 2015; '''10''' (4):e0122797
Identification of Promising Mutants Associated with Egg Production Traits Revealed by Genome-Wide Association Study. Description: Yuan, Jingwei, et al. Identification of Promising Mutants Associated with Egg Production Traits Revealed by Genome-Wide Association Study. ''PLoS One''. 2015; '''10''' (10):e0140615
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR). Description: De, Rishika, et al. Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR). ''BioData Min''. 2015; '''8''': 41
IL10 Variant g.5311A Is Associated with Visceral Leishmaniasis in Indian Population. Description: Mishra, Anshuman, et al. IL10 Variant g.5311A Is Associated with Visceral Leishmaniasis in Indian Population. ''PLoS One''. 2015; '''10''' (5):e0124559
Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort. Description: Hoffmann, Thomas J, et al. Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort. ''PLoS Genet''. 2015 Jan; '''11''' (1):e1004930
Increased Insulin following an Oral Glucose Load, Genetic Variation near the Melatonin Receptor MTNR1B, but No Biochemical Evidence of Endothelial Dysfunction in Young Asian Men and Women. Description: Matuszek, Maria A, et al. Increased Insulin following an Oral Glucose Load, Genetic Variation near the Melatonin Receptor MTNR1B, but No Biochemical Evidence of Endothelial Dysfunction in Young Asian Men and Women. ''PLoS One''. 2015; '''10''' (7):e0133611
Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population. Description: Zhou, Sirui, et al. Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population. ''PLoS One''. 2015; '''10''' (5):e0128255
Increase in Dickkopf-1 Serum Level in Recent Spondyloarthritis. Data from the DESIR Cohort. Description: Nocturne, Gaetane, et al. Increase in Dickkopf-1 Serum Level in Recent Spondyloarthritis. Data from the DESIR Cohort. ''PLoS One''. 2015; '''10''' (8):e0134974
Indications for potential parent-of-origin effects within the FTO gene. Description: Liu, Xuanshi, et al. Indications for potential parent-of-origin effects within the FTO gene. ''PLoS One''. 2015; '''10''' (3):e0119206
Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation. Description: Avramopoulos, Dimitrios, et al. Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation. ''PLoS One''. 2015; '''10''' (3):e0116696
Influence of Feature Encoding and Choice of Classifier on Disease Risk Prediction in Genome-Wide Association Studies. Description: Mittag, Florian, et al. Influence of Feature Encoding and Choice of Classifier on Disease Risk Prediction in Genome-Wide Association Studies. ''PLoS One''. 2015; '''10''' (8):e0135832
Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach. Description: Kim, Yun Kyoung, et al. Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach. ''Biomed Res Int''. 2015; '''2015''': 914965
Influences of gestational obesity on associations between genotypes and gene expression levels in offspring following maternal gastrointestinal bypass surgery for obesity. Description: Guenard, Frederic, et al. Influences of gestational obesity on associations between genotypes and gene expression levels in offspring following maternal gastrointestinal bypass surgery for obesity. ''PLoS One''. 2015; '''10''' (1):e0117011
In Search for the Genetic Basis of Quality of Life in Healthy Swedish Women--A GWAS Study Using the iCOGS Custom Genotyping Array. Description: Schoormans, Dounya, et al. In Search for the Genetic Basis of Quality of Life in Healthy Swedish Women--A GWAS Study Using the iCOGS Custom Genotyping Array. ''PLoS One''. 2015; '''10''' (10):e0140563
Integrating mRNA and miRNA Weighted Gene Co-Expression Networks with eQTLs in the Nucleus Accumbens of Subjects with Alcohol Dependence. Description: Mamdani, Mohammed, et al. Integrating mRNA and miRNA Weighted Gene Co-Expression Networks with eQTLs in the Nucleus Accumbens of Subjects with Alcohol Dependence. ''PLoS One''. 2015; '''10''' (9):e0137671
Interaction of genetic markers associated with serum alkaline phosphatase levels in the Japanese population. Description: Masuda, Masatoshi, et al. Interaction of genetic markers associated with serum alkaline phosphatase levels in the Japanese population. ''Hum Genome Var''. 2015; '''2''': 15019
Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population. Description: Sun, Yifan, et al. Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population. ''Cancer Cell Int''. 2015; '''15''': 35
Investigating the genetics of hippocampal volume in older adults without dementia. Description: Mather, Karen A, et al. Investigating the genetics of hippocampal volume in older adults without dementia. ''PLoS One''. 2015; '''10''' (1):e0116920
Investigation of associations between NR1D1, RORA and RORB genes and bipolar disorder. Description: Lai, Yin-Chieh, et al. Investigation of associations between NR1D1, RORA and RORB genes and bipolar disorder. ''PLoS One''. 2015; '''10''' (3):e0121245
Lack of Associations of CHRNA5-A3-B4 Genetic Variants with Smoking Cessation Treatment Outcomes in Caucasian Smokers despite Associations with Baseline Smoking. Description: Tyndale, Rachel F, et al. Lack of Associations of CHRNA5-A3-B4 Genetic Variants with Smoking Cessation Treatment Outcomes in Caucasian Smokers despite Associations with Baseline Smoking. ''PLoS One''. 2015; '''10''' (5):e0128109
Landscape genomics reveal signatures of local adaptation in barley (Hordeum vulgare L.). Description: Abebe, Tiegist D, et al. Landscape genomics reveal signatures of local adaptation in barley (Hordeum vulgare L.). ''Front Plant Sci''. 2015; '''6''': 813
Leveraging an Electronic Health Record-Linked Biorepository to Generate a Metformin Pharmacogenomics Hypothesis. Description: Breitenstein, Matthew K, et al. Leveraging an Electronic Health Record-Linked Biorepository to Generate a Metformin Pharmacogenomics Hypothesis. ''AMIA Jt Summits Transl Sci Proc''. 2015; '''2015''': 26-30
Loss of TLR3 aggravates CHIKV replication and pathology due to an altered virus-specific neutralizing antibody response. Description: Her, Zhisheng, et al. Loss of TLR3 aggravates CHIKV replication and pathology due to an altered virus-specific neutralizing antibody response. ''EMBO Mol Med''. 2015 Jan; '''7''' (1):24-41
Meta gene set enrichment analyses link miR-137-regulated pathways with schizophrenia risk. Description: Wright, Carrie, et al. Meta gene set enrichment analyses link miR-137-regulated pathways with schizophrenia risk. ''Front Genet''. 2015; '''6''': 147
Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults. Description: Chen, Fang, et al. Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults. ''PLoS One''. 2015; '''10''' (6):e0131106
Molecular Effects of Polymorphism in the 3'UTR of Unc-5 homolog C Associated with Conception Rate in Holsteins. Description: Sugimoto, Mayumi, et al. Molecular Effects of Polymorphism in the 3'UTR of Unc-5 homolog C Associated with Conception Rate in Holsteins. ''PLoS One''. 2015; '''10''' (7):e0131283
Multilocus heterozygosity and coronary heart disease: nested case-control studies in men and women. Description: Mukamal, Kenneth J, et al. Multilocus heterozygosity and coronary heart disease: nested case-control studies in men and women. ''PLoS One''. 2015; '''10''' (5):e0124847
'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture. Description: Benton, Miles C, et al. 'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture. ''Investig Genet''. 2015; '''6''': 11
Netrin-1 - DCC Signaling Systems and Age-Related Macular Degeneration. Description: SanGiovanni, John Paul, et al. Netrin-1 - DCC Signaling Systems and Age-Related Macular Degeneration. ''PLoS One''. 2015; '''10''' (5):e0125548
Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals. Description: Chang, Suhua, et al. Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals. ''PLoS One''. 2015; '''10''' (7):e0133404
No Additional Prognostic Value of Genetic Information in the Prediction of Vascular Events after Cerebral Ischemia of Arterial Origin: The PROMISe Study. Description: Achterberg, Sefanja, et al. No Additional Prognostic Value of Genetic Information in the Prediction of Vascular Events after Cerebral Ischemia of Arterial Origin: The PROMISe Study. ''PLoS One''. 2015; '''10''' (4):e0119203
No association between apolipoprotein E or N-acetyltransferase 2 gene polymorphisms and age-related hearing loss. Description: Dawes, Piers, et al. No association between apolipoprotein E or N-acetyltransferase 2 gene polymorphisms and age-related hearing loss. ''Laryngoscope''. 2015 Jan; '''125''' (1):E33-8
No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. Description: Garcia-Etxebarria, Koldo, et al. No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. ''PLoS One''. 2015; '''10''' (9):e0135983
Novel loci for non-syndromic coarctation of the aorta in sporadic and familial cases. Description: Moosmann, Julia, et al. Novel loci for non-syndromic coarctation of the aorta in sporadic and familial cases. ''PLoS One''. 2015; '''10''' (5):e0126873
Pathway Analysis Based on a Genome-Wide Association Study of Polycystic Ovary Syndrome. Description: Shim, Unjin, et al. Pathway Analysis Based on a Genome-Wide Association Study of Polycystic Ovary Syndrome. ''PLoS One''. 2015; '''10''' (8):e0136609
Pathway-Based Genome-Wide Association Studies for Plasma Triglycerides in Obese Females and Normal-Weight Controls. Description: Jiao, Hongxiao, et al. Pathway-Based Genome-Wide Association Studies for Plasma Triglycerides in Obese Females and Normal-Weight Controls. ''PLoS One''. 2015; '''10''' (8):e0134923
Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols. Description: Moore, Carrie B, et al. Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols. ''Open Forum Infect Dis''. 2015 Jan; '''2''' (1):ofu113
Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein. Description: Ligthart, Symen, et al. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein. ''PLoS One''. 2015; '''10''' (3):e0118859
Pooled Sequencing of Candidate Genes Implicates Rare Variants in the Development of Asthma Following Severe RSV Bronchiolitis in Infancy. Description: Torgerson, Dara G, et al. Pooled Sequencing of Candidate Genes Implicates Rare Variants in the Development of Asthma Following Severe RSV Bronchiolitis in Infancy. ''PLoS One''. 2015; '''10''' (11):e0142649
Population genetic structure, linkage disequilibrium and effective population size of conserved and extensively raised village chicken populations of Southern Africa. Description: Khanyile, Khulekani S, et al. Population genetic structure, linkage disequilibrium and effective population size of conserved and extensively raised village chicken populations of Southern Africa. ''Front Genet''. 2015; '''6''': 13
Population genomics reveals chromosome-scale heterogeneous evolution in a protoploid yeast. Description: Friedrich, Anne, et al. Population genomics reveals chromosome-scale heterogeneous evolution in a protoploid yeast. ''Mol Biol Evol''. 2015 Jan; '''32''' (1):184-92
Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11. Description: Zanetti, Daniela, et al. Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11. ''PLoS One''. 2015; '''10''' (8):e0134840
Practical Calling Approach for Exome Array-Based Genome-Wide Association Studies in Korean Population. Description: Park, Tae-Joon, et al. Practical Calling Approach for Exome Array-Based Genome-Wide Association Studies in Korean Population. ''Int J Genomics''. 2015; '''2015''': 421715
Prediction of breast cancer survival using clinical and genetic markers by tumor subtypes. Description: Song, Nan, et al. Prediction of breast cancer survival using clinical and genetic markers by tumor subtypes. ''PLoS One''. 2015; '''10''' (4):e0122413
Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus. Description: Hafren, Lena, et al. Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus. ''PLoS One''. 2015; '''10''' (7):e0132551
Promising Loci and Genes for Yolk and Ovary Weight in Chickens Revealed by a Genome-Wide Association Study. Description: Sun, Congjiao, et al. Promising Loci and Genes for Yolk and Ovary Weight in Chickens Revealed by a Genome-Wide Association Study. ''PLoS One''. 2015; '''10''' (9):e0137145
Psoriasis drug development and GWAS interpretation through in silico analysis of transcription factor binding sites. Description: Swindell, William R, et al. Psoriasis drug development and GWAS interpretation through in silico analysis of transcription factor binding sites. ''Clin Transl Med''. 2015; '''4''': 13
Race Does Not Predict Melanocyte Heterogeneous Responses to Dermal Fibroblast-Derived Mediators. Description: Sirimahachaiyakul, Pornthep, et al. Race Does Not Predict Melanocyte Heterogeneous Responses to Dermal Fibroblast-Derived Mediators. ''PLoS One''. 2015; '''10''' (9):e0139135
Rare Variants in Transcript and Potential Regulatory Regions Explain a Small Percentage of the Missing Heritability of Complex Traits in Cattle. Description: Gonzalez-Recio, Oscar, et al. Rare Variants in Transcript and Potential Regulatory Regions Explain a Small Percentage of the Missing Heritability of Complex Traits in Cattle. ''PLoS One''. 2015; '''10''' (12):e0143945
Reduced SNP panels for genetic identification and introgression analysis in the dark honey bee (Apis mellifera mellifera). Description: Munoz, Irene, et al. Reduced SNP panels for genetic identification and introgression analysis in the dark honey bee (Apis mellifera mellifera). ''PLoS One''. 2015; '''10''' (4):e0124365
Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population. Description: Inoue, Emiko, et al. Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population. ''PLoS One''. 2015; '''10''' (12):e0144624
Revisiting demographic processes in cattle with genome-wide population genetic analysis. Description: Orozco-terWengel, Pablo, et al. Revisiting demographic processes in cattle with genome-wide population genetic analysis. ''Front Genet''. 2015; '''6''': 191
Scanning and Filling: Ultra-Dense SNP Genotyping Combining Genotyping-By-Sequencing, SNP Array and Whole-Genome Resequencing Data. Description: Torkamaneh, Davoud, et al. Scanning and Filling: Ultra-Dense SNP Genotyping Combining Genotyping-By-Sequencing, SNP Array and Whole-Genome Resequencing Data. ''PLoS One''. 2015; '''10''' (7):e0131533
Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: evidence from two independent cohorts. Description: Oertel-Knochel, Viola, et al. Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: evidence from two independent cohorts. ''Neuroimage Clin''. 2015; '''7''': 764-70
SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents. Description: White, Marquitta J, et al. SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents. ''PLoS One''. 2015; '''10''' (2):e0116915
Signatures of natural selection at the FTO (fat mass and obesity associated) locus in human populations. Description: Liu, Xuanshi, et al. Signatures of natural selection at the FTO (fat mass and obesity associated) locus in human populations. ''PLoS One''. 2015; '''10''' (2):e0117093
SIRT1 Polymorphisms Associate with Seasonal Weight Variation, Depressive Disorders, and Diastolic Blood Pressure in the General Population. Description: Kovanen, Leena, et al. SIRT1 Polymorphisms Associate with Seasonal Weight Variation, Depressive Disorders, and Diastolic Blood Pressure in the General Population. ''PLoS One''. 2015; '''10''' (10):e0141001
Strong selection for behavioural resilience in Australian stock working dogs identified by selective sweep analysis. Description: Arnott, Elizabeth R, et al. Strong selection for behavioural resilience in Australian stock working dogs identified by selective sweep analysis. ''Canine Genet Epidemiol''. 2015; '''2''': 6
Susceptibility to invasive meningococcal disease: polymorphism of complement system genes and Neisseria meningitidis factor H binding protein. Description: Bradley, Declan T, et al. Susceptibility to invasive meningococcal disease: polymorphism of complement system genes and Neisseria meningitidis factor H binding protein. ''PLoS One''. 2015; '''10''' (3):e0120757
Systematic Evaluation of Genetic Variants for Polycystic Ovary Syndrome in a Chinese Population. Description: Xu, Yuping, et al. Systematic Evaluation of Genetic Variants for Polycystic Ovary Syndrome in a Chinese Population. ''PLoS One''. 2015; '''10''' (10):e0140695
Targeted resequencing of the pericentromere of chromosome 2 linked to constitutional delay of growth and puberty. Description: Cousminer, Diana L, et al. Targeted resequencing of the pericentromere of chromosome 2 linked to constitutional delay of growth and puberty. ''PLoS One''. 2015; '''10''' (6):e0128524
TECPR2 Associated Neuroaxonal Dystrophy in Spanish Water Dogs. Description: Hahn, Kerstin, et al. TECPR2 Associated Neuroaxonal Dystrophy in Spanish Water Dogs. ''PLoS One''. 2015; '''10''' (11):e0141824
The association between carbohydrate-rich foods and risk of cardiovascular disease is not modified by genetic susceptibility to dyslipidemia as determined by 80 validated variants. Description: Sonestedt, Emily, et al. The association between carbohydrate-rich foods and risk of cardiovascular disease is not modified by genetic susceptibility to dyslipidemia as determined by 80 validated variants. ''PLoS One''. 2015; '''10''' (4):e0126104
The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes. Description: Kong, Xiaomu, et al. The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes. ''PLoS One''. 2015; '''10''' (11):e0143607
The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey). Description: Helgeland, Oyvind, et al. The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey). ''Int J Endocrinol''. 2015; '''2015''': 164652
The effects of electronic medical record phenotyping details on genetic association studies: HDL-C as a case study. Description: Dumitrescu, Logan, et al. The effects of electronic medical record phenotyping details on genetic association studies: HDL-C as a case study. ''BioData Min''. 2015; '''8''': 15
The female protective effect in autism spectrum disorder is not mediated by a single genetic locus. Description: Gockley, Jake, et al. The female protective effect in autism spectrum disorder is not mediated by a single genetic locus. ''Mol Autism''. 2015; '''6''': 25
The genetic basis of quality of life in healthy Swedish women: a candidate gene approach. Description: Schoormans, Dounya, et al. The genetic basis of quality of life in healthy Swedish women: a candidate gene approach. ''PLoS One''. 2015; '''10''' (2):e0118292
The Genetic Structure of Marijuana and Hemp. Description: Sawler, Jason, et al. The Genetic Structure of Marijuana and Hemp. ''PLoS One''. 2015; '''10''' (8):e0133292
The Genomic Legacy of the Transatlantic Slave Trade in the Yungas Valley of Bolivia. Description: Heinz, Tanja, et al. The Genomic Legacy of the Transatlantic Slave Trade in the Yungas Valley of Bolivia. ''PLoS One''. 2015; '''10''' (8):e0134129
The identification of loci for immune traits in chickens using a genome-wide association study. Description: Zhang, Lei, et al. The identification of loci for immune traits in chickens using a genome-wide association study. ''PLoS One''. 2015; '''10''' (3):e0117269
The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations. Description: Schnitzler, Fabian, et al. The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations. ''PLoS One''. 2015; '''10''' (7):e0116044
The relationship between dopamine receptor D1 and cognitive performance. Description: Tsang, Jonathan, et al. The relationship between dopamine receptor D1 and cognitive performance. ''NPJ Schizophr''. 2015; '''1''': 14002
The Relationship between Runs of Homozygosity and Inbreeding in Jersey Cattle under Selection. Description: Kim, Eui-Soo, et al. The Relationship between Runs of Homozygosity and Inbreeding in Jersey Cattle under Selection. ''PLoS One''. 2015; '''10''' (7):e0129967
The type 2 diabetes risk allele of TMEM154-rs6813195 associates with decreased beta cell function in a study of 6,486 Danes. Description: Harder, Marie Neergaard, et al. The type 2 diabetes risk allele of TMEM154-rs6813195 associates with decreased beta cell function in a study of 6,486 Danes. ''PLoS One''. 2015; '''10''' (3):e0120890
Toll-Like Receptor Family Polymorphisms Are Associated with Primary Renal Diseases but Not with Renal Outcomes Following Kidney Transplantation. Description: Dessing, Mark C, et al. Toll-Like Receptor Family Polymorphisms Are Associated with Primary Renal Diseases but Not with Renal Outcomes Following Kidney Transplantation. ''PLoS One''. 2015; '''10''' (10):e0139769
Transcriptome Analysis of CD4+ T Cells in Coeliac Disease Reveals Imprint of BACH2 and IFNgamma Regulation. Description: Quinn, Emma M, et al. Transcriptome Analysis of CD4+ T Cells in Coeliac Disease Reveals Imprint of BACH2 and IFNgamma Regulation. ''PLoS One''. 2015; '''10''' (10):e0140049
Triploidy--Observations in 154 Diandric Cases. Description: Scholz, Nanna Brink, et al. Triploidy--Observations in 154 Diandric Cases. ''PLoS One''. 2015; '''10''' (11):e0142545
Trypanosomosis: potential driver of selection in African cattle. Description: Smetko, Anamarija, et al. Trypanosomosis: potential driver of selection in African cattle. ''Front Genet''. 2015; '''6''': 137
Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog. Description: Oliver, James A C, et al. Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog. ''PLoS One''. 2015; '''10''' (10):e0140436
TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits. Description: Diogo, Dorothee, et al. TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits. ''PLoS One''. 2015; '''10''' (4):e0122271
Variability in the effect of 5-HTTLPR on depression in a large European population: the role of age, symptom profile, type and intensity of life stressors. Description: Juhasz, Gabriella, et al. Variability in the effect of 5-HTTLPR on depression in a large European population: the role of age, symptom profile, type and intensity of life stressors. ''PLoS One''. 2015; '''10''' (3):e0116316
Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Abeta1-42 Level. Description: Li, Qingqin S, et al. Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Abeta1-42 Level. ''PLoS One''. 2015; '''10''' (8):e0134000
Visualization of Genome Diversity in German Shepherd Dogs. Description: Mortlock, Sally-Anne, et al. Visualization of Genome Diversity in German Shepherd Dogs. ''Bioinform Biol Insights''. 2015; '''9''' (Suppl 2):37-42
When Does Choice of Accuracy Measure Alter Imputation Accuracy Assessments? Description: Ramnarine, Shelina, et al. When Does Choice of Accuracy Measure Alter Imputation Accuracy Assessments? ''PLoS One''. 2015; '''10''' (10):e0137601
Whole-Genome Analysis of Diversity and SNP-Major Gene Association in Peach Germplasm. Description: Micheletti, Diego, et al. Whole-Genome Analysis of Diversity and SNP-Major Gene Association in Peach Germplasm. ''PLoS One''. 2015; '''10''' (9):e0136803
Whole genome sequencing of elite rice cultivars as a comprehensive information resource for marker assisted selection. Description: Duitama, Jorge, et al. Whole genome sequencing of elite rice cultivars as a comprehensive information resource for marker assisted selection. ''PLoS One''. 2015; '''10''' (4):e0124617
A genome-wide association study of marginal zone lymphoma shows association to the HLA region. Description: Vijai, Joseph, et al. A genome-wide association study of marginal zone lymphoma shows association to the HLA region. ''Nat Commun''. 2015 Jan 8; '''6''': 5751
A genome-wide association study for nutritional indices in Drosophila. Description: Unckless, Robert L, et al. A genome-wide association study for nutritional indices in Drosophila. ''G3 (Bethesda)''. 2015 Jan 12; '''5''' (3):417-25
Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma. Description: Igartua, Catherine, et al. Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma. ''Nat Commun''. 2015 Jan 16; '''6''': 5965
Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations. Description: Bansal, Vikas, et al. Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations. ''BMC Bioinformatics''. 2015 Jan 16; '''16''': 4
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios. Description: Besenbacher, Soren, et al. Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios. ''Nat Commun''. 2015 Jan 19; '''6''': 5969
Paging through history: parchment as a reservoir of ancient DNA for next generation sequencing. Description: Teasdale, M D, et al. Paging through history: parchment as a reservoir of ancient DNA for next generation sequencing. ''Philos Trans R Soc Lond B Biol Sci''. 2015 Jan 19; '''370''' (1660):20130379
Unravelling genes and pathways implicated in working memory of schizophrenia in Han Chinese. Description: Ren, Hongyan, et al. Unravelling genes and pathways implicated in working memory of schizophrenia in Han Chinese. ''Int J Mol Sci''. 2015 Jan 20; '''16''' (1):2145-61
A medium density genetic map and QTL for behavioral and production traits in Japanese quail. Description: Recoquillay, Julien, et al. A medium density genetic map and QTL for behavioral and production traits in Japanese quail. ''BMC Genomics''. 2015 Jan 22; '''16''': 10
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. Description: Betz, Regina C, et al. Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. ''Nat Commun''. 2015 Jan 22; '''6''': 5966
Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation. Description: Lock, Eric F, et al. Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation. ''BMC Genomics''. 2015 Jan 22; '''16''': 11
Pharmacogenomics of hypertension: a genome-wide, placebo-controlled cross-over study, using four classes of antihypertensive drugs. Description: Hiltunen, Timo P, et al. Pharmacogenomics of hypertension: a genome-wide, placebo-controlled cross-over study, using four classes of antihypertensive drugs. ''J Am Heart Assoc''. 2015 Jan 26; '''4''' (1):e001521
New loci and coding variants confer risk for age-related macular degeneration in East Asians. Description: Cheng, Ching-Yu, et al. New loci and coding variants confer risk for age-related macular degeneration in East Asians. ''Nat Commun''. 2015 Jan 28; '''6''': 6063
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Description: Wessel, Jennifer, et al. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. ''Nat Commun''. 2015 Jan 29; '''6''': 5897
Genome-wide detection and characterization of positive selection in Korean Native Black Pig from Jeju Island. Description: Kim, Jaemin, et al. Genome-wide detection and characterization of positive selection in Korean Native Black Pig from Jeju Island. ''BMC Genet''. 2015 Jan 30; '''16''': 3
Highlighting nonlinear patterns in population genetics datasets. Description: Alanis-Lobato, Gregorio, et al. Highlighting nonlinear patterns in population genetics datasets. ''Sci Rep''. 2015 Jan 30; '''5''': 8140
A clinicogenetic model to predict lymph node invasion by use of genome-based biomarkers from exome arrays in prostate cancer patients. Description: Oh, Jong Jin, et al. A clinicogenetic model to predict lymph node invasion by use of genome-based biomarkers from exome arrays in prostate cancer patients. ''Korean J Urol''. 2015 Feb; '''56''' (2):109-16
A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions. Description: Oikkonen, J, et al. A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions. ''Mol Psychiatry''. 2015 Feb; '''20''' (2):275-82
Bovine Genome-wide Association Study for Genetic Elements to Resist the Infection of Foot-and-mouth Disease in the Field. Description: Lee, Bo-Young, et al. Bovine Genome-wide Association Study for Genetic Elements to Resist the Infection of Foot-and-mouth Disease in the Field. ''Asian-Australas J Anim Sci''. 2015 Feb; '''28''' (2):166-70
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk. Description: Carvajal-Carmona, Luis G, et al. Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk. ''Hum Genet''. 2015 Feb; '''134''' (2):231-45
Characterization of expression quantitative trait loci in the human colon. Description: Singh, Tarjinder, et al. Characterization of expression quantitative trait loci in the human colon. ''Inflamm Bowel Dis''. 2015 Feb; '''21''' (2):251-6
Genes from a translational analysis support a multifactorial nature of white matter hyperintensities. Description: Lopez, Lorna M, et al. Genes from a translational analysis support a multifactorial nature of white matter hyperintensities. ''Stroke''. 2015 Feb; '''46''' (2):341-7
Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke. Description: Adib-Samii, Poneh, et al. Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke. ''Stroke''. 2015 Feb; '''46''' (2):348-53
Genetic associations with brain cortical thickness in multiple sclerosis. Description: Matsushita, T, et al. Genetic associations with brain cortical thickness in multiple sclerosis. ''Genes Brain Behav''. 2015 Feb; '''14''' (2):217-27
Genetic variants associated with sleep disorders. Description: Kripke, Daniel F, et al. Genetic variants associated with sleep disorders. ''Sleep Med''. 2015 Feb; '''16''' (2):217-24
Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers. Description: Tonomura, Noriko, et al. Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers. ''PLoS Genet''. 2015 Feb; '''11''' (2):e1004922
Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients. Description: Wesolowska-Andersen, A, et al. Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients. ''Leukemia''. 2015 Feb; '''29''' (2):297-303
Identification of additive, dominant, and epistatic variation conferred by key genes in cellulose biosynthesis pathway in Populus tomentosadagger. Description: Du, Qingzhang, et al. Identification of additive, dominant, and epistatic variation conferred by key genes in cellulose biosynthesis pathway in Populus tomentosadagger. ''DNA Res''. 2015 Feb; '''22''' (1):53-67
Impact of cross-disorder polygenic risk on frontal brain activation with specific effect of schizophrenia risk. Description: Whalley, Heather C, et al. Impact of cross-disorder polygenic risk on frontal brain activation with specific effect of schizophrenia risk. ''Schizophr Res''. 2015 Feb; '''161''' (2-3):484-9
Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry. Description: Subaran, Ryan L, et al. Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry. ''Epilepsia''. 2015 Feb; '''56''' (2):188-94
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes. Description: Prescott, Natalie J, et al. Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes. ''PLoS Genet''. 2015 Feb; '''11''' (2):e1004955
Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents. Description: Desrivieres, S, et al. Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents. ''Mol Psychiatry''. 2015 Feb; '''20''' (2):263-74
The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy. Description: Hosseini, S Mohsen, et al. The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy. ''Hum Genet''. 2015 Feb; '''134''' (2):247-57
Heritable variation in courtship patterns in Drosophila melanogaster. Description: Gaertner, Bryn E, et al. Heritable variation in courtship patterns in Drosophila melanogaster. ''G3 (Bethesda)''. 2015 Feb 3; '''5''' (4):531-9
LRP5 regulates human body fat distribution by modulating adipose progenitor biology in a dose- and depot-specific fashion. Description: Loh, Nellie Y, et al. LRP5 regulates human body fat distribution by modulating adipose progenitor biology in a dose- and depot-specific fashion. ''Cell Metab''. 2015 Feb 3; '''21''' (2):262-273
Looking for adaptive footprints in the HSP90AA1 ovine gene. Description: Salces-Ortiz, Judit, et al. Looking for adaptive footprints in the HSP90AA1 ovine gene. ''BMC Evol Biol''. 2015 Feb 4; '''15''': 7
Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis. Description: Bowes, John, et al. Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis. ''Nat Commun''. 2015 Feb 5; '''6''': 6046
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Description: Do, Ron, et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. ''Nature''. 2015 Feb 5; '''518''' (7537):102-6
Filter-free exhaustive odds ratio-based genome-wide interaction approach pinpoints evidence for interaction in the HLA region in psoriasis. Description: Grange, Laura, et al. Filter-free exhaustive odds ratio-based genome-wide interaction approach pinpoints evidence for interaction in the HLA region in psoriasis. ''BMC Genet''. 2015 Feb 6; '''16''': 11
Epidermolysis bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene. Description: Murgiano, Leonardo, et al. Epidermolysis bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene. ''BMC Vet Res''. 2015 Feb 7; '''11''': 23
Apolipoprotein L1, income and early kidney damage. Description: Tamrat, Ruth, et al. Apolipoprotein L1, income and early kidney damage. ''BMC Nephrol''. 2015 Feb 10; '''16''': 14
Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy. Description: Lei, Jieping, et al. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy. ''Breast Cancer Res''. 2015 Feb 10; '''17''': 18
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer. Description: Mtatiro, Siana N, et al. Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer. ''BMC Med Genet''. 2015 Feb 10; '''16''': 4
Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases. Description: Maciag, Anna, et al. Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases. ''BMC Genet''. 2015 Feb 11; '''16''': 15
The genetics of POAG in black South Africans: a candidate gene association study. Description: Williams, Susan E I, et al. The genetics of POAG in black South Africans: a candidate gene association study. ''Sci Rep''. 2015 Feb 11; '''5''': 8378
New genetic loci link adipose and insulin biology to body fat distribution. Description: Shungin, Dmitry, et al. New genetic loci link adipose and insulin biology to body fat distribution. ''Nature''. 2015 Feb 12; '''518''' (7538):187-196
Association between genetic polymorphisms and carotid atherosclerosis in patients treated with radiotherapy for nasopharyngeal carcinoma. Description: Yuan, Chuang, et al. Association between genetic polymorphisms and carotid atherosclerosis in patients treated with radiotherapy for nasopharyngeal carcinoma. ''Radiat Oncol''. 2015 Feb 13; '''10''': 39
MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. Description: Nischwitz, S, et al. MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. ''J Neuroimmunol''. 2015 Feb 15; '''279''': 46-9
Genetic variants in the inositol phosphate metabolism pathway and risk of different types of cancer. Description: Tan, Juan, et al. Genetic variants in the inositol phosphate metabolism pathway and risk of different types of cancer. ''Sci Rep''. 2015 Feb 16; '''5''': 8473
Saving more teeth-a case for personalized care. Description: Vieira, Alexandre R, et al. Saving more teeth-a case for personalized care. ''J Pers Med''. 2015 Feb 16; '''5''' (1):30-5
Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9). Description: Chen, Yu, et al. Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9). ''Sci Rep''. 2015 Feb 17; '''5''': 8517
c.620C>T mutation in GATA4 is associated with congenital heart disease in South India. Description: Mattapally, Saidulu, et al. c.620C>T mutation in GATA4 is associated with congenital heart disease in South India. ''BMC Med Genet''. 2015 Feb 18; '''16''': 7
Genome-wide epistatic expression quantitative trait loci discovery in four human tissues reveals the importance of local chromosomal interactions governing gene expression. Description: Fitzpatrick, Darren J, et al. Genome-wide epistatic expression quantitative trait loci discovery in four human tissues reveals the importance of local chromosomal interactions governing gene expression. ''BMC Genomics''. 2015 Feb 21; '''16''': 109
A genome-wide scan for signatures of directional selection in domesticated pigs. Description: Moon, Sunjin, et al. A genome-wide scan for signatures of directional selection in domesticated pigs. ''BMC Genomics''. 2015 Feb 25; '''16''': 130
Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci. Description: Lemire, Mathieu, et al. Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci. ''Nat Commun''. 2015 Feb 26; '''6''': 6326
Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fat. Description: Lehnert, Klaus, et al. Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fat. ''Sci Rep''. 2015 Feb 26; '''5''': 8484
Non-coding genomic regions possessing enhancer and silencer potential are associated with healthy aging and exceptional survival. Description: Kim, Sangkyu, et al. Non-coding genomic regions possessing enhancer and silencer potential are associated with healthy aging and exceptional survival. ''Oncotarget''. 2015 Feb 28; '''6''' (6):3600-12
Association of symptoms and severity of rift valley fever with genetic polymorphisms in human innate immune pathways. Description: Hise, Amy G, et al. Association of symptoms and severity of rift valley fever with genetic polymorphisms in human innate immune pathways. ''PLoS Negl Trop Dis''. 2015 Mar; '''9''' (3):e0003584
CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs. Description: Putku, Margus, et al. CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs. ''Hum Genet''. 2015 Mar; '''134''' (3):291-303
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. Description: Villanueva, Pia, et al. Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. ''PLoS Genet''. 2015 Mar; '''11''' (3):e1004925
Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate. Description: Wolf, Zena T, et al. Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate. ''PLoS Genet''. 2015 Mar; '''11''' (3):e1005059
Genome-wide association study identifies three novel genetic markers associated with elite endurance performance. Description: Ahmetov, Ii, et al. Genome-wide association study identifies three novel genetic markers associated with elite endurance performance. ''Biol Sport''. 2015 Mar; '''32''' (1):3-9
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. Description: Mattheisen, M, et al. Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. ''Mol Psychiatry''. 2015 Mar; '''20''' (3):337-44
Influence of genetic variants in SORL1 gene on the manifestation of Alzheimer's disease. Description: Louwersheimer, Eva, et al. Influence of genetic variants in SORL1 gene on the manifestation of Alzheimer's disease. ''Neurobiol Aging''. 2015 Mar; '''36''' (3):1605.e13-20
*Insights into the origin of rare haplogroup C3 Y chromosomes in South America from high-density autosomal SNP genotyping.** Description: Mezzavilla, Massimo, et al. Insights into the origin of rare haplogroup C3* Y chromosomes in South America from high-density autosomal SNP genotyping. ''Forensic Sci Int Genet''. 2015 Mar; '''15''': 115-20
Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance. Description: Esparza-Gordillo, Jorge, et al. Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance. ''PLoS Genet''. 2015 Mar; '''11''' (3):e1005076
Meta-analysis of the TNFAIP3 region in psoriasis reveals a risk haplotype that is distinct from other autoimmune diseases. Description: Nititham, J, et al. Meta-analysis of the TNFAIP3 region in psoriasis reveals a risk haplotype that is distinct from other autoimmune diseases. ''Genes Immun''. 2015 Mar; '''16''' (2):120-6
Rare variation facilitates inferences of fine-scale population structure in humans. Description: O'Connor, Timothy D, et al. Rare variation facilitates inferences of fine-scale population structure in humans. ''Mol Biol Evol''. 2015 Mar; '''32''' (3):653-60
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes. Description: Wood, Andrew R, et al. Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes. ''Hum Mol Genet''. 2015 Mar 1; '''24''' (5):1504-12
Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems. Description: Iqbal, Zafar, et al. Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems. ''Am J Hum Genet''. 2015 Mar 5; '''96''' (3):386-96
Whole-genome sequence-based analysis of thyroid function. Description: Taylor, Peter N, et al. Whole-genome sequence-based analysis of thyroid function. ''Nat Commun''. 2015 Mar 6; '''6''': 5681
Comparing variant calling algorithms for target-exon sequencing in a large sample. Description: Lo, Yancy, et al. Comparing variant calling algorithms for target-exon sequencing in a large sample. ''BMC Bioinformatics''. 2015 Mar 7; '''16''': 75
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. Description: van Leeuwen, Elisabeth M, et al. Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. ''Nat Commun''. 2015 Mar 9; '''6''': 6065
A polymorphism at the translation start site of the vitamin D receptor gene is associated with the response to anti-osteoporotic therapy in postmenopausal women from southern Italy. Description: Conti, Valeria, et al. A polymorphism at the translation start site of the vitamin D receptor gene is associated with the response to anti-osteoporotic therapy in postmenopausal women from southern Italy. ''Int J Mol Sci''. 2015 Mar 10; '''16''' (3):5452-66
Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies. Description: Levine, Adam P, et al. Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies. ''BMC Genomics''. 2015 Mar 10; '''16''': 163
CYB5A polymorphism increases androgens and reduces risk of rheumatoid arthritis in women. Description: Stark, Klaus, et al. CYB5A polymorphism increases androgens and reduces risk of rheumatoid arthritis in women. ''Arthritis Res Ther''. 2015 Mar 11; '''17''': 56
Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan. Description: Ilyas, Muhammad, et al. Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan. ''BMC Genomics''. 2015 Mar 12; '''16''': 172
Association of FPGS genetic polymorphisms with primary retroperitoneal liposarcoma. Description: Miao, Chengli, et al. Association of FPGS genetic polymorphisms with primary retroperitoneal liposarcoma. ''Sci Rep''. 2015 Mar 13; '''5''': 9079
Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder. Description: Kember, Rachel L, et al. Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder. ''BMC Genet''. 2015 Mar 15; '''16''': 27
Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes. Description: Cooper, Nicholas J, et al. Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes. ''Hum Mol Genet''. 2015 Mar 15; '''24''' (6):1774-90
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. Description: Barrett, Jennifer H, et al. Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. ''Int J Cancer''. 2015 Mar 15; '''136''' (6):1351-60
Validation study of candidate single nucleotide polymorphisms associated with left ventricular hypertrophy in the Korean population. Description: Park, Jin-Kyu, et al. Validation study of candidate single nucleotide polymorphisms associated with left ventricular hypertrophy in the Korean population. ''BMC Med Genet''. 2015 Mar 15; '''16''': 13
Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS. Description: Steinberg, Karyn Meltz, et al. Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS. ''Sci Rep''. 2015 Mar 16; '''5''': 9124
Genome-wide analysis reveals population structure and selection in Chinese indigenous sheep breeds. Description: Wei, Caihong, et al. Genome-wide analysis reveals population structure and selection in Chinese indigenous sheep breeds. ''BMC Genomics''. 2015 Mar 17; '''16''': 194
A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females. Description: Sharma, Swarkar, et al. A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females. ''Nat Commun''. 2015 Mar 18; '''6''': 6452
Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus. Description: Zhang, Yan, et al. Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus. ''Arthritis Res Ther''. 2015 Mar 20; '''17''': 67
Identification of NF-kappaB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis. Description: Arismendi, Maria, et al. Identification of NF-kappaB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis. ''Arthritis Res Ther''. 2015 Mar 21; '''17''': 71
Ethnic differences in the association of SERPING1 with age-related macular degeneration and polypoidal choroidal vasculopathy. Description: Liu, Ke, et al. Ethnic differences in the association of SERPING1 with age-related macular degeneration and polypoidal choroidal vasculopathy. ''Sci Rep''. 2015 Mar 24; '''5''': 9424
Unravelling the hidden ancestry of American admixed populations. Description: Montinaro, Francesco, et al. Unravelling the hidden ancestry of American admixed populations. ''Nat Commun''. 2015 Mar 24; '''6''': 6596
X-inactivation informs variance-based testing for X-linked association of a quantitative trait. Description: Ma, Li, et al. X-inactivation informs variance-based testing for X-linked association of a quantitative trait. ''BMC Genomics''. 2015 Mar 25; '''16''': 241
Association analyses confirm five susceptibility loci for systemic lupus erythematosus in the Han Chinese population. Description: Sheng, Yu-jun, et al. Association analyses confirm five susceptibility loci for systemic lupus erythematosus in the Han Chinese population. ''Arthritis Res Ther''. 2015 Mar 28; '''17''': 85
Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease. Description: Yokoyama, Jennifer S, et al. Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease. ''BMC Neurol''. 2015 Mar 28; '''15''': 47
Genomic signatures of human and animal disease in the zoonotic pathogen Streptococcus suis. Description: Weinert, Lucy A, et al. Genomic signatures of human and animal disease in the zoonotic pathogen Streptococcus suis. ''Nat Commun''. 2015 Mar 31; '''6''': 6740
RNA expression profiling in depressed patients suggests retinoid-related orphan receptor alpha as a biomarker for antidepressant response. Description: Hennings, J M, et al. RNA expression profiling in depressed patients suggests retinoid-related orphan receptor alpha as a biomarker for antidepressant response. ''Transl Psychiatry''. 2015 Mar 31; '''5''': e538
A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease. Description: Kyostila, Kaisa, et al. A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease. ''PLoS Genet''. 2015 Apr; '''11''' (4):e1005169
Associations of epithelial sodium channel genes with blood pressure: the GenSalt study. Description: Liu, F, et al. Associations of epithelial sodium channel genes with blood pressure: the GenSalt study. ''J Hum Hypertens''. 2015 Apr; '''29''' (4):224-8
Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study. Description: Medina-Gomez, Carolina, et al. Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study. ''Eur J Epidemiol''. 2015 Apr; '''30''' (4):317-30
Contribution of large region joint associations to complex traits genetics. Description: Pare, Guillaume, et al. Contribution of large region joint associations to complex traits genetics. ''PLoS Genet''. 2015 Apr; '''11''' (4):e1005103
Genetic modifiers of ambulation in the Cooperative International Neuromuscular Research Group Duchenne Natural History Study. Description: Bello, Luca, et al. Genetic modifiers of ambulation in the Cooperative International Neuromuscular Research Group Duchenne Natural History Study. ''Ann Neurol''. 2015 Apr; '''77''' (4):684-96
Immunogenetic influences on acquisition of HIV-1 infection: consensus findings from two African cohorts point to an enhancer element in IL19 (1q32.2). Description: Li, X, et al. Immunogenetic influences on acquisition of HIV-1 infection: consensus findings from two African cohorts point to an enhancer element in IL19 (1q32.2). ''Genes Immun''. 2015 Apr-May; '''16''' (3):213-20
MAGMA: generalized gene-set analysis of GWAS data. Description: de Leeuw, Christiaan A, et al. MAGMA: generalized gene-set analysis of GWAS data. ''PLoS Comput Biol''. 2015 Apr; '''11''' (4):e1004219
MGAS: a powerful tool for multivariate gene-based genome-wide association analysis. Description: Van der Sluis, Sophie, et al. MGAS: a powerful tool for multivariate gene-based genome-wide association analysis. ''Bioinformatics''. 2015 Apr 1; '''31''' (7):1007-15
Polygenic risk of Parkinson disease is correlated with disease age at onset. Description: Escott-Price, Valentina, et al. Polygenic risk of Parkinson disease is correlated with disease age at onset. ''Ann Neurol''. 2015 Apr; '''77''' (4):582-91
SERPINB11 frameshift variant associated with novel hoof specific phenotype in Connemara ponies. Description: Finno, Carrie J, et al. SERPINB11 frameshift variant associated with novel hoof specific phenotype in Connemara ponies. ''PLoS Genet''. 2015 Apr; '''11''' (4):e1005122
Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD. Description: Stergiakouli, Evie, et al. Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD. ''J Am Acad Child Adolesc Psychiatry''. 2015 Apr; '''54''' (4):322-7
Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model. Description: Moser, Gerhard, et al. Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model. ''PLoS Genet''. 2015 Apr; '''11''' (4):e1004969
The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk. Description: Tang, R, et al. The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk. ''Genes Immun''. 2015 Apr-May; '''16''' (3):193-8
The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. Description: Eicher, J D, et al. The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. ''Genes Brain Behav''. 2015 Apr; '''14''' (4):377-85
The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. Description: Robinson, E B, et al. The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. ''Mol Psychiatry''. 2015 Apr; '''20''' (4):454-8
Relative extended haplotype homozygosity signals across breeds reveal dairy and beef specific signatures of selection. Description: Bomba, Lorenzo, et al. Relative extended haplotype homozygosity signals across breeds reveal dairy and beef specific signatures of selection. ''Genet Sel Evol''. 2015 Apr 2; '''47''': 25
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. Description: Tapper, William, et al. Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. ''Nat Commun''. 2015 Apr 7; '''6''': 6691
Genome-wide association studies (GWAS) identify a QTL close to PRKAG3 affecting meat pH and colour in crossbred commercial pigs. Description: Zhang, Chunyan, et al. Genome-wide association studies (GWAS) identify a QTL close to PRKAG3 affecting meat pH and colour in crossbred commercial pigs. ''BMC Genet''. 2015 Apr 7; '''16''': 33
Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies. Description: Wojcik, Genevieve L, et al. Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies. ''BMC Genet''. 2015 Apr 8; '''16''': 34
Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis. Description: Zuo, Xianbo, et al. Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis. ''Nat Commun''. 2015 Apr 9; '''6''': 6793
*Association of HLA-B41:02 with Henoch-Schonlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA-DRB1 status.** Description: Lopez-Mejias, Raquel, et al. Association of HLA-B*41:02 with Henoch-Schonlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA-DRB1 status. ''Arthritis Res Ther''. 2015 Apr 14; '''17''': 102
Unravelling the genetic history of Negritos and indigenous populations of Southeast Asia. Description: Aghakhanian, Farhang, et al. Unravelling the genetic history of Negritos and indigenous populations of Southeast Asia. ''Genome Biol Evol''. 2015 Apr 14; '''7''' (5):1206-15
The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses. Description: Cha, Seongwon, et al. The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses. ''BMC Complement Altern Med''. 2015 Apr 15; '''15''': 120
Genome-Wide Association Study on Resistance to Stalk Rot Diseases in Grain Sorghum. Description: Adeyanju, Adedayo, et al. Genome-Wide Association Study on Resistance to Stalk Rot Diseases in Grain Sorghum. ''G3 (Bethesda)''. 2015 Apr 16; '''5''' (6):1165-75
Low levels of taurine introgression in the current Brazilian Nelore and Gir indicine cattle populations. Description: O'Brien, Ana M Perez, et al. Low levels of taurine introgression in the current Brazilian Nelore and Gir indicine cattle populations. ''Genet Sel Evol''. 2015 Apr 17; '''47''': 31
ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide. Description: Graae, Lisette, et al. ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide. ''Genet Res (Camb)''. 2015 Apr 17; '''97''': e8
Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population. Description: Terao, Chikashi, et al. Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population. ''Arthritis Res Ther''. 2015 Apr 18; '''17''': 104
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. Description: Li, Jin, et al. Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. ''Nat Commun''. 2015 Apr 20; '''6''': 6804
Genome-wide association study of behavioural and psychiatric features in human prion disease. Description: Thompson, A G B, et al. Genome-wide association study of behavioural and psychiatric features in human prion disease. ''Transl Psychiatry''. 2015 Apr 21; '''5''': e552
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. Description: Yin, Xianyong, et al. Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. ''Nat Commun''. 2015 Apr 23; '''6''': 6916
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism. Description: Scholl, Ute I, et al. Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism. ''Elife''. 2015 Apr 24; '''4''': e06315
Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior. Description: Salvatore, J E, et al. Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior. ''Transl Psychiatry''. 2015 Apr 28; '''5''': e558
Composite Selection Signals for Complex Traits Exemplified Through Bovine Stature Using Multibreed Cohorts of European and African Bos taurus. Description: Randhawa, Imtiaz A S, et al. Composite Selection Signals for Complex Traits Exemplified Through Bovine Stature Using Multibreed Cohorts of European and African Bos taurus. ''G3 (Bethesda)''. 2015 Apr 30; '''5''' (7):1391-401
Associations of EDNRA and EDN1 polymorphisms with carotid intima media thickness through interactions with gender, regular exercise, and obesity in subjects in Taiwan: Taichung Community Health Study (TCHS). Description: Li, Tsai-Chung, et al. Associations of EDNRA and EDN1 polymorphisms with carotid intima media thickness through interactions with gender, regular exercise, and obesity in subjects in Taiwan: Taichung Community Health Study (TCHS). ''Biomedicine (Taipei)''. 2015 May; '''5''' (2):8
'Carriers of variant luteinizing hormone (V-LH) among 1593 Baltic men have significantly higher serum LH'. Description: Punab, A M, et al. 'Carriers of variant luteinizing hormone (V-LH) among 1593 Baltic men have significantly higher serum LH'. ''Andrology''. 2015 May; '''3''' (3):512-9
Genetic and phenotypic differentiation of an Andean intermediate altitude population. Description: Eichstaedt, Christina A, et al. Genetic and phenotypic differentiation of an Andean intermediate altitude population. ''Physiol Rep''. 2015 May; '''3''' (5):
Identity-by-descent mapping in a Scandinavian multiple sclerosis cohort. Description: Westerlind, Helga, et al. Identity-by-descent mapping in a Scandinavian multiple sclerosis cohort. ''Eur J Hum Genet''. 2015 May; '''23''' (5):688-92
IL28B is associated with outcomes of chronic HBV infection. Description: Shi, Xiaodong, et al. IL28B is associated with outcomes of chronic HBV infection. ''Yonsei Med J''. 2015 May; '''56''' (3):625-33
Investigation of association between hip osteoarthritis susceptibility loci and radiographic proximal femur shape. Description: Lindner, Claudia, et al. Investigation of association between hip osteoarthritis susceptibility loci and radiographic proximal femur shape. ''Arthritis Rheumatol''. 2015 May; '''67''' (8):2076-84
Psoriasis and cardiometabolic traits: modest association but distinct genetic architectures. Description: Koch, Manja, et al. Psoriasis and cardiometabolic traits: modest association but distinct genetic architectures. ''J Invest Dermatol''. 2015 May; '''135''' (5):1283-1293
Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk. Description: Smyth, Conor, et al. Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk. ''Mol Genet Genomic Med''. 2015 May; '''3''' (3):182-8
Rare structural genetic variation in human prion diseases. Description: Lukic, Ana, et al. Rare structural genetic variation in human prion diseases. ''Neurobiol Aging''. 2015 May; '''36''' (5):2004.e1-8
Role of Type 1 Diabetes-Associated SNPs on Risk of Autoantibody Positivity in the TEDDY Study. Description: Torn, Carina, et al. Role of Type 1 Diabetes-Associated SNPs on Risk of Autoantibody Positivity in the TEDDY Study. ''Diabetes''. 2015 May; '''64''' (5):1818-29
The cerebellum ages slowly according to the epigenetic clock. Description: Horvath, Steve, et al. The cerebellum ages slowly according to the epigenetic clock. ''Aging (Albany NY)''. 2015 May; '''7''' (5):294-306
Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery. Description: Kertai, Miklos D, et al. Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery. ''BMJ Open''. 2015 May 6; '''5''' (5):e006920
Genome-wide association mapping in a wild avian population identifies a link between genetic and phenotypic variation in a life-history trait. Description: Husby, Arild, et al. Genome-wide association mapping in a wild avian population identifies a link between genetic and phenotypic variation in a life-history trait. ''Proc Biol Sci''. 2015 May 7; '''282''' (1806):20150156
Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population. Description: Chen, Shanshan, et al. Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population. ''J Am Heart Assoc''. 2015 May 7; '''4''' (5):
Performance of a blockwise approach in variable selection using linkage disequilibrium information. Description: Dehman, Alia, et al. Performance of a blockwise approach in variable selection using linkage disequilibrium information. ''BMC Bioinformatics''. 2015 May 8; '''16''': 148
Insm1 cooperates with Neurod1 and Foxa2 to maintain mature pancreatic beta-cell function. Description: Jia, Shiqi, et al. Insm1 cooperates with Neurod1 and Foxa2 to maintain mature pancreatic beta-cell function. ''EMBO J''. 2015 May 12; '''34''' (10):1417-33
Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese. Description: Li, Changgui, et al. Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese. ''Nat Commun''. 2015 May 13; '''6''': 7041
A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. Description: Wang, Yi-Ting, et al. A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. ''BMC Genomics''. 2015 May 15; '''16''': 381
Mosaic structural variation in children with developmental disorders. Description: King, Daniel A, et al. Mosaic structural variation in children with developmental disorders. ''Hum Mol Genet''. 2015 May 15; '''24''' (10):2733-45
Application of high-dimensional feature selection: evaluation for genomic prediction in man. Description: Bermingham, M L, et al. Application of high-dimensional feature selection: evaluation for genomic prediction in man. ''Sci Rep''. 2015 May 19; '''5''': 10312
Genetic association study of circadian genes with seasonal pattern in bipolar disorders. Description: Geoffroy, Pierre Alexis, et al. Genetic association study of circadian genes with seasonal pattern in bipolar disorders. ''Sci Rep''. 2015 May 19; '''5''': 10232
Adaptation to Low Salinity Promotes Genomic Divergence in Atlantic Cod (Gadus morhua L.). Description: Berg, Paul R, et al. Adaptation to Low Salinity Promotes Genomic Divergence in Atlantic Cod (Gadus morhua L.). ''Genome Biol Evol''. 2015 May 20; '''7''' (6):1644-63
affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling. Description: Hernandez-Ferrer, Carles, et al. affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling. ''BMC Bioinformatics''. 2015 May 20; '''16''': 167
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer. Description: Al-Tassan, Nada A, et al. A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer. ''Sci Rep''. 2015 May 20; '''5''': 10442
Lack of Association between the TSPAN18 Gene and Schizophrenia Based on New Data from Han Chinese and a Meta-Analysis. Description: Zhang, Bao, et al. Lack of Association between the TSPAN18 Gene and Schizophrenia Based on New Data from Han Chinese and a Meta-Analysis. ''Int J Mol Sci''. 2015 May 26; '''16''' (6):11864-72
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. Description: Swaminathan, Bhairavi, et al. Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. ''Nat Commun''. 2015 May 26; '''6''': 7213
Exploring the relationship between lifestyles, diets and genetic adaptations in humans. Description: Valente, Cristina, et al. Exploring the relationship between lifestyles, diets and genetic adaptations in humans. ''BMC Genet''. 2015 May 28; '''16''': 55
A variant of PSMD6 is associated with the therapeutic efficacy of oral antidiabetic drugs in Chinese type 2 diabetes patients. Description: Chen, Miao, et al. A variant of PSMD6 is associated with the therapeutic efficacy of oral antidiabetic drugs in Chinese type 2 diabetes patients. ''Sci Rep''. 2015 May 29; '''5''': 10701
Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study. Description: Tin, Adrienne, et al. Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study. ''BMC Genet''. 2015 May 29; '''16''': 56
Adaptive divergence in the monkey flower Mimulus guttatus is maintained by a chromosomal inversion. Description: Twyford, Alex D, et al. Adaptive divergence in the monkey flower Mimulus guttatus is maintained by a chromosomal inversion. ''Evolution''. 2015 Jun; '''69''' (6):1476-1486
A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. Description: Evans, P D, et al. A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. ''Genes Brain Behav''. 2015 Jun; '''14''' (5):387-97
Common NOTCH3 Variants and Cerebral Small-Vessel Disease. Description: Rutten-Jacobs, Loes C A, et al. Common NOTCH3 Variants and Cerebral Small-Vessel Disease. ''Stroke''. 2015 Jun; '''46''' (6):1482-7
Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor. Description: Ayuso, Pedro, et al. Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor. ''Medicine (Baltimore)''. 2015 Jun; '''94''' (24):e968
Identification of new susceptibility loci for IgA nephropathy in Han Chinese. Description: Li, Ming, et al. Identification of new susceptibility loci for IgA nephropathy in Han Chinese. ''Nat Commun''. 2015 Jun 1; '''6''': 7270
Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease. Description: Wilbe, Maria, et al. Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease. ''PLoS Genet''. 2015 Jun; '''11''' (6):e1005248
Multiple Genes Related to Muscle Identified through a Joint Analysis of a Two-stage Genome-wide Association Study for Racing Performance of 1,156 Thoroughbreds. Description: Shin, Dong-Hyun, et al. Multiple Genes Related to Muscle Identified through a Joint Analysis of a Two-stage Genome-wide Association Study for Racing Performance of 1,156 Thoroughbreds. ''Asian-Australas J Anim Sci''. 2015 Jun; '''28''' (6):771-81
Reconstructing Past Admixture Processes from Local Genomic Ancestry Using Wavelet Transformation. Description: Sanderson, Jean, et al. Reconstructing Past Admixture Processes from Local Genomic Ancestry Using Wavelet Transformation. ''Genetics''. 2015 Jun; '''200''' (2):469-81
Single nucleotide polymorphisms in the FAM167A-BLK gene are associated with polymyositis/dermatomyositis in the Han Chinese population. Description: Chen, Si, et al. Single nucleotide polymorphisms in the FAM167A-BLK gene are associated with polymyositis/dermatomyositis in the Han Chinese population. ''Immunol Res''. 2015 Jun; '''62''' (2):153-62
Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone. Description: Vallet, Maheva, et al. Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone. ''Hum Mol Genet''. 2015 Jun 1; '''24''' (11):3286-95
Understanding the molecular mechanisms of human microtia via a pig model of HOXA1 syndrome. Description: Qiao, Ruimin, et al. Understanding the molecular mechanisms of human microtia via a pig model of HOXA1 syndrome. ''Dis Model Mech''. 2015 Jun; '''8''' (6):611-22
Interaction between common variants of FTO and MC4R is associated with risk of PCOS. Description: Yuan, Huiqin, et al. Interaction between common variants of FTO and MC4R is associated with risk of PCOS. ''Reprod Biol Endocrinol''. 2015 Jun 2; '''13''': 55
Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders. Description: Arloth, Janine, et al. Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders. ''Neuron''. 2015 Jun 3; '''86''' (5):1189-202
Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations. Description: Wei, Zejun, et al. Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations. ''Sci Rep''. 2015 Jun 3; '''5''': 10879
Identification of two novel mammographic density loci at 6Q25.1. Description: Brand, Judith S, et al. Identification of two novel mammographic density loci at 6Q25.1. ''Breast Cancer Res''. 2015 Jun 3; '''17''': 75
Recent genomic heritage in Scotland. Description: Amador, Carmen, et al. Recent genomic heritage in Scotland. ''BMC Genomics''. 2015 Jun 6; '''16''': 437
Do nuclear-encoded core subunits of mitochondrial complex I confer genetic susceptibility to schizophrenia in Han Chinese populations? Description: Li, Xiao, et al. Do nuclear-encoded core subunits of mitochondrial complex I confer genetic susceptibility to schizophrenia in Han Chinese populations? ''Sci Rep''. 2015 Jun 8; '''5''': 11076
In silico phenotyping via co-training for improved phenotype prediction from genotype. Description: Roqueiro, Damian, et al. In silico phenotyping via co-training for improved phenotype prediction from genotype. ''Bioinformatics''. 2015 Jun 15; '''31''' (12):i303-10
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Description: Kouri, Naomi, et al. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. ''Nat Commun''. 2015 Jun 16; '''6''': 7247
Polymerase Theta is a key driver of genome evolution and of CRISPR/Cas9-mediated mutagenesis. Description: van Schendel, Robin, et al. Polymerase Theta is a key driver of genome evolution and of CRISPR/Cas9-mediated mutagenesis. ''Nat Commun''. 2015 Jun 16; '''6''': 7394
The glucagon-like peptide-1 receptor as a potential treatment target in alcohol use disorder: evidence from human genetic association studies and a mouse model of alcohol dependence. Description: Suchankova, P, et al. The glucagon-like peptide-1 receptor as a potential treatment target in alcohol use disorder: evidence from human genetic association studies and a mouse model of alcohol dependence. ''Transl Psychiatry''. 2015 Jun 16; '''5''': e583
Population structure and history of the Welsh sheep breeds determined by whole genome genotyping. Description: Beynon, Sarah E, et al. Population structure and history of the Welsh sheep breeds determined by whole genome genotyping. ''BMC Genet''. 2015 Jun 20; '''16''': 65
Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits. Description: Huang, Yu S, et al. Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits. ''BMC Biol''. 2015 Jun 20; '''13''': 41
Frequency of alcohol consumption in humans; the role of metabotropic glutamate receptors and downstream signaling pathways. Description: Meyers, J L, et al. Frequency of alcohol consumption in humans; the role of metabotropic glutamate receptors and downstream signaling pathways. ''Transl Psychiatry''. 2015 Jun 23; '''5''': e586
Genome-wide Association Study on Platinum-induced Hepatotoxicity in Non-Small Cell Lung Cancer Patients. Description: Cao, Songyu, et al. Genome-wide Association Study on Platinum-induced Hepatotoxicity in Non-Small Cell Lung Cancer Patients. ''Sci Rep''. 2015 Jun 23; '''5''': 11556
Study of genetic variability in Vitis vinifera L. germplasm by high-throughput Vitis18kSNP array: the case of Georgian genetic resources. Description: De Lorenzis, Gabriella, et al. Study of genetic variability in Vitis vinifera L. germplasm by high-throughput Vitis18kSNP array: the case of Georgian genetic resources. ''BMC Plant Biol''. 2015 Jun 23; '''15''': 154
A genome-wide association study identifies multiple loci for variation in human ear morphology. Description: Adhikari, Kaustubh, et al. A genome-wide association study identifies multiple loci for variation in human ear morphology. ''Nat Commun''. 2015 Jun 24; '''6''': 7500
Allelic variation at the rpv1 locus controls partial resistance to Plum pox virus infection in Arabidopsis thaliana. Description: Poque, S, et al. Allelic variation at the rpv1 locus controls partial resistance to Plum pox virus infection in Arabidopsis thaliana. ''BMC Plant Biol''. 2015 Jun 25; '''15''': 159
Demographic, psychosocial, and genetic risk associated with smokeless tobacco use among Mexican heritage youth. Description: Wilkinson, Anna V, et al. Demographic, psychosocial, and genetic risk associated with smokeless tobacco use among Mexican heritage youth. ''BMC Med Genet''. 2015 Jun 26; '''16''': 43
Single-copy gene based 50 K SNP chip for genetic studies and molecular breeding in rice. Description: Singh, Nisha, et al. Single-copy gene based 50 K SNP chip for genetic studies and molecular breeding in rice. ''Sci Rep''. 2015 Jun 26; '''5''': 11600
An analysis of the association between prostate cancer risk loci, PSA levels, disease aggressiveness and disease-specific mortality. Description: Sullivan, J, et al. An analysis of the association between prostate cancer risk loci, PSA levels, disease aggressiveness and disease-specific mortality. ''Br J Cancer''. 2015 Jun 30; '''113''' (1):166-72
Association between IL7R polymorphisms and severe liver disease in HIV/HCV coinfected patients: a cross-sectional study. Description: Guzman-Fulgencio, Maria, et al. Association between IL7R polymorphisms and severe liver disease in HIV/HCV coinfected patients: a cross-sectional study. ''J Transl Med''. 2015 Jun 30; '''13''': 206
A common variant near TGFBR3 is associated with primary open angle glaucoma. Description: Li, Zheng, et al. A common variant near TGFBR3 is associated with primary open angle glaucoma. ''Hum Mol Genet''. 2015 Jul 1; '''24''' (13):3880-92
A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment. Description: Nyegaard, Mette, et al. A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment. ''PLoS Genet''. 2015 Jul; '''11''' (7):e1005386
Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral density. Description: Veldhuis-Vlug, A G, et al. Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral density. ''Osteoporos Int''. 2015 Jul; '''26''' (7):2019-27
Association of serotonin transporter (SLC6A4) and receptor (5HTR1A, 5HTR2A) polymorphisms with response to treatment with escitalopram in patients with major depressive disorder: A preliminary study. Description: Basu, Aniruddha, et al. Association of serotonin transporter (SLC6A4) and receptor (5HTR1A, 5HTR2A) polymorphisms with response to treatment with escitalopram in patients with major depressive disorder: A preliminary study. ''Indian J Med Res''. 2015 Jul; '''142''' (1):40-5
Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network. Description: Hall, Molly A, et al. Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network. ''Genet Epidemiol''. 2015 Jul; '''39''' (5):376-84
CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis. Description: Cho, Chul-Hyun, et al. CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis. ''Psychiatry Investig''. 2015 Jul; '''12''' (3):402-7
Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood. Description: Hatzimanolis, Alex, et al. Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood. ''Am J Med Genet B Neuropsychiatr Genet''. 2015 Jul; '''168B''' (5):392-401
Familiality and SNP heritability of age at onset and episodicity in major depressive disorder. Description: Ferentinos, P, et al. Familiality and SNP heritability of age at onset and episodicity in major depressive disorder. ''Psychol Med''. 2015 Jul; '''45''' (10):2215-25
Glutamate Networks Implicate Cognitive Impairments in Schizophrenia: Genome-Wide Association Studies of 52 Cognitive Phenotypes. Description: Ohi, Kazutaka, et al. Glutamate Networks Implicate Cognitive Impairments in Schizophrenia: Genome-Wide Association Studies of 52 Cognitive Phenotypes. ''Schizophr Bull''. 2015 Jul; '''41''' (4):909-18
Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation. Description: Murgiano, Leonardo, et al. Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation. ''PLoS Genet''. 2015 Jul; '''11''' (7):e1005427
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels. Description: Kavanagh, David, et al. Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels. ''Hum Mol Genet''. 2015 Jul 1; '''24''' (13):3861-70
TOX and CDKN2A/B Gene Polymorphisms Are Associated with Type 2 Diabetes in Han Chinese. Description: Wei, Fengjiang, et al. TOX and CDKN2A/B Gene Polymorphisms Are Associated with Type 2 Diabetes in Han Chinese. ''Sci Rep''. 2015 Jul 3; '''5''': 11900
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. Description: Chen, Pei-Lung, et al. Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. ''Nat Commun''. 2015 Jul 7; '''6''': 7633
Response and inbreeding from a genomic selection experiment in layer chickens. Description: Wolc, Anna, et al. Response and inbreeding from a genomic selection experiment in layer chickens. ''Genet Sel Evol''. 2015 Jul 7; '''47''': 59
Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse. Description: Perrocheau, Maelle, et al. Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse. ''J Cardiovasc Dev Dis''. 2015 Jul 10; '''2''' (3):176-189
Iron and hepcidin as risk factors in atherosclerosis: what do the genes say? Description: Galesloot, Tessel E, et al. Iron and hepcidin as risk factors in atherosclerosis: what do the genes say? ''BMC Genet''. 2015 Jul 11; '''16''': 79
Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Description: Lin, Bochao Danae, et al. Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. ''Genes (Basel)''. 2015 Jul 13; '''6''' (3):559-76
Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine. Description: Huang, Kuo-Chin, et al. Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine. ''BMC Complement Altern Med''. 2015 Jul 14; '''15''': 229
Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels. Description: Setoh, Kazuya, et al. Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels. ''Nat Commun''. 2015 Jul 15; '''6''': 7754
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome. Description: Kelmemi, W, et al. Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome. ''BMC Med Genet''. 2015 Jul 20; '''16''': 50
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. Description: Ramachandran, Dhanya, et al. Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. ''G3 (Bethesda)''. 2015 Jul 20; '''5''' (10):1961-71
Large-scale genomics unveil polygenic architecture of human cortical surface area. Description: Chen, Chi-Hua, et al. Large-scale genomics unveil polygenic architecture of human cortical surface area. ''Nat Commun''. 2015 Jul 20; '''6''': 7549
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome. Description: Dai, Yufei, et al. Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome. ''Sci Rep''. 2015 Jul 20; '''5''': 12169
Ancestry, admixture and fitness in Colombian genomes. Description: Rishishwar, Lavanya, et al. Ancestry, admixture and fitness in Colombian genomes. ''Sci Rep''. 2015 Jul 21; '''5''': 12376
Estimation of inbreeding using pedigree, 50k SNP chip genotypes and full sequence data in three cattle breeds. Description: Zhang, Qianqian, et al. Estimation of inbreeding using pedigree, 50k SNP chip genotypes and full sequence data in three cattle breeds. ''BMC Genet''. 2015 Jul 22; '''16''': 88
Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies. Description: Hoh, Boon-Peng, et al. Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies. ''Hum Genomics''. 2015 Jul 22; '''9''': 16
Genetic variation in insulin-induced kinase signaling. Description: Wang, Isabel Xiaorong, et al. Genetic variation in insulin-induced kinase signaling. ''Mol Syst Biol''. 2015 Jul 22; '''11''' (7):820
Impact of genetic similarity on imputation accuracy. Description: Roshyara, Nab Raj, et al. Impact of genetic similarity on imputation accuracy. ''BMC Genet''. 2015 Jul 22; '''16''': 90
Genome-wide high-throughput SNP discovery and genotyping for understanding natural (functional) allelic diversity and domestication patterns in wild chickpea. Description: Bajaj, Deepak, et al. Genome-wide high-throughput SNP discovery and genotyping for understanding natural (functional) allelic diversity and domestication patterns in wild chickpea. ''Sci Rep''. 2015 Jul 24; '''5''': 12468
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy. Description: Ruggieri, Alessandra, et al. Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy. ''Acta Neuropathol Commun''. 2015 Jul 25; '''3''': 44
Genetic, molecular and physiological basis of variation in Drosophila gut immunocompetence. Description: Bou Sleiman, Maroun S, et al. Genetic, molecular and physiological basis of variation in Drosophila gut immunocompetence. ''Nat Commun''. 2015 Jul 27; '''6''': 7829
A double amino-acid change in the HLA-A peptide-binding groove is associated with response to psychotropic treatment in patients with schizophrenia. Description: Le Clerc, S, et al. A double amino-acid change in the HLA-A peptide-binding groove is associated with response to psychotropic treatment in patients with schizophrenia. ''Transl Psychiatry''. 2015 Jul 28; '''5''': e608
Fingerprinting Soybean Germplasm and Its Utility in Genomic Research. Description: Song, Qijian, et al. Fingerprinting Soybean Germplasm and Its Utility in Genomic Research. ''G3 (Bethesda)''. 2015 Jul 28; '''5''' (10):1999-2006
Genetic contribution to multiple sclerosis risk among Ashkenazi Jews. Description: Khankhanian, Pouya, et al. Genetic contribution to multiple sclerosis risk among Ashkenazi Jews. ''BMC Med Genet''. 2015 Jul 28; '''16''': 55
Genome-wide association study revealed a promising region and candidate genes for eggshell quality in an F2 resource population. Description: Sun, Congjiao, et al. Genome-wide association study revealed a promising region and candidate genes for eggshell quality in an F2 resource population. ''BMC Genomics''. 2015 Jul 31; '''16''': 565
Genetic risk factors affecting mitochondrial function are associated with kidney disease in people with Type 1 diabetes. Description: Swan, E J, et al. Genetic risk factors affecting mitochondrial function are associated with kidney disease in people with Type 1 diabetes. ''Diabet Med''. 2015 Aug; '''32''' (8):1104-9
Across language families: Genome diversity mirrors linguistic variation within Europe. Description: Longobardi, Giuseppe, et al. Across language families: Genome diversity mirrors linguistic variation within Europe. ''Am J Phys Anthropol''. 2015 Aug; '''157''' (4):630-40
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. Description: Childs, Erica J, et al. Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. ''Nat Genet''. 2015 Aug; '''47''' (8):911-6
CREB-BDNF pathway influences alcohol cue-elicited activation in drinkers. Description: Chen, Jiayu, et al. CREB-BDNF pathway influences alcohol cue-elicited activation in drinkers. ''Hum Brain Mapp''. 2015 Aug; '''36''' (8):3007-19
Dimethylglycine Deficiency and the Development of Diabetes. Description: Magnusson, Martin, et al. Dimethylglycine Deficiency and the Development of Diabetes. ''Diabetes''. 2015 Aug; '''64''' (8):3010-6
Evidence for a Common Origin of Blacksmiths and Cultivators in the Ethiopian Ari within the Last 4500 Years: Lessons for Clustering-Based Inference. Description: van Dorp, Lucy, et al. Evidence for a Common Origin of Blacksmiths and Cultivators in the Ethiopian Ari within the Last 4500 Years: Lessons for Clustering-Based Inference. ''PLoS Genet''. 2015 Aug; '''11''' (8):e1005397
F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease. Description: Tosto, Giuseppe, et al. F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease. ''Ann Clin Transl Neurol''. 2015 Aug; '''2''' (8):810-20
Genome-Wide Association Study of HIV-Related Lipoatrophy in Thai Patients: Association of a DLGAP1 Polymorphism with Fat Loss. Description: Uttayamakul, Sumonmal, et al. Genome-Wide Association Study of HIV-Related Lipoatrophy in Thai Patients: Association of a DLGAP1 Polymorphism with Fat Loss. ''AIDS Res Hum Retroviruses''. 2015 Aug; '''31''' (8):792-6
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome. Description: Garcia-Martin, Elena, et al. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome. ''Medicine (Baltimore)''. 2015 Aug; '''94''' (34):e1448
Making a chocolate chip: development and evaluation of a 6K SNP array for Theobroma cacao. Description: Livingstone, Donald, et al. Making a chocolate chip: development and evaluation of a 6K SNP array for Theobroma cacao. ''DNA Res''. 2015 Aug; '''22''' (4):279-91
Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes. Description: Brorsson, Caroline A, et al. Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes. ''Diabetes''. 2015 Aug; '''64''' (8):3017-27
Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. Description: Usher, Christina L, et al. Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. ''Nat Genet''. 2015 Aug; '''47''' (8):921-5
Clinically relevant copy number variations detected in cerebral palsy. Description: Oskoui, Maryam, et al. Clinically relevant copy number variations detected in cerebral palsy. ''Nat Commun''. 2015 Aug 3; '''6''': 7949
Genetic diversity of Italian goat breeds assessed with a medium-density SNP chip. Description: Nicoloso, Letizia, et al. Genetic diversity of Italian goat breeds assessed with a medium-density SNP chip. ''Genet Sel Evol''. 2015 Aug 4; '''47''': 62
Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. Description: Ma, Yuanlin, et al. Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. ''Sci Rep''. 2015 Aug 5; '''5''': 10299
A Validated Phenotyping Algorithm for Genetic Association Studies in Age-related Macular Degeneration. Description: Simonett, Joseph M, et al. A Validated Phenotyping Algorithm for Genetic Association Studies in Age-related Macular Degeneration. ''Sci Rep''. 2015 Aug 10; '''5''': 12875
Two novel genetic variants in the mineralocorticoid receptor gene associated with spontaneous preterm birth. Description: Christiaens, Inge, et al. Two novel genetic variants in the mineralocorticoid receptor gene associated with spontaneous preterm birth. ''BMC Med Genet''. 2015 Aug 11; '''16''': 59
Pathway analysis of body mass index genome-wide association study highlights risk pathways in cardiovascular disease. Description: Zhao, Xin, et al. Pathway analysis of body mass index genome-wide association study highlights risk pathways in cardiovascular disease. ''Sci Rep''. 2015 Aug 12; '''5''': 13025
Merino and Merino-derived sheep breeds: a genome-wide intercontinental study. Description: Ciani, Elena, et al. Merino and Merino-derived sheep breeds: a genome-wide intercontinental study. ''Genet Sel Evol''. 2015 Aug 14; '''47''': 64
Sex-Specific Effects of Adiponectin on Carotid Intima-Media Thickness and Incident Cardiovascular Disease. Description: Persson, Jonas, et al. Sex-Specific Effects of Adiponectin on Carotid Intima-Media Thickness and Incident Cardiovascular Disease. ''J Am Heart Assoc''. 2015 Aug 14; '''4''' (8):e001853
Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding locidagger. Description: Kirsten, Holger, et al. Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding locidagger. ''Hum Mol Genet''. 2015 Aug 15; '''24''' (16):4746-63
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Description: Hayes, M Geoffrey, et al. Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. ''Nat Commun''. 2015 Aug 18; '''6''': 7502
Associations between the orexin (hypocretin) receptor 2 gene polymorphism Val308Ile and nicotine dependence in genome-wide and subsequent association studies. Description: Nishizawa, Daisuke, et al. Associations between the orexin (hypocretin) receptor 2 gene polymorphism Val308Ile and nicotine dependence in genome-wide and subsequent association studies. ''Mol Brain''. 2015 Aug 20; '''8''': 50
Exploring evidence of positive selection reveals genetic basis of meat quality traits in Berkshire pigs through whole genome sequencing. Description: Jeong, Hyeonsoo, et al. Exploring evidence of positive selection reveals genetic basis of meat quality traits in Berkshire pigs through whole genome sequencing. ''BMC Genet''. 2015 Aug 20; '''16''': 104
Gender-specific associations between ADIPOQ gene polymorphisms and adiponectin levels and obesity in the Jackson Heart Study cohort. Description: Riestra, Pia, et al. Gender-specific associations between ADIPOQ gene polymorphisms and adiponectin levels and obesity in the Jackson Heart Study cohort. ''BMC Med Genet''. 2015 Aug 20; '''16''': 65
Barley landraces are characterized by geographically heterogeneous genomic origins. Description: Poets, Ana M, et al. Barley landraces are characterized by geographically heterogeneous genomic origins. ''Genome Biol''. 2015 Aug 21; '''16''': 173
CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations. Description: Dajani, Rana, et al. CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations. ''Sci Rep''. 2015 Aug 21; '''5''': 13391
Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels. Description: Li, Wei-Dong, et al. Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels. ''Sci Rep''. 2015 Aug 24; '''5''': 13422
Polymorphisms of PRLHR and HSPA12A and risk of gastric and colorectal cancer in the Chinese Han population. Description: Su, Qinghua, et al. Polymorphisms of PRLHR and HSPA12A and risk of gastric and colorectal cancer in the Chinese Han population. ''BMC Gastroenterol''. 2015 Aug 25; '''15''': 107
Detection of Selection Signatures on the X Chromosome in Three Sheep Breeds. Description: Zhu, Caiye, et al. Detection of Selection Signatures on the X Chromosome in Three Sheep Breeds. ''Int J Mol Sci''. 2015 Aug 28; '''16''' (9):20360-74
LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients. Description: Alvarez, Lydia, et al. LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients. ''BMC Med Genet''. 2015 Aug 31; '''16''': 72
A common oxytocin receptor gene (OXTR) polymorphism modulates intranasal oxytocin effects on the neural response to social cooperation in humans. Description: Feng, C, et al. A common oxytocin receptor gene (OXTR) polymorphism modulates intranasal oxytocin effects on the neural response to social cooperation in humans. ''Genes Brain Behav''. 2015 Sep; '''14''' (7):516-25
Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia. Description: Fiorentino, Alessia, et al. Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia. ''Eur J Hum Genet''. 2015 Sep; '''23''' (9):1200-6
Data in support of association study of the brain-derived neurotrophic factor gene SNPs and completed suicide in the Slovenian sample. Description: Ropret, Sandra, et al. Data in support of association study of the brain-derived neurotrophic factor gene SNPs and completed suicide in the Slovenian sample. ''Data Brief''. 2015 Sep; '''4''': 529-33
Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE. Description: Jacobsen, Kaya K, et al. Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE. ''Am J Med Genet B Neuropsychiatr Genet''. 2015 Sep; '''168''' (6):423-432
Estimation of Genetic Relationships Between Individuals Across Cohorts and Platforms: Application to Childhood Height. Description: Fedko, Iryna O, et al. Estimation of Genetic Relationships Between Individuals Across Cohorts and Platforms: Application to Childhood Height. ''Behav Genet''. 2015 Sep; '''45''' (5):514-28
Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity. Description: Jiao, Hong, et al. Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity. ''Eur J Hum Genet''. 2015 Sep; '''23''' (9):1216-22
Gene-gene and gene-environment interactions in the etiology of type 2 diabetes mellitus in the population of Hyderabad, India. Description: Uma Jyothi, Kommoju, et al. Gene-gene and gene-environment interactions in the etiology of type 2 diabetes mellitus in the population of Hyderabad, India. ''Meta Gene''. 2015 Sep; '''5''': 9-20
Genome-wide association study of neocortical Lewy-related pathology. Description: Peuralinna, Terhi, et al. Genome-wide association study of neocortical Lewy-related pathology. ''Ann Clin Transl Neurol''. 2015 Sep; '''2''' (9):920-31
Genome-wide association study of rice (Oryza sativa L.) leaf traits with a high-throughput leaf scorer. Description: Yang, Wanneng, et al. Genome-wide association study of rice (Oryza sativa L.) leaf traits with a high-throughput leaf scorer. ''J Exp Bot''. 2015 Sep; '''66''' (18):5605-15
Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality. Description: Raffler, Johannes, et al. Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality. ''PLoS Genet''. 2015 Sep; '''11''' (9):e1005487
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Description: Law, Matthew H, et al. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. ''Nat Genet''. 2015 Sep; '''47''' (9):987-995
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy. Description: Leu, Costin, et al. Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy. ''EBioMedicine''. 2015 Sep; '''2''' (9):1063-70
Heritability of Individual Psychotic Experiences Captured by Common Genetic Variants in a Community Sample of Adolescents. Description: Sieradzka, Dominika, et al. Heritability of Individual Psychotic Experiences Captured by Common Genetic Variants in a Community Sample of Adolescents. ''Behav Genet''. 2015 Sep; '''45''' (5):493-502
Heritability of liver enzyme levels estimated from genome-wide SNP data. Description: van Beek, Jenny H D A, et al. Heritability of liver enzyme levels estimated from genome-wide SNP data. ''Eur J Hum Genet''. 2015 Sep; '''23''' (9):1223-8
Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset. Description: Minica, Camelia C, et al. Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset. ''Behav Genet''. 2015 Sep; '''45''' (5):503-13
Screening for UGT1A1 Genotype in Study A5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia. Description: Vardhanabhuti, Saran, et al. Screening for UGT1A1 Genotype in Study A5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia. ''Open Forum Infect Dis''. 2015 Sep; '''2''' (3):ofv085
The metabolomics of asthma control: a promising link between genetics and disease. Description: McGeachie, Michael J, et al. The metabolomics of asthma control: a promising link between genetics and disease. ''Immun Inflamm Dis''. 2015 Sep; '''3''' (3):224-38
Mutations in DCHS1 cause mitral valve prolapse. Description: Durst, Ronen, et al. Mutations in DCHS1 cause mitral valve prolapse. ''Nature''. 2015 Sep 3; '''525''' (7567):109-13
Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations. Description: Pengelly, Reuben J, et al. Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations. ''BMC Genomics''. 2015 Sep 3; '''16''': 666
Genome-wide insights into population structure and genetic history of Tunisian local cattle using the illumina bovinesnp50 beadchip. Description: Ben Jemaa, Slim, et al. Genome-wide insights into population structure and genetic history of Tunisian local cattle using the illumina bovinesnp50 beadchip. ''BMC Genomics''. 2015 Sep 4; '''16''': 677
Polymorphisms in MTHFD1 Gene and Susceptibility to Neural Tube Defects: A Case-Control Study in a Chinese Han Population with Relatively Low Folate Levels. Description: Wu, Jian, et al. Polymorphisms in MTHFD1 Gene and Susceptibility to Neural Tube Defects: A Case-Control Study in a Chinese Han Population with Relatively Low Folate Levels. ''Med Sci Monit''. 2015 Sep 4; '''21''': 2630-7
Variation at interleukin-6 receptor gene is associated to joint damage in rheumatoid arthritis. Description: Lopez-Lasanta, Maria, et al. Variation at interleukin-6 receptor gene is associated to joint damage in rheumatoid arthritis. ''Arthritis Res Ther''. 2015 Sep 4; '''17''': 242
A genome-wide association study of antidepressant response in Koreans. Description: Myung, W, et al. A genome-wide association study of antidepressant response in Koreans. ''Transl Psychiatry''. 2015 Sep 8; '''5''': e633
Canine MPV17 truncation without clinical manifestations. Description: Hanninen, Reetta L, et al. Canine MPV17 truncation without clinical manifestations. ''Biol Open''. 2015 Sep 9; '''4''' (10):1253-8
Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches. Description: Litchfield, Kevin, et al. Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches. ''Sci Rep''. 2015 Sep 9; '''5''': 13889
Genome-Wide SNP Analysis of Southern African Populations Provides New Insights into the Dispersal of Bantu-Speaking Groups. Description: Gonzalez-Santos, Miguel, et al. Genome-Wide SNP Analysis of Southern African Populations Provides New Insights into the Dispersal of Bantu-Speaking Groups. ''Genome Biol Evol''. 2015 Sep 11; '''7''' (9):2560-8
Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men. Description: Son, Ki Young, et al. Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men. ''Lipids Health Dis''. 2015 Sep 13; '''14''': 105
Genome-Wide Association Study of Ureide Concentration in Diverse Maturity Group IV Soybean [Glycine max (L.) Merr.] Accessions. Description: Ray, Jeffery D, et al. Genome-Wide Association Study of Ureide Concentration in Diverse Maturity Group IV Soybean [Glycine max (L.) Merr.] Accessions. ''G3 (Bethesda)''. 2015 Sep 14; '''5''' (11):2391-403
Association of Nicotinamide Phosphoribosyltransferase (NAMPT) Gene Polymorphisms and of Serum NAMPT Levels with Dilated Cardiomyopathy in a Chinese Population. Description: Dou, Qingyu, et al. Association of Nicotinamide Phosphoribosyltransferase (NAMPT) Gene Polymorphisms and of Serum NAMPT Levels with Dilated Cardiomyopathy in a Chinese Population. ''Int J Mol Sci''. 2015 Sep 15; '''16''' (9):22299-318
CPAG: software for leveraging pleiotropy in GWAS to reveal similarity between human traits links plasma fatty acids and intestinal inflammation. Description: Wang, Liuyang, et al. CPAG: software for leveraging pleiotropy in GWAS to reveal similarity between human traits links plasma fatty acids and intestinal inflammation. ''Genome Biol''. 2015 Sep 15; '''16''': 190
Host genetic variation impacts microbiome composition across human body sites. Description: Blekhman, Ran, et al. Host genetic variation impacts microbiome composition across human body sites. ''Genome Biol''. 2015 Sep 15; '''16''': 191
Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome. Description: Zilina, Olga, et al. Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome. ''BMC Genomics''. 2015 Sep 16; '''16''': 703
P16INK4a Upregulation Mediated by SIX6 Defines Retinal Ganglion Cell Pathogenesis in Glaucoma. Description: Skowronska-Krawczyk, Dorota, et al. P16INK4a Upregulation Mediated by SIX6 Defines Retinal Ganglion Cell Pathogenesis in Glaucoma. ''Mol Cell''. 2015 Sep 17; '''59''' (6):931-40
SeqMule: automated pipeline for analysis of human exome/genome sequencing data. Description: Guo, Yunfei, et al. SeqMule: automated pipeline for analysis of human exome/genome sequencing data. ''Sci Rep''. 2015 Sep 18; '''5''': 14283
A transposable element in a NAC gene is associated with drought tolerance in maize seedlings. Description: Mao, Hude, et al. A transposable element in a NAC gene is associated with drought tolerance in maize seedlings. ''Nat Commun''. 2015 Sep 21; '''6''': 8326
A genome-wide assessment of rare copy number variants in colorectal cancer. Description: Li, Zhenli, et al. A genome-wide assessment of rare copy number variants in colorectal cancer. ''Oncotarget''. 2015 Sep 22; '''6''' (28):26411-23
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls. Description: Zhu, Zezhang, et al. Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls. ''Nat Commun''. 2015 Sep 22; '''6''': 8355
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways. Description: Cordell, Heather J, et al. International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways. ''Nat Commun''. 2015 Sep 22; '''6''': 8019
Dissecting the genetic structure and admixture of four geographical Malay populations. Description: Deng, Lian, et al. Dissecting the genetic structure and admixture of four geographical Malay populations. ''Sci Rep''. 2015 Sep 23; '''5''': 14375
Leveraging existing data sets to generate new insights into Alzheimer's disease biology in specific patient subsets. Description: Fowler, Kevin D, et al. Leveraging existing data sets to generate new insights into Alzheimer's disease biology in specific patient subsets. ''Sci Rep''. 2015 Sep 23; '''5''': 14324
Tracking crop varieties using genotyping-by-sequencing markers: a case study using cassava (Manihot esculenta Crantz). Description: Rabbi, Ismail Y, et al. Tracking crop varieties using genotyping-by-sequencing markers: a case study using cassava (Manihot esculenta Crantz). ''BMC Genet''. 2015 Sep 23; '''16''': 115
Association of CELF2 polymorphism and the prognosis of nasopharyngeal carcinoma in southern Chinese population. Description: Guo, Yun-Miao, et al. Association of CELF2 polymorphism and the prognosis of nasopharyngeal carcinoma in southern Chinese population. ''Oncotarget''. 2015 Sep 29; '''6''' (29):27176-86
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia. Description: Ferrari, Raffaele, et al. A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia. ''Neurobiol Aging''. 2015 Oct; '''36''' (10):2904.e13-26
A New Method for Detecting Associations with Rare Copy-Number Variants. Description: Tzeng, Jung-Ying, et al. A New Method for Detecting Associations with Rare Copy-Number Variants. ''PLoS Genet''. 2015 Oct; '''11''' (10):e1005403
A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers. Description: Benton, Miles C, et al. A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers. ''PLoS Genet''. 2015 Oct; '''11''' (10):e1005593
Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals. Description: Fullerton, Janice M, et al. Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals. ''Am J Med Genet B Neuropsychiatr Genet''. 2015 Oct; '''168''' (7):617-29
CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma. Description: Dahlin, Anna M, et al. CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma. ''J Neurooncol''. 2015 Oct; '''125''' (1):75-8
Common variants in the ARC gene are not associated with cognitive abilities. Description: Myrum, Craig, et al. Common variants in the ARC gene are not associated with cognitive abilities. ''Brain Behav''. 2015 Oct; '''5''' (10):e00376
COMT gene locus: new functional variants. Description: Meloto, Carolina B, et al. COMT gene locus: new functional variants. ''Pain''. 2015 Oct; '''156''' (10):2072-83
Contrasting the Genetic Background of Type 1 Diabetes and Celiac Disease Autoimmunity. Description: Gutierrez-Achury, Javier, et al. Contrasting the Genetic Background of Type 1 Diabetes and Celiac Disease Autoimmunity. ''Diabetes Care''. 2015 Oct; '''38 Suppl 2''': S37-44
Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease. Description: Won, Hong-Hee, et al. Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease. ''PLoS Genet''. 2015 Oct; '''11''' (10):e1005622
Do personality traits moderate the manifestation of type 2 diabetes genetic risk? Description: Cukic, Iva, et al. Do personality traits moderate the manifestation of type 2 diabetes genetic risk? ''J Psychosom Res''. 2015 Oct; '''79''' (4):303-8
FASTKD2 is associated with memory and hippocampal structure in older adults. Description: Ramanan, V K, et al. FASTKD2 is associated with memory and hippocampal structure in older adults. ''Mol Psychiatry''. 2015 Oct; '''20''' (10):1197-204
Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients. Description: Lareau, Caleb A, et al. Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients. ''Ann Clin Transl Neurol''. 2015 Oct; '''2''' (10):972-7
Genetic association analyses highlight biological pathways underlying mitral valve prolapse. Description: Dina, Christian, et al. Genetic association analyses highlight biological pathways underlying mitral valve prolapse. ''Nat Genet''. 2015 Oct; '''47''' (10):1206-11
Genome-wide analyses suggest parallel selection for universal traits may eclipse local environmental selection in a highly mobile carnivore. Description: Stronen, Astrid Vik, et al. Genome-wide analyses suggest parallel selection for universal traits may eclipse local environmental selection in a highly mobile carnivore. ''Ecol Evol''. 2015 Oct; '''5''' (19):4410-25
Genome-wide analysis identifies a role for common copy number variants in specific language impairment. Description: Simpson, Nuala H, et al. Genome-wide analysis identifies a role for common copy number variants in specific language impairment. ''Eur J Hum Genet''. 2015 Oct; '''23''' (10):1370-7
Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci. Description: Stafford-Smith, Mark, et al. Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci. ''Kidney Int''. 2015 Oct; '''88''' (4):823-32
Homozygous loss-of-function variants in European cosmopolitan and isolate populations. Description: Kaiser, Vera B, et al. Homozygous loss-of-function variants in European cosmopolitan and isolate populations. ''Hum Mol Genet''. 2015 Oct 1; '''24''' (19):5464-74
Inherited mtDNA variations are not strong risk factors in human prion disease. Description: Hudson, Gavin, et al. Inherited mtDNA variations are not strong risk factors in human prion disease. ''Neurobiol Aging''. 2015 Oct; '''36''' (10):2908.e1-3
Lack of association of polymorphisms in six candidate genes in colombian adhd patients. Description: Fonseca, Dora J, et al. Lack of association of polymorphisms in six candidate genes in colombian adhd patients. ''Ann Neurosci''. 2015 Oct; '''22''' (4):217-21
Pharmacogenomic study in patients with multiple sclerosis: Responders and nonresponders to IFN-beta. Description: Bustamante, Marta F, et al. Pharmacogenomic study in patients with multiple sclerosis: Responders and nonresponders to IFN-beta. ''Neurol Neuroimmunol Neuroinflamm''. 2015 Oct; '''2''' (5):e154
PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus. Description: Bowes, John, et al. PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus. ''Ann Rheum Dis''. 2015 Oct; '''74''' (10):1882-5
The Genetic Architecture of Arsenic Metabolism Efficiency:A SNP-Based Heritability Study of Bangladeshi Adults. Description: Gao, Jianjun, et al. The Genetic Architecture of Arsenic Metabolism Efficiency:A SNP-Based Heritability Study of Bangladeshi Adults. ''Environ Health Perspect''. 2015 Oct; '''123''' (10):985-92
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Description: Winkler, Thomas W, et al. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. ''PLoS Genet''. 2015 Oct; '''11''' (10):e1005378
A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy. Description: Steffen, Frank, et al. A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy. ''G3 (Bethesda)''. 2015 Oct 4; '''5''' (12):2611-7
Angiogenesis related genes NOS3, CD14, MMP3 and IL4R are associated to VEGF gene expression and circulating levels in healthy adults. Description: Saleh, Abdelsalam, et al. Angiogenesis related genes NOS3, CD14, MMP3 and IL4R are associated to VEGF gene expression and circulating levels in healthy adults. ''BMC Med Genet''. 2015 Oct 5; '''16''': 90
Genome-wide association study dissects genetic architecture underlying longitudinal egg weights in chickens. Description: Yi, Guoqiang, et al. Genome-wide association study dissects genetic architecture underlying longitudinal egg weights in chickens. ''BMC Genomics''. 2015 Oct 5; '''16''': 746
The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape. Description: Busby, George B J, et al. The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape. ''Curr Biol''. 2015 Oct 5; '''25''' (19):2518-26
Quantitative trait locus analysis of parasite density reveals that HbS gene carriage protects severe malaria patients against Plasmodium falciparum hyperparasitaemia. Description: do Sambo, Maria Rosario, et al. Quantitative trait locus analysis of parasite density reveals that HbS gene carriage protects severe malaria patients against Plasmodium falciparum hyperparasitaemia. ''Malar J''. 2015 Oct 7; '''14''': 393
Runs of homozygosity reveal signatures of positive selection for reproduction traits in breed and non-breed horses. Description: Metzger, Julia, et al. Runs of homozygosity reveal signatures of positive selection for reproduction traits in breed and non-breed horses. ''BMC Genomics''. 2015 Oct 9; '''16''': 764
Association of GWAS-supported loci rs2107595 in HDAC9 gene with ischemic stroke in southern Han Chinese. Description: Su, Li, et al. Association of GWAS-supported loci rs2107595 in HDAC9 gene with ischemic stroke in southern Han Chinese. ''Gene''. 2015 Oct 10; '''570''' (2):282-7
Bayesian integration of genetics and epigenetics detects causal regulatory SNPs underlying expression variability. Description: Das, Avinash, et al. Bayesian integration of genetics and epigenetics detects causal regulatory SNPs underlying expression variability. ''Nat Commun''. 2015 Oct 12; '''6''': 8555
CA1 contributes to microcalcification and tumourigenesis in breast cancer. Description: Zheng, Yabing, et al. CA1 contributes to microcalcification and tumourigenesis in breast cancer. ''BMC Cancer''. 2015 Oct 12; '''15''': 679
Comparative genome-wide association studies of a depressive symptom phenotype in a repeated measures setting by race/ethnicity in the Multi-Ethnic Study of Atherosclerosis. Description: Ware, Erin B, et al. Comparative genome-wide association studies of a depressive symptom phenotype in a repeated measures setting by race/ethnicity in the Multi-Ethnic Study of Atherosclerosis. ''BMC Genet''. 2015 Oct 12; '''16''': 118
Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae. Description: Redmond, Seth N, et al. Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae. ''BMC Genomics''. 2015 Oct 13; '''16''': 779
Necdin is a breast cancer metastasis suppressor that regulates the transcription of c-Myc. Description: Lee, Minnkyong, et al. Necdin is a breast cancer metastasis suppressor that regulates the transcription of c-Myc. ''Oncotarget''. 2015 Oct 13; '''6''' (31):31557-68
Development of a SNP-based assay for measuring genetic diversity in the Tasmanian devil insurance population. Description: Wright, Belinda, et al. Development of a SNP-based assay for measuring genetic diversity in the Tasmanian devil insurance population. ''BMC Genomics''. 2015 Oct 14; '''16''': 791
The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A. Description: Vijayakrishnan, Jayaram, et al. The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A. ''Sci Rep''. 2015 Oct 14; '''5''': 15065
Genome-wide association study identifies SNPs in the MHC class II loci that are associated with self-reported history of whooping cough. Description: McMahon, George, et al. Genome-wide association study identifies SNPs in the MHC class II loci that are associated with self-reported history of whooping cough. ''Hum Mol Genet''. 2015 Oct 15; '''24''' (20):5930-9
Expanding the toolbox of ADHD genetics. How can we make sense of parent of origin effects in ADHD and related behavioral phenotypes? Description: Zayats, Tetyana, et al. Expanding the toolbox of ADHD genetics. How can we make sense of parent of origin effects in ADHD and related behavioral phenotypes? ''Behav Brain Funct''. 2015 Oct 16; '''11''' (1):33
Genome-wide association studies for feed intake and efficiency in two laying periods of chickens. Description: Yuan, Jingwei, et al. Genome-wide association studies for feed intake and efficiency in two laying periods of chickens. ''Genet Sel Evol''. 2015 Oct 16; '''47''': 82
Genomic inbreeding coefficients based on the distribution of the length of runs of homozygosity in a closed line of Iberian pigs. Description: Gomez-Raya, Luis, et al. Genomic inbreeding coefficients based on the distribution of the length of runs of homozygosity in a closed line of Iberian pigs. ''Genet Sel Evol''. 2015 Oct 16; '''47''': 81
MC1R diversity in Northern Island Melanesia has not been constrained by strong purifying selection and cannot explain pigmentation phenotype variation in the region. Description: Norton, Heather L, et al. MC1R diversity in Northern Island Melanesia has not been constrained by strong purifying selection and cannot explain pigmentation phenotype variation in the region. ''BMC Genet''. 2015 Oct 19; '''16''': 122
Genetic variants in the upstream region of activin receptor IIA are associated with female fertility in Japanese Black cattle. Description: Sasaki, Shinji, et al. Genetic variants in the upstream region of activin receptor IIA are associated with female fertility in Japanese Black cattle. ''BMC Genet''. 2015 Oct 20; '''16''': 123
Copy number variations in the genome of the Qatari population. Description: Fakhro, Khalid A, et al. Copy number variations in the genome of the Qatari population. ''BMC Genomics''. 2015 Oct 22; '''16''': 834
Early divergent strains of Yersinia pestis in Eurasia 5,000 years ago. Description: Rasmussen, Simon, et al. Early divergent strains of Yersinia pestis in Eurasia 5,000 years ago. ''Cell''. 2015 Oct 22; '''163''' (3):571-82
Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population. Description: Kimura, Hiroki, et al. Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population. ''Sci Rep''. 2015 Oct 23; '''5''': 15705
Genome-wide association analysis reveals loci associated with resistance against Piscirickettsia salmonis in two Atlantic salmon (Salmo salar L.) chromosomes. Description: Correa, Katharina, et al. Genome-wide association analysis reveals loci associated with resistance against Piscirickettsia salmonis in two Atlantic salmon (Salmo salar L.) chromosomes. ''BMC Genomics''. 2015 Oct 24; '''16''': 854
Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk. Description: Wang, Zhanwei, et al. Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk. ''Sci Rep''. 2015 Oct 26; '''5''': 15582
A functional variant in HOXA11-AS, a novel long non-coding RNA, inhibits the oncogenic phenotype of epithelial ovarian cancer. Description: Richards, Edward J, et al. A functional variant in HOXA11-AS, a novel long non-coding RNA, inhibits the oncogenic phenotype of epithelial ovarian cancer. ''Oncotarget''. 2015 Oct 27; '''6''' (33):34745-57
Identification of potential mutations and genomic alterations in the epithelial and spindle cell components of biphasic synovial sarcomas using a human exome SNP chip. Description: Qi, Yan, et al. Identification of potential mutations and genomic alterations in the epithelial and spindle cell components of biphasic synovial sarcomas using a human exome SNP chip. ''BMC Med Genomics''. 2015 Oct 27; '''8''': 69
Transcriptomic and genetic studies identify NFAT5 as a candidate gene for cocaine dependence. Description: Fernandez-Castillo, N, et al. Transcriptomic and genetic studies identify NFAT5 as a candidate gene for cocaine dependence. ''Transl Psychiatry''. 2015 Oct 27; '''5''': e667
Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese. Description: Gu, Zhuqin, et al. Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese. ''Sci Rep''. 2015 Oct 28; '''5''': 15891
Evaluation of regulatory genetic variants in POU5F1 and risk of congenital heart disease in Han Chinese. Description: Lin, Yuan, et al. Evaluation of regulatory genetic variants in POU5F1 and risk of congenital heart disease in Han Chinese. ''Sci Rep''. 2015 Oct 28; '''5''': 15860
A Genome-wide Scan for Selective Sweeps in Racing Horses. Description: Moon, Sunjin, et al. A Genome-wide Scan for Selective Sweeps in Racing Horses. ''Asian-Australas J Anim Sci''. 2015 Nov; '''28''' (11):1525-31
Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population. Description: Jimenez-Jimenez, Felix Javier, et al. Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population. ''Medicine (Baltimore)''. 2015 Nov; '''94''' (47):e2125
BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection Pressures. Description: Medina-Gomez, Carolina, et al. BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection Pressures. ''Mol Biol Evol''. 2015 Nov; '''32''' (11):2961-72
CD33 modulates TREM2: convergence of Alzheimer loci. Description: Chan, Gail, et al. CD33 modulates TREM2: convergence of Alzheimer loci. ''Nat Neurosci''. 2015 Nov; '''18''' (11):1556-8
Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data. Description: Saad, M, et al. Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data. ''Genes Brain Behav''. 2015 Nov; '''14''' (8):607-17
Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population. Description: Edelman, Deborah, et al. Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population. ''Mol Genet Genomic Med''. 2015 Nov; '''3''' (6):558-69
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers. Description: Sidore, Carlo, et al. Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers. ''Nat Genet''. 2015 Nov; '''47''' (11):1272-1281
Genome-wide Association Study (GWAS) and Its Application for Improving the Genomic Estimated Breeding Values (GEBV) of the Berkshire Pork Quality Traits. Description: Lee, Young-Sup, et al. Genome-wide Association Study (GWAS) and Its Application for Improving the Genomic Estimated Breeding Values (GEBV) of the Berkshire Pork Quality Traits. ''Asian-Australas J Anim Sci''. 2015 Nov; '''28''' (11):1551-7
Genome-Wide Association Study of Golden Retrievers Identifies Germ-Line Risk Factors Predisposing to Mast Cell Tumours. Description: Arendt, Maja L, et al. Genome-Wide Association Study of Golden Retrievers Identifies Germ-Line Risk Factors Predisposing to Mast Cell Tumours. ''PLoS Genet''. 2015 Nov; '''11''' (11):e1005647
Genome-wide Association Study to Identify Quantitative Trait Loci for Meat and Carcass Quality Traits in Berkshire. Description: Iqbal, Asif, et al. Genome-wide Association Study to Identify Quantitative Trait Loci for Meat and Carcass Quality Traits in Berkshire. ''Asian-Australas J Anim Sci''. 2015 Nov; '''28''' (11):1537-44
G-protein genomic association with normal variation in gray matter density. Description: Chen, Jiayu, et al. G-protein genomic association with normal variation in gray matter density. ''Hum Brain Mapp''. 2015 Nov; '''36''' (11):4272-86
Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Description: Kraus, William E, et al. Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. ''PLoS Genet''. 2015 Nov; '''11''' (11):e1005553
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates. Description: Guimier, Anne, et al. MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates. ''Nat Genet''. 2015 Nov; '''47''' (11):1260-3
Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event. Description: Poirier, Julia G, et al. Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event. ''Genet Epidemiol''. 2015 Nov; '''39''' (7):518-28
SCN9A Variants May be Implicated in Neuropathic Pain Associated With Diabetic Peripheral Neuropathy and Pain Severity. Description: Li, Qingqin S, et al. SCN9A Variants May be Implicated in Neuropathic Pain Associated With Diabetic Peripheral Neuropathy and Pain Severity. ''Clin J Pain''. 2015 Nov; '''31''' (11):976-82
Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma. Description: Becker, Jessica, et al. Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma. ''Cancer Med''. 2015 Nov; '''4''' (11):1700-4
The vgll3 Locus Controls Age at Maturity in Wild and Domesticated Atlantic Salmon (Salmo salar L.) Males. Description: Ayllon, Fernando, et al. The vgll3 Locus Controls Age at Maturity in Wild and Domesticated Atlantic Salmon (Salmo salar L.) Males. ''PLoS Genet''. 2015 Nov; '''11''' (11):e1005628
Whole-genome sequencing suggests a chemokine gene cluster that modifies age at onset in familial Alzheimer's disease. Description: Lalli, M A, et al. Whole-genome sequencing suggests a chemokine gene cluster that modifies age at onset in familial Alzheimer's disease. ''Mol Psychiatry''. 2015 Nov; '''20''' (11):1294-300
NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment. Description: Casey, Jillian P, et al. NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment. ''Sci Rep''. 2015 Nov 2; '''5''': 16022
Genomic population structure and prevalence of copy number variations in South African Nguni cattle. Description: Wang, Magretha Diane, et al. Genomic population structure and prevalence of copy number variations in South African Nguni cattle. ''BMC Genomics''. 2015 Nov 4; '''16''': 894
Genetic variations in STAT4,C2,HLA-DRB1 and HLA-DQ associated with risk of hepatitis B virus-related liver cirrhosis. Description: Jiang, De-Ke, et al. Genetic variations in STAT4,C2,HLA-DRB1 and HLA-DQ associated with risk of hepatitis B virus-related liver cirrhosis. ''Sci Rep''. 2015 Nov 5; '''5''': 16278
High-density P300 enhancers control cell state transitions. Description: Witte, Steven, et al. High-density P300 enhancers control cell state transitions. ''BMC Genomics''. 2015 Nov 6; '''16''': 903
Meta-analysis identifies seven susceptibility loci involved in the atopic march. Description: Marenholz, Ingo, et al. Meta-analysis identifies seven susceptibility loci involved in the atopic march. ''Nat Commun''. 2015 Nov 6; '''6''': 8804
Pachychoroid neovasculopathy and age-related macular degeneration. Description: Miyake, Masahiro, et al. Pachychoroid neovasculopathy and age-related macular degeneration. ''Sci Rep''. 2015 Nov 6; '''5''': 16204
Characterization of the biological processes shaping the genetic structure of the Italian population. Description: Parolo, Silvia, et al. Characterization of the biological processes shaping the genetic structure of the Italian population. ''BMC Genet''. 2015 Nov 9; '''16''': 132
Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism. Description: Maekawa, Motoko, et al. Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism. ''Sci Rep''. 2015 Nov 9; '''5''': 16239
Risk prediction for sporadic Alzheimer's disease using genetic risk score in the Han Chinese population. Description: Xiao, Qianyi, et al. Risk prediction for sporadic Alzheimer's disease using genetic risk score in the Han Chinese population. ''Oncotarget''. 2015 Nov 10; '''6''' (35):36955-64
The genomics of ecological vicariance in threespine stickleback fish. Description: Roesti, Marius, et al. The genomics of ecological vicariance in threespine stickleback fish. ''Nat Commun''. 2015 Nov 10; '''6''': 8767
Reassessing the Evolutionary History of the 17q21 Inversion Polymorphism. Description: Alves, Joao M, et al. Reassessing the Evolutionary History of the 17q21 Inversion Polymorphism. ''Genome Biol Evol''. 2015 Nov 11; '''7''' (12):3239-48
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease. Description: Luzon-Toro, Berta, et al. Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease. ''Sci Rep''. 2015 Nov 12; '''5''': 16473
Inbreeding and homozygosity in breast cancer survival. Description: Thomsen, Hauke, et al. Inbreeding and homozygosity in breast cancer survival. ''Sci Rep''. 2015 Nov 12; '''5''': 16467
The role of common genetic variation in educational attainment and income: evidence from the National Child Development Study. Description: Davies, Neil M, et al. The role of common genetic variation in educational attainment and income: evidence from the National Child Development Study. ''Sci Rep''. 2015 Nov 12; '''5''': 16509
Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility. Description: Guo, Ren Yu, et al. Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility. ''Med Sci Monit''. 2015 Nov 16; '''21''': 3536-9
Upper Palaeolithic genomes reveal deep roots of modern Eurasians. Description: Jones, Eppie R, et al. Upper Palaeolithic genomes reveal deep roots of modern Eurasians. ''Nat Commun''. 2015 Nov 16; '''6''': 8912
Genetic association analysis of miRNA SNPs implicates MIR145 in breast cancer susceptibility. Description: Chacon-Cortes, Diego, et al. Genetic association analysis of miRNA SNPs implicates MIR145 in breast cancer susceptibility. ''BMC Med Genet''. 2015 Nov 17; '''16''': 107
Multi-breed genome-wide association study reveals novel loci associated with the weight of internal organs. Description: He, Yuna, et al. Multi-breed genome-wide association study reveals novel loci associated with the weight of internal organs. ''Genet Sel Evol''. 2015 Nov 17; '''47''': 87
Genome wide association and genomic prediction for growth traits in juvenile farmed Atlantic salmon using a high density SNP array. Description: Tsai, Hsin-Yuan, et al. Genome wide association and genomic prediction for growth traits in juvenile farmed Atlantic salmon using a high density SNP array. ''BMC Genomics''. 2015 Nov 18; '''16''': 969
Collective effects of common SNPs in foraging decisions in Caenorhabditis elegans and an integrative method of identification of candidate genes. Description: Zhu, Zuobin, et al. Collective effects of common SNPs in foraging decisions in Caenorhabditis elegans and an integrative method of identification of candidate genes. ''Sci Rep''. 2015 Nov 19; '''5''': 16904
SNPTracker: A Swift Tool for Comprehensive Tracking and Unifying dbSNP rs IDs and Genomic Coordinates of Massive Sequence Variants. Description: Deng, Jia-En, et al. SNPTracker: A Swift Tool for Comprehensive Tracking and Unifying dbSNP rs IDs and Genomic Coordinates of Massive Sequence Variants. ''G3 (Bethesda)''. 2015 Nov 19; '''6''' (1):205-7
A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities, and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1). Description: Wiedmer, Michaela, et al. A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities, and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1). ''G3 (Bethesda)''. 2015 Nov 23; '''6''' (2):255-62
Genetic associations and shared environmental effects on the skin microbiome of Korean twins. Description: Si, Jiyeon, et al. Genetic associations and shared environmental effects on the skin microbiome of Korean twins. ''BMC Genomics''. 2015 Nov 23; '''16''': 992
Intrahaplotypic Variants Differentiate Complex Linkage Disequilibrium within Human MHC Haplotypes. Description: Lam, Tze Hau, et al. Intrahaplotypic Variants Differentiate Complex Linkage Disequilibrium within Human MHC Haplotypes. ''Sci Rep''. 2015 Nov 23; '''5''': 16972
Discovery of URAT1 SNPs and association between serum uric acid levels and URAT1. Description: Cho, Sung Kweon, et al. Discovery of URAT1 SNPs and association between serum uric acid levels and URAT1. ''BMJ Open''. 2015 Nov 24; '''5''' (11):e009360
Genome-wide association study identifies two new susceptibility loci for colorectal cancer at 5q23.3 and 17q12 in Han Chinese. Description: Jiang, Kewei, et al. Genome-wide association study identifies two new susceptibility loci for colorectal cancer at 5q23.3 and 17q12 in Han Chinese. ''Oncotarget''. 2015 Nov 24; '''6''' (37):40327-36
Genome-wide linkage disequilibrium and genetic diversity in five populations of Australian domestic sheep. Description: Al-Mamun, Hawlader Abdullah, et al. Genome-wide linkage disequilibrium and genetic diversity in five populations of Australian domestic sheep. ''Genet Sel Evol''. 2015 Nov 24; '''47''': 90
A Bayesian model for detection of high-order interactions among genetic variants in genome-wide association studies. Description: Wang, Juexin, et al. A Bayesian model for detection of high-order interactions among genetic variants in genome-wide association studies. ''BMC Genomics''. 2015 Nov 25; '''16''': 1011
Compatibility between mitochondrial and nuclear genomes correlates with the quantitative trait of lifespan in Caenorhabditis elegans. Description: Zhu, Zuobin, et al. Compatibility between mitochondrial and nuclear genomes correlates with the quantitative trait of lifespan in Caenorhabditis elegans. ''Sci Rep''. 2015 Nov 25; '''5''': 17303
Genome-wide association study and biological pathway analysis of the Eimeria maxima response in broilers. Description: Hamzic, Edin, et al. Genome-wide association study and biological pathway analysis of the Eimeria maxima response in broilers. ''Genet Sel Evol''. 2015 Nov 25; '''47''': 91
ORMDL3 contributes to the risk of atherosclerosis in Chinese Han population and mediates oxidized low-density lipoprotein-induced autophagy in endothelial cells. Description: Ma, Xiaochun, et al. ORMDL3 contributes to the risk of atherosclerosis in Chinese Han population and mediates oxidized low-density lipoprotein-induced autophagy in endothelial cells. ''Sci Rep''. 2015 Nov 25; '''5''': 17194
Extensive Admixture and Selective Pressure Across the Sahel Belt. Description: Triska, Petr, et al. Extensive Admixture and Selective Pressure Across the Sahel Belt. ''Genome Biol Evol''. 2015 Nov 26; '''7''' (12):3484-95
Genome-wide scan for selection signatures in six cattle breeds in South Africa. Description: Makina, Sithembile O, et al. Genome-wide scan for selection signatures in six cattle breeds in South Africa. ''Genet Sel Evol''. 2015 Nov 26; '''47''': 92
Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set. Description: Thibodeau, S N, et al. Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set. ''Nat Commun''. 2015 Nov 27; '''6''': 8653
PExFInS: An Integrative Post-GWAS Explorer for Functional Indels and SNPs. Description: Cheng, Zhongshan, et al. PExFInS: An Integrative Post-GWAS Explorer for Functional Indels and SNPs. ''Sci Rep''. 2015 Nov 27; '''5''': 17302
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study. Description: Roberts, Chrissy h, et al. Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study. ''Sci Rep''. 2015 Nov 30; '''5''': 17447
A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits. Description: Asimit, Jennifer L, et al. A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits. ''Genet Epidemiol''. 2015 Dec; '''39''' (8):624-34
Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes. Description: Stepniak, Beata, et al. Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes. ''EMBO Mol Med''. 2015 Dec; '''7''' (12):1565-79
A Common Genetic Origin for Early Farmers from Mediterranean Cardial and Central European LBK Cultures. Description: Olalde, Inigo, et al. A Common Genetic Origin for Early Farmers from Mediterranean Cardial and Central European LBK Cultures. ''Mol Biol Evol''. 2015 Dec; '''32''' (12):3132-42
A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease. Description: Kun-Rodrigues, Celia, et al. A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease. ''Hum Mol Genet''. 2015 Dec 1; '''24''' (23):6711-20
CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroids. Description: Dahlin, Amber, et al. CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroids. ''Immun Inflamm Dis''. 2015 Dec; '''3''' (4):350-9
Effects of APOE promoter polymorphism on the topological organization of brain structural connectome in nondemented elderly. Description: Shu, Ni, et al. Effects of APOE promoter polymorphism on the topological organization of brain structural connectome in nondemented elderly. ''Hum Brain Mapp''. 2015 Dec; '''36''' (12):4847-58
Epistasis analysis links immune cascades and cerebral amyloidosis. Description: Benedet, Andrea L, et al. Epistasis analysis links immune cascades and cerebral amyloidosis. ''J Neuroinflammation''. 2015 Dec 1; '''12''': 227
Genetic associations of leptin-related polymorphisms with systemic lupus erythematosus. Description: Zhao, Jian, et al. Genetic associations of leptin-related polymorphisms with systemic lupus erythematosus. ''Clin Immunol''. 2015 Dec; '''161''' (2):157-62
Genomic Insights into the Ancestry and Demographic History of South America. Description: Homburger, Julian R, et al. Genomic Insights into the Ancestry and Demographic History of South America. ''PLoS Genet''. 2015 Dec; '''11''' (12):e1005602
Heritability Estimated Using 50K SNPs Indicates Missing Heritability Problem in Holstein Breeding. Description: Shin, Donghyun, et al. Heritability Estimated Using 50K SNPs Indicates Missing Heritability Problem in Holstein Breeding. ''Genomics Inform''. 2015 Dec; '''13''' (4):146-51
Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1. Description: Coppieters, Frauke, et al. Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1. ''Hum Mutat''. 2015 Dec; '''36''' (12):1188-96
Longevity GWAS Using the Drosophila Genetic Reference Panel. Description: Ivanov, Dobril K, et al. Longevity GWAS Using the Drosophila Genetic Reference Panel. ''J Gerontol A Biol Sci Med Sci''. 2015 Dec; '''70''' (12):1470-8
O015. Evaluation of the genetic polymorphism of the alpha3 (CHRNA3) and alpha5 (CHRNA5) nicotinic receptor subunits, in patients with cluster headache. Description: Cainazzo, Maria Michela, et al. O015. Evaluation of the genetic polymorphism of the alpha3 (CHRNA3) and alpha5 (CHRNA5) nicotinic receptor subunits, in patients with cluster headache. ''J Headache Pain''. 2015 Dec; '''16''' (Suppl 1):A88
Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder. Description: Minelli, A, et al. Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder. ''Transl Psychiatry''. 2015 Dec 1; '''5''': e687
Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration. Description: Scheinfeldt, Laura B, et al. Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration. ''Am J Med Genet B Neuropsychiatr Genet''. 2015 Dec; '''168''' (8):697-705
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsy. Description: Schoeler, Natasha E, et al. Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsy. ''Epilepsy Res''. 2015 Dec; '''118''': 22-8
High level of inbreeding in final phase of 1000 Genomes Project. Description: Gazal, Steven, et al. High level of inbreeding in final phase of 1000 Genomes Project. ''Sci Rep''. 2015 Dec 2; '''5''': 17453
Quantifying the heritability of glioma using genome-wide complex trait analysis. Description: Kinnersley, Ben, et al. Quantifying the heritability of glioma using genome-wide complex trait analysis. ''Sci Rep''. 2015 Dec 2; '''5''': 17267
Serum bilirubin concentration is modified by UGT1A1 haplotypes and influences risk of type-2 diabetes in the Norfolk Island genetic isolate. Description: Benton, M C, et al. Serum bilirubin concentration is modified by UGT1A1 haplotypes and influences risk of type-2 diabetes in the Norfolk Island genetic isolate. ''BMC Genet''. 2015 Dec 2; '''16''': 136
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. Description: Lutz, Sharon M, et al. A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. ''BMC Genet''. 2015 Dec 3; '''16''': 138
DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression. Description: Wingo, Aliza P, et al. DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression. ''Nat Commun''. 2015 Dec 3; '''6''': 10106
Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosus. Description: Zhu, Zhengwei, et al. Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosus. ''Arthritis Res Ther''. 2015 Dec 3; '''17''': 349
Population Variation Reveals Independent Selection toward Small Body Size in Chinese Debao Pony. Description: Kader, Adiljan, et al. Population Variation Reveals Independent Selection toward Small Body Size in Chinese Debao Pony. ''Genome Biol Evol''. 2015 Dec 3; '''8''' (1):42-50
Association between genetic risk scoring for schizophrenia and bipolar disorder with regional subcortical volumes. Description: Caseras, X, et al. Association between genetic risk scoring for schizophrenia and bipolar disorder with regional subcortical volumes. ''Transl Psychiatry''. 2015 Dec 8; '''5''': e692
Two-stage comprehensive evaluation of genetic susceptibility of common variants in FBXO38, AP3B2 and WHAMM to severe chronic periodontitis. Description: Shang, Dong, et al. Two-stage comprehensive evaluation of genetic susceptibility of common variants in FBXO38, AP3B2 and WHAMM to severe chronic periodontitis. ''Sci Rep''. 2015 Dec 8; '''5''': 17882
Population genomics of pearl millet (Pennisetum glaucum (L.) R. Br.): Comparative analysis of global accessions and Senegalese landraces. Description: Hu, Zhenbin, et al. Population genomics of pearl millet (Pennisetum glaucum (L.) R. Br.): Comparative analysis of global accessions and Senegalese landraces. ''BMC Genomics''. 2015 Dec 9; '''16''': 1048
Genome-wide SNP analysis explains coral diversity and recovery in the Ryukyu Archipelago. Description: Shinzato, Chuya, et al. Genome-wide SNP analysis explains coral diversity and recovery in the Ryukyu Archipelago. ''Sci Rep''. 2015 Dec 10; '''5''': 18211
Genomic legacy of the African cheetah, Acinonyx jubatus. Description: Dobrynin, Pavel, et al. Genomic legacy of the African cheetah, Acinonyx jubatus. ''Genome Biol''. 2015 Dec 10; '''16''': 277
Genetic basis of maize kernel starch content revealed by high-density single nucleotide polymorphism markers in a recombinant inbred line population. Description: Wang, Tingting, et al. Genetic basis of maize kernel starch content revealed by high-density single nucleotide polymorphism markers in a recombinant inbred line population. ''BMC Plant Biol''. 2015 Dec 12; '''15''': 288
Discover hidden splicing variations by mapping personal transcriptomes to personal genomes. Description: Stein, Shayna, et al. Discover hidden splicing variations by mapping personal transcriptomes to personal genomes. ''Nucleic Acids Res''. 2015 Dec 15; '''43''' (22):10612-22
Increased co-expression of genes harboring the damaging de novo mutations in Chinese schizophrenic patients during prenatal development. Description: Wang, Qiang, et al. Increased co-expression of genes harboring the damaging de novo mutations in Chinese schizophrenic patients during prenatal development. ''Sci Rep''. 2015 Dec 15; '''5''': 18209
Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS. Description: Schrewe, L, et al. Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS. ''J Neuroinflammation''. 2015 Dec 16; '''12''': 234
Pathway-Based Genome-Wide Association Studies for Two Meat Production Traits in Simmental Cattle. Description: Fan, Huizhong, et al. Pathway-Based Genome-Wide Association Studies for Two Meat Production Traits in Simmental Cattle. ''Sci Rep''. 2015 Dec 17; '''5''': 18389
Methylation quantitative trait locus analysis of osteoarthritis links epigenetics with genetic risk. Description: Rushton, Michael D, et al. Methylation quantitative trait locus analysis of osteoarthritis links epigenetics with genetic risk. ''Hum Mol Genet''. 2015 Dec 20; '''24''' (25):7432-44
A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia. Description: Jorgenson, Eric, et al. A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia. ''Nat Commun''. 2015 Dec 21; '''6''': 10130
Genetic differences among ethnic groups. Description: Huang, Tao, et al. Genetic differences among ethnic groups. ''BMC Genomics''. 2015 Dec 21; '''16''': 1093
Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children. Description: Chang, Xiao, et al. Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children. ''Sci Rep''. 2015 Dec 21; '''5''': 18792
Identification of epistatic interactions through genome-wide association studies in sporadic medullary and juvenile papillary thyroid carcinomas. Description: Luzon-Toro, Berta, et al. Identification of epistatic interactions through genome-wide association studies in sporadic medullary and juvenile papillary thyroid carcinomas. ''BMC Med Genomics''. 2015 Dec 21; '''8''': 83
Gene map of large yellow croaker (Larimichthys crocea) provides insights into teleost genome evolution and conserved regions associated with growth. Description: Xiao, Shijun, et al. Gene map of large yellow croaker (Larimichthys crocea) provides insights into teleost genome evolution and conserved regions associated with growth. ''Sci Rep''. 2015 Dec 22; '''5''': 18661
Yak whole-genome resequencing reveals domestication signatures and prehistoric population expansions. Description: Qiu, Qiang, et al. Yak whole-genome resequencing reveals domestication signatures and prehistoric population expansions. ''Nat Commun''. 2015 Dec 22; '''6''': 10283
Association of ADIPOQ gene with type 2 diabetes and related phenotypes in African American men and women: the Jackson Heart Study. Description: Davis, Sharon K, et al. Association of ADIPOQ gene with type 2 diabetes and related phenotypes in African American men and women: the Jackson Heart Study. ''BMC Genet''. 2015 Dec 23; '''16''': 147
High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction. Description: McClay, Joseph L, et al. High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction. ''Genome Biol''. 2015 Dec 23; '''16''': 291
Genome-wide patterns of selection in 230 ancient Eurasians. Description: Mathieson, Iain, et al. Genome-wide patterns of selection in 230 ancient Eurasians. ''Nature''. 2015 Dec 24; '''528''' (7583):499-503
The Effects of Both Recent and Long-Term Selection and Genetic Drift Are Readily Evident in North American Barley Breeding Populations. Description: Poets, Ana M, et al. The Effects of Both Recent and Long-Term Selection and Genetic Drift Are Readily Evident in North American Barley Breeding Populations. ''G3 (Bethesda)''. 2015 Dec 29; '''6''' (3):609-22
A combined association test for rare variants using family and case-control data. Description: Lin, Peng-Lin, et al. A combined association test for rare variants using family and case-control data. ''BMC Proc''. 2016; '''10''' (Suppl 7):215-219
A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus. Description: Woo, Young Jae, et al. A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus. ''PLoS One''. 2016; '''11''' (6):e0158036
Additive Effects of the Risk Alleles of PNPLA3 and TM6SF2 on Non-alcoholic Fatty Liver Disease (NAFLD) in a Chinese Population. Description: Wang, Xiaoliang, et al. Additive Effects of the Risk Alleles of PNPLA3 and TM6SF2 on Non-alcoholic Fatty Liver Disease (NAFLD) in a Chinese Population. ''Front Genet''. 2016; '''7''': 140
A genetic assessment of the English bulldog. Description: Pedersen, Niels C, et al. A genetic assessment of the English bulldog. ''Canine Genet Epidemiol''. 2016; '''3''': 6
A Genome-Wide Association Study of Attention Function in a Population-Based Sample of Children. Description: Alemany, Silvia, et al. A Genome-Wide Association Study of Attention Function in a Population-Based Sample of Children. ''PLoS One''. 2016; '''11''' (9):e0163048
A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits. Description: Volkov, Petr, et al. A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits. ''PLoS One''. 2016; '''11''' (6):e0157776
A Genome-Wide SNP Linkage Analysis Suggests a Susceptibility Locus on 6p21 for Ankylosing Spondylitis and Inflammatory Back Pain Trait. Description: Zhang, Yanli, et al. A Genome-Wide SNP Linkage Analysis Suggests a Susceptibility Locus on 6p21 for Ankylosing Spondylitis and Inflammatory Back Pain Trait. ''PLoS One''. 2016; '''11''' (12):e0166888
A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci. Description: Low, Joyce Siew Yong, et al. A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci. ''PLoS One''. 2016; '''11''' (1):e0145774
A Genome-Wide Test of the Differential Susceptibility Hypothesis Reveals a Genetic Predictor of Differential Response to Psychological Treatments for Child Anxiety Disorders. Description: Keers, Robert, et al. A Genome-Wide Test of the Differential Susceptibility Hypothesis Reveals a Genetic Predictor of Differential Response to Psychological Treatments for Child Anxiety Disorders. ''Psychother Psychosom''. 2016; '''85''' (3):146-58
A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis. Description: Markowitz, Sanford D, et al. A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis. ''PLoS One''. 2016; '''11''' (1):e0146435
Analysis of binary responses with outcome-specific misclassification probability in genome-wide association studies. Description: Rekaya, Romdhane, et al. Analysis of binary responses with outcome-specific misclassification probability in genome-wide association studies. ''Appl Clin Genet''. 2016; '''9''': 169-177
Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations. Description: Sazzini, Marco, et al. Ancient pathogen-driven adaptation triggers increased susceptibility to non-celiac wheat sensitivity in present-day European populations. ''Genes Nutr''. 2016; '''11''': 15
A Novel Variant in CMAH Is Associated with Blood Type AB in Ragdoll Cats. Description: Gandolfi, Barbara, et al. A Novel Variant in CMAH Is Associated with Blood Type AB in Ragdoll Cats. ''PLoS One''. 2016; '''11''' (5):e0154973
A Parallel Population Genomic and Hydrodynamic Approach to Fishery Management of Highly-Dispersive Marine Invertebrates: The Case of the Fijian Black-Lip Pearl Oyster Pinctada margaritifera. Description: Lal, Monal M, et al. A Parallel Population Genomic and Hydrodynamic Approach to Fishery Management of Highly-Dispersive Marine Invertebrates: The Case of the Fijian Black-Lip Pearl Oyster Pinctada margaritifera. ''PLoS One''. 2016; '''11''' (8):e0161390
A Protein Domain and Family Based Approach to Rare Variant Association Analysis. Description: Richardson, Tom G, et al. A Protein Domain and Family Based Approach to Rare Variant Association Analysis. ''PLoS One''. 2016; '''11''' (4):e0153803
A rare nonsynonymous variant in the lipid metabolic gene HELZ2 related to primary biliary cirrhosis in Chinese Han. Description: Li, Ping, et al. A rare nonsynonymous variant in the lipid metabolic gene HELZ2 related to primary biliary cirrhosis in Chinese Han. ''Allergy Asthma Clin Immunol''. 2016; '''12''': 14
ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin-AVPR1A, AVPR1B, and OXTR. Description: Francis, Sunday M, et al. ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin-AVPR1A, AVPR1B, and OXTR. ''Front Neurosci''. 2016; '''10''': 516
Assessing transmission ratio distortion in extended families: a comparison of analysis methods. Description: Bhatnagar, Sahir R, et al. Assessing transmission ratio distortion in extended families: a comparison of analysis methods. ''BMC Proc''. 2016; '''10''' (Suppl 7):197-202
Association between RANK, RANKL and OPG polymorphisms with ACPA and erosions in rheumatoid arthritis: results from a meta-analysis involving three French cohorts. Description: Ruyssen-Witrand, Adeline, et al. Association between RANK, RANKL and OPG polymorphisms with ACPA and erosions in rheumatoid arthritis: results from a meta-analysis involving three French cohorts. ''RMD Open''. 2016; '''2''' (2):e000226
Association between Single Nucleotide Polymorphisms in Gamma-Aminobutyric Acid B Receptor, Insulin Receptor Substrate-1, and Hypocretin Neuropeptide Precursor Genes and Susceptibility to Obstructive Sleep Apnea Hypopnea Syndrome in a Chinese Han Popu... Description: Li, Zhijun, et al. Association between Single Nucleotide Polymorphisms in Gamma-Aminobutyric Acid B Receptor, Insulin Receptor Substrate-1, and Hypocretin Neuropeptide Precursor Genes and Susceptibility to Obstructive Sleep Apnea Hypopnea Syndrome in a Chinese Han Population. ''Med Princ Pract''. 2016; '''25''' (6):517-524
Association between UGT2B7 gene polymorphisms and fentanyl sensitivity in patients undergoing painful orthognathic surgery. Description: Muraoka, Wataru, et al. Association between UGT2B7 gene polymorphisms and fentanyl sensitivity in patients undergoing painful orthognathic surgery. ''Mol Pain''. 2016 Jan-Dec; '''12''': 1744806916683182
Association of common variants in MTAP with susceptibility and overall survival of osteosarcoma: a two-stage population-based study in Han Chinese. Description: Zhi, Liqiang, et al. Association of common variants in MTAP with susceptibility and overall survival of osteosarcoma: a two-stage population-based study in Han Chinese. ''J Cancer''. 2016; '''7''' (15):2179-2186
Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population. Description: Zhang, Yuping, et al. Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population. ''PLoS One''. 2016; '''11''' (4):e0153603
Association of Forced Vital Capacity with the Developmental Gene NCOR2. Description: Minelli, Cosetta, et al. Association of Forced Vital Capacity with the Developmental Gene NCOR2. ''PLoS One''. 2016; '''11''' (2):e0147388
Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma. Description: Chen, Xueli, et al. Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma. ''PLoS One''. 2016; '''11''' (6):e0157093
Association of Nuclear Factor-Erythroid 2-Related Factor 2, Thioredoxin Interacting Protein, and Heme Oxygenase-1 Gene Polymorphisms with Diabetes and Obesity in Mexican Patients. Description: Jimenez-Osorio, Angelica Sarai, et al. Association of Nuclear Factor-Erythroid 2-Related Factor 2, Thioredoxin Interacting Protein, and Heme Oxygenase-1 Gene Polymorphisms with Diabetes and Obesity in Mexican Patients. ''Oxid Med Cell Longev''. 2016; '''2016''': 7367641
Association of Polymorphisms in STRA6 and RARRES2 Genes with Type 2 Diabetes in Southern Han Chinese. Description: Huang, Han-Wei, et al. Association of Polymorphisms in STRA6 and RARRES2 Genes with Type 2 Diabetes in Southern Han Chinese. ''Biomed Res Int''. 2016; '''2016''': 6589793
Association of polymorphisms in the aldosterone-regulated sodium reabsorption pathway with blood pressure among Hispanics. Description: Tayo, Bamidele O, et al. Association of polymorphisms in the aldosterone-regulated sodium reabsorption pathway with blood pressure among Hispanics. ''BMC Proc''. 2016; '''10''' (Suppl 7):343-348
Associations between Polygenic Risk for Psychiatric Disorders and Substance Involvement. Description: Carey, Caitlin E, et al. Associations between Polygenic Risk for Psychiatric Disorders and Substance Involvement. ''Front Genet''. 2016; '''7''': 149
Associations of Toll-Like Receptor and beta-Defensin Polymorphisms with Measures of Periodontal Disease (PD) in HIV+ North American Adults: An Exploratory Study. Description: Mehlotra, Rajeev K, et al. Associations of Toll-Like Receptor and beta-Defensin Polymorphisms with Measures of Periodontal Disease (PD) in HIV+ North American Adults: An Exploratory Study. ''PLoS One''. 2016; '''11''' (10):e0164075
A Systems View of the Differences between APOE epsilon4 Carriers and Non-carriers in Alzheimer's Disease. Description: Jiang, Shan, et al. A Systems View of the Differences between APOE epsilon4 Carriers and Non-carriers in Alzheimer's Disease. ''Front Aging Neurosci''. 2016; '''8''': 171
Automated quality control for genome wide association studies. Description: Ellingson, Sally R, et al. Automated quality control for genome wide association studies. ''F1000Res''. 2016; '''5''': 1889
Biomass traits and candidate genes for bioenergy revealed through association genetics in coppiced European Populus nigra (L.). Description: Allwright, Mike Robert, et al. Biomass traits and candidate genes for bioenergy revealed through association genetics in coppiced European Populus nigra (L.). ''Biotechnol Biofuels''. 2016; '''9''' (1):195
Burden of genetic risk variants in multiple sclerosis families in the Netherlands. Description: Mescheriakova, Julia Y, et al. Burden of genetic risk variants in multiple sclerosis families in the Netherlands. ''Mult Scler J Exp Transl Clin''. 2016 Jan-Dec; '''2''': 2055217316648721
*c.84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.** Description: Ganesan, Mala, et al. c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians. ''PLoS One''. 2016; '''11''' (10):e0164151
Calcium Signaling Pathway Is Associated with the Long-Term Clinical Response to Selective Serotonin Reuptake Inhibitors (SSRI) and SSRI with Antipsychotics in Patients with Obsessive-Compulsive Disorder. Description: Umehara, Hidehiro, et al. Calcium Signaling Pathway Is Associated with the Long-Term Clinical Response to Selective Serotonin Reuptake Inhibitors (SSRI) and SSRI with Antipsychotics in Patients with Obsessive-Compulsive Disorder. ''PLoS One''. 2016; '''11''' (6):e0157232
Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2. Description: Henmyr, Viktor, et al. Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2. ''PLoS One''. 2016; '''11''' (6):e0158202
Circulating n-3 fatty acids and trans-fatty acids, PLA2G2A gene variation and sudden cardiac arrest. Description: Lemaitre, Rozenn N, et al. Circulating n-3 fatty acids and trans-fatty acids, PLA2G2A gene variation and sudden cardiac arrest. ''J Nutr Sci''. 2016; '''5''': e12
Common Genetic Variant in VIT Is Associated with Human Brain Asymmetry. Description: Tadayon, Sayed H, et al. Common Genetic Variant in VIT Is Associated with Human Brain Asymmetry. ''Front Hum Neurosci''. 2016; '''10''': 236
Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development. Description: Mueller, Kathryn L, et al. Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development. ''PLoS One''. 2016; '''11''' (4):e0152576
Common Variants in CLDN2 and MORC4 Genes Confer Disease Susceptibility in Patients with Chronic Pancreatitis. Description: Giri, Anil K, et al. Common Variants in CLDN2 and MORC4 Genes Confer Disease Susceptibility in Patients with Chronic Pancreatitis. ''PLoS One''. 2016; '''11''' (1):e0147345
Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population. Description: Zhang, Rongfeng, et al. Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population. ''PLoS One''. 2016; '''11''' (8):e0160467
Comparative Analysis of Genome Diversity in Bullmastiff Dogs. Description: Mortlock, Sally-Anne, et al. Comparative Analysis of Genome Diversity in Bullmastiff Dogs. ''PLoS One''. 2016; '''11''' (1):e0147941
Comparing Analytic Methods for Longitudinal GWAS and a Case-Study Evaluating Chemotherapy Course Length in Pediatric AML. A Report from the Children's Oncology Group. Description: Vujkovic, Marijana, et al. Comparing Analytic Methods for Longitudinal GWAS and a Case-Study Evaluating Chemotherapy Course Length in Pediatric AML. A Report from the Children's Oncology Group. ''Front Genet''. 2016; '''7''': 139
Creative Activities in Music--A Genome-Wide Linkage Analysis. Description: Oikkonen, Jaana, et al. Creative Activities in Music--A Genome-Wide Linkage Analysis. ''PLoS One''. 2016; '''11''' (2):e0148679
Deficiency of ATP6V1H Causes Bone Loss by Inhibiting Bone Resorption and Bone Formation through the TGF-beta1 Pathway. Description: Duan, Xiaohong, et al. Deficiency of ATP6V1H Causes Bone Loss by Inhibiting Bone Resorption and Bone Formation through the TGF-beta1 Pathway. ''Theranostics''. 2016; '''6''' (12):2183-2195
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. Description: Irum, Bushra, et al. Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. ''PLoS One''. 2016; '''11''' (12):e0167562
Deltex1 Polymorphisms Are Associated with Hepatitis B Vaccination Non-Response in Southwest China. Description: Xie, Bin, et al. Deltex1 Polymorphisms Are Associated with Hepatitis B Vaccination Non-Response in Southwest China. ''PLoS One''. 2016; '''11''' (2):e0149199
Differential effects of hydrocortisone, prednisone, and dexamethasone on hormonal and pharmacokinetic profiles: a pilot study in children with congenital adrenal hyperplasia. Description: Nebesio, Todd D, et al. Differential effects of hydrocortisone, prednisone, and dexamethasone on hormonal and pharmacokinetic profiles: a pilot study in children with congenital adrenal hyperplasia. ''Int J Pediatr Endocrinol''. 2016; '''2016''': 17
Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India. Description: Pranav Chand, Rayabarapu, et al. Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India. ''PLoS One''. 2016; '''11''' (6):e0153720
DNA methylation signature of human fetal alcohol spectrum disorder. Description: Portales-Casamar, Elodie, et al. DNA methylation signature of human fetal alcohol spectrum disorder. ''Epigenetics Chromatin''. 2016; '''9''': 25
Effects of Genetic Loci Associated with Central Obesity on Adipocyte Lipolysis. Description: Strawbridge, Rona J, et al. Effects of Genetic Loci Associated with Central Obesity on Adipocyte Lipolysis. ''PLoS One''. 2016; '''11''' (4):e0153990
Efficient genotype compression and analysis of large genetic-variation data sets. Description: Layer, Ryan M, et al. Efficient genotype compression and analysis of large genetic-variation data sets. ''Nat Methods''. 2016 Jan; '''13''' (1):63-5
Epigenome-wide association data implicates DNA methylation-mediated genetic risk in psoriasis. Description: Zhou, Fusheng, et al. Epigenome-wide association data implicates DNA methylation-mediated genetic risk in psoriasis. ''Clin Epigenetics''. 2016; '''8''': 131
Estimating relationships between phenotypes and subjects drawn from admixed families. Description: Blue, Elizabeth M, et al. Estimating relationships between phenotypes and subjects drawn from admixed families. ''BMC Proc''. 2016; '''10''' (Suppl 7):357-362
Evaluating pathogenic dementia variants in posterior cortical atrophy. Description: Carrasquillo, Minerva M, et al. Evaluating pathogenic dementia variants in posterior cortical atrophy. ''Neurobiol Aging''. 2016 Jan; '''37''': 38-44
Evaluation of genetic association of neurodevelopment and neuroimmunological genes with antipsychotic treatment response in schizophrenia in Indian populations. Description: Jajodia, Ajay, et al. Evaluation of genetic association of neurodevelopment and neuroimmunological genes with antipsychotic treatment response in schizophrenia in Indian populations. ''Mol Genet Genomic Med''. 2016 Jan; '''4''' (1):18-27
Evaluation of Linkage Disequilibrium Pattern and Association Study on Seed Oil Content in Brassica napus Using ddRAD Sequencing. Description: Wu, Zhikun, et al. Evaluation of Linkage Disequilibrium Pattern and Association Study on Seed Oil Content in Brassica napus Using ddRAD Sequencing. ''PLoS One''. 2016; '''11''' (1):e0146383
Evidence of Inbreeding in Hodgkin Lymphoma. Description: Thomsen, Hauke, et al. Evidence of Inbreeding in Hodgkin Lymphoma. ''PLoS One''. 2016; '''11''' (4):e0154259
Evidence of Polygenic Adaptation in the Systems Genetics of Anthropometric Traits. Description: Polimanti, Renato, et al. Evidence of Polygenic Adaptation in the Systems Genetics of Anthropometric Traits. ''PLoS One''. 2016; '''11''' (8):e0160654
Examination of previously identified associations within the Genetic Analysis Workshop 19 data. Description: Howey, Richard A J, et al. Examination of previously identified associations within the Genetic Analysis Workshop 19 data. ''BMC Proc''. 2016; '''10''' (Suppl 7):97-101
Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences. Description: Hill, W D, et al. Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences. ''Intelligence''. 2016 Jan-Feb; '''54''': 80-89
Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population. Description: de Kovel, Carolien G, et al. Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population. ''PLoS One''. 2016; '''11''' (2):e0146502
FCGR2C Polymorphisms Associated with HIV-1 Vaccine Protection Are Linked to Altered Gene Expression of Fc-gamma Receptors in Human B Cells. Description: Peng, Xinxia, et al. FCGR2C Polymorphisms Associated with HIV-1 Vaccine Protection Are Linked to Altered Gene Expression of Fc-gamma Receptors in Human B Cells. ''PLoS One''. 2016; '''11''' (3):e0152425
Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate. Description: Mitra, Amit K, et al. Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate. ''Front Genet''. 2016; '''7''': 88
Gender-Dependent Association of FTO Polymorphisms with Body Mass Index in Mexicans. Description: Saldana-Alvarez, Yolanda, et al. Gender-Dependent Association of FTO Polymorphisms with Body Mass Index in Mexicans. ''PLoS One''. 2016; '''11''' (1):e0145984
Genetic Analysis with the Immunochip Platform in Behcet Disease. Identification of Residues Associated in the HLA Class I Region and New Susceptibility Loci. Description: Ortiz-Fernandez, Lourdes, et al. Genetic Analysis with the Immunochip Platform in Behcet Disease. Identification of Residues Associated in the HLA Class I Region and New Susceptibility Loci. ''PLoS One''. 2016; '''11''' (8):e0161305
Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. Description: Peter, Beate, et al. Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. ''PLoS One''. 2016; '''11''' (4):e0153864
Genetic Diversity and Population Structure in South African, French and Argentinian Angora Goats from Genome-Wide SNP Data. Description: Visser, Carina, et al. Genetic Diversity and Population Structure in South African, French and Argentinian Angora Goats from Genome-Wide SNP Data. ''PLoS One''. 2016; '''11''' (5):e0154353
Genetic Evaluation of Schizophrenia Using the Illumina HumanExome Chip. Description: Moons, Tim, et al. Genetic Evaluation of Schizophrenia Using the Illumina HumanExome Chip. ''PLoS One''. 2016; '''11''' (3):e0150464
Genetic Loci and Novel Discrimination Measures Associated with Blood Pressure Variation in African Americans Living in Tallahassee. Description: Quinlan, Jacklyn, et al. Genetic Loci and Novel Discrimination Measures Associated with Blood Pressure Variation in African Americans Living in Tallahassee. ''PLoS One''. 2016; '''11''' (12):e0167700
Genetic polymorphisms that affect selenium status and response to selenium supplementation in United Kingdom pregnant women. Description: Mao, Jinyuan, et al. Genetic polymorphisms that affect selenium status and response to selenium supplementation in United Kingdom pregnant women. ''Am J Clin Nutr''. 2016 Jan; '''103''' (1):100-6
Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi Consortium. Description: Assimes, Themistocles L, et al. Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi Consortium. ''PLoS One''. 2016; '''11''' (3):e0138014
Genetic susceptibility to dyslipidemia and incidence of cardiovascular disease depending on a diet quality index in the Malmo Diet and Cancer cohort. Description: Hellstrand, Sophie, et al. Genetic susceptibility to dyslipidemia and incidence of cardiovascular disease depending on a diet quality index in the Malmo Diet and Cancer cohort. ''Genes Nutr''. 2016; '''11''': 20
Genetic Variants Associated with Colorectal Adenoma Susceptibility. Description: Abuli, Anna, et al. Genetic Variants Associated with Colorectal Adenoma Susceptibility. ''PLoS One''. 2016; '''11''' (4):e0153084
Genetic Variants in CHIA and CHI3L1 Are Associated with the IgE Response to the Ascaris Resistance Marker ABA-1 and the Birch Pollen Allergen Bet v 1. Description: Acevedo, Nathalie, et al. Genetic Variants in CHIA and CHI3L1 Are Associated with the IgE Response to the Ascaris Resistance Marker ABA-1 and the Birch Pollen Allergen Bet v 1. ''PLoS One''. 2016; '''11''' (12):e0167453
Genetic Variants of TPCN2 Associated with Type 2 Diabetes Risk in the Chinese Population. Description: Fan, Yujuan, et al. Genetic Variants of TPCN2 Associated with Type 2 Diabetes Risk in the Chinese Population. ''PLoS One''. 2016; '''11''' (2):e0149614
Genetic Variation in the IL-6 and HLA-DQB1 Genes Is Associated with Spontaneous Clearance of Hepatitis C Virus Infection. Description: Waldron, Paul Ravi, et al. Genetic Variation in the IL-6 and HLA-DQB1 Genes Is Associated with Spontaneous Clearance of Hepatitis C Virus Infection. ''J Immunol Res''. 2016; '''2016''': 6530436
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium. Description: Lei, Jieping, et al. Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium. ''Hum Genet''. 2016 Jan; '''135''' (1):137-54
Genetic variation in the insulin, insulin-like growth factor, growth hormone, and leptin pathways in relation to breast cancer in African-American women: the AMBER consortium. Description: Ruiz-Narvaez, Edward A, et al. Genetic variation in the insulin, insulin-like growth factor, growth hormone, and leptin pathways in relation to breast cancer in African-American women: the AMBER consortium. ''NPJ Breast Cancer''. 2016; '''2''':
Genetic Variation in the TAS2R38 Bitter Taste Receptor and Smoking Behaviors. Description: Risso, Davide S, et al. Genetic Variation in the TAS2R38 Bitter Taste Receptor and Smoking Behaviors. ''PLoS One''. 2016; '''11''' (10):e0164157
Genome-Wide Analysis Identifies IL-18 and FUCA2 as Novel Genes Associated with Diastolic Function in African Americans with Sickle Cell Disease. Description: Duarte, Julio D, et al. Genome-Wide Analysis Identifies IL-18 and FUCA2 as Novel Genes Associated with Diastolic Function in African Americans with Sickle Cell Disease. ''PLoS One''. 2016; '''11''' (9):e0163013
Genome-Wide Analysis of the Lysine Biosynthesis Pathway Network during Maize Seed Development. Description: Liu, Yuwei, et al. Genome-Wide Analysis of the Lysine Biosynthesis Pathway Network during Maize Seed Development. ''PLoS One''. 2016; '''11''' (2):e0148287
Genome-Wide Association of Heroin Dependence in Han Chinese. Description: Kalsi, Gursharan, et al. Genome-Wide Association of Heroin Dependence in Han Chinese. ''PLoS One''. 2016; '''11''' (12):e0167388
Genome-Wide Association Studies for Comb Traits in Chickens. Description: Shen, Manman, et al. Genome-Wide Association Studies for Comb Traits in Chickens. ''PLoS One''. 2016; '''11''' (7):e0159081
Genome Wide Association Studies (GWAS) Identify QTL on SSC2 and SSC17 Affecting Loin Peak Shear Force in Crossbred Commercial Pigs. Description: Zhang, Chunyan, et al. Genome Wide Association Studies (GWAS) Identify QTL on SSC2 and SSC17 Affecting Loin Peak Shear Force in Crossbred Commercial Pigs. ''PLoS One''. 2016; '''11''' (2):e0145082
Genome-Wide Association Study for Muscle Fat Content and Abdominal Fat Traits in Common Carp (Cyprinus carpio). Description: Zheng, Xianhu, et al. Genome-Wide Association Study for Muscle Fat Content and Abdominal Fat Traits in Common Carp (Cyprinus carpio). ''PLoS One''. 2016; '''11''' (12):e0169127
Genome-wide Association Study Identifies Loci for the Polled Phenotype in Yak. Description: Liang, Chunnian, et al. Genome-wide Association Study Identifies Loci for the Polled Phenotype in Yak. ''PLoS One''. 2016; '''11''' (7):e0158642
Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease. Description: Kuo, Ho-Chang, et al. Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease. ''PLoS One''. 2016; '''11''' (5):e0154943
Genome-Wide Association Study Identifies ZNF354C Variants Associated with Depression from Interferon-Based Therapy for Chronic Hepatitis C. Description: Matsunami, Kayoko, et al. Genome-Wide Association Study Identifies ZNF354C Variants Associated with Depression from Interferon-Based Therapy for Chronic Hepatitis C. ''PLoS One''. 2016; '''11''' (10):e0164418
Genome-Wide Association Study in Immunocompetent Patients with Delayed Hypersensitivity to Sulfonamide Antimicrobials. Description: Reinhart, Jennifer M, et al. Genome-Wide Association Study in Immunocompetent Patients with Delayed Hypersensitivity to Sulfonamide Antimicrobials. ''PLoS One''. 2016; '''11''' (6):e0156000
Genome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population. Description: Sano, Motoaki, et al. Genome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population. ''PLoS One''. 2016; '''11''' (5):e0155550
Genome-Wide Association Study of HIV Whole Genome Sequences Validated using Drug Resistance. Description: Power, Robert A, et al. Genome-Wide Association Study of HIV Whole Genome Sequences Validated using Drug Resistance. ''PLoS One''. 2016; '''11''' (9):e0163746
Genome Wide Association Study of Seedling and Adult Plant Leaf Rust Resistance in Elite Spring Wheat Breeding Lines. Description: Gao, Liangliang, et al. Genome Wide Association Study of Seedling and Adult Plant Leaf Rust Resistance in Elite Spring Wheat Breeding Lines. ''PLoS One''. 2016; '''11''' (2):e0148671
Genome-Wide Association Study Reveals the PLAG1 Gene for Knuckle, Biceps and Shank Weight in Simmental Beef Cattle. Description: Song, Yuxin, et al. Genome-Wide Association Study Reveals the PLAG1 Gene for Knuckle, Biceps and Shank Weight in Simmental Beef Cattle. ''PLoS One''. 2016; '''11''' (12):e0168316
Genome-Wide Association Study Singles Out SCD and LEPR as the Two Main Loci Influencing Intramuscular Fat Content and Fatty Acid Composition in Duroc Pigs. Description: Ros-Freixedes, Roger, et al. Genome-Wide Association Study Singles Out SCD and LEPR as the Two Main Loci Influencing Intramuscular Fat Content and Fatty Acid Composition in Duroc Pigs. ''PLoS One''. 2016; '''11''' (3):e0152496
Genome-Wide Detection of CNVs and Their Association with Meat Tenderness in Nelore Cattle. Description: Silva, Vinicius Henrique da, et al. Genome-Wide Detection of CNVs and Their Association with Meat Tenderness in Nelore Cattle. ''PLoS One''. 2016; '''11''' (6):e0157711
Genome-Wide Detection of Selective Signatures in Chicken through High Density SNPs. Description: Liu, Zhuang, et al. Genome-Wide Detection of Selective Signatures in Chicken through High Density SNPs. ''PLoS One''. 2016; '''11''' (11):e0166146
Genome-Wide Interaction with Insulin Secretion Loci Reveals Novel Loci for Type 2 Diabetes in African Americans. Description: Keaton, Jacob M, et al. Genome-Wide Interaction with Insulin Secretion Loci Reveals Novel Loci for Type 2 Diabetes in African Americans. ''PLoS One''. 2016; '''11''' (7):e0159977
Genome-Wide Meta-Analysis of Sciatica in Finnish Population. Description: Lemmela, Susanna, et al. Genome-Wide Meta-Analysis of Sciatica in Finnish Population. ''PLoS One''. 2016; '''11''' (10):e0163877
Genome-Wide Scans for Delineation of Candidate Genes Regulating Seed-Protein Content in Chickpea. Description: Upadhyaya, Hari D, et al. Genome-Wide Scans for Delineation of Candidate Genes Regulating Seed-Protein Content in Chickpea. ''Front Plant Sci''. 2016; '''7''': 302
Genomic ancestry as a predictor of haemodynamic profile in heart failure. Description: Bernardez-Pereira, Sabrina, et al. Genomic ancestry as a predictor of haemodynamic profile in heart failure. ''Open Heart''. 2016; '''3''' (2):e000434
Genomic and Metabolomic Profile Associated to Clustering of Cardio-Metabolic Risk Factors. Description: Marrachelli, Vannina G, et al. Genomic and Metabolomic Profile Associated to Clustering of Cardio-Metabolic Risk Factors. ''PLoS One''. 2016; '''11''' (9):e0160656
Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders. Description: Lee, Sol Moe, et al. Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders. ''PLoS One''. 2016; '''11''' (6):e0157540
Genomic Contributors to Rhythm Outcome of Atrial Fibrillation Catheter Ablation - Pathway Enrichment Analysis of GWAS Data. Description: Husser, Daniela, et al. Genomic Contributors to Rhythm Outcome of Atrial Fibrillation Catheter Ablation - Pathway Enrichment Analysis of GWAS Data. ''PLoS One''. 2016; '''11''' (11):e0167008
Genomic diversity and differentiation of a managed island wild boar population. Description: Iacolina, L, et al. Genomic diversity and differentiation of a managed island wild boar population. ''Heredity (Edinb)''. 2016 Jan; '''116''' (1):60-7
Genomic Inbreeding and Relatedness in Wild Panda Populations. Description: Garbe, John R, et al. Genomic Inbreeding and Relatedness in Wild Panda Populations. ''PLoS One''. 2016; '''11''' (8):e0160496
Germline TERT promoter mutations are rare in familial melanoma. Description: Harland, Mark, et al. Germline TERT promoter mutations are rare in familial melanoma. ''Fam Cancer''. 2016 Jan; '''15''' (1):139-44
Heterogenous Distribution of MTHFR Gene Variants among Mestizos and Diverse Amerindian Groups from Mexico. Description: Contreras-Cubas, Cecilia, et al. Heterogenous Distribution of MTHFR Gene Variants among Mestizos and Diverse Amerindian Groups from Mexico. ''PLoS One''. 2016; '''11''' (9):e0163248
Hypomethylation of FAM63B in bipolar disorder patients. Description: Starnawska, Anna, et al. Hypomethylation of FAM63B in bipolar disorder patients. ''Clin Epigenetics''. 2016; '''8''': 52
Identification of QTL on Chromosome 18 Associated with Non-Coagulating Milk in Swedish Red Cows. Description: Duchemin, Sandrine I, et al. Identification of QTL on Chromosome 18 Associated with Non-Coagulating Milk in Swedish Red Cows. ''Front Genet''. 2016; '''7''': 57
Identification of Susceptibility Genes of Adult Asthma in French Canadian Women. Description: Berube, Jean-Christophe, et al. Identification of Susceptibility Genes of Adult Asthma in French Canadian Women. ''Can Respir J''. 2016; '''2016''': 3564341
Identity-by-descent mapping for diastolic blood pressure in unrelated Mexican Americans. Description: Liu, Xiao-Qing, et al. Identity-by-descent mapping for diastolic blood pressure in unrelated Mexican Americans. ''BMC Proc''. 2016; '''10''' (Suppl 7):263-267
Imputing rare variants in families using a two-stage approach. Description: Lent, Samantha, et al. Imputing rare variants in families using a two-stage approach. ''BMC Proc''. 2016; '''10''' (Suppl 7):209-214
Incidence and Determinants of Ventilation Tubes in Denmark. Description: Pedersen, Tine Marie, et al. Incidence and Determinants of Ventilation Tubes in Denmark. ''PLoS One''. 2016; '''11''' (11):e0165657
Individual Differences in Scotopic Visual Acuity and Contrast Sensitivity: Genetic and Non-Genetic Influences. Description: Bartholomew, Alex J, et al. Individual Differences in Scotopic Visual Acuity and Contrast Sensitivity: Genetic and Non-Genetic Influences. ''PLoS One''. 2016; '''11''' (2):e0148192
In Search of the judische Typus: A Proposed Benchmark to Test the Genetic Basis of Jewishness Challenges Notions of "Jewish Biomarkers". Description: Elhaik, Eran. In Search of the judische Typus: A Proposed Benchmark to Test the Genetic Basis of Jewishness Challenges Notions of "Jewish Biomarkers". ''Front Genet''. 2016; '''7''': 141
Integrative genomics analyses unveil downstream biological effectors of disease-specific polymorphisms buried in intergenic regions. Description: Li, Haiquan, et al. Integrative genomics analyses unveil downstream biological effectors of disease-specific polymorphisms buried in intergenic regions. ''NPJ Genom Med''. 2016; '''1''':
Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot Study. Description: Trotta, Antonella, et al. Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot Study. ''PLoS One''. 2016; '''11''' (9):e0163319
Investigating the effects of copy number variants on reading and language performance. Description: Gialluisi, Alessandro, et al. Investigating the effects of copy number variants on reading and language performance. ''J Neurodev Disord''. 2016; '''8''': 17
Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Description: Padmanabhuni, Shanmukha S, et al. Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. ''Front Neurosci''. 2016; '''10''': 531
LDLR and PCSK9 Are Associated with the Presence of Antiphospholipid Antibodies and the Development of Thrombosis in aPLA Carriers. Description: Ochoa, Eguzkine, et al. LDLR and PCSK9 Are Associated with the Presence of Antiphospholipid Antibodies and the Development of Thrombosis in aPLA Carriers. ''PLoS One''. 2016; '''11''' (1):e0146990
Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS. Description: Wang, Yunpeng, et al. Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS. ''PLoS Genet''. 2016 Jan; '''12''' (1):e1005803
Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. Description: Bacelis, Jonas, et al. Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. ''PLoS One''. 2016; '''11''' (8):e0160335
Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin. Description: Galesloot, Tessel E, et al. Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin. ''PLoS One''. 2016; '''11''' (11):e0166628
MetaNetVar: Pipeline for applying network analysis tools for genomic variants analysis. Description: Moyer, Eric, et al. MetaNetVar: Pipeline for applying network analysis tools for genomic variants analysis. ''F1000Res''. 2016; '''5''': 674
Methylation quantitative trait loci within the TOMM20 gene are associated with metabolic syndrome-related lipid alterations in severely obese subjects. Description: de Toro-Martin, Juan, et al. Methylation quantitative trait loci within the TOMM20 gene are associated with metabolic syndrome-related lipid alterations in severely obese subjects. ''Diabetol Metab Syndr''. 2016; '''8''': 55
Missense Variant in MAPK Inactivator PTPN5 Is Associated with Decreased Severity of Post-Burn Hypertrophic Scarring. Description: Sood, Ravi F, et al. Missense Variant in MAPK Inactivator PTPN5 Is Associated with Decreased Severity of Post-Burn Hypertrophic Scarring. ''PLoS One''. 2016; '''11''' (2):e0149206
Multipoint association mapping for longitudinal family data: an application to hypertension phenotypes. Description: Chiu, Yen-Feng, et al. Multipoint association mapping for longitudinal family data: an application to hypertension phenotypes. ''BMC Proc''. 2016; '''10''' (Suppl 7):315-320
Multivariate Analysis of Anthropometric Traits Using Summary Statistics of Genome-Wide Association Studies from GIANT Consortium. Description: Park, Haeil, et al. Multivariate Analysis of Anthropometric Traits Using Summary Statistics of Genome-Wide Association Studies from GIANT Consortium. ''PLoS One''. 2016; '''11''' (10):e0163912
Multivariate Imaging Genetics Study of MRI Gray Matter Volume and SNPs Reveals Biological Pathways Correlated with Brain Structural Differences in Attention Deficit Hyperactivity Disorder. Description: Khadka, Sabin, et al. Multivariate Imaging Genetics Study of MRI Gray Matter Volume and SNPs Reveals Biological Pathways Correlated with Brain Structural Differences in Attention Deficit Hyperactivity Disorder. ''Front Psychiatry''. 2016; '''7''': 128
Multivariate Methods for Genetic Variants Selection and Risk Prediction in Cardiovascular Diseases. Description: Malovini, Alberto, et al. Multivariate Methods for Genetic Variants Selection and Risk Prediction in Cardiovascular Diseases. ''Front Cardiovasc Med''. 2016; '''3''': 17
Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts. Description: Irum, Bushra, et al. Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts. ''PLoS One''. 2016; '''11''' (11):e0162620
NABIC: A New Access Portal to Search, Visualize, and Share Agricultural Genomics Data. Description: Seol, Young-Joo, et al. NABIC: A New Access Portal to Search, Visualize, and Share Agricultural Genomics Data. ''Evol Bioinform Online''. 2016; '''12''': 51-8
NALP3-Inflammasome-Related Gene Polymorphisms in Patients with Prehypertension and Coronary Atherosclerosis. Description: Zhao, Xin, et al. NALP3-Inflammasome-Related Gene Polymorphisms in Patients with Prehypertension and Coronary Atherosclerosis. ''Biomed Res Int''. 2016; '''2016''': 7395627
Natural killer cells and single nucleotide polymorphisms of specific ion channels and receptor genes in myalgic encephalomyelitis/chronic fatigue syndrome. Description: Marshall-Gradisnik, Sonya, et al. Natural killer cells and single nucleotide polymorphisms of specific ion channels and receptor genes in myalgic encephalomyelitis/chronic fatigue syndrome. ''Appl Clin Genet''. 2016; '''9''': 39-47
North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene. Description: Bowne, Sara J, et al. North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene. ''Mol Vis''. 2016; '''22''': 1239-1247
Novel Graphical Analyses of Runs of Homozygosity among Species and Livestock Breeds. Description: Iacolina, Laura, et al. Novel Graphical Analyses of Runs of Homozygosity among Species and Livestock Breeds. ''Int J Genomics''. 2016; '''2016''': 2152847
Nucleotide Variants of the BH4 Biosynthesis Pathway Gene GCH1 and the Risk of Orofacial Clefts. Description: Hozyasz, Kamil K, et al. Nucleotide Variants of the BH4 Biosynthesis Pathway Gene GCH1 and the Risk of Orofacial Clefts. ''Mol Neurobiol''. 2016 Jan; '''53''' (1):769-776
PADI2 gene confers susceptibility to breast cancer and plays tumorigenic role via ACSL4, BINC3 and CA9 signaling. Description: Wang, Huifeng, et al. PADI2 gene confers susceptibility to breast cancer and plays tumorigenic role via ACSL4, BINC3 and CA9 signaling. ''Cancer Cell Int''. 2016; '''16''': 61
Pairwise Kinship Analysis by the Index of Chromosome Sharing Using High-Density Single Nucleotide Polymorphisms. Description: Morimoto, Chie, et al. Pairwise Kinship Analysis by the Index of Chromosome Sharing Using High-Density Single Nucleotide Polymorphisms. ''PLoS One''. 2016; '''11''' (7):e0160287
Parallel Evolution of Polydactyly Traits in Chinese and European Chickens. Description: Zhang, Zebin, et al. Parallel Evolution of Polydactyly Traits in Chinese and European Chickens. ''PLoS One''. 2016; '''11''' (2):e0149010
Pathway Analysis Incorporating Protein-Protein Interaction Networks Identified Candidate Pathways for the Seven Common Diseases. Description: Lin, Peng-Lin, et al. Pathway Analysis Incorporating Protein-Protein Interaction Networks Identified Candidate Pathways for the Seven Common Diseases. ''PLoS One''. 2016; '''11''' (9):e0162910
Phenome-Wide Association Study to Explore Relationships between Immune System Related Genetic Loci and Complex Traits and Diseases. Description: Verma, Anurag, et al. Phenome-Wide Association Study to Explore Relationships between Immune System Related Genetic Loci and Complex Traits and Diseases. ''PLoS One''. 2016; '''11''' (8):e0160573
PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism. Description: Giri, Anamika, et al. PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism. ''Tremor Other Hyperkinet Mov (N Y)''. 2016; '''6''': 363
Pleiotropic Genes Affecting Carcass Traits in Bos indicus (Nellore) Cattle Are Modulators of Growth. Description: G T Pereira, Anirene, et al. Pleiotropic Genes Affecting Carcass Traits in Bos indicus (Nellore) Cattle Are Modulators of Growth. ''PLoS One''. 2016; '''11''' (7):e0158165
Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. Description: He, Liang, et al. Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. ''Front Genet''. 2016; '''7''': 179
Polymorphisms of Insulin-Like Growth Factor 1 Pathway Genes and Breast Cancer Risk. Description: Shi, Joy, et al. Polymorphisms of Insulin-Like Growth Factor 1 Pathway Genes and Breast Cancer Risk. ''Front Oncol''. 2016; '''6''': 136
Polymorphisms of Vitamin D Signaling Pathway Genes and Calcium-Sensing Receptor Gene in respect to Survival of Hemodialysis Patients: A Prospective Observational Study. Description: Grzegorzewska, Alicja E, et al. Polymorphisms of Vitamin D Signaling Pathway Genes and Calcium-Sensing Receptor Gene in respect to Survival of Hemodialysis Patients: A Prospective Observational Study. ''Int J Endocrinol''. 2016; '''2016''': 2383216
QTL analysis of soft scald in two apple populations. Description: McClure, Kendra A, et al. QTL analysis of soft scald in two apple populations. ''Hortic Res''. 2016; '''3''': 16043
r2VIM: A new variable selection method for random forests in genome-wide association studies. Description: Szymczak, Silke, et al. r2VIM: A new variable selection method for random forests in genome-wide association studies. ''BioData Min''. 2016; '''9''': 7
Random Projection for Fast and Efficient Multivariate Correlation Analysis of High-Dimensional Data: A New Approach. Description: Grellmann, Claudia, et al. Random Projection for Fast and Efficient Multivariate Correlation Analysis of High-Dimensional Data: A New Approach. ''Front Genet''. 2016; '''7''': 102
Ranking factors involved in diabetes remission after bariatric surgery using machine-learning integrating clinical and genomic biomarkers. Description: Pedersen, Helle Krogh, et al. Ranking factors involved in diabetes remission after bariatric surgery using machine-learning integrating clinical and genomic biomarkers. ''NPJ Genom Med''. 2016; '''1''': 16035
Relation between Established Glioma Risk Variants and DNA Methylation in the Tumor. Description: Dahlin, Anna M, et al. Relation between Established Glioma Risk Variants and DNA Methylation in the Tumor. ''PLoS One''. 2016; '''11''' (10):e0163067
Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study. Description: Sohani, Zahra N, et al. Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study. ''PLoS One''. 2016; '''11''' (4):e0152107
Serological and Genetic Evidence for Altered Complement System Functionality in Systemic Lupus Erythematosus: Findings of the GAPAID Consortium. Description: Prechl, Jozsef, et al. Serological and Genetic Evidence for Altered Complement System Functionality in Systemic Lupus Erythematosus: Findings of the GAPAID Consortium. ''PLoS One''. 2016; '''11''' (3):e0150685
Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study. Description: Christensen, Carol H, et al. Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study. ''Front Oncol''. 2016; '''6''': 237
Significant association of GRM7 and GRM8 genes with schizophrenia and major depressive disorder in the Han Chinese population. Description: Li, Wenjin, et al. Significant association of GRM7 and GRM8 genes with schizophrenia and major depressive disorder in the Han Chinese population. ''Eur Neuropsychopharmacol''. 2016 Jan; '''26''' (1):136-146
Single Nucleotide Polymorphism Clustering in Systemic Autoimmune Diseases. Description: Charlon, Thomas, et al. Single Nucleotide Polymorphism Clustering in Systemic Autoimmune Diseases. ''PLoS One''. 2016; '''11''' (8):e0160270
Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis. Description: Gorski, Marcin M, et al. Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis. ''PLoS One''. 2016; '''11''' (3):e0151347
Surfactant Protein A and B Gene Polymorphisms and Risk of Respiratory Distress Syndrome in Late-Preterm Neonates. Description: Tsitoura, Maria-Eleni I, et al. Surfactant Protein A and B Gene Polymorphisms and Risk of Respiratory Distress Syndrome in Late-Preterm Neonates. ''PLoS One''. 2016; '''11''' (11):e0166516
Targeted genomic enrichment and sequencing of CyHV-3 from carp tissues confirms low nucleotide diversity and mixed genotype infections. Description: Hammoumi, Saliha, et al. Targeted genomic enrichment and sequencing of CyHV-3 from carp tissues confirms low nucleotide diversity and mixed genotype infections. ''PeerJ''. 2016; '''4''': e2516
The Adapting Mind in the Genomic Era. Description: Fieder, Martin, et al. The Adapting Mind in the Genomic Era. ''Front Psychol''. 2016; '''7''': 78
The Association of DRD2 with Insight Problem Solving. Description: Zhang, Shun, et al. The Association of DRD2 with Insight Problem Solving. ''Front Psychol''. 2016; '''7''': 1865
The Association of Mitofusion-2 Gene Polymorphisms with Susceptibility of Essential Hypertension in Northern Han Chinese Population. Description: Li, Mei, et al. The Association of Mitofusion-2 Gene Polymorphisms with Susceptibility of Essential Hypertension in Northern Han Chinese Population. ''Int J Med Sci''. 2016; '''13''' (1):39-47
The effect of the top 20 Alzheimer disease risk genes on gray-matter density and FDG PET brain metabolism. Description: Stage, Eddie, et al. The effect of the top 20 Alzheimer disease risk genes on gray-matter density and FDG PET brain metabolism. ''Alzheimers Dement (Amst)''. 2016; '''5''': 53-66
The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population. Description: Otowa, Takeshi, et al. The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population. ''PLoS One''. 2016; '''11''' (8):e0160823
The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry. Description: Waldman, Yedael Y, et al. The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry. ''PLoS One''. 2016; '''11''' (3):e0152056
The impact of IL-6 and IL-28B gene polymorphisms on treatment outcome of chronic hepatitis C infection among intravenous drug users in Croatia. Description: Bogdanovic, Zoran, et al. The impact of IL-6 and IL-28B gene polymorphisms on treatment outcome of chronic hepatitis C infection among intravenous drug users in Croatia. ''PeerJ''. 2016; '''4''': e2576
The Impact of Variable Degrees of Freedom and Scale Parameters in Bayesian Methods for Genomic Prediction in Chinese Simmental Beef Cattle. Description: Zhu, Bo, et al. The Impact of Variable Degrees of Freedom and Scale Parameters in Bayesian Methods for Genomic Prediction in Chinese Simmental Beef Cattle. ''PLoS One''. 2016; '''11''' (5):e0154118
The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration. Description: Farhan, Sali M K, et al. The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration. ''NPJ Genom Med''. 2016; '''1''': 16032
The polygenic risk for bipolar disorder influences brain regional function relating to visual and default state processing of emotional information. Description: Dima, Danai, et al. The polygenic risk for bipolar disorder influences brain regional function relating to visual and default state processing of emotional information. ''Neuroimage Clin''. 2016; '''12''': 838-844
The projack: a resampling approach to correct for ranking bias in high-throughput studies. Description: Zhou, Yi-Hui, et al. The projack: a resampling approach to correct for ranking bias in high-throughput studies. ''Biostatistics''. 2016 Jan; '''17''' (1):54-64
The Use of Genomics in Conservation Management of the Endangered Visayan Warty Pig (Sus cebifrons). Description: Nuijten, Rascha J M, et al. The Use of Genomics in Conservation Management of the Endangered Visayan Warty Pig (Sus cebifrons). ''Int J Genomics''. 2016; '''2016''': 5613862
Thrombosis Related ABO, F5, MTHFR, and FGG Gene Polymorphisms in Morbidly Obese Patients. Description: Kupcinskiene, Kristina, et al. Thrombosis Related ABO, F5, MTHFR, and FGG Gene Polymorphisms in Morbidly Obese Patients. ''Dis Markers''. 2016; '''2016''': 7853424
TLR1 Variant H305L Associated with Protection from Pulmonary Tuberculosis. Description: Meyer, Christian G, et al. TLR1 Variant H305L Associated with Protection from Pulmonary Tuberculosis. ''PLoS One''. 2016; '''11''' (5):e0156046
To Cheat or Not To Cheat: Tryptophan Hydroxylase 2 SNP Variants Contribute to Dishonest Behavior. Description: Shen, Qiang, et al. To Cheat or Not To Cheat: Tryptophan Hydroxylase 2 SNP Variants Contribute to Dishonest Behavior. ''Front Behav Neurosci''. 2016; '''10''': 82
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism. Description: Harley, Margaret E, et al. TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism. ''Nat Genet''. 2016 Jan; '''48''' (1):36-43
Type 2 Diabetes Risk Allele Loci in the Qatari Population. Description: O'Beirne, Sarah L, et al. Type 2 Diabetes Risk Allele Loci in the Qatari Population. ''PLoS One''. 2016; '''11''' (7):e0156834
Type I error rates of rare single nucleotide variants are inflated in tests of association with non-normally distributed traits using simple linear regression methods. Description: Schwantes-An, Tae-Hwi, et al. Type I error rates of rare single nucleotide variants are inflated in tests of association with non-normally distributed traits using simple linear regression methods. ''BMC Proc''. 2016; '''10''' (Suppl 7):385-388
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation. Description: Gazzellone, Matthew J, et al. Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation. ''J Neurodev Disord''. 2016; '''8''': 36
Using Incomplete Trios to Boost Confidence in Family Based Association Studies. Description: Dhankani, Varsha, et al. Using Incomplete Trios to Boost Confidence in Family Based Association Studies. ''Front Genet''. 2016; '''7''': 34
Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes. Description: Francis, Sunday M, et al. Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes. ''Front Neurosci''. 2016; '''10''': 195
Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression. Description: Davis, Albert A, et al. Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression. ''Neurobiol Aging''. 2016 Jan; '''37''': 209.e1-209.e7
Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent. Description: Chen, Fei, et al. Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent. ''Mol Vis''. 2016; '''22''': 783-96
Von Willebrand Factor Gene Variants Associate with Herpes simplex Encephalitis. Description: Abdelmagid, Nada, et al. Von Willebrand Factor Gene Variants Associate with Herpes simplex Encephalitis. ''PLoS One''. 2016; '''11''' (5):e0155832
Whole exome sequencing of extreme age-related macular degeneration phenotypes. Description: Sardell, Rebecca J, et al. Whole exome sequencing of extreme age-related macular degeneration phenotypes. ''Mol Vis''. 2016; '''22''': 1062-76
Whole-genome single-nucleotide polymorphism (SNP) marker discovery and association analysis with the eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) content in Larimichthys crocea. Description: Xiao, Shijun, et al. Whole-genome single-nucleotide polymorphism (SNP) marker discovery and association analysis with the eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) content in Larimichthys crocea. ''PeerJ''. 2016; '''4''': e2664
Common variations in TERT-CLPTM1L locus are reproducibly associated with the risk of nasopharyngeal carcinoma in Chinese populations. Description: Zhang, Yang, et al. Common variations in TERT-CLPTM1L locus are reproducibly associated with the risk of nasopharyngeal carcinoma in Chinese populations. ''Oncotarget''. 2016 Jan 5; '''7''' (1):759-70
A multi-factorial analysis of response to warfarin in a UK prospective cohort. Description: Bourgeois, Stephane, et al. A multi-factorial analysis of response to warfarin in a UK prospective cohort. ''Genome Med''. 2016 Jan 6; '''8''' (1):2
Heterogeneous alleles comprising G6PD deficiency trait in West Africa exert contrasting effects on two major clinical presentations of severe malaria. Description: Shah, Shivang S, et al. Heterogeneous alleles comprising G6PD deficiency trait in West Africa exert contrasting effects on two major clinical presentations of severe malaria. ''Malar J''. 2016 Jan 7; '''15''': 13
Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brain. Description: Chen, Li, et al. Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brain. ''Sci Rep''. 2016 Jan 8; '''6''': 19010
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study. Description: Cleynen, Isabelle, et al. Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study. ''Lancet''. 2016 Jan 9; '''387''' (10014):156-67
1,25D3 prevents CD8(+)Tc2 skewing and asthma development through VDR binding changes to the Cyp11a1 promoter. Description: Schedel, Michaela, et al. 1,25D3 prevents CD8(+)Tc2 skewing and asthma development through VDR binding changes to the Cyp11a1 promoter. ''Nat Commun''. 2016 Jan 11; '''7''': 10213
Characterizing redescriptions using persistent homology to isolate genetic pathways contributing to pathogenesis. Description: Platt, Daniel E, et al. Characterizing redescriptions using persistent homology to isolate genetic pathways contributing to pathogenesis. ''BMC Syst Biol''. 2016 Jan 11; '''10 Suppl 1''': 10
Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. Description: Traylor, Matthew, et al. Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. ''Neurology''. 2016 Jan 12; '''86''' (2):146-53
Identification and validation of risk loci for osteochondrosis in standardbreds. Description: McCoy, Annette M, et al. Identification and validation of risk loci for osteochondrosis in standardbreds. ''BMC Genomics''. 2016 Jan 12; '''17''': 41
Oxidative phosphorylation and lacunar stroke: Genome-wide enrichment analysis of common variants. Description: Traylor, Matthew, et al. Oxidative phosphorylation and lacunar stroke: Genome-wide enrichment analysis of common variants. ''Neurology''. 2016 Jan 12; '''86''' (2):141-5
Genetic affinities of the Jewish populations of India. Description: Chaubey, Gyaneshwer, et al. Genetic affinities of the Jewish populations of India. ''Sci Rep''. 2016 Jan 13; '''6''': 19166
Association of MMP-2 gene haplotypes with thoracic aortic dissection in chinese han population. Description: Liu, Ou, et al. Association of MMP-2 gene haplotypes with thoracic aortic dissection in chinese han population. ''BMC Cardiovasc Disord''. 2016 Jan 14; '''16''': 11
Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males. Description: Perry, John R B, et al. Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males. ''Hum Mol Genet''. 2016 Jan 15; '''25''' (2):382-8
A longitudinal genome-wide association study of anti-tumor necrosis factor response among Japanese patients with rheumatoid arthritis. Description: Honne, Kyoko, et al. A longitudinal genome-wide association study of anti-tumor necrosis factor response among Japanese patients with rheumatoid arthritis. ''Arthritis Res Ther''. 2016 Jan 18; '''18''': 12
A comparison of genomic profiles of complex diseases under different models. Description: Potenciano, Victor, et al. A comparison of genomic profiles of complex diseases under different models. ''BMC Med Genomics''. 2016 Jan 19; '''9''': 3
Genetic determination of height-mediated mate choice. Description: Tenesa, Albert, et al. Genetic determination of height-mediated mate choice. ''Genome Biol''. 2016 Jan 19; '''16''': 269
Genomic signals of migration and continuity in Britain before the Anglo-Saxons. Description: Martiniano, Rui, et al. Genomic signals of migration and continuity in Britain before the Anglo-Saxons. ''Nat Commun''. 2016 Jan 19; '''7''': 10326
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. Description: Below, Jennifer E, et al. Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. ''Sci Rep''. 2016 Jan 19; '''6''': 19429
Machine learning derived risk prediction of anorexia nervosa. Description: Guo, Yiran, et al. Machine learning derived risk prediction of anorexia nervosa. ''BMC Med Genomics''. 2016 Jan 20; '''9''': 4
Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome. Description: Billing-Ross, Paul, et al. Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome. ''J Transl Med''. 2016 Jan 20; '''14''': 19
A Nonsynonymous FCER1B SNP is Associated with Risk of Developing Allergic Rhinitis and with IgE Levels. Description: Amo, Gemma, et al. A Nonsynonymous FCER1B SNP is Associated with Risk of Developing Allergic Rhinitis and with IgE Levels. ''Sci Rep''. 2016 Jan 21; '''6''': 19724
Genetic architecture of fatty acid composition in the longissimus dorsi muscle revealed by genome-wide association studies on diverse pig populations. Description: Zhang, Wanchang, et al. Genetic architecture of fatty acid composition in the longissimus dorsi muscle revealed by genome-wide association studies on diverse pig populations. ''Genet Sel Evol''. 2016 Jan 21; '''48''': 5
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Description: Pattaro, Cristian, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. ''Nat Commun''. 2016 Jan 21; '''7''': 10023
Complex disease and phenotype mapping in the domestic dog. Description: Hayward, Jessica J, et al. Complex disease and phenotype mapping in the domestic dog. ''Nat Commun''. 2016 Jan 22; '''7''': 10460
Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations. Description: Cocca, Massimiliano, et al. Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations. ''J Transl Med''. 2016 Jan 22; '''14''': 22
A genome-wide association study identifies WT1 variant with better response to 5-fluorouracil, pirarubicin and cyclophosphamide neoadjuvant chemotherapy in breast cancer patients. Description: Wu, Lina, et al. A genome-wide association study identifies WT1 variant with better response to 5-fluorouracil, pirarubicin and cyclophosphamide neoadjuvant chemotherapy in breast cancer patients. ''Oncotarget''. 2016 Jan 26; '''7''' (4):5042-52
Application of linear mixed models to study genetic stability of height and body mass index across countries and time. Description: Trzaskowski, Maciej, et al. Application of linear mixed models to study genetic stability of height and body mass index across countries and time. ''Int J Epidemiol''. 2016 Jan 27;
Genetic determinants of pig birth weight variability. Description: Wang, Xuemin, et al. Genetic determinants of pig birth weight variability. ''BMC Genet''. 2016 Jan 27; '''17 Suppl 1''': 15
Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease. Description: Hartiala, Jaana A, et al. Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease. ''Nat Commun''. 2016 Jan 29; '''7''': 10558
A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. Description: Wakil, Salma M, et al. A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. ''Atherosclerosis''. 2016 Feb; '''245''': 62-70
Association of single nucleotide polymorphism rs2076185 in chromosome 6P24.1 with premature coronary artery diseases in Chinese Han population. Description: Liu, Xin, et al. Association of single nucleotide polymorphism rs2076185 in chromosome 6P24.1 with premature coronary artery diseases in Chinese Han population. ''J Geriatr Cardiol''. 2016 Feb; '''13''' (2):138-44
Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals. Description: Lancaster, Thomas M, et al. Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals. ''Hum Brain Mapp''. 2016 Feb; '''37''' (2):491-500
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. Description: Coleman, Ciara, et al. Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. ''Eur J Hum Genet''. 2016 Feb; '''24''' (2):291-7
Copy number variation associates with mortality in long-lived individuals: a genome-wide assessment. Description: Nygaard, Marianne, et al. Copy number variation associates with mortality in long-lived individuals: a genome-wide assessment. ''Aging Cell''. 2016 Feb; '''15''' (1):49-55
Effects of ambient and preceding temperatures and metabolic genes on flight metabolism in the Glanville fritillary butterfly. Description: Wong, Swee Chong, et al. Effects of ambient and preceding temperatures and metabolic genes on flight metabolism in the Glanville fritillary butterfly. ''J Insect Physiol''. 2016 Feb; '''85''': 23-31
Evaluation of pleiotropic effects among common genetic loci identified for cardio-metabolic traits in a Korean population. Description: Kim, Yun Kyoung, et al. Evaluation of pleiotropic effects among common genetic loci identified for cardio-metabolic traits in a Korean population. ''Cardiovasc Diabetol''. 2016 Feb 1; '''15''': 20
Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans. Description: David, Sean P, et al. Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans. ''EBioMedicine''. 2016 Feb; '''4''': 153-61
Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight. Description: Lee, Myoungsook, et al. Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight. ''Nutr Res Pract''. 2016 Feb; '''10''' (1):115-24
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. Description: Kilpelainen, Tuomas O, et al. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. ''Nat Commun''. 2016 Feb 1; '''7''': 10494
Genomics of Rapid Incipient Speciation in Sympatric Threespine Stickleback. Description: Marques, David A, et al. Genomics of Rapid Incipient Speciation in Sympatric Threespine Stickleback. ''PLoS Genet''. 2016 Feb; '''12''' (2):e1005887
Inverse relationship between a genetic risk score of 31 BMI loci and weight change before and after reaching middle age. Description: Rukh, G, et al. Inverse relationship between a genetic risk score of 31 BMI loci and weight change before and after reaching middle age. ''Int J Obes (Lond)''. 2016 Feb; '''40''' (2):252-9
Iterative Usage of Fixed and Random Effect Models for Powerful and Efficient Genome-Wide Association Studies. Description: Liu, Xiaolei, et al. Iterative Usage of Fixed and Random Effect Models for Powerful and Efficient Genome-Wide Association Studies. ''PLoS Genet''. 2016 Feb; '''12''' (2):e1005767
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. Description: Lu, Yingchang, et al. New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. ''Nat Commun''. 2016 Feb 1; '''7''': 10495
Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation. Description: Xia, Charley, et al. Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation. ''PLoS Genet''. 2016 Feb; '''12''' (2):e1005804
Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies. Description: Choi, Seung Hoan, et al. Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies. ''PLoS Genet''. 2016 Feb; '''12''' (2):e1005874
Whole-genome association analysis of treatment response in obsessive-compulsive disorder. Description: Qin, H, et al. Whole-genome association analysis of treatment response in obsessive-compulsive disorder. ''Mol Psychiatry''. 2016 Feb; '''21''' (2):270-6
Genetic variants near MLST8 and DHX57 affect the epigenetic age of the cerebellum. Description: Lu, Ake T, et al. Genetic variants near MLST8 and DHX57 affect the epigenetic age of the cerebellum. ''Nat Commun''. 2016 Feb 2; '''7''': 10561
Joint mouse-human phenome-wide association to test gene function and disease risk. Description: Wang, Xusheng, et al. Joint mouse-human phenome-wide association to test gene function and disease risk. ''Nat Commun''. 2016 Feb 2; '''7''': 10464
Polymorphisms in MIR137HG and microRNA-137-regulated genes influence gray matter structure in schizophrenia. Description: Wright, C, et al. Polymorphisms in MIR137HG and microRNA-137-regulated genes influence gray matter structure in schizophrenia. ''Transl Psychiatry''. 2016 Feb 2; '''6''': e724
Differential contribution of genomic regions to marked genetic variation and prediction of quantitative traits in broiler chickens. Description: Abdollahi-Arpanahi, Rostam, et al. Differential contribution of genomic regions to marked genetic variation and prediction of quantitative traits in broiler chickens. ''Genet Sel Evol''. 2016 Feb 3; '''48''': 10
A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density. Description: Tang, Ruqi, et al. A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density. ''Sci Rep''. 2016 Feb 4; '''6''': 19877
Genome-wide association and high-resolution phenotyping link Oryza sativa panicle traits to numerous trait-specific QTL clusters. Description: Crowell, Samuel, et al. Genome-wide association and high-resolution phenotyping link Oryza sativa panicle traits to numerous trait-specific QTL clusters. ''Nat Commun''. 2016 Feb 4; '''7''': 10527
Effects of Obesity Related Genetic Variations on Visceral and Subcutaneous Fat Distribution in a Chinese Population. Description: Wang, Tao, et al. Effects of Obesity Related Genetic Variations on Visceral and Subcutaneous Fat Distribution in a Chinese Population. ''Sci Rep''. 2016 Feb 5; '''6''': 20691
Genome-wide association reveals QTL for growth, bone and in vivo carcass traits as assessed by computed tomography in Scottish Blackface lambs. Description: Matika, Oswald, et al. Genome-wide association reveals QTL for growth, bone and in vivo carcass traits as assessed by computed tomography in Scottish Blackface lambs. ''Genet Sel Evol''. 2016 Feb 8; '''48''': 11
Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. Description: Zhang, Yong-Biao, et al. Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. ''Nat Commun''. 2016 Feb 8; '''7''': 10605
Development and application of a novel genome-wide SNP array reveals domestication history in soybean. Description: Wang, Jiao, et al. Development and application of a novel genome-wide SNP array reveals domestication history in soybean. ''Sci Rep''. 2016 Feb 9; '''6''': 20728
Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer. Description: French, Juliet D, et al. Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer. ''Oncotarget''. 2016 Feb 9; '''7''' (6):6353-68
Natural selection in a population of Drosophila melanogaster explained by changes in gene expression caused by sequence variation in core promoter regions. Description: Sato, Mitsuhiko P, et al. Natural selection in a population of Drosophila melanogaster explained by changes in gene expression caused by sequence variation in core promoter regions. ''BMC Evol Biol''. 2016 Feb 9; '''16''': 35
Obsessive-compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs. Description: den Braber, A, et al. Obsessive-compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs. ''Transl Psychiatry''. 2016 Feb 9; '''6''': e731
Genomic study of the Ket: a Paleo-Eskimo-related ethnic group with significant ancient North Eurasian ancestry. Description: Flegontov, Pavel, et al. Genomic study of the Ket: a Paleo-Eskimo-related ethnic group with significant ancient North Eurasian ancestry. ''Sci Rep''. 2016 Feb 11; '''6''': 20768
A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology. Description: Hungate, Eric A, et al. A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology. ''Nat Commun''. 2016 Feb 12; '''7''': 10635
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis. Description: Agundez, Jose A G, et al. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis. ''Sci Rep''. 2016 Feb 12; '''6''': 20830
MAPK1/ERK2 as novel target genes for pain in head and neck cancer patients. Description: Reyes-Gibby, Cielito C, et al. MAPK1/ERK2 as novel target genes for pain in head and neck cancer patients. ''BMC Genet''. 2016 Feb 13; '''17''': 40
Chronic gastroesophageal reflux disease shares genetic background with esophageal adenocarcinoma and Barrett's esophagus. Description: Gharahkhani, Puya, et al. Chronic gastroesophageal reflux disease shares genetic background with esophageal adenocarcinoma and Barrett's esophagus. ''Hum Mol Genet''. 2016 Feb 15; '''25''' (4):828-35
Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder. Description: Rucker, James J H, et al. Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder. ''Biol Psychiatry''. 2016 Feb 15; '''79''' (4):329-36
Associations of Plasma FGF2 Levels and Polymorphisms in the FGF2 Gene with Obesity Phenotypes in Han Chinese Population. Description: Hao, Ruo-Han, et al. Associations of Plasma FGF2 Levels and Polymorphisms in the FGF2 Gene with Obesity Phenotypes in Han Chinese Population. ''Sci Rep''. 2016 Feb 16; '''6''': 19868
Detecting signatures of positive selection associated with musical aptitude in the human genome. Description: Liu, Xuanyao, et al. Detecting signatures of positive selection associated with musical aptitude in the human genome. ''Sci Rep''. 2016 Feb 16; '''6''': 21198
FADS1-FADS2 gene cluster confers risk to polycystic ovary syndrome. Description: Tian, Ye, et al. FADS1-FADS2 gene cluster confers risk to polycystic ovary syndrome. ''Sci Rep''. 2016 Feb 16; '''6''': 21195
A genome-wide association study identifies a genomic region for the polycerate phenotype in sheep (Ovis aries). Description: Ren, Xue, et al. A genome-wide association study identifies a genomic region for the polycerate phenotype in sheep (Ovis aries). ''Sci Rep''. 2016 Feb 17; '''6''': 21111
Genetic predisposition to ductal carcinoma in situ of the breast. Description: Petridis, Christos, et al. Genetic predisposition to ductal carcinoma in situ of the breast. ''Breast Cancer Res''. 2016 Feb 17; '''18''' (1):22
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7. Description: Van Schil, Kristof, et al. Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7. ''Sci Rep''. 2016 Feb 18; '''6''': 21307
Genome-wide data reveal cryptic diversity and genetic introgression in an Oriental cynopterine fruit bat radiation. Description: Chattopadhyay, Balaji, et al. Genome-wide data reveal cryptic diversity and genetic introgression in an Oriental cynopterine fruit bat radiation. ''BMC Evol Biol''. 2016 Feb 18; '''16''': 41
Genome-wide association mapping of partial resistance to Aphanomyces euteiches in pea. Description: Desgroux, Aurore, et al. Genome-wide association mapping of partial resistance to Aphanomyces euteiches in pea. ''BMC Genomics''. 2016 Feb 20; '''17''': 124
Antipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes. Description: Stevenson, J M, et al. Antipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes. ''Transl Psychiatry''. 2016 Feb 23; '''6''': e739
Genome Resequencing Identifies Unique Adaptations of Tibetan Chickens to Hypoxia and High-Dose Ultraviolet Radiation in High-Altitude Environments. Description: Zhang, Qian, et al. Genome Resequencing Identifies Unique Adaptations of Tibetan Chickens to Hypoxia and High-Dose Ultraviolet Radiation in High-Altitude Environments. ''Genome Biol Evol''. 2016 Feb 23; '''8''' (3):765-76
Genome wide association study of uric acid in Indian population and interaction of identified variants with Type 2 diabetes. Description: Giri, Anil K, et al. Genome wide association study of uric acid in Indian population and interaction of identified variants with Type 2 diabetes. ''Sci Rep''. 2016 Feb 23; '''6''': 21440
A common functional variant on the pro-inflammatory Interleukin-6 gene may modify the association between long-term PM10 exposure and diabetes. Description: Eze, Ikenna C, et al. A common functional variant on the pro-inflammatory Interleukin-6 gene may modify the association between long-term PM10 exposure and diabetes. ''Environ Health''. 2016 Feb 24; '''15''': 39
Genetic diversity, linkage disequilibrium, population structure and construction of a core collection of Prunus avium L. landraces and bred cultivars. Description: Campoy, Jose Antonio, et al. Genetic diversity, linkage disequilibrium, population structure and construction of a core collection of Prunus avium L. landraces and bred cultivars. ''BMC Plant Biol''. 2016 Feb 24; '''16''': 49
Assessing the Causality between Blood Pressure and Retinal Vascular Caliber through Mendelian Randomisation. Description: Li, Ling-Jun, et al. Assessing the Causality between Blood Pressure and Retinal Vascular Caliber through Mendelian Randomisation. ''Sci Rep''. 2016 Feb 25; '''6''': 22031
Chlamydia trachomatis from Australian Aboriginal people with trachoma are polyphyletic composed of multiple distinctive lineages. Description: Andersson, Patiyan, et al. Chlamydia trachomatis from Australian Aboriginal people with trachoma are polyphyletic composed of multiple distinctive lineages. ''Nat Commun''. 2016 Feb 25; '''7''': 10688
Novel loci and pathways significantly associated with longevity. Description: Zeng, Yi, et al. Novel loci and pathways significantly associated with longevity. ''Sci Rep''. 2016 Feb 25; '''6''': 21243
Exploiting biological priors and sequence variants enhances QTL discovery and genomic prediction of complex traits. Description: MacLeod, I M, et al. Exploiting biological priors and sequence variants enhances QTL discovery and genomic prediction of complex traits. ''BMC Genomics''. 2016 Feb 27; '''17''': 144
A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Description: Adhikari, Kaustubh, et al. A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. ''Nat Commun''. 2016 Mar 1; '''7''': 10815
Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease Subtype. Description: Rutten-Jacobs, Loes C A, et al. Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease Subtype. ''Stroke''. 2016 Mar; '''47''' (3):646-51
Association of rs17042171 with chromosome 4q25 with atrial fibrillation in Chinese Han populations. Description: Zhao, Liyan, et al. Association of rs17042171 with chromosome 4q25 with atrial fibrillation in Chinese Han populations. ''Anatol J Cardiol''. 2016 Mar; '''16''' (3):165-9
*Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB115:01 Status.** Description: Binder, Michele D, et al. Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status. ''PLoS Genet''. 2016 Mar; '''12''' (3):e1005853
Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1. Description: Choquet, Helene, et al. Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1. ''Free Radic Biol Med''. 2016 Mar; '''92''': 100-109
Distinct effects of folate pathway genes MTHFR and MTHFD1L on ruminative response style: a potential risk mechanism for depression. Description: Eszlari, N, et al. Distinct effects of folate pathway genes MTHFR and MTHFD1L on ruminative response style: a potential risk mechanism for depression. ''Transl Psychiatry''. 2016 Mar 1; '''6''': e745
Exome arrays capture polygenic rare variant contributions to schizophrenia. Description: Richards, A L, et al. Exome arrays capture polygenic rare variant contributions to schizophrenia. ''Hum Mol Genet''. 2016 Mar 1; '''25''' (5):1001-7
Gene signatures of postoperative atrial fibrillation in atrial tissue after coronary artery bypass grafting surgery in patients receiving beta-blockers. Description: Kertai, Miklos D, et al. Gene signatures of postoperative atrial fibrillation in atrial tissue after coronary artery bypass grafting surgery in patients receiving beta-blockers. ''J Mol Cell Cardiol''. 2016 Mar; '''92''': 109-15
Genetic link between family socioeconomic status and children's educational achievement estimated from genome-wide SNPs. Description: Krapohl, E, et al. Genetic link between family socioeconomic status and children's educational achievement estimated from genome-wide SNPs. ''Mol Psychiatry''. 2016 Mar; '''21''' (3):437-43
Genetic loci for serum lipid fractions and intracerebral hemorrhage. Description: Akoudad, Saloua, et al. Genetic loci for serum lipid fractions and intracerebral hemorrhage. ''Atherosclerosis''. 2016 Mar; '''246''': 287-92
Genome-wide association study of 8 carcass traits in Jinghai Yellow chickens using specific-locus amplified fragment sequencing technology. Description: Wang, Wenhao, et al. Genome-wide association study of 8 carcass traits in Jinghai Yellow chickens using specific-locus amplified fragment sequencing technology. ''Poult Sci''. 2016 Mar; '''95''' (3):500-6
Genome-Wide Pharmacogenomic Study on Methadone Maintenance Treatment Identifies SNP rs17180299 and Multiple Haplotypes on CYP2B6, SPON1, and GSG1L Associated with Plasma Concentrations of Methadone R- and S-enantiomers in Heroin-Dependent Patients. Description: Yang, Hsin-Chou, et al. Genome-Wide Pharmacogenomic Study on Methadone Maintenance Treatment Identifies SNP rs17180299 and Multiple Haplotypes on CYP2B6, SPON1, and GSG1L Associated with Plasma Concentrations of Methadone R- and S-enantiomers in Heroin-Dependent Patients. ''PLoS Genet''. 2016 Mar; '''12''' (3):e1005910
Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction. Description: Chen, Shanshan, et al. Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction. ''Atherosclerosis''. 2016 Mar; '''246''': 148-156
Genomic variation in recently collected maize landraces from Mexico. Description: Arteaga, Maria Clara, et al. Genomic variation in recently collected maize landraces from Mexico. ''Genom Data''. 2016 Mar; '''7''': 38-45
High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry. Description: Sun, Celi, et al. High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry. ''Nat Genet''. 2016 Mar; '''48''' (3):323-30
HLA class II sequence variants influence tuberculosis risk in populations of European ancestry. Description: Sveinbjornsson, Gardar, et al. HLA class II sequence variants influence tuberculosis risk in populations of European ancestry. ''Nat Genet''. 2016 Mar; '''48''' (3):318-22
Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants. Description: Pilling, Luke C, et al. Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants. ''Aging (Albany NY)''. 2016 Mar; '''8''' (3):547-60
IL18 Gene Variants Influence the Susceptibility to Chagas Disease. Description: Leon Rodriguez, Daniel A, et al. IL18 Gene Variants Influence the Susceptibility to Chagas Disease. ''PLoS Negl Trop Dis''. 2016 Mar; '''10''' (3):e0004583
Innate biology versus lifestyle behaviour in the aetiology of obesity and type 2 diabetes: the GLACIER Study. Description: Poveda, Alaitz, et al. Innate biology versus lifestyle behaviour in the aetiology of obesity and type 2 diabetes: the GLACIER Study. ''Diabetologia''. 2016 Mar; '''59''' (3):462-71
Insight into Genotype-Phenotype Associations through eQTL Mapping in Multiple Cell Types in Health and Immune-Mediated Disease. Description: Peters, James E, et al. Insight into Genotype-Phenotype Associations through eQTL Mapping in Multiple Cell Types in Health and Immune-Mediated Disease. ''PLoS Genet''. 2016 Mar; '''12''' (3):e1005908
Meta analysis identifies a novel susceptibility locus associated with heel bone strength in the Korean population. Description: Hwang, Joo-Yeon, et al. Meta analysis identifies a novel susceptibility locus associated with heel bone strength in the Korean population. ''Bone''. 2016 Mar; '''84''': 47-51
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Description: van den Berg, Stephanie M, et al. Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. ''Behav Genet''. 2016 Mar; '''46''' (2):170-82
Natural Selection and Recombination Rate Variation Shape Nucleotide Polymorphism Across the Genomes of Three Related Populus Species. Description: Wang, Jing, et al. Natural Selection and Recombination Rate Variation Shape Nucleotide Polymorphism Across the Genomes of Three Related Populus Species. ''Genetics''. 2016 Mar; '''202''' (3):1185-200
Polygenic interactions with environmental adversity in the aetiology of major depressive disorder. Description: Mullins, N, et al. Polygenic interactions with environmental adversity in the aetiology of major depressive disorder. ''Psychol Med''. 2016 Mar; '''46''' (4):759-70
Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort. Description: Clarke, Toni-Kim, et al. Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort. ''Addict Biol''. 2016 Mar; '''21''' (2):469-80
Population structure and genome characterization of local pig breeds in Russia, Belorussia, Kazakhstan and Ukraine. Description: Traspov, Aleksei, et al. Population structure and genome characterization of local pig breeds in Russia, Belorussia, Kazakhstan and Ukraine. ''Genet Sel Evol''. 2016 Mar 1; '''48''': 16
Resolving the ancestry of Austronesian-speaking populations. Description: Soares, Pedro A, et al. Resolving the ancestry of Austronesian-speaking populations. ''Hum Genet''. 2016 Mar; '''135''' (3):309-26
Significant impact of miRNA-target gene networks on genetics of human complex traits. Description: Okada, Yukinori, et al. Significant impact of miRNA-target gene networks on genetics of human complex traits. ''Sci Rep''. 2016 Mar 1; '''6''': 22223
Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes. Description: Ge, Yan, et al. Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes. ''Diabetes''. 2016 Mar; '''65''' (3):794-802
GWASeq: targeted re-sequencing follow up to GWAS. Description: Salomon, Matthew P, et al. GWASeq: targeted re-sequencing follow up to GWAS. ''BMC Genomics''. 2016 Mar 3; '''17''': 176
A genome-wide association study for genetic susceptibility to Mycobacterium bovis infection in dairy cattle identifies a susceptibility QTL on chromosome 23. Description: Richardson, Ian W, et al. A genome-wide association study for genetic susceptibility to Mycobacterium bovis infection in dairy cattle identifies a susceptibility QTL on chromosome 23. ''Genet Sel Evol''. 2016 Mar 9; '''48''': 19
Mapping the genomic mosaic of two 'Afro-Bolivians' from the isolated Yungas valleys. Description: Pardo-Seco, Jacobo, et al. Mapping the genomic mosaic of two 'Afro-Bolivians' from the isolated Yungas valleys. ''BMC Genomics''. 2016 Mar 9; '''17''': 207
Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system. Description: Biswas, Nilima, et al. Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system. ''BMC Med Genet''. 2016 Mar 11; '''17''': 21
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. Description: Hou, Liping, et al. Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. ''Lancet''. 2016 Mar 12; '''387''' (10023):1085-1093
Polymorphisms of the IL27 gene in a Chinese Han population complicated with pre-eclampsia. Description: Liu, Bin, et al. Polymorphisms of the IL27 gene in a Chinese Han population complicated with pre-eclampsia. ''Sci Rep''. 2016 Mar 14; '''6''': 23029
Genomic structure and marker-derived gene networks for growth and meat quality traits of Brazilian Nelore beef cattle. Description: Mudadu, Mauricio A, et al. Genomic structure and marker-derived gene networks for growth and meat quality traits of Brazilian Nelore beef cattle. ''BMC Genomics''. 2016 Mar 15; '''17''': 235
Runs of homozygosity and inbreeding in thyroid cancer. Description: Thomsen, Hauke, et al. Runs of homozygosity and inbreeding in thyroid cancer. ''BMC Cancer''. 2016 Mar 16; '''16''': 227
Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke. Description: Seppala, Ilkka, et al. Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke. ''Sci Rep''. 2016 Mar 17; '''6''': 23207
Joint effects of diabetic-related genomic loci on the therapeutic efficacy of oral anti-diabetic drugs in Chinese type 2 diabetes patients. Description: Chen, Miao, et al. Joint effects of diabetic-related genomic loci on the therapeutic efficacy of oral anti-diabetic drugs in Chinese type 2 diabetes patients. ''Sci Rep''. 2016 Mar 17; '''6''': 23266
Three chromosomal rearrangements promote genomic divergence between migratory and stationary ecotypes of Atlantic cod. Description: Berg, Paul R, et al. Three chromosomal rearrangements promote genomic divergence between migratory and stationary ecotypes of Atlantic cod. ''Sci Rep''. 2016 Mar 17; '''6''': 23246
Effect of HMGCR genetic variation on neuroimaging biomarkers in healthy, mild cognitive impairment and Alzheimer's disease cohorts. Description: Cao, Lei, et al. Effect of HMGCR genetic variation on neuroimaging biomarkers in healthy, mild cognitive impairment and Alzheimer's disease cohorts. ''Oncotarget''. 2016 Mar 22; '''7''' (12):13319-27
Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma. Description: Vishal, Mansi, et al. Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma. ''BMC Med Genomics''. 2016 Mar 22; '''9''': 15
Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility. Description: Finkel, Terri H, et al. Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility. ''BMC Med Genet''. 2016 Mar 22; '''17''': 24
Population-genetic properties of differentiated copy number variations in cattle. Description: Xu, Lingyang, et al. Population-genetic properties of differentiated copy number variations in cattle. ''Sci Rep''. 2016 Mar 23; '''6''': 23161
Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia. Description: Costas, J, et al. Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia. ''Transl Psychiatry''. 2016 Mar 29; '''6''': e768
Identification of PTCSC3 as a Novel Locus for Large-Vessel Ischemic Stroke: A Genome-Wide Association Study. Description: Lee, Tsong-Hai, et al. Identification of PTCSC3 as a Novel Locus for Large-Vessel Ischemic Stroke: A Genome-Wide Association Study. ''J Am Heart Assoc''. 2016 Mar 29; '''5''' (3):e003003
Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways. Description: Cappi, C, et al. Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways. ''Transl Psychiatry''. 2016 Mar 29; '''6''': e764
Genetic diversity analysis of two commercial breeds of pigs using genomic and pedigree data. Description: Zanella, Ricardo, et al. Genetic diversity analysis of two commercial breeds of pigs using genomic and pedigree data. ''Genet Sel Evol''. 2016 Mar 30; '''48''': 24
Epistatic interactions between at least three loci determine the "rat-tail" phenotype in cattle. Description: Knaust, Jacqueline, et al. Epistatic interactions between at least three loci determine the "rat-tail" phenotype in cattle. ''Genet Sel Evol''. 2016 Mar 31; '''48''': 26
Genome-wide significant results identified for plasma apolipoprotein H levels in middle-aged and older adults. Description: Mather, Karen A, et al. Genome-wide significant results identified for plasma apolipoprotein H levels in middle-aged and older adults. ''Sci Rep''. 2016 Mar 31; '''6''': 23675
Systematic identification of genetic influences on methylation across the human life course. Description: Gaunt, Tom R, et al. Systematic identification of genetic influences on methylation across the human life course. ''Genome Biol''. 2016 Mar 31; '''17''': 61
Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan. Description: Joshi, Peter K, et al. Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan. ''Nat Commun''. 2016 Mar 31; '''7''': 11174
A Genome-Wide Association Study Provides New Evidence That CACNA1C Gene is Associated With Diabetic Cataract. Description: Chang, Cheng, et al. A Genome-Wide Association Study Provides New Evidence That CACNA1C Gene is Associated With Diabetic Cataract. ''Invest Ophthalmol Vis Sci''. 2016 Apr 1; '''57''' (4):2246-50
A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients. Description: Morales, Fernando, et al. A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients. ''DNA Repair (Amst)''. 2016 Apr; '''40''': 57-66
Association of Toll-like receptor 4 (TLR4) with chronic plaque type psoriasis and psoriatic arthritis. Description: Smith, Rh Ll, et al. Association of Toll-like receptor 4 (TLR4) with chronic plaque type psoriasis and psoriatic arthritis. ''Arch Dermatol Res''. 2016 Apr; '''308''' (3):201-5
Coexpression network analysis of the genes regulated by two types of resistance responses to powdery mildew in wheat. Description: Zhang, Juncheng, et al. Coexpression network analysis of the genes regulated by two types of resistance responses to powdery mildew in wheat. ''Sci Rep''. 2016 Apr 1; '''6''': 23805
Contribution of Genetic Background and Clinical Risk Factors to Low-Trauma Fractures in Human Immunodeficiency Virus (HIV)-Positive Persons: The Swiss HIV Cohort Study. Description: Junier, Thomas, et al. Contribution of Genetic Background and Clinical Risk Factors to Low-Trauma Fractures in Human Immunodeficiency Virus (HIV)-Positive Persons: The Swiss HIV Cohort Study. ''Open Forum Infect Dis''. 2016 Apr; '''3''' (2):ofw101
Genetic factors influencing the risk of multiple myeloma bone disease. Description: Johnson, D C, et al. Genetic factors influencing the risk of multiple myeloma bone disease. ''Leukemia''. 2016 Apr; '''30''' (4):883-8
Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study. Description: Sapkota, Bishwa R, et al. Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study. ''J Steroid Biochem Mol Biol''. 2016 Apr; '''158''': 149-156
Genome-wide association study of leukotriene modifier response in asthma. Description: Dahlin, A, et al. Genome-wide association study of leukotriene modifier response in asthma. ''Pharmacogenomics J''. 2016 Apr; '''16''' (2):151-7
Genome-wide prediction models that incorporate de novo GWAS are a powerful new tool for tropical rice improvement. Description: Spindel, J E, et al. Genome-wide prediction models that incorporate de novo GWAS are a powerful new tool for tropical rice improvement. ''Heredity (Edinb)''. 2016 Apr; '''116''' (4):395-408
Genomic landscape of the individual host response and outcomes in sepsis: a prospective cohort study. Description: Davenport, Emma E, et al. Genomic landscape of the individual host response and outcomes in sepsis: a prospective cohort study. ''Lancet Respir Med''. 2016 Apr; '''4''' (4):259-71
JAM: A Scalable Bayesian Framework for Joint Analysis of Marginal SNP Effects. Description: Newcombe, Paul J, et al. JAM: A Scalable Bayesian Framework for Joint Analysis of Marginal SNP Effects. ''Genet Epidemiol''. 2016 Apr; '''40''' (3):188-201
Melatonin Pathway and Atenolol-Related Glucose Dysregulation: Is There a Correlation? Description: Chang, S W, et al. Melatonin Pathway and Atenolol-Related Glucose Dysregulation: Is There a Correlation? ''Clin Transl Sci''. 2016 Apr; '''9''' (2):114-22
Mutations in pregnancy-associated plasma protein A2 cause short stature due to low IGF-I availability. Description: Dauber, Andrew, et al. Mutations in pregnancy-associated plasma protein A2 cause short stature due to low IGF-I availability. ''EMBO Mol Med''. 2016 Apr 1; '''8''' (4):363-74
Organic cation transporter 1 variants and gastrointestinal side effects of metformin in patients with Type 2 diabetes. Description: Dujic, T, et al. Organic cation transporter 1 variants and gastrointestinal side effects of metformin in patients with Type 2 diabetes. ''Diabet Med''. 2016 Apr; '''33''' (4):511-4
Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels. Description: Boettger, Linda M, et al. Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels. ''Nat Genet''. 2016 Apr; '''48''' (4):359-66
Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs. Description: Ricano-Ponce, Isis, et al. Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs. ''J Autoimmun''. 2016 Apr; '''68''': 62-74
Relationship Among Chlamydia and Mycoplasma Pneumoniae Seropositivity, IKZF1 Genotype and Chronic Obstructive Pulmonary Disease in A General Japanese Population: The Nagahama Study. Description: Muro, Shigeo, et al. Relationship Among Chlamydia and Mycoplasma Pneumoniae Seropositivity, IKZF1 Genotype and Chronic Obstructive Pulmonary Disease in A General Japanese Population: The Nagahama Study. ''Medicine (Baltimore)''. 2016 Apr; '''95''' (15):e3371
Replication study of 34 common SNPs associated with prostate cancer in the Romanian population. Description: Jinga, Viorel, et al. Replication study of 34 common SNPs associated with prostate cancer in the Romanian population. ''J Cell Mol Med''. 2016 Apr; '''20''' (4):594-600
Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes. Description: Porta, Massimo, et al. Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes. ''Diabetes''. 2016 Apr; '''65''' (4):1022-30
Wide distribution and altitude correlation of an archaic high-altitude-adaptive EPAS1 haplotype in the Himalayas. Description: Hackinger, Sophie, et al. Wide distribution and altitude correlation of an archaic high-altitude-adaptive EPAS1 haplotype in the Himalayas. ''Hum Genet''. 2016 Apr; '''135''' (4):393-402
Genetic scores based on risk-associated single nucleotide polymorphisms (SNPs) can reveal inherited risk of renal cell carcinoma. Description: Wu, Yishuo, et al. Genetic scores based on risk-associated single nucleotide polymorphisms (SNPs) can reveal inherited risk of renal cell carcinoma. ''Oncotarget''. 2016 Apr 5; '''7''' (14):18631-7
Efficient Software for Multi-marker, Region-Based Analysis of GWAS Data. Description: Sanjak, Jaleal S, et al. Efficient Software for Multi-marker, Region-Based Analysis of GWAS Data. ''G3 (Bethesda)''. 2016 Apr 7; '''6''' (4):1023-30
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study. Description: Balendra, Rubika, et al. Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study. ''BMC Med Genet''. 2016 Apr 7; '''17''': 28
Reference genotype and exome data from an Australian Aboriginal population for health-based research. Description: Tang, Dave, et al. Reference genotype and exome data from an Australian Aboriginal population for health-based research. ''Sci Data''. 2016 Apr 12; '''3''': 160023
Genome-wide association study of antidepressant response: involvement of the inorganic cation transmembrane transporter activity pathway. Description: Cocchi, Enrico, et al. Genome-wide association study of antidepressant response: involvement of the inorganic cation transmembrane transporter activity pathway. ''BMC Psychiatry''. 2016 Apr 18; '''16''': 106
Sex-Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction. Description: Yoshino, Satoshi, et al. Sex-Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction. ''J Am Heart Assoc''. 2016 Apr 18; '''5''' (4):e002544
The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens. Description: Psifidi, A, et al. The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens. ''BMC Genomics''. 2016 Apr 18; '''17''': 293
A genetic study and meta-analysis of the genetic predisposition of prostate cancer in a Chinese population. Description: Marzec, Jacek, et al. A genetic study and meta-analysis of the genetic predisposition of prostate cancer in a Chinese population. ''Oncotarget''. 2016 Apr 19; '''7''' (16):21393-403
Germline genetics of cancer of unknown primary (CUP) and its specific subtypes. Description: Hemminki, Kari, et al. Germline genetics of cancer of unknown primary (CUP) and its specific subtypes. ''Oncotarget''. 2016 Apr 19; '''7''' (16):22140-9
Maternal mid-pregnancy C-reactive protein and risk of autism spectrum disorders: the early markers for autism study. Description: Zerbo, O, et al. Maternal mid-pregnancy C-reactive protein and risk of autism spectrum disorders: the early markers for autism study. ''Transl Psychiatry''. 2016 Apr 19; '''6''': e783
SNP- and haplotype-based genome-wide association studies for growth, carcass, and meat quality traits in a Duroc multigenerational population. Description: Sato, Shuji, et al. SNP- and haplotype-based genome-wide association studies for growth, carcass, and meat quality traits in a Duroc multigenerational population. ''BMC Genet''. 2016 Apr 19; '''17''': 60
Identifying genetically driven clinical phenotypes using linear mixed models. Description: Mosley, Jonathan D, et al. Identifying genetically driven clinical phenotypes using linear mixed models. ''Nat Commun''. 2016 Apr 25; '''7''': 11433
Major histocompatibility complex harbors widespread genotypic variability of non-additive risk of rheumatoid arthritis including epistasis. Description: Wei, Wen-Hua, et al. Major histocompatibility complex harbors widespread genotypic variability of non-additive risk of rheumatoid arthritis including epistasis. ''Sci Rep''. 2016 Apr 25; '''6''': 25014
The impact of PICALM genetic variations on reserve capacity of posterior cingulate in AD continuum. Description: Xu, Wei, et al. The impact of PICALM genetic variations on reserve capacity of posterior cingulate in AD continuum. ''Sci Rep''. 2016 Apr 27; '''6''': 24480
A Genetic Mechanism for Convergent Skin Lightening during Recent Human Evolution. Description: Yang, Zhaohui, et al. A Genetic Mechanism for Convergent Skin Lightening during Recent Human Evolution. ''Mol Biol Evol''. 2016 May; '''33''' (5):1177-87
Analysis of Association between MAP2K4 Gene Polymorphism rs3826392 and IL-1b Serum Level in Southern Chinese Han Ischemic Stroke Patients. Description: Gu, Lian, et al. Analysis of Association between MAP2K4 Gene Polymorphism rs3826392 and IL-1b Serum Level in Southern Chinese Han Ischemic Stroke Patients. ''J Stroke Cerebrovasc Dis''. 2016 May; '''25''' (5):1096-1101
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. Description: Ellinghaus, David, et al. Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. ''Nat Genet''. 2016 May; '''48''' (5):510-8
A pilot exome-wide association study of age-related cataract in Koreans. Description: Eom, Sang-Yong, et al. A pilot exome-wide association study of age-related cataract in Koreans. ''J Biomed Res''. 2016 May; '''30''' (3):186-90
Association of IL12A Expression Quantitative Trait Loci (eQTL) With Primary Biliary Cirrhosis in a Chinese Han Population. Description: Li, Ping, et al. Association of IL12A Expression Quantitative Trait Loci (eQTL) With Primary Biliary Cirrhosis in a Chinese Han Population. ''Medicine (Baltimore)''. 2016 May; '''95''' (19):e3665
Evidence of Common Genetic Overlap Between Schizophrenia and Cognition. Description: Hubbard, Leon, et al. Evidence of Common Genetic Overlap Between Schizophrenia and Cognition. ''Schizophr Bull''. 2016 May; '''42''' (3):832-42
Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease. Description: McLeod, Olga, et al. Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease. ''Cytokine''. 2016 May; '''81''': 1-9
Genome-Wide Analysis Identifies Germ-Line Risk Factors Associated with Canine Mammary Tumours. Description: Melin, Malin, et al. Genome-Wide Analysis Identifies Germ-Line Risk Factors Associated with Canine Mammary Tumours. ''PLoS Genet''. 2016 May; '''12''' (5):e1006029
Interleukin-6 promoter polymorphism interacts with pain and life stress influencing depression phenotypes. Description: Kovacs, David, et al. Interleukin-6 promoter polymorphism interacts with pain and life stress influencing depression phenotypes. ''J Neural Transm (Vienna)''. 2016 May; '''123''' (5):541-8
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes. Description: Hytonen, Marjo K, et al. Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes. ''PLoS Genet''. 2016 May; '''12''' (5):e1006037
mRNA GPR162 changes are associated with decreased food intake in rat, and its human genetic variants with impairments in glucose homeostasis in two Swedish cohorts. Description: Caruso, Vanni, et al. mRNA GPR162 changes are associated with decreased food intake in rat, and its human genetic variants with impairments in glucose homeostasis in two Swedish cohorts. ''Gene''. 2016 May 1; '''581''' (2):139-45
No Significant Effect of ASAP1 Gene Variants on the Susceptibility to Tuberculosis in Chinese Population. Description: Hu, Xuejiao, et al. No Significant Effect of ASAP1 Gene Variants on the Susceptibility to Tuberculosis in Chinese Population. ''Medicine (Baltimore)''. 2016 May; '''95''' (21):e3703
Previously reported PDE3A-SLCO1C1 genetic variant does not correlate with anti-TNF response in a large UK rheumatoid arthritis cohort. Description: Smith, Samantha Louise, et al. Previously reported PDE3A-SLCO1C1 genetic variant does not correlate with anti-TNF response in a large UK rheumatoid arthritis cohort. ''Pharmacogenomics''. 2016 May; '''17''' (7):715-20
Screening of Two ADH4 Variations in a Swedish Cluster Headache Case-Control Material. Description: Fourier, Carmen, et al. Screening of Two ADH4 Variations in a Swedish Cluster Headache Case-Control Material. ''Headache''. 2016 May; '''56''' (5):835-840
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis. Description: Kinnersley, Ben, et al. Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis. ''Eur J Hum Genet''. 2016 May; '''24''' (5):717-24
Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration Risk. Description: Hughes, Anne E, et al. Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration Risk. ''Invest Ophthalmol Vis Sci''. 2016 May 1; '''57''' (6):2763-9
The Great Migration and African-American Genomic Diversity. Description: Baharian, Soheil, et al. The Great Migration and African-American Genomic Diversity. ''PLoS Genet''. 2016 May; '''12''' (5):e1006059
The HABP2 G534E polymorphism does not increase nonmedullary thyroid cancer risk in Hispanics. Description: Bohorquez, Mabel E, et al. The HABP2 G534E polymorphism does not increase nonmedullary thyroid cancer risk in Hispanics. ''Endocr Connect''. 2016 May; '''5''' (3):123-7
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts. Description: Shore, Robert, et al. The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts. ''Hum Mol Genet''. 2016 May 1; '''25''' (9):1771-9
Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus. Description: Truve, Katarina, et al. Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus. ''PLoS Genet''. 2016 May; '''12''' (5):e1006000
Conflation of Short Identity-by-Descent Segments Bias Their Inferred Length Distribution. Description: Chiang, Charleston W K, et al. Conflation of Short Identity-by-Descent Segments Bias Their Inferred Length Distribution. ''G3 (Bethesda)''. 2016 May 3; '''6''' (5):1287-96
Financial difficulties but not other types of recent negative life events show strong interactions with 5-HTTLPR genotype in the development of depressive symptoms. Description: Gonda, X, et al. Financial difficulties but not other types of recent negative life events show strong interactions with 5-HTTLPR genotype in the development of depressive symptoms. ''Transl Psychiatry''. 2016 May 3; '''6''': e798
Global diversity in the TAS2R38 bitter taste receptor: revisiting a classic evolutionary PROPosal. Description: Risso, Davide S, et al. Global diversity in the TAS2R38 bitter taste receptor: revisiting a classic evolutionary PROPosal. ''Sci Rep''. 2016 May 3; '''6''': 25506
Latitudinal Clines of the Human Vitamin D Receptor and Skin Color Genes. Description: Tiosano, Dov, et al. Latitudinal Clines of the Human Vitamin D Receptor and Skin Color Genes. ''G3 (Bethesda)''. 2016 May 3; '''6''' (5):1251-66
Schizophrenia and subsequent neighborhood deprivation: revisiting the social drift hypothesis using population, twin and molecular genetic data. Description: Sariaslan, A, et al. Schizophrenia and subsequent neighborhood deprivation: revisiting the social drift hypothesis using population, twin and molecular genetic data. ''Transl Psychiatry''. 2016 May 3; '''6''': e796
Genetic polymorphism rs3760396 of the chemokine (C-C motif) ligand 2 gene (CCL2) associated with the susceptibility of lung cancer in a pathological subtype-specific manner in Han-ancestry Chinese: a case control study. Description: Li, Xu, et al. Genetic polymorphism rs3760396 of the chemokine (C-C motif) ligand 2 gene (CCL2) associated with the susceptibility of lung cancer in a pathological subtype-specific manner in Han-ancestry Chinese: a case control study. ''BMC Cancer''. 2016 May 4; '''16''': 298
A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin. Description: Molloy, Anne M, et al. A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin. ''Am J Hum Genet''. 2016 May 5; '''98''' (5):869-882
Analysis of Genomic Regions Associated With Coronary Artery Disease Reveals Continent-Specific Single Nucleotide Polymorphisms in North African Populations. Description: Zanetti, Daniela, et al. Analysis of Genomic Regions Associated With Coronary Artery Disease Reveals Continent-Specific Single Nucleotide Polymorphisms in North African Populations. ''J Epidemiol''. 2016 May 5; '''26''' (5):264-71
Common genetic variation in ETV6 is associated with colorectal cancer susceptibility. Description: Wang, Meilin, et al. Common genetic variation in ETV6 is associated with colorectal cancer susceptibility. ''Nat Commun''. 2016 May 5; '''7''': 11478
Sequence-based Association Analysis Reveals an MGST1 eQTL with Pleiotropic Effects on Bovine Milk Composition. Description: Littlejohn, Mathew D, et al. Sequence-based Association Analysis Reveals an MGST1 eQTL with Pleiotropic Effects on Bovine Milk Composition. ''Sci Rep''. 2016 May 5; '''6''': 25376
The Pharmacogenomics of Bipolar Disorder study (PGBD): identification of genes for lithium response in a prospective sample. Description: Oedegaard, Ketil J, et al. The Pharmacogenomics of Bipolar Disorder study (PGBD): identification of genes for lithium response in a prospective sample. ''BMC Psychiatry''. 2016 May 5; '''16''': 129
Diet Quality and Change in Blood Lipids during 16 Years of Follow-up and Their Interaction with Genetic Risk for Dyslipidemia. Description: Sonestedt, Emily, et al. Diet Quality and Change in Blood Lipids during 16 Years of Follow-up and Their Interaction with Genetic Risk for Dyslipidemia. ''Nutrients''. 2016 May 9; '''8''' (5):
Genetic Relationship between Schizophrenia and Nicotine Dependence. Description: Chen, Jingchun, et al. Genetic Relationship between Schizophrenia and Nicotine Dependence. ''Sci Rep''. 2016 May 10; '''6''': 25671
FILTUS: a desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector. Description: Vigeland, Magnus D, et al. FILTUS: a desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector. ''Bioinformatics''. 2016 May 15; '''32''' (10):1592-4
Testing the role of predicted gene knockouts in human anthropometric trait variation. Description: Lessard, Samuel, et al. Testing the role of predicted gene knockouts in human anthropometric trait variation. ''Hum Mol Genet''. 2016 May 15; '''25''' (10):2082-2092
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram. Description: Verweij, Niek, et al. Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram. ''Hum Mol Genet''. 2016 May 15; '''25''' (10):2093-2103
Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus. Description: Sakiyama, Masayuki, et al. Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus. ''Sci Rep''. 2016 May 16; '''6''': 25360
CHI3L1 polymorphisms, cord blood YKL-40 levels and later asthma development. Description: Usemann, Jakob, et al. CHI3L1 polymorphisms, cord blood YKL-40 levels and later asthma development. ''BMC Pulm Med''. 2016 May 18; '''16''' (1):81
Contrasting Linguistic and Genetic Origins of the Asian Source Populations of Malagasy. Description: Kusuma, Pradiptajati, et al. Contrasting Linguistic and Genetic Origins of the Asian Source Populations of Malagasy. ''Sci Rep''. 2016 May 18; '''6''': 26066
Exploring the interaction among EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population. Description: An, Li, et al. Exploring the interaction among EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population. ''Hum Genomics''. 2016 May 18; '''10''' (1):13
V-akt murine thymoma viral oncogene homolog 3 (AKT3) contributes to poor disease outcome in humans and mice with pneumococcal meningitis. Description: Valls Seron, Mercedes, et al. V-akt murine thymoma viral oncogene homolog 3 (AKT3) contributes to poor disease outcome in humans and mice with pneumococcal meningitis. ''Acta Neuropathol Commun''. 2016 May 18; '''4''' (1):50
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. Description: Adhikari, Kaustubh, et al. A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. ''Nat Commun''. 2016 May 19; '''7''': 11616
NLRP3 Inflammasome Expression and Activation in Human Atherosclerosis. Description: Paramel Varghese, Geena, et al. NLRP3 Inflammasome Expression and Activation in Human Atherosclerosis. ''J Am Heart Assoc''. 2016 May 20; '''5''' (5):
Association of common genetic variation in the protein C pathway genes with clinical outcomes in acute respiratory distress syndrome. Description: Sapru, Anil, et al. Association of common genetic variation in the protein C pathway genes with clinical outcomes in acute respiratory distress syndrome. ''Crit Care''. 2016 May 23; '''20''' (1):151
Genome-wide gene-based analysis suggests an association between Neuroligin 1 (NLGN1) and post-traumatic stress disorder. Description: Kilaru, V, et al. Genome-wide gene-based analysis suggests an association between Neuroligin 1 (NLGN1) and post-traumatic stress disorder. ''Transl Psychiatry''. 2016 May 24; '''6''': e820
Multiple analyses of large-scale genome-wide association study highlight new risk pathways in lumbar spine bone mineral density. Description: Wei, Jinsong, et al. Multiple analyses of large-scale genome-wide association study highlight new risk pathways in lumbar spine bone mineral density. ''Oncotarget''. 2016 May 24; '''7''' (21):31429-39
Accuracy of heritability estimations in presence of hidden population stratification. Description: Dandine-Roulland, Claire, et al. Accuracy of heritability estimations in presence of hidden population stratification. ''Sci Rep''. 2016 May 25; '''6''': 26471
An ultra-high density linkage map and QTL mapping for sex and growth-related traits of common carp (Cyprinus carpio). Description: Peng, Wenzhu, et al. An ultra-high density linkage map and QTL mapping for sex and growth-related traits of common carp (Cyprinus carpio). ''Sci Rep''. 2016 May 26; '''6''': 26693
Genome-wide resequencing of KRICE_CORE reveals their potential for future breeding, as well as functional and evolutionary studies in the post-genomic era. Description: Kim, Tae-Sung, et al. Genome-wide resequencing of KRICE_CORE reveals their potential for future breeding, as well as functional and evolutionary studies in the post-genomic era. ''BMC Genomics''. 2016 May 26; '''17''': 408
Genomic analysis of Ugandan and Rwandan chicken ecotypes using a 600 k genotyping array. Description: Fleming, D S, et al. Genomic analysis of Ugandan and Rwandan chicken ecotypes using a 600 k genotyping array. ''BMC Genomics''. 2016 May 26; '''17''': 407
Effect of CLU genetic variants on cerebrospinal fluid and neuroimaging markers in healthy, mild cognitive impairment and Alzheimer's disease cohorts. Description: Tan, Lin, et al. Effect of CLU genetic variants on cerebrospinal fluid and neuroimaging markers in healthy, mild cognitive impairment and Alzheimer's disease cohorts. ''Sci Rep''. 2016 May 27; '''6''': 26027
Genome-wide analysis reveals adaptation to high altitudes in Tibetan sheep. Description: Wei, Caihong, et al. Genome-wide analysis reveals adaptation to high altitudes in Tibetan sheep. ''Sci Rep''. 2016 May 27; '''6''': 26770
Clinical Significance of Long Non-Coding RNA CASC8 rs10505477 Polymorphism in Lung Cancer Susceptibility, Platinum-Based Chemotherapy Response, and Toxicity. Description: Hu, Lei, et al. Clinical Significance of Long Non-Coding RNA CASC8 rs10505477 Polymorphism in Lung Cancer Susceptibility, Platinum-Based Chemotherapy Response, and Toxicity. ''Int J Environ Res Public Health''. 2016 May 30; '''13''' (6):
Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese. Description: Li, Yuanfeng, et al. Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese. ''Nat Commun''. 2016 May 31; '''7''': 11664
Impact of SORL1 genetic variations on MRI markers in non-demented elders. Description: Yin, Rui-Hua, et al. Impact of SORL1 genetic variations on MRI markers in non-demented elders. ''Oncotarget''. 2016 May 31; '''7''' (22):31689-98
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. Description: Mosley, J D, et al. A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. ''Pharmacogenomics J''. 2016 Jun; '''16''' (3):231-7
Analysis of ABCG2 and other urate transporters in uric acid homeostasis in chronic kidney disease: potential role of remote sensing and signaling. Description: Bhatnagar, Vibha, et al. Analysis of ABCG2 and other urate transporters in uric acid homeostasis in chronic kidney disease: potential role of remote sensing and signaling. ''Clin Kidney J''. 2016 Jun; '''9''' (3):444-53
Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population. Description: Kreile, Madara, et al. Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population. ''Arch Med Sci''. 2016 Jun 1; '''12''' (3):479-85
Analysis of single nucleotide polymorphisms implicate mTOR signalling in the development of new-onset diabetes after transplantation. Description: Chand, S, et al. Analysis of single nucleotide polymorphisms implicate mTOR signalling in the development of new-onset diabetes after transplantation. ''BBA Clin''. 2016 Jun; '''5''': 41-5
Bias Characterization in Probabilistic Genotype Data and Improved Signal Detection with Multiple Imputation. Description: Palmer, Cameron, et al. Bias Characterization in Probabilistic Genotype Data and Improved Signal Detection with Multiple Imputation. ''PLoS Genet''. 2016 Jun; '''12''' (6):e1006091
Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs. Description: Wakil, Salma M, et al. Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs. ''Data Brief''. 2016 Jun; '''7''': 172-176
Diversity and population-genetic properties of copy number variations and multicopy genes in cattle. Description: Bickhart, Derek M, et al. Diversity and population-genetic properties of copy number variations and multicopy genes in cattle. ''DNA Res''. 2016 Jun; '''23''' (3):253-62
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases. Description: Bettencourt, Conceicao, et al. DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases. ''Ann Neurol''. 2016 Jun; '''79''' (6):983-90
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12. Description: Jackson, Victoria E, et al. Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12. ''Thorax''. 2016 Jun; '''71''' (6):501-9
Five endometrial cancer risk loci identified through genome-wide association analysis. Description: Cheng, Timothy Ht, et al. Five endometrial cancer risk loci identified through genome-wide association analysis. ''Nat Genet''. 2016 Jun; '''48''' (6):667-674
Genetically reduced FAAH activity may be a risk for the development of anxiety and depression in persons with repetitive childhood trauma. Description: Lazary, Judit, et al. Genetically reduced FAAH activity may be a risk for the development of anxiety and depression in persons with repetitive childhood trauma. ''Eur Neuropsychopharmacol''. 2016 Jun; '''26''' (6):1020-8
Genetic variants associated with lean and obese type 2 diabetes in a Han Chinese population: A case-control study. Description: Kong, Xiaomu, et al. Genetic variants associated with lean and obese type 2 diabetes in a Han Chinese population: A case-control study. ''Medicine (Baltimore)''. 2016 Jun; '''95''' (23):e3841
Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci. Description: Smith, D J, et al. Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci. ''Mol Psychiatry''. 2016 Jun; '''21''' (6):749-57
Genome-Wide Association Study of Bone Mineral Density in Korean Men. Description: Bae, Ye Seul, et al. Genome-Wide Association Study of Bone Mineral Density in Korean Men. ''Genomics Inform''. 2016 Jun; '''14''' (2):62-8
Genome-wide association study of colorectal cancer in Hispanics. Description: Schmit, Stephanie L, et al. Genome-wide association study of colorectal cancer in Hispanics. ''Carcinogenesis''. 2016 Jun; '''37''' (6):547-556
Genome-wide view of genetic diversity reveals paths of selection and cultivar differentiation in peach domestication. Description: Akagi, Takashi, et al. Genome-wide view of genetic diversity reveals paths of selection and cultivar differentiation in peach domestication. ''DNA Res''. 2016 Jun; '''23''' (3):271-82
Human genetic variation database, a reference database of genetic variations in the Japanese population. Description: Higasa, Koichiro, et al. Human genetic variation database, a reference database of genetic variations in the Japanese population. ''J Hum Genet''. 2016 Jun; '''61''' (6):547-53
Impact of Common Diabetes Risk Variant in MTNR1B on Sleep, Circadian, and Melatonin Physiology. Description: Lane, Jacqueline M, et al. Impact of Common Diabetes Risk Variant in MTNR1B on Sleep, Circadian, and Melatonin Physiology. ''Diabetes''. 2016 Jun; '''65''' (6):1741-51
No Association between Variation in Longevity Candidate Genes and Aging-related Phenotypes in Oldest-old Danes. Description: Soerensen, Mette, et al. No Association between Variation in Longevity Candidate Genes and Aging-related Phenotypes in Oldest-old Danes. ''Exp Gerontol''. 2016 Jun; '''78''': 57-61
Obesity and Multiple Sclerosis: A Mendelian Randomization Study. Description: Mokry, Lauren E, et al. Obesity and Multiple Sclerosis: A Mendelian Randomization Study. ''PLoS Med''. 2016 Jun; '''13''' (6):e1002053
Origins of cattle on Chirikof Island, Alaska, elucidated from genome-wide SNP genotypes. Description: Decker, J E, et al. Origins of cattle on Chirikof Island, Alaska, elucidated from genome-wide SNP genotypes. ''Heredity (Edinb)''. 2016 Jun; '''116''' (6):502-5
R2d2 Drives Selfish Sweeps in the House Mouse. Description: Didion, John P, et al. R2d2 Drives Selfish Sweeps in the House Mouse. ''Mol Biol Evol''. 2016 Jun; '''33''' (6):1381-95
The population genomic basis of geographic differentiation in North American common ragweed (Ambrosia artemisiifolia L.). Description: Martin, Michael D, et al. The population genomic basis of geographic differentiation in North American common ragweed (Ambrosia artemisiifolia L.). ''Ecol Evol''. 2016 Jun; '''6''' (11):3760-3771
Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease. Description: Orlando, Giulia, et al. Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease. ''Hum Mol Genet''. 2016 Jun 1; '''25''' (11):2349-2359
Detection of Allelic Frequency Differences between the Sexes in Humans: A Signature of Sexually Antagonistic Selection. Description: Lucotte, Elise A, et al. Detection of Allelic Frequency Differences between the Sexes in Humans: A Signature of Sexually Antagonistic Selection. ''Genome Biol Evol''. 2016 Jun 2; '''8''' (5):1489-500
Antibodies directed against endogenous and exogenous citrullinated antigens pre-date the onset of rheumatoid arthritis. Description: Johansson, Linda, et al. Antibodies directed against endogenous and exogenous citrullinated antigens pre-date the onset of rheumatoid arthritis. ''Arthritis Res Ther''. 2016 Jun 3; '''18''' (1):127
CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens. Description: Wang, Binbin, et al. CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens. ''Sci Rep''. 2016 Jun 3; '''6''': 25954
Whole-genome resequencing of honeybee drones to detect genomic selection in a population managed for royal jelly. Description: Wragg, David, et al. Whole-genome resequencing of honeybee drones to detect genomic selection in a population managed for royal jelly. ''Sci Rep''. 2016 Jun 3; '''6''': 27168
CACNA1C hypermethylation is associated with bipolar disorder. Description: Starnawska, A, et al. CACNA1C hypermethylation is associated with bipolar disorder. ''Transl Psychiatry''. 2016 Jun 7; '''6''' (6):e831
Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia. Description: Fingerlin, Tasha E, et al. Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia. ''BMC Genet''. 2016 Jun 7; '''17''' (1):74
NPR-C gene polymorphism is associated with increased susceptibility to coronary artery disease in Chinese Han population: a multicenter study. Description: Hu, Qin, et al. NPR-C gene polymorphism is associated with increased susceptibility to coronary artery disease in Chinese Han population: a multicenter study. ''Oncotarget''. 2016 Jun 7; '''7''' (23):33662-74
Population structure of eleven Spanish ovine breeds and detection of selective sweeps with BayeScan and hapFLK. Description: Manunza, A, et al. Population structure of eleven Spanish ovine breeds and detection of selective sweeps with BayeScan and hapFLK. ''Sci Rep''. 2016 Jun 7; '''6''': 27296
Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population. Description: Zholdybayeva, Elena V, et al. Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population. ''Hum Genomics''. 2016 Jun 8; '''10''' (1):15
Genetic variations associated with six-white-point coat pigmentation in Diannan small-ear pigs. Description: Lu, Meng-Die, et al. Genetic variations associated with six-white-point coat pigmentation in Diannan small-ear pigs. ''Sci Rep''. 2016 Jun 8; '''6''': 27534
SNPConvert: SNP Array Standardization and Integration in Livestock Species. Description: Nicolazzi, Ezequiel Luis, et al. SNPConvert: SNP Array Standardization and Integration in Livestock Species. ''Microarrays (Basel)''. 2016 Jun 9; '''5''' (2):
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe. Description: Blauwendraat, Cornelis, et al. Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe. ''Genome Med''. 2016 Jun 10; '''8''' (1):65
Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans. Description: Salinas, Yasmmyn D, et al. Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans. ''BMC Genet''. 2016 Jun 13; '''17''' (1):78
Association of HLA class I and II genes with cutaneous leishmaniasis: a case control study from Sri Lanka and a systematic review. Description: Samaranayake, Nilakshi, et al. Association of HLA class I and II genes with cutaneous leishmaniasis: a case control study from Sri Lanka and a systematic review. ''BMC Infect Dis''. 2016 Jun 14; '''16''': 292
Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma. Description: Rong, Shi Song, et al. Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma. ''Sci Rep''. 2016 Jun 14; '''6''': 27837
Full circumpolar migration ensures evolutionary unity in the Emperor penguin. Description: Cristofari, Robin, et al. Full circumpolar migration ensures evolutionary unity in the Emperor penguin. ''Nat Commun''. 2016 Jun 14; '''7''': 11842
Association of Genetic Risk for Schizophrenia With Nonparticipation Over Time in a Population-Based Cohort Study. Description: Martin, Joanna, et al. Association of Genetic Risk for Schizophrenia With Nonparticipation Over Time in a Population-Based Cohort Study. ''Am J Epidemiol''. 2016 Jun 15; '''183''' (12):1149-58
Genetic analysis of advanced glycation end products in the DHS MIND study. Description: Adams, Jeremy N, et al. Genetic analysis of advanced glycation end products in the DHS MIND study. ''Gene''. 2016 Jun 15; '''584''' (2):173-9
The heritability and patterns of DNA methylation in normal human colorectum. Description: Rowlatt, Amy, et al. The heritability and patterns of DNA methylation in normal human colorectum. ''Hum Mol Genet''. 2016 Jun 15; '''25''' (12):2600-2611
The Relationship of Common Risk Variants and Polygenic Risk for Schizophrenia to Sensorimotor Gating. Description: Roussos, Panos, et al. The Relationship of Common Risk Variants and Polygenic Risk for Schizophrenia to Sensorimotor Gating. ''Biol Psychiatry''. 2016 Jun 15; '''79''' (12):988-96
Complement gene variants in relation to autoantibodies to beta cell specific antigens and type 1 diabetes in the TEDDY Study. Description: Torn, Carina, et al. Complement gene variants in relation to autoantibodies to beta cell specific antigens and type 1 diabetes in the TEDDY Study. ''Sci Rep''. 2016 Jun 16; '''6''': 27887
Rare coding TTN variants are associated with electrocardiographic QT interval in the general population. Description: Kapoor, Ashish, et al. Rare coding TTN variants are associated with electrocardiographic QT interval in the general population. ''Sci Rep''. 2016 Jun 20; '''6''': 28356
Serum Uric Acid Levels were Dynamically Coupled with Hemoglobin A1c in the Development of Type 2 Diabetes. Description: Wei, Fengjiang, et al. Serum Uric Acid Levels were Dynamically Coupled with Hemoglobin A1c in the Development of Type 2 Diabetes. ''Sci Rep''. 2016 Jun 22; '''6''': 28549
The impact of genotype calling errors on family-based studies. Description: Yan, Qi, et al. The impact of genotype calling errors on family-based studies. ''Sci Rep''. 2016 Jun 22; '''6''': 28323
Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study. Description: Rizzi, Federica, et al. Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study. ''J Transl Med''. 2016 Jun 23; '''14''' (1):186
Pathway Analyses Identify Novel Variants in the WNT Signaling Pathway Associated with Tuberculosis in Chinese Population. Description: Hu, Xuejiao, et al. Pathway Analyses Identify Novel Variants in the WNT Signaling Pathway Associated with Tuberculosis in Chinese Population. ''Sci Rep''. 2016 Jun 23; '''6''': 28530
A practical approach to detect ancestral haplotypes in livestock populations. Description: Sanchez-Molano, Enrique, et al. A practical approach to detect ancestral haplotypes in livestock populations. ''BMC Genet''. 2016 Jun 24; '''17''' (1):91
Exploiting expression patterns across multiple tissues to map expression quantitative trait loci. Description: Acharya, Chaitanya R, et al. Exploiting expression patterns across multiple tissues to map expression quantitative trait loci. ''BMC Bioinformatics''. 2016 Jun 24; '''17''': 257
A de novo silencer causes elimination of MITF-M expression and profound hearing loss in pigs. Description: Chen, Lei, et al. A de novo silencer causes elimination of MITF-M expression and profound hearing loss in pigs. ''BMC Biol''. 2016 Jun 27; '''14''': 52
Cardio-metabolic parameters are associated with genetic admixture estimates in a pediatric population from Colombia. Description: Munoz, Angelica M, et al. Cardio-metabolic parameters are associated with genetic admixture estimates in a pediatric population from Colombia. ''BMC Genet''. 2016 Jun 27; '''17''' (1):93
Genetic polymorphisms in TNIP1 increase the risk of gastric carcinoma. Description: Liu, Zhao, et al. Genetic polymorphisms in TNIP1 increase the risk of gastric carcinoma. ''Oncotarget''. 2016 Jun 28; '''7''' (26):40500-40507
Variants in human papillomavirus receptor and associated genes are associated with type-specific HPV infection and lesion progression of the cervix. Description: Zou, Jian, et al. Variants in human papillomavirus receptor and associated genes are associated with type-specific HPV infection and lesion progression of the cervix. ''Oncotarget''. 2016 Jun 28; '''7''' (26):40135-40147
Genome-wide association study of prolactin levels in blood plasma and cerebrospinal fluid. Description: Staley, Lyndsay A, et al. Genome-wide association study of prolactin levels in blood plasma and cerebrospinal fluid. ''BMC Genomics''. 2016 Jun 29; '''17 Suppl 3''': 436
Genomic prediction of host resistance to sea lice in farmed Atlantic salmon populations. Description: Tsai, Hsin-Yuan, et al. Genomic prediction of host resistance to sea lice in farmed Atlantic salmon populations. ''Genet Sel Evol''. 2016 Jun 29; '''48''' (1):47
Variants in ACPP are associated with cerebrospinal fluid Prostatic Acid Phosphatase levels. Description: Staley, Lyndsay A, et al. Variants in ACPP are associated with cerebrospinal fluid Prostatic Acid Phosphatase levels. ''BMC Genomics''. 2016 Jun 29; '''17 Suppl 3''': 439
Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels. Description: Ebbert, Mark T W, et al. Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels. ''BMC Genomics''. 2016 Jun 29; '''17 Suppl 3''': 437
A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle. Description: Agerholm, Jorgen S, et al. A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle. ''BMC Genomics''. 2016 Jun 30; '''17''': 479
Genomic ancestry estimation quantifies use of wild species in grape breeding. Description: Migicovsky, Zoe, et al. Genomic ancestry estimation quantifies use of wild species in grape breeding. ''BMC Genomics''. 2016 Jun 30; '''17''': 478
A Genetic Variant of the Sortilin 1 Gene is Associated with Reduced Risk of Alzheimer's Disease. Description: Andersson, Carl-Henrik, et al. A Genetic Variant of the Sortilin 1 Gene is Associated with Reduced Risk of Alzheimer's Disease. ''J Alzheimers Dis''. 2016 Jul 1; '''53''' (4):1353-63
Allele Frequencies of the Single Nucleotide Polymorphisms Related to the Body Burden of Heavy Metals in the Korean Population and Their Ethnic Differences. Description: Eom, Sang-Yong, et al. Allele Frequencies of the Single Nucleotide Polymorphisms Related to the Body Burden of Heavy Metals in the Korean Population and Their Ethnic Differences. ''Toxicol Res''. 2016 Jul; '''32''' (3):195-205
A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy. Description: Panjwani, Naim, et al. A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy. ''Ann Clin Transl Neurol''. 2016 Jul; '''3''' (7):512-22
Expression Quantitative Trait Locus Mapping Studies in Mid-secretory Phase Endometrial Cells Identifies HLA-F and TAP2 as Fecundability-Associated Genes. Description: Burrows, Courtney K, et al. Expression Quantitative Trait Locus Mapping Studies in Mid-secretory Phase Endometrial Cells Identifies HLA-F and TAP2 as Fecundability-Associated Genes. ''PLoS Genet''. 2016 Jul; '''12''' (7):e1005858
FKBP5 polymorphisms, childhood abuse, and PTSD symptoms: Results from the National Health and Resilience in Veterans Study. Description: Watkins, Laura E, et al. FKBP5 polymorphisms, childhood abuse, and PTSD symptoms: Results from the National Health and Resilience in Veterans Study. ''Psychoneuroendocrinology''. 2016 Jul; '''69''': 98-105
Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder. Description: Aebi, Marcel, et al. Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder. ''Am J Med Genet B Neuropsychiatr Genet''. 2016 Jul; '''171''' (5):573-88
Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder. Description: Brevik, Erlend J, et al. Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder. ''Am J Med Genet B Neuropsychiatr Genet''. 2016 Jul; '''171''' (5):733-47
Identification of genetic variants associated with susceptibility to West Nile virus neuroinvasive disease. Description: Long, D, et al. Identification of genetic variants associated with susceptibility to West Nile virus neuroinvasive disease. ''Genes Immun''. 2016 Jul; '''17''' (5):298-304
New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins. Description: Roshandel, Delnaz, et al. New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins. ''Diabetes''. 2016 Jul; '''65''' (7):2060-71
Pathway analysis of bladder cancer genome-wide association study identifies novel pathways involved in bladder cancer development. Description: Chen, Meng, et al. Pathway analysis of bladder cancer genome-wide association study identifies novel pathways involved in bladder cancer development. ''Genes Cancer''. 2016 Jul; '''7''' (7-8):229-239
Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. Description: Krishnan, Michelle L, et al. Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. ''Brain Behav''. 2016 Jul; '''6''' (7):e00434
Replication of Associations of Genetic Loci Outside the HLA Region With Susceptibility to Anti-Cyclic Citrullinated Peptide-Negative Rheumatoid Arthritis. Description: Viatte, Sebastien, et al. Replication of Associations of Genetic Loci Outside the HLA Region With Susceptibility to Anti-Cyclic Citrullinated Peptide-Negative Rheumatoid Arthritis. ''Arthritis Rheumatol''. 2016 Jul; '''68''' (7):1603-13
Synergistic association of STX1A and VAMP2 with cryptogenic epilepsy in North Indian population. Description: Baghel, Ruchi, et al. Synergistic association of STX1A and VAMP2 with cryptogenic epilepsy in North Indian population. ''Brain Behav''. 2016 Jul; '''6''' (7):e00490
Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution. Description: Patel, Aniruddh P, et al. Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution. ''Atherosclerosis''. 2016 Jul; '''250''': 63-8
The Bell Curve Revisited: Testing Controversial Hypotheses with Molecular Genetic Data. Description: Conley, Dalton, et al. The Bell Curve Revisited: Testing Controversial Hypotheses with Molecular Genetic Data. ''Sociol Sci''. 2016 Jul; '''3''': 520-539
The Complex Admixture History and Recent Southern Origins of Siberian Populations. Description: Pugach, Irina, et al. The Complex Admixture History and Recent Southern Origins of Siberian Populations. ''Mol Biol Evol''. 2016 Jul; '''33''' (7):1777-95
Variants near the HLA complex group 22 gene (HCG22) confer increased susceptibility to late-onset asthma in Japanese populations. Description: Yatagai, Yohei, et al. Variants near the HLA complex group 22 gene (HCG22) confer increased susceptibility to late-onset asthma in Japanese populations. ''J Allergy Clin Immunol''. 2016 Jul; '''138''' (1):281-283.e13
Pooled analysis of genome-wide association studies of cervical intraepithelial neoplasia 3 (CIN3) identifies a new susceptibility locus. Description: Chen, Dan, et al. Pooled analysis of genome-wide association studies of cervical intraepithelial neoplasia 3 (CIN3) identifies a new susceptibility locus. ''Oncotarget''. 2016 Jul 5; '''7''' (27):42216-42224
Tumor Necrosis Factor-alpha Induced Protein 3 Interacting Protein 1 Gene Polymorphisms and Pustular Psoriasis in Chinese Han Population. Description: Han, Jian-Wen, et al. Tumor Necrosis Factor-alpha Induced Protein 3 Interacting Protein 1 Gene Polymorphisms and Pustular Psoriasis in Chinese Han Population. ''Chin Med J (Engl)''. 2016 Jul 5; '''129''' (13):1519-24
The Power of Inbreeding: NGS-Based GWAS of Rice Reveals Convergent Evolution during Rice Domestication. Description: Wang, Hongru, et al. The Power of Inbreeding: NGS-Based GWAS of Rice Reveals Convergent Evolution during Rice Domestication. ''Mol Plant''. 2016 Jul 6; '''9''' (7):975-85
Construction and Annotation of a High Density SNP Linkage Map of the Atlantic Salmon (Salmo salar) Genome. Description: Tsai, Hsin Y, et al. Construction and Annotation of a High Density SNP Linkage Map of the Atlantic Salmon (Salmo salar) Genome. ''G3 (Bethesda)''. 2016 Jul 7; '''6''' (7):2173-9
Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases. Description: Murk, William, et al. Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases. ''G3 (Bethesda)''. 2016 Jul 7; '''6''' (7):2043-50
Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants. Description: Kaartokallio, Tea, et al. Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants. ''Sci Rep''. 2016 Jul 7; '''6''': 29085
Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma. Description: Murk, William, et al. Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma. ''BMC Genet''. 2016 Jul 7; '''17''' (1):102
Immunophenotyping of rheumatoid arthritis reveals a linkage between HLA-DRB1 genotype, CXCR4 expression on memory CD4(+) T cells, and disease activity. Description: Nagafuchi, Yasuo, et al. Immunophenotyping of rheumatoid arthritis reveals a linkage between HLA-DRB1 genotype, CXCR4 expression on memory CD4(+) T cells, and disease activity. ''Sci Rep''. 2016 Jul 7; '''6''': 29338
A comprehensive study of the genomic differentiation between temperate Dent and Flint maize. Description: Unterseer, Sandra, et al. A comprehensive study of the genomic differentiation between temperate Dent and Flint maize. ''Genome Biol''. 2016 Jul 8; '''17''' (1):137
Exome Array Analysis of Susceptibility to Pneumococcal Meningitis. Description: Kloek, Anne T, et al. Exome Array Analysis of Susceptibility to Pneumococcal Meningitis. ''Sci Rep''. 2016 Jul 8; '''6''': 29351
Prediction models for platinum-based chemotherapy response and toxicity in advanced NSCLC patients. Description: Yin, Ji-Ye, et al. Prediction models for platinum-based chemotherapy response and toxicity in advanced NSCLC patients. ''Cancer Lett''. 2016 Jul 10; '''377''' (1):65-73
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms. Description: van 't Hof, Femke N G, et al. Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms. ''J Am Heart Assoc''. 2016 Jul 14; '''5''' (7):
Two-stage association study to identify the genetic susceptibility of a novel common variant of rs2075290 in ZPR1 to type 2 diabetes. Description: Guan, Fanglin, et al. Two-stage association study to identify the genetic susceptibility of a novel common variant of rs2075290 in ZPR1 to type 2 diabetes. ''Sci Rep''. 2016 Jul 14; '''6''': 29586
Analysis of copy number variation at DMBT1 and age-related macular degeneration. Description: Polley, Shamik, et al. Analysis of copy number variation at DMBT1 and age-related macular degeneration. ''BMC Med Genet''. 2016 Jul 15; '''17''' (1):44
Romanian wild boars and Mangalitza pigs have a European ancestry and harbour genetic signatures compatible with past population bottlenecks. Description: Manunza, A, et al. Romanian wild boars and Mangalitza pigs have a European ancestry and harbour genetic signatures compatible with past population bottlenecks. ''Sci Rep''. 2016 Jul 15; '''6''': 29913
Markers associated with heading and aftermath heading in perennial ryegrass full-sib families. Description: Arojju, Sai Krishna, et al. Markers associated with heading and aftermath heading in perennial ryegrass full-sib families. ''BMC Plant Biol''. 2016 Jul 16; '''16''' (1):160
Targeted genomic analysis reveals widespread autoimmune disease association with regulatory variants in the TNF superfamily cytokine signalling network. Description: Richard, Arianne C, et al. Targeted genomic analysis reveals widespread autoimmune disease association with regulatory variants in the TNF superfamily cytokine signalling network. ''Genome Med''. 2016 Jul 19; '''8''' (1):76
An integrated genomic and transcriptomic survey of mucormycosis-causing fungi. Description: Chibucos, Marcus C, et al. An integrated genomic and transcriptomic survey of mucormycosis-causing fungi. ''Nat Commun''. 2016 Jul 22; '''7''': 12218
Genomic analysis identified a potential novel molecular mechanism for high-altitude adaptation in sheep at the Himalayas. Description: Gorkhali, Neena Amatya, et al. Genomic analysis identified a potential novel molecular mechanism for high-altitude adaptation in sheep at the Himalayas. ''Sci Rep''. 2016 Jul 22; '''6''': 29963
A genome-wide perspective about the diversity and demographic history of seven Spanish goat breeds. Description: Manunza, Arianna, et al. A genome-wide perspective about the diversity and demographic history of seven Spanish goat breeds. ''Genet Sel Evol''. 2016 Jul 25; '''48''' (1):52
East Eurasian ancestry in the middle of Europe: genetic footprints of Steppe nomads in the genomes of Belarusian Lipka Tatars. Description: Pankratov, Vasili, et al. East Eurasian ancestry in the middle of Europe: genetic footprints of Steppe nomads in the genomes of Belarusian Lipka Tatars. ''Sci Rep''. 2016 Jul 25; '''6''': 30197
Associations between smoking behavior-related alleles and the risk of melanoma. Description: Wu, Wenting, et al. Associations between smoking behavior-related alleles and the risk of melanoma. ''Oncotarget''. 2016 Jul 26; '''7''' (30):47366-47375
Association study of C-reactive protein associated gene HNF1A with ischemic stroke in Chinese population. Description: Shi, Haibin, et al. Association study of C-reactive protein associated gene HNF1A with ischemic stroke in Chinese population. ''BMC Med Genet''. 2016 Jul 26; '''17''' (1):51
Genetic architecture dissection by genome-wide association analysis reveals avian eggshell ultrastructure traits. Description: Duan, Zhongyi, et al. Genetic architecture dissection by genome-wide association analysis reveals avian eggshell ultrastructure traits. ''Sci Rep''. 2016 Jul 26; '''6''': 28836
Haplotyping the human leukocyte antigen system from single chromosomes. Description: Murphy, Nicholas M, et al. Haplotyping the human leukocyte antigen system from single chromosomes. ''Sci Rep''. 2016 Jul 27; '''6''': 30381
Integrating Epigenomic Elements and GWASs Identifies BDNF Gene Affecting Bone Mineral Density and Osteoporotic Fracture Risk. Description: Guo, Yan, et al. Integrating Epigenomic Elements and GWASs Identifies BDNF Gene Affecting Bone Mineral Density and Osteoporotic Fracture Risk. ''Sci Rep''. 2016 Jul 28; '''6''': 30558
Analysis of the association of VIPR2 polymorphisms with susceptibility to schizophrenia. Description: Jin, Chunhui, et al. Analysis of the association of VIPR2 polymorphisms with susceptibility to schizophrenia. ''Psychiatry Res''. 2016 Jul 30; '''241''': 104-7
ABO blood group associations with markers of endothelial dysfunction in the Multi-Ethnic Study of Atherosclerosis. Description: Larson, Nicholas B, et al. ABO blood group associations with markers of endothelial dysfunction in the Multi-Ethnic Study of Atherosclerosis. ''Atherosclerosis''. 2016 Aug; '''251''': 422-429
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease. Description: Verheijen, Jan, et al. A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease. ''Acta Neuropathol''. 2016 Aug; '''132''' (2):213-224
A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence. Description: Spain, S L, et al. A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence. ''Mol Psychiatry''. 2016 Aug; '''21''' (8):1145-51
Beyond main effects of gene-sets: harsh parenting moderates the association between a dopamine gene-set and child externalizing behavior. Description: Windhorst, Dafna A, et al. Beyond main effects of gene-sets: harsh parenting moderates the association between a dopamine gene-set and child externalizing behavior. ''Brain Behav''. 2016 Aug; '''6''' (8):e00498
Clinical features of Hispanic thyroid cancer cases and the role of known genetic variants on disease risk. Description: Estrada-Florez, Ana P, et al. Clinical features of Hispanic thyroid cancer cases and the role of known genetic variants on disease risk. ''Medicine (Baltimore)''. 2016 Aug; '''95''' (32):e4148
Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD. Description: Sun, Wei, et al. Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD. ''PLoS Genet''. 2016 Aug; '''12''' (8):e1006011
Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases. Description: Tsuiko, O, et al. Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases. ''Hum Reprod''. 2016 Aug; '''31''' (8):1913-25
Development and Validation of a High-Density SNP Genotyping Array for African Oil Palm. Description: Kwong, Qi Bin, et al. Development and Validation of a High-Density SNP Genotyping Array for African Oil Palm. ''Mol Plant''. 2016 Aug 1; '''9''' (8):1132-1141
Differential frequency of NKG2C/KLRC2 deletion in distinct African populations and susceptibility to Trachoma: a new method for imputation of KLRC2 genotypes from SNP genotyping data. Description: Goncalves, Adriana, et al. Differential frequency of NKG2C/KLRC2 deletion in distinct African populations and susceptibility to Trachoma: a new method for imputation of KLRC2 genotypes from SNP genotyping data. ''Hum Genet''. 2016 Aug; '''135''' (8):939-51
Doublesex and mab-3 related transcription factor 1 (DMRT1) is a sex-specific genetic determinant of childhood-onset asthma and is expressed in testis and macrophages. Description: Schieck, Maximilian, et al. Doublesex and mab-3 related transcription factor 1 (DMRT1) is a sex-specific genetic determinant of childhood-onset asthma and is expressed in testis and macrophages. ''J Allergy Clin Immunol''. 2016 Aug; '''138''' (2):421-31
Evidence for genetic regulation of the human parieto-occipital 10-Hz rhythmic activity. Description: Salmela, Elina, et al. Evidence for genetic regulation of the human parieto-occipital 10-Hz rhythmic activity. ''Eur J Neurosci''. 2016 Aug; '''44''' (3):1963-71
Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent. Description: Guo, Yan, et al. Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent. ''PLoS Med''. 2016 Aug; '''13''' (8):e1002105
Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis. Description: McIntosh, Andrew M, et al. Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis. ''PLoS Med''. 2016 Aug; '''13''' (8):e1002090
Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease. Description: Schott, Jonathan M, et al. Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease. ''Alzheimers Dement''. 2016 Aug; '''12''' (8):862-71
Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing. Description: Nicod, Jerome, et al. Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing. ''Nat Genet''. 2016 Aug; '''48''' (8):912-8
Genome-wide association study for semen quality traits in German Warmblood stallions. Description: Gottschalk, Maren, et al. Genome-wide association study for semen quality traits in German Warmblood stallions. ''Anim Reprod Sci''. 2016 Aug; '''171''': 81-6
Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape. Description: Cole, Joanne B, et al. Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape. ''PLoS Genet''. 2016 Aug; '''12''' (8):e1006174
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Description: Shaffer, John R, et al. Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. ''PLoS Genet''. 2016 Aug; '''12''' (8):e1006149
Genomic analysis of local variation and recent evolution in Plasmodium vivax. Description: Pearson, Richard D, et al. Genomic analysis of local variation and recent evolution in Plasmodium vivax. ''Nat Genet''. 2016 Aug; '''48''' (8):959-964
The genetic association of RUNX3 with ankylosing spondylitis can be explained by allele-specific effects on IRF4 recruitment that alter gene expression. Description: Vecellio, Matteo, et al. The genetic association of RUNX3 with ankylosing spondylitis can be explained by allele-specific effects on IRF4 recruitment that alter gene expression. ''Ann Rheum Dis''. 2016 Aug; '''75''' (8):1534-40
TREM2 p.R47H substitution is not associated with dementia with Lewy bodies. Description: Walton, Ronald L, et al. TREM2 p.R47H substitution is not associated with dementia with Lewy bodies. ''Neurol Genet''. 2016 Aug; '''2''' (4):e85
Variation of 46 Innate Immune Genes Evaluated for their Contribution in Pneumococcal Meningitis Susceptibility and Outcome. Description: Ferwerda, Bart, et al. Variation of 46 Innate Immune Genes Evaluated for their Contribution in Pneumococcal Meningitis Susceptibility and Outcome. ''EBioMedicine''. 2016 Aug; '''10''': 77-84
An enzyme in the kynurenine pathway that governs vulnerability to suicidal behavior by regulating excitotoxicity and neuroinflammation. Description: Brundin, L, et al. An enzyme in the kynurenine pathway that governs vulnerability to suicidal behavior by regulating excitotoxicity and neuroinflammation. ''Transl Psychiatry''. 2016 Aug 2; '''6''' (8):e865
Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension. Description: Liu, Xin, et al. Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension. ''Sci Rep''. 2016 Aug 2; '''6''': 30811
Variant detection and runs of homozygosity in next generation sequencing data elucidate the genetic background of Lundehund syndrome. Description: Metzger, Julia, et al. Variant detection and runs of homozygosity in next generation sequencing data elucidate the genetic background of Lundehund syndrome. ''BMC Genomics''. 2016 Aug 2; '''17''': 535
Genome-wide association study of aggressive behaviour in chicken. Description: Li, Zhenhui, et al. Genome-wide association study of aggressive behaviour in chicken. ''Sci Rep''. 2016 Aug 3; '''6''': 30981
Challenges in Translating GWAS Results to Clinical Care. Description: Scheinfeldt, Laura B, et al. Challenges in Translating GWAS Results to Clinical Care. ''Int J Mol Sci''. 2016 Aug 4; '''17''' (8):
Genome-wide association study revealed genomic regions related to white/red earlobe color trait in the Rhode Island Red chickens. Description: Nie, Changsheng, et al. Genome-wide association study revealed genomic regions related to white/red earlobe color trait in the Rhode Island Red chickens. ''BMC Genet''. 2016 Aug 5; '''17''' (1):115
Genetic mapping of canine fear and aggression. Description: Zapata, Isain, et al. Genetic mapping of canine fear and aggression. ''BMC Genomics''. 2016 Aug 8; '''17''': 572
Genetic markers of pigmentation are novel risk loci for uveal melanoma. Description: Ferguson, Robert, et al. Genetic markers of pigmentation are novel risk loci for uveal melanoma. ''Sci Rep''. 2016 Aug 8; '''6''': 31191
Genomic characterization of the Atlantic cod sex-locus. Description: Star, Bastiaan, et al. Genomic characterization of the Atlantic cod sex-locus. ''Sci Rep''. 2016 Aug 8; '''6''': 31235
Evaluation of VDR gene polymorphisms in Trypanosoma cruzi infection and chronic Chagasic cardiomyopathy. Description: Leon Rodriguez, Daniel A, et al. Evaluation of VDR gene polymorphisms in Trypanosoma cruzi infection and chronic Chagasic cardiomyopathy. ''Sci Rep''. 2016 Aug 9; '''6''': 31263
Impact of polygenic schizophrenia-related risk and hippocampal volumes on the onset of psychosis. Description: Harrisberger, F, et al. Impact of polygenic schizophrenia-related risk and hippocampal volumes on the onset of psychosis. ''Transl Psychiatry''. 2016 Aug 9; '''6''' (8):e868
The genetics of an early Neolithic pastoralist from the Zagros, Iran. Description: Gallego-Llorente, M, et al. The genetics of an early Neolithic pastoralist from the Zagros, Iran. ''Sci Rep''. 2016 Aug 9; '''6''': 31326
Epidermal growth factor gene is a newly identified candidate gene for gout. Description: Han, Lin, et al. Epidermal growth factor gene is a newly identified candidate gene for gout. ''Sci Rep''. 2016 Aug 10; '''6''': 31082
High density genome wide genotyping-by-sequencing and association identifies common and low frequency SNPs, and novel candidate genes influencing cow milk traits. Description: Ibeagha-Awemu, Eveline M, et al. High density genome wide genotyping-by-sequencing and association identifies common and low frequency SNPs, and novel candidate genes influencing cow milk traits. ''Sci Rep''. 2016 Aug 10; '''6''': 31109
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants. Description: Verma, Anurag, et al. eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants. ''BMC Med Genomics''. 2016 Aug 12; '''9 Suppl 1''': 32
Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease. Description: Nho, Kwangsik, et al. Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease. ''BMC Med Genomics''. 2016 Aug 12; '''9 Suppl 1''': 30
Identification of plexin A4 as a novel clusterin receptor links two Alzheimer's disease risk genes. Description: Kang, Silvia S, et al. Identification of plexin A4 as a novel clusterin receptor links two Alzheimer's disease risk genes. ''Hum Mol Genet''. 2016 Aug 15; '''25''' (16):3467-3475
Vitamin D receptor polymorphisms and Parkinson's disease in a Korean population: Revisited. Description: Kang, Seo Young, et al. Vitamin D receptor polymorphisms and Parkinson's disease in a Korean population: Revisited. ''Neurosci Lett''. 2016 Aug 15; '''628''': 230-5
Association study of polymorphisms in the ABO gene with ischemic stroke in the Chinese population. Description: Ling, Xiaoming, et al. Association study of polymorphisms in the ABO gene with ischemic stroke in the Chinese population. ''BMC Neurol''. 2016 Aug 19; '''16''' (1):146
A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease. Description: Hao, Jingcan, et al. A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease. ''Sci Rep''. 2016 Aug 22; '''6''': 31792
Crowdsourced assessment of common genetic contribution to predicting anti-TNF treatment response in rheumatoid arthritis. Description: Sieberts, Solveig K, et al. Crowdsourced assessment of common genetic contribution to predicting anti-TNF treatment response in rheumatoid arthritis. ''Nat Commun''. 2016 Aug 23; '''7''': 12460
Meta-dimensional data integration identifies critical pathways for susceptibility, tumorigenesis and progression of endometrial cancer. Description: Wei, Runmin, et al. Meta-dimensional data integration identifies critical pathways for susceptibility, tumorigenesis and progression of endometrial cancer. ''Oncotarget''. 2016 Aug 23; '''7''' (34):55249-55263
Pharmacogenomics of platinum-based chemotherapy response in NSCLC: a genotyping study and a pooled analysis. Description: Chen, Juan, et al. Pharmacogenomics of platinum-based chemotherapy response in NSCLC: a genotyping study and a pooled analysis. ''Oncotarget''. 2016 Aug 23; '''7''' (34):55741-55756
An RGS2 3'UTR polymorphism is associated with preeclampsia in overweight women. Description: Karppanen, Tiina, et al. An RGS2 3'UTR polymorphism is associated with preeclampsia in overweight women. ''BMC Genet''. 2016 Aug 24; '''17''' (1):121
Characterisation of the global transcriptional response to heat shock and the impact of individual genetic variation. Description: Humburg, Peter, et al. Characterisation of the global transcriptional response to heat shock and the impact of individual genetic variation. ''Genome Med''. 2016 Aug 24; '''8''' (1):87
Bioinformatics Identification of Drug Resistance-Associated Gene Pairs in Mycobacterium tuberculosis. Description: Cui, Ze-Jia, et al. Bioinformatics Identification of Drug Resistance-Associated Gene Pairs in Mycobacterium tuberculosis. ''Int J Mol Sci''. 2016 Aug 27; '''17''' (9):
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation. Description: Hannon, Eilis, et al. An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation. ''Genome Biol''. 2016 Aug 30; '''17''' (1):176
CRY1 and CRY2 genetic variants in seasonality: A longitudinal and cross-sectional study. Description: Kovanen, Leena, et al. CRY1 and CRY2 genetic variants in seasonality: A longitudinal and cross-sectional study. ''Psychiatry Res''. 2016 Aug 30; '''242''': 101-110
Genotype distribution-based inference of collective effects in genome-wide association studies: insights to age-related macular degeneration disease mechanism. Description: Woo, Hyung Jun, et al. Genotype distribution-based inference of collective effects in genome-wide association studies: insights to age-related macular degeneration disease mechanism. ''BMC Genomics''. 2016 Aug 30; '''17''': 695
A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia. Description: Moskowitz, Abby M, et al. A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia. ''Cold Spring Harb Mol Case Stud''. 2016 Sep; '''2''' (5):a000851
Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses. Description: Khawaja, Anthony P, et al. Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses. ''Invest Ophthalmol Vis Sci''. 2016 Sep 1; '''57''' (11):5046-5052
Bipartite Community Structure of eQTLs. Description: Platig, John, et al. Bipartite Community Structure of eQTLs. ''PLoS Comput Biol''. 2016 Sep; '''12''' (9):e1005033
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Description: Scott, Eric M, et al. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. ''Nat Genet''. 2016 Sep; '''48''' (9):1071-6
Complex interplay between neutral and adaptive evolution shaped differential genomic background and disease susceptibility along the Italian peninsula. Description: Sazzini, Marco, et al. Complex interplay between neutral and adaptive evolution shaped differential genomic background and disease susceptibility along the Italian peninsula. ''Sci Rep''. 2016 Sep 1; '''6''': 32513
Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium. Description: Verma, Shefali Setia, et al. Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium. ''PLoS Genet''. 2016 Sep; '''12''' (9):e1006186
Evolutionary Analyses of Hanwoo (Korean Cattle)-Specific Single-Nucleotide Polymorphisms and Genes Using Whole-Genome Resequencing Data of a Hanwoo Population. Description: Lee, Daehwan, et al. Evolutionary Analyses of Hanwoo (Korean Cattle)-Specific Single-Nucleotide Polymorphisms and Genes Using Whole-Genome Resequencing Data of a Hanwoo Population. ''Mol Cells''. 2016 Sep; '''39''' (9):692-8
Genetic Modifiers of Patent Ductus Arteriosus in Term Infants. Description: Patel, Priti M, et al. Genetic Modifiers of Patent Ductus Arteriosus in Term Infants. ''J Pediatr''. 2016 Sep; '''176''': 57-61.e1
Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans. Description: Melroy-Greif, Whitney E, et al. Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans. ''Drug Alcohol Depend''. 2016 Sep 1; '''166''': 249-53
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Description: Song, J, et al. Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. ''Mol Psychiatry''. 2016 Sep; '''21''' (9):1290-7
Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines. Description: McCarthy, Nina S, et al. Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines. ''Genom Data''. 2016 Sep; '''9''': 18-21
Mitochondrial genome association study with peripheral arterial disease and venous thromboembolism. Description: Abrantes, Patricia, et al. Mitochondrial genome association study with peripheral arterial disease and venous thromboembolism. ''Atherosclerosis''. 2016 Sep; '''252''': 97-105
No associations of a set of SNPs in the Vascular Endothelial Growth Factor (VEGF) and Matrix Metalloproteinase (MMP) genes with survival of colorectal cancer patients. Description: Dan, Lydia A, et al. No associations of a set of SNPs in the Vascular Endothelial Growth Factor (VEGF) and Matrix Metalloproteinase (MMP) genes with survival of colorectal cancer patients. ''Cancer Med''. 2016 Sep; '''5''' (9):2221-31
Pharmacogenetic predictors of toxicity to platinum based chemotherapy in non-small cell lung cancer patients. Description: Perez-Ramirez, Cristina, et al. Pharmacogenetic predictors of toxicity to platinum based chemotherapy in non-small cell lung cancer patients. ''Pharmacol Res''. 2016 Sep; '''111''': 877-884
Population-specific single-nucleotide polymorphism confers increased risk of venous thromboembolism in African Americans. Description: Daneshjou, Roxana, et al. Population-specific single-nucleotide polymorphism confers increased risk of venous thromboembolism in African Americans. ''Mol Genet Genomic Med''. 2016 Sep; '''4''' (5):513-20
Replication of Early B-cell Factor 1 (EBF1) Gene-by-psychosocial Stress Interaction Effects on Central Adiposity in a Korean Population. Description: Kim, Hyun-Jin, et al. Replication of Early B-cell Factor 1 (EBF1) Gene-by-psychosocial Stress Interaction Effects on Central Adiposity in a Korean Population. ''J Prev Med Public Health''. 2016 Sep; '''49''' (5):253-259
Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort. Description: Gonzalez, Suzanne, et al. Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort. ''Bipolar Disord''. 2016 Sep; '''18''' (6):520-527
Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden. Description: Ran, Caroline, et al. Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden. ''Neurobiol Aging''. 2016 Sep; '''45''': 212.e5-212.e11
THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome. Description: Tsai, Ellen A, et al. THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome. ''Cell Mol Gastroenterol Hepatol''. 2016 Sep; '''2''' (5):663-675.e2
The Genetic Basis of Host Preference and Resting Behavior in the Major African Malaria Vector, Anopheles arabiensis. Description: Main, Bradley J, et al. The Genetic Basis of Host Preference and Resting Behavior in the Major African Malaria Vector, Anopheles arabiensis. ''PLoS Genet''. 2016 Sep; '''12''' (9):e1006303
Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin. Description: Zhou, Kaixin, et al. Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin. ''Nat Genet''. 2016 Sep; '''48''' (9):1055-1059
Associations of genetic polymorphisms of the transporters organic cation transporter 2 (OCT2), multidrug and toxin extrusion 1 (MATE1), and ATP-binding cassette subfamily C member 2 (ABCC2) with platinum-based chemotherapy response and toxicity in non... Description: Qian, Chen-Yue, et al. Associations of genetic polymorphisms of the transporters organic cation transporter 2 (OCT2), multidrug and toxin extrusion 1 (MATE1), and ATP-binding cassette subfamily C member 2 (ABCC2) with platinum-based chemotherapy response and toxicity in non-small cell lung cancer patients. ''Chin J Cancer''. 2016 Sep 2; '''35''' (1):85
Integration of transcriptomic and genomic data suggests candidate mechanisms for APOE4-mediated pathogenic action in Alzheimer's disease. Description: Caberlotto, Laura, et al. Integration of transcriptomic and genomic data suggests candidate mechanisms for APOE4-mediated pathogenic action in Alzheimer's disease. ''Sci Rep''. 2016 Sep 2; '''6''': 32583
Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression. Description: Sirkis, Daniel W, et al. Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression. ''Acta Neuropathol Commun''. 2016 Sep 2; '''4''' (1):98
Relationship of TRIM5 and TRIM22 polymorphisms with liver disease and HCV clearance after antiviral therapy in HIV/HCV coinfected patients. Description: Medrano, Luz M, et al. Relationship of TRIM5 and TRIM22 polymorphisms with liver disease and HCV clearance after antiviral therapy in HIV/HCV coinfected patients. ''J Transl Med''. 2016 Sep 2; '''14''': 257
Association Study of a Proliferation-inducing Ligand, Spermatogenesis Associated 8, Platelet-derived Growth Factor Receptor-alpha, and POLB Polymorphisms with Systemic Lupus Erythematosus in Chinese Han Population. Description: Li, Ping, et al. Association Study of a Proliferation-inducing Ligand, Spermatogenesis Associated 8, Platelet-derived Growth Factor Receptor-alpha, and POLB Polymorphisms with Systemic Lupus Erythematosus in Chinese Han Population. ''Chin Med J (Engl)''. 2016 Sep 5; '''129''' (17):2085-90
Revealing misassembled segments in the bovine reference genome by high resolution linkage disequilibrium scan. Description: Utsunomiya, Adam T H, et al. Revealing misassembled segments in the bovine reference genome by high resolution linkage disequilibrium scan. ''BMC Genomics''. 2016 Sep 5; '''17''': 705
Genome-wide association study of antisocial personality disorder. Description: Rautiainen, M-R, et al. Genome-wide association study of antisocial personality disorder. ''Transl Psychiatry''. 2016 Sep 6; '''6''' (9):e883
An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed. Description: Forman, Oliver P, et al. An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed. ''G3 (Bethesda)''. 2016 Sep 8; '''6''' (9):2687-92
A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype. Description: Waluk, Dominik P, et al. A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype. ''G3 (Bethesda)''. 2016 Sep 8; '''6''' (9):2949-54
Domestication and Divergence of Saccharomyces cerevisiae Beer Yeasts. Description: Gallone, Brigida, et al. Domestication and Divergence of Saccharomyces cerevisiae Beer Yeasts. ''Cell''. 2016 Sep 8; '''166''' (6):1397-1410.e16
Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits. Description: Bakshi, Andrew, et al. Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits. ''Sci Rep''. 2016 Sep 8; '''6''': 32894
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles. Description: Timberlake, Andrew T, et al. Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles. ''Elife''. 2016 Sep 8; '''5''':
Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Description: Li, Q S, et al. Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. ''Transl Psychiatry''. 2016 Sep 13; '''6''' (9):e889
Exome genotyping, linkage disequilibrium and population structure in loblolly pine (Pinus taeda L.). Description: Lu, Mengmeng, et al. Exome genotyping, linkage disequilibrium and population structure in loblolly pine (Pinus taeda L.). ''BMC Genomics''. 2016 Sep 13; '''17''' (1):730
MS4A6A genotypes are associated with the atrophy rates of Alzheimer's disease related brain structures. Description: Ma, Jing, et al. MS4A6A genotypes are associated with the atrophy rates of Alzheimer's disease related brain structures. ''Oncotarget''. 2016 Sep 13; '''7''' (37):58779-58788
An integrative study identifies KCNC2 as a novel predisposing factor for childhood obesity and the risk of diabetes in the Korean population. Description: Hwang, Joo-Yeon, et al. An integrative study identifies KCNC2 as a novel predisposing factor for childhood obesity and the risk of diabetes in the Korean population. ''Sci Rep''. 2016 Sep 14; '''6''': 33043
Genetically Low Vitamin D Levels, Bone Mineral Density, and Bone Metabolism Markers: a Mendelian Randomisation Study. Description: Li, Shan-Shan, et al. Genetically Low Vitamin D Levels, Bone Mineral Density, and Bone Metabolism Markers: a Mendelian Randomisation Study. ''Sci Rep''. 2016 Sep 14; '''6''': 33202
Genetic basis of nitrogen use efficiency and yield stability across environments in winter rapeseed. Description: Bouchet, Anne-Sophie, et al. Genetic basis of nitrogen use efficiency and yield stability across environments in winter rapeseed. ''BMC Genet''. 2016 Sep 15; '''17''' (1):131
UGT2B4 previously implicated in the risk of breast cancer is associated with menarche timing in Ukrainian females. Description: Yermachenko, Anna, et al. UGT2B4 previously implicated in the risk of breast cancer is associated with menarche timing in Ukrainian females. ''Gene''. 2016 Sep 15; '''590''' (1):85-9
Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion. Description: Einarsdottir, Elisabet, et al. Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion. ''Sci Rep''. 2016 Sep 16; '''6''': 33240
Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples. Description: Wang, Jingwen, et al. Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples. ''Sci Rep''. 2016 Sep 16; '''6''': 33256
Fine-mapping markers of lung cancer susceptibility in a sub-region of chromosome 19q13.3 among Chinese. Description: Yin, Jiaoyang, et al. Fine-mapping markers of lung cancer susceptibility in a sub-region of chromosome 19q13.3 among Chinese. ''Oncotarget''. 2016 Sep 20; '''7''' (38):60929-60939
Genetic variants of genes in the Notch signaling pathway predict overall survival of non-small cell lung cancer patients in the PLCO study. Description: Xu, Yinghui, et al. Genetic variants of genes in the Notch signaling pathway predict overall survival of non-small cell lung cancer patients in the PLCO study. ''Oncotarget''. 2016 Sep 20; '''7''' (38):61716-61727
PADI4 has genetic susceptibility to gastric carcinoma and upregulates CXCR2, KRT14 and TNF-alpha expression levels. Description: Zheng, Yabing, et al. PADI4 has genetic susceptibility to gastric carcinoma and upregulates CXCR2, KRT14 and TNF-alpha expression levels. ''Oncotarget''. 2016 Sep 20; '''7''' (38):62159-62176
A hybrid expectation maximisation and MCMC sampling algorithm to implement Bayesian mixture model based genomic prediction and QTL mapping. Description: Wang, Tingting, et al. A hybrid expectation maximisation and MCMC sampling algorithm to implement Bayesian mixture model based genomic prediction and QTL mapping. ''BMC Genomics''. 2016 Sep 21; '''17''' (1):744
Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity. Description: Petros, Zelalem, et al. Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity. ''BMC Genomics''. 2016 Sep 26; '''17''' (1):755
Common genetic variations in cell cycle and DNA repair pathways associated with pediatric brain tumor susceptibility. Description: Adel Fahmideh, Maral, et al. Common genetic variations in cell cycle and DNA repair pathways associated with pediatric brain tumor susceptibility. ''Oncotarget''. 2016 Sep 27; '''7''' (39):63640-63650
Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients. Description: Reyes-Gibby, Cielito C, et al. Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients. ''Sci Rep''. 2016 Sep 27; '''6''': 34206
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene. Description: van Ingen, Gijs, et al. Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene. ''Nat Commun''. 2016 Sep 28; '''7''': 12792
Genome-wide association studies of immune, disease and production traits in indigenous chicken ecotypes. Description: Psifidi, Androniki, et al. Genome-wide association studies of immune, disease and production traits in indigenous chicken ecotypes. ''Genet Sel Evol''. 2016 Sep 29; '''48''' (1):74
Genomic Regions Associated With Interspecies Communication in Dogs Contain Genes Related to Human Social Disorders. Description: Persson, Mia E, et al. Genomic Regions Associated With Interspecies Communication in Dogs Contain Genes Related to Human Social Disorders. ''Sci Rep''. 2016 Sep 29; '''6''': 33439
Feralisation targets different genomic loci to domestication in the chicken. Description: Johnsson, M, et al. Feralisation targets different genomic loci to domestication in the chicken. ''Nat Commun''. 2016 Sep 30; '''7''': 12950
A 3'UTR polymorphism marks differential KLRG1 mRNA levels through disruption of a miR-584-5p binding site and associates with pemphigus foliaceus susceptibility. Description: Cipolla, Gabriel A, et al. A 3'UTR polymorphism marks differential KLRG1 mRNA levels through disruption of a miR-584-5p binding site and associates with pemphigus foliaceus susceptibility. ''Biochim Biophys Acta''. 2016 Oct; '''1859''' (10):1306-13
A Genome-wide Association Analysis in Four Populations Reveals Strong Genetic Heterogeneity For Birth Weight. Description: Luo, Tiane, et al. A Genome-wide Association Analysis in Four Populations Reveals Strong Genetic Heterogeneity For Birth Weight. ''Curr Genomics''. 2016 Oct; '''17''' (5):416-426
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records. Description: Hoffmann, Thomas J, et al. A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records. ''PLoS Genet''. 2016 Oct; '''12''' (10):e1006371
CD6 gene polymorphism rs17824933 is associated with multiple sclerosis in Indian population. Description: D'Cunha, Mary Anitha, et al. CD6 gene polymorphism rs17824933 is associated with multiple sclerosis in Indian population. ''Ann Indian Acad Neurol''. 2016 Oct-Dec; '''19''' (4):491-494
Collapsed methylation quantitative trait loci analysis for low frequency and rare variants. Description: Richardson, Tom G, et al. Collapsed methylation quantitative trait loci analysis for low frequency and rare variants. ''Hum Mol Genet''. 2016 Oct 1; '''25''' (19):4339-4349
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers. Description: Ghorbanoghli, Z, et al. Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers. ''Fam Cancer''. 2016 Oct; '''15''' (4):563-70
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction. Description: Hastings, Robert, et al. Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction. ''Circ Cardiovasc Genet''. 2016 Oct; '''9''' (5):426-435
Commonalities in Development of Pure Breeds and Population Isolates Revealed in the Genome of the Sardinian Fonni's Dog. Description: Dreger, Dayna L, et al. Commonalities in Development of Pure Breeds and Population Isolates Revealed in the Genome of the Sardinian Fonni's Dog. ''Genetics''. 2016 Oct; '''204''' (2):737-755
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing. Description: Kumar, Kishore R, et al. Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing. ''Neurogenetics''. 2016 Oct; '''17''' (4):265-270
Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study. Description: Nowak, Christoph, et al. Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study. ''PLoS Genet''. 2016 Oct; '''12''' (10):e1006379
Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set. Description: Kanai, Masahiro, et al. Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set. ''J Hum Genet''. 2016 Oct; '''61''' (10):861-866
Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland. Description: Trotta, Luca, et al. Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland. ''Eur J Hum Genet''. 2016 Oct; '''24''' (10):1473-8
Gene and Network Analysis of Common Variants Reveals Novel Associations in Multiple Complex Diseases. Description: Nakka, Priyanka, et al. Gene and Network Analysis of Common Variants Reveals Novel Associations in Multiple Complex Diseases. ''Genetics''. 2016 Oct; '''204''' (2):783-798
Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families. Description: Levine, Adam P, et al. Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families. ''Gastroenterology''. 2016 Oct; '''151''' (4):698-709
Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density. Description: Pei, Yu-Fang, et al. Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density. ''Bone''. 2016 Oct; '''91''': 1-10
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis. Description: Gharahkhani, Puya, et al. Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis. ''Lancet Oncol''. 2016 Oct; '''17''' (10):1363-1373
Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits. Description: Teumer, Alexander, et al. Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits. ''Aging Cell''. 2016 Oct; '''15''' (5):811-24
Local Adaptation of Sun-Exposure-Dependent Gene Expression Regulation in Human Skin. Description: Kita, Ryosuke, et al. Local Adaptation of Sun-Exposure-Dependent Gene Expression Regulation in Human Skin. ''PLoS Genet''. 2016 Oct; '''12''' (10):e1006382
MMP-2 gene polymorphisms are associated with type A aortic dissection and aortic diameters in patients. Description: Liu, Ou, et al. MMP-2 gene polymorphisms are associated with type A aortic dissection and aortic diameters in patients. ''Medicine (Baltimore)''. 2016 Oct; '''95''' (42):e5175
No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. Description: Johnson, Emma C, et al. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. ''PLoS Genet''. 2016 Oct; '''12''' (10):e1006343
Personality Polygenes, Positive Affect, and Life Satisfaction. Description: Weiss, Alexander, et al. Personality Polygenes, Positive Affect, and Life Satisfaction. ''Twin Res Hum Genet''. 2016 Oct; '''19''' (5):407-17
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance. Description: Kiando, Soto Romuald, et al. PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance. ''PLoS Genet''. 2016 Oct; '''12''' (10):e1006367
Polygenic risk scores for cigarettes smoked per day do not generalize to a Native American population. Description: Otto, Jacqueline M, et al. Polygenic risk scores for cigarettes smoked per day do not generalize to a Native American population. ''Drug Alcohol Depend''. 2016 Oct 1; '''167''': 95-102
Soluble CD93 Is Involved in Metabolic Dysregulation but Does Not Influence Carotid Intima-Media Thickness. Description: Strawbridge, Rona J, et al. Soluble CD93 Is Involved in Metabolic Dysregulation but Does Not Influence Carotid Intima-Media Thickness. ''Diabetes''. 2016 Oct; '''65''' (10):2888-99
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Description: Ehret, Georg B, et al. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. ''Nat Genet''. 2016 Oct; '''48''' (10):1171-1184
Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children. Description: Kemp, John P, et al. Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children. ''Int J Epidemiol''. 2016 Oct; '''45''' (5):1560-1572
Whole-exome sequencing in an isolated population from the Dalmatian island of Vis. Description: Jeroncic, Ana, et al. Whole-exome sequencing in an isolated population from the Dalmatian island of Vis. ''Eur J Hum Genet''. 2016 Oct; '''24''' (10):1479-87
Whole-Genome Sequencing of Native Sheep Provides Insights into Rapid Adaptations to Extreme Environments. Description: Yang, Ji, et al. Whole-Genome Sequencing of Native Sheep Provides Insights into Rapid Adaptations to Extreme Environments. ''Mol Biol Evol''. 2016 Oct; '''33''' (10):2576-92
Genome-wide association analysis identifies genetic loci associated with resistance to multiple antimalarials in Plasmodium falciparum from China-Myanmar border. Description: Wang, Zenglei, et al. Genome-wide association analysis identifies genetic loci associated with resistance to multiple antimalarials in Plasmodium falciparum from China-Myanmar border. ''Sci Rep''. 2016 Oct 3; '''6''': 33891
Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study. Description: Dankowski, Theresa, et al. Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study. ''BMC Gastroenterol''. 2016 Oct 3; '''16''' (1):118
A functional variant of TLR10 modifies the activity of NFkB and may help predict a worse prognosis in patients with rheumatoid arthritis. Description: Torices, Silvia, et al. A functional variant of TLR10 modifies the activity of NFkB and may help predict a worse prognosis in patients with rheumatoid arthritis. ''Arthritis Res Ther''. 2016 Oct 4; '''18''' (1):221
SP110 and PMP22 polymorphisms are associated with tuberculosis risk in a Chinese-Tibetan population. Description: Ren, Guoxia, et al. SP110 and PMP22 polymorphisms are associated with tuberculosis risk in a Chinese-Tibetan population. ''Oncotarget''. 2016 Oct 4; '''7''' (40):66100-66108
Identification of selective sweeps reveals divergent selection between Chinese Holstein and Simmental cattle populations. Description: Chen, Minhui, et al. Identification of selective sweeps reveals divergent selection between Chinese Holstein and Simmental cattle populations. ''Genet Sel Evol''. 2016 Oct 6; '''48''' (1):76
The genetic map of goldfish (Carassius auratus) provided insights to the divergent genome evolutions in the Cyprinidae family. Description: Kuang, You-Yi, et al. The genetic map of goldfish (Carassius auratus) provided insights to the divergent genome evolutions in the Cyprinidae family. ''Sci Rep''. 2016 Oct 6; '''6''': 34849
A Novel Genetic Variant in Long Non-coding RNA Gene NEXN-AS1 is Associated with Risk of Lung Cancer. Description: Yuan, Hua, et al. A Novel Genetic Variant in Long Non-coding RNA Gene NEXN-AS1 is Associated with Risk of Lung Cancer. ''Sci Rep''. 2016 Oct 7; '''6''': 34234
Identifying molecular signatures of hypoxia adaptation from sex chromosomes: A case for Tibetan Mastiff based on analyses of X chromosome. Description: Wu, Hong, et al. Identifying molecular signatures of hypoxia adaptation from sex chromosomes: A case for Tibetan Mastiff based on analyses of X chromosome. ''Sci Rep''. 2016 Oct 7; '''6''': 35004
Genome-wide association study for hereditary ataxia in the Parson Russell Terrier and DNA-testing for ataxia-associated mutations in the Parson and Jack Russell Terrier. Description: Gast, Alana Christina, et al. Genome-wide association study for hereditary ataxia in the Parson Russell Terrier and DNA-testing for ataxia-associated mutations in the Parson and Jack Russell Terrier. ''BMC Vet Res''. 2016 Oct 10; '''12''' (1):225
Genomics-assisted characterization of a breeding collection of Apios americana, an edible tuberous legume. Description: Belamkar, Vikas, et al. Genomics-assisted characterization of a breeding collection of Apios americana, an edible tuberous legume. ''Sci Rep''. 2016 Oct 10; '''6''': 34908
The Demographic Development of the First Farmers in Anatolia. Description: Kilinc, Gulsah Merve, et al. The Demographic Development of the First Farmers in Anatolia. ''Curr Biol''. 2016 Oct 10; '''26''' (19):2659-2666
A genome-wide association study in multiple system atrophy. Description: Sailer, Anna, et al. A genome-wide association study in multiple system atrophy. ''Neurology''. 2016 Oct 11; '''87''' (15):1591-1598
Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases. Description: Allen, Mariet, et al. Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases. ''Sci Data''. 2016 Oct 11; '''3''': 160089
A Genome-Wide Association Study Identifies Multiple Regions Associated with Head Size in Catfish. Description: Geng, Xin, et al. A Genome-Wide Association Study Identifies Multiple Regions Associated with Head Size in Catfish. ''G3 (Bethesda)''. 2016 Oct 13; '''6''' (10):3389-3398
Preservation Analysis of Macrophage Gene Coexpression Between Human and Mouse Identifies PARK2 as a Genetically Controlled Master Regulator of Oxidative Phosphorylation in Humans. Description: Codoni, Veronica, et al. Preservation Analysis of Macrophage Gene Coexpression Between Human and Mouse Identifies PARK2 as a Genetically Controlled Master Regulator of Oxidative Phosphorylation in Humans. ''G3 (Bethesda)''. 2016 Oct 13; '''6''' (10):3361-3371
Transcriptional regulation of PNPLA3 and its impact on susceptibility to nonalcoholic fatty liver Disease (NAFLD) in humans. Description: Liu, Wanqing, et al. Transcriptional regulation of PNPLA3 and its impact on susceptibility to nonalcoholic fatty liver Disease (NAFLD) in humans. ''Aging (Albany NY)''. 2016 Oct 13; '''9''' (1):26-40
Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients. Description: Grzegorzewska, Alicja E, et al. Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients. ''Sci Rep''. 2016 Oct 14; '''6''': 35188
Pharmacogenomic Study of Clozapine-Induced Agranulocytosis/Granulocytopenia in a Japanese Population. Description: Saito, Takeo, et al. Pharmacogenomic Study of Clozapine-Induced Agranulocytosis/Granulocytopenia in a Japanese Population. ''Biol Psychiatry''. 2016 Oct 15; '''80''' (8):636-42
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations. Description: Wang, Yi, et al. Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations. ''J Exp Med''. 2016 Oct 17; '''213''' (11):2413-2435
Exome chip analyses in adult attention deficit hyperactivity disorder. Description: Zayats, T, et al. Exome chip analyses in adult attention deficit hyperactivity disorder. ''Transl Psychiatry''. 2016 Oct 18; '''6''' (10):e923
A genome-wide assessment of genetic diversity and population structure of Korean native cattle breeds. Description: Sharma, Aditi, et al. A genome-wide assessment of genetic diversity and population structure of Korean native cattle breeds. ''BMC Genet''. 2016 Oct 20; '''17''' (1):139
Genetic Adaptation and Neandertal Admixture Shaped the Immune System of Human Populations. Description: Quach, Helene, et al. Genetic Adaptation and Neandertal Admixture Shaped the Immune System of Human Populations. ''Cell''. 2016 Oct 20; '''167''' (3):643-656.e17
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism. Description: Wang, Yanping, et al. Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism. ''BMC Urol''. 2016 Oct 21; '''16''' (1):62
Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort. Description: Landini, Martina, et al. Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort. ''Int J Mol Sci''. 2016 Oct 22; '''17''' (10):
Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer. Description: Hampras, Shalaka S, et al. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer. ''Oncotarget''. 2016 Oct 25; '''7''' (43):69097-69110
Polygenic sex determination in the cichlid fish Astatotilapia burtoni. Description: Roberts, Natalie B, et al. Polygenic sex determination in the cichlid fish Astatotilapia burtoni. ''BMC Genomics''. 2016 Oct 26; '''17''' (1):835
Genotyping-by-sequencing provides the discriminating power to investigate the subspecies of Daucus carota (Apiaceae). Description: Arbizu, Carlos I, et al. Genotyping-by-sequencing provides the discriminating power to investigate the subspecies of Daucus carota (Apiaceae). ''BMC Evol Biol''. 2016 Oct 28; '''16''' (1):234
On the performance of tests for the detection of signatures of selection: a case study with the Spanish autochthonous beef cattle populations. Description: Gonzalez-Rodriguez, Aldemar, et al. On the performance of tests for the detection of signatures of selection: a case study with the Spanish autochthonous beef cattle populations. ''Genet Sel Evol''. 2016 Oct 28; '''48''' (1):81
Candidate gene study reveals DRD1 and DRD2 as putative interacting risk factors for youth depression. Description: Corrales, Eyleen, et al. Candidate gene study reveals DRD1 and DRD2 as putative interacting risk factors for youth depression. ''Psychiatry Res''. 2016 Oct 30; '''244''': 71-7
A childhood acute lymphoblastic leukemia genome-wide association study identifies novel sex-specific risk variants. Description: Singh, Sandeep K, et al. A childhood acute lymphoblastic leukemia genome-wide association study identifies novel sex-specific risk variants. ''Medicine (Baltimore)''. 2016 Nov; '''95''' (46):e5300
A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans. Description: Pazderska, Agnieszka, et al. A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans. ''J Clin Endocrinol Metab''. 2016 Nov; '''101''' (11):3865-3869
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. Description: Bronson, Paola G, et al. Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. ''Nat Genet''. 2016 Nov; '''48''' (11):1425-1429
Contribution of oxytocin receptor polymorphisms to amygdala activation in schizophrenia spectrum disorders. Description: Haram, Marit, et al. Contribution of oxytocin receptor polymorphisms to amygdala activation in schizophrenia spectrum disorders. ''BJPsych Open''. 2016 Nov; '''2''' (6):353-358
Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. Description: Herold, C, et al. Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. ''Mol Psychiatry''. 2016 Nov; '''21''' (11):1608-1612
Gene expression elucidates functional impact of polygenic risk for schizophrenia. Description: Fromer, Menachem, et al. Gene expression elucidates functional impact of polygenic risk for schizophrenia. ''Nat Neurosci''. 2016 Nov; '''19''' (11):1442-1453
Genetic polymorphisms of CYP3A4 among Chinese patients with steroid-induced osteonecrosis of the femoral head. Description: Wang, Yuan, et al. Genetic polymorphisms of CYP3A4 among Chinese patients with steroid-induced osteonecrosis of the femoral head. ''Medicine (Baltimore)''. 2016 Nov; '''95''' (44):e5332
Genetic variants in CETP increase risk of intracerebral hemorrhage. Description: Anderson, Christopher D, et al. Genetic variants in CETP increase risk of intracerebral hemorrhage. ''Ann Neurol''. 2016 Nov; '''80''' (5):730-740
Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. Description: Jin, Ying, et al. Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. ''Nat Genet''. 2016 Nov; '''48''' (11):1418-1424
Genome-wide DNA methylation analysis in multiple tissues in primary Sjogren's syndrome reveals regulatory effects at interferon-induced genes. Description: Imgenberg-Kreuz, Juliana, et al. Genome-wide DNA methylation analysis in multiple tissues in primary Sjogren's syndrome reveals regulatory effects at interferon-induced genes. ''Ann Rheum Dis''. 2016 Nov; '''75''' (11):2029-2036
Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs. Description: Kukita, Yoji, et al. Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs. ''Cold Spring Harb Mol Case Stud''. 2016 Nov; '''2''' (6):a001032
Identifying significant gene-environment interactions using a combination of screening testing and hierarchical false discovery rate control. Description: Frost, H Robert, et al. Identifying significant gene-environment interactions using a combination of screening testing and hierarchical false discovery rate control. ''Genet Epidemiol''. 2016 Nov; '''40''' (7):544-557
Neurotrophin Genes and Antidepressant-Worsening Suicidal Ideation: A Prospective Case-Control Study. Description: Voegeli, Geraldine, et al. Neurotrophin Genes and Antidepressant-Worsening Suicidal Ideation: A Prospective Case-Control Study. ''Int J Neuropsychopharmacol''. 2016 Nov; '''19''' (11):
Pleiotropic Mechanisms Indicated for Sex Differences in Autism. Description: Mitra, Ileena, et al. Pleiotropic Mechanisms Indicated for Sex Differences in Autism. ''PLoS Genet''. 2016 Nov; '''12''' (11):e1006425
TGFbeta regulates persistent neuroinflammation by controlling Th1 polarization and ROS production via monocyte-derived dendritic cells. Description: Parsa, Roham, et al. TGFbeta regulates persistent neuroinflammation by controlling Th1 polarization and ROS production via monocyte-derived dendritic cells. ''Glia''. 2016 Nov; '''64''' (11):1925-37
Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies. Description: Martinon-Torres, Federico, et al. Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies. ''Sci Rep''. 2016 Nov 2; '''6''': 35842
Performance Metrics for Selecting Single Nucleotide Polymorphisms in Late-onset Alzheimer's Disease. Description: Chen, Yen-Ching, et al. Performance Metrics for Selecting Single Nucleotide Polymorphisms in Late-onset Alzheimer's Disease. ''Sci Rep''. 2016 Nov 2; '''6''': 36155
Leveraging genetically simple traits to identify small-effect variants for complex phenotypes. Description: Kemper, K E, et al. Leveraging genetically simple traits to identify small-effect variants for complex phenotypes. ''BMC Genomics''. 2016 Nov 3; '''17''' (1):858
A sequence variant associating with educational attainment also affects childhood cognition. Description: Gunnarsson, Bjarni, et al. A sequence variant associating with educational attainment also affects childhood cognition. ''Sci Rep''. 2016 Nov 4; '''6''': 36189
Genomic Variants Associated with Resistance to High Fat Diet Induced Obesity in a Primate Model. Description: Harris, R Alan, et al. Genomic Variants Associated with Resistance to High Fat Diet Induced Obesity in a Primate Model. ''Sci Rep''. 2016 Nov 4; '''6''': 36123
Sequence variants selected from a multi-breed GWAS can improve the reliability of genomic predictions in dairy cattle. Description: van den Berg, Irene, et al. Sequence variants selected from a multi-breed GWAS can improve the reliability of genomic predictions in dairy cattle. ''Genet Sel Evol''. 2016 Nov 4; '''48''' (1):83
Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicities. Description: Lindstrom, Sara, et al. Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicities. ''Breast Cancer Res''. 2016 Nov 5; '''18''' (1):109
A Pedigree-Based Map of Recombination in the Domestic Dog Genome. Description: Campbell, Christopher L, et al. A Pedigree-Based Map of Recombination in the Domestic Dog Genome. ''G3 (Bethesda)''. 2016 Nov 8; '''6''' (11):3517-3524
Association of ATP6V1B2 rs1106634 with lifetime risk of depression and hippocampal neurocognitive deficits: possible novel mechanisms in the etiopathology of depression. Description: Gonda, X, et al. Association of ATP6V1B2 rs1106634 with lifetime risk of depression and hippocampal neurocognitive deficits: possible novel mechanisms in the etiopathology of depression. ''Transl Psychiatry''. 2016 Nov 8; '''6''' (11):e945
Genome-wide association study of 12 agronomic traits in peach. Description: Cao, Ke, et al. Genome-wide association study of 12 agronomic traits in peach. ''Nat Commun''. 2016 Nov 8; '''7''': 13246
Genomic continuity of Argentinean Mennonites. Description: Pardo-Seco, Jacobo, et al. Genomic continuity of Argentinean Mennonites. ''Sci Rep''. 2016 Nov 8; '''6''': 36392
Chitinase-3-like 1 protein (CHI3L1) locus influences cerebrospinal fluid levels of YKL-40. Description: Deming, Yuetiva, et al. Chitinase-3-like 1 protein (CHI3L1) locus influences cerebrospinal fluid levels of YKL-40. ''BMC Neurol''. 2016 Nov 10; '''16''' (1):217
A targeted genome association study examining transient receptor potential ion channels, acetylcholine receptors, and adrenergic receptors in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis. Description: Johnston, Samantha, et al. A targeted genome association study examining transient receptor potential ion channels, acetylcholine receptors, and adrenergic receptors in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis. ''BMC Med Genet''. 2016 Nov 11; '''17''' (1):79
Assessing genotype-phenotype associations in three dorsal colour morphs in the meadow spittlebug Philaenus spumarius (L.) (Hemiptera: Aphrophoridae) using genomic and transcriptomic resources. Description: Rodrigues, Ana S B, et al. Assessing genotype-phenotype associations in three dorsal colour morphs in the meadow spittlebug Philaenus spumarius (L.) (Hemiptera: Aphrophoridae) using genomic and transcriptomic resources. ''BMC Genet''. 2016 Nov 15; '''17''' (1):144
Defining the role of corticotropin releasing factor binding protein in alcohol consumption. Description: Haass-Koffler, C L, et al. Defining the role of corticotropin releasing factor binding protein in alcohol consumption. ''Transl Psychiatry''. 2016 Nov 15; '''6''' (11):e953
IMPA2 polymorphisms and risk of ischemic stroke in a northwest Han Chinese population. Description: Ma, Qiaoya, et al. IMPA2 polymorphisms and risk of ischemic stroke in a northwest Han Chinese population. ''Oncotarget''. 2016 Nov 15; '''7''' (46):75273-75278
Insight into the genetic composition of South African Sanga cattle using SNP data from cattle breeds worldwide. Description: Makina, Sithembile O, et al. Insight into the genetic composition of South African Sanga cattle using SNP data from cattle breeds worldwide. ''Genet Sel Evol''. 2016 Nov 15; '''48''' (1):88
LAMPLINK: detection of statistically significant SNP combinations from GWAS data. Description: Terada, Aika, et al. LAMPLINK: detection of statistically significant SNP combinations from GWAS data. ''Bioinformatics''. 2016 Nov 15; '''32''' (22):3513-3515
Multidimensional heritability analysis of neuroanatomical shape. Description: Ge, Tian, et al. Multidimensional heritability analysis of neuroanatomical shape. ''Nat Commun''. 2016 Nov 15; '''7''': 13291
Reconstructing Druze population history. Description: Marshall, Scarlett, et al. Reconstructing Druze population history. ''Sci Rep''. 2016 Nov 16; '''6''': 35837
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells. Description: Chen, Lu, et al. Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells. ''Cell''. 2016 Nov 17; '''167''' (5):1398-1414.e24
Salinity tolerance loci revealed in rice using high-throughput non-invasive phenotyping. Description: Al-Tamimi, Nadia, et al. Salinity tolerance loci revealed in rice using high-throughput non-invasive phenotyping. ''Nat Commun''. 2016 Nov 17; '''7''': 13342
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Description: Astle, William J, et al. The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. ''Cell''. 2016 Nov 17; '''167''' (5):1415-1429.e19
Genomic contributors to atrial electroanatomical remodeling and atrial fibrillation progression: Pathway enrichment analysis of GWAS data. Description: Husser, Daniela, et al. Genomic contributors to atrial electroanatomical remodeling and atrial fibrillation progression: Pathway enrichment analysis of GWAS data. ''Sci Rep''. 2016 Nov 18; '''6''': 36630
Pooled genome wide association detects association upstream of FCRL3 with Graves' disease. Description: Khong, Jwu Jin, et al. Pooled genome wide association detects association upstream of FCRL3 with Graves' disease. ''BMC Genomics''. 2016 Nov 18; '''17''' (1):939
Re-evaluating data quality of dog mitochondrial, Y chromosomal, and autosomal SNPs genotyped by SNP array. Description: O Otecko, Newton, et al. Re-evaluating data quality of dog mitochondrial, Y chromosomal, and autosomal SNPs genotyped by SNP array. ''Zool Res''. 2016 Nov 18; '''37''' (6):356-360
Genome-wide association study (GWAS) reveals the genetic architecture of four husk traits in maize. Description: Cui, Zhenhai, et al. Genome-wide association study (GWAS) reveals the genetic architecture of four husk traits in maize. ''BMC Genomics''. 2016 Nov 21; '''17''' (1):946
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. Description: Ried, Janina S, et al. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. ''Nat Commun''. 2016 Nov 23; '''7''': 13357
Common variants in the PARL and PINK1 genes increase the risk to leprosy in Han Chinese from South China. Description: Wang, Dong, et al. Common variants in the PARL and PINK1 genes increase the risk to leprosy in Han Chinese from South China. ''Sci Rep''. 2016 Nov 23; '''6''': 37086
An ethnically relevant consensus Korean reference genome is a step towards personal reference genomes. Description: Cho, Yun Sung, et al. An ethnically relevant consensus Korean reference genome is a step towards personal reference genomes. ''Nat Commun''. 2016 Nov 24; '''7''': 13637
Rapid scoring of genes in microbial pan-genome-wide association studies with Scoary. Description: Brynildsrud, Ola, et al. Rapid scoring of genes in microbial pan-genome-wide association studies with Scoary. ''Genome Biol''. 2016 Nov 25; '''17''' (1):238
Characterization of variations in IL23A and IL23R genes: possible roles in multiple sclerosis and other neuroinflammatory demyelinating diseases. Description: Li, Fei-Feng, et al. Characterization of variations in IL23A and IL23R genes: possible roles in multiple sclerosis and other neuroinflammatory demyelinating diseases. ''Aging (Albany NY)''. 2016 Nov 26; '''8''' (11):2734-2746
GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration. Description: Riaz, Moeen, et al. GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration. ''Sci Rep''. 2016 Nov 28; '''6''': 37924
Multi-strategy genome-wide association studies identify the DCAF16-NCAPG region as a susceptibility locus for average daily gain in cattle. Description: Zhang, Wengang, et al. Multi-strategy genome-wide association studies identify the DCAF16-NCAPG region as a susceptibility locus for average daily gain in cattle. ''Sci Rep''. 2016 Nov 28; '''6''': 38073
Differentially expressed miRNAs in triple negative breast cancer between African-American and non-Hispanic white women. Description: Sugita, Bruna, et al. Differentially expressed miRNAs in triple negative breast cancer between African-American and non-Hispanic white women. ''Oncotarget''. 2016 Nov 29; '''7''' (48):79274-79291
Evaluation of association of common variants in HTR1A and HTR5A with schizophrenia and executive function. Description: Guan, Fanglin, et al. Evaluation of association of common variants in HTR1A and HTR5A with schizophrenia and executive function. ''Sci Rep''. 2016 Nov 29; '''6''': 38048
Genetic polymorphisms of FAS and EVER genes in a Greek population and their susceptibility to cervical cancer: a case control study. Description: Pavlidou, Evangelia, et al. Genetic polymorphisms of FAS and EVER genes in a Greek population and their susceptibility to cervical cancer: a case control study. ''BMC Cancer''. 2016 Nov 29; '''16''' (1):923
Multi-variant study of obesity risk genes in African Americans: The Jackson Heart Study. Description: Liu, Shijian, et al. Multi-variant study of obesity risk genes in African Americans: The Jackson Heart Study. ''Gene''. 2016 Nov 30; '''593''' (2):315-21
An efficient linear mixed model framework for meta-analytic association studies across multiple contexts. Description: Jew, Brandon, et al. An efficient linear mixed model framework for meta-analytic association studies across multiple contexts. ''Lebniz Int Proc Inform''. 2016 Dec; '''2016''':
Activating KIR2DS4 Is Expressed by Uterine NK Cells and Contributes to Successful Pregnancy. Description: Kennedy, Philippa R, et al. Activating KIR2DS4 Is Expressed by Uterine NK Cells and Contributes to Successful Pregnancy. ''J Immunol''. 2016 Dec 1; '''197''' (11):4292-4300
A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants. Description: Bacchelli, Elena, et al. A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants. ''J Headache Pain''. 2016 Dec; '''17''' (1):114
A global test for gene-gene interactions based on random matrix theory. Description: Frost, H Robert, et al. A global test for gene-gene interactions based on random matrix theory. ''Genet Epidemiol''. 2016 Dec; '''40''' (8):689-701
A GWAS follow-up of obesity-related SNPs in SYPL2 reveals sex-specific association with hip circumference. Description: de Toro-Martin, J, et al. A GWAS follow-up of obesity-related SNPs in SYPL2 reveals sex-specific association with hip circumference. ''Obes Sci Pract''. 2016 Dec; '''2''' (4):407-414
An ankylosing spondylitis-associated genetic variant in the IL23R-IL12RB2 intergenic region modulates enhancer activity and is associated with increased Th1-cell differentiation. Description: Roberts, Amity R, et al. An ankylosing spondylitis-associated genetic variant in the IL23R-IL12RB2 intergenic region modulates enhancer activity and is associated with increased Th1-cell differentiation. ''Ann Rheum Dis''. 2016 Dec; '''75''' (12):2150-2156
A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies. Description: Plassais, Jocelyn, et al. A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies. ''PLoS Genet''. 2016 Dec; '''12''' (12):e1006482
Assessing polar bear (Ursus maritimus) population structure in the Hudson Bay region using SNPs. Description: Viengkone, Michelle, et al. Assessing polar bear (Ursus maritimus) population structure in the Hudson Bay region using SNPs. ''Ecol Evol''. 2016 Dec; '''6''' (23):8474-8484
Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population. Description: Sun, Ying, et al. Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population. ''J Clin Res Pediatr Endocrinol''. 2016 Dec 1; '''8''' (4):405-410
Autosomal genetic control of human gene expression does not differ across the sexes. Description: Kassam, Irfahan, et al. Autosomal genetic control of human gene expression does not differ across the sexes. ''Genome Biol''. 2016 Dec 1; '''17''' (1):248
Demographic Trends in Korean Native Cattle Explained Using Bovine SNP50 Beadchip. Description: Sharma, Aditi, et al. Demographic Trends in Korean Native Cattle Explained Using Bovine SNP50 Beadchip. ''Genomics Inform''. 2016 Dec; '''14''' (4):230-233
Detecting Positive Selection of Korean Native Goat Populations Using Next-Generation Sequencing. Description: Lee, Wonseok, et al. Detecting Positive Selection of Korean Native Goat Populations Using Next-Generation Sequencing. ''Mol Cells''. 2016 Dec; '''39''' (12):862-868
Effects of Single Nucleotide Polymorphism Marker Density on Haplotype Block Partition. Description: Kim, Sun Ah, et al. Effects of Single Nucleotide Polymorphism Marker Density on Haplotype Block Partition. ''Genomics Inform''. 2016 Dec; '''14''' (4):196-204
Genetic Diversity and Population Structure of Rice Varieties Cultivated in Temperate Regions. Description: Reig-Valiente, Juan L, et al. Genetic Diversity and Population Structure of Rice Varieties Cultivated in Temperate Regions. ''Rice (N Y)''. 2016 Dec; '''9''' (1):58
Genetic risk score based on the prevalence of vertebral fracture in Japanese women with osteoporosis. Description: Zhou, Heying, et al. Genetic risk score based on the prevalence of vertebral fracture in Japanese women with osteoporosis. ''Bone Rep''. 2016 Dec; '''5''': 168-172
Genetics of structural connectivity and information processing in the brain. Description: Giddaluru, Sudheer, et al. Genetics of structural connectivity and information processing in the brain. ''Brain Struct Funct''. 2016 Dec; '''221''' (9):4643-4661
genipe: an automated genome-wide imputation pipeline with automatic reporting and statistical tools. Description: Lemieux Perreault, Louis-Philippe, et al. genipe: an automated genome-wide imputation pipeline with automatic reporting and statistical tools. ''Bioinformatics''. 2016 Dec 1; '''32''' (23):3661-3663
Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Description: Lesseur, Corina, et al. Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. ''Nat Genet''. 2016 Dec; '''48''' (12):1544-1550
Genome-wide association study in essential tremor identifies three new loci. Description: Muller, Stefanie H, et al. Genome-wide association study in essential tremor identifies three new loci. ''Brain''. 2016 Dec; '''139''' (Pt 12):3163-3169
Genomic prediction using preselected DNA variants from a GWAS with whole-genome sequence data in Holstein-Friesian cattle. Description: Veerkamp, Roel F, et al. Genomic prediction using preselected DNA variants from a GWAS with whole-genome sequence data in Holstein-Friesian cattle. ''Genet Sel Evol''. 2016 Dec 1; '''48''' (1):95
Identification of Risk Pathways and Functional Modules for Coronary Artery Disease Based on Genome-wide SNP Data. Description: Zhao, Xiang, et al. Identification of Risk Pathways and Functional Modules for Coronary Artery Disease Based on Genome-wide SNP Data. ''Genomics Proteomics Bioinformatics''. 2016 Dec; '''14''' (6):349-356
Identification of Susceptible Loci and Enriched Pathways for Bipolar II Disorder Using Genome-Wide Association Studies. Description: Kao, Chung-Feng, et al. Identification of Susceptible Loci and Enriched Pathways for Bipolar II Disorder Using Genome-Wide Association Studies. ''Int J Neuropsychopharmacol''. 2016 Dec; '''19''' (12):
IREB2, CHRNA5, CHRNA3, FAM13A & hedgehog interacting protein genes polymorphisms & risk of chronic obstructive pulmonary disease in Tatar population from Russia. Description: Korytina, Gulnaz Faritovna, et al. IREB2, CHRNA5, CHRNA3, FAM13A & hedgehog interacting protein genes polymorphisms & risk of chronic obstructive pulmonary disease in Tatar population from Russia. ''Indian J Med Res''. 2016 Dec; '''144''' (6):865-876
Population Dynamics Among six Major Groups of the Oryza rufipogon Species Complex, Wild Relative of Cultivated Asian Rice. Description: Kim, HyunJung, et al. Population Dynamics Among six Major Groups of the Oryza rufipogon Species Complex, Wild Relative of Cultivated Asian Rice. ''Rice (N Y)''. 2016 Dec; '''9''' (1):56
Single nucleotide polymorphisms and genotypes of transient receptor potential ion channel and acetylcholine receptor genes from isolated B lymphocytes in myalgic encephalomyelitis/chronic fatigue syndrome patients. Description: Marshall-Gradisnik, Sonya, et al. Single nucleotide polymorphisms and genotypes of transient receptor potential ion channel and acetylcholine receptor genes from isolated B lymphocytes in myalgic encephalomyelitis/chronic fatigue syndrome patients. ''J Int Med Res''. 2016 Dec; '''44''' (6):1381-1394
Stanniocalcin-1 Hormone in Nonpreeclamptic and Preeclamptic Pregnancy: Clinical, Life-Style, and Genetic Modulators. Description: Juhanson, Peeter, et al. Stanniocalcin-1 Hormone in Nonpreeclamptic and Preeclamptic Pregnancy: Clinical, Life-Style, and Genetic Modulators. ''J Clin Endocrinol Metab''. 2016 Dec; '''101''' (12):4799-4807
Strong cis-acting expression quantitative trait loci for the genes encoding SNHG5 and PEX6. Description: Lee, Jihyeon, et al. Strong cis-acting expression quantitative trait loci for the genes encoding SNHG5 and PEX6. ''Medicine (Baltimore)''. 2016 Dec; '''95''' (52):e5793
Structural and genomic variation in preterm birth. Description: Uzun, Alper, et al. Structural and genomic variation in preterm birth. ''Pediatr Res''. 2016 Dec; '''80''' (6):829-836
Targeted exome sequencing for the identification of a protective variant against Internet gaming disorder at rs2229910 of neurotrophic tyrosine kinase receptor, type 3 (NTRK3): A pilot study. Description: Kim, Jeong-Yu, et al. Targeted exome sequencing for the identification of a protective variant against Internet gaming disorder at rs2229910 of neurotrophic tyrosine kinase receptor, type 3 (NTRK3): A pilot study. ''J Behav Addict''. 2016 Dec; '''5''' (4):631-638
The disappearing San of southeastern Africa and their genetic affinities. Description: Schlebusch, Carina M, et al. The disappearing San of southeastern Africa and their genetic affinities. ''Hum Genet''. 2016 Dec; '''135''' (12):1365-1373
Utility of blood pressure genetic risk score in admixed Hispanic samples. Description: Beecham, A H, et al. Utility of blood pressure genetic risk score in admixed Hispanic samples. ''J Hum Hypertens''. 2016 Dec; '''30''' (12):772-777
Variation in the oxytocin receptor gene (OXTR) is associated with differences in moral judgment. Description: Bernhard, Regan M, et al. Variation in the oxytocin receptor gene (OXTR) is associated with differences in moral judgment. ''Soc Cogn Affect Neurosci''. 2016 Dec; '''11''' (12):1872-1881
Whole-genome sequence, SNP chips and pedigree structure: building demographic profiles in domestic dog breeds to optimize genetic-trait mapping. Description: Dreger, Dayna L, et al. Whole-genome sequence, SNP chips and pedigree structure: building demographic profiles in domestic dog breeds to optimize genetic-trait mapping. ''Dis Model Mech''. 2016 Dec 1; '''9''' (12):1445-1460
Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data. Description: Shi, Jianxin, et al. Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data. ''PLoS Genet''. 2016 Dec; '''12''' (12):e1006493
A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle. Description: Murgiano, Leonardo, et al. A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle. ''BMC Vet Res''. 2016 Dec 5; '''12''' (1):276
The psoriasis-associated deletion of late cornified envelope genes LCE3B and LCE3C has been maintained under balancing selection since Human Denisovan divergence. Description: Pajic, Petar, et al. The psoriasis-associated deletion of late cornified envelope genes LCE3B and LCE3C has been maintained under balancing selection since Human Denisovan divergence. ''BMC Evol Biol''. 2016 Dec 5; '''16''' (1):265
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21. Description: Hamdi, Yosr, et al. Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21. ''Oncotarget''. 2016 Dec 6; '''7''' (49):80140-80163
Genome-Wide Association Study and QTL Mapping Reveal Genomic Loci Associated with Fusarium Ear Rot Resistance in Tropical Maize Germplasm. Description: Chen, Jiafa, et al. Genome-Wide Association Study and QTL Mapping Reveal Genomic Loci Associated with Fusarium Ear Rot Resistance in Tropical Maize Germplasm. ''G3 (Bethesda)''. 2016 Dec 7; '''6''' (12):3803-3815
Genome-Wide Association Study of Meiotic Recombination Phenotypes. Description: Begum, Ferdouse, et al. Genome-Wide Association Study of Meiotic Recombination Phenotypes. ''G3 (Bethesda)''. 2016 Dec 7; '''6''' (12):3995-4007
An integrated genomic approach for the study of mandibular prognathism in the European seabass (Dicentrarchus labrax). Description: Babbucci, Massimiliano, et al. An integrated genomic approach for the study of mandibular prognathism in the European seabass (Dicentrarchus labrax). ''Sci Rep''. 2016 Dec 8; '''6''': 38673
Effect of TREM-1 blockade and single nucleotide variants in experimental renal injury and kidney transplantation. Description: Tammaro, Alessandra, et al. Effect of TREM-1 blockade and single nucleotide variants in experimental renal injury and kidney transplantation. ''Sci Rep''. 2016 Dec 8; '''6''': 38275
High-density Association Mapping and Interaction Analysis of PLA2R1 and HLA Regions with Idiopathic Membranous Nephropathy in Japanese. Description: Thiri, Myo, et al. High-density Association Mapping and Interaction Analysis of PLA2R1 and HLA Regions with Idiopathic Membranous Nephropathy in Japanese. ''Sci Rep''. 2016 Dec 9; '''6''': 38189
CDKN2BAS polymorphisms are associated with coronary heart disease risk a Han Chinese population. Description: Zhao, Qingbin, et al. CDKN2BAS polymorphisms are associated with coronary heart disease risk a Han Chinese population. ''Oncotarget''. 2016 Dec 13; '''7''' (50):82046-82054
Genetic polymorphisms of Wnt/beta-catenin pathway genes are associated with the efficacy and toxicities of radiotherapy in patients with nasopharyngeal carcinoma. Description: Yu, Jingjing, et al. Genetic polymorphisms of Wnt/beta-catenin pathway genes are associated with the efficacy and toxicities of radiotherapy in patients with nasopharyngeal carcinoma. ''Oncotarget''. 2016 Dec 13; '''7''' (50):82528-82537
Genetic variants in TERT are associated with risk of gastric cancer in a Chinese Han population. Description: Duan, Xianglong, et al. Genetic variants in TERT are associated with risk of gastric cancer in a Chinese Han population. ''Oncotarget''. 2016 Dec 13; '''7''' (50):82727-82732
Implication of NOTCH1 gene in susceptibility to anxiety and depression among sexual abuse victims. Description: Steine, I M, et al. Implication of NOTCH1 gene in susceptibility to anxiety and depression among sexual abuse victims. ''Transl Psychiatry''. 2016 Dec 13; '''6''' (12):e977
Trans-ethnic follow-up of breast cancer GWAS hits using the preferential linkage disequilibrium approach. Description: Zhu, Qianqian, et al. Trans-ethnic follow-up of breast cancer GWAS hits using the preferential linkage disequilibrium approach. ''Oncotarget''. 2016 Dec 13; '''7''' (50):83160-83176
A large-scale genome-wide association and meta-analysis identified four novel susceptibility loci for leprosy. Description: Wang, Zhenzhen, et al. A large-scale genome-wide association and meta-analysis identified four novel susceptibility loci for leprosy. ''Nat Commun''. 2016 Dec 15; '''7''': 13760
STAMS: STRING-assisted module search for genome wide association studies and application to autism. Description: Hillenmeyer, Sara, et al. STAMS: STRING-assisted module search for genome wide association studies and application to autism. ''Bioinformatics''. 2016 Dec 15; '''32''' (24):3815-3822
Heterotaxy in Caenorhabditis: widespread natural variation in left-right arrangement of the major organs. Description: Alcorn, Melissa R, et al. Heterotaxy in Caenorhabditis: widespread natural variation in left-right arrangement of the major organs. ''Philos Trans R Soc Lond B Biol Sci''. 2016 Dec 19; '''371''' (1710):
Impact of diabetes-related gene polymorphisms on the clinical characteristics of type 2 diabetes Chinese Han population. Description: Li, Jing, et al. Impact of diabetes-related gene polymorphisms on the clinical characteristics of type 2 diabetes Chinese Han population. ''Oncotarget''. 2016 Dec 20; '''7''' (51):85464-85471
SLINGER: large-scale learning for predicting gene expression. Description: Vervier, Kevin, et al. SLINGER: large-scale learning for predicting gene expression. ''Sci Rep''. 2016 Dec 20; '''6''': 39360
A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples. Description: Chou, Wen-Chi, et al. A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples. ''Sci Rep''. 2016 Dec 22; '''6''': 39313
Sacral agenesis: a pilot whole exome sequencing and copy number study. Description: Porsch, Robert M, et al. Sacral agenesis: a pilot whole exome sequencing and copy number study. ''BMC Med Genet''. 2016 Dec 22; '''17''' (1):98
Validation of a genome-wide association study implied that SHTIN1 may involve in the pathogenesis of NSCL/P in Chinese population. Description: Wang, Yirui, et al. Validation of a genome-wide association study implied that SHTIN1 may involve in the pathogenesis of NSCL/P in Chinese population. ''Sci Rep''. 2016 Dec 23; '''6''': 38872
Genetic variants in the acylphosphatase 2 gene and the risk of breast cancer in a Han Chinese population. Description: Zhang, Fuli, et al. Genetic variants in the acylphosphatase 2 gene and the risk of breast cancer in a Han Chinese population. ''Oncotarget''. 2016 Dec 27; '''7''' (52):86704-86712
The association of variants in PNPLA3 and GRP78 and the risk of developing hepatocellular carcinoma in an Italian population. Description: Balasus, Daniele, et al. The association of variants in PNPLA3 and GRP78 and the risk of developing hepatocellular carcinoma in an Italian population. ''Oncotarget''. 2016 Dec 27; '''7''' (52):86791-86802
Common variants in the chromosome 2p23 region containing the SLC30A3 (ZnT3) gene are associated with schizophrenia in female but not male individuals in a large collection of European samples. Description: Perez-Becerril, C, et al. Common variants in the chromosome 2p23 region containing the SLC30A3 (ZnT3) gene are associated with schizophrenia in female but not male individuals in a large collection of European samples. ''Psychiatry Res''. 2016 Dec 30; '''246''': 335-340
Population Stratification and Underrepresentation of Indian Subcontinent Genetic Diversity in the 1000 Genomes Project Dataset. Description: Sengupta, Dhriti, et al. Population Stratification and Underrepresentation of Indian Subcontinent Genetic Diversity in the 1000 Genomes Project Dataset. ''Genome Biol Evol''. 2016 Dec 31; '''8''' (11):3460-3470
Post-concussion symptoms and chronic pain after mild traumatic brain injury are modulated by multiple locus effect in the BDNF gene through the expression of antisense: A pilot prospective control study. Description: Khoury, Samar, et al. Post-concussion symptoms and chronic pain after mild traumatic brain injury are modulated by multiple locus effect in the BDNF gene through the expression of antisense: A pilot prospective control study. ''Can J Pain''. 2017; '''1''' (1):112-126
ACE gene variants and sarcoidosis in a Finnish population. Description: Lahtela, Elisa, et al. ACE gene variants and sarcoidosis in a Finnish population. ''Sarcoidosis Vasc Diffuse Lung Dis''. 2017; '''34''' (2):104-114
A CREB1 Gene Polymorphism (rs2253206) Is Associated with Prospective Memory in a Healthy Cohort. Description: Avgan, Nesli, et al. A CREB1 Gene Polymorphism (rs2253206) Is Associated with Prospective Memory in a Healthy Cohort. ''Front Behav Neurosci''. 2017; '''11''': 86
Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal. Description: Parra, Esteban J, et al. Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal. ''PLoS One''. 2017; '''12''' (2):e0172880
Admixture mapping of pelvic organ prolapse in African Americans from the Women's Health Initiative Hormone Therapy trial. Description: Giri, Ayush, et al. Admixture mapping of pelvic organ prolapse in African Americans from the Women's Health Initiative Hormone Therapy trial. ''PLoS One''. 2017; '''12''' (6):e0178839
Adult onset asthma and interaction between genes and active tobacco smoking: The GABRIEL consortium. Description: Vonk, J M, et al. Adult onset asthma and interaction between genes and active tobacco smoking: The GABRIEL consortium. ''PLoS One''. 2017; '''12''' (3):e0172716
A family-based genome-wide association study of chronic rhinosinusitis with nasal polyps implicates several genes in the disease pathogenesis. Description: Bohman, Anton, et al. A family-based genome-wide association study of chronic rhinosinusitis with nasal polyps implicates several genes in the disease pathogenesis. ''PLoS One''. 2017; '''12''' (12):e0185244
A framework to identify contributing genes in patients with Phelan-McDermid syndrome. Description: Tabet, Anne-Claude, et al. A framework to identify contributing genes in patients with Phelan-McDermid syndrome. ''NPJ Genom Med''. 2017; '''2''': 32
Age-Dependent Association of TNFSF15/TNFSF8 Variants and Leprosy Type 1 Reaction. Description: Fava, Vinicius M, et al. Age-Dependent Association of TNFSF15/TNFSF8 Variants and Leprosy Type 1 Reaction. ''Front Immunol''. 2017; '''8''': 155
A Gene-Based Analysis of Acoustic Startle Latency. Description: Smith, Alicia K, et al. A Gene-Based Analysis of Acoustic Startle Latency. ''Front Psychiatry''. 2017; '''8''': 117
A genome-wide association study for body weight in Japanese Thoroughbred racehorses clarifies candidate regions on chromosomes 3, 9, 15, and 18. Description: Tozaki, Teruaki, et al. A genome-wide association study for body weight in Japanese Thoroughbred racehorses clarifies candidate regions on chromosomes 3, 9, 15, and 18. ''J Equine Sci''. 2017; '''28''' (4):127-134
A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents. Description: Nielsen, Tenna Ruest Haarmark, et al. A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents. ''PLoS One''. 2017; '''12''' (3):e0174204
A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population. Description: Nannini, Drew R, et al. A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population. ''Invest Ophthalmol Vis Sci''. 2017 Jan 1; '''58''' (1):87-95
A genome-wide study to identify genes responsible for oviduct development in chickens. Description: Shen, Manman, et al. A genome-wide study to identify genes responsible for oviduct development in chickens. ''PLoS One''. 2017; '''12''' (12):e0189955
A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus. Description: Mobuchon, Lenha, et al. A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus. ''NPJ Genom Med''. 2017; '''2''':
A longitudinal cline characterizes the genetic structure of human populations in the Tibetan plateau. Description: Jeong, Choongwon, et al. A longitudinal cline characterizes the genetic structure of human populations in the Tibetan plateau. ''PLoS One''. 2017; '''12''' (4):e0175885
A Model of Compound Heterozygous, Loss-of-Function Alleles Is Broadly Consistent with Observations from Complex-Disease GWAS Datasets. Description: Sanjak, Jaleal S, et al. A Model of Compound Heterozygous, Loss-of-Function Alleles Is Broadly Consistent with Observations from Complex-Disease GWAS Datasets. ''PLoS Genet''. 2017 Jan; '''13''' (1):e1006573
Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia. Description: Lokki, A Inkeri, et al. Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia. ''Front Immunol''. 2017; '''8''': 589
Analysis of the prion protein gene in multiple system atrophy. Description: Chelban, Viorica, et al. Analysis of the prion protein gene in multiple system atrophy. ''Neurobiol Aging''. 2017 Jan; '''49''': 216.e15-216.e18
An ancestral human genetic variant linked to an ancient disease: A novel association of FMO2 polymorphisms with tuberculosis (TB) in Ethiopian populations provides new insight into the differential ethno-geographic distribution of FMO21. Description: Mekonnen, Ephrem, et al. An ancestral human genetic variant linked to an ancient disease: A novel association of FMO2 polymorphisms with tuberculosis (TB) in Ethiopian populations provides new insight into the differential ethno-geographic distribution of FMO21. ''PLoS One''. 2017; '''12''' (10):e0184931
An autosomal recessive mutation in SCL24A4 causing enamel hypoplasia in Samoyed and its relationship to breed-wide genetic diversity. Description: Pedersen, Niels C, et al. An autosomal recessive mutation in SCL24A4 causing enamel hypoplasia in Samoyed and its relationship to breed-wide genetic diversity. ''Canine Genet Epidemiol''. 2017; '''4''': 11
Ancestors' dietary patterns and environments could drive positive selection in genes involved in micronutrient metabolism-the case of cofactor transporters. Description: Parolo, Silvia, et al. Ancestors' dietary patterns and environments could drive positive selection in genes involved in micronutrient metabolism-the case of cofactor transporters. ''Genes Nutr''. 2017; '''12''': 28
An epigenome-wide association study in whole blood of measures of adiposity among Ghanaians: the RODAM study. Description: Meeks, Karlijn A C, et al. An epigenome-wide association study in whole blood of measures of adiposity among Ghanaians: the RODAM study. ''Clin Epigenetics''. 2017; '''9''': 103
A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts. Description: Skare, Oivind, et al. A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts. ''PLoS One''. 2017; '''12''' (9):e0183772
A novel iterative mixed model to remap three complex orthopedic traits in dogs. Description: Huang, Meng, et al. A novel iterative mixed model to remap three complex orthopedic traits in dogs. ''PLoS One''. 2017; '''12''' (6):e0176932
A Pilot Genome-Wide Association Study Identifies Potential Metabolic Pathways Involved in Tinnitus. Description: Gilles, Annick, et al. A Pilot Genome-Wide Association Study Identifies Potential Metabolic Pathways Involved in Tinnitus. ''Front Neurosci''. 2017; '''11''': 71
A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density. Description: Villalobos-Comparan, Marisela, et al. A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density. ''Int J Genomics''. 2017; '''2017''': 5831020
A pilot study on the impact of dopamine, serotonin, and brain-derived neurotrophic factor genotype on long-term functional outcomes after subarachnoid hemorrhage. Description: Stanfill, Ansley, et al. A pilot study on the impact of dopamine, serotonin, and brain-derived neurotrophic factor genotype on long-term functional outcomes after subarachnoid hemorrhage. ''SAGE Open Med''. 2017; '''5''': 2050312117726725
APOE allele frequencies in suspected non-amyloid pathophysiology (SNAP) and the prodromal stages of Alzheimer's Disease. Description: Hohman, Timothy J, et al. APOE allele frequencies in suspected non-amyloid pathophysiology (SNAP) and the prodromal stages of Alzheimer's Disease. ''PLoS One''. 2017; '''12''' (11):e0188501
Apolipoprotein L1 risk variants associate with prevalent atherosclerotic disease in African American systemic lupus erythematosus patients. Description: Blazer, Ashira, et al. Apolipoprotein L1 risk variants associate with prevalent atherosclerotic disease in African American systemic lupus erythematosus patients. ''PLoS One''. 2017; '''12''' (8):e0182483
A Powerful Gene-Based Test Accommodating Common and Low-Frequency Variants to Detect Both Main Effects and Gene-Gene Interaction Effects in Case-Control Studies. Description: Chung, Ren-Hua, et al. A Powerful Gene-Based Test Accommodating Common and Low-Frequency Variants to Detect Both Main Effects and Gene-Gene Interaction Effects in Case-Control Studies. ''Front Genet''. 2017; '''8''': 228
A Pragmatic Study Shows Failure of Dental Composite Fillings Is Genetically Determined: A Contribution to the Discussion on Dental Amalgams. Description: Vieira, Alexandre R, et al. A Pragmatic Study Shows Failure of Dental Composite Fillings Is Genetically Determined: A Contribution to the Discussion on Dental Amalgams. ''Front Med (Lausanne)''. 2017; '''4''': 186
A promoter variant of the APOA5 gene increases atherogenic LDL levels and arterial stiffness in hypertriglyceridemic patients. Description: Kim, Minjoo, et al. A promoter variant of the APOA5 gene increases atherogenic LDL levels and arterial stiffness in hypertriglyceridemic patients. ''PLoS One''. 2017; '''12''' (12):e0186693
Association and clinical utility of NAT2 in the prediction of isoniazid-induced liver injury in Singaporean patients. Description: Chan, Sze Ling, et al. Association and clinical utility of NAT2 in the prediction of isoniazid-induced liver injury in Singaporean patients. ''PLoS One''. 2017; '''12''' (10):e0186200
Association of angiotensinogen gene SNPs and haplotypes with risk of hypertension in eastern Indian population. Description: Purkait, Pulakes, et al. Association of angiotensinogen gene SNPs and haplotypes with risk of hypertension in eastern Indian population. ''Clin Hypertens''. 2017; '''23''': 12
Association of ATG16L1 gene haplotype with inflammatory bowel disease in Indians. Description: Pugazhendhi, Srinivasan, et al. Association of ATG16L1 gene haplotype with inflammatory bowel disease in Indians. ''PLoS One''. 2017; '''12''' (5):e0178291
Association of FLG single nucleotide variations with clinical phenotypes of atopic dermatitis. Description: Kim, Myungshin, et al. Association of FLG single nucleotide variations with clinical phenotypes of atopic dermatitis. ''PLoS One''. 2017; '''12''' (12):e0190077
Association of prediabetes-associated single nucleotide polymorphisms with microalbuminuria. Description: Choi, Jong Wook, et al. Association of prediabetes-associated single nucleotide polymorphisms with microalbuminuria. ''PLoS One''. 2017; '''12''' (2):e0171367
Assortative Mating by Ethnicity in Longevous Families. Description: Sebastiani, Paola, et al. Assortative Mating by Ethnicity in Longevous Families. ''Front Genet''. 2017; '''8''': 186
A targeted approach to genome-wide studies reveals new genetic associations with central corneal thickness. Description: Benson, Matthew D, et al. A targeted approach to genome-wide studies reveals new genetic associations with central corneal thickness. ''Mol Vis''. 2017; '''23''': 952-962
Brain insulin resistance deteriorates cognition by altering the topological features of brain networks. Description: Su, Fan, et al. Brain insulin resistance deteriorates cognition by altering the topological features of brain networks. ''Neuroimage Clin''. 2017; '''13''': 280-287
Candidate Gene Identification of Feed Efficiency and Coat Color Traits in a C57BL/6J x Kunming F2 Mice Population Using Genome-Wide Association Study. Description: Miao, Yuanxin, et al. Candidate Gene Identification of Feed Efficiency and Coat Color Traits in a C57BL/6J x Kunming F2 Mice Population Using Genome-Wide Association Study. ''Biomed Res Int''. 2017; '''2017''': 7132941
CELSR2 is a candidate susceptibility gene in idiopathic scoliosis. Description: Einarsdottir, Elisabet, et al. CELSR2 is a candidate susceptibility gene in idiopathic scoliosis. ''PLoS One''. 2017; '''12''' (12):e0189591
Characterization and functional analysis of hypoxia-inducible factor HIF1alpha and its inhibitor HIF1alphan in tilapia. Description: Li, Hong Lian, et al. Characterization and functional analysis of hypoxia-inducible factor HIF1alpha and its inhibitor HIF1alphan in tilapia. ''PLoS One''. 2017; '''12''' (3):e0173478
Climate Clever Clovers: New Paradigm to Reduce the Environmental Footprint of Ruminants by Breeding Low Methanogenic Forages Utilizing Haplotype Variation. Description: Kaur, Parwinder, et al. Climate Clever Clovers: New Paradigm to Reduce the Environmental Footprint of Ruminants by Breeding Low Methanogenic Forages Utilizing Haplotype Variation. ''Front Plant Sci''. 2017; '''8''': 1463
Close genetic relationships between a spousal pair with autism-affected children and high minor allele content in cases in autism-associated SNPs. Description: Zhu, Zuobin, et al. Close genetic relationships between a spousal pair with autism-affected children and high minor allele content in cases in autism-associated SNPs. ''Genomics''. 2017 Jan; '''109''' (1):9-15
Collective Genetic Interaction Effects and the Role of Antigen-Presenting Cells in Autoimmune Diseases. Description: Woo, Hyung Jun, et al. Collective Genetic Interaction Effects and the Role of Antigen-Presenting Cells in Autoimmune Diseases. ''PLoS One''. 2017; '''12''' (1):e0169918
Colorectal Cancer and Long-Term Exposure to Trihalomethanes in Drinking Water: A Multicenter Case-Control Study in Spain and Italy. Description: Villanueva, Cristina M, et al. Colorectal Cancer and Long-Term Exposure to Trihalomethanes in Drinking Water: A Multicenter Case-Control Study in Spain and Italy. ''Environ Health Perspect''. 2017 Jan; '''125''' (1):56-65
Combined approach for finding susceptibility genes in DISH/chondrocalcinosis families: whole-genome-wide linkage and IBS/IBD studies. Description: Couto, Ana Rita, et al. Combined approach for finding susceptibility genes in DISH/chondrocalcinosis families: whole-genome-wide linkage and IBS/IBD studies. ''Hum Genome Var''. 2017; '''4''': 17041
Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families. Description: Woodbury-Smith, M, et al. Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families. ''J Neurodev Disord''. 2017; '''9''': 5
Common and rare exonic MUC5B variants associated with type 2 diabetes in Han Chinese. Description: Chen, Guanjie, et al. Common and rare exonic MUC5B variants associated with type 2 diabetes in Han Chinese. ''PLoS One''. 2017; '''12''' (3):e0173784
Common and rare genetic markers of lipid variation in subjects with type 2 diabetes from the ACCORD clinical trial. Description: Marvel, Skylar W, et al. Common and rare genetic markers of lipid variation in subjects with type 2 diabetes from the ACCORD clinical trial. ''PeerJ''. 2017; '''5''': e3187
Common Expression Quantitative Trait Loci Shared by Histone Genes. Description: Kim, Hanseol, et al. Common Expression Quantitative Trait Loci Shared by Histone Genes. ''Int J Genomics''. 2017; '''2017''': 6202567
Common Genetic Variation Near Melatonin Receptor 1A Gene Linked to Job-Related Exhaustion in Shift Workers. Description: Sulkava, Sonja, et al. Common Genetic Variation Near Melatonin Receptor 1A Gene Linked to Job-Related Exhaustion in Shift Workers. ''Sleep''. 2017 Jan 1; '''40''' (1):
Common variants near IKZF1 are associated with primary Sjogren's syndrome in Han Chinese. Description: Qu, Susu, et al. Common variants near IKZF1 are associated with primary Sjogren's syndrome in Han Chinese. ''PLoS One''. 2017; '''12''' (5):e0177320
Comparative Genome-Wide-Association Mapping Identifies Common Loci Controlling Root System Architecture and Resistance to Aphanomyces euteiches in Pea. Description: Desgroux, Aurore, et al. Comparative Genome-Wide-Association Mapping Identifies Common Loci Controlling Root System Architecture and Resistance to Aphanomyces euteiches in Pea. ''Front Plant Sci''. 2017; '''8''': 2195
Comparing distributions of polygenic risk scores of type 2 diabetes and coronary heart disease within different populations. Description: Reisberg, Sulev, et al. Comparing distributions of polygenic risk scores of type 2 diabetes and coronary heart disease within different populations. ''PLoS One''. 2017; '''12''' (7):e0179238
*Comparison between the HLA-B( )58 : 01 Allele and Single-Nucleotide Polymorphisms in Chromosome 6 for Prediction of Allopurinol-Induced Severe Cutaneous Adverse Reactions.** Description: Saksit, Niwat, et al. Comparison between the HLA-B( *)58 : 01 Allele and Single-Nucleotide Polymorphisms in Chromosome 6 for Prediction of Allopurinol-Induced Severe Cutaneous Adverse Reactions. ''J Immunol Res''. 2017; '''2017''': 2738784
Complex Ancient Genetic Structure and Cultural Transitions in Southern African Populations. Description: Montinaro, Francesco, et al. Complex Ancient Genetic Structure and Cultural Transitions in Southern African Populations. ''Genetics''. 2017 Jan; '''205''' (1):303-316
Controlling the Rate of GWAS False Discoveries. Description: Brzyski, Damian, et al. Controlling the Rate of GWAS False Discoveries. ''Genetics''. 2017 Jan; '''205''' (1):61-75
cophesim: a comprehensive phenotype simulator for testing novel association methods. Description: Zhbannikov, Ilya Y, et al. cophesim: a comprehensive phenotype simulator for testing novel association methods. ''F1000Res''. 2017; '''6''': 1294
Copy Number Variants in Alzheimer's Disease. Description: Cuccaro, Denis, et al. Copy Number Variants in Alzheimer's Disease. ''J Alzheimers Dis''. 2017; '''55''' (1):37-52
Coronary collateralization shows sex and racial-ethnic differences in obstructive artery disease patients. Description: Liu, Zhi, et al. Coronary collateralization shows sex and racial-ethnic differences in obstructive artery disease patients. ''PLoS One''. 2017; '''12''' (10):e0183836
Determination of Genetic Structure and Signatures of Selection in Three Strains of Tanzania Shorthorn Zebu, Boran and Friesian Cattle by Genome-Wide SNP Analyses. Description: Msalya, George, et al. Determination of Genetic Structure and Signatures of Selection in Three Strains of Tanzania Shorthorn Zebu, Boran and Friesian Cattle by Genome-Wide SNP Analyses. ''PLoS One''. 2017; '''12''' (1):e0171088
Development of a maize 55 K SNP array with improved genome coverage for molecular breeding. Description: Xu, Cheng, et al. Development of a maize 55 K SNP array with improved genome coverage for molecular breeding. ''Mol Breed''. 2017; '''37''' (3):20
Development of next generation sequencing panel for UMOD and association with kidney disease. Description: Bailie, Caitlin, et al. Development of next generation sequencing panel for UMOD and association with kidney disease. ''PLoS One''. 2017; '''12''' (6):e0178321
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals. Description: Holzinger, Emily R, et al. Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals. ''BioData Min''. 2017; '''10''': 25
Dissociation between skin test reactivity and anti-aeroallergen IgE: Determinants among urban Brazilian children. Description: Alcantara-Neves, Neuza M, et al. Dissociation between skin test reactivity and anti-aeroallergen IgE: Determinants among urban Brazilian children. ''PLoS One''. 2017; '''12''' (3):e0174089
Domestication Genomics of the Open-Pollinated Scarlet Runner Bean (Phaseolus coccineus L.). Description: Guerra-Garcia, Azalea, et al. Domestication Genomics of the Open-Pollinated Scarlet Runner Bean (Phaseolus coccineus L.). ''Front Plant Sci''. 2017; '''8''': 1891
Drosophila Genotype Influences Commensal Bacterial Levels. Description: Early, Angela M, et al. Drosophila Genotype Influences Commensal Bacterial Levels. ''PLoS One''. 2017; '''12''' (1):e0170332
Ecological genomics of local adaptation in Cornus florida L. by genotyping by sequencing. Description: Pais, Andrew L, et al. Ecological genomics of local adaptation in Cornus florida L. by genotyping by sequencing. ''Ecol Evol''. 2017 Jan; '''7''' (1):441-465
Effect of Genetic Variability in the CYP4F2, CYP4F11, and CYP4F12 Genes on Liver mRNA Levels and Warfarin Response. Description: Zhang, J E, et al. Effect of Genetic Variability in the CYP4F2, CYP4F11, and CYP4F12 Genes on Liver mRNA Levels and Warfarin Response. ''Front Pharmacol''. 2017; '''8''': 323
Effects of overweight and the PLA2G7 V279F polymorphism on the association of age with systolic blood pressure. Description: Kim, Minjoo, et al. Effects of overweight and the PLA2G7 V279F polymorphism on the association of age with systolic blood pressure. ''PLoS One''. 2017; '''12''' (3):e0173611
Enrichment of minor allele of SNPs and genetic prediction of type 2 diabetes risk in British population. Description: Lei, Xiaoyun, et al. Enrichment of minor allele of SNPs and genetic prediction of type 2 diabetes risk in British population. ''PLoS One''. 2017; '''12''' (11):e0187644
Environment-Dependent Genotype-Phenotype Associations in Avian Breeding Time. Description: Gienapp, Phillip, et al. Environment-Dependent Genotype-Phenotype Associations in Avian Breeding Time. ''Front Genet''. 2017; '''8''': 102
Estimates of linkage disequilibrium and effective population sizes in Chinese Merino (Xinjiang type) sheep by genome-wide SNPs. Description: Liu, Shudong, et al. Estimates of linkage disequilibrium and effective population sizes in Chinese Merino (Xinjiang type) sheep by genome-wide SNPs. ''Genes Genomics''. 2017; '''39''' (7):733-745
Evaluating the glucose raising effect of established loci via a genetic risk score. Description: Marouli, Eirini, et al. Evaluating the glucose raising effect of established loci via a genetic risk score. ''PLoS One''. 2017; '''12''' (11):e0186669
Evolutionary Insights Based on SNP Haplotypes of Red Pericarp, Grain Size and Starch Synthase Genes in Wild and Cultivated Rice. Description: Singh, Nisha, et al. Evolutionary Insights Based on SNP Haplotypes of Red Pericarp, Grain Size and Starch Synthase Genes in Wild and Cultivated Rice. ''Front Plant Sci''. 2017; '''8''': 972
Examining for an association between candidate gene polymorphisms in the metabolic syndrome components on excess weight and adiposity measures in youth: a cross-sectional study. Description: Munoz, Angelica Maria, et al. Examining for an association between candidate gene polymorphisms in the metabolic syndrome components on excess weight and adiposity measures in youth: a cross-sectional study. ''Genes Nutr''. 2017; '''12''': 19
Exome Sequencing Identified CCER2 as a Novel Candidate Gene for Moyamoya Disease. Description: Mukawa, Maki, et al. Exome Sequencing Identified CCER2 as a Novel Candidate Gene for Moyamoya Disease. ''J Stroke Cerebrovasc Dis''. 2017 Jan; '''26''' (1):150-161
Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea. Description: van der Spek, Ashley, et al. Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea. ''Front Genet''. 2017; '''8''': 151
Expression of D-Amino Acid Oxidase (DAO/DAAO) and D-Amino Acid Oxidase Activator (DAOA/G72) during Development and Aging in the Human Post-mortem Brain. Description: Jagannath, Vinita, et al. Expression of D-Amino Acid Oxidase (DAO/DAAO) and D-Amino Acid Oxidase Activator (DAOA/G72) during Development and Aging in the Human Post-mortem Brain. ''Front Neuroanat''. 2017; '''11''': 31
Expression quantitative trait loci for PI3K/AKT pathway. Description: Ryu, Dongchan, et al. Expression quantitative trait loci for PI3K/AKT pathway. ''Medicine (Baltimore)''. 2017 Jan; '''96''' (1):e5817
Extending the use of GWAS data by combining data from different genetic platforms. Description: van Iperen, E P A, et al. Extending the use of GWAS data by combining data from different genetic platforms. ''PLoS One''. 2017; '''12''' (2):e0172082
Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations. Description: Olafsson, Sigurgeir, et al. Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations. ''NPJ Genom Med''. 2017; '''2''': 24
GBA2 Mutations Cause a Marinesco-Sjogren-Like Syndrome: Genetic and Biochemical Studies. Description: Haugarvoll, Kristoffer, et al. GBA2 Mutations Cause a Marinesco-Sjogren-Like Syndrome: Genetic and Biochemical Studies. ''PLoS One''. 2017; '''12''' (1):e0169309
Genetic Analysis of Mitochondrial Ribosomal Proteins and Cognitive Aging in Postmenopausal Women. Description: Mozhui, Khyobeni, et al. Genetic Analysis of Mitochondrial Ribosomal Proteins and Cognitive Aging in Postmenopausal Women. ''Front Genet''. 2017; '''8''': 127
Genetic and Quantitative Trait Locus Analysis of Cell Wall Components and Forage Digestibility in the Zheng58 x HD568 Maize RIL Population at Anthesis Stage. Description: Li, Kun, et al. Genetic and Quantitative Trait Locus Analysis of Cell Wall Components and Forage Digestibility in the Zheng58 x HD568 Maize RIL Population at Anthesis Stage. ''Front Plant Sci''. 2017; '''8''': 1472
Genetic association of FTO/IRX region with obesity and overweight in the Polish population. Description: Sobalska-Kwapis, Marta, et al. Genetic association of FTO/IRX region with obesity and overweight in the Polish population. ''PLoS One''. 2017; '''12''' (6):e0180295
Genetic Association Study of KCNQ5 Polymorphisms with High Myopia. Description: Liao, Xuan, et al. Genetic Association Study of KCNQ5 Polymorphisms with High Myopia. ''Biomed Res Int''. 2017; '''2017''': 3024156
Genetic Diversity and Population Structure of Ethiopian Sheep Populations Revealed by High-Density SNP Markers. Description: Edea, Zewdu, et al. Genetic Diversity and Population Structure of Ethiopian Sheep Populations Revealed by High-Density SNP Markers. ''Front Genet''. 2017; '''8''': 218
Genetic Diversity and Population Structure of Two Tomato Species from the Galapagos Islands. Description: Pailles, Yveline, et al. Genetic Diversity and Population Structure of Two Tomato Species from the Galapagos Islands. ''Front Plant Sci''. 2017; '''8''': 138
Genetic Diversity, Population Structure and Ancestral Origin of Australian Wheat. Description: Joukhadar, Reem, et al. Genetic Diversity, Population Structure and Ancestral Origin of Australian Wheat. ''Front Plant Sci''. 2017; '''8''': 2115
Genetic Diversity, Population Structure, and Linkage Disequilibrium of an Association-Mapping Panel Revealed by Genome-Wide SNP Markers in Sesame. Description: Cui, Chengqi, et al. Genetic Diversity, Population Structure, and Linkage Disequilibrium of an Association-Mapping Panel Revealed by Genome-Wide SNP Markers in Sesame. ''Front Plant Sci''. 2017; '''8''': 1189
Genetic factors affecting EBV copy number in lymphoblastoid cell lines derived from the 1000 Genome Project samples. Description: Mandage, Rajendra, et al. Genetic factors affecting EBV copy number in lymphoblastoid cell lines derived from the 1000 Genome Project samples. ''PLoS One''. 2017; '''12''' (6):e0179446
Genetic factors influencing frontostriatal dysfunction and the development of dementia in Parkinson's disease. Description: Huertas, Ismael, et al. Genetic factors influencing frontostriatal dysfunction and the development of dementia in Parkinson's disease. ''PLoS One''. 2017; '''12''' (4):e0175560
Genetic mapping of principal components of canine pelvic morphology. Description: Fealey, Mark J, et al. Genetic mapping of principal components of canine pelvic morphology. ''Canine Genet Epidemiol''. 2017; '''4''': 4
Genetic Parameters and the Impact of Off-Types for Theobroma cacao L. in a Breeding Program in Brazil. Description: DuVal, Ashley, et al. Genetic Parameters and the Impact of Off-Types for Theobroma cacao L. in a Breeding Program in Brazil. ''Front Plant Sci''. 2017; '''8''': 2059
Genetic pattern and gene localization of polydactyly in Beijing fatty chicken. Description: He, Chuan, et al. Genetic pattern and gene localization of polydactyly in Beijing fatty chicken. ''PLoS One''. 2017; '''12''' (5):e0176113
Genetic rescue of an endangered domestic animal through outcrossing with closely related breeds: A case study of the Norwegian Lundehund. Description: Stronen, Astrid V, et al. Genetic rescue of an endangered domestic animal through outcrossing with closely related breeds: A case study of the Norwegian Lundehund. ''PLoS One''. 2017; '''12''' (6):e0177429
Genetic Stratification to Identify Risk Groups for Alzheimer's Disease. Description: Marioni, Riccardo E, et al. Genetic Stratification to Identify Risk Groups for Alzheimer's Disease. ''J Alzheimers Dis''. 2017; '''57''' (1):275-283
Genetic variants in ALDH1B1 and alcohol dependence risk in a British and Irish population: A bioinformatic and genetic study. Description: Way, Michael J, et al. Genetic variants in ALDH1B1 and alcohol dependence risk in a British and Irish population: A bioinformatic and genetic study. ''PLoS One''. 2017; '''12''' (6):e0177009
Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. Description: Arpawong, Thalida E, et al. Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. ''PLoS One''. 2017; '''12''' (8):e0182448
Genetic variation in the eicosanoid pathway is associated with non-small-cell lung cancer (NSCLC) survival. Description: Sausville, Lindsay N, et al. Genetic variation in the eicosanoid pathway is associated with non-small-cell lung cancer (NSCLC) survival. ''PLoS One''. 2017; '''12''' (7):e0180471
Genetic Variations and mRNA Expression of NRF2 in Parkinson's Disease. Description: Ran, Caroline, et al. Genetic Variations and mRNA Expression of NRF2 in Parkinson's Disease. ''Parkinsons Dis''. 2017; '''2017''': 4020198
Genomes of Fasciola hepatica from the Americas Reveal Colonization with Neorickettsia Endobacteria Related to the Agents of Potomac Horse and Human Sennetsu Fevers. Description: McNulty, Samantha N, et al. Genomes of Fasciola hepatica from the Americas Reveal Colonization with Neorickettsia Endobacteria Related to the Agents of Potomac Horse and Human Sennetsu Fevers. ''PLoS Genet''. 2017 Jan; '''13''' (1):e1006537
Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS). Description: Shendre, Aditi, et al. Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS). ''PLoS One''. 2017; '''12''' (12):e0188725
Genome-wide analysis of parent-of-origin interaction effects with environmental exposure (PoOxE): An application to European and Asian cleft palate trios. Description: Haaland, Oystein A, et al. Genome-wide analysis of parent-of-origin interaction effects with environmental exposure (PoOxE): An application to European and Asian cleft palate trios. ''PLoS One''. 2017; '''12''' (9):e0184358
GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. Description: Salem, Joe-Elie, et al. GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. ''PLoS One''. 2017; '''12''' (8):e0181875
Genome-wide analysis of the diversity and ancestry of Korean dogs. Description: Choi, Bong Hwan, et al. Genome-wide analysis of the diversity and ancestry of Korean dogs. ''PLoS One''. 2017; '''12''' (11):e0188676
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Description: Hoffmann, Thomas J, et al. Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. ''Nat Genet''. 2017 Jan; '''49''' (1):54-64
Genome-wide association analysis identifies resistance loci for bacterial blight in a diverse collection of indica rice germplasm. Description: Zhang, Fan, et al. Genome-wide association analysis identifies resistance loci for bacterial blight in a diverse collection of indica rice germplasm. ''PLoS One''. 2017; '''12''' (3):e0174598
Genome-wide association analysis in dogs implicates 99 loci as risk variants for anterior cruciate ligament rupture. Description: Baker, Lauren A, et al. Genome-wide association analysis in dogs implicates 99 loci as risk variants for anterior cruciate ligament rupture. ''PLoS One''. 2017; '''12''' (4):e0173810
Genome wide association analysis of cold tolerance at germination in temperate japonica rice (Oryza sativa L.) varieties. Description: Sales, Ester, et al. Genome wide association analysis of cold tolerance at germination in temperate japonica rice (Oryza sativa L.) varieties. ''PLoS One''. 2017; '''12''' (8):e0183416
Genome-wide association analysis reveals genetic loci and candidate genes for feeding behavior and eating efficiency in Duroc boars. Description: Ding, Rongrong, et al. Genome-wide association analysis reveals genetic loci and candidate genes for feeding behavior and eating efficiency in Duroc boars. ''PLoS One''. 2017; '''12''' (8):e0183244
Genome-Wide Association Mapping of Flowering and Ripening Periods in Apple. Description: Urrestarazu, Jorge, et al. Genome-Wide Association Mapping of Flowering and Ripening Periods in Apple. ''Front Plant Sci''. 2017; '''8''': 1923
Genome-wide association screens for Achilles tendon and ACL tears and tendinopathy. Description: Kim, Stuart K, et al. Genome-wide association screens for Achilles tendon and ACL tears and tendinopathy. ''PLoS One''. 2017; '''12''' (3):e0170422
Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD). Description: Ritter, McKenzie L, et al. Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD). ''Front Mol Neurosci''. 2017; '''10''': 83
Genome-wide association study identifies a locus associated with rotator cuff injury. Description: Roos, Thomas R, et al. Genome-wide association study identifies a locus associated with rotator cuff injury. ''PLoS One''. 2017; '''12''' (12):e0189317
Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations. Description: Dajani, Rana, et al. Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations. ''PeerJ''. 2017; '''5''': e3618
Genome-Wide Association Study of Acute Renal Graft Rejection. Description: Ghisdal, L, et al. Genome-Wide Association Study of Acute Renal Graft Rejection. ''Am J Transplant''. 2017 Jan; '''17''' (1):201-209
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Description: Lee, Myoung Keun, et al. Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. ''PLoS One''. 2017; '''12''' (4):e0176566
Genome-wide association study of paliperidone efficacy. Description: Li, Qingqin, et al. Genome-wide association study of paliperidone efficacy. ''Pharmacogenet Genomics''. 2017 Jan; '''27''' (1):7-18
Genome-Wide Association Study of Piglet Uniformity and Farrowing Interval. Description: Wang, Yuan, et al. Genome-Wide Association Study of Piglet Uniformity and Farrowing Interval. ''Front Genet''. 2017; '''8''': 194
Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry. Description: Rawofi, Lida, et al. Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry. ''PeerJ''. 2017; '''5''': e3951
Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup. Description: Kim, Taehyeung, et al. Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup. ''PLoS One''. 2017; '''12''' (1):e0168137
Genome-Wide Association Study Reveals Novel Loci for SC7 Resistance in a Soybean Mutant Panel. Description: Che, Zhijun, et al. Genome-Wide Association Study Reveals Novel Loci for SC7 Resistance in a Soybean Mutant Panel. ''Front Plant Sci''. 2017; '''8''': 1771
Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate. Description: Matovinovic, Elizabeth, et al. Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate. ''Mol Vis''. 2017; '''23''': 660-665
Genome-Wide SNP Markers Based on SLAF-Seq Uncover Breeding Traces in Rapeseed (Brassica napus L.). Description: Zhou, Qinghong, et al. Genome-Wide SNP Markers Based on SLAF-Seq Uncover Breeding Traces in Rapeseed (Brassica napus L.). ''Front Plant Sci''. 2017; '''8''': 648
Genome-wide study of resistant hypertension identified from electronic health records. Description: Dumitrescu, Logan, et al. Genome-wide study of resistant hypertension identified from electronic health records. ''PLoS One''. 2017; '''12''' (2):e0171745
Genomic ancestry and education level independently influence abdominal fat distributions in a Brazilian admixed population. Description: Franca, Giovanny Vinicius Araujo de, et al. Genomic ancestry and education level independently influence abdominal fat distributions in a Brazilian admixed population. ''PLoS One''. 2017; '''12''' (6):e0179085
Genomic Basis of Adaptive Evolution: The Survival of Amur Ide (Leuciscus waleckii) in an Extremely Alkaline Environment. Description: Xu, Jian, et al. Genomic Basis of Adaptive Evolution: The Survival of Amur Ide (Leuciscus waleckii) in an Extremely Alkaline Environment. ''Mol Biol Evol''. 2017 Jan; '''34''' (1):145-159
Genomic prediction with parallel computing for slaughter traits in Chinese Simmental beef cattle using high-density genotypes. Description: Guo, Peng, et al. Genomic prediction with parallel computing for slaughter traits in Chinese Simmental beef cattle using high-density genotypes. ''PLoS One''. 2017; '''12''' (7):e0179885
Genomics of a revived breed: Case study of the Belgian campine cattle. Description: Francois, Liesbeth, et al. Genomics of a revived breed: Case study of the Belgian campine cattle. ''PLoS One''. 2017; '''12''' (4):e0175916
Grid-based stochastic search for hierarchical gene-gene interactions in population-based genetic studies of common human diseases. Description: Moore, Jason H, et al. Grid-based stochastic search for hierarchical gene-gene interactions in population-based genetic studies of common human diseases. ''BioData Min''. 2017; '''10''': 19
Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank. Description: Howard, David M, et al. Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank. ''Wellcome Open Res''. 2017; '''2''': 61
Haplotype dependent association of rs7927894 (11q13.5) with atopic dermatitis and chronic allergic rhinitis: A study in ECAP cohort. Description: Poninska, Joanna Kinga, et al. Haplotype dependent association of rs7927894 (11q13.5) with atopic dermatitis and chronic allergic rhinitis: A study in ECAP cohort. ''PLoS One''. 2017; '''12''' (9):e0183922
Haplotypes on pig chromosome 3 distinguish metabolically healthy from unhealthy obese individuals. Description: Frederiksen, Simona D, et al. Haplotypes on pig chromosome 3 distinguish metabolically healthy from unhealthy obese individuals. ''PLoS One''. 2017; '''12''' (6):e0178828
High-Throughput Resequencing of Maize Landraces at Genomic Regions Associated with Flowering Time. Description: Jamann, Tiffany M, et al. High-Throughput Resequencing of Maize Landraces at Genomic Regions Associated with Flowering Time. ''PLoS One''. 2017; '''12''' (1):e0168910
HLA and non-HLA genes and familial predisposition to autoimmune diseases in families with a child affected by type 1 diabetes. Description: Parkkola, Anna, et al. HLA and non-HLA genes and familial predisposition to autoimmune diseases in families with a child affected by type 1 diabetes. ''PLoS One''. 2017; '''12''' (11):e0188402
Identification of key contributors in complex population structures. Description: Neuditschko, Markus, et al. Identification of key contributors in complex population structures. ''PLoS One''. 2017; '''12''' (5):e0177638
Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. Description: Forstner, Andreas J, et al. Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. ''PLoS One''. 2017; '''12''' (2):e0171595
Identifying novel genes and biological processes relevant to the development of cancer therapy-induced mucositis: An informative gene network analysis. Description: Reyes-Gibby, Cielito C, et al. Identifying novel genes and biological processes relevant to the development of cancer therapy-induced mucositis: An informative gene network analysis. ''PLoS One''. 2017; '''12''' (7):e0180396
Identifying patterns of dispersal, connectivity and selection in the sea scallop, Placopecten magellanicus, using RADseq-derived SNPs. Description: Van Wyngaarden, Mallory, et al. Identifying patterns of dispersal, connectivity and selection in the sea scallop, Placopecten magellanicus, using RADseq-derived SNPs. ''Evol Appl''. 2017 Jan; '''10''' (1):102-117
Implication of the APP Gene in Intellectual Abilities. Description: Myrum, Craig, et al. Implication of the APP Gene in Intellectual Abilities. ''J Alzheimers Dis''. 2017; '''59''' (2):723-735
Improved Progression-Free Survival in Irinotecan-Treated Metastatic Colorectal Cancer Patients Carrying the HNF1A Coding Variant p.I27L. Description: Labriet, Adrien, et al. Improved Progression-Free Survival in Irinotecan-Treated Metastatic Colorectal Cancer Patients Carrying the HNF1A Coding Variant p.I27L. ''Front Pharmacol''. 2017; '''8''': 712
Inbreeding depression by environment interactions in a free-living mammal population. Description: Pemberton, J M, et al. Inbreeding depression by environment interactions in a free-living mammal population. ''Heredity (Edinb)''. 2017 Jan; '''118''' (1):64-77
Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder. Description: Reis, Viviane Neri de Souza, et al. Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder. ''PLoS One''. 2017; '''12''' (1):e0170386
Integrity of Induced Pluripotent Stem Cell (iPSC) Derived Megakaryocytes as Assessed by Genetic and Transcriptomic Analysis. Description: Kammers, Kai, et al. Integrity of Induced Pluripotent Stem Cell (iPSC) Derived Megakaryocytes as Assessed by Genetic and Transcriptomic Analysis. ''PLoS One''. 2017; '''12''' (1):e0167794
Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes. Description: Kim, Jihye, et al. Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes. ''PLoS One''. 2017; '''12''' (4):e0175681
Interactions within the MHC contribute to the genetic architecture of celiac disease. Description: Goudey, Benjamin, et al. Interactions within the MHC contribute to the genetic architecture of celiac disease. ''PLoS One''. 2017; '''12''' (3):e0172826
In Vitro Acid-Mediated Initial Dental Enamel Loss Is Associated with Genetic Variants Previously Linked to Caries Experience. Description: Vieira, Alexandre R, et al. In Vitro Acid-Mediated Initial Dental Enamel Loss Is Associated with Genetic Variants Previously Linked to Caries Experience. ''Front Physiol''. 2017; '''8''': 104
Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations. Description: Ben Halima, Yosra, et al. Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations. ''Genes Nutr''. 2017; '''12''': 20
Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease. Description: Kwon, Young-Chang, et al. Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease. ''PLoS One''. 2017; '''12''' (9):e0184248
Mapping the sensory perception of apple using descriptive sensory evaluation in a genome wide association study. Description: Amyotte, Beatrice, et al. Mapping the sensory perception of apple using descriptive sensory evaluation in a genome wide association study. ''PLoS One''. 2017; '''12''' (2):e0171710
Maternal prenatal anxiety and child COMT genotype predict working memory and symptoms of ADHD. Description: O'Donnell, Kieran J, et al. Maternal prenatal anxiety and child COMT genotype predict working memory and symptoms of ADHD. ''PLoS One''. 2017; '''12''' (6):e0177506
Mediating Role of the Reward Network in the Relationship between the Dopamine Multilocus Genetic Profile and Depression. Description: Gong, Liang, et al. Mediating Role of the Reward Network in the Relationship between the Dopamine Multilocus Genetic Profile and Depression. ''Front Mol Neurosci''. 2017; '''10''': 292
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Description: Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. ''Mol Autism''. 2017; '''8''': 21
MGST2 and WNT2 are candidate genes for comitant strabismus susceptibility in Japanese patients. Description: Zhang, Jingjing, et al. MGST2 and WNT2 are candidate genes for comitant strabismus susceptibility in Japanese patients. ''PeerJ''. 2017; '''5''': e3935
Missense mutation at CLDN8 associated with a high plasma interferon gamma-inducible protein 10 level in methadone-maintained patients with urine test positive for morphine. Description: Liu, Tung-Hsia, et al. Missense mutation at CLDN8 associated with a high plasma interferon gamma-inducible protein 10 level in methadone-maintained patients with urine test positive for morphine. ''PLoS One''. 2017; '''12''' (11):e0187639
Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students. Description: Webb, Bradley T, et al. Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students. ''Front Genet''. 2017; '''8''': 30
Morgagnian cataract resulting from a naturally occurring nonsense mutation elucidates a role of CPAMD8 in mammalian lens development. Description: Hollmann, Anne K, et al. Morgagnian cataract resulting from a naturally occurring nonsense mutation elucidates a role of CPAMD8 in mammalian lens development. ''PLoS One''. 2017; '''12''' (7):e0180665
Morphometrics Reveals Complex and Heritable Apple Leaf Shapes. Description: Migicovsky, Zoe, et al. Morphometrics Reveals Complex and Heritable Apple Leaf Shapes. ''Front Plant Sci''. 2017; '''8''': 2185
NCOA1 is a novel susceptibility gene for multiple myeloma in the Chinese population: A case-control study. Description: Peng, Mengle, et al. NCOA1 is a novel susceptibility gene for multiple myeloma in the Chinese population: A case-control study. ''PLoS One''. 2017; '''12''' (3):e0173298
Neuropeptide S (NPS) variants modify the signaling and risk effects of NPS Receptor 1 (NPSR1) variants in asthma. Description: Acevedo, Nathalie, et al. Neuropeptide S (NPS) variants modify the signaling and risk effects of NPS Receptor 1 (NPSR1) variants in asthma. ''PLoS One''. 2017; '''12''' (5):e0176568
Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis. Description: Martin-Fernandez, Laura, et al. Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis. ''PLoS One''. 2017; '''12''' (4):e0176301
OCA2 splice site variant in German Spitz dogs with oculocutaneous albinism. Description: Caduff, Madleina, et al. OCA2 splice site variant in German Spitz dogs with oculocutaneous albinism. ''PLoS One''. 2017; '''12''' (10):e0185944
Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study. Description: Robiou-du-Pont, Sebastien, et al. Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study. ''PLoS One''. 2017; '''12''' (10):e0186218
PARP-1 Variant Rs1136410 Confers Protection against Coronary Artery Disease in a Chinese Han Population: A Two-Stage Case-Control Study Involving 5643 Subjects. Description: Wang, Xue-Bin, et al. PARP-1 Variant Rs1136410 Confers Protection against Coronary Artery Disease in a Chinese Han Population: A Two-Stage Case-Control Study Involving 5643 Subjects. ''Front Physiol''. 2017; '''8''': 916
Patterns of genomic and phenomic diversity in wine and table grapes. Description: Migicovsky, Zoe, et al. Patterns of genomic and phenomic diversity in wine and table grapes. ''Hortic Res''. 2017; '''4''': 17035
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Description: Yeo, Astrid, et al. Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. ''PLoS One''. 2017; '''12''' (7):e0182115
Pharmacogenetic Variation in Over 100 Genes in Patients Receiving Acenocumarol. Description: Gonzalez-Covarrubias, Vanessa, et al. Pharmacogenetic Variation in Over 100 Genes in Patients Receiving Acenocumarol. ''Front Pharmacol''. 2017; '''8''': 863
PNPLA3 rs1010023 Predisposes Chronic Hepatitis B to Hepatic Steatosis but Improves Insulin Resistance and Glucose Metabolism. Description: Pan, Qin, et al. PNPLA3 rs1010023 Predisposes Chronic Hepatitis B to Hepatic Steatosis but Improves Insulin Resistance and Glucose Metabolism. ''J Diabetes Res''. 2017; '''2017''': 4740124
Polygenic risk for five psychiatric disorders and cross-disorder and disorder-specific neural connectivity in two independent populations. Description: Wang, Tianqi, et al. Polygenic risk for five psychiatric disorders and cross-disorder and disorder-specific neural connectivity in two independent populations. ''Neuroimage Clin''. 2017; '''14''': 441-449
Polymorphisms in HTR2A and DRD4 Predispose to Smoking and Smoking Quantity. Description: Perez-Rubio, Gloria, et al. Polymorphisms in HTR2A and DRD4 Predispose to Smoking and Smoking Quantity. ''PLoS One''. 2017; '''12''' (1):e0170019
Positive Association between ANKRD55 Polymorphism 7731626 and Dermatomyositis/Polymyositis with Interstitial Lung Disease in Chinese Han Population. Description: Li, Liubing, et al. Positive Association between ANKRD55 Polymorphism 7731626 and Dermatomyositis/Polymyositis with Interstitial Lung Disease in Chinese Han Population. ''Biomed Res Int''. 2017; '''2017''': 2905987
Prediction Analysis for Transition to Schizophrenia in Individuals at Clinical High Risk for Psychosis: The Relationship of DAO, DAOA, and NRG1 Variants with Negative Symptoms and Cognitive Deficits. Description: Jagannath, Vinita, et al. Prediction Analysis for Transition to Schizophrenia in Individuals at Clinical High Risk for Psychosis: The Relationship of DAO, DAOA, and NRG1 Variants with Negative Symptoms and Cognitive Deficits. ''Front Psychiatry''. 2017; '''8''': 292
PR Interval Associated Genes, Atrial Remodeling and Rhythm Outcome of Catheter Ablation of Atrial Fibrillation-A Gene-Based Analysis of GWAS Data. Description: Husser, Daniela, et al. PR Interval Associated Genes, Atrial Remodeling and Rhythm Outcome of Catheter Ablation of Atrial Fibrillation-A Gene-Based Analysis of GWAS Data. ''Front Genet''. 2017; '''8''': 224
QTL Mapping for Pest and Disease Resistance in Cassava and Coincidence of Some QTL with Introgression Regions Derived from Manihot glaziovii. Description: Nzuki, Inosters, et al. QTL Mapping for Pest and Disease Resistance in Cassava and Coincidence of Some QTL with Introgression Regions Derived from Manihot glaziovii. ''Front Plant Sci''. 2017; '''8''': 1168
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. Description: Pilling, Luke C, et al. Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. ''PLoS One''. 2017; '''12''' (9):e0185083
Regulation of Fn14 Receptor and NF-kappaB Underlies Inflammation in Meniere's Disease. Description: Frejo, Lidia, et al. Regulation of Fn14 Receptor and NF-kappaB Underlies Inflammation in Meniere's Disease. ''Front Immunol''. 2017; '''8''': 1739
Risk-Conferring Glutamatergic Genes and Brain Glutamate Plus Glutamine in Schizophrenia. Description: Bustillo, Juan R, et al. Risk-Conferring Glutamatergic Genes and Brain Glutamate Plus Glutamine in Schizophrenia. ''Front Psychiatry''. 2017; '''8''': 79
Risk prediction of pulmonary tuberculosis using genetic and conventional risk factors in adult Korean population. Description: Hong, Eun Pyo, et al. Risk prediction of pulmonary tuberculosis using genetic and conventional risk factors in adult Korean population. ''PLoS One''. 2017; '''12''' (3):e0174642
Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions. Description: Viana, Joana, et al. Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions. ''Hum Mol Genet''. 2017 Jan 1; '''26''' (1):210-225
Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development. Description: Stergiakouli, Evie, et al. Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development. ''Mol Autism''. 2017; '''8''': 18
Sherpas share genetic variations with Tibetans for high-altitude adaptation. Description: Bhandari, Sushil, et al. Sherpas share genetic variations with Tibetans for high-altitude adaptation. ''Mol Genet Genomic Med''. 2017 Jan; '''5''' (1):76-84
Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease. Description: Morimoto, Takaaki, et al. Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease. ''PLoS One''. 2017; '''12''' (4):e0175649
Single Nucleotide Polymorphism in the COL11A2 Gene Associated with Heat Pain Sensitivity in Knee Osteoarthritis. Description: Ho, Kwo Wei David, et al. Single Nucleotide Polymorphism in the COL11A2 Gene Associated with Heat Pain Sensitivity in Knee Osteoarthritis. ''Mol Pain''. 2017 Jan-Dec; '''13''': 1744806917724259
Single-nucleotide polymorphisms are associated with cognitive decline at Alzheimer's disease conversion within mild cognitive impairment patients. Description: Lee, Eunjee, et al. Single-nucleotide polymorphisms are associated with cognitive decline at Alzheimer's disease conversion within mild cognitive impairment patients. ''Alzheimers Dement (Amst)''. 2017; '''8''': 86-95
Single Nucleotide Variants of Candidate Genes in Aggrecan Metabolic Pathway Are Associated with Lumbar Disc Degeneration and Modic Changes. Description: Perera, Romain Shanil, et al. Single Nucleotide Variants of Candidate Genes in Aggrecan Metabolic Pathway Are Associated with Lumbar Disc Degeneration and Modic Changes. ''PLoS One''. 2017; '''12''' (1):e0169835
SNP-Discovery by RAD-Sequencing in a Germplasm Collection of Wild and Cultivated Grapevines (V. vinifera L.). Description: Marrano, Annarita, et al. SNP-Discovery by RAD-Sequencing in a Germplasm Collection of Wild and Cultivated Grapevines (V. vinifera L.). ''PLoS One''. 2017; '''12''' (1):e0170655
SNP-SNP interactions as risk factors for aggressive prostate cancer. Description: Vaidyanathan, Venkatesh, et al. SNP-SNP interactions as risk factors for aggressive prostate cancer. ''F1000Res''. 2017; '''6''': 621
SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations. Description: Wolin, Annika, et al. SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations. ''Front Immunol''. 2017; '''8''': 422
Socioeconomic Status Is Not Related with Facial Fluctuating Asymmetry: Evidence from Latin-American Populations. Description: Quinto-Sanchez, Mirsha, et al. Socioeconomic Status Is Not Related with Facial Fluctuating Asymmetry: Evidence from Latin-American Populations. ''PLoS One''. 2017; '''12''' (1):e0169287
Study on the introgression of beef breeds in Canchim cattle using single nucleotide polymorphism markers. Description: Buzanskas, Marcos Eli, et al. Study on the introgression of beef breeds in Canchim cattle using single nucleotide polymorphism markers. ''PLoS One''. 2017; '''12''' (2):e0171660
Systematic Profiling of Short Tandem Repeats in the Cattle Genome. Description: Xu, Lingyang, et al. Systematic Profiling of Short Tandem Repeats in the Cattle Genome. ''Genome Biol Evol''. 2017 Jan 1; '''9''' (1):20-31
Temporal Genetic Dynamics of an Experimental, Biparental Field Population of Phytophthora capsici. Description: Carlson, Maryn O, et al. Temporal Genetic Dynamics of an Experimental, Biparental Field Population of Phytophthora capsici. ''Front Genet''. 2017; '''8''': 26
TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases. Description: Kuot, Abraham, et al. TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases. ''PLoS One''. 2017; '''12''' (8):e0183719
The ADAMTS9 gene is associated with cognitive aging in the elderly in a Taiwanese population. Description: Lin, Eugene, et al. The ADAMTS9 gene is associated with cognitive aging in the elderly in a Taiwanese population. ''PLoS One''. 2017; '''12''' (2):e0172440
The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia. Description: Thomsen, Liv Cecilie V, et al. The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia. ''J Hypertens''. 2017 Jan; '''35''' (1):132-139
The association between 38 previously reported polymorphisms and psoriasis in a Polish population: High predicative accuracy of a genetic risk score combining 16 loci. Description: Kisiel, Bartlomiej, et al. The association between 38 previously reported polymorphisms and psoriasis in a Polish population: High predicative accuracy of a genetic risk score combining 16 loci. ''PLoS One''. 2017; '''12''' (6):e0179348
The association between the nicotinic acetylcholine receptor alpha4 subunit gene (CHRNA4) rs1044396 and Internet gaming disorder in Korean male adults. Description: Jeong, Jo-Eun, et al. The association between the nicotinic acetylcholine receptor alpha4 subunit gene (CHRNA4) rs1044396 and Internet gaming disorder in Korean male adults. ''PLoS One''. 2017; '''12''' (12):e0188358
The Association of a Genetic Variant in SCAF8-CNKSR3 with Diabetic Kidney Disease and Diabetic Retinopathy in a Chinese Population. Description: Jin, Li, et al. The Association of a Genetic Variant in SCAF8-CNKSR3 with Diabetic Kidney Disease and Diabetic Retinopathy in a Chinese Population. ''J Diabetes Res''. 2017; '''2017''': 6542689
The Association of Genetic Predisposition to Depressive Symptoms with Non-suicidal and Suicidal Self-Injuries. Description: Maciejewski, Dominique F, et al. The Association of Genetic Predisposition to Depressive Symptoms with Non-suicidal and Suicidal Self-Injuries. ''Behav Genet''. 2017 Jan; '''47''' (1):3-10
The Bos taurus-Bos indicus balance in fertility and milk related genes. Description: Kasarapu, Parthan, et al. The Bos taurus-Bos indicus balance in fertility and milk related genes. ''PLoS One''. 2017; '''12''' (8):e0181930
The distribution of runs of homozygosity and selection signatures in six commercial meat sheep breeds. Description: Purfield, Deirdre C, et al. The distribution of runs of homozygosity and selection signatures in six commercial meat sheep breeds. ''PLoS One''. 2017; '''12''' (5):e0176780
The fine-scale genetic structure and evolution of the Japanese population. Description: Takeuchi, Fumihiko, et al. The fine-scale genetic structure and evolution of the Japanese population. ''PLoS One''. 2017; '''12''' (11):e0185487
The impact of methylation quantitative trait loci (mQTLs) on active smoking-related DNA methylation changes. Description: Gao, Xu, et al. The impact of methylation quantitative trait loci (mQTLs) on active smoking-related DNA methylation changes. ''Clin Epigenetics''. 2017; '''9''': 87
TMEM187-IRAK1 Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic Origin. Description: Khalifa, Olfa, et al. TMEM187-IRAK1 Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic Origin. ''J Immunol Res''. 2017; '''2017''': 4915950
Transmission between Archaic and Modern Human Ancestors during the Evolution of the Oncogenic Human Papillomavirus 16. Description: Pimenoff, Ville N, et al. Transmission between Archaic and Modern Human Ancestors during the Evolution of the Oncogenic Human Papillomavirus 16. ''Mol Biol Evol''. 2017 Jan; '''34''' (1):4-19
Unveiling the Identity of Wenwan Walnuts and Phylogenetic Relationships of Asian Juglans Species Using Restriction Site-Associated DNA-Sequencing. Description: Mu, Xian-Yun, et al. Unveiling the Identity of Wenwan Walnuts and Phylogenetic Relationships of Asian Juglans Species Using Restriction Site-Associated DNA-Sequencing. ''Front Plant Sci''. 2017; '''8''': 1708
Using Genetic Variation to Explore the Causal Effect of Maternal Pregnancy Adiposity on Future Offspring Adiposity: A Mendelian Randomisation Study. Description: Richmond, Rebecca C, et al. Using Genetic Variation to Explore the Causal Effect of Maternal Pregnancy Adiposity on Future Offspring Adiposity: A Mendelian Randomisation Study. ''PLoS Med''. 2017 Jan; '''14''' (1):e1002221
Using spatio-temporal surveillance data to test the infectious environment of children before type 1 diabetes diagnosis. Description: Bougneres, Pierre, et al. Using spatio-temporal surveillance data to test the infectious environment of children before type 1 diabetes diagnosis. ''PLoS One''. 2017; '''12''' (2):e0170658
Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants. Description: Kantojarvi, Katri, et al. Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants. ''PLoS One''. 2017; '''12''' (8):e0180652
Variants of ACAN are associated with severity of lumbar disc herniation in patients with chronic low back pain. Description: Perera, Romain Shanil, et al. Variants of ACAN are associated with severity of lumbar disc herniation in patients with chronic low back pain. ''PLoS One''. 2017; '''12''' (7):e0181580
Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study. Description: Claudio-Campos, Karla, et al. Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study. ''Front Pharmacol''. 2017; '''8''': 347
Whole exome sequencing as a diagnostic tool for patients with ciliopathy-like phenotypes. Description: Castro-Sanchez, Sheila, et al. Whole exome sequencing as a diagnostic tool for patients with ciliopathy-like phenotypes. ''PLoS One''. 2017; '''12''' (8):e0183081
Whole genome structural analysis of Caribbean hair sheep reveals quantitative link to West African ancestry. Description: Spangler, Gordon L, et al. Whole genome structural analysis of Caribbean hair sheep reveals quantitative link to West African ancestry. ''PLoS One''. 2017; '''12''' (6):e0179021
XX Disorder of Sex Development is associated with an insertion on chromosome 9 and downregulation of RSPO1 in dogs (Canis lupus familiaris). Description: Meyers-Wallen, Vicki N, et al. XX Disorder of Sex Development is associated with an insertion on chromosome 9 and downregulation of RSPO1 in dogs (Canis lupus familiaris). ''PLoS One''. 2017; '''12''' (10):e0186331
Building a genetic risk model for bipolar disorder from genome-wide association data with random forest algorithm. Description: Chuang, Li-Chung, et al. Building a genetic risk model for bipolar disorder from genome-wide association data with random forest algorithm. ''Sci Rep''. 2017 Jan 3; '''7''': 39943
TIMP-2 SNPs rs7342880 and rs4789936 are linked to risk of knee osteoarthritis in the Chinese Han Population. Description: Xu, Pengcheng, et al. TIMP-2 SNPs rs7342880 and rs4789936 are linked to risk of knee osteoarthritis in the Chinese Han Population. ''Oncotarget''. 2017 Jan 3; '''8''' (1):1166-1176
Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes. Description: Karyadi, Danielle M, et al. Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes. ''Oncotarget''. 2017 Jan 3; '''8''' (1):1495-1507
Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus. Description: Pritchard, Victoria L, et al. Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus. ''G3 (Bethesda)''. 2017 Jan 5; '''7''' (1):165-178
Genome-wide association study identifies COL2A1 locus involved in the hand development failure of Kashin-Beck disease. Description: Hao, Jingcan, et al. Genome-wide association study identifies COL2A1 locus involved in the hand development failure of Kashin-Beck disease. ''Sci Rep''. 2017 Jan 6; '''7''': 40020
Mapping Post-Glacial expansions: The Peopling of Southwest Asia. Description: Platt, Daniel E, et al. Mapping Post-Glacial expansions: The Peopling of Southwest Asia. ''Sci Rep''. 2017 Jan 6; '''7''': 40338
Type 2 Diabetes Susceptibility in the Greek-Cypriot Population: Replication of Associations with TCF7L2, FTO, HHEX, SLC30A8 and IGF2BP2 Polymorphisms. Description: Votsi, Christina, et al. Type 2 Diabetes Susceptibility in the Greek-Cypriot Population: Replication of Associations with TCF7L2, FTO, HHEX, SLC30A8 and IGF2BP2 Polymorphisms. ''Genes (Basel)''. 2017 Jan 6; '''8''' (1):
SLC11A1 polymorphisms and host susceptibility to cutaneous leishmaniasis in Pakistan. Description: Sophie, Mariam, et al. SLC11A1 polymorphisms and host susceptibility to cutaneous leishmaniasis in Pakistan. ''Parasit Vectors''. 2017 Jan 7; '''10''' (1):12
No convincing association between genetic markers and respiratory symptoms: results of a GWA study. Description: Zeng, Xiang, et al. No convincing association between genetic markers and respiratory symptoms: results of a GWA study. ''Respir Res''. 2017 Jan 10; '''18''' (1):11
Development of a 690 K SNP array in catfish and its application for genetic mapping and validation of the reference genome sequence. Description: Zeng, Qifan, et al. Development of a 690 K SNP array in catfish and its application for genetic mapping and validation of the reference genome sequence. ''Sci Rep''. 2017 Jan 12; '''7''': 40347
SNP rs11185644 of RXRA gene is identified for dose-response variability to vitamin D3 supplementation: a randomized clinical trial. Description: Zhang, Mingzhi, et al. SNP rs11185644 of RXRA gene is identified for dose-response variability to vitamin D3 supplementation: a randomized clinical trial. ''Sci Rep''. 2017 Jan 12; '''7''': 40593
Germline compound heterozygous poly-glutamine deletion in USF3 may be involved in predisposition to heritable and sporadic epithelial thyroid carcinoma. Description: Ni, Ying, et al. Germline compound heterozygous poly-glutamine deletion in USF3 may be involved in predisposition to heritable and sporadic epithelial thyroid carcinoma. ''Hum Mol Genet''. 2017 Jan 15; '''26''' (2):243-257
Multimodal Brain Imaging Reveals Structural Differences in Alzheimer's Disease Polygenic Risk Carriers: A Study in Healthy Young Adults. Description: Foley, Sonya F, et al. Multimodal Brain Imaging Reveals Structural Differences in Alzheimer's Disease Polygenic Risk Carriers: A Study in Healthy Young Adults. ''Biol Psychiatry''. 2017 Jan 15; '''81''' (2):154-161
A mast cell-ILC2-Th9 pathway promotes lung inflammation in cystic fibrosis. Description: Moretti, Silvia, et al. A mast cell-ILC2-Th9 pathway promotes lung inflammation in cystic fibrosis. ''Nat Commun''. 2017 Jan 16; '''8''': 14017
Association between DNA mismatch repair gene polymorphisms and platinum-based chemotherapy toxicity in non-small cell lung cancer patients. Description: Liu, Jun-Yan, et al. Association between DNA mismatch repair gene polymorphisms and platinum-based chemotherapy toxicity in non-small cell lung cancer patients. ''Chin J Cancer''. 2017 Jan 16; '''36''' (1):12
Phage-Derived Protein Induces Increased Platelet Activation and Is Associated with Mortality in Patients with Invasive Pneumococcal Disease. Description: Tunjungputri, Rahajeng N, et al. Phage-Derived Protein Induces Increased Platelet Activation and Is Associated with Mortality in Patients with Invasive Pneumococcal Disease. ''MBio''. 2017 Jan 17; '''8''' (1):
Genetic structure in the Sherpa and neighboring Nepalese populations. Description: Cole, Amy M, et al. Genetic structure in the Sherpa and neighboring Nepalese populations. ''BMC Genomics''. 2017 Jan 19; '''18''' (1):102
Genetic risk variants for metabolic traits in Arab populations. Description: Hebbar, Prashantha, et al. Genetic risk variants for metabolic traits in Arab populations. ''Sci Rep''. 2017 Jan 20; '''7''': 40988
Genetic diversity, extent of linkage disequilibrium and persistence of gametic phase in Canadian pigs. Description: Grossi, Daniela A, et al. Genetic diversity, extent of linkage disequilibrium and persistence of gametic phase in Canadian pigs. ''BMC Genet''. 2017 Jan 21; '''18''' (1):6
Fine mapping genetic associations between the HLA region and extremely high intelligence. Description: Zabaneh, Delilah, et al. Fine mapping genetic associations between the HLA region and extremely high intelligence. ''Sci Rep''. 2017 Jan 24; '''7''': 41182
Whole-exome sequencing of 228 patients with sporadic Parkinson's disease. Description: Sandor, Cynthia, et al. Whole-exome sequencing of 228 patients with sporadic Parkinson's disease. ''Sci Rep''. 2017 Jan 24; '''7''': 41188
Genome-wide association study identifies four SNPs associated with response to platinum-based neoadjuvant chemotherapy for cervical cancer. Description: Li, Xiong, et al. Genome-wide association study identifies four SNPs associated with response to platinum-based neoadjuvant chemotherapy for cervical cancer. ''Sci Rep''. 2017 Jan 25; '''7''': 41103
Identification of RAN1 orthologue associated with sex determination through whole genome sequencing analysis in fig (Ficus carica L.). Description: Mori, Kazuki, et al. Identification of RAN1 orthologue associated with sex determination through whole genome sequencing analysis in fig (Ficus carica L.). ''Sci Rep''. 2017 Jan 25; '''7''': 41124
Integrating GWAS and Co-expression Network Data Identifies Bone Mineral Density Genes SPTBN1 and MARK3 and an Osteoblast Functional Module. Description: Calabrese, Gina M, et al. Integrating GWAS and Co-expression Network Data Identifies Bone Mineral Density Genes SPTBN1 and MARK3 and an Osteoblast Functional Module. ''Cell Syst''. 2017 Jan 25; '''4''' (1):46-59.e4
De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease. Description: Takahashi, Shinichi, et al. De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease. ''Genome Med''. 2017 Jan 26; '''9''' (1):8
Genomic characterization of a core set of the USDA-NPGS Ethiopian sorghum germplasm collection: implications for germplasm conservation, evaluation, and utilization in crop improvement. Description: Cuevas, Hugo E, et al. Genomic characterization of a core set of the USDA-NPGS Ethiopian sorghum germplasm collection: implications for germplasm conservation, evaluation, and utilization in crop improvement. ''BMC Genomics''. 2017 Jan 26; '''18''' (1):108
Evaluation of 10 SLE susceptibility loci in Asian populations, which were initially identified in European populations. Description: Zhang, Yue-Miao, et al. Evaluation of 10 SLE susceptibility loci in Asian populations, which were initially identified in European populations. ''Sci Rep''. 2017 Jan 27; '''7''': 41399
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Description: Jansen, Iris E, et al. Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. ''Genome Biol''. 2017 Jan 30; '''18''' (1):22
The Identification of a 1916 Irish Rebel: New Approach for Estimating Relatedness From Low Coverage Homozygous Genomes. Description: Fernandes, Daniel, et al. The Identification of a 1916 Irish Rebel: New Approach for Estimating Relatedness From Low Coverage Homozygous Genomes. ''Sci Rep''. 2017 Jan 30; '''7''': 41529
ADAM23 is a common risk gene for canine idiopathic epilepsy. Description: Koskinen, Lotta L E, et al. ADAM23 is a common risk gene for canine idiopathic epilepsy. ''BMC Genet''. 2017 Jan 31; '''18''' (1):8
A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria. Description: Marquet, Sandrine, et al. A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria. ''Sci Rep''. 2017 Jan 31; '''7''': 41636
Genome-Wide Association Study of Polymorphisms Predisposing to Bronchiolitis. Description: Pasanen, Anu, et al. Genome-Wide Association Study of Polymorphisms Predisposing to Bronchiolitis. ''Sci Rep''. 2017 Jan 31; '''7''': 41653
Medical history of discordant twins and environmental etiologies of autism. Description: Willfors, C, et al. Medical history of discordant twins and environmental etiologies of autism. ''Transl Psychiatry''. 2017 Jan 31; '''7''' (1):e1014
Mx1, OAS1 and OAS2 polymorphisms are associated with the severity of liver disease in HIV/HCV-coinfected patients: A cross-sectional study. Description: Garcia-Alvarez, Monica, et al. Mx1, OAS1 and OAS2 polymorphisms are associated with the severity of liver disease in HIV/HCV-coinfected patients: A cross-sectional study. ''Sci Rep''. 2017 Jan 31; '''7''': 41516
SNP variants associated with non-Hodgkin lymphoma (NHL) correlate with human leukocyte antigen (HLA) class II expression. Description: Ten, Lik-Chin, et al. SNP variants associated with non-Hodgkin lymphoma (NHL) correlate with human leukocyte antigen (HLA) class II expression. ''Sci Rep''. 2017 Jan 31; '''7''': 41400
A Common Polymorphism in a Williams Syndrome Gene Predicts Amygdala Reactivity and Extraversion in Healthy Adults. Description: Swartz, Johnna R, et al. A Common Polymorphism in a Williams Syndrome Gene Predicts Amygdala Reactivity and Extraversion in Healthy Adults. ''Biol Psychiatry''. 2017 Feb 1; '''81''' (3):203-210
Adenylyl cyclase type 9 gene polymorphisms are associated with asthma and allergy in Brazilian children. Description: Teixeira, Helena M P, et al. Adenylyl cyclase type 9 gene polymorphisms are associated with asthma and allergy in Brazilian children. ''Mol Immunol''. 2017 Feb; '''82''': 137-145
A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy. Description: Fava, Vinicius M, et al. A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy. ''PLoS Genet''. 2017 Feb; '''13''' (2):e1006637
A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. Description: Zazo Seco, Celia, et al. A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. ''Dis Model Mech''. 2017 Feb 1; '''10''' (2):105-118
ANLN truncation causes a familial fatal acute respiratory distress syndrome in Dalmatian dogs. Description: Holopainen, Saila, et al. ANLN truncation causes a familial fatal acute respiratory distress syndrome in Dalmatian dogs. ''PLoS Genet''. 2017 Feb; '''13''' (2):e1006625
A novel locus on chromosome 1 underlies the evolution of a melanic plumage polymorphism in a wild songbird. Description: Bourgeois, Yann X C, et al. A novel locus on chromosome 1 underlies the evolution of a melanic plumage polymorphism in a wild songbird. ''R Soc Open Sci''. 2017 Feb; '''4''' (2):160805
A two-stage inter-rater approach for enrichment testing of variants associated with multiple traits. Description: Asimit, Jennifer L, et al. A two-stage inter-rater approach for enrichment testing of variants associated with multiple traits. ''Eur J Hum Genet''. 2017 Feb; '''25''' (3):341-349
Complement receptor 1 gene polymorphisms are associated with cardiovascular risk. Description: de Vries, Marijke A, et al. Complement receptor 1 gene polymorphisms are associated with cardiovascular risk. ''Atherosclerosis''. 2017 Feb; '''257''': 16-21
Genetic analysis of CHCHD2 in a southern Spanish population. Description: Tejera-Parrado, Cristina, et al. Genetic analysis of CHCHD2 in a southern Spanish population. ''Neurobiol Aging''. 2017 Feb; '''50''': 169.e1-169.e2
Genetic architecture of age-related cognitive decline in African Americans. Description: Raj, Towfique, et al. Genetic architecture of age-related cognitive decline in African Americans. ''Neurol Genet''. 2017 Feb; '''3''' (1):e125
Genetic origin, admixture and population history of aurochs (Bos primigenius) and primitive European cattle. Description: Upadhyay, M R, et al. Genetic origin, admixture and population history of aurochs (Bos primigenius) and primitive European cattle. ''Heredity (Edinb)''. 2017 Feb; '''118''' (2):169-176
Genetic polymorphism of nonsyndromic cleft lip with or without cleft palate is associated with developmental dyslexia in Chinese school-aged populations. Description: Wang, Bin, et al. Genetic polymorphism of nonsyndromic cleft lip with or without cleft palate is associated with developmental dyslexia in Chinese school-aged populations. ''J Hum Genet''. 2017 Feb; '''62''' (2):265-268
Genetic prediction of male pattern baldness. Description: Hagenaars, Saskia P, et al. Genetic prediction of male pattern baldness. ''PLoS Genet''. 2017 Feb; '''13''' (2):e1006594
Genetic variants alter T-bet binding and gene expression in mucosal inflammatory disease. Description: Soderquest, Katrina, et al. Genetic variants alter T-bet binding and gene expression in mucosal inflammatory disease. ''PLoS Genet''. 2017 Feb; '''13''' (2):e1006587
Genome-wide association scans for idiopathic osteonecrosis of the femoral head in a Korean population. Description: Baek, Seung-Hoon, et al. Genome-wide association scans for idiopathic osteonecrosis of the femoral head in a Korean population. ''Mol Med Rep''. 2017 Feb; '''15''' (2):750-758
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease. Description: Ji, Sun-Gou, et al. Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease. ''Nat Genet''. 2017 Feb; '''49''' (2):269-273
Genome-wide data from two early Neolithic East Asian individuals dating to 7700 years ago. Description: Siska, Veronika, et al. Genome-wide data from two early Neolithic East Asian individuals dating to 7700 years ago. ''Sci Adv''. 2017 Feb; '''3''' (2):e1601877
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway. Description: Kiryluk, Krzysztof, et al. GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway. ''PLoS Genet''. 2017 Feb; '''13''' (2):e1006609
Host genetic variation in mucosal immunity pathways influences the upper airway microbiome. Description: Igartua, Catherine, et al. Host genetic variation in mucosal immunity pathways influences the upper airway microbiome. ''Microbiome''. 2017 Feb 1; '''5''' (1):16
Improving polygenic risk prediction from summary statistics by an empirical Bayes approach. Description: So, Hon-Cheong, et al. Improving polygenic risk prediction from summary statistics by an empirical Bayes approach. ''Sci Rep''. 2017 Feb 1; '''7''': 41262
MicroRNA-146a suppresses IL-17-mediated skin inflammation and is genetically associated with psoriasis. Description: Srivastava, Ankit, et al. MicroRNA-146a suppresses IL-17-mediated skin inflammation and is genetically associated with psoriasis. ''J Allergy Clin Immunol''. 2017 Feb; '''139''' (2):550-561
Multiple rare genetic variants co-segregating with familial IgA nephropathy all act within a single immune-related network. Description: Cox, S N, et al. Multiple rare genetic variants co-segregating with familial IgA nephropathy all act within a single immune-related network. ''J Intern Med''. 2017 Feb; '''281''' (2):189-205
New genetic signatures associated with cancer cachexia as defined by low skeletal muscle index and weight loss. Description: Johns, Neil, et al. New genetic signatures associated with cancer cachexia as defined by low skeletal muscle index and weight loss. ''J Cachexia Sarcopenia Muscle''. 2017 Feb; '''8''' (1):122-130
OSBPL10, RXRA and lipid metabolism confer African-ancestry protection against dengue haemorrhagic fever in admixed Cubans. Description: Sierra, Beatriz, et al. OSBPL10, RXRA and lipid metabolism confer African-ancestry protection against dengue haemorrhagic fever in admixed Cubans. ''PLoS Pathog''. 2017 Feb; '''13''' (2):e1006220
Overcoming the dichotomy between open and isolated populations using genomic data from a large European dataset. Description: Anagnostou, Paolo, et al. Overcoming the dichotomy between open and isolated populations using genomic data from a large European dataset. ''Sci Rep''. 2017 Feb 1; '''7''': 41614
Recent Historical Migrations Have Shaped the Gene Pool of Arabs and Berbers in North Africa. Description: Arauna, Lara R, et al. Recent Historical Migrations Have Shaped the Gene Pool of Arabs and Berbers in North Africa. ''Mol Biol Evol''. 2017 Feb 1; '''34''' (2):318-329
Systolic Blood Pressure and Risk of Type 2 Diabetes: A Mendelian Randomization Study. Description: Aikens, Rachael C, et al. Systolic Blood Pressure and Risk of Type 2 Diabetes: A Mendelian Randomization Study. ''Diabetes''. 2017 Feb; '''66''' (2):543-550
Targeted capture to assess neutral genomic variation in the narrow-leaf hopbush across a continental biodiversity refugium. Description: Christmas, Matthew J, et al. Targeted capture to assess neutral genomic variation in the narrow-leaf hopbush across a continental biodiversity refugium. ''Sci Rep''. 2017 Feb 1; '''7''': 41367
The ultimate and proximate mechanisms driving the evolution of long tails in forest deer mice. Description: Kingsley, Evan P, et al. The ultimate and proximate mechanisms driving the evolution of long tails in forest deer mice. ''Evolution''. 2017 Feb; '''71''' (2):261-273
A genome-wide association study in a large F2-cross of laying hens reveals novel genomic regions associated with feather pecking and aggressive pecking behavior. Description: Lutz, Vanessa, et al. A genome-wide association study in a large F2-cross of laying hens reveals novel genomic regions associated with feather pecking and aggressive pecking behavior. ''Genet Sel Evol''. 2017 Feb 3; '''49''' (1):18
Diversity analysis of cotton (Gossypium hirsutum L.) germplasm using the CottonSNP63K Array. Description: Hinze, Lori L, et al. Diversity analysis of cotton (Gossypium hirsutum L.) germplasm using the CottonSNP63K Array. ''BMC Plant Biol''. 2017 Feb 3; '''17''' (1):37
IL1B-CGTC haplotype is associated with colorectal cancer in admixed individuals with increased African ancestry. Description: Sanabria-Salas, Maria Carolina, et al. IL1B-CGTC haplotype is associated with colorectal cancer in admixed individuals with increased African ancestry. ''Sci Rep''. 2017 Feb 3; '''7''': 41920
Associations of PARP-1 variant rs1136410 with PARP activities, oxidative DNA damage, and the risk of age-related cataract in a Chinese Han population: A two-stage case-control analysis. Description: Cui, Ning-Hua, et al. Associations of PARP-1 variant rs1136410 with PARP activities, oxidative DNA damage, and the risk of age-related cataract in a Chinese Han population: A two-stage case-control analysis. ''Gene''. 2017 Feb 5; '''600''': 70-76
Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes. Description: Xu, Hongqin, et al. Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes. ''Sci Rep''. 2017 Feb 6; '''7''': 41816
Associations between genetic variants in immunoregulatory genes and risk of non-Hodgkin lymphoma in a Chinese population. Description: Ye, Xibiao, et al. Associations between genetic variants in immunoregulatory genes and risk of non-Hodgkin lymphoma in a Chinese population. ''Oncotarget''. 2017 Feb 7; '''8''' (6):10450-10457
Searching for new loci and candidate genes for economically important traits through gene-based association analysis of Simmental cattle. Description: Xia, Jiangwei, et al. Searching for new loci and candidate genes for economically important traits through gene-based association analysis of Simmental cattle. ''Sci Rep''. 2017 Feb 7; '''7''': 42048
Susceptibility to type 2 diabetes may be modulated by haplotypes in G6PC2, a target of positive selection. Description: Al-Daghri, Nasser M, et al. Susceptibility to type 2 diabetes may be modulated by haplotypes in G6PC2, a target of positive selection. ''BMC Evol Biol''. 2017 Feb 7; '''17''' (1):43
Comparative genomics of canine hemoglobin genes reveals primacy of beta subunit delta in adult carnivores. Description: Zaldivar-Lopez, Sara, et al. Comparative genomics of canine hemoglobin genes reveals primacy of beta subunit delta in adult carnivores. ''BMC Genomics''. 2017 Feb 8; '''18''' (1):141
Implications of human evolution and admixture for mitochondrial replacement therapy. Description: Rishishwar, Lavanya, et al. Implications of human evolution and admixture for mitochondrial replacement therapy. ''BMC Genomics''. 2017 Feb 8; '''18''' (1):140
A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1). Description: Mauri, Nico, et al. A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1). ''G3 (Bethesda)''. 2017 Feb 9; '''7''' (2):663-669
Assessing the risk for suicide in schizophrenia according to migration, ethnicity and geographical ancestry. Description: Hettige, Nuwan C, et al. Assessing the risk for suicide in schizophrenia according to migration, ethnicity and geographical ancestry. ''BMC Psychiatry''. 2017 Feb 9; '''17''' (1):63
Genetic susceptibility variants for lung cancer: replication study and assessment as expression quantitative trait loci. Description: Pintarelli, Giulia, et al. Genetic susceptibility variants for lung cancer: replication study and assessment as expression quantitative trait loci. ''Sci Rep''. 2017 Feb 9; '''7''': 42185
Genomic insights into the population structure and history of the Irish Travellers. Description: Gilbert, Edmund, et al. Genomic insights into the population structure and history of the Irish Travellers. ''Sci Rep''. 2017 Feb 9; '''7''': 42187
Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease. Description: Yin, Dan, et al. Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease. ''Sci Rep''. 2017 Feb 9; '''7''': 42175
Unveiling genomic regions that underlie differences between Afec-Assaf sheep and its parental Awassi breed. Description: Seroussi, Eyal, et al. Unveiling genomic regions that underlie differences between Afec-Assaf sheep and its parental Awassi breed. ''Genet Sel Evol''. 2017 Feb 10; '''49''' (1):19
Evolutionary selected Tibetan variants of HIF pathway and risk of lung cancer. Description: Lanikova, Lucie, et al. Evolutionary selected Tibetan variants of HIF pathway and risk of lung cancer. ''Oncotarget''. 2017 Feb 14; '''8''' (7):11739-11747
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder. Description: Lescai, F, et al. Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder. ''Transl Psychiatry''. 2017 Feb 14; '''7''' (2):e1034
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. Description: Power, Robert A, et al. Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. ''Biol Psychiatry''. 2017 Feb 15; '''81''' (4):325-335
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip +/- cleft palate and cleft palate only. Description: Ludwig, Kerstin U, et al. Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip +/- cleft palate and cleft palate only. ''Hum Mol Genet''. 2017 Feb 15; '''26''' (4):829-842
Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data. Description: Mobegi, Fredrick M, et al. Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data. ''Sci Rep''. 2017 Feb 16; '''7''': 42808
The origin of chow chows in the light of the East Asian breeds. Description: Yang, Hechuan, et al. The origin of chow chows in the light of the East Asian breeds. ''BMC Genomics''. 2017 Feb 16; '''18''' (1):174
Exome-wide association study identifies genetic polymorphisms of C12orf51, MYL2, and ALDH2 associated with blood lead levels in the general Korean population. Description: Eom, Sang-Yong, et al. Exome-wide association study identifies genetic polymorphisms of C12orf51, MYL2, and ALDH2 associated with blood lead levels in the general Korean population. ''Environ Health''. 2017 Feb 17; '''16''' (1):11
Origin and phylogenetic status of the local Ashanti Dwarf pig (ADP) of Ghana based on genetic analysis. Description: Osei-Amponsah, Richard, et al. Origin and phylogenetic status of the local Ashanti Dwarf pig (ADP) of Ghana based on genetic analysis. ''BMC Genomics''. 2017 Feb 20; '''18''' (1):193
The genome landscape of indigenous African cattle. Description: Kim, Jaemin, et al. The genome landscape of indigenous African cattle. ''Genome Biol''. 2017 Feb 20; '''18''' (1):34
Association between PPAP2B gene polymorphisms and coronary heart disease susceptibility in Chinese Han males and females. Description: Sun, Yu-Xiao, et al. Association between PPAP2B gene polymorphisms and coronary heart disease susceptibility in Chinese Han males and females. ''Oncotarget''. 2017 Feb 21; '''8''' (8):13166-13173
TLR4 rs41426344 increases susceptibility of rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA) in a central south Chinese Han population. Description: Wang, Yan, et al. TLR4 rs41426344 increases susceptibility of rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA) in a central south Chinese Han population. ''Pediatr Rheumatol Online J''. 2017 Feb 21; '''15''' (1):12
Characterizing a region on BTA11 affecting beta-lactoglobulin content of milk using high-density genotyping and haplotype grouping. Description: Bedere, Nicolas, et al. Characterizing a region on BTA11 affecting beta-lactoglobulin content of milk using high-density genotyping and haplotype grouping. ''BMC Genet''. 2017 Feb 22; '''18''' (1):17
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. Description: Yu, Yanqin, et al. Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. ''Nat Commun''. 2017 Feb 24; '''8''': 14364
TCF21 is related to testis growth and development in broiler chickens. Description: Zhang, Hui, et al. TCF21 is related to testis growth and development in broiler chickens. ''Genet Sel Evol''. 2017 Feb 24; '''49''' (1):25
Connecting genetic risk to disease end points through the human blood plasma proteome. Description: Suhre, Karsten, et al. Connecting genetic risk to disease end points through the human blood plasma proteome. ''Nat Commun''. 2017 Feb 27; '''8''': 14357
Genome-wide identification of splicing QTLs in the human brain and their enrichment among schizophrenia-associated loci. Description: Takata, Atsushi, et al. Genome-wide identification of splicing QTLs in the human brain and their enrichment among schizophrenia-associated loci. ''Nat Commun''. 2017 Feb 27; '''8''': 14519
ABCC3 genetic variants are associated with postoperative morphine-induced respiratory depression and morphine pharmacokinetics in children. Description: Chidambaran, V, et al. ABCC3 genetic variants are associated with postoperative morphine-induced respiratory depression and morphine pharmacokinetics in children. ''Pharmacogenomics J''. 2017 Mar; '''17''' (2):162-169
A few sequence polymorphisms among isolates of Maize bushy stunt phytoplasma associate with organ proliferation symptoms of infected maize plants. Description: Orlovskis, Zigmunds, et al. A few sequence polymorphisms among isolates of Maize bushy stunt phytoplasma associate with organ proliferation symptoms of infected maize plants. ''Ann Bot''. 2017 Mar 1; '''119''' (5):869-884
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1. Description: Vijayakrishnan, J, et al. A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1. ''Leukemia''. 2017 Mar; '''31''' (3):573-579
A molecular census of arcuate hypothalamus and median eminence cell types. Description: Campbell, John N, et al. A molecular census of arcuate hypothalamus and median eminence cell types. ''Nat Neurosci''. 2017 Mar; '''20''' (3):484-496
Analysis of large versus small dogs reveals three genes on the canine X chromosome associated with body weight, muscling and back fat thickness. Description: Plassais, Jocelyn, et al. Analysis of large versus small dogs reveals three genes on the canine X chromosome associated with body weight, muscling and back fat thickness. ''PLoS Genet''. 2017 Mar; '''13''' (3):e1006661
A pharmacogenetic investigation of intravenous furosemide in decompensated heart failure: a meta-analysis of three clinical trials. Description: de Denus, S, et al. A pharmacogenetic investigation of intravenous furosemide in decompensated heart failure: a meta-analysis of three clinical trials. ''Pharmacogenomics J''. 2017 Mar; '''17''' (2):192-200
Characterization of ADME gene variation in 21 populations by exome sequencing. Description: Hovelson, Daniel H, et al. Characterization of ADME gene variation in 21 populations by exome sequencing. ''Pharmacogenet Genomics''. 2017 Mar; '''27''' (3):89-100
Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk. Description: Hoffman, Joshua D, et al. Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk. ''PLoS Genet''. 2017 Mar; '''13''' (3):e1006690
Evaluation of genome-wide genotyping concordance between tumor tissues and peripheral blood. Description: Shao, Wei, et al. Evaluation of genome-wide genotyping concordance between tumor tissues and peripheral blood. ''Genomics''. 2017 Mar; '''109''' (2):108-112
Evolved genetic and phenotypic differences due to mitochondrial-nuclear interactions. Description: Baris, Tara Z, et al. Evolved genetic and phenotypic differences due to mitochondrial-nuclear interactions. ''PLoS Genet''. 2017 Mar; '''13''' (3):e1006517
Exome-wide Association Study Identifies CLEC3B Missense Variant p.S106G as Being Associated With Extreme Longevity in East Asian Populations. Description: Tanisawa, Kumpei, et al. Exome-wide Association Study Identifies CLEC3B Missense Variant p.S106G as Being Associated With Extreme Longevity in East Asian Populations. ''J Gerontol A Biol Sci Med Sci''. 2017 Mar 1; '''72''' (3):309-318
Gene-centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility. Description: Stuart, Shani, et al. Gene-centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility. ''Mol Genet Genomic Med''. 2017 Mar; '''5''' (2):157-163
Genetic, physiological and comparative genomic studies of hypertension and insulin resistance in the spontaneously hypertensive rat. Description: Coan, Philip M, et al. Genetic, physiological and comparative genomic studies of hypertension and insulin resistance in the spontaneously hypertensive rat. ''Dis Model Mech''. 2017 Mar 1; '''10''' (3):297-306
Genetic Predisposition of Polymorphisms in HMGB1-Related Genes to Breast Cancer Prognosis in Korean Women. Description: Lee, Junsu, et al. Genetic Predisposition of Polymorphisms in HMGB1-Related Genes to Breast Cancer Prognosis in Korean Women. ''J Breast Cancer''. 2017 Mar; '''20''' (1):27-34
Genetic variation in the endocannabinoid system and response to Cognitive Behavior Therapy for child anxiety disorders. Description: Lester, Kathryn J, et al. Genetic variation in the endocannabinoid system and response to Cognitive Behavior Therapy for child anxiety disorders. ''Am J Med Genet B Neuropsychiatr Genet''. 2017 Mar; '''174''' (2):144-155
Genome-association analysis of Korean Holstein milk traits using genomic estimated breeding value. Description: Shin, Donghyun, et al. Genome-association analysis of Korean Holstein milk traits using genomic estimated breeding value. ''Asian-Australas J Anim Sci''. 2017 Mar; '''30''' (3):309-319
Germline miRNA DNA variants and the risk of colorectal cancer by subtype. Description: Lindor, Noralane M, et al. Germline miRNA DNA variants and the risk of colorectal cancer by subtype. ''Genes Chromosomes Cancer''. 2017 Mar; '''56''' (3):177-184
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. Description: Trampush, J W, et al. GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. ''Mol Psychiatry''. 2017 Mar; '''22''' (3):336-345
High resolution HLA haplotyping by imputation for a British population bioresource. Description: Neville, Matt J, et al. High resolution HLA haplotyping by imputation for a British population bioresource. ''Hum Immunol''. 2017 Mar; '''78''' (3):242-251
Human genetic and metabolite variation reveals that methylthioadenosine is a prognostic biomarker and an inflammatory regulator in sepsis. Description: Wang, Liuyang, et al. Human genetic and metabolite variation reveals that methylthioadenosine is a prognostic biomarker and an inflammatory regulator in sepsis. ''Sci Adv''. 2017 Mar; '''3''' (3):e1602096
Human ROBO1 regulates white matter structure in corpus callosum. Description: Darki, Fahimeh, et al. Human ROBO1 regulates white matter structure in corpus callosum. ''Brain Struct Funct''. 2017 Mar; '''222''' (2):707-716
Investigating the case of human nose shape and climate adaptation. Description: Zaidi, Arslan A, et al. Investigating the case of human nose shape and climate adaptation. ''PLoS Genet''. 2017 Mar; '''13''' (3):e1006616
Investigation of a possible extended risk haplotype in the IL23R region associated with ankylosing spondylitis. Description: Roberts, A R, et al. Investigation of a possible extended risk haplotype in the IL23R region associated with ankylosing spondylitis. ''Genes Immun''. 2017 Mar; '''18''' (2):105-108
Molecular Population Genetics. Description: Casillas, Sonia, et al. Molecular Population Genetics. ''Genetics''. 2017 Mar; '''205''' (3):1003-1035
Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202. Description: Verma, Anurag, et al. Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202. ''Pharmacogenet Genomics''. 2017 Mar; '''27''' (3):101-111
New insights from GWAS for the cleft palate among han Chinese population. Description: Duan, S-J, et al. New insights from GWAS for the cleft palate among han Chinese population. ''Med Oral Patol Oral Cir Bucal''. 2017 Mar 1; '''22''' (2):e219-e227
Population genetic analysis of the DARC locus (Duffy) reveals adaptation from standing variation associated with malaria resistance in humans. Description: McManus, Kimberly F, et al. Population genetic analysis of the DARC locus (Duffy) reveals adaptation from standing variation associated with malaria resistance in humans. ''PLoS Genet''. 2017 Mar; '''13''' (3):e1006560
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure. Description: He, Karen Y, et al. Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure. ''PLoS Genet''. 2017 Mar; '''13''' (3):e1006678
Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes. Description: Rhead, Brooke, et al. Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes. ''Arthritis Rheumatol''. 2017 Mar; '''69''' (3):550-559
Shared regulatory sites are abundant in the human genome and shed light on genome evolution and disease pleiotropy. Description: Tong, Pin, et al. Shared regulatory sites are abundant in the human genome and shed light on genome evolution and disease pleiotropy. ''PLoS Genet''. 2017 Mar; '''13''' (3):e1006673
Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular Degeneration. Description: Tan, Perciliz L, et al. Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular Degeneration. ''Invest Ophthalmol Vis Sci''. 2017 Mar 1; '''58''' (3):1570-1576
Two-dimensional enrichment analysis for mining high-level imaging genetic associations. Description: Yao, Xiaohui, et al. Two-dimensional enrichment analysis for mining high-level imaging genetic associations. ''Brain Inform''. 2017 Mar; '''4''' (1):27-37
Variants in the CNR1 gene predispose to headache with nausea in the presence of life stress. Description: Juhasz, G, et al. Variants in the CNR1 gene predispose to headache with nausea in the presence of life stress. ''Genes Brain Behav''. 2017 Mar; '''16''' (3):384-393
Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India. Description: Pranavchand, Rayabarapu, et al. Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India. ''Hum Genomics''. 2017 Mar 4; '''11''' (1):3
Interaction between Single Nucleotide Polymorphism and Urinary Sodium, Potassium, and Sodium-Potassium Ratio on the Risk of Hypertension in Korean Adults. Description: Park, Yeong Mi, et al. Interaction between Single Nucleotide Polymorphism and Urinary Sodium, Potassium, and Sodium-Potassium Ratio on the Risk of Hypertension in Korean Adults. ''Nutrients''. 2017 Mar 5; '''9''' (3):
Genetic contribution to lipid levels in early life based on 158 loci validated in adults: the FAMILY study. Description: Christie, Shanice, et al. Genetic contribution to lipid levels in early life based on 158 loci validated in adults: the FAMILY study. ''Sci Rep''. 2017 Mar 6; '''7''' (1):68
Population genomics of an endemic Mediterranean fish: differentiation by fine scale dispersal and adaptation. Description: Carreras, Carlos, et al. Population genomics of an endemic Mediterranean fish: differentiation by fine scale dispersal and adaptation. ''Sci Rep''. 2017 Mar 6; '''7''': 43417
Association of FCGR2A/FCGR3A variant rs2099684 with Takayasu arteritis in the Han Chinese population. Description: Chen, Si, et al. Association of FCGR2A/FCGR3A variant rs2099684 with Takayasu arteritis in the Han Chinese population. ''Oncotarget''. 2017 Mar 7; '''8''' (10):17239-17245
Developmental pathways to adiposity begin before birth and are influenced by genotype, prenatal environment and epigenome. Description: Lin, Xinyi, et al. Developmental pathways to adiposity begin before birth and are influenced by genotype, prenatal environment and epigenome. ''BMC Med''. 2017 Mar 7; '''15''' (1):50
Estimation of breeding values for uniformity of growth in Atlantic salmon (Salmo salar) using pedigree relationships or single-step genomic evaluation. Description: Sae-Lim, Panya, et al. Estimation of breeding values for uniformity of growth in Atlantic salmon (Salmo salar) using pedigree relationships or single-step genomic evaluation. ''Genet Sel Evol''. 2017 Mar 7; '''49''' (1):33
Efficient and reliable establishment of lymphoblastoid cell lines by Epstein-Barr virus transformation from a limited amount of peripheral blood. Description: Omi, Natsue, et al. Efficient and reliable establishment of lymphoblastoid cell lines by Epstein-Barr virus transformation from a limited amount of peripheral blood. ''Sci Rep''. 2017 Mar 8; '''7''': 43833
Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock. Description: Vilander, Laura M, et al. Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock. ''Crit Care''. 2017 Mar 8; '''21''' (1):47
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness. Description: Heilmann-Heimbach, Stefanie, et al. Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness. ''Nat Commun''. 2017 Mar 8; '''8''': 14694
SNP-SNP interactions between WNT4 and WNT5A were associated with obesity related traits in Han Chinese Population. Description: Dong, Shan-Shan, et al. SNP-SNP interactions between WNT4 and WNT5A were associated with obesity related traits in Han Chinese Population. ''Sci Rep''. 2017 Mar 8; '''7''': 43939
Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes. Description: Gui, Hongsheng, et al. Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes. ''Genome Biol''. 2017 Mar 8; '''18''' (1):48
Analysis of the common genetic component of large-vessel vasculitides through a meta-Immunochip strategy. Description: Carmona, F David, et al. Analysis of the common genetic component of large-vessel vasculitides through a meta-Immunochip strategy. ''Sci Rep''. 2017 Mar 9; '''7''': 43953
Lack of Association of CD55 Receptor Genetic Variants and Severe Malaria in Ghanaian Children. Description: Schuldt, Kathrin, et al. Lack of Association of CD55 Receptor Genetic Variants and Severe Malaria in Ghanaian Children. ''G3 (Bethesda)''. 2017 Mar 10; '''7''' (3):859-864
Functional interactors of three genome-wide association study genes are differentially expressed in severe chronic obstructive pulmonary disease lung tissue. Description: Morrow, Jarrett D, et al. Functional interactors of three genome-wide association study genes are differentially expressed in severe chronic obstructive pulmonary disease lung tissue. ''Sci Rep''. 2017 Mar 13; '''7''': 44232
Multivariate simulation framework reveals performance of multi-trait GWAS methods. Description: Porter, Heather F, et al. Multivariate simulation framework reveals performance of multi-trait GWAS methods. ''Sci Rep''. 2017 Mar 13; '''7''': 38837
Exome sequencing identifies a novel TTC37 mutation in the first reported case of Trichohepatoenteric syndrome (THE-S) in South Africa. Description: Kinnear, Craig, et al. Exome sequencing identifies a novel TTC37 mutation in the first reported case of Trichohepatoenteric syndrome (THE-S) in South Africa. ''BMC Med Genet''. 2017 Mar 14; '''18''' (1):26
Genetic diversity and signatures of selection in various goat breeds revealed by genome-wide SNP markers. Description: Brito, Luiz F, et al. Genetic diversity and signatures of selection in various goat breeds revealed by genome-wide SNP markers. ''BMC Genomics''. 2017 Mar 14; '''18''' (1):229
Genetic diversity of a New Zealand multi-breed sheep population and composite breeds' history revealed by a high-density SNP chip. Description: Brito, Luiz F, et al. Genetic diversity of a New Zealand multi-breed sheep population and composite breeds' history revealed by a high-density SNP chip. ''BMC Genet''. 2017 Mar 14; '''18''' (1):25
SNP by SNP by environment interaction network of alcoholism. Description: Zollanvari, Amin, et al. SNP by SNP by environment interaction network of alcoholism. ''BMC Syst Biol''. 2017 Mar 14; '''11''' (Suppl 3):19
Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. Description: Ransohoff, Katherine J, et al. Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. ''Oncotarget''. 2017 Mar 14; '''8''' (11):17586-17592
An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis. Description: Vassos, Evangelos, et al. An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis. ''Biol Psychiatry''. 2017 Mar 15; '''81''' (6):470-477
C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten. Description: Stopford, Matthew J, et al. C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten. ''Hum Mol Genet''. 2017 Mar 15; '''26''' (6):1133-1145
A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosis. Description: Cooper-Knock, Johnathan, et al. A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosis. ''Acta Neuropathol Commun''. 2017 Mar 16; '''5''' (1):23
Identification of a novel locus associated with skin colour in African-admixed populations. Description: Hernandez-Pacheco, Natalia, et al. Identification of a novel locus associated with skin colour in African-admixed populations. ''Sci Rep''. 2017 Mar 16; '''7''': 44548
Associations between genetic variants in mRNA splicing-related genes and risk of lung cancer: a pathway-based analysis from published GWASs. Description: Pan, Yongchu, et al. Associations between genetic variants in mRNA splicing-related genes and risk of lung cancer: a pathway-based analysis from published GWASs. ''Sci Rep''. 2017 Mar 17; '''7''': 44634
BDNF Variants May Modulate Long-Term Visual Memory Performance in a Healthy Cohort. Description: Avgan, Nesli, et al. BDNF Variants May Modulate Long-Term Visual Memory Performance in a Healthy Cohort. ''Int J Mol Sci''. 2017 Mar 17; '''18''' (3):
Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip. Description: Basit, Sulman, et al. Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip. ''BMC Med Genet''. 2017 Mar 21; '''18''' (1):34
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Description: McLaughlin, Russell L, et al. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. ''Nat Commun''. 2017 Mar 21; '''8''': 14774
A genetic chronology for the Indian Subcontinent points to heavily sex-biased dispersals. Description: Silva, Marina, et al. A genetic chronology for the Indian Subcontinent points to heavily sex-biased dispersals. ''BMC Evol Biol''. 2017 Mar 23; '''17''' (1):88
Genomic regions underlying susceptibility to bovine tuberculosis in Holstein-Friesian cattle. Description: Raphaka, Kethusegile, et al. Genomic regions underlying susceptibility to bovine tuberculosis in Holstein-Friesian cattle. ''BMC Genet''. 2017 Mar 23; '''18''' (1):27
Human Epistatic Interaction Controls IL7R Splicing and Increases Multiple Sclerosis Risk. Description: Galarza-Munoz, Gaddiel, et al. Human Epistatic Interaction Controls IL7R Splicing and Increases Multiple Sclerosis Risk. ''Cell''. 2017 Mar 23; '''169''' (1):72-84.e13
Integrative variants, haplotypes and diplotypes of the CAPN3 and FRMD5 genes and several environmental exposures associate with serum lipid variables. Description: Guo, Tao, et al. Integrative variants, haplotypes and diplotypes of the CAPN3 and FRMD5 genes and several environmental exposures associate with serum lipid variables. ''Sci Rep''. 2017 Mar 23; '''7''': 45119
Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis. Description: Iorio, Andrea, et al. Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis. ''BMC Genomics''. 2017 Mar 23; '''18''' (1):254
Variants in the host genome may inhibit tumour growth in devil facial tumours: evidence from genome-wide association. Description: Wright, Belinda, et al. Variants in the host genome may inhibit tumour growth in devil facial tumours: evidence from genome-wide association. ''Sci Rep''. 2017 Mar 24; '''7''' (1):423
Genome-wide association study and accuracy of genomic prediction for teat number in Duroc pigs using genotyping-by-sequencing. Description: Tan, Cheng, et al. Genome-wide association study and accuracy of genomic prediction for teat number in Duroc pigs using genotyping-by-sequencing. ''Genet Sel Evol''. 2017 Mar 29; '''49''' (1):35
Genomic history of the origin and domestication of common bean unveils its closest sister species. Description: Rendon-Anaya, Martha, et al. Genomic history of the origin and domestication of common bean unveils its closest sister species. ''Genome Biol''. 2017 Mar 29; '''18''' (1):60
Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Description: Afshari, Natalie A, et al. Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. ''Nat Commun''. 2017 Mar 30; '''8''': 14898
ADP ribosyl-cyclases (CD38/CD157), social skills and friendship. Description: Chong, Anne, et al. ADP ribosyl-cyclases (CD38/CD157), social skills and friendship. ''Psychoneuroendocrinology''. 2017 Apr; '''78''': 185-192
A promoter polymorphism rs2075824 within IMPA2 gene affecting the transcription activity: possible relationship with schizophrenia. Description: Li, Jia, et al. A promoter polymorphism rs2075824 within IMPA2 gene affecting the transcription activity: possible relationship with schizophrenia. ''J Cell Mol Med''. 2017 Apr; '''21''' (4):658-664
Association between polygenic risk scores for attention-deficit hyperactivity disorder and educational and cognitive outcomes in the general population. Description: Stergiakouli, Evie, et al. Association between polygenic risk scores for attention-deficit hyperactivity disorder and educational and cognitive outcomes in the general population. ''Int J Epidemiol''. 2017 Apr 1; '''46''' (2):421-428
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium. Description: Ng, Maggie C Y, et al. Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium. ''PLoS Genet''. 2017 Apr; '''13''' (4):e1006719
Down-Regulation of EPAS1 Transcription and Genetic Adaptation of Tibetans to High-Altitude Hypoxia. Description: Peng, Yi, et al. Down-Regulation of EPAS1 Transcription and Genetic Adaptation of Tibetans to High-Altitude Hypoxia. ''Mol Biol Evol''. 2017 Apr 1; '''34''' (4):818-830
Gene co-expression network connectivity is an important determinant of selective constraint. Description: Mahler, Niklas, et al. Gene co-expression network connectivity is an important determinant of selective constraint. ''PLoS Genet''. 2017 Apr; '''13''' (4):e1006402
Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study. Description: Traylor, Matthew, et al. Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study. ''Neurol Genet''. 2017 Apr; '''3''' (2):e142
Genome Sequencing Reveals the Origin of the Allotetraploid Arabidopsis suecica. Description: Novikova, Polina Yu, et al. Genome Sequencing Reveals the Origin of the Allotetraploid Arabidopsis suecica. ''Mol Biol Evol''. 2017 Apr 1; '''34''' (4):957-968
Genome-wide meta-analysis identifies novel loci of plaque burden in carotid artery. Description: Pott, Janne, et al. Genome-wide meta-analysis identifies novel loci of plaque burden in carotid artery. ''Atherosclerosis''. 2017 Apr; '''259''': 32-40
Genomic variants at 20p11 associated with body fat mass in the European population. Description: Pei, Yu-Fang, et al. Genomic variants at 20p11 associated with body fat mass in the European population. ''Obesity (Silver Spring)''. 2017 Apr; '''25''' (4):757-764
Identification of genes associated with dissociation of cognitive performance and neuropathological burden: Multistep analysis of genetic, epigenetic, and transcriptional data. Description: White, Charles C, et al. Identification of genes associated with dissociation of cognitive performance and neuropathological burden: Multistep analysis of genetic, epigenetic, and transcriptional data. ''PLoS Med''. 2017 Apr; '''14''' (4):e1002287
Identification of growth trait related genes in a Yorkshire purebred pig population by genome-wide association studies. Description: Meng, Qingli, et al. Identification of growth trait related genes in a Yorkshire purebred pig population by genome-wide association studies. ''Asian-Australas J Anim Sci''. 2017 Apr; '''30''' (4):462-469
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies. Description: Wang, Zhaoming, et al. Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies. ''Gut''. 2017 Apr; '''66''' (4):581-587
Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort. Description: Clarke, Toni-Kim, et al. Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort. ''Am J Med Genet B Neuropsychiatr Genet''. 2017 Apr; '''174''' (3):227-234
In Vitro Effects of Lead on Gene Expression in Neural Stem Cells and Associations between Up-regulated Genes and Cognitive Scores in Children. Description: Wagner, Peter J, et al. In Vitro Effects of Lead on Gene Expression in Neural Stem Cells and Associations between Up-regulated Genes and Cognitive Scores in Children. ''Environ Health Perspect''. 2017 Apr; '''125''' (4):721-729
Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease. Description: Folkersen, Lasse, et al. Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease. ''PLoS Genet''. 2017 Apr; '''13''' (4):e1006706
Phenome-wide heritability analysis of the UK Biobank. Description: Ge, Tian, et al. Phenome-wide heritability analysis of the UK Biobank. ''PLoS Genet''. 2017 Apr; '''13''' (4):e1006711
Polymorphic variants in VAX1 and the risk of nonsyndromic cleft lip with or without cleft palate in a population from northern China. Description: Li, Dongmei, et al. Polymorphic variants in VAX1 and the risk of nonsyndromic cleft lip with or without cleft palate in a population from northern China. ''Medicine (Baltimore)''. 2017 Apr; '''96''' (14):e6550
Population genetic analysis and genome-wide association study of patellar luxation in a Thai population of Pomeranian dogs. Description: Wangdee, C, et al. Population genetic analysis and genome-wide association study of patellar luxation in a Thai population of Pomeranian dogs. ''Res Vet Sci''. 2017 Apr; '''111''': 9-13
RAD sequencing reveals genomewide divergence between independent invasions of the European green crab (Carcinus maenas) in the Northwest Atlantic. Description: Jeffery, Nicholas W, et al. RAD sequencing reveals genomewide divergence between independent invasions of the European green crab (Carcinus maenas) in the Northwest Atlantic. ''Ecol Evol''. 2017 Apr; '''7''' (8):2513-2524
Rs12941170 at SOX9 gene associated with orofacial clefts in Chinese. Description: Jia, Zhong-Lin, et al. Rs12941170 at SOX9 gene associated with orofacial clefts in Chinese. ''Arch Oral Biol''. 2017 Apr; '''76''': 14-19
Rs4265085 in GPER1 gene increases the risk for unexplained recurrent spontaneous abortion in Dai and Bai ethnic groups in China. Description: Tang, Liang, et al. Rs4265085 in GPER1 gene increases the risk for unexplained recurrent spontaneous abortion in Dai and Bai ethnic groups in China. ''Reprod Biomed Online''. 2017 Apr; '''34''' (4):399-405
Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci. Description: Canver, Matthew C, et al. Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci. ''Nat Genet''. 2017 Apr; '''49''' (4):625-634
A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome. Description: Bauer, Anina, et al. A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome. ''G3 (Bethesda)''. 2017 Apr 3; '''7''' (4):1315-1321
Functional implications of Neandertal introgression in modern humans. Description: Dannemann, Michael, et al. Functional implications of Neandertal introgression in modern humans. ''Genome Biol''. 2017 Apr 3; '''18''' (1):61
Genome-wide Association Analyses Reveal the Genetic Basis of Stigma Exsertion in Rice. Description: Zhou, Hao, et al. Genome-wide Association Analyses Reveal the Genetic Basis of Stigma Exsertion in Rice. ''Mol Plant''. 2017 Apr 3; '''10''' (4):634-644
Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. Description: Traglia, Michela, et al. Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. ''G3 (Bethesda)''. 2017 Apr 3; '''7''' (4):1287-1299
Pharmacogenetics of antidepressant response: A polygenic approach. Description: Garcia-Gonzalez, Judit, et al. Pharmacogenetics of antidepressant response: A polygenic approach. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2017 Apr 3; '''75''': 128-134
Polymorphisms of STS gene and SULT2A1 gene and neurosteroid levels in Han Chinese boys with attention-deficit/hyperactivity disorder: an exploratory investigation. Description: Wang, Liang-Jen, et al. Polymorphisms of STS gene and SULT2A1 gene and neurosteroid levels in Han Chinese boys with attention-deficit/hyperactivity disorder: an exploratory investigation. ''Sci Rep''. 2017 Apr 3; '''7''': 45595
Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci. Description: Ellinghaus, Eva, et al. Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci. ''Sci Rep''. 2017 Apr 4; '''7''': 45652
Imputation-Based Whole-Genome Sequence Association Study Rediscovered the Missing QTL for Lumbar Number in Sutai Pigs. Description: Yan, Guorong, et al. Imputation-Based Whole-Genome Sequence Association Study Rediscovered the Missing QTL for Lumbar Number in Sutai Pigs. ''Sci Rep''. 2017 Apr 4; '''7''' (1):615
Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk. Description: Suchon, P, et al. Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk. ''Sci Rep''. 2017 Apr 4; '''7''': 45507
Association of atrial fibrillation susceptibility genes, atrial fibrillation phenotypes and response to catheter ablation: a gene-based analysis of GWAS data. Description: Husser, Daniela, et al. Association of atrial fibrillation susceptibility genes, atrial fibrillation phenotypes and response to catheter ablation: a gene-based analysis of GWAS data. ''J Transl Med''. 2017 Apr 5; '''15''' (1):71
Genetic architecture of bone quality variation in layer chickens revealed by a genome-wide association study. Description: Guo, Jun, et al. Genetic architecture of bone quality variation in layer chickens revealed by a genome-wide association study. ''Sci Rep''. 2017 Apr 6; '''7''': 45317
Phenotypic and genotypic correlation between myopia and intelligence. Description: Williams, Katie M, et al. Phenotypic and genotypic correlation between myopia and intelligence. ''Sci Rep''. 2017 Apr 6; '''7''': 45977
Comprehensive analysis of the association between UBAC2 polymorphisms and Behcet's disease in a Japanese population. Description: Yamazoe, Kyoko, et al. Comprehensive analysis of the association between UBAC2 polymorphisms and Behcet's disease in a Japanese population. ''Sci Rep''. 2017 Apr 7; '''7''' (1):742
Local Ancestry and Clinical Cardiovascular Events Among African Americans From the Atherosclerosis Risk in Communities Study. Description: Shendre, Aditi, et al. Local Ancestry and Clinical Cardiovascular Events Among African Americans From the Atherosclerosis Risk in Communities Study. ''J Am Heart Assoc''. 2017 Apr 10; '''6''' (4):
Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium. Description: Feng, Yun, et al. Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium. ''Sci Rep''. 2017 Apr 11; '''7''' (1):825
Germline genetic variations in PDZD2 and ITPR2 genes are associated with clear cell renal cell carcinoma in Chinese population. Description: Zhang, Ning, et al. Germline genetic variations in PDZD2 and ITPR2 genes are associated with clear cell renal cell carcinoma in Chinese population. ''Oncotarget''. 2017 Apr 11; '''8''' (15):24196-24201
Leukocyte telomere length-related genetic variants in ACYP2 contribute to the risk of esophageal carcinoma in Chinese Han population. Description: Fang, Quan, et al. Leukocyte telomere length-related genetic variants in ACYP2 contribute to the risk of esophageal carcinoma in Chinese Han population. ''Oncotarget''. 2017 Apr 11; '''8''' (15):25564-25570
SIRT6 polymorphism rs117385980 is associated with longevity and healthy aging in Finnish men. Description: Hirvonen, Katariina, et al. SIRT6 polymorphism rs117385980 is associated with longevity and healthy aging in Finnish men. ''BMC Med Genet''. 2017 Apr 11; '''18''' (1):41
The impacts of single nucleotide polymorphisms in genes of cell cycle and NF-kB pathways on the efficacy and acute toxicities of radiotherapy in patients with nasopharyngeal carcinoma. Description: Guo, Chengxian, et al. The impacts of single nucleotide polymorphisms in genes of cell cycle and NF-kB pathways on the efficacy and acute toxicities of radiotherapy in patients with nasopharyngeal carcinoma. ''Oncotarget''. 2017 Apr 11; '''8''' (15):25334-25344
Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity. Description: Saleheen, Danish, et al. Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity. ''Nature''. 2017 Apr 12; '''544''' (7649):235-239
Additional evidence supports association of common genetic variants in VTI1A and ETFA with increased risk of glioma susceptibility. Description: Wang, Ning, et al. Additional evidence supports association of common genetic variants in VTI1A and ETFA with increased risk of glioma susceptibility. ''J Neurol Sci''. 2017 Apr 15; '''375''': 282-288
Genetic predisposition to advanced biological ageing increases risk for childhood-onset recurrent major depressive disorder in a large UK sample. Description: Michalek, Julia E, et al. Genetic predisposition to advanced biological ageing increases risk for childhood-onset recurrent major depressive disorder in a large UK sample. ''J Affect Disord''. 2017 Apr 15; '''213''': 207-213
Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations. Description: Amin, Najaf, et al. Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations. ''Biol Psychiatry''. 2017 Apr 15; '''81''' (8):702-707
Genome-wide detection of copy number variation in Chinese indigenous sheep using an ovine high-density 600 K SNP array. Description: Ma, Qing, et al. Genome-wide detection of copy number variation in Chinese indigenous sheep using an ovine high-density 600 K SNP array. ''Sci Rep''. 2017 Apr 19; '''7''' (1):912
Significance of genetic polymorphisms in long non-coding RNA AC079767.4 in tuberculosis susceptibility and clinical phenotype in Western Chinese Han population. Description: Zhao, Zhenzhen, et al. Significance of genetic polymorphisms in long non-coding RNA AC079767.4 in tuberculosis susceptibility and clinical phenotype in Western Chinese Han population. ''Sci Rep''. 2017 Apr 19; '''7''' (1):965
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis. Description: Qiu, Fang, et al. A genome-wide association study identifies six novel risk loci for primary biliary cholangitis. ''Nat Commun''. 2017 Apr 20; '''8''': 14828
Detection of QTL for traits related to adaptation to sub-optimal climatic conditions in chickens. Description: Lien, Ching-Yi, et al. Detection of QTL for traits related to adaptation to sub-optimal climatic conditions in chickens. ''Genet Sel Evol''. 2017 Apr 20; '''49''' (1):39
Comprehensive assessment showed no associations of variants at the SLC10A1 locus with susceptibility to persistent HBV infection among Southern Chinese. Description: Zhang, Ying, et al. Comprehensive assessment showed no associations of variants at the SLC10A1 locus with susceptibility to persistent HBV infection among Southern Chinese. ''Sci Rep''. 2017 Apr 21; '''7''': 46490
Effects of the common polymorphism in the human aldehyde dehydrogenase 2 (ALDH2) gene on the lung. Description: Kuroda, Aoi, et al. Effects of the common polymorphism in the human aldehyde dehydrogenase 2 (ALDH2) gene on the lung. ''Respir Res''. 2017 Apr 21; '''18''' (1):69
Imaging genetics approach to Parkinson's disease and its correlation with clinical score. Description: Kim, Mansu, et al. Imaging genetics approach to Parkinson's disease and its correlation with clinical score. ''Sci Rep''. 2017 Apr 21; '''7''': 46700
Phenome-wide association study for CYP2A6 alleles: rs113288603 is associated with hearing loss symptoms in elderly smokers. Description: Polimanti, Renato, et al. Phenome-wide association study for CYP2A6 alleles: rs113288603 is associated with hearing loss symptoms in elderly smokers. ''Sci Rep''. 2017 Apr 21; '''7''' (1):1034
Improved phylogenetic resolution for Y-chromosome Haplogroup O2a1c-002611. Description: Yao, Xiaotian, et al. Improved phylogenetic resolution for Y-chromosome Haplogroup O2a1c-002611. ''Sci Rep''. 2017 Apr 25; '''7''' (1):1146
Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes. Description: Mishra, Rajashree, et al. Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes. ''BMC Med''. 2017 Apr 25; '''15''' (1):88
TCF7L2 polymorphisms and the risk of schizophrenia in the Chinese Han population. Description: Liu, Lijun, et al. TCF7L2 polymorphisms and the risk of schizophrenia in the Chinese Han population. ''Oncotarget''. 2017 Apr 25; '''8''' (17):28614-28620
Whole-exome sequencing identifies SGCD and ACVRL1 mutations associated with total anomalous pulmonary venous return (TAPVR) in Chinese population. Description: Li, Jun, et al. Whole-exome sequencing identifies SGCD and ACVRL1 mutations associated with total anomalous pulmonary venous return (TAPVR) in Chinese population. ''Oncotarget''. 2017 Apr 25; '''8''' (17):27812-27819
A peripheral epigenetic signature of immune system genes is linked to neocortical thickness and memory. Description: Freytag, Virginie, et al. A peripheral epigenetic signature of immune system genes is linked to neocortical thickness and memory. ''Nat Commun''. 2017 Apr 26; '''8''': 15193
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Description: Justice, Anne E, et al. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. ''Nat Commun''. 2017 Apr 26; '''8''': 14977
Association between PAX7 and NTN1 gene polymorphisms and nonsyndromic orofacial clefts in a northern Chinese population. Description: Guo, Qiang, et al. Association between PAX7 and NTN1 gene polymorphisms and nonsyndromic orofacial clefts in a northern Chinese population. ''Medicine (Baltimore)''. 2017 May; '''96''' (19):e6724
Association of early onset myasthenia gravis in Newfoundland dogs with the canine major histocompatibility complex class I. Description: Wolf, Zena, et al. Association of early onset myasthenia gravis in Newfoundland dogs with the canine major histocompatibility complex class I. ''Neuromuscul Disord''. 2017 May; '''27''' (5):409-416
Association of Variants of Arginine Vasopressin and Arginine Vasopressin Receptor 1A With Severe Acetaminophen Liver Injury. Description: Randesi, Matthew, et al. Association of Variants of Arginine Vasopressin and Arginine Vasopressin Receptor 1A With Severe Acetaminophen Liver Injury. ''Cell Mol Gastroenterol Hepatol''. 2017 May; '''3''' (3):500-505
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma. Description: McDaniel, Lee D, et al. Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma. ''PLoS Genet''. 2017 May; '''13''' (5):e1006787
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. Description: Hu, Yao, et al. Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. ''J Lipid Res''. 2017 May; '''58''' (5):974-981
Effects of Antenatal Maternal Depressive Symptoms and Socio-Economic Status on Neonatal Brain Development are Modulated by Genetic Risk. Description: Qiu, Anqi, et al. Effects of Antenatal Maternal Depressive Symptoms and Socio-Economic Status on Neonatal Brain Development are Modulated by Genetic Risk. ''Cereb Cortex''. 2017 May 1; '''27''' (5):3080-3092
Ethnicity of Patients With Germline GCM2-Activating Variants and Primary Hyperparathyroidism. Description: Guan, Bin, et al. Ethnicity of Patients With Germline GCM2-Activating Variants and Primary Hyperparathyroidism. ''J Endocr Soc''. 2017 May 1; '''1''' (5):488-499
Genetic Architecture of Natural Variation Underlying Adult Foraging Behavior That Is Essential for Survival of Drosophila melanogaster. Description: Lee, Yuh Chwen G, et al. Genetic Architecture of Natural Variation Underlying Adult Foraging Behavior That Is Essential for Survival of Drosophila melanogaster. ''Genome Biol Evol''. 2017 May 1; '''9''' (5):1357-1369
Genetic variants affecting cross-sectional lung function in adults show little or no effect on longitudinal lung function decline. Description: John, Catherine, et al. Genetic variants affecting cross-sectional lung function in adults show little or no effect on longitudinal lung function decline. ''Thorax''. 2017 May; '''72''' (5):400-408
Genome-wide association study of positive emotion identifies a genetic variant and a role for microRNAs. Description: Wingo, A P, et al. Genome-wide association study of positive emotion identifies a genetic variant and a role for microRNAs. ''Mol Psychiatry''. 2017 May; '''22''' (5):774-783
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis. Description: Merkel, Peter A, et al. Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis. ''Arthritis Rheumatol''. 2017 May; '''69''' (5):1054-1066
Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum. Description: Rothwell, Simon, et al. Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum. ''Arthritis Rheumatol''. 2017 May; '''69''' (5):1090-1099
Natural Variation in the Promoter of GSE5 Contributes to Grain Size Diversity in Rice. Description: Duan, Penggen, et al. Natural Variation in the Promoter of GSE5 Contributes to Grain Size Diversity in Rice. ''Mol Plant''. 2017 May 1; '''10''' (5):685-694
Novel linkage disequilibrium clustering algorithm identifies new lupus genes on meta-analysis of GWAS datasets. Description: Saeed, Mohammad. Novel linkage disequilibrium clustering algorithm identifies new lupus genes on meta-analysis of GWAS datasets. ''Immunogenetics''. 2017 May; '''69''' (5):295-302
Pollutants and Insecticides Drive Local Adaptation in African Malaria Mosquitoes. Description: Kamdem, Colince, et al. Pollutants and Insecticides Drive Local Adaptation in African Malaria Mosquitoes. ''Mol Biol Evol''. 2017 May 1; '''34''' (5):1261-1275
PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study. Description: Hamet, Pavel, et al. PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study. ''J Hypertens''. 2017 May; '''35 Suppl 1''': S24-S32
Receptor activator of nuclear factor kappa-B ligand (RANKL) but not sclerostin or gene polymorphisms is related to joint destruction in early rheumatoid arthritis. Description: Boman, Antonia, et al. Receptor activator of nuclear factor kappa-B ligand (RANKL) but not sclerostin or gene polymorphisms is related to joint destruction in early rheumatoid arthritis. ''Clin Rheumatol''. 2017 May; '''36''' (5):1005-1012
Stepwise Distributed Open Innovation Contests for Software Development: Acceleration of Genome-Wide Association Analysis. Description: Hill, Andrew, et al. Stepwise Distributed Open Innovation Contests for Software Development: Acceleration of Genome-Wide Association Analysis. ''Gigascience''. 2017 May 1; '''6''' (5):1-10
The Relation Between Inflation in Type-I and Type-II Error Rate and Population Divergence in Genome-Wide Association Analysis of Multi-Ethnic Populations. Description: Derks, E M, et al. The Relation Between Inflation in Type-I and Type-II Error Rate and Population Divergence in Genome-Wide Association Analysis of Multi-Ethnic Populations. ''Behav Genet''. 2017 May; '''47''' (3):360-368
Two extended haplotype blocks are associated with adaptation to high altitude habitats in East African honey bees. Description: Wallberg, Andreas, et al. Two extended haplotype blocks are associated with adaptation to high altitude habitats in East African honey bees. ''PLoS Genet''. 2017 May; '''13''' (5):e1006792
Post-operative atrial fibrillation examined using whole-genome RNA sequencing in human left atrial tissue. Description: Sigurdsson, Martin I, et al. Post-operative atrial fibrillation examined using whole-genome RNA sequencing in human left atrial tissue. ''BMC Med Genomics''. 2017 May 2; '''10''' (1):25
A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity. Description: Somers, Metten, et al. A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity. ''Genes (Basel)''. 2017 May 4; '''8''' (5):
Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. Description: Serie, Daniel J, et al. Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. ''J Cardiovasc Dev Dis''. 2017 May 4; '''4''' (2):
Whole genome sequencing identifies missense mutation in MTBP in Shar-Pei affected with Autoinflammatory Disease (SPAID). Description: Metzger, Julia, et al. Whole genome sequencing identifies missense mutation in MTBP in Shar-Pei affected with Autoinflammatory Disease (SPAID). ''BMC Genomics''. 2017 May 4; '''18''' (1):348
Human ancestry correlates with language and reveals that race is not an objective genomic classifier. Description: Baker, Jennifer L, et al. Human ancestry correlates with language and reveals that race is not an objective genomic classifier. ''Sci Rep''. 2017 May 8; '''7''' (1):1572
A missense variant of the ABCC11 gene is associated with Axillary Osmidrosis susceptibility and clinical phenotypes in the Chinese Han Population. Description: Ren, Yunqing, et al. A missense variant of the ABCC11 gene is associated with Axillary Osmidrosis susceptibility and clinical phenotypes in the Chinese Han Population. ''Sci Rep''. 2017 May 9; '''7''': 46335
Correlation between polymorphisms in microRNA-regulated genes and cervical cancer susceptibility in a Xinjiang Uygur population. Description: Fang, Jing, et al. Correlation between polymorphisms in microRNA-regulated genes and cervical cancer susceptibility in a Xinjiang Uygur population. ''Oncotarget''. 2017 May 9; '''8''' (19):31758-31764
Genome-wide association study of high-altitude pulmonary edema in a Han Chinese population. Description: Li, Xun, et al. Genome-wide association study of high-altitude pulmonary edema in a Han Chinese population. ''Oncotarget''. 2017 May 9; '''8''' (19):31568-31580
Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease. Description: Kunkle, B W, et al. Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease. ''Neurosci Lett''. 2017 May 10; '''649''': 124-129
Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania. Description: Parks, Tom, et al. Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania. ''Nat Commun''. 2017 May 11; '''8''': 14946
Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation. Description: Lonjou, Christine, et al. Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation. ''BMC Cancer''. 2017 May 12; '''17''' (1):328
Ancient and recent admixture layers in Sicily and Southern Italy trace multiple migration routes along the Mediterranean. Description: Sarno, Stefania, et al. Ancient and recent admixture layers in Sicily and Southern Italy trace multiple migration routes along the Mediterranean. ''Sci Rep''. 2017 May 16; '''7''' (1):1984
Combination analysis of NOS3, ABCB1 and IL23R polymorphisms with alcohol-induced osteonecrosis of the femoral head risk in Chinese males. Description: Wang, Yuan, et al. Combination analysis of NOS3, ABCB1 and IL23R polymorphisms with alcohol-induced osteonecrosis of the femoral head risk in Chinese males. ''Oncotarget''. 2017 May 16; '''8''' (20):33770-33778
Obesity-related CpG Methylation (cg07814318) of Kruppel-like Factor-13 (KLF13) Gene with Childhood Obesity and its cis-Methylation Quantitative Loci. Description: Koh, In-Uk, et al. Obesity-related CpG Methylation (cg07814318) of Kruppel-like Factor-13 (KLF13) Gene with Childhood Obesity and its cis-Methylation Quantitative Loci. ''Sci Rep''. 2017 May 16; '''7''': 45368
Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data. Description: Wu, Yang, et al. Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data. ''Genome Biol''. 2017 May 16; '''18''' (1):86
Association of 4p14 and 6q27 variation with Graves disease: a case-control study and a meta-analysis of available evidence. Description: Li, Fa-Mei, et al. Association of 4p14 and 6q27 variation with Graves disease: a case-control study and a meta-analysis of available evidence. ''BMC Med Genet''. 2017 May 18; '''18''' (1):56
Endothelial TLR4 and the microbiome drive cerebral cavernous malformations. Description: Tang, Alan T, et al. Endothelial TLR4 and the microbiome drive cerebral cavernous malformations. ''Nature''. 2017 May 18; '''545''' (7654):305-310
EP300 contributes to high-altitude adaptation in Tibetans by regulating nitric oxide production. Description: Zheng, Wang-Shan, et al. EP300 contributes to high-altitude adaptation in Tibetans by regulating nitric oxide production. ''Zool Res''. 2017 May 18; '''38''' (3):163-170
Fast diffusion of domesticated maize to temperate zones. Description: Li, Xiaolong, et al. Fast diffusion of domesticated maize to temperate zones. ''Sci Rep''. 2017 May 18; '''7''' (1):2077
GCH1 plays a role in the high-altitude adaptation of Tibetans. Description: Guo, Yong-Bo, et al. GCH1 plays a role in the high-altitude adaptation of Tibetans. ''Zool Res''. 2017 May 18; '''38''' (3):155-162
Genetic architecture of epigenetic and neuronal ageing rates in human brain regions. Description: Lu, Ake T, et al. Genetic architecture of epigenetic and neuronal ageing rates in human brain regions. ''Nat Commun''. 2017 May 18; '''8''': 15353
Polymorphisms of T helper cell cytokine-associated genes and survival of hemodialysis patients - a prospective study. Description: Grzegorzewska, Alicja E, et al. Polymorphisms of T helper cell cytokine-associated genes and survival of hemodialysis patients - a prospective study. ''BMC Nephrol''. 2017 May 19; '''18''' (1):165
Polymorphisms of microRNA target genes IL12B, INSR, CCND1 and IL10 in gastric cancer. Description: Petkevicius, Vytenis, et al. Polymorphisms of microRNA target genes IL12B, INSR, CCND1 and IL10 in gastric cancer. ''World J Gastroenterol''. 2017 May 21; '''23''' (19):3480-3487
Extremely low-coverage whole genome sequencing in South Asians captures population genomics information. Description: Rustagi, Navin, et al. Extremely low-coverage whole genome sequencing in South Asians captures population genomics information. ''BMC Genomics''. 2017 May 22; '''18''' (1):396
The effect of glucose-dependent insulinotropic polypeptide (GIP) variants on visceral fat accumulation in Han Chinese populations. Description: Wang, T, et al. The effect of glucose-dependent insulinotropic polypeptide (GIP) variants on visceral fat accumulation in Han Chinese populations. ''Nutr Diabetes''. 2017 May 22; '''7''' (5):e278
Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1. Description: Pasutto, Francesca, et al. Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1. ''Nat Commun''. 2017 May 23; '''8''': 15466
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. Description: Sapkota, Yadav, et al. Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. ''Nat Commun''. 2017 May 24; '''8''': 15539
Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve. Description: Yang, Bo, et al. Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve. ''Nat Commun''. 2017 May 25; '''8''': 15481
Development of a SNP panel dedicated to parentage assignment in French sheep populations. Description: Tortereau, F, et al. Development of a SNP panel dedicated to parentage assignment in French sheep populations. ''BMC Genet''. 2017 May 26; '''18''' (1):50
Genome-wide network-based pathway analysis of CSF t-tau/Abeta1-42 ratio in the ADNI cohort. Description: Cong, Wang, et al. Genome-wide network-based pathway analysis of CSF t-tau/Abeta1-42 ratio in the ADNI cohort. ''BMC Genomics''. 2017 May 30; '''18''' (1):421
Search for rare protein altering variants influencing susceptibility to multiple myeloma. Description: Scales, Matthew, et al. Search for rare protein altering variants influencing susceptibility to multiple myeloma. ''Oncotarget''. 2017 May 30; '''8''' (22):36203-36210
A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK. Description: Morgan, Sarah, et al. A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK. ''Brain''. 2017 Jun 1; '''140''' (6):1611-1618
A Dopamine Receptor genetic variant enhances perceptual speed in cognitive healthy subjects. Description: Barral, S, et al. A Dopamine Receptor genetic variant enhances perceptual speed in cognitive healthy subjects. ''Alzheimers Dement (N Y)''. 2017 Jun; '''3''' (2):254-261
A Variant in RUNX3 Is Associated with the Risk of Ankylosing Spondylitis in Koreans. Description: Cho, Sung-Min, et al. A Variant in RUNX3 Is Associated with the Risk of Ankylosing Spondylitis in Koreans. ''Genomics Inform''. 2017 Jun; '''15''' (2):65-68
Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study. Description: Noyce, Alastair J, et al. Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study. ''PLoS Med''. 2017 Jun; '''14''' (6):e1002314
Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality. Description: Baekvad-Hansen, Marie, et al. Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality. ''Mol Genet Metab Rep''. 2017 Jun; '''11''': 36-45
Fetal and postnatal metal dysregulation in autism. Description: Arora, Manish, et al. Fetal and postnatal metal dysregulation in autism. ''Nat Commun''. 2017 Jun 1; '''8''': 15493
Genetic Characterization of Dog Personality Traits. Description: Ilska, Joanna, et al. Genetic Characterization of Dog Personality Traits. ''Genetics''. 2017 Jun; '''206''' (2):1101-1111
Genetic Indicators of Drug Resistance in the Highly Repetitive Genome of Trichomonas vaginalis. Description: Bradic, Martina, et al. Genetic Indicators of Drug Resistance in the Highly Repetitive Genome of Trichomonas vaginalis. ''Genome Biol Evol''. 2017 Jun 1; '''9''' (6):1658-1672
Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy. Description: Byars, Sean G, et al. Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy. ''PLoS Genet''. 2017 Jun; '''13''' (6):e1006328
Genetics of ancestry-specific risk for relapse in acute lymphoblastic leukemia. Description: Karol, S E, et al. Genetics of ancestry-specific risk for relapse in acute lymphoblastic leukemia. ''Leukemia''. 2017 Jun; '''31''' (6):1325-1332
Genetics of Sex Hormone-Binding Globulin and Testosterone Levels in Fertile and Infertile Men of Reproductive Age. Description: Grigorova, Marina, et al. Genetics of Sex Hormone-Binding Globulin and Testosterone Levels in Fertile and Infertile Men of Reproductive Age. ''J Endocr Soc''. 2017 Jun 1; '''1''' (6):560-576
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjogren's Syndrome According to Ancestry. Description: Taylor, Kimberly E, et al. Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjogren's Syndrome According to Ancestry. ''Arthritis Rheumatol''. 2017 Jun; '''69''' (6):1294-1305
Genome-wide, high-content siRNA screening identifies the Alzheimer's genetic risk factor FERMT2 as a major modulator of APP metabolism. Description: Chapuis, Julien, et al. Genome-wide, high-content siRNA screening identifies the Alzheimer's genetic risk factor FERMT2 as a major modulator of APP metabolism. ''Acta Neuropathol''. 2017 Jun; '''133''' (6):955-966
Identification of a Sjogren's syndrome susceptibility locus at OAS1 that influences isoform switching, protein expression, and responsiveness to type I interferons. Description: Li, He, et al. Identification of a Sjogren's syndrome susceptibility locus at OAS1 that influences isoform switching, protein expression, and responsiveness to type I interferons. ''PLoS Genet''. 2017 Jun; '''13''' (6):e1006820
Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel. Description: Mitt, Mario, et al. Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel. ''Eur J Hum Genet''. 2017 Jun; '''25''' (7):869-876
Molecular genetic contributions to self-rated health. Description: Harris, Sarah E, et al. Molecular genetic contributions to self-rated health. ''Int J Epidemiol''. 2017 Jun 1; '''46''' (3):994-1009
Population genomics reveals high gene flow in grass rockfish (Sebastes rastrelliger). Description: Martinez, Edith, et al. Population genomics reveals high gene flow in grass rockfish (Sebastes rastrelliger). ''Mar Genomics''. 2017 Jun; '''33''': 57-63
Potassium channel gene associations with joint processing speed and white matter impairments in schizophrenia. Description: Bruce, H A, et al. Potassium channel gene associations with joint processing speed and white matter impairments in schizophrenia. ''Genes Brain Behav''. 2017 Jun; '''16''' (5):515-521
Selection in Europeans on Fatty Acid Desaturases Associated with Dietary Changes. Description: Buckley, Matthew T, et al. Selection in Europeans on Fatty Acid Desaturases Associated with Dietary Changes. ''Mol Biol Evol''. 2017 Jun 1; '''34''' (6):1307-1318
SUMO-Targeted DNA Translocase Rrp2 Protects the Genome from Top2-Induced DNA Damage. Description: Wei, Yi, et al. SUMO-Targeted DNA Translocase Rrp2 Protects the Genome from Top2-Induced DNA Damage. ''Mol Cell''. 2017 Jun 1; '''66''' (5):581-596.e6
Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. Description: Zhu, Yimin, et al. Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. ''J Cell Mol Med''. 2017 Jun; '''21''' (6):1106-1116
The genomic mosaicism of hybrid speciation. Description: Elgvin, Tore O, et al. The genomic mosaicism of hybrid speciation. ''Sci Adv''. 2017 Jun; '''3''' (6):e1602996
Unraveling the Population History of Indian Siddis. Description: Das, Ranajit, et al. Unraveling the Population History of Indian Siddis. ''Genome Biol Evol''. 2017 Jun 1; '''9''' (6):1385-1392
Variants in Pharmacokinetic Transporters and Glycemic Response to Metformin: A Metgen Meta-Analysis. Description: Dujic, T, et al. Variants in Pharmacokinetic Transporters and Glycemic Response to Metformin: A Metgen Meta-Analysis. ''Clin Pharmacol Ther''. 2017 Jun; '''101''' (6):763-772
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Description: Tachmazidou, Ioanna, et al. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. ''Am J Hum Genet''. 2017 Jun 1; '''100''' (6):865-884
Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2. Description: Marchant, Thomas W, et al. Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2. ''Curr Biol''. 2017 Jun 5; '''27''' (11):1573-1584.e6
Identification of 15 novel risk loci for coronary artery disease and genetic risk of recurrent events, atrial fibrillation and heart failure. Description: Verweij, Niek, et al. Identification of 15 novel risk loci for coronary artery disease and genetic risk of recurrent events, atrial fibrillation and heart failure. ''Sci Rep''. 2017 Jun 5; '''7''' (1):2761
Improved detection of gene-microbe interactions in the mouse skin microbiota using high-resolution QTL mapping of 16S rRNA transcripts. Description: Belheouane, Meriem, et al. Improved detection of gene-microbe interactions in the mouse skin microbiota using high-resolution QTL mapping of 16S rRNA transcripts. ''Microbiome''. 2017 Jun 6; '''5''' (1):59
Predicting attention-deficit/hyperactivity disorder severity from psychosocial stress and stress-response genes: a random forest regression approach. Description: van der Meer, D, et al. Predicting attention-deficit/hyperactivity disorder severity from psychosocial stress and stress-response genes: a random forest regression approach. ''Transl Psychiatry''. 2017 Jun 6; '''7''' (6):e1145
A Chromosome-Scale Assembly of the Bactrocera cucurbitae Genome Provides Insight to the Genetic Basis of white pupae. Description: Sim, Sheina B, et al. A Chromosome-Scale Assembly of the Bactrocera cucurbitae Genome Provides Insight to the Genetic Basis of white pupae. ''G3 (Bethesda)''. 2017 Jun 7; '''7''' (6):1927-1940
Genomic admixture tracks pulses of economic activity over 2,000 years in the Indian Ocean trading network. Description: Brucato, Nicolas, et al. Genomic admixture tracks pulses of economic activity over 2,000 years in the Indian Ocean trading network. ''Sci Rep''. 2017 Jun 7; '''7''' (1):2919
Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth. Description: Hong, Xiumei, et al. Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth. ''Nat Commun''. 2017 Jun 9; '''8''': 15608
Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls. Description: Buckley, Alexandra R, et al. Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls. ''BMC Genomics''. 2017 Jun 12; '''18''' (1):458
Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India. Description: Pranavchand, Rayabarapu, et al. Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India. ''Lipids Health Dis''. 2017 Jun 13; '''16''' (1):116
Experimental and Human Evidence for Lipocalin-2 (Neutrophil Gelatinase-Associated Lipocalin [NGAL]) in the Development of Cardiac Hypertrophy and heart failure. Description: Marques, Francine Z, et al. Experimental and Human Evidence for Lipocalin-2 (Neutrophil Gelatinase-Associated Lipocalin [NGAL]) in the Development of Cardiac Hypertrophy and heart failure. ''J Am Heart Assoc''. 2017 Jun 14; '''6''' (6):
Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Description: Nolte, Ilja M, et al. Genetic loci associated with heart rate variability and their effects on cardiac disease risk. ''Nat Commun''. 2017 Jun 14; '''8''': 15805
Genome wide association study and genomic prediction for fatty acid composition in Chinese Simmental beef cattle using high density SNP array. Description: Zhu, Bo, et al. Genome wide association study and genomic prediction for fatty acid composition in Chinese Simmental beef cattle using high density SNP array. ''BMC Genomics''. 2017 Jun 14; '''18''' (1):464
"Like sugar in milk": reconstructing the genetic history of the Parsi population. Description: Chaubey, Gyaneshwer, et al. "Like sugar in milk": reconstructing the genetic history of the Parsi population. ''Genome Biol''. 2017 Jun 14; '''18''' (1):110
Discovery of novel heart rate-associated loci using the Exome Chip. Description: van den Berg, Marten E, et al. Discovery of novel heart rate-associated loci using the Exome Chip. ''Hum Mol Genet''. 2017 Jun 15; '''26''' (12):2346-2363
Gene-physical activity interactions in lower extremity performance: inflammatory genes CRP, TNF-alpha, and LTA in community-dwelling elders. Description: Liu, Chiu-Shong, et al. Gene-physical activity interactions in lower extremity performance: inflammatory genes CRP, TNF-alpha, and LTA in community-dwelling elders. ''Sci Rep''. 2017 Jun 15; '''7''' (1):3585
Genome-wide pathway analysis identifies VEGF pathway association with oral ulceration in systemic lupus erythematosus. Description: Aterido, Adria, et al. Genome-wide pathway analysis identifies VEGF pathway association with oral ulceration in systemic lupus erythematosus. ''Arthritis Res Ther''. 2017 Jun 15; '''19''' (1):138
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling. Description: Li, Dong, et al. A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling. ''Sci Rep''. 2017 Jun 19; '''7''' (1):3847
Paleogenomic Evidence for Multi-generational Mixing between Neolithic Farmers and Mesolithic Hunter-Gatherers in the Lower Danube Basin. Description: Gonzalez-Fortes, Gloria, et al. Paleogenomic Evidence for Multi-generational Mixing between Neolithic Farmers and Mesolithic Hunter-Gatherers in the Lower Danube Basin. ''Curr Biol''. 2017 Jun 19; '''27''' (12):1801-1810.e10
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Description: Huang, Alden Y, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. ''Neuron''. 2017 Jun 21; '''94''' (6):1101-1111.e7
Circadian CLOCK gene polymorphisms in relation to sleep patterns and obesity in African Americans: findings from the Jackson heart study. Description: Riestra, Pia, et al. Circadian CLOCK gene polymorphisms in relation to sleep patterns and obesity in African Americans: findings from the Jackson heart study. ''BMC Genet''. 2017 Jun 23; '''18''' (1):58
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations. Description: Xue, Yali, et al. Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations. ''Nat Commun''. 2017 Jun 23; '''8''': 15927
Genome-Wide Association Study of Dietary Pattern Scores. Description: Guenard, Frederic, et al. Genome-Wide Association Study of Dietary Pattern Scores. ''Nutrients''. 2017 Jun 23; '''9''' (7):
Characterizing sleep spindles in 11,630 individuals from the National Sleep Research Resource. Description: Purcell, S M, et al. Characterizing sleep spindles in 11,630 individuals from the National Sleep Research Resource. ''Nat Commun''. 2017 Jun 26; '''8''': 15930
Polygenic risk has an impact on the structural plasticity of hippocampal subfields during aerobic exercise combined with cognitive remediation in multi-episode schizophrenia. Description: Papiol, S, et al. Polygenic risk has an impact on the structural plasticity of hippocampal subfields during aerobic exercise combined with cognitive remediation in multi-episode schizophrenia. ''Transl Psychiatry''. 2017 Jun 27; '''7''' (6):e1159
Association of SIX1/SIX6 locus polymorphisms with regional circumpapillary retinal nerve fibre layer thickness: The Nagahama study. Description: Yoshikawa, Munemitsu, et al. Association of SIX1/SIX6 locus polymorphisms with regional circumpapillary retinal nerve fibre layer thickness: The Nagahama study. ''Sci Rep''. 2017 Jun 29; '''7''' (1):4393
Evaluating the accuracy of genomic prediction of growth and wood traits in two Eucalyptus species and their F1 hybrids. Description: Tan, Biyue, et al. Evaluating the accuracy of genomic prediction of growth and wood traits in two Eucalyptus species and their F1 hybrids. ''BMC Plant Biol''. 2017 Jun 29; '''17''' (1):110
Inherited determinants of early recurrent somatic mutations in prostate cancer. Description: Romanel, Alessandro, et al. Inherited determinants of early recurrent somatic mutations in prostate cancer. ''Nat Commun''. 2017 Jun 29; '''8''' (1):48
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity. Description: Hendricks, Audrey E, et al. Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity. ''Sci Rep''. 2017 Jun 29; '''7''' (1):4394
An integrated hyperspectral imaging and genome-wide association analysis platform provides spectral and genetic insights into the natural variation in rice. Description: Feng, Hui, et al. An integrated hyperspectral imaging and genome-wide association analysis platform provides spectral and genetic insights into the natural variation in rice. ''Sci Rep''. 2017 Jun 30; '''7''' (1):4401
African genetic ancestry interacts with body mass index to modify risk for uterine fibroids. Description: Giri, Ayush, et al. African genetic ancestry interacts with body mass index to modify risk for uterine fibroids. ''PLoS Genet''. 2017 Jul; '''13''' (7):e1006871
A rare coding allele in IFIH1 is protective for psoriatic arthritis. Description: Budu-Aggrey, Ashley, et al. A rare coding allele in IFIH1 is protective for psoriatic arthritis. ''Ann Rheum Dis''. 2017 Jul; '''76''' (7):1321-1324
Associations between ABO blood groups and pancreatic ductal adenocarcinoma: influence on resection status and survival. Description: El Jellas, Khadija, et al. Associations between ABO blood groups and pancreatic ductal adenocarcinoma: influence on resection status and survival. ''Cancer Med''. 2017 Jul; '''6''' (7):1531-1540
Associations between serotonin transporter and behavioral traits and diagnoses related to anxiety. Description: Talati, Ardesheer, et al. Associations between serotonin transporter and behavioral traits and diagnoses related to anxiety. ''Psychiatry Res''. 2017 Jul; '''253''': 211-219
Detecting epistasis with the marginal epistasis test in genetic mapping studies of quantitative traits. Description: Crawford, Lorin, et al. Detecting epistasis with the marginal epistasis test in genetic mapping studies of quantitative traits. ''PLoS Genet''. 2017 Jul; '''13''' (7):e1006869
Genetics of Hereditary Ataxia in Scottish Terriers. Description: Urkasemsin, G, et al. Genetics of Hereditary Ataxia in Scottish Terriers. ''J Vet Intern Med''. 2017 Jul; '''31''' (4):1132-1139
Genetic variation in the alpha1B-adrenergic receptor and vascular response. Description: Adefurin, A, et al. Genetic variation in the alpha1B-adrenergic receptor and vascular response. ''Pharmacogenomics J''. 2017 Jul; '''17''' (4):366-371
Genome-wide analysis of ivermectin response by Onchocerca volvulus reveals that genetic drift and soft selective sweeps contribute to loss of drug sensitivity. Description: Doyle, Stephen R, et al. Genome-wide analysis of ivermectin response by Onchocerca volvulus reveals that genetic drift and soft selective sweeps contribute to loss of drug sensitivity. ''PLoS Negl Trop Dis''. 2017 Jul; '''11''' (7):e0005816
Genome-wide diversity and differentiation in New World populations of the human malaria parasite Plasmodium vivax. Description: de Oliveira, Thais C, et al. Genome-wide diversity and differentiation in New World populations of the human malaria parasite Plasmodium vivax. ''PLoS Negl Trop Dis''. 2017 Jul; '''11''' (7):e0005824
GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians. Description: Nongmaithem, Suraj S, et al. GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians. ''Hum Mol Genet''. 2017 Jul 1; '''26''' (13):2551-2564
Identification and characterization of variants and a novel 4 bp deletion in the regulatory region of SIX6, a risk factor for primary open-angle glaucoma. Description: Shah, Mohd Hussain, et al. Identification and characterization of variants and a novel 4 bp deletion in the regulatory region of SIX6, a risk factor for primary open-angle glaucoma. ''Mol Genet Genomic Med''. 2017 Jul; '''5''' (4):323-335
IFITM3, TLR3, and CD55 Gene SNPs and Cumulative Genetic Risks for Severe Outcomes in Chinese Patients With H7N9/H1N1pdm09 Influenza. Description: Lee, Nelson, et al. IFITM3, TLR3, and CD55 Gene SNPs and Cumulative Genetic Risks for Severe Outcomes in Chinese Patients With H7N9/H1N1pdm09 Influenza. ''J Infect Dis''. 2017 Jul 1; '''216''' (1):97-104
Immunoglobulin M gene association with autoantibody reactivity and type 1 diabetes. Description: Rolim, Ines, et al. Immunoglobulin M gene association with autoantibody reactivity and type 1 diabetes. ''Immunogenetics''. 2017 Jul; '''69''' (7):429-437
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Description: McKay, James D, et al. Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. ''Nat Genet''. 2017 Jul; '''49''' (7):1126-1132
Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor. Description: Wang, Zhaoming, et al. Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor. ''Nat Genet''. 2017 Jul; '''49''' (7):1141-1147
Paroxysmal Dyskinesia in Border Terriers: Clinical, Epidemiological, and Genetic Investigations. Description: Stassen, Q E M, et al. Paroxysmal Dyskinesia in Border Terriers: Clinical, Epidemiological, and Genetic Investigations. ''J Vet Intern Med''. 2017 Jul; '''31''' (4):1123-1131
Reevaluation of SNP heritability in complex human traits. Description: Speed, Doug, et al. Reevaluation of SNP heritability in complex human traits. ''Nat Genet''. 2017 Jul; '''49''' (7):986-992
Strong association of SLC1A1 and DPF3 gene variants with idiopathic male infertility in Han Chinese. Description: Liu, Shu-Yuan, et al. Strong association of SLC1A1 and DPF3 gene variants with idiopathic male infertility in Han Chinese. ''Asian J Androl''. 2017 Jul-Aug; '''19''' (4):486-492
Structural variants in genes associated with human Williams-Beuren syndrome underlie stereotypical hypersociability in domestic dogs. Description: vonHoldt, Bridgett M, et al. Structural variants in genes associated with human Williams-Beuren syndrome underlie stereotypical hypersociability in domestic dogs. ''Sci Adv''. 2017 Jul; '''3''' (7):e1700398
The A946T variant of the RNA sensor IFIH1 mediates an interferon program that limits viral infection but increases the risk for autoimmunity. Description: Gorman, Jacquelyn A, et al. The A946T variant of the RNA sensor IFIH1 mediates an interferon program that limits viral infection but increases the risk for autoimmunity. ''Nat Immunol''. 2017 Jul; '''18''' (7):744-752
The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based methods. Description: Martiniano, Rui, et al. The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based methods. ''PLoS Genet''. 2017 Jul; '''13''' (7):e1006852
The Relationship Between Mental Health, Disease Severity, and Genetic Risk for Depression in Early Rheumatoid Arthritis. Description: Euesden, Jack, et al. The Relationship Between Mental Health, Disease Severity, and Genetic Risk for Depression in Early Rheumatoid Arthritis. ''Psychosom Med''. 2017 Jul/Aug; '''79''' (6):638-645
Whole genome sequencing predicts novel human disease models in rhesus macaques. Description: Bimber, Benjamin N, et al. Whole genome sequencing predicts novel human disease models in rhesus macaques. ''Genomics''. 2017 Jul; '''109''' (3-4):214-220
Genetic association analysis of the RTK/ERK pathway with aggressive prostate cancer highlights the potential role of CCND2 in disease progression. Description: Chen, Yang, et al. Genetic association analysis of the RTK/ERK pathway with aggressive prostate cancer highlights the potential role of CCND2 in disease progression. ''Sci Rep''. 2017 Jul 3; '''7''' (1):4538
MBOAT7 rs641738 variant and hepatocellular carcinoma in non-cirrhotic individuals. Description: Donati, Benedetta, et al. MBOAT7 rs641738 variant and hepatocellular carcinoma in non-cirrhotic individuals. ''Sci Rep''. 2017 Jul 3; '''7''' (1):4492
Recurrent rhinovirus infections in a child with inherited MDA5 deficiency. Description: Lamborn, Ian T, et al. Recurrent rhinovirus infections in a child with inherited MDA5 deficiency. ''J Exp Med''. 2017 Jul 3; '''214''' (7):1949-1972
Exome-based genome-wide association study and risk assessment using genetic risk score to prostate cancer in the Korean population. Description: Oh, Jong Jin, et al. Exome-based genome-wide association study and risk assessment using genetic risk score to prostate cancer in the Korean population. ''Oncotarget''. 2017 Jul 4; '''8''' (27):43934-43943
Identifying pathways modulating sleep duration: from genomics to transcriptomics. Description: Allebrandt, Karla V, et al. Identifying pathways modulating sleep duration: from genomics to transcriptomics. ''Sci Rep''. 2017 Jul 4; '''7''' (1):4555
Whole-exome sequencing identified genetic risk factors for asparaginase-related complications in childhood ALL patients. Description: Abaji, Rachid, et al. Whole-exome sequencing identified genetic risk factors for asparaginase-related complications in childhood ALL patients. ''Oncotarget''. 2017 Jul 4; '''8''' (27):43752-43767
A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy. Description: Chew, Tracy, et al. A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy. ''G3 (Bethesda)''. 2017 Jul 5; '''7''' (7):2327-2335
A Pathway-Centered Analysis of Pig Domestication and Breeding in Eurasia. Description: Leno-Colorado, Jordi, et al. A Pathway-Centered Analysis of Pig Domestication and Breeding in Eurasia. ''G3 (Bethesda)''. 2017 Jul 5; '''7''' (7):2171-2184
Genome-wide association study identifies candidate genes for piglet splay leg syndrome in different populations. Description: Hao, Xingjie, et al. Genome-wide association study identifies candidate genes for piglet splay leg syndrome in different populations. ''BMC Genet''. 2017 Jul 5; '''18''' (1):64
The Genetic Architecture of Ovariole Number in Drosophila melanogaster: Genes with Major, Quantitative, and Pleiotropic Effects. Description: Lobell, Amanda S, et al. The Genetic Architecture of Ovariole Number in Drosophila melanogaster: Genes with Major, Quantitative, and Pleiotropic Effects. ''G3 (Bethesda)''. 2017 Jul 5; '''7''' (7):2391-2403
Genomic and phenotypic analysis of Vavilov's historic landraces reveals the impact of environment and genomic islands of agronomic traits. Description: Plekhanova, Elena, et al. Genomic and phenotypic analysis of Vavilov's historic landraces reveals the impact of environment and genomic islands of agronomic traits. ''Sci Rep''. 2017 Jul 6; '''7''' (1):4816
A genome-wide association study suggests the HLA Class II region as the major susceptibility locus for IgA vasculitis. Description: Lopez-Mejias, Raquel, et al. A genome-wide association study suggests the HLA Class II region as the major susceptibility locus for IgA vasculitis. ''Sci Rep''. 2017 Jul 11; '''7''' (1):5088
Gene-gene and gene-environment interactions influence platinum-based chemotherapy response and toxicity in non-small cell lung cancer patients. Description: Cui, Jia-Jia, et al. Gene-gene and gene-environment interactions influence platinum-based chemotherapy response and toxicity in non-small cell lung cancer patients. ''Sci Rep''. 2017 Jul 11; '''7''' (1):5082
Genomic prediction in contrast to a genome-wide association study in explaining heritable variation of complex growth traits in breeding populations of Eucalyptus. Description: Muller, Barbara S F, et al. Genomic prediction in contrast to a genome-wide association study in explaining heritable variation of complex growth traits in breeding populations of Eucalyptus. ''BMC Genomics''. 2017 Jul 11; '''18''' (1):524
The genetic architecture of water-soluble protein content and its genetic relationship to total protein content in soybean. Description: Zhang, Dan, et al. The genetic architecture of water-soluble protein content and its genetic relationship to total protein content in soybean. ''Sci Rep''. 2017 Jul 11; '''7''' (1):5053
Identification of QTL with large effect on seed weight in a selective population of soybean with genome-wide association and fixation index analyses. Description: Yan, Long, et al. Identification of QTL with large effect on seed weight in a selective population of soybean with genome-wide association and fixation index analyses. ''BMC Genomics''. 2017 Jul 12; '''18''' (1):529
Fine-mapping inflammatory bowel disease loci to single-variant resolution. Description: Huang, Hailiang, et al. Fine-mapping inflammatory bowel disease loci to single-variant resolution. ''Nature''. 2017 Jul 13; '''547''' (7662):173-178
Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer. Description: Son, Ho-Young, et al. Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer. ''Nat Commun''. 2017 Jul 13; '''8''': 15966
ddRADseq reveals determinants for temperature-dependent sex reversal in Nile tilapia on LG23. Description: Wessels, Stephan, et al. ddRADseq reveals determinants for temperature-dependent sex reversal in Nile tilapia on LG23. ''BMC Genomics''. 2017 Jul 14; '''18''' (1):531
Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder. Description: Garcia-Martinez, Iris, et al. Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder. ''Sci Rep''. 2017 Jul 14; '''7''' (1):5407
Common variants of T-cells contribute differently to phenotypic variation in sarcoidosis. Description: Rivera, Natalia V, et al. Common variants of T-cells contribute differently to phenotypic variation in sarcoidosis. ''Sci Rep''. 2017 Jul 17; '''7''' (1):5623
Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. Description: Treutlein, Jens, et al. Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. ''Genes (Basel)''. 2017 Jul 17; '''8''' (7):
RADseq provides evidence for parallel ecotypic divergence in the autotetraploid Cochlearia officinalis in Northern Norway. Description: Brandrud, Marie K, et al. RADseq provides evidence for parallel ecotypic divergence in the autotetraploid Cochlearia officinalis in Northern Norway. ''Sci Rep''. 2017 Jul 17; '''7''' (1):5573
Association between genetic variants and esophageal cancer risk. Description: Yue, Chenli, et al. Association between genetic variants and esophageal cancer risk. ''Oncotarget''. 2017 Jul 18; '''8''' (29):47167-47174
Common shared genetic variation behind decreased risk of breast cancer in celiac disease. Description: Ugalde-Morales, Emilio, et al. Common shared genetic variation behind decreased risk of breast cancer in celiac disease. ''Sci Rep''. 2017 Jul 19; '''7''' (1):5942
Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes. Description: Jager, Susanne, et al. Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes. ''Sci Rep''. 2017 Jul 20; '''7''' (1):6037
Genome-wide association study identifies a major gene for beech bark disease resistance in American beech (Fagus grandifolia Ehrh.). Description: Calic, Irina, et al. Genome-wide association study identifies a major gene for beech bark disease resistance in American beech (Fagus grandifolia Ehrh.). ''BMC Genomics''. 2017 Jul 20; '''18''' (1):547
Variants in the Promoter Region of HLA-DQA1 were Associated with Idiopathic Membranous Nephropathy in a Chinese Han Population. Description: Qin, Xiao-Song, et al. Variants in the Promoter Region of HLA-DQA1 were Associated with Idiopathic Membranous Nephropathy in a Chinese Han Population. ''Chin Med J (Engl)''. 2017 Jul 20; '''130''' (14):1677-1682
Novel efficient genome-wide SNP panels for the conservation of the highly endangered Iberian lynx. Description: Kleinman-Ruiz, Daniel, et al. Novel efficient genome-wide SNP panels for the conservation of the highly endangered Iberian lynx. ''BMC Genomics''. 2017 Jul 21; '''18''' (1):556
Genes and pathways underlying susceptibility to impaired lung function in the context of environmental tobacco smoke exposure. Description: de Jong, K, et al. Genes and pathways underlying susceptibility to impaired lung function in the context of environmental tobacco smoke exposure. ''Respir Res''. 2017 Jul 24; '''18''' (1):142
Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families. Description: Maatta, Kirsi M, et al. Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families. ''BMC Cancer''. 2017 Jul 24; '''17''' (1):496
Identifying and mitigating batch effects in whole genome sequencing data. Description: Tom, Jennifer A, et al. Identifying and mitigating batch effects in whole genome sequencing data. ''BMC Bioinformatics''. 2017 Jul 24; '''18''' (1):351
Neanderthal-Derived Genetic Variation Shapes Modern Human Cranium and Brain. Description: Gregory, Michael D, et al. Neanderthal-Derived Genetic Variation Shapes Modern Human Cranium and Brain. ''Sci Rep''. 2017 Jul 24; '''7''' (1):6308
Novel risk genes for systemic lupus erythematosus predicted by random forest classification. Description: Almlof, Jonas Carlsson, et al. Novel risk genes for systemic lupus erythematosus predicted by random forest classification. ''Sci Rep''. 2017 Jul 24; '''7''' (1):6236
Genetic loci associated with an earlier age at onset in multiplex schizophrenia. Description: Woolston, Annemarie L, et al. Genetic loci associated with an earlier age at onset in multiplex schizophrenia. ''Sci Rep''. 2017 Jul 25; '''7''' (1):6486
The DCDC2 deletion is not a risk factor for dyslexia. Description: Scerri, T S, et al. The DCDC2 deletion is not a risk factor for dyslexia. ''Transl Psychiatry''. 2017 Jul 25; '''7''' (7):e1182
Inclusion of Population-specific Reference Panel from India to the 1000 Genomes Phase 3 Panel Improves Imputation Accuracy. Description: Ahmad, Meraj, et al. Inclusion of Population-specific Reference Panel from India to the 1000 Genomes Phase 3 Panel Improves Imputation Accuracy. ''Sci Rep''. 2017 Jul 27; '''7''' (1):6733
The practical use of genome sequencing data in the management of a feline colony pedigree. Description: Farias, Fabiana H G, et al. The practical use of genome sequencing data in the management of a feline colony pedigree. ''BMC Vet Res''. 2017 Jul 27; '''13''' (1):225
Design and implementation of a custom next generation sequencing panel for selected vitamin D associated genes. Description: Benson, Katherine Angela, et al. Design and implementation of a custom next generation sequencing panel for selected vitamin D associated genes. ''BMC Res Notes''. 2017 Jul 28; '''10''' (1):348
Efficiency of ddRAD target enriched sequencing across spiny rock lobster species (Palinuridae: Jasus). Description: Souza, Carla A, et al. Efficiency of ddRAD target enriched sequencing across spiny rock lobster species (Palinuridae: Jasus). ''Sci Rep''. 2017 Jul 28; '''7''' (1):6781
Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment. Description: Wang, Zhaoxi, et al. Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment. ''Environ Health''. 2017 Jul 28; '''16''' (1):81
Diurnal preference, mood and the response to morning light in relation to polymorphisms in the human clock gene PER3. Description: Turco, M, et al. Diurnal preference, mood and the response to morning light in relation to polymorphisms in the human clock gene PER3. ''Sci Rep''. 2017 Jul 31; '''7''' (1):6967
Adaptive introgression from distant Caribbean islands contributed to the diversification of a microendemic adaptive radiation of trophic specialist pupfishes. Description: Richards, Emilie J, et al. Adaptive introgression from distant Caribbean islands contributed to the diversification of a microendemic adaptive radiation of trophic specialist pupfishes. ''PLoS Genet''. 2017 Aug; '''13''' (8):e1006919
A gene-environment interaction analysis of plasma selenium with prevalent and incident diabetes: The Hortega study. Description: Galan-Chilet, Inmaculada, et al. A gene-environment interaction analysis of plasma selenium with prevalent and incident diabetes: The Hortega study. ''Redox Biol''. 2017 Aug; '''12''': 798-805
A normal genetic variation modulates synaptic MMP-9 protein levels and the severity of schizophrenia symptoms. Description: Lepeta, Katarzyna, et al. A normal genetic variation modulates synaptic MMP-9 protein levels and the severity of schizophrenia symptoms. ''EMBO Mol Med''. 2017 Aug; '''9''' (8):1100-1116
Association Study Confirmed Three Breast Cancer-Specific Molecular Subtype-Associated Susceptibility Loci in Chinese Han Women. Description: Xu, Yihui, et al. Association Study Confirmed Three Breast Cancer-Specific Molecular Subtype-Associated Susceptibility Loci in Chinese Han Women. ''Oncologist''. 2017 Aug; '''22''' (8):890-894
Candidate gene polymorphisms study between human African trypanosomiasis clinical phenotypes in Guinea. Description: Kabore, Justin Windingoudi, et al. Candidate gene polymorphisms study between human African trypanosomiasis clinical phenotypes in Guinea. ''PLoS Negl Trop Dis''. 2017 Aug; '''11''' (8):e0005833
Composite likelihood method for inferring local pedigrees. Description: Ko, Amy, et al. Composite likelihood method for inferring local pedigrees. ''PLoS Genet''. 2017 Aug; '''13''' (8):e1006963
CYP2A6 Polymorphisms Associate with Outcomes of S-1 Plus Oxaliplatin Chemotherapy in Chinese Gastric Cancer Patients. Description: Yang, Lin, et al. CYP2A6 Polymorphisms Associate with Outcomes of S-1 Plus Oxaliplatin Chemotherapy in Chinese Gastric Cancer Patients. ''Genomics Proteomics Bioinformatics''. 2017 Aug; '''15''' (4):255-262
Deconstructing isolation-by-distance: The genomic consequences of limited dispersal. Description: Aguillon, Stepfanie M, et al. Deconstructing isolation-by-distance: The genomic consequences of limited dispersal. ''PLoS Genet''. 2017 Aug; '''13''' (8):e1006911
Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study. Description: Leo, Paul J, et al. Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study. ''PLoS Genet''. 2017 Aug; '''13''' (8):e1006866
Discerning the Origins of the Negritos, First Sundaland People: Deep Divergence and Archaic Admixture. Description: Jinam, Timothy A, et al. Discerning the Origins of the Negritos, First Sundaland People: Deep Divergence and Archaic Admixture. ''Genome Biol Evol''. 2017 Aug 1; '''9''' (8):2013-2022
Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function. Description: Cukier, H N, et al. Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function. ''J Alzheimers Dis Parkinsonism''. 2017 Aug; '''7''' (4):
Genetic factors exist behind the high prevalence of reduced high-density lipoprotein cholesterol levels in the Roma population. Description: Piko, Peter, et al. Genetic factors exist behind the high prevalence of reduced high-density lipoprotein cholesterol levels in the Roma population. ''Atherosclerosis''. 2017 Aug; '''263''': 119-126
Genetic interplay between human longevity and metabolic pathways - a large-scale eQTL study. Description: Hasler, Robert, et al. Genetic interplay between human longevity and metabolic pathways - a large-scale eQTL study. ''Aging Cell''. 2017 Aug; '''16''' (4):716-725
Genome-wide association analysis identifies common variants influencing infant brain volumes. Description: Xia, K, et al. Genome-wide association analysis identifies common variants influencing infant brain volumes. ''Transl Psychiatry''. 2017 Aug 1; '''7''' (8):e1188
Genome-wide association study for 13 agronomic traits reveals distribution of superior alleles in bread wheat from the Yellow and Huai Valley of China. Description: Sun, Congwei, et al. Genome-wide association study for 13 agronomic traits reveals distribution of superior alleles in bread wheat from the Yellow and Huai Valley of China. ''Plant Biotechnol J''. 2017 Aug; '''15''' (8):953-969
Genome-wide association study identifies 22 new loci for body dimension and body weight traits in a White DurocxErhualian F2 intercross population. Description: Ji, Jiuxiu, et al. Genome-wide association study identifies 22 new loci for body dimension and body weight traits in a White DurocxErhualian F2 intercross population. ''Asian-Australas J Anim Sci''. 2017 Aug; '''30''' (8):1066-1073
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals. Description: Rivera, Margarita, et al. Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals. ''Br J Psychiatry''. 2017 Aug; '''211''' (2):70-76
Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Description: Persad, Patrice J, et al. Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. ''Invest Ophthalmol Vis Sci''. 2017 Aug 1; '''58''' (10):4027-4038
Multiple introductions of the dengue vector, Aedes aegypti, into California. Description: Pless, Evlyn, et al. Multiple introductions of the dengue vector, Aedes aegypti, into California. ''PLoS Negl Trop Dis''. 2017 Aug; '''11''' (8):e0005718
Northeast African genomic variation shaped by the continuity of indigenous groups and Eurasian migrations. Description: Hollfelder, Nina, et al. Northeast African genomic variation shaped by the continuity of indigenous groups and Eurasian migrations. ''PLoS Genet''. 2017 Aug; '''13''' (8):e1006976
Prevalence, Patterns, and Genetic Association Analysis of Modic Vertebral Endplate Changes. Description: Kanna, Rishi Mugesh, et al. Prevalence, Patterns, and Genetic Association Analysis of Modic Vertebral Endplate Changes. ''Asian Spine J''. 2017 Aug; '''11''' (4):594-600
Quantification of transplant-derived circulating cell-free DNA in absence of a donor genotype. Description: Sharon, Eilon, et al. Quantification of transplant-derived circulating cell-free DNA in absence of a donor genotype. ''PLoS Comput Biol''. 2017 Aug; '''13''' (8):e1005629
Rare coding variants pinpoint genes that control human hematological traits. Description: Mousas, Abdou, et al. Rare coding variants pinpoint genes that control human hematological traits. ''PLoS Genet''. 2017 Aug; '''13''' (8):e1006925
Resurgence of cucurbit downy mildew in the United States: Insights from comparative genomic analysis of Pseudoperonospora cubensis. Description: Thomas, Anna, et al. Resurgence of cucurbit downy mildew in the United States: Insights from comparative genomic analysis of Pseudoperonospora cubensis. ''Ecol Evol''. 2017 Aug; '''7''' (16):6231-6246
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Description: Singh, Tarjinder, et al. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. ''Nat Genet''. 2017 Aug; '''49''' (8):1167-1173
The last sea nomads of the Indonesian archipelago: genomic origins and dispersal. Description: Kusuma, Pradiptajati, et al. The last sea nomads of the Indonesian archipelago: genomic origins and dispersal. ''Eur J Hum Genet''. 2017 Aug; '''25''' (8):1004-1010
The susceptible HLA class II alleles and their presenting epitope(s) in Goodpasture's disease. Description: Xie, Li-Jun, et al. The susceptible HLA class II alleles and their presenting epitope(s) in Goodpasture's disease. ''Immunology''. 2017 Aug; '''151''' (4):395-404
UNC5C variants are associated with cerebral amyloid angiopathy. Description: Yang, Hyun-Sik, et al. UNC5C variants are associated with cerebral amyloid angiopathy. ''Neurol Genet''. 2017 Aug; '''3''' (4):e176
A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle. Description: Agerholm, Jorgen S, et al. A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle. ''BMC Genet''. 2017 Aug 2; '''18''' (1):74
A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration. Description: Kawashima-Kumagai, Kyoko, et al. A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration. ''Sci Rep''. 2017 Aug 3; '''7''' (1):7173
De Novo FGF12 (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia. Description: Li, Qianqian, et al. De Novo FGF12 (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia. ''J Am Heart Assoc''. 2017 Aug 3; '''6''' (8):
Effect of carboxylesterase 1 S75N on clopidogrel therapy among acute coronary syndrome patients. Description: Xiao, Fei-Yan, et al. Effect of carboxylesterase 1 S75N on clopidogrel therapy among acute coronary syndrome patients. ''Sci Rep''. 2017 Aug 3; '''7''' (1):7244
Leptin Receptor Gene Variant rs11804091 Is Associated with BMI and Insulin Resistance in Spanish Female Obese Children: A Case-Control Study. Description: Olza, Josune, et al. Leptin Receptor Gene Variant rs11804091 Is Associated with BMI and Insulin Resistance in Spanish Female Obese Children: A Case-Control Study. ''Int J Mol Sci''. 2017 Aug 3; '''18''' (8):
Effects of four novel genetic polymorphisms on clopidogrel efficacy in Chinese acute coronary syndromes patients. Description: Xiao, Fei-Yan, et al. Effects of four novel genetic polymorphisms on clopidogrel efficacy in Chinese acute coronary syndromes patients. ''Gene''. 2017 Aug 5; '''623''': 63-71
A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2). Description: Mauri, Nico, et al. A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2). ''G3 (Bethesda)''. 2017 Aug 7; '''7''' (8):2729-2737
Genome-Wide Associations for Water-Soluble Carbohydrate Concentration and Relative Maturity in Wheat Using SNP and DArT Marker Arrays. Description: Ovenden, Ben, et al. Genome-Wide Associations for Water-Soluble Carbohydrate Concentration and Relative Maturity in Wheat Using SNP and DArT Marker Arrays. ''G3 (Bethesda)''. 2017 Aug 7; '''7''' (8):2821-2830
Genome-wide Association Study Reveals that the Aquaporin NIP1;1 Contributes to Variation in Hydrogen Peroxide Sensitivity in Arabidopsis thaliana. Description: Sadhukhan, Ayan, et al. Genome-wide Association Study Reveals that the Aquaporin NIP1;1 Contributes to Variation in Hydrogen Peroxide Sensitivity in Arabidopsis thaliana. ''Mol Plant''. 2017 Aug 7; '''10''' (8):1082-1094
Associations of high altitude polycythemia with polymorphisms in EPHA2 and AGT in Chinese Han and Tibetan populations. Description: Liu, Lijun, et al. Associations of high altitude polycythemia with polymorphisms in EPHA2 and AGT in Chinese Han and Tibetan populations. ''Oncotarget''. 2017 Aug 8; '''8''' (32):53234-53243
Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population. Description: Chung, Ren-Hua, et al. Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population. ''BMC Genomics''. 2017 Aug 8; '''18''' (1):591
Genomic signatures of adaptive introgression from European mouflon into domestic sheep. Description: Barbato, Mario, et al. Genomic signatures of adaptive introgression from European mouflon into domestic sheep. ''Sci Rep''. 2017 Aug 8; '''7''' (1):7623
Mitochondrial DNA sequencing and large-scale genotyping identifies MT-ND4 gene mutation m.11696G>A associated with idiopathic oligoasthenospermia. Description: Ji, Juan, et al. Mitochondrial DNA sequencing and large-scale genotyping identifies MT-ND4 gene mutation m.11696G>A associated with idiopathic oligoasthenospermia. ''Oncotarget''. 2017 Aug 8; '''8''' (32):52975-52982
Genome-wide dissection of heterosis for yield traits in two-line hybrid rice populations. Description: Zhen, Gang, et al. Genome-wide dissection of heterosis for yield traits in two-line hybrid rice populations. ''Sci Rep''. 2017 Aug 9; '''7''' (1):7635
Performance of gout definitions for genetic epidemiological studies: analysis of UK Biobank. Description: Cadzow, Murray, et al. Performance of gout definitions for genetic epidemiological studies: analysis of UK Biobank. ''Arthritis Res Ther''. 2017 Aug 9; '''19''' (1):181
A phased SNP-based classification of sickle cell anemia HBB haplotypes. Description: Shaikho, Elmutaz M, et al. A phased SNP-based classification of sickle cell anemia HBB haplotypes. ''BMC Genomics''. 2017 Aug 11; '''18''' (1):608
Risk and predictors of psoriasis in patients with breast cancer: a Swedish population-based cohort study. Description: Yang, Haomin, et al. Risk and predictors of psoriasis in patients with breast cancer: a Swedish population-based cohort study. ''BMC Med''. 2017 Aug 11; '''15''' (1):154
Genomic data illuminates demography, genetic structure and selection of a popular dog breed. Description: Wiener, Pamela, et al. Genomic data illuminates demography, genetic structure and selection of a popular dog breed. ''BMC Genomics''. 2017 Aug 14; '''18''' (1):609
Application of a Bayesian non-linear model hybrid scheme to sequence data for genomic prediction and QTL mapping. Description: Wang, Tingting, et al. Application of a Bayesian non-linear model hybrid scheme to sequence data for genomic prediction and QTL mapping. ''BMC Genomics''. 2017 Aug 15; '''18''' (1):618
Do regional brain volumes and major depressive disorder share genetic architecture? A study of Generation Scotland (n=19 762), UK Biobank (n=24 048) and the English Longitudinal Study of Ageing (n=5766). Description: Wigmore, E M, et al. Do regional brain volumes and major depressive disorder share genetic architecture? A study of Generation Scotland (n=19 762), UK Biobank (n=24 048) and the English Longitudinal Study of Ageing (n=5766). ''Transl Psychiatry''. 2017 Aug 15; '''7''' (8):e1205
Heritable Bovine Rumen Bacteria Are Phylogenetically Related and Correlated with the Cow's Capacity To Harvest Energy from Its Feed. Description: Sasson, Goor, et al. Heritable Bovine Rumen Bacteria Are Phylogenetically Related and Correlated with the Cow's Capacity To Harvest Energy from Its Feed. ''MBio''. 2017 Aug 15; '''8''' (4):
Risk assessment models for genetic risk predictors of lung cancer using two-stage replication for Asian and European populations. Description: Cheng, Yang, et al. Risk assessment models for genetic risk predictors of lung cancer using two-stage replication for Asian and European populations. ''Oncotarget''. 2017 Aug 15; '''8''' (33):53959-53967
Variants in the CXCL12 gene was associated with coronary artery disease susceptibility in Chinese Han population. Description: Zhang, Junbo, et al. Variants in the CXCL12 gene was associated with coronary artery disease susceptibility in Chinese Han population. ''Oncotarget''. 2017 Aug 15; '''8''' (33):54518-54527
The genomic architecture of mastitis resistance in dairy sheep. Description: Banos, G, et al. The genomic architecture of mastitis resistance in dairy sheep. ''BMC Genomics''. 2017 Aug 16; '''18''' (1):624
Convergent and divergent genetic changes in the genome of Chinese and European pigs. Description: Wang, Jing, et al. Convergent and divergent genetic changes in the genome of Chinese and European pigs. ''Sci Rep''. 2017 Aug 17; '''7''' (1):8662
Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat. Description: Qiao, Xian, et al. Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat. ''Sci Rep''. 2017 Aug 17; '''7''' (1):8621
CDKAL1 rs7756992 is associated with diabetic retinopathy in a Chinese population with type 2 diabetes. Description: Peng, Danfeng, et al. CDKAL1 rs7756992 is associated with diabetic retinopathy in a Chinese population with type 2 diabetes. ''Sci Rep''. 2017 Aug 18; '''7''' (1):8812
Prioritizing tests of epistasis through hierarchical representation of genomic redundancies. Description: Cowman, Tyler, et al. Prioritizing tests of epistasis through hierarchical representation of genomic redundancies. ''Nucleic Acids Res''. 2017 Aug 21; '''45''' (14):e131
The genetic variation rs12143842 in NOS1AP increases idiopathic ventricular tachycardia risk in Chinese Han populations. Description: Zhang, Ronfeng, et al. The genetic variation rs12143842 in NOS1AP increases idiopathic ventricular tachycardia risk in Chinese Han populations. ''Sci Rep''. 2017 Aug 21; '''7''' (1):8356
Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium. Description: Lophatananon, Artitaya, et al. Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium. ''Br J Cancer''. 2017 Aug 22; '''117''' (5):734-743
RNA-Seq reveals MicroRNA expression signature and genetic polymorphism associated with growth and muscle quality traits in rainbow trout. Description: Paneru, Bam Dev, et al. RNA-Seq reveals MicroRNA expression signature and genetic polymorphism associated with growth and muscle quality traits in rainbow trout. ''Sci Rep''. 2017 Aug 22; '''7''' (1):9078
A prospective multicenter study on genome wide associations to ranibizumab treatment outcome for age-related macular degeneration. Description: Yamashiro, Kenji, et al. A prospective multicenter study on genome wide associations to ranibizumab treatment outcome for age-related macular degeneration. ''Sci Rep''. 2017 Aug 23; '''7''' (1):9196
High-density 80 K SNP array is a powerful tool for genotyping G. hirsutum accessions and genome analysis. Description: Cai, Caiping, et al. High-density 80 K SNP array is a powerful tool for genotyping G. hirsutum accessions and genome analysis. ''BMC Genomics''. 2017 Aug 23; '''18''' (1):654
Genetic association analysis of serotonin and signal transduction pathways in suicide attempters from an Italian sample of psychiatric patients. Description: Pompili, Maurizio, et al. Genetic association analysis of serotonin and signal transduction pathways in suicide attempters from an Italian sample of psychiatric patients. ''Neurosci Lett''. 2017 Aug 24; '''656''': 94-102
Genetic influences on the human oral microbiome. Description: Demmitt, Brittany A, et al. Genetic influences on the human oral microbiome. ''BMC Genomics''. 2017 Aug 24; '''18''' (1):659
Genome-wide association studies dissect the genetic networks underlying agronomical traits in soybean. Description: Fang, Chao, et al. Genome-wide association studies dissect the genetic networks underlying agronomical traits in soybean. ''Genome Biol''. 2017 Aug 24; '''18''' (1):161
Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene. Description: Mahlman, Mari, et al. Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene. ''Sci Rep''. 2017 Aug 24; '''7''' (1):9271
Identifying highly informative genetic markers for quantification of ancestry proportions in crossbred sheep populations: implications for choosing optimum levels of admixture. Description: Getachew, Tesfaye, et al. Identifying highly informative genetic markers for quantification of ancestry proportions in crossbred sheep populations: implications for choosing optimum levels of admixture. ''BMC Genet''. 2017 Aug 24; '''18''' (1):80
Lack of association between AKAP2 and the susceptibility of adolescent idiopathic scoliosis in the Chinese population. Description: Xu, Leilei, et al. Lack of association between AKAP2 and the susceptibility of adolescent idiopathic scoliosis in the Chinese population. ''BMC Musculoskelet Disord''. 2017 Aug 24; '''18''' (1):368
A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs. Description: Becker, Doreen, et al. A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs. ''BMC Genomics''. 2017 Aug 25; '''18''' (1):662
Influence of epistasis on response to genomic selection using complete sequence data. Description: Forneris, Natalia S, et al. Influence of epistasis on response to genomic selection using complete sequence data. ''Genet Sel Evol''. 2017 Aug 25; '''49''' (1):66
Organ damage in sickle cell disease study (ORDISS): protocol for a longitudinal cohort study based in Ghana. Description: Anie, Kofi A, et al. Organ damage in sickle cell disease study (ORDISS): protocol for a longitudinal cohort study based in Ghana. ''BMJ Open''. 2017 Aug 28; '''7''' (8):e016727
A rare genetic variant of BPIFB4 predisposes to high blood pressure via impairment of nitric oxide signaling. Description: Vecchione, Carmine, et al. A rare genetic variant of BPIFB4 predisposes to high blood pressure via impairment of nitric oxide signaling. ''Sci Rep''. 2017 Aug 29; '''7''' (1):9706
Influence of estrogen-related receptor gamma (ESRRG) rs1890552 A > G polymorphism on changes in fasting glucose and arterial stiffness. Description: Kim, Minjoo, et al. Influence of estrogen-related receptor gamma (ESRRG) rs1890552 A > G polymorphism on changes in fasting glucose and arterial stiffness. ''Sci Rep''. 2017 Aug 29; '''7''' (1):9787
Nonsteroidal Anti-inflammatory Drug Interaction with Prostacyclin Synthase Protects from Miscarriage. Description: Velez Edwards, Digna R, et al. Nonsteroidal Anti-inflammatory Drug Interaction with Prostacyclin Synthase Protects from Miscarriage. ''Sci Rep''. 2017 Aug 29; '''7''' (1):9874
Performance of risk prediction for inflammatory bowel disease based on genotyping platform and genomic risk score method. Description: Chen, Guo-Bo, et al. Performance of risk prediction for inflammatory bowel disease based on genotyping platform and genomic risk score method. ''BMC Med Genet''. 2017 Aug 29; '''18''' (1):94
Significant association of the CHRNB3-CHRNA6 gene cluster with nicotine dependence in the Chinese Han population. Description: Wen, Li, et al. Significant association of the CHRNB3-CHRNA6 gene cluster with nicotine dependence in the Chinese Han population. ''Sci Rep''. 2017 Aug 29; '''7''' (1):9745
A candidate gene approach to study nematode resistance traits in naturally infected sheep. Description: Wilkie, Hazel, et al. A candidate gene approach to study nematode resistance traits in naturally infected sheep. ''Vet Parasitol''. 2017 Aug 30; '''243''': 71-74
A comprehensive analysis of the association of common variants of ABCG2 with gout. Description: Yu, Kuang-Hui, et al. A comprehensive analysis of the association of common variants of ABCG2 with gout. ''Sci Rep''. 2017 Aug 30; '''7''' (1):9988
Attempts to replicate genetic associations with schizophrenia in a cohort from north India. Description: Prasad, Suman, et al. Attempts to replicate genetic associations with schizophrenia in a cohort from north India. ''NPJ Schizophr''. 2017 Aug 30; '''3''' (1):28
Genome-wide genetic structure and differentially selected regions among Landrace, Erhualian, and Meishan pigs using specific-locus amplified fragment sequencing. Description: Li, Zhen, et al. Genome-wide genetic structure and differentially selected regions among Landrace, Erhualian, and Meishan pigs using specific-locus amplified fragment sequencing. ''Sci Rep''. 2017 Aug 30; '''7''' (1):10063
Prenatal Serum Concentrations of Brominated Flame Retardants and Autism Spectrum Disorder and Intellectual Disability in the Early Markers of Autism Study: A Population-Based Case-Control Study in California. Description: Lyall, Kristen, et al. Prenatal Serum Concentrations of Brominated Flame Retardants and Autism Spectrum Disorder and Intellectual Disability in the Early Markers of Autism Study: A Population-Based Case-Control Study in California. ''Environ Health Perspect''. 2017 Aug 30; '''125''' (8):087023
The Genetic Origin of Short Tail in Endangered Korean Dog, DongGyeongi. Description: Yoo, DongAhn, et al. The Genetic Origin of Short Tail in Endangered Korean Dog, DongGyeongi. ''Sci Rep''. 2017 Aug 30; '''7''' (1):10048
The molecular basis of differential morphology and bleaching thresholds in two morphs of the coral Pocillopora acuta. Description: Smith, Hillary, et al. The molecular basis of differential morphology and bleaching thresholds in two morphs of the coral Pocillopora acuta. ''Sci Rep''. 2017 Aug 30; '''7''' (1):10066
A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors. Description: Braenne, Ingrid, et al. A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors. ''Sci Rep''. 2017 Aug 31; '''7''' (1):10252
Refining the South Asian Origin of the Romani people. Description: Melegh, Bela I, et al. Refining the South Asian Origin of the Romani people. ''BMC Genet''. 2017 Aug 31; '''18''' (1):82
ABCG2 Polymorphism Is Associated with Hyperuricemia in a Study of a Community-Based Korean Cohort. Description: Son, Chang Nam, et al. ABCG2 Polymorphism Is Associated with Hyperuricemia in a Study of a Community-Based Korean Cohort. ''J Korean Med Sci''. 2017 Sep; '''32''' (9):1451-1459
A Novel Association between Lysyl Oxidase Gene Polymorphism and Intracranial Aneurysm in Koreans. Description: Hong, Eun Pyo, et al. A Novel Association between Lysyl Oxidase Gene Polymorphism and Intracranial Aneurysm in Koreans. ''Yonsei Med J''. 2017 Sep; '''58''' (5):1006-1011
Association analysis of APO gene polymorphisms with ischemic stroke risk: a case-control study in a Chinese Han population. Description: Xiao, Rongjun, et al. Association analysis of APO gene polymorphisms with ischemic stroke risk: a case-control study in a Chinese Han population. ''Oncotarget''. 2017 Sep 1; '''8''' (36):60496-60503
Association of candidate gene polymorphisms with clinical subtypes of preterm birth in a Latin American population. Description: Gimenez, Lucas G, et al. Association of candidate gene polymorphisms with clinical subtypes of preterm birth in a Latin American population. ''Pediatr Res''. 2017 Sep; '''82''' (3):554-559
C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis. Description: Lepik, Kaido, et al. C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis. ''PLoS Comput Biol''. 2017 Sep; '''13''' (9):e1005766
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease. Description: De Roeck, Arne, et al. Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease. ''Acta Neuropathol''. 2017 Sep; '''134''' (3):475-487
Family-specific aggregation of lipid GWAS variants confers the susceptibility to familial hypercholesterolemia in a large Austrian family. Description: Nikkola, Elina, et al. Family-specific aggregation of lipid GWAS variants confers the susceptibility to familial hypercholesterolemia in a large Austrian family. ''Atherosclerosis''. 2017 Sep; '''264''': 58-66
Fine scale mapping of genomic introgressions within the Drosophila yakuba clade. Description: Turissini, David A, et al. Fine scale mapping of genomic introgressions within the Drosophila yakuba clade. ''PLoS Genet''. 2017 Sep; '''13''' (9):e1006971
Genome-wide association study of language performance in Alzheimer's disease. Description: Deters, Kacie D, et al. Genome-wide association study of language performance in Alzheimer's disease. ''Brain Lang''. 2017 Sep; '''172''': 22-29
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. Description: Zeng, Yanni, et al. Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. ''Biol Psychiatry''. 2017 Sep 1; '''82''' (5):312-321
Genomic analyses of African Trypanozoon strains to assess evolutionary relationships and identify markers for strain identification. Description: Richardson, Joshua Brian, et al. Genomic analyses of African Trypanozoon strains to assess evolutionary relationships and identify markers for strain identification. ''PLoS Negl Trop Dis''. 2017 Sep; '''11''' (9):e0005949
Genomic Reconstruction of the History of Native Sheep Reveals the Peopling Patterns of Nomads and the Expansion of Early Pastoralism in East Asia. Description: Zhao, Yong-Xin, et al. Genomic Reconstruction of the History of Native Sheep Reveals the Peopling Patterns of Nomads and the Expansion of Early Pastoralism in East Asia. ''Mol Biol Evol''. 2017 Sep 1; '''34''' (9):2380-2395
Identifying genetic variants that affect viability in large cohorts. Description: Mostafavi, Hakhamanesh, et al. Identifying genetic variants that affect viability in large cohorts. ''PLoS Biol''. 2017 Sep; '''15''' (9):e2002458
Identifying new susceptibility genes on dopaminergic and serotonergic pathways for the framing effect in decision-making. Description: Gao, Xiaoxue, et al. Identifying new susceptibility genes on dopaminergic and serotonergic pathways for the framing effect in decision-making. ''Soc Cogn Affect Neurosci''. 2017 Sep 1; '''12''' (9):1534-1544
MergeReference: A Tool for Merging Reference Panels for HLA Imputation. Description: Cook, Seungho, et al. MergeReference: A Tool for Merging Reference Panels for HLA Imputation. ''Genomics Inform''. 2017 Sep; '''15''' (3):108-111
Population Genomics Reveals Speciation and Introgression between Brown Norway Rats and Their Sibling Species. Description: Teng, Huajing, et al. Population Genomics Reveals Speciation and Introgression between Brown Norway Rats and Their Sibling Species. ''Mol Biol Evol''. 2017 Sep 1; '''34''' (9):2214-2228
Potential contribution of the neurodegenerative disorders risk loci to cognitive performance in an elderly male gout population. Description: Han, Lin, et al. Potential contribution of the neurodegenerative disorders risk loci to cognitive performance in an elderly male gout population. ''Medicine (Baltimore)''. 2017 Sep; '''96''' (39):e8195
The eBioKit, a stand-alone educational platform for bioinformatics. Description: Hernandez-de-Diego, Rafael, et al. The eBioKit, a stand-alone educational platform for bioinformatics. ''PLoS Comput Biol''. 2017 Sep; '''13''' (9):e1005616
A functional IFN-lambda4-generating DNA polymorphism could protect older asthmatic women from aeroallergen sensitization and associate with clinical features of asthma. Description: Chinnaswamy, Sreedhar, et al. A functional IFN-lambda4-generating DNA polymorphism could protect older asthmatic women from aeroallergen sensitization and associate with clinical features of asthma. ''Sci Rep''. 2017 Sep 5; '''7''' (1):10500
Vitamin D receptor and calcium-sensing receptor polymorphisms and colorectal cancer survival in the Newfoundland population. Description: Zhu, Yun, et al. Vitamin D receptor and calcium-sensing receptor polymorphisms and colorectal cancer survival in the Newfoundland population. ''Br J Cancer''. 2017 Sep 5; '''117''' (6):898-906
Genome-wide association study reveals putative role of gga-miR-15a in controlling feed conversion ratio in layer chickens. Description: Yuan, Jingwei, et al. Genome-wide association study reveals putative role of gga-miR-15a in controlling feed conversion ratio in layer chickens. ''BMC Genomics''. 2017 Sep 6; '''18''' (1):699
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis. Description: Ng, Michael, et al. A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis. ''Am J Hum Genet''. 2017 Sep 7; '''101''' (3):417-427
Genome-wide association study Identified multiple Genetic Loci on Chilling Resistance During Germination in Maize. Description: Hu, Guanghui, et al. Genome-wide association study Identified multiple Genetic Loci on Chilling Resistance During Germination in Maize. ''Sci Rep''. 2017 Sep 7; '''7''' (1):10840
The Genetic Legacy of Zoroastrianism in Iran and India: Insights into Population Structure, Gene Flow, and Selection. Description: Lopez, Saioa, et al. The Genetic Legacy of Zoroastrianism in Iran and India: Insights into Population Structure, Gene Flow, and Selection. ''Am J Hum Genet''. 2017 Sep 7; '''101''' (3):353-368
Association between alcohol-induced osteonecrosis of femoral head and risk variants of MMPS in Han population based on a case-control study. Description: Wang, Jianzhong, et al. Association between alcohol-induced osteonecrosis of femoral head and risk variants of MMPS in Han population based on a case-control study. ''Oncotarget''. 2017 Sep 8; '''8''' (38):64490-64498
Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Description: Prins, Bram P, et al. Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. ''Sci Rep''. 2017 Sep 8; '''7''' (1):11008
Neurogenetic plasticity and sex influence the link between corticolimbic structural connectivity and trait anxiety. Description: Kim, M Justin, et al. Neurogenetic plasticity and sex influence the link between corticolimbic structural connectivity and trait anxiety. ''Sci Rep''. 2017 Sep 8; '''7''' (1):10959
Predictive single nucleotide polymorphism markers for acute oral mucositis in patients with nasopharyngeal carcinoma treated with radiotherapy. Description: Le, Ziyu, et al. Predictive single nucleotide polymorphism markers for acute oral mucositis in patients with nasopharyngeal carcinoma treated with radiotherapy. ''Oncotarget''. 2017 Sep 8; '''8''' (38):63026-63037
Association of common genetic variants in VEGFA with biliary atresia susceptibility in Northwestern Han Chinese. Description: Liu, Bailing, et al. Association of common genetic variants in VEGFA with biliary atresia susceptibility in Northwestern Han Chinese. ''Gene''. 2017 Sep 10; '''628''': 87-92
A variant on chromosome 2p13.3 is associated with atopic dermatitis in Chinese Han population. Description: Cai, Xin-Ying, et al. A variant on chromosome 2p13.3 is associated with atopic dermatitis in Chinese Han population. ''Gene''. 2017 Sep 10; '''628''': 281-285
A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol. Description: Chang, Chia-Jung, et al. A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol. ''Nat Commun''. 2017 Sep 12; '''8''' (1):522
Analyses of germline variants associated with ovarian cancer survival identify functional candidates at the 1q22 and 19p12 outcome loci. Description: Glubb, Dylan M, et al. Analyses of germline variants associated with ovarian cancer survival identify functional candidates at the 1q22 and 19p12 outcome loci. ''Oncotarget''. 2017 Sep 12; '''8''' (39):64670-64684
Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system. Description: Belbin, Gillian Morven, et al. Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system. ''Elife''. 2017 Sep 12; '''6''':
Deletion variant rs35153737 in TOR1A is associated with isolated dystonia in a Southwestern Chinese Population. Description: Li, Jiang, et al. Deletion variant rs35153737 in TOR1A is associated with isolated dystonia in a Southwestern Chinese Population. ''Neurosci Lett''. 2017 Sep 14; '''657''': 1-4
Y Chromosome, Mitochondrial DNA and Childhood Behavioural Traits. Description: Howe, Laurence J, et al. Y Chromosome, Mitochondrial DNA and Childhood Behavioural Traits. ''Sci Rep''. 2017 Sep 14; '''7''' (1):11655
Accumulation of minor alleles and risk prediction in schizophrenia. Description: He, Pei, et al. Accumulation of minor alleles and risk prediction in schizophrenia. ''Sci Rep''. 2017 Sep 15; '''7''' (1):11661
ACYP2 polymorphisms are associated with the risk of liver cancer in a Han Chinese population. Description: Chen, Zhong, et al. ACYP2 polymorphisms are associated with the risk of liver cancer in a Han Chinese population. ''Oncotarget''. 2017 Sep 15; '''8''' (40):67723-67731
Haplotype of the Interleukin 17A gene is associated with osteitis after Bacillus Calmette-Guerin vaccination. Description: Korppi, Matti, et al. Haplotype of the Interleukin 17A gene is associated with osteitis after Bacillus Calmette-Guerin vaccination. ''Sci Rep''. 2017 Sep 15; '''7''' (1):11691
Positive correlation of cg16672562 methylation with obesity-related traits in childhood obesity, and its independence with underlying HIF3A (hypoxia-inducible factor 3a) genetic background. Description: Lee, Suman, et al. Positive correlation of cg16672562 methylation with obesity-related traits in childhood obesity, and its independence with underlying HIF3A (hypoxia-inducible factor 3a) genetic background. ''Oncotarget''. 2017 Sep 15; '''8''' (40):67473-67481
Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution. Description: Magi, Reedik, et al. Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution. ''Hum Mol Genet''. 2017 Sep 15; '''26''' (18):3639-3650
5-hydroxymethylcytosine is highly dynamic across human fetal brain development. Description: Spiers, Helen, et al. 5-hydroxymethylcytosine is highly dynamic across human fetal brain development. ''BMC Genomics''. 2017 Sep 18; '''18''' (1):738
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk. Description: Chang, Xiao, et al. Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk. ''Nat Commun''. 2017 Sep 18; '''8''' (1):569
Single nucleotide polymorphisms of nucleotide excision repair pathway are significantly associated with outcomes of platinum-based chemotherapy in lung cancer. Description: Song, Xiao, et al. Single nucleotide polymorphisms of nucleotide excision repair pathway are significantly associated with outcomes of platinum-based chemotherapy in lung cancer. ''Sci Rep''. 2017 Sep 18; '''7''' (1):11785
Different effection of p.1125Val>Ala and rs11954856 in APC on Wnt signaling pathway. Description: Li, Fei-Feng, et al. Different effection of p.1125Val>Ala and rs11954856 in APC on Wnt signaling pathway. ''Oncotarget''. 2017 Sep 19; '''8''' (41):70854-70864
Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. Description: Qian, David C, et al. Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. ''BMC Genomics''. 2017 Sep 19; '''18''' (1):740
Polygenic loading for major depression is associated with specific medical comorbidity. Description: McCoy, T H, et al. Polygenic loading for major depression is associated with specific medical comorbidity. ''Transl Psychiatry''. 2017 Sep 19; '''7''' (9):e1238
Alpha TC1 and Beta-TC-6 genomic profiling uncovers both shared and distinct transcriptional regulatory features with their primary islet counterparts. Description: Lawlor, Nathan, et al. Alpha TC1 and Beta-TC-6 genomic profiling uncovers both shared and distinct transcriptional regulatory features with their primary islet counterparts. ''Sci Rep''. 2017 Sep 20; '''7''' (1):11959
Association of HLA-B and HLA-DRB1 polymorphisms with antithyroid drug-induced agranulocytosis in a Han population from northern China. Description: He, Yayi, et al. Association of HLA-B and HLA-DRB1 polymorphisms with antithyroid drug-induced agranulocytosis in a Han population from northern China. ''Sci Rep''. 2017 Sep 20; '''7''' (1):11950
Large-scale replication study identified multiple independent SNPs in RET synergistically associated with Hirschsprung disease in Southern Chinese population. Description: Zhang, Yan, et al. Large-scale replication study identified multiple independent SNPs in RET synergistically associated with Hirschsprung disease in Southern Chinese population. ''Aging (Albany NY)''. 2017 Sep 20; '''9''' (9):1996-2009
Genome-wide SNP data unveils the globalization of domesticated pigs. Description: Yang, Bin, et al. Genome-wide SNP data unveils the globalization of domesticated pigs. ''Genet Sel Evol''. 2017 Sep 21; '''49''' (1):71
Multi-breed genomic prediction using Bayes R with sequence data and dropping variants with a small effect. Description: van den Berg, Irene, et al. Multi-breed genomic prediction using Bayes R with sequence data and dropping variants with a small effect. ''Genet Sel Evol''. 2017 Sep 21; '''49''' (1):70
A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study. Description: Hauer, Allard J, et al. A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study. ''Sci Rep''. 2017 Sep 22; '''7''' (1):12175
A genome-wide association analysis identifies PDE1A\|DNAJC10 locus on chromosome 2 associated with idiopathic pulmonary arterial hypertension in a Japanese population. Description: Kimura, Mai, et al. A genome-wide association analysis identifies PDE1A\|DNAJC10 locus on chromosome 2 associated with idiopathic pulmonary arterial hypertension in a Japanese population. ''Oncotarget''. 2017 Sep 26; '''8''' (43):74917-74926
The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal. Description: Berge-Seidl, Victoria, et al. The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal. ''Neurosci Lett''. 2017 Sep 29; '''658''': 48-52
Whole genome sequencing-based association study to unravel genetic architecture of cooked grain width and length traits in rice. Description: Misra, Gopal, et al. Whole genome sequencing-based association study to unravel genetic architecture of cooked grain width and length traits in rice. ''Sci Rep''. 2017 Sep 29; '''7''' (1):12478
6q12 and 11p14 variants are associated with postnatal exhaled nitric oxide levels and respiratory symptoms. Description: Fuchs, Oliver, et al. 6q12 and 11p14 variants are associated with postnatal exhaled nitric oxide levels and respiratory symptoms. ''J Allergy Clin Immunol''. 2017 Oct; '''140''' (4):1015-1023
A multi-stage genome-wide association study of uterine fibroids in African Americans. Description: Hellwege, Jacklyn N, et al. A multi-stage genome-wide association study of uterine fibroids in African Americans. ''Hum Genet''. 2017 Oct; '''136''' (10):1363-1373
A polymorphism in the haptoglobin, haptoglobin related protein locus is associated with risk of human sleeping sickness within Cameroonian populations. Description: Ofon, Elvis, et al. A polymorphism in the haptoglobin, haptoglobin related protein locus is associated with risk of human sleeping sickness within Cameroonian populations. ''PLoS Negl Trop Dis''. 2017 Oct; '''11''' (10):e0005979
Candidate genes-based investigation of susceptibility to Human African Trypanosomiasis in Cote d'Ivoire. Description: Ahouty, Bernardin, et al. Candidate genes-based investigation of susceptibility to Human African Trypanosomiasis in Cote d'Ivoire. ''PLoS Negl Trop Dis''. 2017 Oct; '''11''' (10):e0005992
Correlation of PON1 polymorphisms with ankylosing spondylitis susceptibility: A case-control study in Chinese Han population. Description: Xu, Haitao, et al. Correlation of PON1 polymorphisms with ankylosing spondylitis susceptibility: A case-control study in Chinese Han population. ''Medicine (Baltimore)''. 2017 Oct; '''96''' (42):e7416
FKBP5 moderation of the relationship between childhood trauma and maladaptive emotion regulation strategies in adolescents. Description: Halldorsdottir, Thorhildur, et al. FKBP5 moderation of the relationship between childhood trauma and maladaptive emotion regulation strategies in adolescents. ''Psychoneuroendocrinology''. 2017 Oct; '''84''': 61-65
Genetic polymorphisms and valproic acid plasma concentration in children with epilepsy on valproic acid monotherapy. Description: Mei, Shenghui, et al. Genetic polymorphisms and valproic acid plasma concentration in children with epilepsy on valproic acid monotherapy. ''Seizure''. 2017 Oct; '''51''': 22-26
Genome-scale identification of microRNA-related SNPs associated with risk of head and neck squamous cell carcinoma. Description: Wilkins, Owen M, et al. Genome-scale identification of microRNA-related SNPs associated with risk of head and neck squamous cell carcinoma. ''Carcinogenesis''. 2017 Oct 1; '''38''' (10):986-993
Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117). Description: Clarke, T-K, et al. Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117). ''Mol Psychiatry''. 2017 Oct; '''22''' (10):1376-1384
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Description: Legge, S E, et al. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. ''Mol Psychiatry''. 2017 Oct; '''22''' (10):1502-1508
Genome-wide interaction study of dust mite allergen on lung function in children with asthma. Description: Forno, Erick, et al. Genome-wide interaction study of dust mite allergen on lung function in children with asthma. ''J Allergy Clin Immunol''. 2017 Oct; '''140''' (4):996-1003.e7
Genome-wide scan in Hispanics highlights candidate loci for brain white matter hyperintensities. Description: Beecham, Ashley, et al. Genome-wide scan in Hispanics highlights candidate loci for brain white matter hyperintensities. ''Neurol Genet''. 2017 Oct; '''3''' (5):e185
Genomic insights into adaptive divergence and speciation among malaria vectors of the Anopheles nili group. Description: Fouet, Caroline, et al. Genomic insights into adaptive divergence and speciation among malaria vectors of the Anopheles nili group. ''Evol Appl''. 2017 Oct; '''10''' (9):897-906
Hidden heritability due to heterogeneity across seven populations. Description: Tropf, Felix C, et al. Hidden heritability due to heterogeneity across seven populations. ''Nat Hum Behav''. 2017 Oct; '''1''' (10):757-765
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis. Description: Kemp, John P, et al. Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis. ''Nat Genet''. 2017 Oct; '''49''' (10):1468-1475
Identification of a single nucleotide polymorphism indicative of high risk in acute myocardial infarction. Description: Shalia, Kavita, et al. Identification of a single nucleotide polymorphism indicative of high risk in acute myocardial infarction. ''Indian J Med Res''. 2017 Oct; '''146''' (4):505-513
Meta-analysis of genome-wide SNP- and pathway-based associations for facets of neuroticism. Description: Kim, Song E, et al. Meta-analysis of genome-wide SNP- and pathway-based associations for facets of neuroticism. ''J Hum Genet''. 2017 Oct; '''62''' (10):903-909
Multimodal Neuroimaging in Schizophrenia: Description and Dissemination. Description: Aine, C J, et al. Multimodal Neuroimaging in Schizophrenia: Description and Dissemination. ''Neuroinformatics''. 2017 Oct; '''15''' (4):343-364
No rare deleterious variants from STK32B, PPARGC1A, and CTNNA3 are associated with essential tremor. Description: Houle, Gabrielle, et al. No rare deleterious variants from STK32B, PPARGC1A, and CTNNA3 are associated with essential tremor. ''Neurol Genet''. 2017 Oct; '''3''' (5):e195
Polymorphisms in DENND1B gene are associated with asthma and atopy phenotypes in Brazilian children. Description: Fiuza, Bianca S D, et al. Polymorphisms in DENND1B gene are associated with asthma and atopy phenotypes in Brazilian children. ''Mol Immunol''. 2017 Oct; '''90''': 33-41
Profiling RNA-Seq at multiple resolutions markedly increases the number of causal eQTLs in autoimmune disease. Description: Odhams, Christopher A, et al. Profiling RNA-Seq at multiple resolutions markedly increases the number of causal eQTLs in autoimmune disease. ''PLoS Genet''. 2017 Oct; '''13''' (10):e1007071
Replication and fine-mapping of genetic predictors of lipid traits in African-Americans. Description: Feng, QiPing, et al. Replication and fine-mapping of genetic predictors of lipid traits in African-Americans. ''J Hum Genet''. 2017 Oct; '''62''' (10):895-901
Risk alleles for IgA nephropathy-associated SNPs conferred completely opposite effects to idiopathic membranous nephropathy in Chinese Han. Description: Qin, Xiaosong, et al. Risk alleles for IgA nephropathy-associated SNPs conferred completely opposite effects to idiopathic membranous nephropathy in Chinese Han. ''Immunol Res''. 2017 Oct; '''65''' (5):1059-1064
Signatures of Selection and Interspecies Introgression in the Genome of Chinese Domestic Pigs. Description: Zhu, Yaling, et al. Signatures of Selection and Interspecies Introgression in the Genome of Chinese Domestic Pigs. ''Genome Biol Evol''. 2017 Oct 1; '''9''' (10):2592-2603
Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease. Description: Marigorta, Urko M, et al. Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease. ''Nat Genet''. 2017 Oct; '''49''' (10):1517-1521
A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11. Description: Bhutta, Mahmood F, et al. A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11. ''Sci Rep''. 2017 Oct 2; '''7''' (1):12496
A pathway analysis of genome-wide association study highlights novel type 2 diabetes risk pathways. Description: Liu, Yang, et al. A pathway analysis of genome-wide association study highlights novel type 2 diabetes risk pathways. ''Sci Rep''. 2017 Oct 2; '''7''' (1):12546
Associations between SNPs and immune-related circulating proteins in schizophrenia. Description: Chan, Man K, et al. Associations between SNPs and immune-related circulating proteins in schizophrenia. ''Sci Rep''. 2017 Oct 3; '''7''' (1):12586
A Comparative Analysis of Genetic Ancestry and Admixture in the Colombian Populations of Choco and Medellin. Description: Conley, Andrew B, et al. A Comparative Analysis of Genetic Ancestry and Admixture in the Colombian Populations of Choco and Medellin. ''G3 (Bethesda)''. 2017 Oct 5; '''7''' (10):3435-3447
Fine-Scale Genetic Structure in Finland. Description: Kerminen, Sini, et al. Fine-Scale Genetic Structure in Finland. ''G3 (Bethesda)''. 2017 Oct 5; '''7''' (10):3459-3468
The Contribution of Neanderthals to Phenotypic Variation in Modern Humans. Description: Dannemann, Michael, et al. The Contribution of Neanderthals to Phenotypic Variation in Modern Humans. ''Am J Hum Genet''. 2017 Oct 5; '''101''' (4):578-589
Clinical utility of the low-density Infinium QC genotyping Array in a genomics-based diagnostics laboratory. Description: Ponomarenko, Petr, et al. Clinical utility of the low-density Infinium QC genotyping Array in a genomics-based diagnostics laboratory. ''BMC Med Genomics''. 2017 Oct 6; '''10''' (1):57
Regional variation in health is predominantly driven by lifestyle rather than genetics. Description: Amador, Carmen, et al. Regional variation in health is predominantly driven by lifestyle rather than genetics. ''Nat Commun''. 2017 Oct 6; '''8''' (1):801
ADAR1 polymorphisms are related to severity of liver fibrosis in HIV/HCV-coinfected patients. Description: Medrano, Luz M, et al. ADAR1 polymorphisms are related to severity of liver fibrosis in HIV/HCV-coinfected patients. ''Sci Rep''. 2017 Oct 10; '''7''' (1):12918
A new stress sensor and risk factor for suicide: the T allele of the functional genetic variant in the GABRA6 gene. Description: Gonda, Xenia, et al. A new stress sensor and risk factor for suicide: the T allele of the functional genetic variant in the GABRA6 gene. ''Sci Rep''. 2017 Oct 10; '''7''' (1):12887
Germline mutation within COL2A1 associated with lethal chondrodysplasia in a polled Holstein family. Description: Reinartz, Sina, et al. Germline mutation within COL2A1 associated with lethal chondrodysplasia in a polled Holstein family. ''BMC Genomics''. 2017 Oct 10; '''18''' (1):762
Association of red cell distribution width with all-cause and cardiovascular-specific mortality in African American and white adults: a prospective cohort study. Description: Tajuddin, Salman M, et al. Association of red cell distribution width with all-cause and cardiovascular-specific mortality in African American and white adults: a prospective cohort study. ''J Transl Med''. 2017 Oct 13; '''15''' (1):208
CCDC88B is required for pathogenesis of inflammatory bowel disease. Description: Fodil, Nassima, et al. CCDC88B is required for pathogenesis of inflammatory bowel disease. ''Nat Commun''. 2017 Oct 13; '''8''' (1):932
Single nucleotide polymorphisms in the ETS1 gene are associated with idiopathic inflammatory myopathies in a northern Chinese Han population. Description: Chen, Si, et al. Single nucleotide polymorphisms in the ETS1 gene are associated with idiopathic inflammatory myopathies in a northern Chinese Han population. ''Sci Rep''. 2017 Oct 13; '''7''' (1):13128
Mapping eQTL by leveraging multiple tissues and DNA methylation. Description: Acharya, Chaitanya R, et al. Mapping eQTL by leveraging multiple tissues and DNA methylation. ''BMC Bioinformatics''. 2017 Oct 18; '''18''' (1):455
Genetic association study identified a 20 kb regulatory element in WLS associated with osteoporosis and bone mineral density in Han Chinese. Description: Zhang, Dangfeng, et al. Genetic association study identified a 20 kb regulatory element in WLS associated with osteoporosis and bone mineral density in Han Chinese. ''Sci Rep''. 2017 Oct 20; '''7''' (1):13668
Identification of polymorphisms in cancer patients that differentially affect survival with age. Description: Doherty, Aoife, et al. Identification of polymorphisms in cancer patients that differentially affect survival with age. ''Aging (Albany NY)''. 2017 Oct 20; '''9''' (10):2117-2136
Genetic determinants of growth hormone and GH-related phenotypes. Description: Hallengren, Erik, et al. Genetic determinants of growth hormone and GH-related phenotypes. ''BMC Genomics''. 2017 Oct 24; '''18''' (1):822
Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study. Description: Lencer, R, et al. Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study. ''Transl Psychiatry''. 2017 Oct 24; '''7''' (10):e1249
The value of blood cytokines and chemokines in assessing COPD. Description: Bradford, Eric, et al. The value of blood cytokines and chemokines in assessing COPD. ''Respir Res''. 2017 Oct 24; '''18''' (1):180
Toll-like receptor 5 gene polymorphism is associated with breast cancer susceptibility. Description: Shuang, Chen, et al. Toll-like receptor 5 gene polymorphism is associated with breast cancer susceptibility. ''Oncotarget''. 2017 Oct 24; '''8''' (51):88622-88629
Biological function integrated prediction of severe radiographic progression in rheumatoid arthritis: a nested case control study. Description: Joo, Young Bin, et al. Biological function integrated prediction of severe radiographic progression in rheumatoid arthritis: a nested case control study. ''Arthritis Res Ther''. 2017 Oct 25; '''19''' (1):244
Sex influences eQTL effects of SLE and Sjogren's syndrome-associated genetic polymorphisms. Description: Linden, Magdalena, et al. Sex influences eQTL effects of SLE and Sjogren's syndrome-associated genetic polymorphisms. ''Biol Sex Differ''. 2017 Oct 25; '''8''' (1):34
Male fertility restored by transplanting primordial germ cells into testes: a new way towards efficient transgenesis in chicken. Description: Trefil, Pavel, et al. Male fertility restored by transplanting primordial germ cells into testes: a new way towards efficient transgenesis in chicken. ''Sci Rep''. 2017 Oct 27; '''7''' (1):14246
PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies. Description: Hall, Molly A, et al. PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies. ''Nat Commun''. 2017 Oct 27; '''8''' (1):1167
Genetic associations with adverse events from anti-tumor necrosis factor therapy in inflammatory bowel disease patients. Description: Lew, Daniel, et al. Genetic associations with adverse events from anti-tumor necrosis factor therapy in inflammatory bowel disease patients. ''World J Gastroenterol''. 2017 Oct 28; '''23''' (40):7265-7273
Genome-wide analysis reveals differential selection involved with copy number variation in diverse Chinese Cattle. Description: Yang, Liu, et al. Genome-wide analysis reveals differential selection involved with copy number variation in diverse Chinese Cattle. ''Sci Rep''. 2017 Oct 30; '''7''' (1):14299
The RS4939827 polymorphism in the SMAD7 GENE and its association with Mediterranean diet in colorectal carcinogenesis. Description: Alonso-Molero, Jessica, et al. The RS4939827 polymorphism in the SMAD7 GENE and its association with Mediterranean diet in colorectal carcinogenesis. ''BMC Med Genet''. 2017 Oct 30; '''18''' (1):122
TXNDC5 is a cervical tumor susceptibility gene that stimulates cell migration, vasculogenic mimicry and angiogenesis by down-regulating SERPINF1 and TRAF1 expression. Description: Xu, Bing, et al. TXNDC5 is a cervical tumor susceptibility gene that stimulates cell migration, vasculogenic mimicry and angiogenesis by down-regulating SERPINF1 and TRAF1 expression. ''Oncotarget''. 2017 Oct 31; '''8''' (53):91009-91024
2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio. Description: Lin, Bochao Danae, et al. 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio. ''J Hum Genet''. 2017 Nov; '''62''' (11):979-988
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations. Description: Zhu, Xiaolin, et al. A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations. ''PLoS Genet''. 2017 Nov; '''13''' (11):e1007104
A Genome-Wide Association Study Identifies UTRN Gene Polymorphism for Restless Legs Syndrome in a Korean Population. Description: Cho, Chul-Hyun, et al. A Genome-Wide Association Study Identifies UTRN Gene Polymorphism for Restless Legs Syndrome in a Korean Population. ''Psychiatry Investig''. 2017 Nov; '''14''' (6):830-838
ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR. Description: Muller, Bent, et al. ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR. ''Brain Behav''. 2017 Nov; '''7''' (11):e00851
Complex genetic control of lung tumorigenesis in resistant mice strains. Description: Dassano, Alice, et al. Complex genetic control of lung tumorigenesis in resistant mice strains. ''Cancer Sci''. 2017 Nov; '''108''' (11):2281-2286
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands. Description: Jin, Sheng Chih, et al. Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands. ''Nat Genet''. 2017 Nov; '''49''' (11):1593-1601
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling. Description: Dand, Nick, et al. Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling. ''Hum Mol Genet''. 2017 Nov 1; '''26''' (21):4301-4313
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. Description: van Hulzen, Kimm J E, et al. Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. ''Biol Psychiatry''. 2017 Nov 1; '''82''' (9):634-641
Genetic variations at the human growth hormone receptor (GHR) gene locus are associated with idiopathic short stature. Description: Dias, Christel, et al. Genetic variations at the human growth hormone receptor (GHR) gene locus are associated with idiopathic short stature. ''J Cell Mol Med''. 2017 Nov; '''21''' (11):2985-2999
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Description: Hammerschlag, Anke R, et al. Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. ''Nat Genet''. 2017 Nov; '''49''' (11):1584-1592
Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys. Description: Wattacheril, Julia, et al. Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys. ''J Pediatr''. 2017 Nov; '''190''': 100-107.e2
Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans. Description: Zhong, Kaiyin, et al. Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans. ''Hum Genet''. 2017 Nov; '''136''' (11-12):1407-1417
Genomic regions controlling shape variation in the first upper molar of the house mouse. Description: Pallares, Luisa F, et al. Genomic regions controlling shape variation in the first upper molar of the house mouse. ''Elife''. 2017 Nov 1; '''6''':
Genotype-based recall to study metabolic effects of genetic variation: a pilot study of PPARG Pro12Ala carriers. Description: Kamble, Prasad G, et al. Genotype-based recall to study metabolic effects of genetic variation: a pilot study of PPARG Pro12Ala carriers. ''Ups J Med Sci''. 2017 Nov; '''122''' (4):234-242
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation. Description: Strawbridge, Rona J, et al. Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation. ''Atherosclerosis''. 2017 Nov; '''266''': 196-204
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. Description: Schormair, Barbara, et al. Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. ''Lancet Neurol''. 2017 Nov; '''16''' (11):898-907
Insights into DDT Resistance from the Drosophila melanogaster Genetic Reference Panel. Description: Schmidt, Joshua M, et al. Insights into DDT Resistance from the Drosophila melanogaster Genetic Reference Panel. ''Genetics''. 2017 Nov; '''207''' (3):1181-1193
Is there an optimum level of diversity in utilization of genetic resources? Description: Mayer, Manfred, et al. Is there an optimum level of diversity in utilization of genetic resources? ''Theor Appl Genet''. 2017 Nov; '''130''' (11):2283-2295
Japanese genome-wide association study identifies a significant colorectal cancer susceptibility locus at chromosome 10p14. Description: Takahashi, Yusuke, et al. Japanese genome-wide association study identifies a significant colorectal cancer susceptibility locus at chromosome 10p14. ''Cancer Sci''. 2017 Nov; '''108''' (11):2239-2247
Landscape genomic approach to detect selection signatures in locally adapted Brazilian swine genetic groups. Description: Cesconeto, Robson Jose, et al. Landscape genomic approach to detect selection signatures in locally adapted Brazilian swine genetic groups. ''Ecol Evol''. 2017 Nov; '''7''' (22):9544-9556
Population genomics of the eastern cottonwood (Populus deltoides). Description: Fahrenkrog, Annette M, et al. Population genomics of the eastern cottonwood (Populus deltoides). ''Ecol Evol''. 2017 Nov; '''7''' (22):9426-9440
Range-wide parallel climate-associated genomic clines in Atlantic salmon. Description: Jeffery, Nicholas W, et al. Range-wide parallel climate-associated genomic clines in Atlantic salmon. ''R Soc Open Sci''. 2017 Nov; '''4''' (11):171394
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population. Description: Ameur, Adam, et al. SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population. ''Eur J Hum Genet''. 2017 Nov; '''25''' (11):1253-1260
The role of ST2 and ST2 genetic variants in schistosomiasis. Description: Long, Xin, et al. The role of ST2 and ST2 genetic variants in schistosomiasis. ''J Allergy Clin Immunol''. 2017 Nov; '''140''' (5):1416-1422.e6
Tracing the breeding farm of domesticated pig using feature selection (Sus scrofa). Description: Kwon, Taehyung, et al. Tracing the breeding farm of domesticated pig using feature selection (Sus scrofa). ''Asian-Australas J Anim Sci''. 2017 Nov; '''30''' (11):1540-1549
Unravelling the Genetic Diversity among Cassava Bemisia tabaci Whiteflies Using NextRAD Sequencing. Description: Wosula, Everlyne N, et al. Unravelling the Genetic Diversity among Cassava Bemisia tabaci Whiteflies Using NextRAD Sequencing. ''Genome Biol Evol''. 2017 Nov 1; '''9''' (11):2958-2973
Will Big Data Close the Missing Heritability Gap? Description: Kim, Hwasoon, et al. Will Big Data Close the Missing Heritability Gap? ''Genetics''. 2017 Nov; '''207''' (3):1135-1145
Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/beta-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials. Description: Magvanjav, Oyunbileg, et al. Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/beta-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials. ''J Am Heart Assoc''. 2017 Nov 2; '''6''' (11):
Genetic dissection of Sharka disease tolerance in peach (P. persica L. Batsch). Description: Cirilli, Marco, et al. Genetic dissection of Sharka disease tolerance in peach (P. persica L. Batsch). ''BMC Plant Biol''. 2017 Nov 3; '''17''' (1):192
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux. Description: Darlow, John M, et al. Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux. ''Sci Rep''. 2017 Nov 6; '''7''' (1):14595
Genome-wide association studies and genomic prediction of breeding values for calving performance and body conformation traits in Holstein cattle. Description: Abo-Ismail, Mohammed K, et al. Genome-wide association studies and genomic prediction of breeding values for calving performance and body conformation traits in Holstein cattle. ''Genet Sel Evol''. 2017 Nov 7; '''49''' (1):82
High-resolution analysis of selection sweeps identified between fine-wool Merino and coarse-wool Churra sheep breeds. Description: Gutierrez-Gil, Beatriz, et al. High-resolution analysis of selection sweeps identified between fine-wool Merino and coarse-wool Churra sheep breeds. ''Genet Sel Evol''. 2017 Nov 7; '''49''' (1):81
Population structure and genomic inbreeding in nine Swiss dairy cattle populations. Description: Signer-Hasler, Heidi, et al. Population structure and genomic inbreeding in nine Swiss dairy cattle populations. ''Genet Sel Evol''. 2017 Nov 7; '''49''' (1):83
The effect of artificial selection on phenotypic plasticity in maize. Description: Gage, Joseph L, et al. The effect of artificial selection on phenotypic plasticity in maize. ''Nat Commun''. 2017 Nov 7; '''8''' (1):1348
Tracing the origin and evolution of supergene mimicry in butterflies. Description: Zhang, Wei, et al. Tracing the origin and evolution of supergene mimicry in butterflies. ''Nat Commun''. 2017 Nov 7; '''8''' (1):1269
A systematic survey to identify lethal recessive variation in highly managed pig populations. Description: Derks, Martijn F L, et al. A systematic survey to identify lethal recessive variation in highly managed pig populations. ''BMC Genomics''. 2017 Nov 9; '''18''' (1):858
Identification of selection signals by large-scale whole-genome resequencing of cashmere goats. Description: Li, Xiaokai, et al. Identification of selection signals by large-scale whole-genome resequencing of cashmere goats. ''Sci Rep''. 2017 Nov 9; '''7''' (1):15142
Genomic determinants of long-term cardiometabolic complications in childhood acute lymphoblastic leukemia survivors. Description: England, Jade, et al. Genomic determinants of long-term cardiometabolic complications in childhood acute lymphoblastic leukemia survivors. ''BMC Cancer''. 2017 Nov 10; '''17''' (1):751
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes. Description: Rietschel, Liz, et al. Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes. ''Sci Rep''. 2017 Nov 10; '''7''' (1):15351
Effect of two non-synonymous ecto-5'-nucleotidase variants on the genetic architecture of inosine 5'-monophosphate (IMP) and its degradation products in Japanese Black beef. Description: Uemoto, Yoshinobu, et al. Effect of two non-synonymous ecto-5'-nucleotidase variants on the genetic architecture of inosine 5'-monophosphate (IMP) and its degradation products in Japanese Black beef. ''BMC Genomics''. 2017 Nov 13; '''18''' (1):874
The interplay of demography and selection during maize domestication and expansion. Description: Wang, Li, et al. The interplay of demography and selection during maize domestication and expansion. ''Genome Biol''. 2017 Nov 13; '''18''' (1):215
A genetic variant in SLC28A3, rs56350726, is associated with progression to castration-resistant prostate cancer in a Korean population with metastatic prostate cancer. Description: Jo, Jung Ki, et al. A genetic variant in SLC28A3, rs56350726, is associated with progression to castration-resistant prostate cancer in a Korean population with metastatic prostate cancer. ''Oncotarget''. 2017 Nov 14; '''8''' (57):96893-96902
Epistasis, physical capacity-related genes and exceptional longevity: FNDC5 gene interactions with candidate genes FOXOA3 and APOE. Description: Fuku, Noriyuki, et al. Epistasis, physical capacity-related genes and exceptional longevity: FNDC5 gene interactions with candidate genes FOXOA3 and APOE. ''BMC Genomics''. 2017 Nov 14; '''18''' (Suppl 8):803
Genome-wide scan for runs of homozygosity identifies potential candidate genes associated with local adaptation in Valle del Belice sheep. Description: Mastrangelo, Salvatore, et al. Genome-wide scan for runs of homozygosity identifies potential candidate genes associated with local adaptation in Valle del Belice sheep. ''Genet Sel Evol''. 2017 Nov 14; '''49''' (1):84
Genomic Variation and Evolution of Vibrio parahaemolyticus ST36 over the Course of a Transcontinental Epidemic Expansion. Description: Martinez-Urtaza, Jaime, et al. Genomic Variation and Evolution of Vibrio parahaemolyticus ST36 over the Course of a Transcontinental Epidemic Expansion. ''MBio''. 2017 Nov 14; '''8''' (6):
The genomic landscape of Nepalese Tibeto-Burmans reveals new insights into the recent peopling of Southern Himalayas. Description: Gnecchi-Ruscone, Guido A, et al. The genomic landscape of Nepalese Tibeto-Burmans reveals new insights into the recent peopling of Southern Himalayas. ''Sci Rep''. 2017 Nov 14; '''7''' (1):15512
An exome sequencing based approach for genome-wide association studies in the dog. Description: Broeckx, Bart J G, et al. An exome sequencing based approach for genome-wide association studies in the dog. ''Sci Rep''. 2017 Nov 15; '''7''' (1):15680
An intronic single-nucleotide polymorphism (rs13217795) in FOXO3 is associated with asthma and allergic rhinitis: a case-case-control study. Description: Amarin, Justin Z, et al. An intronic single-nucleotide polymorphism (rs13217795) in FOXO3 is associated with asthma and allergic rhinitis: a case-case-control study. ''BMC Med Genet''. 2017 Nov 15; '''18''' (1):132
Genetic polymorphism related to monocyte-macrophage function is associated with graft-versus-host disease. Description: Hyvarinen, Kati, et al. Genetic polymorphism related to monocyte-macrophage function is associated with graft-versus-host disease. ''Sci Rep''. 2017 Nov 15; '''7''' (1):15666
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. Description: Schulz, Herbert, et al. Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. ''Nat Commun''. 2017 Nov 15; '''8''' (1):1511
Long-term balancing selection contributes to adaptation in Arabidopsis and its relatives. Description: Wu, Qiong, et al. Long-term balancing selection contributes to adaptation in Arabidopsis and its relatives. ''Genome Biol''. 2017 Nov 15; '''18''' (1):217
Parkinson disease polygenic risk score is associated with Parkinson disease status and age at onset but not with alpha-synuclein cerebrospinal fluid levels. Description: Ibanez, Laura, et al. Parkinson disease polygenic risk score is associated with Parkinson disease status and age at onset but not with alpha-synuclein cerebrospinal fluid levels. ''BMC Neurol''. 2017 Nov 15; '''17''' (1):198
Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. Description: Hofer, Philipp, et al. Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. ''Oncotarget''. 2017 Nov 17; '''8''' (58):98623-98634
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. Description: Pirastu, Nicola, et al. GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. ''Nat Commun''. 2017 Nov 17; '''8''' (1):1584
Regulation of gene expression and RNA editing in Drosophila adapting to divergent microclimates. Description: Yablonovitch, Arielle L, et al. Regulation of gene expression and RNA editing in Drosophila adapting to divergent microclimates. ''Nat Commun''. 2017 Nov 17; '''8''' (1):1570
Transcriptome sequencing and differential gene expression analysis of the schistosome-transmitting snail Oncomelania hupensis inhabiting hilly and marshland regions. Description: Zhao, Jin-Song, et al. Transcriptome sequencing and differential gene expression analysis of the schistosome-transmitting snail Oncomelania hupensis inhabiting hilly and marshland regions. ''Sci Rep''. 2017 Nov 17; '''7''' (1):15809
Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection. Description: Huang, Hailiang, et al. Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection. ''Sci Rep''. 2017 Nov 20; '''7''' (1):15843
Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. Description: Heckerman, David, et al. Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. ''Sci Rep''. 2017 Nov 20; '''7''' (1):15879
MAPK and ERK polymorphisms are associated with PCOS risk in Chinese women. Description: Hu, Lingmin, et al. MAPK and ERK polymorphisms are associated with PCOS risk in Chinese women. ''Oncotarget''. 2017 Nov 21; '''8''' (59):100261-100268
The peptidylglycine-alpha-amidating monooxygenase (PAM) gene rs13175330 A>G polymorphism is associated with hypertension in a Korean population. Description: Yoo, Hye Jin, et al. The peptidylglycine-alpha-amidating monooxygenase (PAM) gene rs13175330 A>G polymorphism is associated with hypertension in a Korean population. ''Hum Genomics''. 2017 Nov 21; '''11''' (1):29
Evidence of high-altitude adaptation in the glyptosternoid fish, Creteuchiloglanis macropterus from the Nujiang River obtained through transcriptome analysis. Description: Kang, Jingliang, et al. Evidence of high-altitude adaptation in the glyptosternoid fish, Creteuchiloglanis macropterus from the Nujiang River obtained through transcriptome analysis. ''BMC Evol Biol''. 2017 Nov 23; '''17''' (1):229
Genome-wide meta-analysis in Japanese populations identifies novel variants at the TMC6-TMC8 and SIX3-SIX2 loci associated with HbA1c. Description: Hachiya, Tsuyoshi, et al. Genome-wide meta-analysis in Japanese populations identifies novel variants at the TMC6-TMC8 and SIX3-SIX2 loci associated with HbA1c. ''Sci Rep''. 2017 Nov 23; '''7''' (1):16147
Genome-wide association studies of fertility and calving traits in Brown Swiss cattle using imputed whole-genome sequences. Description: Frischknecht, Mirjam, et al. Genome-wide association studies of fertility and calving traits in Brown Swiss cattle using imputed whole-genome sequences. ''BMC Genomics''. 2017 Nov 25; '''18''' (1):910
A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder. Description: Polimanti, Renato, et al. A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder. ''Genome Med''. 2017 Nov 27; '''9''' (1):99
Genetic Architecture and Candidate Genes Identified for Follicle Number in Chicken. Description: Shen, Manman, et al. Genetic Architecture and Candidate Genes Identified for Follicle Number in Chicken. ''Sci Rep''. 2017 Nov 27; '''7''' (1):16412
Evaluation of the association of UBASH3A and SYNGR1 with rheumatoid arthritis and disease activity and severity in Han Chinese. Description: Liu, Dan, et al. Evaluation of the association of UBASH3A and SYNGR1 with rheumatoid arthritis and disease activity and severity in Han Chinese. ''Oncotarget''. 2017 Nov 28; '''8''' (61):103385-103392
High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder. Description: Grunblatt, Edna, et al. High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder. ''BMC Med Genomics''. 2017 Nov 28; '''10''' (1):68
Genome diversity in the Neolithic Globular Amphorae culture and the spread of Indo-European languages. Description: Tassi, Francesca, et al. Genome diversity in the Neolithic Globular Amphorae culture and the spread of Indo-European languages. ''Proc Biol Sci''. 2017 Nov 29; '''284''' (1867):
Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience. Description: Ridge, Perry G, et al. Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience. ''Genome Med''. 2017 Nov 29; '''9''' (1):100
Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders. Description: Glessner, Joseph T, et al. Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders. ''Genome Med''. 2017 Nov 30; '''9''' (1):106
Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia. Description: Ward, Joey, et al. Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia. ''Transl Psychiatry''. 2017 Nov 30; '''7''' (11):1264
Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Description: Morey, Rajendra A, et al. Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. ''Transl Psychiatry''. 2017 Nov 30; '''7''' (11):1265
Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank. Description: Howard, David M, et al. Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank. ''Transl Psychiatry''. 2017 Nov 30; '''7''' (11):1263
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia. Description: Lowther, Chelsea, et al. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia. ''Genome Med''. 2017 Nov 30; '''9''' (1):105
A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers. Description: Meng, W, et al. A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers. ''Br J Dermatol''. 2017 Dec; '''177''' (6):1664-1670
Associations of the Intellectual Disability Gene MYT1L with Helix-Loop-Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval. Description: Kepa, Agnieszka, et al. Associations of the Intellectual Disability Gene MYT1L with Helix-Loop-Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval. ''Neuropsychopharmacology''. 2017 Dec; '''42''' (13):2516-2526
BDNF Val66Met polymorphism modulates the effect of loneliness on white matter microstructure in young adults. Description: Meng, Jie, et al. BDNF Val66Met polymorphism modulates the effect of loneliness on white matter microstructure in young adults. ''Biol Psychol''. 2017 Dec; '''130''': 41-49
CXCL9-11 polymorphisms are associated with liver fibrosis in patients with chronic hepatitis C: a cross-sectional study. Description: Jimenez-Sousa, Maria Angeles, et al. CXCL9-11 polymorphisms are associated with liver fibrosis in patients with chronic hepatitis C: a cross-sectional study. ''Clin Transl Med''. 2017 Dec; '''6''' (1):26
Genetic variants of increased waist circumference in psychosis. Description: Hukic, Dzana S, et al. Genetic variants of increased waist circumference in psychosis. ''Psychiatr Genet''. 2017 Dec; '''27''' (6):210-218
Genetic Variants of RAMP2 and CLR are Associated with Stroke. Description: Koyama, Teruhide, et al. Genetic Variants of RAMP2 and CLR are Associated with Stroke. ''J Atheroscler Thromb''. 2017 Dec 1; '''24''' (12):1267-1281
Genetic variations of NTCP are associated with susceptibility to HBV infection and related hepatocellular carcinoma. Description: Wang, Peng, et al. Genetic variations of NTCP are associated with susceptibility to HBV infection and related hepatocellular carcinoma. ''Oncotarget''. 2017 Dec 1; '''8''' (62):105407-105424
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population. Description: Salo, Perttu P, et al. Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population. ''Circ Cardiovasc Genet''. 2017 Dec; '''10''' (6):
Identification of bakanae disease resistance loci in japonica rice through genome wide association study. Description: Volante, Andrea, et al. Identification of bakanae disease resistance loci in japonica rice through genome wide association study. ''Rice (N Y)''. 2017 Dec; '''10''' (1):29
IVAG: An Integrative Visualization Application for Various Types of Genomic Data Based on R-Shiny and the Docker Platform. Description: Lee, Tae-Rim, et al. IVAG: An Integrative Visualization Application for Various Types of Genomic Data Based on R-Shiny and the Docker Platform. ''Genomics Inform''. 2017 Dec; '''15''' (4):178-182
Pharmacogenetic study of seven polymorphisms in three nicotinic acetylcholine receptor subunits in smoking-cessation therapies. Description: Pintarelli, Giulia, et al. Pharmacogenetic study of seven polymorphisms in three nicotinic acetylcholine receptor subunits in smoking-cessation therapies. ''Sci Rep''. 2017 Dec 1; '''7''' (1):16730
Screening study for genetic polymorphisms affecting pharmacokinetics of talniflumate. Description: Jin, Li Hua, et al. Screening study for genetic polymorphisms affecting pharmacokinetics of talniflumate. ''Transl Clin Pharmacol''. 2017 Dec; '''25''' (4):166-172
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Description: Ferreira, Manuel A, et al. Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. ''Nat Genet''. 2017 Dec; '''49''' (12):1752-1757
The Diversity of REcent and Ancient huMan (DREAM): A New Microarray for Genetic Anthropology and Genealogy, Forensics, and Personalized Medicine. Description: Elhaik, Eran, et al. The Diversity of REcent and Ancient huMan (DREAM): A New Microarray for Genetic Anthropology and Genealogy, Forensics, and Personalized Medicine. ''Genome Biol Evol''. 2017 Dec 1; '''9''' (12):3225-3237
The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma. Description: Capasso, Mario, et al. The functional variant rs34330 of CDKN1B is associated with risk of neuroblastoma. ''J Cell Mol Med''. 2017 Dec; '''21''' (12):3224-3230
Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. Description: Bien, Stephanie A, et al. Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. ''Diabetologia''. 2017 Dec; '''60''' (12):2384-2398
Trans-oceanic genomic divergence of Atlantic cod ecotypes is associated with large inversions. Description: Berg, P R, et al. Trans-oceanic genomic divergence of Atlantic cod ecotypes is associated with large inversions. ''Heredity (Edinb)''. 2017 Dec; '''119''' (6):418-428
Weighted likelihood inference of genomic autozygosity patterns in dense genotype data. Description: Blant, Alexandra, et al. Weighted likelihood inference of genomic autozygosity patterns in dense genotype data. ''BMC Genomics''. 2017 Dec 1; '''18''' (1):928
Heterogeneous Patterns of Genetic Diversity and Differentiation in European and Siberian Chiffchaff (Phylloscopus collybita abietinus/P. tristis). Description: Talla, Venkat, et al. Heterogeneous Patterns of Genetic Diversity and Differentiation in European and Siberian Chiffchaff (Phylloscopus collybita abietinus/P. tristis). ''G3 (Bethesda)''. 2017 Dec 4; '''7''' (12):3983-3998
Long-Term Impact of Optimum Contribution Selection Strategies on Local Livestock Breeds with Historical Introgression Using the Example of German Angler Cattle. Description: Wang, Yu, et al. Long-Term Impact of Optimum Contribution Selection Strategies on Local Livestock Breeds with Historical Introgression Using the Example of German Angler Cattle. ''G3 (Bethesda)''. 2017 Dec 4; '''7''' (12):4009-4018
Genome Sequences Reveal Cryptic Speciation in the Human Pathogen Histoplasma capsulatum. Description: Sepulveda, Victoria E, et al. Genome Sequences Reveal Cryptic Speciation in the Human Pathogen Histoplasma capsulatum. ''MBio''. 2017 Dec 5; '''8''' (6):
Mountain hare transcriptome and diagnostic markers as resources to monitor hybridization with European hares. Description: Marques, Joao P, et al. Mountain hare transcriptome and diagnostic markers as resources to monitor hybridization with European hares. ''Sci Data''. 2017 Dec 5; '''4''': 170178
Pharmacogenetics of response to neoadjuvant paclitaxel treatment for locally advanced breast cancer. Description: Perez-Ortiz, Andric C, et al. Pharmacogenetics of response to neoadjuvant paclitaxel treatment for locally advanced breast cancer. ''Oncotarget''. 2017 Dec 5; '''8''' (63):106454-106467
Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects. Description: de Jesus Ascencio-Montiel, Ivan, et al. Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects. ''Sci Rep''. 2017 Dec 6; '''7''' (1):17105
EPHA6 rs4857055 C > T polymorphism associates with hypertension through triglyceride and LDL particle size in the Korean population. Description: Kim, Minjoo, et al. EPHA6 rs4857055 C > T polymorphism associates with hypertension through triglyceride and LDL particle size in the Korean population. ''Lipids Health Dis''. 2017 Dec 6; '''16''' (1):230
Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. Description: Pilling, Luke C, et al. Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. ''Aging (Albany NY)''. 2017 Dec 6; '''9''' (12):2504-2520
Maternal variant in the upstream of FOXP3 gene on the X chromosome is associated with recurrent infertility in Japanese Black cattle. Description: Arishima, Taichi, et al. Maternal variant in the upstream of FOXP3 gene on the X chromosome is associated with recurrent infertility in Japanese Black cattle. ''BMC Genet''. 2017 Dec 6; '''18''' (1):103
A PLAG1 mutation contributed to stature recovery in modern cattle. Description: Utsunomiya, Yuri Tani, et al. A PLAG1 mutation contributed to stature recovery in modern cattle. ''Sci Rep''. 2017 Dec 7; '''7''' (1):17140
Association of ARMS2 genotype with response to anti-vascular endothelial growth factor treatment in polypoidal choroidal vasculopathy. Description: Park, Un Chul, et al. Association of ARMS2 genotype with response to anti-vascular endothelial growth factor treatment in polypoidal choroidal vasculopathy. ''BMC Ophthalmol''. 2017 Dec 7; '''17''' (1):241
Influence of genetic ancestry and socioeconomic status on type 2 diabetes in the diverse Colombian populations of Choco and Antioquia. Description: Chande, Aroon T, et al. Influence of genetic ancestry and socioeconomic status on type 2 diabetes in the diverse Colombian populations of Choco and Antioquia. ''Sci Rep''. 2017 Dec 7; '''7''' (1):17127
Dissecting the Genetic Basis of Local Adaptation in Soybean. Description: Bandillo, Nonoy B, et al. Dissecting the Genetic Basis of Local Adaptation in Soybean. ''Sci Rep''. 2017 Dec 8; '''7''' (1):17195
Lack of association between the APLNR variant rs9943582 with ischemic stroke in the Chinese Han GeneID population. Description: Wang, Pengyun, et al. Lack of association between the APLNR variant rs9943582 with ischemic stroke in the Chinese Han GeneID population. ''Oncotarget''. 2017 Dec 8; '''8''' (64):107678-107684
The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within Ireland. Description: Gilbert, Edmund, et al. The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within Ireland. ''Sci Rep''. 2017 Dec 8; '''7''' (1):17199
Rationale and design of GENEiUS: a prospective observational study on the genetic and environmental determinants of body mass index evolution in Canadian undergraduate students. Description: Morassut, Rita E, et al. Rationale and design of GENEiUS: a prospective observational study on the genetic and environmental determinants of body mass index evolution in Canadian undergraduate students. ''BMJ Open''. 2017 Dec 10; '''7''' (12):e019365
Elevated peripheral expression of neuregulin-1 (NRG1) mRNA isoforms in clozapine-treated schizophrenia patients. Description: Mostaid, Md Shaki, et al. Elevated peripheral expression of neuregulin-1 (NRG1) mRNA isoforms in clozapine-treated schizophrenia patients. ''Transl Psychiatry''. 2017 Dec 11; '''7''' (12):1280
Use and optimization of different sources of information for genomic prediction. Description: Ilska, Joanna J, et al. Use and optimization of different sources of information for genomic prediction. ''Genet Sel Evol''. 2017 Dec 11; '''49''' (1):90
Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head. Description: Qi, Yuxin, et al. Association between MMP-3 polymorphisms among Chinese patients with osteonecrosis of the femoral head. ''Oncotarget''. 2017 Dec 12; '''8''' (65):108859-108866
Identification and characterization of two functional variants in the human longevity gene FOXO3. Description: Flachsbart, Friederike, et al. Identification and characterization of two functional variants in the human longevity gene FOXO3. ''Nat Commun''. 2017 Dec 12; '''8''' (1):2063
Whole-genome sequencing for an enhanced understanding of genetic variation among South Africans. Description: Choudhury, Ananyo, et al. Whole-genome sequencing for an enhanced understanding of genetic variation among South Africans. ''Nat Commun''. 2017 Dec 12; '''8''' (1):2062
Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family. Description: Ajmal, Muhammad, et al. Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family. ''BMC Med Genet''. 2017 Dec 13; '''18''' (1):148
A functional variant in the OAS1 gene is associated with Sjogren's syndrome complicated with HBV infection. Description: Liu, Xianjun, et al. A functional variant in the OAS1 gene is associated with Sjogren's syndrome complicated with HBV infection. ''Sci Rep''. 2017 Dec 14; '''7''' (1):17571
Association of ALDH3B2 gene polymorphism and risk factors with susceptibility of esophageal squamous cell carcinoma in a Chinese population: a case-control study involving 2,358 subjects. Description: Yin, Jun, et al. Association of ALDH3B2 gene polymorphism and risk factors with susceptibility of esophageal squamous cell carcinoma in a Chinese population: a case-control study involving 2,358 subjects. ''Oncotarget''. 2017 Dec 15; '''8''' (66):110153-110165
Cancer risk susceptibility loci in a Swedish population. Description: Liu, Wen, et al. Cancer risk susceptibility loci in a Swedish population. ''Oncotarget''. 2017 Dec 15; '''8''' (66):110300-110310
DNA and RNA-sequence based GWAS highlights membrane-transport genes as key modulators of milk lactose content. Description: Lopdell, Thomas J, et al. DNA and RNA-sequence based GWAS highlights membrane-transport genes as key modulators of milk lactose content. ''BMC Genomics''. 2017 Dec 15; '''18''' (1):968
Genomic footprints of dryland stress adaptation in Egyptian fat-tail sheep and their divergence from East African and western Asia cohorts. Description: Mwacharo, Joram M, et al. Genomic footprints of dryland stress adaptation in Egyptian fat-tail sheep and their divergence from East African and western Asia cohorts. ''Sci Rep''. 2017 Dec 15; '''7''' (1):17647
Association analysis of ILVBL gene polymorphisms with aspirin-exacerbated respiratory disease in asthma. Description: Chang, Hun Soo, et al. Association analysis of ILVBL gene polymorphisms with aspirin-exacerbated respiratory disease in asthma. ''BMC Pulm Med''. 2017 Dec 16; '''17''' (1):210
Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. Description: Polushina, Tatiana, et al. Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. ''Transl Psychiatry''. 2017 Dec 18; '''7''' (12):1289
"DNA Methylation signatures in panic disorder". Description: Iurato, Stella, et al. "DNA Methylation signatures in panic disorder". ''Transl Psychiatry''. 2017 Dec 18; '''7''' (12):1287
A Genome-Wide Association Study and Complex Network Identify Four Core Hub Genes in Bipolar Disorder. Description: Xie, Zengyan, et al. A Genome-Wide Association Study and Complex Network Identify Four Core Hub Genes in Bipolar Disorder. ''Int J Mol Sci''. 2017 Dec 19; '''18''' (12):
Identification of potential genetic causal variants for rheumatoid arthritis by whole-exome sequencing. Description: Li, Ying, et al. Identification of potential genetic causal variants for rheumatoid arthritis by whole-exome sequencing. ''Oncotarget''. 2017 Dec 19; '''8''' (67):111119-111129
PDE1A polymorphism contributes to the susceptibility of nephrolithiasis. Description: Yang, Zhenxing, et al. PDE1A polymorphism contributes to the susceptibility of nephrolithiasis. ''BMC Genomics''. 2017 Dec 20; '''18''' (1):982
Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease. Description: Senhaji, Nezha, et al. Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease. ''World J Gastroenterol''. 2017 Dec 21; '''23''' (47):8300-8307
Machine learning shows association between genetic variability in PPARG and cerebral connectivity in preterm infants. Description: Krishnan, Michelle L, et al. Machine learning shows association between genetic variability in PPARG and cerebral connectivity in preterm infants. ''Proc Natl Acad Sci U S A''. 2017 Dec 26; '''114''' (52):13744-13749
Novel methods for genotype imputation to whole-genome sequence and a simple linear model to predict imputation accuracy. Description: Larmer, Steven G, et al. Novel methods for genotype imputation to whole-genome sequence and a simple linear model to predict imputation accuracy. ''BMC Genet''. 2017 Dec 27; '''18''' (1):120
Application of geographic population structure (GPS) algorithm for biogeographical analyses of populations with complex ancestries: a case study of South Asians from 1000 genomes project. Description: Das, Ranajit, et al. Application of geographic population structure (GPS) algorithm for biogeographical analyses of populations with complex ancestries: a case study of South Asians from 1000 genomes project. ''BMC Genet''. 2017 Dec 28; '''18''' (Suppl 1):109
Highly accurate sequence imputation enables precise QTL mapping in Brown Swiss cattle. Description: Frischknecht, Mirjam, et al. Highly accurate sequence imputation enables precise QTL mapping in Brown Swiss cattle. ''BMC Genomics''. 2017 Dec 29; '''18''' (1):999
Sphingolipid Metabolic Pathway Impacts Thiazide Diuretics Blood Pressure Response: Insights From Genomics, Metabolomics, and Lipidomics. Description: Shahin, Mohamed H, et al. Sphingolipid Metabolic Pathway Impacts Thiazide Diuretics Blood Pressure Response: Insights From Genomics, Metabolomics, and Lipidomics. ''J Am Heart Assoc''. 2017 Dec 29; '''7''' (1):
A CARD9 Founder Mutation Disrupts NF-kappaB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome Formation. Description: De Bruyne, Marieke, et al. A CARD9 Founder Mutation Disrupts NF-kappaB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome Formation. ''Front Immunol''. 2018; '''9''': 2366
A DRD2/ANNK1-COMT Interaction, Consisting of Functional Variants, Confers Risk of Post-traumatic Stress Disorder in Traumatized Chinese. Description: Zhang, Kunlin, et al. A DRD2/ANNK1-COMT Interaction, Consisting of Functional Variants, Confers Risk of Post-traumatic Stress Disorder in Traumatized Chinese. ''Front Psychiatry''. 2018; '''9''': 170
A genome-wide association study identifies three novel genetic markers for response to tamoxifen: A prospective multicenter study. Description: Onishi, Hiroshi, et al. A genome-wide association study identifies three novel genetic markers for response to tamoxifen: A prospective multicenter study. ''PLoS One''. 2018; '''13''' (8):e0201606
A genome-wide association study of corneal astigmatism: The CREAM Consortium. Description: Shah, Rupal L, et al. A genome-wide association study of corneal astigmatism: The CREAM Consortium. ''Mol Vis''. 2018; '''24''': 127-142
A genome-wide data assessment of the African lion (Panthera leo) population genetic structure and diversity in Tanzania. Description: Smitz, Nathalie, et al. A genome-wide data assessment of the African lion (Panthera leo) population genetic structure and diversity in Tanzania. ''PLoS One''. 2018; '''13''' (11):e0205395
A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants. Description: Nedeljkovic, Ivana, et al. A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants. ''Front Genet''. 2018; '''9''': 133
A Large Panel of Drosophila simulans Reveals an Abundance of Common Variants. Description: Signor, Sarah A, et al. A Large Panel of Drosophila simulans Reveals an Abundance of Common Variants. ''Genome Biol Evol''. 2018 Jan 1; '''10''' (1):189-206
AmpliSeq Screening of Genes Encoding the C-Type Lectin Receptors and Their Signaling Components Reveals a Common Variant in MASP1 Associated with Pulmonary Tuberculosis in an Indian Population. Description: Klassert, Tilman E, et al. AmpliSeq Screening of Genes Encoding the C-Type Lectin Receptors and Their Signaling Components Reveals a Common Variant in MASP1 Associated with Pulmonary Tuberculosis in an Indian Population. ''Front Immunol''. 2018; '''9''': 242
Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia. Description: Charles, Bashira A, et al. Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia. ''PLoS One''. 2018; '''13''' (3):e0194400
Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2. Description: Skare, Oivind, et al. Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2. ''Front Genet''. 2018; '''9''': 25
An integrated framework to identify wildlife populations under threat from climate change. Description: Razgour, Orly, et al. An integrated framework to identify wildlife populations under threat from climate change. ''Mol Ecol Resour''. 2018 Jan; '''18''' (1):18-31
An Integration of Genome-Wide Association Study and Gene Co-expression Network Analysis Identifies Candidate Genes of Stem Lodging-Related Traits in Brassica napus. Description: Li, Hongge, et al. An Integration of Genome-Wide Association Study and Gene Co-expression Network Analysis Identifies Candidate Genes of Stem Lodging-Related Traits in Brassica napus. ''Front Plant Sci''. 2018; '''9''': 796
A non-coding CRHR2 SNP rs255105, a cis-eQTL for a downstream lincRNA AC005154.6, is associated with heroin addiction. Description: Levran, Orna, et al. A non-coding CRHR2 SNP rs255105, a cis-eQTL for a downstream lincRNA AC005154.6, is associated with heroin addiction. ''PLoS One''. 2018; '''13''' (6):e0199951
A non-synonymous polymorphism in NBS1 is associated with progression from chronic hepatitis B virus infection to hepatocellular carcinoma in a Chinese population. Description: Zhen, Ya'nan, et al. A non-synonymous polymorphism in NBS1 is associated with progression from chronic hepatitis B virus infection to hepatocellular carcinoma in a Chinese population. ''Onco Targets Ther''. 2018; '''11''': 563-569
A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains. Description: Ranlund, Siri, et al. A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains. ''Am J Med Genet B Neuropsychiatr Genet''. 2018 Jan; '''177''' (1):21-34
A polymorphism in the OPRM1 3'-untranslated region is associated with methadone efficacy in treating opioid dependence. Description: Crist, R C, et al. A polymorphism in the OPRM1 3'-untranslated region is associated with methadone efficacy in treating opioid dependence. ''Pharmacogenomics J''. 2018 Jan; '''18''' (1):173-179
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Description: de Jong, Simone, et al. Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. ''Commun Biol''. 2018; '''1''': 163
A Sex-Stratified Genome-Wide Association Study of Tuberculosis Using a Multi-Ethnic Genotyping Array. Description: Schurz, Haiko, et al. A Sex-Stratified Genome-Wide Association Study of Tuberculosis Using a Multi-Ethnic Genotyping Array. ''Front Genet''. 2018; '''9''': 678
Assessing the association between hypoxia during craniofacial development and oral clefts. Description: Kuchler, Erika Calvano, et al. Assessing the association between hypoxia during craniofacial development and oral clefts. ''J Appl Oral Sci''. 2018; '''26''': e20170234
Association between diacylglycerol kinase kappa variants and hypospadias susceptibility in a Han Chinese population. Description: Xie, Hua, et al. Association between diacylglycerol kinase kappa variants and hypospadias susceptibility in a Han Chinese population. ''Asian J Androl''. 2018 Jan-Feb; '''20''' (1):85-89
Association between functional lactase variants and a high abundance of Bifidobacterium in the gut of healthy Japanese people. Description: Kato, Kumiko, et al. Association between functional lactase variants and a high abundance of Bifidobacterium in the gut of healthy Japanese people. ''PLoS One''. 2018; '''13''' (10):e0206189
Association of Copy Number Variation at Intron 3 of HMGA2 With Navel Length in Bos indicus. Description: Aguiar, Tamiris Sayuri, et al. Association of Copy Number Variation at Intron 3 of HMGA2 With Navel Length in Bos indicus. ''Front Genet''. 2018; '''9''': 627
Association of Crohn's disease-related chromosome 1q32 with ankylosing spondylitis is independent of bowel symptoms and faecal calprotectin. Description: Roberts, Rebecca L, et al. Association of Crohn's disease-related chromosome 1q32 with ankylosing spondylitis is independent of bowel symptoms and faecal calprotectin. ''PeerJ''. 2018; '''6''': e5088
Association of genetic variants in RAB23 and ANXA11 with uveitis in sarcoidosis. Description: Davoudi, Samaneh, et al. Association of genetic variants in RAB23 and ANXA11 with uveitis in sarcoidosis. ''Mol Vis''. 2018; '''24''': 59-74
Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder. Description: Amare, Azmeraw T, et al. Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder. ''Front Psychiatry''. 2018; '''9''': 65
Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry. Description: Rolfe, Sara, et al. Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry. ''Front Genet''. 2018; '''9''': 659
Associations between polygenic risk scores for four psychiatric illnesses and brain structure using multivariate pattern recognition. Description: Ranlund, Siri, et al. Associations between polygenic risk scores for four psychiatric illnesses and brain structure using multivariate pattern recognition. ''Neuroimage Clin''. 2018; '''20''': 1026-1036
Associations between single-nucleotide polymorphisms in the NTRK1 gene and basal pain sensitivity in young Han Chinese women. Description: Li, Ningbo, et al. Associations between single-nucleotide polymorphisms in the NTRK1 gene and basal pain sensitivity in young Han Chinese women. ''Neurosci Lett''. 2018 Jan 1; '''662''': 312-317
Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers. Description: Huentelman, Matthew J, et al. Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers. ''Front Aging Neurosci''. 2018; '''10''': 155
Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses. Description: Penney, Michelle E, et al. Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses. ''Biomark Res''. 2018; '''6''': 17
Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population. Description: Kobayashi, Momoko, et al. Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population. ''PLoS One''. 2018; '''13''' (1):e0190991
A TNFSF13B functional variant is not involved in systemic sclerosis and giant cell arteritis susceptibility. Description: Gonzalez-Serna, David, et al. A TNFSF13B functional variant is not involved in systemic sclerosis and giant cell arteritis susceptibility. ''PLoS One''. 2018; '''13''' (12):e0209343
Autosomal and Mitochondrial Adaptation Following Admixture: A Case Study on the Honeybees of Reunion Island. Description: Wragg, David, et al. Autosomal and Mitochondrial Adaptation Following Admixture: A Case Study on the Honeybees of Reunion Island. ''Genome Biol Evol''. 2018 Jan 1; '''10''' (1):220-238
Bowel Location Rather Than Disease Subtype Dominates Transcriptomic Heterogeneity in Pediatric IBD. Description: Venkateswaran, Suresh, et al. Bowel Location Rather Than Disease Subtype Dominates Transcriptomic Heterogeneity in Pediatric IBD. ''Cell Mol Gastroenterol Hepatol''. 2018; '''6''' (4):474-476.e3
Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes. Description: Luukkonen, Tiia Maria, et al. Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes. ''Mol Genet Genomic Med''. 2018 Jan; '''6''' (1):56-68
Cancer- and behavior-related genes are targeted by selection in the Tasmanian devil (Sarcophilus harrisii). Description: Hubert, Jean-Noel, et al. Cancer- and behavior-related genes are targeted by selection in the Tasmanian devil (Sarcophilus harrisii). ''PLoS One''. 2018; '''13''' (8):e0201838
Cerebral Artery Diameter in Inbred Mice Varies as a Function of Strain. Description: Qian, Baogang, et al. Cerebral Artery Diameter in Inbred Mice Varies as a Function of Strain. ''Front Neuroanat''. 2018; '''12''': 10
Clinical Implication and the Hereditary Factors of NM23 in Hepatocellular Carcinoma Based on Bioinformatics Analysis and Genome-Wide Association Study. Description: Yang, Chengkun, et al. Clinical Implication and the Hereditary Factors of NM23 in Hepatocellular Carcinoma Based on Bioinformatics Analysis and Genome-Wide Association Study. ''J Oncol''. 2018; '''2018''': 6594169
Combined GWAS and LDLA approaches to improve genome-wide quantitative trait loci detection affecting carcass and meat quality traits in pig. Description: Herault, Frederic, et al. Combined GWAS and LDLA approaches to improve genome-wide quantitative trait loci detection affecting carcass and meat quality traits in pig. ''Meat Sci''. 2018 Jan; '''135''': 148-158
Common Variants in PLXNA4 and Correlation to CSF-related Phenotypes in Alzheimer's Disease. Description: Han, Qiu, et al. Common Variants in PLXNA4 and Correlation to CSF-related Phenotypes in Alzheimer's Disease. ''Front Neurosci''. 2018; '''12''': 946
Comparative study for haplotype block partitioning methods - Evidence from chromosome 6 of the North American Rheumatoid Arthritis Consortium (NARAC) dataset. Description: Saad, Mohamed N, et al. Comparative study for haplotype block partitioning methods - Evidence from chromosome 6 of the North American Rheumatoid Arthritis Consortium (NARAC) dataset. ''PLoS One''. 2018; '''13''' (12):e0209603
Comparison of Genetic and Self-Identified Ancestry in Modeling Intracerebral Hemorrhage Risk. Description: Marini, Sandro, et al. Comparison of Genetic and Self-Identified Ancestry in Modeling Intracerebral Hemorrhage Risk. ''Front Neurol''. 2018; '''9''': 514
Complex patterns of direct and indirect association between the transcription Factor-7 like 2 gene, body mass index and type 2 diabetes diagnosis in adulthood in the Hispanic Community Health Study/Study of Latinos. Description: Fernandez-Rhodes, Lindsay, et al. Complex patterns of direct and indirect association between the transcription Factor-7 like 2 gene, body mass index and type 2 diabetes diagnosis in adulthood in the Hispanic Community Health Study/Study of Latinos. ''BMC Obes''. 2018; '''5''': 26
Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes. Description: Bybjerg-Grauholm, Jonas, et al. Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes. ''PLoS One''. 2018; '''13''' (12):e0208829
Contribution of Host Genetics to the Variation of Microbial Composition of Cecum Lumen and Feces in Pigs. Description: Chen, Congying, et al. Contribution of Host Genetics to the Variation of Microbial Composition of Cecum Lumen and Feces in Pigs. ''Front Microbiol''. 2018; '''9''': 2626
Decomposing Additive Genetic Variance Revealed Novel Insights into Trait Evolution in Synthetic Hexaploid Wheat. Description: Jighly, Abdulqader, et al. Decomposing Additive Genetic Variance Revealed Novel Insights into Trait Evolution in Synthetic Hexaploid Wheat. ''Front Genet''. 2018; '''9''': 27
Detection of Selection Signatures Among Brazilian, Sri Lankan, and Egyptian Chicken Populations Under Different Environmental Conditions. Description: Walugembe, Muhammed, et al. Detection of Selection Signatures Among Brazilian, Sri Lankan, and Egyptian Chicken Populations Under Different Environmental Conditions. ''Front Genet''. 2018; '''9''': 737
Detection of Selection Signatures in Chinese Landrace and Yorkshire Pigs Based on Genotyping-by-Sequencing Data. Description: Wang, Kai, et al. Detection of Selection Signatures in Chinese Landrace and Yorkshire Pigs Based on Genotyping-by-Sequencing Data. ''Front Genet''. 2018; '''9''': 119
Detection of Significant Association Between Variants in Cannabinoid Receptor 1 Gene (CNR1) and Personality in African-American Population. Description: Yao, Yinghao, et al. Detection of Significant Association Between Variants in Cannabinoid Receptor 1 Gene (CNR1) and Personality in African-American Population. ''Front Genet''. 2018; '''9''': 199
Development of Target Sequence Capture and Estimation of Genomic Relatedness in a Mixed Oak Stand. Description: Lesur, Isabelle, et al. Development of Target Sequence Capture and Estimation of Genomic Relatedness in a Mixed Oak Stand. ''Front Plant Sci''. 2018; '''9''': 996
Dietary and genetic risk scores and incidence of type 2 diabetes. Description: Ericson, Ulrika, et al. Dietary and genetic risk scores and incidence of type 2 diabetes. ''Genes Nutr''. 2018; '''13''': 13
Discovery of SNPs for individual identification by reduced representation sequencing of moose (Alces alces). Description: Blahed, Ida-Maria, et al. Discovery of SNPs for individual identification by reduced representation sequencing of moose (Alces alces). ''PLoS One''. 2018; '''13''' (5):e0197364
Dissecting the Genomic Architecture of Resistance to Eimeria maxima Parasitism in the Chicken. Description: Boulton, Kay, et al. Dissecting the Genomic Architecture of Resistance to Eimeria maxima Parasitism in the Chicken. ''Front Genet''. 2018; '''9''': 528
Diversity analysis and genome-wide association studies of grain shape and eating quality traits in rice (Oryza sativa L.) using DArT markers. Description: Mogga, Maurice, et al. Diversity analysis and genome-wide association studies of grain shape and eating quality traits in rice (Oryza sativa L.) using DArT markers. ''PLoS One''. 2018; '''13''' (6):e0198012
Diversity and Genome Analysis of Australian and Global Oilseed Brassica napus L. Germplasm Using Transcriptomics and Whole Genome Re-sequencing. Description: Malmberg, M Michelle, et al. Diversity and Genome Analysis of Australian and Global Oilseed Brassica napus L. Germplasm Using Transcriptomics and Whole Genome Re-sequencing. ''Front Plant Sci''. 2018; '''9''': 508
Elucidating biogeographical patterns in Australian native canids using genome wide SNPs. Description: Cairns, Kylie M, et al. Elucidating biogeographical patterns in Australian native canids using genome wide SNPs. ''PLoS One''. 2018; '''13''' (6):e0198754
Ensemble learning for detecting gene-gene interactions in colorectal cancer. Description: Dorani, Faramarz, et al. Ensemble learning for detecting gene-gene interactions in colorectal cancer. ''PeerJ''. 2018; '''6''': e5854
Epigenetic alterations of a novel antioxidant gene SLC22A3 predispose susceptible individuals to increased risk of esophageal cancer. Description: Xiong, Ji-Xian, et al. Epigenetic alterations of a novel antioxidant gene SLC22A3 predispose susceptible individuals to increased risk of esophageal cancer. ''Int J Biol Sci''. 2018; '''14''' (12):1658-1668
Estimating the mutational load for cardiovascular diseases in Pakistani population. Description: Shakeel, Muhammad, et al. Estimating the mutational load for cardiovascular diseases in Pakistani population. ''PLoS One''. 2018; '''13''' (2):e0192446
Estimation of linkage disequilibrium and analysis of genetic diversity in Korean chicken lines. Description: Seo, Dongwon, et al. Estimation of linkage disequilibrium and analysis of genetic diversity in Korean chicken lines. ''PLoS One''. 2018; '''13''' (2):e0192063
Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression. Description: Li, Binglan, et al. Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression. ''Pac Symp Biocomput''. 2018; '''23''': 448-459
Evidence for a second ankylosing spondylitis-associated RUNX3 regulatory polymorphism. Description: Vecellio, Matteo, et al. Evidence for a second ankylosing spondylitis-associated RUNX3 regulatory polymorphism. ''RMD Open''. 2018; '''4''' (1):e000628
Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer. Description: Traylor, Matthew, et al. Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer. ''PLoS One''. 2018; '''13''' (5):e0188911
Exome sequencing in large, multiplex bipolar disorder families from Cuba. Description: Maaser, Anna, et al. Exome sequencing in large, multiplex bipolar disorder families from Cuba. ''PLoS One''. 2018; '''13''' (10):e0205895
Exploring Genetic Associations of Alzheimer's Disease Loci With Mild Cognitive Impairment Neurocognitive Endophenotypes. Description: Espinosa, Ana, et al. Exploring Genetic Associations of Alzheimer's Disease Loci With Mild Cognitive Impairment Neurocognitive Endophenotypes. ''Front Aging Neurosci''. 2018; '''10''': 340
Exploring the Genetic Correlation Between Growth and Immunity Based on Summary Statistics of Genome-Wide Association Studies. Description: Zhang, Zhe, et al. Exploring the Genetic Correlation Between Growth and Immunity Based on Summary Statistics of Genome-Wide Association Studies. ''Front Genet''. 2018; '''9''': 393
Extended diversity analysis of cultivated grapevine Vitis vinifera with 10K genome-wide SNPs. Description: Laucou, Valerie, et al. Extended diversity analysis of cultivated grapevine Vitis vinifera with 10K genome-wide SNPs. ''PLoS One''. 2018; '''13''' (2):e0192540
Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits. Description: Wu, Baolin, et al. Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits. ''Comput Math Methods Med''. 2018; '''2018''': 2564531
Frailty Index associates with GRIN2B in two representative samples from the United States and the United Kingdom. Description: Mekli, Krisztina, et al. Frailty Index associates with GRIN2B in two representative samples from the United States and the United Kingdom. ''PLoS One''. 2018; '''13''' (11):e0207824
Functional Partitioning of Genomic Variance and Genome-Wide Association Study for Carcass Traits in Korean Hanwoo Cattle Using Imputed Sequence Level SNP Data. Description: Bhuiyan, Mohammad S A, et al. Functional Partitioning of Genomic Variance and Genome-Wide Association Study for Carcass Traits in Korean Hanwoo Cattle Using Imputed Sequence Level SNP Data. ''Front Genet''. 2018; '''9''': 217
Further evidence for the genetic association between CACNA1I and schizophrenia. Description: Xie, Yijun, et al. Further evidence for the genetic association between CACNA1I and schizophrenia. ''Hereditas''. 2018; '''155''': 16
FUT2 secretor genotype and susceptibility to infections and chronic conditions in the ALSPAC cohort. Description: Azad, Meghan B, et al. FUT2 secretor genotype and susceptibility to infections and chronic conditions in the ALSPAC cohort. ''Wellcome Open Res''. 2018; '''3''': 65
Gender-specific association of functional prodynorphin 68 bp repeats with cannabis exposure in an African American cohort. Description: Yuferov, Vadim, et al. Gender-specific association of functional prodynorphin 68 bp repeats with cannabis exposure in an African American cohort. ''Neuropsychiatr Dis Treat''. 2018; '''14''': 1025-1034
Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. Description: Andaleon, Angela, et al. Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. ''PeerJ''. 2018; '''6''': e4314
Gene expression and single nucleotide polymorphism of ATP7B are associated with platinum-based chemotherapy response in non-small cell lung cancer patients. Description: Li, Yue-Qin, et al. Gene expression and single nucleotide polymorphism of ATP7B are associated with platinum-based chemotherapy response in non-small cell lung cancer patients. ''J Cancer''. 2018; '''9''' (19):3532-3539
Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Description: Gorlova, Olga Y, et al. Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. ''PLoS One''. 2018; '''13''' (1):e0189498
Genetic analysis of impulsive personality traits: Examination of a priori candidates and genome-wide variation. Description: Gray, Joshua C, et al. Genetic analysis of impulsive personality traits: Examination of a priori candidates and genome-wide variation. ''Psychiatry Res''. 2018 Jan; '''259''': 398-404
Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism. Description: Clarke, Toni-Kim, et al. Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism. ''Wellcome Open Res''. 2018; '''3''': 11
Genetic Architecture of Feeding Behavior and Feed Efficiency in a Duroc Pig Population. Description: Ding, Rongrong, et al. Genetic Architecture of Feeding Behavior and Feed Efficiency in a Duroc Pig Population. ''Front Genet''. 2018; '''9''': 220
Genetic assessment of inbred chicken lines indicates genomic signatures of resistance to Marek's disease. Description: Xu, Lingyang, et al. Genetic assessment of inbred chicken lines indicates genomic signatures of resistance to Marek's disease. ''J Anim Sci Biotechnol''. 2018; '''9''': 65
Genetic association of -1562C>T polymorphism in the MMP9 gene with primary glaucoma in a north Indian population. Description: Thakur, Nanamika, et al. Genetic association of -1562C>T polymorphism in the MMP9 gene with primary glaucoma in a north Indian population. ''PLoS One''. 2018; '''13''' (2):e0192636
Genetic association study of dyslexia and ADHD candidate genes in a Spanish cohort: Implications of comorbid samples. Description: Sanchez-Moran, Mirian, et al. Genetic association study of dyslexia and ADHD candidate genes in a Spanish cohort: Implications of comorbid samples. ''PLoS One''. 2018; '''13''' (10):e0206431
Genetic association study of NLRP1, CARD, and CASP1 inflammasome genes with chronic Chagas cardiomyopathy among Trypanosoma cruzi seropositive patients in Bolivia. Description: Clipman, Steven J, et al. Genetic association study of NLRP1, CARD, and CASP1 inflammasome genes with chronic Chagas cardiomyopathy among Trypanosoma cruzi seropositive patients in Bolivia. ''PLoS One''. 2018; '''13''' (2):e0192378
Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients. Description: Lanata, Cristina M, et al. Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients. ''PLoS One''. 2018; '''13''' (6):e0199003
Genetic diversity and population structure of domestic and wild reindeer (Rangifer tarandus L. 1758): A novel approach using BovineHD BeadChip. Description: Kharzinova, Veronika Ruslanovna, et al. Genetic diversity and population structure of domestic and wild reindeer (Rangifer tarandus L. 1758): A novel approach using BovineHD BeadChip. ''PLoS One''. 2018; '''13''' (11):e0207944
Genetic diversity, breed composition and admixture of Kenyan domestic pigs. Description: Mujibi, Fidalis Denis, et al. Genetic diversity, breed composition and admixture of Kenyan domestic pigs. ''PLoS One''. 2018; '''13''' (1):e0190080
Genetic homogeneity of North-African goats. Description: Ouchene-Khelifi, Nadjet-Amina, et al. Genetic homogeneity of North-African goats. ''PLoS One''. 2018; '''13''' (8):e0202196
Genetic Insights Into Frailty: Association of 9p21-23 Locus With Frailty. Description: Sathyan, Sanish, et al. Genetic Insights Into Frailty: Association of 9p21-23 Locus With Frailty. ''Front Med (Lausanne)''. 2018; '''5''': 105
Genetic Landscape of Slovenians: Past Admixture and Natural Selection Pattern. Description: Maisano Delser, Pierpaolo, et al. Genetic Landscape of Slovenians: Past Admixture and Natural Selection Pattern. ''Front Genet''. 2018; '''9''': 551
Genetic Mapping of Head Size Related Traits in Common Carp (Cyprinus carpio). Description: Chen, Lin, et al. Genetic Mapping of Head Size Related Traits in Common Carp (Cyprinus carpio). ''Front Genet''. 2018; '''9''': 448
Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort. Description: Chalazan, Brandon, et al. Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort. ''PLoS One''. 2018; '''13''' (4):e0194480
Genetic Patterns of Common-Bean Seed Acquisition and Early-Stage Adoption Among Farmer Groups in Western Uganda. Description: Wilkus, Erin L, et al. Genetic Patterns of Common-Bean Seed Acquisition and Early-Stage Adoption Among Farmer Groups in Western Uganda. ''Front Plant Sci''. 2018; '''9''': 586
Genetic polymorphisms of NOS2 and predisposition to fracture non-union: A case control study based on Han Chinese population. Description: Huang, Wei, et al. Genetic polymorphisms of NOS2 and predisposition to fracture non-union: A case control study based on Han Chinese population. ''PLoS One''. 2018; '''13''' (3):e0193673
Genetic Regulation of the Thymic Stromal Lymphopoietin (TSLP)/TSLP Receptor (TSLPR) Gene Expression and Influence of Epistatic Interactions Between IL-33 and the TSLP/TSLPR Axis on Risk of Coronary Artery Disease. Description: Nie, Shao-Fang, et al. Genetic Regulation of the Thymic Stromal Lymphopoietin (TSLP)/TSLP Receptor (TSLPR) Gene Expression and Influence of Epistatic Interactions Between IL-33 and the TSLP/TSLPR Axis on Risk of Coronary Artery Disease. ''Front Immunol''. 2018; '''9''': 1775
Genetic Risk for Psychiatric Disorders and Telomere Length. Description: Palmos, Alish B, et al. Genetic Risk for Psychiatric Disorders and Telomere Length. ''Front Genet''. 2018; '''9''': 468
Genetic risk score for adult body mass index associations with childhood and adolescent weight gain in an African population. Description: Munthali, Richard J, et al. Genetic risk score for adult body mass index associations with childhood and adolescent weight gain in an African population. ''Genes Nutr''. 2018; '''13''': 24
Genetics Modulate Gray Matter Variation Beyond Disease Burden in Prodromal Huntington's Disease. Description: Liu, Jingyu, et al. Genetics Modulate Gray Matter Variation Beyond Disease Burden in Prodromal Huntington's Disease. ''Front Neurol''. 2018; '''9''': 190
Genetics of Obesity Traits: A Bivariate Genome-Wide Association Analysis. Description: Wu, Yili, et al. Genetics of Obesity Traits: A Bivariate Genome-Wide Association Analysis. ''Front Genet''. 2018; '''9''': 179
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke. Description: Cole, John W, et al. Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke. ''PLoS One''. 2018; '''13''' (11):e0206554
Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies. Description: Pande, Mala, et al. Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies. ''PLoS One''. 2018; '''13''' (4):e0196245
Genetic variants in cellular transport do not affect mesalamine response in ulcerative colitis. Description: Moran, Christopher J, et al. Genetic variants in cellular transport do not affect mesalamine response in ulcerative colitis. ''PLoS One''. 2018; '''13''' (3):e0192806
Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay. Description: Duverger, Olivier, et al. Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay. ''PLoS Genet''. 2018 Jan; '''14''' (1):e1007168
Genetic Variation in the Androgen Receptor and Measures of Plasma Testosterone Levels Suggest Androgen Dysfunction in Alzheimer's Disease. Description: Carr, Jessie S, et al. Genetic Variation in the Androgen Receptor and Measures of Plasma Testosterone Levels Suggest Androgen Dysfunction in Alzheimer's Disease. ''Front Neurosci''. 2018; '''12''': 529
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. Description: Manderstedt, Eric, et al. Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. ''PLoS One''. 2018; '''13''' (2):e0192024
Genome Sequencing of Blacklip and Greenlip Abalone for Development and Validation of a SNP Based Genotyping Tool. Description: Kijas, James, et al. Genome Sequencing of Blacklip and Greenlip Abalone for Development and Validation of a SNP Based Genotyping Tool. ''Front Genet''. 2018; '''9''': 687
Genome-Wide Association Analyses Highlight the Potential for Different Genetic Mechanisms for Litter Size Among Sheep Breeds. Description: Xu, Song-Song, et al. Genome-Wide Association Analyses Highlight the Potential for Different Genetic Mechanisms for Litter Size Among Sheep Breeds. ''Front Genet''. 2018; '''9''': 118
Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations. Description: Lee, Jeonghwan, et al. Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations. ''PLoS One''. 2018; '''13''' (3):e0194044
Genome-Wide Association Analysis of Age-Dependent Egg Weights in Chickens. Description: Liu, Zhuang, et al. Genome-Wide Association Analysis of Age-Dependent Egg Weights in Chickens. ''Front Genet''. 2018; '''9''': 128
Genome Wide Association Mapping of Grain and Straw Biomass Traits in the Rice Bengal and Assam Aus Panel (BAAP) Grown Under Alternate Wetting and Drying and Permanently Flooded Irrigation. Description: Norton, Gareth J, et al. Genome Wide Association Mapping of Grain and Straw Biomass Traits in the Rice Bengal and Assam Aus Panel (BAAP) Grown Under Alternate Wetting and Drying and Permanently Flooded Irrigation. ''Front Plant Sci''. 2018; '''9''': 1223
Genome-wide association studies and meta-analysis uncovers new candidate genes for growth and carcass traits in pigs. Description: Blaj, Iulia, et al. Genome-wide association studies and meta-analysis uncovers new candidate genes for growth and carcass traits in pigs. ''PLoS One''. 2018; '''13''' (10):e0205576
Genome-Wide Association Studies for Dynamic Plant Height and Number of Nodes on the Main Stem in Summer Sowing Soybeans. Description: Chang, Fangguo, et al. Genome-Wide Association Studies for Dynamic Plant Height and Number of Nodes on the Main Stem in Summer Sowing Soybeans. ''Front Plant Sci''. 2018; '''9''': 1184
Genome-Wide Association Studies Identify Candidate Genes for Coat Color and Mohair Traits in the Iranian Markhoz Goat. Description: Nazari-Ghadikolaei, Anahit, et al. Genome-Wide Association Studies Identify Candidate Genes for Coat Color and Mohair Traits in the Iranian Markhoz Goat. ''Front Genet''. 2018; '''9''': 105
Genome-Wide Association Studies of 11 Agronomic Traits in Cassava (Manihot esculenta Crantz). Description: Zhang, Shengkui, et al. Genome-Wide Association Studies of 11 Agronomic Traits in Cassava (Manihot esculenta Crantz). ''Front Plant Sci''. 2018; '''9''': 503
Genome-wide association studies of inflammatory bowel disease in German shepherd dogs. Description: Peiravan, Atiyeh, et al. Genome-wide association studies of inflammatory bowel disease in German shepherd dogs. ''PLoS One''. 2018; '''13''' (7):e0200685
Genome-Wide Association Studies Reveal Genetic Variation and Candidate Genes of Drought Stress Related Traits in Cotton (Gossypium hirsutum L.). Description: Hou, Sen, et al. Genome-Wide Association Studies Reveal Genetic Variation and Candidate Genes of Drought Stress Related Traits in Cotton (Gossypium hirsutum L.). ''Front Plant Sci''. 2018; '''9''': 1276
Genome-Wide Association Study for Susceptibility to and Recoverability From Mastitis in Danish Holstein Cows. Description: Welderufael, B G, et al. Genome-Wide Association Study for Susceptibility to and Recoverability From Mastitis in Danish Holstein Cows. ''Front Genet''. 2018; '''9''': 141
Genome-wide association study identifies pharmacogenomic loci linked with specific antihypertensive drug treatment and new-onset diabetes. Description: Chang, S-W, et al. Genome-wide association study identifies pharmacogenomic loci linked with specific antihypertensive drug treatment and new-onset diabetes. ''Pharmacogenomics J''. 2018 Jan; '''18''' (1):106-112
Genome-Wide Association Study in Vestibular Neuritis: Involvement of the Host Factor for HSV-1 Replication. Description: Rujescu, Dan, et al. Genome-Wide Association Study in Vestibular Neuritis: Involvement of the Host Factor for HSV-1 Replication. ''Front Neurol''. 2018; '''9''': 591
Genome-wide association study of developmental dysplasia of the hip identifies an association with GDF5. Description: Hatzikotoulas, Konstantinos, et al. Genome-wide association study of developmental dysplasia of the hip identifies an association with GDF5. ''Commun Biol''. 2018; '''1''': 56
Genome-Wide Association Study of Serum 25-Hydroxyvitamin D in US Women. Description: O'Brien, Katie M, et al. Genome-Wide Association Study of Serum 25-Hydroxyvitamin D in US Women. ''Front Genet''. 2018; '''9''': 67
Genome-wide association study of telomere length among South Asians identifies a second RTEL1 association signal. Description: Delgado, Dayana A, et al. Genome-wide association study of telomere length among South Asians identifies a second RTEL1 association signal. ''J Med Genet''. 2018 Jan; '''55''' (1):64-71
Genome-wide association study provides insights into genes related with horn development in Nelore beef cattle. Description: Stafuzza, Nedenia Bonvino, et al. Genome-wide association study provides insights into genes related with horn development in Nelore beef cattle. ''PLoS One''. 2018; '''13''' (8):e0202978
Genome-wide association study using haplotype alleles for the evaluation of reproductive traits in Nelore cattle. Description: Nascimento, Andre Vieira do, et al. Genome-wide association study using haplotype alleles for the evaluation of reproductive traits in Nelore cattle. ''PLoS One''. 2018; '''13''' (8):e0201876
Genome-Wide Characterization of Selection Signatures and Runs of Homozygosity in Ugandan Goat Breeds. Description: Onzima, Robert B, et al. Genome-Wide Characterization of Selection Signatures and Runs of Homozygosity in Ugandan Goat Breeds. ''Front Genet''. 2018; '''9''': 318
Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. Description: Arnau-Soler, Aleix, et al. Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. ''PLoS One''. 2018; '''13''' (12):e0209160
Genome-wide linkage scan for loci influencing plasma triglyceride levels. Description: Peralta, Juan M, et al. Genome-wide linkage scan for loci influencing plasma triglyceride levels. ''BMC Proc''. 2018; '''12''' (Suppl 9):52
Genome-Wide Signatures of Selection Reveal Genes Associated With Performance in American Quarter Horse Subpopulations. Description: Avila, Felipe, et al. Genome-Wide Signatures of Selection Reveal Genes Associated With Performance in American Quarter Horse Subpopulations. ''Front Genet''. 2018; '''9''': 249
Genome-Wide SNP Data Revealed the Extent of Linkage Disequilibrium, Persistence of Phase and Effective Population Size in Purebred and Crossbred Buffalo Populations. Description: Deng, Tingxian, et al. Genome-Wide SNP Data Revealed the Extent of Linkage Disequilibrium, Persistence of Phase and Effective Population Size in Purebred and Crossbred Buffalo Populations. ''Front Genet''. 2018; '''9''': 688
Genome-Wide Variation, Candidate Regions and Genes Associated With Fat Deposition and Tail Morphology in Ethiopian Indigenous Sheep. Description: Ahbara, Abulgasim, et al. Genome-Wide Variation, Candidate Regions and Genes Associated With Fat Deposition and Tail Morphology in Ethiopian Indigenous Sheep. ''Front Genet''. 2018; '''9''': 699
Genomic analysis of morphometric traits in bighorn sheep using the Ovine Infinium((R)) HD SNP BeadChip. Description: Miller, Joshua M, et al. Genomic analysis of morphometric traits in bighorn sheep using the Ovine Infinium((R)) HD SNP BeadChip. ''PeerJ''. 2018; '''6''': e4364
Genomic Characterisation of the Indigenous Irish Kerry Cattle Breed. Description: Browett, Sam, et al. Genomic Characterisation of the Indigenous Irish Kerry Cattle Breed. ''Front Genet''. 2018; '''9''': 51
Genomic characterization of the Braque Francais type Pyrenees dog and relationship with other breeds. Description: Mastrangelo, Salvatore, et al. Genomic characterization of the Braque Francais type Pyrenees dog and relationship with other breeds. ''PLoS One''. 2018; '''13''' (12):e0208548
Genomic signatures of different adaptations to environmental stimuli between wild and cultivated Vitis vinifera L. Description: Marrano, Annarita, et al. Genomic signatures of different adaptations to environmental stimuli between wild and cultivated Vitis vinifera L. ''Hortic Res''. 2018; '''5''': 34
Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China. Description: Zhuang, Wenjuan, et al. Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China. ''PLoS One''. 2018; '''13''' (11):e0206935
Genotypic and phenotypic evaluation of off-type grasses in hybrid Bermudagrass [Cynodon dactylon (L.) Pers. x C. transvaalensis Burtt-Davy] putting greens using genotyping-by-sequencing and morphological characterization. Description: Reasor, Eric H, et al. Genotypic and phenotypic evaluation of off-type grasses in hybrid Bermudagrass [Cynodon dactylon (L.) Pers. x C. transvaalensis Burtt-Davy] putting greens using genotyping-by-sequencing and morphological characterization. ''Hereditas''. 2018; '''155''': 8
Genotyping-by-sequencing identifies date palm clone preference in agronomics of the State of Qatar. Description: Thareja, Gaurav, et al. Genotyping-by-sequencing identifies date palm clone preference in agronomics of the State of Qatar. ''PLoS One''. 2018; '''13''' (12):e0207299
Genotyping-by-sequencing of Brassica oleracea vegetables reveals unique phylogenetic patterns, population structure and domestication footprints. Description: Stansell, Zachary, et al. Genotyping-by-sequencing of Brassica oleracea vegetables reveals unique phylogenetic patterns, population structure and domestication footprints. ''Hortic Res''. 2018; '''5''': 38
Global analysis of A-to-I RNA editing reveals association with common disease variants. Description: Franzen, Oscar, et al. Global analysis of A-to-I RNA editing reveals association with common disease variants. ''PeerJ''. 2018; '''6''': e4466
Haplotype-based genome-wide association study identifies loci and candidate genes for milk yield in Holsteins. Description: Chen, Zhenliang, et al. Haplotype-based genome-wide association study identifies loci and candidate genes for milk yield in Holsteins. ''PLoS One''. 2018; '''13''' (2):e0192695
Haplotypic and Genotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Polymorphisms and Treatment Resistance in Schizophrenia. Description: Sagud, Marina, et al. Haplotypic and Genotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Polymorphisms and Treatment Resistance in Schizophrenia. ''Front Pharmacol''. 2018; '''9''': 705
Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships. Description: Blackburn, Nicholas B, et al. Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships. ''BMC Proc''. 2018; '''12''' (Suppl 9):34
HLA Pharmacogenetic Markers of Drug Hypersensitivity in a Thai Population. Description: Nakkam, Nontaya, et al. HLA Pharmacogenetic Markers of Drug Hypersensitivity in a Thai Population. ''Front Genet''. 2018; '''9''': 277
Human Genetic Susceptibility to Native Valve Staphylococcus aureus Endocarditis in Patients With S. aureus Bacteremia: Genome-Wide Association Study. Description: Moreau, Karen, et al. Human Genetic Susceptibility to Native Valve Staphylococcus aureus Endocarditis in Patients With S. aureus Bacteremia: Genome-Wide Association Study. ''Front Microbiol''. 2018; '''9''': 640
Identification of novel susceptibility loci associated with hepatitis B surface antigen seroclearance in chronic hepatitis B. Description: Kim, Tae Hyung, et al. Identification of novel susceptibility loci associated with hepatitis B surface antigen seroclearance in chronic hepatitis B. ''PLoS One''. 2018; '''13''' (7):e0199094
Identifying artificial selection signals in the chicken genome. Description: Ma, Yunlong, et al. Identifying artificial selection signals in the chicken genome. ''PLoS One''. 2018; '''13''' (4):e0196215
Identity-by-descent refines mapping of candidate regions for preaxial polydactyly II /III in a large Chinese pedigree. Description: Yang, Xingyan, et al. Identity-by-descent refines mapping of candidate regions for preaxial polydactyly II /III in a large Chinese pedigree. ''Hereditas''. 2018; '''155''': 2
IGF1 Gene Is Associated With Triglyceride Levels In Subjects With Family History Of Hypertension From The SAPPHIRe And TWB Projects. Description: Wang, Wen-Chang, et al. IGF1 Gene Is Associated With Triglyceride Levels In Subjects With Family History Of Hypertension From The SAPPHIRe And TWB Projects. ''Int J Med Sci''. 2018; '''15''' (10):1035-1042
Importance of human demographic history knowledge in genetic studies involving multi-ethnic cohorts. Description: Kulohoma, Benard W. Importance of human demographic history knowledge in genetic studies involving multi-ethnic cohorts. ''Wellcome Open Res''. 2018; '''3''': 82
Imputation-Based Whole-Genome Sequence Association Study Reveals Constant and Novel Loci for Hematological Traits in a Large-Scale Swine F2 Resource Population. Description: Yan, Guorong, et al. Imputation-Based Whole-Genome Sequence Association Study Reveals Constant and Novel Loci for Hematological Traits in a Large-Scale Swine F2 Resource Population. ''Front Genet''. 2018; '''9''': 401
Inbreeding estimates in human populations: Applying new approaches to an admixed Brazilian isolate. Description: Lemes, Renan B, et al. Inbreeding estimates in human populations: Applying new approaches to an admixed Brazilian isolate. ''PLoS One''. 2018; '''13''' (4):e0196360
Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models. Description: Momen, Mehdi, et al. Including Phenotypic Causal Networks in Genome-Wide Association Studies Using Mixed Effects Structural Equation Models. ''Front Genet''. 2018; '''9''': 455
Incomplete lineage sorting rather than hybridization explains the inconsistent phylogeny of the wisent. Description: Wang, Kun, et al. Incomplete lineage sorting rather than hybridization explains the inconsistent phylogeny of the wisent. ''Commun Biol''. 2018; '''1''': 169
Influence of CRHR1 Polymorphisms and Childhood Abuse on Suicide Attempts in Affective Disorders: A GxE Approach. Description: Ludwig, Birgit, et al. Influence of CRHR1 Polymorphisms and Childhood Abuse on Suicide Attempts in Affective Disorders: A GxE Approach. ''Front Psychiatry''. 2018; '''9''': 165
Influence of Fetal and Maternal Genetic Susceptibility to Obesity on Birthweight in African Ancestry Populations. Description: Shrestha, Deepika, et al. Influence of Fetal and Maternal Genetic Susceptibility to Obesity on Birthweight in African Ancestry Populations. ''Front Genet''. 2018; '''9''': 511
Insular Celtic population structure and genomic footprints of migration. Description: Byrne, Ross P, et al. Insular Celtic population structure and genomic footprints of migration. ''PLoS Genet''. 2018 Jan; '''14''' (1):e1007152
Integration of "omics" Data and Phenotypic Data Within a Unified Extensible Multimodal Framework. Description: Das, Samir, et al. Integration of "omics" Data and Phenotypic Data Within a Unified Extensible Multimodal Framework. ''Front Neuroinform''. 2018; '''12''': 91
Intensive Glucose Control Reduces the Risk Effect of TRIB3, SMARCD3, and ATF6 Genetic Variation on Diabetic Vascular Complications. Description: He, Fazhong, et al. Intensive Glucose Control Reduces the Risk Effect of TRIB3, SMARCD3, and ATF6 Genetic Variation on Diabetic Vascular Complications. ''Front Pharmacol''. 2018; '''9''': 1422
Interaction of childhood urbanicity and variation in dopamine genes alters adult prefrontal function as measured by functional magnetic resonance imaging (fMRI). Description: Reed, Jessica L, et al. Interaction of childhood urbanicity and variation in dopamine genes alters adult prefrontal function as measured by functional magnetic resonance imaging (fMRI). ''PLoS One''. 2018; '''13''' (4):e0195189
Joint Genomic Prediction of Canine Hip Dysplasia in UK and US Labrador Retrievers. Description: Edwards, Stefan M, et al. Joint Genomic Prediction of Canine Hip Dysplasia in UK and US Labrador Retrievers. ''Front Genet''. 2018; '''9''': 101
Jointly Modelling Single Nucleotide Polymorphisms With Longitudinal and Time-to-Event Trait: An Application to Type 2 Diabetes and Fasting Plasma Glucose. Description: Canouil, Mickael, et al. Jointly Modelling Single Nucleotide Polymorphisms With Longitudinal and Time-to-Event Trait: An Application to Type 2 Diabetes and Fasting Plasma Glucose. ''Front Genet''. 2018; '''9''': 210
Leveraging putative enhancer-promoter interactions to investigate two-way epistasis in Type 2 Diabetes GWAS. Description: Manduchi, Elisabetta, et al. Leveraging putative enhancer-promoter interactions to investigate two-way epistasis in Type 2 Diabetes GWAS. ''Pac Symp Biocomput''. 2018; '''23''': 548-558
Mapping genetic variants for cranial vault shape in humans. Description: Roosenboom, Jasmien, et al. Mapping genetic variants for cranial vault shape in humans. ''PLoS One''. 2018; '''13''' (4):e0196148
Maternal human telomerase reverse transcriptase variants are associated with preterm labor and preterm premature rupture of membranes. Description: Marrs, Caroline, et al. Maternal human telomerase reverse transcriptase variants are associated with preterm labor and preterm premature rupture of membranes. ''PLoS One''. 2018; '''13''' (5):e0195963
Meta-Analysis of Genome-Wide Association Studies Identifies Novel Functional CpG-SNPs Associated with Bone Mineral Density at Lumbar Spine. Description: Qiu, Chuan, et al. Meta-Analysis of Genome-Wide Association Studies Identifies Novel Functional CpG-SNPs Associated with Bone Mineral Density at Lumbar Spine. ''Int J Genomics''. 2018; '''2018''': 6407257
Migration-Selection Balance Drives Genetic Differentiation in Genes Associated with High-Altitude Function in the Speckled Teal (Anas flavirostris) in the Andes. Description: Graham, Allie M, et al. Migration-Selection Balance Drives Genetic Differentiation in Genes Associated with High-Altitude Function in the Speckled Teal (Anas flavirostris) in the Andes. ''Genome Biol Evol''. 2018 Jan 1; '''10''' (1):14-32
Milk Composition for Admixed Dairy Cattle in Tanzania. Description: Cheruiyot, Evans K, et al. Milk Composition for Admixed Dairy Cattle in Tanzania. ''Front Genet''. 2018; '''9''': 142
MS4A2-rs573790 Is Associated With Aspirin-Exacerbated Respiratory Disease: Replicative Study Using a Candidate Gene Strategy. Description: Pavon-Romero, Gandhi F, et al. MS4A2-rs573790 Is Associated With Aspirin-Exacerbated Respiratory Disease: Replicative Study Using a Candidate Gene Strategy. ''Front Genet''. 2018; '''9''': 363
Multi-omic Directed Networks Describe Features of Gene Regulation in Aged Brains and Expand the Set of Genes Driving Cognitive Decline. Description: Tasaki, Shinya, et al. Multi-omic Directed Networks Describe Features of Gene Regulation in Aged Brains and Expand the Set of Genes Driving Cognitive Decline. ''Front Genet''. 2018; '''9''': 294
Multiple genomic regions influence root morphology and seedling growth in cultivated sunflower (Helianthus annuus L.) under well-watered and water-limited conditions. Description: Masalia, Rishi R, et al. Multiple genomic regions influence root morphology and seedling growth in cultivated sunflower (Helianthus annuus L.) under well-watered and water-limited conditions. ''PLoS One''. 2018; '''13''' (9):e0204279
Myopia in Chinese families shows linkage to 10q26.13. Description: Musolf, Anthony M, et al. Myopia in Chinese families shows linkage to 10q26.13. ''Mol Vis''. 2018; '''24''': 29-42
No association between IFNL3 (IL28B) genotype and response to peginterferon alfa-2a in HBeAg-positive or -negative chronic hepatitis B. Description: Wei, Lai, et al. No association between IFNL3 (IL28B) genotype and response to peginterferon alfa-2a in HBeAg-positive or -negative chronic hepatitis B. ''PLoS One''. 2018; '''13''' (7):e0199198
Non-classical human leucocyte antigens in ankylosing spondylitis: possible association with HLA-E and HLA-F. Description: Santos, Margarida Rodrigues, et al. Non-classical human leucocyte antigens in ankylosing spondylitis: possible association with HLA-E and HLA-F. ''RMD Open''. 2018; '''4''' (1):e000677
Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania. Description: Ravenhall, Matt, et al. Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania. ''PLoS Genet''. 2018 Jan; '''14''' (1):e1007172
Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort. Description: Baronas, Karolis, et al. Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort. ''Acta Med Litu''. 2018; '''25''' (1):7-13
Novel polymorphisms in TICAM2 and NOD1 associated with tuberculosis progression phenotypes in Ethiopian populations. Description: Mekonnen, E, et al. Novel polymorphisms in TICAM2 and NOD1 associated with tuberculosis progression phenotypes in Ethiopian populations. ''Glob Health Epidemiol Genom''. 2018; '''3''': e1
Out in the Cold: Identification of Genomic Regions Associated With Cold Tolerance in the Biocontrol Fungus Clonostachys rosea Through Genome-Wide Association Mapping. Description: Broberg, Martin, et al. Out in the Cold: Identification of Genomic Regions Associated With Cold Tolerance in the Biocontrol Fungus Clonostachys rosea Through Genome-Wide Association Mapping. ''Front Microbiol''. 2018; '''9''': 2844
Pathway-Based Analysis of Genome-Wide Association Data Identified SNPs in HMMR as Biomarker for Chemotherapy- Induced Neutropenia in Breast Cancer Patients. Description: Bidadi, Behzad, et al. Pathway-Based Analysis of Genome-Wide Association Data Identified SNPs in HMMR as Biomarker for Chemotherapy- Induced Neutropenia in Breast Cancer Patients. ''Front Pharmacol''. 2018; '''9''': 158
Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations. Description: Jmel, Haifa, et al. Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations. ''PLoS One''. 2018; '''13''' (4):e0194842
Pharmacogenetic variation influences sensory neuropathy occurrence in Southern Africans treated with stavudine-containing antiretroviral therapy. Description: Moketla, Marvin Blessings, et al. Pharmacogenetic variation influences sensory neuropathy occurrence in Southern Africans treated with stavudine-containing antiretroviral therapy. ''PLoS One''. 2018; '''13''' (10):e0204111
Pigmentation phototype and prostate and breast cancer in a select Spanish population-A Mendelian randomization analysis in the MCC-Spain study. Description: Gomez-Acebo, Ines, et al. Pigmentation phototype and prostate and breast cancer in a select Spanish population-A Mendelian randomization analysis in the MCC-Spain study. ''PLoS One''. 2018; '''13''' (8):e0201750
Polygenic Basis and Variable Genetic Architectures Contribute to the Complex Nature of Body Weight -A Genome-Wide Study in Four Chinese Indigenous Chicken Breeds. Description: Yuan, Yangyang, et al. Polygenic Basis and Variable Genetic Architectures Contribute to the Complex Nature of Body Weight -A Genome-Wide Study in Four Chinese Indigenous Chicken Breeds. ''Front Genet''. 2018; '''9''': 229
Polygenic risk scores for major depressive disorder and neuroticism as predictors of antidepressant response: Meta-analysis of three treatment cohorts. Description: Ward, Joey, et al. Polygenic risk scores for major depressive disorder and neuroticism as predictors of antidepressant response: Meta-analysis of three treatment cohorts. ''PLoS One''. 2018; '''13''' (9):e0203896
Polymorphism in schizophrenia risk gene MIR137 is associated with the posterior cingulate Cortex's activation and functional and structural connectivity in healthy controls. Description: Zhang, Zhifang, et al. Polymorphism in schizophrenia risk gene MIR137 is associated with the posterior cingulate Cortex's activation and functional and structural connectivity in healthy controls. ''Neuroimage Clin''. 2018; '''19''': 160-166
Population genetic analysis of aquaculture salmonid populations in China using a 57K rainbow trout SNP array. Description: Zhang, Han-Yuan, et al. Population genetic analysis of aquaculture salmonid populations in China using a 57K rainbow trout SNP array. ''PLoS One''. 2018; '''13''' (8):e0202582
Population genomics of Mesolithic Scandinavia: Investigating early postglacial migration routes and high-latitude adaptation. Description: Gunther, Torsten, et al. Population genomics of Mesolithic Scandinavia: Investigating early postglacial migration routes and high-latitude adaptation. ''PLoS Biol''. 2018 Jan; '''16''' (1):e2003703
Population Genomic Structure and Genome-Wide Linkage Disequilibrium in Farmed Atlantic Salmon (Salmo salar L.) Using Dense SNP Genotypes. Description: Barria, Agustin, et al. Population Genomic Structure and Genome-Wide Linkage Disequilibrium in Farmed Atlantic Salmon (Salmo salar L.) Using Dense SNP Genotypes. ''Front Genet''. 2018; '''9''': 649
Population structure in Argentina. Description: Muzzio, Marina, et al. Population structure in Argentina. ''PLoS One''. 2018; '''13''' (5):e0196325
Population structure, relatedness and ploidy levels in an apple gene bank revealed through genotyping-by-sequencing. Description: Larsen, Bjarne, et al. Population structure, relatedness and ploidy levels in an apple gene bank revealed through genotyping-by-sequencing. ''PLoS One''. 2018; '''13''' (8):e0201889
Prediction model for pancreatic cancer risk in the general Japanese population. Description: Nakatochi, Masahiro, et al. Prediction model for pancreatic cancer risk in the general Japanese population. ''PLoS One''. 2018; '''13''' (9):e0203386
Prediction of Cacao (Theobroma cacao) Resistance to Moniliophthora spp. Diseases via Genome-Wide Association Analysis and Genomic Selection. Description: McElroy, Michel S, et al. Prediction of Cacao (Theobroma cacao) Resistance to Moniliophthora spp. Diseases via Genome-Wide Association Analysis and Genomic Selection. ''Front Plant Sci''. 2018; '''9''': 343
Prevalence Rates of ADIPOQ Polymorphisms in Indian Population and a Comparison with Other Populations. Description: Pemmasani, Sandhya Kiran, et al. Prevalence Rates of ADIPOQ Polymorphisms in Indian Population and a Comparison with Other Populations. ''Indian J Endocrinol Metab''. 2018 Jan-Feb; '''22''' (1):36-40
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Description: Turcot, Valerie, et al. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. ''Nat Genet''. 2018 Jan; '''50''' (1):26-41
Race/ethnicity difference in the pharmacogenetics of bilirubin-related atazanavir discontinuation. Description: Leger, Paul, et al. Race/ethnicity difference in the pharmacogenetics of bilirubin-related atazanavir discontinuation. ''Pharmacogenet Genomics''. 2018 Jan; '''28''' (1):1-6
Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder. Description: Fan, Yanjie, et al. Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder. ''Front Genet''. 2018; '''9''': 665
Rare gene deletions in genetic generalized and Rolandic epilepsies. Description: Jabbari, Kamel, et al. Rare gene deletions in genetic generalized and Rolandic epilepsies. ''PLoS One''. 2018; '''13''' (8):e0202022
Real-life helping behaviours in North America: A genome-wide association approach. Description: Primes, Georg, et al. Real-life helping behaviours in North America: A genome-wide association approach. ''PLoS One''. 2018; '''13''' (1):e0190950
Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population. Description: Jiao, Xiang, et al. Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population. ''PLoS One''. 2018; '''13''' (3):e0193547
Retrospective Evaluation of Marker-Assisted Selection for Resistance to Bacterial Cold Water Disease in Three Generations of a Commercial Rainbow Trout Breeding Population. Description: Liu, Sixin, et al. Retrospective Evaluation of Marker-Assisted Selection for Resistance to Bacterial Cold Water Disease in Three Generations of a Commercial Rainbow Trout Breeding Population. ''Front Genet''. 2018; '''9''': 286
Revealing the impact of the Caucasus region on the genetic legacy of Romani people from genome-wide data. Description: Banfai, Zsolt, et al. Revealing the impact of the Caucasus region on the genetic legacy of Romani people from genome-wide data. ''PLoS One''. 2018; '''13''' (9):e0202890
Runs of homozygosity associate with decreased risks of lung cancer in never-smoking East Asian females. Description: Chen, Yi-Xiao, et al. Runs of homozygosity associate with decreased risks of lung cancer in never-smoking East Asian females. ''J Cancer''. 2018; '''9''' (21):3858-3866
SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes. Description: Hariprakash, Judith Mary, et al. SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes. ''Database (Oxford)''. 2018 Jan 1; '''2018''': 1-10
Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease. Description: Hagen, Christian M, et al. Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease. ''PLoS One''. 2018; '''13''' (12):e0208828
Screening and verification of genes associated with leaf angle and leaf orientation value in inbred maize lines. Description: Lu, Shi, et al. Screening and verification of genes associated with leaf angle and leaf orientation value in inbred maize lines. ''PLoS One''. 2018; '''13''' (12):e0208386
Shared Biological Pathways Between Alzheimer's Disease and Ischemic Stroke. Description: Cui, Pan, et al. Shared Biological Pathways Between Alzheimer's Disease and Ischemic Stroke. ''Front Neurosci''. 2018; '''12''': 605
Sickening or Healing the Heart? The Association of Ficolin-1 and Rheumatic Fever. Description: Catarino, Sandra Jeremias, et al. Sickening or Healing the Heart? The Association of Ficolin-1 and Rheumatic Fever. ''Front Immunol''. 2018; '''9''': 3009
Signatures of Selection in Admixed Dairy Cattle in Tanzania. Description: Cheruiyot, Evans Kiptoo, et al. Signatures of Selection in Admixed Dairy Cattle in Tanzania. ''Front Genet''. 2018; '''9''': 607
Single nucleotide polymorphisms in candidate genes associated with milk yield in Argentinean Holstein and Holstein x Jersey cows. Description: Raschia, Maria Agustina, et al. Single nucleotide polymorphisms in candidate genes associated with milk yield in Argentinean Holstein and Holstein x Jersey cows. ''J Anim Sci Technol''. 2018; '''60''': 31
Single nucleotide polymorphisms in the MYLKP1 pseudogene are associated with increased colon cancer risk in African Americans. Description: Lynn, Heather, et al. Single nucleotide polymorphisms in the MYLKP1 pseudogene are associated with increased colon cancer risk in African Americans. ''PLoS One''. 2018; '''13''' (8):e0200916
Single nucleotide polymorphisms within HLA region are associated with disease relapse for patients with unrelated cord blood transplantation. Description: Chen, Ding-Ping, et al. Single nucleotide polymorphisms within HLA region are associated with disease relapse for patients with unrelated cord blood transplantation. ''PeerJ''. 2018; '''6''': e5228
Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation. Description: Indencleef, Karlijne, et al. Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation. ''Front Genet''. 2018; '''9''': 502
SNPs Associated With Testosterone Levels Influence Human Facial Morphology. Description: Roosenboom, Jasmien, et al. SNPs Associated With Testosterone Levels Influence Human Facial Morphology. ''Front Genet''. 2018; '''9''': 497
Spatial and Temporal Scales of Range Expansion in Wild Phaseolus vulgaris. Description: Ariani, Andrea, et al. Spatial and Temporal Scales of Range Expansion in Wild Phaseolus vulgaris. ''Mol Biol Evol''. 2018 Jan 1; '''35''' (1):119-131
Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis. Description: Newbury, Dianne F, et al. Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis. ''Wellcome Open Res''. 2018; '''3''': 10
Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis. Description: Newbury, Dianne F, et al. Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis. ''Wellcome Open Res''. 2018; '''3''': 85
Staphylococcus aureus from patients with chronic rhinosinusitis show minimal genetic association between polyp and non-polyp phenotypes. Description: Bardy, Jake Jervis, et al. Staphylococcus aureus from patients with chronic rhinosinusitis show minimal genetic association between polyp and non-polyp phenotypes. ''BMC Ear Nose Throat Disord''. 2018; '''18''': 16
Systems genomics study reveals expression quantitative trait loci, regulator genes and pathways associated with boar taint in pigs. Description: Drag, Markus, et al. Systems genomics study reveals expression quantitative trait loci, regulator genes and pathways associated with boar taint in pigs. ''PLoS One''. 2018; '''13''' (2):e0192673
Targeted Sequencing of Alzheimer Disease Genes in African Americans Implicates Novel Risk Variants. Description: Logue, Mark W, et al. Targeted Sequencing of Alzheimer Disease Genes in African Americans Implicates Novel Risk Variants. ''Front Neurosci''. 2018; '''12''': 592
The Application of Multi-Locus GWAS for the Detection of Salt-Tolerance Loci in Rice. Description: Cui, Yanru, et al. The Application of Multi-Locus GWAS for the Detection of Salt-Tolerance Loci in Rice. ''Front Plant Sci''. 2018; '''9''': 1464
The genetic connectedness calculated from genomic information and its effect on the accuracy of genomic prediction. Description: Zhang, Suo-Yu, et al. The genetic connectedness calculated from genomic information and its effect on the accuracy of genomic prediction. ''PLoS One''. 2018; '''13''' (7):e0201400
The genomic ancestry, landscape genetics and invasion history of introduced mice in New Zealand. Description: Veale, Andrew J, et al. The genomic ancestry, landscape genetics and invasion history of introduced mice in New Zealand. ''R Soc Open Sci''. 2018 Jan; '''5''' (1):170879
The Genomic Architecture of Fowl Typhoid Resistance in Commercial Layers. Description: Psifidi, Androniki, et al. The Genomic Architecture of Fowl Typhoid Resistance in Commercial Layers. ''Front Genet''. 2018; '''9''': 519
The global spectrum of protein-coding pharmacogenomic diversity. Description: Wright, G E B, et al. The global spectrum of protein-coding pharmacogenomic diversity. ''Pharmacogenomics J''. 2018 Jan; '''18''' (1):187-195
The IL7RA rs6897932 polymorphism is associated with progression of liver fibrosis in patients with chronic hepatitis C: Repeated measurements design. Description: Jimenez-Sousa, Maria Angeles, et al. The IL7RA rs6897932 polymorphism is associated with progression of liver fibrosis in patients with chronic hepatitis C: Repeated measurements design. ''PLoS One''. 2018; '''13''' (5):e0197115
The Impact of IL-16 3'UTR Polymorphism rs859 on Lung Carcinoma Susceptibility among Chinese Han Individuals. Description: Zhuo, Manyun, et al. The Impact of IL-16 3'UTR Polymorphism rs859 on Lung Carcinoma Susceptibility among Chinese Han Individuals. ''Biomed Res Int''. 2018; '''2018''': 8305745
The Influence of Genetic Variation on Social Disposition, Romantic Relationships and Social Networks: a Replication Study. Description: Pearce, Eiluned, et al. The Influence of Genetic Variation on Social Disposition, Romantic Relationships and Social Networks: a Replication Study. ''Adapt Human Behav Physiol''. 2018; '''4''' (4):400-422
The Mega2R package: R tools for accessing and processing genetic data in common formats. Description: Baron, Robert V, et al. The Mega2R package: R tools for accessing and processing genetic data in common formats. ''F1000Res''. 2018; '''7''': 1352
TPH-2 Gene Polymorphism in Major Depressive Disorder Patients With Early-Wakening Symptom. Description: Tao, Shiwan, et al. TPH-2 Gene Polymorphism in Major Depressive Disorder Patients With Early-Wakening Symptom. ''Front Neurosci''. 2018; '''12''': 827
Tracking a serial killer: Integrating phylogenetic relationships, epidemiology, and geography for two invasive meningococcal disease outbreaks. Description: Ezeoke, Ifeoma, et al. Tracking a serial killer: Integrating phylogenetic relationships, epidemiology, and geography for two invasive meningococcal disease outbreaks. ''PLoS One''. 2018; '''13''' (11):e0202615
Traditional Norwegian Kveik Are a Genetically Distinct Group of Domesticated Saccharomyces cerevisiae Brewing Yeasts. Description: Preiss, Richard, et al. Traditional Norwegian Kveik Are a Genetically Distinct Group of Domesticated Saccharomyces cerevisiae Brewing Yeasts. ''Front Microbiol''. 2018; '''9''': 2137
Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density. Description: Zhou, Xueya, et al. Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density. ''Front Genet''. 2018; '''9''': 267
Transition-transversion encoding and genetic relationship metric in ReliefF feature selection improves pathway enrichment in GWAS. Description: Arabnejad, M, et al. Transition-transversion encoding and genetic relationship metric in ReliefF feature selection improves pathway enrichment in GWAS. ''BioData Min''. 2018; '''11''': 23
UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population. Description: Wisnumurti, Dewi A, et al. UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population. ''Biomed Res Int''. 2018; '''2018''': 9425843
Use of High Density Single Nucleotide Polymorphism (SNP) Arrays to Assess Genetic Diversity and Population Structure of Dairy Cattle in Smallholder Dairy Systems: The Case of Girinka Programme in Rwanda. Description: Chagunda, Mizeck G G, et al. Use of High Density Single Nucleotide Polymorphism (SNP) Arrays to Assess Genetic Diversity and Population Structure of Dairy Cattle in Smallholder Dairy Systems: The Case of Girinka Programme in Rwanda. ''Front Genet''. 2018; '''9''': 438
Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery. Description: Cha, Elliot D K, et al. Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery. ''J Obes''. 2018; '''2018''': 3253096
Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype. Description: Manley, William, et al. Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype. ''PLoS One''. 2018; '''13''' (3):e0194233
Variability in Resting State Network and Functional Network Connectivity Associated With Schizophrenia Genetic Risk: A Pilot Study. Description: Chen, Jiayu, et al. Variability in Resting State Network and Functional Network Connectivity Associated With Schizophrenia Genetic Risk: A Pilot Study. ''Front Neurosci''. 2018; '''12''': 114
viGEN: An Open Source Pipeline for the Detection and Quantification of Viral RNA in Human Tumors. Description: Bhuvaneshwar, Krithika, et al. viGEN: An Open Source Pipeline for the Detection and Quantification of Viral RNA in Human Tumors. ''Front Microbiol''. 2018; '''9''': 1172
Vitamin D metabolic loci and preeclampsia risk in multi-ethnic pregnant women. Description: Baca, Katharyn M, et al. Vitamin D metabolic loci and preeclampsia risk in multi-ethnic pregnant women. ''Physiol Rep''. 2018 Jan; '''6''' (2):
Whole-Genome Resequencing of Red Junglefowl and Indigenous Village Chicken Reveal New Insights on the Genome Dynamics of the Species. Description: Lawal, Raman A, et al. Whole-Genome Resequencing of Red Junglefowl and Indigenous Village Chicken Reveal New Insights on the Genome Dynamics of the Species. ''Front Genet''. 2018; '''9''': 264
Prenatal Maternal Serum Concentrations of Per- and Polyfluoroalkyl Substances in Association with Autism Spectrum Disorder and Intellectual Disability. Description: Lyall, Kristen, et al. Prenatal Maternal Serum Concentrations of Per- and Polyfluoroalkyl Substances in Association with Autism Spectrum Disorder and Intellectual Disability. ''Environ Health Perspect''. 2018 Jan 2; '''126''' (1):017001
SNPs related to vitamin D and breast cancer risk: a case-control study. Description: Huss, Linnea, et al. SNPs related to vitamin D and breast cancer risk: a case-control study. ''Breast Cancer Res''. 2018 Jan 2; '''20''' (1):1
Fast genomic prediction of breeding values using parallel Markov chain Monte Carlo with convergence diagnosis. Description: Guo, Peng, et al. Fast genomic prediction of breeding values using parallel Markov chain Monte Carlo with convergence diagnosis. ''BMC Bioinformatics''. 2018 Jan 3; '''19''' (1):3
Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. Description: Rambo-Martin, Benjamin L, et al. Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. ''G3 (Bethesda)''. 2018 Jan 4; '''8''' (1):105-111
PGG.Population: a database for understanding the genomic diversity and genetic ancestry of human populations. Description: Zhang, Chao, et al. PGG.Population: a database for understanding the genomic diversity and genetic ancestry of human populations. ''Nucleic Acids Res''. 2018 Jan 4; '''46''' (D1):D984-D993
Efficiency of different strategies to mitigate ascertainment bias when using SNP panels in diversity studies. Description: Malomane, Dorcus Kholofelo, et al. Efficiency of different strategies to mitigate ascertainment bias when using SNP panels in diversity studies. ''BMC Genomics''. 2018 Jan 5; '''19''' (1):22
TLR1 polymorphisms are significantly associated with the occurrence, presentation and drug-adverse reactions of tuberculosis in Western Chinese adults. Description: Peng, Wu, et al. TLR1 polymorphisms are significantly associated with the occurrence, presentation and drug-adverse reactions of tuberculosis in Western Chinese adults. ''Oncotarget''. 2018 Jan 5; '''9''' (2):1691-1704
Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population. Description: Zhou, Feng, et al. Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population. ''Oncotarget''. 2018 Jan 5; '''9''' (2):2249-2254
A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth. Description: Rappoport, Nadav, et al. A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth. ''Sci Rep''. 2018 Jan 9; '''8''' (1):226
Assessment of runs of homozygosity islands and estimates of genomic inbreeding in Gyr (Bos indicus) dairy cattle. Description: Peripolli, Elisa, et al. Assessment of runs of homozygosity islands and estimates of genomic inbreeding in Gyr (Bos indicus) dairy cattle. ''BMC Genomics''. 2018 Jan 9; '''19''' (1):34
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank. Description: Hall, Lynsey S, et al. Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank. ''Transl Psychiatry''. 2018 Jan 10; '''8''' (1):9
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes. Description: Astuti, Galuh D N, et al. Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes. ''Genes (Basel)''. 2018 Jan 10; '''9''' (1):
Preliminary evidence for genetic overlap between body mass index and striatal reward response. Description: Lancaster, T M, et al. Preliminary evidence for genetic overlap between body mass index and striatal reward response. ''Transl Psychiatry''. 2018 Jan 10; '''8''' (1):19
The Association Between Variants of Receptor for Advanced Glycation End Products (RAGE) Gene Polymorphisms and Age-Related Macular Degeneration. Description: Banevicius, Mantas, et al. The Association Between Variants of Receptor for Advanced Glycation End Products (RAGE) Gene Polymorphisms and Age-Related Macular Degeneration. ''Med Sci Monit''. 2018 Jan 10; '''24''': 190-199
Causal associations between risk factors and common diseases inferred from GWAS summary data. Description: Zhu, Zhihong, et al. Causal associations between risk factors and common diseases inferred from GWAS summary data. ''Nat Commun''. 2018 Jan 15; '''9''' (1):224
Ensemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease. Description: Morrow, Jarrett D, et al. Ensemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease. ''Hum Genomics''. 2018 Jan 15; '''12''' (1):1
Multi-omics differentially classify disease state and treatment outcome in pediatric Crohn's disease. Description: Douglas, Gavin M, et al. Multi-omics differentially classify disease state and treatment outcome in pediatric Crohn's disease. ''Microbiome''. 2018 Jan 15; '''6''' (1):13
Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome. Description: Yabe, Ichiro, et al. Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome. ''Sci Rep''. 2018 Jan 16; '''8''' (1):819
Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort. Description: Hendry, Liesl M, et al. Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort. ''BMC Med Genomics''. 2018 Jan 17; '''11''' (1):2
Genome-wide association study of self-reported food reactions in Japanese identifies shrimp and peach specific loci in the HLA-DR/DQ gene region. Description: Khor, Seik-Soon, et al. Genome-wide association study of self-reported food reactions in Japanese identifies shrimp and peach specific loci in the HLA-DR/DQ gene region. ''Sci Rep''. 2018 Jan 18; '''8''' (1):1069
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. Description: Wiemels, Joseph L, et al. GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. ''Nat Commun''. 2018 Jan 18; '''9''' (1):286
Identifying genome-wide immune gene variation underlying infectious disease in wildlife populations - a next generation sequencing approach in the gopher tortoise. Description: Elbers, Jean P, et al. Identifying genome-wide immune gene variation underlying infectious disease in wildlife populations - a next generation sequencing approach in the gopher tortoise. ''BMC Genomics''. 2018 Jan 19; '''19''' (1):64
Gene variants and educational attainment in cannabis use: mediating role of DNA methylation. Description: Gerra, Maria Carla, et al. Gene variants and educational attainment in cannabis use: mediating role of DNA methylation. ''Transl Psychiatry''. 2018 Jan 22; '''8''' (1):23
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Description: Bonas-Guarch, Silvia, et al. Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. ''Nat Commun''. 2018 Jan 22; '''9''' (1):321
Using Y-Chromosomal Haplogroups in Genetic Association Studies and Suggested Implications. Description: Erzurumluoglu, A Mesut, et al. Using Y-Chromosomal Haplogroups in Genetic Association Studies and Suggested Implications. ''Genes (Basel)''. 2018 Jan 22; '''9''' (1):
Revealing the selection history of adaptive loci using genome-wide scans for selection: an example from domestic sheep. Description: Rochus, Christina Marie, et al. Revealing the selection history of adaptive loci using genome-wide scans for selection: an example from domestic sheep. ''BMC Genomics''. 2018 Jan 23; '''19''' (1):71
A genome-wide association study in the Japanese population identifies the 12q24 locus for habitual coffee consumption: The J-MICC Study. Description: Nakagawa-Senda, Hiroko, et al. A genome-wide association study in the Japanese population identifies the 12q24 locus for habitual coffee consumption: The J-MICC Study. ''Sci Rep''. 2018 Jan 24; '''8''' (1):1493
GWAS of epigenetic aging rates in blood reveals a critical role for TERT. Description: Lu, Ake T, et al. GWAS of epigenetic aging rates in blood reveals a critical role for TERT. ''Nat Commun''. 2018 Jan 26; '''9''' (1):387
Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia Description: Kreile, Madara, et al. Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia ''Asian Pac J Cancer Prev''. 2018 Jan 27; '''19''' (1):91-95
Identification of Genetic Regions Associated with Scrotal Hernias in a Commercial Swine Herd. Description: Lago, Luisa Vitoria, et al. Identification of Genetic Regions Associated with Scrotal Hernias in a Commercial Swine Herd. ''Vet Sci''. 2018 Jan 27; '''5''' (1):
Inbreeding and runs of homozygosity before and after genomic selection in North American Holstein cattle. Description: Forutan, Mehrnush, et al. Inbreeding and runs of homozygosity before and after genomic selection in North American Holstein cattle. ''BMC Genomics''. 2018 Jan 27; '''19''' (1):98
Host genetic variation and its microbiome interactions within the Human Microbiome Project. Description: Kolde, Raivo, et al. Host genetic variation and its microbiome interactions within the Human Microbiome Project. ''Genome Med''. 2018 Jan 29; '''10''' (1):6
Integrated ovarian mRNA and miRNA transcriptome profiling characterizes the genetic basis of prolificacy traits in sheep (Ovis aries). Description: Pokharel, Kisun, et al. Integrated ovarian mRNA and miRNA transcriptome profiling characterizes the genetic basis of prolificacy traits in sheep (Ovis aries). ''BMC Genomics''. 2018 Jan 29; '''19''' (1):104
Assessing runs of Homozygosity: a comparison of SNP Array and whole genome sequence low coverage data. Description: Ceballos, Francisco C, et al. Assessing runs of Homozygosity: a comparison of SNP Array and whole genome sequence low coverage data. ''BMC Genomics''. 2018 Jan 30; '''19''' (1):106
Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder. Description: Pagerols, Mireia, et al. Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder. ''Sci Rep''. 2018 Jan 30; '''8''' (1):1881
Population-Wide Genetic Risk Prediction of Complex Diseases: A Pilot Feasibility Study in Macau Population for Precision Public Healthcare Planning. Description: Tsui, Nancy B Y, et al. Population-Wide Genetic Risk Prediction of Complex Diseases: A Pilot Feasibility Study in Macau Population for Precision Public Healthcare Planning. ''Sci Rep''. 2018 Jan 30; '''8''' (1):1853
The genetic prehistory of the Baltic Sea region. Description: Mittnik, Alissa, et al. The genetic prehistory of the Baltic Sea region. ''Nat Commun''. 2018 Jan 30; '''9''' (1):442
Genome-wide associations identify novel candidate loci associated with genetic susceptibility to tuberculosis in wild boar. Description: Queiros, Joao, et al. Genome-wide associations identify novel candidate loci associated with genetic susceptibility to tuberculosis in wild boar. ''Sci Rep''. 2018 Jan 31; '''8''' (1):1980
A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor. Description: Stanne, Tara M, et al. A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor. ''Thromb Haemost''. 2018 Feb; '''118''' (2):298-308
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+). Description: Makela, Mira, et al. Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+). ''Neurol Genet''. 2018 Feb; '''4''' (1):e211
A phylogenetic method to perform genome-wide association studies in microbes that accounts for population structure and recombination. Description: Collins, Caitlin, et al. A phylogenetic method to perform genome-wide association studies in microbes that accounts for population structure and recombination. ''PLoS Comput Biol''. 2018 Feb; '''14''' (2):e1005958
Applications of random forest feature selection for fine-scale genetic population assignment. Description: Sylvester, Emma V A, et al. Applications of random forest feature selection for fine-scale genetic population assignment. ''Evol Appl''. 2018 Feb; '''11''' (2):153-165
Applying landscape genomic tools to forest management and restoration of Hawaiian koa (Acacia koa) in a changing environment. Description: Gugger, Paul F, et al. Applying landscape genomic tools to forest management and restoration of Hawaiian koa (Acacia koa) in a changing environment. ''Evol Appl''. 2018 Feb; '''11''' (2):231-242
ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties. Description: St Pourcain, B, et al. ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties. ''Mol Psychiatry''. 2018 Feb; '''23''' (2):263-270
Association of interleukin-6 polymorphisms with obesity or metabolic traits in young Mexican-Americans. Description: Boeta-Lopez, K, et al. Association of interleukin-6 polymorphisms with obesity or metabolic traits in young Mexican-Americans. ''Obes Sci Pract''. 2018 Feb; '''4''' (1):85-96
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy. Description: Zarrei, Mehdi, et al. De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy. ''Genet Med''. 2018 Feb; '''20''' (2):172-180
De novo mutations implicate novel genes in systemic lupus erythematosus. Description: Pullabhatla, Venu, et al. De novo mutations implicate novel genes in systemic lupus erythematosus. ''Hum Mol Genet''. 2018 Feb 1; '''27''' (3):421-429
DLGAP1 and NMDA receptor-associated postsynaptic density protein genes influence executive function in attention deficit hyperactivity disorder. Description: Fan, Zili, et al. DLGAP1 and NMDA receptor-associated postsynaptic density protein genes influence executive function in attention deficit hyperactivity disorder. ''Brain Behav''. 2018 Feb; '''8''' (2):e00914
Expression of CPPED1 in human trophoblasts is associated with timing of term birth. Description: Haapalainen, Antti M, et al. Expression of CPPED1 in human trophoblasts is associated with timing of term birth. ''J Cell Mol Med''. 2018 Feb; '''22''' (2):968-981
Expression of the PPM1F Gene Is Regulated by Stress and Associated With Anxiety and Depression. Description: Wingo, Aliza P, et al. Expression of the PPM1F Gene Is Regulated by Stress and Associated With Anxiety and Depression. ''Biol Psychiatry''. 2018 Feb 1; '''83''' (3):284-295
Genetic variants in PPARGC1B and CNTN4 are associated with thromboxane A2 formation and with cardiovascular event free survival in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT). Description: McCarthy, Nina S, et al. Genetic variants in PPARGC1B and CNTN4 are associated with thromboxane A2 formation and with cardiovascular event free survival in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT). ''Atherosclerosis''. 2018 Feb; '''269''': 42-49
Genome-wide association study for pollinosis identified two novel loci in interleukin (IL)-1B in a Japanese population. Description: Fujii, Ryosuke, et al. Genome-wide association study for pollinosis identified two novel loci in interleukin (IL)-1B in a Japanese population. ''Nagoya J Med Sci''. 2018 Feb; '''80''' (1):109-120
Genomic associations with bill length and disease reveal drift and selection across island bird populations. Description: Armstrong, Claire, et al. Genomic associations with bill length and disease reveal drift and selection across island bird populations. ''Evol Lett''. 2018 Feb; '''2''' (1):22-36
Genomic basis and evolutionary potential for extreme drought adaptation in Arabidopsis thaliana. Description: Exposito-Alonso, Moises, et al. Genomic basis and evolutionary potential for extreme drought adaptation in Arabidopsis thaliana. ''Nat Ecol Evol''. 2018 Feb; '''2''' (2):352-358
Identification of polymorphisms in MITF and DCT genes and their associations with plumage colors in Asian duck breeds. Description: Sultana, Hasina, et al. Identification of polymorphisms in MITF and DCT genes and their associations with plumage colors in Asian duck breeds. ''Asian-Australas J Anim Sci''. 2018 Feb; '''31''' (2):180-188
Joint ancestry and association test indicate two distinct pathogenic pathways involved in classical dengue fever and dengue shock syndrome. Description: Oliveira, Marisa, et al. Joint ancestry and association test indicate two distinct pathogenic pathways involved in classical dengue fever and dengue shock syndrome. ''PLoS Negl Trop Dis''. 2018 Feb; '''12''' (2):e0006202
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair. Description: Liu, Fan, et al. Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair. ''Hum Mol Genet''. 2018 Feb 1; '''27''' (3):559-575
Multi-trait analysis of genome-wide association summary statistics using MTAG. Description: Turley, Patrick, et al. Multi-trait analysis of genome-wide association summary statistics using MTAG. ''Nat Genet''. 2018 Feb; '''50''' (2):229-237
No evidence for association between APOL1 kidney disease risk alleles and Human African Trypanosomiasis in two Ugandan populations. Description: Kimuda, Magambo Phillip, et al. No evidence for association between APOL1 kidney disease risk alleles and Human African Trypanosomiasis in two Ugandan populations. ''PLoS Negl Trop Dis''. 2018 Feb; '''12''' (2):e0006300
Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk. Description: Waller, Rosalie G, et al. Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk. ''PLoS Genet''. 2018 Feb; '''14''' (2):e1007111
OTTO: a new strategy to extract mental disease-relevant combinations of GWAS hits from individuals. Description: Ehrenreich, H, et al. OTTO: a new strategy to extract mental disease-relevant combinations of GWAS hits from individuals. ''Mol Psychiatry''. 2018 Feb; '''23''' (2):476-486
Serine Racemase and D-serine in the Amygdala Are Dynamically Involved in Fear Learning. Description: Balu, Darrick T, et al. Serine Racemase and D-serine in the Amygdala Are Dynamically Involved in Fear Learning. ''Biol Psychiatry''. 2018 Feb 1; '''83''' (3):273-283
Single-nucleotide polymorphism discovery and panel characterization in the African forest elephant. Description: Bourgeois, Stephanie, et al. Single-nucleotide polymorphism discovery and panel characterization in the African forest elephant. ''Ecol Evol''. 2018 Feb; '''8''' (4):2207-2217
The Interactive Effects of Age and PICALM rs541458 Polymorphism on Cognitive Performance, Brain Structure, and Function in Non-demented Elderly. Description: Liu, Zhen, et al. The Interactive Effects of Age and PICALM rs541458 Polymorphism on Cognitive Performance, Brain Structure, and Function in Non-demented Elderly. ''Mol Neurobiol''. 2018 Feb; '''55''' (2):1271-1283
The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. Description: Chang, H, et al. The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. ''Mol Psychiatry''. 2018 Feb; '''23''' (2):400-412
Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. Description: McElroy, Susan L, et al. Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. ''Transl Psychiatry''. 2018 Feb 2; '''8''' (1):40
Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort. Description: Strawbridge, Rona J, et al. Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort. ''Transl Psychiatry''. 2018 Feb 2; '''8''' (1):39
Genomic Prediction and Association Mapping of Curd-Related Traits in Gene Bank Accessions of Cauliflower. Description: Thorwarth, Patrick, et al. Genomic Prediction and Association Mapping of Curd-Related Traits in Gene Bank Accessions of Cauliflower. ''G3 (Bethesda)''. 2018 Feb 2; '''8''' (2):707-718
Identifying Genetic Differences Between Dongxiang Blue-Shelled and White Leghorn Chickens Using Sequencing Data. Description: Zhao, Qing-Bo, et al. Identifying Genetic Differences Between Dongxiang Blue-Shelled and White Leghorn Chickens Using Sequencing Data. ''G3 (Bethesda)''. 2018 Feb 2; '''8''' (2):469-476
Sequencing of Linkage Region on Chromosome 12p11 Identifies PKP2 as a Candidate Gene for Left Ventricular Mass in Dominican Families. Description: Dueker, Nicole D, et al. Sequencing of Linkage Region on Chromosome 12p11 Identifies PKP2 as a Candidate Gene for Left Ventricular Mass in Dominican Families. ''G3 (Bethesda)''. 2018 Feb 2; '''8''' (2):659-668
Sequence analysis of European maize inbred line F2 provides new insights into molecular and chromosomal characteristics of presence/absence variants. Description: Darracq, Aude, et al. Sequence analysis of European maize inbred line F2 provides new insights into molecular and chromosomal characteristics of presence/absence variants. ''BMC Genomics''. 2018 Feb 5; '''19''' (1):119
QTL mapping and GWAS reveal candidate genes controlling capsaicinoid content in Capsicum. Description: Han, Koeun, et al. QTL mapping and GWAS reveal candidate genes controlling capsaicinoid content in Capsicum. ''Plant Biotechnol J''. 2018 Feb 6;
Vitamin D-Binding Protein Polymorphisms, 25-Hydroxyvitamin D, Sunshine and Multiple Sclerosis. Description: Langer-Gould, Annette, et al. Vitamin D-Binding Protein Polymorphisms, 25-Hydroxyvitamin D, Sunshine and Multiple Sclerosis. ''Nutrients''. 2018 Feb 7; '''10''' (2):
Integrated Systems Approach Reveals Sphingolipid Metabolism Pathway Dysregulation in Association with Late-Onset Alzheimer's Disease. Description: Malamon, John Stephen, et al. Integrated Systems Approach Reveals Sphingolipid Metabolism Pathway Dysregulation in Association with Late-Onset Alzheimer's Disease. ''Biology (Basel)''. 2018 Feb 9; '''7''' (1):
Genetic determinants of sporadic breast cancer in Sri Lankan women. Description: Sirisena, Nirmala Dushyanthi, et al. Genetic determinants of sporadic breast cancer in Sri Lankan women. ''BMC Cancer''. 2018 Feb 13; '''18''' (1):180
Genome-wide scan for commons SNPs affecting bovine leukemia virus infection level in dairy cattle. Description: Carignano, Hugo A, et al. Genome-wide scan for commons SNPs affecting bovine leukemia virus infection level in dairy cattle. ''BMC Genomics''. 2018 Feb 13; '''19''' (1):142
Validation of genotype imputation in Southeast Asian populations and the effect of single nucleotide polymorphism annotation on imputation outcome. Description: Lert-Itthiporn, Worachart, et al. Validation of genotype imputation in Southeast Asian populations and the effect of single nucleotide polymorphism annotation on imputation outcome. ''BMC Med Genet''. 2018 Feb 13; '''19''' (1):23
Colorectal Cancer-Associated Genes Are Associated with Tooth Agenesis and May Have a Role in Tooth Development. Description: Williams, Meredith A, et al. Colorectal Cancer-Associated Genes Are Associated with Tooth Agenesis and May Have a Role in Tooth Development. ''Sci Rep''. 2018 Feb 14; '''8''' (1):2979
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Description: Gharahkhani, Puya, et al. Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. ''Sci Rep''. 2018 Feb 15; '''8''' (1):3124
A recurrent de novo missense mutation in UBTF causes developmental neuroregression. Description: Toro, Camilo, et al. A recurrent de novo missense mutation in UBTF causes developmental neuroregression. ''Hum Mol Genet''. 2018 Feb 15; '''27''' (4):691-705
Assessment of interaction between maternal polycyclic aromatic hydrocarbons exposure and genetic polymorphisms on the risk of congenital heart diseases. Description: Li, Nana, et al. Assessment of interaction between maternal polycyclic aromatic hydrocarbons exposure and genetic polymorphisms on the risk of congenital heart diseases. ''Sci Rep''. 2018 Feb 15; '''8''' (1):3075
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. Description: Beaumont, Robin N, et al. Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. ''Hum Mol Genet''. 2018 Feb 15; '''27''' (4):742-756
Two novel colorectal cancer risk loci in the region on chromosome 9q22.32. Description: Thutkawkorapin, Jessada, et al. Two novel colorectal cancer risk loci in the region on chromosome 9q22.32. ''Oncotarget''. 2018 Feb 16; '''9''' (13):11170-11179
Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation. Description: Wang, Pengxia, et al. Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation. ''Sci Rep''. 2018 Feb 19; '''8''' (1):3297
Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer's disease pathogenesis. Description: Zhou, Xiaopu, et al. Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer's disease pathogenesis. ''Proc Natl Acad Sci U S A''. 2018 Feb 20; '''115''' (8):1697-1706
Risk variants of the alpha-synuclein locus and REM sleep behavior disorder in Parkinson's disease: a genetic association study. Description: Bjornara, Kari Anne, et al. Risk variants of the alpha-synuclein locus and REM sleep behavior disorder in Parkinson's disease: a genetic association study. ''BMC Neurol''. 2018 Feb 21; '''18''' (1):20
Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to beta-Blockers. Description: Shahin, Mohamed H, et al. Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to beta-Blockers. ''J Am Heart Assoc''. 2018 Feb 24; '''7''' (5):
A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans. Description: Xu, Huichun, et al. A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans. ''J Pers Med''. 2018 Feb 26; '''8''' (1):
Characterization of cross-tissue genetic-epigenetic effects and their patterns in schizophrenia. Description: Lin, Dongdong, et al. Characterization of cross-tissue genetic-epigenetic effects and their patterns in schizophrenia. ''Genome Med''. 2018 Feb 26; '''10''' (1):13
Impact of Genetic Variants on the Individual Potential for Body Fat Loss. Description: Cha, Soyeon, et al. Impact of Genetic Variants on the Individual Potential for Body Fat Loss. ''Nutrients''. 2018 Feb 26; '''10''' (3):
Evaluation of three polygenic risk score models for the prediction of breast cancer risk in Singapore Chinese. Description: Chan, Claire Hian Tzer, et al. Evaluation of three polygenic risk score models for the prediction of breast cancer risk in Singapore Chinese. ''Oncotarget''. 2018 Feb 27; '''9''' (16):12796-12804
MS Sunshine Study: Sun Exposure But Not Vitamin D Is Associated with Multiple Sclerosis Risk in Blacks and Hispanics. Description: Langer-Gould, Annette, et al. MS Sunshine Study: Sun Exposure But Not Vitamin D Is Associated with Multiple Sclerosis Risk in Blacks and Hispanics. ''Nutrients''. 2018 Feb 27; '''10''' (3):
Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels. Description: O'Brien, Timothy D, et al. Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels. ''Genome Med''. 2018 Feb 27; '''10''' (1):16
Dietary n-3 and n-6 polyunsaturated fatty acids, the FADS gene, and the risk of gastric cancer in a Korean population. Description: Lee, Sunghee, et al. Dietary n-3 and n-6 polyunsaturated fatty acids, the FADS gene, and the risk of gastric cancer in a Korean population. ''Sci Rep''. 2018 Feb 28; '''8''' (1):3823
Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis. Description: Onoufriadis, Alexandros, et al. Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis. ''J Crohns Colitis''. 2018 Feb 28; '''12''' (3):321-326
Sheep genome functional annotation reveals proximal regulatory elements contributed to the evolution of modern breeds. Description: Naval-Sanchez, Marina, et al. Sheep genome functional annotation reveals proximal regulatory elements contributed to the evolution of modern breeds. ''Nat Commun''. 2018 Feb 28; '''9''' (1):859
Accuracy of Imputation of Microsatellite Markers from BovineSNP50 and BovineHD BeadChip in Hanwoo Population of Korea. Description: Sharma, Aditi, et al. Accuracy of Imputation of Microsatellite Markers from BovineSNP50 and BovineHD BeadChip in Hanwoo Population of Korea. ''Genomics Inform''. 2018 Mar; '''16''' (1):10-13
A large electronic-health-record-based genome-wide study of serum lipids. Description: Hoffmann, Thomas J, et al. A large electronic-health-record-based genome-wide study of serum lipids. ''Nat Genet''. 2018 Mar; '''50''' (3):401-413
CCR5Delta32 (rs333) polymorphism is associated with decreased risk of chronic and aggressive periodontitis: A case-control analysis based in disease resistance and susceptibility phenotypes. Description: Cavalla, Franco, et al. CCR5Delta32 (rs333) polymorphism is associated with decreased risk of chronic and aggressive periodontitis: A case-control analysis based in disease resistance and susceptibility phenotypes. ''Cytokine''. 2018 Mar; '''103''': 142-149
Cleaner fish escape salmon farms and hybridize with local wrasse populations. Description: Faust, Ellika, et al. Cleaner fish escape salmon farms and hybridize with local wrasse populations. ''R Soc Open Sci''. 2018 Mar; '''5''' (3):171752
Comprehensive description of genomewide nucleotide and structural variation in short-season soya bean. Description: Torkamaneh, Davoud, et al. Comprehensive description of genomewide nucleotide and structural variation in short-season soya bean. ''Plant Biotechnol J''. 2018 Mar; '''16''' (3):749-759
Dysregulation of C-X-C motif ligand 10 during aging and association with cognitive performance. Description: Bradburn, Steven, et al. Dysregulation of C-X-C motif ligand 10 during aging and association with cognitive performance. ''Neurobiol Aging''. 2018 Mar; '''63''': 54-64
Genetic Ancestry of Hadza and Sandawe Peoples Reveals Ancient Population Structure in Africa. Description: Shriner, Daniel, et al. Genetic Ancestry of Hadza and Sandawe Peoples Reveals Ancient Population Structure in Africa. ''Genome Biol Evol''. 2018 Mar 1; '''10''' (3):875-882
Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population. Description: Liu, Gang, et al. Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population. ''J Cell Mol Med''. 2018 Mar; '''22''' (3):1964-1971
Genetic variations of IL-10: Identification of novel variations and evaluation of the impact of the SNPs/haplotype in the promoter region with the progression of Oral Squamous Cell Carcinoma in Indian population. Description: Sharma, Upma, et al. Genetic variations of IL-10: Identification of novel variations and evaluation of the impact of the SNPs/haplotype in the promoter region with the progression of Oral Squamous Cell Carcinoma in Indian population. ''Cytokine''. 2018 Mar; '''103''': 99-108
Identification of novel loci associated with maturity and yield traits in early maturity soybean plant introduction lines. Description: Copley, Tanya R, et al. Identification of novel loci associated with maturity and yield traits in early maturity soybean plant introduction lines. ''BMC Genomics''. 2018 Mar 1; '''19''' (1):167
Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability. Description: Duncan, L E, et al. Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability. ''Mol Psychiatry''. 2018 Mar; '''23''' (3):666-673
Madeiran Arabidopsis thaliana Reveals Ancient Long-Range Colonization and Clarifies Demography in Eurasia. Description: Fulgione, Andrea, et al. Madeiran Arabidopsis thaliana Reveals Ancient Long-Range Colonization and Clarifies Demography in Eurasia. ''Mol Biol Evol''. 2018 Mar 1; '''35''' (3):564-574
Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells. Description: Smets, Ide, et al. Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells. ''Brain''. 2018 Mar 1; '''141''' (3):786-796
Nucleotide variation in ATG4A and susceptibility to cervical cancer in Southwestern Chinese women. Description: Mao, Jin-Ju, et al. Nucleotide variation in ATG4A and susceptibility to cervical cancer in Southwestern Chinese women. ''Oncol Lett''. 2018 Mar; '''15''' (3):2992-3000
Oceanographic variation influences spatial genomic structure in the sea scallop, Placopecten magellanicus. Description: Van Wyngaarden, Mallory, et al. Oceanographic variation influences spatial genomic structure in the sea scallop, Placopecten magellanicus. ''Ecol Evol''. 2018 Mar; '''8''' (5):2824-2841
Pharmacogenetic Analysis of the Model-Based Pharmacokinetics of Five Anti-HIV Drugs: How Does This Influence the Effect of Aging? Description: Chen, Jingxian, et al. Pharmacogenetic Analysis of the Model-Based Pharmacokinetics of Five Anti-HIV Drugs: How Does This Influence the Effect of Aging? ''Clin Transl Sci''. 2018 Mar; '''11''' (2):226-236
Profile of common prostate cancer risk variants in an unscreened Romanian population. Description: Iordache, Paul D, et al. Profile of common prostate cancer risk variants in an unscreened Romanian population. ''J Cell Mol Med''. 2018 Mar; '''22''' (3):1574-1582
Single Nucleotide Polymorphism Facilitated Down-Regulation of the Cohesin Stromal Antigen-1: Implications for Colorectal Cancer Racial Disparities. Description: Datta, Somenath, et al. Single Nucleotide Polymorphism Facilitated Down-Regulation of the Cohesin Stromal Antigen-1: Implications for Colorectal Cancer Racial Disparities. ''Neoplasia''. 2018 Mar; '''20''' (3):289-294
Studies of modern Italian dog populations reveal multiple patterns for domestic breed evolution. Description: Talenti, Andrea, et al. Studies of modern Italian dog populations reveal multiple patterns for domestic breed evolution. ''Ecol Evol''. 2018 Mar; '''8''' (5):2911-2925
The Arf6 activator Efa6/PSD3 confers regional specificity and modulates ethanol consumption in Drosophila and humans. Description: Gonzalez, D A, et al. The Arf6 activator Efa6/PSD3 confers regional specificity and modulates ethanol consumption in Drosophila and humans. ''Mol Psychiatry''. 2018 Mar; '''23''' (3):621-628
Common variants of ARID1A and KAT2B are associated with obesity in Indian adolescents. Description: Giri, Anil K, et al. Common variants of ARID1A and KAT2B are associated with obesity in Indian adolescents. ''Sci Rep''. 2018 Mar 2; '''8''' (1):3964
Computational modeling suggests impaired interactions between NKX2.5 and GATA4 in individuals carrying a novel pathogenic D16N NKX2.5 mutation. Description: Mattapally, Saidulu, et al. Computational modeling suggests impaired interactions between NKX2.5 and GATA4 in individuals carrying a novel pathogenic D16N NKX2.5 mutation. ''Oncotarget''. 2018 Mar 2; '''9''' (17):13713-13732
Exploring the pathogenesis of canine epilepsy using a systems genetics method and implications for anti-epilepsy drug discovery. Description: Cui, Ze-Jia, et al. Exploring the pathogenesis of canine epilepsy using a systems genetics method and implications for anti-epilepsy drug discovery. ''Oncotarget''. 2018 Mar 2; '''9''' (17):13181-13192
Genetic Diversity, Molecular Phylogeny, and Selection Evidence of Jinchuan Yak Revealed by Whole-Genome Resequencing. Description: Lan, Daoliang, et al. Genetic Diversity, Molecular Phylogeny, and Selection Evidence of Jinchuan Yak Revealed by Whole-Genome Resequencing. ''G3 (Bethesda)''. 2018 Mar 2; '''8''' (3):945-952
Genomic evidence of speciation reversal in ravens. Description: Kearns, Anna M, et al. Genomic evidence of speciation reversal in ravens. ''Nat Commun''. 2018 Mar 2; '''9''' (1):906
IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in Uruguayan patients. Description: Echeverria, Natalia, et al. IL28B gene polymorphism rs12979860, but not rs8099917, contributes to the occurrence of chronic HCV infection in Uruguayan patients. ''Virol J''. 2018 Mar 2; '''15''' (1):40
Item-level analyses reveal genetic heterogeneity in neuroticism. Description: Nagel, Mats, et al. Item-level analyses reveal genetic heterogeneity in neuroticism. ''Nat Commun''. 2018 Mar 2; '''9''' (1):905
Strong selection during the last millennium for African ancestry in the admixed population of Madagascar. Description: Pierron, Denis, et al. Strong selection during the last millennium for African ancestry in the admixed population of Madagascar. ''Nat Commun''. 2018 Mar 2; '''9''' (1):932
Uncovering Genomic Regions Associated with Trypanosoma Infections in Wild Populations of the Tsetse Fly Glossina fuscipes. Description: Gloria-Soria, Andrea, et al. Uncovering Genomic Regions Associated with Trypanosoma Infections in Wild Populations of the Tsetse Fly Glossina fuscipes. ''G3 (Bethesda)''. 2018 Mar 2; '''8''' (3):887-897
Crossed beaks in a local Swiss chicken breed. Description: Joller, Sara, et al. Crossed beaks in a local Swiss chicken breed. ''BMC Vet Res''. 2018 Mar 5; '''14''' (1):68
Origins and genetic legacies of the Caribbean Taino. Description: Schroeder, Hannes, et al. Origins and genetic legacies of the Caribbean Taino. ''Proc Natl Acad Sci U S A''. 2018 Mar 6; '''115''' (10):2341-2346
A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis. Description: Theriault, Sebastien, et al. A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis. ''Nat Commun''. 2018 Mar 7; '''9''' (1):988
Genome-wide analysis yields new loci associating with aortic valve stenosis. Description: Helgadottir, Anna, et al. Genome-wide analysis yields new loci associating with aortic valve stenosis. ''Nat Commun''. 2018 Mar 7; '''9''' (1):987
Improving genetic prediction by leveraging genetic correlations among human diseases and traits. Description: Maier, Robert M, et al. Improving genetic prediction by leveraging genetic correlations among human diseases and traits. ''Nat Commun''. 2018 Mar 7; '''9''' (1):989
Risk of nontyphoidal Salmonella bacteraemia in African children is modified by STAT4. Description: Gilchrist, James J, et al. Risk of nontyphoidal Salmonella bacteraemia in African children is modified by STAT4. ''Nat Commun''. 2018 Mar 9; '''9''' (1):1014
Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa. Description: Warrier, Varun, et al. Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa. ''Transl Psychiatry''. 2018 Mar 12; '''8''' (1):35
Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. Description: Zhou, Sirui, et al. Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. ''Sci Rep''. 2018 Mar 12; '''8''' (1):4356
Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Description: Meijsen, Joeri J, et al. Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. ''Transl Psychiatry''. 2018 Mar 13; '''8''' (1):63
Genetic Contributions to The Association Between Adult Height and Head and Neck Cancer: A Mendelian Randomization Analysis. Description: Pastorino, Roberta, et al. Genetic Contributions to The Association Between Adult Height and Head and Neck Cancer: A Mendelian Randomization Analysis. ''Sci Rep''. 2018 Mar 14; '''8''' (1):4534
pedigreejs: a web-based graphical pedigree editor. Description: Carver, Tim, et al. pedigreejs: a web-based graphical pedigree editor. ''Bioinformatics''. 2018 Mar 15; '''34''' (6):1069-1071
The integrated landscape of causal genes and pathways in schizophrenia. Description: Ma, Changguo, et al. The integrated landscape of causal genes and pathways in schizophrenia. ''Transl Psychiatry''. 2018 Mar 15; '''8''' (1):67
An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis. Description: Ogura, Yoji, et al. An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis. ''Sci Rep''. 2018 Mar 16; '''8''' (1):4730
Phylogenetic Relationships, Breeding Implications, and Cultivation History of Hawaiian Taro (Colocasia Esculenta) Through Genome-Wide SNP Genotyping. Description: Helmkampf, Martin, et al. Phylogenetic Relationships, Breeding Implications, and Cultivation History of Hawaiian Taro (Colocasia Esculenta) Through Genome-Wide SNP Genotyping. ''J Hered''. 2018 Mar 16; '''109''' (3):272-282
Mapping QTL for white striping in relation to breast muscle yield and meat quality traits in broiler chickens. Description: Pampouille, Eva, et al. Mapping QTL for white striping in relation to breast muscle yield and meat quality traits in broiler chickens. ''BMC Genomics''. 2018 Mar 20; '''19''' (1):202
A genome-wide association study identifies candidate loci associated to syringomyelia secondary to Chiari-like malformation in Cavalier King Charles Spaniels. Description: Ancot, Frederic, et al. A genome-wide association study identifies candidate loci associated to syringomyelia secondary to Chiari-like malformation in Cavalier King Charles Spaniels. ''BMC Genet''. 2018 Mar 22; '''19''' (1):16
Early and late feathering in turkey and chicken: same gene but different mutations. Description: Derks, Martijn F L, et al. Early and late feathering in turkey and chicken: same gene but different mutations. ''Genet Sel Evol''. 2018 Mar 22; '''50''' (1):7
Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes. Description: Quan, Yuan, et al. Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes. ''Molecules''. 2018 Mar 23; '''23''' (4):
Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians. Description: Gurung, Resham Lal, et al. Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians. ''Sci Rep''. 2018 Mar 23; '''8''' (1):5109
Eigen decomposition expedites longitudinal genome-wide association studies for milk production traits in Chinese Holstein. Description: Ning, Chao, et al. Eigen decomposition expedites longitudinal genome-wide association studies for milk production traits in Chinese Holstein. ''Genet Sel Evol''. 2018 Mar 26; '''50''' (1):12
Local adaptation in European populations affected the genetics of psychiatric disorders and behavioral traits. Description: Polimanti, Renato, et al. Local adaptation in European populations affected the genetics of psychiatric disorders and behavioral traits. ''Genome Med''. 2018 Mar 26; '''10''' (1):24
Adaptive diversification of growth allometry in the plant Arabidopsis thaliana. Description: Vasseur, Francois, et al. Adaptive diversification of growth allometry in the plant Arabidopsis thaliana. ''Proc Natl Acad Sci U S A''. 2018 Mar 27; '''115''' (13):3416-3421
Effects on gene expression and behavior of untagged short tandem repeats: the case of arginine vasopressin receptor 1a (AVPR1a) and externalizing behaviors. Description: Landefeld, Clare C, et al. Effects on gene expression and behavior of untagged short tandem repeats: the case of arginine vasopressin receptor 1a (AVPR1a) and externalizing behaviors. ''Transl Psychiatry''. 2018 Mar 27; '''8''' (1):72
Low-frequency and rare variants may contribute to elucidate the genetics of major depressive disorder. Description: Yu, Chenglong, et al. Low-frequency and rare variants may contribute to elucidate the genetics of major depressive disorder. ''Transl Psychiatry''. 2018 Mar 27; '''8''' (1):70
A Genomic Reference Panel for Drosophila serrata. Description: Reddiex, Adam J, et al. A Genomic Reference Panel for Drosophila serrata. ''G3 (Bethesda)''. 2018 Mar 28; '''8''' (4):1335-1346
Genome-Wide Association and Genomic Selection for Resistance to Amoebic Gill Disease in Atlantic Salmon. Description: Robledo, Diego, et al. Genome-Wide Association and Genomic Selection for Resistance to Amoebic Gill Disease in Atlantic Salmon. ''G3 (Bethesda)''. 2018 Mar 28; '''8''' (4):1195-1203
Multilocus genetic profile in dopaminergic pathway modulates the striatum and working memory. Description: Wang, Chao, et al. Multilocus genetic profile in dopaminergic pathway modulates the striatum and working memory. ''Sci Rep''. 2018 Mar 29; '''8''' (1):5372
Fine-mapping analysis of the MHC region for vitiligo based on a new Han-MHC reference panel. Description: Yang, Chao, et al. Fine-mapping analysis of the MHC region for vitiligo based on a new Han-MHC reference panel. ''Gene''. 2018 Mar 30; '''648''': 76-81
Pharmacogenetics-based area-under-curve model can predict efficacy and adverse events from axitinib in individual patients with advanced renal cell carcinoma. Description: Yamamoto, Yoshiaki, et al. Pharmacogenetics-based area-under-curve model can predict efficacy and adverse events from axitinib in individual patients with advanced renal cell carcinoma. ''Oncotarget''. 2018 Mar 30; '''9''' (24):17160-17170
A genetic association study of carotid intima-media thickness (CIMT) and plaque in Mexican Americans and European Americans with rheumatoid arthritis. Description: Arya, Rector, et al. A genetic association study of carotid intima-media thickness (CIMT) and plaque in Mexican Americans and European Americans with rheumatoid arthritis. ''Atherosclerosis''. 2018 Apr; '''271''': 92-101
A genetic risk score for fasting plasma glucose is independently associated with arterial stiffness: a Mendelian randomization study. Description: Gottsater, Mikael, et al. A genetic risk score for fasting plasma glucose is independently associated with arterial stiffness: a Mendelian randomization study. ''J Hypertens''. 2018 Apr; '''36''' (4):809-814
An Autoimmune Disease-Associated Risk Variant in the TNFAIP3 Gene Plays a Protective Role in Brucellosis That Is Mediated by the NF-kappaB Signaling Pathway. Description: Lou, Lixin, et al. An Autoimmune Disease-Associated Risk Variant in the TNFAIP3 Gene Plays a Protective Role in Brucellosis That Is Mediated by the NF-kappaB Signaling Pathway. ''J Clin Microbiol''. 2018 Apr; '''56''' (4):
Association of AGTR1 (A1166C) and ACE (I/D) Polymorphisms with Breast Cancer Risk in North Indian Population. Description: Singh, Anukriti, et al. Association of AGTR1 (A1166C) and ACE (I/D) Polymorphisms with Breast Cancer Risk in North Indian Population. ''Transl Oncol''. 2018 Apr; '''11''' (2):233-242
Association of genetic variants of PD1 with recurrent pregnancy loss. Description: Hayashi, Yuko, et al. Association of genetic variants of PD1 with recurrent pregnancy loss. ''Reprod Med Biol''. 2018 Apr; '''17''' (2):195-202
Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population. Description: Zhang, Yan, et al. Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population. ''J Cell Mol Med''. 2018 Apr; '''22''' (4):2190-2199
Associations of NADPH oxidase-related genes with blood pressure changes and incident hypertension: The GenSalt Study. Description: Li, Hongfan, et al. Associations of NADPH oxidase-related genes with blood pressure changes and incident hypertension: The GenSalt Study. ''J Hum Hypertens''. 2018 Apr; '''32''' (4):287-293
Comparative analysis examining patterns of genomic differentiation across multiple episodes of population divergence in birds. Description: Delmore, Kira E, et al. Comparative analysis examining patterns of genomic differentiation across multiple episodes of population divergence in birds. ''Evol Lett''. 2018 Apr; '''2''' (2):76-87
CYP3A4 genotype is associated with sildenafil concentrations in patients with heart failure with preserved ejection fraction. Description: de Denus, S, et al. CYP3A4 genotype is associated with sildenafil concentrations in patients with heart failure with preserved ejection fraction. ''Pharmacogenomics J''. 2018 Apr; '''18''' (2):232-237
Data on genetic associations of carotid atherosclerosis markers in Mexican American and European American rheumatoid arthritis subjects. Description: Arya, Rector, et al. Data on genetic associations of carotid atherosclerosis markers in Mexican American and European American rheumatoid arthritis subjects. ''Data Brief''. 2018 Apr; '''17''': 820-829
Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis. Description: Suzuki, Akiko, et al. Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis. ''Mech Dev''. 2018 Apr; '''150''': 21-27
Genetic risk for schizophrenia and psychosis in Alzheimer disease. Description: DeMichele-Sweet, M A A, et al. Genetic risk for schizophrenia and psychosis in Alzheimer disease. ''Mol Psychiatry''. 2018 Apr; '''23''' (4):963-972
Genome evolution across 1,011 Saccharomyces cerevisiae isolates. Description: Peter, Jackson, et al. Genome evolution across 1,011 Saccharomyces cerevisiae isolates. ''Nature''. 2018 Apr; '''556''' (7701):339-344
Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths. Description: Kweon, Kukju, et al. Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths. ''Soa Chongsonyon Chongsin Uihak''. 2018 Apr 1; '''29''' (2):62-72
Genome-wide association study reveals genetic loci and candidate genes for average daily gain in Duroc pigs. Description: Quan, Jianping, et al. Genome-wide association study reveals genetic loci and candidate genes for average daily gain in Duroc pigs. ''Asian-Australas J Anim Sci''. 2018 Apr; '''31''' (4):480-488
Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey. Description: Spracklen, Cassandra N, et al. Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey. ''PLoS Genet''. 2018 Apr; '''14''' (4):e1007275
Identification of novel alleles associated with insulin resistance in childhood obesity using pooled-DNA genome-wide association study approach. Description: Kotnik, P, et al. Identification of novel alleles associated with insulin resistance in childhood obesity using pooled-DNA genome-wide association study approach. ''Int J Obes (Lond)''. 2018 Apr; '''42''' (4):686-695
Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. Description: Abdulkadir, Mohamed, et al. Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. ''Eur Arch Psychiatry Clin Neurosci''. 2018 Apr; '''268''' (3):301-316
Linkage disequilibrium levels and allele frequency distribution in Blanco Orejinegro and Romosinuano Creole cattle using medium density SNP chip data. Description: Bejarano, Diego, et al. Linkage disequilibrium levels and allele frequency distribution in Blanco Orejinegro and Romosinuano Creole cattle using medium density SNP chip data. ''Genet Mol Biol''. 2018 Apr./Jun; '''41''' (2):426-433
Modification of the association between antipsychotic treatment response and childhood adversity by MMP9 gene variants in a first-episode schizophrenia cohort. Description: McGregor, Nathaniel, et al. Modification of the association between antipsychotic treatment response and childhood adversity by MMP9 gene variants in a first-episode schizophrenia cohort. ''Psychiatry Res''. 2018 Apr; '''262''': 141-148
One for all and all for One: Improving replication of genetic studies through network diffusion. Description: Lancour, Daniel, et al. One for all and all for One: Improving replication of genetic studies through network diffusion. ''PLoS Genet''. 2018 Apr; '''14''' (4):e1007306
Rare ABCA7 variants in 2 German families with Alzheimer disease. Description: May, Patrick, et al. Rare ABCA7 variants in 2 German families with Alzheimer disease. ''Neurol Genet''. 2018 Apr; '''4''' (2):e224
The Gateway from Near into Remote Oceania: New Insights from Genome-Wide Data. Description: Pugach, Irina, et al. The Gateway from Near into Remote Oceania: New Insights from Genome-Wide Data. ''Mol Biol Evol''. 2018 Apr 1; '''35''' (4):871-886
Whole-genome resequencing reveals signatures of selection and timing of duck domestication. Description: Zhang, Zebin, et al. Whole-genome resequencing reveals signatures of selection and timing of duck domestication. ''Gigascience''. 2018 Apr 1; '''7''' (4):
Whole-genome sequences of 89 Chinese sheep suggest role of RXFP2 in the development of unique horn phenotype as response to semi-feralization. Description: Pan, Zhangyuan, et al. Whole-genome sequences of 89 Chinese sheep suggest role of RXFP2 in the development of unique horn phenotype as response to semi-feralization. ''Gigascience''. 2018 Apr 1; '''7''' (4):
Evolution of Sex Determination Loci in Atlantic Salmon. Description: Kijas, James, et al. Evolution of Sex Determination Loci in Atlantic Salmon. ''Sci Rep''. 2018 Apr 4; '''8''' (1):5664
KoVariome: Korean National Standard Reference Variome database of whole genomes with comprehensive SNV, indel, CNV, and SV analyses. Description: Kim, Jungeun, et al. KoVariome: Korean National Standard Reference Variome database of whole genomes with comprehensive SNV, indel, CNV, and SV analyses. ''Sci Rep''. 2018 Apr 4; '''8''' (1):5677
Variance explained by whole genome sequence variants in coding and regulatory genome annotations for six dairy traits. Description: Koufariotis, Lambros T, et al. Variance explained by whole genome sequence variants in coding and regulatory genome annotations for six dairy traits. ''BMC Genomics''. 2018 Apr 5; '''19''' (1):237
Association of EGLN1 genetic polymorphisms with SpO2 responses to acute hypobaric hypoxia in a Japanese cohort. Description: Yasukochi, Yoshiki, et al. Association of EGLN1 genetic polymorphisms with SpO2 responses to acute hypobaric hypoxia in a Japanese cohort. ''J Physiol Anthropol''. 2018 Apr 6; '''37''' (1):9
Genomic evaluation of feed efficiency component traits in Duroc pigs using 80K, 650K and whole-genome sequence variants. Description: Zhang, Chunyan, et al. Genomic evaluation of feed efficiency component traits in Duroc pigs using 80K, 650K and whole-genome sequence variants. ''Genet Sel Evol''. 2018 Apr 6; '''50''' (1):14
Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. Description: Vijayakrishnan, Jayaram, et al. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. ''Nat Commun''. 2018 Apr 9; '''9''' (1):1340
Polygenic risk for schizophrenia and measured domains of cognition in individuals with psychosis and controls. Description: Shafee, Rebecca, et al. Polygenic risk for schizophrenia and measured domains of cognition in individuals with psychosis and controls. ''Transl Psychiatry''. 2018 Apr 12; '''8''' (1):78
A survey of functional genomic variation in domesticated chickens. Description: Derks, Martijn F L, et al. A survey of functional genomic variation in domesticated chickens. ''Genet Sel Evol''. 2018 Apr 16; '''50''' (1):17
Combined linkage and association analysis of classical Hodgkin lymphoma. Description: Lawrie, Alastair, et al. Combined linkage and association analysis of classical Hodgkin lymphoma. ''Oncotarget''. 2018 Apr 17; '''9''' (29):20377-20385
Common genetic variation and novel loci associated with volumetric mammographic density. Description: Brand, Judith S, et al. Common genetic variation and novel loci associated with volumetric mammographic density. ''Breast Cancer Res''. 2018 Apr 17; '''20''' (1):30
Human bony labyrinth is an indicator of population history and dispersal from Africa. Description: Ponce de Leon, Marcia S, et al. Human bony labyrinth is an indicator of population history and dispersal from Africa. ''Proc Natl Acad Sci U S A''. 2018 Apr 17; '''115''' (16):4128-4133
Association and cis-mQTL analysis of variants in CHRNA3-A5, CHRNA7, CHRNB2, and CHRNB4 in relation to nicotine dependence in a Chinese Han population. Description: Liu, Qiang, et al. Association and cis-mQTL analysis of variants in CHRNA3-A5, CHRNA7, CHRNB2, and CHRNB4 in relation to nicotine dependence in a Chinese Han population. ''Transl Psychiatry''. 2018 Apr 18; '''8''' (1):83
Founder-specific inbreeding depression affects racing performance in Thoroughbred horses. Description: Todd, Evelyn T, et al. Founder-specific inbreeding depression affects racing performance in Thoroughbred horses. ''Sci Rep''. 2018 Apr 18; '''8''' (1):6167
Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records. Description: Chen, Chia-Yen, et al. Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records. ''Transl Psychiatry''. 2018 Apr 18; '''8''' (1):86
The NRP1 migraine risk variant shows evidence of association with menstrual migraine. Description: Pollock, Charmaine E, et al. The NRP1 migraine risk variant shows evidence of association with menstrual migraine. ''J Headache Pain''. 2018 Apr 18; '''19''' (1):31
Haplotype analysis of APOE intragenic SNPs. Description: Babenko, Vladimir N, et al. Haplotype analysis of APOE intragenic SNPs. ''BMC Neurosci''. 2018 Apr 19; '''19''' (Suppl 1):16
WISARD: workbench for integrated superfast association studies for related datasets. Description: Lee, Sungyoung, et al. WISARD: workbench for integrated superfast association studies for related datasets. ''BMC Med Genomics''. 2018 Apr 20; '''11''' (Suppl 2):39
An epistatic effect of KRT25 on SP6 is involved in curly coat in horses. Description: Thomer, Annika, et al. An epistatic effect of KRT25 on SP6 is involved in curly coat in horses. ''Sci Rep''. 2018 Apr 23; '''8''' (1):6374
Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease. Description: Emdin, Connor A, et al. Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease. ''Nat Commun''. 2018 Apr 24; '''9''' (1):1613
Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study. Description: DeBoever, Christopher, et al. Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study. ''Nat Commun''. 2018 Apr 24; '''9''' (1):1612
Association of VAMP5 and MCC genetic polymorphisms with increased risk of Hirschsprung disease susceptibility in Southern Chinese children. Description: Zhao, Jinglu, et al. Association of VAMP5 and MCC genetic polymorphisms with increased risk of Hirschsprung disease susceptibility in Southern Chinese children. ''Aging (Albany NY)''. 2018 Apr 25; '''10''' (4):689-700
Identification of genomic regions and candidate genes for chicken meat ultimate pH by combined detection of selection signatures and QTL. Description: Bihan-Duval, Elisabeth Le, et al. Identification of genomic regions and candidate genes for chicken meat ultimate pH by combined detection of selection signatures and QTL. ''BMC Genomics''. 2018 Apr 25; '''19''' (1):294
Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes. Description: Charmet, Romain, et al. Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes. ''Cardiovasc Diabetol''. 2018 Apr 25; '''17''' (1):61
Bayesian nonparametric discovery of isoforms and individual specific quantification. Description: Aguiar, Derek, et al. Bayesian nonparametric discovery of isoforms and individual specific quantification. ''Nat Commun''. 2018 Apr 27; '''9''' (1):1681
A Bayesian Framework for Generalized Linear Mixed Modeling Identifies New Candidate Loci for Late-Onset Alzheimer's Disease. Description: Wang, Xulong, et al. A Bayesian Framework for Generalized Linear Mixed Modeling Identifies New Candidate Loci for Late-Onset Alzheimer's Disease. ''Genetics''. 2018 May; '''209''' (1):51-64
A potential regulatory region near the EDN3 gene may control both harness racing performance and coat color variation in horses. Description: Jaderkvist Fegraeus, Kim, et al. A potential regulatory region near the EDN3 gene may control both harness racing performance and coat color variation in horses. ''Physiol Rep''. 2018 May; '''6''' (10):e13700
Association between LCE gene polymorphisms and psoriasis vulgaris among Mongolians from Inner Mongolia. Description: Sun, Li, et al. Association between LCE gene polymorphisms and psoriasis vulgaris among Mongolians from Inner Mongolia. ''Arch Dermatol Res''. 2018 May; '''310''' (4):321-327
Autism spectrum disorders and autistic traits share genetics and biology. Description: Bralten, J, et al. Autism spectrum disorders and autistic traits share genetics and biology. ''Mol Psychiatry''. 2018 May; '''23''' (5):1205-1212
Clinical, Social, and Genetic Factors Associated with Obesity at 12 Months of Age. Description: Hazrati, Sahel, et al. Clinical, Social, and Genetic Factors Associated with Obesity at 12 Months of Age. ''J Pediatr''. 2018 May; '''196''': 175-181.e7
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. Description: Heinzen, Erin L, et al. De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. ''PLoS Genet''. 2018 May; '''14''' (5):e1007281
DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus. Description: Imgenberg-Kreuz, Juliana, et al. DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus. ''Ann Rheum Dis''. 2018 May; '''77''' (5):736-743
Effects of UGT2B7, SCN1A and CYP3A4 on the therapeutic response of sodium valproate treatment in children with generalized seizures. Description: Feng, Weixing, et al. Effects of UGT2B7, SCN1A and CYP3A4 on the therapeutic response of sodium valproate treatment in children with generalized seizures. ''Seizure''. 2018 May; '''58''': 96-100
EFhd2/Swiprosin-1 is a common genetic determinator for sensation-seeking/low anxiety and alcohol addiction. Description: Mielenz, D, et al. EFhd2/Swiprosin-1 is a common genetic determinator for sensation-seeking/low anxiety and alcohol addiction. ''Mol Psychiatry''. 2018 May; '''23''' (5):1303-1319
Evaluating the genetic susceptibility to peer reported bullying behaviors. Description: Musci, Rashelle J, et al. Evaluating the genetic susceptibility to peer reported bullying behaviors. ''Psychiatry Res''. 2018 May; '''263''': 193-198
Evidence of evolutionary history and selective sweeps in the genome of Meishan pig reveals its genetic and phenotypic characterization. Description: Zhao, Pengju, et al. Evidence of evolutionary history and selective sweeps in the genome of Meishan pig reveals its genetic and phenotypic characterization. ''Gigascience''. 2018 May 1; '''7''' (5):
Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. Description: Fan, Bao Jian, et al. Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. ''Invest Ophthalmol Vis Sci''. 2018 May 1; '''59''' (6):2495-2502
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. Description: Painter, Jodie N, et al. Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. ''Cancer Med''. 2018 May; '''7''' (5):1978-1987
Genetics and Crime: Integrating New Genomic Discoveries Into Psychological Research About Antisocial Behavior. Description: Wertz, J, et al. Genetics and Crime: Integrating New Genomic Discoveries Into Psychological Research About Antisocial Behavior. ''Psychol Sci''. 2018 May; '''29''' (5):791-803
Genetic variant repressing ADH1A expression confers susceptibility to esophageal squamous-cell carcinoma. Description: Cui, Qionghua, et al. Genetic variant repressing ADH1A expression confers susceptibility to esophageal squamous-cell carcinoma. ''Cancer Lett''. 2018 May 1; '''421''': 43-50
Genome-wide association study identifies a novel locus for cannabis dependence. Description: Agrawal, A, et al. Genome-wide association study identifies a novel locus for cannabis dependence. ''Mol Psychiatry''. 2018 May; '''23''' (5):1293-1302
Genomic Response to Vitamin D Supplementation in the Setting of a Randomized, Placebo-Controlled Trial. Description: Berlanga-Taylor, Antonio J, et al. Genomic Response to Vitamin D Supplementation in the Setting of a Randomized, Placebo-Controlled Trial. ''EBioMedicine''. 2018 May; '''31''': 133-142
Genomic variation in 3,010 diverse accessions of Asian cultivated rice. Description: Wang, Wensheng, et al. Genomic variation in 3,010 diverse accessions of Asian cultivated rice. ''Nature''. 2018 May; '''557''' (7703):43-49
Height and overall cancer risk and mortality: evidence from a Mendelian randomisation study on 310,000 UK Biobank participants. Description: Ong, Jue-Sheng, et al. Height and overall cancer risk and mortality: evidence from a Mendelian randomisation study on 310,000 UK Biobank participants. ''Br J Cancer''. 2018 May; '''118''' (9):1262-1267
Insights into Platypus Population Structure and History from Whole-Genome Sequencing. Description: Martin, Hilary C, et al. Insights into Platypus Population Structure and History from Whole-Genome Sequencing. ''Mol Biol Evol''. 2018 May 1; '''35''' (5):1238-1252
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. Description: Rivas, Manuel A, et al. Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. ''PLoS Genet''. 2018 May; '''14''' (5):e1007329
Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density. Description: Pei, Yu-Fang, et al. Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density. ''Bone''. 2018 May; '''110''': 378-385
Parallel altitudinal clines reveal trends in adaptive evolution of genome size in Zea mays. Description: Bilinski, Paul, et al. Parallel altitudinal clines reveal trends in adaptive evolution of genome size in Zea mays. ''PLoS Genet''. 2018 May; '''14''' (5):e1007162
Population genomic data reveal genes related to important traits of quail. Description: Wu, Yan, et al. Population genomic data reveal genes related to important traits of quail. ''Gigascience''. 2018 May 1; '''7''' (5):
Population-specific genetic modification of Huntington's disease in Venezuela. Description: Chao, Michael J, et al. Population-specific genetic modification of Huntington's disease in Venezuela. ''PLoS Genet''. 2018 May; '''14''' (5):e1007274
Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus. Description: Wadelius, Mia, et al. Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus. ''Clin Pharmacol Ther''. 2018 May; '''103''' (5):843-853
Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8. Description: Jilling, Tamas, et al. Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8. ''Pediatr Res''. 2018 May; '''83''' (5):943-953
Ventral striatal regulation of CREM mediates impulsive action and drug addiction vulnerability. Description: Miller, M L, et al. Ventral striatal regulation of CREM mediates impulsive action and drug addiction vulnerability. ''Mol Psychiatry''. 2018 May; '''23''' (5):1328-1335
Complex patterns of response to oral hygiene instructions: longitudinal evaluation of periodontal patients. Description: Amoo-Achampong, Felice, et al. Complex patterns of response to oral hygiene instructions: longitudinal evaluation of periodontal patients. ''BMC Oral Health''. 2018 May 2; '''18''' (1):72
Effect of smoking on the association of HHEX (rs5015480) with diabetes among Korean women and heavy smoking men. Description: Sull, Jae Woong, et al. Effect of smoking on the association of HHEX (rs5015480) with diabetes among Korean women and heavy smoking men. ''BMC Med Genet''. 2018 May 2; '''19''' (1):68
Genome-wide scan reveals population stratification and footprints of recent selection in Nelore cattle. Description: Cardoso, Diercles F, et al. Genome-wide scan reveals population stratification and footprints of recent selection in Nelore cattle. ''Genet Sel Evol''. 2018 May 2; '''50''' (1):22
Plasmepsin II-III copy number accounts for bimodal piperaquine resistance among Cambodian Plasmodium falciparum. Description: Bopp, Selina, et al. Plasmepsin II-III copy number accounts for bimodal piperaquine resistance among Cambodian Plasmodium falciparum. ''Nat Commun''. 2018 May 2; '''9''' (1):1769
CCDC102B confers risk of low vision and blindness in high myopia. Description: Hosoda, Yoshikatsu, et al. CCDC102B confers risk of low vision and blindness in high myopia. ''Nat Commun''. 2018 May 3; '''9''' (1):1782
Gene-based analysis of genes related to neurotrophic pathway suggests association of BDNF and VEGFA with antidepressant treatment-response in depressed patients. Description: Kao, Chung-Feng, et al. Gene-based analysis of genes related to neurotrophic pathway suggests association of BDNF and VEGFA with antidepressant treatment-response in depressed patients. ''Sci Rep''. 2018 May 3; '''8''' (1):6983
Whole Exome Sequencing Identifies New Host Genomic Susceptibility Factors in Empyema Caused by Streptococcus pneumoniae in Children: A Pilot Study. Description: Salas, Antonio, et al. Whole Exome Sequencing Identifies New Host Genomic Susceptibility Factors in Empyema Caused by Streptococcus pneumoniae in Children: A Pilot Study. ''Genes (Basel)''. 2018 May 3; '''9''' (5):
Applications and efficiencies of the first cat 63K DNA array. Description: Gandolfi, Barbara, et al. Applications and efficiencies of the first cat 63K DNA array. ''Sci Rep''. 2018 May 4; '''8''' (1):7024
Evaluating the association between calpastatin (CAST) gene and keratoconus in the Han Chinese population. Description: Zhang, Jing, et al. Evaluating the association between calpastatin (CAST) gene and keratoconus in the Han Chinese population. ''Gene''. 2018 May 5; '''653''': 10-13
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Description: Barbeira, Alvaro N, et al. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. ''Nat Commun''. 2018 May 8; '''9''' (1):1825
Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy. Description: Graham, Patricia S, et al. Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy. ''BMC Med Genet''. 2018 May 8; '''19''' (1):71
Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. Description: Visconti, Alessia, et al. Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. ''Nat Commun''. 2018 May 8; '''9''' (1):1684
Hybridization and gene flow in the mega-pest lineage of moth, Helicoverpa. Description: Anderson, Craig J, et al. Hybridization and gene flow in the mega-pest lineage of moth, Helicoverpa. ''Proc Natl Acad Sci U S A''. 2018 May 8; '''115''' (19):5034-5039
The polymorphism rs6918289 located in the downstream region of the TREM2 gene is associated with TNF-alpha levels and IMT-F. Description: Gorenjak, Vesna, et al. The polymorphism rs6918289 located in the downstream region of the TREM2 gene is associated with TNF-alpha levels and IMT-F. ''Sci Rep''. 2018 May 8; '''8''' (1):7160
Genome-wide association study identifies two loci influencing plasma neurofilament light levels. Description: Li, Jie-Qiong, et al. Genome-wide association study identifies two loci influencing plasma neurofilament light levels. ''BMC Med Genomics''. 2018 May 10; '''11''' (1):47
Genome-wide association study identified ATP6V1H locus influencing cerebrospinal fluid BACE activity. Description: Hu, Hao, et al. Genome-wide association study identified ATP6V1H locus influencing cerebrospinal fluid BACE activity. ''BMC Med Genet''. 2018 May 11; '''19''' (1):75
Association of Genetic Variation in the Epithelial Sodium Channel Gene with Urinary Sodium Excretion and Blood Pressure. Description: Yang, Yoon Jung, et al. Association of Genetic Variation in the Epithelial Sodium Channel Gene with Urinary Sodium Excretion and Blood Pressure. ''Nutrients''. 2018 May 14; '''10''' (5):
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Description: Iglesias, Adriana I, et al. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. ''Nat Commun''. 2018 May 14; '''9''' (1):1864
Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy. Description: Lacey, Cameron J, et al. Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy. ''Sci Rep''. 2018 May 15; '''8''' (1):7548
Genetic Polymorphisms of PNPLA3 and SAMM50 Are Associated with Nonalcoholic Fatty Liver Disease in a Korean Population. Description: Chung, Goh Eun, et al. Genetic Polymorphisms of PNPLA3 and SAMM50 Are Associated with Nonalcoholic Fatty Liver Disease in a Korean Population. ''Gut Liver''. 2018 May 15; '''12''' (3):316-323
Genome-wide significant risk factors on chromosome 19 and the APOE locus. Description: Moreno-Grau, Sonia, et al. Genome-wide significant risk factors on chromosome 19 and the APOE locus. ''Oncotarget''. 2018 May 15; '''9''' (37):24590-24600
A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. Description: Estrada, Karol, et al. A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. ''Nat Commun''. 2018 May 16; '''9''' (1):1929
Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system. Description: Ramirez, Julia, et al. Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system. ''Nat Commun''. 2018 May 16; '''9''' (1):1947
Genome-wide detection of selection signatures in Chinese indigenous Laiwu pigs revealed candidate genes regulating fat deposition in muscle. Description: Chen, Minhui, et al. Genome-wide detection of selection signatures in Chinese indigenous Laiwu pigs revealed candidate genes regulating fat deposition in muscle. ''BMC Genet''. 2018 May 18; '''19''' (1):31
A genome-wide association study reveals novel genomic regions and positional candidate genes for fat deposition in broiler chickens. Description: Moreira, Gabriel Costa Monteiro, et al. A genome-wide association study reveals novel genomic regions and positional candidate genes for fat deposition in broiler chickens. ''BMC Genomics''. 2018 May 21; '''19''' (1):374
Genome-wide association study identified new susceptible genetic variants in HLA class I region for hepatitis B virus-related hepatocellular carcinoma. Description: Sawai, Hiromi, et al. Genome-wide association study identified new susceptible genetic variants in HLA class I region for hepatitis B virus-related hepatocellular carcinoma. ''Sci Rep''. 2018 May 21; '''8''' (1):7958
Brain APOE expression quantitative trait loci-based association study identified one susceptibility locus for Alzheimer's disease by interacting with APOE epsilon4. Description: Zhang, Aiqian, et al. Brain APOE expression quantitative trait loci-based association study identified one susceptibility locus for Alzheimer's disease by interacting with APOE epsilon4. ''Sci Rep''. 2018 May 23; '''8''' (1):8068
Genetic Association with Subgingival Bacterial Colonization in Chronic Periodontitis. Description: Cavalla, Franco, et al. Genetic Association with Subgingival Bacterial Colonization in Chronic Periodontitis. ''Genes (Basel)''. 2018 May 23; '''9''' (6):
High burden of birthweight-lowering genetic variants in Africans and Asians. Description: Tekola-Ayele, Fasil, et al. High burden of birthweight-lowering genetic variants in Africans and Asians. ''BMC Med''. 2018 May 24; '''16''' (1):70
Population structure and genetic diversity of 25 Russian sheep breeds based on whole-genome genotyping. Description: Deniskova, Tatiana E, et al. Population structure and genetic diversity of 25 Russian sheep breeds based on whole-genome genotyping. ''Genet Sel Evol''. 2018 May 24; '''50''' (1):29
Blood lipid-related low-frequency variants in LDLR and PCSK9 are associated with onset age and risk of myocardial infarction in Japanese. Description: Tajima, Tomoyuki, et al. Blood lipid-related low-frequency variants in LDLR and PCSK9 are associated with onset age and risk of myocardial infarction in Japanese. ''Sci Rep''. 2018 May 25; '''8''' (1):8107
Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus. Description: Gonzalez-Serna, David, et al. Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus. ''Sci Rep''. 2018 May 29; '''8''' (1):8195
Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden. Description: Eriksson, Daniel, et al. Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden. ''Sci Rep''. 2018 May 30; '''8''' (1):8395
Genome-wide association study meta-analysis identifies five new loci for systemic lupus erythematosus. Description: Julia, Antonio, et al. Genome-wide association study meta-analysis identifies five new loci for systemic lupus erythematosus. ''Arthritis Res Ther''. 2018 May 30; '''20''' (1):100
Signatures of balancing selection in toll-like receptor (TLRs) genes - novel insights from a free-living rodent. Description: Kloch, Agnieszka, et al. Signatures of balancing selection in toll-like receptor (TLRs) genes - novel insights from a free-living rodent. ''Sci Rep''. 2018 May 30; '''8''' (1):8361
Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Description: Hirata, Tetsuya, et al. Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. ''Sci Rep''. 2018 May 31; '''8''' (1):8502
A genome-wide association study of social genetic effects in Landrace pigs. Description: Hong, Joon Ki, et al. A genome-wide association study of social genetic effects in Landrace pigs. ''Asian-Australas J Anim Sci''. 2018 Jun; '''31''' (6):784-790
A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. Description: Zhu, Zhaozhong, et al. A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. ''Nat Genet''. 2018 Jun; '''50''' (6):857-864
Capturing variation in Lens (Fabaceae): Development and utility of an exome capture array for lentil. Description: Ogutcen, Ezgi, et al. Capturing variation in Lens (Fabaceae): Development and utility of an exome capture array for lentil. ''Appl Plant Sci''. 2018 Jun; '''6''' (7):e01165
Cholesteryl ester transfer protein gene variations and macronutrient intakes interaction in relation to metabolic syndrome: Tehran lipid and glucose study. Description: Esfandiar, Zohre, et al. Cholesteryl ester transfer protein gene variations and macronutrient intakes interaction in relation to metabolic syndrome: Tehran lipid and glucose study. ''Iran J Basic Med Sci''. 2018 Jun; '''21''' (6):586-592
Discovering variation of secondary metabolite diversity and its relationship with disease resistance in Cornus florida L. Description: Pais, Andrew L, et al. Discovering variation of secondary metabolite diversity and its relationship with disease resistance in Cornus florida L. ''Ecol Evol''. 2018 Jun; '''8''' (11):5619-5636
Effect of genetic architecture on the prediction accuracy of quantitative traits in samples of unrelated individuals. Description: Morgante, Fabio, et al. Effect of genetic architecture on the prediction accuracy of quantitative traits in samples of unrelated individuals. ''Heredity (Edinb)''. 2018 Jun; '''120''' (6):500-514
Elucidating Gene-by-Environment Interactions Associated with Differential Susceptibility to Chemical Exposure. Description: Balik-Meisner, Michele, et al. Elucidating Gene-by-Environment Interactions Associated with Differential Susceptibility to Chemical Exposure. ''Environ Health Perspect''. 2018 Jun; '''126''' (6):067010
Exploring the genetics of lesion and nodal resistance in pea (Pisum sativum L.) to Sclerotinia sclerotiorum using genome-wide association studies and RNA-Seq. Description: Chang, Hao-Xun, et al. Exploring the genetics of lesion and nodal resistance in pea (Pisum sativum L.) to Sclerotinia sclerotiorum using genome-wide association studies and RNA-Seq. ''Plant Direct''. 2018 Jun; '''2''' (6):e00064
Genetic ancestry and population differences in levels of inflammatory cytokines in women: Role for evolutionary selection and environmental factors. Description: Yao, Song, et al. Genetic ancestry and population differences in levels of inflammatory cytokines in women: Role for evolutionary selection and environmental factors. ''PLoS Genet''. 2018 Jun; '''14''' (6):e1007368
Genetic correlation of antisocial behaviour with alcohol, nicotine, and cannabis use. Description: Tielbeek, Jorim J, et al. Genetic correlation of antisocial behaviour with alcohol, nicotine, and cannabis use. ''Drug Alcohol Depend''. 2018 Jun 1; '''187''': 296-299
Genetic Variants Associated with Clinicopathological Profiles in Sporadic Breast Cancer in Sri Lankan Women. Description: Sirisena, Nirmala Dushyanthi, et al. Genetic Variants Associated with Clinicopathological Profiles in Sporadic Breast Cancer in Sri Lankan Women. ''J Breast Cancer''. 2018 Jun; '''21''' (2):165-172
Genome-wide analysis of adolescent psychotic-like experiences shows genetic overlap with psychiatric disorders. Description: Pain, Oliver, et al. Genome-wide analysis of adolescent psychotic-like experiences shows genetic overlap with psychiatric disorders. ''Am J Med Genet B Neuropsychiatr Genet''. 2018 Jun; '''177''' (4):416-425
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Description: Tedja, Milly S, et al. Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. ''Nat Genet''. 2018 Jun; '''50''' (6):834-848
Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men. Description: Sato, Youichi, et al. Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men. ''J Med Genet''. 2018 Jun; '''55''' (6):415-421
Genomic signatures of parasite-driven natural selection in north European Atlantic salmon (Salmo salar). Description: Zueva, Ksenia J, et al. Genomic signatures of parasite-driven natural selection in north European Atlantic salmon (Salmo salar). ''Mar Genomics''. 2018 Jun; '''39''': 26-38
Genotyping by sequencing reveals contrasting patterns of population structure, ecologically mediated divergence, and long-distance dispersal in North American palms. Description: Klimova, Anastasia, et al. Genotyping by sequencing reveals contrasting patterns of population structure, ecologically mediated divergence, and long-distance dispersal in North American palms. ''Ecol Evol''. 2018 Jun; '''8''' (11):5873-5890
Identification of LEF1 as a Susceptibility Locus for Kawasaki Disease in Patients Younger than 6 Months of Age. Description: Kim, Hea-Ji, et al. Identification of LEF1 as a Susceptibility Locus for Kawasaki Disease in Patients Younger than 6 Months of Age. ''Genomics Inform''. 2018 Jun; '''16''' (2):36-41
Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma. Description: Wang, Zhaoxi, et al. Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma. ''EBioMedicine''. 2018 Jun; '''32''': 93-101
Novel caries loci in children and adults implicated by genome-wide analysis of families. Description: Govil, Manika, et al. Novel caries loci in children and adults implicated by genome-wide analysis of families. ''BMC Oral Health''. 2018 Jun 1; '''18''' (1):98
Optimized distributed systems achieve significant performance improvement on sorted merging of massive VCF files. Description: Sun, Xiaobo, et al. Optimized distributed systems achieve significant performance improvement on sorted merging of massive VCF files. ''Gigascience''. 2018 Jun 1; '''7''' (6):
POLARIS: Polygenic LD-adjusted risk score approach for set-based analysis of GWAS data. Description: Baker, Emily, et al. POLARIS: Polygenic LD-adjusted risk score approach for set-based analysis of GWAS data. ''Genet Epidemiol''. 2018 Jun; '''42''' (4):366-377
Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic Stroke. Description: Xiong, Xin, et al. Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic Stroke. ''J Stroke Cerebrovasc Dis''. 2018 Jun; '''27''' (6):1683-1691
Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Description: Chibnik, L B, et al. Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. ''Mol Psychiatry''. 2018 Jun; '''23''' (6):1521-1529
Widespread, long-term admixture between grey wolves and domestic dogs across Eurasia and its implications for the conservation status of hybrids. Description: Pilot, Malgorzata, et al. Widespread, long-term admixture between grey wolves and domestic dogs across Eurasia and its implications for the conservation status of hybrids. ''Evol Appl''. 2018 Jun; '''11''' (5):662-680
A major locus controls local adaptation and adaptive life history variation in a perennial plant. Description: Wang, Jing, et al. A major locus controls local adaptation and adaptive life history variation in a perennial plant. ''Genome Biol''. 2018 Jun 4; '''19''' (1):72
A survey of microRNA single nucleotide polymorphisms identifies novel breast cancer susceptibility loci in a case-control, population-based study of African-American women. Description: Bensen, Jeannette T, et al. A survey of microRNA single nucleotide polymorphisms identifies novel breast cancer susceptibility loci in a case-control, population-based study of African-American women. ''Breast Cancer Res''. 2018 Jun 5; '''20''' (1):45
Collective interaction effects associated with mammalian behavioral traits reveal genetic factors connecting fear and hemostasis. Description: Woo, Hyung Jun, et al. Collective interaction effects associated with mammalian behavioral traits reveal genetic factors connecting fear and hemostasis. ''BMC Psychiatry''. 2018 Jun 5; '''18''' (1):175
The inference of gray whale (Eschrichtius robustus) historical population attributes from whole-genome sequences. Description: Bruniche-Olsen, Anna, et al. The inference of gray whale (Eschrichtius robustus) historical population attributes from whole-genome sequences. ''BMC Evol Biol''. 2018 Jun 7; '''18''' (1):87
Gene flow contributes to diversification of the major fungal pathogen Candida albicans. Description: Ropars, Jeanne, et al. Gene flow contributes to diversification of the major fungal pathogen Candida albicans. ''Nat Commun''. 2018 Jun 8; '''9''' (1):2253
Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer. Description: Reyes-Gibby, Cielito C, et al. Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer. ''Sci Rep''. 2018 Jun 8; '''8''' (1):8789
Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes. Description: Fan, Chun Chieh, et al. Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes. ''Transl Psychiatry''. 2018 Jun 8; '''8''' (1):114
A genome-wide scan for signatures of selection in Azeri and Khuzestani buffalo breeds. Description: Mokhber, Mahdi, et al. A genome-wide scan for signatures of selection in Azeri and Khuzestani buffalo breeds. ''BMC Genomics''. 2018 Jun 11; '''19''' (1):449
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. Description: Choquet, Helene, et al. A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. ''Nat Commun''. 2018 Jun 11; '''9''' (1):2278
Linkage disequilibrium in Brazilian Santa Ines breed, Ovis aries. Description: Alvarenga, Amanda Botelho, et al. Linkage disequilibrium in Brazilian Santa Ines breed, Ovis aries. ''Sci Rep''. 2018 Jun 11; '''8''' (1):8851
Modifier locus mapping of a transgenic F2 mouse population identifies CCDC115 as a novel aggressive prostate cancer modifier gene in humans. Description: Winter, Jean M, et al. Modifier locus mapping of a transgenic F2 mouse population identifies CCDC115 as a novel aggressive prostate cancer modifier gene in humans. ''BMC Genomics''. 2018 Jun 11; '''19''' (1):450
CFH and VIPR2 as susceptibility loci in choroidal thickness and pachychoroid disease central serous chorioretinopathy. Description: Hosoda, Yoshikatsu, et al. CFH and VIPR2 as susceptibility loci in choroidal thickness and pachychoroid disease central serous chorioretinopathy. ''Proc Natl Acad Sci U S A''. 2018 Jun 12; '''115''' (24):6261-6266
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. Description: Endo, Chihiro, et al. Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. ''Sci Rep''. 2018 Jun 12; '''8''' (1):8974
Dissection of complicate genetic architecture and breeding perspective of cottonseed traits by genome-wide association study. Description: Du, Xiongming, et al. Dissection of complicate genetic architecture and breeding perspective of cottonseed traits by genome-wide association study. ''BMC Genomics''. 2018 Jun 13; '''19''' (1):451
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. Description: Gusarova, Viktoria, et al. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. ''Nat Commun''. 2018 Jun 13; '''9''' (1):2252
Resurrecting Darwin's Niata - anatomical, biomechanical, genetic, and morphometric studies of morphological novelty in cattle. Description: Veitschegger, Kristof, et al. Resurrecting Darwin's Niata - anatomical, biomechanical, genetic, and morphometric studies of morphological novelty in cattle. ''Sci Rep''. 2018 Jun 14; '''8''' (1):9129
Whole-genome resequencing reveals world-wide ancestry and adaptive introgression events of domesticated cattle in East Asia. Description: Chen, Ningbo, et al. Whole-genome resequencing reveals world-wide ancestry and adaptive introgression events of domesticated cattle in East Asia. ''Nat Commun''. 2018 Jun 14; '''9''' (1):2337
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Description: Martin, Joanna, et al. A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. ''Biol Psychiatry''. 2018 Jun 15; '''83''' (12):1044-1053
NAFLD risk alleles in PNPLA3, TM6SF2, GCKR and LYPLAL1 show divergent metabolic effects. Description: Sliz, Eeva, et al. NAFLD risk alleles in PNPLA3, TM6SF2, GCKR and LYPLAL1 show divergent metabolic effects. ''Hum Mol Genet''. 2018 Jun 15; '''27''' (12):2214-2223
Associations between hypertension and the peroxisome proliferator-activated receptor-delta (PPARD) gene rs7770619 C>T polymorphism in a Korean population. Description: Kim, Minjoo, et al. Associations between hypertension and the peroxisome proliferator-activated receptor-delta (PPARD) gene rs7770619 C>T polymorphism in a Korean population. ''Hum Genomics''. 2018 Jun 18; '''12''' (1):28
Value of multilocus genetic risk score for atrial fibrillation in end-stage kidney disease patients in a Polish population. Description: Saracyn, Marek, et al. Value of multilocus genetic risk score for atrial fibrillation in end-stage kidney disease patients in a Polish population. ''Sci Rep''. 2018 Jun 18; '''8''' (1):9284
*DNA methylation as a mediator of HLA-DRB115:01 and a protective variant in multiple sclerosis.** Description: Kular, Lara, et al. DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis. ''Nat Commun''. 2018 Jun 19; '''9''' (1):2397
Genome-wide mapping of quantitative trait loci in admixed populations using mixed linear model and Bayesian multiple regression analysis. Description: Toosi, Ali, et al. Genome-wide mapping of quantitative trait loci in admixed populations using mixed linear model and Bayesian multiple regression analysis. ''Genet Sel Evol''. 2018 Jun 19; '''50''' (1):32
Identification of five novel genetic loci related to facial morphology by genome-wide association studies. Description: Cha, Seongwon, et al. Identification of five novel genetic loci related to facial morphology by genome-wide association studies. ''BMC Genomics''. 2018 Jun 19; '''19''' (1):481
Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies. Description: Sa, Ana Caroline C, et al. Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies. ''BMC Med Genomics''. 2018 Jun 20; '''11''' (1):55
Genetic Diversity of Cryptosporidium hominis in a Bangladeshi Community as Revealed by Whole-Genome Sequencing. Description: Gilchrist, Carol A, et al. Genetic Diversity of Cryptosporidium hominis in a Bangladeshi Community as Revealed by Whole-Genome Sequencing. ''J Infect Dis''. 2018 Jun 20; '''218''' (2):259-264
Genetic interaction effects reveal lipid-metabolic and inflammatory pathways underlying common metabolic disease risks. Description: Woo, Hyung Jun, et al. Genetic interaction effects reveal lipid-metabolic and inflammatory pathways underlying common metabolic disease risks. ''BMC Med Genomics''. 2018 Jun 20; '''11''' (1):54
Population genomics provide insights into the evolution and adaptation of the eastern honey bee (Apis cerana). Description: Chen, Chao, et al. Population genomics provide insights into the evolution and adaptation of the eastern honey bee (Apis cerana). ''Mol Biol Evol''. 2018 Jun 20;
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes. Description: Momozawa, Yukihide, et al. IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes. ''Nat Commun''. 2018 Jun 21; '''9''' (1):2427
High and Low Levels of an NTRK2-Driven Genetic Profile Affect Motor- and Cognition-Associated Frontal Gray Matter in Prodromal Huntington's Disease. Description: Ciarochi, Jennifer A, et al. High and Low Levels of an NTRK2-Driven Genetic Profile Affect Motor- and Cognition-Associated Frontal Gray Matter in Prodromal Huntington's Disease. ''Brain Sci''. 2018 Jun 22; '''8''' (7):
The contribution of common genetic risk variants for ADHD to a general factor of childhood psychopathology. Description: Brikell, Isabell, et al. The contribution of common genetic risk variants for ADHD to a general factor of childhood psychopathology. ''Mol Psychiatry''. 2018 Jun 22;
A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework. Description: LeBlanc, Marissa, et al. A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework. ''BMC Genomics''. 2018 Jun 25; '''19''' (1):494
Common variants in the GNL3 contribute to the increasing risk of knee osteoarthritis in Han Chinese population. Description: Liu, Bo, et al. Common variants in the GNL3 contribute to the increasing risk of knee osteoarthritis in Han Chinese population. ''Sci Rep''. 2018 Jun 25; '''8''' (1):9610
Genome data uncover four synergistic key regulators for extremely small body size in horses. Description: Metzger, Julia, et al. Genome data uncover four synergistic key regulators for extremely small body size in horses. ''BMC Genomics''. 2018 Jun 25; '''19''' (1):492
Conservation status and historical relatedness of Italian cattle breeds. Description: Mastrangelo, Salvatore, et al. Conservation status and historical relatedness of Italian cattle breeds. ''Genet Sel Evol''. 2018 Jun 26; '''50''' (1):35
Multivariate genome-wide association analysis identifies novel and relevant variants associated with anterior cruciate ligament rupture risk in the dog model. Description: Baker, Lauren A, et al. Multivariate genome-wide association analysis identifies novel and relevant variants associated with anterior cruciate ligament rupture risk in the dog model. ''BMC Genet''. 2018 Jun 26; '''19''' (1):39
SNPrune: an efficient algorithm to prune large SNP array and sequence datasets based on high linkage disequilibrium. Description: Calus, Mario P L, et al. SNPrune: an efficient algorithm to prune large SNP array and sequence datasets based on high linkage disequilibrium. ''Genet Sel Evol''. 2018 Jun 26; '''50''' (1):34
Disease-specific regulation of gene expression in a comparative analysis of juvenile idiopathic arthritis and inflammatory bowel disease. Description: Mo, Angela, et al. Disease-specific regulation of gene expression in a comparative analysis of juvenile idiopathic arthritis and inflammatory bowel disease. ''Genome Med''. 2018 Jun 27; '''10''' (1):48
Identification of putative regulatory regions and transcription factors associated with intramuscular fat content traits. Description: Cesar, Aline S M, et al. Identification of putative regulatory regions and transcription factors associated with intramuscular fat content traits. ''BMC Genomics''. 2018 Jun 27; '''19''' (1):499
Comparison of village dog and wolf genomes highlights the role of the neural crest in dog domestication. Description: Pendleton, Amanda L, et al. Comparison of village dog and wolf genomes highlights the role of the neural crest in dog domestication. ''BMC Biol''. 2018 Jun 28; '''16''' (1):64
Single SNP- and pathway-based genome-wide association studies for beak deformity in chickens using high-density 600K SNP arrays. Description: Bai, Hao, et al. Single SNP- and pathway-based genome-wide association studies for beak deformity in chickens using high-density 600K SNP arrays. ''BMC Genomics''. 2018 Jun 28; '''19''' (1):501
The intragenic epistatic association of ADD3 with biliary atresia in Southern Han Chinese population. Description: Wang, Zhe, et al. The intragenic epistatic association of ADD3 with biliary atresia in Southern Han Chinese population. ''Biosci Rep''. 2018 Jun 29; '''38''' (3):
Interactions between ALDH2 rs671 polymorphism and lifestyle behaviors on coronary artery disease risk in a Chinese Han population with dyslipidemia: A guide to targeted heart health management. Description: Huang, Liu, et al. Interactions between ALDH2 rs671 polymorphism and lifestyle behaviors on coronary artery disease risk in a Chinese Han population with dyslipidemia: A guide to targeted heart health management. ''Environ Health Prev Med''. 2018 Jun 30; '''23''' (1):29
Association of copy number variation across the genome with neuropsychiatric traits in the general population. Description: Guyatt, Anna L, et al. Association of copy number variation across the genome with neuropsychiatric traits in the general population. ''Am J Med Genet B Neuropsychiatr Genet''. 2018 Jul; '''177''' (5):489-502
Association of MCP-1 rs1024611 polymorphism with diabetic foot ulcers. Description: Su, Na, et al. Association of MCP-1 rs1024611 polymorphism with diabetic foot ulcers. ''Medicine (Baltimore)''. 2018 Jul; '''97''' (28):e11232
Associations of Y chromosomal haplogroups with cardiometabolic risk factors and subclinical vascular measures in males during childhood and adolescence. Description: O'Keeffe, Linda M, et al. Associations of Y chromosomal haplogroups with cardiometabolic risk factors and subclinical vascular measures in males during childhood and adolescence. ''Atherosclerosis''. 2018 Jul; '''274''': 94-103
Causal association of body mass index with hypertension using a Mendelian randomization design. Description: Lee, Mee-Ri, et al. Causal association of body mass index with hypertension using a Mendelian randomization design. ''Medicine (Baltimore)''. 2018 Jul; '''97''' (30):e11252
Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use. Description: Marees, Andries T, et al. Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use. ''Drug Alcohol Depend''. 2018 Jul 1; '''188''': 94-101
Genetic Risk Score Is Associated With Prevalence of Advanced Neoplasms in a Colorectal Cancer Screening Population. Description: Weigl, Korbinian, et al. Genetic Risk Score Is Associated With Prevalence of Advanced Neoplasms in a Colorectal Cancer Screening Population. ''Gastroenterology''. 2018 Jul; '''155''' (1):88-98.e10
Genetic study of multimodal imaging Alzheimer's disease progression score implicates novel loci. Description: Scelsi, Marzia A, et al. Genetic study of multimodal imaging Alzheimer's disease progression score implicates novel loci. ''Brain''. 2018 Jul 1; '''141''' (7):2167-2180
Genomewide evidence of environmentally mediated secondary contact of European green crab (Carcinus maenas) lineages in eastern North America. Description: Jeffery, Nicholas W, et al. Genomewide evidence of environmentally mediated secondary contact of European green crab (Carcinus maenas) lineages in eastern North America. ''Evol Appl''. 2018 Jul; '''11''' (6):869-882
Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses. Description: Bakker, Olivier B, et al. Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses. ''Nat Immunol''. 2018 Jul; '''19''' (7):776-786
Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits. Description: Hormozdiari, Farhad, et al. Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits. ''Nat Genet''. 2018 Jul; '''50''' (7):1041-1047
Melatonin receptor type 1A gene linked to Alzheimer's disease in old age. Description: Sulkava, Sonja, et al. Melatonin receptor type 1A gene linked to Alzheimer's disease in old age. ''Sleep''. 2018 Jul 1; '''41''' (7):
Polygenic risk score of SERPINA6/SERPINA1 associates with diurnal and stress-induced HPA axis activity in children. Description: Utge, Siddheshwar, et al. Polygenic risk score of SERPINA6/SERPINA1 associates with diurnal and stress-induced HPA axis activity in children. ''Psychoneuroendocrinology''. 2018 Jul; '''93''': 1-7
Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease. Description: Mijuskovic, Martina, et al. Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease. ''Br J Cancer''. 2018 Jul; '''119''' (1):96-104
Relationships between estimated autozygosity and complex traits in the UK Biobank. Description: Johnson, Emma C, et al. Relationships between estimated autozygosity and complex traits in the UK Biobank. ''PLoS Genet''. 2018 Jul; '''14''' (7):e1007556
Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. Description: Gamazon, Eric R, et al. Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. ''Nat Genet''. 2018 Jul; '''50''' (7):956-967
A High-Resolution Genetic Map for the Laboratory Rat. Description: Littrell, John, et al. A High-Resolution Genetic Map for the Laboratory Rat. ''G3 (Bethesda)''. 2018 Jul 2; '''8''' (7):2241-2248
Genetic variants in systemic lupus erythematosus susceptibility loci, XKR6 and GLT1D1 are associated with childhood-onset SLE in a Korean cohort. Description: Joo, Young Bin, et al. Genetic variants in systemic lupus erythematosus susceptibility loci, XKR6 and GLT1D1 are associated with childhood-onset SLE in a Korean cohort. ''Sci Rep''. 2018 Jul 2; '''8''' (1):9962
Cardiolipin Synthesis in Brown and Beige Fat Mitochondria Is Essential for Systemic Energy Homeostasis. Description: Sustarsic, Elahu G, et al. Cardiolipin Synthesis in Brown and Beige Fat Mitochondria Is Essential for Systemic Energy Homeostasis. ''Cell Metab''. 2018 Jul 3; '''28''' (1):159-174.e11
GSTP1 rs1695 is associated with both hematological toxicity and prognosis of ovarian cancer treated with paclitaxel plus carboplatin combination chemotherapy: a comprehensive analysis using targeted resequencing of 100 pharmacogenes. Description: Yoshihama, Tomoko, et al. GSTP1 rs1695 is associated with both hematological toxicity and prognosis of ovarian cancer treated with paclitaxel plus carboplatin combination chemotherapy: a comprehensive analysis using targeted resequencing of 100 pharmacogenes. ''Oncotarget''. 2018 Jul 3; '''9''' (51):29789-29800
TMEM106B haplotypes have distinct gene expression patterns in aged brain. Description: Ren, Yingxue, et al. TMEM106B haplotypes have distinct gene expression patterns in aged brain. ''Mol Neurodegener''. 2018 Jul 3; '''13''' (1):35
Genome-wide association study of nocturnal blood pressure dipping in hypertensive patients. Description: Rimpela, Jenni M, et al. Genome-wide association study of nocturnal blood pressure dipping in hypertensive patients. ''BMC Med Genet''. 2018 Jul 4; '''19''' (1):110
Age at first birth in women is genetically associated with increased risk of schizophrenia. Description: Ni, Guiyan, et al. Age at first birth in women is genetically associated with increased risk of schizophrenia. ''Sci Rep''. 2018 Jul 5; '''8''' (1):10168
Mediation analysis to understand genetic relationships between habitual coffee intake and gout. Description: Hutton, Joseph, et al. Mediation analysis to understand genetic relationships between habitual coffee intake and gout. ''Arthritis Res Ther''. 2018 Jul 5; '''20''' (1):135
Aedes aegypti in the Black Sea: recent introduction or ancient remnant? Description: Kotsakiozi, Panayiota, et al. Aedes aegypti in the Black Sea: recent introduction or ancient remnant? ''Parasit Vectors''. 2018 Jul 6; '''11''' (1):396
TLR10 and NFKBIA contributed to the risk of hip osteoarthritis: systematic evaluation based on Han Chinese population. Description: Tang, Hongtao, et al. TLR10 and NFKBIA contributed to the risk of hip osteoarthritis: systematic evaluation based on Han Chinese population. ''Sci Rep''. 2018 Jul 6; '''8''' (1):10243
A vascular endothelial growth factor receptor gene variant is associated with susceptibility to acute respiratory distress syndrome. Description: Hernandez-Pacheco, Natalia, et al. A vascular endothelial growth factor receptor gene variant is associated with susceptibility to acute respiratory distress syndrome. ''Intensive Care Med Exp''. 2018 Jul 9; '''6''' (1):16
High-density Genotyping reveals Genomic Characterization, Population Structure and Genetic Diversity of Indian Mithun (Bos frontalis). Description: Mukherjee, Anupama, et al. High-density Genotyping reveals Genomic Characterization, Population Structure and Genetic Diversity of Indian Mithun (Bos frontalis). ''Sci Rep''. 2018 Jul 9; '''8''' (1):10316
Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci. Description: Sanchez-Contreras, Monica Y, et al. Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci. ''Mol Neurodegener''. 2018 Jul 9; '''13''' (1):37
Stepwise approach to SNP-set analysis illustrated with the Metabochip and colorectal cancer in Japanese Americans of the Multiethnic Cohort. Description: Cologne, John, et al. Stepwise approach to SNP-set analysis illustrated with the Metabochip and colorectal cancer in Japanese Americans of the Multiethnic Cohort. ''BMC Genomics''. 2018 Jul 9; '''19''' (1):524
A promoter interaction map for cardiovascular disease genetics. Description: Montefiori, Lindsey E, et al. A promoter interaction map for cardiovascular disease genetics. ''Elife''. 2018 Jul 10; '''7''':
Whole-genome sequencing reveals selection signatures associated with important traits in six goat breeds. Description: Guo, Jiazhong, et al. Whole-genome sequencing reveals selection signatures associated with important traits in six goat breeds. ''Sci Rep''. 2018 Jul 10; '''8''' (1):10405
Whole-genome SNP analysis elucidates the genetic structure of Russian cattle and its relationship with Eurasian taurine breeds. Description: Sermyagin, Alexander A, et al. Whole-genome SNP analysis elucidates the genetic structure of Russian cattle and its relationship with Eurasian taurine breeds. ''Genet Sel Evol''. 2018 Jul 11; '''50''' (1):37
The origin and adaptive evolution of domesticated populations of yeast from Far East Asia. Description: Duan, Shou-Fu, et al. The origin and adaptive evolution of domesticated populations of yeast from Far East Asia. ''Nat Commun''. 2018 Jul 12; '''9''' (1):2690
Association between DSCAM polymorphisms and non-syndromic Hirschsprung disease in Chinese population. Description: Wang, Yong, et al. Association between DSCAM polymorphisms and non-syndromic Hirschsprung disease in Chinese population. ''BMC Med Genet''. 2018 Jul 13; '''19''' (1):116
Downregulation of plasma SELENBP1 protein in patients with recent-onset schizophrenia. Description: Chau, Edith J, et al. Downregulation of plasma SELENBP1 protein in patients with recent-onset schizophrenia. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2018 Jul 13; '''85''': 1-6
The DNA-polymorphism rs849142 is associated with skin toxicity induced by targeted anti-EGFR therapy using cetuximab. Description: Froelich, Matthias F, et al. The DNA-polymorphism rs849142 is associated with skin toxicity induced by targeted anti-EGFR therapy using cetuximab. ''Oncotarget''. 2018 Jul 13; '''9''' (54):30279-30288
The major depressive disorder GWAS-supported variant rs10514299 in TMEM161B-MEF2C predicts putamen activation during reward processing in alcohol dependence. Description: Muench, Christine, et al. The major depressive disorder GWAS-supported variant rs10514299 in TMEM161B-MEF2C predicts putamen activation during reward processing in alcohol dependence. ''Transl Psychiatry''. 2018 Jul 13; '''8''' (1):131
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium. Description: Peyrot, Wouter J, et al. Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium. ''Biol Psychiatry''. 2018 Jul 15; '''84''' (2):138-147
Replication in Imaging Genetics: The Case of Threat-Related Amygdala Reactivity. Description: Avinun, Reut, et al. Replication in Imaging Genetics: The Case of Threat-Related Amygdala Reactivity. ''Biol Psychiatry''. 2018 Jul 15; '''84''' (2):148-159
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Description: Prins, Bram P, et al. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. ''Genome Biol''. 2018 Jul 17; '''19''' (1):87
Genetic variations for egg quality of chickens at late laying period revealed by genome-wide association study. Description: Liu, Zhuang, et al. Genetic variations for egg quality of chickens at late laying period revealed by genome-wide association study. ''Sci Rep''. 2018 Jul 17; '''8''' (1):10832
Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA. Description: Yokoyama, Maho, et al. Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA. ''Genome Biol''. 2018 Jul 18; '''19''' (1):94
Arylsulphatase A Pseudodeficiency (ARSA-PD), hypertension and chronic renal disease in Aboriginal Australians. Description: Tang, Dave, et al. Arylsulphatase A Pseudodeficiency (ARSA-PD), hypertension and chronic renal disease in Aboriginal Australians. ''Sci Rep''. 2018 Jul 19; '''8''' (1):10912
Common and rare variants of WNT16, DKK1 and SOST and their relationship with bone mineral density. Description: Martinez-Gil, Nuria, et al. Common and rare variants of WNT16, DKK1 and SOST and their relationship with bone mineral density. ''Sci Rep''. 2018 Jul 19; '''8''' (1):10951
Genetic variants in SEC16B are associated with body composition in black South Africans. Description: Sahibdeen, Venesa, et al. Genetic variants in SEC16B are associated with body composition in black South Africans. ''Nutr Diabetes''. 2018 Jul 19; '''8''' (1):43
Genetic diversity and selection signatures of the beef 'Charolais de Cuba' breed. Description: Rodriguez-Valera, Yoel, et al. Genetic diversity and selection signatures of the beef 'Charolais de Cuba' breed. ''Sci Rep''. 2018 Jul 20; '''8''' (1):11005
MDM4 contributes to the increased risk of glioma susceptibility in Han Chinese population. Description: Sun, Peng, et al. MDM4 contributes to the increased risk of glioma susceptibility in Han Chinese population. ''Sci Rep''. 2018 Jul 23; '''8''' (1):11093
The genetic architecture of socially-affected traits: a GWAS for direct and indirect genetic effects on survival time in laying hens showing cannibalism. Description: Brinker, Tessa, et al. The genetic architecture of socially-affected traits: a GWAS for direct and indirect genetic effects on survival time in laying hens showing cannibalism. ''Genet Sel Evol''. 2018 Jul 23; '''50''' (1):38
Genetic selection of athletic success in sport-hunting dogs. Description: Kim, Jaemin, et al. Genetic selection of athletic success in sport-hunting dogs. ''Proc Natl Acad Sci U S A''. 2018 Jul 24; '''115''' (30):E7212-E7221
Polygenic analysis of inflammatory disease variants and effects on microglia in the aging brain. Description: Felsky, Daniel, et al. Polygenic analysis of inflammatory disease variants and effects on microglia in the aging brain. ''Mol Neurodegener''. 2018 Jul 24; '''13''' (1):38
Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank Project. Description: Yasuda, Jun, et al. Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank Project. ''BMC Genomics''. 2018 Jul 24; '''19''' (1):551
Using Multi-Scale Genetic, Neuroimaging and Clinical Data for Predicting Alzheimer's Disease and Reconstruction of Relevant Biological Mechanisms. Description: Khanna, Shashank, et al. Using Multi-Scale Genetic, Neuroimaging and Clinical Data for Predicting Alzheimer's Disease and Reconstruction of Relevant Biological Mechanisms. ''Sci Rep''. 2018 Jul 24; '''8''' (1):11173
Unperturbed expression bias of imprinted genes in schizophrenia. Description: Gulyas-Kovacs, Attila, et al. Unperturbed expression bias of imprinted genes in schizophrenia. ''Nat Commun''. 2018 Jul 25; '''9''' (1):2914
Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Description: Scepanovic, Petar, et al. Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. ''Genome Med''. 2018 Jul 27; '''10''' (1):59
Using whole genome scores to compare three clinical phenotyping methods in complex diseases. Description: Song, Wenyu, et al. Using whole genome scores to compare three clinical phenotyping methods in complex diseases. ''Sci Rep''. 2018 Jul 27; '''8''' (1):11360
Copy number variations in Friesian horses and genetic risk factors for insect bite hypersensitivity. Description: Schurink, Anouk, et al. Copy number variations in Friesian horses and genetic risk factors for insect bite hypersensitivity. ''BMC Genet''. 2018 Jul 30; '''19''' (1):49
Exploring Cuba's population structure and demographic history using genome-wide data. Description: Fortes-Lima, Cesar, et al. Exploring Cuba's population structure and demographic history using genome-wide data. ''Sci Rep''. 2018 Jul 30; '''8''' (1):11422
Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome. Description: Fung, Jenny N, et al. Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndrome. ''Sci Rep''. 2018 Jul 30; '''8''' (1):11424
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Description: Wyss, Annah B, et al. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. ''Nat Commun''. 2018 Jul 30; '''9''' (1):2976
The genomic impact of historical hybridization with massive mitochondrial DNA introgression. Description: Seixas, Fernando A, et al. The genomic impact of historical hybridization with massive mitochondrial DNA introgression. ''Genome Biol''. 2018 Jul 30; '''19''' (1):91
A Missense Mutation in the Vacuolar Protein Sorting 11 (VPS11) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs. Description: Lucot, Katherine L, et al. A Missense Mutation in the Vacuolar Protein Sorting 11 (VPS11) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs. ''G3 (Bethesda)''. 2018 Jul 31; '''8''' (8):2773-2780
RAD Sequencing and a Hybrid Antarctic Fur Seal Genome Assembly Reveal Rapidly Decaying Linkage Disequilibrium, Global Population Structure and Evidence for Inbreeding. Description: Humble, Emily, et al. RAD Sequencing and a Hybrid Antarctic Fur Seal Genome Assembly Reveal Rapidly Decaying Linkage Disequilibrium, Global Population Structure and Evidence for Inbreeding. ''G3 (Bethesda)''. 2018 Jul 31; '''8''' (8):2709-2722
A genetics-based approach confirms immune associations with life history across multiple populations of an aquatic vertebrate (Gasterosteus aculeatus). Description: Whiting, James R, et al. A genetics-based approach confirms immune associations with life history across multiple populations of an aquatic vertebrate (Gasterosteus aculeatus). ''Mol Ecol''. 2018 Aug; '''27''' (15):3174-3191
A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1. Description: Chen, Ying, et al. A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1. ''PLoS Genet''. 2018 Aug; '''14''' (8):e1007532
A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis. Description: Kou, Ikuyo, et al. A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis. ''Sci Rep''. 2018 Aug 1; '''8''' (1):11575
Analysis of cross-population differentiation between Thoroughbred and Jeju horses. Description: Lee, Wonseok, et al. Analysis of cross-population differentiation between Thoroughbred and Jeju horses. ''Asian-Australas J Anim Sci''. 2018 Aug; '''31''' (8):1110-1118
A regulatory mutant on TRIM26 conferring the risk of nasopharyngeal carcinoma by inducing low immune response. Description: Lyu, Xiao-Ming, et al. A regulatory mutant on TRIM26 conferring the risk of nasopharyngeal carcinoma by inducing low immune response. ''Cancer Med''. 2018 Aug; '''7''' (8):3848-3861
Deep learning sequence-based ab initio prediction of variant effects on expression and disease risk. Description: Zhou, Jian, et al. Deep learning sequence-based ab initio prediction of variant effects on expression and disease risk. ''Nat Genet''. 2018 Aug; '''50''' (8):1171-1179
Demographic History and Genetic Adaptation in the Himalayan Region Inferred from Genome-Wide SNP Genotypes of 49 Populations. Description: Arciero, Elena, et al. Demographic History and Genetic Adaptation in the Himalayan Region Inferred from Genome-Wide SNP Genotypes of 49 Populations. ''Mol Biol Evol''. 2018 Aug 1; '''35''' (8):1916-1933
De novo MYH9 mutation in congenital scalp hemangioma. Description: Fomchenko, Elena I, et al. De novo MYH9 mutation in congenital scalp hemangioma. ''Cold Spring Harb Mol Case Stud''. 2018 Aug; '''4''' (4):
Extent of linkage disequilibrium and effective population size of the Landrace population in Korea. Description: Shin, Donghyun, et al. Extent of linkage disequilibrium and effective population size of the Landrace population in Korea. ''Asian-Australas J Anim Sci''. 2018 Aug; '''31''' (8):1078-1087
Genetic architecture of gene expression traits across diverse populations. Description: Mogil, Lauren S, et al. Genetic architecture of gene expression traits across diverse populations. ''PLoS Genet''. 2018 Aug; '''14''' (8):e1007586
Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy. Description: Schoeler, Natasha E, et al. Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy. ''Epilepsia''. 2018 Aug; '''59''' (8):1557-1566
Genome wide association study of fatty acid composition in Duroc swine. Description: Viterbo, Vanessa S, et al. Genome wide association study of fatty acid composition in Duroc swine. ''Asian-Australas J Anim Sci''. 2018 Aug; '''31''' (8):1127-1133
Genome-wide association study of lung function and clinical implication in heavy smokers. Description: Li, Xingnan, et al. Genome-wide association study of lung function and clinical implication in heavy smokers. ''BMC Med Genet''. 2018 Aug 1; '''19''' (1):134
Genome-wide SNP analysis unveils genetic structure and phylogeographic history of snow sheep (Ovis nivicola) populations inhabiting the Verkhoyansk Mountains and Momsky Ridge (northeastern Siberia). Description: Dotsev, Arsen V, et al. Genome-wide SNP analysis unveils genetic structure and phylogeographic history of snow sheep (Ovis nivicola) populations inhabiting the Verkhoyansk Mountains and Momsky Ridge (northeastern Siberia). ''Ecol Evol''. 2018 Aug; '''8''' (16):8000-8010
Glucose and Insulin-Related Traits, Type 2 Diabetes and Risk of Schizophrenia: A Mendelian Randomization Study. Description: Li, Zhiqiang, et al. Glucose and Insulin-Related Traits, Type 2 Diabetes and Risk of Schizophrenia: A Mendelian Randomization Study. ''EBioMedicine''. 2018 Aug; '''34''': 182-188
*HLA-C06:02-independent, gender-related association of PSORS1C3 and PSORS1C1/CDSN single-nucleotide polymorphisms with risk and severity of psoriasis.** Description: Wisniewski, Andrzej, et al. HLA-C*06:02-independent, gender-related association of PSORS1C3 and PSORS1C1/CDSN single-nucleotide polymorphisms with risk and severity of psoriasis. ''Mol Genet Genomics''. 2018 Aug; '''293''' (4):957-966
Influence of puberty timing on adiposity and cardiometabolic traits: A Mendelian randomisation study. Description: Bell, Joshua A, et al. Influence of puberty timing on adiposity and cardiometabolic traits: A Mendelian randomisation study. ''PLoS Med''. 2018 Aug; '''15''' (8):e1002641
Integration of summary data from GWAS and eQTL studies identified novel causal BMD genes with functional predictions. Description: Meng, Xiang-He, et al. Integration of summary data from GWAS and eQTL studies identified novel causal BMD genes with functional predictions. ''Bone''. 2018 Aug; '''113''': 41-48
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology. Description: Howe, Laurence J, et al. Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology. ''PLoS Genet''. 2018 Aug; '''14''' (8):e1007501
Loci and natural alleles underlying robust roots and adaptive domestication of upland ecotype rice in aerobic conditions. Description: Zhao, Yan, et al. Loci and natural alleles underlying robust roots and adaptive domestication of upland ecotype rice in aerobic conditions. ''PLoS Genet''. 2018 Aug; '''14''' (8):e1007521
Nonclonal coloniality: Genetically chimeric colonies through fusion of sexually produced polyps in the hydrozoan Ectopleura larynx. Description: Chang, E Sally, et al. Nonclonal coloniality: Genetically chimeric colonies through fusion of sexually produced polyps in the hydrozoan Ectopleura larynx. ''Evol Lett''. 2018 Aug; '''2''' (4):442-455
Population genomics of Culiseta melanura, the principal vector of Eastern equine encephalitis virus in the United States. Description: Soghigian, John, et al. Population genomics of Culiseta melanura, the principal vector of Eastern equine encephalitis virus in the United States. ''PLoS Negl Trop Dis''. 2018 Aug; '''12''' (8):e0006698
Possible Role of Single Stranded DNA Binding Protein 3 on Skin Hydration by Regulating Epidermal Differentiation. Description: Choi, Mi-Ra, et al. Possible Role of Single Stranded DNA Binding Protein 3 on Skin Hydration by Regulating Epidermal Differentiation. ''Ann Dermatol''. 2018 Aug; '''30''' (4):432-440
RBPJ polymorphisms associated with cerebral infarction diseases in Chinese Han population: A Clinical Trial/Experimental Study (CONSORT Compliant). Description: Zhang, Qiong, et al. RBPJ polymorphisms associated with cerebral infarction diseases in Chinese Han population: A Clinical Trial/Experimental Study (CONSORT Compliant). ''Medicine (Baltimore)''. 2018 Aug; '''97''' (31):e11420
Theory, practice, and conservation in the age of genomics: The Galapagos giant tortoise as a case study. Description: Gaughran, Stephen J, et al. Theory, practice, and conservation in the age of genomics: The Galapagos giant tortoise as a case study. ''Evol Appl''. 2018 Aug; '''11''' (7):1084-1093
Traffic-Related Air Pollution, APOEepsilon4 Status, and Neurodevelopmental Outcomes among School Children Enrolled in the BREATHE Project (Catalonia, Spain). Description: Alemany, Silvia, et al. Traffic-Related Air Pollution, APOEepsilon4 Status, and Neurodevelopmental Outcomes among School Children Enrolled in the BREATHE Project (Catalonia, Spain). ''Environ Health Perspect''. 2018 Aug; '''126''' (8):087001
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection. Description: Vuckovic, Dragana, et al. Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection. ''Eur J Hum Genet''. 2018 Aug; '''26''' (8):1167-1179
Global genomic diversity and conservation priorities for domestic animals are associated with the economies of their regions of origin. Description: Zhang, Min, et al. Global genomic diversity and conservation priorities for domestic animals are associated with the economies of their regions of origin. ''Sci Rep''. 2018 Aug 3; '''8''' (1):11677
Genome-wide association study results for educational attainment aid in identifying genetic heterogeneity of schizophrenia. Description: Bansal, V, et al. Genome-wide association study results for educational attainment aid in identifying genetic heterogeneity of schizophrenia. ''Nat Commun''. 2018 Aug 6; '''9''' (1):3078
Reduced-representation sequencing identifies small effective population sizes of Anopheles gambiae in the north-western Lake Victoria basin, Uganda. Description: Wiltshire, Rachel M, et al. Reduced-representation sequencing identifies small effective population sizes of Anopheles gambiae in the north-western Lake Victoria basin, Uganda. ''Malar J''. 2018 Aug 6; '''17''' (1):285
A multi-omic atlas of the human frontal cortex for aging and Alzheimer's disease research. Description: De Jager, Philip L, et al. A multi-omic atlas of the human frontal cortex for aging and Alzheimer's disease research. ''Sci Data''. 2018 Aug 7; '''5''': 180142
Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. Description: Yilmaz, Zeynep, et al. Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. ''Mol Psychiatry''. 2018 Aug 7;
Genetic association and meta-analysis of a schizophrenia GWAS variant rs10489202 in East Asian populations. Description: Yang, Yongfeng, et al. Genetic association and meta-analysis of a schizophrenia GWAS variant rs10489202 in East Asian populations. ''Transl Psychiatry''. 2018 Aug 7; '''8''' (1):144
Putative functional variants of lncRNA identified by RegulomeDB were associated with knee osteoarthritis susceptibility. Description: Wang, Kejie, et al. Putative functional variants of lncRNA identified by RegulomeDB were associated with knee osteoarthritis susceptibility. ''BMC Musculoskelet Disord''. 2018 Aug 7; '''19''' (1):284
Genetic Polymorphisms Associated with the Neutrophil(-)Lymphocyte Ratio and Their Clinical Implications for Metabolic Risk Factors. Description: Park, Boram, et al. Genetic Polymorphisms Associated with the Neutrophil(-)Lymphocyte Ratio and Their Clinical Implications for Metabolic Risk Factors. ''J Clin Med''. 2018 Aug 8; '''7''' (8):
Impact of demography and population dynamics on the genetic architecture of human longevity. Description: Giuliani, Cristina, et al. Impact of demography and population dynamics on the genetic architecture of human longevity. ''Aging (Albany NY)''. 2018 Aug 8; '''10''' (8):1947-1963
Investigating the genetic architecture of general and specific psychopathology in adolescence. Description: Jones, Hannah J, et al. Investigating the genetic architecture of general and specific psychopathology in adolescence. ''Transl Psychiatry''. 2018 Aug 8; '''8''' (1):145
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases. Description: Chen, Jason A, et al. Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases. ''Mol Neurodegener''. 2018 Aug 8; '''13''' (1):41
Trans-Ethnic Mapping of BANK1 Identifies Two Independent SLE-Risk Linkage Groups Enriched for Co-Transcriptional Splicing Marks. Description: Martinez-Bueno, Manuel, et al. Trans-Ethnic Mapping of BANK1 Identifies Two Independent SLE-Risk Linkage Groups Enriched for Co-Transcriptional Splicing Marks. ''Int J Mol Sci''. 2018 Aug 8; '''19''' (8):
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility. Description: Machiela, Mitchell J, et al. Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility. ''Nat Commun''. 2018 Aug 9; '''9''' (1):3184
Genomic diversity dynamics in conserved chicken populations are revealed by genome-wide SNPs. Description: Zhang, Mengmeng, et al. Genomic diversity dynamics in conserved chicken populations are revealed by genome-wide SNPs. ''BMC Genomics''. 2018 Aug 9; '''19''' (1):598
Long-term exposure to insulin and volumetric mammographic density: observational and genetic associations in the Karma study. Description: Borgquist, Signe, et al. Long-term exposure to insulin and volumetric mammographic density: observational and genetic associations in the Karma study. ''Breast Cancer Res''. 2018 Aug 9; '''20''' (1):93
Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP). Description: Ren, Hongyan, et al. Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP). ''Transl Psychiatry''. 2018 Aug 13; '''8''' (1):150
Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Description: Ji, Xuemei, et al. Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. ''Nat Commun''. 2018 Aug 13; '''9''' (1):3221
A tutorial on how not to over-interpret STRUCTURE and ADMIXTURE bar plots. Description: Lawson, Daniel J, et al. A tutorial on how not to over-interpret STRUCTURE and ADMIXTURE bar plots. ''Nat Commun''. 2018 Aug 14; '''9''' (1):3258
Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study. Description: He, Yazhou, et al. Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study. ''BMC Med''. 2018 Aug 14; '''16''' (1):142
Pervasive Modulation of Obesity Risk by the Environment and Genomic Background. Description: Nagpal, Sini, et al. Pervasive Modulation of Obesity Risk by the Environment and Genomic Background. ''Genes (Basel)''. 2018 Aug 14; '''9''' (8):
A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1. Description: Catoire, Helene, et al. A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1. ''Sci Rep''. 2018 Aug 15; '''8''' (1):12173
Efficient analysis of large-scale genome-wide data with two R packages: bigstatsr and bigsnpr. Description: Prive, Florian, et al. Efficient analysis of large-scale genome-wide data with two R packages: bigstatsr and bigsnpr. ''Bioinformatics''. 2018 Aug 15; '''34''' (16):2781-2787
Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Description: Kikuchi, Masataka, et al. Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. ''Sci Rep''. 2018 Aug 17; '''8''' (1):12347
Identification of novel loci associated with infant cognitive ability. Description: Sun, Ryan, et al. Identification of novel loci associated with infant cognitive ability. ''Mol Psychiatry''. 2018 Aug 17;
Food Consumption as a Modifier of the Association between LEPR Gene Variants and Excess Body Weight in Children and Adolescents: A Study of the SCAALA Cohort. Description: Dos Santos Rocha, Aline, et al. Food Consumption as a Modifier of the Association between LEPR Gene Variants and Excess Body Weight in Children and Adolescents: A Study of the SCAALA Cohort. ''Nutrients''. 2018 Aug 18; '''10''' (8):
Whole genome sequencing and bioinformatics analysis of two Egyptian genomes. Description: ElHefnawi, Mahmoud, et al. Whole genome sequencing and bioinformatics analysis of two Egyptian genomes. ''Gene''. 2018 Aug 20; '''668''': 129-134
Harnessing genetic potential of wheat germplasm banks through impact-oriented-prebreeding for future food and nutritional security. Description: Singh, Sukhwinder, et al. Harnessing genetic potential of wheat germplasm banks through impact-oriented-prebreeding for future food and nutritional security. ''Sci Rep''. 2018 Aug 21; '''8''' (1):12527
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol. Description: Low-Kam, Cecile, et al. Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol. ''J Am Heart Assoc''. 2018 Aug 21; '''7''' (16):e009545
Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. Description: Traglia, Michela, et al. Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. ''Genome Med''. 2018 Aug 22; '''10''' (1):67
Fitness Loss under Amino Acid Starvation in Artemisinin-Resistant Plasmodium falciparum Isolates from Cambodia. Description: Bunditvorapoom, Duangkamon, et al. Fitness Loss under Amino Acid Starvation in Artemisinin-Resistant Plasmodium falciparum Isolates from Cambodia. ''Sci Rep''. 2018 Aug 22; '''8''' (1):12622
Misidentification of runs of homozygosity islands in cattle caused by interference with copy number variation or large intermarker distances. Description: Nandolo, Wilson, et al. Misidentification of runs of homozygosity islands in cattle caused by interference with copy number variation or large intermarker distances. ''Genet Sel Evol''. 2018 Aug 22; '''50''' (1):43
Novel genome and genome-wide SNPs reveal early fragmentation effects in an edge-tolerant songbird population across an urbanized tropical metropolis. Description: Tan, David J X, et al. Novel genome and genome-wide SNPs reveal early fragmentation effects in an edge-tolerant songbird population across an urbanized tropical metropolis. ''Sci Rep''. 2018 Aug 24; '''8''' (1):12804
A genome-wide association study for harness racing success in the Norwegian-Swedish coldblooded trotter reveals genes for learning and energy metabolism. Description: Velie, Brandon D, et al. A genome-wide association study for harness racing success in the Norwegian-Swedish coldblooded trotter reveals genes for learning and energy metabolism. ''BMC Genet''. 2018 Aug 29; '''19''' (1):80
FADS1-FADS2 genetic polymorphisms are associated with fatty acid metabolism through changes in DNA methylation and gene expression. Description: He, Zhen, et al. FADS1-FADS2 genetic polymorphisms are associated with fatty acid metabolism through changes in DNA methylation and gene expression. ''Clin Epigenetics''. 2018 Aug 29; '''10''' (1):113
The demographic history of African Drosophila melanogaster. Description: Kapopoulou, Adamandia, et al. The demographic history of African Drosophila melanogaster. ''Genome Biol Evol''. 2018 Aug 29;
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers. Description: Mosley, Jonathan D, et al. A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers. ''Nat Commun''. 2018 Aug 30; '''9''' (1):3522
High-resolution genetic linkage map of European pear (Pyrus communis) and QTL fine-mapping of vegetative budbreak time. Description: Gabay, Gilad, et al. High-resolution genetic linkage map of European pear (Pyrus communis) and QTL fine-mapping of vegetative budbreak time. ''BMC Plant Biol''. 2018 Aug 31; '''18''' (1):175
Balancing selection on a recessive lethal deletion with pleiotropic effects on two neighboring genes in the porcine genome. Description: Derks, Martijn F L, et al. Balancing selection on a recessive lethal deletion with pleiotropic effects on two neighboring genes in the porcine genome. ''PLoS Genet''. 2018 Sep; '''14''' (9):e1007661
Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Description: Jeong, Choongwon, et al. Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. ''PLoS Genet''. 2018 Sep; '''14''' (9):e1007650
Developing reduced SNP assays from whole-genome sequence data to estimate introgression in an organism with complex genetic patterns, the Iberian honeybee (Apis mellifera iberiensis). Description: Henriques, Dora, et al. Developing reduced SNP assays from whole-genome sequence data to estimate introgression in an organism with complex genetic patterns, the Iberian honeybee (Apis mellifera iberiensis). ''Evol Appl''. 2018 Sep; '''11''' (8):1270-1282
Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency. Description: Kong, Xiao-Fei, et al. Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency. ''Nat Immunol''. 2018 Sep; '''19''' (9):973-985
Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior. Description: Kopp, Nathan D, et al. Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior. ''Mol Genet Genomic Med''. 2018 Sep; '''6''' (5):749-765
Genetic analysis of CHARGE syndrome identifies overlapping molecular biology. Description: Moccia, Amanda, et al. Genetic analysis of CHARGE syndrome identifies overlapping molecular biology. ''Genet Med''. 2018 Sep; '''20''' (9):1022-1029
Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans. Description: Wu, Sijie, et al. Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans. ''PLoS Genet''. 2018 Sep; '''14''' (9):e1007640
Genome-Wide Association Studies Associated with Backfat Thickness in Landrace and Yorkshire Pigs. Description: Lee, Young-Sup, et al. Genome-Wide Association Studies Associated with Backfat Thickness in Landrace and Yorkshire Pigs. ''Genomics Inform''. 2018 Sep; '''16''' (3):59-64
Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability. Description: Ferguson, Amy, et al. Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability. ''EBioMedicine''. 2018 Sep; '''35''': 279-287
Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. Description: Gregson, Celia L, et al. Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. ''Bone''. 2018 Sep; '''114''': 62-71
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. Description: Khera, Amit V, et al. Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. ''Nat Genet''. 2018 Sep; '''50''' (9):1219-1224
NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Description: Kakuta, Yoichi, et al. NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. ''J Gastroenterol''. 2018 Sep; '''53''' (9):1065-1078
Polymorphisms in the DAD1 and OXA1L genes are associated with asthma and atopy in a South American population. Description: Pires, Anaque de Oliveira, et al. Polymorphisms in the DAD1 and OXA1L genes are associated with asthma and atopy in a South American population. ''Mol Immunol''. 2018 Sep; '''101''': 294-302
Prediction of leprosy in the Chinese population based on a weighted genetic risk score. Description: Wang, Na, et al. Prediction of leprosy in the Chinese population based on a weighted genetic risk score. ''PLoS Negl Trop Dis''. 2018 Sep; '''12''' (9):e0006789
Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease. Description: Schiff, E R, et al. Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease. ''Hum Genet''. 2018 Sep; '''137''' (9):723-734
Reduced representation sequencing detects only subtle regional structure in a heavily exploited and rapidly recolonizing marine mammal species. Description: Dussex, Nicolas, et al. Reduced representation sequencing detects only subtle regional structure in a heavily exploited and rapidly recolonizing marine mammal species. ''Ecol Evol''. 2018 Sep; '''8''' (17):8736-8749
The Fas Signaling Pathway Is a Common Genetic Risk Factor for Severe Cutaneous Drug Adverse Reactions Across Diverse Drugs. Description: Park, Heung Woo, et al. The Fas Signaling Pathway Is a Common Genetic Risk Factor for Severe Cutaneous Drug Adverse Reactions Across Diverse Drugs. ''Allergy Asthma Immunol Res''. 2018 Sep; '''10''' (5):555-561
The molecular genetic basis of herbivory between butterflies and their host plants. Description: Nallu, Sumitha, et al. The molecular genetic basis of herbivory between butterflies and their host plants. ''Nat Ecol Evol''. 2018 Sep; '''2''' (9):1418-1427
The phosphatidylinositide 3-kinase (PI3K) signaling pathway is a determinant of zileuton response in adults with asthma. Description: Dahlin, Amber, et al. The phosphatidylinositide 3-kinase (PI3K) signaling pathway is a determinant of zileuton response in adults with asthma. ''Pharmacogenomics J''. 2018 Sep; '''18''' (5):665-677
Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane. Description: Corominas, Jordi, et al. Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane. ''Ophthalmology''. 2018 Sep; '''125''' (9):1433-1443
The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to beta-papillomaviruses. Description: de Jong, Sarah Jill, et al. The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to beta-papillomaviruses. ''J Exp Med''. 2018 Sep 3; '''215''' (9):2289-2310
TLR5 decoy receptor as a novel anti-amyloid therapeutic for Alzheimer's disease. Description: Chakrabarty, Paramita, et al. TLR5 decoy receptor as a novel anti-amyloid therapeutic for Alzheimer's disease. ''J Exp Med''. 2018 Sep 3; '''215''' (9):2247-2264
Draft genome sequence of wild Prunus yedoensis reveals massive inter-specific hybridization between sympatric flowering cherries. Description: Baek, Seunghoon, et al. Draft genome sequence of wild Prunus yedoensis reveals massive inter-specific hybridization between sympatric flowering cherries. ''Genome Biol''. 2018 Sep 4; '''19''' (1):127
Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression. Description: Strawbridge, Rona J, et al. Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression. ''Transl Psychiatry''. 2018 Sep 4; '''8''' (1):178
Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma. Description: Singh, Larry N, et al. Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma. ''Invest Ophthalmol Vis Sci''. 2018 Sep 4; '''59''' (11):4598-4602
Analysis of evolution and genetic diversity of sweetpotato and its related different polyploidy wild species I. trifida using RAD-seq. Description: Feng, J Y, et al. Analysis of evolution and genetic diversity of sweetpotato and its related different polyploidy wild species I. trifida using RAD-seq. ''BMC Plant Biol''. 2018 Sep 5; '''18''' (1):181
Body mass index modulates the association between CDKAL1 rs10946398 variant and type 2 diabetes among Taiwanese women. Description: Nfor, Oswald Ndi, et al. Body mass index modulates the association between CDKAL1 rs10946398 variant and type 2 diabetes among Taiwanese women. ''Sci Rep''. 2018 Sep 5; '''8''' (1):13235
Genetic Determinants of Telomere Length in African American Youth. Description: Zeiger, Andrew M, et al. Genetic Determinants of Telomere Length in African American Youth. ''Sci Rep''. 2018 Sep 5; '''8''' (1):13265
Genomic analysis reveals genes affecting distinct phenotypes among different Chinese and western pig breeds. Description: Zhang, Zhe, et al. Genomic analysis reveals genes affecting distinct phenotypes among different Chinese and western pig breeds. ''Sci Rep''. 2018 Sep 6; '''8''' (1):13352
Prioritizing candidate genes post-GWAS using multiple sources of data for mastitis resistance in dairy cattle. Description: Cai, Zexi, et al. Prioritizing candidate genes post-GWAS using multiple sources of data for mastitis resistance in dairy cattle. ''BMC Genomics''. 2018 Sep 6; '''19''' (1):656
Association of schizophrenia polygenic risk score with manic and depressive psychosis in bipolar disorder. Description: Markota, Matej, et al. Association of schizophrenia polygenic risk score with manic and depressive psychosis in bipolar disorder. ''Transl Psychiatry''. 2018 Sep 10; '''8''' (1):188
Cancer expression quantitative trait loci (eQTLs) can be determined from heterogeneous tumor gene expression data by modeling variation in tumor purity. Description: Geeleher, Paul, et al. Cancer expression quantitative trait loci (eQTLs) can be determined from heterogeneous tumor gene expression data by modeling variation in tumor purity. ''Genome Biol''. 2018 Sep 11; '''19''' (1):130
Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations. Description: Chang, Jiang, et al. Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations. ''Nat Commun''. 2018 Sep 11; '''9''' (1):3688
Conditional and interaction gene-set analysis reveals novel functional pathways for blood pressure. Description: de Leeuw, Christiaan A, et al. Conditional and interaction gene-set analysis reveals novel functional pathways for blood pressure. ''Nat Commun''. 2018 Sep 14; '''9''' (1):3768
Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas. Description: Buckley, Alexandra R, et al. Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas. ''Genome Med''. 2018 Sep 14; '''10''' (1):69
High cryptic species diversity is revealed by genome-wide polymorphisms in a wild relative of banana, Musa itinerans, and implications for its conservation in subtropical China. Description: Wu, Wei, et al. High cryptic species diversity is revealed by genome-wide polymorphisms in a wild relative of banana, Musa itinerans, and implications for its conservation in subtropical China. ''BMC Plant Biol''. 2018 Sep 14; '''18''' (1):194
Pharmacogenetics analysis of serotonin receptor gene variants and clinical response to risperidone in Han Chinese schizophrenic patients. Description: Zhou, Wei, et al. Pharmacogenetics analysis of serotonin receptor gene variants and clinical response to risperidone in Han Chinese schizophrenic patients. ''Neurosci Lett''. 2018 Sep 14; '''683''': 202-206
Autozygosity islands and ROH patterns in Nellore lineages: evidence of selection for functionally important traits. Description: Peripolli, Elisa, et al. Autozygosity islands and ROH patterns in Nellore lineages: evidence of selection for functionally important traits. ''BMC Genomics''. 2018 Sep 17; '''19''' (1):680
Characterization of the contribution of shared environmental and genetic factors to metabolic syndrome methylation heritability and familial correlations. Description: Fernandez-Rhodes, Lindsay, et al. Characterization of the contribution of shared environmental and genetic factors to metabolic syndrome methylation heritability and familial correlations. ''BMC Genet''. 2018 Sep 17; '''19''' (Suppl 1):69
Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability. Description: Valimaki, Niko, et al. Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability. ''Elife''. 2018 Sep 18; '''7''':
Genome-Wide Association Study Reveals Genetic Link between Diarrhea-Associated Entamoeba histolytica Infection and Inflammatory Bowel Disease. Description: Wojcik, Genevieve L, et al. Genome-Wide Association Study Reveals Genetic Link between Diarrhea-Associated Entamoeba histolytica Infection and Inflammatory Bowel Disease. ''MBio''. 2018 Sep 18; '''9''' (5):
Analysis of porcine body size variation using re-sequencing data of miniature and large pigs. Description: Reimer, C, et al. Analysis of porcine body size variation using re-sequencing data of miniature and large pigs. ''BMC Genomics''. 2018 Sep 19; '''19''' (1):687
Genome-wide SNP analyses reveal high gene flow and signatures of local adaptation among the scalloped spiny lobster (Panulirus homarus) along the Omani coastline. Description: Al-Breiki, Rufaida Dhuhai, et al. Genome-wide SNP analyses reveal high gene flow and signatures of local adaptation among the scalloped spiny lobster (Panulirus homarus) along the Omani coastline. ''BMC Genomics''. 2018 Sep 19; '''19''' (1):690
Genome-wide analysis of polymorphism x sodium interaction effect on blood pressure identifies a novel 3'-BCL11B gene desert locus. Description: Hachiya, Tsuyoshi, et al. Genome-wide analysis of polymorphism x sodium interaction effect on blood pressure identifies a novel 3'-BCL11B gene desert locus. ''Sci Rep''. 2018 Sep 21; '''8''' (1):14162
Association of APOB and LIPC polymorphisms with type 2 diabetes in Chinese Han population. Description: Long, Tianzhu, et al. Association of APOB and LIPC polymorphisms with type 2 diabetes in Chinese Han population. ''Gene''. 2018 Sep 25; '''672''': 150-155
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Description: Wang, Sheng, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. ''Cell Rep''. 2018 Sep 25; '''24''' (13):3441-3454.e12
Significant Association Between Variant in SGCD and Age-Related Macular Degeneration. Description: Perez-Ortiz, Andric Christopher, et al. Significant Association Between Variant in SGCD and Age-Related Macular Degeneration. ''Genes (Basel)''. 2018 Sep 25; '''9''' (10):
Genome-wide burden and association analyses implicate copy number variations in asthma risk among children and young adults from Latin America. Description: Oliveira, Pablo, et al. Genome-wide burden and association analyses implicate copy number variations in asthma risk among children and young adults from Latin America. ''Sci Rep''. 2018 Sep 27; '''8''' (1):14475
INFERNO: inferring the molecular mechanisms of noncoding genetic variants. Description: Amlie-Wolf, Alexandre, et al. INFERNO: inferring the molecular mechanisms of noncoding genetic variants. ''Nucleic Acids Res''. 2018 Sep 28; '''46''' (17):8740-8753
Ancient genomes suggest the eastern Pontic-Caspian steppe as the source of western Iron Age nomads. Description: Krzewinska, Maja, et al. Ancient genomes suggest the eastern Pontic-Caspian steppe as the source of western Iron Age nomads. ''Sci Adv''. 2018 Oct; '''4''' (10):eaat4457
A neurobiological pathway to smoking in adolescence: TTC12-ANKK1-DRD2 variants and reward response. Description: Macare, Christine, et al. A neurobiological pathway to smoking in adolescence: TTC12-ANKK1-DRD2 variants and reward response. ''Eur Neuropsychopharmacol''. 2018 Oct; '''28''' (10):1103-1114
ANKRD9 is associated with tumor suppression as a substrate receptor subunit of ubiquitin ligase. Description: Lee, Yejin, et al. ANKRD9 is associated with tumor suppression as a substrate receptor subunit of ubiquitin ligase. ''Biochim Biophys Acta Mol Basis Dis''. 2018 Oct; '''1864''' (10):3145-3153
Assessment of shared alleles in drought-associated candidate genes among southern California white oak species (Quercus sect. Quercus). Description: Oney-Birol, Signem, et al. Assessment of shared alleles in drought-associated candidate genes among southern California white oak species (Quercus sect. Quercus). ''BMC Genet''. 2018 Oct 1; '''19''' (1):88
Design and evaluation of a sequence capture system for genome-wide SNP genotyping in highly heterozygous plant genomes: a case study with a keystone Neotropical hardwood tree genome. Description: Silva-Junior, Orzenil Bonfim, et al. Design and evaluation of a sequence capture system for genome-wide SNP genotyping in highly heterozygous plant genomes: a case study with a keystone Neotropical hardwood tree genome. ''DNA Res''. 2018 Oct 1; '''25''' (5):535-545
Direct-to-consumer DNA testing of 6,000 dogs reveals 98.6-kb duplication associated with blue eyes and heterochromia in Siberian Huskies. Description: Deane-Coe, Petra E, et al. Direct-to-consumer DNA testing of 6,000 dogs reveals 98.6-kb duplication associated with blue eyes and heterochromia in Siberian Huskies. ''PLoS Genet''. 2018 Oct; '''14''' (10):e1007648
Fine mapping MHC associations in Graves' disease and its clinical subtypes in Han Chinese. Description: Chu, Xun, et al. Fine mapping MHC associations in Graves' disease and its clinical subtypes in Han Chinese. ''J Med Genet''. 2018 Oct; '''55''' (10):685-692
Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier bipolar disorder patient. Description: Palladino, Viola Stella, et al. Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier bipolar disorder patient. ''Stem Cell Res''. 2018 Oct; '''32''': 104-109
Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease. Description: Maguire, Lillias H, et al. Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease. ''Nat Genet''. 2018 Oct; '''50''' (10):1359-1365
Genome-wide association studies of brain imaging phenotypes in UK Biobank. Description: Elliott, Lloyd T, et al. Genome-wide association studies of brain imaging phenotypes in UK Biobank. ''Nature''. 2018 Oct; '''562''' (7726):210-216
Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. Description: Rosendahl, Jonas, et al. Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. ''Gut''. 2018 Oct; '''67''' (10):1855-1863
Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank. Description: Fall, Tove, et al. Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank. ''Diabetologia''. 2018 Oct; '''61''' (10):2174-2179
Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations. Description: Bonnemaijer, Pieter W M, et al. Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations. ''Hum Genet''. 2018 Oct; '''137''' (10):847-862
Genomic history of the Sardinian population. Description: Chiang, Charleston W K, et al. Genomic history of the Sardinian population. ''Nat Genet''. 2018 Oct; '''50''' (10):1426-1434
GRK5 Is Associated with the Regulation of Methadone Dosage in Heroin Dependence. Description: Wang, Sheng-Chang, et al. GRK5 Is Associated with the Regulation of Methadone Dosage in Heroin Dependence. ''Int J Neuropsychopharmacol''. 2018 Oct 1; '''21''' (10):910-917
Heterogeneity in association of remote herpesvirus infections and pediatric MS. Description: Nourbakhsh, Bardia, et al. Heterogeneity in association of remote herpesvirus infections and pediatric MS. ''Ann Clin Transl Neurol''. 2018 Oct; '''5''' (10):1222-1228
Human mitochondrial DNA haplogroup M8a influences the penetrance of m.8684C>T in Han Chinese men with non-obstructive azoospermia. Description: Ji, Juan, et al. Human mitochondrial DNA haplogroup M8a influences the penetrance of m.8684C>T in Han Chinese men with non-obstructive azoospermia. ''Reprod Biomed Online''. 2018 Oct; '''37''' (4):480-488
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency. Description: Hernandez, Nicholas, et al. Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency. ''J Exp Med''. 2018 Oct 1; '''215''' (10):2567-2585
Plasticity-related gene 3 (LPPR1) and age at diagnosis of Parkinson disease. Description: Wallen, Zachary D, et al. Plasticity-related gene 3 (LPPR1) and age at diagnosis of Parkinson disease. ''Neurol Genet''. 2018 Oct; '''4''' (5):e271
Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis. Description: Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis. ''Eur J Hum Genet''. 2018 Oct; '''26''' (10):1537-1546
ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls. Description: Hendricks, Audrey E, et al. ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls. ''PLoS Genet''. 2018 Oct; '''14''' (10):e1007591
Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease. Description: Gaare, Johannes J, et al. Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease. ''Mov Disord''. 2018 Oct; '''33''' (10):1591-1600
Recovery of novel association loci in Arabidopsis thaliana and Drosophila melanogaster through leveraging INDELs association and integrated burden test. Description: Song, Baoxing, et al. Recovery of novel association loci in Arabidopsis thaliana and Drosophila melanogaster through leveraging INDELs association and integrated burden test. ''PLoS Genet''. 2018 Oct; '''14''' (10):e1007699
The role of local adaptation in sustainable village chicken production. Description: Bettridge, Judy M, et al. The role of local adaptation in sustainable village chicken production. ''Nat Sustain''. 2018 Oct; '''1''' (10):574-582
The UK Biobank resource with deep phenotyping and genomic data. Description: Bycroft, Clare, et al. The UK Biobank resource with deep phenotyping and genomic data. ''Nature''. 2018 Oct; '''562''' (7726):203-209
TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome. Description: Corbitt, Holly, et al. TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome. ''PLoS Genet''. 2018 Oct; '''14''' (10):e1007692
Value of DNA methylation in predicting curve progression in patients with adolescent idiopathic scoliosis. Description: Meng, Yichen, et al. Value of DNA methylation in predicting curve progression in patients with adolescent idiopathic scoliosis. ''EBioMedicine''. 2018 Oct; '''36''': 489-496
Variants in Notch signalling pathway genes, PSEN1 and MAML2, predict overall survival in Chinese patients with epithelial ovarian cancer. Description: Xu, Yuan, et al. Variants in Notch signalling pathway genes, PSEN1 and MAML2, predict overall survival in Chinese patients with epithelial ovarian cancer. ''J Cell Mol Med''. 2018 Oct; '''22''' (10):4975-4984
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype. Description: Jabbari, Edwin, et al. Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype. ''Ann Neurol''. 2018 Oct; '''84''' (4):485-496
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Description: van der Meer, Dennis, et al. Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. ''Mol Psychiatry''. 2018 Oct 2;
Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin. Description: Tuteja, Sony, et al. Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin. ''J Am Heart Assoc''. 2018 Oct 2; '''7''' (19):e03488
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series. Description: Koriath, C, et al. Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series. ''Mol Psychiatry''. 2018 Oct 2;
Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. Description: Wojcik, Genevieve L, et al. Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. ''G3 (Bethesda)''. 2018 Oct 3; '''8''' (10):3255-3267
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese. Description: Zheng, Ruijuan, et al. Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese. ''Nat Commun''. 2018 Oct 4; '''9''' (1):4072
Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time. Description: Pinar, Ari, et al. Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time. ''Transl Psychiatry''. 2018 Oct 4; '''8''' (1):207
Large-scale transcriptome-wide association study identifies new prostate cancer risk regions. Description: Mancuso, Nicholas, et al. Large-scale transcriptome-wide association study identifies new prostate cancer risk regions. ''Nat Commun''. 2018 Oct 4; '''9''' (1):4079
A genomic Neolithic time transect of hunter-farmer admixture in central Poland. Description: Fernandes, D M, et al. A genomic Neolithic time transect of hunter-farmer admixture in central Poland. ''Sci Rep''. 2018 Oct 5; '''8''' (1):14879
Evaluating the effect of multiple genetic risk score models on colorectal cancer risk prediction. Description: Xin, Junyi, et al. Evaluating the effect of multiple genetic risk score models on colorectal cancer risk prediction. ''Gene''. 2018 Oct 5; '''673''': 174-180
Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder. Description: Hughes, Timothy, et al. Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder. ''Transl Psychiatry''. 2018 Oct 8; '''8''' (1):210
Genetic signature to provide robust risk assessment of psoriatic arthritis development in psoriasis patients. Description: Patrick, Matthew T, et al. Genetic signature to provide robust risk assessment of psoriatic arthritis development in psoriasis patients. ''Nat Commun''. 2018 Oct 9; '''9''' (1):4178
Genetic variations in TAS2R3 and TAS2R4 bitterness receptors modify papillary carcinoma risk and thyroid function in Korean females. Description: Choi, Jeong-Hwa, et al. Genetic variations in TAS2R3 and TAS2R4 bitterness receptors modify papillary carcinoma risk and thyroid function in Korean females. ''Sci Rep''. 2018 Oct 9; '''8''' (1):15004
Genome-wide association analysis identifies SNPs predictive of in vitro leukemic cell sensitivity to cytarabine in pediatric AML. Description: Bargal, Salma A, et al. Genome-wide association analysis identifies SNPs predictive of in vitro leukemic cell sensitivity to cytarabine in pediatric AML. ''Oncotarget''. 2018 Oct 9; '''9''' (79):34859-34875
ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans. Description: Conway, Olivia J, et al. ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans. ''Mol Neurodegener''. 2018 Oct 11; '''13''' (1):53
VEGFA GENE variation influences hallucinations and frontotemporal morphology in psychotic disorders: a B-SNIP study. Description: Lizano, Paulo, et al. VEGFA GENE variation influences hallucinations and frontotemporal morphology in psychotic disorders: a B-SNIP study. ''Transl Psychiatry''. 2018 Oct 11; '''8''' (1):215
BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts. Description: Lee, Joo-Yeon, et al. BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts. ''Sci Rep''. 2018 Oct 15; '''8''' (1):15263
High prevalence of focal and multi-focal somatic genetic variants in the human brain. Description: Keogh, Michael J, et al. High prevalence of focal and multi-focal somatic genetic variants in the human brain. ''Nat Commun''. 2018 Oct 15; '''9''' (1):4257
Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators. Description: Lagou, Vasiliki, et al. Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators. ''Cell Rep''. 2018 Oct 16; '''25''' (3):798-810.e6
Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention. Description: Inouye, Michael, et al. Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention. ''J Am Coll Cardiol''. 2018 Oct 16; '''72''' (16):1883-1893
Phenome-wide association studies across large population cohorts support drug target validation. Description: Diogo, Dorothee, et al. Phenome-wide association studies across large population cohorts support drug target validation. ''Nat Commun''. 2018 Oct 16; '''9''' (1):4285
Extracting stability increases the SNP heritability of emotional problems in young people. Description: Cheesman, Rosa, et al. Extracting stability increases the SNP heritability of emotional problems in young people. ''Transl Psychiatry''. 2018 Oct 17; '''8''' (1):223
The genetic basis of a social polymorphism in halictid bees. Description: Kocher, Sarah D, et al. The genetic basis of a social polymorphism in halictid bees. ''Nat Commun''. 2018 Oct 18; '''9''' (1):4338
Discovering in vivo cytokine-eQTL interactions from a lupus clinical trial. Description: Davenport, Emma E, et al. Discovering in vivo cytokine-eQTL interactions from a lupus clinical trial. ''Genome Biol''. 2018 Oct 19; '''19''' (1):168
Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth. Description: Hamvas, Aaron, et al. Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth. ''BMC Genet''. 2018 Oct 20; '''19''' (1):94
Identification of three novel loci of ALDH2 Gene for Serum Folate levels in a Male Chinese Population by Genome-Wide Association Study. Description: Deng, Caiwang, et al. Identification of three novel loci of ALDH2 Gene for Serum Folate levels in a Male Chinese Population by Genome-Wide Association Study. ''Gene''. 2018 Oct 20; '''674''': 121-126
A role for genes in the 'caregiver stress process'? Description: Wolf, Douglas A, et al. A role for genes in the 'caregiver stress process'? ''Transl Psychiatry''. 2018 Oct 22; '''8''' (1):228
Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population. Description: Wang, Shaolin, et al. Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population. ''BMC Ophthalmol''. 2018 Oct 22; '''18''' (1):271
Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous Nephropathy. Description: Latt, Khun Zaw, et al. Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous Nephropathy. ''Sci Rep''. 2018 Oct 22; '''8''' (1):15576
A striking new species of leaf warbler from the Lesser Sundas as uncovered through morphology and genomics. Description: Ng, Nathaniel S R, et al. A striking new species of leaf warbler from the Lesser Sundas as uncovered through morphology and genomics. ''Sci Rep''. 2018 Oct 23; '''8''' (1):15646
Genetic variation in the SIM1 locus is associated with erectile dysfunction. Description: Jorgenson, Eric, et al. Genetic variation in the SIM1 locus is associated with erectile dysfunction. ''Proc Natl Acad Sci U S A''. 2018 Oct 23; '''115''' (43):11018-11023
Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide. Description: Coon, Hilary, et al. Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide. ''Mol Psychiatry''. 2018 Oct 23;
Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study. Description: Hayden, Lystra P, et al. Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study. ''Respir Res''. 2018 Oct 29; '''19''' (1):209
Associations between polymorphisms of the CXCL12 and CNNM2 gene and hypertension risk: A case-control study. Description: Liu, Xianxia, et al. Associations between polymorphisms of the CXCL12 and CNNM2 gene and hypertension risk: A case-control study. ''Gene''. 2018 Oct 30; '''675''': 185-190
A functional splice variant associated with decreased asthma risk abolishes the ability of gasdermin B to induce epithelial cell pyroptosis. Description: Panganiban, Ronald A, et al. A functional splice variant associated with decreased asthma risk abolishes the ability of gasdermin B to induce epithelial cell pyroptosis. ''J Allergy Clin Immunol''. 2018 Nov; '''142''' (5):1469-1478.e2
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes. Description: Meng, Weihua, et al. A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes. ''Acta Ophthalmol''. 2018 Nov; '''96''' (7):e811-e819
A Schizophrenia-Related Genetic-Brain-Cognition Pathway Revealed in a Large Chinese Population. Description: Luo, Na, et al. A Schizophrenia-Related Genetic-Brain-Cognition Pathway Revealed in a Large Chinese Population. ''EBioMedicine''. 2018 Nov; '''37''': 471-482
Associations of genetic variants in endocytic trafficking of epidermal growth factor receptor super pathway with risk of nonsyndromic cleft lip with or without cleft palate. Description: Li, Bing, et al. Associations of genetic variants in endocytic trafficking of epidermal growth factor receptor super pathway with risk of nonsyndromic cleft lip with or without cleft palate. ''Mol Genet Genomic Med''. 2018 Nov; '''6''' (6):1157-1167
Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy. Description: Allen, Mariet, et al. Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy. ''Acta Neuropathol''. 2018 Nov; '''136''' (5):709-727
Evidence of Polygenic Adaptation to High Altitude from Tibetan and Sherpa Genomes. Description: Gnecchi-Ruscone, Guido A, et al. Evidence of Polygenic Adaptation to High Altitude from Tibetan and Sherpa Genomes. ''Genome Biol Evol''. 2018 Nov 1; '''10''' (11):2919-2930
Exploring the genetic correlations of antisocial behaviour and life history traits. Description: Tielbeek, Jorim J, et al. Exploring the genetic correlations of antisocial behaviour and life history traits. ''BJPsych Open''. 2018 Nov; '''4''' (6):467-470
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. Description: Klarin, Derek, et al. Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. ''Nat Genet''. 2018 Nov; '''50''' (11):1514-1523
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. Description: Ligthart, Symen, et al. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. ''Am J Hum Genet''. 2018 Nov 1; '''103''' (5):691-706
Genome-wide analysis of insomnia disorder. Description: Stein, Murray B, et al. Genome-wide analysis of insomnia disorder. ''Mol Psychiatry''. 2018 Nov; '''23''' (11):2238-2250
Influence of proinflammatory cytokine gene polymorphisms on the risk of COPD and the levels of plasma protein. Description: Ambrocio-Ortiz, Enrique, et al. Influence of proinflammatory cytokine gene polymorphisms on the risk of COPD and the levels of plasma protein. ''Cytokine''. 2018 Nov; '''111''': 364-370
Integration of genome wide association studies and whole genome sequencing provides novel insights into fat deposition in chicken. Description: Moreira, Gabriel Costa Monteiro, et al. Integration of genome wide association studies and whole genome sequencing provides novel insights into fat deposition in chicken. ''Sci Rep''. 2018 Nov 1; '''8''' (1):16222
Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. Description: Raj, Towfique, et al. Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. ''Nat Genet''. 2018 Nov; '''50''' (11):1584-1592
Investigation of the CADM2 polymorphism rs17518584 in memory and executive functions measures in a cohort of young healthy individuals. Description: Ibrahim, Omar, et al. Investigation of the CADM2 polymorphism rs17518584 in memory and executive functions measures in a cohort of young healthy individuals. ''Neurobiol Learn Mem''. 2018 Nov; '''155''': 330-336
Leveraging DNA-Methylation Quantitative-Trait Loci to Characterize the Relationship between Methylomic Variation, Gene Expression, and Complex Traits. Description: Hannon, Eilis, et al. Leveraging DNA-Methylation Quantitative-Trait Loci to Characterize the Relationship between Methylomic Variation, Gene Expression, and Complex Traits. ''Am J Hum Genet''. 2018 Nov 1; '''103''' (5):654-665
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Description: Galvan-Femenia, Ivan, et al. Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. ''J Med Genet''. 2018 Nov; '''55''' (11):765-778
Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development. Description: Konjikusic, Mia J, et al. Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development. ''PLoS Genet''. 2018 Nov; '''14''' (11):e1007817
Neurocognitive Endophenotypes of Schizophrenia and Bipolar Disorder and Possible Associations with FKBP Variant rs3800373. Description: Memic, Amra, et al. Neurocognitive Endophenotypes of Schizophrenia and Bipolar Disorder and Possible Associations with FKBP Variant rs3800373. ''Med Arch''. 2018 Nov; '''72''' (5):352-356
Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease. Description: Qiu, Chengxiang, et al. Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease. ''Nat Med''. 2018 Nov; '''24''' (11):1721-1731
Selection Signatures Underlying Dramatic Male Inflorescence Transformation During Modern Hybrid Maize Breeding. Description: Gage, Joseph L, et al. Selection Signatures Underlying Dramatic Male Inflorescence Transformation During Modern Hybrid Maize Breeding. ''Genetics''. 2018 Nov; '''210''' (3):1125-1138
The biological embedding of early-life socioeconomic status and family adversity in children's genome-wide DNA methylation. Description: Bush, Nicole R, et al. The biological embedding of early-life socioeconomic status and family adversity in children's genome-wide DNA methylation. ''Epigenomics''. 2018 Nov; '''10''' (11):1445-1461
The optimal mating distance resulting from heterosis and genetic incompatibility. Description: Wei, Xinzhu, et al. The optimal mating distance resulting from heterosis and genetic incompatibility. ''Sci Adv''. 2018 Nov; '''4''' (11):eaau5518
The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease. Description: Zaid, Younes, et al. The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease. ''BMC Res Notes''. 2018 Nov 1; '''11''' (1):783
Type 2 Diabetes-Associated Genetic Variants Regulate Chromatin Accessibility in Human Islets. Description: Khetan, Shubham, et al. Type 2 Diabetes-Associated Genetic Variants Regulate Chromatin Accessibility in Human Islets. ''Diabetes''. 2018 Nov; '''67''' (11):2466-2477
VAX1 gene associated non-syndromic cleft lip with or without palate in Western Han Chinese. Description: Zhang, Bi-He, et al. VAX1 gene associated non-syndromic cleft lip with or without palate in Western Han Chinese. ''Arch Oral Biol''. 2018 Nov; '''95''': 40-43
DNA methylation levels are associated with CRF1 receptor antagonist treatment outcome in women with post-traumatic stress disorder. Description: Pape, Julius C, et al. DNA methylation levels are associated with CRF1 receptor antagonist treatment outcome in women with post-traumatic stress disorder. ''Clin Epigenetics''. 2018 Nov 3; '''10''' (1):136
A Genomic Variation Map Provides Insights into the Genetic Basis of Spring Chinese Cabbage (Brassica rapa ssp. pekinensis) Selection. Description: Su, Tongbing, et al. A Genomic Variation Map Provides Insights into the Genetic Basis of Spring Chinese Cabbage (Brassica rapa ssp. pekinensis) Selection. ''Mol Plant''. 2018 Nov 5; '''11''' (11):1360-1376
Bayesian variable selection for parametric survival model with applications to cancer omics data. Description: Duan, Weiwei, et al. Bayesian variable selection for parametric survival model with applications to cancer omics data. ''Hum Genomics''. 2018 Nov 6; '''12''' (1):49
Empirical Comparisons of Different Statistical Models To Identify and Validate Kernel Row Number-Associated Variants from Structured Multi-parent Mapping Populations of Maize. Description: Yang, Jinliang, et al. Empirical Comparisons of Different Statistical Models To Identify and Validate Kernel Row Number-Associated Variants from Structured Multi-parent Mapping Populations of Maize. ''G3 (Bethesda)''. 2018 Nov 6; '''8''' (11):3567-3575
Exploring the genetic basis of gene transcript abundance and metabolite levels in loblolly pine (Pinus taeda L.) using association mapping and network construction. Description: Lu, Mengmeng, et al. Exploring the genetic basis of gene transcript abundance and metabolite levels in loblolly pine (Pinus taeda L.) using association mapping and network construction. ''BMC Genet''. 2018 Nov 6; '''19''' (1):100
Genomic Analysis To Identify Signatures of Artificial Selection and Loci Associated with Important Economic Traits in Duroc Pigs. Description: Ma, Yunlong, et al. Genomic Analysis To Identify Signatures of Artificial Selection and Loci Associated with Important Economic Traits in Duroc Pigs. ''G3 (Bethesda)''. 2018 Nov 6; '''8''' (11):3617-3625
Association and cis-mQTL analysis of variants in serotonergic genes associated with nicotine dependence in Chinese Han smokers. Description: Han, Haijun, et al. Association and cis-mQTL analysis of variants in serotonergic genes associated with nicotine dependence in Chinese Han smokers. ''Transl Psychiatry''. 2018 Nov 7; '''8''' (1):243
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. Description: Gilly, Arthur, et al. Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. ''Nat Commun''. 2018 Nov 7; '''9''' (1):4674
K-variant BCHE and pesticide exposure: Gene-environment interactions in a case-control study of Parkinson's disease in Egypt. Description: Rosler, Thomas W, et al. K-variant BCHE and pesticide exposure: Gene-environment interactions in a case-control study of Parkinson's disease in Egypt. ''Sci Rep''. 2018 Nov 8; '''8''' (1):16525
Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations. Description: de Farias, Allysson Allan, et al. Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations. ''Sci Rep''. 2018 Nov 8; '''8''' (1):16552
Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders. Description: O'Brien, Heath E, et al. Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders. ''Genome Biol''. 2018 Nov 12; '''19''' (1):194
Novel insights into the genetic basis of buffalo reproductive performance. Description: Li, Jun, et al. Novel insights into the genetic basis of buffalo reproductive performance. ''BMC Genomics''. 2018 Nov 12; '''19''' (1):814
Functional and evolutionary genomic inferences in Populus through genome and population sequencing of American and European aspen. Description: Lin, Yao-Cheng, et al. Functional and evolutionary genomic inferences in Populus through genome and population sequencing of American and European aspen. ''Proc Natl Acad Sci U S A''. 2018 Nov 13; '''115''' (46):E10970-E10978
Nonsense mutation in PMEL is associated with yellowish plumage colour phenotype in Japanese quail. Description: Ishishita, Satoshi, et al. Nonsense mutation in PMEL is associated with yellowish plumage colour phenotype in Japanese quail. ''Sci Rep''. 2018 Nov 13; '''8''' (1):16732
Genomes reveal marked differences in the adaptive evolution between orangutan species. Description: Mattle-Greminger, Maja P, et al. Genomes reveal marked differences in the adaptive evolution between orangutan species. ''Genome Biol''. 2018 Nov 15; '''19''' (1):193
Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans. Description: Cheng, Zhongshan, et al. Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans. ''Biol Psychiatry''. 2018 Nov 15; '''84''' (10):762-770
Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity. Description: Niazi, Robina Khan, et al. Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity. ''BMC Med Genet''. 2018 Nov 15; '''19''' (1):199
Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity. Description: Marklund, Matti, et al. Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity. ''Nutrients''. 2018 Nov 17; '''10''' (11):
Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta. Description: Kausar, Mehran, et al. Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta. ''J Biomed Sci''. 2018 Nov 17; '''25''' (1):82
Functional SNP panel for parentage assessment and assignment in worldwide goat breeds. Description: Talenti, Andrea, et al. Functional SNP panel for parentage assessment and assignment in worldwide goat breeds. ''Genet Sel Evol''. 2018 Nov 19; '''50''' (1):55
Genome-wide patterns of homozygosity provide clues about the population history and adaptation of goats. Description: Bertolini, Francesca, et al. Genome-wide patterns of homozygosity provide clues about the population history and adaptation of goats. ''Genet Sel Evol''. 2018 Nov 19; '''50''' (1):59
Genome-wide SNP profiling of worldwide goat populations reveals strong partitioning of diversity and highlights post-domestication migration routes. Description: Colli, Licia, et al. Genome-wide SNP profiling of worldwide goat populations reveals strong partitioning of diversity and highlights post-domestication migration routes. ''Genet Sel Evol''. 2018 Nov 19; '''50''' (1):58
Patterns of homozygosity in insular and continental goat breeds. Description: Cardoso, Taina F, et al. Patterns of homozygosity in insular and continental goat breeds. ''Genet Sel Evol''. 2018 Nov 19; '''50''' (1):56
A high-density genetic linkage map and QTL mapping for growth and sex of yellow drum (Nibea albiflora). Description: Qiu, Changliang, et al. A high-density genetic linkage map and QTL mapping for growth and sex of yellow drum (Nibea albiflora). ''Sci Rep''. 2018 Nov 22; '''8''' (1):17271
Genetic variation is associated with PTSD risk and aversive memory: Evidence from two trauma-Exposed African samples and one healthy European sample. Description: Wilker, Sarah, et al. Genetic variation is associated with PTSD risk and aversive memory: Evidence from two trauma-Exposed African samples and one healthy European sample. ''Transl Psychiatry''. 2018 Nov 22; '''8''' (1):251
Inferring phenotypes from substance use via collaborative matrix completion. Description: Lu, Jin, et al. Inferring phenotypes from substance use via collaborative matrix completion. ''BMC Syst Biol''. 2018 Nov 22; '''12''' (Suppl 6):104
Characterisation of the British honey bee metagenome. Description: Regan, Tim, et al. Characterisation of the British honey bee metagenome. ''Nat Commun''. 2018 Nov 26; '''9''' (1):4995
GRIPT: a novel case-control analysis method for Mendelian disease gene discovery. Description: Wang, Jun, et al. GRIPT: a novel case-control analysis method for Mendelian disease gene discovery. ''Genome Biol''. 2018 Nov 26; '''19''' (1):203
Hotspots of recent hybridization between pigs and wild boars in Europe. Description: Iacolina, Laura, et al. Hotspots of recent hybridization between pigs and wild boars in Europe. ''Sci Rep''. 2018 Nov 26; '''8''' (1):17372
Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression. Description: Schmiedel, Benjamin J, et al. Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression. ''Cell''. 2018 Nov 29; '''175''' (6):1701-1715.e16
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk. Description: Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk. ''Cell''. 2018 Nov 29; '''175''' (6):1679-1687.e7
Association of IL18 genetic polymorphisms with increased risk of Biliary atresia susceptibility in Southern Chinese children. Description: Liang, Jiankun, et al. Association of IL18 genetic polymorphisms with increased risk of Biliary atresia susceptibility in Southern Chinese children. ''Gene''. 2018 Nov 30; '''677''': 228-231
GT-repeat extension in the IL11 promoter is associated with Hirschsprung's disease (HSCR). Description: Haase, Michael G, et al. GT-repeat extension in the IL11 promoter is associated with Hirschsprung's disease (HSCR). ''Gene''. 2018 Nov 30; '''677''': 163-168
Identification on novel locus of dairy traits of Kazakh horse in Xinjiang. Description: Liu, Ling-Ling, et al. Identification on novel locus of dairy traits of Kazakh horse in Xinjiang. ''Gene''. 2018 Nov 30; '''677''': 105-110
Gamma-aminobutyric acid transaminase genetic polymorphism is a candidate locus for responsiveness to opioid analgesics in patients with cancer pain: An exploratory study. Description: Yokoshima, Yaeko, et al. Gamma-aminobutyric acid transaminase genetic polymorphism is a candidate locus for responsiveness to opioid analgesics in patients with cancer pain: An exploratory study. ''Neuropsychopharmacol Rep''. 2018 Dec; '''38''' (4):175-181
Ancestral origin of ApoE epsilon4 Alzheimer disease risk in Puerto Rican and African American populations. Description: Rajabli, Farid, et al. Ancestral origin of ApoE epsilon4 Alzheimer disease risk in Puerto Rican and African American populations. ''PLoS Genet''. 2018 Dec; '''14''' (12):e1007791
A whole-genome sequence based association study on pork eating quality traits and cooking loss in a specially designed heterogeneous F6 pig population. Description: Ji, Jiuxiu, et al. A whole-genome sequence based association study on pork eating quality traits and cooking loss in a specially designed heterogeneous F6 pig population. ''Meat Sci''. 2018 Dec; '''146''': 160-167
Axon guidance pathway genes are associated with schizophrenia risk. Description: Wang, Zhichao, et al. Axon guidance pathway genes are associated with schizophrenia risk. ''Exp Ther Med''. 2018 Dec; '''16''' (6):4519-4526
Combining mitochondrial and nuclear genome analyses to dissect the effects of colonization, environment, and geography on population structure in Pinus tabuliformis. Description: Xia, Hanhan, et al. Combining mitochondrial and nuclear genome analyses to dissect the effects of colonization, environment, and geography on population structure in Pinus tabuliformis. ''Evol Appl''. 2018 Dec; '''11''' (10):1931-1945
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. Description: Toma, Claudio, et al. Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. ''PLoS Genet''. 2018 Dec; '''14''' (12):e1007535
Correlation analysis between SNPs in microRNA-machinery genes and tuberculosis susceptibility in the Chinese Uygur population. Description: Cheng, Hong, et al. Correlation analysis between SNPs in microRNA-machinery genes and tuberculosis susceptibility in the Chinese Uygur population. ''Medicine (Baltimore)''. 2018 Dec; '''97''' (52):e13637
Endangered Pere David's deer genome provides insights into population recovering. Description: Zhu, Lifeng, et al. Endangered Pere David's deer genome provides insights into population recovering. ''Evol Appl''. 2018 Dec; '''11''' (10):2040-2053
Expression reflects population structure. Description: Brown, Brielin C, et al. Expression reflects population structure. ''PLoS Genet''. 2018 Dec; '''14''' (12):e1007841
Extent of linkage disequilibrium and effective population size of Korean Yorkshire swine. Description: Shin, Donghyun, et al. Extent of linkage disequilibrium and effective population size of Korean Yorkshire swine. ''Asian-Australas J Anim Sci''. 2018 Dec; '''31''' (12):1843-1851
Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. Description: Shah, Rupal L, et al. Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. ''Hum Genet''. 2018 Dec; '''137''' (11-12):881-896
Genomewide Association Study of Leisure-Time Exercise Behavior in Japanese Adults. Description: Hara, Megumi, et al. Genomewide Association Study of Leisure-Time Exercise Behavior in Japanese Adults. ''Med Sci Sports Exerc''. 2018 Dec; '''50''' (12):2433-2441
Genomic Analyses of Human European Diversity at the Southwestern Edge: Isolation, African Influence and Disease Associations in the Canary Islands. Description: Guillen-Guio, Beatriz, et al. Genomic Analyses of Human European Diversity at the Southwestern Edge: Isolation, African Influence and Disease Associations in the Canary Islands. ''Mol Biol Evol''. 2018 Dec 1; '''35''' (12):3010-3026
How much of the predisposition to Hashimoto's thyroiditis can be explained based on previously reported associations? Description: Jabrocka-Hybel, A, et al. How much of the predisposition to Hashimoto's thyroiditis can be explained based on previously reported associations? ''J Endocrinol Invest''. 2018 Dec; '''41''' (12):1409-1416
Major changes of cell function and toxicant sensitivity in cultured cells undergoing mild, quasi-natural genetic drift. Description: Gutbier, Simon, et al. Major changes of cell function and toxicant sensitivity in cultured cells undergoing mild, quasi-natural genetic drift. ''Arch Toxicol''. 2018 Dec; '''92''' (12):3487-3503
Metabolic Syndrome Prediction Using Machine Learning Models with Genetic and Clinical Information from a Nonobese Healthy Population. Description: Choe, Eun Kyung, et al. Metabolic Syndrome Prediction Using Machine Learning Models with Genetic and Clinical Information from a Nonobese Healthy Population. ''Genomics Inform''. 2018 Dec; '''16''' (4):e31
Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC. Description: Smajlagic, Dinka, et al. Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC. ''Brain Behav''. 2018 Dec; '''8''' (12):e01144
Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP data. Description: Cherlin, Svetlana, et al. Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP data. ''Genet Epidemiol''. 2018 Dec; '''42''' (8):754-771
Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease. Description: Beecham, Gary W, et al. Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease. ''Neurol Genet''. 2018 Dec; '''4''' (6):e286
snpEnrichR: analyzing co-localization of SNPs and their proxies in genomic regions. Description: Nousiainen, Kari, et al. snpEnrichR: analyzing co-localization of SNPs and their proxies in genomic regions. ''Bioinformatics''. 2018 Dec 1; '''34''' (23):4112-4114
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes. Description: de Haan, H G, et al. Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes. ''J Thromb Haemost''. 2018 Dec; '''16''' (12):2432-2441
The hSNM1B/Apollo variant rs11552449 is associated with cellular sensitivity towards mitomycin C and ionizing radiation. Description: Herwest, Sarah, et al. The hSNM1B/Apollo variant rs11552449 is associated with cellular sensitivity towards mitomycin C and ionizing radiation. ''DNA Repair (Amst)''. 2018 Dec; '''72''': 93-98
The impact of GJA8 SNPs on susceptibility to age-related cataract. Description: Yu, Xiaoning, et al. The impact of GJA8 SNPs on susceptibility to age-related cataract. ''Hum Genet''. 2018 Dec; '''137''' (11-12):897-904
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Description: Walters, Raymond K, et al. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. ''Nat Neurosci''. 2018 Dec; '''21''' (12):1656-1669
Whole genome variant association across 100 dogs identifies a frame shift mutation in DISHEVELLED 2 which contributes to Robinow-like syndrome in Bulldogs and related screw tail dog breeds. Description: Mansour, Tamer A, et al. Whole genome variant association across 100 dogs identifies a frame shift mutation in DISHEVELLED 2 which contributes to Robinow-like syndrome in Bulldogs and related screw tail dog breeds. ''PLoS Genet''. 2018 Dec; '''14''' (12):e1007850
Genetic Characterization of Indubrasil Cattle Breed Population. Description: Zanella, Ricardo, et al. Genetic Characterization of Indubrasil Cattle Breed Population. ''Vet Sci''. 2018 Dec 3; '''5''' (4):
Long-term experimental hybridisation results in the evolution of a new sex chromosome in swordtail fish. Description: Franchini, Paolo, et al. Long-term experimental hybridisation results in the evolution of a new sex chromosome in swordtail fish. ''Nat Commun''. 2018 Dec 3; '''9''' (1):5136
Design of low density SNP chips for genotype imputation in layer chicken. Description: Herry, Florian, et al. Design of low density SNP chips for genotype imputation in layer chicken. ''BMC Genet''. 2018 Dec 4; '''19''' (1):108
Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. Description: Mukherjee, Shubhabrata, et al. Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. ''Mol Psychiatry''. 2018 Dec 4;
Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study. Description: Hollensted, Mette, et al. Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study. ''BMC Med Genet''. 2018 Dec 4; '''19''' (1):207
The origins of malaria artemisinin resistance defined by a genetic and transcriptomic background. Description: Zhu, Lei, et al. The origins of malaria artemisinin resistance defined by a genetic and transcriptomic background. ''Nat Commun''. 2018 Dec 4; '''9''' (1):5158
A phylogenetic framework of the legume genus Aeschynomene for comparative genetic analysis of the Nod-dependent and Nod-independent symbioses. Description: Brottier, Laurent, et al. A phylogenetic framework of the legume genus Aeschynomene for comparative genetic analysis of the Nod-dependent and Nod-independent symbioses. ''BMC Plant Biol''. 2018 Dec 5; '''18''' (1):333
Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing. Description: Husson, Thomas, et al. Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing. ''Transl Psychiatry''. 2018 Dec 5; '''8''' (1):268
The association between neonatal vitamin D status and risk of schizophrenia. Description: Eyles, Darryl W, et al. The association between neonatal vitamin D status and risk of schizophrenia. ''Sci Rep''. 2018 Dec 6; '''8''' (1):17692
The Genetic Ancestry of Modern Indus Valley Populations from Northwest India. Description: Pathak, Ajai K, et al. The Genetic Ancestry of Modern Indus Valley Populations from Northwest India. ''Am J Hum Genet''. 2018 Dec 6; '''103''' (6):918-929
Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population. Description: Zhao, Lijuan, et al. Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population. ''Transl Psychiatry''. 2018 Dec 7; '''8''' (1):270
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Description: Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. ''Nat Commun''. 2018 Dec 10; '''9''' (1):5269
Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. Description: Morgan, Michael D, et al. Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. ''Nat Commun''. 2018 Dec 10; '''9''' (1):5271
Rediscovery of Red Wolf Ghost Alleles in a Canid Population Along the American Gulf Coast. Description: Heppenheimer, Elizabeth, et al. Rediscovery of Red Wolf Ghost Alleles in a Canid Population Along the American Gulf Coast. ''Genes (Basel)''. 2018 Dec 10; '''9''' (12):
Genetic ancestry, admixture and health determinants in Latin America. Description: Norris, Emily T, et al. Genetic ancestry, admixture and health determinants in Latin America. ''BMC Genomics''. 2018 Dec 11; '''19''' (Suppl 8):861
Accuracy of RNAseq based SNP discovery and genotyping in Populusnigra. Description: Rogier, Odile, et al. Accuracy of RNAseq based SNP discovery and genotyping in Populusnigra. ''BMC Genomics''. 2018 Dec 12; '''19''' (1):909
Ancient Ancestry Informative Markers for Identifying Fine-Scale Ancient Population Structure in Eurasians. Description: Esposito, Umberto, et al. Ancient Ancestry Informative Markers for Identifying Fine-Scale Ancient Population Structure in Eurasians. ''Genes (Basel)''. 2018 Dec 12; '''9''' (12):
Identification of deleterious and regulatory genomic variations in known asthma loci. Description: Neville, Matthew D C, et al. Identification of deleterious and regulatory genomic variations in known asthma loci. ''Respir Res''. 2018 Dec 12; '''19''' (1):248
Screening of Streptococcus Suis serotype 2 resistance genes with GWAS and transcriptomic microarray analysis. Description: Ma, Zhe, et al. Screening of Streptococcus Suis serotype 2 resistance genes with GWAS and transcriptomic microarray analysis. ''BMC Genomics''. 2018 Dec 12; '''19''' (1):907
Association between Polymorphisms in Inflammatory Response-Related Genes and the Susceptibility, Progression and Prognosis of the Diffuse Histological Subtype of Gastric Cancer. Description: Furuya, Tatiane K, et al. Association between Polymorphisms in Inflammatory Response-Related Genes and the Susceptibility, Progression and Prognosis of the Diffuse Histological Subtype of Gastric Cancer. ''Genes (Basel)''. 2018 Dec 13; '''9''' (12):
Dopamine perturbation of gene co-expression networks reveals differential response in schizophrenia for translational machinery. Description: Kos, Mark Z, et al. Dopamine perturbation of gene co-expression networks reveals differential response in schizophrenia for translational machinery. ''Transl Psychiatry''. 2018 Dec 13; '''8''' (1):278
Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP. Description: Jiang, Shan, et al. Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP. ''Transl Psychiatry''. 2018 Dec 13; '''8''' (1):265
Clinical and genetic associations of renal function and diabetic kidney disease in the United Arab Emirates: a cross-sectional study. Description: Osman, Wael M, et al. Clinical and genetic associations of renal function and diabetic kidney disease in the United Arab Emirates: a cross-sectional study. ''BMJ Open''. 2018 Dec 14; '''8''' (12):e020759
Exploratory genome-wide association analysis of response to ketamine and a polygenic analysis of response to scopolamine in depression. Description: Guo, Wei, et al. Exploratory genome-wide association analysis of response to ketamine and a polygenic analysis of response to scopolamine in depression. ''Transl Psychiatry''. 2018 Dec 14; '''8''' (1):280
Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis. Description: Kuiper, Jonas J W, et al. Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis. ''Hum Mol Genet''. 2018 Dec 15; '''27''' (24):4333-4343
Genetic variants within 17q12 are associated with the risk of cervical cancer in the Han Chinese population. Description: Hu, Lingmin, et al. Genetic variants within 17q12 are associated with the risk of cervical cancer in the Han Chinese population. ''Gene''. 2018 Dec 15; '''678''': 124-128
The Muskox Lost a Substantial Part of Its Genetic Diversity on Its Long Road to Greenland. Description: Hansen, Charles Christian Riis, et al. The Muskox Lost a Substantial Part of Its Genetic Diversity on Its Long Road to Greenland. ''Curr Biol''. 2018 Dec 17; '''28''' (24):4022-4028.e5
A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene. Description: Hawi, Ziarih, et al. A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene. ''Transl Psychiatry''. 2018 Dec 18; '''8''' (1):284
Accuracy of genomic selection for growth and wood quality traits in two control-pollinated progeny trials using exome capture as the genotyping platform in Norway spruce. Description: Chen, Zhi-Qiang, et al. Accuracy of genomic selection for growth and wood quality traits in two control-pollinated progeny trials using exome capture as the genotyping platform in Norway spruce. ''BMC Genomics''. 2018 Dec 18; '''19''' (1):946
Blood-Based Biomarkers for Predicting the Risk for Five-Year Incident Coronary Heart Disease in the Framingham Heart Study via Machine Learning. Description: Dogan, Meeshanthini V, et al. Blood-Based Biomarkers for Predicting the Risk for Five-Year Incident Coronary Heart Disease in the Framingham Heart Study via Machine Learning. ''Genes (Basel)''. 2018 Dec 18; '''9''' (12):
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients. Description: Cardamone, Giulia, et al. Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients. ''Biomedicines''. 2018 Dec 18; '''6''' (4):
Genetic investigation into an increased susceptibility to biliary atresia in an extended New Zealand Maori family. Description: Cameron-Christie, Sophia R, et al. Genetic investigation into an increased susceptibility to biliary atresia in an extended New Zealand Maori family. ''BMC Med Genomics''. 2018 Dec 18; '''11''' (1):121
Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance. Description: Chacon-Duque, Juan-Camilo, et al. Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance. ''Nat Commun''. 2018 Dec 19; '''9''' (1):5388
A novel deletion in KRT75L4 mediates the frizzle trait in a Chinese indigenous chicken. Description: Dong, Jing, et al. A novel deletion in KRT75L4 mediates the frizzle trait in a Chinese indigenous chicken. ''Genet Sel Evol''. 2018 Dec 20; '''50''' (1):68
Dissection of genetic variation and evidence for pleiotropy in male pattern baldness. Description: Yap, Chloe X, et al. Dissection of genetic variation and evidence for pleiotropy in male pattern baldness. ''Nat Commun''. 2018 Dec 20; '''9''' (1):5407
Genome re-sequencing reveals the evolutionary history of peach fruit edibility. Description: Yu, Yang, et al. Genome re-sequencing reveals the evolutionary history of peach fruit edibility. ''Nat Commun''. 2018 Dec 20; '''9''' (1):5404
Genome-wide assessment of genetic diversity and population structure insights into admixture and introgression in Chinese indigenous cattle. Description: Zhang, Wengang, et al. Genome-wide assessment of genetic diversity and population structure insights into admixture and introgression in Chinese indigenous cattle. ''BMC Genet''. 2018 Dec 20; '''19''' (1):114
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations. Description: Marquez, Ana, et al. Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations. ''Genome Med''. 2018 Dec 20; '''10''' (1):97
The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma. Description: Loohuis, Loes M, et al. The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma. ''Genes (Basel)''. 2018 Dec 22; '''10''' (1):
Copy number variation in the MSRB3 gene enlarges porcine ear size through a mechanism involving miR-584-5p. Description: Chen, Congying, et al. Copy number variation in the MSRB3 gene enlarges porcine ear size through a mechanism involving miR-584-5p. ''Genet Sel Evol''. 2018 Dec 27; '''50''' (1):72
Genome-wide association study of Mycobacterium avium subspecies Paratuberculosis infection in Chinese Holstein. Description: Gao, Yahui, et al. Genome-wide association study of Mycobacterium avium subspecies Paratuberculosis infection in Chinese Holstein. ''BMC Genomics''. 2018 Dec 27; '''19''' (1):972
Meta-analysis of Alzheimer's disease on 9,751 samples from Norway and IGAP study identifies four risk loci. Description: Witoelar, Aree, et al. Meta-analysis of Alzheimer's disease on 9,751 samples from Norway and IGAP study identifies four risk loci. ''Sci Rep''. 2018 Dec 27; '''8''' (1):18088
Polymorphisms in RAS/RAF/MEK/ERK Pathway Are Associated with Gastric Cancer. Description: Gonzalez-Hormazabal, Patricio, et al. Polymorphisms in RAS/RAF/MEK/ERK Pathway Are Associated with Gastric Cancer. ''Genes (Basel)''. 2018 Dec 28; '''10''' (1):
A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci. Description: Hamdi, Yosr, et al. A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci. ''BMC Cancer''. 2018 Dec 29; '''18''' (1):1295
Associations of Homer Scaffolding Protein 1 gene and psychological correlates with suicide attempts in Chinese: A pilot study of multifactorial risk model. Description: Rao, Shitao, et al. Associations of Homer Scaffolding Protein 1 gene and psychological correlates with suicide attempts in Chinese: A pilot study of multifactorial risk model. ''Gene''. 2018 Dec 30; '''679''': 382-388
Gene variants in AKT1, GCKR and SOCS3 are differentially associated with metabolic traits in Mexican Amerindians and Mestizos. Description: Cid-Soto, Miguel A, et al. Gene variants in AKT1, GCKR and SOCS3 are differentially associated with metabolic traits in Mexican Amerindians and Mestizos. ''Gene''. 2018 Dec 30; '''679''': 160-171
Precision Phenotyping Reveals Novel Loci for Quantitative Resistance to Septoria Tritici Blotch. Description: Yates, Steven, et al. Precision Phenotyping Reveals Novel Loci for Quantitative Resistance to Septoria Tritici Blotch. ''Plant Phenomics''. 2019; '''2019''': 3285904
Using Polygenic Scores in Social Science Research: Unraveling Childlessness. Description: Verweij, Renske M, et al. Using Polygenic Scores in Social Science Research: Unraveling Childlessness. ''Front Sociol''. 2019; '''4''': 74
3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosome. Description: Tadaka, Shu, et al. 3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosome. ''Hum Genome Var''. 2019; '''6''': 28
A 3' UTR SNP rs885863, a cis-eQTL for the circadian gene VIPR2 and lincRNA 689, is associated with opioid addiction. Description: Levran, Orna, et al. A 3' UTR SNP rs885863, a cis-eQTL for the circadian gene VIPR2 and lincRNA 689, is associated with opioid addiction. ''PLoS One''. 2019; '''14''' (11):e0224399
A Combined Multi-Cohort Approach Reveals Novel and Known Genome-Wide Selection Signatures for Wool Traits in Merino and Merino-Derived Sheep Breeds. Description: Megdiche, Sami, et al. A Combined Multi-Cohort Approach Reveals Novel and Known Genome-Wide Selection Signatures for Wool Traits in Merino and Merino-Derived Sheep Breeds. ''Front Genet''. 2019; '''10''': 1025
A Combined Transcriptomic and Genomic Analysis Identifies a Gene Signature Associated With the Response to Anti-TNF Therapy in Rheumatoid Arthritis. Description: Aterido, Adria, et al. A Combined Transcriptomic and Genomic Analysis Identifies a Gene Signature Associated With the Response to Anti-TNF Therapy in Rheumatoid Arthritis. ''Front Immunol''. 2019; '''10''': 1459
Adaptation to milking agropastoralism in Chilean goat herders and nutritional benefit of lactase persistence. Description: Montalva, Nicolas, et al. Adaptation to milking agropastoralism in Chilean goat herders and nutritional benefit of lactase persistence. ''Ann Hum Genet''. 2019 Jan; '''83''' (1):11-22
Additive and heterozygous (dis)advantage GWAS models reveal candidate genes involved in the genotypic variation of maize hybrids to Azospirillum brasilense. Description: Vidotti, Miriam Suzane, et al. Additive and heterozygous (dis)advantage GWAS models reveal candidate genes involved in the genotypic variation of maize hybrids to Azospirillum brasilense. ''PLoS One''. 2019; '''14''' (9):e0222788
Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry. Description: Chi, Calvin, et al. Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry. ''PLoS Genet''. 2019 Jan; '''15''' (1):e1007808
Affected Sib-Pair Analyses Identify Signaling Networks Associated With Social Behavioral Deficits in Autism. Description: Pirooznia, Mehdi, et al. Affected Sib-Pair Analyses Identify Signaling Networks Associated With Social Behavioral Deficits in Autism. ''Front Genet''. 2019; '''10''': 1186
A framework for linking resting-state chronnectome/genome features in schizophrenia: A pilot study. Description: Rashid, Barnaly, et al. A framework for linking resting-state chronnectome/genome features in schizophrenia: A pilot study. ''Neuroimage''. 2019 Jan 1; '''184''': 843-854
A genetic sum score of risk alleles associated with body mass index interacts with socioeconomic position in the Heinz Nixdorf Recall Study. Description: Frank, Mirjam, et al. A genetic sum score of risk alleles associated with body mass index interacts with socioeconomic position in the Heinz Nixdorf Recall Study. ''PLoS One''. 2019; '''14''' (8):e0221252
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Description: van der Lee, Sven J, et al. A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. ''Commun Biol''. 2019; '''2''': 285
A geographically matched control population efficiently limits the number of candidate disease-causing variants in an unbiased whole-genome analysis. Description: Rentoft, Matilda, et al. A geographically matched control population efficiently limits the number of candidate disease-causing variants in an unbiased whole-genome analysis. ''PLoS One''. 2019; '''14''' (3):e0213350
A large data resource of genomic copy number variation across neurodevelopmental disorders. Description: Zarrei, Mehdi, et al. A large data resource of genomic copy number variation across neurodevelopmental disorders. ''NPJ Genom Med''. 2019; '''4''': 26
A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska. Description: Weinstein, Spencer Y, et al. A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska. ''PLoS One''. 2019; '''14''' (9):e0223018
A Large-Scale Genome-Wide Association Analyses of Ethiopian Sorghum Landrace Collection Reveal Loci Associated With Important Traits. Description: Girma, Gezahegn, et al. A Large-Scale Genome-Wide Association Analyses of Ethiopian Sorghum Landrace Collection Reveal Loci Associated With Important Traits. ''Front Plant Sci''. 2019; '''10''': 691
Allele frequency-free inference of close familial relationships from genotypes or low-depth sequencing data. Description: Waples, Ryan K, et al. Allele frequency-free inference of close familial relationships from genotypes or low-depth sequencing data. ''Mol Ecol''. 2019 Jan; '''28''' (1):35-48
A Mutation in the Mitochondrial Aspartate/Glutamate Carrier Leads to a More Oxidizing Intramitochondrial Environment and an Inflammatory Myopathy in Dutch Shepherd Dogs. Description: Shelton, G Diane, et al. A Mutation in the Mitochondrial Aspartate/Glutamate Carrier Leads to a More Oxidizing Intramitochondrial Environment and an Inflammatory Myopathy in Dutch Shepherd Dogs. ''J Neuromuscul Dis''. 2019; '''6''' (4):485-501
Analysis of genome-wide DNA arrays reveals the genomic population structure and diversity in autochthonous Greek goat breeds. Description: Michailidou, S, et al. Analysis of genome-wide DNA arrays reveals the genomic population structure and diversity in autochthonous Greek goat breeds. ''PLoS One''. 2019; '''14''' (12):e0226179
Analysis of porcine IGF2 gene expression in adipose tissue and its effect on fatty acid composition. Description: Criado-Mesas, Lourdes, et al. Analysis of porcine IGF2 gene expression in adipose tissue and its effect on fatty acid composition. ''PLoS One''. 2019; '''14''' (8):e0220708
Ancient DNA from mastics solidifies connection between material culture and genetics of mesolithic hunter-gatherers in Scandinavia. Description: Kashuba, Natalija, et al. Ancient DNA from mastics solidifies connection between material culture and genetics of mesolithic hunter-gatherers in Scandinavia. ''Commun Biol''. 2019; '''2''': 185
Ancient introgression drives adaptation to cooler and drier mountain habitats in a cypress species complex. Description: Ma, Yazhen, et al. Ancient introgression drives adaptation to cooler and drier mountain habitats in a cypress species complex. ''Commun Biol''. 2019; '''2''': 213
An expanded variant list and assembly annotation identifies multiple novel coding and noncoding genes for prostate cancer risk using a normal prostate tissue eQTL data set. Description: DeRycke, Melissa S, et al. An expanded variant list and assembly annotation identifies multiple novel coding and noncoding genes for prostate cancer risk using a normal prostate tissue eQTL data set. ''PLoS One''. 2019; '''14''' (4):e0214588
An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank. Description: James, Glen, et al. An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank. ''PLoS One''. 2019; '''14''' (4):e0215026
A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans. Description: Pendergrass, Sarah A, et al. A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans. ''PLoS One''. 2019; '''14''' (12):e0226771
Apolipoprotein E Homozygous epsilon4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain Structure. Description: Goltermann, Janik, et al. Apolipoprotein E Homozygous epsilon4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain Structure. ''Front Neurol''. 2019; '''10''': 552
A Population Genomics Analysis of the Native Irish Galway Sheep Breed. Description: McHugo, Gillian P, et al. A Population Genomics Analysis of the Native Irish Galway Sheep Breed. ''Front Genet''. 2019; '''10''': 927
Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine. Description: Cowan, Karen, et al. Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine. ''PLoS One''. 2019; '''14''' (12):e0226564
A preliminary investigation of rare variants associated with genetic risk for PTSD in a natural disaster-exposed adolescent sample. Description: Sheerin, Christina M, et al. A preliminary investigation of rare variants associated with genetic risk for PTSD in a natural disaster-exposed adolescent sample. ''Eur J Psychotraumatol''. 2019; '''10''' (1):1688935
A Rare Genetic Defect of MBL2 Increased the Risk for Progression of IgA Nephropathy. Description: Ouyang, Yan, et al. A Rare Genetic Defect of MBL2 Increased the Risk for Progression of IgA Nephropathy. ''Front Immunol''. 2019; '''10''': 537
Architecture of population-differentiated polymorphisms in the human genome. Description: Bachtiar, Maulana, et al. Architecture of population-differentiated polymorphisms in the human genome. ''PLoS One''. 2019; '''14''' (10):e0224089
ARHGEF10L contributes to liver tumorigenesis through RhoA-ROCK1 signaling and the epithelial-mesenchymal transition. Description: Tang, Junyi, et al. ARHGEF10L contributes to liver tumorigenesis through RhoA-ROCK1 signaling and the epithelial-mesenchymal transition. ''Exp Cell Res''. 2019 Jan 1; '''374''' (1):46-68
A set of novel SNP loci for differentiating continental populations and three Chinese populations. Description: Jin, Xiao-Ye, et al. A set of novel SNP loci for differentiating continental populations and three Chinese populations. ''PeerJ''. 2019; '''7''': e6508
A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population. Description: Hollister, Brittany M, et al. A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population. ''Front Genet''. 2019; '''10''': 428
Assessment of Autozygosity Derived From Runs of Homozygosity in Jinhua Pigs Disclosed by Sequencing Data. Description: Xu, Zhong, et al. Assessment of Autozygosity Derived From Runs of Homozygosity in Jinhua Pigs Disclosed by Sequencing Data. ''Front Genet''. 2019; '''10''': 274
Assessment of the Clinical Heterogeneity of Kawasaki Disease Using Genetic Variants of BLK and FCGR2A. Description: Sim, Bo Kyung, et al. Assessment of the Clinical Heterogeneity of Kawasaki Disease Using Genetic Variants of BLK and FCGR2A. ''Korean Circ J''. 2019 Jan; '''49''' (1):99-108
Association analysis of polymorphisms in STARD6 and near ECHDC3 in Alzheimer's disease patients carrying the APOE epsilon4 Allele. Description: Yin, Jiajun, et al. Association analysis of polymorphisms in STARD6 and near ECHDC3 in Alzheimer's disease patients carrying the APOE epsilon4 Allele. ''Neuropsychiatr Dis Treat''. 2019; '''15''': 213-218
Association and Interaction Effects of Interleukin-12 Related Genes and Physical Activity on Cognitive Aging in Old Adults in the Taiwanese Population. Description: Lin, Eugene, et al. Association and Interaction Effects of Interleukin-12 Related Genes and Physical Activity on Cognitive Aging in Old Adults in the Taiwanese Population. ''Front Neurol''. 2019; '''10''': 1065
Association between oral cleft and transcobalamin 2 polymorphism in a sample study from Nassiriya, Iraq. Description: Carinci, Francesco, et al. Association between oral cleft and transcobalamin 2 polymorphism in a sample study from Nassiriya, Iraq. ''Int J Immunopathol Pharmacol''. 2019 Jan-Dec; '''33''': 2058738419855571
Association of SYNE1 locus with bipolar disorder in Chinese population. Description: Li, Wenqiang, et al. Association of SYNE1 locus with bipolar disorder in Chinese population. ''Hereditas''. 2019; '''156''': 19
Association of TIMP4 gene variants with steroid-induced osteonecrosis of the femoral head in the population of northern China. Description: Wang, Jiaqi, et al. Association of TIMP4 gene variants with steroid-induced osteonecrosis of the femoral head in the population of northern China. ''PeerJ''. 2019; '''7''': e6270
Association study between CCR2-CCR5 genes polymorphisms and chronic Chagas heart disease in Wichi and in admixed populations from Argentina. Description: Juiz, Natalia Anahi, et al. Association study between CCR2-CCR5 genes polymorphisms and chronic Chagas heart disease in Wichi and in admixed populations from Argentina. ''PLoS Negl Trop Dis''. 2019 Jan; '''13''' (1):e0007033
Association Study of KCNH7 Polymorphisms and Individual Responses to Risperidone Treatment in Schizophrenia. Description: Wang, Xueping, et al. Association Study of KCNH7 Polymorphisms and Individual Responses to Risperidone Treatment in Schizophrenia. ''Front Psychiatry''. 2019; '''10''': 633
Association Study Reveals Genetic Loci Responsible for Arsenic, Cadmium and Lead Accumulation in Rice Grain in Contaminated Farmlands. Description: Liu, Xiuyan, et al. Association Study Reveals Genetic Loci Responsible for Arsenic, Cadmium and Lead Accumulation in Rice Grain in Contaminated Farmlands. ''Front Plant Sci''. 2019; '''10''': 61
Assortative Mating on Ancestry-Variant Traits in Admixed Latin American Populations. Description: Norris, Emily T, et al. Assortative Mating on Ancestry-Variant Traits in Admixed Latin American Populations. ''Front Genet''. 2019; '''10''': 359
A whole genome scan of SNP data suggests a lack of abundant hard selective sweeps in the genome of the broad host range plant pathogenic fungus Sclerotinia sclerotiorum. Description: Derbyshire, Mark Charles, et al. A whole genome scan of SNP data suggests a lack of abundant hard selective sweeps in the genome of the broad host range plant pathogenic fungus Sclerotinia sclerotiorum. ''PLoS One''. 2019; '''14''' (3):e0214201
Beta2-Adrenergic Receptor Polymorphisms and Haplotypes Associate With Chronic Pain in Sickle Cell Disease. Description: Jhun, Ellie H, et al. Beta2-Adrenergic Receptor Polymorphisms and Haplotypes Associate With Chronic Pain in Sickle Cell Disease. ''Front Pharmacol''. 2019; '''10''': 84
Bilirubin and risk of ischemic heart disease in Korea: a two-sample Mendelian randomization study. Description: Jeon, Christina, et al. Bilirubin and risk of ischemic heart disease in Korea: a two-sample Mendelian randomization study. ''Epidemiol Health''. 2019; '''41''': e2019034
Both rare and common genetic variants contribute to autism in the Faroe Islands. Description: Leblond, Claire S, et al. Both rare and common genetic variants contribute to autism in the Faroe Islands. ''NPJ Genom Med''. 2019; '''4''': 1
Brain function, structure and genomic data are linked but show different sensitivity to duration of illness and disease stage in schizophrenia. Description: Luo, Na, et al. Brain function, structure and genomic data are linked but show different sensitivity to duration of illness and disease stage in schizophrenia. ''Neuroimage Clin''. 2019; '''23''': 101887
Causal Effects of Genetically Predicted Cardiovascular Risk Factors on Chronic Kidney Disease: A Two-Sample Mendelian Randomization Study. Description: Liu, Hui-Min, et al. Causal Effects of Genetically Predicted Cardiovascular Risk Factors on Chronic Kidney Disease: A Two-Sample Mendelian Randomization Study. ''Front Genet''. 2019; '''10''': 415
Chronic Immune Activation in Systemic Lupus Erythematosus and the Autoimmune PTPN22 Trp(620) Risk Allele Drive the Expansion of FOXP3(+) Regulatory T Cells and PD-1 Expression. Description: Ferreira, Ricardo C, et al. Chronic Immune Activation in Systemic Lupus Erythematosus and the Autoimmune PTPN22 Trp(620) Risk Allele Drive the Expansion of FOXP3(+) Regulatory T Cells and PD-1 Expression. ''Front Immunol''. 2019; '''10''': 2606
Circulating mitochondrial DNA: New indices of type 2 diabetes-related cognitive impairment in Mexican Americans. Description: Silzer, Talisa, et al. Circulating mitochondrial DNA: New indices of type 2 diabetes-related cognitive impairment in Mexican Americans. ''PLoS One''. 2019; '''14''' (3):e0213527
Common and rare GCH1 variants are associated with Parkinson's disease. Description: Rudakou, Uladzislau, et al. Common and rare GCH1 variants are associated with Parkinson's disease. ''Neurobiol Aging''. 2019 Jan; '''73''': 231.e1-231.e6
Common oxytocin polymorphisms interact with maternal verbal aggression in early infancy impacting blood pressure at age 5-6: The ABCD study. Description: Smarius, Laetitia J C A, et al. Common oxytocin polymorphisms interact with maternal verbal aggression in early infancy impacting blood pressure at age 5-6: The ABCD study. ''PLoS One''. 2019; '''14''' (6):e0216035
Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese. Description: Zhou, Zhaowei, et al. Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese. ''Hereditas''. 2019; '''156''': 4
Comparative Genomic Analysis Reveals the Potential Risk of Vibrio parahaemolyticus Isolated From Ready-To-Eat Foods in China. Description: Pang, Rui, et al. Comparative Genomic Analysis Reveals the Potential Risk of Vibrio parahaemolyticus Isolated From Ready-To-Eat Foods in China. ''Front Microbiol''. 2019; '''10''': 186
Comparing genomic signatures of domestication in two Atlantic salmon (Salmo salar L.) populations with different geographical origins. Description: Lopez, Maria E, et al. Comparing genomic signatures of domestication in two Atlantic salmon (Salmo salar L.) populations with different geographical origins. ''Evol Appl''. 2019 Jan; '''12''' (1):137-156
Comparison Between Flat and Round Peaches, Genomic Evidences of Heterozygosity Events. Description: Tan, Qiuping, et al. Comparison Between Flat and Round Peaches, Genomic Evidences of Heterozygosity Events. ''Front Plant Sci''. 2019; '''10''': 592
Comparison of quantitative trait loci methods: Total expression and allelic imbalance method in brain RNA-seq. Description: Gadin, Jesper R, et al. Comparison of quantitative trait loci methods: Total expression and allelic imbalance method in brain RNA-seq. ''PLoS One''. 2019; '''14''' (6):e0217765
Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of "Fogo Selvagem" Pemphigus Foliaceus. Description: Oliveira, Luana Caroline, et al. Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of "Fogo Selvagem" Pemphigus Foliaceus. ''Front Immunol''. 2019; '''10''': 2585
Confounding of linkage disequilibrium patterns in large scale DNA based gene-gene interaction studies. Description: Joiret, Marc, et al. Confounding of linkage disequilibrium patterns in large scale DNA based gene-gene interaction studies. ''BioData Min''. 2019; '''12''': 11
Consequences of PCA graphs, SNP codings, and PCA variants for elucidating population structure. Description: Gauch, Hugh G Jr, et al. Consequences of PCA graphs, SNP codings, and PCA variants for elucidating population structure. ''PLoS One''. 2019; '''14''' (6):e0218306
Conservation, Extensive Heterozygosity, and Convergence of Signaling Potential All Indicate a Critical Role for KIR3DL3 in Higher Primates. Description: Leaton, Laura A, et al. Conservation, Extensive Heterozygosity, and Convergence of Signaling Potential All Indicate a Critical Role for KIR3DL3 in Higher Primates. ''Front Immunol''. 2019; '''10''': 24
Coverage rate of ADME genes from commercial sequencing arrays. Description: Zaid, Nabil, et al. Coverage rate of ADME genes from commercial sequencing arrays. ''Medicine (Baltimore)''. 2019 Jan; '''98''' (3):e13975
CRUMBLER: A tool for the prediction of ancestry in cattle. Description: Crum, Tamar E, et al. CRUMBLER: A tool for the prediction of ancestry in cattle. ''PLoS One''. 2019; '''14''' (8):e0221471
CYP2B6 genetic polymorphisms influence chronic obstructive pulmonary disease susceptibility in the Hainan population. Description: Ding, Yipeng, et al. CYP2B6 genetic polymorphisms influence chronic obstructive pulmonary disease susceptibility in the Hainan population. ''Int J Chron Obstruct Pulmon Dis''. 2019; '''14''': 2103-2115
Deep Genome Resequencing Reveals Artificial and Natural Selection for Visual Deterioration, Plateau Adaptability and High Prolificacy in Chinese Domestic Sheep. Description: Wang, Weimin, et al. Deep Genome Resequencing Reveals Artificial and Natural Selection for Visual Deterioration, Plateau Adaptability and High Prolificacy in Chinese Domestic Sheep. ''Front Genet''. 2019; '''10''': 300
Deleterious alleles in the context of domestication, inbreeding, and selection. Description: Bosse, Mirte, et al. Deleterious alleles in the context of domestication, inbreeding, and selection. ''Evol Appl''. 2019 Jan; '''12''' (1):6-17
Demography and rapid local adaptation shape Creole cattle genome diversity in the tropics. Description: Pitt, Daniel, et al. Demography and rapid local adaptation shape Creole cattle genome diversity in the tropics. ''Evol Appl''. 2019 Jan; '''12''' (1):105-122
Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network. Description: Zhang, Xinyuan, et al. Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network. ''Pac Symp Biocomput''. 2019; '''24''': 272-283
Detection of a Frameshift Deletion in the SPTBN4 Gene Leads to Prevention of Severe Myopathy and Postnatal Mortality in Pigs. Description: Derks, Martijn F L, et al. Detection of a Frameshift Deletion in the SPTBN4 Gene Leads to Prevention of Severe Myopathy and Postnatal Mortality in Pigs. ''Front Genet''. 2019; '''10''': 1226
Discovery of Genomic Characteristics and Selection Signatures in Korean Indigenous Goats Through Comparison of 10 Goat Breeds. Description: Kim, Jae-Yoon, et al. Discovery of Genomic Characteristics and Selection Signatures in Korean Indigenous Goats Through Comparison of 10 Goat Breeds. ''Front Genet''. 2019; '''10''': 699
Discovery of Novel Biomarkers of Therapeutic Responses in Han Chinese Pemetrexed-Based Treated Advanced NSCLC Patients. Description: Zhang, Xiaoqing, et al. Discovery of Novel Biomarkers of Therapeutic Responses in Han Chinese Pemetrexed-Based Treated Advanced NSCLC Patients. ''Front Pharmacol''. 2019; '''10''': 944
Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach. Description: Portilla-Fernandez, Eliana, et al. Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach. ''PLoS One''. 2019; '''14''' (3):e0214137
Diverse Effects of the NTCP p.Ser267Phe Variant on Disease Progression During Chronic HBV Infection and on HBV preS1 Variability. Description: Yang, Fangji, et al. Diverse Effects of the NTCP p.Ser267Phe Variant on Disease Progression During Chronic HBV Infection and on HBV preS1 Variability. ''Front Cell Infect Microbiol''. 2019; '''9''': 18
Diversity, Virulence, and Antimicrobial Resistance in Isolates From the Newly Emerging Klebsiella pneumoniae ST101 Lineage. Description: Roe, Chandler C, et al. Diversity, Virulence, and Antimicrobial Resistance in Isolates From the Newly Emerging Klebsiella pneumoniae ST101 Lineage. ''Front Microbiol''. 2019; '''10''': 542
Do age-related macular degeneration genes show association with keratoconus? Description: Cao, Ke, et al. Do age-related macular degeneration genes show association with keratoconus? ''Eye Vis (Lond)''. 2019; '''6''': 38
Domestication of cattle: Two or three events? Description: Pitt, Daniel, et al. Domestication of cattle: Two or three events? ''Evol Appl''. 2019 Jan; '''12''' (1):123-136
Effective Diagnosis of Alzheimer's Disease via Multimodal Fusion Analysis Framework. Description: Bi, Xia-An, et al. Effective Diagnosis of Alzheimer's Disease via Multimodal Fusion Analysis Framework. ''Front Genet''. 2019; '''10''': 976
Effectiveness of imaging genetics analysis to explain degree of depression in Parkinson's disease. Description: Won, Ji Hye, et al. Effectiveness of imaging genetics analysis to explain degree of depression in Parkinson's disease. ''PLoS One''. 2019; '''14''' (2):e0211699
Effect of SNPs in HSP Family Genes, Variation in the mRNA and Intracellular Hsp Levels in COPD Secondary to Tobacco Smoking and Biomass-Burning Smoke. Description: Ambrocio-Ortiz, Enrique, et al. Effect of SNPs in HSP Family Genes, Variation in the mRNA and Intracellular Hsp Levels in COPD Secondary to Tobacco Smoking and Biomass-Burning Smoke. ''Front Genet''. 2019; '''10''': 1307
Effects of CYP3A4 Polymorphisms on Drug Addiction Risk Among the Chinese Han Population. Description: Wang, Li, et al. Effects of CYP3A4 Polymorphisms on Drug Addiction Risk Among the Chinese Han Population. ''Front Public Health''. 2019; '''7''': 315
Epigenome-Wide Comparative Study Reveals Key Differences Between Mixed Connective Tissue Disease and Related Systemic Autoimmune Diseases. Description: Carnero-Montoro, Elena, et al. Epigenome-Wide Comparative Study Reveals Key Differences Between Mixed Connective Tissue Disease and Related Systemic Autoimmune Diseases. ''Front Immunol''. 2019; '''10''': 1880
Evaluating the Accuracy of Imputation Methods in a Five-Way Admixed Population. Description: Schurz, Haiko, et al. Evaluating the Accuracy of Imputation Methods in a Five-Way Admixed Population. ''Front Genet''. 2019; '''10''': 34
Evaluation of Mannose Binding Lectin Gene Variants in Pediatric Influenza Virus-Related Critical Illness. Description: Levy, Emily R, et al. Evaluation of Mannose Binding Lectin Gene Variants in Pediatric Influenza Virus-Related Critical Illness. ''Front Immunol''. 2019; '''10''': 1005
Evaluation of the association of C5 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. Description: Liu, Ke, et al. Evaluation of the association of C5 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. ''Eye Vis (Lond)''. 2019; '''6''': 34
Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. Description: Foo, Jerome C, et al. Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. ''Am J Med Genet B Neuropsychiatr Genet''. 2019 Jan; '''180''' (1):35-45
Evidence of a causal relationship between body mass index and psoriasis: A mendelian randomization study. Description: Budu-Aggrey, Ashley, et al. Evidence of a causal relationship between body mass index and psoriasis: A mendelian randomization study. ''PLoS Med''. 2019 Jan; '''16''' (1):e1002739
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations. Description: van de Putte, Romy, et al. Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations. ''PLoS One''. 2019; '''14''' (5):e0217477
Exome Sequencing Identifies Susceptibility Loci for Sarcoidosis Prognosis. Description: Lahtela, Elisa, et al. Exome Sequencing Identifies Susceptibility Loci for Sarcoidosis Prognosis. ''Front Immunol''. 2019; '''10''': 2964
Exploration of a diversity of computational and statistical measures of association for genome-wide genetic studies. Description: Manduchi, Elisabetta, et al. Exploration of a diversity of computational and statistical measures of association for genome-wide genetic studies. ''BioData Min''. 2019; '''12''': 14
Exploring Impact of Rare Variation in Systemic Lupus Erythematosus by a Genome Wide Imputation Approach. Description: Martinez-Bueno, Manuel, et al. Exploring Impact of Rare Variation in Systemic Lupus Erythematosus by a Genome Wide Imputation Approach. ''Front Immunol''. 2019; '''10''': 258
Exploring the Causal Pathway From Telomere Length to Alzheimer's Disease: An Update Mendelian Randomization Study. Description: Gao, Kai, et al. Exploring the Causal Pathway From Telomere Length to Alzheimer's Disease: An Update Mendelian Randomization Study. ''Front Psychiatry''. 2019; '''10''': 843
Exploring the Structure of Haplotype Blocks and Genetic Diversity in Chinese Indigenous Pig Populations for Conservation Purpose. Description: Zhao, Qing-Bo, et al. Exploring the Structure of Haplotype Blocks and Genetic Diversity in Chinese Indigenous Pig Populations for Conservation Purpose. ''Evol Bioinform Online''. 2019; '''15''': 1176934318825082
Extending Classification Algorithms to Case-Control Studies. Description: Stanfill, Bryan, et al. Extending Classification Algorithms to Case-Control Studies. ''Biomed Eng Comput Biol''. 2019; '''10''': 1179597219858954
Fasciola hepatica Infection in Cattle: Analyzing Responses of Peripheral Blood Mononuclear Cells (PBMC) Using a Transcriptomics Approach. Description: Garcia-Campos, Andres, et al. Fasciola hepatica Infection in Cattle: Analyzing Responses of Peripheral Blood Mononuclear Cells (PBMC) Using a Transcriptomics Approach. ''Front Immunol''. 2019; '''10''': 2081
Financial Stress Interacts With CLOCK Gene to Affect Migraine. Description: Baksa, Daniel, et al. Financial Stress Interacts With CLOCK Gene to Affect Migraine. ''Front Behav Neurosci''. 2019; '''13''': 284
Finding New Cell Wall Regulatory Genes in Populus trichocarpa Using Multiple Lines of Evidence. Description: Furches, Anna, et al. Finding New Cell Wall Regulatory Genes in Populus trichocarpa Using Multiple Lines of Evidence. ''Front Plant Sci''. 2019; '''10''': 1249
Fine Mapping in Chromosome 3q28 Identified Two Variants Associated with Lung Cancer Risk in Asian Population. Description: Wen, Yang, et al. Fine Mapping in Chromosome 3q28 Identified Two Variants Associated with Lung Cancer Risk in Asian Population. ''J Cancer''. 2019; '''10''' (8):1862-1869
FTO Variant rs1421085 Associates With Increased Body Weight, Soft Lean Mass, and Total Body Water Through Interaction With Ghrelin and Apolipoproteins in Arab Population. Description: Hebbar, Prashantha, et al. FTO Variant rs1421085 Associates With Increased Body Weight, Soft Lean Mass, and Total Body Water Through Interaction With Ghrelin and Apolipoproteins in Arab Population. ''Front Genet''. 2019; '''10''': 1411
Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects. Description: Sewda, Anshuman, et al. Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects. ''PLoS One''. 2019; '''14''' (7):e0219926
Genetically regulated gene expression underlies lipid traits in Hispanic cohorts. Description: Andaleon, Angela, et al. Genetically regulated gene expression underlies lipid traits in Hispanic cohorts. ''PLoS One''. 2019; '''14''' (8):e0220827
Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms. Description: Liu, Boxiang, et al. Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms. ''Commun Biol''. 2019; '''2''': 186
Genetic and Expression Analysis of COPI Genes and Alzheimer's Disease Susceptibility. Description: Yang, Yu, et al. Genetic and Expression Analysis of COPI Genes and Alzheimer's Disease Susceptibility. ''Front Genet''. 2019; '''10''': 866
Genetic and genomic analyses of testicular hypoplasia in Nellore cattle. Description: Neves, Haroldo H R, et al. Genetic and genomic analyses of testicular hypoplasia in Nellore cattle. ''PLoS One''. 2019; '''14''' (1):e0211159
Genetic and genomic analyses underpin the feasibility of concomitant genetic improvement of milk yield and mastitis resistance in dairy sheep. Description: Banos, Georgios, et al. Genetic and genomic analyses underpin the feasibility of concomitant genetic improvement of milk yield and mastitis resistance in dairy sheep. ''PLoS One''. 2019; '''14''' (11):e0214346
Genetic architecture of human thinness compared to severe obesity. Description: Riveros-McKay, Fernando, et al. Genetic architecture of human thinness compared to severe obesity. ''PLoS Genet''. 2019 Jan; '''15''' (1):e1007603
Genetic association and differential expression of PITX2 with acute appendicitis. Description: Orlova, Ekaterina, et al. Genetic association and differential expression of PITX2 with acute appendicitis. ''Hum Genet''. 2019 Jan; '''138''' (1):37-47
Genetic Association of Olanzapine Treatment Response in Han Chinese Schizophrenia Patients. Description: Zhou, Wei, et al. Genetic Association of Olanzapine Treatment Response in Han Chinese Schizophrenia Patients. ''Front Pharmacol''. 2019; '''10''': 177
Genetic associations of perinatal pain and depression. Description: McClain, Lora, et al. Genetic associations of perinatal pain and depression. ''Mol Pain''. 2019 Jan-Dec; '''15''': 1744806919882139
Genetic Associations With Diabetic Retinopathy and Coronary Artery Disease in Emirati Patients With Type-2 Diabetes Mellitus. Description: Azzam, Sarah K, et al. Genetic Associations With Diabetic Retinopathy and Coronary Artery Disease in Emirati Patients With Type-2 Diabetes Mellitus. ''Front Endocrinol (Lausanne)''. 2019; '''10''': 283
Genetic Basis of Fiber Improvement and Decreased Stress Tolerance in Cultivated Versus Semi-Domesticated Upland Cotton. Description: Zhu, Guozhong, et al. Genetic Basis of Fiber Improvement and Decreased Stress Tolerance in Cultivated Versus Semi-Domesticated Upland Cotton. ''Front Plant Sci''. 2019; '''10''': 1572
Genetic Connectivity of the Sky Emperor, Lethrinus mahsena Populations Across a Gradient of Exploitation Rates in Coastal Kenya. Description: Mzingirwa, Fatuma Ali, et al. Genetic Connectivity of the Sky Emperor, Lethrinus mahsena Populations Across a Gradient of Exploitation Rates in Coastal Kenya. ''Front Genet''. 2019; '''10''': 1003
Genetic Diversities and Differentially Selected Regions Between Shandong Indigenous Pig Breeds and Western Pig Breeds. Description: Qin, Ming, et al. Genetic Diversities and Differentially Selected Regions Between Shandong Indigenous Pig Breeds and Western Pig Breeds. ''Front Genet''. 2019; '''10''': 1351
Genetic diversity and population structure of four Chinese rabbit breeds. Description: Ren, Anyong, et al. Genetic diversity and population structure of four Chinese rabbit breeds. ''PLoS One''. 2019; '''14''' (9):e0222503
Genetic Diversity and Signatures of Selection in 15 Chinese Indigenous Dog Breeds Revealed by Genome-Wide SNPs. Description: Yang, Qianyong, et al. Genetic Diversity and Signatures of Selection in 15 Chinese Indigenous Dog Breeds Revealed by Genome-Wide SNPs. ''Front Genet''. 2019; '''10''': 1174
Genetic Diversity Linked to Haplotype Variation in the World Core Collection of Trifolium subterraneum for Boron Toxicity Tolerance Provides Valuable Markers for Pasture Breeding. Description: Tahghighi, Hediyeh, et al. Genetic Diversity Linked to Haplotype Variation in the World Core Collection of Trifolium subterraneum for Boron Toxicity Tolerance Provides Valuable Markers for Pasture Breeding. ''Front Plant Sci''. 2019; '''10''': 1043
Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach. Description: Kurowski, Brad G, et al. Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach. ''Front Genet''. 2019; '''10''': 481
Genetic mapping of distal femoral, stifle, and tibial radiographic morphology in dogs with cranial cruciate ligament disease. Description: Healey, Eleni, et al. Genetic mapping of distal femoral, stifle, and tibial radiographic morphology in dogs with cranial cruciate ligament disease. ''PLoS One''. 2019; '''14''' (10):e0223094
Genetic Polymorphisms Affecting IDO1 or IDO2 Activity Differently Associate With Aspergillosis in Humans. Description: Napolioni, Valerio, et al. Genetic Polymorphisms Affecting IDO1 or IDO2 Activity Differently Associate With Aspergillosis in Humans. ''Front Immunol''. 2019; '''10''': 890
Genetic polymorphisms in IL-7 and IL-7R are correlated with lung cancer risk in the Chinese Han population. Description: Zhang, Chan, et al. Genetic polymorphisms in IL-7 and IL-7R are correlated with lung cancer risk in the Chinese Han population. ''Cancer Manag Res''. 2019; '''11''': 5393-5401
Genetic polymorphisms in PXR and NF-kappaB1 influence susceptibility to anti-tuberculosis drug-induced liver injury. Description: Zhang, Jingwei, et al. Genetic polymorphisms in PXR and NF-kappaB1 influence susceptibility to anti-tuberculosis drug-induced liver injury. ''PLoS One''. 2019; '''14''' (9):e0222033
Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate. Description: Sangurdekar, Dipen, et al. Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate. ''Front Genet''. 2019; '''10''': 1039
Genetic variability of five ADRB2 polymorphisms among Mexican Amerindian ethnicities and the Mestizo population. Description: Salas-Martinez, Maria Guadalupe, et al. Genetic variability of five ADRB2 polymorphisms among Mexican Amerindian ethnicities and the Mestizo population. ''PLoS One''. 2019; '''14''' (12):e0225030
Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk. Description: Schuetz, Johanna M, et al. Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk. ''PLoS One''. 2019; '''14''' (1):e0209010
Genetic variation drives seasonal onset of hibernation in the 13-lined ground squirrel. Description: Grabek, Katharine R, et al. Genetic variation drives seasonal onset of hibernation in the 13-lined ground squirrel. ''Commun Biol''. 2019; '''2''': 478
Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia. Description: Rhie, Arang, et al. Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia. ''PLoS One''. 2019; '''14''' (9):e0222533
Genome Analysis Reveals Genetic Admixture and Signature of Selection for Productivity and Environmental Traits in Iraqi Cattle. Description: Alshawi, Akil, et al. Genome Analysis Reveals Genetic Admixture and Signature of Selection for Productivity and Environmental Traits in Iraqi Cattle. ''Front Genet''. 2019; '''10''': 609
Genome Diversity and Signatures of Selection for Production and Performance Traits in Dromedary Camels. Description: Bahbahani, Hussain, et al. Genome Diversity and Signatures of Selection for Production and Performance Traits in Dromedary Camels. ''Front Genet''. 2019; '''10''': 893
Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease. Description: Frenkel, Svetlana, et al. Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease. ''PLoS One''. 2019; '''14''' (6):e0217846
Genome-Wide Analysis of Genetic Diversity in Plasmodium falciparum Isolates From China-Myanmar Border. Description: Ye, Run, et al. Genome-Wide Analysis of Genetic Diversity in Plasmodium falciparum Isolates From China-Myanmar Border. ''Front Genet''. 2019; '''10''': 1065
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy. Description: Hosoda, Yoshikatsu, et al. Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy. ''Commun Biol''. 2019; '''2''': 468
Genome-Wide Association Mapping and Gene Expression Analyses Reveal Genetic Mechanisms of Disease Resistance Variations in Cynoglossus semilaevis. Description: Zhou, Qian, et al. Genome-Wide Association Mapping and Gene Expression Analyses Reveal Genetic Mechanisms of Disease Resistance Variations in Cynoglossus semilaevis. ''Front Genet''. 2019; '''10''': 1167
Genome-wide association studies for yield-related traits in soft red winter wheat grown in Virginia. Description: Ward, Brian P, et al. Genome-wide association studies for yield-related traits in soft red winter wheat grown in Virginia. ''PLoS One''. 2019; '''14''' (2):e0208217
Genome-wide association study and a post replication analysis revealed a promising genomic region and candidate genes for chicken eggshell blueness. Description: Darwish, Hesham Y A, et al. Genome-wide association study and a post replication analysis revealed a promising genomic region and candidate genes for chicken eggshell blueness. ''PLoS One''. 2019; '''14''' (1):e0209181
Genome-wide association study for proliferative diabetic retinopathy in Africans. Description: Liu, Chang, et al. Genome-wide association study for proliferative diabetic retinopathy in Africans. ''NPJ Genom Med''. 2019; '''4''': 20
Genome-Wide Association Study Identifies Genomic Loci Affecting Filet Firmness and Protein Content in Rainbow Trout. Description: Ali, Ali, et al. Genome-Wide Association Study Identifies Genomic Loci Affecting Filet Firmness and Protein Content in Rainbow Trout. ''Front Genet''. 2019; '''10''': 386
Genome wide association study identifies SNPs associated with fatty acid composition in Chinese Wagyu cattle. Description: Wang, Zezhao, et al. Genome wide association study identifies SNPs associated with fatty acid composition in Chinese Wagyu cattle. ''J Anim Sci Biotechnol''. 2019; '''10''': 27
Genome-wide association study of berry-related traits in grape [Vitis vinifera L.] based on genotyping-by-sequencing markers. Description: Guo, Da-Long, et al. Genome-wide association study of berry-related traits in grape [Vitis vinifera L.] based on genotyping-by-sequencing markers. ''Hortic Res''. 2019; '''6''': 11
Genome-wide association study of coronary artery calcification in asymptomatic Korean populations. Description: Choi, Su-Yeon, et al. Genome-wide association study of coronary artery calcification in asymptomatic Korean populations. ''PLoS One''. 2019; '''14''' (3):e0214370
Genome-Wide Association Study of Growth and Feeding Traits in Pekin Ducks. Description: Zhu, Feng, et al. Genome-Wide Association Study of Growth and Feeding Traits in Pekin Ducks. ''Front Genet''. 2019; '''10''': 702
Genome-Wide Association Study of Meat Quality Traits in Hanwoo Beef Cattle Using Imputed Whole-Genome Sequence Data. Description: Bedhane, Mohammed, et al. Genome-Wide Association Study of Meat Quality Traits in Hanwoo Beef Cattle Using Imputed Whole-Genome Sequence Data. ''Front Genet''. 2019; '''10''': 1235
Genome-Wide Association Study of Tacrolimus Pharmacokinetics Identifies Novel Single Nucleotide Polymorphisms in the Convalescence and Stabilization Periods of Post-transplant Liver Function. Description: Liu, Yuan, et al. Genome-Wide Association Study of Tacrolimus Pharmacokinetics Identifies Novel Single Nucleotide Polymorphisms in the Convalescence and Stabilization Periods of Post-transplant Liver Function. ''Front Genet''. 2019; '''10''': 528
Genome-Wide Association Study Reveals Candidate Genes for Flowering Time Variation in Common Bean (Phaseolus vulgaris L.). Description: Raggi, Lorenzo, et al. Genome-Wide Association Study Reveals Candidate Genes for Flowering Time Variation in Common Bean (Phaseolus vulgaris L.). ''Front Plant Sci''. 2019; '''10''': 962
Genome-Wide Association Study Reveals Candidate Genes for Growth Relevant Traits in Pigs. Description: Tang, Zhenshuang, et al. Genome-Wide Association Study Reveals Candidate Genes for Growth Relevant Traits in Pigs. ''Front Genet''. 2019; '''10''': 302
Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia. Description: Kornilov, Sergey A, et al. Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia. ''Front Genet''. 2019; '''10''': 888
Genome-Wide Interaction and Pathway Association Studies for Body Mass Index. Description: Jiao, Hongxiao, et al. Genome-Wide Interaction and Pathway Association Studies for Body Mass Index. ''Front Genet''. 2019; '''10''': 404
Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma. Description: Chattopadhyay, Subhayan, et al. Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma. ''Commun Biol''. 2019; '''2''': 89
Genome-Wide Patterns of Population Structure and Linkage Disequilibrium in Farmed Nile Tilapia (Oreochromis niloticus). Description: Yoshida, Grazyella M, et al. Genome-Wide Patterns of Population Structure and Linkage Disequilibrium in Farmed Nile Tilapia (Oreochromis niloticus). ''Front Genet''. 2019; '''10''': 745
Genome-wide SNP analysis of Japanese Thoroughbred racehorses. Description: Fawcett, Jeffrey A, et al. Genome-wide SNP analysis of Japanese Thoroughbred racehorses. ''PLoS One''. 2019; '''14''' (7):e0218407
Genomic analyses provide insights into breed-of-origin effects from purebreds on three-way crossbred pigs. Description: Lin, Yu, et al. Genomic analyses provide insights into breed-of-origin effects from purebreds on three-way crossbred pigs. ''PeerJ''. 2019; '''7''': e8009
Genomic Analysis Reveals Pleiotropic Alleles at EDN3 and BMP7 Involved in Chicken Comb Color and Egg Production. Description: Dong, Xianggui, et al. Genomic Analysis Reveals Pleiotropic Alleles at EDN3 and BMP7 Involved in Chicken Comb Color and Egg Production. ''Front Genet''. 2019; '''10''': 612
Genomic and Transcriptomic Analysis of Amoebic Gill Disease Resistance in Atlantic Salmon (Salmo salar L.). Description: Boison, Solomon Antwi, et al. Genomic and Transcriptomic Analysis of Amoebic Gill Disease Resistance in Atlantic Salmon (Salmo salar L.). ''Front Genet''. 2019; '''10''': 68
Genomic prediction of relapse in recipients of allogeneic haematopoietic stem cell transplantation. Description: Ritari, J, et al. Genomic prediction of relapse in recipients of allogeneic haematopoietic stem cell transplantation. ''Leukemia''. 2019 Jan; '''33''' (1):240-248
Genomic structure of a crossbred Landrace pig population. Description: Joaquim, Leticia Borges, et al. Genomic structure of a crossbred Landrace pig population. ''PLoS One''. 2019; '''14''' (2):e0212266
Genomic, Transcriptomic, and Epigenomic Features Differentiate Genes That Are Relevant for Muscular Polyunsaturated Fatty Acids in the Common Carp. Description: Zhang, Hanyuan, et al. Genomic, Transcriptomic, and Epigenomic Features Differentiate Genes That Are Relevant for Muscular Polyunsaturated Fatty Acids in the Common Carp. ''Front Genet''. 2019; '''10''': 217
Glycated Serum Protein Genetics and Pleiotropy with Cardiometabolic Risk Factors. Description: Johnson, Matthew P, et al. Glycated Serum Protein Genetics and Pleiotropy with Cardiometabolic Risk Factors. ''J Diabetes Res''. 2019; '''2019''': 2310235
GmBRC1 is a Candidate Gene for Branching in Soybean (Glycine max (L.) Merrill). Description: Shim, Sangrea, et al. GmBRC1 is a Candidate Gene for Branching in Soybean (Glycine max (L.) Merrill). ''Int J Mol Sci''. 2019 Jan 1; '''20''' (1):
GWAS Follow-up Study Discovers a Novel Genetic Signal on 10q21.2 for Atopic Dermatitis in Chinese Han Population. Description: Cai, Xin-Ying, et al. GWAS Follow-up Study Discovers a Novel Genetic Signal on 10q21.2 for Atopic Dermatitis in Chinese Han Population. ''Front Genet''. 2019; '''10''': 174
Haplotypes of HTRA1 rs1120638, TIMP3 rs9621532, VEGFA rs833068, CFI rs10033900, ERCC6 rs3793784, and KCTD10 rs56209061 Gene Polymorphisms in Age-Related Macular Degeneration. Description: Liutkeviciene, Rasa, et al. Haplotypes of HTRA1 rs1120638, TIMP3 rs9621532, VEGFA rs833068, CFI rs10033900, ERCC6 rs3793784, and KCTD10 rs56209061 Gene Polymorphisms in Age-Related Macular Degeneration. ''Dis Markers''. 2019; '''2019''': 9602949
Heme oxygenase-1 repeat polymorphism in septic acute kidney injury. Description: Vilander, Laura M, et al. Heme oxygenase-1 repeat polymorphism in septic acute kidney injury. ''PLoS One''. 2019; '''14''' (5):e0217291
Hepatocyte gene expression and DNA methylation as ancestry-dependent mechanisms in African Americans. Description: Park, C S, et al. Hepatocyte gene expression and DNA methylation as ancestry-dependent mechanisms in African Americans. ''NPJ Genom Med''. 2019; '''4''': 29
Hidden Rice Diversity in the Guianas. Description: Van Andel, Tinde, et al. Hidden Rice Diversity in the Guianas. ''Front Plant Sci''. 2019; '''10''': 1161
High-quality, genome-wide SNP genotypic data for pedigreed germplasm of the diploid outbreeding species apple, peach, and sweet cherry through a common workflow. Description: Vanderzande, Stijn, et al. High-quality, genome-wide SNP genotypic data for pedigreed germplasm of the diploid outbreeding species apple, peach, and sweet cherry through a common workflow. ''PLoS One''. 2019; '''14''' (6):e0210928
Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers. Description: Cunningham, Patrick N, et al. Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers. ''PLoS One''. 2019; '''14''' (9):e0221957
Identification of Candidate Signature Genes and Key Regulators Associated With Trypanotolerance in the Sheko Breed. Description: Mekonnen, Yonatan Ayalew, et al. Identification of Candidate Signature Genes and Key Regulators Associated With Trypanotolerance in the Sheko Breed. ''Front Genet''. 2019; '''10''': 1095
Identification of muscle-specific candidate genes in Simmental beef cattle using imputed next generation sequencing. Description: Bordbar, Farhad, et al. Identification of muscle-specific candidate genes in Simmental beef cattle using imputed next generation sequencing. ''PLoS One''. 2019; '''14''' (10):e0223671
Identification of recombination hotspots and quantitative trait loci for recombination rate in layer chickens. Description: Weng, Ziqing, et al. Identification of recombination hotspots and quantitative trait loci for recombination rate in layer chickens. ''J Anim Sci Biotechnol''. 2019; '''10''': 20
Identification of Shared Genes Between Ischemic Stroke and Parkinson's Disease Using Genome-Wide Association Studies. Description: Lang, Wenjing, et al. Identification of Shared Genes Between Ischemic Stroke and Parkinson's Disease Using Genome-Wide Association Studies. ''Front Neurol''. 2019; '''10''': 297
Identification of Specific Nuclear Genetic Loci and Genes That Interact With the Mitochondrial Genome and Contribute to Fecundity in Caenorhabditis elegans. Description: Zhu, Zuobin, et al. Identification of Specific Nuclear Genetic Loci and Genes That Interact With the Mitochondrial Genome and Contribute to Fecundity in Caenorhabditis elegans. ''Front Genet''. 2019; '''10''': 28
Identification of the 12q24 locus associated with fish intake frequency by genome-wide meta-analysis in Japanese populations. Description: Igarashi, Maki, et al. Identification of the 12q24 locus associated with fish intake frequency by genome-wide meta-analysis in Japanese populations. ''Genes Nutr''. 2019; '''14''': 21
Important gene-gene interaction of TNF-alpha and VDR on osteoporosis in community-dwelling elders. Description: Liao, Li-Na, et al. Important gene-gene interaction of TNF-alpha and VDR on osteoporosis in community-dwelling elders. ''PLoS One''. 2019; '''14''' (12):e0226973
Increased Adaptive Variation Despite Reduced Overall Genetic Diversity in a Rapidly Adapting Invader. Description: Selechnik, Daniel, et al. Increased Adaptive Variation Despite Reduced Overall Genetic Diversity in a Rapidly Adapting Invader. ''Front Genet''. 2019; '''10''': 1221
Increased Serological Response Against Human Herpesvirus 6A Is Associated With Risk for Multiple Sclerosis. Description: Engdahl, Elin, et al. Increased Serological Response Against Human Herpesvirus 6A Is Associated With Risk for Multiple Sclerosis. ''Front Immunol''. 2019; '''10''': 2715
INDEL variation in the regulatory region of the major flowering time gene LanFTc1 is associated with vernalization response and flowering time in narrow-leafed lupin (Lupinus angustifolius L.). Description: Taylor, Candy M, et al. INDEL variation in the regulatory region of the major flowering time gene LanFTc1 is associated with vernalization response and flowering time in narrow-leafed lupin (Lupinus angustifolius L.). ''Plant Cell Environ''. 2019 Jan; '''42''' (1):174-187
Influence of genetic factors on long-term treatment related neurocognitive complications, and on anxiety and depression in survivors of childhood acute lymphoblastic leukemia: The Petale study. Description: Petrykey, Kateryna, et al. Influence of genetic factors on long-term treatment related neurocognitive complications, and on anxiety and depression in survivors of childhood acute lymphoblastic leukemia: The Petale study. ''PLoS One''. 2019; '''14''' (6):e0217314
Integrated genetic and methylomic analyses identify shared biology between autism and autistic traits. Description: Massrali, Aicha, et al. Integrated genetic and methylomic analyses identify shared biology between autism and autistic traits. ''Mol Autism''. 2019; '''10''': 31
Inter-individual genomic heterogeneity within European population isolates. Description: Anagnostou, Paolo, et al. Inter-individual genomic heterogeneity within European population isolates. ''PLoS One''. 2019; '''14''' (10):e0214564
Interrogating the Evolutionary Paradox of Schizophrenia: A Novel Framework and Evidence Supporting Recent Negative Selection of Schizophrenia Risk Alleles. Description: Liu, Chenxing, et al. Interrogating the Evolutionary Paradox of Schizophrenia: A Novel Framework and Evidence Supporting Recent Negative Selection of Schizophrenia Risk Alleles. ''Front Genet''. 2019; '''10''': 389
ITGAM is a risk factor to systemic lupus erythematosus and possibly a protection factor to rheumatoid arthritis in patients from Mexico. Description: Ramirez-Bello, Julian, et al. ITGAM is a risk factor to systemic lupus erythematosus and possibly a protection factor to rheumatoid arthritis in patients from Mexico. ''PLoS One''. 2019; '''14''' (11):e0224543
Landscape of Loci and Candidate Genes for Muscle Fatty Acid Composition in Pigs Revealed by Multiple Population Association Analysis. Description: Zhang, Junjie, et al. Landscape of Loci and Candidate Genes for Muscle Fatty Acid Composition in Pigs Revealed by Multiple Population Association Analysis. ''Front Genet''. 2019; '''10''': 1067
LD-annot: A Bioinformatics Tool to Automatically Provide Candidate SNPs With Annotations for Genetically Linked Genes. Description: Prunier, Julien, et al. LD-annot: A Bioinformatics Tool to Automatically Provide Candidate SNPs With Annotations for Genetically Linked Genes. ''Front Genet''. 2019; '''10''': 1192
Linkage disequilibrium and past effective population size in native Tunisian cattle. Description: Jemaa, Slim Ben, et al. Linkage disequilibrium and past effective population size in native Tunisian cattle. ''Genet Mol Biol''. 2019 Jan-Mar; '''42''' (1):52-61
Locus 5p13.1 may be associated with the selection of cancer-related HBV core promoter mutations. Description: Chen, Qin-Yan, et al. Locus 5p13.1 may be associated with the selection of cancer-related HBV core promoter mutations. ''Int J Med Sci''. 2019; '''16''' (7):990-997
LRP1B Polymorphisms Are Associated with Multiple Myeloma Risk in a Chinese Han Population. Description: Li, Bingjie, et al. LRP1B Polymorphisms Are Associated with Multiple Myeloma Risk in a Chinese Han Population. ''J Cancer''. 2019; '''10''' (3):577-582
MAGI2 Gene Region and Celiac Disease. Description: Jauregi-Miguel, Amaia, et al. MAGI2 Gene Region and Celiac Disease. ''Front Nutr''. 2019; '''6''': 187
Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study. Description: Pechlivanis, Sonali, et al. Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study. ''PLoS One''. 2019; '''14''' (11):e0225521
MC4R Single Nucleotide Polymorphisms Were Associated with Metabolically Healthy and Unhealthy Obesity in Chinese Northern Han Populations. Description: Gao, Luying, et al. MC4R Single Nucleotide Polymorphisms Were Associated with Metabolically Healthy and Unhealthy Obesity in Chinese Northern Han Populations. ''Int J Endocrinol''. 2019; '''2019''': 4328909
Mechanistic Characterization of RASGRP1 Variants Identifies an hnRNP-K-Regulated Transcriptional Enhancer Contributing to SLE Susceptibility. Description: Molineros, Julio E, et al. Mechanistic Characterization of RASGRP1 Variants Identifies an hnRNP-K-Regulated Transcriptional Enhancer Contributing to SLE Susceptibility. ''Front Immunol''. 2019; '''10''': 1066
Mendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery disease. Description: Marouli, Eirini, et al. Mendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery disease. ''Commun Biol''. 2019; '''2''': 119
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. Description: Pulit, Sara L, et al. Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. ''Hum Mol Genet''. 2019 Jan 1; '''28''' (1):166-174
Meta-analysis of genome-wide association studies for loin muscle area and loin muscle depth in two Duroc pig populations. Description: Zhuang, Zhanwei, et al. Meta-analysis of genome-wide association studies for loin muscle area and loin muscle depth in two Duroc pig populations. ''PLoS One''. 2019; '''14''' (6):e0218263
Minor alleles are associated with white rust (Albugo occidentalis) susceptibility in spinach (Spinacia oleracea). Description: Awika, Henry O, et al. Minor alleles are associated with white rust (Albugo occidentalis) susceptibility in spinach (Spinacia oleracea). ''Hortic Res''. 2019; '''6''': 129
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset. Description: Billingsley, Kimberley J, et al. Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset. ''NPJ Parkinsons Dis''. 2019; '''5''': 8
Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Description: Tao, Feifei, et al. Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. ''J Neuromuscul Dis''. 2019; '''6''' (2):201-211
Multi-breed genome-wide association studies across countries for electronically recorded behavior traits in local dual-purpose cows. Description: Yin, Tong, et al. Multi-breed genome-wide association studies across countries for electronically recorded behavior traits in local dual-purpose cows. ''PLoS One''. 2019; '''14''' (10):e0221973
Multiple Epistasis Interactions Within MHC Are Associated With Ulcerative Colitis. Description: Zhang, Jie, et al. Multiple Epistasis Interactions Within MHC Are Associated With Ulcerative Colitis. ''Front Genet''. 2019; '''10''': 257
Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels. Description: Khlebus, Eleonora, et al. Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels. ''PLoS One''. 2019; '''14''' (5):e0217620
Multiple Selection Signatures in Farmed Atlantic Salmon Adapted to Different Environments Across Hemispheres. Description: Lopez, Maria Eugenia, et al. Multiple Selection Signatures in Farmed Atlantic Salmon Adapted to Different Environments Across Hemispheres. ''Front Genet''. 2019; '''10''': 901
Mutational landscape of canine B-cell lymphoma profiled at single nucleotide resolution by RNA-seq. Description: Giannuzzi, Diana, et al. Mutational landscape of canine B-cell lymphoma profiled at single nucleotide resolution by RNA-seq. ''PLoS One''. 2019; '''14''' (4):e0215154
Natural Selection Footprints Among African Chicken Breeds and Village Ecotypes. Description: Elbeltagy, Ahmed R, et al. Natural Selection Footprints Among African Chicken Breeds and Village Ecotypes. ''Front Genet''. 2019; '''10''': 376
Next generation sequencing (NGS) to improve the diagnosis and management of patients with disorders of sex development (DSD). Description: Hughes, Lowri A, et al. Next generation sequencing (NGS) to improve the diagnosis and management of patients with disorders of sex development (DSD). ''Endocr Connect''. 2019 Jan 1;
No association of COMT with insight problem solving in Chinese college students. Description: Yang, Xiaolei, et al. No association of COMT with insight problem solving in Chinese college students. ''PeerJ''. 2019; '''7''': e6755
Non-syndromic cleft palate: Association analysis on three gene polymorphisms of the folate pathway in Asian and Italian populations. Description: Carinci, Francesco, et al. Non-syndromic cleft palate: Association analysis on three gene polymorphisms of the folate pathway in Asian and Italian populations. ''Int J Immunopathol Pharmacol''. 2019 Jan-Dec; '''33''': 2058738419858572
Novel and known signals of selection for fat deposition in domestic sheep breeds from Africa and Eurasia. Description: Mastrangelo, Salvatore, et al. Novel and known signals of selection for fat deposition in domestic sheep breeds from Africa and Eurasia. ''PLoS One''. 2019; '''14''' (6):e0209632
Origins and geographic diversification of African rice (Oryza glaberrima). Description: Veltman, Margaretha A, et al. Origins and geographic diversification of African rice (Oryza glaberrima). ''PLoS One''. 2019; '''14''' (3):e0203508
Patterns of Geographical and Potential Adaptive Divergence in the Genome of the Common Carp (Cyprinus carpio). Description: Xu, Jian, et al. Patterns of Geographical and Potential Adaptive Divergence in the Genome of the Common Carp (Cyprinus carpio). ''Front Genet''. 2019; '''10''': 660
Performance Evaluation of Highly Admixed Tanzanian Smallholder Dairy Cattle Using SNP Derived Kinship Matrix. Description: Mujibi, Fidalis D N, et al. Performance Evaluation of Highly Admixed Tanzanian Smallholder Dairy Cattle Using SNP Derived Kinship Matrix. ''Front Genet''. 2019; '''10''': 375
Phylotranscriptomic Insights into the Diversification of Endothermic Thunnus Tunas. Description: Ciezarek, Adam G, et al. Phylotranscriptomic Insights into the Diversification of Endothermic Thunnus Tunas. ''Mol Biol Evol''. 2019 Jan 1; '''36''' (1):84-96
Polygenic Risk Score for Alzheimer's Disease Is Associated With Ch4 Volume in Normal Subjects. Description: Wang, Tao, et al. Polygenic Risk Score for Alzheimer's Disease Is Associated With Ch4 Volume in Normal Subjects. ''Front Genet''. 2019; '''10''': 519
Population Genetic Analysis of Modern and Ancient DNA Variations Yields New Insights Into the Formation, Genetic Structure, and Phylogenetic Relationship of Northern Han Chinese. Description: Chen, Pengyu, et al. Population Genetic Analysis of Modern and Ancient DNA Variations Yields New Insights Into the Formation, Genetic Structure, and Phylogenetic Relationship of Northern Han Chinese. ''Front Genet''. 2019; '''10''': 1045
Population Pharmacogenomics for Precision Public Health in Colombia. Description: Nagar, Shashwat Deepali, et al. Population Pharmacogenomics for Precision Public Health in Colombia. ''Front Genet''. 2019; '''10''': 241
Population Structure and Genetic Diversity of Sheep Breeds in the Kyrgyzstan. Description: Deniskova, Tatiana, et al. Population Structure and Genetic Diversity of Sheep Breeds in the Kyrgyzstan. ''Front Genet''. 2019; '''10''': 1311
Primary closed angle glaucoma in the Basset Hound: Genetic investigations using genome-wide association and RNA sequencing strategies. Description: Oliver, James A C, et al. Primary closed angle glaucoma in the Basset Hound: Genetic investigations using genome-wide association and RNA sequencing strategies. ''Mol Vis''. 2019; '''25''': 93-105
Proprotein convertase subtilisin/kexin type 9 (PCSK9) in Alzheimer's disease: A genetic and proteomic multi-cohort study. Description: Picard, Cynthia, et al. Proprotein convertase subtilisin/kexin type 9 (PCSK9) in Alzheimer's disease: A genetic and proteomic multi-cohort study. ''PLoS One''. 2019; '''14''' (8):e0220254
Quantile regression analysis reveals widespread evidence for gene-environment or gene-gene interactions in myopia development. Description: Pozarickij, Alfred, et al. Quantile regression analysis reveals widespread evidence for gene-environment or gene-gene interactions in myopia development. ''Commun Biol''. 2019; '''2''': 167
Quantitative Trait Loci Mapping for Lameness Associated Phenotypes in Holstein-Friesian Dairy Cattle. Description: Sanchez-Molano, Enrique, et al. Quantitative Trait Loci Mapping for Lameness Associated Phenotypes in Holstein-Friesian Dairy Cattle. ''Front Genet''. 2019; '''10''': 926
Quick assessment for systematic test statistic inflation/deflation due to null model misspecifications in genome-wide environment interaction studies. Description: Ueki, Masao, et al. Quick assessment for systematic test statistic inflation/deflation due to null model misspecifications in genome-wide environment interaction studies. ''PLoS One''. 2019; '''14''' (7):e0219825
RAD genotyping reveals fine-scale population structure and provides evidence for adaptive divergence in a commercially important fish from the northwestern Pacific Ocean. Description: Zhang, Bai-Dong, et al. RAD genotyping reveals fine-scale population structure and provides evidence for adaptive divergence in a commercially important fish from the northwestern Pacific Ocean. ''PeerJ''. 2019; '''7''': e7242
Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools. Description: Sariya, Sanjeev, et al. Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools. ''Front Genet''. 2019; '''10''': 239
Reducing inbreeding rates with a breeding circle: Theory and practice in Veluws Heideschaap. Description: Windig, Jack J, et al. Reducing inbreeding rates with a breeding circle: Theory and practice in Veluws Heideschaap. ''J Anim Breed Genet''. 2019 Jan; '''136''' (1):51-62
Regional fat depot masses are influenced by protein-coding gene variants. Description: Neville, Matt J, et al. Regional fat depot masses are influenced by protein-coding gene variants. ''PLoS One''. 2019; '''14''' (5):e0217644
Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area. Description: Banfai, Zsolt, et al. Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area. ''Front Genet''. 2019; '''10''': 558
Role of PCK1 gene on oil tea-induced glucose homeostasis and type 2 diabetes: an animal experiment and a case-control study. Description: Hu, Qiantu, et al. Role of PCK1 gene on oil tea-induced glucose homeostasis and type 2 diabetes: an animal experiment and a case-control study. ''Nutr Metab (Lond)''. 2019; '''16''': 12
Runs of Homozygosity and NetView analyses provide new insight into the genome-wide diversity and admixture of three German cattle breeds. Description: Addo, Sowah, et al. Runs of Homozygosity and NetView analyses provide new insight into the genome-wide diversity and admixture of three German cattle breeds. ''PLoS One''. 2019; '''14''' (12):e0225847
Schizophrenia liability shares common molecular genetic risk factors with sleep duration and nightmares in childhood. Description: Reed, Zoe E, et al. Schizophrenia liability shares common molecular genetic risk factors with sleep duration and nightmares in childhood. ''Wellcome Open Res''. 2019; '''4''': 15
Selecting RAD-Seq Data Analysis Parameters for Population Genetics: The More the Better? Description: Diaz-Arce, Natalia, et al. Selecting RAD-Seq Data Analysis Parameters for Population Genetics: The More the Better? ''Front Genet''. 2019; '''10''': 533
Selection footprints reflect genomic changes associated with breeding efforts in 56 cucumber inbred lines. Description: Liu, Bin, et al. Selection footprints reflect genomic changes associated with breeding efforts in 56 cucumber inbred lines. ''Hortic Res''. 2019; '''6''': 127
Sex-Interacting mRNA- and miRNA-eQTLs and Their Implications in Gene Expression Regulation and Disease. Description: Shen, Jiangshan J, et al. Sex-Interacting mRNA- and miRNA-eQTLs and Their Implications in Gene Expression Regulation and Disease. ''Front Genet''. 2019; '''10''': 313
Single-Locus and Multi-Locus Genome-Wide Association Studies for Intramuscular Fat in Duroc Pigs. Description: Ding, Rongrong, et al. Single-Locus and Multi-Locus Genome-Wide Association Studies for Intramuscular Fat in Duroc Pigs. ''Front Genet''. 2019; '''10''': 619
Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C. Description: Kato, Keizo, et al. Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C. ''PLoS One''. 2019; '''14''' (7):e0219022
SNP-based mixed model association of growth- and yield-related traits in popcorn. Description: Mafra, Gabrielle Sousa, et al. SNP-based mixed model association of growth- and yield-related traits in popcorn. ''PLoS One''. 2019; '''14''' (6):e0218552
Social and non-social autism symptoms and trait domains are genetically dissociable. Description: Warrier, Varun, et al. Social and non-social autism symptoms and trait domains are genetically dissociable. ''Commun Biol''. 2019; '''2''': 328
Strategies for Obtaining and Pruning Imputed Whole-Genome Sequence Data for Genomic Prediction. Description: Ye, Shaopan, et al. Strategies for Obtaining and Pruning Imputed Whole-Genome Sequence Data for Genomic Prediction. ''Front Genet''. 2019; '''10''': 673
Study of whole genome linkage disequilibrium patterns of Iranian water buffalo breeds using the Axiom Buffalo Genotyping 90K Array. Description: Mokhber, Mahdi, et al. Study of whole genome linkage disequilibrium patterns of Iranian water buffalo breeds using the Axiom Buffalo Genotyping 90K Array. ''PLoS One''. 2019; '''14''' (5):e0217687
Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations. Description: Simba, Hannah, et al. Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations. ''Front Genet''. 2019; '''10''': 642
TB DEPOT (Data Exploration Portal): A multi-domain tuberculosis data analysis resource. Description: Gabrielian, Andrei, et al. TB DEPOT (Data Exploration Portal): A multi-domain tuberculosis data analysis resource. ''PLoS One''. 2019; '''14''' (5):e0217410
Testing gene by community disadvantage moderation of sexual health outcomes among urban women. Description: Powell, Terrinieka W, et al. Testing gene by community disadvantage moderation of sexual health outcomes among urban women. ''PLoS One''. 2019; '''14''' (10):e0223311
The Association Between Schizophrenia Risk Variants and Creativity in Healthy Han Chinese Subjects. Description: Wang, Dan, et al. The Association Between Schizophrenia Risk Variants and Creativity in Healthy Han Chinese Subjects. ''Front Psychol''. 2019; '''10''': 2218
The Challenge of Stratifying Obesity: Attempts in the Quebec Family Study. Description: de Toro-Martin, Juan, et al. The Challenge of Stratifying Obesity: Attempts in the Quebec Family Study. ''Front Genet''. 2019; '''10''': 994
The concept of exposure when selecting comparison groups for determining individual susceptibility to addiction to cigarette smoking. Description: Henn, Indiara W, et al. The concept of exposure when selecting comparison groups for determining individual susceptibility to addiction to cigarette smoking. ''PLoS One''. 2019; '''14''' (4):e0214946
The Effect of Genetic Variation on the Placental Transcriptome in Humans. Description: Kikas, Triin, et al. The Effect of Genetic Variation on the Placental Transcriptome in Humans. ''Front Genet''. 2019; '''10''': 550
The Genetic Architecture of Bovine Telomere Length in Early Life and Association With Animal Fitness. Description: Ilska-Warner, Joanna J, et al. The Genetic Architecture of Bovine Telomere Length in Early Life and Association With Animal Fitness. ''Front Genet''. 2019; '''10''': 1048
The Genetic Architecture of Chronic Mountain Sickness in Peru. Description: Gazal, Steven, et al. The Genetic Architecture of Chronic Mountain Sickness in Peru. ''Front Genet''. 2019; '''10''': 690
The Genetic Architecture of Early Body Temperature and Its Correlation With Salmonella Pullorum Resistance in Three Chicken Breeds. Description: Li, Xinghua, et al. The Genetic Architecture of Early Body Temperature and Its Correlation With Salmonella Pullorum Resistance in Three Chicken Breeds. ''Front Genet''. 2019; '''10''': 1287
The impact of genetic variants in IL1R2 on cervical cancer risk among Uygur females from China: A case-control study. Description: Niu, Fanglin, et al. The impact of genetic variants in IL1R2 on cervical cancer risk among Uygur females from China: A case-control study. ''Mol Genet Genomic Med''. 2019 Jan; '''7''' (1):e00516
The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study. Description: Johansson, Mattias, et al. The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study. ''PLoS Med''. 2019 Jan; '''16''' (1):e1002724
The Landscape of Copia and Gypsy Retrotransposon During Maize Domestication and Improvement. Description: Zhang, Xiangbo, et al. The Landscape of Copia and Gypsy Retrotransposon During Maize Domestication and Improvement. ''Front Plant Sci''. 2019; '''10''': 1533
The Length of the Expressed 3' UTR Is an Intermediate Molecular Phenotype Linking Genetic Variants to Complex Diseases. Description: Mariella, Elisa, et al. The Length of the Expressed 3' UTR Is an Intermediate Molecular Phenotype Linking Genetic Variants to Complex Diseases. ''Front Genet''. 2019; '''10''': 714
The Local South American Chicken Populations Are a Melting-Pot of Genomic Diversity. Description: Luzuriaga-Neira, Agusto, et al. The Local South American Chicken Populations Are a Melting-Pot of Genomic Diversity. ''Front Genet''. 2019; '''10''': 1172
The MAPT H1 Haplotype Is a Risk Factor for Alzheimer's Disease in APOE epsilon4 Non-carriers. Description: Sanchez-Juan, Pascual, et al. The MAPT H1 Haplotype Is a Risk Factor for Alzheimer's Disease in APOE epsilon4 Non-carriers. ''Front Aging Neurosci''. 2019; '''11''': 327
The Potential Role of Regulatory Genes (DNMT3A, HDAC5, and HDAC9) in Antipsychotic Treatment Response in South African Schizophrenia Patients. Description: O'Connell, Kevin Sean, et al. The Potential Role of Regulatory Genes (DNMT3A, HDAC5, and HDAC9) in Antipsychotic Treatment Response in South African Schizophrenia Patients. ''Front Genet''. 2019; '''10''': 641
The Puerto Rico Alzheimer Disease Initiative (PRADI): A Multisource Ascertainment Approach. Description: Feliciano-Astacio, Briseida E, et al. The Puerto Rico Alzheimer Disease Initiative (PRADI): A Multisource Ascertainment Approach. ''Front Genet''. 2019; '''10''': 538
The radial expansion of the Diego blood group system polymorphisms in Asia: mark of co-migration with the Mongol conquests. Description: Petit, Florence, et al. The radial expansion of the Diego blood group system polymorphisms in Asia: mark of co-migration with the Mongol conquests. ''Eur J Hum Genet''. 2019 Jan; '''27''' (1):125-132
The Vaccinia virion: Filling the gap between atomic and ultrastructure. Description: Mirzakhanyan, Yeva, et al. The Vaccinia virion: Filling the gap between atomic and ultrastructure. ''PLoS Pathog''. 2019 Jan; '''15''' (1):e1007508
The Variant at TGFBRAP1 but Not TGFBR2 Is Associated with Antituberculosis Drug-Induced Liver Injury. Description: Zhang, Jingwei, et al. The Variant at TGFBRAP1 but Not TGFBR2 Is Associated with Antituberculosis Drug-Induced Liver Injury. ''Evid Based Complement Alternat Med''. 2019; '''2019''': 1685128
Transcriptome association studies of neuropsychiatric traits in African Americans implicate PRMT7 in schizophrenia. Description: Fiorica, Peter N, et al. Transcriptome association studies of neuropsychiatric traits in African Americans implicate PRMT7 in schizophrenia. ''PeerJ''. 2019; '''7''': e7778
Uncovering Genomic Regions Associated With 36 Agro-Morphological Traits in Indian Spring Wheat Using GWAS. Description: Sheoran, Sonia, et al. Uncovering Genomic Regions Associated With 36 Agro-Morphological Traits in Indian Spring Wheat Using GWAS. ''Front Plant Sci''. 2019; '''10''': 527
Using Ancestry Informative Markers (AIMs) to Detect Fine Structures Within Gorilla Populations. Description: Das, Ranajit, et al. Using Ancestry Informative Markers (AIMs) to Detect Fine Structures Within Gorilla Populations. ''Front Genet''. 2019; '''10''': 43
Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Description: Geidenstam, Nina, et al. Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. ''PLoS One''. 2019; '''14''' (9):e0222445
Using Whole Genome Sequencing in an African Subphenotype of Myasthenia Gravis to Generate a Pathogenetic Hypothesis. Description: Nel, Melissa, et al. Using Whole Genome Sequencing in an African Subphenotype of Myasthenia Gravis to Generate a Pathogenetic Hypothesis. ''Front Genet''. 2019; '''10''': 136
Utilizing trait networks and structural equation models as tools to interpret multi-trait genome-wide association studies. Description: Momen, Mehdi, et al. Utilizing trait networks and structural equation models as tools to interpret multi-trait genome-wide association studies. ''Plant Methods''. 2019; '''15''': 107
Validation of Candidate Gene-Based Markers and Identification of Novel Loci for Thousand-Grain Weight in Spring Bread Wheat. Description: Sehgal, Deepmala, et al. Validation of Candidate Gene-Based Markers and Identification of Novel Loci for Thousand-Grain Weight in Spring Bread Wheat. ''Front Plant Sci''. 2019; '''10''': 1189
Variants in the IL17 pathway genes are associated with atopic asthma and atopy makers in a South American population. Description: Silva, Milca de J, et al. Variants in the IL17 pathway genes are associated with atopic asthma and atopy makers in a South American population. ''Allergy Asthma Clin Immunol''. 2019; '''15''': 28
Variation in Actionable Pharmacogenetic Markers in Natives and Mestizos From Mexico. Description: Gonzalez-Covarrubias, Vanessa, et al. Variation in Actionable Pharmacogenetic Markers in Natives and Mestizos From Mexico. ''Front Pharmacol''. 2019; '''10''': 1169
Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population. Description: Gialluisi, Alessandro, et al. Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population. ''Front Neurol''. 2019; '''10''': 1362
Whole Genome Linkage Disequilibrium and Effective Population Size in a Coho Salmon (Oncorhynchus kisutch) Breeding Population Using a High-Density SNP Array. Description: Barria, Agustin, et al. Whole Genome Linkage Disequilibrium and Effective Population Size in a Coho Salmon (Oncorhynchus kisutch) Breeding Population Using a High-Density SNP Array. ''Front Genet''. 2019; '''10''': 498
Whole-Genome Resequencing Identifies KIT New Alleles That Affect Coat Color Phenotypes in Pigs. Description: Wu, Zhongping, et al. Whole-Genome Resequencing Identifies KIT New Alleles That Affect Coat Color Phenotypes in Pigs. ''Front Genet''. 2019; '''10''': 218
Whole Genome Resequencing Reveals Selection Signatures Associated With Important Traits in Ethiopian Indigenous Goat Populations. Description: Berihulay, Haile, et al. Whole Genome Resequencing Reveals Selection Signatures Associated With Important Traits in Ethiopian Indigenous Goat Populations. ''Front Genet''. 2019; '''10''': 1190
Widespread subcortical grey matter degeneration in primary lateral sclerosis: a multimodal imaging study with genetic profiling. Description: Finegan, Eoin, et al. Widespread subcortical grey matter degeneration in primary lateral sclerosis: a multimodal imaging study with genetic profiling. ''Neuroimage Clin''. 2019; '''24''': 102089
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. Description: Kraja, Aldi T, et al. Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. ''Am J Hum Genet''. 2019 Jan 3; '''104''' (1):112-138
Genome-wide association study reveals novel loci associated with body size and carcass yields in Pekin ducks. Description: Deng, Meng-Ting, et al. Genome-wide association study reveals novel loci associated with body size and carcass yields in Pekin ducks. ''BMC Genomics''. 2019 Jan 3; '''20''' (1):1
Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Description: Kichaev, Gleb, et al. Leveraging Polygenic Functional Enrichment to Improve GWAS Power. ''Am J Hum Genet''. 2019 Jan 3; '''104''' (1):65-75
Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population. Description: Coltell, Oscar, et al. Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population. ''Nutrients''. 2019 Jan 4; '''11''' (1):
Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide. Description: Ruderfer, Douglas M, et al. Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide. ''Mol Psychiatry''. 2019 Jan 4;
SNP genotyping elucidates the genetic diversity of Magna Graecia grapevine germplasm and its historical origin and dissemination. Description: De Lorenzis, Gabriella, et al. SNP genotyping elucidates the genetic diversity of Magna Graecia grapevine germplasm and its historical origin and dissemination. ''BMC Plant Biol''. 2019 Jan 6; '''19''' (1):7
Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity. Description: Gunz, Philipp, et al. Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity. ''Curr Biol''. 2019 Jan 7; '''29''' (1):120-127.e5
Whole-Genome Resequencing of a Worldwide Collection of Rapeseed Accessions Reveals the Genetic Basis of Ecotype Divergence. Description: Wu, Dezhi, et al. Whole-Genome Resequencing of a Worldwide Collection of Rapeseed Accessions Reveals the Genetic Basis of Ecotype Divergence. ''Mol Plant''. 2019 Jan 7; '''12''' (1):30-43
A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos. Description: Huerta-Chagoya, Alicia, et al. A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos. ''BMC Genet''. 2019 Jan 8; '''20''' (1):5
Genetic legacy of state centralization in the Kuba Kingdom of the Democratic Republic of the Congo. Description: van Dorp, Lucy, et al. Genetic legacy of state centralization in the Kuba Kingdom of the Democratic Republic of the Congo. ''Proc Natl Acad Sci U S A''. 2019 Jan 8; '''116''' (2):593-598
Non-additive effects of ACVR2A in preeclampsia in a Philippine population. Description: Amosco, Melissa D, et al. Non-additive effects of ACVR2A in preeclampsia in a Philippine population. ''BMC Pregnancy Childbirth''. 2019 Jan 8; '''19''' (1):11
Fine-Scale Resolution of Runs of Homozygosity Reveal Patterns of Inbreeding and Substantial Overlap with Recessive Disease Genotypes in Domestic Dogs. Description: Sams, Aaron J, et al. Fine-Scale Resolution of Runs of Homozygosity Reveal Patterns of Inbreeding and Substantial Overlap with Recessive Disease Genotypes in Domestic Dogs. ''G3 (Bethesda)''. 2019 Jan 9; '''9''' (1):117-123
Emergence and Spread of Basal Lineages of Yersinia pestis during the Neolithic Decline. Description: Rascovan, Nicolas, et al. Emergence and Spread of Basal Lineages of Yersinia pestis during the Neolithic Decline. ''Cell''. 2019 Jan 10; '''176''' (1-2):295-305.e10
Genome-wide analysis of genetic predisposition to Alzheimer's disease and related sex disparities. Description: Nazarian, Alireza, et al. Genome-wide analysis of genetic predisposition to Alzheimer's disease and related sex disparities. ''Alzheimers Res Ther''. 2019 Jan 12; '''11''' (1):5
Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations. Description: Gouder, Laura, et al. Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations. ''Sci Rep''. 2019 Jan 14; '''9''' (1):94
Genome-wide association analyses of invasive pneumococcal isolates identify a missense bacterial mutation associated with meningitis. Description: Li, Yuan, et al. Genome-wide association analyses of invasive pneumococcal isolates identify a missense bacterial mutation associated with meningitis. ''Nat Commun''. 2019 Jan 14; '''10''' (1):178
Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas. Description: Hoffman, Joshua, et al. Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas. ''Breast Cancer Res''. 2019 Jan 14; '''21''' (1):3
Pattern Recognition Receptor Polymorphisms as Predictors of Oxaliplatin Benefit in Colorectal Cancer. Description: Gray, Victoria, et al. Pattern Recognition Receptor Polymorphisms as Predictors of Oxaliplatin Benefit in Colorectal Cancer. ''J Natl Cancer Inst''. 2019 Jan 14;
POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33. Description: Hitomi, Yuki, et al. POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33. ''Sci Rep''. 2019 Jan 14; '''9''' (1):102
An exonic splicing enhancer mutation in DUOX2 causes aberrant alternative splicing and severe congenital hypothyroidism in Bama pigs. Description: Cao, Chunwei, et al. An exonic splicing enhancer mutation in DUOX2 causes aberrant alternative splicing and severe congenital hypothyroidism in Bama pigs. ''Dis Model Mech''. 2019 Jan 15; '''12''' (1):
Association between IL23R and ERAP1 polymorphisms and sacroiliac or spinal MRI inflammation in spondyloarthritis: DESIR cohort data. Description: Ruyssen-Witrand, Adeline, et al. Association between IL23R and ERAP1 polymorphisms and sacroiliac or spinal MRI inflammation in spondyloarthritis: DESIR cohort data. ''Arthritis Res Ther''. 2019 Jan 15; '''21''' (1):22
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis. Description: Fadista, Joao, et al. Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis. ''Hum Mol Genet''. 2019 Jan 15; '''28''' (2):332-340
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances. Description: Timmers, Paul Rhj, et al. Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances. ''Elife''. 2019 Jan 15; '''8''':
Multiomic Profiling Identifies cis-Regulatory Networks Underlying Human Pancreatic beta Cell Identity and Function. Description: Lawlor, Nathan, et al. Multiomic Profiling Identifies cis-Regulatory Networks Underlying Human Pancreatic beta Cell Identity and Function. ''Cell Rep''. 2019 Jan 15; '''26''' (3):788-801.e6
Rare variant of HSPG2 is not involved in the development of adolescent idiopathic scoliosis: evidence from a large-scale replication study. Description: Xia, Chao, et al. Rare variant of HSPG2 is not involved in the development of adolescent idiopathic scoliosis: evidence from a large-scale replication study. ''BMC Musculoskelet Disord''. 2019 Jan 15; '''20''' (1):24
Genetic associations with suicide attempt severity and genetic overlap with major depression. Description: Levey, Daniel F, et al. Genetic associations with suicide attempt severity and genetic overlap with major depression. ''Transl Psychiatry''. 2019 Jan 17; '''9''' (1):22
Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci. Description: Sarviaho, R, et al. Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci. ''Transl Psychiatry''. 2019 Jan 17; '''9''' (1):18
Apparent latent structure within the UK Biobank sample has implications for epidemiological analysis. Description: Haworth, Simon, et al. Apparent latent structure within the UK Biobank sample has implications for epidemiological analysis. ''Nat Commun''. 2019 Jan 18; '''10''' (1):333
A validation of the diathesis-stress model for depression in Generation Scotland. Description: Arnau-Soler, Aleix, et al. A validation of the diathesis-stress model for depression in Generation Scotland. ''Transl Psychiatry''. 2019 Jan 18; '''9''' (1):25
Genetics and Genomic Regions Affecting Response to Newcastle Disease Virus Infection under Heat Stress in Layer Chickens. Description: Saelao, Perot, et al. Genetics and Genomic Regions Affecting Response to Newcastle Disease Virus Infection under Heat Stress in Layer Chickens. ''Genes (Basel)''. 2019 Jan 18; '''10''' (1):
A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Description: Adhikari, Kaustubh, et al. A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. ''Nat Commun''. 2019 Jan 21; '''10''' (1):358
Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. Description: Rask-Andersen, Mathias, et al. Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. ''Nat Commun''. 2019 Jan 21; '''10''' (1):339
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume. Description: Haworth, Simon, et al. Low-frequency variation in TP53 has large effects on head circumference and intracranial volume. ''Nat Commun''. 2019 Jan 21; '''10''' (1):357
The Genomic Footprints of the Fall and Recovery of the Crested Ibis. Description: Feng, Shaohong, et al. The Genomic Footprints of the Fall and Recovery of the Crested Ibis. ''Curr Biol''. 2019 Jan 21; '''29''' (2):340-349.e7
Genome-wide association study for salinity tolerance at the flowering stage in a panel of rice accessions from Thailand. Description: Lekklar, Chakkree, et al. Genome-wide association study for salinity tolerance at the flowering stage in a panel of rice accessions from Thailand. ''BMC Genomics''. 2019 Jan 22; '''20''' (1):76
Cellular and animal models of skin alterations in the autism-related ADNP syndrome. Description: Mollinedo, Pilar, et al. Cellular and animal models of skin alterations in the autism-related ADNP syndrome. ''Sci Rep''. 2019 Jan 24; '''9''' (1):736
Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study. Description: Westphal, Sabine, et al. Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study. ''BMC Cardiovasc Disord''. 2019 Jan 24; '''19''' (1):26
Genome-wide signatures of local adaptation among seven stoneflies species along a nationwide latitudinal gradient in Japan. Description: Gamboa, Maribet, et al. Genome-wide signatures of local adaptation among seven stoneflies species along a nationwide latitudinal gradient in Japan. ''BMC Genomics''. 2019 Jan 24; '''20''' (1):84
Polygenic impact of common genetic risk loci for Alzheimer's disease on cerebral blood flow in young individuals. Description: Chandler, Hannah L, et al. Polygenic impact of common genetic risk loci for Alzheimer's disease on cerebral blood flow in young individuals. ''Sci Rep''. 2019 Jan 24; '''9''' (1):467
Scanning the genomes of parents for imprinted loci acting in their un-genotyped progeny. Description: Blunk, Inga, et al. Scanning the genomes of parents for imprinted loci acting in their un-genotyped progeny. ''Sci Rep''. 2019 Jan 24; '''9''' (1):654
CLOCK Polymorphisms in Attention-Deficit/Hyperactivity Disorder (ADHD): Further Evidence Linking Sleep and Circadian Disturbances and ADHD. Description: Carpena, Marina Xavier, et al. CLOCK Polymorphisms in Attention-Deficit/Hyperactivity Disorder (ADHD): Further Evidence Linking Sleep and Circadian Disturbances and ADHD. ''Genes (Basel)''. 2019 Jan 28; '''10''' (2):
Identification of sequence variants associated with severe microtia-astresia by targeted sequencing. Description: Wang, Pu, et al. Identification of sequence variants associated with severe microtia-astresia by targeted sequencing. ''BMC Med Genomics''. 2019 Jan 28; '''12''' (1):28
Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry. Description: Bustos, Bernabe I, et al. Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry. ''Sci Rep''. 2019 Jan 28; '''9''' (1):772
Dissecting closely linked association signals in combination with the mammalian phenotype database can identify candidate genes in dairy cattle. Description: Cai, Zexi, et al. Dissecting closely linked association signals in combination with the mammalian phenotype database can identify candidate genes in dairy cattle. ''BMC Genet''. 2019 Jan 29; '''20''' (1):15
Using phenome-wide association to investigate the function of a schizophrenia risk locus at SLC39A8. Description: McCoy, Thomas H Jr, et al. Using phenome-wide association to investigate the function of a schizophrenia risk locus at SLC39A8. ''Transl Psychiatry''. 2019 Jan 29; '''9''' (1):45
A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Description: Guyatt, Anna L, et al. A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. ''Hum Genomics''. 2019 Jan 31; '''13''' (1):6
A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study. Description: Zhao, Xueyan, et al. A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study. ''BMC Med Genomics''. 2019 Jan 31; '''12''' (Suppl 1):26
Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families. Description: Simpson, Claire L, et al. Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families. ''BMC Med Genet''. 2019 Jan 31; '''20''' (1):27
Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget's disease of bone. Description: Mullin, Benjamin H, et al. Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget's disease of bone. ''Sci Rep''. 2019 Jan 31; '''9''' (1):1052
Genome-wide association study identifies a novel locus associated with psychological distress in the Japanese population. Description: Koshimizu, Hisatsugu, et al. Genome-wide association study identifies a novel locus associated with psychological distress in the Japanese population. ''Transl Psychiatry''. 2019 Jan 31; '''9''' (1):52
MAPT rs242557 variant is associated with hippocampus tau uptake on (18)F-AV-1451 PET in non-demented elders. Description: Shen, Xue-Ning, et al. MAPT rs242557 variant is associated with hippocampus tau uptake on (18)F-AV-1451 PET in non-demented elders. ''Aging (Albany NY)''. 2019 Jan 31; '''11''' (3):874-884
The association between peroxisome proliferator-activated receptor Delta rs3777744, rs3798343, and rs6922548 and coronary artery disease. Description: Zhang, Jing, et al. The association between peroxisome proliferator-activated receptor Delta rs3777744, rs3798343, and rs6922548 and coronary artery disease. ''Biosci Rep''. 2019 Jan 31; '''39''' (1):
Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease. Description: Dalmasso, Maria Carolina, et al. Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease. ''Transl Psychiatry''. 2019 Jan 31; '''9''' (1):55
A Genome-Wide Association Study for Susceptibility to Visual Experience-Induced Myopia. Description: Huang, Yu, et al. A Genome-Wide Association Study for Susceptibility to Visual Experience-Induced Myopia. ''Invest Ophthalmol Vis Sci''. 2019 Feb 1; '''60''' (2):559-569
An African-specific haplotype in MRGPRX4 is associated with menthol cigarette smoking. Description: Kozlitina, Julia, et al. An African-specific haplotype in MRGPRX4 is associated with menthol cigarette smoking. ''PLoS Genet''. 2019 Feb; '''15''' (2):e1007916
Association of GTF2IRD1-GTF2I polymorphisms with neuromyelitis optica spectrum disorders in Han Chinese patients. Description: Xie, Jing-Lu, et al. Association of GTF2IRD1-GTF2I polymorphisms with neuromyelitis optica spectrum disorders in Han Chinese patients. ''Neural Regen Res''. 2019 Feb; '''14''' (2):346-353
Associations between schizophrenia genetic risk, anxiety disorders and manic/hypomanic episode in a longitudinal population cohort study. Description: Richards, Alexander, et al. Associations between schizophrenia genetic risk, anxiety disorders and manic/hypomanic episode in a longitudinal population cohort study. ''Br J Psychiatry''. 2019 Feb; '''214''' (2):96-102
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Description: Liu, Mengzhen, et al. Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. ''Nat Genet''. 2019 Feb; '''51''' (2):237-244
Bactericidal/Permeability-Increasing Fold-Containing Family B Member 4 May Be Associated with NSAID-Induced Enteropathy. Description: Fujimori, Shunji, et al. Bactericidal/Permeability-Increasing Fold-Containing Family B Member 4 May Be Associated with NSAID-Induced Enteropathy. ''Dig Dis Sci''. 2019 Feb; '''64''' (2):401-408
BLINK: a package for the next level of genome-wide association studies with both individuals and markers in the millions. Description: Huang, Meng, et al. BLINK: a package for the next level of genome-wide association studies with both individuals and markers in the millions. ''Gigascience''. 2019 Feb 1; '''8''' (2):
Characterization of Proteome Variation During Modern Maize Breeding. Description: Jiang, Lu-Guang, et al. Characterization of Proteome Variation During Modern Maize Breeding. ''Mol Cell Proteomics''. 2019 Feb; '''18''' (2):263-276
Dysregulated protocadherin-pathway activity as an intrinsic defect in induced pluripotent stem cell-derived cortical interneurons from subjects with schizophrenia. Description: Shao, Zhicheng, et al. Dysregulated protocadherin-pathway activity as an intrinsic defect in induced pluripotent stem cell-derived cortical interneurons from subjects with schizophrenia. ''Nat Neurosci''. 2019 Feb; '''22''' (2):229-242
Eleven loci with new reproducible genetic associations with allergic disease risk. Description: Ferreira, Manuel A R, et al. Eleven loci with new reproducible genetic associations with allergic disease risk. ''J Allergy Clin Immunol''. 2019 Feb; '''143''' (2):691-699
Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate. Description: Howe, Laurence J, et al. Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate. ''Epigenomics''. 2019 Feb; '''11''' (2):133-145
Exome Resequencing Reveals Evolutionary History, Genomic Diversity, and Targets of Selection in the Conifers Pinus taeda and Pinus elliottii. Description: Acosta, Juan J, et al. Exome Resequencing Reveals Evolutionary History, Genomic Diversity, and Targets of Selection in the Conifers Pinus taeda and Pinus elliottii. ''Genome Biol Evol''. 2019 Feb 1; '''11''' (2):508-520
Gene variants of adhesion molecules predispose to MS: A case-control study. Description: Dardiotis, Efthimios, et al. Gene variants of adhesion molecules predispose to MS: A case-control study. ''Neurol Genet''. 2019 Feb; '''5''' (1):e304
Genome-wide association study (GWAS) of human host factors influencing viral severity of herpes simplex virus type 2 (HSV-2). Description: Kleinstein, Sarah E, et al. Genome-wide association study (GWAS) of human host factors influencing viral severity of herpes simplex virus type 2 (HSV-2). ''Genes Immun''. 2019 Feb; '''20''' (2):112-120
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. Description: Tachmazidou, Ioanna, et al. Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. ''Nat Genet''. 2019 Feb; '''51''' (2):230-236
Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies. Description: Baird, Denis A, et al. Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies. ''J Bone Miner Res''. 2019 Feb; '''34''' (2):241-251
Investigating mitonuclear interactions in human admixed populations. Description: Zaidi, Arslan A, et al. Investigating mitonuclear interactions in human admixed populations. ''Nat Ecol Evol''. 2019 Feb; '''3''' (2):213-222
Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study. Description: Kalman, Janos L, et al. Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study. ''Bipolar Disord''. 2019 Feb; '''21''' (1):68-75
Modulation of homologous recombination repair gene polymorphisms on genetic damage in chromate exposed workers. Description: Long, Changmao, et al. Modulation of homologous recombination repair gene polymorphisms on genetic damage in chromate exposed workers. ''Environ Toxicol Pharmacol''. 2019 Feb; '''66''': 126-132
No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease. Description: Berge-Seidl, Victoria, et al. No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease. ''Neurobiol Aging''. 2019 Feb; '''74''': 236.e1-236.e5
Nonequivalent lethal equivalents: Models and inbreeding metrics for unbiased estimation of inbreeding load. Description: Nietlisbach, Pirmin, et al. Nonequivalent lethal equivalents: Models and inbreeding metrics for unbiased estimation of inbreeding load. ''Evol Appl''. 2019 Feb; '''12''' (2):266-279
Overcoming challenges in variant calling: exploring sequence diversity in candidate genes for plant development in perennial ryegrass (Lolium perenne). Description: Veeckman, Elisabeth, et al. Overcoming challenges in variant calling: exploring sequence diversity in candidate genes for plant development in perennial ryegrass (Lolium perenne). ''DNA Res''. 2019 Feb 1; '''26''' (1):1-12
Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival. Description: Hallberg, Par, et al. Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival. ''EBioMedicine''. 2019 Feb; '''40''': 595-604
Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula. Description: Bycroft, Clare, et al. Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula. ''Nat Commun''. 2019 Feb 1; '''10''' (1):551
Polymorphism in the PBX1 gene is related to cystinuria in Brazilian families. Description: Reis, Sabrina T, et al. Polymorphism in the PBX1 gene is related to cystinuria in Brazilian families. ''J Cell Mol Med''. 2019 Feb; '''23''' (2):1593-1597
Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms. Description: Haug-Baltzell, Asher, et al. Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms. ''Genes Immun''. 2019 Feb; '''20''' (2):172-179
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype. Description: Stanaway, Ian B, et al. The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype. ''Genet Epidemiol''. 2019 Feb; '''43''' (1):63-81
Towards population genomics in non-model species with large genomes: a case study of the marine zooplankton Calanus finmarchicus. Description: Choquet, Marvin, et al. Towards population genomics in non-model species with large genomes: a case study of the marine zooplankton Calanus finmarchicus. ''R Soc Open Sci''. 2019 Feb; '''6''' (2):180608
Translating Alzheimer's disease-associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs. Description: Katsumata, Yuriko, et al. Translating Alzheimer's disease-associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs. ''Neurobiol Aging''. 2019 Feb; '''74''': 135-146
Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene-environment interaction approach. Description: Alemany-Navarro, Maria, et al. Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene-environment interaction approach. ''Transl Psychiatry''. 2019 Feb 4; '''9''' (1):70
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. Description: Moon, Sanghoon, et al. The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. ''Sci Rep''. 2019 Feb 4; '''9''' (1):1382
Application of the geographic population structure (GPS) algorithm for biogeographical analyses of wild and captive gorillas. Description: Das, Ranajit, et al. Application of the geographic population structure (GPS) algorithm for biogeographical analyses of wild and captive gorillas. ''BMC Bioinformatics''. 2019 Feb 5; '''20''' (Suppl 1):35
Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults. Description: Bittner, Nora, et al. Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults. ''Nat Commun''. 2019 Feb 6; '''10''' (1):621
Genome-wide associations and detection of potential candidate genes for direct genetic and maternal genetic effects influencing dairy cattle body weight at different ages. Description: Yin, Tong, et al. Genome-wide associations and detection of potential candidate genes for direct genetic and maternal genetic effects influencing dairy cattle body weight at different ages. ''Genet Sel Evol''. 2019 Feb 6; '''51''' (1):4
A Genome Wide Association Study Reveals Markers and Genes Associated with Resistance to Fusarium verticillioides Infection of Seedlings in a Maize Diversity Panel. Description: Stagnati, Lorenzo, et al. A Genome Wide Association Study Reveals Markers and Genes Associated with Resistance to Fusarium verticillioides Infection of Seedlings in a Maize Diversity Panel. ''G3 (Bethesda)''. 2019 Feb 7; '''9''' (2):571-579
Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting. Description: Wright, Caroline F, et al. Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting. ''Am J Hum Genet''. 2019 Feb 7; '''104''' (2):275-286
Complex Structural PPT1 Variant Associated with Non-syndromic Canine Retinal Degeneration. Description: Murgiano, Leonardo, et al. Complex Structural PPT1 Variant Associated with Non-syndromic Canine Retinal Degeneration. ''G3 (Bethesda)''. 2019 Feb 7; '''9''' (2):425-437
Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance. Description: van der Klaauw, Agatha A, et al. Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance. ''Cell''. 2019 Feb 7; '''176''' (4):729-742.e18
Identification of copy number variations using high density whole-genome SNP markers in Chinese Dongxiang spotted pigs. Description: Wang, Chengbin, et al. Identification of copy number variations using high density whole-genome SNP markers in Chinese Dongxiang spotted pigs. ''Asian-Australas J Anim Sci''. 2019 Feb 7; 1809-1815
Selection signature reveals genes associated with susceptibility loci affecting respiratory disease due to pleiotropic and hitchhiking effect in Chinese indigenous pigs. Description: Xu, Zhong, et al. Selection signature reveals genes associated with susceptibility loci affecting respiratory disease due to pleiotropic and hitchhiking effect in Chinese indigenous pigs. ''Asian-Australas J Anim Sci''. 2019 Feb 7; 187-196
Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk. Description: Huo, Yongxia, et al. Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk. ''Nat Commun''. 2019 Feb 8; '''10''' (1):670
Inositol Polyphosphate Multikinase (IPMK), a Gene Coding for a Potential Moonlighting Protein, Contributes to Human Female Longevity. Description: De Rango, Francesco, et al. Inositol Polyphosphate Multikinase (IPMK), a Gene Coding for a Potential Moonlighting Protein, Contributes to Human Female Longevity. ''Genes (Basel)''. 2019 Feb 8; '''10''' (2):
A genome-wide association study identifies single nucleotide polymorphisms associated with time-to-metastasis in colorectal cancer. Description: Penney, Michelle E, et al. A genome-wide association study identifies single nucleotide polymorphisms associated with time-to-metastasis in colorectal cancer. ''BMC Cancer''. 2019 Feb 9; '''19''' (1):133
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Description: Gialluisi, Alessandro, et al. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. ''Transl Psychiatry''. 2019 Feb 11; '''9''' (1):77
Revisit Population-based and Family-based Genotype Imputation. Description: Liu, Ching-Ti, et al. Revisit Population-based and Family-based Genotype Imputation. ''Sci Rep''. 2019 Feb 12; '''9''' (1):1800
Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development. Description: Cullen, Harriet, et al. Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development. ''Sci Rep''. 2019 Feb 13; '''9''' (1):1976
Unexpected population fragmentation in an endangered seabird: the case of the Peruvian diving-petrel. Description: Cristofari, Robin, et al. Unexpected population fragmentation in an endangered seabird: the case of the Peruvian diving-petrel. ''Sci Rep''. 2019 Feb 14; '''9''' (1):2021
Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans. Description: Vidal, Elena A, et al. Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans. ''Sci Rep''. 2019 Feb 14; '''9''' (1):2132
Causal effects of blood lipids on amyotrophic lateral sclerosis: a Mendelian randomization study. Description: Zeng, Ping, et al. Causal effects of blood lipids on amyotrophic lateral sclerosis: a Mendelian randomization study. ''Hum Mol Genet''. 2019 Feb 15; '''28''' (4):688-697
Genome-wide association and gene-environment interaction study identifies variants in ALDH2 associated with serum ferritin in a Chinese population. Description: Tao, Yuting, et al. Genome-wide association and gene-environment interaction study identifies variants in ALDH2 associated with serum ferritin in a Chinese population. ''Gene''. 2019 Feb 15; '''685''': 196-201
Haplotype and Haplotype-Environment Interaction Analysis Revealed Roles of SPRY2 for NSCL/P among Chinese Populations. Description: Zhou, Ren, et al. Haplotype and Haplotype-Environment Interaction Analysis Revealed Roles of SPRY2 for NSCL/P among Chinese Populations. ''Int J Environ Res Public Health''. 2019 Feb 15; '''16''' (4):
Polygenic and sex specific architecture for two maturation traits in farmed Atlantic salmon. Description: Mohamed, Amin R, et al. Polygenic and sex specific architecture for two maturation traits in farmed Atlantic salmon. ''BMC Genomics''. 2019 Feb 15; '''20''' (1):139
Polygenic Risk Scores Derived From a Tourette Syndrome Genome-wide Association Study Predict Presence of Tics in the Avon Longitudinal Study of Parents and Children Cohort. Description: Abdulkadir, Mohamed, et al. Polygenic Risk Scores Derived From a Tourette Syndrome Genome-wide Association Study Predict Presence of Tics in the Avon Longitudinal Study of Parents and Children Cohort. ''Biol Psychiatry''. 2019 Feb 15; '''85''' (4):298-304
Nuclear genetic regulation of the human mitochondrial transcriptome. Description: Ali, Aminah T, et al. Nuclear genetic regulation of the human mitochondrial transcriptome. ''Elife''. 2019 Feb 18; '''8''':
Neuropsychiatric Genetics of African Populations-Psychosis (NeuroGAP-Psychosis): a case-control study protocol and GWAS in Ethiopia, Kenya, South Africa and Uganda. Description: Stevenson, Anne, et al. Neuropsychiatric Genetics of African Populations-Psychosis (NeuroGAP-Psychosis): a case-control study protocol and GWAS in Ethiopia, Kenya, South Africa and Uganda. ''BMJ Open''. 2019 Feb 19; '''9''' (2):e025469
Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. Description: Daya, Michelle, et al. Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. ''Nat Commun''. 2019 Feb 20; '''10''' (1):880
SIRT1 rs12778366, FGFR2 rs2981582, STAT3 rs744166, LIPC rs10468017, rs493258 and LPL rs12678919 genotypes and haplotype evaluation in patients with age-related macular degeneration. Description: Liutkeviciene, Rasa, et al. SIRT1 rs12778366, FGFR2 rs2981582, STAT3 rs744166, LIPC rs10468017, rs493258 and LPL rs12678919 genotypes and haplotype evaluation in patients with age-related macular degeneration. ''Gene''. 2019 Feb 20; '''686''': 8-15
Blood groups A and AB are associated with increased gastric cancer risk: evidence from a large genetic study and systematic review. Description: Mao, Yingying, et al. Blood groups A and AB are associated with increased gastric cancer risk: evidence from a large genetic study and systematic review. ''BMC Cancer''. 2019 Feb 21; '''19''' (1):164
Chronic Inflammation Permanently Reshapes Tissue-Resident Immunity in Celiac Disease. Description: Mayassi, Toufic, et al. Chronic Inflammation Permanently Reshapes Tissue-Resident Immunity in Celiac Disease. ''Cell''. 2019 Feb 21; '''176''' (5):967-981.e19
Genomic analyses of an extensive collection of wild and cultivated accessions provide new insights into peach breeding history. Description: Li, Yong, et al. Genomic analyses of an extensive collection of wild and cultivated accessions provide new insights into peach breeding history. ''Genome Biol''. 2019 Feb 21; '''20''' (1):36
New alleles for chlorophyll content and stay-green traits revealed by a genome wide association study in rice (Oryza sativa). Description: Zhao, Yan, et al. New alleles for chlorophyll content and stay-green traits revealed by a genome wide association study in rice (Oryza sativa). ''Sci Rep''. 2019 Feb 22; '''9''' (1):2541
Pleiotropic effect of common PHOX2B variants in Hirschsprung disease and neuroblastoma. Description: Zhao, Jinglu, et al. Pleiotropic effect of common PHOX2B variants in Hirschsprung disease and neuroblastoma. ''Aging (Albany NY)''. 2019 Feb 22; '''11''' (4):1252-1261
Longitudinal plasma metabolomics of aging and sex. Description: Darst, Burcu F, et al. Longitudinal plasma metabolomics of aging and sex. ''Aging (Albany NY)''. 2019 Feb 24; '''11''' (4):1262-1282
Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population. Description: Hong, Eun Pyo, et al. Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population. ''J Clin Med''. 2019 Feb 25; '''8''' (2):
Hybridization is a recurrent evolutionary stimulus in wild yeast speciation. Description: Eberlein, Chris, et al. Hybridization is a recurrent evolutionary stimulus in wild yeast speciation. ''Nat Commun''. 2019 Feb 25; '''10''' (1):923
Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort. Description: Underwood, Jack F G, et al. Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort. ''Br J Psychiatry''. 2019 Feb 26; 1-7
*Behcet's disease and genetic interactions between HLA-B51 and variants in genes of autoinflammatory syndromes.** Description: Burillo-Sanz, Sergio, et al. Behcet's disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes. ''Sci Rep''. 2019 Feb 26; '''9''' (1):2777
Genome-wide association study suggests impact of chromosome 10 rs139401390 on kidney function in patients with coronary artery disease. Description: Schmitz, Boris, et al. Genome-wide association study suggests impact of chromosome 10 rs139401390 on kidney function in patients with coronary artery disease. ''Sci Rep''. 2019 Feb 26; '''9''' (1):2750
Long-term balancing selection drives evolution of immunity genes in Capsella. Description: Koenig, Daniel, et al. Long-term balancing selection drives evolution of immunity genes in Capsella. ''Elife''. 2019 Feb 26; '''8''':
TNFAIP3, TNIP1, and MyD88 Polymorphisms Predict Septic-Shock-Related Death in Patients Who Underwent Major Surgery. Description: Jimenez-Sousa, Maria Angeles, et al. TNFAIP3, TNIP1, and MyD88 Polymorphisms Predict Septic-Shock-Related Death in Patients Who Underwent Major Surgery. ''J Clin Med''. 2019 Feb 26; '''8''' (3):
Single Nucleotide Polymorphisms in MIR143 Contribute to Protection Against Non-Hodgkin Lymphoma (NHL) in Caucasian Populations. Description: Bradshaw, Gabrielle, et al. Single Nucleotide Polymorphisms in MIR143 Contribute to Protection Against Non-Hodgkin Lymphoma (NHL) in Caucasian Populations. ''Genes (Basel)''. 2019 Feb 27; '''10''' (3):
Leveraging brain cortex-derived molecular data to elucidate epigenetic and transcriptomic drivers of complex traits and disease. Description: Hatcher, Charlie, et al. Leveraging brain cortex-derived molecular data to elucidate epigenetic and transcriptomic drivers of complex traits and disease. ''Transl Psychiatry''. 2019 Feb 28; '''9''' (1):105
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Description: Berghuis, Bianca, et al. A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. ''Epilepsia Open''. 2019 Mar; '''4''' (1):102-109
A longitudinal approach to biological psychiatric research: The PsyCourse study. Description: Budde, Monika, et al. A longitudinal approach to biological psychiatric research: The PsyCourse study. ''Am J Med Genet B Neuropsychiatr Genet''. 2019 Mar; '''180''' (2):89-102
Analysis of HCRTR2 Gene Variants and Cluster Headache in Sweden. Description: Fourier, Carmen, et al. Analysis of HCRTR2 Gene Variants and Cluster Headache in Sweden. ''Headache''. 2019 Mar; '''59''' (3):410-417
Association Between rs3833912/rs16944 SNPs and Risk for Cerebral Palsy in Mexican Children. Description: Torres-Merino, Sofia, et al. Association Between rs3833912/rs16944 SNPs and Risk for Cerebral Palsy in Mexican Children. ''Mol Neurobiol''. 2019 Mar; '''56''' (3):1800-1811
Association of Genetic Risk Factors for Psychiatric Disorders and Traits of These Disorders in a Swedish Population Twin Sample. Description: Taylor, Mark J, et al. Association of Genetic Risk Factors for Psychiatric Disorders and Traits of These Disorders in a Swedish Population Twin Sample. ''JAMA Psychiatry''. 2019 Mar 1; '''76''' (3):280-289
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry. Description: Patel, Devanshi, et al. Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry. ''JAMA Netw Open''. 2019 Mar 1; '''2''' (3):e191350
Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese. Description: Rong, Shi Song, et al. Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese. ''Exp Eye Res''. 2019 Mar; '''180''': 129-136
Association study of variants in genes FTO, SLC6A4, DRD2, BDNF and GHRL with binge eating disorder (BED) in Portuguese women. Description: Palmeira, Lara, et al. Association study of variants in genes FTO, SLC6A4, DRD2, BDNF and GHRL with binge eating disorder (BED) in Portuguese women. ''Psychiatry Res''. 2019 Mar; '''273''': 309-311
A synonymous germline variant in a gene encoding a cell adhesion molecule is associated with cutaneous mast cell tumour development in Labrador and Golden Retrievers. Description: Biasoli, Deborah, et al. A synonymous germline variant in a gene encoding a cell adhesion molecule is associated with cutaneous mast cell tumour development in Labrador and Golden Retrievers. ''PLoS Genet''. 2019 Mar; '''15''' (3):e1007967
Biological and clinical insights from genetics of insomnia symptoms. Description: Lane, Jacqueline M, et al. Biological and clinical insights from genetics of insomnia symptoms. ''Nat Genet''. 2019 Mar; '''51''' (3):387-393
Clinical Utility and Practical Considerations of a Coronary Artery Disease Genetic Risk Score. Description: Liu, Robin, et al. Clinical Utility and Practical Considerations of a Coronary Artery Disease Genetic Risk Score. ''CJC Open''. 2019 Mar; '''1''' (2):69-75
Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese. Description: Zhang, Deng-Feng, et al. Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese. ''Natl Sci Rev''. 2019 Mar; '''6''' (2):257-274
Deleterious Mutation Burden and Its Association with Complex Traits in Sorghum (Sorghum bicolor). Description: Valluru, Ravi, et al. Deleterious Mutation Burden and Its Association with Complex Traits in Sorghum (Sorghum bicolor). ''Genetics''. 2019 Mar; '''211''' (3):1075-1087
Detailed insights into pan-European population structure and inbreeding in wild and hatchery Pacific oysters (Crassostrea gigas) revealed by genome-wide SNP data. Description: Vendrami, David L J, et al. Detailed insights into pan-European population structure and inbreeding in wild and hatchery Pacific oysters (Crassostrea gigas) revealed by genome-wide SNP data. ''Evol Appl''. 2019 Mar; '''12''' (3):519-534
Distinguishing the victim from the threat: SNP-based methods reveal the extent of introgressive hybridization between wildcats and domestic cats in Scotland and inform future in situ and ex situ management options for species restoration. Description: Senn, Helen V, et al. Distinguishing the victim from the threat: SNP-based methods reveal the extent of introgressive hybridization between wildcats and domestic cats in Scotland and inform future in situ and ex situ management options for species restoration. ''Evol Appl''. 2019 Mar; '''12''' (3):399-414
Effect of increased body mass index on risk of diagnosis or death from cancer. Description: Gharahkhani, Puya, et al. Effect of increased body mass index on risk of diagnosis or death from cancer. ''Br J Cancer''. 2019 Mar; '''120''' (5):565-570
eQTL of KCNK2 regionally influences the brain sulcal widening: evidence from 15,597 UK Biobank participants with neuroimaging data. Description: Le Guen, Yann, et al. eQTL of KCNK2 regionally influences the brain sulcal widening: evidence from 15,597 UK Biobank participants with neuroimaging data. ''Brain Struct Funct''. 2019 Mar; '''224''' (2):847-857
Evaluation of an HMGA2 variant for pleiotropic effects on height and metabolic traits in ponies. Description: Norton, Elaine M, et al. Evaluation of an HMGA2 variant for pleiotropic effects on height and metabolic traits in ponies. ''J Vet Intern Med''. 2019 Mar; '''33''' (2):942-952
Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia. Description: Brucato, Nicolas, et al. Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia. ''Genome Biol Evol''. 2019 Mar 1; '''11''' (3):748-758
GAD1 gene polymorphisms are associated with bipolar I disorder and with blood homovanillic acid levels but not with plasma GABA levels. Description: Arrue, Aurora, et al. GAD1 gene polymorphisms are associated with bipolar I disorder and with blood homovanillic acid levels but not with plasma GABA levels. ''Neurochem Int''. 2019 Mar; '''124''': 152-161
Genetic analysis of the relation of telomere length-related gene (RTEL1) and coronary heart disease risk. Description: Lu, Shijuan, et al. Genetic analysis of the relation of telomere length-related gene (RTEL1) and coronary heart disease risk. ''Mol Genet Genomic Med''. 2019 Mar; '''7''' (3):e550
Genetic architecture and candidate genes detected for chicken internal organ weight with a 600 K single nucleotide polymorphism array. Description: Dou, Taocun, et al. Genetic architecture and candidate genes detected for chicken internal organ weight with a 600 K single nucleotide polymorphism array. ''Asian-Australas J Anim Sci''. 2019 Mar; '''32''' (3):341-349
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. Description: Sakornsakolpat, Phuwanat, et al. Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. ''Nat Genet''. 2019 Mar; '''51''' (3):494-505
Genetic signatures of gene flow and malaria-driven natural selection in sub-Saharan populations of the "endemic Burkitt Lymphoma belt". Description: Gouveia, Mateus H, et al. Genetic signatures of gene flow and malaria-driven natural selection in sub-Saharan populations of the "endemic Burkitt Lymphoma belt". ''PLoS Genet''. 2019 Mar; '''15''' (3):e1008027
Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. Description: Tasa, Tonis, et al. Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. ''Eur J Hum Genet''. 2019 Mar; '''27''' (3):442-454
Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males. Description: Smith, Shad B, et al. Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males. ''Pain''. 2019 Mar; '''160''' (3):579-591
Genotyping-by-sequencing performance in selected livestock species. Description: Gurgul, Artur, et al. Genotyping-by-sequencing performance in selected livestock species. ''Genomics''. 2019 Mar; '''111''' (2):186-195
High expression of FAM13A was associated with increasing the liver cirrhosis risk. Description: Zhang, Yingai, et al. High expression of FAM13A was associated with increasing the liver cirrhosis risk. ''Mol Genet Genomic Med''. 2019 Mar; '''7''' (3):e543
Identification of a 3'-Untranslated Genetic Variant of RARB Associated With Carotid Intima-Media Thickness in Rheumatoid Arthritis: A Genome-Wide Association Study. Description: Lopez-Mejias, Raquel, et al. Identification of a 3'-Untranslated Genetic Variant of RARB Associated With Carotid Intima-Media Thickness in Rheumatoid Arthritis: A Genome-Wide Association Study. ''Arthritis Rheumatol''. 2019 Mar; '''71''' (3):351-360
Integrative Genomics Reveals the Genetics and Evolution of the Honey Bee's Social Immune System. Description: Harpur, Brock A, et al. Integrative Genomics Reveals the Genetics and Evolution of the Honey Bee's Social Immune System. ''Genome Biol Evol''. 2019 Mar 1; '''11''' (3):937-948
Integrative omics analysis identifies macrophage migration inhibitory factor signaling pathways underlying human hepatic fibrogenesis and fibrosis. Description: Liu, Zhipeng, et al. Integrative omics analysis identifies macrophage migration inhibitory factor signaling pathways underlying human hepatic fibrogenesis and fibrosis. ''J BioX Res''. 2019 Mar; '''2''' (1):16-24
Interactions of CDH13 gene polymorphisms and ambient PM10 air pollution exposure with blood pressure and hypertension in Korean men. Description: Kim, Hyun-Jin, et al. Interactions of CDH13 gene polymorphisms and ambient PM10 air pollution exposure with blood pressure and hypertension in Korean men. ''Chemosphere''. 2019 Mar; '''218''': 292-298
Loss of function mutations in essential genes cause embryonic lethality in pigs. Description: Derks, Martijn F L, et al. Loss of function mutations in essential genes cause embryonic lethality in pigs. ''PLoS Genet''. 2019 Mar; '''15''' (3):e1008055
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Description: Shrine, Nick, et al. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. ''Nat Genet''. 2019 Mar; '''51''' (3):481-493
New insights into host adaptation to swine respiratory disease revealed by genetic differentiation and RNA sequencing analyses. Description: Zhang, Mingpeng, et al. New insights into host adaptation to swine respiratory disease revealed by genetic differentiation and RNA sequencing analyses. ''Evol Appl''. 2019 Mar; '''12''' (3):535-548
Origin of the Aromatic Group of Cultivated Rice (Oryza sativa L.) Traced to the Indian Subcontinent. Description: Civan, Peter, et al. Origin of the Aromatic Group of Cultivated Rice (Oryza sativa L.) Traced to the Indian Subcontinent. ''Genome Biol Evol''. 2019 Mar 1; '''11''' (3):832-843
Population Genomics and Structure of the Critically Endangered Mariana Crow (Corvus kubaryi). Description: Cortes-Rodriguez, Nandadevi, et al. Population Genomics and Structure of the Critically Endangered Mariana Crow (Corvus kubaryi). ''Genes (Basel)''. 2019 Mar 1; '''10''' (3):
Population genomics of rapidly invading lionfish in the Caribbean reveals signals of range expansion in the absence of spatial population structure. Description: Bors, Eleanor K, et al. Population genomics of rapidly invading lionfish in the Caribbean reveals signals of range expansion in the absence of spatial population structure. ''Ecol Evol''. 2019 Mar; '''9''' (6):3306-3320
Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic. Description: Sun, Ryan, et al. Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic. ''PLoS Genet''. 2019 Mar; '''15''' (3):e1007530
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Description: Justice, Anne E, et al. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. ''Nat Genet''. 2019 Mar; '''51''' (3):452-469
Schizophrenia risk and reproductive success: a Mendelian randomization study. Description: Lawn, Rebecca B, et al. Schizophrenia risk and reproductive success: a Mendelian randomization study. ''R Soc Open Sci''. 2019 Mar; '''6''' (3):181049
Seascape genomics of eastern oyster (Crassostrea virginica) along the Atlantic coast of Canada. Description: Bernatchez, Simon, et al. Seascape genomics of eastern oyster (Crassostrea virginica) along the Atlantic coast of Canada. ''Evol Appl''. 2019 Mar; '''12''' (3):587-609
The complex geography of domestication of the African rice Oryza glaberrima. Description: Choi, Jae Young, et al. The complex geography of domestication of the African rice Oryza glaberrima. ''PLoS Genet''. 2019 Mar; '''15''' (3):e1007414
The polygenic nature of telomere length and the anti-ageing properties of lithium. Description: Coutts, Fiona, et al. The polygenic nature of telomere length and the anti-ageing properties of lithium. ''Neuropsychopharmacology''. 2019 Mar; '''44''' (4):757-765
Trypsin-encoding PRSS1-PRSS2 variations influence the risk of asparaginase-associated pancreatitis in children with acute lymphoblastic leukemia: a Ponte di Legno toxicity working group report. Description: Wolthers, Benjamin O, et al. Trypsin-encoding PRSS1-PRSS2 variations influence the risk of asparaginase-associated pancreatitis in children with acute lymphoblastic leukemia: a Ponte di Legno toxicity working group report. ''Haematologica''. 2019 Mar; '''104''' (3):556-563
Whole exome sequencing identifies hemizygous deletions in the UGT2B28 and USP17L2 genes in a threegeneration family with endometriosis. Description: Albertsen, Hans M, et al. Whole exome sequencing identifies hemizygous deletions in the UGT2B28 and USP17L2 genes in a threegeneration family with endometriosis. ''Mol Med Rep''. 2019 Mar; '''19''' (3):1716-1720
Widespread introgression in Chinese indigenous chicken breeds from commercial broiler. Description: Zhang, Chunyuan, et al. Widespread introgression in Chinese indigenous chicken breeds from commercial broiler. ''Evol Appl''. 2019 Mar; '''12''' (3):610-621
A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome. Description: Wiberg, Akira, et al. A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome. ''Nat Commun''. 2019 Mar 4; '''10''' (1):1030
Comparing the mRNA expression profile and the genetic determinism of intramuscular fat traits in the porcine gluteus medius and longissimus dorsi muscles. Description: Gonzalez-Prendes, Rayner, et al. Comparing the mRNA expression profile and the genetic determinism of intramuscular fat traits in the porcine gluteus medius and longissimus dorsi muscles. ''BMC Genomics''. 2019 Mar 4; '''20''' (1):170
Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development. Description: Li, Yafang, et al. Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development. ''Oncotarget''. 2019 Mar 5; '''10''' (19):1760-1774
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. Description: Dudding, Tom, et al. Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. ''Nat Commun''. 2019 Mar 5; '''10''' (1):1052
High-resolution population structure and runs of homozygosity reveal the genetic architecture of complex traits in the Lipizzan horse. Description: Grilz-Seger, Gertrud, et al. High-resolution population structure and runs of homozygosity reveal the genetic architecture of complex traits in the Lipizzan horse. ''BMC Genomics''. 2019 Mar 5; '''20''' (1):174
Evaluation of Linkage Disequilibrium, Effective Population Size and Haplotype Block Structure in Chinese Cattle. Description: Xu, Lei, et al. Evaluation of Linkage Disequilibrium, Effective Population Size and Haplotype Block Structure in Chinese Cattle. ''Animals (Basel)''. 2019 Mar 6; '''9''' (3):
Genome-wide data from the Bubi of Bioko Island clarifies the Atlantic fringe of the Bantu dispersal. Description: Gelabert, Pere, et al. Genome-wide data from the Bubi of Bioko Island clarifies the Atlantic fringe of the Bantu dispersal. ''BMC Genomics''. 2019 Mar 6; '''20''' (1):179
Arginine to Glutamine Variant in Olfactomedin Like 3 (OLFML3) Is a Candidate for Severe Goniodysgenesis and Glaucoma in the Border Collie Dog Breed. Description: Pugh, Carys A, et al. Arginine to Glutamine Variant in Olfactomedin Like 3 (OLFML3) Is a Candidate for Severe Goniodysgenesis and Glaucoma in the Border Collie Dog Breed. ''G3 (Bethesda)''. 2019 Mar 7; '''9''' (3):943-954
Discovery of Allele-Specific Protein-RNA Interactions in Human Transcriptomes. Description: Bahrami-Samani, Emad, et al. Discovery of Allele-Specific Protein-RNA Interactions in Human Transcriptomes. ''Am J Hum Genet''. 2019 Mar 7; '''104''' (3):492-502
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. Description: Dashti, Hassan S, et al. Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. ''Nat Commun''. 2019 Mar 7; '''10''' (1):1100
Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population. Description: van der Plaat, Diana A, et al. Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population. ''BMC Pulm Med''. 2019 Mar 7; '''19''' (1):58
Structural and Functional Neuroimaging of Polygenic Risk for Schizophrenia: A Recall-by-Genotype-Based Approach. Description: Lancaster, Thomas M, et al. Structural and Functional Neuroimaging of Polygenic Risk for Schizophrenia: A Recall-by-Genotype-Based Approach. ''Schizophr Bull''. 2019 Mar 7; '''45''' (2):405-414
Effects of X-chromosome Tenomodulin Genetic Variants on Obesity in a Children's Cohort and Implications of the Gene in Adipocyte Metabolism. Description: Ruiz-Ojeda, Francisco Javier, et al. Effects of X-chromosome Tenomodulin Genetic Variants on Obesity in a Children's Cohort and Implications of the Gene in Adipocyte Metabolism. ''Sci Rep''. 2019 Mar 8; '''9''' (1):3979
*Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B07:02.** Description: Tziotzios, Christos, et al. Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02. ''Nat Commun''. 2019 Mar 8; '''10''' (1):1150
No interaction between polygenic scores and childhood trauma in predicting suicide attempt in schizophrenia. Description: Bani-Fatemi, Ali, et al. No interaction between polygenic scores and childhood trauma in predicting suicide attempt in schizophrenia. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2019 Mar 8; '''89''': 169-173
Population Substructure Has Implications in Validating Next-Generation Cancer Genomics Studies with TCGA. Description: Miller, Marina D, et al. Population Substructure Has Implications in Validating Next-Generation Cancer Genomics Studies with TCGA. ''Int J Mol Sci''. 2019 Mar 8; '''20''' (5):
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population. Description: Liu, Gang, et al. Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population. ''Gene''. 2019 Mar 10; '''688''': 215-220
Common Inflammation-Related Candidate Gene Variants and Acute Kidney Injury in 2647 Critically Ill Finnish Patients. Description: Vilander, Laura M, et al. Common Inflammation-Related Candidate Gene Variants and Acute Kidney Injury in 2647 Critically Ill Finnish Patients. ''J Clin Med''. 2019 Mar 11; '''8''' (3):
Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy. Description: Nutile, T, et al. Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy. ''Sci Rep''. 2019 Mar 11; '''9''' (1):4059
Whole-genome resequencing reveals Brassica napus origin and genetic loci involved in its improvement. Description: Lu, Kun, et al. Whole-genome resequencing reveals Brassica napus origin and genetic loci involved in its improvement. ''Nat Commun''. 2019 Mar 11; '''10''' (1):1154
Alcohol-responsive genes identified in human iPSC-derived neural cultures. Description: Jensen, Kevin P, et al. Alcohol-responsive genes identified in human iPSC-derived neural cultures. ''Transl Psychiatry''. 2019 Mar 12; '''9''' (1):96
Mitotic Recombination and Rapid Genome Evolution in the Invasive Forest Pathogen Phytophthora ramorum. Description: Dale, Angela L, et al. Mitotic Recombination and Rapid Genome Evolution in the Invasive Forest Pathogen Phytophthora ramorum. ''MBio''. 2019 Mar 12; '''10''' (2):
Survey of allele specific expression in bovine muscle. Description: Guillocheau, Gabriel M, et al. Survey of allele specific expression in bovine muscle. ''Sci Rep''. 2019 Mar 12; '''9''' (1):4297
Whole-genome resequencing of 472 Vitis accessions for grapevine diversity and demographic history analyses. Description: Liang, Zhenchang, et al. Whole-genome resequencing of 472 Vitis accessions for grapevine diversity and demographic history analyses. ''Nat Commun''. 2019 Mar 13; '''10''' (1):1190
Genetic regulation of methylation in human endometrium and blood and gene targets for reproductive diseases. Description: Mortlock, Sally, et al. Genetic regulation of methylation in human endometrium and blood and gene targets for reproductive diseases. ''Clin Epigenetics''. 2019 Mar 14; '''11''' (1):49
Genome-wide tracts of homozygosity and exome analyses reveal repetitive elements with Barrets esophagus/esophageal adenocarcinoma risk. Description: Wanchai, Visanu, et al. Genome-wide tracts of homozygosity and exome analyses reveal repetitive elements with Barrets esophagus/esophageal adenocarcinoma risk. ''BMC Bioinformatics''. 2019 Mar 14; '''20''' (Suppl 2):98
TM6SF2 and MBOAT7 Gene Variants in Liver Fibrosis and Cirrhosis. Description: Basyte-Bacevice, Viktorija, et al. TM6SF2 and MBOAT7 Gene Variants in Liver Fibrosis and Cirrhosis. ''Int J Mol Sci''. 2019 Mar 14; '''20''' (6):
A functional variant in the serotonin receptor 7 gene (HTR7), rs7905446, is associated with good response to SSRIs in bipolar and unipolar depression. Description: Wei, Ya Bin, et al. A functional variant in the serotonin receptor 7 gene (HTR7), rs7905446, is associated with good response to SSRIs in bipolar and unipolar depression. ''Mol Psychiatry''. 2019 Mar 15;
Genomewide Study of Epigenetic Biomarkers of Opioid Dependence in European- American Women. Description: Montalvo-Ortiz, Janitza L, et al. Genomewide Study of Epigenetic Biomarkers of Opioid Dependence in European- American Women. ''Sci Rep''. 2019 Mar 15; '''9''' (1):4660
Exceptional Longevity and Polygenic Risk for Cardiovascular Health. Description: Revelas, Mary, et al. Exceptional Longevity and Polygenic Risk for Cardiovascular Health. ''Genes (Basel)''. 2019 Mar 18; '''10''' (3):
Genome-wide association study and scan for signatures of selection point to candidate genes for body temperature maintenance under the cold stress in Siberian cattle populations. Description: Igoshin, Alexander V, et al. Genome-wide association study and scan for signatures of selection point to candidate genes for body temperature maintenance under the cold stress in Siberian cattle populations. ''BMC Genet''. 2019 Mar 18; '''20''' (Suppl 1):26
Association of Human FOS Promoter Variants with the Occurrence of Knee-Osteoarthritis in a Case Control Association Study. Description: Huber, Rene, et al. Association of Human FOS Promoter Variants with the Occurrence of Knee-Osteoarthritis in a Case Control Association Study. ''Int J Mol Sci''. 2019 Mar 19; '''20''' (6):
Genome-wide association meta-analysis of functional outcome after ischemic stroke. Description: Soderholm, Martin, et al. Genome-wide association meta-analysis of functional outcome after ischemic stroke. ''Neurology''. 2019 Mar 19; '''92''' (12):e1271-e1283
Late Pleistocene human genome suggests a local origin for the first farmers of central Anatolia. Description: Feldman, Michal, et al. Late Pleistocene human genome suggests a local origin for the first farmers of central Anatolia. ''Nat Commun''. 2019 Mar 19; '''10''' (1):1218
Risk-modeling of dog osteosarcoma genome scans shows individuals with Mendelian-level polygenic risk are common. Description: Zapata, Isain, et al. Risk-modeling of dog osteosarcoma genome scans shows individuals with Mendelian-level polygenic risk are common. ''BMC Genomics''. 2019 Mar 19; '''20''' (1):226
Vitamin D levels and risk of delirium: A mendelian randomization study in the UK Biobank. Description: Bowman, Kirsty, et al. Vitamin D levels and risk of delirium: A mendelian randomization study in the UK Biobank. ''Neurology''. 2019 Mar 19; '''92''' (12):e1387-e1394
Integrative Genome-Wide Association Studies of eQTL and GWAS Data for Gout Disease Susceptibility. Description: Lee, Meng-Tse Gabriel, et al. Integrative Genome-Wide Association Studies of eQTL and GWAS Data for Gout Disease Susceptibility. ''Sci Rep''. 2019 Mar 21; '''9''' (1):4981
Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies. Description: Sohail, Mashaal, et al. Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies. ''Elife''. 2019 Mar 21; '''8''':
The Origin of a Coastal Indigenous Horse Breed in China Revealed by Genome-Wide SNP Data. Description: Ma, Hongying, et al. The Origin of a Coastal Indigenous Horse Breed in China Revealed by Genome-Wide SNP Data. ''Genes (Basel)''. 2019 Mar 21; '''10''' (3):
A Genome-Wide Analysis of the Penumbral Volume in Inbred Mice following Middle Cerebral Artery Occlusion. Description: Rudy, Robert F, et al. A Genome-Wide Analysis of the Penumbral Volume in Inbred Mice following Middle Cerebral Artery Occlusion. ''Sci Rep''. 2019 Mar 25; '''9''' (1):5070
Genetic polymorphisms in MTR are associated with non-syndromic congenital heart disease from a family-based case-control study in the Chinese population. Description: Deng, Changfei, et al. Genetic polymorphisms in MTR are associated with non-syndromic congenital heart disease from a family-based case-control study in the Chinese population. ''Sci Rep''. 2019 Mar 25; '''9''' (1):5065
X-chromosome association study reveals genetic susceptibility loci of nasopharyngeal carcinoma. Description: Zuo, Xiao-Yu, et al. X-chromosome association study reveals genetic susceptibility loci of nasopharyngeal carcinoma. ''Biol Sex Differ''. 2019 Mar 25; '''10''' (1):13
Parent of origin genetic effects on methylation in humans are common and influence complex trait variation. Description: Zeng, Yanni, et al. Parent of origin genetic effects on methylation in humans are common and influence complex trait variation. ''Nat Commun''. 2019 Mar 27; '''10''' (1):1383
Identifying Selection Signatures for Backfat Thickness in Yorkshire Pigs Highlights New Regions Affecting Fat Metabolism. Description: Ma, Haoran, et al. Identifying Selection Signatures for Backfat Thickness in Yorkshire Pigs Highlights New Regions Affecting Fat Metabolism. ''Genes (Basel)''. 2019 Mar 28; '''10''' (4):
Association of rs10830962 polymorphism with gestational diabetes mellitus risk in a Chinese population. Description: Xie, Kaipeng, et al. Association of rs10830962 polymorphism with gestational diabetes mellitus risk in a Chinese population. ''Sci Rep''. 2019 Mar 29; '''9''' (1):5357
Chronotype Genetic Variant in PER2 is Associated with Intrinsic Circadian Period in Humans. Description: Chang, Anne-Marie, et al. Chronotype Genetic Variant in PER2 is Associated with Intrinsic Circadian Period in Humans. ''Sci Rep''. 2019 Mar 29; '''9''' (1):5350
Genetic Risk Score Predictive of the Plasma Triglyceride Response to an Omega-3 Fatty Acid Supplementation in a Mexican Population. Description: Vallee Marcotte, Bastien, et al. Genetic Risk Score Predictive of the Plasma Triglyceride Response to an Omega-3 Fatty Acid Supplementation in a Mexican Population. ''Nutrients''. 2019 Mar 29; '''11''' (4):
Genome-wide association study of four yield-related traits at the R6 stage in soybean. Description: Li, Xiangnan, et al. Genome-wide association study of four yield-related traits at the R6 stage in soybean. ''BMC Genet''. 2019 Mar 29; '''20''' (1):39
Prioritizing candidate genes for fertility in dairy cows using gene-based analysis, functional annotation and differential gene expression. Description: Cai, Zexi, et al. Prioritizing candidate genes for fertility in dairy cows using gene-based analysis, functional annotation and differential gene expression. ''BMC Genomics''. 2019 Mar 29; '''20''' (1):255
A biologically-informed polygenic score identifies endophenotypes and clinical conditions associated with the insulin receptor function on specific brain regions. Description: Hari Dass, Shantala A, et al. A biologically-informed polygenic score identifies endophenotypes and clinical conditions associated with the insulin receptor function on specific brain regions. ''EBioMedicine''. 2019 Apr; '''42''': 188-202
Association study and a systematic meta-analysis of the VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention-deficit hyperactivity disorder. Description: Grunblatt, Edna, et al. Association study and a systematic meta-analysis of the VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention-deficit hyperactivity disorder. ''J Neural Transm (Vienna)''. 2019 Apr; '''126''' (4):517-529
Discovering heritable modes of MEG spectral power. Description: Leppaaho, Eemeli, et al. Discovering heritable modes of MEG spectral power. ''Hum Brain Mapp''. 2019 Apr 1; '''40''' (5):1391-1402
Epistatic mutations under divergent selection govern phenotypic variation in the crow hybrid zone. Description: Knief, Ulrich, et al. Epistatic mutations under divergent selection govern phenotypic variation in the crow hybrid zone. ''Nat Ecol Evol''. 2019 Apr; '''3''' (4):570-576
Gene-environment interaction and maternal arsenic methylation efficiency during pregnancy. Description: Gao, Shangzhi, et al. Gene-environment interaction and maternal arsenic methylation efficiency during pregnancy. ''Environ Int''. 2019 Apr; '''125''': 43-50
Genetic analysis of neurodegenerative diseases in a pathology cohort. Description: Blauwendraat, Cornelis, et al. Genetic analysis of neurodegenerative diseases in a pathology cohort. ''Neurobiol Aging''. 2019 Apr; '''76''': 214.e1-214.e9
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. Description: Imaizumi, Akira, et al. Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. ''Eur J Hum Genet''. 2019 Apr; '''27''' (4):621-630
Genetic correlation of fatty acid composition with growth, carcass, fat deposition and meat quality traits based on GWAS data in six pig populations. Description: Zhang, Yifeng, et al. Genetic correlation of fatty acid composition with growth, carcass, fat deposition and meat quality traits based on GWAS data in six pig populations. ''Meat Sci''. 2019 Apr; '''150''': 47-55
Genetic Determinants of Glycated Hemoglobin in Type 1 Diabetes. Description: Syreeni, Anna, et al. Genetic Determinants of Glycated Hemoglobin in Type 1 Diabetes. ''Diabetes''. 2019 Apr; '''68''' (4):858-867
Genetic diversity patterns and domestication origin of soybean. Description: Jeong, Soon-Chun, et al. Genetic diversity patterns and domestication origin of soybean. ''Theor Appl Genet''. 2019 Apr; '''132''' (4):1179-1193
Genetics of response to cognitive behavior therapy in adults with major depression: a preliminary report. Description: Andersson, Evelyn, et al. Genetics of response to cognitive behavior therapy in adults with major depression: a preliminary report. ''Mol Psychiatry''. 2019 Apr; '''24''' (4):484-490
Genetic variation in CRHR1 is associated with short-term respiratory response to corticosteroids in preterm infants at risk for bronchopulmonary dysplasia. Description: Lewis, Tamorah, et al. Genetic variation in CRHR1 is associated with short-term respiratory response to corticosteroids in preterm infants at risk for bronchopulmonary dysplasia. ''Pediatr Res''. 2019 Apr; '''85''' (5):625-633
Genome-Wide Association of Genetic Variation in the PSCA Gene with Gastric Cancer Susceptibility in a Korean Population. Description: Park, Boyoung, et al. Genome-Wide Association of Genetic Variation in the PSCA Gene with Gastric Cancer Susceptibility in a Korean Population. ''Cancer Res Treat''. 2019 Apr; '''51''' (2):748-757
Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis. Description: Li, Zhixiu, et al. Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis. ''PLoS Genet''. 2019 Apr; '''15''' (4):e1008038
Genome wide association study on feed conversion ratio using imputed sequence data in chickens. Description: Wang, Jiaying, et al. Genome wide association study on feed conversion ratio using imputed sequence data in chickens. ''Asian-Australas J Anim Sci''. 2019 Apr; '''32''' (4):494-500
Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. Description: Hu, Bowen, et al. Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. ''PLoS Genet''. 2019 Apr; '''15''' (4):e1007973
Genome-wide sexually antagonistic variants reveal long-standing constraints on sexual dimorphism in fruit flies. Description: Ruzicka, Filip, et al. Genome-wide sexually antagonistic variants reveal long-standing constraints on sexual dimorphism in fruit flies. ''PLoS Biol''. 2019 Apr; '''17''' (4):e3000244
Identification of epistasis loci underlying rice flowering time by controlling population stratification and polygenic effect. Description: Ahsan, Asif, et al. Identification of epistasis loci underlying rice flowering time by controlling population stratification and polygenic effect. ''DNA Res''. 2019 Apr 1; '''26''' (2):119-130
Interrogation of human hematopoiesis at single-cell and single-variant resolution. Description: Ulirsch, Jacob C, et al. Interrogation of human hematopoiesis at single-cell and single-variant resolution. ''Nat Genet''. 2019 Apr; '''51''' (4):683-693
Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus. Description: Vergara, Candelaria, et al. Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus. ''Gastroenterology''. 2019 Apr; '''156''' (5):1496-1507.e7
Nonlinear phenotypic variation uncovers the emergence of heterosis in Arabidopsis thaliana. Description: Vasseur, Francois, et al. Nonlinear phenotypic variation uncovers the emergence of heterosis in Arabidopsis thaliana. ''PLoS Biol''. 2019 Apr; '''17''' (4):e3000214
Novel idiopathic pulmonary fibrosis susceptibility variants revealed by deep sequencing. Description: Lorenzo-Salazar, Jose M, et al. Novel idiopathic pulmonary fibrosis susceptibility variants revealed by deep sequencing. ''ERJ Open Res''. 2019 Apr; '''5''' (2):
Nuclear receptor gene polymorphisms and warfarin dose requirements in the Quebec Warfarin Cohort. Description: Shahabi, Payman, et al. Nuclear receptor gene polymorphisms and warfarin dose requirements in the Quebec Warfarin Cohort. ''Pharmacogenomics J''. 2019 Apr; '''19''' (2):147-156
Patterns of genetic differentiation in Colorado potato beetle correlate with contemporary, not historic, potato land cover. Description: Crossley, Michael S, et al. Patterns of genetic differentiation in Colorado potato beetle correlate with contemporary, not historic, potato land cover. ''Evol Appl''. 2019 Apr; '''12''' (4):804-814
Polygenic Risk Score Is Associated With Intraocular Pressure and Improves Glaucoma Prediction in the UK Biobank Cohort. Description: Gao, X Raymond, et al. Polygenic Risk Score Is Associated With Intraocular Pressure and Improves Glaucoma Prediction in the UK Biobank Cohort. ''Transl Vis Sci Technol''. 2019 Apr; '''8''' (2):10
SeqSQC: A Bioconductor Package for Evaluating the Sample Quality of Next-generation Sequencing Data. Description: Liu, Qian, et al. SeqSQC: A Bioconductor Package for Evaluating the Sample Quality of Next-generation Sequencing Data. ''Genomics Proteomics Bioinformatics''. 2019 Apr; '''17''' (2):211-218
The combined effects of FADS gene variation and dietary fats in obesity-related traits in a population from the far north of Sweden: the GLACIER Study. Description: Chen, Yan, et al. The combined effects of FADS gene variation and dietary fats in obesity-related traits in a population from the far north of Sweden: the GLACIER Study. ''Int J Obes (Lond)''. 2019 Apr; '''43''' (4):808-820
The Cortical Neuroimmune Regulator TANK Affects Emotional Processing and Enhances Alcohol Drinking: A Translational Study. Description: Muller, Christian P, et al. The Cortical Neuroimmune Regulator TANK Affects Emotional Processing and Enhances Alcohol Drinking: A Translational Study. ''Cereb Cortex''. 2019 Apr 1; '''29''' (4):1736-1751
Varicose veins of lower extremities: Insights from the first large-scale genetic study. Description: Shadrina, Alexandra S, et al. Varicose veins of lower extremities: Insights from the first large-scale genetic study. ''PLoS Genet''. 2019 Apr; '''15''' (4):e1008110
Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes. Description: Choi, Jihoon, et al. Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes. ''Pharmacogenomics J''. 2019 Apr; '''19''' (2):127-135
Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. Description: Zhu, Zhaozhong, et al. Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. ''Respir Res''. 2019 Apr 2; '''20''' (1):64
Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. Description: Kranzler, Henry R, et al. Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. ''Nat Commun''. 2019 Apr 2; '''10''' (1):1499
Rapid evolution of a retro-transposable hotspot of ovine genome underlies the alteration of BMP2 expression and development of fat tails. Description: Pan, Zhangyuan, et al. Rapid evolution of a retro-transposable hotspot of ovine genome underlies the alteration of BMP2 expression and development of fat tails. ''BMC Genomics''. 2019 Apr 2; '''20''' (1):261
Comparing the Utility of Mitochondrial and Nuclear DNA to Adjust for Genetic Ancestry in Association Studies. Description: Miller, Brendan, et al. Comparing the Utility of Mitochondrial and Nuclear DNA to Adjust for Genetic Ancestry in Association Studies. ''Cells''. 2019 Apr 3; '''8''' (4):
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. Description: Ferreira, Manuel A R, et al. Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. ''Am J Hum Genet''. 2019 Apr 4; '''104''' (4):665-684
Genome-wide association studies targeting the yield of extraembryonic fluid and production traits in Russian White chickens. Description: Kudinov, Andrei A, et al. Genome-wide association studies targeting the yield of extraembryonic fluid and production traits in Russian White chickens. ''BMC Genomics''. 2019 Apr 4; '''20''' (1):270
Genome-Wide Association Study Identifies a Genetic Prediction Model for Postoperative Survival in Patients with Hepatocellular Carcinoma. Description: Wei, Jinwang, et al. Genome-Wide Association Study Identifies a Genetic Prediction Model for Postoperative Survival in Patients with Hepatocellular Carcinoma. ''Med Sci Monit''. 2019 Apr 4; '''25''': 2452-2478
Meta-analysis of genome-wide association studies provides insights into genetic control of tomato flavor. Description: Zhao, Jiantao, et al. Meta-analysis of genome-wide association studies provides insights into genetic control of tomato flavor. ''Nat Commun''. 2019 Apr 4; '''10''' (1):1534
Adjustment for index event bias in genome-wide association studies of subsequent events. Description: Dudbridge, Frank, et al. Adjustment for index event bias in genome-wide association studies of subsequent events. ''Nat Commun''. 2019 Apr 5; '''10''' (1):1561
Association of Circulating YKL-40 Levels and CHI3L1 Variants with the Risk of Spinal Deformity Progression in Adolescent Idiopathic Scoliosis. Description: Nada, Dina, et al. Association of Circulating YKL-40 Levels and CHI3L1 Variants with the Risk of Spinal Deformity Progression in Adolescent Idiopathic Scoliosis. ''Sci Rep''. 2019 Apr 5; '''9''' (1):5712
Genome-wide associations and functional gene analyses for endoparasite resistance in an endangered population of native German Black Pied cattle. Description: May, Katharina, et al. Genome-wide associations and functional gene analyses for endoparasite resistance in an endangered population of native German Black Pied cattle. ''BMC Genomics''. 2019 Apr 8; '''20''' (1):277
Natural variation in C. elegans arsenic toxicity is explained by differences in branched chain amino acid metabolism. Description: Zdraljevic, Stefan, et al. Natural variation in C. elegans arsenic toxicity is explained by differences in branched chain amino acid metabolism. ''Elife''. 2019 Apr 8; '''8''':
Analysis of Genetic Diversity and Population Structure in Three Forest Musk Deer Captive Populations with Different Origins. Description: Fan, Jiamin, et al. Analysis of Genetic Diversity and Population Structure in Three Forest Musk Deer Captive Populations with Different Origins. ''G3 (Bethesda)''. 2019 Apr 9; '''9''' (4):1037-1044
A specific amino acid motif of HLA-DRB1 mediates risk and interacts with smoking history in Parkinson's disease. Description: Hollenbach, Jill A, et al. A specific amino acid motif of HLA-DRB1 mediates risk and interacts with smoking history in Parkinson's disease. ''Proc Natl Acad Sci U S A''. 2019 Apr 9; '''116''' (15):7419-7424
Exome-wide survey of the Siberian Caucasian population. Description: Yurchenko, Andrey A, et al. Exome-wide survey of the Siberian Caucasian population. ''BMC Med Genet''. 2019 Apr 9; '''20''' (Suppl 1):51
High-Density Linkage Map and QTLs for Growth in Snapper (Chrysophrys auratus). Description: Ashton, David T, et al. High-Density Linkage Map and QTLs for Growth in Snapper (Chrysophrys auratus). ''G3 (Bethesda)''. 2019 Apr 9; '''9''' (4):1027-1035
Reconstructing recent population history while mapping rare variants using haplotypes. Description: Yunusbaev, Ural, et al. Reconstructing recent population history while mapping rare variants using haplotypes. ''Sci Rep''. 2019 Apr 10; '''9''' (1):5849
The lysosomal disease caused by mutant VPS33A. Description: Pavlova, Elena V, et al. The lysosomal disease caused by mutant VPS33A. ''Hum Mol Genet''. 2019 Apr 10;
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis. Description: Dekker, Annelot M, et al. Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis. ''Sci Rep''. 2019 Apr 11; '''9''' (1):5931
Genome-wide association study of suicide attempt in a Mexican population: a study protocol. Description: Gonzalez-Castro, Thelma Beatriz, et al. Genome-wide association study of suicide attempt in a Mexican population: a study protocol. ''BMJ Open''. 2019 Apr 11; '''9''' (4):e025335
Associations of the NRF2/KEAP1 pathway and antioxidant defense gene polymorphisms with chronic obstructive pulmonary disease. Description: Korytina, Gulnaz F, et al. Associations of the NRF2/KEAP1 pathway and antioxidant defense gene polymorphisms with chronic obstructive pulmonary disease. ''Gene''. 2019 Apr 15; '''692''': 102-112
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer. Description: Ferreira, Manuel A, et al. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer. ''Nat Commun''. 2019 Apr 15; '''10''' (1):1741
Telomere length as a predictor of emotional processing in the brain. Description: Powell, Timothy R, et al. Telomere length as a predictor of emotional processing in the brain. ''Hum Brain Mapp''. 2019 Apr 15; '''40''' (6):1750-1759
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome. Description: Berner, Daniel, et al. The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome. ''Hum Mol Genet''. 2019 Apr 15;
Polygenic prediction via Bayesian regression and continuous shrinkage priors. Description: Ge, Tian, et al. Polygenic prediction via Bayesian regression and continuous shrinkage priors. ''Nat Commun''. 2019 Apr 16; '''10''' (1):1776
Association of Rare Copy Number Variants With Risk of Depression. Description: Kendall, Kimberley Marie, et al. Association of Rare Copy Number Variants With Risk of Depression. ''JAMA Psychiatry''. 2019 Apr 17;
Genome-wide association study of endo-parasite phenotypes using imputed whole-genome sequence data in dairy and beef cattle. Description: Twomey, Alan J, et al. Genome-wide association study of endo-parasite phenotypes using imputed whole-genome sequence data in dairy and beef cattle. ''Genet Sel Evol''. 2019 Apr 18; '''51''' (1):15
Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood. Description: Khera, Amit V, et al. Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood. ''Cell''. 2019 Apr 18; '''177''' (3):587-596.e9
Sequence imputation from low density single nucleotide polymorphism panel in a black poplar breeding population. Description: Pegard, Marie, et al. Sequence imputation from low density single nucleotide polymorphism panel in a black poplar breeding population. ''BMC Genomics''. 2019 Apr 18; '''20''' (1):302
Evaluation of a Chicken 600K SNP genotyping array in non-model species of grouse. Description: Minias, Piotr, et al. Evaluation of a Chicken 600K SNP genotyping array in non-model species of grouse. ''Sci Rep''. 2019 Apr 23; '''9''' (1):6407
Genetics and evidence for balancing selection of a sex-linked colour polymorphism in a songbird. Description: Kim, Kang-Wook, et al. Genetics and evidence for balancing selection of a sex-linked colour polymorphism in a songbird. ''Nat Commun''. 2019 Apr 23; '''10''' (1):1852
Genome-wide association study of medication-use and associated disease in the UK Biobank. Description: Wu, Yeda, et al. Genome-wide association study of medication-use and associated disease in the UK Biobank. ''Nat Commun''. 2019 Apr 23; '''10''' (1):1891
Genome-wide patterns of population structure and association mapping of nut-related traits in Persian walnut populations from Iran using the Axiom J. regia 700K SNP array. Description: Arab, Mohammad Mehdi, et al. Genome-wide patterns of population structure and association mapping of nut-related traits in Persian walnut populations from Iran using the Axiom J. regia 700K SNP array. ''Sci Rep''. 2019 Apr 23; '''9''' (1):6376
Investigation and genome-wide association study for Fusarium crown rot resistance in Chinese common wheat. Description: Yang, Xia, et al. Investigation and genome-wide association study for Fusarium crown rot resistance in Chinese common wheat. ''BMC Plant Biol''. 2019 Apr 23; '''19''' (1):153
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. Description: Graham, Sarah E, et al. Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. ''Nat Commun''. 2019 Apr 23; '''10''' (1):1847
African evolutionary history inferred from whole genome sequence data of 44 indigenous African populations. Description: Fan, Shaohua, et al. African evolutionary history inferred from whole genome sequence data of 44 indigenous African populations. ''Genome Biol''. 2019 Apr 26; '''20''' (1):82
Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition. Description: Whitaker, D Thad, et al. Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition. ''Genes (Basel)''. 2019 Apr 26; '''10''' (5):
Genome-wide association analysis for fumonisin content in maize kernels. Description: Samayoa, L F, et al. Genome-wide association analysis for fumonisin content in maize kernels. ''BMC Plant Biol''. 2019 Apr 27; '''19''' (1):166
Reliability of genomic prediction for milk fatty acid composition by using a multi-population reference and incorporating GWAS results. Description: Gebreyesus, Grum, et al. Reliability of genomic prediction for milk fatty acid composition by using a multi-population reference and incorporating GWAS results. ''Genet Sel Evol''. 2019 Apr 27; '''51''' (1):16
Exome sequencing in patients with chronic central serous chorioretinopathy. Description: Schellevis, Rosa L, et al. Exome sequencing in patients with chronic central serous chorioretinopathy. ''Sci Rep''. 2019 Apr 29; '''9''' (1):6598
Genetic architecture of grain yield in bread wheat based on genome-wide association studies. Description: Li, Faji, et al. Genetic architecture of grain yield in bread wheat based on genome-wide association studies. ''BMC Plant Biol''. 2019 Apr 29; '''19''' (1):168
Genetic risk score has added value over initial clinical grading stage in predicting disease progression in age-related macular degeneration. Description: Heesterbeek, Thomas J, et al. Genetic risk score has added value over initial clinical grading stage in predicting disease progression in age-related macular degeneration. ''Sci Rep''. 2019 Apr 29; '''9''' (1):6611
Linkage-based genome assembly improvement of oil palm (Elaeis guineensis). Description: Ong, Ai-Ling, et al. Linkage-based genome assembly improvement of oil palm (Elaeis guineensis). ''Sci Rep''. 2019 Apr 29; '''9''' (1):6619
Genome-Wide Investigation and Functional Analysis of Sus scrofa RNA Editing Sites across Eleven Tissues. Description: Wang, Zishuai, et al. Genome-Wide Investigation and Functional Analysis of Sus scrofa RNA Editing Sites across Eleven Tissues. ''Genes (Basel)''. 2019 Apr 30; '''10''' (5):
Genomic analysis on pygmy hog reveals extensive interbreeding during wild boar expansion. Description: Liu, Langqing, et al. Genomic analysis on pygmy hog reveals extensive interbreeding during wild boar expansion. ''Nat Commun''. 2019 Apr 30; '''10''' (1):1992
High-Throughput Genotype, Morphology, and Quality Traits Evaluation for the Assessment of Genetic Diversity of Wheat Landraces from Sicily. Description: Fiore, Maria Carola, et al. High-Throughput Genotype, Morphology, and Quality Traits Evaluation for the Assessment of Genetic Diversity of Wheat Landraces from Sicily. ''Plants (Basel)''. 2019 Apr 30; '''8''' (5):
Reliable heritability estimation using sparse regularization in ultrahigh dimensional genome-wide association studies. Description: Li, Xin, et al. Reliable heritability estimation using sparse regularization in ultrahigh dimensional genome-wide association studies. ''BMC Bioinformatics''. 2019 Apr 30; '''20''' (1):219
A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions. Description: Hytonen, Marjo K, et al. A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions. ''Hum Genet''. 2019 May; '''138''' (5):535-539
A Genetic Investigation of the Well-Being Spectrum. Description: Baselmans, B M L, et al. A Genetic Investigation of the Well-Being Spectrum. ''Behav Genet''. 2019 May; '''49''' (3):286-297
An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome. Description: Marchant, Thomas W, et al. An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome. ''PLoS Genet''. 2019 May; '''15''' (5):e1008102
A novel rice grain size gene OsSNB was identified by genome-wide association study in natural population. Description: Ma, Xiaosong, et al. A novel rice grain size gene OsSNB was identified by genome-wide association study in natural population. ''PLoS Genet''. 2019 May; '''15''' (5):e1008191
Association of Maternal Neurodevelopmental Risk Alleles With Early-Life Exposures. Description: Leppert, Beate, et al. Association of Maternal Neurodevelopmental Risk Alleles With Early-Life Exposures. ''JAMA Psychiatry''. 2019 May 1;
Association study between genetic polymorphisms in folate metabolism and gastric cancer susceptibility in Chinese Han population: A case-control study. Description: Wei, Lusha, et al. Association study between genetic polymorphisms in folate metabolism and gastric cancer susceptibility in Chinese Han population: A case-control study. ''Mol Genet Genomic Med''. 2019 May; '''7''' (5):e633
Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants. Description: Hytonen, Marjo K, et al. Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants. ''Hum Genet''. 2019 May; '''138''' (5):525-533
Evaluating and sharing global genetic ancestry in biomedical datasets. Description: Harismendy, Olivier, et al. Evaluating and sharing global genetic ancestry in biomedical datasets. ''J Am Med Inform Assoc''. 2019 May 1; '''26''' (5):457-461
Genome-wide association study for intramuscular fat content in Chinese Lulai black pigs. Description: Wang, Yanping, et al. Genome-wide association study for intramuscular fat content in Chinese Lulai black pigs. ''Asian-Australas J Anim Sci''. 2019 May; '''32''' (5):607-613
Genome-wide association study identifies 30 loci associated with bipolar disorder. Description: Stahl, Eli A, et al. Genome-wide association study identifies 30 loci associated with bipolar disorder. ''Nat Genet''. 2019 May; '''51''' (5):793-803
Genomic comparisons reveal biogeographic and anthropogenic impacts in the koala (Phascolarctos cinereus): a dietary-specialist species distributed across heterogeneous environments. Description: Kjeldsen, Shannon R, et al. Genomic comparisons reveal biogeographic and anthropogenic impacts in the koala (Phascolarctos cinereus): a dietary-specialist species distributed across heterogeneous environments. ''Heredity (Edinb)''. 2019 May; '''122''' (5):525-544
Genomic evidence for the population genetic differentiation of Misgurnus anguillicaudatus in the Yangtze River basin of China. Description: Yi, Shaokui, et al. Genomic evidence for the population genetic differentiation of Misgurnus anguillicaudatus in the Yangtze River basin of China. ''Genomics''. 2019 May; '''111''' (3):367-374
Genomic signatures of adaptation to Sahelian and Soudanian climates in sorghum landraces of Senegal. Description: Faye, Jacques M, et al. Genomic signatures of adaptation to Sahelian and Soudanian climates in sorghum landraces of Senegal. ''Ecol Evol''. 2019 May; '''9''' (10):6038-6051
Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. Description: Grotzinger, Andrew D, et al. Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. ''Nat Hum Behav''. 2019 May; '''3''' (5):513-525
Gigwa v2-Extended and improved genotype investigator. Description: Sempere, Guilhem, et al. Gigwa v2-Extended and improved genotype investigator. ''Gigascience''. 2019 May 1; '''8''' (5):
High-frequency marker haplotypes in the genomic selection of dairy cattle. Description: Mucha, Anna, et al. High-frequency marker haplotypes in the genomic selection of dairy cattle. ''J Appl Genet''. 2019 May; '''60''' (2):179-186
Identification and validation of genetic variants predictive of gait in standardbred horses. Description: McCoy, Annette M, et al. Identification and validation of genetic variants predictive of gait in standardbred horses. ''PLoS Genet''. 2019 May; '''15''' (5):e1008146
Influence of IL-1R2 polymorphisms on endometrial cancer susceptibility in the Chinese Han population. Description: Wu, Jiamin, et al. Influence of IL-1R2 polymorphisms on endometrial cancer susceptibility in the Chinese Han population. ''Mol Genet Genomic Med''. 2019 May; '''7''' (5):e650
Multi-omics of the gut microbial ecosystem in inflammatory bowel diseases. Description: Lloyd-Price, Jason, et al. Multi-omics of the gut microbial ecosystem in inflammatory bowel diseases. ''Nature''. 2019 May; '''569''' (7758):655-662
Sexual reproduction in a natural Trypanosoma cruzi population. Description: Berry, Alexander S F, et al. Sexual reproduction in a natural Trypanosoma cruzi population. ''PLoS Negl Trop Dis''. 2019 May; '''13''' (5):e0007392
Genes with High Network Connectivity Are Enriched for Disease Heritability. Description: Kim, Samuel S, et al. Genes with High Network Connectivity Are Enriched for Disease Heritability. ''Am J Hum Genet''. 2019 May 2; '''104''' (5):896-913
Multiple Deeply Divergent Denisovan Ancestries in Papuans. Description: Jacobs, Guy S, et al. Multiple Deeply Divergent Denisovan Ancestries in Papuans. ''Cell''. 2019 May 2; '''177''' (4):1010-1021.e32
Association and interaction of genetic variants with occurrence of ischemic stroke among Brazilian patients. Description: Ferreira, Leslie Ecker, et al. Association and interaction of genetic variants with occurrence of ischemic stroke among Brazilian patients. ''Gene''. 2019 May 5; '''695''': 84-91
Genomic structural diversity in Criollo Argentino horses: Analysis of copy number variations. Description: Corbi-Botto, Claudia M, et al. Genomic structural diversity in Criollo Argentino horses: Analysis of copy number variations. ''Gene''. 2019 May 5; '''695''': 26-31
A highly flexible and repeatable genotyping method for aquaculture studies based on target amplicon sequencing using next-generation sequencing technology. Description: Sato, Mana, et al. A highly flexible and repeatable genotyping method for aquaculture studies based on target amplicon sequencing using next-generation sequencing technology. ''Sci Rep''. 2019 May 6; '''9''' (1):6904
Genotyping by sequencing provides new insights into the diversity of Napier grass (Cenchrus purpureus) and reveals variation in genome-wide LD patterns between collections. Description: Muktar, Meki S, et al. Genotyping by sequencing provides new insights into the diversity of Napier grass (Cenchrus purpureus) and reveals variation in genome-wide LD patterns between collections. ''Sci Rep''. 2019 May 6; '''9''' (1):6936
Identification of regulatory variants associated with genetic susceptibility to meningococcal disease. Description: Borghini, Lisa, et al. Identification of regulatory variants associated with genetic susceptibility to meningococcal disease. ''Sci Rep''. 2019 May 6; '''9''' (1):6966
Early stages of phase selection in MOF formation observed in molecular Monte Carlo simulations. Description: Wells, Stephen A, et al. Early stages of phase selection in MOF formation observed in molecular Monte Carlo simulations. ''RSC Adv''. 2019 May 7; '''9''' (25):14382-14390
BGData - A Suite of R Packages for Genomic Analysis with Big Data. Description: Grueneberg, Alexander, et al. BGData - A Suite of R Packages for Genomic Analysis with Big Data. ''G3 (Bethesda)''. 2019 May 7; '''9''' (5):1377-1383
Copy number variation-based gene set analysis reveals cytokine signalling pathways associated with psychiatric comorbidity in patients with inflammatory bowel disease. Description: Frenkel, Svetlana, et al. Copy number variation-based gene set analysis reveals cytokine signalling pathways associated with psychiatric comorbidity in patients with inflammatory bowel disease. ''Genomics''. 2019 May 7;
GBA and APOE epsilon4 associate with sporadic dementia with Lewy bodies in European genome wide association study. Description: Rongve, Arvid, et al. GBA and APOE epsilon4 associate with sporadic dementia with Lewy bodies in European genome wide association study. ''Sci Rep''. 2019 May 7; '''9''' (1):7013
Genome-wide association studies for 30 haematological and blood clinical-biochemical traits in Large White pigs reveal genomic regions affecting intermediate phenotypes. Description: Bovo, Samuele, et al. Genome-wide association studies for 30 haematological and blood clinical-biochemical traits in Large White pigs reveal genomic regions affecting intermediate phenotypes. ''Sci Rep''. 2019 May 7; '''9''' (1):7003
Genome-Wide Signatures of Selection Detection in Three South China Indigenous Pigs. Description: Diao, Shuqi, et al. Genome-Wide Signatures of Selection Detection in Three South China Indigenous Pigs. ''Genes (Basel)''. 2019 May 7; '''10''' (5):
Chromosomal imbalance in pigs showing a syndromic form of cleft palate. Description: Grahofer, Alexander, et al. Chromosomal imbalance in pigs showing a syndromic form of cleft palate. ''BMC Genomics''. 2019 May 8; '''20''' (1):349
High-density genotyping reveals signatures of selection related to acclimation and economically important traits in 15 local sheep breeds from Russia. Description: Yurchenko, Andrey A, et al. High-density genotyping reveals signatures of selection related to acclimation and economically important traits in 15 local sheep breeds from Russia. ''BMC Genomics''. 2019 May 8; '''20''' (Suppl 3):294
Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesis. Description: Nandakumar, Satish K, et al. Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesis. ''Elife''. 2019 May 9; '''8''':
A Missense Variant in SCN8A in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia. Description: Letko, Anna, et al. A Missense Variant in SCN8A in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia. ''Genes (Basel)''. 2019 May 10; '''10''' (5):
Development of Three Sets of High-Throughput Genotyped Rice Chromosome Segment Substitution Lines and QTL Mapping for Eleven Traits. Description: Zhang, Bin, et al. Development of Three Sets of High-Throughput Genotyped Rice Chromosome Segment Substitution Lines and QTL Mapping for Eleven Traits. ''Rice (N Y)''. 2019 May 10; '''12''' (1):33
Weighting sequence variants based on their annotation increases the power of genome-wide association studies in dairy cattle. Description: Cai, Zexi, et al. Weighting sequence variants based on their annotation increases the power of genome-wide association studies in dairy cattle. ''Genet Sel Evol''. 2019 May 10; '''51''' (1):20
Association analyses identify 31 new risk loci for colorectal cancer susceptibility. Description: Law, Philip J, et al. Association analyses identify 31 new risk loci for colorectal cancer susceptibility. ''Nat Commun''. 2019 May 14; '''10''' (1):2154
Association between TIMP-2 gene polymorphism and breast cancer in Han Chinese women. Description: Wang, Kai, et al. Association between TIMP-2 gene polymorphism and breast cancer in Han Chinese women. ''BMC Cancer''. 2019 May 14; '''19''' (1):446
Genetic variation in CADM2 as a link between psychological traits and obesity. Description: Morris, Julia, et al. Genetic variation in CADM2 as a link between psychological traits and obesity. ''Sci Rep''. 2019 May 14; '''9''' (1):7339
Genome-Wide Association Studies Based on Equine Joint Angle Measurements Reveal New QTL Affecting the Conformation of Horses. Description: Gmel, Annik Imogen, et al. Genome-Wide Association Studies Based on Equine Joint Angle Measurements Reveal New QTL Affecting the Conformation of Horses. ''Genes (Basel)''. 2019 May 14; '''10''' (5):
Genome-wide association study of right-sided colonic diverticulosis in a Korean population. Description: Choe, Eun Kyung, et al. Genome-wide association study of right-sided colonic diverticulosis in a Korean population. ''Sci Rep''. 2019 May 14; '''9''' (1):7360
Identification of genetic association between cardiorespiratory fitness and the trainability genes in childhood acute lymphoblastic leukemia survivors. Description: Caru, Maxime, et al. Identification of genetic association between cardiorespiratory fitness and the trainability genes in childhood acute lymphoblastic leukemia survivors. ''BMC Cancer''. 2019 May 14; '''19''' (1):443
Interferon inducible X-linked gene CXorf21 may contribute to sexual dimorphism in Systemic Lupus Erythematosus. Description: Odhams, Christopher A, et al. Interferon inducible X-linked gene CXorf21 may contribute to sexual dimorphism in Systemic Lupus Erythematosus. ''Nat Commun''. 2019 May 15; '''10''' (1):2164
RAD sequencing sheds new light on the genetic structure and local adaptation of European scallops and resolves their demographic histories. Description: Vendrami, David L J, et al. RAD sequencing sheds new light on the genetic structure and local adaptation of European scallops and resolves their demographic histories. ''Sci Rep''. 2019 May 15; '''9''' (1):7455
Usefulness of COMT gene polymorphisms in North African populations. Description: Boussetta, Sami, et al. Usefulness of COMT gene polymorphisms in North African populations. ''Gene''. 2019 May 15; '''696''': 186-196
APOE Variant (rs405509) might Modulate the Effect of Sex and Educational Level on Cognitive Impairment Risk in a Taiwanese Population. Description: Hsu, Tsui-Wen, et al. APOE Variant (rs405509) might Modulate the Effect of Sex and Educational Level on Cognitive Impairment Risk in a Taiwanese Population. ''Int J Environ Res Public Health''. 2019 May 16; '''16''' (10):
Refining the Genomic Region Containing a Major Locus Controlling Fruit Maturity in Peach. Description: Elsadr, H, et al. Refining the Genomic Region Containing a Major Locus Controlling Fruit Maturity in Peach. ''Sci Rep''. 2019 May 17; '''9''' (1):7522
Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex. Description: Liu, Zelin, et al. Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex. ''Genome Biol''. 2019 May 20; '''20''' (1):99
Ice-Age Climate Adaptations Trap the Alpine Marmot in a State of Low Genetic Diversity. Description: Gossmann, Toni I, et al. Ice-Age Climate Adaptations Trap the Alpine Marmot in a State of Low Genetic Diversity. ''Curr Biol''. 2019 May 20; '''29''' (10):1712-1720.e7
The Arrival of Siberian Ancestry Connecting the Eastern Baltic to Uralic Speakers further East. Description: Saag, Lehti, et al. The Arrival of Siberian Ancestry Connecting the Eastern Baltic to Uralic Speakers further East. ''Curr Biol''. 2019 May 20; '''29''' (10):1701-1711.e16
Genome-Wide Association Study of H/L Traits in Chicken. Description: Zhu, Bo, et al. Genome-Wide Association Study of H/L Traits in Chicken. ''Animals (Basel)''. 2019 May 21; '''9''' (5):
Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration. Description: Hitti, Rebekkah J, et al. Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration. ''Genes (Basel)''. 2019 May 21; '''10''' (5):
A new chicken 55K SNP genotyping array. Description: Liu, Ranran, et al. A new chicken 55K SNP genotyping array. ''BMC Genomics''. 2019 May 22; '''20''' (1):410
A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders. Description: Rayner, Christopher, et al. A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders. ''Transl Psychiatry''. 2019 May 23; '''9''' (1):150
MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip. Description: Gajera, Mona, et al. MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip. ''BMC Med Genomics''. 2019 May 23; '''12''' (1):70
Alzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairment. Description: Chaudhury, Sultan, et al. Alzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairment. ''Transl Psychiatry''. 2019 May 24; '''9''' (1):154
Exome-wide search and functional annotation of genes associated in patients with severe tick-borne encephalitis in a Russian population. Description: Ignatieva, Elena V, et al. Exome-wide search and functional annotation of genes associated in patients with severe tick-borne encephalitis in a Russian population. ''BMC Med Genomics''. 2019 May 24; '''12''' (Suppl 3):61
Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula. Description: Pimenta, Joao, et al. Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula. ''Sci Rep''. 2019 May 24; '''9''' (1):7825
Differential BDNF methylation in combat exposed veterans and the association with exercise. Description: Voisey, Joanne, et al. Differential BDNF methylation in combat exposed veterans and the association with exercise. ''Gene''. 2019 May 25; '''698''': 107-112
Genomic measures of inbreeding in the Norwegian-Swedish Coldblooded Trotter and their associations with known QTL for reproduction and health traits. Description: Velie, Brandon D, et al. Genomic measures of inbreeding in the Norwegian-Swedish Coldblooded Trotter and their associations with known QTL for reproduction and health traits. ''Genet Sel Evol''. 2019 May 27; '''51''' (1):22
Rare variant phasing using paired tumor:normal sequence data. Description: Buckley, Alexandra R, et al. Rare variant phasing using paired tumor:normal sequence data. ''BMC Bioinformatics''. 2019 May 27; '''20''' (1):265
Genetic homogenization of indigenous sheep breeds in Northwest Africa. Description: Belabdi, Ibrahim, et al. Genetic homogenization of indigenous sheep breeds in Northwest Africa. ''Sci Rep''. 2019 May 28; '''9''' (1):7920
Human pancreatic cancer cell exosomes, but not human normal cell exosomes, act as an initiator in cell transformation. Description: Stefanius, Karoliina, et al. Human pancreatic cancer cell exosomes, but not human normal cell exosomes, act as an initiator in cell transformation. ''Elife''. 2019 May 28; '''8''':
WhoGEM: an admixture-based prediction machine accurately predicts quantitative functional traits in plants. Description: Gentzbittel, Laurent, et al. WhoGEM: an admixture-based prediction machine accurately predicts quantitative functional traits in plants. ''Genome Biol''. 2019 May 28; '''20''' (1):106
Genome-Wide Scan Identifies Selection Signatures in Chinese Wagyu Cattle Using a High-Density SNP Array. Description: Wang, Zezhao, et al. Genome-Wide Scan Identifies Selection Signatures in Chinese Wagyu Cattle Using a High-Density SNP Array. ''Animals (Basel)''. 2019 May 30; '''9''' (6):
Tracking Five Millennia of Horse Management with Extensive Ancient Genome Time Series. Description: Fages, Antoine, et al. Tracking Five Millennia of Horse Management with Extensive Ancient Genome Time Series. ''Cell''. 2019 May 30; '''177''' (6):1419-1435.e31
A Fast and Powerful Empirical Bayes Method for Genome-Wide Association Studies. Description: Chang, Tianpeng, et al. A Fast and Powerful Empirical Bayes Method for Genome-Wide Association Studies. ''Animals (Basel)''. 2019 May 31; '''9''' (6):
Polymorphisms in the CCR5 promoter associated with cervical intraepithelial neoplasia in a Chinese Han population. Description: Liu, Shuyuan, et al. Polymorphisms in the CCR5 promoter associated with cervical intraepithelial neoplasia in a Chinese Han population. ''BMC Cancer''. 2019 May 31; '''19''' (1):525
Acute effects of 9-tetrahydrocannabinol (THC) on resting state brain function and their modulation by COMT genotype. Description: Bossong, Matthijs G, et al. Acute effects of 9-tetrahydrocannabinol (THC) on resting state brain function and their modulation by COMT genotype. ''Eur Neuropsychopharmacol''. 2019 Jun; '''29''' (6):766-776
A new genomic tool for walnut (Juglans regia L.): development and validation of the high-density Axiom J. regia 700K SNP genotyping array. Description: Marrano, Annarita, et al. A new genomic tool for walnut (Juglans regia L.): development and validation of the high-density Axiom J. regia 700K SNP genotyping array. ''Plant Biotechnol J''. 2019 Jun; '''17''' (6):1027-1036
Association between polymorphisms of MIR17HG and risk of colorectal cancer in the Chinese Han population. Description: Chen, Peng, et al. Association between polymorphisms of MIR17HG and risk of colorectal cancer in the Chinese Han population. ''Mol Genet Genomic Med''. 2019 Jun; '''7''' (6):e667
Association of OPG gene polymorphisms with the risk of knee osteoarthritis among Chinese people. Description: Qi, Yuxin, et al. Association of OPG gene polymorphisms with the risk of knee osteoarthritis among Chinese people. ''Mol Genet Genomic Med''. 2019 Jun; '''7''' (6):e662
Blood-Derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation. Description: Somineni, Hari K, et al. Blood-Derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation. ''Gastroenterology''. 2019 Jun; '''156''' (8):2254-2265.e3
Cardiometabolic Polygenic Risk Scores and Osteoarthritis Outcomes: A Mendelian Randomization Study Using Data From the Malmo Diet and Cancer Study and the UK Biobank. Description: Hindy, George, et al. Cardiometabolic Polygenic Risk Scores and Osteoarthritis Outcomes: A Mendelian Randomization Study Using Data From the Malmo Diet and Cancer Study and the UK Biobank. ''Arthritis Rheumatol''. 2019 Jun; '''71''' (6):925-934
Comparative transcriptomics reveals the selection patterns of domesticated ramie. Description: Huang, Kun-Yong, et al. Comparative transcriptomics reveals the selection patterns of domesticated ramie. ''Ecol Evol''. 2019 Jun; '''9''' (12):7057-7068
Deciphering the patterns of genetic admixture and diversity in southern European cattle using genome-wide SNPs. Description: Upadhyay, Maulik, et al. Deciphering the patterns of genetic admixture and diversity in southern European cattle using genome-wide SNPs. ''Evol Appl''. 2019 Jun; '''12''' (5):951-963
Dissecting the Pre-Columbian Genomic Ancestry of Native Americans along the Andes-Amazonia Divide. Description: Gnecchi-Ruscone, Guido Alberto, et al. Dissecting the Pre-Columbian Genomic Ancestry of Native Americans along the Andes-Amazonia Divide. ''Mol Biol Evol''. 2019 Jun 1; '''36''' (6):1254-1269
Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb. Description: Fritsche, Lars G, et al. Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb. ''PLoS Genet''. 2019 Jun; '''15''' (6):e1008202
Genetic polymorphisms of long noncoding RNA RP11-37B2.1 associate with susceptibility of tuberculosis and adverse events of antituberculosis drugs in west China. Description: Song, Jiajia, et al. Genetic polymorphisms of long noncoding RNA RP11-37B2.1 associate with susceptibility of tuberculosis and adverse events of antituberculosis drugs in west China. ''J Clin Lab Anal''. 2019 Jun; '''33''' (5):e22880
Genomic analyses suggest adaptive differentiation of northern European native cattle breeds. Description: Stronen, Astrid V, et al. Genomic analyses suggest adaptive differentiation of northern European native cattle breeds. ''Evol Appl''. 2019 Jun; '''12''' (6):1096-1113
Genomic Analysis Reveals Specific Patterns of Homozygosity and Heterozygosity in Inbred Pigs. Description: Wang, Ligang, et al. Genomic Analysis Reveals Specific Patterns of Homozygosity and Heterozygosity in Inbred Pigs. ''Animals (Basel)''. 2019 Jun 1; '''9''' (6):
Genomic changes in the biological control agent Cryptolaemus montrouzieri associated with introduction. Description: Li, Hao-Sen, et al. Genomic changes in the biological control agent Cryptolaemus montrouzieri associated with introduction. ''Evol Appl''. 2019 Jun; '''12''' (5):989-1000
Genomic determinants of speciation and spread of the Mycobacterium tuberculosis complex. Description: Chiner-Oms, A, et al. Genomic determinants of speciation and spread of the Mycobacterium tuberculosis complex. ''Sci Adv''. 2019 Jun; '''5''' (6):eaaw3307
HMGCLL1 is a predictive biomarker for deep molecular response to imatinib therapy in chronic myeloid leukemia. Description: Park, Jong-Ho, et al. HMGCLL1 is a predictive biomarker for deep molecular response to imatinib therapy in chronic myeloid leukemia. ''Leukemia''. 2019 Jun; '''33''' (6):1439-1450
Identification of the primate-specific gene BTN3A2 as an additional schizophrenia risk gene in the MHC loci. Description: Wu, Yong, et al. Identification of the primate-specific gene BTN3A2 as an additional schizophrenia risk gene in the MHC loci. ''EBioMedicine''. 2019 Jun; '''44''': 530-541
miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS. Description: Rhead, Brooke, et al. miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS. ''Ann Clin Transl Neurol''. 2019 Jun; '''6''' (6):1053-1061
Parallel Molecular Evolution in Pathways, Genes, and Sites in High-Elevation Hummingbirds Revealed by Comparative Transcriptomics. Description: Lim, Marisa C W, et al. Parallel Molecular Evolution in Pathways, Genes, and Sites in High-Elevation Hummingbirds Revealed by Comparative Transcriptomics. ''Genome Biol Evol''. 2019 Jun 1; '''11''' (6):1552-1572
Parents of early-maturing girls die younger. Description: Horak, Peeter, et al. Parents of early-maturing girls die younger. ''Evol Appl''. 2019 Jun; '''12''' (5):1050-1061
Polymorphisms of the DNA repair gene EXO1 modulate cognitive aging in old adults in a Taiwanese population. Description: Lin, Eugene, et al. Polymorphisms of the DNA repair gene EXO1 modulate cognitive aging in old adults in a Taiwanese population. ''DNA Repair (Amst)''. 2019 Jun; '''78''': 1-6
Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. Description: Tiensuu, Heli, et al. Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. ''PLoS Genet''. 2019 Jun; '''15''' (6):e1008107
Screening of Genetic Factor in the Interaction Between Periodontitis and Metabolic Traits Using Candidate Gene Association Study (CGAS). Description: Moon, Kyung-Hui. Screening of Genetic Factor in the Interaction Between Periodontitis and Metabolic Traits Using Candidate Gene Association Study (CGAS). ''Biochem Genet''. 2019 Jun; '''57''' (3):466-474
Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Description: Zhou, Wei-Zhen, et al. Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. ''Hum Mutat''. 2019 Jun; '''40''' (6):801-815
The genetic history of admixture across inner Eurasia. Description: Jeong, Choongwon, et al. The genetic history of admixture across inner Eurasia. ''Nat Ecol Evol''. 2019 Jun; '''3''' (6):966-976
The Role of Stressful Parenting and Mineralocorticoid Receptor Haplotypes on Social Development During Adolescence and Young Adulthood. Description: Endedijk, H M, et al. The Role of Stressful Parenting and Mineralocorticoid Receptor Haplotypes on Social Development During Adolescence and Young Adulthood. ''J Youth Adolesc''. 2019 Jun; '''48''' (6):1082-1099
Three novel genetic variants in NRF2 signaling pathway genes are associated with pancreatic cancer risk. Description: Yang, Wenjun, et al. Three novel genetic variants in NRF2 signaling pathway genes are associated with pancreatic cancer risk. ''Cancer Sci''. 2019 Jun; '''110''' (6):2022-2032
Unprecedented reorganization of holocentric chromosomes provides insights into the enigma of lepidopteran chromosome evolution. Description: Hill, Jason, et al. Unprecedented reorganization of holocentric chromosomes provides insights into the enigma of lepidopteran chromosome evolution. ''Sci Adv''. 2019 Jun; '''5''' (6):eaau3648
Using dried blood spot samples from a trio for linked-read whole-exome sequencing. Description: Mortensen, Olavur, et al. Using dried blood spot samples from a trio for linked-read whole-exome sequencing. ''Eur J Hum Genet''. 2019 Jun; '''27''' (6):980-988
Whole Genome Analyses of Chinese Population and De Novo Assembly of A Northern Han Genome. Description: Du, Zhenglin, et al. Whole Genome Analyses of Chinese Population and De Novo Assembly of A Northern Han Genome. ''Genomics Proteomics Bioinformatics''. 2019 Jun; '''17''' (3):229-247
A SNP in a Steroidogenic Enzyme Is Associated with Phenotypic Sex in Seriola Fishes. Description: Koyama, Takashi, et al. A SNP in a Steroidogenic Enzyme Is Associated with Phenotypic Sex in Seriola Fishes. ''Curr Biol''. 2019 Jun 3; '''29''' (11):1901-1909.e8
Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation. Description: Frei, Oleksandr, et al. Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation. ''Nat Commun''. 2019 Jun 3; '''10''' (1):2417
From reference genomes to population genomics: comparing three reference-aligned reduced-representation sequencing pipelines in two wildlife species. Description: Wright, Belinda, et al. From reference genomes to population genomics: comparing three reference-aligned reduced-representation sequencing pipelines in two wildlife species. ''BMC Genomics''. 2019 Jun 3; '''20''' (1):453
Identification of selection signatures involved in performance traits in a paternal broiler line. Description: Almeida, Octavio Augusto Costa, et al. Identification of selection signatures involved in performance traits in a paternal broiler line. ''BMC Genomics''. 2019 Jun 3; '''20''' (1):449
A practical guide to methods controlling false discoveries in computational biology. Description: Korthauer, Keegan, et al. A practical guide to methods controlling false discoveries in computational biology. ''Genome Biol''. 2019 Jun 4; '''20''' (1):118
Association of BUD13-ZNF259-APOA5-APOA1-SIK3 cluster polymorphism in 11q23.3 and structure of APOA5 with increased plasma triglyceride levels in a Korean population. Description: Kim, Han-Kyul, et al. Association of BUD13-ZNF259-APOA5-APOA1-SIK3 cluster polymorphism in 11q23.3 and structure of APOA5 with increased plasma triglyceride levels in a Korean population. ''Sci Rep''. 2019 Jun 5; '''9''' (1):8296
Genome-Wide Analyses Reveal Footprints of Divergent Selection and Drought Adaptive Traits in Synthetic-Derived Wheats. Description: Afzal, Fakiha, et al. Genome-Wide Analyses Reveal Footprints of Divergent Selection and Drought Adaptive Traits in Synthetic-Derived Wheats. ''G3 (Bethesda)''. 2019 Jun 5; '''9''' (6):1957-1973
Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia. Description: Tobar, Hugo E, et al. Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia. ''Lipids Health Dis''. 2019 Jun 5; '''18''' (1):132
Genome-wide estimates of genetic diversity, inbreeding and effective size of experimental and commercial rainbow trout lines undergoing selective breeding. Description: D'Ambrosio, Jonathan, et al. Genome-wide estimates of genetic diversity, inbreeding and effective size of experimental and commercial rainbow trout lines undergoing selective breeding. ''Genet Sel Evol''. 2019 Jun 6; '''51''' (1):26
Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland. Description: Kerminen, Sini, et al. Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland. ''Am J Hum Genet''. 2019 Jun 6; '''104''' (6):1169-1181
Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. Description: Kong, Sokanha, et al. Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. ''BMC Med Genet''. 2019 Jun 6; '''20''' (1):99
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease. Description: Wright, Galen E B, et al. Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease. ''Am J Hum Genet''. 2019 Jun 6; '''104''' (6):1116-1126
On Using Local Ancestry to Characterize the Genetic Architecture of Human Traits: Genetic Regulation of Gene Expression in Multiethnic or Admixed Populations. Description: Zhong, Yizhen, et al. On Using Local Ancestry to Characterize the Genetic Architecture of Human Traits: Genetic Regulation of Gene Expression in Multiethnic or Admixed Populations. ''Am J Hum Genet''. 2019 Jun 6; '''104''' (6):1097-1115
BarkBase: Epigenomic Annotation of Canine Genomes. Description: Megquier, Kate, et al. BarkBase: Epigenomic Annotation of Canine Genomes. ''Genes (Basel)''. 2019 Jun 7; '''10''' (6):
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy. Description: Takata, Atsushi, et al. Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy. ''Nat Commun''. 2019 Jun 7; '''10''' (1):2506
Investigation of bidirectional longitudinal associations between advanced epigenetic age and peripheral biomarkers of inflammation and metabolic syndrome. Description: Morrison, Filomene G, et al. Investigation of bidirectional longitudinal associations between advanced epigenetic age and peripheral biomarkers of inflammation and metabolic syndrome. ''Aging (Albany NY)''. 2019 Jun 7; '''11''' (11):3487-3504
Polygenic risk associated with post-traumatic stress disorder onset and severity. Description: Misganaw, Burook, et al. Polygenic risk associated with post-traumatic stress disorder onset and severity. ''Transl Psychiatry''. 2019 Jun 7; '''9''' (1):165
Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk. Description: Wang, Alex W, et al. Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2019 Jun 8; '''92''': 133-147
Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population. Description: Chen, Wenlong C, et al. Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population. ''Carcinogenesis''. 2019 Jun 10; '''40''' (4):513-520
Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization. Description: O'Connor, Daniel, et al. Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization. ''Cell Rep''. 2019 Jun 11; '''27''' (11):3241-3253.e4
Evaluation of linkage disequilibrium, population structure, and genetic diversity in the U.S. peanut mini core collection. Description: Otyama, Paul I, et al. Evaluation of linkage disequilibrium, population structure, and genetic diversity in the U.S. peanut mini core collection. ''BMC Genomics''. 2019 Jun 11; '''20''' (1):481
Population divergence and gene flow in two East Asian shorebirds on the verge of speciation. Description: Sadanandan, Keren R, et al. Population divergence and gene flow in two East Asian shorebirds on the verge of speciation. ''Sci Rep''. 2019 Jun 12; '''9''' (1):8546
Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study. Description: Lee, Eunkyung, et al. Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study. ''Hum Genomics''. 2019 Jun 13; '''13''' (1):28
Genome-Wide Linkage Disequilibrium and the Extent of Effective Population Sizes in Six Chinese Goat Populations Using a 50K Single Nucleotide Polymorphism Panel. Description: Berihulay, Haile, et al. Genome-Wide Linkage Disequilibrium and the Extent of Effective Population Sizes in Six Chinese Goat Populations Using a 50K Single Nucleotide Polymorphism Panel. ''Animals (Basel)''. 2019 Jun 13; '''9''' (6):
Genome-wide scan reveals genetic divergence and diverse adaptive selection in Chinese local cattle. Description: Xu, Lingyang, et al. Genome-wide scan reveals genetic divergence and diverse adaptive selection in Chinese local cattle. ''BMC Genomics''. 2019 Jun 14; '''20''' (1):494
Influence of Genetic and Non-Genetic Risk Factors for Serum Uric Acid Levels and Hyperuricemia in Mexicans. Description: Rivera-Paredez, Berenice, et al. Influence of Genetic and Non-Genetic Risk Factors for Serum Uric Acid Levels and Hyperuricemia in Mexicans. ''Nutrients''. 2019 Jun 14; '''11''' (6):
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts. Description: Zhang, Xianglong, et al. Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts. ''Biol Psychiatry''. 2019 Jun 15; '''85''' (12):1065-1073
The genetic susceptibility profile of the South Indian women with polycystic ovary syndrome and the universality of the lack of association of type 2 diabetes genes. Description: Irgam, Kumuda, et al. The genetic susceptibility profile of the South Indian women with polycystic ovary syndrome and the universality of the lack of association of type 2 diabetes genes. ''Gene''. 2019 Jun 15; '''701''': 113-120
Genetic Diversity of Indigenous Pigs from South China Area Revealed by SNP Array. Description: Diao, Shuqi, et al. Genetic Diversity of Indigenous Pigs from South China Area Revealed by SNP Array. ''Animals (Basel)''. 2019 Jun 16; '''9''' (6):
Analysis of Hematological Traits in Polled Yak by Genome-Wide Association Studies Using Individual SNPs and Haplotypes. Description: Ma, Xiaoming, et al. Analysis of Hematological Traits in Polled Yak by Genome-Wide Association Studies Using Individual SNPs and Haplotypes. ''Genes (Basel)''. 2019 Jun 17; '''10''' (6):
Genome-wide association study of important agronomic traits within a core collection of rice (Oryza sativa L.). Description: Zhang, Peng, et al. Genome-wide association study of important agronomic traits within a core collection of rice (Oryza sativa L.). ''BMC Plant Biol''. 2019 Jun 17; '''19''' (1):259
Genomic structure and diversity of Plasmodium falciparum in Southeast Asia reveal recent parasite migration patterns. Description: Shetty, Amol C, et al. Genomic structure and diversity of Plasmodium falciparum in Southeast Asia reveal recent parasite migration patterns. ''Nat Commun''. 2019 Jun 17; '''10''' (1):2665
Association between the pig genome and its gut microbiota composition. Description: Crespo-Piazuelo, Daniel, et al. Association between the pig genome and its gut microbiota composition. ''Sci Rep''. 2019 Jun 19; '''9''' (1):8791
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1. Description: Flower, Michael, et al. MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1. ''Brain''. 2019 Jun 19;
Ancient polymorphisms contribute to genome-wide variation by long-term balancing selection and divergent sorting in Boechera stricta. Description: Wang, Baosheng, et al. Ancient polymorphisms contribute to genome-wide variation by long-term balancing selection and divergent sorting in Boechera stricta. ''Genome Biol''. 2019 Jun 21; '''20''' (1):126
Genetic markers of lipid metabolism genes associated with low susceptibility to HCV infection. Description: Real, Luis Miguel, et al. Genetic markers of lipid metabolism genes associated with low susceptibility to HCV infection. ''Sci Rep''. 2019 Jun 21; '''9''' (1):9054
Polymorphisms of the cryptochrome 2 and mitoguardin 2 genes are associated with the variation of lipid-related traits in Duroc pigs. Description: Marmol-Sanchez, Emilio, et al. Polymorphisms of the cryptochrome 2 and mitoguardin 2 genes are associated with the variation of lipid-related traits in Duroc pigs. ''Sci Rep''. 2019 Jun 21; '''9''' (1):9025
About the existence of common determinants of gene expression in the porcine liver and skeletal muscle. Description: Gonzalez-Prendes, Rayner, et al. About the existence of common determinants of gene expression in the porcine liver and skeletal muscle. ''BMC Genomics''. 2019 Jun 24; '''20''' (1):518
Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants. Description: Fung, Kenneth, et al. Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants. ''Sci Rep''. 2019 Jun 24; '''9''' (1):9143
Patterns of genetic structure and adaptive positive selection in the Lithuanian population from high-density SNP data. Description: Urnikyte, A, et al. Patterns of genetic structure and adaptive positive selection in the Lithuanian population from high-density SNP data. ''Sci Rep''. 2019 Jun 24; '''9''' (1):9163
RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprinting. Description: Jadhav, Bharati, et al. RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprinting. ''BMC Biol''. 2019 Jun 24; '''17''' (1):50
The Genomic Makeup of Nine Horse Populations Sampled in the Netherlands. Description: Schurink, Anouk, et al. The Genomic Makeup of Nine Horse Populations Sampled in the Netherlands. ''Genes (Basel)''. 2019 Jun 25; '''10''' (6):
Genome-wide associations and epistatic interactions for internode number, plant height, seed weight and seed yield in soybean. Description: Assefa, Teshale, et al. Genome-wide associations and epistatic interactions for internode number, plant height, seed weight and seed yield in soybean. ''BMC Genomics''. 2019 Jun 26; '''20''' (1):527
Using imputed whole-genome sequence data to improve the accuracy of genomic prediction for parasite resistance in Australian sheep. Description: Al Kalaldeh, Mohammad, et al. Using imputed whole-genome sequence data to improve the accuracy of genomic prediction for parasite resistance in Australian sheep. ''Genet Sel Evol''. 2019 Jun 26; '''51''' (1):32
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy. Description: Nikopoulos, Konstantinos, et al. A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy. ''Nat Commun''. 2019 Jun 28; '''10''' (1):2884
Genome-Wide Homozygosity Patterns and Evidence for Selection in a Set of European and Near Eastern Horse Breeds. Description: Grilz-Seger, Gertrud, et al. Genome-Wide Homozygosity Patterns and Evidence for Selection in a Set of European and Near Eastern Horse Breeds. ''Genes (Basel)''. 2019 Jun 28; '''10''' (7):
Odyssey: a semi-automated pipeline for phasing, imputation, and analysis of genome-wide genetic data. Description: Eller, Ryan J, et al. Odyssey: a semi-automated pipeline for phasing, imputation, and analysis of genome-wide genetic data. ''BMC Bioinformatics''. 2019 Jun 28; '''20''' (1):364
Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus. Description: An, Hong, et al. Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus. ''Nat Commun''. 2019 Jun 28; '''10''' (1):2878
A carotenoid oxygenase is responsible for muscle coloration in scallop. Description: Li, Xue, et al. A carotenoid oxygenase is responsible for muscle coloration in scallop. ''Biochim Biophys Acta Mol Cell Biol Lipids''. 2019 Jul; '''1864''' (7):966-975
A commonly occurring genetic variant within the NPLOC4-TSPAN10-PDE6G gene cluster is associated with the risk of strabismus. Description: Plotnikov, Denis, et al. A commonly occurring genetic variant within the NPLOC4-TSPAN10-PDE6G gene cluster is associated with the risk of strabismus. ''Hum Genet''. 2019 Jul; '''138''' (7):723-737
A heritable subset of the core rumen microbiome dictates dairy cow productivity and emissions. Description: Wallace, R John, et al. A heritable subset of the core rumen microbiome dictates dairy cow productivity and emissions. ''Sci Adv''. 2019 Jul; '''5''' (7):eaav8391
Anastrozole Aromatase Inhibitor Plasma Drug Concentration Genome-Wide Association Study: Functional Epistatic Interaction Between SLC38A7 and ALPPL2. Description: Dudenkov, Tanda M, et al. Anastrozole Aromatase Inhibitor Plasma Drug Concentration Genome-Wide Association Study: Functional Epistatic Interaction Between SLC38A7 and ALPPL2. ''Clin Pharmacol Ther''. 2019 Jul; '''106''' (1):219-227
Ancient DNA sheds light on the genetic origins of early Iron Age Philistines. Description: Feldman, Michal, et al. Ancient DNA sheds light on the genetic origins of early Iron Age Philistines. ''Sci Adv''. 2019 Jul; '''5''' (7):eaax0061
Association of glypican-6 polymorphisms with lumbar disk herniation risk in the Han Chinese population. Description: Hu, Baoyang, et al. Association of glypican-6 polymorphisms with lumbar disk herniation risk in the Han Chinese population. ''Mol Genet Genomic Med''. 2019 Jul; '''7''' (7):e00747
Associations between polymorphisms of the ACYP2 gene and Liver cancer risk: A case-control study and meta-analysis. Description: Zhao, Wenhui, et al. Associations between polymorphisms of the ACYP2 gene and Liver cancer risk: A case-control study and meta-analysis. ''Mol Genet Genomic Med''. 2019 Jul; '''7''' (7):e00716
Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro-oculo-facio-skeletal syndrome. Description: Ben Haj Ali, Abir, et al. Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro-oculo-facio-skeletal syndrome. ''Mol Genet Genomic Med''. 2019 Jul; '''7''' (7):e00694
Determining Possible Shared Genetic Architecture Between Myopia and Primary Open-Angle Glaucoma. Description: Iglesias, Adriana I, et al. Determining Possible Shared Genetic Architecture Between Myopia and Primary Open-Angle Glaucoma. ''Invest Ophthalmol Vis Sci''. 2019 Jul 1; '''60''' (8):3142-3149
Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait. Description: Chundru, V Kartik, et al. Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait. ''Genetics''. 2019 Jul; '''212''' (3):577-586
Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa. Description: Walton, E, et al. Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa. ''Mol Neurobiol''. 2019 Jul; '''56''' (7):5146-5156
Fine-mapping analysis of a chromosome 2 region linked to resistance to Mycobacterium tuberculosis infection in Uganda reveals potential regulatory variants. Description: Igo, Robert P Jr, et al. Fine-mapping analysis of a chromosome 2 region linked to resistance to Mycobacterium tuberculosis infection in Uganda reveals potential regulatory variants. ''Genes Immun''. 2019 Jul; '''20''' (6):473-483
Genetic analysis of Taishu horses on and off Tsushima Island: Implications for conservation. Description: Tezuka, Ayumi, et al. Genetic analysis of Taishu horses on and off Tsushima Island: Implications for conservation. ''J Equine Sci''. 2019 Jul; '''30''' (2):33-40
Genetic analysis of the relation between IL2RA/IL2RB and rheumatoid arthritis risk. Description: Yang, Yonghui, et al. Genetic analysis of the relation between IL2RA/IL2RB and rheumatoid arthritis risk. ''Mol Genet Genomic Med''. 2019 Jul; '''7''' (7):e00754
Genetic variability and history of a native Finnish horse breed. Description: Kvist, Laura, et al. Genetic variability and history of a native Finnish horse breed. ''Genet Sel Evol''. 2019 Jul 1; '''51''' (1):35
Genetic variants in p53 signaling pathway genes predict chemotherapy efficacy in colorectal cancer. Description: Zhang, Ke, et al. Genetic variants in p53 signaling pathway genes predict chemotherapy efficacy in colorectal cancer. ''Cancer Med''. 2019 Jul; '''8''' (7):3428-3436
Genetic variants in the ITPR2 gene are associated with Kashin-Beck Disease in Tibetan. Description: He, Xue, et al. Genetic variants in the ITPR2 gene are associated with Kashin-Beck Disease in Tibetan. ''Mol Genet Genomic Med''. 2019 Jul; '''7''' (7):e00715
Genome sequencing analysis identifies Epstein-Barr virus subtypes associated with high risk of nasopharyngeal carcinoma. Description: Xu, Miao, et al. Genome sequencing analysis identifies Epstein-Barr virus subtypes associated with high risk of nasopharyngeal carcinoma. ''Nat Genet''. 2019 Jul; '''51''' (7):1131-1136
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis. Description: Wang, Chan, et al. Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis. ''Hepatology''. 2019 Jul; '''70''' (1):294-307
Genome-Wide Single-Nucleotide Polymorphism Data Unveil Admixture of Chinese Indigenous Chicken Breeds with Commercial Breeds. Description: Nie, Changsheng, et al. Genome-Wide Single-Nucleotide Polymorphism Data Unveil Admixture of Chinese Indigenous Chicken Breeds with Commercial Breeds. ''Genome Biol Evol''. 2019 Jul 1; '''11''' (7):1847-1856
IL-7R gene polymorphisms among patients with rheumatoid arthritis: A case-control study. Description: Bai, Mei, et al. IL-7R gene polymorphisms among patients with rheumatoid arthritis: A case-control study. ''Mol Genet Genomic Med''. 2019 Jul; '''7''' (7):e00738
Joint Estimates of Heterozygosity and Runs of Homozygosity for Modern and Ancient Samples. Description: Renaud, Gabriel, et al. Joint Estimates of Heterozygosity and Runs of Homozygosity for Modern and Ancient Samples. ''Genetics''. 2019 Jul; '''212''' (3):587-614
Mitogenome types of two Lentinula edodes sensu lato populations in China. Description: Song, Xiaoxia, et al. Mitogenome types of two Lentinula edodes sensu lato populations in China. ''Sci Rep''. 2019 Jul 1; '''9''' (1):9421
Noncoding deletions reveal a gene that is critical for intestinal function. Description: Oz-Levi, Danit, et al. Noncoding deletions reveal a gene that is critical for intestinal function. ''Nature''. 2019 Jul; '''571''' (7763):107-111
Novel protective and risk loci in hip dysplasia in German Shepherds. Description: Mikkola, Lea I, et al. Novel protective and risk loci in hip dysplasia in German Shepherds. ''PLoS Genet''. 2019 Jul; '''15''' (7):e1008197
Pair Matcher (PaM): fast model-based optimization of treatment/case-control matches. Description: Elhaik, Eran, et al. Pair Matcher (PaM): fast model-based optimization of treatment/case-control matches. ''Bioinformatics''. 2019 Jul 1; '''35''' (13):2243-2250
Population Genomic Signatures of Genetic Structure and Environmental Selection in the Catadromous Roughskin Sculpin Trachidermus fasciatus. Description: Li, Yu-Long, et al. Population Genomic Signatures of Genetic Structure and Environmental Selection in the Catadromous Roughskin Sculpin Trachidermus fasciatus. ''Genome Biol Evol''. 2019 Jul 1; '''11''' (7):1751-1764
Regions of homozygosity as risk factors for multiple myeloma. Description: Went, Molly, et al. Regions of homozygosity as risk factors for multiple myeloma. ''Ann Hum Genet''. 2019 Jul; '''83''' (4):231-238
Studying the effects of haplotype partitioning methods on the RA-associated genomic results from the North American Rheumatoid Arthritis Consortium (NARAC) dataset. Description: Saad, Mohamed N, et al. Studying the effects of haplotype partitioning methods on the RA-associated genomic results from the North American Rheumatoid Arthritis Consortium (NARAC) dataset. ''J Adv Res''. 2019 Jul; '''18''': 113-126
The effect on congenital heart diseases of maternal EPHX1 polymorphisms modified by polycyclic aromatic hydrocarbons exposure. Description: Tao, Jing, et al. The effect on congenital heart diseases of maternal EPHX1 polymorphisms modified by polycyclic aromatic hydrocarbons exposure. ''Medicine (Baltimore)''. 2019 Jul; '''98''' (30):e16556
EPAS1 gain-of-function mutation contributes to high-altitude adaptation in Tibetan horses. Description: Liu, Xuexue, et al. EPAS1 gain-of-function mutation contributes to high-altitude adaptation in Tibetan horses. ''Mol Biol Evol''. 2019 Jul 2;
Genome-wide analysis indicates association between heterozygote advantage and healthy aging in humans. Description: Xu, Ke, et al. Genome-wide analysis indicates association between heterozygote advantage and healthy aging in humans. ''BMC Genet''. 2019 Jul 2; '''20''' (1):52
ImmuneRegulation: a web-based tool for identifying human immune regulatory elements. Description: Kalayci, Selim, et al. ImmuneRegulation: a web-based tool for identifying human immune regulatory elements. ''Nucleic Acids Res''. 2019 Jul 2; '''47''' (W1):W142-W150
Common BACE2 Polymorphisms are Associated with Altered Risk for Alzheimer's Disease and CSF Amyloid Biomarkers in APOE epsilon4 Non-Carriers. Description: Huentelman, Matt, et al. Common BACE2 Polymorphisms are Associated with Altered Risk for Alzheimer's Disease and CSF Amyloid Biomarkers in APOE epsilon4 Non-Carriers. ''Sci Rep''. 2019 Jul 3; '''9''' (1):9640
Metabolomic signature of exposure and response to citalopram/escitalopram in depressed outpatients. Description: Bhattacharyya, Sudeepa, et al. Metabolomic signature of exposure and response to citalopram/escitalopram in depressed outpatients. ''Transl Psychiatry''. 2019 Jul 4; '''9''' (1):173
Effect of the interleukin 10 polymorphisms on interleukin 10 production and visceral hypersensitivity in Chinese patients with diarrhea-predominant irritable bowel syndrome. Description: Zhu, Shi-Wei, et al. Effect of the interleukin 10 polymorphisms on interleukin 10 production and visceral hypersensitivity in Chinese patients with diarrhea-predominant irritable bowel syndrome. ''Chin Med J (Engl)''. 2019 Jul 5; '''132''' (13):1524-1532
A single nucleotide variant in the promoter region of the CCR5 gene increases susceptibility to arthritis encephalitis virus in goats. Description: Colussi, Silvia, et al. A single nucleotide variant in the promoter region of the CCR5 gene increases susceptibility to arthritis encephalitis virus in goats. ''BMC Vet Res''. 2019 Jul 6; '''15''' (1):230
COL6A3 polymorphisms were associated with lung cancer risk in a Chinese population. Description: Duan, Ying, et al. COL6A3 polymorphisms were associated with lung cancer risk in a Chinese population. ''Respir Res''. 2019 Jul 8; '''20''' (1):143
The effect of X-linked dosage compensation on complex trait variation. Description: Sidorenko, Julia, et al. The effect of X-linked dosage compensation on complex trait variation. ''Nat Commun''. 2019 Jul 8; '''10''' (1):3009
Identifying candidate genes for Phytophthora capsici resistance in pepper (Capsicum annuum) via genotyping-by-sequencing-based QTL mapping and genome-wide association study. Description: Siddique, Muhammad Irfan, et al. Identifying candidate genes for Phytophthora capsici resistance in pepper (Capsicum annuum) via genotyping-by-sequencing-based QTL mapping and genome-wide association study. ''Sci Rep''. 2019 Jul 10; '''9''' (1):9962
Genome-wide association study identifies CD1A associated with rate of increase in plasma neurofilament light in non-demented elders. Description: Wang, Zuo-Teng, et al. Genome-wide association study identifies CD1A associated with rate of increase in plasma neurofilament light in non-demented elders. ''Aging (Albany NY)''. 2019 Jul 11; '''11''' (13):4521-4535
Frequent intra- and inter-species introgression shapes the landscape of genetic variation in bread wheat. Description: Cheng, Hong, et al. Frequent intra- and inter-species introgression shapes the landscape of genetic variation in bread wheat. ''Genome Biol''. 2019 Jul 12; '''20''' (1):136
Therapeutic efficacy of dimethyl fumarate in relapsing-remitting multiple sclerosis associates with ROS pathway in monocytes. Description: Carlstrom, Karl E, et al. Therapeutic efficacy of dimethyl fumarate in relapsing-remitting multiple sclerosis associates with ROS pathway in monocytes. ''Nat Commun''. 2019 Jul 12; '''10''' (1):3081
Genome-wide association and evolutionary analyses reveal the formation of swine facial wrinkles in Chinese Erhualian pigs. Description: Huang, Tao, et al. Genome-wide association and evolutionary analyses reveal the formation of swine facial wrinkles in Chinese Erhualian pigs. ''Aging (Albany NY)''. 2019 Jul 15; '''11''' (13):4672-4687
Immunomodulatory germline variation associated with the development of multiple primary melanoma (MPM). Description: Ferguson, Robert, et al. Immunomodulatory germline variation associated with the development of multiple primary melanoma (MPM). ''Sci Rep''. 2019 Jul 15; '''9''' (1):10173
Predicting Polygenic Risk of Psychiatric Disorders. Description: Martin, Alicia R, et al. Predicting Polygenic Risk of Psychiatric Disorders. ''Biol Psychiatry''. 2019 Jul 15; '''86''' (2):97-109
ARMC 5 Variants and Risk of Hypertension in Blacks: MH- GRID Study. Description: Zilbermint, Mihail, et al. ARMC 5 Variants and Risk of Hypertension in Blacks: MH- GRID Study. ''J Am Heart Assoc''. 2019 Jul 16; '''8''' (14):e012508
Defective HNF4alpha-dependent gene expression as a driver of hepatocellular failure in alcoholic hepatitis. Description: Argemi, Josepmaria, et al. Defective HNF4alpha-dependent gene expression as a driver of hepatocellular failure in alcoholic hepatitis. ''Nat Commun''. 2019 Jul 16; '''10''' (1):3126
Genetic Analyses of Tanzanian Local Chicken Ecotypes Challenged with Newcastle Disease Virus. Description: Walugembe, Muhammed, et al. Genetic Analyses of Tanzanian Local Chicken Ecotypes Challenged with Newcastle Disease Virus. ''Genes (Basel)''. 2019 Jul 17; '''10''' (7):
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Description: Namjou, Bahram, et al. GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. ''BMC Med''. 2019 Jul 17; '''17''' (1):135
Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. Description: Lona-Durazo, Frida, et al. Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. ''BMC Genet''. 2019 Jul 17; '''20''' (1):59
Phasing quality assessment in a brown layer population through family- and population-based software. Description: Frioni, N, et al. Phasing quality assessment in a brown layer population through family- and population-based software. ''BMC Genet''. 2019 Jul 17; '''20''' (1):57
Evaluating the Potential of Younger Cases and Older Controls Cohorts to Improve Discovery Power in Genome-Wide Association Studies of Late-Onset Diseases. Description: Oliynyk, Roman Teo. Evaluating the Potential of Younger Cases and Older Controls Cohorts to Improve Discovery Power in Genome-Wide Association Studies of Late-Onset Diseases. ''J Pers Med''. 2019 Jul 22; '''9''' (3):
Genetic loci regulating arsenic content in rice grains when grown flooded or under alternative wetting and drying irrigation. Description: Norton, Gareth J, et al. Genetic loci regulating arsenic content in rice grains when grown flooded or under alternative wetting and drying irrigation. ''Rice (N Y)''. 2019 Jul 22; '''12''' (1):54
Protocol for the Emory University African American maternal stress and infant gut microbiome cohort study. Description: Brennan, Patricia A, et al. Protocol for the Emory University African American maternal stress and infant gut microbiome cohort study. ''BMC Pediatr''. 2019 Jul 22; '''19''' (1):246
Genetic diversity, linkage disequilibrium, and population structure analysis of the tea plant (Camellia sinensis) from an origin center, Guizhou plateau, using genome-wide SNPs developed by genotyping-by-sequencing. Description: Niu, Suzhen, et al. Genetic diversity, linkage disequilibrium, and population structure analysis of the tea plant (Camellia sinensis) from an origin center, Guizhou plateau, using genome-wide SNPs developed by genotyping-by-sequencing. ''BMC Plant Biol''. 2019 Jul 23; '''19''' (1):328
Genetic polymorphisms and transcription profiles associated with intracranial aneurysm: a key role for NOTCH3. Description: Li, Mengqi, et al. Genetic polymorphisms and transcription profiles associated with intracranial aneurysm: a key role for NOTCH3. ''Aging (Albany NY)''. 2019 Jul 23; '''11''' (14):5173-5191
Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects. Description: Gill, Dipender, et al. Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects. ''Circulation''. 2019 Jul 23; '''140''' (4):270-279
Genomic differentiation tracks earth-historic isolation in an Indo-Australasian archipelagic pitta (Pittidae; Aves) complex. Description: Ericson, Per G P, et al. Genomic differentiation tracks earth-historic isolation in an Indo-Australasian archipelagic pitta (Pittidae; Aves) complex. ''BMC Evol Biol''. 2019 Jul 24; '''19''' (1):151
Identification of an emphysema-associated genetic variant near TGFB2 with regulatory effects in lung fibroblasts. Description: Parker, Margaret M, et al. Identification of an emphysema-associated genetic variant near TGFB2 with regulatory effects in lung fibroblasts. ''Elife''. 2019 Jul 25; '''8''':
Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits. Description: Glicksberg, Benjamin S, et al. Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits. ''BMC Med Genomics''. 2019 Jul 25; '''12''' (Suppl 6):108
Non-coding variability at the APOE locus contributes to the Alzheimer's risk. Description: Zhou, Xiaopu, et al. Non-coding variability at the APOE locus contributes to the Alzheimer's risk. ''Nat Commun''. 2019 Jul 25; '''10''' (1):3310
AKNA Frameshift Variant in Three Dogs with Recurrent Inflammatory Pulmonary Disease. Description: Hug, Petra, et al. AKNA Frameshift Variant in Three Dogs with Recurrent Inflammatory Pulmonary Disease. ''Genes (Basel)''. 2019 Jul 26; '''10''' (8):
Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence. Description: Cruz, Pedro R S, et al. Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence. ''Sci Rep''. 2019 Jul 26; '''9''' (1):10896
GWAS of habitual coffee consumption reveals a sex difference in the genetic effect of the 12q24 locus in the Japanese population. Description: Jia, Huijuan, et al. GWAS of habitual coffee consumption reveals a sex difference in the genetic effect of the 12q24 locus in the Japanese population. ''BMC Genet''. 2019 Jul 26; '''20''' (1):61
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. Description: Kerr, Shona M, et al. An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. ''Sci Rep''. 2019 Jul 29; '''9''' (1):10964
LRRTM4 and PCSK5 Genetic Polymorphisms as Markers for Cognitive Impairment in A Hypotensive Aging Population: A Genome-Wide Association Study in Taiwan. Description: Chen, Yi-Chun, et al. LRRTM4 and PCSK5 Genetic Polymorphisms as Markers for Cognitive Impairment in A Hypotensive Aging Population: A Genome-Wide Association Study in Taiwan. ''J Clin Med''. 2019 Jul 29; '''8''' (8):
Genome-Wide Association Study of Metabolic Syndrome Reveals Primary Genetic Variants at CETP Locus in Indians. Description: Prasad, Gauri, et al. Genome-Wide Association Study of Metabolic Syndrome Reveals Primary Genetic Variants at CETP Locus in Indians. ''Biomolecules''. 2019 Jul 30; '''9''' (8):
Multilocus associations of inflammatory genes with the risk of type 1 diabetes. Description: Timasheva, Yanina R, et al. Multilocus associations of inflammatory genes with the risk of type 1 diabetes. ''Gene''. 2019 Jul 30; '''707''': 1-8
Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and Parkinson's disease. Description: Fava, Vinicius M, et al. Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and Parkinson's disease. ''Proc Natl Acad Sci U S A''. 2019 Jul 30; '''116''' (31):15616-15624
Spatial chromatin architecture alteration by structural variations in human genomes at the population scale. Description: Sadowski, Michal, et al. Spatial chromatin architecture alteration by structural variations in human genomes at the population scale. ''Genome Biol''. 2019 Jul 30; '''20''' (1):148
Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population. Description: Figueroa-Ildefonso, Erick, et al. Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population. ''Genes (Basel)''. 2019 Jul 31; '''10''' (8):
Accurate estimation of SNP-heritability from biobank-scale data irrespective of genetic architecture. Description: Hou, Kangcheng, et al. Accurate estimation of SNP-heritability from biobank-scale data irrespective of genetic architecture. ''Nat Genet''. 2019 Aug; '''51''' (8):1244-1251
A conserved role of the insulin-like signaling pathway in diet-dependent uric acid pathologies in Drosophila melanogaster. Description: Lang, Sven, et al. A conserved role of the insulin-like signaling pathway in diet-dependent uric acid pathologies in Drosophila melanogaster. ''PLoS Genet''. 2019 Aug; '''15''' (8):e1008318
Analysis of MIR155HG variants and colorectal cancer susceptibility in Han Chinese population. Description: Wu, Huangfu, et al. Analysis of MIR155HG variants and colorectal cancer susceptibility in Han Chinese population. ''Mol Genet Genomic Med''. 2019 Aug; '''7''' (8):e778
Ancestry-Specific Analyses Reveal Differential Demographic Histories and Opposite Selective Pressures in Modern South Asian Populations. Description: Yelmen, Burak, et al. Ancestry-Specific Analyses Reveal Differential Demographic Histories and Opposite Selective Pressures in Modern South Asian Populations. ''Mol Biol Evol''. 2019 Aug 1; '''36''' (8):1628-1642
A Novel Gene Underlies Bleomycin-Response Variation in Caenorhabditis elegans. Description: Brady, Shannon C, et al. A Novel Gene Underlies Bleomycin-Response Variation in Caenorhabditis elegans. ''Genetics''. 2019 Aug; '''212''' (4):1453-1468
Association of APOL1 renal disease risk alleles with Trypanosoma brucei rhodesiense infection outcomes in the northern part of Malawi. Description: Kamoto, Kelita, et al. Association of APOL1 renal disease risk alleles with Trypanosoma brucei rhodesiense infection outcomes in the northern part of Malawi. ''PLoS Negl Trop Dis''. 2019 Aug; '''13''' (8):e0007603
Development of an integrated 200K SNP genotyping array and application for genetic mapping, genome assembly improvement and genome wide association studies in pear (Pyrus). Description: Li, Xiaolong, et al. Development of an integrated 200K SNP genotyping array and application for genetic mapping, genome assembly improvement and genome wide association studies in pear (Pyrus). ''Plant Biotechnol J''. 2019 Aug; '''17''' (8):1582-1594
Differences in brain-derived neurotrophic factor gene polymorphisms between acute ischemic stroke patients and healthy controls in the Han population of southwest China. Description: Zhou, Jie, et al. Differences in brain-derived neurotrophic factor gene polymorphisms between acute ischemic stroke patients and healthy controls in the Han population of southwest China. ''Neural Regen Res''. 2019 Aug; '''14''' (8):1404-1411
Does gene flow aggravate or alleviate maladaptation to environmental stress in small populations? Description: Fitzpatrick, Sarah W, et al. Does gene flow aggravate or alleviate maladaptation to environmental stress in small populations? ''Evol Appl''. 2019 Aug; '''12''' (7):1402-1416
Galectin-3, a novel endogenous TREM2 ligand, detrimentally regulates inflammatory response in Alzheimer's disease. Description: Boza-Serrano, Antonio, et al. Galectin-3, a novel endogenous TREM2 ligand, detrimentally regulates inflammatory response in Alzheimer's disease. ''Acta Neuropathol''. 2019 Aug; '''138''' (2):251-273
Gene polymorphism of cytochrome P450 significantly affects lung cancer susceptibility. Description: Li, Meng, et al. Gene polymorphism of cytochrome P450 significantly affects lung cancer susceptibility. ''Cancer Med''. 2019 Aug; '''8''' (10):4892-4905
Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts. Description: Iwaki, Hirotaka, et al. Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts. ''Neurol Genet''. 2019 Aug; '''5''' (4):e348
Genome-wide association study identifies CBFA2T3 affecting the rate of CSF Abeta42 decline in non-demented elders. Description: Dou, Kai-Xin, et al. Genome-wide association study identifies CBFA2T3 affecting the rate of CSF Abeta42 decline in non-demented elders. ''Aging (Albany NY)''. 2019 Aug 1; '''11''' (15):5433-5444
Genome-wide copy number variant data for inflammatory bowel disease in a caucasian population. Description: Frenkel, Svetlana, et al. Genome-wide copy number variant data for inflammatory bowel disease in a caucasian population. ''Data Brief''. 2019 Aug; '''25''': 104203
Genome-Wide Scan for Runs of Homozygosity Identifies Candidate Genes in Three Pig Breeds. Description: Xie, Rui, et al. Genome-Wide Scan for Runs of Homozygosity Identifies Candidate Genes in Three Pig Breeds. ''Animals (Basel)''. 2019 Aug 1; '''9''' (8):
Genomic diversity and admixture patterns among six Chinese indigenous cattle breeds in Yunnan. Description: Li, Rong, et al. Genomic diversity and admixture patterns among six Chinese indigenous cattle breeds in Yunnan. ''Asian-Australas J Anim Sci''. 2019 Aug; '''32''' (8):1069-1076
HaploBlocker: Creation of Subgroup-Specific Haplotype Blocks and Libraries. Description: Pook, Torsten, et al. HaploBlocker: Creation of Subgroup-Specific Haplotype Blocks and Libraries. ''Genetics''. 2019 Aug; '''212''' (4):1045-1061
Identification of the master sex determining gene in Northern pike (Esox lucius) reveals restricted sex chromosome differentiation. Description: Pan, Qiaowei, et al. Identification of the master sex determining gene in Northern pike (Esox lucius) reveals restricted sex chromosome differentiation. ''PLoS Genet''. 2019 Aug; '''15''' (8):e1008013
Interaction between lifestyle and genetic susceptibility in myopia: the Generation R study. Description: Enthoven, Clair A, et al. Interaction between lifestyle and genetic susceptibility in myopia: the Generation R study. ''Eur J Epidemiol''. 2019 Aug; '''34''' (8):777-784
Interactions between FKBP5 variation and environmental stressors in adolescent Major Depression. Description: Piechaczek, Charlotte Elisabeth, et al. Interactions between FKBP5 variation and environmental stressors in adolescent Major Depression. ''Psychoneuroendocrinology''. 2019 Aug; '''106''': 28-37
Intraspecific Diversity of Fission Yeast Mitochondrial Genomes. Description: Tao, Yu-Tian, et al. Intraspecific Diversity of Fission Yeast Mitochondrial Genomes. ''Genome Biol Evol''. 2019 Aug 1; '''11''' (8):2312-2329
Linkage analysis revealed risk loci on 6p21 and 18p11.2-q11.2 in familial colon and rectal cancer, respectively. Description: von Holst, Susanna, et al. Linkage analysis revealed risk loci on 6p21 and 18p11.2-q11.2 in familial colon and rectal cancer, respectively. ''Eur J Hum Genet''. 2019 Aug; '''27''' (8):1286-1295
Mitochondrial DNA variability of the Polish population. Description: Jarczak, Justyna, et al. Mitochondrial DNA variability of the Polish population. ''Eur J Hum Genet''. 2019 Aug; '''27''' (8):1304-1314
Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Description: Truong, Dongnhu Thuy, et al. Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. ''J Med Genet''. 2019 Aug; '''56''' (8):557-566
Performing different kinds of physical exercise differentially attenuates the genetic effects on obesity measures: Evidence from 18,424 Taiwan Biobank participants. Description: Lin, Wan-Yu, et al. Performing different kinds of physical exercise differentially attenuates the genetic effects on obesity measures: Evidence from 18,424 Taiwan Biobank participants. ''PLoS Genet''. 2019 Aug; '''15''' (8):e1008277
Polygenic risk for circulating reproductive hormone levels and their influence on hippocampal volume and depression susceptibility. Description: Smeeth, Demelza M, et al. Polygenic risk for circulating reproductive hormone levels and their influence on hippocampal volume and depression susceptibility. ''Psychoneuroendocrinology''. 2019 Aug; '''106''': 284-292
PRDM9 Diversity at Fine Geographical Scale Reveals Contrasting Evolutionary Patterns and Functional Constraints in Natural Populations of House Mice. Description: Vara, Covadonga, et al. PRDM9 Diversity at Fine Geographical Scale Reveals Contrasting Evolutionary Patterns and Functional Constraints in Natural Populations of House Mice. ''Mol Biol Evol''. 2019 Aug 1; '''36''' (8):1686-1700
Shared genes between Alzheimer's disease and ischemic stroke. Description: Wei, Chang-Juan, et al. Shared genes between Alzheimer's disease and ischemic stroke. ''CNS Neurosci Ther''. 2019 Aug; '''25''' (8):855-864
Significant association between RETN genetic polymorphisms and alcohol-induced osteonecrosis of femoral head. Description: Liu, Chang, et al. Significant association between RETN genetic polymorphisms and alcohol-induced osteonecrosis of femoral head. ''Mol Genet Genomic Med''. 2019 Aug; '''7''' (8):e822
The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population. Description: Szentkereszty-Kovacs, Zita, et al. The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population. ''Arch Dermatol Res''. 2019 Aug; '''311''' (6):435-442
The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. Description: Liu, Xiumin, et al. The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. ''Mol Genet Genomic Med''. 2019 Aug; '''7''' (8):e835
The role of FOXO3 polymorphisms in susceptibility to tuberculosis in a Chinese population. Description: Wang, Bo, et al. The role of FOXO3 polymorphisms in susceptibility to tuberculosis in a Chinese population. ''Mol Genet Genomic Med''. 2019 Aug; '''7''' (8):e770
The role of polygenic risk score gene-set analysis in the context of the omnigenic model of schizophrenia. Description: Rammos, Alexandros, et al. The role of polygenic risk score gene-set analysis in the context of the omnigenic model of schizophrenia. ''Neuropsychopharmacology''. 2019 Aug; '''44''' (9):1562-1569
ASD Phenotype-Genotype Associations in Concordant and Discordant Monozygotic and Dizygotic Twins Stratified by Severity of Autistic Traits. Description: Hu, Valerie W, et al. ASD Phenotype-Genotype Associations in Concordant and Discordant Monozygotic and Dizygotic Twins Stratified by Severity of Autistic Traits. ''Int J Mol Sci''. 2019 Aug 3; '''20''' (15):
A New Pedigree-Based SNP Haplotype Method for Genomic Polymorphism and Genetic Studies. Description: Vadva, Zareen, et al. A New Pedigree-Based SNP Haplotype Method for Genomic Polymorphism and Genetic Studies. ''Cells''. 2019 Aug 5; '''8''' (8):
Genetic diversity and population structure of the Sapsaree, a native Korean dog breed. Description: Gajaweera, Chandima, et al. Genetic diversity and population structure of the Sapsaree, a native Korean dog breed. ''BMC Genet''. 2019 Aug 5; '''20''' (1):66
Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. Description: Liu, Xu, et al. Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. ''Respir Res''. 2019 Aug 5; '''20''' (1):174
CAG Repeat Not Polyglutamine Length Determines Timing of Huntington's Disease Onset. Description: CAG Repeat Not Polyglutamine Length Determines Timing of Huntington's Disease Onset. ''Cell''. 2019 Aug 8; '''178''' (4):887-900.e14
Genome-Wide Association Study and Cost-Efficient Genomic Predictions for Growth and Fillet Yield in Nile Tilapia (Oreochromis niloticus). Description: Yoshida, Grazyella M, et al. Genome-Wide Association Study and Cost-Efficient Genomic Predictions for Growth and Fillet Yield in Nile Tilapia (Oreochromis niloticus). ''G3 (Bethesda)''. 2019 Aug 8; '''9''' (8):2597-2607
GRAF-pop: A Fast Distance-Based Method To Infer Subject Ancestry from Multiple Genotype Datasets Without Principal Components Analysis. Description: Jin, Yumi, et al. GRAF-pop: A Fast Distance-Based Method To Infer Subject Ancestry from Multiple Genotype Datasets Without Principal Components Analysis. ''G3 (Bethesda)''. 2019 Aug 8; '''9''' (8):2447-2461
Population Genome Sequencing of the Scab Fungal Species Venturia inaequalis, Venturia pirina, Venturia aucupariae and Venturia asperata. Description: Le Cam, Bruno, et al. Population Genome Sequencing of the Scab Fungal Species Venturia inaequalis, Venturia pirina, Venturia aucupariae and Venturia asperata. ''G3 (Bethesda)''. 2019 Aug 8; '''9''' (8):2405-2414
Signatures of Recent Positive Selection in Enhancers Across 41 Human Tissues. Description: Moon, Jiyun M, et al. Signatures of Recent Positive Selection in Enhancers Across 41 Human Tissues. ''G3 (Bethesda)''. 2019 Aug 8; '''9''' (8):2761-2774
Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomics. Description: Speedy, Helen E, et al. Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomics. ''Nat Commun''. 2019 Aug 9; '''10''' (1):3615
Is Hyperuricemia, an Early-Onset Metabolic Disorder, Causally Associated with Cardiovascular Disease Events in Han Chinese? Description: Chiang, Kuang-Mao, et al. Is Hyperuricemia, an Early-Onset Metabolic Disorder, Causally Associated with Cardiovascular Disease Events in Han Chinese? ''J Clin Med''. 2019 Aug 12; '''8''' (8):
Targeted sequencing of linkage region in Dominican families implicates PRIMA1 and the SPATA7-PTPN21-ZC3H14-EML5-TTC8 locus in carotid-intima media thickness and atherosclerotic events. Description: Wang, Liyong, et al. Targeted sequencing of linkage region in Dominican families implicates PRIMA1 and the SPATA7-PTPN21-ZC3H14-EML5-TTC8 locus in carotid-intima media thickness and atherosclerotic events. ''Sci Rep''. 2019 Aug 12; '''9''' (1):11621
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes. Description: Wang, Heming, et al. Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes. ''Nat Commun''. 2019 Aug 13; '''10''' (1):3503
Genome-wide association analysis of egg production performance in chickens across the whole laying period. Description: Liu, Zhuang, et al. Genome-wide association analysis of egg production performance in chickens across the whole laying period. ''BMC Genet''. 2019 Aug 14; '''20''' (1):67
Signatures of differential selection in chloroplast genome between japonica and indica. Description: Cheng, Lin, et al. Signatures of differential selection in chloroplast genome between japonica and indica. ''Rice (N Y)''. 2019 Aug 14; '''12''' (1):65
Extensive intraspecies cryptic variation in an ancient embryonic gene regulatory network. Description: Torres Cleuren, Yamila N, et al. Extensive intraspecies cryptic variation in an ancient embryonic gene regulatory network. ''Elife''. 2019 Aug 15; '''8''':
Novel Insight Into the Etiology of Autism Spectrum Disorder Gained by Integrating Expression Data With Genome-wide Association Statistics. Description: Pain, Oliver, et al. Novel Insight Into the Etiology of Autism Spectrum Disorder Gained by Integrating Expression Data With Genome-wide Association Statistics. ''Biol Psychiatry''. 2019 Aug 15; '''86''' (4):265-273
Genome-wide association study identifies new susceptible loci of IgA nephropathy in Koreans. Description: Jeong, Kyung Hwan, et al. Genome-wide association study identifies new susceptible loci of IgA nephropathy in Koreans. ''BMC Med Genomics''. 2019 Aug 19; '''12''' (1):122
GWAS for Starch-Related Parameters in Japonica Rice (Oryza sativa L.). Description: Biselli, Chiara, et al. GWAS for Starch-Related Parameters in Japonica Rice (Oryza sativa L.). ''Plants (Basel)''. 2019 Aug 19; '''8''' (8):
The genetic relationship between female reproductive traits and six psychiatric disorders. Description: Ni, Guiyan, et al. The genetic relationship between female reproductive traits and six psychiatric disorders. ''Sci Rep''. 2019 Aug 19; '''9''' (1):12041
Ancient DNA from the skeletons of Roopkund Lake reveals Mediterranean migrants in India. Description: Harney, Eadaoin, et al. Ancient DNA from the skeletons of Roopkund Lake reveals Mediterranean migrants in India. ''Nat Commun''. 2019 Aug 20; '''10''' (1):3670
The Role of MIR9-2 in Shared Susceptibility of Psychiatric Disorders during Childhood: A Population-Based Birth Cohort Study. Description: Tovo-Rodrigues, Luciana, et al. The Role of MIR9-2 in Shared Susceptibility of Psychiatric Disorders during Childhood: A Population-Based Birth Cohort Study. ''Genes (Basel)''. 2019 Aug 20; '''10''' (8):
Catalytically Impaired TYK2 Variants are Protective Against Childhood- and Adult-Onset Systemic Lupus Erythematosus in Mexicans. Description: Contreras-Cubas, Cecilia, et al. Catalytically Impaired TYK2 Variants are Protective Against Childhood- and Adult-Onset Systemic Lupus Erythematosus in Mexicans. ''Sci Rep''. 2019 Aug 21; '''9''' (1):12165
Genome-wide association scan for QTL and their positional candidate genes associated with internal organ traits in chickens. Description: Moreira, Gabriel Costa Monteiro, et al. Genome-wide association scan for QTL and their positional candidate genes associated with internal organ traits in chickens. ''BMC Genomics''. 2019 Aug 22; '''20''' (1):669
Novel Locus Associated with Symmetrical Lupoid Onychodystrophy in the Bearded Collie. Description: Gershony, Liza C, et al. Novel Locus Associated with Symmetrical Lupoid Onychodystrophy in the Bearded Collie. ''Genes (Basel)''. 2019 Aug 22; '''10''' (9):
Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits. Description: Zhang, Wen, et al. Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits. ''Nat Commun''. 2019 Aug 23; '''10''' (1):3834
Muscle glycogen level and occurrence of acid meat in commercial hybrid pigs are regulated by two low-frequency causal variants with large effects and multiple common variants with small effects. Description: Liu, Xianxian, et al. Muscle glycogen level and occurrence of acid meat in commercial hybrid pigs are regulated by two low-frequency causal variants with large effects and multiple common variants with small effects. ''Genet Sel Evol''. 2019 Aug 23; '''51''' (1):46
Mutant Huntingtin Affects Diabetes and Alzheimer's Markers in Human and Cell Models of Huntington's Disease. Description: Chaves, Gepoliano, et al. Mutant Huntingtin Affects Diabetes and Alzheimer's Markers in Human and Cell Models of Huntington's Disease. ''Cells''. 2019 Aug 23; '''8''' (9):
Evaluating Neighborhood, Social, and Genetic Influences on Precursors of Alcohol Use Risk Behavior in African American Adolescents. Description: Compton, Kimberly S, et al. Evaluating Neighborhood, Social, and Genetic Influences on Precursors of Alcohol Use Risk Behavior in African American Adolescents. ''Int J Environ Res Public Health''. 2019 Aug 24; '''16''' (17):
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. Description: Hellwege, Jacklyn N, et al. Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. ''Nat Commun''. 2019 Aug 26; '''10''' (1):3842
Bos taurus-indicus hybridization correlates with intralocus sexual-conflict effects of PRDM9 on male and female fertility in Holstein cattle. Description: Seroussi, Eyal, et al. Bos taurus-indicus hybridization correlates with intralocus sexual-conflict effects of PRDM9 on male and female fertility in Holstein cattle. ''BMC Genet''. 2019 Aug 28; '''20''' (1):71
Dissecting genetic factors affecting phenylephrine infusion rates during anesthesia: a genome-wide association study employing EHR data. Description: Zhang, Yanfei, et al. Dissecting genetic factors affecting phenylephrine infusion rates during anesthesia: a genome-wide association study employing EHR data. ''BMC Med''. 2019 Aug 28; '''17''' (1):168
The genetic relationship between educational attainment and cognitive performance in major psychiatric disorders. Description: Comes, Ashley L, et al. The genetic relationship between educational attainment and cognitive performance in major psychiatric disorders. ''Transl Psychiatry''. 2019 Aug 28; '''9''' (1):210
A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus. Description: Lanata, Cristina M, et al. A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus. ''Nat Commun''. 2019 Aug 29; '''10''' (1):3902
Associations of SLC6A20 genetic polymorphisms with Hirschsprung's disease in a Southern Chinese population. Description: Xie, Xiaoli, et al. Associations of SLC6A20 genetic polymorphisms with Hirschsprung's disease in a Southern Chinese population. ''Biosci Rep''. 2019 Aug 30; '''39''' (8):
The association between SYT1-rs2251214 and cocaine use disorder further supports its role in psychiatry. Description: da Silva, Bruna S, et al. The association between SYT1-rs2251214 and cocaine use disorder further supports its role in psychiatry. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2019 Aug 30; '''94''': 109642
Association between rs2303861 polymorphism in CD82 gene and non-alcoholic fatty liver disease: a preliminary case-control study. Description: Habibzadeh, Parham, et al. Association between rs2303861 polymorphism in CD82 gene and non-alcoholic fatty liver disease: a preliminary case-control study. ''Croat Med J''. 2019 Aug 31; '''60''' (4):361-368
Adaptation to Extreme Environments in an Admixed Human Population from the Atacama Desert. Description: Vicuna, Lucas, et al. Adaptation to Extreme Environments in an Admixed Human Population from the Atacama Desert. ''Genome Biol Evol''. 2019 Sep 1; '''11''' (9):2468-2479
Analysis of differences in human leukocyte antigen between the two Wellcome Trust Case Control Consortium control datasets. Description: Jang, Chloe Soohyun, et al. Analysis of differences in human leukocyte antigen between the two Wellcome Trust Case Control Consortium control datasets. ''Genomics Inform''. 2019 Sep; '''17''' (3):e29
Association of genetic variants at 22q11.2 chromosomal region with cognitive performance in Japanese patients with schizophrenia. Description: Akiyama, Kazufumi, et al. Association of genetic variants at 22q11.2 chromosomal region with cognitive performance in Japanese patients with schizophrenia. ''Schizophr Res Cogn''. 2019 Sep; '''17''': 100134
Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population. Description: Ji, Demin, et al. Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population. ''Mol Genet Genomic Med''. 2019 Sep; '''7''' (9):e890
Distinct genetic variation and heterogeneity of the Iranian population. Description: Mehrjoo, Zohreh, et al. Distinct genetic variation and heterogeneity of the Iranian population. ''PLoS Genet''. 2019 Sep; '''15''' (9):e1008385
European Roma groups show complex West Eurasian admixture footprints and a common South Asian genetic origin. Description: Font-Porterias, Neus, et al. European Roma groups show complex West Eurasian admixture footprints and a common South Asian genetic origin. ''PLoS Genet''. 2019 Sep; '''15''' (9):e1008417
Genetic Affinities among Southern Africa Hunter-Gatherers and the Impact of Admixing Farmer and Herder Populations. Description: Vicente, Mario, et al. Genetic Affinities among Southern Africa Hunter-Gatherers and the Impact of Admixing Farmer and Herder Populations. ''Mol Biol Evol''. 2019 Sep 1; '''36''' (9):1849-1861
Genetic dissection of drought and heat-responsive agronomic traits in wheat. Description: Li, Long, et al. Genetic dissection of drought and heat-responsive agronomic traits in wheat. ''Plant Cell Environ''. 2019 Sep; '''42''' (9):2540-2553
Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration. Description: Wilman, Henry R, et al. Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration. ''J Hepatol''. 2019 Sep; '''71''' (3):594-602
Imputation of canine genotype array data using 365 whole-genome sequences improves power of genome-wide association studies. Description: Hayward, Jessica J, et al. Imputation of canine genotype array data using 365 whole-genome sequences improves power of genome-wide association studies. ''PLoS Genet''. 2019 Sep; '''15''' (9):e1008003
Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI. Description: Major, Megan, et al. Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI. ''Genet Epidemiol''. 2019 Sep; '''43''' (6):629-645
Interplay between genome-wide implicated genetic variants and environmental factors related to childhood antisocial behavior in the UK ALSPAC cohort. Description: Ruisch, I Hyun, et al. Interplay between genome-wide implicated genetic variants and environmental factors related to childhood antisocial behavior in the UK ALSPAC cohort. ''Eur Arch Psychiatry Clin Neurosci''. 2019 Sep; '''269''' (6):741-752
Last exit before the brink: Conservation genomics of the Cambodian population of the critically endangered southern river terrapin. Description: Cilingir, F Gozde, et al. Last exit before the brink: Conservation genomics of the Cambodian population of the critically endangered southern river terrapin. ''Ecol Evol''. 2019 Sep; '''9''' (17):9500-9510
Maternal genomic variability of the wild boar (Sus scrofa) reveals the uniqueness of East-Caucasian and Central Italian populations. Description: Khederzadeh, Saber, et al. Maternal genomic variability of the wild boar (Sus scrofa) reveals the uniqueness of East-Caucasian and Central Italian populations. ''Ecol Evol''. 2019 Sep; '''9''' (17):9467-9478
Native American admixture recapitulates population-specific migration and settlement of the continental United States. Description: Jordan, I King, et al. Native American admixture recapitulates population-specific migration and settlement of the continental United States. ''PLoS Genet''. 2019 Sep; '''15''' (9):e1008225
NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia. Description: Anderegg, Linda, et al. NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia. ''PLoS Genet''. 2019 Sep; '''15''' (9):e1008378
Old divergence and restricted gene flow between torrent duck (Merganetta armata) subspecies in the Central and Southern Andes. Description: Alza, Luis, et al. Old divergence and restricted gene flow between torrent duck (Merganetta armata) subspecies in the Central and Southern Andes. ''Ecol Evol''. 2019 Sep; '''9''' (17):9961-9976
Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe. Description: Raveane, A, et al. Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe. ''Sci Adv''. 2019 Sep; '''5''' (9):eaaw3492
Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage. Description: Lee, Changhoon, et al. Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage. ''Nat Neurosci''. 2019 Sep; '''22''' (9):1521-1532
Reconstructed Lost Native American Populations from Eastern Brazil Are Shaped by Differential Je/Tupi Ancestry. Description: Mas-Sandoval, Alex, et al. Reconstructed Lost Native American Populations from Eastern Brazil Are Shaped by Differential Je/Tupi Ancestry. ''Genome Biol Evol''. 2019 Sep 1; '''11''' (9):2593-2604
SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus. Description: Jin, Sheng Chih, et al. SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus. ''Mol Genet Genomic Med''. 2019 Sep; '''7''' (9):e892
Targeted ultra-deep sequencing of a South African Bantu-speaking cohort to comprehensively map and characterize common and novel variants in 65 pharmacologically-related genes. Description: Tshabalala, Sibongile, et al. Targeted ultra-deep sequencing of a South African Bantu-speaking cohort to comprehensively map and characterize common and novel variants in 65 pharmacologically-related genes. ''Pharmacogenet Genomics''. 2019 Sep; '''29''' (7):167-178
The ferroportin Q248H mutation protects from anemia, but not malaria or bacteremia. Description: Muriuki, John Muthii, et al. The ferroportin Q248H mutation protects from anemia, but not malaria or bacteremia. ''Sci Adv''. 2019 Sep; '''5''' (9):eaaw0109
The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy. Description: Jabbari, Edwin, et al. The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy. ''Mov Disord''. 2019 Sep; '''34''' (9):1307-1314
The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis. Description: Grunblatt, Edna, et al. The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis. ''Am J Med Genet B Neuropsychiatr Genet''. 2019 Sep; '''180''' (6):365-376
Ultrarare variants drive substantial cis heritability of human gene expression. Description: Hernandez, Ryan D, et al. Ultrarare variants drive substantial cis heritability of human gene expression. ''Nat Genet''. 2019 Sep; '''51''' (9):1349-1355
Gene set enrichment analysis to create polygenic scores: a developmental examination of aggression. Description: Elam, Kit K, et al. Gene set enrichment analysis to create polygenic scores: a developmental examination of aggression. ''Transl Psychiatry''. 2019 Sep 2; '''9''' (1):212
Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines. Description: Hernandez, Nicholas, et al. Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines. ''J Exp Med''. 2019 Sep 2; '''216''' (9):2057-2070
Integrating genome-wide co-association and gene expression to identify putative regulators and predictors of feed efficiency in pigs. Description: Ramayo-Caldas, Yuliaxis, et al. Integrating genome-wide co-association and gene expression to identify putative regulators and predictors of feed efficiency in pigs. ''Genet Sel Evol''. 2019 Sep 2; '''51''' (1):48
Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responses. Description: Spencer, Sarah, et al. Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responses. ''J Exp Med''. 2019 Sep 2; '''216''' (9):1986-1998
Single-cell transcriptomic analysis of tissue-resident memory T cells in human lung cancer. Description: Clarke, James, et al. Single-cell transcriptomic analysis of tissue-resident memory T cells in human lung cancer. ''J Exp Med''. 2019 Sep 2; '''216''' (9):2128-2149
Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. Description: Liu, Xueping, et al. Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. ''Nat Commun''. 2019 Sep 2; '''10''' (1):3927
Extreme inbreeding in a European ancestry sample from the contemporary UK population. Description: Yengo, Loic, et al. Extreme inbreeding in a European ancestry sample from the contemporary UK population. ''Nat Commun''. 2019 Sep 3; '''10''' (1):3719
A Genetic Approach to the Association Between PCSK9 and Sepsis. Description: Feng, QiPing, et al. A Genetic Approach to the Association Between PCSK9 and Sepsis. ''JAMA Netw Open''. 2019 Sep 4; '''2''' (9):e1911130
A Prospective Analysis of Genetic Variants Associated with Human Lifespan. Description: Wright, Kevin M, et al. A Prospective Analysis of Genetic Variants Associated with Human Lifespan. ''G3 (Bethesda)''. 2019 Sep 4; '''9''' (9):2863-2878
Genome-Wide Association Mapping of Anthracnose (Colletotrichum sublineolum) Resistance in NPGS Ethiopian Sorghum Germplasm. Description: Cuevas, Hugo E, et al. Genome-Wide Association Mapping of Anthracnose (Colletotrichum sublineolum) Resistance in NPGS Ethiopian Sorghum Germplasm. ''G3 (Bethesda)''. 2019 Sep 4; '''9''' (9):2879-2885
A Transcriptomic Study of the Tail Fat Deposition in Two Types of Hulun Buir Sheep According to Tail Size and Sex. Description: Fan, Hongying, et al. A Transcriptomic Study of the Tail Fat Deposition in Two Types of Hulun Buir Sheep According to Tail Size and Sex. ''Animals (Basel)''. 2019 Sep 5; '''9''' (9):
Distinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype. Description: Terao, Chikashi, et al. Distinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype. ''Am J Hum Genet''. 2019 Sep 5; '''105''' (3):616-624
Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report. Description: Niazi, Robina Khan, et al. Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report. ''BMC Med Genet''. 2019 Sep 5; '''20''' (1):152
Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology. Description: Tanigawa, Yosuke, et al. Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology. ''Nat Commun''. 2019 Sep 6; '''10''' (1):4064
Functional disease architectures reveal unique biological role of transposable elements. Description: Hormozdiari, Farhad, et al. Functional disease architectures reveal unique biological role of transposable elements. ''Nat Commun''. 2019 Sep 6; '''10''' (1):4054
Serotonin is elevated in risk-genotype carriers of TCF7L2 - rs7903146. Description: Leiherer, Andreas, et al. Serotonin is elevated in risk-genotype carriers of TCF7L2 - rs7903146. ''Sci Rep''. 2019 Sep 6; '''9''' (1):12863
HLA-G Polymorphisms Are Associated with Non-segmental Vitiligo among Brazilians. Description: Veiga-Castelli, Luciana, et al. HLA-G Polymorphisms Are Associated with Non-segmental Vitiligo among Brazilians. ''Biomolecules''. 2019 Sep 9; '''9''' (9):
A Unique Epigenomic Landscape Defines Human Erythropoiesis. Description: Schulz, Vincent P, et al. A Unique Epigenomic Landscape Defines Human Erythropoiesis. ''Cell Rep''. 2019 Sep 10; '''28''' (11):2996-3009.e7
Germline variability and tumor expression level of ribosomal protein gene RPL28 are associated with survival of metastatic colorectal cancer patients. Description: Labriet, Adrien, et al. Germline variability and tumor expression level of ribosomal protein gene RPL28 are associated with survival of metastatic colorectal cancer patients. ''Sci Rep''. 2019 Sep 10; '''9''' (1):13008
Genetic variants in CYP4F2 were significantly correlated with susceptibility to ischemic stroke. Description: Wu, Yuan, et al. Genetic variants in CYP4F2 were significantly correlated with susceptibility to ischemic stroke. ''BMC Med Genet''. 2019 Sep 11; '''20''' (1):155
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Description: Teumer, Alexander, et al. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. ''Nat Commun''. 2019 Sep 11; '''10''' (1):4130
Identification of transcriptome-wide, nut weight-associated SNPs in Castanea crenata. Description: Kang, Min-Jeong, et al. Identification of transcriptome-wide, nut weight-associated SNPs in Castanea crenata. ''Sci Rep''. 2019 Sep 11; '''9''' (1):13161
The Interplay of Diet Quality and Alzheimer's Disease Genetic Risk Score in Relation to Cognitive Performance Among Urban African Americans. Description: Hossain, Sharmin, et al. The Interplay of Diet Quality and Alzheimer's Disease Genetic Risk Score in Relation to Cognitive Performance Among Urban African Americans. ''Nutrients''. 2019 Sep 11; '''11''' (9):
A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals. Description: Scepanovic, Petar, et al. A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals. ''Microbiome''. 2019 Sep 13; '''7''' (1):130
Resequencing 545 ginkgo genomes across the world reveals the evolutionary history of the living fossil. Description: Zhao, Yun-Peng, et al. Resequencing 545 ginkgo genomes across the world reveals the evolutionary history of the living fossil. ''Nat Commun''. 2019 Sep 13; '''10''' (1):4201
Combined analysis of keratinocyte cancers identifies novel genome-wide loci. Description: Liyanage, Upekha E, et al. Combined analysis of keratinocyte cancers identifies novel genome-wide loci. ''Hum Mol Genet''. 2019 Sep 15; '''28''' (18):3148-3160
Mendelian randomization analysis of celiac GWAS reveals a blood expression signature with diagnostic potential in absence of gluten consumption. Description: Fernandez-Jimenez, Nora, et al. Mendelian randomization analysis of celiac GWAS reveals a blood expression signature with diagnostic potential in absence of gluten consumption. ''Hum Mol Genet''. 2019 Sep 15; '''28''' (18):3037-3042
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases. Description: An, Jiyuan, et al. Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases. ''Nat Commun''. 2019 Sep 16; '''10''' (1):4219
A chromosome-level genome assembly of Cydia pomonella provides insights into chemical ecology and insecticide resistance. Description: Wan, Fanghao, et al. A chromosome-level genome assembly of Cydia pomonella provides insights into chemical ecology and insecticide resistance. ''Nat Commun''. 2019 Sep 17; '''10''' (1):4237
Identification and characterization of SEC24D as a susceptibility gene for hepatitis B virus infection. Description: Jiang, Xianzhong, et al. Identification and characterization of SEC24D as a susceptibility gene for hepatitis B virus infection. ''Sci Rep''. 2019 Sep 17; '''9''' (1):13425
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Description: Alliey-Rodriguez, Ney, et al. NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. ''Transl Psychiatry''. 2019 Sep 17; '''9''' (1):230
The polymorphic variant rs1800734 influences methylation acquisition and allele-specific TFAP4 binding in the MLH1 promoter leading to differential mRNA expression. Description: Thomas, Rachael, et al. The polymorphic variant rs1800734 influences methylation acquisition and allele-specific TFAP4 binding in the MLH1 promoter leading to differential mRNA expression. ''Sci Rep''. 2019 Sep 17; '''9''' (1):13463
A genome-wide association study explores the genetic determinism of host resistance to Salmonella pullorum infection in chickens. Description: Li, Xinghua, et al. A genome-wide association study explores the genetic determinism of host resistance to Salmonella pullorum infection in chickens. ''Genet Sel Evol''. 2019 Sep 18; '''51''' (1):51
Pilot GWAS of caries in African-Americans shows genetic heterogeneity. Description: Orlova, E, et al. Pilot GWAS of caries in African-Americans shows genetic heterogeneity. ''BMC Oral Health''. 2019 Sep 18; '''19''' (1):215
Signatures of selection in the genome of Swedish warmblood horses selected for sport performance. Description: Ablondi, Michela, et al. Signatures of selection in the genome of Swedish warmblood horses selected for sport performance. ''BMC Genomics''. 2019 Sep 18; '''20''' (1):717
Depression genetic risk score is associated with anhedonia-related markers across units of analysis. Description: Guffanti, Guia, et al. Depression genetic risk score is associated with anhedonia-related markers across units of analysis. ''Transl Psychiatry''. 2019 Sep 19; '''9''' (1):236
Discovering genetic interactions bridging pathways in genome-wide association studies. Description: Fang, Gang, et al. Discovering genetic interactions bridging pathways in genome-wide association studies. ''Nat Commun''. 2019 Sep 19; '''10''' (1):4274
Evidence of a Causal Association Between Cancer and Alzheimer's Disease: a Mendelian Randomization Analysis. Description: Seddighi, Sahba, et al. Evidence of a Causal Association Between Cancer and Alzheimer's Disease: a Mendelian Randomization Analysis. ''Sci Rep''. 2019 Sep 19; '''9''' (1):13548
Genome-wide analysis of Corsican population reveals a close affinity with Northern and Central Italy. Description: Tamm, Erika, et al. Genome-wide analysis of Corsican population reveals a close affinity with Northern and Central Italy. ''Sci Rep''. 2019 Sep 19; '''9''' (1):13581
Genomic diversity, linkage disequilibrium and selection signatures in European local pig breeds assessed with a high density SNP chip. Description: Munoz, M, et al. Genomic diversity, linkage disequilibrium and selection signatures in European local pig breeds assessed with a high density SNP chip. ''Sci Rep''. 2019 Sep 19; '''9''' (1):13546
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement. Description: Nethononda, Richard M, et al. Marked variation in heritability estimates of left ventricular mass depending on modality of measurement. ''Sci Rep''. 2019 Sep 19; '''9''' (1):13556
Using Polygenic Profiles to Predict Variation in Language and Psychosocial Outcomes in Early and Middle Childhood. Description: Newbury, Dianne F, et al. Using Polygenic Profiles to Predict Variation in Language and Psychosocial Outcomes in Early and Middle Childhood. ''J Speech Lang Hear Res''. 2019 Sep 20; '''62''' (9):3381-3396
Genetic Parameter Estimation and Genomic Prediction of Duroc Boars' Sperm Morphology Abnormalities. Description: Zhao, Yunxiang, et al. Genetic Parameter Estimation and Genomic Prediction of Duroc Boars' Sperm Morphology Abnormalities. ''Animals (Basel)''. 2019 Sep 23; '''9''' (10):
KLB gene polymorphism is associated with obesity and non-alcoholic fatty liver disease in the Han Chinese. Description: Ji, Fang, et al. KLB gene polymorphism is associated with obesity and non-alcoholic fatty liver disease in the Han Chinese. ''Aging (Albany NY)''. 2019 Sep 23; '''11''' (18):7847-7858
The impact of genomic selection on genetic diversity and genetic gain in three French dairy cattle breeds. Description: Doublet, Anna-Charlotte, et al. The impact of genomic selection on genetic diversity and genetic gain in three French dairy cattle breeds. ''Genet Sel Evol''. 2019 Sep 23; '''51''' (1):52
Distribution of local ancestry and evidence of adaptation in admixed populations. Description: Secolin, Rodrigo, et al. Distribution of local ancestry and evidence of adaptation in admixed populations. ''Sci Rep''. 2019 Sep 25; '''9''' (1):13900
Associations of SNPs of the ADIPOQ Gene with Serum Adiponectin Levels, Unstable Angina, and Coronary Artery Disease. Description: Smetnev, Stepan, et al. Associations of SNPs of the ADIPOQ Gene with Serum Adiponectin Levels, Unstable Angina, and Coronary Artery Disease. ''Biomolecules''. 2019 Sep 26; '''9''' (10):
Genome-Wide Association Study for Reproductive Traits in a Duroc Pig Population. Description: Zhang, Zhe, et al. Genome-Wide Association Study for Reproductive Traits in a Duroc Pig Population. ''Animals (Basel)''. 2019 Sep 26; '''9''' (10):
Characterizing rare and low-frequency height-associated variants in the Japanese population. Description: Akiyama, Masato, et al. Characterizing rare and low-frequency height-associated variants in the Japanese population. ''Nat Commun''. 2019 Sep 27; '''10''' (1):4393
Inbreeding depression due to recent and ancient inbreeding in Dutch Holstein-Friesian dairy cattle. Description: Doekes, Harmen P, et al. Inbreeding depression due to recent and ancient inbreeding in Dutch Holstein-Friesian dairy cattle. ''Genet Sel Evol''. 2019 Sep 27; '''51''' (1):54
A variant of the castor zinc finger 1 (CASZ1) gene is differentially associated with the clinical classification of chronic venous disease. Description: Jones, Gregory T, et al. A variant of the castor zinc finger 1 (CASZ1) gene is differentially associated with the clinical classification of chronic venous disease. ''Sci Rep''. 2019 Sep 30; '''9''' (1):14011
Distinct patterns of natural selection determine sub-population structure in the fire blight pathogen, Erwinia amylovora. Description: Singh, Jugpreet, et al. Distinct patterns of natural selection determine sub-population structure in the fire blight pathogen, Erwinia amylovora. ''Sci Rep''. 2019 Sep 30; '''9''' (1):14017
HPO-Shuffle: an associated gene prioritization strategy and its application in drug repurposing for the treatment of canine epilepsy. Description: Wang, Shuguang, et al. HPO-Shuffle: an associated gene prioritization strategy and its application in drug repurposing for the treatment of canine epilepsy. ''Biosci Rep''. 2019 Sep 30; '''39''' (9):
A functional regulatory variant of MYH3 influences muscle fiber-type composition and intramuscular fat content in pigs. Description: Cho, In-Cheol, et al. A functional regulatory variant of MYH3 influences muscle fiber-type composition and intramuscular fat content in pigs. ''PLoS Genet''. 2019 Oct; '''15''' (10):e1008279
A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. Description: Ciosi, Marc, et al. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. ''EBioMedicine''. 2019 Oct; '''48''': 568-580
A genome-wide association and replication study of blood pressure in Ugandan early adolescents. Description: Lule, Swaib A, et al. A genome-wide association and replication study of blood pressure in Ugandan early adolescents. ''Mol Genet Genomic Med''. 2019 Oct; '''7''' (10):e00950
Ancient Hybridization and Adaptive Introgression of an Invadolysin Gene in Schistosome Parasites. Description: Platt, Roy N, et al. Ancient Hybridization and Adaptive Introgression of an Invadolysin Gene in Schistosome Parasites. ''Mol Biol Evol''. 2019 Oct 1; '''36''' (10):2127-2142
Association Between Perifoveal Drusen Burden Determined by OCT and Genetic Risk in Early and Intermediate Age-Related Macular Degeneration. Description: Seddon, Johanna M, et al. Association Between Perifoveal Drusen Burden Determined by OCT and Genetic Risk in Early and Intermediate Age-Related Macular Degeneration. ''Invest Ophthalmol Vis Sci''. 2019 Oct 1; '''60''' (13):4469-4478
Causal relationships between obesity and the leading causes of death in women and men. Description: Censin, Jenny C, et al. Causal relationships between obesity and the leading causes of death in women and men. ''PLoS Genet''. 2019 Oct; '''15''' (10):e1008405
Common brain disorders are associated with heritable patterns of apparent aging of the brain. Description: Kaufmann, Tobias, et al. Common brain disorders are associated with heritable patterns of apparent aging of the brain. ''Nat Neurosci''. 2019 Oct; '''22''' (10):1617-1623
Dimethylguanidino Valerate: A Lifestyle-Related Metabolite Associated With Future Coronary Artery Disease and Cardiovascular Mortality. Description: Ottosson, Filip, et al. Dimethylguanidino Valerate: A Lifestyle-Related Metabolite Associated With Future Coronary Artery Disease and Cardiovascular Mortality. ''J Am Heart Assoc''. 2019 Oct; '''8''' (19):e012846
Draft genome sequence of Solanum aethiopicum provides insights into disease resistance, drought tolerance, and the evolution of the genome. Description: Song, Bo, et al. Draft genome sequence of Solanum aethiopicum provides insights into disease resistance, drought tolerance, and the evolution of the genome. ''Gigascience''. 2019 Oct 1; '''8''' (10):
Functionalization of the TMEM175 p.M393T variant as a risk factor for Parkinson disease. Description: Jinn, Sarah, et al. Functionalization of the TMEM175 p.M393T variant as a risk factor for Parkinson disease. ''Hum Mol Genet''. 2019 Oct 1; '''28''' (19):3244-3254
Gene-diet quality interactions on haemoglobin A1c and type 2 diabetes risk: The Airwave Health Monitoring Study. Description: Eriksen, Rebeca, et al. Gene-diet quality interactions on haemoglobin A1c and type 2 diabetes risk: The Airwave Health Monitoring Study. ''Endocrinol Diabetes Metab''. 2019 Oct; '''2''' (4):e00074
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft. Description: Huang, Lulin, et al. Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft. ''PLoS Genet''. 2019 Oct; '''15''' (10):e1008357
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout. Description: Kawamura, Yusuke, et al. Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout. ''Ann Rheum Dis''. 2019 Oct; '''78''' (10):1430-1437
Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans. Description: Do, Anh N, et al. Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans. ''Mol Genet Genomic Med''. 2019 Oct; '''7''' (10):e00788
Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing. Description: Toma, Claudio, et al. Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing. ''Clin Transl Gastroenterol''. 2019 Oct; '''10''' (10):e00100
Identification of complement-related host genetic risk factors associated with influenza A(H1N1)pdm09 outcome: challenges ahead. Description: Chatzopoulou, Fani, et al. Identification of complement-related host genetic risk factors associated with influenza A(H1N1)pdm09 outcome: challenges ahead. ''Med Microbiol Immunol''. 2019 Oct; '''208''' (5):631-640
Population genetic analysis of the domestic Bactrian camel in China by RAD-seq. Description: Liu, Chenmiao, et al. Population genetic analysis of the domestic Bactrian camel in China by RAD-seq. ''Ecol Evol''. 2019 Oct; '''9''' (19):11232-11242
Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish. Description: Waksmunski, Andrea R, et al. Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish. ''Hum Genet''. 2019 Oct; '''138''' (10):1171-1182
Sea Turtle Population Genomic Discovery: Global and Locus-Specific Signatures of Polymorphism, Selection, and Adaptive Potential. Description: Chow, Julie C, et al. Sea Turtle Population Genomic Discovery: Global and Locus-Specific Signatures of Polymorphism, Selection, and Adaptive Potential. ''Genome Biol Evol''. 2019 Oct 1; '''11''' (10):2797-2806
Selection and gene flow shape niche-associated variation in pheromone response. Description: Lee, Daehan, et al. Selection and gene flow shape niche-associated variation in pheromone response. ''Nat Ecol Evol''. 2019 Oct; '''3''' (10):1455-1463
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Description: Tin, Adrienne, et al. Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. ''Nat Genet''. 2019 Oct; '''51''' (10):1459-1474
TSEN54 missense variant in Standard Schnauzers with leukodystrophy. Description: Stork, Theresa, et al. TSEN54 missense variant in Standard Schnauzers with leukodystrophy. ''PLoS Genet''. 2019 Oct; '''15''' (10):e1008411
Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness. Description: Das, Rueben G, et al. Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness. ''Sci Rep''. 2019 Oct 2; '''9''' (1):14166
Genomic relatedness and diversity of Swedish native cattle breeds. Description: Upadhyay, Maulik, et al. Genomic relatedness and diversity of Swedish native cattle breeds. ''Genet Sel Evol''. 2019 Oct 2; '''51''' (1):56
Environmental Association Identifies Candidates for Tolerance to Low Temperature and Drought. Description: Lei, Li, et al. Environmental Association Identifies Candidates for Tolerance to Low Temperature and Drought. ''G3 (Bethesda)''. 2019 Oct 7; '''9''' (10):3423-3438
Fine Mapping Using Whole-Genome Sequencing Confirms Anti-Mullerian Hormone as a Major Gene for Sex Determination in Farmed Nile Tilapia (Oreochromis niloticus L.). Description: Caceres, Giovanna, et al. Fine Mapping Using Whole-Genome Sequencing Confirms Anti-Mullerian Hormone as a Major Gene for Sex Determination in Farmed Nile Tilapia (Oreochromis niloticus L.). ''G3 (Bethesda)''. 2019 Oct 7; '''9''' (10):3213-3223
Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss's Wilt of Maize. Description: Singh, Amritpal, et al. Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss's Wilt of Maize. ''G3 (Bethesda)''. 2019 Oct 7; '''9''' (10):3139-3152
Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison. Description: Sun, Yan, et al. Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison. ''Transl Psychiatry''. 2019 Oct 7; '''9''' (1):249
Predicting Longitudinal Traits Derived from High-Throughput Phenomics in Contrasting Environments Using Genomic Legendre Polynomials and B-Splines. Description: Momen, Mehdi, et al. Predicting Longitudinal Traits Derived from High-Throughput Phenomics in Contrasting Environments Using Genomic Legendre Polynomials and B-Splines. ''G3 (Bethesda)''. 2019 Oct 7; '''9''' (10):3369-3380
Improvement of the Pacific bluefin tuna (Thunnus orientalis) reference genome and development of male-specific DNA markers. Description: Suda, Ayako, et al. Improvement of the Pacific bluefin tuna (Thunnus orientalis) reference genome and development of male-specific DNA markers. ''Sci Rep''. 2019 Oct 8; '''9''' (1):14450
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Description: Nievergelt, Caroline M, et al. International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. ''Nat Commun''. 2019 Oct 8; '''10''' (1):4558
Genome-wide association analysis of hippocampal volume identifies enrichment of neurogenesis-related pathways. Description: Horgusluoglu-Moloch, Emrin, et al. Genome-wide association analysis of hippocampal volume identifies enrichment of neurogenesis-related pathways. ''Sci Rep''. 2019 Oct 10; '''9''' (1):14498
Polymorphisms of MTHFR and TYMS predict capecitabine-induced hand-foot syndrome in patients with metastatic breast cancer. Description: Lin, Shaoyan, et al. Polymorphisms of MTHFR and TYMS predict capecitabine-induced hand-foot syndrome in patients with metastatic breast cancer. ''Cancer Commun (Lond)''. 2019 Oct 11; '''39''' (1):57
Theoretical Evaluation of Multi-Breed Genomic Prediction in Chinese Indigenous Cattle. Description: Xu, Lei, et al. Theoretical Evaluation of Multi-Breed Genomic Prediction in Chinese Indigenous Cattle. ''Animals (Basel)''. 2019 Oct 11; '''9''' (10):
Towards genomic database of Alexander disease to identify variations modifying disease phenotype. Description: Yasuda, Rei, et al. Towards genomic database of Alexander disease to identify variations modifying disease phenotype. ''Sci Rep''. 2019 Oct 14; '''9''' (1):14763
Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches. Description: Yao, Shuyang, et al. Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches. ''Biol Psychiatry''. 2019 Oct 15; '''86''' (8):577-586
Whole-genome DNA similarity and population structure of Plasmodiophora brassicae strains from Canada. Description: Sedaghatkish, Afsaneh, et al. Whole-genome DNA similarity and population structure of Plasmodiophora brassicae strains from Canada. ''BMC Genomics''. 2019 Oct 16; '''20''' (1):744
Association of Polygenic Liability for Alcohol Dependence and EEG Connectivity in Adolescence and Young Adulthood. Description: Meyers, Jacquelyn L, et al. Association of Polygenic Liability for Alcohol Dependence and EEG Connectivity in Adolescence and Young Adulthood. ''Brain Sci''. 2019 Oct 17; '''9''' (10):
Puma genomes from North and South America provide insights into the genomic consequences of inbreeding. Description: Saremi, Nedda F, et al. Puma genomes from North and South America provide insights into the genomic consequences of inbreeding. ''Nat Commun''. 2019 Oct 18; '''10''' (1):4769
BDNF genetic variants and methylation: effects on cognition in major depressive disorder. Description: Ferrer, Alex, et al. BDNF genetic variants and methylation: effects on cognition in major depressive disorder. ''Transl Psychiatry''. 2019 Oct 21; '''9''' (1):265
Using imputation-based whole-genome sequencing data to improve the accuracy of genomic prediction for combined populations in pigs. Description: Song, Hailiang, et al. Using imputation-based whole-genome sequencing data to improve the accuracy of genomic prediction for combined populations in pigs. ''Genet Sel Evol''. 2019 Oct 21; '''51''' (1):58
Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer's disease. Description: Creese, Byron, et al. Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer's disease. ''Transl Psychiatry''. 2019 Oct 22; '''9''' (1):273
Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance. Description: Nadella, Ravi K, et al. Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance. ''Hum Genomics''. 2019 Oct 22; '''13''' (1):53
Identification of genomic regions regulating sex determination in Atlantic salmon using high density SNP data. Description: Gabian, Maria, et al. Identification of genomic regions regulating sex determination in Atlantic salmon using high density SNP data. ''BMC Genomics''. 2019 Oct 22; '''20''' (1):764
Integrated copy number and miRNA expression analysis in triple negative breast cancer of Latin American patients. Description: Sugita, Bruna M, et al. Integrated copy number and miRNA expression analysis in triple negative breast cancer of Latin American patients. ''Oncotarget''. 2019 Oct 22; '''10''' (58):6184-6203
DBP rs16846876 and rs12512631 polymorphisms are associated with progression to AIDS naive HIV-infected patients: a retrospective study. Description: Jimenez-Sousa, Maria Angeles, et al. DBP rs16846876 and rs12512631 polymorphisms are associated with progression to AIDS naive HIV-infected patients: a retrospective study. ''J Biomed Sci''. 2019 Oct 23; '''26''' (1):83
Resistin expression in human monocytes is controlled by two linked promoter SNPs mediating NFKB p50/p50 binding and C-methylation. Description: Kumar, Dilip, et al. Resistin expression in human monocytes is controlled by two linked promoter SNPs mediating NFKB p50/p50 binding and C-methylation. ''Sci Rep''. 2019 Oct 23; '''9''' (1):15245
Extensive impact of low-frequency variants on the phenotypic landscape at population-scale. Description: Fournier, Teo, et al. Extensive impact of low-frequency variants on the phenotypic landscape at population-scale. ''Elife''. 2019 Oct 24; '''8''':
Gene-set association and epistatic analyses reveal complex gene interaction networks affecting flowering time in a worldwide barley collection. Description: He, Tianhua, et al. Gene-set association and epistatic analyses reveal complex gene interaction networks affecting flowering time in a worldwide barley collection. ''J Exp Bot''. 2019 Oct 24; '''70''' (20):5603-5616
Genetic mapping and evolutionary analysis of human-expanded cognitive networks. Description: Wei, Yongbin, et al. Genetic mapping and evolutionary analysis of human-expanded cognitive networks. ''Nat Commun''. 2019 Oct 24; '''10''' (1):4839
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Description: Gallagher, C S, et al. Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. ''Nat Commun''. 2019 Oct 24; '''10''' (1):4857
HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases. Description: Jordan, Daniel M, et al. HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases. ''Genome Biol''. 2019 Oct 25; '''20''' (1):222
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders. Description: Oetjens, M T, et al. Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders. ''Nat Commun''. 2019 Oct 25; '''10''' (1):4897
Using DNA From Mothers and Children to Study Parental Investment in Children's Educational Attainment. Description: Wertz, Jasmin, et al. Using DNA From Mothers and Children to Study Parental Investment in Children's Educational Attainment. ''Child Dev''. 2019 Oct 27;
Population Genomics of Bettongia lesueur: Admixing Increases Genetic Diversity with no Evidence of Outbreeding Depression. Description: Rick, Kate, et al. Population Genomics of Bettongia lesueur: Admixing Increases Genetic Diversity with no Evidence of Outbreeding Depression. ''Genes (Basel)''. 2019 Oct 28; '''10''' (11):
Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706). Description: Zhao, Bingxin, et al. Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706). ''Mol Psychiatry''. 2019 Oct 30;
Effects of the MAML2 genetic variants in glioma susceptibility and prognosis. Description: Zhang, Ming, et al. Effects of the MAML2 genetic variants in glioma susceptibility and prognosis. ''Biosci Rep''. 2019 Oct 30; '''39''' (10):
Exploring effective approaches for haplotype block phasing. Description: Al Bkhetan, Ziad, et al. Exploring effective approaches for haplotype block phasing. ''BMC Bioinformatics''. 2019 Oct 30; '''20''' (1):540
Identification of novel non-synonymous variants associated with type 2 diabetes-related metabolites in Korean population. Description: Park, Tae-Joon, et al. Identification of novel non-synonymous variants associated with type 2 diabetes-related metabolites in Korean population. ''Biosci Rep''. 2019 Oct 30; '''39''' (10):
Associations of autozygosity with a broad range of human phenotypes. Description: Clark, David W, et al. Associations of autozygosity with a broad range of human phenotypes. ''Nat Commun''. 2019 Oct 31; '''10''' (1):4957
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways. Description: Lopez-Isac, Elena, et al. GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways. ''Nat Commun''. 2019 Oct 31; '''10''' (1):4955
Prioritizing natural-selection signals from the deep-sequencing genomic data suggests multi-variant adaptation in Tibetan highlanders. Description: Deng, Lian, et al. Prioritizing natural-selection signals from the deep-sequencing genomic data suggests multi-variant adaptation in Tibetan highlanders. ''Natl Sci Rev''. 2019 Nov; '''6''' (6):1201-1222
Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions. Description: Nicoletti, Paola, et al. Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions. ''Clin Pharmacol Ther''. 2019 Nov; '''106''' (5):1028-1036
A 3,000-year-old Egyptian emmer wheat genome reveals dispersal and domestication history. Description: Scott, Michael F, et al. A 3,000-year-old Egyptian emmer wheat genome reveals dispersal and domestication history. ''Nat Plants''. 2019 Nov; '''5''' (11):1120-1128
A Mechanogenetic Model of Exercise-Induced Pulmonary Haemorrhage in the Thoroughbred Horse. Description: Blott, Sarah, et al. A Mechanogenetic Model of Exercise-Induced Pulmonary Haemorrhage in the Thoroughbred Horse. ''Genes (Basel)''. 2019 Nov 1; '''10''' (11):
An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations. Description: Dube, Umber, et al. An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations. ''Nat Neurosci''. 2019 Nov; '''22''' (11):1903-1912
Association between ACYP2 polymorphisms and the risk of renal cell cancer. Description: Wang, Yuhe, et al. Association between ACYP2 polymorphisms and the risk of renal cell cancer. ''Mol Genet Genomic Med''. 2019 Nov; '''7''' (11):e966
Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia. Description: Horsdal, Henriette Thisted, et al. Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia. ''JAMA Netw Open''. 2019 Nov 1; '''2''' (11):e1914401
Association of IL18 genetic polymorphisms with Chagas disease in Latin American populations. Description: Strauss, Mariana, et al. Association of IL18 genetic polymorphisms with Chagas disease in Latin American populations. ''PLoS Negl Trop Dis''. 2019 Nov; '''13''' (11):e0007859
Association of sirtuin 1 gene polymorphisms with nephrolithiasis in Eastern chinese population. Description: Hou, Jiebin, et al. Association of sirtuin 1 gene polymorphisms with nephrolithiasis in Eastern chinese population. ''Ren Fail''. 2019 Nov; '''41''' (1):34-41
Biological characterization of expression quantitative trait loci (eQTLs) showing tissue-specific opposite directional effects. Description: Mizuno, Akira, et al. Biological characterization of expression quantitative trait loci (eQTLs) showing tissue-specific opposite directional effects. ''Eur J Hum Genet''. 2019 Nov; '''27''' (11):1745-1756
Comparison of genomic predictions for carcass and reproduction traits in Berkshire, Duroc and Yorkshire populations in Korea. Description: Iqbal, Asif, et al. Comparison of genomic predictions for carcass and reproduction traits in Berkshire, Duroc and Yorkshire populations in Korea. ''Asian-Australas J Anim Sci''. 2019 Nov; '''32''' (11):1657-1663
Discovery and validation of plasma proteomic biomarkers relating to brain amyloid burden by SOMAscan assay. Description: Shi, Liu, et al. Discovery and validation of plasma proteomic biomarkers relating to brain amyloid burden by SOMAscan assay. ''Alzheimers Dement''. 2019 Nov; '''15''' (11):1478-1488
Effects of CDKN2B-AS1 polymorphisms on the susceptibility to coronary heart disease. Description: Huang, Kang, et al. Effects of CDKN2B-AS1 polymorphisms on the susceptibility to coronary heart disease. ''Mol Genet Genomic Med''. 2019 Nov; '''7''' (11):e955
Evaluation of the major histocompatibility complex (MHC) class II as a candidate for sudden acquired retinal degeneration syndrome (SARDS) in Dachshunds. Description: Stromberg, Stephanie J, et al. Evaluation of the major histocompatibility complex (MHC) class II as a candidate for sudden acquired retinal degeneration syndrome (SARDS) in Dachshunds. ''Vet Ophthalmol''. 2019 Nov; '''22''' (6):751-759
Eye color prediction using single nucleotide polymorphisms in Saudi population. Description: Alghamdi, Jahad, et al. Eye color prediction using single nucleotide polymorphisms in Saudi population. ''Saudi J Biol Sci''. 2019 Nov; '''26''' (7):1607-1612
Genetic analyses supporting colorectal, gastric, and prostate cancer syndromes. Description: Wallander, Karin, et al. Genetic analyses supporting colorectal, gastric, and prostate cancer syndromes. ''Genes Chromosomes Cancer''. 2019 Nov; '''58''' (11):775-782
Genetic history of the population of Crete. Description: Drineas, Petros, et al. Genetic history of the population of Crete. ''Ann Hum Genet''. 2019 Nov; '''83''' (6):373-388
Genome-wide association analyses reveal the genetic basis of combining ability in rice. Description: Chen, Junxiao, et al. Genome-wide association analyses reveal the genetic basis of combining ability in rice. ''Plant Biotechnol J''. 2019 Nov; '''17''' (11):2211-2222
Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits. Description: Zhao, Bingxin, et al. Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits. ''Nat Genet''. 2019 Nov; '''51''' (11):1637-1644
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease. Description: Klarin, Derek, et al. Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease. ''Nat Genet''. 2019 Nov; '''51''' (11):1574-1579
Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population. Description: Otsuka, Ikuo, et al. Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population. ''Neuropsychopharmacology''. 2019 Nov; '''44''' (12):2119-2124
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions. Description: Halachev, Mihail, et al. Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions. ''PLoS Genet''. 2019 Nov; '''15''' (11):e1008480
In search of causal pathways in diabetes: a study using proteomics and genotyping data from a cross-sectional study. Description: Beijer, Kristina, et al. In search of causal pathways in diabetes: a study using proteomics and genotyping data from a cross-sectional study. ''Diabetologia''. 2019 Nov; '''62''' (11):1998-2006
Leveraging Human Genetics to Estimate Clinical Risk Reductions Achievable by Inhibiting Factor XI. Description: Georgi, Benjamin, et al. Leveraging Human Genetics to Estimate Clinical Risk Reductions Achievable by Inhibiting Factor XI. ''Stroke''. 2019 Nov; '''50''' (11):3004-3012
Physiological and genomic evidence that selection on the transcription factor Epas1 has altered cardiovascular function in high-altitude deer mice. Description: Schweizer, Rena M, et al. Physiological and genomic evidence that selection on the transcription factor Epas1 has altered cardiovascular function in high-altitude deer mice. ''PLoS Genet''. 2019 Nov; '''15''' (11):e1008420
Polygenic burden in focal and generalized epilepsies. Description: Leu, Costin, et al. Polygenic burden in focal and generalized epilepsies. ''Brain''. 2019 Nov 1; '''142''' (11):3473-3481
Scaling computational genomics to millions of individuals with GPUs. Description: Taylor-Weiner, Amaro, et al. Scaling computational genomics to millions of individuals with GPUs. ''Genome Biol''. 2019 Nov 1; '''20''' (1):228
TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes. Description: Ganmore, Ithamar, et al. TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes. ''Sci Rep''. 2019 Nov 1; '''9''' (1):15818
The genetic variants in calcium signaling related genes influence anti-tuberculosis drug induced liver injury: A prospective study. Description: Lyu, Mengyuan, et al. The genetic variants in calcium signaling related genes influence anti-tuberculosis drug induced liver injury: A prospective study. ''Medicine (Baltimore)''. 2019 Nov; '''98''' (44):e17821
UMAP reveals cryptic population structure and phenotype heterogeneity in large genomic cohorts. Description: Diaz-Papkovich, Alex, et al. UMAP reveals cryptic population structure and phenotype heterogeneity in large genomic cohorts. ''PLoS Genet''. 2019 Nov; '''15''' (11):e1008432
Cox regression increases power to detect genotype-phenotype associations in genomic studies using the electronic health record. Description: Hughey, Jacob J, et al. Cox regression increases power to detect genotype-phenotype associations in genomic studies using the electronic health record. ''BMC Genomics''. 2019 Nov 4; '''20''' (1):805
Biomarker Research in ADHD: the Impact of Nutrition (BRAIN) - study protocol of an open-label trial to investigate the mechanisms underlying the effects of a few-foods diet on ADHD symptoms in children. Description: Stobernack, Tim, et al. Biomarker Research in ADHD: the Impact of Nutrition (BRAIN) - study protocol of an open-label trial to investigate the mechanisms underlying the effects of a few-foods diet on ADHD symptoms in children. ''BMJ Open''. 2019 Nov 5; '''9''' (11):e029422
Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design. Description: Rokita, Jo Lynne, et al. Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design. ''Cell Rep''. 2019 Nov 5; '''29''' (6):1675-1689.e9
Single-Step Genome-Wide Association Study for Resistance to Piscirickettsia salmonis in Rainbow Trout (Oncorhynchus mykiss). Description: Barria, Agustin, et al. Single-Step Genome-Wide Association Study for Resistance to Piscirickettsia salmonis in Rainbow Trout (Oncorhynchus mykiss). ''G3 (Bethesda)''. 2019 Nov 5; '''9''' (11):3833-3841
Genome-Wide Association Analyses of Equine Metabolic Syndrome Phenotypes in Welsh Ponies and Morgan Horses. Description: Norton, Elaine, et al. Genome-Wide Association Analyses of Equine Metabolic Syndrome Phenotypes in Welsh Ponies and Morgan Horses. ''Genes (Basel)''. 2019 Nov 6; '''10''' (11):
A Study of Genomic Prediction of 12 Important Traits in the Domesticated Yak (Bos grunniens). Description: Fu, Donghai, et al. A Study of Genomic Prediction of 12 Important Traits in the Domesticated Yak (Bos grunniens). ''Animals (Basel)''. 2019 Nov 7; '''9''' (11):
Genome-wide association study of milk and reproductive traits in dual-purpose Xinjiang Brown cattle. Description: Zhou, Jinghang, et al. Genome-wide association study of milk and reproductive traits in dual-purpose Xinjiang Brown cattle. ''BMC Genomics''. 2019 Nov 8; '''20''' (1):827
Improved polygenic prediction by Bayesian multiple regression on summary statistics. Description: Lloyd-Jones, Luke R, et al. Improved polygenic prediction by Bayesian multiple regression on summary statistics. ''Nat Commun''. 2019 Nov 8; '''10''' (1):5086
Association between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank. Description: Cordova-Palomera, Aldo, et al. Association between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank. ''Sci Rep''. 2019 Nov 11; '''9''' (1):16515
Genome-wide association study identifies SIAH3 locus influencing the rate of ventricular enlargement in non-demented elders. Description: Li, Xian, et al. Genome-wide association study identifies SIAH3 locus influencing the rate of ventricular enlargement in non-demented elders. ''Aging (Albany NY)''. 2019 Nov 11; '''11''' (21):9862-9874
Polygenic burden associated to oligodendrocyte precursor cells and radial glia influences the hippocampal volume changes induced by aerobic exercise in schizophrenia patients. Description: Papiol, Sergi, et al. Polygenic burden associated to oligodendrocyte precursor cells and radial glia influences the hippocampal volume changes induced by aerobic exercise in schizophrenia patients. ''Transl Psychiatry''. 2019 Nov 11; '''9''' (1):284
A New Lineage of Cryptococcus gattii (VGV) Discovered in the Central Zambezian Miombo Woodlands. Description: Farrer, Rhys A, et al. A New Lineage of Cryptococcus gattii (VGV) Discovered in the Central Zambezian Miombo Woodlands. ''MBio''. 2019 Nov 12; '''10''' (6):
Genetic polymorphisms associated with sleep-related phenotypes; relationships with individual nocturnal symptoms of insomnia in the HUNT study. Description: Bragantini, Daniela, et al. Genetic polymorphisms associated with sleep-related phenotypes; relationships with individual nocturnal symptoms of insomnia in the HUNT study. ''BMC Med Genet''. 2019 Nov 12; '''20''' (1):179
Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status. Description: Lyons, Paul A, et al. Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status. ''Nat Commun''. 2019 Nov 12; '''10''' (1):5120
Mining candidate gene for rice aluminum tolerance through genome wide association study and transcriptomic analysis. Description: Zhang, Peng, et al. Mining candidate gene for rice aluminum tolerance through genome wide association study and transcriptomic analysis. ''BMC Plant Biol''. 2019 Nov 12; '''19''' (1):490
Candidate Gene and Genome-Wide Association Studies for Circulating Leptin Levels Reveal Population and Sex-Specific Associations in High Cardiovascular Risk Mediterranean Subjects. Description: Ortega-Azorin, Carolina, et al. Candidate Gene and Genome-Wide Association Studies for Circulating Leptin Levels Reveal Population and Sex-Specific Associations in High Cardiovascular Risk Mediterranean Subjects. ''Nutrients''. 2019 Nov 13; '''11''' (11):
Comprehensive genome and transcriptome analyses reveal genetic relationship, selection signature, and transcriptome landscape of small-sized Korean native Jeju horse. Description: Srikanth, Krishnamoorthy, et al. Comprehensive genome and transcriptome analyses reveal genetic relationship, selection signature, and transcriptome landscape of small-sized Korean native Jeju horse. ''Sci Rep''. 2019 Nov 13; '''9''' (1):16672
Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer's disease. Description: Saez, M E, et al. Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer's disease. ''Sci Rep''. 2019 Nov 13; '''9''' (1):16665
Improved power and precision with whole genome sequencing data in genome-wide association studies of inflammatory biomarkers. Description: Hoglund, Julia, et al. Improved power and precision with whole genome sequencing data in genome-wide association studies of inflammatory biomarkers. ''Sci Rep''. 2019 Nov 14; '''9''' (1):16844
Novel risk genes and mechanisms implicated by exome sequencing of 2572 individuals with pulmonary arterial hypertension. Description: Zhu, Na, et al. Novel risk genes and mechanisms implicated by exome sequencing of 2572 individuals with pulmonary arterial hypertension. ''Genome Med''. 2019 Nov 14; '''11''' (1):69
Type 1 diabetes loci display a variety of native American and African ancestries in diseased individuals from Northwest Colombia. Description: Gomez-Lopera, Natalia, et al. Type 1 diabetes loci display a variety of native American and African ancestries in diseased individuals from Northwest Colombia. ''World J Diabetes''. 2019 Nov 15; '''10''' (11):534-545
Genome-Wide Runs of Homozygosity, Effective Population Size, and Detection of Positive Selection Signatures in Six Chinese Goat Breeds. Description: Islam, Rabiul, et al. Genome-Wide Runs of Homozygosity, Effective Population Size, and Detection of Positive Selection Signatures in Six Chinese Goat Breeds. ''Genes (Basel)''. 2019 Nov 17; '''10''' (11):
Genomic Patterns of Homozygosity in Chinese Local Cattle. Description: Xu, Lingyang, et al. Genomic Patterns of Homozygosity in Chinese Local Cattle. ''Sci Rep''. 2019 Nov 18; '''9''' (1):16977
Genome-Wide Association Study of Body Mass Index and Body Fat in Mexican-Mestizo Children. Description: Costa-Urrutia, Paula, et al. Genome-Wide Association Study of Body Mass Index and Body Fat in Mexican-Mestizo Children. ''Genes (Basel)''. 2019 Nov 19; '''10''' (11):
Exome resequencing and GWAS for growth, ecophysiology, and chemical and metabolomic composition of wood of Populus trichocarpa. Description: Guerra, Fernando P, et al. Exome resequencing and GWAS for growth, ecophysiology, and chemical and metabolomic composition of wood of Populus trichocarpa. ''BMC Genomics''. 2019 Nov 20; '''20''' (1):875
Identification of novel common variants associated with chronic pain using conditional false discovery rate analysis with major depressive disorder and assessment of pleiotropic effects of LRFN5. Description: Johnston, Keira J A, et al. Identification of novel common variants associated with chronic pain using conditional false discovery rate analysis with major depressive disorder and assessment of pleiotropic effects of LRFN5. ''Transl Psychiatry''. 2019 Nov 20; '''9''' (1):310
SIRT1 (rs3740051) role in pituitary adenoma development. Description: Liutkeviciene, Rasa, et al. SIRT1 (rs3740051) role in pituitary adenoma development. ''BMC Med Genet''. 2019 Nov 20; '''20''' (1):185
Comparison of Genetic Liability for Sleep Traits Among Individuals With Bipolar Disorder I or II and Control Participants. Description: Lewis, Katie J S, et al. Comparison of Genetic Liability for Sleep Traits Among Individuals With Bipolar Disorder I or II and Control Participants. ''JAMA Psychiatry''. 2019 Nov 21;
Genome-wide associated study identifies NAC42-activated nitrate transporter conferring high nitrogen use efficiency in rice. Description: Tang, Weijie, et al. Genome-wide associated study identifies NAC42-activated nitrate transporter conferring high nitrogen use efficiency in rice. ''Nat Commun''. 2019 Nov 21; '''10''' (1):5279
Identification of QTN and Candidate Gene for Seed-flooding Tolerance in Soybean [Glycine max (L.) Merr.] using Genome-Wide Association Study (GWAS). Description: Yu, Zheping, et al. Identification of QTN and Candidate Gene for Seed-flooding Tolerance in Soybean [Glycine max (L.) Merr.] using Genome-Wide Association Study (GWAS). ''Genes (Basel)''. 2019 Nov 21; '''10''' (12):
Are personalities genetically determined? Inferences from subsocial spiders. Description: Purcell, Jessica, et al. Are personalities genetically determined? Inferences from subsocial spiders. ''BMC Genomics''. 2019 Nov 22; '''20''' (1):867
Global Phylogeographic and Admixture Patterns in Grey Wolves and Genetic Legacy of An Ancient Siberian Lineage. Description: Pilot, Malgorzata, et al. Global Phylogeographic and Admixture Patterns in Grey Wolves and Genetic Legacy of An Ancient Siberian Lineage. ''Sci Rep''. 2019 Nov 22; '''9''' (1):17328
Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population. Description: Low, Siew-Kee, et al. Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population. ''Sci Rep''. 2019 Nov 22; '''9''' (1):17332
Genome-wide association study of hippocampal atrophy rate in non-demented elders. Description: Guo, Yu, et al. Genome-wide association study of hippocampal atrophy rate in non-demented elders. ''Aging (Albany NY)''. 2019 Nov 23; '''11''' (22):10468-10484
Impact of AKAP6 polymorphisms on Glioma susceptibility and prognosis. Description: Zhang, Ming, et al. Impact of AKAP6 polymorphisms on Glioma susceptibility and prognosis. ''BMC Neurol''. 2019 Nov 23; '''19''' (1):296
Two functional variants at 6p21.1 were associated with lean mass. Description: Pei, Yu-Fang, et al. Two functional variants at 6p21.1 were associated with lean mass. ''Skelet Muscle''. 2019 Nov 23; '''9''' (1):28
A Combined Linkage and GWAS Analysis Identifies QTLs Linked to Soybean Seed Protein and Oil Content. Description: Zhang, Tengfei, et al. A Combined Linkage and GWAS Analysis Identifies QTLs Linked to Soybean Seed Protein and Oil Content. ''Int J Mol Sci''. 2019 Nov 25; '''20''' (23):
Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk. Description: Vijayakrishnan, Jayaram, et al. Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk. ''Nat Commun''. 2019 Nov 25; '''10''' (1):5348
Quantitative Trait Module-Based Genetic Analysis of Alzheimer's Disease. Description: Yuan, Shaoxun, et al. Quantitative Trait Module-Based Genetic Analysis of Alzheimer's Disease. ''Int J Mol Sci''. 2019 Nov 25; '''20''' (23):
Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds. Description: Guo, Jiazhong, et al. Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds. ''Genet Sel Evol''. 2019 Nov 26; '''51''' (1):70
Novel genetic loci affecting facial shape variation in humans. Description: Xiong, Ziyi, et al. Novel genetic loci affecting facial shape variation in humans. ''Elife''. 2019 Nov 26; '''8''':
Calcium-sensing receptor gene (CASR) polymorphisms and CASR transcript level concerning dyslipidemia in hemodialysis patients: a cross-sectional study. Description: Grzegorzewska, Alicja E, et al. Calcium-sensing receptor gene (CASR) polymorphisms and CASR transcript level concerning dyslipidemia in hemodialysis patients: a cross-sectional study. ''BMC Nephrol''. 2019 Nov 27; '''20''' (1):436
Genome-wide association study reveals genomic regions controlling root and shoot traits at late growth stages in wheat. Description: Li, Long, et al. Genome-wide association study reveals genomic regions controlling root and shoot traits at late growth stages in wheat. ''Ann Bot''. 2019 Nov 27; '''124''' (6):993-1006
Genomic Divergence in Swedish Warmblood Horses Selected for Equestrian Disciplines. Description: Ablondi, Michela, et al. Genomic Divergence in Swedish Warmblood Horses Selected for Equestrian Disciplines. ''Genes (Basel)''. 2019 Nov 27; '''10''' (12):
Polygenic approaches to detect gene-environment interactions when external information is unavailable. Description: Lin, Wan-Yu, et al. Polygenic approaches to detect gene-environment interactions when external information is unavailable. ''Brief Bioinform''. 2019 Nov 27; '''20''' (6):2236-2252
Root and shoot variation in relation to potential intermittent drought adaptation of Mesoamerican wild common bean (Phaseolus vulgaris L.). Description: Berny Mier Y Teran, Jorge C, et al. Root and shoot variation in relation to potential intermittent drought adaptation of Mesoamerican wild common bean (Phaseolus vulgaris L.). ''Ann Bot''. 2019 Nov 27; '''124''' (6):917-932
A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. Description: Chernus, Jonathan M, et al. A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. ''PLoS Genet''. 2019 Dec; '''15''' (12):e1008414
Accuracies of genomic prediction for twenty economically important traits in Chinese Simmental beef cattle. Description: Zhu, B, et al. Accuracies of genomic prediction for twenty economically important traits in Chinese Simmental beef cattle. ''Anim Genet''. 2019 Dec; '''50''' (6):634-643
Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy. Description: Stevelink, Remi, et al. Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy. ''Mol Genet Metab Rep''. 2019 Dec; '''21''': 100518
Association of Variants in the CP, ATOX1 and COMMD1 Genes with Wilson Disease Symptoms in Latvia. Description: Zarina, A, et al. Association of Variants in the CP, ATOX1 and COMMD1 Genes with Wilson Disease Symptoms in Latvia. ''Balkan J Med Genet''. 2019 Dec; '''22''' (2):37-42
Associations between rare microglia-linked Alzheimer's disease risk variants and subcortical brain volumes in young individuals. Description: Lancaster, Thomas M. Associations between rare microglia-linked Alzheimer's disease risk variants and subcortical brain volumes in young individuals. ''Alzheimers Dement (Amst)''. 2019 Dec; '''11''': 368-373
Dissection of soybean populations according to selection signatures based on whole-genome sequences. Description: Kim, Jae-Yoon, et al. Dissection of soybean populations according to selection signatures based on whole-genome sequences. ''Gigascience''. 2019 Dec 1; '''8''' (12):
Educational attainment and allostatic load in later life: Evidence using genetic markers. Description: Ding, Xuejie, et al. Educational attainment and allostatic load in later life: Evidence using genetic markers. ''Prev Med''. 2019 Dec; '''129''': 105866
Ethnic differences in prevalence of Dupuytren disease can partly be explained by known genetic risk variants. Description: Riesmeijer, Sophie A, et al. Ethnic differences in prevalence of Dupuytren disease can partly be explained by known genetic risk variants. ''Eur J Hum Genet''. 2019 Dec; '''27''' (12):1876-1884
Evaluation of Genomic Selection for Seven Economic Traits in Yellow Drum (Nibea albiflora). Description: Liu, Guijia, et al. Evaluation of Genomic Selection for Seven Economic Traits in Yellow Drum (Nibea albiflora). ''Mar Biotechnol (NY)''. 2019 Dec; '''21''' (6):806-812
Gene-level genome-wide association analysis of suicide attempt, a preliminary study in a psychiatric Mexican population. Description: Gonzalez-Castro, Thelma Beatriz, et al. Gene-level genome-wide association analysis of suicide attempt, a preliminary study in a psychiatric Mexican population. ''Mol Genet Genomic Med''. 2019 Dec; '''7''' (12):e983
Genetic dissection of complex behaviour traits in German Shepherd dogs. Description: Friedrich, Juliane, et al. Genetic dissection of complex behaviour traits in German Shepherd dogs. ''Heredity (Edinb)''. 2019 Dec; '''123''' (6):746-758
Genetic diversity of laboratory strains and implications for research: The case of Aedes aegypti. Description: Gloria-Soria, Andrea, et al. Genetic diversity of laboratory strains and implications for research: The case of Aedes aegypti. ''PLoS Negl Trop Dis''. 2019 Dec; '''13''' (12):e0007930
Genetic risk score predicts risk for overweight and obesity in Finnish preadolescents. Description: Viljakainen, Heli, et al. Genetic risk score predicts risk for overweight and obesity in Finnish preadolescents. ''Clin Obes''. 2019 Dec; '''9''' (6):e12342
Genetics of diabetic kidney disease: A follow-up study in the Arab population of the United Arab Emirates. Description: Osman, Wael M, et al. Genetics of diabetic kidney disease: A follow-up study in the Arab population of the United Arab Emirates. ''Mol Genet Genomic Med''. 2019 Dec; '''7''' (12):e985
Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children. Description: Kampe, Anders, et al. Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children. ''PLoS Genet''. 2019 Dec; '''15''' (12):e1008530
Genome of 'Charleston Gray', the principal American watermelon cultivar, and genetic characterization of 1,365 accessions in the U.S. National Plant Germplasm System watermelon collection. Description: Wu, Shan, et al. Genome of 'Charleston Gray', the principal American watermelon cultivar, and genetic characterization of 1,365 accessions in the U.S. National Plant Germplasm System watermelon collection. ''Plant Biotechnol J''. 2019 Dec; '''17''' (12):2246-2258
Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema. Description: Johansson, Asa, et al. Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema. ''Hum Mol Genet''. 2019 Dec 1; '''28''' (23):4022-4041
Genomewide Association Study of Statin-Induced Myopathy in Patients Recruited Using the UK Clinical Practice Research Datalink. Description: Carr, Daniel F, et al. Genomewide Association Study of Statin-Induced Myopathy in Patients Recruited Using the UK Clinical Practice Research Datalink. ''Clin Pharmacol Ther''. 2019 Dec; '''106''' (6):1353-1361
Genomic and clinical predictors of lacosamide response in refractory epilepsies. Description: Heavin, Sinead B, et al. Genomic and clinical predictors of lacosamide response in refractory epilepsies. ''Epilepsia Open''. 2019 Dec; '''4''' (4):563-571
Genomic Prediction and Association Analysis with Models Including Dominance Effects for Important Traits in Chinese Simmental Beef Cattle. Description: Liu, Ying, et al. Genomic Prediction and Association Analysis with Models Including Dominance Effects for Important Traits in Chinese Simmental Beef Cattle. ''Animals (Basel)''. 2019 Dec 1; '''9''' (12):
Homogeneity in the association of body mass index with type 2 diabetes across the UK Biobank: A Mendelian randomization study. Description: Wainberg, Michael, et al. Homogeneity in the association of body mass index with type 2 diabetes across the UK Biobank: A Mendelian randomization study. ''PLoS Med''. 2019 Dec; '''16''' (12):e1002982
Identification of TYW3/CRYZ and FGD4 as susceptibility genes for amyotrophic lateral sclerosis. Description: Wei, Ling, et al. Identification of TYW3/CRYZ and FGD4 as susceptibility genes for amyotrophic lateral sclerosis. ''Neurol Genet''. 2019 Dec; '''5''' (6):e375
Landscape drivers of genomic diversity and divergence in woodland Eucalyptus. Description: Murray, Kevin D, et al. Landscape drivers of genomic diversity and divergence in woodland Eucalyptus. ''Mol Ecol''. 2019 Dec; '''28''' (24):5232-5247
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies. Description: Zhang, Li, et al. LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies. ''Hum Mutat''. 2019 Dec; '''40''' (12):2221-2229
Mendelian randomization study of telomere length and lung cancer risk in East Asian population. Description: Cao, Xuguang, et al. Mendelian randomization study of telomere length and lung cancer risk in East Asian population. ''Cancer Med''. 2019 Dec; '''8''' (17):7469-7476
Migraine polygenic risk score associates with efficacy of migraine-specific drugs. Description: Kogelman, Lisette J A, et al. Migraine polygenic risk score associates with efficacy of migraine-specific drugs. ''Neurol Genet''. 2019 Dec; '''5''' (6):e364
Morphological and molecular characterization of freshwater prawn of genus Macrobrachium in the coastal area of Cameroon. Description: Makombu, Judith G, et al. Morphological and molecular characterization of freshwater prawn of genus Macrobrachium in the coastal area of Cameroon. ''Ecol Evol''. 2019 Dec; '''9''' (24):14217-14233
Recapitulation of previously reported associations for type 2 diabetes and metabolic traits in the 126K East Asians. Description: Choi, Ji-Young, et al. Recapitulation of previously reported associations for type 2 diabetes and metabolic traits in the 126K East Asians. ''Genomics Inform''. 2019 Dec; '''17''' (4):e48
Sex is determined by XY chromosomes across the radiation of dioecious Nepenthes pitcher plants. Description: Scharmann, Mathias, et al. Sex is determined by XY chromosomes across the radiation of dioecious Nepenthes pitcher plants. ''Evol Lett''. 2019 Dec; '''3''' (6):586-597
Stable longitudinal associations of family income with children's hippocampal volume and memory persist after controlling for polygenic scores of educational attainment. Description: Raffington, Laurel, et al. Stable longitudinal associations of family income with children's hippocampal volume and memory persist after controlling for polygenic scores of educational attainment. ''Dev Cogn Neurosci''. 2019 Dec; '''40''': 100720
Subclinical atherosclerosis and its progression are modulated by PLIN2 through a feed-forward loop between LXR and autophagy. Description: Saliba-Gustafsson, P, et al. Subclinical atherosclerosis and its progression are modulated by PLIN2 through a feed-forward loop between LXR and autophagy. ''J Intern Med''. 2019 Dec; '''286''' (6):660-675
TASUKE+: a web-based platform for exploring genome-wide association studies results and large-scale resequencing data. Description: Kumagai, Masahiko, et al. TASUKE+: a web-based platform for exploring genome-wide association studies results and large-scale resequencing data. ''DNA Res''. 2019 Dec 1; '''26''' (6):445-452
The combined use of raw and phylogenetically independent methods of outlier detection uncovers genome-wide dynamics of local adaptation in a lizard. Description: Llanos-Garrido, Alejandro, et al. The combined use of raw and phylogenetically independent methods of outlier detection uncovers genome-wide dynamics of local adaptation in a lizard. ''Ecol Evol''. 2019 Dec; '''9''' (24):14356-14367
The Current Genomic Landscape of Western South America: Andes, Amazonia, and Pacific Coast. Description: Barbieri, Chiara, et al. The Current Genomic Landscape of Western South America: Andes, Amazonia, and Pacific Coast. ''Mol Biol Evol''. 2019 Dec 1; '''36''' (12):2698-2713
The Genetic Links to Anxiety and Depression (GLAD) Study: Online recruitment into the largest recontactable study of depression and anxiety. Description: Davies, Molly R, et al. The Genetic Links to Anxiety and Depression (GLAD) Study: Online recruitment into the largest recontactable study of depression and anxiety. ''Behav Res Ther''. 2019 Dec; '''123''': 103503
The GenomeAsia 100K Project enables genetic discoveries across Asia. Description: The GenomeAsia 100K Project enables genetic discoveries across Asia. ''Nature''. 2019 Dec; '''576''' (7785):106-111
The impact of the genetic background on gene deletion phenotypes in Saccharomyces cerevisiae. Description: Galardini, Marco, et al. The impact of the genetic background on gene deletion phenotypes in Saccharomyces cerevisiae. ''Mol Syst Biol''. 2019 Dec; '''15''' (12):e8831
The polyamine transporter Slc18b1(VPAT) is important for both short and long time memory and for regulation of polyamine content in the brain. Description: Fredriksson, Robert, et al. The polyamine transporter Slc18b1(VPAT) is important for both short and long time memory and for regulation of polyamine content in the brain. ''PLoS Genet''. 2019 Dec; '''15''' (12):e1008455
Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis. Description: Wong, Karen H Y, et al. Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis. ''Mol Genet Genomic Med''. 2019 Dec; '''7''' (12):e1007
Assessment of kinship detection using RNA-seq data. Description: Blay, Natalia, et al. Assessment of kinship detection using RNA-seq data. ''Nucleic Acids Res''. 2019 Dec 2; '''47''' (21):e136
A Weighted Genetic Risk Score of Adult Glioma Susceptibility Loci Associated with Pediatric Brain Tumor Risk. Description: Adel Fahmideh, Maral, et al. A Weighted Genetic Risk Score of Adult Glioma Susceptibility Loci Associated with Pediatric Brain Tumor Risk. ''Sci Rep''. 2019 Dec 2; '''9''' (1):18142
Population history and genetic adaptation of the Fulani nomads: inferences from genome-wide data and the lactase persistence trait. Description: Vicente, Mario, et al. Population history and genetic adaptation of the Fulani nomads: inferences from genome-wide data and the lactase persistence trait. ''BMC Genomics''. 2019 Dec 2; '''20''' (1):915
Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease. Description: Dennis, Jessica, et al. Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease. ''Mol Psychiatry''. 2019 Dec 3;
Deep sampling of Hawaiian Caenorhabditis elegans reveals high genetic diversity and admixture with global populations. Description: Crombie, Tim A, et al. Deep sampling of Hawaiian Caenorhabditis elegans reveals high genetic diversity and admixture with global populations. ''Elife''. 2019 Dec 3; '''8''':
Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death. Description: Mitchell, Rebecca N, et al. Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death. ''J Am Heart Assoc''. 2019 Dec 3; '''8''' (23):e013751
Machine Learning Enables High-Throughput Phenotyping for Analyses of the Genetic Architecture of Bulliform Cell Patterning in Maize. Description: Qiao, Pengfei, et al. Machine Learning Enables High-Throughput Phenotyping for Analyses of the Genetic Architecture of Bulliform Cell Patterning in Maize. ''G3 (Bethesda)''. 2019 Dec 3; '''9''' (12):4235-4243
Phenotypic and molecular assessment of genetic structure and diversity in a panel of winged yam (Dioscorea alata) clones and cultivars. Description: Agre, Paterne, et al. Phenotypic and molecular assessment of genetic structure and diversity in a panel of winged yam (Dioscorea alata) clones and cultivars. ''Sci Rep''. 2019 Dec 3; '''9''' (1):18221
Population genomics of two congeneric Palaearctic shorebirds reveals differential impacts of Quaternary climate oscillations across habitats types. Description: Tan, Hui Zhen, et al. Population genomics of two congeneric Palaearctic shorebirds reveals differential impacts of Quaternary climate oscillations across habitats types. ''Sci Rep''. 2019 Dec 3; '''9''' (1):18172
The myopia susceptibility locus vasoactive intestinal peptide receptor 2 (VIPR2) contains variants with opposite effects. Description: Leung, Kim Hung, et al. The myopia susceptibility locus vasoactive intestinal peptide receptor 2 (VIPR2) contains variants with opposite effects. ''Sci Rep''. 2019 Dec 3; '''9''' (1):18165
Association of Leukotriene A4 Hydrolase with Tuberculosis Susceptibility Using Genomic Data in Portugal. Description: Rito, Teresa, et al. Association of Leukotriene A4 Hydrolase with Tuberculosis Susceptibility Using Genomic Data in Portugal. ''Microorganisms''. 2019 Dec 4; '''7''' (12):
Genome-wide association and genotype by environment interactions for growth traits in U.S. Gelbvieh cattle. Description: Smith, Johanna L, et al. Genome-wide association and genotype by environment interactions for growth traits in U.S. Gelbvieh cattle. ''BMC Genomics''. 2019 Dec 4; '''20''' (1):926
Trio deep-sequencing does not reveal unexpected off-target and on-target mutations in Cas9-edited rhesus monkeys. Description: Luo, Xin, et al. Trio deep-sequencing does not reveal unexpected off-target and on-target mutations in Cas9-edited rhesus monkeys. ''Nat Commun''. 2019 Dec 4; '''10''' (1):5525
Genomic prediction based on selected variants from imputed whole-genome sequence data in Australian sheep populations. Description: Moghaddar, Nasir, et al. Genomic prediction based on selected variants from imputed whole-genome sequence data in Australian sheep populations. ''Genet Sel Evol''. 2019 Dec 5; '''51''' (1):72
Combining information from genome-wide association and multi-tissue gene expression studies to elucidate factors underlying genetic variation for residual feed intake in Australian Angus cattle. Description: de Las Heras-Saldana, Sara, et al. Combining information from genome-wide association and multi-tissue gene expression studies to elucidate factors underlying genetic variation for residual feed intake in Australian Angus cattle. ''BMC Genomics''. 2019 Dec 6; '''20''' (1):939
A Gene-Environment Interaction Between Smoking and Gene polymorphisms Provides a High Risk of Two Subgroups of Sarcoidosis. Description: Rivera, Natalia V, et al. A Gene-Environment Interaction Between Smoking and Gene polymorphisms Provides a High Risk of Two Subgroups of Sarcoidosis. ''Sci Rep''. 2019 Dec 9; '''9''' (1):18633
Investigating the relationship between melatonin levels, melatonin system, microbiota composition and bipolar disorder psychopathology across the different phases of the disease. Description: Manchia, Mirko, et al. Investigating the relationship between melatonin levels, melatonin system, microbiota composition and bipolar disorder psychopathology across the different phases of the disease. ''Int J Bipolar Disord''. 2019 Dec 9; '''7''' (1):27
Statistical methods for testing X chromosome variant associations: application to sex-specific characteristics of bipolar disorder. Description: Jons, William A, et al. Statistical methods for testing X chromosome variant associations: application to sex-specific characteristics of bipolar disorder. ''Biol Sex Differ''. 2019 Dec 9; '''10''' (1):57
Linking glycemic dysregulation in diabetes to symptoms, comorbidities, and genetics through EHR data mining. Description: Kirk, Isa Kristina, et al. Linking glycemic dysregulation in diabetes to symptoms, comorbidities, and genetics through EHR data mining. ''Elife''. 2019 Dec 10; '''8''':
WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene. Description: Nersisyan, Lilit, et al. WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene. ''Sci Rep''. 2019 Dec 10; '''9''' (1):18758
Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis. Description: Siitonen, Ari, et al. Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis. ''Sci Rep''. 2019 Dec 11; '''9''' (1):18865
Tempo and mode of allopatric divergence in the weakly electric fish Sternopygus dariensis in the Isthmus of Panama. Description: Aguilar, Celestino, et al. Tempo and mode of allopatric divergence in the weakly electric fish Sternopygus dariensis in the Isthmus of Panama. ''Sci Rep''. 2019 Dec 11; '''9''' (1):18828
WNT gene polymorphisms and predisposition to apical periodontitis. Description: de Souza, Leticia Chaves, et al. WNT gene polymorphisms and predisposition to apical periodontitis. ''Sci Rep''. 2019 Dec 12; '''9''' (1):18980
Genetic variations in olfactory receptor gene OR2AG2 in a large multigenerational family with asthma. Description: Chakraborty, Samarpana, et al. Genetic variations in olfactory receptor gene OR2AG2 in a large multigenerational family with asthma. ''Sci Rep''. 2019 Dec 13; '''9''' (1):19029
Benchmarking machine learning models for late-onset alzheimer's disease prediction from genomic data. Description: De Velasco Oriol, Javier, et al. Benchmarking machine learning models for late-onset alzheimer's disease prediction from genomic data. ''BMC Bioinformatics''. 2019 Dec 16; '''20''' (1):709
Level-biases in estimated breeding values due to the use of different SNP panels over time in ssGBLUP. Description: Nordbo, Oyvind, et al. Level-biases in estimated breeding values due to the use of different SNP panels over time in ssGBLUP. ''Genet Sel Evol''. 2019 Dec 16; '''51''' (1):76
An epistasis between dopaminergic and oxytocinergic systems confers risk of post-traumatic stress disorder in a traumatized Chinese cohort. Description: Zhang, Kunlin, et al. An epistasis between dopaminergic and oxytocinergic systems confers risk of post-traumatic stress disorder in a traumatized Chinese cohort. ''Sci Rep''. 2019 Dec 17; '''9''' (1):19252
An Exploratory Association Analysis of the Insulin Gene Region With Diabetes Mellitus in Two Dog Breeds. Description: Hess, Rebecka, et al. An Exploratory Association Analysis of the Insulin Gene Region With Diabetes Mellitus in Two Dog Breeds. ''J Hered''. 2019 Dec 17; '''110''' (7):793-800
Effect of Divergent Selection for Intramuscular Fat Content on Muscle Lipid Metabolism in Chickens. Description: Liu, Lu, et al. Effect of Divergent Selection for Intramuscular Fat Content on Muscle Lipid Metabolism in Chickens. ''Animals (Basel)''. 2019 Dec 18; '''10''' (1):
GBS Data Identify Pigmentation-Specific Genes of Potential Role in Skin-Photosensitization in Two Tunisian Sheep Breeds. Description: Baazaoui, Imen, et al. GBS Data Identify Pigmentation-Specific Genes of Potential Role in Skin-Photosensitization in Two Tunisian Sheep Breeds. ''Animals (Basel)''. 2019 Dec 18; '''10''' (1):
Genome-Wide Association Analysis of the Genetic Basis for Sheath Blight Resistance in Rice. Description: Zhang, Fan, et al. Genome-Wide Association Analysis of the Genetic Basis for Sheath Blight Resistance in Rice. ''Rice (N Y)''. 2019 Dec 18; '''12''' (1):93
Genome-wide association study of morbid obesity in Han Chinese. Description: Chiang, Kuang-Mao, et al. Genome-wide association study of morbid obesity in Han Chinese. ''BMC Genet''. 2019 Dec 18; '''20''' (1):97
A harlequin ichthyosis pig model with a novel ABCA12 mutation can be rescued by acitretin treatment. Description: Wang, Xiao, et al. A harlequin ichthyosis pig model with a novel ABCA12 mutation can be rescued by acitretin treatment. ''J Mol Cell Biol''. 2019 Dec 19; '''11''' (12):1029-1041
Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13. Description: Chen, Zhongzhong, et al. Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13. ''BMC Med Genomics''. 2019 Dec 19; '''12''' (1):196
Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome. Description: Jabbari, Edwin, et al. Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome. ''JAMA Neurol''. 2019 Dec 20;
G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population. Description: Wisnumurti, Dewi A, et al. G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population. ''BMC Pediatr''. 2019 Dec 20; '''19''' (1):506
Genetic Screening of Plasticity Regulating Nogo-Type Signaling Genes in Migraine. Description: Smedfors, Gabriella, et al. Genetic Screening of Plasticity Regulating Nogo-Type Signaling Genes in Migraine. ''Brain Sci''. 2019 Dec 20; '''10''' (1):
Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke. Description: Abraham, Gad, et al. Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke. ''Nat Commun''. 2019 Dec 20; '''10''' (1):5819
Exploring the Genetic Landscape of Retinal Diseases in North-Western Pakistan Reveals a High Degree of Autozygosity and a Prevalent Founder Mutation in ABCA4. Description: Rehman, Atta Ur, et al. Exploring the Genetic Landscape of Retinal Diseases in North-Western Pakistan Reveals a High Degree of Autozygosity and a Prevalent Founder Mutation in ABCA4. ''Genes (Basel)''. 2019 Dec 21; '''11''' (1):
Ecological genomics of adaptation to unpredictability in experimental rotifer populations. Description: Tarazona, Eva, et al. Ecological genomics of adaptation to unpredictability in experimental rotifer populations. ''Sci Rep''. 2019 Dec 23; '''9''' (1):19646
Integrative genomic analysis identified common regulatory networks underlying the correlation between coronary artery disease and plasma lipid levels. Description: Chen, Liuying, et al. Integrative genomic analysis identified common regulatory networks underlying the correlation between coronary artery disease and plasma lipid levels. ''BMC Cardiovasc Disord''. 2019 Dec 23; '''19''' (1):310
A multi-breed reference panel and additional rare variants maximize imputation accuracy in cattle. Description: Rowan, Troy N, et al. A multi-breed reference panel and additional rare variants maximize imputation accuracy in cattle. ''Genet Sel Evol''. 2019 Dec 26; '''51''' (1):77
Whole-Genome Signatures of Selection in Sport Horses Revealed Selection Footprints Related to Musculoskeletal System Development Processes. Description: Salek Ardestani, Siavash, et al. Whole-Genome Signatures of Selection in Sport Horses Revealed Selection Footprints Related to Musculoskeletal System Development Processes. ''Animals (Basel)''. 2019 Dec 26; '''10''' (1):
Chronic heavy alcohol consumption influences the association between genetic variants of GCK or INSR and the development of diabetes in men: A 12-year follow-up study. Description: Jang, Han Byul, et al. Chronic heavy alcohol consumption influences the association between genetic variants of GCK or INSR and the development of diabetes in men: A 12-year follow-up study. ''Sci Rep''. 2019 Dec 27; '''9''' (1):20029
Genetic dissection of canine hip dysplasia phenotypes and osteoarthritis reveals three novel loci. Description: Mikkola, Lea, et al. Genetic dissection of canine hip dysplasia phenotypes and osteoarthritis reveals three novel loci. ''BMC Genomics''. 2019 Dec 27; '''20''' (1):1027
Genetic risk score for risk prediction of diabetic nephropathy in Han Chinese type 2 diabetes patients. Description: Liao, Li-Na, et al. Genetic risk score for risk prediction of diabetic nephropathy in Han Chinese type 2 diabetes patients. ''Sci Rep''. 2019 Dec 27; '''9''' (1):19897
Haplotype in SERPINA1 (AAT) Is Associated with Reduced Risk for COPD in a Mexican Mestizo Population. Description: Ponce-Gallegos, Marco Antonio, et al. Haplotype in SERPINA1 (AAT) Is Associated with Reduced Risk for COPD in a Mexican Mestizo Population. ''Int J Mol Sci''. 2019 Dec 27; '''21''' (1):
Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Description: Al-Khelaifi, Fatima, et al. Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. ''Sci Rep''. 2019 Dec 27; '''9''' (1):19889
An ancestry informative marker panel design for individual ancestry estimation of Hispanic population using whole exome sequencing data. Description: Wang, Li-Ju, et al. An ancestry informative marker panel design for individual ancestry estimation of Hispanic population using whole exome sequencing data. ''BMC Genomics''. 2019 Dec 30; '''20''' (Suppl 12):1007
Genome-Wide Association Analysis Dissects the Genetic Basis of the Grain Carbon and Nitrogen Contents in Milled Rice. Description: Tang, Liang, et al. Genome-Wide Association Analysis Dissects the Genetic Basis of the Grain Carbon and Nitrogen Contents in Milled Rice. ''Rice (N Y)''. 2019 Dec 30; '''12''' (1):101
The VNTR 48 bp Polymorphism in the DRD4 Gene Is Associated with Higher Tobacco Smoking in Male Mexican Mestizo Smokers with and without COPD. Description: Perez-Rubio, Gloria, et al. The VNTR 48 bp Polymorphism in the DRD4 Gene Is Associated with Higher Tobacco Smoking in Male Mexican Mestizo Smokers with and without COPD. ''Diagnostics (Basel)''. 2019 Dec 30; '''10''' (1):
Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank. Description: Abul-Husn, Noura S, et al. Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank. ''Genome Med''. 2019 Dec 31; '''12''' (1):2
A Genome-Wide Association Study in Early COPD: Identification of One Major Susceptibility Loci. Description: Lee, Ye-Jin, et al. A Genome-Wide Association Study in Early COPD: Identification of One Major Susceptibility Loci. ''Int J Chron Obstruct Pulmon Dis''. 2020; '''15''': 2967-2975
Alcohol Use and Depression: A Mendelian Randomization Study From China. Description: Zhu, Chen, et al. Alcohol Use and Depression: A Mendelian Randomization Study From China. ''Front Genet''. 2020; '''11''': 585351
All thresholds of maternal hyperglycaemia from the WHO 2013 criteria for gestational diabetes identify women with a higher genetic risk for type 2 diabetes. Description: Hughes, Alice E, et al. All thresholds of maternal hyperglycaemia from the WHO 2013 criteria for gestational diabetes identify women with a higher genetic risk for type 2 diabetes. ''Wellcome Open Res''. 2020; '''5''': 175
Alzheimer Disease Pathology-Associated Polymorphism in a Complex Variable Number of Tandem Repeat Region Within the MUC6 Gene, Near the AP2A2 Gene. Description: Katsumata, Yuriko, et al. Alzheimer Disease Pathology-Associated Polymorphism in a Complex Variable Number of Tandem Repeat Region Within the MUC6 Gene, Near the AP2A2 Gene. ''J Neuropathol Exp Neurol''. 2020 Jan 1; '''79''' (1):3-21
An insight into the evolutionary history of Indonesian cattle assessed by whole genome data analysis. Description: Sudrajad, Pita, et al. An insight into the evolutionary history of Indonesian cattle assessed by whole genome data analysis. ''PLoS One''. 2020; '''15''' (11):e0241038
Association of Genes Involved in the Metabolic Pathways of Amyloid-beta and Tau Proteins With Sporadic Late-Onset Alzheimer's Disease in the Southern Han Chinese Population. Description: Xiao, Xuewen, et al. Association of Genes Involved in the Metabolic Pathways of Amyloid-beta and Tau Proteins With Sporadic Late-Onset Alzheimer's Disease in the Southern Han Chinese Population. ''Front Aging Neurosci''. 2020; '''12''': 584801
Association of PARP1-specific polymorphisms and haplotypes with non-small cell lung cancer subtypes. Description: Jin, Jing, et al. Association of PARP1-specific polymorphisms and haplotypes with non-small cell lung cancer subtypes. ''PLoS One''. 2020; '''15''' (12):e0243509
Association of the Lactase Persistence Haplotype Block With Disease Risk in Populations of European Descent. Description: Joslin, Shannon E K, et al. Association of the Lactase Persistence Haplotype Block With Disease Risk in Populations of European Descent. ''Front Genet''. 2020; '''11''': 558762
A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients. Description: Wu, Tao, et al. A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients. ''Front Genet''. 2020; '''11''': 539862
BDNF Gene's Role in Schizophrenia: From Risk Allele to Methylation Implications. Description: Fu, Xiaoqian, et al. BDNF Gene's Role in Schizophrenia: From Risk Allele to Methylation Implications. ''Front Psychiatry''. 2020; '''11''': 564277
Blood pressure and bladder cancer risk in men by use of survival analysis and in interaction with NAT2 genotype, and by Mendelian randomization analysis. Description: Teleka, Stanley, et al. Blood pressure and bladder cancer risk in men by use of survival analysis and in interaction with NAT2 genotype, and by Mendelian randomization analysis. ''PLoS One''. 2020; '''15''' (11):e0241711
Breed Ancestry, Divergence, Admixture, and Selection Patterns of the Simbra Crossbreed. Description: van der Nest, Magriet A, et al. Breed Ancestry, Divergence, Admixture, and Selection Patterns of the Simbra Crossbreed. ''Front Genet''. 2020; '''11''': 608650
Candidate Gene Analysis Reveals Strong Association of CETP Variants With High Density Lipoprotein Cholesterol and PCSK9 Variants With Low Density Lipoprotein Cholesterol in Ghanaian Adults: An AWI-Gen Sub-Study. Description: Agongo, Godfred, et al. Candidate Gene Analysis Reveals Strong Association of CETP Variants With High Density Lipoprotein Cholesterol and PCSK9 Variants With Low Density Lipoprotein Cholesterol in Ghanaian Adults: An AWI-Gen Sub-Study. ''Front Genet''. 2020; '''11''': 456661
Candidate Genes for Age at Menarche Are Associated With Uterine Leiomyoma. Description: Ponomarenko, Irina, et al. Candidate Genes for Age at Menarche Are Associated With Uterine Leiomyoma. ''Front Genet''. 2020; '''11''': 512940
Causal Effect of the Triglyceride-Glucose Index and the Joint Exposure of Higher Glucose and Triglyceride With Extensive Cardio-Cerebrovascular Metabolic Outcomes in the UK Biobank: A Mendelian Randomization Study. Description: Si, Shucheng, et al. Causal Effect of the Triglyceride-Glucose Index and the Joint Exposure of Higher Glucose and Triglyceride With Extensive Cardio-Cerebrovascular Metabolic Outcomes in the UK Biobank: A Mendelian Randomization Study. ''Front Cardiovasc Med''. 2020; '''7''': 583473
CCR5 Promoter Polymorphisms Associated With Pulmonary Tuberculosis in a Chinese Han Population. Description: Liu, Shuyuan, et al. CCR5 Promoter Polymorphisms Associated With Pulmonary Tuberculosis in a Chinese Han Population. ''Front Immunol''. 2020; '''11''': 544548
Characterization of Autozygosity in Pigs in Three-Way Crossbreeding. Description: Ganteil, Audrey, et al. Characterization of Autozygosity in Pigs in Three-Way Crossbreeding. ''Front Genet''. 2020; '''11''': 584556
Cis- and Trans-Acting Expression Quantitative Trait Loci of Long Non-Coding RNA in 2,549 Cancers With Potential Clinical and Therapeutic Implications. Description: Li, Wenzhi, et al. Cis- and Trans-Acting Expression Quantitative Trait Loci of Long Non-Coding RNA in 2,549 Cancers With Potential Clinical and Therapeutic Implications. ''Front Oncol''. 2020; '''10''': 602104
Classification of Grain Amaranths Using Chromosome-Level Genome Assembly of Ramdana, A. hypochondriacus. Description: Deb, Saptarathi, et al. Classification of Grain Amaranths Using Chromosome-Level Genome Assembly of Ramdana, A. hypochondriacus. ''Front Plant Sci''. 2020; '''11''': 579529
Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank. Description: Kolin, David A, et al. Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank. ''PLoS One''. 2020; '''15''' (11):e0241264
Comparing Genomic Signatures of Selection Between the Abbassa Strain and Eight Wild Populations of Nile Tilapia (Oreochromis niloticus) in Egypt. Description: Nayfa, Maria G, et al. Comparing Genomic Signatures of Selection Between the Abbassa Strain and Eight Wild Populations of Nile Tilapia (Oreochromis niloticus) in Egypt. ''Front Genet''. 2020; '''11''': 567969
Development and Evaluation of a High-Throughput Single-Nucleotide Polymorphism Array for Large Yellow Croaker (Larimichthys crocea). Description: Zhou, Tao, et al. Development and Evaluation of a High-Throughput Single-Nucleotide Polymorphism Array for Large Yellow Croaker (Larimichthys crocea). ''Front Genet''. 2020; '''11''': 571751
Development of SNP-Based Genomic Tools for the Canadian Bison Industry: Parentage Verification and Subspecies Composition. Description: Yang, Tianfu, et al. Development of SNP-Based Genomic Tools for the Canadian Bison Industry: Parentage Verification and Subspecies Composition. ''Front Genet''. 2020; '''11''': 585999
Dickkopf-1 Overexpression in vitro Nominates Candidate Blood Biomarkers Relating to Alzheimer's Disease Pathology. Description: Shi, Liu, et al. Dickkopf-1 Overexpression in vitro Nominates Candidate Blood Biomarkers Relating to Alzheimer's Disease Pathology. ''J Alzheimers Dis''. 2020; '''77''' (3):1353-1368
Differential admixture in Latin American populations and its impact on the study of colorectal cancer. Description: Colistro, Valentina, et al. Differential admixture in Latin American populations and its impact on the study of colorectal cancer. ''Genet Mol Biol''. 2020; '''43''' (4):e20200143
Dissecting seed pigmentation-associated genomic loci and genes by employing dual approaches of reference-based and k-mer-based GWAS with 438 Glycine accessions. Description: Kim, Jin-Hyun, et al. Dissecting seed pigmentation-associated genomic loci and genes by employing dual approaches of reference-based and k-mer-based GWAS with 438 Glycine accessions. ''PLoS One''. 2020; '''15''' (12):e0243085
Dopamine Multilocus Genetic Profile, Spontaneous Activity of Left Superior Temporal Gyrus, and Early Therapeutic Effect in Major Depressive Disorder. Description: Liu, Xiaoyun, et al. Dopamine Multilocus Genetic Profile, Spontaneous Activity of Left Superior Temporal Gyrus, and Early Therapeutic Effect in Major Depressive Disorder. ''Front Psychiatry''. 2020; '''11''': 591407
Effects of the Openness to Experience Polygenic Score on Cortical Thickness and Functional Connectivity. Description: Ren, Zhiting, et al. Effects of the Openness to Experience Polygenic Score on Cortical Thickness and Functional Connectivity. ''Front Neurosci''. 2020; '''14''': 607912
Evaluation of Polygenic Risk Scores for Prediction of Prostate Cancer in Korean Men. Description: Oh, Jong Jin, et al. Evaluation of Polygenic Risk Scores for Prediction of Prostate Cancer in Korean Men. ''Front Oncol''. 2020; '''10''': 583625
Exome Sequencing of Native Populations From the Amazon Reveals Patterns on the Peopling of South America. Description: Ribeiro-Dos-Santos, Andre M, et al. Exome Sequencing of Native Populations From the Amazon Reveals Patterns on the Peopling of South America. ''Front Genet''. 2020; '''11''': 548507
Exploring the Relationship Between Psychiatric Traits and the Risk of Mouth Ulcers Using Bi-Directional Mendelian Randomization. Description: Wang, Kai, et al. Exploring the Relationship Between Psychiatric Traits and the Risk of Mouth Ulcers Using Bi-Directional Mendelian Randomization. ''Front Genet''. 2020; '''11''': 608630
First evaluation of the population structure, genetic diversity and landscape connectivity of the Endangered Arabian tahr. Description: Ross, Steven, et al. First evaluation of the population structure, genetic diversity and landscape connectivity of the Endangered Arabian tahr. ''Mamm Biol''. 2020; '''100''' (6):659-673
Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation. Description: Koponen, Mikael, et al. Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation. ''PLoS One''. 2020; '''15''' (12):e0243649
Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients. Description: Kao, Chung-Feng, et al. Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients. ''Front Pharmacol''. 2020; '''11''': 559601
Genetic diversity and population structure of eddoe taro in China using genome-wide SNP markers. Description: Wang, Zhixin, et al. Genetic diversity and population structure of eddoe taro in China using genome-wide SNP markers. ''PeerJ''. 2020; '''8''': e10485
Genetic Diversity, Inbreeding Level, and Genetic Load in Endangered Snub-Nosed Monkeys (Rhinopithecus). Description: Kuang, Weimin, et al. Genetic Diversity, Inbreeding Level, and Genetic Load in Endangered Snub-Nosed Monkeys (Rhinopithecus). ''Front Genet''. 2020; '''11''': 615926
Genetic Diversity of Bubalus bubalis in Germany and Global Relations of Its Genetic Background. Description: Noce, Antonia, et al. Genetic Diversity of Bubalus bubalis in Germany and Global Relations of Its Genetic Background. ''Front Genet''. 2020; '''11''': 610353
Genetic liability in individuals at ultra-high risk of psychosis: A comparison study of 9 psychiatric traits. Description: Lim, Keane, et al. Genetic liability in individuals at ultra-high risk of psychosis: A comparison study of 9 psychiatric traits. ''PLoS One''. 2020; '''15''' (12):e0243104
Genetic Susceptibility to Antisynthetase Syndrome Associated With Single-Nucleotide Variants in the IL1B Gene That Lead Variation in IL-1beta Serum Levels. Description: Ponce-Gallegos, Marco Antonio, et al. Genetic Susceptibility to Antisynthetase Syndrome Associated With Single-Nucleotide Variants in the IL1B Gene That Lead Variation in IL-1beta Serum Levels. ''Front Med (Lausanne)''. 2020; '''7''': 547186
GenomeChronicler: The Personal Genome Project UK Genomic Report Generator Pipeline. Description: Guerra-Assuncao, Jose Afonso, et al. GenomeChronicler: The Personal Genome Project UK Genomic Report Generator Pipeline. ''Front Genet''. 2020; '''11''': 518644
Genome-Wide Association Analysis for Phosphorus Use Efficiency Traits in Mungbean (Vigna radiata L. Wilczek) Using Genotyping by Sequencing Approach. Description: Reddy, Venkata Ravi Prakash, et al. Genome-Wide Association Analysis for Phosphorus Use Efficiency Traits in Mungbean (Vigna radiata L. Wilczek) Using Genotyping by Sequencing Approach. ''Front Plant Sci''. 2020; '''11''': 537766
Genome-wide association analysis of Russian wheat aphid (Diuraphis noxia) resistance in Dn4 derived wheat lines evaluated in South Africa. Description: Kisten, Lavinia, et al. Genome-wide association analysis of Russian wheat aphid (Diuraphis noxia) resistance in Dn4 derived wheat lines evaluated in South Africa. ''PLoS One''. 2020; '''15''' (12):e0244455
Genome-Wide Association Mapping for Salt Tolerance of Rice Seedlings Grown in Hydroponic and Soil Systems Using the Bengal and Assam Aus Panel. Description: Chen, Caijin, et al. Genome-Wide Association Mapping for Salt Tolerance of Rice Seedlings Grown in Hydroponic and Soil Systems Using the Bengal and Assam Aus Panel. ''Front Plant Sci''. 2020; '''11''': 576479
Genome-Wide Association Studies Detect Multiple QTLs for Productivity in Mesoamerican Diversity Panel of Common Bean Under Drought Stress. Description: Valdisser, Paula Arielle Mendes Ribeiro, et al. Genome-Wide Association Studies Detect Multiple QTLs for Productivity in Mesoamerican Diversity Panel of Common Bean Under Drought Stress. ''Front Plant Sci''. 2020; '''11''': 574674
Genome Wide Association Studies in Multiple Spinach Breeding Populations Refine Downy Mildew Race 13 Resistance Genes. Description: Bhattarai, Gehendra, et al. Genome Wide Association Studies in Multiple Spinach Breeding Populations Refine Downy Mildew Race 13 Resistance Genes. ''Front Plant Sci''. 2020; '''11''': 563187
Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens. Description: Liu, Xiayi, et al. Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens. ''Front Genet''. 2020; '''11''': 613078
Genome-wide linkage analysis of families with primary hyperhidrosis. Description: Schote, Andrea B, et al. Genome-wide linkage analysis of families with primary hyperhidrosis. ''PLoS One''. 2020; '''15''' (12):e0244565
Genomic analysis of GBS data reveals genes associated with facial pigmentation in Xinyang blue-shelled layers. Description: Hou, Haobin, et al. Genomic analysis of GBS data reveals genes associated with facial pigmentation in Xinyang blue-shelled layers. ''Arch Anim Breed''. 2020; '''63''' (2):483-491
Genomic Association Study for Cognitive Impairment in Parkinson's Disease. Description: Park, Kye Won, et al. Genomic Association Study for Cognitive Impairment in Parkinson's Disease. ''Front Neurol''. 2020; '''11''': 579268
Genomic Prediction Based on SNP Functional Annotation Using Imputed Whole-Genome Sequence Data in Korean Hanwoo Cattle. Description: Lopez, Bryan Irvine M, et al. Genomic Prediction Based on SNP Functional Annotation Using Imputed Whole-Genome Sequence Data in Korean Hanwoo Cattle. ''Front Genet''. 2020; '''11''': 603822
Genomic Prediction of Additive and Dominant Effects on Wool and Blood Traits in Alpine Merino Sheep. Description: Zhu, Shaohua, et al. Genomic Prediction of Additive and Dominant Effects on Wool and Blood Traits in Alpine Merino Sheep. ''Front Vet Sci''. 2020; '''7''': 573692
Genomic Selection for Prediction of Fruit-Related Traits in Pepper (Capsicum spp.). Description: Hong, Ju-Pyo, et al. Genomic Selection for Prediction of Fruit-Related Traits in Pepper (Capsicum spp.). ''Front Plant Sci''. 2020; '''11''': 570871
Haplotype-Based, Genome-Wide Association Study Reveals Stable Genomic Regions for Grain Yield in CIMMYT Spring Bread Wheat. Description: Sehgal, Deepmala, et al. Haplotype-Based, Genome-Wide Association Study Reveals Stable Genomic Regions for Grain Yield in CIMMYT Spring Bread Wheat. ''Front Genet''. 2020; '''11''': 589490
Homozygosity Mapping Reveals Population History and Trait Architecture in Self-Incompatible Pear (Pyrus spp.). Description: Kumar, Satish, et al. Homozygosity Mapping Reveals Population History and Trait Architecture in Self-Incompatible Pear (Pyrus spp.). ''Front Plant Sci''. 2020; '''11''': 590846
How Well Can Multivariate and Univariate GWAS Distinguish Between True and Spurious Pleiotropy? Description: Fernandes, Samuel B, et al. How Well Can Multivariate and Univariate GWAS Distinguish Between True and Spurious Pleiotropy? ''Front Genet''. 2020; '''11''': 602526
Identification of Maturity-Onset Diabetes of the Young Caused by Mutation in FOXM1 via Whole-Exome Sequencing in Northern China. Description: Zhong, Liang, et al. Identification of Maturity-Onset Diabetes of the Young Caused by Mutation in FOXM1 via Whole-Exome Sequencing in Northern China. ''Front Endocrinol (Lausanne)''. 2020; '''11''': 534362
Identification of New Helicobacter pylori Subpopulations in Native Americans and Mestizos From Peru. Description: Gutierrez-Escobar, Andres Julian, et al. Identification of New Helicobacter pylori Subpopulations in Native Americans and Mestizos From Peru. ''Front Microbiol''. 2020; '''11''': 601839
Improving Genomic Prediction of Crossbred and Purebred Dairy Cattle. Description: Khansefid, Majid, et al. Improving Genomic Prediction of Crossbred and Purebred Dairy Cattle. ''Front Genet''. 2020; '''11''': 598580
Integrating Genetic and Genomic Analyses of Combined Health Data Across Ecotypes to Improve Disease Resistance in Indigenous African Chickens. Description: Banos, Georgios, et al. Integrating Genetic and Genomic Analyses of Combined Health Data Across Ecotypes to Improve Disease Resistance in Indigenous African Chickens. ''Front Genet''. 2020; '''11''': 543890
Integration of SNP Disease Association, eQTL, and Enrichment Analyses to Identify Risk SNPs and Susceptibility Genes in Chronic Obstructive Pulmonary Disease. Description: Liu, Yang, et al. Integration of SNP Disease Association, eQTL, and Enrichment Analyses to Identify Risk SNPs and Susceptibility Genes in Chronic Obstructive Pulmonary Disease. ''Biomed Res Int''. 2020; '''2020''': 3854196
Interactive Effect of IGF2BP2 rs4402960 Variant, Smoking and Type 2 Diabetes. Description: Nfor, Oswald Ndi, et al. Interactive Effect of IGF2BP2 rs4402960 Variant, Smoking and Type 2 Diabetes. ''Diabetes Metab Syndr Obes''. 2020; '''13''': 5097-5102
Investigating Mitonuclear Genetic Interactions Through Machine Learning: A Case Study on Cold Adaptation Genes in Human Populations From Different European Climate Regions. Description: Kalyakulina, Alena, et al. Investigating Mitonuclear Genetic Interactions Through Machine Learning: A Case Study on Cold Adaptation Genes in Human Populations From Different European Climate Regions. ''Front Physiol''. 2020; '''11''': 575968
Loci Associated With Antibody Response in Feral Swine (Sus scrofa) Infected With Brucella suis. Description: Pierce, Courtney F, et al. Loci Associated With Antibody Response in Feral Swine (Sus scrofa) Infected With Brucella suis. ''Front Vet Sci''. 2020; '''7''': 554674
Male-Dominated Migration and Massive Assimilation of Indigenous East Asians in the Formation of Muslim Hui People in Southwest China. Description: Wang, Qiyan, et al. Male-Dominated Migration and Massive Assimilation of Indigenous East Asians in the Formation of Muslim Hui People in Southwest China. ''Front Genet''. 2020; '''11''': 618614
Network preservation reveals shared and unique biological processes associated with chronic alcohol abuse in NAc and PFC. Description: Vornholt, Eric, et al. Network preservation reveals shared and unique biological processes associated with chronic alcohol abuse in NAc and PFC. ''PLoS One''. 2020; '''15''' (12):e0243857
Non-classical human leukocyte antigen class I in Tunisian children with autism. Description: Kharrat, Najla, et al. Non-classical human leukocyte antigen class I in Tunisian children with autism. ''Cent Eur J Immunol''. 2020; '''45''' (2):176-183
Novel methods for epistasis detection in genome-wide association studies. Description: Slim, Lotfi, et al. Novel methods for epistasis detection in genome-wide association studies. ''PLoS One''. 2020; '''15''' (11):e0242927
NRG1, PIP4K2A, and HTR2C as Potential Candidate Biomarker Genes for Several Clinical Subphenotypes of Depression and Bipolar Disorder. Description: Levchenko, Anastasia, et al. NRG1, PIP4K2A, and HTR2C as Potential Candidate Biomarker Genes for Several Clinical Subphenotypes of Depression and Bipolar Disorder. ''Front Genet''. 2020; '''11''': 936
Parentage Atlas of Italian Grapevine Varieties as Inferred From SNP Genotyping. Description: D'Onofrio, Claudio, et al. Parentage Atlas of Italian Grapevine Varieties as Inferred From SNP Genotyping. ''Front Plant Sci''. 2020; '''11''': 605934
Polymorphisms in STING Affect Human Innate Immune Responses to Poxviruses. Description: Kennedy, Richard B, et al. Polymorphisms in STING Affect Human Innate Immune Responses to Poxviruses. ''Front Immunol''. 2020; '''11''': 567348
Polymorphisms in TLR4 Gene Associated With Somatic Cell Score in Water Buffaloes (Bubalus bubalis). Description: Roldan-Montes, Valentina, et al. Polymorphisms in TLR4 Gene Associated With Somatic Cell Score in Water Buffaloes (Bubalus bubalis). ''Front Vet Sci''. 2020; '''7''': 568249
RAI14 in the blood feather regulates chicken pigmentation. Description: Adetula, Adeyinka Abiola, et al. RAI14 in the blood feather regulates chicken pigmentation. ''Arch Anim Breed''. 2020; '''63''' (2):231-239
Rapid phenotypic evolution with shallow genomic differentiation during early stages of high elevation adaptation in Eurasian Tree Sparrows. Description: Qu, Yanhua, et al. Rapid phenotypic evolution with shallow genomic differentiation during early stages of high elevation adaptation in Eurasian Tree Sparrows. ''Natl Sci Rev''. 2020 Jan; '''7''' (1):113-127
Recent Consanguinity and Outbred Autozygosity Are Associated With Increased Risk of Late-Onset Alzheimer's Disease. Description: Napolioni, Valerio, et al. Recent Consanguinity and Outbred Autozygosity Are Associated With Increased Risk of Late-Onset Alzheimer's Disease. ''Front Genet''. 2020; '''11''': 629373
Risk Stratification for Bipolar Disorder Using Polygenic Risk Scores Among Young High-Risk Adults. Description: Biere, Silvia, et al. Risk Stratification for Bipolar Disorder Using Polygenic Risk Scores Among Young High-Risk Adults. ''Front Psychiatry''. 2020; '''11''': 552532
Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera. Description: Sargolzaei, Maryam, et al. Rpv29, Rpv30 and Rpv31: Three Novel Genomic Loci Associated With Resistance to Plasmopara viticola in Vitis vinifera. ''Front Plant Sci''. 2020; '''11''': 562432
Screening of Microbes Associated With Swine Growth and Fat Deposition Traits Across the Intestinal Tract. Description: Tang, Shi, et al. Screening of Microbes Associated With Swine Growth and Fat Deposition Traits Across the Intestinal Tract. ''Front Microbiol''. 2020; '''11''': 586776
Selection signatures in two oldest Russian native cattle breeds revealed using high-density single nucleotide polymorphism analysis. Description: Zinovieva, Natalia Anatolievna, et al. Selection signatures in two oldest Russian native cattle breeds revealed using high-density single nucleotide polymorphism analysis. ''PLoS One''. 2020; '''15''' (11):e0242200
Selective Sweeps Lead to Evolutionary Success in an Amazonian Hyperdominant Palm. Description: Melo, Warita A, et al. Selective Sweeps Lead to Evolutionary Success in an Amazonian Hyperdominant Palm. ''Front Genet''. 2020; '''11''': 596662
Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children. Description: Zheng, Yi, et al. Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children. ''Biomed Res Int''. 2020; '''2020''': 5956412
Single-Nucleotide Polymorphisms in Genes Predisposing to Leprosy in Leprosy Household Contacts in Zhejiang Province, China. Description: Shen, Yun-Liang, et al. Single-Nucleotide Polymorphisms in Genes Predisposing to Leprosy in Leprosy Household Contacts in Zhejiang Province, China. ''Pharmgenomics Pers Med''. 2020; '''13''': 767-773
Systematic Prioritization of Candidate Genes in Disease Loci Identifies TRAFD1 as a Master Regulator of IFNgamma Signaling in Celiac Disease. Description: van der Graaf, Adriaan, et al. Systematic Prioritization of Candidate Genes in Disease Loci Identifies TRAFD1 as a Master Regulator of IFNgamma Signaling in Celiac Disease. ''Front Genet''. 2020; '''11''': 562434
The Contribution of Genetic Variants to the Risk of Papillary Thyroid Carcinoma in the Kazakh Population: Study of Common Single Nucleotide Polymorphisms and Their Clinicopathological Correlations. Description: Mussazhanova, Zhanna, et al. The Contribution of Genetic Variants to the Risk of Papillary Thyroid Carcinoma in the Kazakh Population: Study of Common Single Nucleotide Polymorphisms and Their Clinicopathological Correlations. ''Front Endocrinol (Lausanne)''. 2020; '''11''': 543500
The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages. Description: Li, Shuo, et al. The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages. ''Brain Commun''. 2020; '''2''' (2):fcaa176
The homeland of Proto-Tungusic inferred from contemporary words and ancient genomes. Description: Wang, Chuan-Chao, et al. The homeland of Proto-Tungusic inferred from contemporary words and ancient genomes. ''Evol Hum Sci''. 2020; '''2''': e8
The relationship between donor-recipient genetic distance and long-term kidney transplant outcome. Description: Stapleton, Caragh P, et al. The relationship between donor-recipient genetic distance and long-term kidney transplant outcome. ''HRB Open Res''. 2020; '''3''': 47
The SNP rs13147758 in the HHIP Gene Is Associated With COPD Susceptibility, Serum, and Sputum Protein Levels in Smokers. Description: Ortega-Martinez, Alejandro, et al. The SNP rs13147758 in the HHIP Gene Is Associated With COPD Susceptibility, Serum, and Sputum Protein Levels in Smokers. ''Front Genet''. 2020; '''11''': 882
THI Modulation of Genetic and Non-genetic Variance Components for Carcass Traits in Hanwoo Cattle. Description: Chung, Yoonji, et al. THI Modulation of Genetic and Non-genetic Variance Components for Carcass Traits in Hanwoo Cattle. ''Front Genet''. 2020; '''11''': 576377
Validation of Susceptibility Loci for Vitiligo Identified by GWAS in the Chinese Han Population. Description: Cheng, Lu, et al. Validation of Susceptibility Loci for Vitiligo Identified by GWAS in the Chinese Han Population. ''Front Genet''. 2020; '''11''': 542275
Variants associated with HHIP expression have sex-differential effects on lung function. Description: Fawcett, Katherine A, et al. Variants associated with HHIP expression have sex-differential effects on lung function. ''Wellcome Open Res''. 2020; '''5''': 111
Variants in ACE2 and TMPRSS2 Genes Are Not Major Determinants of COVID-19 Severity in UK Biobank Subjects. Description: Curtis, David. Variants in ACE2 and TMPRSS2 Genes Are Not Major Determinants of COVID-19 Severity in UK Biobank Subjects. ''Hum Hered''. 2020; '''85''' (2):66-68
Variants in PPP2R2B and IGF2BP3 are associated with higher tau deposition. Description: Ramanan, Vijay K, et al. Variants in PPP2R2B and IGF2BP3 are associated with higher tau deposition. ''Brain Commun''. 2020; '''2''' (2):fcaa159
Whole Transcriptome Analysis Identifies the Taxonomic Status of a New Chinese Native Cattle Breed and Reveals Genes Related to Body Size. Description: Zheng, Xiao-Dong, et al. Whole Transcriptome Analysis Identifies the Taxonomic Status of a New Chinese Native Cattle Breed and Reveals Genes Related to Body Size. ''Front Genet''. 2020; '''11''': 562855
ABCB1 Genetic Variants as Predictors of Irinotecan-Induced Severe Gastrointestinal Toxicity in Metastatic Colorectal Cancer Patients. Description: Riera, Pau, et al. ABCB1 Genetic Variants as Predictors of Irinotecan-Induced Severe Gastrointestinal Toxicity in Metastatic Colorectal Cancer Patients. ''Front Pharmacol''. 2020; '''11''': 973
A Between Ethnicities Comparison of Chronic Obstructive Pulmonary Disease Genetic Risk. Description: Gim, Jungsoo, et al. A Between Ethnicities Comparison of Chronic Obstructive Pulmonary Disease Genetic Risk. ''Front Genet''. 2020; '''11''': 329
A Case-Control Study of ADCY9 Gene Polymorphisms and the Risk of Hepatocellular Carcinoma in the Chinese Han Population. Description: Chao, Xu, et al. A Case-Control Study of ADCY9 Gene Polymorphisms and the Risk of Hepatocellular Carcinoma in the Chinese Han Population. ''Front Oncol''. 2020; '''10''': 1450
A cost-effective barcode system for maize genetic discrimination based on bi-allelic InDel markers. Description: Liang, Shuaiqiang, et al. A cost-effective barcode system for maize genetic discrimination based on bi-allelic InDel markers. ''Plant Methods''. 2020; '''16''': 101
ADAMTS12, a new candidate gene for pediatric stroke. Description: Witten, Anika, et al. ADAMTS12, a new candidate gene for pediatric stroke. ''PLoS One''. 2020; '''15''' (8):e0237928
A different view on fine-scale population structure in Western African populations. Description: Chaichoompu, Kridsadakorn, et al. A different view on fine-scale population structure in Western African populations. ''Hum Genet''. 2020 Jan; '''139''' (1):45-59
Adiponectin receptor 1 gene is potentially associated with severity of postoperative pain but not cancer pain. Description: Ninagawa, Jun, et al. Adiponectin receptor 1 gene is potentially associated with severity of postoperative pain but not cancer pain. ''Medicine (Baltimore)''. 2020 Jan; '''99''' (5):e18924
Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans. Description: Liu, Zhi, et al. Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans. ''PLoS One''. 2020; '''15''' (4):e0232048
A genetically unique Chinese cattle population shows evidence of common ancestry with wild species when analysed with a reduced ascertainment bias SNP panel. Description: Barbato, Mario, et al. A genetically unique Chinese cattle population shows evidence of common ancestry with wild species when analysed with a reduced ascertainment bias SNP panel. ''PLoS One''. 2020; '''15''' (4):e0231162
A Genetic Investigation of Island Jersey Cattle, the Foundation of the Jersey Breed: Comparing Population Structure and Selection to Guernsey, Holstein, and United States Jersey Cattle. Description: Huson, Heather J, et al. A Genetic Investigation of Island Jersey Cattle, the Foundation of the Jersey Breed: Comparing Population Structure and Selection to Guernsey, Holstein, and United States Jersey Cattle. ''Front Genet''. 2020; '''11''': 366
A genome-wide association study of deafness in three canine breeds. Description: Hayward, Jessica J, et al. A genome-wide association study of deafness in three canine breeds. ''PLoS One''. 2020; '''15''' (5):e0232900
A Genome-Wide Association Study on Feed Efficiency Related Traits in Landrace Pigs. Description: Fu, Lu, et al. A Genome-Wide Association Study on Feed Efficiency Related Traits in Landrace Pigs. ''Front Genet''. 2020; '''11''': 692
A genome-wide association study on liver enzymes in Korean population. Description: Seo, Ji Yeon, et al. A genome-wide association study on liver enzymes in Korean population. ''PLoS One''. 2020; '''15''' (2):e0229374
A Genomewide Scan for Genetic Structure and Demographic History of Two Closely Related Species, Rhododendron dauricum and R. mucronulatum (Rhododendron, Ericaceae). Description: Yang, Baiming, et al. A Genomewide Scan for Genetic Structure and Demographic History of Two Closely Related Species, Rhododendron dauricum and R. mucronulatum (Rhododendron, Ericaceae). ''Front Plant Sci''. 2020; '''11''': 1093
A genome-wide scan for pleiotropy between bone mineral density and nonbone phenotypes. Description: Christou, Maria A, et al. A genome-wide scan for pleiotropy between bone mineral density and nonbone phenotypes. ''Bone Res''. 2020; '''8''': 26
Amygdala 5-HTT Gene Network Moderates the Effects of Postnatal Adversity on Attention Problems: Anatomo-Functional Correlation and Epigenetic Changes. Description: de Lima, Randriely Merscher Sobreira, et al. Amygdala 5-HTT Gene Network Moderates the Effects of Postnatal Adversity on Attention Problems: Anatomo-Functional Correlation and Epigenetic Changes. ''Front Neurosci''. 2020; '''14''': 198
Analyzing Genome-Wide Association Study Dataset Highlights Immune Pathways in Lip Bone Mineral Density. Description: Liu, Xiaodong, et al. Analyzing Genome-Wide Association Study Dataset Highlights Immune Pathways in Lip Bone Mineral Density. ''Front Genet''. 2020; '''11''': 4
Analyzing the genomic and transcriptomic architecture of milk traits in Murciano-Granadina goats. Description: Guan, Dailu, et al. Analyzing the genomic and transcriptomic architecture of milk traits in Murciano-Granadina goats. ''J Anim Sci Biotechnol''. 2020; '''11''': 35
An evaluation of machine-learning for predicting phenotype: studies in yeast, rice, and wheat. Description: Grinberg, Nastasiya F, et al. An evaluation of machine-learning for predicting phenotype: studies in yeast, rice, and wheat. ''Mach Learn''. 2020; '''109''' (2):251-277
*A population-specific low-frequency variant of SLC22A12 (p.W258) explains nearby genome-wide association signals for serum uric acid concentrations among Koreans.** Description: Im, Sun-Wha, et al. A population-specific low-frequency variant of SLC22A12 (p.W258*) explains nearby genome-wide association signals for serum uric acid concentrations among Koreans. ''PLoS One''. 2020; '''15''' (4):e0231336
Aquaporin locus (12q13.12) might contribute to susceptibility of temporomandibular joint disorder associated with periodontitis. Description: Bezamat, Mariana, et al. Aquaporin locus (12q13.12) might contribute to susceptibility of temporomandibular joint disorder associated with periodontitis. ''PLoS One''. 2020; '''15''' (3):e0229245
Assessing the Relationship Between Gut Microbiota and Bone Mineral Density. Description: Cheng, Shiqiang, et al. Assessing the Relationship Between Gut Microbiota and Bone Mineral Density. ''Front Genet''. 2020; '''11''': 6
Association analysis between chronic obstructive pulmonary disease and polymorphisms in circadian genes. Description: Chen, Guo, et al. Association analysis between chronic obstructive pulmonary disease and polymorphisms in circadian genes. ''PeerJ''. 2020; '''8''': e9806
Association between Adiponectin Gene Polymorphism and Environmental Risk Factors of Type 2 Diabetes Mellitus among the Chinese Population in Hohhot. Description: Cui, Meng, et al. Association between Adiponectin Gene Polymorphism and Environmental Risk Factors of Type 2 Diabetes Mellitus among the Chinese Population in Hohhot. ''Biomed Res Int''. 2020; '''2020''': 6383906
Association between a TCF4 Polymorphism and Susceptibility to Schizophrenia. Description: Gao, Jia-Yang, et al. Association between a TCF4 Polymorphism and Susceptibility to Schizophrenia. ''Biomed Res Int''. 2020; '''2020''': 1216303
Association between blooming time and climatic adaptation in Prunus mume. Description: Shi, Ting, et al. Association between blooming time and climatic adaptation in Prunus mume. ''Ecol Evol''. 2020 Jan; '''10''' (1):292-306
Association between the rs1544410 polymorphism in the vitamin D receptor (VDR) gene and insulin secretion after gestational diabetes mellitus. Description: Shaat, Nael, et al. Association between the rs1544410 polymorphism in the vitamin D receptor (VDR) gene and insulin secretion after gestational diabetes mellitus. ''PLoS One''. 2020; '''15''' (5):e0232297
Association Mapping of Seed Quality Traits Under Varying Conditions of Nitrogen Application in Brassica juncea L. Czern & Coss. Description: Akhatar, Javed, et al. Association Mapping of Seed Quality Traits Under Varying Conditions of Nitrogen Application in Brassica juncea L. Czern & Coss. ''Front Genet''. 2020; '''11''': 744
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome. Description: Pagliaroli, Luca, et al. Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome. ''Front Neurol''. 2020; '''11''': 803
Association of Race and Major Adverse Cardiac Events (MACE): The Atherosclerosis Risk in Communities (ARIC) Cohort. Description: Franey, Ericha G, et al. Association of Race and Major Adverse Cardiac Events (MACE): The Atherosclerosis Risk in Communities (ARIC) Cohort. ''J Aging Res''. 2020; '''2020''': 7417242
Associations of the intestinal microbiome with the complement system in neovascular age-related macular degeneration. Description: Zysset-Burri, Denise C, et al. Associations of the intestinal microbiome with the complement system in neovascular age-related macular degeneration. ''NPJ Genom Med''. 2020; '''5''': 34
Association Study of Genetic Variants in Autophagy Pathway and Risk of Non-syndromic Cleft Lip With or Without Cleft Palate. Description: Lou, Shu, et al. Association Study of Genetic Variants in Autophagy Pathway and Risk of Non-syndromic Cleft Lip With or Without Cleft Palate. ''Front Cell Dev Biol''. 2020; '''8''': 576
Association Study of MAP3K1 SNPs and Risk Factors with Susceptibility to Esophageal Squamous Cell Carcinoma in a Chinese Population: A Case-Control Study. Description: Yang, Yiling, et al. Association Study of MAP3K1 SNPs and Risk Factors with Susceptibility to Esophageal Squamous Cell Carcinoma in a Chinese Population: A Case-Control Study. ''Pharmgenomics Pers Med''. 2020; '''13''': 189-197
Association Study of Puberty-Related Candidate Genes in Chinese Female Population. Description: Omariba, Gideon, et al. Association Study of Puberty-Related Candidate Genes in Chinese Female Population. ''Int J Genomics''. 2020; '''2020''': 1426761
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics. Description: Magi, Alberto, et al. AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics. ''Comput Struct Biotechnol J''. 2020; '''18''': 1956-1967
A whole-genome sequenced control population in northern Sweden reveals subregional genetic differences. Description: Svensson, Daniel, et al. A whole-genome sequenced control population in northern Sweden reveals subregional genetic differences. ''PLoS One''. 2020; '''15''' (9):e0237721
Birth Weight and Stroke in Adult Life: Genetic Correlation and Causal Inference With Genome-Wide Association Data Sets. Description: Wang, Ting, et al. Birth Weight and Stroke in Adult Life: Genetic Correlation and Causal Inference With Genome-Wide Association Data Sets. ''Front Neurosci''. 2020; '''14''': 479
Blood multiomics reveal insights into population clusters with low prevalence of diabetes, dyslipidemia and hypertension. Description: Su, Ming-Wei, et al. Blood multiomics reveal insights into population clusters with low prevalence of diabetes, dyslipidemia and hypertension. ''PLoS One''. 2020; '''15''' (3):e0229922
CACNA1C Gene rs11832738 Polymorphism Influences Depression Severity by Modulating Spontaneous Activity in the Right Middle Frontal Gyrus in Patients With Major Depressive Disorder. Description: Liu, Xiaoyun, et al. CACNA1C Gene rs11832738 Polymorphism Influences Depression Severity by Modulating Spontaneous Activity in the Right Middle Frontal Gyrus in Patients With Major Depressive Disorder. ''Front Psychiatry''. 2020; '''11''': 73
Changed Patterns of Genomic Variation Following Recent Domestication: Selection Sweeps in Farmed Atlantic Salmon. Description: Naval-Sanchez, Marina, et al. Changed Patterns of Genomic Variation Following Recent Domestication: Selection Sweeps in Farmed Atlantic Salmon. ''Front Genet''. 2020; '''11''': 264
Combining Crop Growth Modeling With Trait-Assisted Prediction Improved the Prediction of Genotype by Environment Interactions. Description: Robert, Pauline, et al. Combining Crop Growth Modeling With Trait-Assisted Prediction Improved the Prediction of Genotype by Environment Interactions. ''Front Plant Sci''. 2020; '''11''': 827
Comparing Alternative Single-Step GBLUP Approaches and Training Population Designs for Genomic Evaluation of Crossbred Animals. Description: Alvarenga, Amanda B, et al. Comparing Alternative Single-Step GBLUP Approaches and Training Population Designs for Genomic Evaluation of Crossbred Animals. ''Front Genet''. 2020; '''11''': 263
Comparing local ancestry inference models in populations of two- and three-way admixture. Description: Schubert, Ryan, et al. Comparing local ancestry inference models in populations of two- and three-way admixture. ''PeerJ''. 2020; '''8''': e10090
Conservation Genomic Analysis of the Croatian Indigenous Black Slavonian and Turopolje Pig Breeds. Description: Lukic, Boris, et al. Conservation Genomic Analysis of the Croatian Indigenous Black Slavonian and Turopolje Pig Breeds. ''Front Genet''. 2020; '''11''': 261
Conservation Genomics of a Threatened Rhododendron: Contrasting Patterns of Population Structure Revealed From Neutral and Selected SNPs. Description: Liu, Detuan, et al. Conservation Genomics of a Threatened Rhododendron: Contrasting Patterns of Population Structure Revealed From Neutral and Selected SNPs. ''Front Genet''. 2020; '''11''': 757
coPLINK: A complementary tool to PLINK. Description: Liu, Han-Ming, et al. coPLINK: A complementary tool to PLINK. ''PLoS One''. 2020; '''15''' (9):e0239144
Detection of Allosteric Effects of lncRNA Secondary Structures Altered by SNPs in Human Diseases. Description: Lu, Xiaoyan, et al. Detection of Allosteric Effects of lncRNA Secondary Structures Altered by SNPs in Human Diseases. ''Front Cell Dev Biol''. 2020; '''8''': 242
Development of a low-density panel for genomic selection of pigs in Russia. Description: Shashkova, Tatiana I, et al. Development of a low-density panel for genomic selection of pigs in Russia. ''Transl Anim Sci''. 2020 Jan; '''4''' (1):264-274
Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgery. Description: Schnitzler, Fabian, et al. Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgery. ''PLoS One''. 2020; '''15''' (7):e0236421
Development of core-collections for Guizhou tea genetic resources and GWAS of leaf size using SNP developed by genotyping-by-sequencing. Description: Niu, Suzhen, et al. Development of core-collections for Guizhou tea genetic resources and GWAS of leaf size using SNP developed by genotyping-by-sequencing. ''PeerJ''. 2020; '''8''': e8572
Development of Genomic Resources and Identification of Genetic Diversity and Genetic Structure of the Domestic Bactrian Camel in China by RAD Sequencing. Description: Liu, Chenmiao, et al. Development of Genomic Resources and Identification of Genetic Diversity and Genetic Structure of the Domestic Bactrian Camel in China by RAD Sequencing. ''Front Genet''. 2020; '''11''': 797
Deviation from Mendelian transmission of autosomal SNPs can be used to estimate germline mutations in humans exposed to ionizing radiation. Description: Leite Filho, Hugo Pereira, et al. Deviation from Mendelian transmission of autosomal SNPs can be used to estimate germline mutations in humans exposed to ionizing radiation. ''PLoS One''. 2020; '''15''' (10):e0233941
Dissecting new genetic components of salinity tolerance in two-row spring barley at the vegetative and reproductive stages. Description: Saade, Stephanie, et al. Dissecting new genetic components of salinity tolerance in two-row spring barley at the vegetative and reproductive stages. ''PLoS One''. 2020; '''15''' (7):e0236037
Effect of apolipoprotein E polymorphism on cognition and brain in the Cambridge Centre for Ageing and Neuroscience cohort. Description: Henson, Richard N, et al. Effect of apolipoprotein E polymorphism on cognition and brain in the Cambridge Centre for Ageing and Neuroscience cohort. ''Brain Neurosci Adv''. 2020 Jan-Dec; '''4''': 2398212820961704
Epigenetic aging is accelerated in alcohol use disorder and regulated by genetic variation in APOL2. Description: Luo, Audrey, et al. Epigenetic aging is accelerated in alcohol use disorder and regulated by genetic variation in APOL2. ''Neuropsychopharmacology''. 2020 Jan; '''45''' (2):327-336
Estimation of inbreeding and identification of regions under heavy selection based on runs of homozygosity in a Large White pig population. Description: Shi, Liangyu, et al. Estimation of inbreeding and identification of regions under heavy selection based on runs of homozygosity in a Large White pig population. ''J Anim Sci Biotechnol''. 2020; '''11''': 46
Evaluation of single nucleotide polymorphisms in 6 candidate genes and carotid intima-media thickness in community-dwelling residents. Description: Wu, Fang-Yang, et al. Evaluation of single nucleotide polymorphisms in 6 candidate genes and carotid intima-media thickness in community-dwelling residents. ''PLoS One''. 2020; '''15''' (3):e0230715
Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length. Description: van der Spek, Ashley, et al. Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length. ''Front Genet''. 2020; '''11''': 337
Exome-Wide Association Study Reveals Several Susceptibility Genes and Pathways Associated With Acute Coronary Syndromes in Han Chinese. Description: Zheng, Qiwen, et al. Exome-Wide Association Study Reveals Several Susceptibility Genes and Pathways Associated With Acute Coronary Syndromes in Han Chinese. ''Front Genet''. 2020; '''11''': 336
Exploring the genetic relationship between hearing impairment and Alzheimer's disease. Description: Mitchell, Brittany L, et al. Exploring the genetic relationship between hearing impairment and Alzheimer's disease. ''Alzheimers Dement (Amst)''. 2020; '''12''' (1):e12108
Fine-Scale Population Genetic Structure and Parapatric Cryptic Species of Kuruma Shrimp (Marsupenaeus japonicus), Along the Northwestern Pacific Coast of China. Description: Wang, Panpan, et al. Fine-Scale Population Genetic Structure and Parapatric Cryptic Species of Kuruma Shrimp (Marsupenaeus japonicus), Along the Northwestern Pacific Coast of China. ''Front Genet''. 2020; '''11''': 118
Frequency of ClinVar Pathogenic Variants in Chronic Kidney Disease Patients Surveyed for Return of Research Results at a Cleveland Public Hospital. Description: Crawford, Dana C, et al. Frequency of ClinVar Pathogenic Variants in Chronic Kidney Disease Patients Surveyed for Return of Research Results at a Cleveland Public Hospital. ''Pac Symp Biocomput''. 2020; '''25''': 575-586
From landrace to modern hybrid broccoli: the genomic and morphological domestication syndrome within a diverse B. oleracea collection. Description: Stansell, Zachary, et al. From landrace to modern hybrid broccoli: the genomic and morphological domestication syndrome within a diverse B. oleracea collection. ''Hortic Res''. 2020; '''7''': 159
Functional genetic variants of CTNNBIP1 predict platinum treatment response of Chinese epithelial ovarian cancer patients. Description: Li, Haoran, et al. Functional genetic variants of CTNNBIP1 predict platinum treatment response of Chinese epithelial ovarian cancer patients. ''J Cancer''. 2020; '''11''' (23):6850-6860
Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects. Description: Sewda, Anshuman, et al. Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects. ''PLoS One''. 2020; '''15''' (6):e0234357
Gene-by-gene interactions associated with the risk of conotruncal heart defects. Description: Lyu, Chen, et al. Gene-by-gene interactions associated with the risk of conotruncal heart defects. ''Mol Genet Genomic Med''. 2020 Jan; '''8''' (1):e1010
Genetic Analysis of Antibody Response to Porcine Reproductive and Respiratory Syndrome Vaccination as an Indicator Trait for Reproductive Performance in Commercial Sows. Description: Sanglard, Leticia P, et al. Genetic Analysis of Antibody Response to Porcine Reproductive and Respiratory Syndrome Vaccination as an Indicator Trait for Reproductive Performance in Commercial Sows. ''Front Genet''. 2020; '''11''': 1011
Genetic Association and Expression Correlation between Colony-Stimulating Factor 1 Gene Encoding M-CSF and Adult-Onset Still's Disease. Description: Chen, Yi-Ming, et al. Genetic Association and Expression Correlation between Colony-Stimulating Factor 1 Gene Encoding M-CSF and Adult-Onset Still's Disease. ''J Immunol Res''. 2020; '''2020''': 8640719
Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India. Description: Srivastava, Anshika, et al. Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India. ''Front Genet''. 2020; '''11''': 564741
Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations. Description: Hayat, Mahtaab, et al. Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations. ''PLoS One''. 2020; '''15''' (2):e0229098
Genetic Basis of Response of Ghanaian Local Chickens to Infection With a Lentogenic Newcastle Disease Virus. Description: Walugembe, Muhammed, et al. Genetic Basis of Response of Ghanaian Local Chickens to Infection With a Lentogenic Newcastle Disease Virus. ''Front Genet''. 2020; '''11''': 739
Genetic Connectedness Between Norwegian White Sheep and New Zealand Composite Sheep Populations With Similar Development History. Description: Oliveira, Hinayah Rojas, et al. Genetic Connectedness Between Norwegian White Sheep and New Zealand Composite Sheep Populations With Similar Development History. ''Front Genet''. 2020; '''11''': 371
Genetic Dissection of Growth Traits in a Unique Chicken Advanced Intercross Line. Description: Wang, Yuzhe, et al. Genetic Dissection of Growth Traits in a Unique Chicken Advanced Intercross Line. ''Front Genet''. 2020; '''11''': 894
Genetic diversity and genetic origin of Lanping black-boned sheep investigated by genome-wide single-nucleotide polymorphisms (SNPs). Description: Xiong, Heli, et al. Genetic diversity and genetic origin of Lanping black-boned sheep investigated by genome-wide single-nucleotide polymorphisms (SNPs). ''Arch Anim Breed''. 2020; '''63''' (1):193-201
Genetic Diversity and Low Stratification of the Population of the United Arab Emirates. Description: Tay, Guan K, et al. Genetic Diversity and Low Stratification of the Population of the United Arab Emirates. ''Front Genet''. 2020; '''11''': 608
Genetic Diversity and Selection Signatures Within Diannan Small-Ear Pigs Revealed by Next-Generation Sequencing. Description: Wu, Fen, et al. Genetic Diversity and Selection Signatures Within Diannan Small-Ear Pigs Revealed by Next-Generation Sequencing. ''Front Genet''. 2020; '''11''': 733
Genetic Polymorphisms and Forensic Efficiencies of a Set of Novel Autosomal InDel Markers in a Chinese Mongolian Group. Description: Zhang, Wenqing, et al. Genetic Polymorphisms and Forensic Efficiencies of a Set of Novel Autosomal InDel Markers in a Chinese Mongolian Group. ''Biomed Res Int''. 2020; '''2020''': 3925189
Genetic risk for dengue hemorrhagic fever and dengue fever in multiple ancestries. Description: Pare, Guillaume, et al. Genetic risk for dengue hemorrhagic fever and dengue fever in multiple ancestries. ''EBioMedicine''. 2020 Jan; '''51''': 102584
Genetic risk scores for coronary artery disease and its traditional risk factors: Their role in the progression of coronary artery calcification-Results of the Heinz Nixdorf Recall study. Description: Pechlivanis, Sonali, et al. Genetic risk scores for coronary artery disease and its traditional risk factors: Their role in the progression of coronary artery calcification-Results of the Heinz Nixdorf Recall study. ''PLoS One''. 2020; '''15''' (5):e0232735
Genetic Underpinnings of Increased BMI and Its Association With Late Midlife Cognitive Abilities. Description: Xian, Hong, et al. Genetic Underpinnings of Increased BMI and Its Association With Late Midlife Cognitive Abilities. ''Gerontol Geriatr Med''. 2020 Jan-Dec; '''6''': 2333721420925267
Genetic Variants in DNA Mismatch Repair Pathway predict prognosis of Lung Cancer patients with receiving Platinum-Based Chemotherapy. Description: Liu, Jun-Yan, et al. Genetic Variants in DNA Mismatch Repair Pathway predict prognosis of Lung Cancer patients with receiving Platinum-Based Chemotherapy. ''J Cancer''. 2020; '''11''' (18):5281-5288
Genetic Variants in miRNAs Are Associated With Risk of Non-syndromic Tooth Agenesis. Description: Gu, Min, et al. Genetic Variants in miRNAs Are Associated With Risk of Non-syndromic Tooth Agenesis. ''Front Physiol''. 2020; '''11''': 1052
Genetic variants in the Folic acid Metabolic Pathway Genes predict outcomes of metastatic Colorectal Cancer patients receiving first-line Chemotherapy. Description: Jiang, Lu, et al. Genetic variants in the Folic acid Metabolic Pathway Genes predict outcomes of metastatic Colorectal Cancer patients receiving first-line Chemotherapy. ''J Cancer''. 2020; '''11''' (22):6507-6515
Genetic variation of the Chilean endemic long-haired mouse Abrothrix longipilis (Rodentia, Supramyomorpha, Cricetidae) in a geographical and environmental context. Description: Valdez, Lourdes, et al. Genetic variation of the Chilean endemic long-haired mouse Abrothrix longipilis (Rodentia, Supramyomorpha, Cricetidae) in a geographical and environmental context. ''PeerJ''. 2020; '''8''': e9517
Genome and population sequencing of a chromosome-level genome assembly of the Chinese tapertail anchovy (Coilia nasus) provides novel insights into migratory adaptation. Description: Xu, Gangchun, et al. Genome and population sequencing of a chromosome-level genome assembly of the Chinese tapertail anchovy (Coilia nasus) provides novel insights into migratory adaptation. ''Gigascience''. 2020 Jan 1; '''9''' (1):
Genome Data Uncover Conservation Status, Historical Relatedness and Candidate Genes Under Selection in Chinese Indigenous Pigs in the Taihu Lake Region. Description: Liu, Chenxi, et al. Genome Data Uncover Conservation Status, Historical Relatedness and Candidate Genes Under Selection in Chinese Indigenous Pigs in the Taihu Lake Region. ''Front Genet''. 2020; '''11''': 591
Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men. Description: Pott, Janne, et al. Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men. ''PLoS One''. 2020; '''15''' (5):e0233728
Genome Wide Assessment of Genetic Variation and Population Distinctiveness of the Pig Family in South Africa. Description: Hlongwane, Nompilo Lucia, et al. Genome Wide Assessment of Genetic Variation and Population Distinctiveness of the Pig Family in South Africa. ''Front Genet''. 2020; '''11''': 344
Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure. Description: Rode, Michael, et al. Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure. ''PLoS One''. 2020; '''15''' (8):e0237237
Genome-wide association and epistatic interactions of flowering time in soybean cultivar. Description: Kim, Kyoung Hyoun, et al. Genome-wide association and epistatic interactions of flowering time in soybean cultivar. ''PLoS One''. 2020; '''15''' (1):e0228114
Genome-Wide Association Study and Fine Mapping Reveals Candidate Genes for Birth Weight of Yorkshire and Landrace Pigs. Description: Li, Yong, et al. Genome-Wide Association Study and Fine Mapping Reveals Candidate Genes for Birth Weight of Yorkshire and Landrace Pigs. ''Front Genet''. 2020; '''11''': 183
Genome-Wide Association Study and Genomic Prediction Elucidate the Distinct Genetic Architecture of Aluminum and Proton Tolerance in Arabidopsis thaliana. Description: Nakano, Yuki, et al. Genome-Wide Association Study and Genomic Prediction Elucidate the Distinct Genetic Architecture of Aluminum and Proton Tolerance in Arabidopsis thaliana. ''Front Plant Sci''. 2020; '''11''': 405
Genome-Wide Association Study Dissects the Genetic Architecture of Maize Husk Tightness. Description: Jiang, Siqi, et al. Genome-Wide Association Study Dissects the Genetic Architecture of Maize Husk Tightness. ''Front Plant Sci''. 2020; '''11''': 861
Genome-Wide Association Study Identifies Genomic Loci Associated With Neurotransmitter Concentration in Cattle. Description: Chen, Qiuming, et al. Genome-Wide Association Study Identifies Genomic Loci Associated With Neurotransmitter Concentration in Cattle. ''Front Genet''. 2020; '''11''': 139
Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse. Description: Hadji-Turdeghal, Katra, et al. Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse. ''Cardiovasc Res''. 2020 Jan 1; '''116''' (1):138-148
Genome-Wide Association Study of Body Weights in Hu Sheep and Population Verification of Related Single-Nucleotide Polymorphisms. Description: Cao, Yuhao, et al. Genome-Wide Association Study of Body Weights in Hu Sheep and Population Verification of Related Single-Nucleotide Polymorphisms. ''Front Genet''. 2020; '''11''': 588
Genome wide association study of incomplete hippocampal inversion in adolescents. Description: Cury, Claire, et al. Genome wide association study of incomplete hippocampal inversion in adolescents. ''PLoS One''. 2020; '''15''' (1):e0227355
Genome-wide association study of metabolic syndrome in Korean populations. Description: Oh, Seung-Won, et al. Genome-wide association study of metabolic syndrome in Korean populations. ''PLoS One''. 2020; '''15''' (1):e0227357
Genome-Wide Association Study of Smoking Behavior Traits in a Chinese Han Population. Description: Li, Meng, et al. Genome-Wide Association Study of Smoking Behavior Traits in a Chinese Han Population. ''Front Psychiatry''. 2020; '''11''': 564239
Genome-Wide Association Study Reveals a Novel Association Between MYBPC3 Gene Polymorphism, Endurance Athlete Status, Aerobic Capacity and Steroid Metabolism. Description: Al-Khelaifi, Fatima, et al. Genome-Wide Association Study Reveals a Novel Association Between MYBPC3 Gene Polymorphism, Endurance Athlete Status, Aerobic Capacity and Steroid Metabolism. ''Front Genet''. 2020; '''11''': 595
Genome-Wide Association Study Using Individual Single-Nucleotide Polymorphisms and Haplotypes for Erythrocyte Traits in Alpine Merino Sheep. Description: Zhu, Shaohua, et al. Genome-Wide Association Study Using Individual Single-Nucleotide Polymorphisms and Haplotypes for Erythrocyte Traits in Alpine Merino Sheep. ''Front Genet''. 2020; '''11''': 848
Genome-Wide Epistatic Interaction Networks Affecting Feed Efficiency in Duroc and Landrace Pigs. Description: Banerjee, Priyanka, et al. Genome-Wide Epistatic Interaction Networks Affecting Feed Efficiency in Duroc and Landrace Pigs. ''Front Genet''. 2020; '''11''': 121
Genome-wide identification and analysis of heterotic loci in three maize hybrids. Description: Liu, Hongjun, et al. Genome-wide identification and analysis of heterotic loci in three maize hybrids. ''Plant Biotechnol J''. 2020 Jan; '''18''' (1):185-194
Genome-wide interaction study reveals age-dependent determinants of responsiveness to inhaled corticosteroids in individuals with asthma. Description: Dahlin, Amber, et al. Genome-wide interaction study reveals age-dependent determinants of responsiveness to inhaled corticosteroids in individuals with asthma. ''PLoS One''. 2020; '''15''' (3):e0229241
Genome-Wide Population Genetic Analysis of Commercial, Indigenous, Game, and Wild Chickens Using 600K SNP Microarray Data. Description: Zhang, Jinxin, et al. Genome-Wide Population Genetic Analysis of Commercial, Indigenous, Game, and Wild Chickens Using 600K SNP Microarray Data. ''Front Genet''. 2020; '''11''': 543294
Genome-Wide Runs of Homozygosity Revealed Selection Signatures in Bos indicus. Description: Dixit, S P, et al. Genome-Wide Runs of Homozygosity Revealed Selection Signatures in Bos indicus. ''Front Genet''. 2020; '''11''': 92
Genome-Wide Search for SNP Interactions in GWAS Data: Algorithm, Feasibility, Replication Using Schizophrenia Datasets. Description: Lee, Kwan-Yeung, et al. Genome-Wide Search for SNP Interactions in GWAS Data: Algorithm, Feasibility, Replication Using Schizophrenia Datasets. ''Front Genet''. 2020; '''11''': 1003
Genome-wide signatures of environmental adaptation in European aspen (Populus tremula) under current and future climate conditions. Description: Ingvarsson, Par K, et al. Genome-wide signatures of environmental adaptation in European aspen (Populus tremula) under current and future climate conditions. ''Evol Appl''. 2020 Jan; '''13''' (1):132-142
Genomic Analysis Identifies New Loci Associated With Motor Complications in Parkinson's Disease. Description: Ryu, Ho-Sung, et al. Genomic Analysis Identifies New Loci Associated With Motor Complications in Parkinson's Disease. ''Front Neurol''. 2020; '''11''': 570
Genomic Characteristics and Selection Signatures in Indigenous Chongming White Goat (Capra hircus). Description: Gao, Jun, et al. Genomic Characteristics and Selection Signatures in Indigenous Chongming White Goat (Capra hircus). ''Front Genet''. 2020; '''11''': 901
Genomic Investigation of the Strawberry Pathogen Phytophthora fragariae Indicates Pathogenicity Is Associated With Transcriptional Variation in Three Key Races. Description: Adams, Thomas M, et al. Genomic Investigation of the Strawberry Pathogen Phytophthora fragariae Indicates Pathogenicity Is Associated With Transcriptional Variation in Three Key Races. ''Front Microbiol''. 2020; '''11''': 490
Genomic landscape of the signals of positive natural selection in populations of Northern Eurasia: A view from Northern Russia. Description: Khrunin, Andrey V, et al. Genomic landscape of the signals of positive natural selection in populations of Northern Eurasia: A view from Northern Russia. ''PLoS One''. 2020; '''15''' (2):e0228778
Genomic mapping identifies two genetic variants in the MC1R gene for coat colour variation in Chinese Tan sheep. Description: Gebreselassie, Gebremedhin, et al. Genomic mapping identifies two genetic variants in the MC1R gene for coat colour variation in Chinese Tan sheep. ''PLoS One''. 2020; '''15''' (8):e0235426
Genomic Prediction of Agronomic Traits in Common Bean (Phaseolus vulgaris L.) Under Environmental Stress. Description: Keller, Beat, et al. Genomic Prediction of Agronomic Traits in Common Bean (Phaseolus vulgaris L.) Under Environmental Stress. ''Front Plant Sci''. 2020; '''11''': 1001
Genomic prediction of depression risk and resilience under stress. Description: Fang, Yu, et al. Genomic prediction of depression risk and resilience under stress. ''Nat Hum Behav''. 2020 Jan; '''4''' (1):111-118
Genomic Prediction Using Low Density Marker Panels in Aquaculture: Performance Across Species, Traits, and Genotyping Platforms. Description: Kriaridou, Christina, et al. Genomic Prediction Using Low Density Marker Panels in Aquaculture: Performance Across Species, Traits, and Genotyping Platforms. ''Front Genet''. 2020; '''11''': 124
Genomic Signatures After Five Generations of Intensive Selective Breeding: Runs of Homozygosity and Genetic Diversity in Representative Domestic and Wild Populations of Turbot (Scophthalmus maximus). Description: Aramburu, Oscar, et al. Genomic Signatures After Five Generations of Intensive Selective Breeding: Runs of Homozygosity and Genetic Diversity in Representative Domestic and Wild Populations of Turbot (Scophthalmus maximus). ''Front Genet''. 2020; '''11''': 296
Genomic signatures of seed mass adaptation to global precipitation gradients in sorghum. Description: Wang, Jianan, et al. Genomic signatures of seed mass adaptation to global precipitation gradients in sorghum. ''Heredity (Edinb)''. 2020 Jan; '''124''' (1):108-121
GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Description: Masuda, Tatsuo, et al. GWAS of five gynecologic diseases and cross-trait analysis in Japanese. ''Eur J Hum Genet''. 2020 Jan; '''28''' (1):95-107
Haplotype Block Analysis Reveals Candidate Genes and QTLs for Meat Quality and Disease Resistance in Chinese Jiangquhai Pig Breed. Description: Oyelami, Favour Oluwapelumi, et al. Haplotype Block Analysis Reveals Candidate Genes and QTLs for Meat Quality and Disease Resistance in Chinese Jiangquhai Pig Breed. ''Front Genet''. 2020; '''11''': 752
Heterozygous Genotype rs17580 AT (PiS) in SERPINA1 is Associated with COPD Secondary to Biomass-Burning and Tobacco Smoking: A Case-Control and Populational Study. Description: Perez-Rubio, Gloria, et al. Heterozygous Genotype rs17580 AT (PiS) in SERPINA1 is Associated with COPD Secondary to Biomass-Burning and Tobacco Smoking: A Case-Control and Populational Study. ''Int J Chron Obstruct Pulmon Dis''. 2020; '''15''': 1181-1190
High-Density Genetic Linkage Mapping of Lepidium Based on Genotyping-by-Sequencing SNPs and Segregating Contig Tag Haplotypes. Description: Geleta, Mulatu, et al. High-Density Genetic Linkage Mapping of Lepidium Based on Genotyping-by-Sequencing SNPs and Segregating Contig Tag Haplotypes. ''Front Plant Sci''. 2020; '''11''': 448
High-Throughput Sequencing to Investigate Associations Between HLA Genes and Metamizole-Induced Agranulocytosis. Description: Cismaru, Anca Liliana, et al. High-Throughput Sequencing to Investigate Associations Between HLA Genes and Metamizole-Induced Agranulocytosis. ''Front Genet''. 2020; '''11''': 951
Host Genetic Variants Potentially Associated With SARS-CoV-2: A Multi-Population Analysis. Description: Smatti, Maria K, et al. Host Genetic Variants Potentially Associated With SARS-CoV-2: A Multi-Population Analysis. ''Front Genet''. 2020; '''11''': 578523
How "simple" methodological decisions affect interpretation of population structure based on reduced representation library DNA sequencing: A case study using the lake whitefish. Description: Graham, Carly F, et al. How "simple" methodological decisions affect interpretation of population structure based on reduced representation library DNA sequencing: A case study using the lake whitefish. ''PLoS One''. 2020; '''15''' (1):e0226608
Hybridization Between Yuccas From Baja California: Genomic and Environmental Patterns. Description: Arteaga, Maria Clara, et al. Hybridization Between Yuccas From Baja California: Genomic and Environmental Patterns. ''Front Plant Sci''. 2020; '''11''': 685
Identification of a Human SOCS1 Polymorphism That Predicts Rheumatoid Arthritis Severity. Description: Lamana, Amalia, et al. Identification of a Human SOCS1 Polymorphism That Predicts Rheumatoid Arthritis Severity. ''Front Immunol''. 2020; '''11''': 1336
Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease. Description: Daida, Kensuke, et al. Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease. ''Front Neurol''. 2020; '''11''': 576465
Identification of Ear Morphology Genes in Maize (Zea mays L.) Using Selective Sweeps and Association Mapping. Description: Li, Ting, et al. Identification of Ear Morphology Genes in Maize (Zea mays L.) Using Selective Sweeps and Association Mapping. ''Front Genet''. 2020; '''11''': 747
Identification of Selective Sweeps in the Domesticated Table and Wine Grape (Vitis vinifera L.). Description: Kui, Ling, et al. Identification of Selective Sweeps in the Domesticated Table and Wine Grape (Vitis vinifera L.). ''Front Plant Sci''. 2020; '''11''': 572
Identifying Pleiotropic SNPs Associated With Femoral Neck and Heel Bone Mineral Density. Description: He, Pei, et al. Identifying Pleiotropic SNPs Associated With Femoral Neck and Heel Bone Mineral Density. ''Front Genet''. 2020; '''11''': 772
Identifying Shared Risk Genes for Asthma, Hay Fever, and Eczema by Multi-Trait and Multiomic Association Analyses. Description: Guo, Hongping, et al. Identifying Shared Risk Genes for Asthma, Hay Fever, and Eczema by Multi-Trait and Multiomic Association Analyses. ''Front Genet''. 2020; '''11''': 270
Impact of Genetic and Nongenetic Factors on Body Mass Index and Waist-Hip Ratio Change in HIV-Infected Individuals Initiating Antiretroviral Therapy. Description: Barcelo, Catalina, et al. Impact of Genetic and Nongenetic Factors on Body Mass Index and Waist-Hip Ratio Change in HIV-Infected Individuals Initiating Antiretroviral Therapy. ''Open Forum Infect Dis''. 2020 Jan; '''7''' (1):ofz464
Incorporating Genome Annotation Into Genomic Prediction for Carcass Traits in Chinese Simmental Beef Cattle. Description: Xu, Ling, et al. Incorporating Genome Annotation Into Genomic Prediction for Carcass Traits in Chinese Simmental Beef Cattle. ''Front Genet''. 2020; '''11''': 481
Incorporating Genome-Wide Association Mapping Results Into Genomic Prediction Models for Grain Yield and Yield Stability in CIMMYT Spring Bread Wheat. Description: Sehgal, Deepmala, et al. Incorporating Genome-Wide Association Mapping Results Into Genomic Prediction Models for Grain Yield and Yield Stability in CIMMYT Spring Bread Wheat. ''Front Plant Sci''. 2020; '''11''': 197
Independent Replication on Genome-Wide Association Study Signals Identifies IRF3 as a Novel Locus for Systemic Lupus Erythematosus. Description: Zhang, Feixia, et al. Independent Replication on Genome-Wide Association Study Signals Identifies IRF3 as a Novel Locus for Systemic Lupus Erythematosus. ''Front Genet''. 2020; '''11''': 600
Individual and joint performance of DNA methylation profiles, genetic risk score and environmental risk scores for predicting breast cancer risk. Description: Guan, Zhong, et al. Individual and joint performance of DNA methylation profiles, genetic risk score and environmental risk scores for predicting breast cancer risk. ''Mol Oncol''. 2020 Jan; '''14''' (1):42-53
Influence of Genetic Variance on Biomarker Levels After Occupational Exposure to 1,6-Hexamethylene Diisocyanate Monomer and 1,6-Hexamethylene Diisocyanate Isocyanurate. Description: Taylor, Laura W, et al. Influence of Genetic Variance on Biomarker Levels After Occupational Exposure to 1,6-Hexamethylene Diisocyanate Monomer and 1,6-Hexamethylene Diisocyanate Isocyanurate. ''Front Genet''. 2020; '''11''': 836
Integrating GWAS and Transcriptomics to Identify the Molecular Underpinnings of Thermal Stress Responses in Drosophila melanogaster. Description: Lecheta, Melise C, et al. Integrating GWAS and Transcriptomics to Identify the Molecular Underpinnings of Thermal Stress Responses in Drosophila melanogaster. ''Front Genet''. 2020; '''11''': 658
Integration of GWAS and eQTL Analysis to Identify Risk Loci and Susceptibility Genes for Gastric Cancer. Description: Ni, Jing, et al. Integration of GWAS and eQTL Analysis to Identify Risk Loci and Susceptibility Genes for Gastric Cancer. ''Front Genet''. 2020; '''11''': 679
Interaction Between Prematurity and the MAOA Gene on Mental Development in Children: A Longitudinal View. Description: Yao, Nai-Jia, et al. Interaction Between Prematurity and the MAOA Gene on Mental Development in Children: A Longitudinal View. ''Front Pediatr''. 2020; '''8''': 92
Interactions among IGF-1, AKT2, FOXO1, and FOXO3 variations and between genes and physical activities on physical performance in community-dwelling elders. Description: Li, Tsai-Chung, et al. Interactions among IGF-1, AKT2, FOXO1, and FOXO3 variations and between genes and physical activities on physical performance in community-dwelling elders. ''PLoS One''. 2020; '''15''' (9):e0239530
Intracranial aneurysm's association with genetic variants, transcription abnormality, and methylation changes in ADAMTS genes. Description: Chen, Shi, et al. Intracranial aneurysm's association with genetic variants, transcription abnormality, and methylation changes in ADAMTS genes. ''PeerJ''. 2020; '''8''': e8596
Introgression Among Cultivated and Wild Grapevine in Tuscany. Description: D'Onofrio, Claudio. Introgression Among Cultivated and Wild Grapevine in Tuscany. ''Front Plant Sci''. 2020; '''11''': 202
Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Description: Zhou, Jiayan, et al. Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. ''PLoS One''. 2020; '''15''' (9):e0238304
Investigation of the STOX1 polymorphism on lumbar disc herniation. Description: Yang, Xuejun, et al. Investigation of the STOX1 polymorphism on lumbar disc herniation. ''Mol Genet Genomic Med''. 2020 Jan; '''8''' (1):e1038
KRGDB: the large-scale variant database of 1722 Koreans based on whole genome sequencing. Description: Jung, Kwang Su, et al. KRGDB: the large-scale variant database of 1722 Koreans based on whole genome sequencing. ''Database (Oxford)''. 2020 Jan 1; '''2020''':
Lack of Association Between Genetic Variants at ACE2 and TMPRSS2 Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes. Description: Lopera Maya, Esteban A, et al. Lack of Association Between Genetic Variants at ACE2 and TMPRSS2 Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes. ''Front Genet''. 2020; '''11''': 613
Lack of association of genetic variants for diabetic retinopathy in Taiwanese patients with diabetic nephropathy. Description: Hsieh, Ai-Ru, et al. Lack of association of genetic variants for diabetic retinopathy in Taiwanese patients with diabetic nephropathy. ''BMJ Open Diabetes Res Care''. 2020 Jan; '''8''' (1):
Maternal environmental risk factors and the development of internalizing and externalizing problems in childhood: The complex role of genetic factors. Description: Ensink, Judith B M, et al. Maternal environmental risk factors and the development of internalizing and externalizing problems in childhood: The complex role of genetic factors. ''Am J Med Genet B Neuropsychiatr Genet''. 2020 Jan; '''183''' (1):17-25
Mendelian Randomization Identifies CpG Methylation Sites With Mediation Effects for Genetic Influences on BMD in Peripheral Blood Monocytes. Description: Yu, Fangtang, et al. Mendelian Randomization Identifies CpG Methylation Sites With Mediation Effects for Genetic Influences on BMD in Peripheral Blood Monocytes. ''Front Genet''. 2020; '''11''': 60
Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci. Description: Gaare, Johannes Jernqvist, et al. Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci. ''PLoS One''. 2020; '''15''' (10):e0239824
Molecular basis for a new bovine model of Niemann-Pick type C disease. Description: Woolley, Shernae A, et al. Molecular basis for a new bovine model of Niemann-Pick type C disease. ''PLoS One''. 2020; '''15''' (9):e0238697
Multi-ethnic transcriptome-wide association study of prostate cancer. Description: Fiorica, Peter N, et al. Multi-ethnic transcriptome-wide association study of prostate cancer. ''PLoS One''. 2020; '''15''' (9):e0236209
Multi-Location Evaluation of Global Wheat Lines Reveal Multiple QTL for Adult Plant Resistance to Septoria Nodorum Blotch (SNB) Detected in Specific Environments and in Response to Different Isolates. Description: Francki, Michael G, et al. Multi-Location Evaluation of Global Wheat Lines Reveal Multiple QTL for Adult Plant Resistance to Septoria Nodorum Blotch (SNB) Detected in Specific Environments and in Response to Different Isolates. ''Front Plant Sci''. 2020; '''11''': 771
Multi-Omics Analysis Reveals MicroRNAs Associated With Cardiometabolic Traits. Description: Mens, Michelle M J, et al. Multi-Omics Analysis Reveals MicroRNAs Associated With Cardiometabolic Traits. ''Front Genet''. 2020; '''11''': 110
Neural correlates of polygenic risk score for autism spectrum disorders in general population. Description: Khundrakpam, Budhachandra, et al. Neural correlates of polygenic risk score for autism spectrum disorders in general population. ''Brain Commun''. 2020; '''2''' (2):fcaa092
Neurophysiological and Genetic Findings in Patients With Juvenile Myoclonic Epilepsy. Description: Stefani, Stefani, et al. Neurophysiological and Genetic Findings in Patients With Juvenile Myoclonic Epilepsy. ''Front Integr Neurosci''. 2020; '''14''': 45
New Insights From Imputed Whole-Genome Sequence-Based Genome-Wide Association Analysis and Transcriptome Analysis: The Genetic Mechanisms Underlying Residual Feed Intake in Chickens. Description: Ye, Shaopan, et al. New Insights From Imputed Whole-Genome Sequence-Based Genome-Wide Association Analysis and Transcriptome Analysis: The Genetic Mechanisms Underlying Residual Feed Intake in Chickens. ''Front Genet''. 2020; '''11''': 243
Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort. Description: Schidlowski, Laire, et al. Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort. ''Front Genet''. 2020; '''11''': 397
Novel genes involved in the genetic architecture of temperament in Brahman cattle. Description: Paredes-Sanchez, Francisco Alejandro, et al. Novel genes involved in the genetic architecture of temperament in Brahman cattle. ''PLoS One''. 2020; '''15''' (8):e0237825
Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma. Description: Rauf, Bushra, et al. Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma. ''Mol Vis''. 2020; '''26''': 14-25
On the usefulness of parental lines GWAS for predicting low heritability traits in tropical maize hybrids. Description: Galli, Giovanni, et al. On the usefulness of parental lines GWAS for predicting low heritability traits in tropical maize hybrids. ''PLoS One''. 2020; '''15''' (2):e0228724
Optimized Whole Genome Association Scanning for Discovery of HLA Class I-Restricted Minor Histocompatibility Antigens. Description: Fuchs, Kyra J, et al. Optimized Whole Genome Association Scanning for Discovery of HLA Class I-Restricted Minor Histocompatibility Antigens. ''Front Immunol''. 2020; '''11''': 659
Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade-off with American chestnut ancestry implies resistance is polygenic. Description: Westbrook, Jared W, et al. Optimizing genomic selection for blight resistance in American chestnut backcross populations: A trade-off with American chestnut ancestry implies resistance is polygenic. ''Evol Appl''. 2020 Jan; '''13''' (1):31-47
"Out, out, brief candle! Life's but a walking shadow": 5-HTTLPR Is Associated With Current Suicidal Ideation but Not With Previous Suicide Attempts and Interacts With Recent Relationship Problems. Description: Bokor, Janos, et al. "Out, out, brief candle! Life's but a walking shadow": 5-HTTLPR Is Associated With Current Suicidal Ideation but Not With Previous Suicide Attempts and Interacts With Recent Relationship Problems. ''Front Psychiatry''. 2020; '''11''': 567
Pharmacogenomics Study for Raloxifene in Postmenopausal Female with Osteoporosis. Description: Lu, Hsing-Fang, et al. Pharmacogenomics Study for Raloxifene in Postmenopausal Female with Osteoporosis. ''Dis Markers''. 2020; '''2020''': 8855423
Phenotypic Responses to and Genetic Architecture of Sterility Following Exposure to Sub-Lethal Temperature During Development. Description: Zwoinska, Martyna K, et al. Phenotypic Responses to and Genetic Architecture of Sterility Following Exposure to Sub-Lethal Temperature During Development. ''Front Genet''. 2020; '''11''': 573
Phosphodiesterase 4D Gene Modifies the Functional Network of Patients With Mild Cognitive Impairment and Alzheimer's Disease. Description: Xiang, Jie, et al. Phosphodiesterase 4D Gene Modifies the Functional Network of Patients With Mild Cognitive Impairment and Alzheimer's Disease. ''Front Genet''. 2020; '''11''': 890
Polygenic Risk Scores for Subtyping of Schizophrenia. Description: Chen, Jingchun, et al. Polygenic Risk Scores for Subtyping of Schizophrenia. ''Schizophr Res Treatment''. 2020; '''2020''': 1638403
Population genetic simulation study of power in association testing across genetic architectures and study designs. Description: Tong, Dominic M H, et al. Population genetic simulation study of power in association testing across genetic architectures and study designs. ''Genet Epidemiol''. 2020 Jan; '''44''' (1):90-103
Population structure analysis and identification of genomic regions under selection associated with low-nitrogen tolerance in tropical maize lines. Description: Sant'Ana, Gustavo Cesar, et al. Population structure analysis and identification of genomic regions under selection associated with low-nitrogen tolerance in tropical maize lines. ''PLoS One''. 2020; '''15''' (9):e0239900
Precise prediction of the radiation pneumonitis in lung cancer: an explorative preliminary mathematical model using genotype information. Description: Du, Lehui, et al. Precise prediction of the radiation pneumonitis in lung cancer: an explorative preliminary mathematical model using genotype information. ''J Cancer''. 2020; '''11''' (8):2329-2338
Predicted DRD4 prefrontal gene expression moderates snack intake and stress perception in response to the environment in adolescents. Description: Portella, Andre Krumel, et al. Predicted DRD4 prefrontal gene expression moderates snack intake and stress perception in response to the environment in adolescents. ''PLoS One''. 2020; '''15''' (6):e0234601
Prediction of Smoking Behavior From Single Nucleotide Polymorphisms With Machine Learning Approaches. Description: Xu, Yi, et al. Prediction of Smoking Behavior From Single Nucleotide Polymorphisms With Machine Learning Approaches. ''Front Psychiatry''. 2020; '''11''': 416
PROC Promoter Single Nucleotide Polymorphisms Associated With Low Protein C Activity But Not Increased Risk of Thromboembolism in Pediatric Population. Description: Udomkittivorakul, Natsumon, et al. PROC Promoter Single Nucleotide Polymorphisms Associated With Low Protein C Activity But Not Increased Risk of Thromboembolism in Pediatric Population. ''Clin Appl Thromb Hemost''. 2020 Jan-Dec; '''26''': 1076029620935206
Quantifying the Predictive Accuracy of a Polygenic Risk Score for Predicting Incident Cancer Cases : Application to the CARTaGENE Cohort. Description: Duhaze, Julianne, et al. Quantifying the Predictive Accuracy of a Polygenic Risk Score for Predicting Incident Cancer Cases : Application to the CARTaGENE Cohort. ''Front Genet''. 2020; '''11''': 408
Quantitative phenotyping of shell suture strength in walnut (Juglans regia L.) enhances precision for detection of QTL and genome-wide association mapping. Description: Sideli, Gina M, et al. Quantitative phenotyping of shell suture strength in walnut (Juglans regia L.) enhances precision for detection of QTL and genome-wide association mapping. ''PLoS One''. 2020; '''15''' (4):e0231144
RAD52 variants influence NSCLC risk in the Chinese population in a high altitude area. Description: Li, Miao, et al. RAD52 variants influence NSCLC risk in the Chinese population in a high altitude area. ''Ther Adv Respir Dis''. 2020 Jan-Dec; '''14''': 1753466620918192
Range reduction of Oblong Rocksnail, Leptoxis compacta, shapes riverscape genetic patterns. Description: Wright, Aaliyah D, et al. Range reduction of Oblong Rocksnail, Leptoxis compacta, shapes riverscape genetic patterns. ''PeerJ''. 2020; '''8''': e9789
Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency. Description: Suratannon, Narissara, et al. Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency. ''Front Immunol''. 2020; '''11''': 614
Replication of the Association Between Keratoconus and Polymorphisms in PNPLA2 and MAML2 in a Han Chinese Population. Description: Zhang, Jing, et al. Replication of the Association Between Keratoconus and Polymorphisms in PNPLA2 and MAML2 in a Han Chinese Population. ''Front Genet''. 2020; '''11''': 827
Response to IL-17A inhibitors secukinumab and ixekizumab cannot be explained by genetic variation in the protein-coding and untranslated regions of the IL-17A gene: results from a multicentre study of four European psoriasis cohorts. Description: van Vugt, L J, et al. Response to IL-17A inhibitors secukinumab and ixekizumab cannot be explained by genetic variation in the protein-coding and untranslated regions of the IL-17A gene: results from a multicentre study of four European psoriasis cohorts. ''J Eur Acad Dermatol Venereol''. 2020 Jan; '''34''' (1):112-118
Robustification of Linear Regression and Its Application in Genome-Wide Association Studies. Description: Alamin, Md, et al. Robustification of Linear Regression and Its Application in Genome-Wide Association Studies. ''Front Genet''. 2020; '''11''': 549
Schizophrenia Polygenic Risk and Brain Structural Changes in Methamphetamine-Associated Psychosis in a South African Population. Description: Passchier, Ruth V, et al. Schizophrenia Polygenic Risk and Brain Structural Changes in Methamphetamine-Associated Psychosis in a South African Population. ''Front Genet''. 2020; '''11''': 1018
Selection in Australian Thoroughbred horses acts on a locus associated with early two-year old speed. Description: Han, Haige, et al. Selection in Australian Thoroughbred horses acts on a locus associated with early two-year old speed. ''PLoS One''. 2020; '''15''' (2):e0227212
Single nucleotide polymorphisms in telomere length-related genes are associated with hepatocellular carcinoma risk in the Chinese Han population. Description: Huang, Peng, et al. Single nucleotide polymorphisms in telomere length-related genes are associated with hepatocellular carcinoma risk in the Chinese Han population. ''Ther Adv Med Oncol''. 2020; '''12''': 1758835920933029
SNPs in IL4 and IFNG show no protective associations with human African trypanosomiasis in the Democratic Republic of the Congo: a case-control study. Description: Fataki Asina, Olivier, et al. SNPs in IL4 and IFNG show no protective associations with human African trypanosomiasis in the Democratic Republic of the Congo: a case-control study. ''AAS Open Res''. 2020; '''3''': 35
Statin Use Associates With Risk of Type 2 Diabetes via Epigenetic Patterns at ABCG1. Description: Liu, Yuwei, et al. Statin Use Associates With Risk of Type 2 Diabetes via Epigenetic Patterns at ABCG1. ''Front Genet''. 2020; '''11''': 622
Stress, Cortisol and NR3C1 in At-Risk Individuals for Psychosis: A Mendelian Randomization Study. Description: Iftimovici, Anton, et al. Stress, Cortisol and NR3C1 in At-Risk Individuals for Psychosis: A Mendelian Randomization Study. ''Front Psychiatry''. 2020; '''11''': 680
SWATH-MS based proteomic profiling of pancreatic ductal adenocarcinoma tumours reveals the interplay between the extracellular matrix and related intracellular pathways. Description: Nweke, Ekene Emmanuel, et al. SWATH-MS based proteomic profiling of pancreatic ductal adenocarcinoma tumours reveals the interplay between the extracellular matrix and related intracellular pathways. ''PLoS One''. 2020; '''15''' (10):e0240453
Systematic analysis of genetic variants in cancer-testis genes identified two novel lung cancer susceptibility loci in Chinese population. Description: Li, Zhihua, et al. Systematic analysis of genetic variants in cancer-testis genes identified two novel lung cancer susceptibility loci in Chinese population. ''J Cancer''. 2020; '''11''' (7):1985-1993
Systems Analysis of Biliary Atresia Through Integration of High-Throughput Biological Data. Description: Min, Jun, et al. Systems Analysis of Biliary Atresia Through Integration of High-Throughput Biological Data. ''Front Physiol''. 2020; '''11''': 966
The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study. Description: van Reij, R R I, et al. The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study. ''Anaesthesia''. 2020 Jan; '''75 Suppl 1''': e111-e120
The Association Between Heat-Shock Protein Polymorphisms and Prognosis in Lung Cancer Patients Treated With Platinum-Based Chemotherapy. Description: Zou, Ting, et al. The Association Between Heat-Shock Protein Polymorphisms and Prognosis in Lung Cancer Patients Treated With Platinum-Based Chemotherapy. ''Front Pharmacol''. 2020; '''11''': 1029
The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations. Description: Rocha, Cristiane S, et al. The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations. ''NPJ Genom Med''. 2020; '''5''': 42
The effects of age at menarche and first sexual intercourse on reproductive and behavioural outcomes: A Mendelian randomization study. Description: Lawn, Rebecca B, et al. The effects of age at menarche and first sexual intercourse on reproductive and behavioural outcomes: A Mendelian randomization study. ''PLoS One''. 2020; '''15''' (6):e0234488
The Genetic Architecture for Phenotypic Plasticity of the Rice Grain Ionome. Description: Tan, Yongjun, et al. The Genetic Architecture for Phenotypic Plasticity of the Rice Grain Ionome. ''Front Plant Sci''. 2020; '''11''': 12
The Genetic Architecture of the Chickens Dropping Moisture by Genetic Parameter Estimation and Genome-Wide Association. Description: Zhu, Tao, et al. The Genetic Architecture of the Chickens Dropping Moisture by Genetic Parameter Estimation and Genome-Wide Association. ''Front Genet''. 2020; '''11''': 806
The Genetic Population Structure of Robinson Crusoe Island, Chile. Description: Mountford, Hayley S, et al. The Genetic Population Structure of Robinson Crusoe Island, Chile. ''Front Genet''. 2020; '''11''': 669
The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population. Description: Soltesz, Beata, et al. The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population. ''PLoS One''. 2020; '''15''' (6):e0234547
The Identification of Admixture Patterns Could Refine Pharmacogenetic Counseling: Analysis of a Population-Based Sample in Mexico. Description: Martinez-Magana, Jose Jaime, et al. The Identification of Admixture Patterns Could Refine Pharmacogenetic Counseling: Analysis of a Population-Based Sample in Mexico. ''Front Pharmacol''. 2020; '''11''': 324
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change. Description: Oni-Orisan, Akinyemi, et al. The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change. ''NPJ Genom Med''. 2020; '''5''': 1
The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder. Description: Li, Danyang, et al. The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder. ''NPJ Genom Med''. 2020; '''5''': 45
The role of 5-HTTLPR in autism spectrum disorder: New evidence and a meta-analysis of this polymorphism in Latin American population with psychiatric disorders. Description: Nunez-Rios, D L, et al. The role of 5-HTTLPR in autism spectrum disorder: New evidence and a meta-analysis of this polymorphism in Latin American population with psychiatric disorders. ''PLoS One''. 2020; '''15''' (7):e0235512
The sockeye salmon genome, transcriptome, and analyses identifying population defining regions of the genome. Description: Christensen, Kris A, et al. The sockeye salmon genome, transcriptome, and analyses identifying population defining regions of the genome. ''PLoS One''. 2020; '''15''' (10):e0240935
Transcriptome-Wide Patterns of the Genetic and Expression Variations in Two Sympatric Schizothoracine Fishes in a Tibetan Plateau Glacier Lake. Description: Chen, Juan, et al. Transcriptome-Wide Patterns of the Genetic and Expression Variations in Two Sympatric Schizothoracine Fishes in a Tibetan Plateau Glacier Lake. ''Genome Biol Evol''. 2020 Jan 1; '''12''' (1):3725-3737
Two Variants in the NOTCH4 and HLA-C Genes Contribute to Familial Clustering of Psoriasis. Description: Cai, Minglong, et al. Two Variants in the NOTCH4 and HLA-C Genes Contribute to Familial Clustering of Psoriasis. ''Int J Genomics''. 2020; '''2020''': 6907378
Uncovering Candidate Genes Controlling Major Fruit-Related Traits in Pepper via Genotype-by-Sequencing Based QTL Mapping and Genome-Wide Association Study. Description: Lee, Hea-Young, et al. Uncovering Candidate Genes Controlling Major Fruit-Related Traits in Pepper via Genotype-by-Sequencing Based QTL Mapping and Genome-Wide Association Study. ''Front Plant Sci''. 2020; '''11''': 1100
Using Genetic Risk Score Approaches to Infer Whether an Environmental Factor Attenuates or Exacerbates the Adverse Influence of a Candidate Gene. Description: Lin, Wan-Yu, et al. Using Genetic Risk Score Approaches to Infer Whether an Environmental Factor Attenuates or Exacerbates the Adverse Influence of a Candidate Gene. ''Front Genet''. 2020; '''11''': 331
Utilization of archived neonatal dried blood spots for genome-wide genotyping. Description: Sok, Pagna, et al. Utilization of archived neonatal dried blood spots for genome-wide genotyping. ''PLoS One''. 2020; '''15''' (2):e0229352
Whole genome re-sequencing of sweet cherry (Prunus avium L.) yields insights into genomic diversity of a fruit species. Description: Xanthopoulou, Aliki, et al. Whole genome re-sequencing of sweet cherry (Prunus avium L.) yields insights into genomic diversity of a fruit species. ''Hortic Res''. 2020; '''7''': 60
Whole Genome Scan Reveals Molecular Signatures of Divergence and Selection Related to Important Traits in Durum Wheat Germplasm. Description: Taranto, Francesca, et al. Whole Genome Scan Reveals Molecular Signatures of Divergence and Selection Related to Important Traits in Durum Wheat Germplasm. ''Front Genet''. 2020; '''11''': 217
Whole Genome Sequence Data Provides Novel Insights Into the Genetic Architecture of Meat Quality Traits in Beef. Description: Leal-Gutierrez, Joel D, et al. Whole Genome Sequence Data Provides Novel Insights Into the Genetic Architecture of Meat Quality Traits in Beef. ''Front Genet''. 2020; '''11''': 538640
Whole Genome Sequencing of Four Representatives From the Admixed Population of the United Arab Emirates. Description: Daw Elbait, Gihan, et al. Whole Genome Sequencing of Four Representatives From the Admixed Population of the United Arab Emirates. ''Front Genet''. 2020; '''11''': 681
Whole genome sequencing of Herpes Simplex Virus 1 directly from human cerebrospinal fluid reveals selective constraints in neurotropic viruses. Description: Lassalle, Florent, et al. Whole genome sequencing of Herpes Simplex Virus 1 directly from human cerebrospinal fluid reveals selective constraints in neurotropic viruses. ''Virus Evol''. 2020 Jan; '''6''' (1):veaa012
Using whole-genome SNP data to reconstruct a large multi-generation pedigree in apple germplasm. Description: Muranty, Helene, et al. Using whole-genome SNP data to reconstruct a large multi-generation pedigree in apple germplasm. ''BMC Plant Biol''. 2020 Jan 2; '''20''' (1):2
A shared genetic basis of mimicry across swallowtail butterflies points to ancestral co-option of doublesex. Description: Palmer, Daniela H, et al. A shared genetic basis of mimicry across swallowtail butterflies points to ancestral co-option of doublesex. ''Nat Commun''. 2020 Jan 3; '''11''' (1):6
Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations. Description: Yehia, Lamis, et al. Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations. ''JAMA Netw Open''. 2020 Jan 3; '''3''' (1):e1920415
Inference of Breed Structure in Farm Animals: Empirical Comparison between SNP and Microsatellite Performance. Description: Laoun, Abbas, et al. Inference of Breed Structure in Farm Animals: Empirical Comparison between SNP and Microsatellite Performance. ''Genes (Basel)''. 2020 Jan 4; '''11''' (1):
A Genome-Wide Association Study Identifies Quantitative Trait Loci Affecting Hematological Traits in Camelus bactrianus. Description: Guo, Fucheng, et al. A Genome-Wide Association Study Identifies Quantitative Trait Loci Affecting Hematological Traits in Camelus bactrianus. ''Animals (Basel)''. 2020 Jan 7; '''10''' (1):
Effect of 15 BMI-Associated Polymorphisms, Reported for Europeans, across Ethnicities and Degrees of Amerindian Ancestry in Mexican Children. Description: Costa-Urrutia, Paula, et al. Effect of 15 BMI-Associated Polymorphisms, Reported for Europeans, across Ethnicities and Degrees of Amerindian Ancestry in Mexican Children. ''Int J Mol Sci''. 2020 Jan 7; '''21''' (2):
Heritability estimates for 361 blood metabolites across 40 genome-wide association studies. Description: Hagenbeek, Fiona A, et al. Heritability estimates for 361 blood metabolites across 40 genome-wide association studies. ''Nat Commun''. 2020 Jan 7; '''11''' (1):39
IL10 rs1800872 Is Associated with Non-Steroidal Anti-Inflammatory Drugs Exacerbated Respiratory Disease in Mexican-Mestizo Patients. Description: Pavon-Romero, Gandhi Fernando, et al. IL10 rs1800872 Is Associated with Non-Steroidal Anti-Inflammatory Drugs Exacerbated Respiratory Disease in Mexican-Mestizo Patients. ''Biomolecules''. 2020 Jan 7; '''10''' (1):
Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility. Description: Kachuri, Linda, et al. Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility. ''Nat Commun''. 2020 Jan 7; '''11''' (1):27
Influence of Genetic Interactions on Polygenic Prediction. Description: Dai, Zhijun, et al. Influence of Genetic Interactions on Polygenic Prediction. ''G3 (Bethesda)''. 2020 Jan 7; '''10''' (1):109-115
Whole-genome sequencing of 128 camels across Asia reveals origin and migration of domestic Bactrian camels. Description: Ming, Liang, et al. Whole-genome sequencing of 128 camels across Asia reveals origin and migration of domestic Bactrian camels. ''Commun Biol''. 2020 Jan 7; '''3''' (1):1
Global evaluation of taxonomic relationships and admixture within the Culex pipiens complex of mosquitoes. Description: Aardema, Matthew L, et al. Global evaluation of taxonomic relationships and admixture within the Culex pipiens complex of mosquitoes. ''Parasit Vectors''. 2020 Jan 8; '''13''' (1):8
Genome-Wide Association Study of Opioid Cessation. Description: Cox, Jiayi W, et al. Genome-Wide Association Study of Opioid Cessation. ''J Clin Med''. 2020 Jan 9; '''9''' (1):
Pigment Intensity in Dogs is Associated with a Copy Number Variant Upstream of KITLG. Description: Weich, Kalie, et al. Pigment Intensity in Dogs is Associated with a Copy Number Variant Upstream of KITLG. ''Genes (Basel)''. 2020 Jan 9; '''11''' (1):
Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population. Description: Corredor, Zuray, et al. Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population. ''Sci Rep''. 2020 Jan 10; '''10''' (1):144
Genome-Wide Association Study and Subsequent Exclusion of ATCAY as a Candidate Gene Involved in Equine Neuroaxonal Dystrophy Using Two Animal Models. Description: Hales, Erin N, et al. Genome-Wide Association Study and Subsequent Exclusion of ATCAY as a Candidate Gene Involved in Equine Neuroaxonal Dystrophy Using Two Animal Models. ''Genes (Basel)''. 2020 Jan 10; '''11''' (1):
The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple Sclerosis. Description: Gomez-Fernandez, Paloma, et al. The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple Sclerosis. ''Cells''. 2020 Jan 10; '''9''' (1):
Longitudinal epigenome-wide association studies of three male military cohorts reveal multiple CpG sites associated with post-traumatic stress disorder. Description: Snijders, Clara, et al. Longitudinal epigenome-wide association studies of three male military cohorts reveal multiple CpG sites associated with post-traumatic stress disorder. ''Clin Epigenetics''. 2020 Jan 13; '''12''' (1):11
Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study. Description: Kim, Yong Woo, et al. Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study. ''Sci Rep''. 2020 Jan 14; '''10''' (1):221
De novo variants in exomes of congenital heart disease patients identify risk genes and pathways. Description: Sevim Bayrak, Cigdem, et al. De novo variants in exomes of congenital heart disease patients identify risk genes and pathways. ''Genome Med''. 2020 Jan 15; '''12''' (1):9
Genomic inbreeding trends, influential sire lines and selection in the global Thoroughbred horse population. Description: McGivney, Beatrice A, et al. Genomic inbreeding trends, influential sire lines and selection in the global Thoroughbred horse population. ''Sci Rep''. 2020 Jan 16; '''10''' (1):466
Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients. Description: Li, Mo, et al. Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients. ''Transl Psychiatry''. 2020 Jan 16; '''10''' (1):5
Identification of genetic polymorphisms modulating nausea and vomiting in two series of opioid-treated cancer patients. Description: Colombo, Francesca, et al. Identification of genetic polymorphisms modulating nausea and vomiting in two series of opioid-treated cancer patients. ''Sci Rep''. 2020 Jan 17; '''10''' (1):542
Using regulatory variants to detect gene-gene interactions identifies networks of genes linked to cell immortalisation. Description: Wragg, D, et al. Using regulatory variants to detect gene-gene interactions identifies networks of genes linked to cell immortalisation. ''Nat Commun''. 2020 Jan 17; '''11''' (1):343
Contribution of Known Genetic Risk Variants to Dyslipidemias and Type 2 Diabetes in Mexico: A Population-Based Nationwide Study. Description: Huerta-Chagoya, Alicia, et al. Contribution of Known Genetic Risk Variants to Dyslipidemias and Type 2 Diabetes in Mexico: A Population-Based Nationwide Study. ''Genes (Basel)''. 2020 Jan 20; '''11''' (1):
FAM222A encodes a protein which accumulates in plaques in Alzheimer's disease. Description: Yan, Tingxiang, et al. FAM222A encodes a protein which accumulates in plaques in Alzheimer's disease. ''Nat Commun''. 2020 Jan 21; '''11''' (1):411
Genetic variants in IL17A and serum levels of IL-17A are associated with COPD related to tobacco smoking and biomass burning. Description: Ponce-Gallegos, Marco A, et al. Genetic variants in IL17A and serum levels of IL-17A are associated with COPD related to tobacco smoking and biomass burning. ''Sci Rep''. 2020 Jan 21; '''10''' (1):784
Integrated genome-wide investigations of the housefly, a global vector of diseases reveal unique dispersal patterns and bacterial communities across farms. Description: Bahrndorff, Simon, et al. Integrated genome-wide investigations of the housefly, a global vector of diseases reveal unique dispersal patterns and bacterial communities across farms. ''BMC Genomics''. 2020 Jan 21; '''21''' (1):66
Personality, lifestyle and job satisfaction: causal association between neuroticism and job satisfaction using Mendelian randomisation in the UK biobank cohort. Description: Rukh, Gull, et al. Personality, lifestyle and job satisfaction: causal association between neuroticism and job satisfaction using Mendelian randomisation in the UK biobank cohort. ''Transl Psychiatry''. 2020 Jan 21; '''10''' (1):11
Targeted exome sequencing identifies five novel loci at genome-wide significance for modulating antidepressant response in patients with major depressive disorder. Description: Xu, Zhi, et al. Targeted exome sequencing identifies five novel loci at genome-wide significance for modulating antidepressant response in patients with major depressive disorder. ''Transl Psychiatry''. 2020 Jan 23; '''10''' (1):30
CUBIC: an atlas of genetic architecture promises directed maize improvement. Description: Liu, Hai-Jun, et al. CUBIC: an atlas of genetic architecture promises directed maize improvement. ''Genome Biol''. 2020 Jan 24; '''21''' (1):20
Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Description: Coltell, Oscar, et al. Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. ''Nutrients''. 2020 Jan 24; '''12''' (2):
Novel Genetic Variants of ALG6 and GALNTL4 of the Glycosylation Pathway Predict Cutaneous Melanoma-Specific Survival. Description: Zhou, Bingrong, et al. Novel Genetic Variants of ALG6 and GALNTL4 of the Glycosylation Pathway Predict Cutaneous Melanoma-Specific Survival. ''Cancers (Basel)''. 2020 Jan 24; '''12''' (2):
Association of Irregular Pigment Epithelial Detachment in Central Serous Chorioretinopathy with Genetic Variants Implicated in Age-related Macular Degeneration. Description: Cho, Soo Chang, et al. Association of Irregular Pigment Epithelial Detachment in Central Serous Chorioretinopathy with Genetic Variants Implicated in Age-related Macular Degeneration. ''Sci Rep''. 2020 Jan 27; '''10''' (1):1203
Genetic associations with clozapine-induced myocarditis in patients with schizophrenia. Description: Lacaze, Paul, et al. Genetic associations with clozapine-induced myocarditis in patients with schizophrenia. ''Transl Psychiatry''. 2020 Jan 27; '''10''' (1):37
Genomic influences on self-reported childhood maltreatment. Description: Dalvie, Shareefa, et al. Genomic influences on self-reported childhood maltreatment. ''Transl Psychiatry''. 2020 Jan 27; '''10''' (1):38
Identification of a novel uterine leiomyoma GWAS locus in a Japanese population. Description: Sakai, Kensuke, et al. Identification of a novel uterine leiomyoma GWAS locus in a Japanese population. ''Sci Rep''. 2020 Jan 27; '''10''' (1):1197
Adaptive introgression from indicine cattle into white cattle breeds from Central Italy. Description: Barbato, Mario, et al. Adaptive introgression from indicine cattle into white cattle breeds from Central Italy. ''Sci Rep''. 2020 Jan 28; '''10''' (1):1279
Deconstructing the genetic architecture of iron deficiency chlorosis in soybean using genome-wide approaches. Description: Assefa, Teshale, et al. Deconstructing the genetic architecture of iron deficiency chlorosis in soybean using genome-wide approaches. ''BMC Plant Biol''. 2020 Jan 28; '''20''' (1):42
Evaluation of genetic diversity, agronomic traits, and anthracnose resistance in the NPGS Sudan Sorghum Core collection. Description: Cuevas, Hugo E, et al. Evaluation of genetic diversity, agronomic traits, and anthracnose resistance in the NPGS Sudan Sorghum Core collection. ''BMC Genomics''. 2020 Jan 28; '''21''' (1):88
Functional and population genetic features of copy number variations in two dairy cattle populations. Description: Lee, Young-Lim, et al. Functional and population genetic features of copy number variations in two dairy cattle populations. ''BMC Genomics''. 2020 Jan 28; '''21''' (1):89
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies. Description: Orme, Tatiana, et al. Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies. ''Acta Neuropathol Commun''. 2020 Jan 29; '''8''' (1):5
Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease. Description: Elsheikh, Samar S M, et al. Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease. ''Sci Rep''. 2020 Jan 29; '''10''' (1):1433
How to study runs of homozygosity using PLINK? A guide for analyzing medium density SNP data in livestock and pet species. Description: Meyermans, R, et al. How to study runs of homozygosity using PLINK? A guide for analyzing medium density SNP data in livestock and pet species. ''BMC Genomics''. 2020 Jan 29; '''21''' (1):94
The association of CASC16 variants with breast Cancer risk in a northwest Chinese female population. Description: Zuo, Xiaoxiao, et al. The association of CASC16 variants with breast Cancer risk in a northwest Chinese female population. ''Mol Med''. 2020 Jan 29; '''26''' (1):11
Association of the genetic ancestry with resistant hypertension in the ReHOT (Resistant Hypertension Optimal Treatment) randomized study. Description: Bueno, Carolina Tosin, et al. Association of the genetic ancestry with resistant hypertension in the ReHOT (Resistant Hypertension Optimal Treatment) randomized study. ''Sci Rep''. 2020 Jan 30; '''10''' (1):1476
Polygenic risk for coronary heart disease acts through atherosclerosis in type 2 diabetes. Description: Lu, Tianyuan, et al. Polygenic risk for coronary heart disease acts through atherosclerosis in type 2 diabetes. ''Cardiovasc Diabetol''. 2020 Jan 30; '''19''' (1):12
Genome-wide association study reveals that different pathways contribute to grain quality variation in sorghum (Sorghum bicolor). Description: Kimani, Wilson, et al. Genome-wide association study reveals that different pathways contribute to grain quality variation in sorghum (Sorghum bicolor). ''BMC Genomics''. 2020 Jan 31; '''21''' (1):112
Stratified analyses of genome wide association study data reveal haplotypes for a candidate gene on chromosome 2 (KIAA1211L) is associated with opioid use in patients of Arabian descent. Description: Alblooshi, Hiba, et al. Stratified analyses of genome wide association study data reveal haplotypes for a candidate gene on chromosome 2 (KIAA1211L) is associated with opioid use in patients of Arabian descent. ''BMC Psychiatry''. 2020 Jan 31; '''20''' (1):41
Along the Indian Ocean Coast: Genomic Variation in Mozambique Provides New Insights into the Bantu Expansion. Description: Semo, Armando, et al. Along the Indian Ocean Coast: Genomic Variation in Mozambique Provides New Insights into the Bantu Expansion. ''Mol Biol Evol''. 2020 Feb 1; '''37''' (2):406-416
Analysis of common and rare VPS13C variants in late-onset Parkinson disease. Description: Rudakou, Uladzislau, et al. Analysis of common and rare VPS13C variants in late-onset Parkinson disease. ''Neurol Genet''. 2020 Feb; '''6''' (1):385
Analysis of the genetic variants associated with circulating levels of sgp130. Results from the IMPROVE study. Description: Bonomi, Alice, et al. Analysis of the genetic variants associated with circulating levels of sgp130. Results from the IMPROVE study. ''Genes Immun''. 2020 Feb; '''21''' (2):100-108
A SNP, Gene, and Polygenic Risk Score Approach of Oxytocin-Vasopressin Genes in Adolescents' Loneliness. Description: Verhagen, Maaike, et al. A SNP, Gene, and Polygenic Risk Score Approach of Oxytocin-Vasopressin Genes in Adolescents' Loneliness. ''J Res Adolesc''. 2020 Feb; '''30 Suppl 2''': 333-348
Assessing connectivity despite high diversity in island populations of a malaria mosquito. Description: Bergey, Christina M, et al. Assessing connectivity despite high diversity in island populations of a malaria mosquito. ''Evol Appl''. 2020 Feb; '''13''' (2):417-431
Autism spectrum disorder polygenic scores are associated with every day executive function in children admitted for clinical assessment. Description: Torske, Tonje, et al. Autism spectrum disorder polygenic scores are associated with every day executive function in children admitted for clinical assessment. ''Autism Res''. 2020 Feb; '''13''' (2):207-220
Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UK Biobank. Description: Strawbridge, Rona J, et al. Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UK Biobank. ''Arterioscler Thromb Vasc Biol''. 2020 Feb; '''40''' (2):446-461
Copy number variants in lipid metabolism genes are associated with gallstones disease in men. Description: Perez-Palma, Eduardo, et al. Copy number variants in lipid metabolism genes are associated with gallstones disease in men. ''Eur J Hum Genet''. 2020 Feb; '''28''' (2):264-273
DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. Description: Arloth, Janine, et al. DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. ''PLoS Comput Biol''. 2020 Feb; '''16''' (2):e1007616
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Description: Rees, Elliott, et al. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. ''Nat Neurosci''. 2020 Feb; '''23''' (2):179-184
Estimating the inbreeding level and genetic relatedness in an isolated population of critically endangered Sichuan taimen (Hucho Bleekeri) using genome-wide SNP markers. Description: Zhang, Yongquan, et al. Estimating the inbreeding level and genetic relatedness in an isolated population of critically endangered Sichuan taimen (Hucho Bleekeri) using genome-wide SNP markers. ''Ecol Evol''. 2020 Feb; '''10''' (3):1390-1400
Evaluation of polymorphisms in microRNA-binding sites and pancreatic cancer risk in Chinese population. Description: Ke, Juntao, et al. Evaluation of polymorphisms in microRNA-binding sites and pancreatic cancer risk in Chinese population. ''J Cell Mol Med''. 2020 Feb; '''24''' (3):2252-2259
Genetic evidence of a northward range expansion in the eastern Bering Sea stock of Pacific cod. Description: Spies, Ingrid, et al. Genetic evidence of a northward range expansion in the eastern Bering Sea stock of Pacific cod. ''Evol Appl''. 2020 Feb; '''13''' (2):362-375
Genetic polymorphisms in collagen-related genes are associated with pelvic organ prolapse. Description: Li, Lei, et al. Genetic polymorphisms in collagen-related genes are associated with pelvic organ prolapse. ''Menopause''. 2020 Feb; '''27''' (2):223-229
Genomic analyses reveal distinct genetic architectures and selective pressures in buffaloes. Description: Sun, Ting, et al. Genomic analyses reveal distinct genetic architectures and selective pressures in buffaloes. ''Gigascience''. 2020 Feb 1; '''9''' (2):
High rate of extrapair paternity in a human population demonstrates diversity in human reproductive strategies. Description: Scelza, B A, et al. High rate of extrapair paternity in a human population demonstrates diversity in human reproductive strategies. ''Sci Adv''. 2020 Feb; '''6''' (8):eaay6195
Identification of loci controlling adaptation in Chinese soya bean landraces via a combination of conventional and bioclimatic GWAS. Description: Li, Ying-Hui, et al. Identification of loci controlling adaptation in Chinese soya bean landraces via a combination of conventional and bioclimatic GWAS. ''Plant Biotechnol J''. 2020 Feb; '''18''' (2):389-401
Increased genetic marker density reveals high levels of admixture between red deer and introduced Japanese sika in Kintyre, Scotland. Description: McFarlane, S Eryn, et al. Increased genetic marker density reveals high levels of admixture between red deer and introduced Japanese sika in Kintyre, Scotland. ''Evol Appl''. 2020 Feb; '''13''' (2):432-441
Influence of Genetic Variation in PDE3A on Endothelial Function and Stroke. Description: Traylor, Matthew, et al. Influence of Genetic Variation in PDE3A on Endothelial Function and Stroke. ''Hypertension''. 2020 Feb; '''75''' (2):365-371
RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method. Description: Hamazaki, Kosuke, et al. RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method. ''PLoS Comput Biol''. 2020 Feb; '''16''' (2):e1007663
SNP genotypes reveal breed substructure, selection signatures and highly inbred regions in Pietrain pigs. Description: Gorssen, W, et al. SNP genotypes reveal breed substructure, selection signatures and highly inbred regions in Pietrain pigs. ''Anim Genet''. 2020 Feb; '''51''' (1):32-42
The association analysis between CYP24A1 genetic polymorphisms and the risk of ischemic stroke in Chinese Han population. Description: Yang, Wei, et al. The association analysis between CYP24A1 genetic polymorphisms and the risk of ischemic stroke in Chinese Han population. ''Brain Behav''. 2020 Feb; '''10''' (2):e01503
The fine-scale genetic structure and selection signals of Chinese indigenous pigs. Description: Huang, Min, et al. The fine-scale genetic structure and selection signals of Chinese indigenous pigs. ''Evol Appl''. 2020 Feb; '''13''' (2):458-475
The type of bottleneck matters: Insights into the deleterious variation landscape of small managed populations. Description: Bortoluzzi, Chiara, et al. The type of bottleneck matters: Insights into the deleterious variation landscape of small managed populations. ''Evol Appl''. 2020 Feb; '''13''' (2):330-341
Whole-chromosome hitchhiking driven by a male-killing endosymbiont. Description: Martin, Simon H, et al. Whole-chromosome hitchhiking driven by a male-killing endosymbiont. ''PLoS Biol''. 2020 Feb; '''18''' (2):e3000610
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21. Description: Mukhopadhyay, Nandita, et al. Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21. ''Hum Genet''. 2020 Feb; '''139''' (2):215-226
Measuring the Microscopic Structures of Human Dental Enamel Can Predict Caries Experience. Description: Kelly, Ariana M, et al. Measuring the Microscopic Structures of Human Dental Enamel Can Predict Caries Experience. ''J Pers Med''. 2020 Feb 2; '''10''' (1):
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Description: Cleynen, Isabelle, et al. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. ''Mol Psychiatry''. 2020 Feb 3;
A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE). Description: Leeb, Tosso, et al. A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE). ''Genes (Basel)''. 2020 Feb 3; '''11''' (2):
A polygenic predictor of treatment-resistant depression using whole exome sequencing and genome-wide genotyping. Description: Fabbri, Chiara, et al. A polygenic predictor of treatment-resistant depression using whole exome sequencing and genome-wide genotyping. ''Transl Psychiatry''. 2020 Feb 3; '''10''' (1):50
AATF and SMARCA2 are associated with thyroid volume in Hashimoto's thyroiditis patients. Description: Brcic, Luka, et al. AATF and SMARCA2 are associated with thyroid volume in Hashimoto's thyroiditis patients. ''Sci Rep''. 2020 Feb 4; '''10''' (1):1754
Functional variants of DOG1 control seed chilling responses and variation in seasonal life-history strategies in Arabidopsis thaliana. Description: Martinez-Berdeja, Alejandra, et al. Functional variants of DOG1 control seed chilling responses and variation in seasonal life-history strategies in Arabidopsis thaliana. ''Proc Natl Acad Sci U S A''. 2020 Feb 4; '''117''' (5):2526-2534
Parental warmth interacts with several genes to affect executive function components: a genome-wide environment interaction study. Description: Chen, Chunhui, et al. Parental warmth interacts with several genes to affect executive function components: a genome-wide environment interaction study. ''BMC Genet''. 2020 Feb 4; '''21''' (1):11
Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants. Description: Pottinger, Tess D, et al. Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants. ''J Am Heart Assoc''. 2020 Feb 4; '''9''' (3):e013808
Systems modeling of white matter microstructural abnormalities in Alzheimer's disease. Description: Horgusluoglu-Moloch, Emrin, et al. Systems modeling of white matter microstructural abnormalities in Alzheimer's disease. ''Neuroimage Clin''. 2020 Feb 4; '''26''': 102203
The whole transcriptome regulation as a function of mitochondrial polymorphisms and aging in Caenorhabditis elegans. Description: Song, Yuanjian, et al. The whole transcriptome regulation as a function of mitochondrial polymorphisms and aging in Caenorhabditis elegans. ''Aging (Albany NY)''. 2020 Feb 4; '''12''' (3):2453-2470
A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn's disease. Description: Gonzalez-Serna, David, et al. A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn's disease. ''Sci Rep''. 2020 Feb 5; '''10''' (1):1862
Genome-wide study of immune biomarkers in cerebrospinal fluid and serum from patients with bipolar disorder and controls. Description: Zhang, Ruyue, et al. Genome-wide study of immune biomarkers in cerebrospinal fluid and serum from patients with bipolar disorder and controls. ''Transl Psychiatry''. 2020 Feb 5; '''10''' (1):58
Interaction between Sex and LDLR rs688 Polymorphism on Hyperlipidemia among Taiwan Biobank Adult Participants. Description: Liu, Yin-Tso, et al. Interaction between Sex and LDLR rs688 Polymorphism on Hyperlipidemia among Taiwan Biobank Adult Participants. ''Biomolecules''. 2020 Feb 5; '''10''' (2):
Nanopore sequencing-based genome assembly and evolutionary genomics of circum-basmati rice. Description: Choi, Jae Young, et al. Nanopore sequencing-based genome assembly and evolutionary genomics of circum-basmati rice. ''Genome Biol''. 2020 Feb 5; '''21''' (1):21
The LCORL Locus is under Selection in Large-Sized Pakistani Goat Breeds. Description: Saif, Rashid, et al. The LCORL Locus is under Selection in Large-Sized Pakistani Goat Breeds. ''Genes (Basel)''. 2020 Feb 5; '''11''' (2):
Genome-wide association study of white matter hyperintensity volume in elderly persons without dementia. Description: Guo, Yu, et al. Genome-wide association study of white matter hyperintensity volume in elderly persons without dementia. ''Neuroimage Clin''. 2020 Feb 6; '''26''': 102209
Admixture-enabled selection for rapid adaptive evolution in the Americas. Description: Norris, Emily T, et al. Admixture-enabled selection for rapid adaptive evolution in the Americas. ''Genome Biol''. 2020 Feb 7; '''21''' (1):29
Association of a Variant in VWA3A with Response to Anti-Vascular Endothelial Growth Factor Treatment in Neovascular AMD. Description: Grunin, Michelle, et al. Association of a Variant in VWA3A with Response to Anti-Vascular Endothelial Growth Factor Treatment in Neovascular AMD. ''Invest Ophthalmol Vis Sci''. 2020 Feb 7; '''61''' (2):48
COMT-Polymorphisms Modulated Functional Profile of the Fusiform Face Area Contributes to Face-Specific Recognition Ability. Description: Wu, Chao, et al. COMT-Polymorphisms Modulated Functional Profile of the Fusiform Face Area Contributes to Face-Specific Recognition Ability. ''Sci Rep''. 2020 Feb 7; '''10''' (1):2134
Conserved defense responses between maize and sorghum to Exserohilum turcicum. Description: Zhang, Xiaoyue, et al. Conserved defense responses between maize and sorghum to Exserohilum turcicum. ''BMC Plant Biol''. 2020 Feb 10; '''20''' (1):67
Genomic measures of inbreeding coefficients and genome-wide scan for runs of homozygosity islands in Iranian river buffalo, Bubalus bubalis. Description: Ghoreishifar, Seyed Mohammad, et al. Genomic measures of inbreeding coefficients and genome-wide scan for runs of homozygosity islands in Iranian river buffalo, Bubalus bubalis. ''BMC Genet''. 2020 Feb 10; '''21''' (1):16
Weighted Single-Step Genome-Wide Association Study for Growth Traits in Chinese Simmental Beef Cattle. Description: Zhuang, Zhanwei, et al. Weighted Single-Step Genome-Wide Association Study for Growth Traits in Chinese Simmental Beef Cattle. ''Genes (Basel)''. 2020 Feb 11; '''11''' (2):
Association of Monogenic vs Polygenic Hypercholesterolemia With Risk of Atherosclerotic Cardiovascular Disease. Description: Trinder, Mark, et al. Association of Monogenic vs Polygenic Hypercholesterolemia With Risk of Atherosclerotic Cardiovascular Disease. ''JAMA Cardiol''. 2020 Feb 12;
Beyond large-effect loci: large-scale GWAS reveals a mixed large-effect and polygenic architecture for age at maturity of Atlantic salmon. Description: Sinclair-Waters, Marion, et al. Beyond large-effect loci: large-scale GWAS reveals a mixed large-effect and polygenic architecture for age at maturity of Atlantic salmon. ''Genet Sel Evol''. 2020 Feb 12; '''52''' (1):9
The wild species genome ancestry of domestic chickens. Description: Lawal, Raman Akinyanju, et al. The wild species genome ancestry of domestic chickens. ''BMC Biol''. 2020 Feb 12; '''18''' (1):13
Effects of Coffee Intake on Dyslipidemia Risk According to Genetic Variants in the ADORA Gene Family among Korean Adults. Description: Han, Jihee, et al. Effects of Coffee Intake on Dyslipidemia Risk According to Genetic Variants in the ADORA Gene Family among Korean Adults. ''Nutrients''. 2020 Feb 14; '''12''' (2):
FADS3 is a Delta14Z sphingoid base desaturase that contributes to gender differences in the human plasma sphingolipidome. Description: Karsai, Gergely, et al. FADS3 is a Delta14Z sphingoid base desaturase that contributes to gender differences in the human plasma sphingolipidome. ''J Biol Chem''. 2020 Feb 14; '''295''' (7):1889-1897
The role of schizotypal traits and the OXTR gene in theory of mind in schizophrenia: A family-based study. Description: Giralt-Lopez, M, et al. The role of schizotypal traits and the OXTR gene in theory of mind in schizophrenia: A family-based study. ''Eur Psychiatry''. 2020 Feb 14; '''63''' (1):e15
Correlation of age-of-onset of Atopic Dermatitis with Filaggrin loss-of-function variant status. Description: Smieszek, S P, et al. Correlation of age-of-onset of Atopic Dermatitis with Filaggrin loss-of-function variant status. ''Sci Rep''. 2020 Feb 17; '''10''' (1):2721
Genomic scan of selective sweeps in Djallonke (West African Dwarf) sheep shed light on adaptation to harsh environments. Description: Alvarez, Isabel, et al. Genomic scan of selective sweeps in Djallonke (West African Dwarf) sheep shed light on adaptation to harsh environments. ''Sci Rep''. 2020 Feb 18; '''10''' (1):2824
A chromosomal connectome for psychiatric and metabolic risk variants in adult dopaminergic neurons. Description: Espeso-Gil, Sergio, et al. A chromosomal connectome for psychiatric and metabolic risk variants in adult dopaminergic neurons. ''Genome Med''. 2020 Feb 19; '''12''' (1):19
A genetic analysis identifies a haplotype at adiponectin locus: Association with obesity and type 2 diabetes. Description: Palit, Sayantani Pramanik, et al. A genetic analysis identifies a haplotype at adiponectin locus: Association with obesity and type 2 diabetes. ''Sci Rep''. 2020 Feb 19; '''10''' (1):2904
Comparative genomics and association analysis identifies virulence genes of Cercospora sojina in soybean. Description: Gu, Xin, et al. Comparative genomics and association analysis identifies virulence genes of Cercospora sojina in soybean. ''BMC Genomics''. 2020 Feb 19; '''21''' (1):172
A framework for transcriptome-wide association studies in breast cancer in diverse study populations. Description: Bhattacharya, Arjun, et al. A framework for transcriptome-wide association studies in breast cancer in diverse study populations. ''Genome Biol''. 2020 Feb 20; '''21''' (1):42
Decimated little brown bats show potential for adaptive change. Description: Auteri, Giorgia G, et al. Decimated little brown bats show potential for adaptive change. ''Sci Rep''. 2020 Feb 20; '''10''' (1):3023
FADS Genetic Variants in Taiwanese Modify Association of DHA Intake and Its Proportions in Human Milk. Description: Wu, Wen-Chieh, et al. FADS Genetic Variants in Taiwanese Modify Association of DHA Intake and Its Proportions in Human Milk. ''Nutrients''. 2020 Feb 20; '''12''' (2):
Seed Weight as a Covariate in Association and Prediction Studies for Biomass Traits in Maize Seedlings. Description: Galic, Vlatko, et al. Seed Weight as a Covariate in Association and Prediction Studies for Biomass Traits in Maize Seedlings. ''Plants (Basel)''. 2020 Feb 20; '''9''' (2):
An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. Description: Bacchelli, Elena, et al. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. ''Sci Rep''. 2020 Feb 21; '''10''' (1):3198
Genome wide association analysis on semen volume and milk yield using different strategies of imputation to whole genome sequence in French dairy goats. Description: Talouarn, Estelle, et al. Genome wide association analysis on semen volume and milk yield using different strategies of imputation to whole genome sequence in French dairy goats. ''BMC Genet''. 2020 Feb 21; '''21''' (1):19
Purging of highly deleterious mutations through severe bottlenecks in Alpine ibex. Description: Grossen, Christine, et al. Purging of highly deleterious mutations through severe bottlenecks in Alpine ibex. ''Nat Commun''. 2020 Feb 21; '''11''' (1):1001
Analysis of Killer Immunoglobulin-Like Receptor Genes in Colorectal Cancer. Description: Diaz-Pena, Roberto, et al. Analysis of Killer Immunoglobulin-Like Receptor Genes in Colorectal Cancer. ''Cells''. 2020 Feb 24; '''9''' (2):
Deep learning versus parametric and ensemble methods for genomic prediction of complex phenotypes. Description: Abdollahi-Arpanahi, Rostam, et al. Deep learning versus parametric and ensemble methods for genomic prediction of complex phenotypes. ''Genet Sel Evol''. 2020 Feb 24; '''52''' (1):12
Discovering weaker genetic associations guided by known associations. Description: Wang, Haohan, et al. Discovering weaker genetic associations guided by known associations. ''BMC Med Genomics''. 2020 Feb 24; '''13''' (Suppl 3):19
Patterns of African and Asian admixture in the Afrikaner population of South Africa. Description: Hollfelder, N, et al. Patterns of African and Asian admixture in the Afrikaner population of South Africa. ''BMC Biol''. 2020 Feb 24; '''18''' (1):16
The behavioral, cellular and immune mediators of HIV-1 acquisition: New insights from population genetics. Description: Powell, Timothy R, et al. The behavioral, cellular and immune mediators of HIV-1 acquisition: New insights from population genetics. ''Sci Rep''. 2020 Feb 24; '''10''' (1):3304
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells. Description: Gil-Varea, Elia, et al. A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells. ''J Clin Med''. 2020 Feb 26; '''9''' (3):
The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia. Description: Richards, Alexander L, et al. The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia. ''Schizophr Bull''. 2020 Feb 26; '''46''' (2):336-344
Loci associated with variation in gene expression and growth in juvenile salmon are influenced by the presence of a growth hormone transgene. Description: McClelland, Erin Kathleen, et al. Loci associated with variation in gene expression and growth in juvenile salmon are influenced by the presence of a growth hormone transgene. ''BMC Genomics''. 2020 Feb 27; '''21''' (1):185
Effect direction meta-analysis of GWAS identifies extreme, prevalent and shared pleiotropy in a large mammal. Description: Xiang, Ruidong, et al. Effect direction meta-analysis of GWAS identifies extreme, prevalent and shared pleiotropy in a large mammal. ''Commun Biol''. 2020 Feb 28; '''3''' (1):88
Natural Sequence Variations and Combinations of GNP1 and NAL1 Determine the Grain Number per Panicle in Rice. Description: Wang, Yun, et al. Natural Sequence Variations and Combinations of GNP1 and NAL1 Determine the Grain Number per Panicle in Rice. ''Rice (N Y)''. 2020 Feb 28; '''13''' (1):14
The genetics of situs inversus without primary ciliary dyskinesia. Description: Postema, Merel C, et al. The genetics of situs inversus without primary ciliary dyskinesia. ''Sci Rep''. 2020 Feb 28; '''10''' (1):3677
Tissue specific regulation of transcription in endometrium and association with disease. Description: Mortlock, Sally, et al. Tissue specific regulation of transcription in endometrium and association with disease. ''Hum Reprod''. 2020 Feb 29; '''35''' (2):377-393
Gene expression networks in the Drosophila Genetic Reference Panel. Description: Everett, Logan J, et al. Gene expression networks in the Drosophila Genetic Reference Panel. ''Genome Res''. 2020 Mar; '''30''' (3):485-496
Genetic susceptibility to asthma increases the vulnerability to indoor air pollution. Description: Huls, Anke, et al. Genetic susceptibility to asthma increases the vulnerability to indoor air pollution. ''Eur Respir J''. 2020 Mar; '''55''' (3):
Mitonuclear interactions influence Alzheimer's disease risk. Description: Andrews, Shea J, et al. Mitonuclear interactions influence Alzheimer's disease risk. ''Neurobiol Aging''. 2020 Mar; '''87''': 138.e7-138.e14
Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci. Description: Gutierrez-Arcelus, Maria, et al. Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci. ''Nat Genet''. 2020 Mar; '''52''' (3):247-253
A Novel Susceptibility Locus Near GRIK2 Associated With Erosive Esophagitis in a Korean Cohort. Description: Jin, Eun Hyo, et al. A Novel Susceptibility Locus Near GRIK2 Associated With Erosive Esophagitis in a Korean Cohort. ''Clin Transl Gastroenterol''. 2020 Mar; '''11''' (3):e00145
A putative silencer variant in a spontaneous canine model of retinitis pigmentosa. Description: Kaukonen, Maria, et al. A putative silencer variant in a spontaneous canine model of retinitis pigmentosa. ''PLoS Genet''. 2020 Mar; '''16''' (3):e1008659
A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease. Description: Hartl, Daniela, et al. A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease. ''Mol Psychiatry''. 2020 Mar; '''25''' (3):629-639
Association of MAPK4 and SOX1-OT gene polymorphisms with cleft lip palate in multiplex families: A genetic study. Description: Neela, Praveen Kumar, et al. Association of MAPK4 and SOX1-OT gene polymorphisms with cleft lip palate in multiplex families: A genetic study. ''J Dent Res Dent Clin Dent Prospects''. 2020 Spring; '''14''' (2):93-96
Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder. Description: Brunet, Theresa, et al. Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder. ''Ann Clin Transl Neurol''. 2020 Mar; '''7''' (3):390-396
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. Description: Glanville, Kylie P, et al. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. ''Biol Psychiatry''. 2020 Mar 1; '''87''' (5):419-430
Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant. Description: Balaraju, Sunitha, et al. Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant. ''Eur J Hum Genet''. 2020 Mar; '''28''' (3):373-377
Divergent Selection and Primary Gene Flow Shape Incipient Speciation of a Riparian Tree on Hawaii Island. Description: Choi, Jae Young, et al. Divergent Selection and Primary Gene Flow Shape Incipient Speciation of a Riparian Tree on Hawaii Island. ''Mol Biol Evol''. 2020 Mar 1; '''37''' (3):695-710
Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis. Description: Richardson, Tom G, et al. Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis. ''PLoS Med''. 2020 Mar; '''17''' (3):e1003062
Fine-mapping of a novel premenopausal breast cancer susceptibility locus at Chr4q31.22 in Caucasian women and validation in African and Chinese women. Description: Kumaran, Mahalakshmi, et al. Fine-mapping of a novel premenopausal breast cancer susceptibility locus at Chr4q31.22 in Caucasian women and validation in African and Chinese women. ''Int J Cancer''. 2020 Mar 1; '''146''' (5):1219-1229
Genetic risk and atrial fibrillation in patients with heart failure. Description: Kloosterman, Marielle, et al. Genetic risk and atrial fibrillation in patients with heart failure. ''Eur J Heart Fail''. 2020 Mar; '''22''' (3):519-527
Genetic structure and admixture in sheep from terminal breeds in the United States. Description: Davenport, K M, et al. Genetic structure and admixture in sheep from terminal breeds in the United States. ''Anim Genet''. 2020 Mar; '''51''' (2):284-291
Genome-Wide Selection Scan in an Arabian Peninsula Population Identifies a TNKS Haplotype Linked to Metabolic Traits and Hypertension. Description: Eaaswarkhanth, Muthukrishnan, et al. Genome-Wide Selection Scan in an Arabian Peninsula Population Identifies a TNKS Haplotype Linked to Metabolic Traits and Hypertension. ''Genome Biol Evol''. 2020 Mar 1; '''12''' (3):77-87
Genomic Resources for Darters (Percidae: Etheostominae) Provide Insight into Postzygotic Barriers Implicated in Speciation. Description: Moran, Rachel L, et al. Genomic Resources for Darters (Percidae: Etheostominae) Provide Insight into Postzygotic Barriers Implicated in Speciation. ''Mol Biol Evol''. 2020 Mar 1; '''37''' (3):711-729
INTERACTIONS AMONG INTERLEUKIN-6, C-REACTIVE PROTEIN AND INTERLEUKIN-6 (-174) G/C POLYMORPHISM IN THE PATHOGENESIS OF CROHN'S DISEASE AND ULCERATIVE COLITIS. Description: Takac, Boris, et al. INTERACTIONS AMONG INTERLEUKIN-6, C-REACTIVE PROTEIN AND INTERLEUKIN-6 (-174) G/C POLYMORPHISM IN THE PATHOGENESIS OF CROHN'S DISEASE AND ULCERATIVE COLITIS. ''Acta Clin Croat''. 2020 Mar; '''59''' (1):67-80
Introgression of Eastern Chinese and Southern Chinese haplotypes contributes to the improvement of fertility and immunity in European modern pigs. Description: Chen, Hao, et al. Introgression of Eastern Chinese and Southern Chinese haplotypes contributes to the improvement of fertility and immunity in European modern pigs. ''Gigascience''. 2020 Mar 1; '''9''' (3):
Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk. Description: Nudel, Ron, et al. Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk. ''Autism Res''. 2020 Mar; '''13''' (3):369-381
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases. Description: Perenthaler, Elena, et al. Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases. ''Acta Neuropathol''. 2020 Mar; '''139''' (3):415-442
Quantitative genetic analysis deciphers the impact of cis and trans regulation on cell-to-cell variability in protein expression levels. Description: Morgan, Michael D, et al. Quantitative genetic analysis deciphers the impact of cis and trans regulation on cell-to-cell variability in protein expression levels. ''PLoS Genet''. 2020 Mar; '''16''' (3):e1008686
Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs. Description: Dillard, Kati J, et al. Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs. ''PLoS Genet''. 2020 Mar; '''16''' (3):e1008651
The association of HFE gene H63D polymorphism with endurance athlete status and aerobic capacity: novel findings and a meta-analysis. Description: Semenova, Ekaterina A, et al. The association of HFE gene H63D polymorphism with endurance athlete status and aerobic capacity: novel findings and a meta-analysis. ''Eur J Appl Physiol''. 2020 Mar; '''120''' (3):665-673
Twin introductions by independent invader mussel lineages are both associated with recent admixture with a native congener in Australia. Description: Popovic, Iva, et al. Twin introductions by independent invader mussel lineages are both associated with recent admixture with a native congener in Australia. ''Evol Appl''. 2020 Mar; '''13''' (3):515-532
Unraveling the genetic diversity of Belgian Milk Sheep using medium-density SNP genotypes. Description: Meyermans, R, et al. Unraveling the genetic diversity of Belgian Milk Sheep using medium-density SNP genotypes. ''Anim Genet''. 2020 Mar; '''51''' (2):258-265
Identification of runs of homozygosity affecting female fertility and milk production traits in Finnish Ayrshire cattle. Description: Martikainen, K, et al. Identification of runs of homozygosity affecting female fertility and milk production traits in Finnish Ayrshire cattle. ''Sci Rep''. 2020 Mar 2; '''10''' (1):3804
Comparison of the Efficiency of BLUP and GBLUP in Genomic Prediction of Immune Traits in Chickens. Description: Zhang, Jin, et al. Comparison of the Efficiency of BLUP and GBLUP in Genomic Prediction of Immune Traits in Chickens. ''Animals (Basel)''. 2020 Mar 3; '''10''' (3):
Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity. Description: Hernandez, Leanna M, et al. Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity. ''Transl Psychiatry''. 2020 Mar 3; '''10''' (1):82
Transcriptomic resources for evolutionary studies in flat periwinkles and related species. Description: Marques, Joao P, et al. Transcriptomic resources for evolutionary studies in flat periwinkles and related species. ''Sci Data''. 2020 Mar 3; '''7''' (1):73
Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia. Description: Liang, Wei, et al. Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia. ''Transl Psychiatry''. 2020 Mar 3; '''10''' (1):83
CYP3A4 and CYP11A1 variants are risk factors for ischemic stroke: a case control study. Description: Gao, Ning, et al. CYP3A4 and CYP11A1 variants are risk factors for ischemic stroke: a case control study. ''BMC Neurol''. 2020 Mar 4; '''20''' (1):77
Genetic Characterization of Endometriosis Patients: Review of the Literature and a Prospective Cohort Study on a Mediterranean Population. Description: Angioni, Stefano, et al. Genetic Characterization of Endometriosis Patients: Review of the Literature and a Prospective Cohort Study on a Mediterranean Population. ''Int J Mol Sci''. 2020 Mar 4; '''21''' (5):
Genome-Wide Analysis Reveals Human-Mediated Introgression from Western Pigs to Indigenous Chinese Breeds. Description: Wang, Jue, et al. Genome-Wide Analysis Reveals Human-Mediated Introgression from Western Pigs to Indigenous Chinese Breeds. ''Genes (Basel)''. 2020 Mar 4; '''11''' (3):
Genome-wide analysis reveals molecular convergence underlying domestication in 7 bird and mammals. Description: Hou, Yali, et al. Genome-wide analysis reveals molecular convergence underlying domestication in 7 bird and mammals. ''BMC Genomics''. 2020 Mar 4; '''21''' (1):204
Genome-Wide Association Study Reveals Candidate Genes for Litter Size Traits in Pelibuey Sheep. Description: Hernandez-Montiel, Wilber, et al. Genome-Wide Association Study Reveals Candidate Genes for Litter Size Traits in Pelibuey Sheep. ''Animals (Basel)''. 2020 Mar 4; '''10''' (3):
Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians. Description: Arbeeva, Liubov, et al. Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians. ''J Foot Ankle Res''. 2020 Mar 4; '''13''' (1):11
Insight into unique somitogenesis of yak (Bos grunniens) with one additional thoracic vertebra. Description: Wang, Yu, et al. Insight into unique somitogenesis of yak (Bos grunniens) with one additional thoracic vertebra. ''BMC Genomics''. 2020 Mar 4; '''21''' (1):201
A Possible Link of Genetic Variations in ER/IGF1R Pathway and Risk of Melanoma. Description: Yuan, Tze-An, et al. A Possible Link of Genetic Variations in ER/IGF1R Pathway and Risk of Melanoma. ''Int J Mol Sci''. 2020 Mar 5; '''21''' (5):
Genetic and phenotypic landscape of the mitochondrial genome in the Japanese population. Description: Yamamoto, Kenichi, et al. Genetic and phenotypic landscape of the mitochondrial genome in the Japanese population. ''Commun Biol''. 2020 Mar 5; '''3''' (1):104
Genome-Wide Association Study in Two Cohorts from a Multi-generational Mouse Advanced Intercross Line Highlights the Difficulty of Replication Due to Study-Specific Heterogeneity. Description: Zhou, Xinzhu, et al. Genome-Wide Association Study in Two Cohorts from a Multi-generational Mouse Advanced Intercross Line Highlights the Difficulty of Replication Due to Study-Specific Heterogeneity. ''G3 (Bethesda)''. 2020 Mar 5; '''10''' (3):951-965
Genome-wide identification of loci associated with growth in rainbow trout. Description: Ali, Ali, et al. Genome-wide identification of loci associated with growth in rainbow trout. ''BMC Genomics''. 2020 Mar 5; '''21''' (1):209
Gene-flow from steppe individuals into Cucuteni-Trypillia associated populations indicates long-standing contacts and gradual admixture. Description: Immel, Alexander, et al. Gene-flow from steppe individuals into Cucuteni-Trypillia associated populations indicates long-standing contacts and gradual admixture. ''Sci Rep''. 2020 Mar 6; '''10''' (1):4253
Genetic Diversity, Population Structure and Linkage Disequilibrium Assessment among International Sunflower Breeding Collections. Description: Filippi, Carla V, et al. Genetic Diversity, Population Structure and Linkage Disequilibrium Assessment among International Sunflower Breeding Collections. ''Genes (Basel)''. 2020 Mar 6; '''11''' (3):
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. Description: Wang, Yang, et al. Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. ''Aging (Albany NY)''. 2020 Mar 6; '''12''' (5):4379-4393
Population structure of five native sheep breeds of Sweden estimated with high density SNP genotypes. Description: Rochus, Christina Marie, et al. Population structure of five native sheep breeds of Sweden estimated with high density SNP genotypes. ''BMC Genet''. 2020 Mar 6; '''21''' (1):27
Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features. Description: Ray, John P, et al. Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features. ''Nat Commun''. 2020 Mar 6; '''11''' (1):1237
Variants in RETN gene are associated with steroid-induced osteonecrosis of the femoral head risk among Han Chinese people. Description: An, Feimeng, et al. Variants in RETN gene are associated with steroid-induced osteonecrosis of the femoral head risk among Han Chinese people. ''J Orthop Surg Res''. 2020 Mar 6; '''15''' (1):96
Population Genomic Analysis of Two Endemic Schizothoracins Reveals Their Genetic Differences and Underlying Selection Associated with Altitude and Temperature. Description: Yang, Tianyan, et al. Population Genomic Analysis of Two Endemic Schizothoracins Reveals Their Genetic Differences and Underlying Selection Associated with Altitude and Temperature. ''Animals (Basel)''. 2020 Mar 7; '''10''' (3):
Can education be personalised using pupils' genetic data? Description: Morris, Tim T, et al. Can education be personalised using pupils' genetic data? ''Elife''. 2020 Mar 10; '''9''':
Identification of Novel Genomic Regions and Superior Alleles Associated with Zn Accumulation in Wheat Using a Genome-Wide Association Analysis Method. Description: Zhou, Zhengfu, et al. Identification of Novel Genomic Regions and Superior Alleles Associated with Zn Accumulation in Wheat Using a Genome-Wide Association Analysis Method. ''Int J Mol Sci''. 2020 Mar 11; '''21''' (6):
Integrating Casein Complex SNPs Additive, Dominance and Epistatic Effects on Genetic Parameters and Breeding Values Estimation for Murciano-Granadina Goat Milk Yield and Components. Description: Pizarro Inostroza, Maria Gabriela, et al. Integrating Casein Complex SNPs Additive, Dominance and Epistatic Effects on Genetic Parameters and Breeding Values Estimation for Murciano-Granadina Goat Milk Yield and Components. ''Genes (Basel)''. 2020 Mar 14; '''11''' (3):
Multiple association analysis of loci and candidate genes that regulate body size at three growth stages in Simmental beef cattle. Description: An, Bingxing, et al. Multiple association analysis of loci and candidate genes that regulate body size at three growth stages in Simmental beef cattle. ''BMC Genet''. 2020 Mar 14; '''21''' (1):32
YARS2 Missense Variant in Belgian Shepherd Dogs with Cardiomyopathy and Juvenile Mortality. Description: Gurtner, Corinne, et al. YARS2 Missense Variant in Belgian Shepherd Dogs with Cardiomyopathy and Juvenile Mortality. ''Genes (Basel)''. 2020 Mar 14; '''11''' (3):
Genome-wide Analyses Identifies Known and New Markers Responsible of Chicken Plumage Color. Description: Mastrangelo, Salvatore, et al. Genome-wide Analyses Identifies Known and New Markers Responsible of Chicken Plumage Color. ''Animals (Basel)''. 2020 Mar 15; '''10''' (3):
Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer. Description: Toma, Claudio, et al. Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer. ''Int J Cancer''. 2020 Mar 15; '''146''' (6):1568-1577
A Gene-Set Enrichment and Protein-Protein Interaction Network-Based GWAS with Regulatory SNPs Identifies Candidate Genes and Pathways Associated with Carcass Traits in Hanwoo Cattle. Description: Srikanth, Krishnamoorthy, et al. A Gene-Set Enrichment and Protein-Protein Interaction Network-Based GWAS with Regulatory SNPs Identifies Candidate Genes and Pathways Associated with Carcass Traits in Hanwoo Cattle. ''Genes (Basel)''. 2020 Mar 16; '''11''' (3):
Enabling population assignment from cancer genomes with SNP2pop. Description: Huang, Qingyao, et al. Enabling population assignment from cancer genomes with SNP2pop. ''Sci Rep''. 2020 Mar 16; '''10''' (1):4846
Effects of acute sleep loss on diurnal plasma dynamics of CNS health biomarkers in young men. Description: Benedict, Christian, et al. Effects of acute sleep loss on diurnal plasma dynamics of CNS health biomarkers in young men. ''Neurology''. 2020 Mar 17; '''94''' (11):e1181-e1189
On rare variants in principal component analysis of population stratification. Description: Ma, Shengqing, et al. On rare variants in principal component analysis of population stratification. ''BMC Genet''. 2020 Mar 17; '''21''' (1):34
Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis. Description: Chen, Hao Yu, et al. Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis. ''JAMA Cardiol''. 2020 Mar 18;
Population structure of Apodemus flavicollis and comparison to Apodemus sylvaticus in northern Poland based on RAD-seq. Description: Martin Cerezo, Maria Luisa, et al. Population structure of Apodemus flavicollis and comparison to Apodemus sylvaticus in northern Poland based on RAD-seq. ''BMC Genomics''. 2020 Mar 18; '''21''' (1):241
Stable species boundaries despite ten million years of hybridization in tropical eels. Description: Barth, Julia M I, et al. Stable species boundaries despite ten million years of hybridization in tropical eels. ''Nat Commun''. 2020 Mar 18; '''11''' (1):1433
Collagen type VI alpha5 gene variations may predict the risk of lung cancer development in Chinese Han population. Description: Duan, Ying, et al. Collagen type VI alpha5 gene variations may predict the risk of lung cancer development in Chinese Han population. ''Sci Rep''. 2020 Mar 19; '''10''' (1):5010
Genetic polymorphisms of IL17A associated with Chagas disease: results from a meta-analysis in Latin American populations. Description: Strauss, Mariana, et al. Genetic polymorphisms of IL17A associated with Chagas disease: results from a meta-analysis in Latin American populations. ''Sci Rep''. 2020 Mar 19; '''10''' (1):5015
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Description: Fan, Qiao, et al. Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. ''Commun Biol''. 2020 Mar 19; '''3''' (1):133
Genome-Wide Scan for Runs of Homozygosity Identifies Candidate Genes Related to Economically Important Traits in Chinese Merino. Description: He, Sangang, et al. Genome-Wide Scan for Runs of Homozygosity Identifies Candidate Genes Related to Economically Important Traits in Chinese Merino. ''Animals (Basel)''. 2020 Mar 20; '''10''' (3):
Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease. Description: Akcimen, Fulya, et al. Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease. ''Aging (Albany NY)''. 2020 Mar 23; '''12''' (6):4742-4756
Genetic Differentiation of the Two Types of Polish Cold-blooded Horses Included in the National Conservation Program. Description: Gurgul, Artur, et al. Genetic Differentiation of the Two Types of Polish Cold-blooded Horses Included in the National Conservation Program. ''Animals (Basel)''. 2020 Mar 24; '''10''' (3):
EDN1 gene potentially involved in the development of acute mountain sickness. Description: Yu, Jie, et al. EDN1 gene potentially involved in the development of acute mountain sickness. ''Sci Rep''. 2020 Mar 25; '''10''' (1):5414
Identification of slit3 as a locus affecting nicotine preference in zebrafish and human smoking behaviour. Description: Garcia-Gonzalez, Judit, et al. Identification of slit3 as a locus affecting nicotine preference in zebrafish and human smoking behaviour. ''Elife''. 2020 Mar 25; '''9''':
Dimensionality reduction reveals fine-scale structure in the Japanese population with consequences for polygenic risk prediction. Description: Sakaue, Saori, et al. Dimensionality reduction reveals fine-scale structure in the Japanese population with consequences for polygenic risk prediction. ''Nat Commun''. 2020 Mar 26; '''11''' (1):1569
Analysis of mitochondrial m1A/G RNA modification reveals links to nuclear genetic variants and associated disease processes. Description: Ali, Aminah Tasnim, et al. Analysis of mitochondrial m1A/G RNA modification reveals links to nuclear genetic variants and associated disease processes. ''Commun Biol''. 2020 Mar 27; '''3''' (1):147
Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification. Description: Pechlivanis, Sonali, et al. Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification. ''BMC Med Genet''. 2020 Mar 27; '''21''' (1):62
Genome-wide analyses disclose the distinctive HLA architecture and the pharmacogenetic landscape of the Somali population. Description: Ali, Abshir A, et al. Genome-wide analyses disclose the distinctive HLA architecture and the pharmacogenetic landscape of the Somali population. ''Sci Rep''. 2020 Mar 27; '''10''' (1):5652
Single-nucleotide polymorphisms of HLA and Polygonum multiflorum-induced liver injury in the Han Chinese population. Description: Yang, Wan-Na, et al. Single-nucleotide polymorphisms of HLA and Polygonum multiflorum-induced liver injury in the Han Chinese population. ''World J Gastroenterol''. 2020 Mar 28; '''26''' (12):1329-1339
The Effect of Integrating Genomic Information into Genetic Evaluations of Chinese Merino Sheep. Description: Wei, Chen, et al. The Effect of Integrating Genomic Information into Genetic Evaluations of Chinese Merino Sheep. ''Animals (Basel)''. 2020 Mar 28; '''10''' (4):
Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases. Description: Yamasaki, Maria, et al. Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases. ''BMC Med Genomics''. 2020 Mar 29; '''13''' (1):55
Genome and Transcriptome Sequencing of casper and roy Zebrafish Mutants Provides Novel Genetic Clues for Iridophore Loss. Description: Bian, Chao, et al. Genome and Transcriptome Sequencing of casper and roy Zebrafish Mutants Provides Novel Genetic Clues for Iridophore Loss. ''Int J Mol Sci''. 2020 Mar 30; '''21''' (7):
Identification of Ancestry Informative Marker (AIM) Panels to Assess Hybridisation between Feral and Domestic Sheep. Description: Somenzi, Elisa, et al. Identification of Ancestry Informative Marker (AIM) Panels to Assess Hybridisation between Feral and Domestic Sheep. ''Animals (Basel)''. 2020 Mar 30; '''10''' (4):
The association of DNA methylation with body mass index: distinguishing between predictors and biomarkers. Description: Reed, Zoe E, et al. The association of DNA methylation with body mass index: distinguishing between predictors and biomarkers. ''Clin Epigenetics''. 2020 Mar 30; '''12''' (1):50
Whole genome resequencing reveals an association of ABCC4 variants with preaxial polydactyly in pigs. Description: Ma, Cheng, et al. Whole genome resequencing reveals an association of ABCC4 variants with preaxial polydactyly in pigs. ''BMC Genomics''. 2020 Mar 30; '''21''' (1):268
Comparison and development of machine learning tools for the prediction of chronic obstructive pulmonary disease in the Chinese population. Description: Ma, Xia, et al. Comparison and development of machine learning tools for the prediction of chronic obstructive pulmonary disease in the Chinese population. ''J Transl Med''. 2020 Mar 31; '''18''' (1):146
Genomic consequences of population decline in critically endangered pangolins and their demographic histories. Description: Hu, Jing-Yang, et al. Genomic consequences of population decline in critically endangered pangolins and their demographic histories. ''Natl Sci Rev''. 2020 Apr; '''7''' (4):798-814
SR4R: An Integrative SNP Resource for Genomic Breeding and Population Research in Rice. Description: Yan, Jun, et al. SR4R: An Integrative SNP Resource for Genomic Breeding and Population Research in Rice. ''Genomics Proteomics Bioinformatics''. 2020 Apr; '''18''' (2):173-185
A bird's-eye view of Italian genomic variation through whole-genome sequencing. Description: Cocca, Massimiliano, et al. A bird's-eye view of Italian genomic variation through whole-genome sequencing. ''Eur J Hum Genet''. 2020 Apr; '''28''' (4):435-444
A genome-wide association study of prostate cancer in Latinos. Description: Du, Zhaohui, et al. A genome-wide association study of prostate cancer in Latinos. ''Int J Cancer''. 2020 Apr 1; '''146''' (7):1819-1826
A genome-wide association study on medulloblastoma. Description: Dahlin, Anna M, et al. A genome-wide association study on medulloblastoma. ''J Neurooncol''. 2020 Apr; '''147''' (2):309-315
A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease. Description: Emdin, Connor A, et al. A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease. ''PLoS Genet''. 2020 Apr; '''16''' (4):e1008629
Association of ECE1 gene polymorphisms and essential hypertension risk in the Northern Han Chinese: A case-control study. Description: Wang, Hao, et al. Association of ECE1 gene polymorphisms and essential hypertension risk in the Northern Han Chinese: A case-control study. ''Mol Genet Genomic Med''. 2020 Apr; '''8''' (4):e1188
A TREML2 missense variant influences specific hippocampal subfield volumes in cognitively normal elderly subjects. Description: Wang, Si-Yu, et al. A TREML2 missense variant influences specific hippocampal subfield volumes in cognitively normal elderly subjects. ''Brain Behav''. 2020 Apr; '''10''' (4):e01573
CHIT1 at Diagnosis Reflects Long-Term Multiple Sclerosis Disease Activity. Description: Oldoni, Emanuela, et al. CHIT1 at Diagnosis Reflects Long-Term Multiple Sclerosis Disease Activity. ''Ann Neurol''. 2020 Apr; '''87''' (4):633-645
Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels. Description: Misawa, Kazuharu, et al. Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels. ''Genetics''. 2020 Apr; '''214''' (4):1079-1090
Discovery of novel hepatocyte eQTLs in African Americans. Description: Zhong, Yizhen, et al. Discovery of novel hepatocyte eQTLs in African Americans. ''PLoS Genet''. 2020 Apr; '''16''' (4):e1008662
Divergent northern and southern populations and demographic history of the pearl oyster in the western Pacific revealed with genomic SNPs. Description: Takeuchi, Takeshi, et al. Divergent northern and southern populations and demographic history of the pearl oyster in the western Pacific revealed with genomic SNPs. ''Evol Appl''. 2020 Apr; '''13''' (4):837-853
DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data. Description: Jiang, Yi, et al. DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data. ''PLoS Comput Biol''. 2020 Apr; '''16''' (4):e1007522
Endothelin-1 rs9296344 associates with the susceptibility of childhood primary nephrotic syndrome. Description: Zhang, Ruifeng, et al. Endothelin-1 rs9296344 associates with the susceptibility of childhood primary nephrotic syndrome. ''J Clin Lab Anal''. 2020 Apr; '''34''' (4):e23134
Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP. Description: Wigmore, Eleanor M, et al. Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP. ''Pharmacogenomics J''. 2020 Apr; '''20''' (2):329-341
Genomic analysis of natural intra-specific hybrids among Ethiopian isolates of Leishmania donovani. Description: Cotton, James A, et al. Genomic analysis of natural intra-specific hybrids among Ethiopian isolates of Leishmania donovani. ''PLoS Negl Trop Dis''. 2020 Apr; '''14''' (4):e0007143
Genomic Evidence for Complex Domestication History of the Cultivated Tomato in Latin America. Description: Razifard, Hamid, et al. Genomic Evidence for Complex Domestication History of the Cultivated Tomato in Latin America. ''Mol Biol Evol''. 2020 Apr 1; '''37''' (4):1118-1132
Human Genomic Diversity Where the Mediterranean Joins the Atlantic. Description: Hernandez, Candela L, et al. Human Genomic Diversity Where the Mediterranean Joins the Atlantic. ''Mol Biol Evol''. 2020 Apr 1; '''37''' (4):1041-1055
Integrating GWAS with bulk and single-cell RNA-sequencing reveals a role for LY86 in the anti-Candida host response. Description: de Vries, Dylan H, et al. Integrating GWAS with bulk and single-cell RNA-sequencing reveals a role for LY86 in the anti-Candida host response. ''PLoS Pathog''. 2020 Apr; '''16''' (4):e1008408
Large-scale GWAS in sorghum reveals common genetic control of grain size among cereals. Description: Tao, Yongfu, et al. Large-scale GWAS in sorghum reveals common genetic control of grain size among cereals. ''Plant Biotechnol J''. 2020 Apr; '''18''' (4):1093-1105
Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia. Description: Hysi, Pirro G, et al. Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia. ''Nat Genet''. 2020 Apr; '''52''' (4):401-407
One-year Mediterranean diet promotes epigenetic rejuvenation with country- and sex-specific effects: a pilot study from the NU-AGE project. Description: Gensous, Noemie, et al. One-year Mediterranean diet promotes epigenetic rejuvenation with country- and sex-specific effects: a pilot study from the NU-AGE project. ''Geroscience''. 2020 Apr; '''42''' (2):687-701
Parallelism in eco-morphology and gene expression despite variable evolutionary and genomic backgrounds in a Holarctic fish. Description: Jacobs, Arne, et al. Parallelism in eco-morphology and gene expression despite variable evolutionary and genomic backgrounds in a Holarctic fish. ''PLoS Genet''. 2020 Apr; '''16''' (4):e1008658
Polygenic disruption of retinoid signalling in schizophrenia and a severe cognitive deficit subtype. Description: Reay, William R, et al. Polygenic disruption of retinoid signalling in schizophrenia and a severe cognitive deficit subtype. ''Mol Psychiatry''. 2020 Apr; '''25''' (4):719-731
Population phenomena inflate genetic associations of complex social traits. Description: Morris, Tim T, et al. Population phenomena inflate genetic associations of complex social traits. ''Sci Adv''. 2020 Apr; '''6''' (16):eaay0328
Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Description: Li, Donghe, et al. Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. ''Genes Genomics''. 2020 Apr; '''42''' (4):393-403
Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity. Description: Su, Chun-Lang, et al. Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity. ''Menopause''. 2020 Apr; '''27''' (4):459-462
The relevance of gene flow with wild relatives in understanding the domestication process. Description: Moreno-Letelier, Alejandra, et al. The relevance of gene flow with wild relatives in understanding the domestication process. ''R Soc Open Sci''. 2020 Apr; '''7''' (4):191545
Use of local genetic ancestry to assess TOMM40-523' and risk for Alzheimer disease. Description: Bussies, Parker L, et al. Use of local genetic ancestry to assess TOMM40-523' and risk for Alzheimer disease. ''Neurol Genet''. 2020 Apr; '''6''' (2):e404
Ancestry deconvolution and partial polygenic score can improve susceptibility predictions in recently admixed individuals. Description: Marnetto, Davide, et al. Ancestry deconvolution and partial polygenic score can improve susceptibility predictions in recently admixed individuals. ''Nat Commun''. 2020 Apr 2; '''11''' (1):1628
Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes. Description: Subramanian, Deepak N, et al. Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes. ''Nat Commun''. 2020 Apr 2; '''11''' (1):1640
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Description: Revez, Joana A, et al. Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. ''Nat Commun''. 2020 Apr 2; '''11''' (1):1647
Association between craniofacial morphological patterns and tooth agenesis-related genes. Description: Rodrigues, Amanda Silva, et al. Association between craniofacial morphological patterns and tooth agenesis-related genes. ''Prog Orthod''. 2020 Apr 6; '''21''' (1):9
The association of genetic polymorphisms in interleukin-1 receptors type 1 and type 2 with age-related hearing impairment in a Taiwanese population: a case control study. Description: Chang, Ning-Chia, et al. The association of genetic polymorphisms in interleukin-1 receptors type 1 and type 2 with age-related hearing impairment in a Taiwanese population: a case control study. ''J Otolaryngol Head Neck Surg''. 2020 Apr 6; '''49''' (1):16
A platinum standard pan-genome resource that represents the population structure of Asian rice. Description: Zhou, Yong, et al. A platinum standard pan-genome resource that represents the population structure of Asian rice. ''Sci Data''. 2020 Apr 7; '''7''' (1):113
Development of Single Nucleotide Polymorphism (SNP) Markers for Analysis of Population Structure and Invasion Pathway in the Coconut Leaf Beetle Brontispa longissima (Gestro) Using Restriction Site-Associated DNA (RAD) Genotyping in Southern China. Description: Chen, Zhiming, et al. Development of Single Nucleotide Polymorphism (SNP) Markers for Analysis of Population Structure and Invasion Pathway in the Coconut Leaf Beetle Brontispa longissima (Gestro) Using Restriction Site-Associated DNA (RAD) Genotyping in Southern China. ''Insects''. 2020 Apr 7; '''11''' (4):
Germline burden of rare damaging variants negatively affects human healthspan and lifespan. Description: Shindyapina, Anastasia V, et al. Germline burden of rare damaging variants negatively affects human healthspan and lifespan. ''Elife''. 2020 Apr 7; '''9''':
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Description: Werling, Donna M, et al. Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. ''Cell Rep''. 2020 Apr 7; '''31''' (1):107489
Genomic Dissection of Anthracnose (Colletotrichum sublineolum) Resistance Response in Sorghum Differential Line SC112-14. Description: Cruet-Burgos, Clara M, et al. Genomic Dissection of Anthracnose (Colletotrichum sublineolum) Resistance Response in Sorghum Differential Line SC112-14. ''G3 (Bethesda)''. 2020 Apr 9; '''10''' (4):1403-1412
MHC associations of ankylosing spondylitis in East Asians are complex and involve non-HLA-B27 HLA contributions. Description: Wang, Geng, et al. MHC associations of ankylosing spondylitis in East Asians are complex and involve non-HLA-B27 HLA contributions. ''Arthritis Res Ther''. 2020 Apr 9; '''22''' (1):74
Natural Genetic Variation Underlying Tiller Development in Barley (Hordeum vulgare L). Description: Haaning, Allison M, et al. Natural Genetic Variation Underlying Tiller Development in Barley (Hordeum vulgare L). ''G3 (Bethesda)''. 2020 Apr 9; '''10''' (4):1197-1212
RIPK1 polymorphisms alter the susceptibility to cervical Cancer among the Uyghur population in China. Description: Tuoheti, Zulipiyamu, et al. RIPK1 polymorphisms alter the susceptibility to cervical Cancer among the Uyghur population in China. ''BMC Cancer''. 2020 Apr 9; '''20''' (1):299
Copy number variation in human genomes from three major ethno-linguistic groups in Africa. Description: Nyangiri, Oscar A, et al. Copy number variation in human genomes from three major ethno-linguistic groups in Africa. ''BMC Genomics''. 2020 Apr 10; '''21''' (1):289
Association of germline genetic variants with TMPRSS2-ERG fusion status in prostate cancer. Description: Kohaar, Indu, et al. Association of germline genetic variants with TMPRSS2-ERG fusion status in prostate cancer. ''Oncotarget''. 2020 Apr 14; '''11''' (15):1321-1333
Genome-wide association mapping and accuracy of predictions for amoebic gill disease in Atlantic salmon (Salmo salar). Description: Aslam, Muhammad L, et al. Genome-wide association mapping and accuracy of predictions for amoebic gill disease in Atlantic salmon (Salmo salar). ''Sci Rep''. 2020 Apr 15; '''10''' (1):6435
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Description: Halvorsen, Matthew, et al. Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. ''Nat Commun''. 2020 Apr 15; '''11''' (1):1842
Telomere Maintenance Genes are associated with Type 2 Diabetes Susceptibility in Northwest Indian Population Group. Description: Sethi, Itty, et al. Telomere Maintenance Genes are associated with Type 2 Diabetes Susceptibility in Northwest Indian Population Group. ''Sci Rep''. 2020 Apr 15; '''10''' (1):6444
The correlation between CYP4F2 variants and chronic obstructive pulmonary disease risk in Hainan Han population. Description: Ding, Yipeng, et al. The correlation between CYP4F2 variants and chronic obstructive pulmonary disease risk in Hainan Han population. ''Respir Res''. 2020 Apr 15; '''21''' (1):86
Genome wide association study of 40 clinical measurements in eight dog breeds. Description: Momozawa, Yukihide, et al. Genome wide association study of 40 clinical measurements in eight dog breeds. ''Sci Rep''. 2020 Apr 16; '''10''' (1):6520
Role of aldehyde dehydrogenases, alcohol dehydrogenase 1B genotype, alcohol consumption, and their combination in breast cancer in East-Asian women. Description: Park, Boyoung, et al. Role of aldehyde dehydrogenases, alcohol dehydrogenase 1B genotype, alcohol consumption, and their combination in breast cancer in East-Asian women. ''Sci Rep''. 2020 Apr 16; '''10''' (1):6564
Paternity Assignment in White Guinea Yam (Dioscorea Rotundata) Half-Sib Progenies from Polycross Mating Design Using SNP Markers. Description: Norman, Prince E, et al. Paternity Assignment in White Guinea Yam (Dioscorea Rotundata) Half-Sib Progenies from Polycross Mating Design Using SNP Markers. ''Plants (Basel)''. 2020 Apr 19; '''9''' (4):
Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway. Description: Manry, Jeremy, et al. Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway. ''Commun Biol''. 2020 Apr 20; '''3''' (1):177
Genome-wide genetic structure and selection signatures for color in 10 traditional Chinese yellow-feathered chicken breeds. Description: Huang, Xunhe, et al. Genome-wide genetic structure and selection signatures for color in 10 traditional Chinese yellow-feathered chicken breeds. ''BMC Genomics''. 2020 Apr 20; '''21''' (1):316
Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes. Description: Perrino, Peter A, et al. Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes. ''Commun Biol''. 2020 Apr 20; '''3''' (1):180
Association of common variation in ADD3 and GPC1 with biliary atresia susceptibility. Description: Bai, Mei-Rong, et al. Association of common variation in ADD3 and GPC1 with biliary atresia susceptibility. ''Aging (Albany NY)''. 2020 Apr 21; '''12''' (8):7163-7182
Epigenomic Assessment of Cardiovascular Disease Risk and Interactions With Traditional Risk Metrics. Description: Westerman, Kenneth, et al. Epigenomic Assessment of Cardiovascular Disease Risk and Interactions With Traditional Risk Metrics. ''J Am Heart Assoc''. 2020 Apr 21; '''9''' (8):e015299
Polygenetic Risk Scores for Major Psychiatric Disorders Among Schizophrenia Patients, Their First-Degree Relatives, and Healthy Participants. Description: Ohi, Kazutaka, et al. Polygenetic Risk Scores for Major Psychiatric Disorders Among Schizophrenia Patients, Their First-Degree Relatives, and Healthy Participants. ''Int J Neuropsychopharmacol''. 2020 Apr 21; '''23''' (3):157-164
Polygenic Score for Body Mass Index Is Associated with Disordered Eating in a General Population Cohort. Description: Abdulkadir, Mohamed, et al. Polygenic Score for Body Mass Index Is Associated with Disordered Eating in a General Population Cohort. ''J Clin Med''. 2020 Apr 21; '''9''' (4):
Mapping co-ancestry connections between the genome of a Medieval individual and modern Europeans. Description: Ferrando-Bernal, Manuel, et al. Mapping co-ancestry connections between the genome of a Medieval individual and modern Europeans. ''Sci Rep''. 2020 Apr 22; '''10''' (1):6843
Admixture and natural selection shaped genomes of an Austronesian-speaking population in the Solomon Islands. Description: Isshiki, Mariko, et al. Admixture and natural selection shaped genomes of an Austronesian-speaking population in the Solomon Islands. ''Sci Rep''. 2020 Apr 23; '''10''' (1):6872
Modified entropy-based procedure detects gene-gene-interactions in unconventional genetic models. Description: Malten, Jorg, et al. Modified entropy-based procedure detects gene-gene-interactions in unconventional genetic models. ''BMC Med Genomics''. 2020 Apr 23; '''13''' (1):65
Phenotypic and functional translation of IL1RL1 locus polymorphisms in lung tissue and asthmatic airway epithelium. Description: Portelli, Michael A, et al. Phenotypic and functional translation of IL1RL1 locus polymorphisms in lung tissue and asthmatic airway epithelium. ''JCI Insight''. 2020 Apr 23; '''5''' (8):
Genome-wide association analysis of insomnia using data from Partners Biobank. Description: Song, Wenyu, et al. Genome-wide association analysis of insomnia using data from Partners Biobank. ''Sci Rep''. 2020 Apr 24; '''10''' (1):6928
The TAGA Study: A Study of Factors Determining Aortic Diameter in Families at High Risk of Abdominal Aortic Aneurysm Reveal Two New Candidate Genes. Description: Peypoch, Olga, et al. The TAGA Study: A Study of Factors Determining Aortic Diameter in Families at High Risk of Abdominal Aortic Aneurysm Reveal Two New Candidate Genes. ''J Clin Med''. 2020 Apr 24; '''9''' (4):
NAF1 rs4691896 Is Significantly Associated with Coal Workers' Pneumoconiosis in a Chinese Han Population: A Case-Control Study. Description: Yuan, Baojun, et al. NAF1 rs4691896 Is Significantly Associated with Coal Workers' Pneumoconiosis in a Chinese Han Population: A Case-Control Study. ''Med Sci Monit''. 2020 Apr 25; '''26''': e918709
Synergistic activation of NF-kappaB by TNFAIP3 (A20) reduction and UBE2L3 (UBCH7) augment that synergistically elevate lupus risk. Description: Kim, Taehyeung, et al. Synergistic activation of NF-kappaB by TNFAIP3 (A20) reduction and UBE2L3 (UBCH7) augment that synergistically elevate lupus risk. ''Arthritis Res Ther''. 2020 Apr 25; '''22''' (1):93
Genetic Diversity and Ancestral Study for Korean Native Pigs Using 60K SNP Chip. Description: Lee, Soo Hyun, et al. Genetic Diversity and Ancestral Study for Korean Native Pigs Using 60K SNP Chip. ''Animals (Basel)''. 2020 Apr 27; '''10''' (5):
Genome-Wide Association Study of Diabetogenic Adipose Morphology in the GENetics of Adipocyte Lipolysis (GENiAL) Cohort. Description: Lundback, Veroniqa, et al. Genome-Wide Association Study of Diabetogenic Adipose Morphology in the GENetics of Adipocyte Lipolysis (GENiAL) Cohort. ''Cells''. 2020 Apr 27; '''9''' (5):
Assessing the power of principal components and wright's fixation index analyzes applied to reveal the genome-wide genetic differences between herds of Holstein cows. Description: Smaragdov, M G, et al. Assessing the power of principal components and wright's fixation index analyzes applied to reveal the genome-wide genetic differences between herds of Holstein cows. ''BMC Genet''. 2020 Apr 28; '''21''' (1):47
Contribution of common and rare damaging variants in familial forms of bipolar disorder and phenotypic outcome. Description: Courtois, Elisa, et al. Contribution of common and rare damaging variants in familial forms of bipolar disorder and phenotypic outcome. ''Transl Psychiatry''. 2020 Apr 28; '''10''' (1):124
Evolutionary history of modern Samoans. Description: Harris, Daniel N, et al. Evolutionary history of modern Samoans. ''Proc Natl Acad Sci U S A''. 2020 Apr 28; '''117''' (17):9458-9465
No correlation between the variants of exostosin 2 gene and type 2 diabetes in Burkina Faso population. Description: Ouedraogo, Serge Yannick, et al. No correlation between the variants of exostosin 2 gene and type 2 diabetes in Burkina Faso population. ''J Public Health Afr''. 2020 Apr 29; '''11''' (1):1233
Genome Wide Analysis for Growth at Two Growth Stages in A New Fast-Growing Common Carp Strain (Cyprinus carpio L.). Description: Su, Shengyan, et al. Genome Wide Analysis for Growth at Two Growth Stages in A New Fast-Growing Common Carp Strain (Cyprinus carpio L.). ''Sci Rep''. 2020 Apr 29; '''10''' (1):7259
Unraveling the genetic origin of 'Glera', 'Ribolla Gialla' and other autochthonous grapevine varieties from Friuli Venezia Giulia (northeastern Italy). Description: Crespan, Manna, et al. Unraveling the genetic origin of 'Glera', 'Ribolla Gialla' and other autochthonous grapevine varieties from Friuli Venezia Giulia (northeastern Italy). ''Sci Rep''. 2020 Apr 29; '''10''' (1):7206
Estimates of Autozygosity Through Runs of Homozygosity in Farmed Coho Salmon. Description: Yoshida, Grazyella M, et al. Estimates of Autozygosity Through Runs of Homozygosity in Farmed Coho Salmon. ''Genes (Basel)''. 2020 Apr 30; '''11''' (5):
Genome-Wide Association Study of Muscle Glycogen in Jingxing Yellow Chicken. Description: Liu, Xiaojing, et al. Genome-Wide Association Study of Muscle Glycogen in Jingxing Yellow Chicken. ''Genes (Basel)''. 2020 Apr 30; '''11''' (5):
Genomic Diversity, Population Structure, and Signature of Selection in Five Chinese Native Sheep Breeds Adapted to Extreme Environments. Description: Abied, Adam, et al. Genomic Diversity, Population Structure, and Signature of Selection in Five Chinese Native Sheep Breeds Adapted to Extreme Environments. ''Genes (Basel)''. 2020 Apr 30; '''11''' (5):
Identification of epigenetic factor KAT2B gene variants for possible roles in congenital heart diseases. Description: Hou, Yong-Sheng, et al. Identification of epigenetic factor KAT2B gene variants for possible roles in congenital heart diseases. ''Biosci Rep''. 2020 Apr 30; '''40''' (4):
Single Nucleotide and Copy-Number Variants in IL4 and IL13 Are Not Associated with Asthma Susceptibility or Inflammatory Markers: A Case-Control Study in a Mexican-Mestizo Population. Description: Ambrocio-Ortiz, Enrique, et al. Single Nucleotide and Copy-Number Variants in IL4 and IL13 Are Not Associated with Asthma Susceptibility or Inflammatory Markers: A Case-Control Study in a Mexican-Mestizo Population. ''Diagnostics (Basel)''. 2020 Apr 30; '''10''' (5):
Determining the impact of uncharacterized inversions in the human genome by droplet digital PCR. Description: Puig, Marta, et al. Determining the impact of uncharacterized inversions in the human genome by droplet digital PCR. ''Genome Res''. 2020 May; '''30''' (5):724-735
Identifying genetic variants underlying phenotypic variation in plants without complete genomes. Description: Voichek, Yoav, et al. Identifying genetic variants underlying phenotypic variation in plants without complete genomes. ''Nat Genet''. 2020 May; '''52''' (5):534-540
A new genetic locus for antipsychotic-induced weight gain: A genome-wide study of first-episode psychosis patients using amisulpride (from the OPTiMiSE cohort). Description: Ter Hark, Sophie E, et al. A new genetic locus for antipsychotic-induced weight gain: A genome-wide study of first-episode psychosis patients using amisulpride (from the OPTiMiSE cohort). ''J Psychopharmacol''. 2020 May; '''34''' (5):524-531
An Out-of-Patagonia migration explains the worldwide diversity and distribution of Saccharomyces eubayanus lineages. Description: Nespolo, Roberto F, et al. An Out-of-Patagonia migration explains the worldwide diversity and distribution of Saccharomyces eubayanus lineages. ''PLoS Genet''. 2020 May; '''16''' (5):e1008777
ASPM-lexical tone association in speakers of a tone language: Direct evidence for the genetic-biasing hypothesis of language evolution. Description: Wong, Patrick C M, et al. ASPM-lexical tone association in speakers of a tone language: Direct evidence for the genetic-biasing hypothesis of language evolution. ''Sci Adv''. 2020 May; '''6''' (22):eaba5090
Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE). Description: Ouyang, Hui, et al. Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE). ''Medicine (Baltimore)''. 2020 May; '''99''' (18):e19985
Decoding a highly mixed Kazakh genome. Description: Seidualy, Madina, et al. Decoding a highly mixed Kazakh genome. ''Hum Genet''. 2020 May; '''139''' (5):557-568
Deletion of beta-fructofuranosidase (invertase) genes is associated with sucrose content in Date Palm fruit. Description: Malek, Joel A, et al. Deletion of beta-fructofuranosidase (invertase) genes is associated with sucrose content in Date Palm fruit. ''Plant Direct''. 2020 May; '''4''' (5):e00214
Family-based genome-wide association study of leprosy in Vietnam. Description: Gzara, Chaima, et al. Family-based genome-wide association study of leprosy in Vietnam. ''PLoS Pathog''. 2020 May; '''16''' (5):e1008565
Fine-scale barriers to connectivity across a fragmented South-East Asian landscape in six songbird species. Description: Cros, Emilie, et al. Fine-scale barriers to connectivity across a fragmented South-East Asian landscape in six songbird species. ''Evol Appl''. 2020 May; '''13''' (5):1026-1036
Genetic polymorphism association analysis of SNPs on the species conservation genes of Tan sheep and Hu sheep. Description: EEr, Hehua, et al. Genetic polymorphism association analysis of SNPs on the species conservation genes of Tan sheep and Hu sheep. ''Trop Anim Health Prod''. 2020 May; '''52''' (3):915-926
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Description: Landi, Maria Teresa, et al. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. ''Nat Genet''. 2020 May; '''52''' (5):494-504
Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants. Description: Persyn, Elodie, et al. Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants. ''Nat Commun''. 2020 May 1; '''11''' (1):2175
Genome-wide association study to identify canine hip dysplasia loci in dogs. Description: Kang, Ji Min, et al. Genome-wide association study to identify canine hip dysplasia loci in dogs. ''J Anim Sci Technol''. 2020 May; '''62''' (3):306-312
Genome-wide DNA methylation and gene expression patterns reflect genetic ancestry and environmental differences across the Indonesian archipelago. Description: Natri, Heini M, et al. Genome-wide DNA methylation and gene expression patterns reflect genetic ancestry and environmental differences across the Indonesian archipelago. ''PLoS Genet''. 2020 May; '''16''' (5):e1008749
Genomic analysis reveals selection signatures of the Wannan Black pig during domestication and breeding. Description: Zhang, Wei, et al. Genomic analysis reveals selection signatures of the Wannan Black pig during domestication and breeding. ''Asian-Australas J Anim Sci''. 2020 May; '''33''' (5):712-721
Genomic characterization of Ugandan smallholder farmer-preferred cassava varieties. Description: Iragaba, Paula, et al. Genomic characterization of Ugandan smallholder farmer-preferred cassava varieties. ''Crop Sci''. 2020 May-Jun; '''60''' (3):1450-1461
Germline Polymorphisms and Length of Survival of Nasopharyngeal Carcinoma: An Exome-Wide Association Study in Multiple Cohorts. Description: Guo, Yun-Miao, et al. Germline Polymorphisms and Length of Survival of Nasopharyngeal Carcinoma: An Exome-Wide Association Study in Multiple Cohorts. ''Adv Sci (Weinh)''. 2020 May; '''7''' (10):1903727
Haplotype-based genome-wide association studies for carcass and growth traits in chicken. Description: Zhang, Hui, et al. Haplotype-based genome-wide association studies for carcass and growth traits in chicken. ''Poult Sci''. 2020 May; '''99''' (5):2349-2361
Integrated GWAS and mRNA Microarray Analysis Identified IFNG and CD40L as the Central Upstream Regulators in Primary Biliary Cholangitis. Description: Ueno, Kazuko, et al. Integrated GWAS and mRNA Microarray Analysis Identified IFNG and CD40L as the Central Upstream Regulators in Primary Biliary Cholangitis. ''Hepatol Commun''. 2020 May; '''4''' (5):724-738
Korean Genome Project: 1094 Korean personal genomes with clinical information. Description: Jeon, Sungwon, et al. Korean Genome Project: 1094 Korean personal genomes with clinical information. ''Sci Adv''. 2020 May; '''6''' (22):eaaz7835
Mitochondrial genome-wide association study of migraine - the HUNT Study. Description: Borte, Sigrid, et al. Mitochondrial genome-wide association study of migraine - the HUNT Study. ''Cephalalgia''. 2020 May; '''40''' (6):625-634
Polygenic liability for schizophrenia and childhood adversity influences daily-life emotion dysregulation and psychosis proneness. Description: Pries, L-K, et al. Polygenic liability for schizophrenia and childhood adversity influences daily-life emotion dysregulation and psychosis proneness. ''Acta Psychiatr Scand''. 2020 May; '''141''' (5):465-475
Polygenic Multiple Sclerosis Risk and Population-Based Childhood Brain Imaging. Description: de Mol, C Louk, et al. Polygenic Multiple Sclerosis Risk and Population-Based Childhood Brain Imaging. ''Ann Neurol''. 2020 May; '''87''' (5):774-787
Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma. Description: Tanigawa, Yosuke, et al. Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma. ''PLoS Genet''. 2020 May; '''16''' (5):e1008682
Rattus population genomics across the Haida Gwaii archipelago provides a framework for guiding invasive species management. Description: Sjodin, Bryson M F, et al. Rattus population genomics across the Haida Gwaii archipelago provides a framework for guiding invasive species management. ''Evol Appl''. 2020 May; '''13''' (5):889-904
Reduction of slaughter age of Hanwoo steers by early genotyping based on meat yield index. Description: Jeong, Chang Dae, et al. Reduction of slaughter age of Hanwoo steers by early genotyping based on meat yield index. ''Asian-Australas J Anim Sci''. 2020 May; '''33''' (5):770-777
Remote modulation of lncRNA GCLET by risk variant at 16p13 underlying genetic susceptibility to gastric cancer. Description: Du, Mulong, et al. Remote modulation of lncRNA GCLET by risk variant at 16p13 underlying genetic susceptibility to gastric cancer. ''Sci Adv''. 2020 May; '''6''' (21):eaay5525
Resolving fine-scale population structure and fishery exploitation using sequenced microsatellites in a northern fish. Description: Layton, Kara K S, et al. Resolving fine-scale population structure and fishery exploitation using sequenced microsatellites in a northern fish. ''Evol Appl''. 2020 May; '''13''' (5):1055-1068
Scalable probabilistic PCA for large-scale genetic variation data. Description: Agrawal, Aman, et al. Scalable probabilistic PCA for large-scale genetic variation data. ''PLoS Genet''. 2020 May; '''16''' (5):e1008773
Shared genetic susceptibilities for irritable bowel syndrome and depressive disorder in Chinese patients uncovered by pooled whole-exome sequencing. Description: Zhu, Shiwei, et al. Shared genetic susceptibilities for irritable bowel syndrome and depressive disorder in Chinese patients uncovered by pooled whole-exome sequencing. ''J Adv Res''. 2020 May; '''23''': 113-121
Signatures of positive selection underlying beef production traits in Korean cattle breeds. Description: Edea, Zewdu, et al. Signatures of positive selection underlying beef production traits in Korean cattle breeds. ''J Anim Sci Technol''. 2020 May; '''62''' (3):293-305
Space is the Place: Effects of Continuous Spatial Structure on Analysis of Population Genetic Data. Description: Battey, C J, et al. Space is the Place: Effects of Continuous Spatial Structure on Analysis of Population Genetic Data. ''Genetics''. 2020 May; '''215''' (1):193-214
The origin of domestication genes in goats. Description: Zheng, Zhuqing, et al. The origin of domestication genes in goats. ''Sci Adv''. 2020 May; '''6''' (21):eaaz5216
Trans-ethnic meta-analysis of genome-wide association studies identifies maternal ITPR1 as a novel locus influencing fetal growth during sensitive periods in pregnancy. Description: Tekola-Ayele, Fasil, et al. Trans-ethnic meta-analysis of genome-wide association studies identifies maternal ITPR1 as a novel locus influencing fetal growth during sensitive periods in pregnancy. ''PLoS Genet''. 2020 May; '''16''' (5):e1008747
Interaction between Coffee Drinking and TRIB1 rs17321515 Single Nucleotide Polymorphism on Coronary Heart Disease in a Taiwanese Population. Description: Liu, Yin-Tso, et al. Interaction between Coffee Drinking and TRIB1 rs17321515 Single Nucleotide Polymorphism on Coronary Heart Disease in a Taiwanese Population. ''Nutrients''. 2020 May 2; '''12''' (5):
A Genome-Wide Association Study To Understand the Effect of Fusarium verticillioides Infection on Seedlings of a Maize Diversity Panel. Description: Stagnati, Lorenzo, et al. A Genome-Wide Association Study To Understand the Effect of Fusarium verticillioides Infection on Seedlings of a Maize Diversity Panel. ''G3 (Bethesda)''. 2020 May 4; '''10''' (5):1685-1696
Genome-Wide Association Study for Maize Leaf Cuticular Conductance Identifies Candidate Genes Involved in the Regulation of Cuticle Development. Description: Lin, Meng, et al. Genome-Wide Association Study for Maize Leaf Cuticular Conductance Identifies Candidate Genes Involved in the Regulation of Cuticle Development. ''G3 (Bethesda)''. 2020 May 4; '''10''' (5):1671-1683
Mutations in a Novel Cadherin Gene Associated with Bt Resistance in Helicoverpa zea. Description: Fritz, Megan L, et al. Mutations in a Novel Cadherin Gene Associated with Bt Resistance in Helicoverpa zea. ''G3 (Bethesda)''. 2020 May 4; '''10''' (5):1563-1574
The metabolome as a link in the genotype-phenotype map for peroxide resistance in the fruit fly, Drosophila melanogaster. Description: Harrison, Benjamin R, et al. The metabolome as a link in the genotype-phenotype map for peroxide resistance in the fruit fly, Drosophila melanogaster. ''BMC Genomics''. 2020 May 4; '''21''' (1):341
Whole-genome homozygosity mapping reveals candidate regions affecting bull fertility in US Holstein cattle. Description: Nani, Juan Pablo, et al. Whole-genome homozygosity mapping reveals candidate regions affecting bull fertility in US Holstein cattle. ''BMC Genomics''. 2020 May 4; '''21''' (1):338
Historic recombination in a durum wheat breeding panel enables high-resolution mapping of Fusarium head blight resistance quantitative trait loci. Description: Sari, Ehsan, et al. Historic recombination in a durum wheat breeding panel enables high-resolution mapping of Fusarium head blight resistance quantitative trait loci. ''Sci Rep''. 2020 May 5; '''10''' (1):7567
The polygenic architecture of left ventricular mass mirrors the clinical epidemiology. Description: Mosley, Jonathan D, et al. The polygenic architecture of left ventricular mass mirrors the clinical epidemiology. ''Sci Rep''. 2020 May 5; '''10''' (1):7561
Genetic Association Reveals Protection against Recurrence of Clostridium difficile Infection with Bezlotoxumab Treatment. Description: Shen, Judong, et al. Genetic Association Reveals Protection against Recurrence of Clostridium difficile Infection with Bezlotoxumab Treatment. ''mSphere''. 2020 May 6; '''5''' (3):
Identification of functional mutations associated with environmental variance of litter size in rabbits. Description: Casto-Rebollo, Cristina, et al. Identification of functional mutations associated with environmental variance of litter size in rabbits. ''Genet Sel Evol''. 2020 May 6; '''52''' (1):22
Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study. Description: Richardson, Tom G, et al. Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study. ''BMJ''. 2020 May 6; '''369''': m1203
Genome-wide association analyses identify known and novel loci for teat number in Duroc pigs using single-locus and multi-locus models. Description: Zhuang, Zhanwei, et al. Genome-wide association analyses identify known and novel loci for teat number in Duroc pigs using single-locus and multi-locus models. ''BMC Genomics''. 2020 May 7; '''21''' (1):344
Genome-wide association mapping of Sclerotinia sclerotiorum resistance in soybean using whole-genome resequencing data. Description: Boudhrioua, Chiheb, et al. Genome-wide association mapping of Sclerotinia sclerotiorum resistance in soybean using whole-genome resequencing data. ''BMC Plant Biol''. 2020 May 7; '''20''' (1):195
Identifying novel associations in GWAS by hierarchical Bayesian latent variable detection of differentially misclassified phenotypes. Description: Shafquat, Afrah, et al. Identifying novel associations in GWAS by hierarchical Bayesian latent variable detection of differentially misclassified phenotypes. ''BMC Bioinformatics''. 2020 May 7; '''21''' (1):178
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank. Description: Shen, Xueyi, et al. A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank. ''Nat Commun''. 2020 May 8; '''11''' (1):2301
Differentiation of Hispanic biogeographic ancestry with 80 ancestry informative markers. Description: Setser, Casandra H, et al. Differentiation of Hispanic biogeographic ancestry with 80 ancestry informative markers. ''Sci Rep''. 2020 May 8; '''10''' (1):7745
DNA methylation QTL analysis identifies new regulators of human longevity. Description: Szymczak, Silke, et al. DNA methylation QTL analysis identifies new regulators of human longevity. ''Hum Mol Genet''. 2020 May 8; '''29''' (7):1154-1167
Discordant evolution of mitochondrial and nuclear yeast genomes at population level. Description: De Chiara, Matteo, et al. Discordant evolution of mitochondrial and nuclear yeast genomes at population level. ''BMC Biol''. 2020 May 11; '''18''' (1):49
Protein-altering germline mutations implicate novel genes related to lung cancer development. Description: Ji, Xuemei, et al. Protein-altering germline mutations implicate novel genes related to lung cancer development. ''Nat Commun''. 2020 May 11; '''11''' (1):2220
A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder. Description: Martin, Joanna, et al. A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder. ''Transl Psychiatry''. 2020 May 12; '''10''' (1):135
Association analysis in a Latin American population revealed ethnic differences in rheumatoid arthritis-associated SNPs in Caucasian and Asian populations. Description: Castro-Santos, P, et al. Association analysis in a Latin American population revealed ethnic differences in rheumatoid arthritis-associated SNPs in Caucasian and Asian populations. ''Sci Rep''. 2020 May 12; '''10''' (1):7879
Genetic susceptibility, inflammation and specific types of depressive symptoms: evidence from the English Longitudinal Study of Ageing. Description: Frank, Philipp, et al. Genetic susceptibility, inflammation and specific types of depressive symptoms: evidence from the English Longitudinal Study of Ageing. ''Transl Psychiatry''. 2020 May 12; '''10''' (1):140
Computational strategies for the preconditioned conjugate gradient method applied to ssSNPBLUP, with an application to a multivariate maternal model. Description: Vandenplas, Jeremie, et al. Computational strategies for the preconditioned conjugate gradient method applied to ssSNPBLUP, with an application to a multivariate maternal model. ''Genet Sel Evol''. 2020 May 13; '''52''' (1):24
Dynamic alterations of genome and transcriptome in KRAS G13D mutant CRC PDX model treated with cetuximab. Description: Zhang, Hangyu, et al. Dynamic alterations of genome and transcriptome in KRAS G13D mutant CRC PDX model treated with cetuximab. ''BMC Cancer''. 2020 May 13; '''20''' (1):416
Gene networks and expression quantitative trait loci associated with adjuvant chemotherapy response in high-grade serous ovarian cancer. Description: Choi, Jihoon, et al. Gene networks and expression quantitative trait loci associated with adjuvant chemotherapy response in high-grade serous ovarian cancer. ''BMC Cancer''. 2020 May 13; '''20''' (1):413
Identification of Immune complement function as a determinant of adverse SARS-CoV-2 infection outcome. Description: Ramlall, Vijendra, et al. Identification of Immune complement function as a determinant of adverse SARS-CoV-2 infection outcome. ''medRxiv''. 2020 May 13;
Haplotype-Based Genome-Wide Association Study and Identification of Candidate Genes Associated with Carcass Traits in Hanwoo Cattle. Description: Srivastava, Swati, et al. Haplotype-Based Genome-Wide Association Study and Identification of Candidate Genes Associated with Carcass Traits in Hanwoo Cattle. ''Genes (Basel)''. 2020 May 14; '''11''' (5):
On the origin of European sheep as revealed by the diversity of the Balkan breeds and by optimizing population-genetic analysis tools. Description: Ciani, Elena, et al. On the origin of European sheep as revealed by the diversity of the Balkan breeds and by optimizing population-genetic analysis tools. ''Genet Sel Evol''. 2020 May 14; '''52''' (1):25
Tropomyosin 1 genetically constrains in vitro hematopoiesis. Description: Thom, Christopher Stephen, et al. Tropomyosin 1 genetically constrains in vitro hematopoiesis. ''BMC Biol''. 2020 May 14; '''18''' (1):52
Identification of single-nucleotide variants associated with susceptibility to Salmonella in pigs using a genome-wide association approach. Description: Schut, Corinne H, et al. Identification of single-nucleotide variants associated with susceptibility to Salmonella in pigs using a genome-wide association approach. ''BMC Vet Res''. 2020 May 15; '''16''' (1):138
Interindividual Variation in Cardiorespiratory Fitness: A Candidate Gene Study in Han Chinese People. Description: Gaowa, et al. Interindividual Variation in Cardiorespiratory Fitness: A Candidate Gene Study in Han Chinese People. ''Genes (Basel)''. 2020 May 15; '''11''' (5):
Metabolite Genome-Wide Association Study (mGWAS) and Gene-Metabolite Interaction Network Analysis Reveal Potential Biomarkers for Feed Efficiency in Pigs. Description: Wang, Xiao, et al. Metabolite Genome-Wide Association Study (mGWAS) and Gene-Metabolite Interaction Network Analysis Reveal Potential Biomarkers for Feed Efficiency in Pigs. ''Metabolites''. 2020 May 15; '''10''' (5):
Mitochondrial tRNA methylation in Alzheimer's disease and progressive supranuclear palsy. Description: Silzer, Talisa K, et al. Mitochondrial tRNA methylation in Alzheimer's disease and progressive supranuclear palsy. ''BMC Med Genomics''. 2020 May 19; '''13''' (1):71
Genome-Wide Patterns of Homozygosity and Relevant Characterizations on the Population Structure in Pietrain Pigs. Description: Zhan, Huiwen, et al. Genome-Wide Patterns of Homozygosity and Relevant Characterizations on the Population Structure in Pietrain Pigs. ''Genes (Basel)''. 2020 May 21; '''11''' (5):
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Description: Ntalla, Ioanna, et al. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. ''Nat Commun''. 2020 May 21; '''11''' (1):2542
Genomic history of the Italian population recapitulates key evolutionary dynamics of both Continental and Southern Europeans. Description: Sazzini, Marco, et al. Genomic history of the Italian population recapitulates key evolutionary dynamics of both Continental and Southern Europeans. ''BMC Biol''. 2020 May 22; '''18''' (1):51
Genetic stratification of depression in UK Biobank. Description: Howard, David M, et al. Genetic stratification of depression in UK Biobank. ''Transl Psychiatry''. 2020 May 24; '''10''' (1):163
A case of Usher syndrome type IIA caused by a rare USH2A homozygous frameshift variant with maternal uniparental disomy (UPD) in a Chinese family. Description: Fu, Jiewen, et al. A case of Usher syndrome type IIA caused by a rare USH2A homozygous frameshift variant with maternal uniparental disomy (UPD) in a Chinese family. ''J Cell Mol Med''. 2020 May 25;
Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples. Description: Esteller-Cucala, Paula, et al. Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples. ''Sci Rep''. 2020 May 25; '''10''' (1):8622
Bruxism Throughout the Lifespan and Variants in MMP2, MMP9 and COMT. Description: Vieira, Alexandre R, et al. Bruxism Throughout the Lifespan and Variants in MMP2, MMP9 and COMT. ''J Pers Med''. 2020 May 27; '''10''' (2):
Combination of Exercise and Vegetarian Diet: Relationship with High Density-Lipoprotein Cholesterol in Taiwanese Adults Based on MTHFR rs1801133 Polymorphism. Description: Chang, Shu-Lin, et al. Combination of Exercise and Vegetarian Diet: Relationship with High Density-Lipoprotein Cholesterol in Taiwanese Adults Based on MTHFR rs1801133 Polymorphism. ''Nutrients''. 2020 May 27; '''12''' (6):
Selection signatures in tropical cattle are enriched for promoter and coding regions and reveal missense mutations in the damage response gene HELB. Description: Naval-Sanchez, Marina, et al. Selection signatures in tropical cattle are enriched for promoter and coding regions and reveal missense mutations in the damage response gene HELB. ''Genet Sel Evol''. 2020 May 27; '''52''' (1):27
A novel genomic region on chromosome 11 associated with fearfulness in dogs. Description: Sarviaho, R, et al. A novel genomic region on chromosome 11 associated with fearfulness in dogs. ''Transl Psychiatry''. 2020 May 28; '''10''' (1):169
Polygenic risk scores for coronary artery disease and subsequent event risk amongst established cases. Description: Howe, Laurence J, et al. Polygenic risk scores for coronary artery disease and subsequent event risk amongst established cases. ''Hum Mol Genet''. 2020 May 28; '''29''' (8):1388-1395
Ancestry-specific predisposing germline variants in cancer. Description: Oak, Ninad, et al. Ancestry-specific predisposing germline variants in cancer. ''Genome Med''. 2020 May 29; '''12''' (1):51
Influence of IGF2BP2, HMG20A, and HNF1B genetic polymorphisms on the susceptibility to Type 2 diabetes mellitus in Chinese Han population. Description: Huang, Ting, et al. Influence of IGF2BP2, HMG20A, and HNF1B genetic polymorphisms on the susceptibility to Type 2 diabetes mellitus in Chinese Han population. ''Biosci Rep''. 2020 May 29; '''40''' (5):
Uncovering Sub-Structure and Genomic Profiles in Across-Countries Subpopulations of Angus Cattle. Description: Cardoso, Diercles Francisco, et al. Uncovering Sub-Structure and Genomic Profiles in Across-Countries Subpopulations of Angus Cattle. ''Sci Rep''. 2020 May 29; '''10''' (1):8770
An Independent Locus Upstream of ASIP Controls Variation in the Shade of the Bay Coat Colour in Horses. Description: Corbin, Laura J, et al. An Independent Locus Upstream of ASIP Controls Variation in the Shade of the Bay Coat Colour in Horses. ''Genes (Basel)''. 2020 May 30; '''11''' (6):
Genome-Wide Association Study Confirms Previous Findings of Major Loci Affecting Resistance to Piscine myocarditis virus in Atlantic Salmon (Salmo salar L.). Description: Hillestad, Borghild, et al. Genome-Wide Association Study Confirms Previous Findings of Major Loci Affecting Resistance to Piscine myocarditis virus in Atlantic Salmon (Salmo salar L.). ''Genes (Basel)''. 2020 May 30; '''11''' (6):
The landscape of host genetic factors involved in infection to common viruses and SARS-CoV-2. Description: Kachuri, Linda, et al. The landscape of host genetic factors involved in infection to common viruses and SARS-CoV-2. ''medRxiv''. 2020 May 30;
TERC Variants Associated with Short Leukocyte Telomeres: Implication of Higher Early Life Leukocyte Telomere Attrition as Assessed by the Blood-and-Muscle Model. Description: Toupance, Simon, et al. TERC Variants Associated with Short Leukocyte Telomeres: Implication of Higher Early Life Leukocyte Telomere Attrition as Assessed by the Blood-and-Muscle Model. ''Cells''. 2020 May 31; '''9''' (6):
Gene-environment interaction with smoking for increased non-muscle-invasive bladder cancer tumor size. Description: Lipunova, Nadezda, et al. Gene-environment interaction with smoking for increased non-muscle-invasive bladder cancer tumor size. ''Transl Androl Urol''. 2020 Jun; '''9''' (3):1329-1337
Novel genetic variants in genes of the Fc gamma receptor-mediated phagocytosis pathway predict non-small cell lung cancer survival. Description: Qian, Danwen, et al. Novel genetic variants in genes of the Fc gamma receptor-mediated phagocytosis pathway predict non-small cell lung cancer survival. ''Transl Lung Cancer Res''. 2020 Jun; '''9''' (3):575-586
A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma. Description: Ruffieux, Helene, et al. A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma. ''PLoS Comput Biol''. 2020 Jun; '''16''' (6):e1007882
Age-of-onset information helps identify 76 genetic variants associated with allergic disease. Description: Ferreira, Manuel A R, et al. Age-of-onset information helps identify 76 genetic variants associated with allergic disease. ''PLoS Genet''. 2020 Jun; '''16''' (6):e1008725
Ancient genomes from northern China suggest links between subsistence changes and human migration. Description: Ning, Chao, et al. Ancient genomes from northern China suggest links between subsistence changes and human migration. ''Nat Commun''. 2020 Jun 1; '''11''' (1):2700
Association Between Lifelong Premature Ejaculation and Polymorphism of Tryptophan Hydroxylase 2 Gene in the Han Population. Description: Fu, Xu, et al. Association Between Lifelong Premature Ejaculation and Polymorphism of Tryptophan Hydroxylase 2 Gene in the Han Population. ''Sex Med''. 2020 Jun; '''8''' (2):223-229
Association between the MUC1 rs4072037 Polymorphism and Risk of Gastric Cancer and Clinical Outcomes. Description: Kim, Beom Su, et al. Association between the MUC1 rs4072037 Polymorphism and Risk of Gastric Cancer and Clinical Outcomes. ''J Gastric Cancer''. 2020 Jun; '''20''' (2):127-138
A Variation in FGF14 Is Associated with Downbeat Nystagmus in a Genome-Wide Association Study. Description: Strupp, Michael, et al. A Variation in FGF14 Is Associated with Downbeat Nystagmus in a Genome-Wide Association Study. ''Cerebellum''. 2020 Jun; '''19''' (3):348-357
Cholinergic neuroplasticity in asthma driven by TrkB signaling. Description: Dragunas, Guilherme, et al. Cholinergic neuroplasticity in asthma driven by TrkB signaling. ''FASEB J''. 2020 Jun; '''34''' (6):7703-7717
CRISPLD2 Gene Polymorphisms with Nonsyndromic Cleft Lip Palate in Indian Population. Description: Neela, Praveen Kumar, et al. CRISPLD2 Gene Polymorphisms with Nonsyndromic Cleft Lip Palate in Indian Population. ''Glob Med Genet''. 2020 Jun; '''7''' (1):22-25
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache. Description: Siewert, Katherine M, et al. Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache. ''Int J Epidemiol''. 2020 Jun 1; '''49''' (3):1022-1031
Differential DNA methylation correlates with response to methotrexate in rheumatoid arthritis. Description: Nair, Nisha, et al. Differential DNA methylation correlates with response to methotrexate in rheumatoid arthritis. ''Rheumatology (Oxford)''. 2020 Jun 1; '''59''' (6):1364-1371
Genetic meta-analysis of obsessive-compulsive disorder and self-report compulsive symptoms. Description: Smit, Dirk J A, et al. Genetic meta-analysis of obsessive-compulsive disorder and self-report compulsive symptoms. ''Am J Med Genet B Neuropsychiatr Genet''. 2020 Jun; '''183''' (4):208-216
Genome-wide study on the polysomic genetic factors conferring plasticity of flower sexuality in hexaploid persimmon. Description: Masuda, Kanae, et al. Genome-wide study on the polysomic genetic factors conferring plasticity of flower sexuality in hexaploid persimmon. ''DNA Res''. 2020 Jun 1; '''27''' (3):
Inspection of real and imputed genotypes reveled 76 SNPs associated to rear udder height in Holstein cattle. Description: Gonzalez, Mirvana, et al. Inspection of real and imputed genotypes reveled 76 SNPs associated to rear udder height in Holstein cattle. ''J Adv Vet Anim Res''. 2020 Jun; '''7''' (2):234-241
Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity. Description: Chu, Benjamin B, et al. Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity. ''Gigascience''. 2020 Jun 1; '''9''' (6):
Longitudinal DNA methylation changes at MET may alter HGF/c-MET signalling in adolescents at risk for depression. Description: Ciuculete, Diana M, et al. Longitudinal DNA methylation changes at MET may alter HGF/c-MET signalling in adolescents at risk for depression. ''Epigenetics''. 2020 Jun - Jul; '''15''' (6-7):646-663
MassARRAY analysis of twelve cancer related SNPs in esophageal squamous cell carcinoma in J&K, India. Description: Shah, Ruchi, et al. MassARRAY analysis of twelve cancer related SNPs in esophageal squamous cell carcinoma in J&K, India. ''BMC Cancer''. 2020 Jun 1; '''20''' (1):497
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export. Description: Martin, Shaun, et al. Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export. ''Acta Neuropathol''. 2020 Jun; '''139''' (6):1001-1024
Negative dominance and dominance-by-dominance epistatic effects reduce grain-yield heterosis in wide crosses in wheat. Description: Boeven, Philipp H G, et al. Negative dominance and dominance-by-dominance epistatic effects reduce grain-yield heterosis in wide crosses in wheat. ''Sci Adv''. 2020 Jun; '''6''' (24):eaay4897
Osteoporosis- and obesity-risk interrelationships: an epigenetic analysis of GWAS-derived SNPs at the developmental gene TBX15. Description: Zhang, Xiao, et al. Osteoporosis- and obesity-risk interrelationships: an epigenetic analysis of GWAS-derived SNPs at the developmental gene TBX15. ''Epigenetics''. 2020 Jun - Jul; '''15''' (6-7):728-749
Patient genetics is linked to chronic wound microbiome composition and healing. Description: Tipton, Craig D, et al. Patient genetics is linked to chronic wound microbiome composition and healing. ''PLoS Pathog''. 2020 Jun; '''16''' (6):e1008511
Polygenic risk for Alzheimer's disease shapes hippocampal scene-selectivity. Description: Chandler, Hannah L, et al. Polygenic risk for Alzheimer's disease shapes hippocampal scene-selectivity. ''Neuropsychopharmacology''. 2020 Jun; '''45''' (7):1171-1178
Polygenic risk scores of several subtypes of epilepsies in a founder population. Description: Moreau, Claudia, et al. Polygenic risk scores of several subtypes of epilepsies in a founder population. ''Neurol Genet''. 2020 Jun; '''6''' (3):e416
Predicted efficacy of a pharmacogenetic passport for inflammatory bowel disease. Description: Bangma, Amber, et al. Predicted efficacy of a pharmacogenetic passport for inflammatory bowel disease. ''Aliment Pharmacol Ther''. 2020 Jun; '''51''' (11):1105-1115
Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population. Description: Eivers, Sarah B, et al. Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population. ''J Glaucoma''. 2020 Jun; '''29''' (6):417-422
Significance of LncRNA CASC8 genetic polymorphisms on the tuberculosis susceptibility in Chinese population. Description: Liu, Guoye, et al. Significance of LncRNA CASC8 genetic polymorphisms on the tuberculosis susceptibility in Chinese population. ''J Clin Lab Anal''. 2020 Jun; '''34''' (6):e23234
Transcript specific regulation of expression influences susceptibility to multiple sclerosis. Description: Ban, Maria, et al. Transcript specific regulation of expression influences susceptibility to multiple sclerosis. ''Eur J Hum Genet''. 2020 Jun; '''28''' (6):826-834
Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription. Description: Marenne, Gaelle, et al. Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription. ''Cell Metab''. 2020 Jun 2; '''31''' (6):1107-1119.e12
Fine-tuning of Genome-Wide Polygenic Risk Scores and Prediction of Gestational Diabetes in South Asian Women. Description: Lamri, Amel, et al. Fine-tuning of Genome-Wide Polygenic Risk Scores and Prediction of Gestational Diabetes in South Asian Women. ''Sci Rep''. 2020 Jun 2; '''10''' (1):8941
G6PD variant distribution in sub-Saharan Africa and potential risks of using chloroquine/hydroxychloroquine based treatments for COVID-19. Description: da Rocha, Jorge, et al. G6PD variant distribution in sub-Saharan Africa and potential risks of using chloroquine/hydroxychloroquine based treatments for COVID-19. ''medRxiv''. 2020 Jun 2;
The Human Leukocyte Antigen Locus and Rheumatic Heart Disease Susceptibility in South Asians and Europeans. Description: Auckland, Kathryn, et al. The Human Leukocyte Antigen Locus and Rheumatic Heart Disease Susceptibility in South Asians and Europeans. ''Sci Rep''. 2020 Jun 2; '''10''' (1):9004
Genomewide Association Study of Acute Anterior Uveitis Identifies New Susceptibility Loci. Description: Huang, Xiu-Feng, et al. Genomewide Association Study of Acute Anterior Uveitis Identifies New Susceptibility Loci. ''Invest Ophthalmol Vis Sci''. 2020 Jun 3; '''61''' (6):3
Identification of genetic loci associated with higher resistance to pancreas disease (PD) in Atlantic salmon (Salmo salar L.). Description: Hillestad, Borghild, et al. Identification of genetic loci associated with higher resistance to pancreas disease (PD) in Atlantic salmon (Salmo salar L.). ''BMC Genomics''. 2020 Jun 3; '''21''' (1):388
RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro. Description: Loh, Nellie Y, et al. RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro. ''Nat Commun''. 2020 Jun 3; '''11''' (1):2797
Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval. Description: Ramirez, Julia, et al. Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval. ''Am J Hum Genet''. 2020 Jun 4; '''106''' (6):764-778
Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement. Description: Mechaussier, Sabrina, et al. Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement. ''Am J Hum Genet''. 2020 Jun 4; '''106''' (6):859-871
Whole-genome resequencing of wild and domestic sheep identifies genes associated with morphological and agronomic traits. Description: Li, Xin, et al. Whole-genome resequencing of wild and domestic sheep identifies genes associated with morphological and agronomic traits. ''Nat Commun''. 2020 Jun 4; '''11''' (1):2815
Cholesterol-binding protein TSPO2 coordinates maturation and proliferation of terminally differentiating erythroblasts. Description: Kiatpakdee, Benjaporn, et al. Cholesterol-binding protein TSPO2 coordinates maturation and proliferation of terminally differentiating erythroblasts. ''J Biol Chem''. 2020 Jun 5; '''295''' (23):8048-8063
Genetic variations associated with telomere length affect the risk of gastric carcinoma. Description: Lili, Ma, et al. Genetic variations associated with telomere length affect the risk of gastric carcinoma. ''Medicine (Baltimore)''. 2020 Jun 5; '''99''' (23):e20551
Genome-wide association study identifies genetic susceptibility loci and pathways of radiation-induced acute oral mucositis. Description: Yang, Da-Wei, et al. Genome-wide association study identifies genetic susceptibility loci and pathways of radiation-induced acute oral mucositis. ''J Transl Med''. 2020 Jun 5; '''18''' (1):224
Identification of Regulatory SNPs Associated with Vicine and Convicine Content of Vicia faba Based on Genotyping by Sequencing Data Using Deep Learning. Description: Heinrich, Felix, et al. Identification of Regulatory SNPs Associated with Vicine and Convicine Content of Vicia faba Based on Genotyping by Sequencing Data Using Deep Learning. ''Genes (Basel)''. 2020 Jun 5; '''11''' (6):
Identification of Genomic Characteristics and Selective Signals in a Du'an Goat Flock. Description: Chen, Qiuming, et al. Identification of Genomic Characteristics and Selective Signals in a Du'an Goat Flock. ''Animals (Basel)''. 2020 Jun 6; '''10''' (6):
High-Throughput Genotyping of Resilient Tomato Landraces to Detect Candidate Genes Involved in the Response to High Temperatures. Description: Olivieri, Fabrizio, et al. High-Throughput Genotyping of Resilient Tomato Landraces to Detect Candidate Genes Involved in the Response to High Temperatures. ''Genes (Basel)''. 2020 Jun 7; '''11''' (6):
Gene-environment interaction: New insights into perceived parenting and social anxiety among adolescents. Description: Chubar, Viktoria, et al. Gene-environment interaction: New insights into perceived parenting and social anxiety among adolescents. ''Eur Psychiatry''. 2020 Jun 8; '''63''' (1):e64
Genetic Diversity and Signatures of Selection in a Native Italian Horse Breed Based on SNP Data. Description: Ablondi, Michela, et al. Genetic Diversity and Signatures of Selection in a Native Italian Horse Breed Based on SNP Data. ''Animals (Basel)''. 2020 Jun 8; '''10''' (6):
Genomic background and genetic relationships between boar taint and fertility traits in German Landrace and Large White. Description: Brinke, Ines, et al. Genomic background and genetic relationships between boar taint and fertility traits in German Landrace and Large White. ''BMC Genet''. 2020 Jun 8; '''21''' (1):61
Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals. Description: Cho, Sung Kweon, et al. Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals. ''Sci Rep''. 2020 Jun 8; '''10''' (1):9179
Transcriptional and imaging-genetic association of cortical interneurons, brain function, and schizophrenia risk. Description: Anderson, Kevin M, et al. Transcriptional and imaging-genetic association of cortical interneurons, brain function, and schizophrenia risk. ''Nat Commun''. 2020 Jun 8; '''11''' (1):2889
Age-dependent effects of body mass index across the adult life span on the risk of dementia: a cohort study with a genetic approach. Description: Karlsson, Ida K, et al. Age-dependent effects of body mass index across the adult life span on the risk of dementia: a cohort study with a genetic approach. ''BMC Med''. 2020 Jun 9; '''18''' (1):131
Pan-GWAS of Streptococcus agalactiae Highlights Lineage-Specific Genes Associated with Virulence and Niche Adaptation. Description: Gori, Andrea, et al. Pan-GWAS of Streptococcus agalactiae Highlights Lineage-Specific Genes Associated with Virulence and Niche Adaptation. ''mBio''. 2020 Jun 9; '''11''' (3):
The genetic basis of sex determination in grapes. Description: Massonnet, Melanie, et al. The genetic basis of sex determination in grapes. ''Nat Commun''. 2020 Jun 9; '''11''' (1):2902
Genetic variations in catechol-O-methyltransferase gene are associated with levodopa response variability in Chinese patients with Parkinson's disease. Description: Zhao, Cuiping, et al. Genetic variations in catechol-O-methyltransferase gene are associated with levodopa response variability in Chinese patients with Parkinson's disease. ''Sci Rep''. 2020 Jun 12; '''10''' (1):9521
Preimplantation Genetic Testing for Polygenic Disease Relative Risk Reduction: Evaluation of Genomic Index Performance in 11,883 Adult Sibling Pairs. Description: Treff, Nathan R, et al. Preimplantation Genetic Testing for Polygenic Disease Relative Risk Reduction: Evaluation of Genomic Index Performance in 11,883 Adult Sibling Pairs. ''Genes (Basel)''. 2020 Jun 12; '''11''' (6):
Conservation Assessment of the State Goat Farms by Using SNP Genotyping Data. Description: Islam, Rabiul, et al. Conservation Assessment of the State Goat Farms by Using SNP Genotyping Data. ''Genes (Basel)''. 2020 Jun 13; '''11''' (6):
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses. Description: Torrico, Barbara, et al. Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses. ''J Clin Med''. 2020 Jun 13; '''9''' (6):
Estimation of Linkage Disequilibrium and Effective Population Size in Three Italian Autochthonous Beef Breeds. Description: Fabbri, Maria Chiara, et al. Estimation of Linkage Disequilibrium and Effective Population Size in Three Italian Autochthonous Beef Breeds. ''Animals (Basel)''. 2020 Jun 14; '''10''' (6):
Genetic risk prediction of the plasma triglyceride response to independent supplementations with eicosapentaenoic and docosahexaenoic acids: the ComparED Study. Description: Vallee Marcotte, Bastien, et al. Genetic risk prediction of the plasma triglyceride response to independent supplementations with eicosapentaenoic and docosahexaenoic acids: the ComparED Study. ''Genes Nutr''. 2020 Jun 15; '''15''' (1):10
Risk of pneumococcal bacteremia in Kenyan children with glucose-6-phosphate dehydrogenase deficiency. Description: Gilchrist, James J, et al. Risk of pneumococcal bacteremia in Kenyan children with glucose-6-phosphate dehydrogenase deficiency. ''BMC Med''. 2020 Jun 15; '''18''' (1):148
Genome Diversity and the Origin of the Arabian Horse. Description: Cosgrove, Elissa J, et al. Genome Diversity and the Origin of the Arabian Horse. ''Sci Rep''. 2020 Jun 16; '''10''' (1):9702
Genomic Structural Diversity in Local Goats: Analysis of Copy-Number Variations. Description: Di Gerlando, Rosalia, et al. Genomic Structural Diversity in Local Goats: Analysis of Copy-Number Variations. ''Animals (Basel)''. 2020 Jun 16; '''10''' (6):
Efficient polygenic risk scores for biobank scale data by exploiting phenotypes from inferred relatives. Description: Truong, Buu, et al. Efficient polygenic risk scores for biobank scale data by exploiting phenotypes from inferred relatives. ''Nat Commun''. 2020 Jun 17; '''11''' (1):3074
Genomewide Association Study of Severe Covid-19 with Respiratory Failure. Description: Ellinghaus, David, et al. Genomewide Association Study of Severe Covid-19 with Respiratory Failure. ''N Engl J Med''. 2020 Jun 17;
Identification of eQTLs associated with lipid metabolism in Longissimus dorsi muscle of pigs with different genetic backgrounds. Description: Criado-Mesas, Lourdes, et al. Identification of eQTLs associated with lipid metabolism in Longissimus dorsi muscle of pigs with different genetic backgrounds. ''Sci Rep''. 2020 Jun 17; '''10''' (1):9845
KAML: improving genomic prediction accuracy of complex traits using machine learning determined parameters. Description: Yin, Lilin, et al. KAML: improving genomic prediction accuracy of complex traits using machine learning determined parameters. ''Genome Biol''. 2020 Jun 17; '''21''' (1):146
Individual and joint contributions of genetic and methylation risk scores for enhancing lung cancer risk stratification: data from a population-based cohort in Germany. Description: Yu, Haixin, et al. Individual and joint contributions of genetic and methylation risk scores for enhancing lung cancer risk stratification: data from a population-based cohort in Germany. ''Clin Epigenetics''. 2020 Jun 18; '''12''' (1):89
A Deletion in GDF7 is Associated with a Heritable Forebrain Commissural Malformation Concurrent with Ventriculomegaly and Interhemispheric Cysts in Cats. Description: Yu, Yoshihiko, et al. A Deletion in GDF7 is Associated with a Heritable Forebrain Commissural Malformation Concurrent with Ventriculomegaly and Interhemispheric Cysts in Cats. ''Genes (Basel)''. 2020 Jun 19; '''11''' (6):
Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits. Description: Smith, Robert Lovsletten, et al. Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits. ''Transl Psychiatry''. 2020 Jun 19; '''10''' (1):198
MiRNA155HG polymorphisms influenced the risk of liver cancer among the Han Chinese population. Description: Chao, Xu, et al. MiRNA155HG polymorphisms influenced the risk of liver cancer among the Han Chinese population. ''BMC Med Genet''. 2020 Jun 19; '''21''' (1):134
Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population. Description: Shi, Xiu-Yu, et al. Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population. ''EBioMedicine''. 2020 Jun 21; '''57''': 102840
Four Loci Are Associated with Cardiorespiratory Fitness and Endurance Performance in Young Chinese Females. Description: Zhao, Ying, et al. Four Loci Are Associated with Cardiorespiratory Fitness and Endurance Performance in Young Chinese Females. ''Sci Rep''. 2020 Jun 22; '''10''' (1):10117
Array-Based Epigenetic Aging Indices May Be Racially Biased. Description: Philibert, Robert, et al. Array-Based Epigenetic Aging Indices May Be Racially Biased. ''Genes (Basel)''. 2020 Jun 22; '''11''' (6):
Asexual Evolution and Forest Conditions Drive Genetic Parallelism in Phytophthora ramorum. Description: Yuzon, Jennifer David, et al. Asexual Evolution and Forest Conditions Drive Genetic Parallelism in Phytophthora ramorum. ''Microorganisms''. 2020 Jun 22; '''8''' (6):
Catechol-O-methyltransferase rs4680 and rs4818 haplotype association with treatment response to olanzapine in patients with schizophrenia. Description: Nikolac Perkovic, Matea, et al. Catechol-O-methyltransferase rs4680 and rs4818 haplotype association with treatment response to olanzapine in patients with schizophrenia. ''Sci Rep''. 2020 Jun 22; '''10''' (1):10049
Coat Color Roan Shows Association with KIT Variants and No Evidence of Lethality in Icelandic Horses. Description: Voss, Katharina, et al. Coat Color Roan Shows Association with KIT Variants and No Evidence of Lethality in Icelandic Horses. ''Genes (Basel)''. 2020 Jun 22; '''11''' (6):
Genome-wide association analysis reveals loci and candidate genes involved in fiber quality traits in sea island cotton (Gossypium barbadense). Description: Su, Xiujuan, et al. Genome-wide association analysis reveals loci and candidate genes involved in fiber quality traits in sea island cotton (Gossypium barbadense). ''BMC Plant Biol''. 2020 Jun 22; '''20''' (1):289
Novel insights on demographic history of tribal and caste groups from West Maharashtra (India) using genome-wide data. Description: Debortoli, Guilherme, et al. Novel insights on demographic history of tribal and caste groups from West Maharashtra (India) using genome-wide data. ''Sci Rep''. 2020 Jun 22; '''10''' (1):10075
Population genomics of Vibrionaceae isolated from an endangered oasis reveals local adaptation after an environmental perturbation. Description: Vazquez-Rosas-Landa, Mirna, et al. Population genomics of Vibrionaceae isolated from an endangered oasis reveals local adaptation after an environmental perturbation. ''BMC Genomics''. 2020 Jun 22; '''21''' (1):418
Allele-specific expression is widespread in Bos indicus muscle and affects meat quality candidate genes. Description: de Souza, Marcela Maria, et al. Allele-specific expression is widespread in Bos indicus muscle and affects meat quality candidate genes. ''Sci Rep''. 2020 Jun 23; '''10''' (1):10204
Whole-genome sequence association analysis of blood proteins in a longitudinal wellness cohort. Description: Zhong, Wen, et al. Whole-genome sequence association analysis of blood proteins in a longitudinal wellness cohort. ''Genome Med''. 2020 Jun 23; '''12''' (1):53
Genomic Tools for the Conservation and Genetic Improvement of a Highly Fragmented Breed-The Ramo Grande Cattle from the Azores. Description: Amaral, Andreia J, et al. Genomic Tools for the Conservation and Genetic Improvement of a Highly Fragmented Breed-The Ramo Grande Cattle from the Azores. ''Animals (Basel)''. 2020 Jun 24; '''10''' (6):
Predicting Health-Related Quality of Life in Trauma-Exposed Male Veterans in Late Midlife: A 20 Year Longitudinal Study. Description: Stevens, Samantha M, et al. Predicting Health-Related Quality of Life in Trauma-Exposed Male Veterans in Late Midlife: A 20 Year Longitudinal Study. ''Int J Environ Res Public Health''. 2020 Jun 24; '''17''' (12):
Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions. Description: Tsepilov, Yakov A, et al. Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions. ''Commun Biol''. 2020 Jun 25; '''3''' (1):329
Ancestry effects on type 2 diabetes genetic risk inference in Hispanic/Latino populations. Description: Chande, Aroon T, et al. Ancestry effects on type 2 diabetes genetic risk inference in Hispanic/Latino populations. ''BMC Med Genet''. 2020 Jun 25; '''21''' (Suppl 2):132
Quantitative trait loci and genes associated with salmonid alphavirus load in Atlantic salmon: implications for pancreas disease resistance and tolerance. Description: Aslam, M L, et al. Quantitative trait loci and genes associated with salmonid alphavirus load in Atlantic salmon: implications for pancreas disease resistance and tolerance. ''Sci Rep''. 2020 Jun 25; '''10''' (1):10393
A genome-wide survey of copy number variations reveals an asymmetric evolution of duplicated genes in rice. Description: Zhao, Fengli, et al. A genome-wide survey of copy number variations reveals an asymmetric evolution of duplicated genes in rice. ''BMC Biol''. 2020 Jun 26; '''18''' (1):73
Common variants in LTBP3 gene contributed to the risk of hip osteoarthritis in Han Chinese population. Description: Zhao, Tianyun, et al. Common variants in LTBP3 gene contributed to the risk of hip osteoarthritis in Han Chinese population. ''Biosci Rep''. 2020 Jun 26; '''40''' (6):
Prioritization of causal genes for coronary artery disease based on cumulative evidence from experimental and in silico studies. Description: Shadrina, Alexandra S, et al. Prioritization of causal genes for coronary artery disease based on cumulative evidence from experimental and in silico studies. ''Sci Rep''. 2020 Jun 26; '''10''' (1):10486
Relationship between the characteristic traits of polycystic ovary syndrome and susceptibility genes. Description: Hong, So-Hyeon, et al. Relationship between the characteristic traits of polycystic ovary syndrome and susceptibility genes. ''Sci Rep''. 2020 Jun 26; '''10''' (1):10479
Genome-wide assessment of genetic risk for systemic lupus erythematosus and disease severity. Description: Chen, Lingyan, et al. Genome-wide assessment of genetic risk for systemic lupus erythematosus and disease severity. ''Hum Mol Genet''. 2020 Jun 27; '''29''' (10):1745-1756
Allele-specific DNA methylation is increased in cancers and its dense mapping in normal plus neoplastic cells increases the yield of disease-associated regulatory SNPs. Description: Do, Catherine, et al. Allele-specific DNA methylation is increased in cancers and its dense mapping in normal plus neoplastic cells increases the yield of disease-associated regulatory SNPs. ''Genome Biol''. 2020 Jun 29; '''21''' (1):153
Genetic colocalization atlas points to common regulatory sites and genes for hematopoietic traits and hematopoietic contributions to disease phenotypes. Description: Thom, Christopher S, et al. Genetic colocalization atlas points to common regulatory sites and genes for hematopoietic traits and hematopoietic contributions to disease phenotypes. ''BMC Med Genomics''. 2020 Jun 29; '''13''' (1):89
Associations between gut microbiota and genetic risk for rheumatoid arthritis in the absence of disease: a cross-sectional study. Description: Wells, Philippa M, et al. Associations between gut microbiota and genetic risk for rheumatoid arthritis in the absence of disease: a cross-sectional study. ''Lancet Rheumatol''. 2020 Jul; '''2''' (7):e418-e427
Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. Description: Zhou, Hang, et al. Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. ''Nat Neurosci''. 2020 Jul; '''23''' (7):809-818
Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program. Description: Kanchan, Kanika, et al. Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program. ''Stem Cell Res''. 2020 Jul; '''46''': 101803
Hepatic NADH reductive stress underlies common variation in metabolic traits. Description: Goodman, Russell P, et al. Hepatic NADH reductive stress underlies common variation in metabolic traits. ''Nature''. 2020 Jul; '''583''' (7814):122-126
Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome. Description: Hsu, Yu-Han H, et al. Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome. ''Int J Obes (Lond)''. 2020 Jul; '''44''' (7):1596-1606
MAPT haplotype-stratified GWAS reveals differential association for AD risk variants. Description: Strickland, Samantha L, et al. MAPT haplotype-stratified GWAS reveals differential association for AD risk variants. ''Alzheimers Dement''. 2020 Jul; '''16''' (7):983-1002
Native American gene flow into Polynesia predating Easter Island settlement. Description: Ioannidis, Alexander G, et al. Native American gene flow into Polynesia predating Easter Island settlement. ''Nature''. 2020 Jul; '''583''' (7817):572-577
Whole-genome sequencing of a sporadic primary immunodeficiency cohort. Description: Thaventhiran, James E D, et al. Whole-genome sequencing of a sporadic primary immunodeficiency cohort. ''Nature''. 2020 Jul; '''583''' (7814):90-95
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Description: von Berg, Joanna, et al. Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. ''Eur J Hum Genet''. 2020 Jul; '''28''' (7):963-972
An atlas of dynamic chromatin landscapes in mouse fetal development. Description: Gorkin, David U, et al. An atlas of dynamic chromatin landscapes in mouse fetal development. ''Nature''. 2020 Jul; '''583''' (7818):744-751
Candidate gene associations reveal sex-specific Graves' disease risk alleles among Chinese Han populations. Description: Yan, Chen-Yan, et al. Candidate gene associations reveal sex-specific Graves' disease risk alleles among Chinese Han populations. ''Mol Genet Genomic Med''. 2020 Jul; '''8''' (7):e1249
Comparison of prediction accuracy for genomic estimated breeding value using the reference pig population of single-breed and admixed-breed. Description: Lee, Soo Hyun, et al. Comparison of prediction accuracy for genomic estimated breeding value using the reference pig population of single-breed and admixed-breed. ''J Anim Sci Technol''. 2020 Jul; '''62''' (4):438-448
Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study. Description: Forgetta, Vincenzo, et al. Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study. ''PLoS Med''. 2020 Jul; '''17''' (7):e1003152
Early Metabolic Features of Genetic Liability to Type 2 Diabetes: Cohort Study With Repeated Metabolomics Across Early Life. Description: Bell, Joshua A, et al. Early Metabolic Features of Genetic Liability to Type 2 Diabetes: Cohort Study With Repeated Metabolomics Across Early Life. ''Diabetes Care''. 2020 Jul; '''43''' (7):1537-1545
Genetic and metabolomic architecture of variation in diet restriction-mediated lifespan extension in Drosophila. Description: Jin, Kelly, et al. Genetic and metabolomic architecture of variation in diet restriction-mediated lifespan extension in Drosophila. ''PLoS Genet''. 2020 Jul; '''16''' (7):e1008835
Identification of male heterogametic sex-determining regions on the Atlantic herring Clupea harengus genome. Description: I Kongsstovu, Sunnvor, et al. Identification of male heterogametic sex-determining regions on the Atlantic herring Clupea harengus genome. ''J Fish Biol''. 2020 Jul; '''97''' (1):190-201
Intergenerational Transmission of Education and ADHD: Effects of Parental Genotypes. Description: de Zeeuw, Eveline L, et al. Intergenerational Transmission of Education and ADHD: Effects of Parental Genotypes. ''Behav Genet''. 2020 Jul; '''50''' (4):221-232
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits. Description: Bretherick, Andrew D, et al. Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits. ''PLoS Genet''. 2020 Jul; '''16''' (7):e1008785
Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand KITLG/SCF and Gene-By-Air-Pollution Interaction. Description: Mak, Angel C Y, et al. Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand KITLG/SCF and Gene-By-Air-Pollution Interaction. ''Genetics''. 2020 Jul; '''215''' (3):869-886
Maternal and paternal effects on offspring internalizing problems: Results from genetic and family-based analyses. Description: Jami, Eshim S, et al. Maternal and paternal effects on offspring internalizing problems: Results from genetic and family-based analyses. ''Am J Med Genet B Neuropsychiatr Genet''. 2020 Jul; '''183''' (5):258-267
Multiple sclerosis risk variants regulate gene expression in innate and adaptive immune cells. Description: Gresle, Melissa M, et al. Multiple sclerosis risk variants regulate gene expression in innate and adaptive immune cells. ''Life Sci Alliance''. 2020 Jul; '''3''' (7):
Non-additive (dominance) effects of genetic variants associated with refractive error and myopia. Description: Pozarickij, Alfred, et al. Non-additive (dominance) effects of genetic variants associated with refractive error and myopia. ''Mol Genet Genomics''. 2020 Jul; '''295''' (4):843-853
Polygenic risk score for obesity and the quality, quantity, and timing of workplace food purchases: A secondary analysis from the ChooseWell 365 randomized trial. Description: Dashti, Hassan S, et al. Polygenic risk score for obesity and the quality, quantity, and timing of workplace food purchases: A secondary analysis from the ChooseWell 365 randomized trial. ''PLoS Med''. 2020 Jul; '''17''' (7):e1003219
Polygenic risk scores indicates genetic overlap between peripheral pain syndromes and chronic postsurgical pain. Description: van Reij, Roel R I, et al. Polygenic risk scores indicates genetic overlap between peripheral pain syndromes and chronic postsurgical pain. ''Neurogenetics''. 2020 Jul; '''21''' (3):205-215
Scleral HIF-1alpha is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis. Description: Zhao, Fei, et al. Scleral HIF-1alpha is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis. ''EBioMedicine''. 2020 Jul; '''57''': 102878
Size reductions and genomic changes within two generations in wild walleye populations: associated with harvest? Description: Bowles, Ella, et al. Size reductions and genomic changes within two generations in wild walleye populations: associated with harvest? ''Evol Appl''. 2020 Jul; '''13''' (6):1128-1144
The role of polygenic susceptibility to obesity among carriers of pathogenic mutations in MC4R in the UK Biobank population. Description: Chami, Nathalie, et al. The role of polygenic susceptibility to obesity among carriers of pathogenic mutations in MC4R in the UK Biobank population. ''PLoS Med''. 2020 Jul; '''17''' (7):e1003196
Genomic analysis of the domestication and post-Spanish conquest evolution of the llama and alpaca. Description: Fan, Ruiwen, et al. Genomic analysis of the domestication and post-Spanish conquest evolution of the llama and alpaca. ''Genome Biol''. 2020 Jul 2; '''21''' (1):159
meQTL and ncRNA functional analyses of 102 GWAS-SNPs associated with depression implicate HACE1 and SHANK2 genes. Description: Ciuculete, Diana M, et al. meQTL and ncRNA functional analyses of 102 GWAS-SNPs associated with depression implicate HACE1 and SHANK2 genes. ''Clin Epigenetics''. 2020 Jul 2; '''12''' (1):99
Cell-to-cell expression dispersion of B-cell surface proteins is linked to genetic variants in humans. Description: Triqueneaux, Gerard, et al. Cell-to-cell expression dispersion of B-cell surface proteins is linked to genetic variants in humans. ''Commun Biol''. 2020 Jul 3; '''3''' (1):346
The roles of hybridization and habitat fragmentation in the evolution of Brazil's enigmatic longwing butterflies, Heliconius nattereri and H. hermathena. Description: Massardo, Darli, et al. The roles of hybridization and habitat fragmentation in the evolution of Brazil's enigmatic longwing butterflies, Heliconius nattereri and H. hermathena. ''BMC Biol''. 2020 Jul 3; '''18''' (1):84
Genome-wide association analysis of canine T zone lymphoma identifies link to hypothyroidism and a shared association with mast-cell tumors. Description: Labadie, Julia D, et al. Genome-wide association analysis of canine T zone lymphoma identifies link to hypothyroidism and a shared association with mast-cell tumors. ''BMC Genomics''. 2020 Jul 6; '''21''' (1):464
Genomic basis of homoploid hybrid speciation within chestnut trees. Description: Sun, Yongshuai, et al. Genomic basis of homoploid hybrid speciation within chestnut trees. ''Nat Commun''. 2020 Jul 6; '''11''' (1):3375
Investigating the influence of mtDNA and nuclear encoded mitochondrial variants on high intensity interval training outcomes. Description: Harvey, N R, et al. Investigating the influence of mtDNA and nuclear encoded mitochondrial variants on high intensity interval training outcomes. ''Sci Rep''. 2020 Jul 6; '''10''' (1):11089
Statistical driver genes as a means to uncover missing heritability for age-related macular degeneration. Description: Waksmunski, Andrea R, et al. Statistical driver genes as a means to uncover missing heritability for age-related macular degeneration. ''BMC Med Genomics''. 2020 Jul 6; '''13''' (1):95
An Investigation into the Genetic History of Japanese Populations of Three Starfish, Acanthaster planci, Linckia laevigata, and Asterias amurensis, Based on Complete Mitochondrial DNA Sequences. Description: Inoue, Jun, et al. An Investigation into the Genetic History of Japanese Populations of Three Starfish, Acanthaster planci, Linckia laevigata, and Asterias amurensis, Based on Complete Mitochondrial DNA Sequences. ''G3 (Bethesda)''. 2020 Jul 7; '''10''' (7):2519-2528
Genomic Heritabilities and Correlations of 17 Traits Related to Obesity and Associated Conditions in the Japanese Population. Description: Gervais, Olivier, et al. Genomic Heritabilities and Correlations of 17 Traits Related to Obesity and Associated Conditions in the Japanese Population. ''G3 (Bethesda)''. 2020 Jul 7; '''10''' (7):2221-2228
Linkage Disequilibrium-Based Inference of Genome Homology and Chromosomal Rearrangements Between Species. Description: de Abreu Santos, Daniel Jordan, et al. Linkage Disequilibrium-Based Inference of Genome Homology and Chromosomal Rearrangements Between Species. ''G3 (Bethesda)''. 2020 Jul 7; '''10''' (7):2327-2343
Mitochondrial GWAS and association of nuclear - mitochondrial epistasis with BMI in T1DM patients. Description: Ludwig-Slomczynska, Agnieszka H, et al. Mitochondrial GWAS and association of nuclear - mitochondrial epistasis with BMI in T1DM patients. ''BMC Med Genomics''. 2020 Jul 7; '''13''' (1):97
Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study. Description: Nudel, Ron, et al. Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study. ''BMC Neurosci''. 2020 Jul 7; '''21''' (1):30
The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instability. Description: Russell, Holly, et al. The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instability. ''Clin Epigenetics''. 2020 Jul 8; '''12''' (1):102
Last Glacial Maximum led to community-wide population expansion in a montane songbird radiation in highland Papua New Guinea. Description: Garg, Kritika M, et al. Last Glacial Maximum led to community-wide population expansion in a montane songbird radiation in highland Papua New Guinea. ''BMC Evol Biol''. 2020 Jul 11; '''20''' (1):82
Ancient Homozygosity Segments in West African Djallonke Sheep Inform on the Genomic Impact of Livestock Adaptation to the Environment. Description: Alvarez, Isabel, et al. Ancient Homozygosity Segments in West African Djallonke Sheep Inform on the Genomic Impact of Livestock Adaptation to the Environment. ''Animals (Basel)''. 2020 Jul 12; '''10''' (7):
Genome-Wide Association Study Unravels LRK1 as a Dark Respiration Regulator in Rice (Oryza sativa L.). Description: Qu, Mingnan, et al. Genome-Wide Association Study Unravels LRK1 as a Dark Respiration Regulator in Rice (Oryza sativa L.). ''Int J Mol Sci''. 2020 Jul 13; '''21''' (14):
Whole genome re-sequencing reveals recent signatures of selection in three strains of farmed Nile tilapia (Oreochromis niloticus). Description: Cadiz, Maria I, et al. Whole genome re-sequencing reveals recent signatures of selection in three strains of farmed Nile tilapia (Oreochromis niloticus). ''Sci Rep''. 2020 Jul 13; '''10''' (1):11514
Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses. Description: Brumpton, Ben, et al. Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses. ''Nat Commun''. 2020 Jul 14; '''11''' (1):3519
Genetic Diversity in Invasive Populations of Argentine Stem Weevil Associated with Adaptation to Biocontrol. Description: Harrop, Thomas W R, et al. Genetic Diversity in Invasive Populations of Argentine Stem Weevil Associated with Adaptation to Biocontrol. ''Insects''. 2020 Jul 14; '''11''' (7):
Heterogeneous Effects of Calorie Content and Nutritional Components Underlie Dietary Influence on Pancreatic Cancer Susceptibility. Description: Dooley, James, et al. Heterogeneous Effects of Calorie Content and Nutritional Components Underlie Dietary Influence on Pancreatic Cancer Susceptibility. ''Cell Rep''. 2020 Jul 14; '''32''' (2):107880
The Frequency of Sex: Population Genomics Reveals Differences in Recombination and Population Structure of the Aflatoxin-Producing Fungus Aspergillus flavus. Description: Drott, Milton T, et al. The Frequency of Sex: Population Genomics Reveals Differences in Recombination and Population Structure of the Aflatoxin-Producing Fungus Aspergillus flavus. ''mBio''. 2020 Jul 14; '''11''' (4):
The genetic heritage of Alpine local cattle breeds using genomic SNP data. Description: Senczuk, Gabriele, et al. The genetic heritage of Alpine local cattle breeds using genomic SNP data. ''Genet Sel Evol''. 2020 Jul 14; '''52''' (1):40
Understanding the genetic determinants of the brain with MOSTest. Description: van der Meer, Dennis, et al. Understanding the genetic determinants of the brain with MOSTest. ''Nat Commun''. 2020 Jul 14; '''11''' (1):3512
Prediction of age at onset in Parkinson's disease using objective specific neuroimaging genetics based on a sparse canonical correlation analysis. Description: Won, Ji Hye, et al. Prediction of age at onset in Parkinson's disease using objective specific neuroimaging genetics based on a sparse canonical correlation analysis. ''Sci Rep''. 2020 Jul 15; '''10''' (1):11662
The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohort. Description: Al Ammari, Maha, et al. The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohort. ''Sci Rep''. 2020 Jul 15; '''10''' (1):11613
Genome-wide diversity and global migration patterns in dromedaries follow ancient caravan routes. Description: Lado, Sara, et al. Genome-wide diversity and global migration patterns in dromedaries follow ancient caravan routes. ''Commun Biol''. 2020 Jul 16; '''3''' (1):387
Novel susceptibility loci for A(H7N9) infection identified by next generation sequencing and functional analysis. Description: Zhao, Baihui, et al. Novel susceptibility loci for A(H7N9) infection identified by next generation sequencing and functional analysis. ''Sci Rep''. 2020 Jul 16; '''10''' (1):11768
QTL mapping and candidate gene analysis of cadmium accumulation in polished rice by genome-wide association study. Description: Pan, Xiaowu, et al. QTL mapping and candidate gene analysis of cadmium accumulation in polished rice by genome-wide association study. ''Sci Rep''. 2020 Jul 16; '''10''' (1):11791
Robust genome-wide ancestry inference for heterogeneous datasets: illustrated using the 1,000 genome project with 3D facial images. Description: Li, Jiarui, et al. Robust genome-wide ancestry inference for heterogeneous datasets: illustrated using the 1,000 genome project with 3D facial images. ''Sci Rep''. 2020 Jul 16; '''10''' (1):11850
Identifying Interactions between Dietary Sodium, Potassium, Sodium-Potassium Ratios, and FGF5 rs16998073 Variants and Their Associated Risk for Hypertension in Korean Adults. Description: Jeong, Hyeyun, et al. Identifying Interactions between Dietary Sodium, Potassium, Sodium-Potassium Ratios, and FGF5 rs16998073 Variants and Their Associated Risk for Hypertension in Korean Adults. ''Nutrients''. 2020 Jul 17; '''12''' (7):
Comparative population genomic analysis uncovers novel genomic footprints and genes associated with small body size in Chinese pony. Description: Asadollahpour Nanaei, Hojjat, et al. Comparative population genomic analysis uncovers novel genomic footprints and genes associated with small body size in Chinese pony. ''BMC Genomics''. 2020 Jul 20; '''21''' (1):496
Identifying Candidate Genes for Hypoxia Adaptation of Tibet Chicken Embryos by Selection Signature Analyses and RNA Sequencing. Description: Liu, Xiayi, et al. Identifying Candidate Genes for Hypoxia Adaptation of Tibet Chicken Embryos by Selection Signature Analyses and RNA Sequencing. ''Genes (Basel)''. 2020 Jul 20; '''11''' (7):
Identifying the fitness costs of a pyrethroid-resistant genotype in the major arboviral vector Aedes aegypti. Description: Rigby, Lisa M, et al. Identifying the fitness costs of a pyrethroid-resistant genotype in the major arboviral vector Aedes aegypti. ''Parasit Vectors''. 2020 Jul 20; '''13''' (1):358
ACE2, TMPRSS2, and Furin variants and SARS-CoV-2 infection in Madrid, Spain. Description: Torre-Fuentes, Laura, et al. ACE2, TMPRSS2, and Furin variants and SARS-CoV-2 infection in Madrid, Spain. ''J Med Virol''. 2020 Jul 21;
Genome-wide association mapping reveals novel genes associated with coleoptile length in a worldwide collection of barley. Description: Luo, Hao, et al. Genome-wide association mapping reveals novel genes associated with coleoptile length in a worldwide collection of barley. ''BMC Plant Biol''. 2020 Jul 22; '''20''' (1):346
Breeding history and candidate genes responsible for black skin of Xichuan black-bone chicken. Description: Li, Donghua, et al. Breeding history and candidate genes responsible for black skin of Xichuan black-bone chicken. ''BMC Genomics''. 2020 Jul 23; '''21''' (1):511
Evaluation of genetic susceptibility of common variants in SOX9 in patients with congenital talipes equinovarus in the Han Chinese population. Description: Li, Jian, et al. Evaluation of genetic susceptibility of common variants in SOX9 in patients with congenital talipes equinovarus in the Han Chinese population. ''J Orthop Surg Res''. 2020 Jul 23; '''15''' (1):276
Temporal Variation in Genetic Composition of Migratory Helicoverpa Zea in Peripheral Populations. Description: Perera, Omaththage P, et al. Temporal Variation in Genetic Composition of Migratory Helicoverpa Zea in Peripheral Populations. ''Insects''. 2020 Jul 23; '''11''' (8):
Accounting for diverse evolutionary forces reveals mosaic patterns of selection on human preterm birth loci. Description: LaBella, Abigail L, et al. Accounting for diverse evolutionary forces reveals mosaic patterns of selection on human preterm birth loci. ''Nat Commun''. 2020 Jul 24; '''11''' (1):3731
Effects of polygenic risk for Alzheimer's disease on rate of cognitive decline in normal aging. Description: Kauppi, Karolina, et al. Effects of polygenic risk for Alzheimer's disease on rate of cognitive decline in normal aging. ''Transl Psychiatry''. 2020 Jul 24; '''10''' (1):250
Evaluating the effect of birth weight on brain volumes and depression: An observational and genetic study using UK Biobank cohort. Description: Ye, Jing, et al. Evaluating the effect of birth weight on brain volumes and depression: An observational and genetic study using UK Biobank cohort. ''Eur Psychiatry''. 2020 Jul 24; '''63''' (1):e73
Sequencing and Analysis of the Sex Determination Region of Populus trichocarpa. Description: Zhou, Ran, et al. Sequencing and Analysis of the Sex Determination Region of Populus trichocarpa. ''Genes (Basel)''. 2020 Jul 24; '''11''' (8):
Interactions of Habitual Coffee Consumption by Genetic Polymorphisms with the Risk of Prediabetes and Type 2 Diabetes Combined. Description: Jin, Taiyue, et al. Interactions of Habitual Coffee Consumption by Genetic Polymorphisms with the Risk of Prediabetes and Type 2 Diabetes Combined. ''Nutrients''. 2020 Jul 26; '''12''' (8):
Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery. Description: Crysnanto, Danang, et al. Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery. ''Genome Biol''. 2020 Jul 27; '''21''' (1):184
Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues. Description: Cao, Xiaolong, et al. Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues. ''Genome Biol''. 2020 Jul 27; '''21''' (1):185
STAGdb: a 30K SNP genotyping array and Science Gateway for Acropora corals and their dinoflagellate symbionts. Description: Kitchen, S A, et al. STAGdb: a 30K SNP genotyping array and Science Gateway for Acropora corals and their dinoflagellate symbionts. ''Sci Rep''. 2020 Jul 27; '''10''' (1):12488
Desaturase Activity and the Risk of Type 2 Diabetes and Coronary Artery Disease: A Mendelian Randomization Study. Description: Jager, Susanne, et al. Desaturase Activity and the Risk of Type 2 Diabetes and Coronary Artery Disease: A Mendelian Randomization Study. ''Nutrients''. 2020 Jul 28; '''12''' (8):
Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women. Description: Mehta, Supriya D, et al. Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women. ''mSystems''. 2020 Jul 28; '''5''' (4):
Identification and validation of a novel candidate gene regulating net meat weight in Simmental beef cattle based on imputed next-generation sequencing. Description: Bordbar, Farhad, et al. Identification and validation of a novel candidate gene regulating net meat weight in Simmental beef cattle based on imputed next-generation sequencing. ''Cell Prolif''. 2020 Jul 28; e12870
The association between serotonin-related gene polymorphisms and susceptibility and early sertraline response in patients with panic disorder. Description: Zou, Zhili, et al. The association between serotonin-related gene polymorphisms and susceptibility and early sertraline response in patients with panic disorder. ''BMC Psychiatry''. 2020 Jul 28; '''20''' (1):388
A minor allele of the haplotype located in the 19q13 loci is associated with a decreased risk of hyper-LDL-cholesterolemia, and a balanced diet and high protein intake can reduce the risk. Description: Park, Sunmin, et al. A minor allele of the haplotype located in the 19q13 loci is associated with a decreased risk of hyper-LDL-cholesterolemia, and a balanced diet and high protein intake can reduce the risk. ''Lipids Health Dis''. 2020 Jul 29; '''19''' (1):178
Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. Description: Morey, Rajendra A, et al. Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. ''Eur J Psychotraumatol''. 2020 Jul 29; '''11''' (1):1785994
Individual-based population genomics reveal different drivers of adaptation in sympatric fish. Description: Torrado, Hector, et al. Individual-based population genomics reveal different drivers of adaptation in sympatric fish. ''Sci Rep''. 2020 Jul 29; '''10''' (1):12683
MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance. Description: Thongpradit, Supranee, et al. MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance. ''Sci Rep''. 2020 Jul 29; '''10''' (1):12712
Population Genetic Analysis of Ten Geographically Isolated Tibetan Pig Populations. Description: Shang, Peng, et al. Population Genetic Analysis of Ten Geographically Isolated Tibetan Pig Populations. ''Animals (Basel)''. 2020 Jul 29; '''10''' (8):
Population structure, genetic diversity, and selective signature of Chaka sheep revealed by whole genome sequencing. Description: Cheng, Jie, et al. Population structure, genetic diversity, and selective signature of Chaka sheep revealed by whole genome sequencing. ''BMC Genomics''. 2020 Jul 29; '''21''' (1):520
Use of the Multivariate Discriminant Analysis for Genome-Wide Association Studies in Cattle. Description: Manca, Elisabetta, et al. Use of the Multivariate Discriminant Analysis for Genome-Wide Association Studies in Cattle. ''Animals (Basel)''. 2020 Jul 29; '''10''' (8):
Genetic Variability in the Italian Heavy Draught Horse from Pedigree Data and Genomic Information. Description: Mancin, Enrico, et al. Genetic Variability in the Italian Heavy Draught Horse from Pedigree Data and Genomic Information. ''Animals (Basel)''. 2020 Jul 30; '''10''' (8):
Hybrid Versus Autochthonous Turkey Populations: Homozygous Genomic Regions Occurrences Due to Artificial and Natural Selection. Description: Strillacci, Maria Giuseppina, et al. Hybrid Versus Autochthonous Turkey Populations: Homozygous Genomic Regions Occurrences Due to Artificial and Natural Selection. ''Animals (Basel)''. 2020 Jul 30; '''10''' (8):
Insight into the Current Genetic Diversity and Population Structure of Domestic Reindeer (Rangifer tarandus) in Russia. Description: Kharzinova, Veronika, et al. Insight into the Current Genetic Diversity and Population Structure of Domestic Reindeer (Rangifer tarandus) in Russia. ''Animals (Basel)''. 2020 Jul 30; '''10''' (8):
Psychiatric comorbidities in Asperger syndrome are related with polygenic overlap and differ from other Autism subtypes. Description: Gonzalez-Penas, Javier, et al. Psychiatric comorbidities in Asperger syndrome are related with polygenic overlap and differ from other Autism subtypes. ''Transl Psychiatry''. 2020 Jul 30; '''10''' (1):258
Genome-Wide Association Analysis for Tuber Dry Matter and Oxidative Browning in Water Yam (Dioscorea alata L.). Description: Gatarira, Cobes, et al. Genome-Wide Association Analysis for Tuber Dry Matter and Oxidative Browning in Water Yam (Dioscorea alata L.). ''Plants (Basel)''. 2020 Jul 31; '''9''' (8):
Genome-wide scan for common variants associated with intramuscular fat and moisture content in rainbow trout. Description: Ali, Ali, et al. Genome-wide scan for common variants associated with intramuscular fat and moisture content in rainbow trout. ''BMC Genomics''. 2020 Jul 31; '''21''' (1):529
Keratoconus-susceptibility gene identification by corneal thickness genome-wide association study and artificial intelligence IBM Watson. Description: Hosoda, Yoshikatsu, et al. Keratoconus-susceptibility gene identification by corneal thickness genome-wide association study and artificial intelligence IBM Watson. ''Commun Biol''. 2020 Jul 31; '''3''' (1):410
PDGFA gene rs9690350 polymorphism increases biliary atresia risk in Chinese children. Description: Liu, Fei, et al. PDGFA gene rs9690350 polymorphism increases biliary atresia risk in Chinese children. ''Biosci Rep''. 2020 Jul 31; '''40''' (7):
Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups. Description: Nedoszytko, Boguslaw, et al. Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups. ''Int J Mol Sci''. 2020 Jul 31; '''21''' (15):
Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations. Description: Ortiz-Fernandez, Lourdes, et al. Genetic variability in the expression of the SARS-CoV-2 host cell entry factors across populations. ''Genes Immun''. 2020 Aug; '''21''' (4):269-272
Genome-wide association study identifies new loci for albuminuria in the Japanese population. Description: Okuda, Hiroshi, et al. Genome-wide association study identifies new loci for albuminuria in the Japanese population. ''Clin Exp Nephrol''. 2020 Aug; '''24''' (8):1-9
Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients. Description: Cha, Pei-Chieng, et al. Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients. ''J Hum Genet''. 2020 Aug; '''65''' (8):693-704
The TP63 Gene Polymorphism rs17506395 is Associated with Early Breast Cancer in Cameroon. Description: Tiofack, Arnol T Z, et al. The TP63 Gene Polymorphism rs17506395 is Associated with Early Breast Cancer in Cameroon. ''Asian Pac J Cancer Prev''. 2020 Aug 1; '''21''' (8):2199-2208
Antioxidant Enzymes Haplotypes and Polymorphisms Associated with Obesity in Mexican Children. Description: Costa-Urrutia, Paula, et al. Antioxidant Enzymes Haplotypes and Polymorphisms Associated with Obesity in Mexican Children. ''Antioxidants (Basel)''. 2020 Aug 1; '''9''' (8):
A scan for genes associated with cancer mortality and longevity in pedigree dog breeds. Description: Doherty, Aoife, et al. A scan for genes associated with cancer mortality and longevity in pedigree dog breeds. ''Mamm Genome''. 2020 Aug; '''31''' (7-8):215-227
Association between osteoporosis and menopause in relation to SOX6 rs297325 variant in Taiwanese women. Description: Hsu, Tzu-Liang, et al. Association between osteoporosis and menopause in relation to SOX6 rs297325 variant in Taiwanese women. ''Menopause''. 2020 Aug; '''27''' (8):887-892
Disease-modifying effects of an SCAF4 structural variant in a predominantly SOD1 ALS cohort. Description: Pytte, Julia, et al. Disease-modifying effects of an SCAF4 structural variant in a predominantly SOD1 ALS cohort. ''Neurol Genet''. 2020 Aug; '''6''' (4):e470
Endogenization and excision of human herpesvirus 6 in human genomes. Description: Liu, Xiaoxi, et al. Endogenization and excision of human herpesvirus 6 in human genomes. ''PLoS Genet''. 2020 Aug; '''16''' (8):e1008915
Epistatic interactions between killer immunoglobulin-like receptors and human leukocyte antigen ligands are associated with ankylosing spondylitis. Description: Hanson, Aimee L, et al. Epistatic interactions between killer immunoglobulin-like receptors and human leukocyte antigen ligands are associated with ankylosing spondylitis. ''PLoS Genet''. 2020 Aug; '''16''' (8):e1008906
Genetic background of ataxia in children younger than 5 years in Finland. Description: Ignatius, Erika, et al. Genetic background of ataxia in children younger than 5 years in Finland. ''Neurol Genet''. 2020 Aug; '''6''' (4):e444
Genetic variants and functional pathways associated with resilience to Alzheimer's disease. Description: Dumitrescu, Logan, et al. Genetic variants and functional pathways associated with resilience to Alzheimer's disease. ''Brain''. 2020 Aug 1; '''143''' (8):2561-2575
Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads. Description: Levis, Nicholas A, et al. Identification of candidate loci for adaptive phenotypic plasticity in natural populations of spadefoot toads. ''Ecol Evol''. 2020 Aug; '''10''' (16):8976-8988
Identifying interactive biological pathways associated with reading disability. Description: Lancaster, Hope Sparks, et al. Identifying interactive biological pathways associated with reading disability. ''Brain Behav''. 2020 Aug; '''10''' (8):e01735
Inferring the ancestry of parents and grandparents from genetic data. Description: Pei, Jingwen, et al. Inferring the ancestry of parents and grandparents from genetic data. ''PLoS Comput Biol''. 2020 Aug; '''16''' (8):e1008065
Machine Learning based histology phenotyping to investigate the epidemiologic and genetic basis of adipocyte morphology and cardiometabolic traits. Description: Glastonbury, Craig A, et al. Machine Learning based histology phenotyping to investigate the epidemiologic and genetic basis of adipocyte morphology and cardiometabolic traits. ''PLoS Comput Biol''. 2020 Aug; '''16''' (8):e1008044
Natural variation in a glucuronosyltransferase modulates propionate sensitivity in a C. elegans propionic acidemia model. Description: Na, Huimin, et al. Natural variation in a glucuronosyltransferase modulates propionate sensitivity in a C. elegans propionic acidemia model. ''PLoS Genet''. 2020 Aug; '''16''' (8):e1008984
Population genomics identifies a distinct Plasmodium vivax population on the China-Myanmar border of Southeast Asia. Description: Brashear, Awtum M, et al. Population genomics identifies a distinct Plasmodium vivax population on the China-Myanmar border of Southeast Asia. ''PLoS Negl Trop Dis''. 2020 Aug; '''14''' (8):e0008506
Postadmixture Selection on Chileans Targets Haplotype Involved in Pigmentation, Thermogenesis and Immune Defense against Pathogens. Description: Vicuna, Lucas, et al. Postadmixture Selection on Chileans Targets Haplotype Involved in Pigmentation, Thermogenesis and Immune Defense against Pathogens. ''Genome Biol Evol''. 2020 Aug 1; '''12''' (8):1459-1470
Recent introgression between Taiga Bean Goose and Tundra Bean Goose results in a largely homogeneous landscape of genetic differentiation. Description: Ottenburghs, Jente, et al. Recent introgression between Taiga Bean Goose and Tundra Bean Goose results in a largely homogeneous landscape of genetic differentiation. ''Heredity (Edinb)''. 2020 Aug; '''125''' (1-2):73-84
Reinforcement learning as an intermediate phenotype in psychosis? Deficits sensitive to illness stage but not associated with polygenic risk of schizophrenia in the general population. Description: Montagnese, Marcella, et al. Reinforcement learning as an intermediate phenotype in psychosis? Deficits sensitive to illness stage but not associated with polygenic risk of schizophrenia in the general population. ''Schizophr Res''. 2020 Aug; '''222''': 389-396
Systematic identification of functional SNPs interrupting 3'UTR polyadenylation signals. Description: Shulman, Eldad David, et al. Systematic identification of functional SNPs interrupting 3'UTR polyadenylation signals. ''PLoS Genet''. 2020 Aug; '''16''' (8):e1008977
The complex pattern of genetic associations of leprosy with HLA class I and class II alleles can be reduced to four amino acid positions. Description: Dallmann-Sauer, Monica, et al. The complex pattern of genetic associations of leprosy with HLA class I and class II alleles can be reduced to four amino acid positions. ''PLoS Pathog''. 2020 Aug; '''16''' (8):e1008818
Translating Discoveries in Attention-Deficit/Hyperactivity Disorder Genomics to an Outpatient Child and Adolescent Psychiatric Cohort. Description: Vuijk, Pieter J, et al. Translating Discoveries in Attention-Deficit/Hyperactivity Disorder Genomics to an Outpatient Child and Adolescent Psychiatric Cohort. ''J Am Acad Child Adolesc Psychiatry''. 2020 Aug; '''59''' (8):964-977
Whole-exome sequencing and genome-wide association studies identify novel sarcopenia risk genes in Han Chinese. Description: Ran, Shu, et al. Whole-exome sequencing and genome-wide association studies identify novel sarcopenia risk genes in Han Chinese. ''Mol Genet Genomic Med''. 2020 Aug; '''8''' (8):e1267
Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study. Description: Chai, Xiaoran, et al. Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study. ''Invest Ophthalmol Vis Sci''. 2020 Aug 3; '''61''' (10):37
Association of WNT7B and RSPO1 with Axial Length in School Children. Description: Lu, Shi Yao, et al. Association of WNT7B and RSPO1 with Axial Length in School Children. ''Invest Ophthalmol Vis Sci''. 2020 Aug 3; '''61''' (10):11
Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism. Description: Matoba, Nana, et al. Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism. ''Transl Psychiatry''. 2020 Aug 3; '''10''' (1):265
Possible Modifying Effect of Hemoglobin A1c on Genetic Susceptibility to Severe Diabetic Retinopathy in Patients With Type 2 Diabetes. Description: Ng, Kelvin K K, et al. Possible Modifying Effect of Hemoglobin A1c on Genetic Susceptibility to Severe Diabetic Retinopathy in Patients With Type 2 Diabetes. ''Invest Ophthalmol Vis Sci''. 2020 Aug 3; '''61''' (10):7
Single nucleotide polymorphisms in tinnitus patients exhibiting severe distress. Description: Watabe, Takahisa, et al. Single nucleotide polymorphisms in tinnitus patients exhibiting severe distress. ''Sci Rep''. 2020 Aug 3; '''10''' (1):13023
A genome-wide scan for candidate lethal variants in Thoroughbred horses. Description: Todd, Evelyn T, et al. A genome-wide scan for candidate lethal variants in Thoroughbred horses. ''Sci Rep''. 2020 Aug 4; '''10''' (1):13153
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study. Description: Pan, Hong-Xu, et al. GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study. ''Transl Neurodegener''. 2020 Aug 4; '''9''' (1):31
Genome-wide association study identifies favorable SNP alleles and candidate genes for frost tolerance in pea. Description: Beji, Sana, et al. Genome-wide association study identifies favorable SNP alleles and candidate genes for frost tolerance in pea. ''BMC Genomics''. 2020 Aug 4; '''21''' (1):536
QTL mapping and GWAS for field kernel water content and kernel dehydration rate before physiological maturity in maize. Description: Li, Shufang, et al. QTL mapping and GWAS for field kernel water content and kernel dehydration rate before physiological maturity in maize. ''Sci Rep''. 2020 Aug 4; '''10''' (1):13114
An 85K SNP Array Uncovers Inbreeding and Cryptic Relatedness in an Antarctic Fur Seal Breeding Colony. Description: Humble, Emily, et al. An 85K SNP Array Uncovers Inbreeding and Cryptic Relatedness in an Antarctic Fur Seal Breeding Colony. ''G3 (Bethesda)''. 2020 Aug 5; '''10''' (8):2787-2799
Bayesian and Machine Learning Models for Genomic Prediction of Anterior Cruciate Ligament Rupture in the Canine Model. Description: Baker, Lauren A, et al. Bayesian and Machine Learning Models for Genomic Prediction of Anterior Cruciate Ligament Rupture in the Canine Model. ''G3 (Bethesda)''. 2020 Aug 5; '''10''' (8):2619-2628
Combining Random Forests and a Signal Detection Method Leads to the Robust Detection of Genotype-Phenotype Associations. Description: Ramzan, Faisal, et al. Combining Random Forests and a Signal Detection Method Leads to the Robust Detection of Genotype-Phenotype Associations. ''Genes (Basel)''. 2020 Aug 5; '''11''' (8):
Development and Validation of an Open Access SNP Array for Nile Tilapia (Oreochromis niloticus). Description: Penaloza, Carolina, et al. Development and Validation of an Open Access SNP Array for Nile Tilapia (Oreochromis niloticus). ''G3 (Bethesda)''. 2020 Aug 5; '''10''' (8):2777-2785
Development and validation of a RAD-Seq target-capture based genotyping assay for routine application in advanced black tiger shrimp (Penaeus monodon) breeding programs. Description: Guppy, Jarrod L, et al. Development and validation of a RAD-Seq target-capture based genotyping assay for routine application in advanced black tiger shrimp (Penaeus monodon) breeding programs. ''BMC Genomics''. 2020 Aug 5; '''21''' (1):541
Dietary Protein and Fat Intake Affects Diabetes Risk with CDKAL1 Genetic Variants in Korean Adults. Description: Choi, Woo Jeong, et al. Dietary Protein and Fat Intake Affects Diabetes Risk with CDKAL1 Genetic Variants in Korean Adults. ''Int J Mol Sci''. 2020 Aug 5; '''21''' (16):
Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data. Description: Pospiech, Ewelina, et al. Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data. ''BMC Genomics''. 2020 Aug 5; '''21''' (1):538
Appraising the Genetic Architecture of Kernel Traits in Hexaploid Wheat Using GWAS. Description: Muhammad, Ali, et al. Appraising the Genetic Architecture of Kernel Traits in Hexaploid Wheat Using GWAS. ''Int J Mol Sci''. 2020 Aug 6; '''21''' (16):
Contribution of CYP24A1 variants in coronary heart disease among the Chinese population. Description: Qian, Peng, et al. Contribution of CYP24A1 variants in coronary heart disease among the Chinese population. ''Lipids Health Dis''. 2020 Aug 6; '''19''' (1):181
Regional Variation of Splicing QTLs in Human Brain. Description: Zhang, Yida, et al. Regional Variation of Splicing QTLs in Human Brain. ''Am J Hum Genet''. 2020 Aug 6; '''107''' (2):196-210
Genetic Diversity and Genetic Structure of the Wild Tsushima Leopard Cat from Genome-Wide Analysis. Description: Ito, Hideyuki, et al. Genetic Diversity and Genetic Structure of the Wild Tsushima Leopard Cat from Genome-Wide Analysis. ''Animals (Basel)''. 2020 Aug 7; '''10''' (8):
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. Description: Zhou, Wei, et al. GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. ''Nat Commun''. 2020 Aug 7; '''11''' (1):3981
Multiscale causal networks identify VGF as a key regulator of Alzheimer's disease. Description: Beckmann, Noam D, et al. Multiscale causal networks identify VGF as a key regulator of Alzheimer's disease. ''Nat Commun''. 2020 Aug 7; '''11''' (1):3942
Meta-analysis of genome-wide association study identifies FBN2 as a novel locus associated with systemic lupus erythematosus in Thai population. Description: Tangtanatakul, Pattarin, et al. Meta-analysis of genome-wide association study identifies FBN2 as a novel locus associated with systemic lupus erythematosus in Thai population. ''Arthritis Res Ther''. 2020 Aug 8; '''22''' (1):185
ContamLD: estimation of ancient nuclear DNA contamination using breakdown of linkage disequilibrium. Description: Nakatsuka, Nathan, et al. ContamLD: estimation of ancient nuclear DNA contamination using breakdown of linkage disequilibrium. ''Genome Biol''. 2020 Aug 10; '''21''' (1):199
Genome-wide pQTL analysis of protein expression regulatory networks in the human liver. Description: He, Bing, et al. Genome-wide pQTL analysis of protein expression regulatory networks in the human liver. ''BMC Biol''. 2020 Aug 10; '''18''' (1):97
Neuronal intranuclear inclusion disease is genetically heterogeneous. Description: Chen, Zhongbo, et al. Neuronal intranuclear inclusion disease is genetically heterogeneous. ''Ann Clin Transl Neurol''. 2020 Aug 10;
The genetic architecture of human brainstem structures and their involvement in common brain disorders. Description: Elvsashagen, Torbjorn, et al. The genetic architecture of human brainstem structures and their involvement in common brain disorders. ''Nat Commun''. 2020 Aug 11; '''11''' (1):4016
Genetic Characterization of Russian Rapeseed Collection and Association Mapping of Novel Loci Affecting Glucosinolate Content. Description: Gubaev, Rim, et al. Genetic Characterization of Russian Rapeseed Collection and Association Mapping of Novel Loci Affecting Glucosinolate Content. ''Genes (Basel)''. 2020 Aug 12; '''11''' (8):
Population analysis of the Korean native duck using whole-genome sequencing data. Description: Lee, Daehwan, et al. Population analysis of the Korean native duck using whole-genome sequencing data. ''BMC Genomics''. 2020 Aug 12; '''21''' (1):554
A transcriptomic variation map provides insights into the genetic basis of Pinus massoniana Lamb. evolution and the association with oleoresin yield. Description: Liu, Qinghua, et al. A transcriptomic variation map provides insights into the genetic basis of Pinus massoniana Lamb. evolution and the association with oleoresin yield. ''BMC Plant Biol''. 2020 Aug 13; '''20''' (1):375
Fifteen Shades of Grey: Combined Analysis of Genome-Wide SNP Data in Steppe and Mediterranean Grey Cattle Sheds New Light on the Molecular Basis of Coat Color. Description: Senczuk, Gabriele, et al. Fifteen Shades of Grey: Combined Analysis of Genome-Wide SNP Data in Steppe and Mediterranean Grey Cattle Sheds New Light on the Molecular Basis of Coat Color. ''Genes (Basel)''. 2020 Aug 13; '''11''' (8):
Genetic structure of the mosquito Aedes aegypti in local forest and domestic habitats in Gabon and Kenya. Description: Xia, Siyang, et al. Genetic structure of the mosquito Aedes aegypti in local forest and domestic habitats in Gabon and Kenya. ''Parasit Vectors''. 2020 Aug 13; '''13''' (1):417
The impact of transposable elements on tomato diversity. Description: Dominguez, Marisol, et al. The impact of transposable elements on tomato diversity. ''Nat Commun''. 2020 Aug 13; '''11''' (1):4058
Genome-Wide Assessment of Runs of Homozygosity in Chinese Wagyu Beef Cattle. Description: Zhao, Guoyao, et al. Genome-Wide Assessment of Runs of Homozygosity in Chinese Wagyu Beef Cattle. ''Animals (Basel)''. 2020 Aug 14; '''10''' (8):
Efficient toolkit implementing best practices for principal component analysis of population genetic data. Description: Prive, Florian, et al. Efficient toolkit implementing best practices for principal component analysis of population genetic data. ''Bioinformatics''. 2020 Aug 15; '''36''' (16):4449-4457
Correlation analysis between CARMEN variants and alcohol-induced osteonecrosis of the femoral head in the Chinese population. Description: Guo, Yongchang, et al. Correlation analysis between CARMEN variants and alcohol-induced osteonecrosis of the femoral head in the Chinese population. ''BMC Musculoskelet Disord''. 2020 Aug 15; '''21''' (1):547
Partitioning heritability analyses unveil the genetic architecture of human brain multidimensional functional connectivity patterns. Description: Feng, Junjiao, et al. Partitioning heritability analyses unveil the genetic architecture of human brain multidimensional functional connectivity patterns. ''Hum Brain Mapp''. 2020 Aug 15; '''41''' (12):3305-3317
Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation. Description: Goodman, Sarah J, et al. Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation. ''J Neurodev Disord''. 2020 Aug 16; '''12''' (1):23
Association of MC4R (rs17782313) with diabetes and cardiovascular disease in Korean men and women. Description: Sull, Jae Woong, et al. Association of MC4R (rs17782313) with diabetes and cardiovascular disease in Korean men and women. ''BMC Med Genet''. 2020 Aug 17; '''21''' (1):160
Clustering by phenotype and genome-wide association study in autism. Description: Narita, Akira, et al. Clustering by phenotype and genome-wide association study in autism. ''Transl Psychiatry''. 2020 Aug 17; '''10''' (1):290
Machine learning for effectively avoiding overfitting is a crucial strategy for the genetic prediction of polygenic psychiatric phenotypes. Description: Takahashi, Yuta, et al. Machine learning for effectively avoiding overfitting is a crucial strategy for the genetic prediction of polygenic psychiatric phenotypes. ''Transl Psychiatry''. 2020 Aug 17; '''10''' (1):294
Polygenic risk score analysis revealed shared genetic background in attention deficit hyperactivity disorder and narcolepsy. Description: Takahashi, Nagahide, et al. Polygenic risk score analysis revealed shared genetic background in attention deficit hyperactivity disorder and narcolepsy. ''Transl Psychiatry''. 2020 Aug 17; '''10''' (1):284
Alcohol Induced Depression: Clinical, Biological and Genetic Features. Description: Farre, Adriana, et al. Alcohol Induced Depression: Clinical, Biological and Genetic Features. ''J Clin Med''. 2020 Aug 18; '''9''' (8):
Amerindian Ancestry Influences Genetic Susceptibility to Chronic Obstructive Pulmonary Disease. Description: Diaz-Pena, Roberto, et al. Amerindian Ancestry Influences Genetic Susceptibility to Chronic Obstructive Pulmonary Disease. ''J Pers Med''. 2020 Aug 18; '''10''' (3):
Basal Levels of CD18 Antigen Presenting Cells in Cow Milk Associate with Copy Number Variation of Fc Gamma Receptors. Description: Seroussi, Eyal, et al. Basal Levels of CD18 Antigen Presenting Cells in Cow Milk Associate with Copy Number Variation of Fc Gamma Receptors. ''Genes (Basel)''. 2020 Aug 18; '''11''' (8):
Genome-Wide SNP Analysis Reveals the Population Structure and the Conservation Status of 23 Italian Chicken Breeds. Description: Cendron, Filippo, et al. Genome-Wide SNP Analysis Reveals the Population Structure and the Conservation Status of 23 Italian Chicken Breeds. ''Animals (Basel)''. 2020 Aug 18; '''10''' (8):
Identification of strong candidate genes for backfat and intramuscular fatty acid composition in three crosses based on the Iberian pig. Description: Crespo-Piazuelo, Daniel, et al. Identification of strong candidate genes for backfat and intramuscular fatty acid composition in three crosses based on the Iberian pig. ''Sci Rep''. 2020 Aug 18; '''10''' (1):13962
Prediction of genomic breeding values based on pre-selected SNPs using ssGBLUP, WssGBLUP and BayesB for Edwardsiellosis resistance in Japanese flounder. Description: Lu, Sheng, et al. Prediction of genomic breeding values based on pre-selected SNPs using ssGBLUP, WssGBLUP and BayesB for Edwardsiellosis resistance in Japanese flounder. ''Genet Sel Evol''. 2020 Aug 18; '''52''' (1):49
Association of CYP19A1 and CYP1A2 genetic polymorphisms with type 2 diabetes mellitus risk in the Chinese Han population. Description: Yang, Yafeng, et al. Association of CYP19A1 and CYP1A2 genetic polymorphisms with type 2 diabetes mellitus risk in the Chinese Han population. ''Lipids Health Dis''. 2020 Aug 19; '''19''' (1):187
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Description: Schmitz-Abe, Klaus, et al. Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. ''Sci Rep''. 2020 Aug 20; '''10''' (1):14045
Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy. Description: Clayton, Joshua S, et al. Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy. ''Acta Neuropathol Commun''. 2020 Aug 20; '''8''' (1):142
Pharmacogenomics of aromatase inhibitors in postmenopausal breast cancer and additional mechanisms of anastrozole action. Description: Cairns, Junmei, et al. Pharmacogenomics of aromatase inhibitors in postmenopausal breast cancer and additional mechanisms of anastrozole action. ''JCI Insight''. 2020 Aug 20; '''5''' (16):
CORE GREML for estimating covariance between random effects in linear mixed models for complex trait analyses. Description: Zhou, Xuan, et al. CORE GREML for estimating covariance between random effects in linear mixed models for complex trait analyses. ''Nat Commun''. 2020 Aug 21; '''11''' (1):4208
GBAT: a gene-based association test for robust detection of trans-gene regulation. Description: Liu, Xuanyao, et al. GBAT: a gene-based association test for robust detection of trans-gene regulation. ''Genome Biol''. 2020 Aug 24; '''21''' (1):211
Integration of postmortem amygdala expression profiling, GWAS, and functional cell culture assays: neuroticism-associated synaptic vesicle glycoprotein 2A (SV2A) gene is regulated by miR-133a and miR-218. Description: Jurkiewicz, Magdalena, et al. Integration of postmortem amygdala expression profiling, GWAS, and functional cell culture assays: neuroticism-associated synaptic vesicle glycoprotein 2A (SV2A) gene is regulated by miR-133a and miR-218. ''Transl Psychiatry''. 2020 Aug 24; '''10''' (1):297
Whole-genome sequencing and gene network modules predict gemcitabine/carboplatin-induced myelosuppression in non-small cell lung cancer patients. Description: Bjorn, Niclas, et al. Whole-genome sequencing and gene network modules predict gemcitabine/carboplatin-induced myelosuppression in non-small cell lung cancer patients. ''NPJ Syst Biol Appl''. 2020 Aug 24; '''6''' (1):25
Identification of Genetic Factors Underlying the Association between Sodium Intake Habits and Hypertension Risk. Description: Kwon, Yu-Jin, et al. Identification of Genetic Factors Underlying the Association between Sodium Intake Habits and Hypertension Risk. ''Nutrients''. 2020 Aug 25; '''12''' (9):
A new mechanism for a familiar mutation - bovine DGAT1 K232A modulates gene expression through multi-junction exon splice enhancement. Description: Fink, Tania, et al. A new mechanism for a familiar mutation - bovine DGAT1 K232A modulates gene expression through multi-junction exon splice enhancement. ''BMC Genomics''. 2020 Aug 26; '''21''' (1):591
Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population. Description: Rodriguez-Arellano, Martha Eunice, et al. Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population. ''Medicina (Kaunas)''. 2020 Aug 26; '''56''' (9):
Population genetic structure and gene flow of rare and endangered Tetraena mongolica Maxim. revealed by reduced representation sequencing. Description: Cheng, Jin, et al. Population genetic structure and gene flow of rare and endangered Tetraena mongolica Maxim. revealed by reduced representation sequencing. ''BMC Plant Biol''. 2020 Aug 26; '''20''' (1):391
SAP30BP gene is associated with the susceptibility of rotator cuff tear: a case-control study based on Han Chinese population. Description: Tian, Bin, et al. SAP30BP gene is associated with the susceptibility of rotator cuff tear: a case-control study based on Han Chinese population. ''J Orthop Surg Res''. 2020 Aug 26; '''15''' (1):356
Genetic Variability in Polish Lowland Sheepdogs Assessed by Pedigree and Genomic Data. Description: Michels, Paula Wiebke, et al. Genetic Variability in Polish Lowland Sheepdogs Assessed by Pedigree and Genomic Data. ''Animals (Basel)''. 2020 Aug 27; '''10''' (9):
Genome-Wide Association Study and Pathway Analysis for Heterophil/Lymphocyte (H/L) Ratio in Chicken. Description: Wang, Jie, et al. Genome-Wide Association Study and Pathway Analysis for Heterophil/Lymphocyte (H/L) Ratio in Chicken. ''Genes (Basel)''. 2020 Aug 27; '''11''' (9):
Association of nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing protein 3 polymorphisms with systemic lupus erythematosus disease activity and biomarker levels: A case-control study in Chinese population. Description: Su, Zhenzhen, et al. Association of nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing protein 3 polymorphisms with systemic lupus erythematosus disease activity and biomarker levels: A case-control study in Chinese population. ''Medicine (Baltimore)''. 2020 Aug 28; '''99''' (35):e21888
Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa. Description: Hechmi, Meriem, et al. Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa. ''Biosci Rep''. 2020 Aug 28; '''40''' (8):
Dynamics behind disjunct distribution, hotspot-edge refugia, and discordant RADseq/mtDNA variability: insights from the Emei mustache toad. Description: Zheng, Yuchi, et al. Dynamics behind disjunct distribution, hotspot-edge refugia, and discordant RADseq/mtDNA variability: insights from the Emei mustache toad. ''BMC Evol Biol''. 2020 Aug 28; '''20''' (1):111
MIR17HG polymorphism (rs7318578) is associated with liver cancer risk in the Chinese Han population. Description: Chao, Xu, et al. MIR17HG polymorphism (rs7318578) is associated with liver cancer risk in the Chinese Han population. ''Biosci Rep''. 2020 Aug 28; '''40''' (8):
Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits. Description: Wang, Yuzhe, et al. Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits. ''Commun Biol''. 2020 Aug 28; '''3''' (1):472
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease. Description: Izarzugaza, Jose M G, et al. Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease. ''Genome Med''. 2020 Aug 28; '''12''' (1):76
Genetic variants in GHR and PLCE1 genes are associated with susceptibility to esophageal cancer. Description: Wang, Rong, et al. Genetic variants in GHR and PLCE1 genes are associated with susceptibility to esophageal cancer. ''Mol Genet Genomic Med''. 2020 Aug 31; e1474
Genome-wide association study of cafe-au-lait macule number in neurofibromatosis type 1. Description: Sung, Heejong, et al. Genome-wide association study of cafe-au-lait macule number in neurofibromatosis type 1. ''Mol Genet Genomic Med''. 2020 Aug 31; e1400
Immune-microbiota interaction in Finnish and Russian Karelia young people with high and low allergy prevalence. Description: Ruokolainen, Lasse, et al. Immune-microbiota interaction in Finnish and Russian Karelia young people with high and low allergy prevalence. ''Clin Exp Allergy''. 2020 Aug 31;
Targeted sequencing of the BDNF gene in young Chinese Han people with major depressive disorder. Description: Zhang, Chenyu, et al. Targeted sequencing of the BDNF gene in young Chinese Han people with major depressive disorder. ''Mol Genet Genomic Med''. 2020 Aug 31; e1484
Common mechanisms for type 2 diabetes and psychosis: Findings from a prospective birth cohort. Description: Perry, Benjamin I, et al. Common mechanisms for type 2 diabetes and psychosis: Findings from a prospective birth cohort. ''Schizophr Res''. 2020 Sep; '''223''': 227-235
Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease. Description: Bandres-Ciga, S, et al. Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease. ''Acta Neuropathol''. 2020 Sep; '''140''' (3):341-358
NG-Circos: next-generation Circos for data visualization and interpretation. Description: Cui, Ya, et al. NG-Circos: next-generation Circos for data visualization and interpretation. ''NAR Genom Bioinform''. 2020 Sep; '''2''' (3):lqaa069
Adaptive Introgression across Semipermeable Species Boundaries between Local Helicoverpa zea and Invasive Helicoverpa armigera Moths. Description: Valencia-Montoya, Wendy A, et al. Adaptive Introgression across Semipermeable Species Boundaries between Local Helicoverpa zea and Invasive Helicoverpa armigera Moths. ''Mol Biol Evol''. 2020 Sep 1; '''37''' (9):2568-2583
Age-dependent effect of APOE and polygenic component on Alzheimer's disease. Description: Bellou, Eftychia, et al. Age-dependent effect of APOE and polygenic component on Alzheimer's disease. ''Neurobiol Aging''. 2020 Sep; '''93''': 69-77
A genome-wide association study of reproduction traits in four pig populations with different genetic backgrounds. Description: Jiang, Yao, et al. A genome-wide association study of reproduction traits in four pig populations with different genetic backgrounds. ''Asian-Australas J Anim Sci''. 2020 Sep; '''33''' (9):1400-1410
An Intronic HCP5 Variant Is Associated With Age of Onset and Susceptibility to Graves Disease in UK and Polish Cohorts. Description: Lane, Laura Claire, et al. An Intronic HCP5 Variant Is Associated With Age of Onset and Susceptibility to Graves Disease in UK and Polish Cohorts. ''J Clin Endocrinol Metab''. 2020 Sep 1; '''105''' (9):
A nonsense variant in Rap Guanine Nucleotide Exchange Factor 5 (RAPGEF5) is associated with equine familial isolated hypoparathyroidism in Thoroughbred foals. Description: Rivas, Victor N, et al. A nonsense variant in Rap Guanine Nucleotide Exchange Factor 5 (RAPGEF5) is associated with equine familial isolated hypoparathyroidism in Thoroughbred foals. ''PLoS Genet''. 2020 Sep; '''16''' (9):e1009028
Biological insights from multi-omic analysis of 31 genomic risk loci for adult hearing difficulty. Description: Kalra, Gurmannat, et al. Biological insights from multi-omic analysis of 31 genomic risk loci for adult hearing difficulty. ''PLoS Genet''. 2020 Sep; '''16''' (9):e1009025
Comparison of genomic diversity and structure of sable antelope (Hippotragus niger) in zoos, conservation centers, and private ranches in North America. Description: Gooley, Rebecca M, et al. Comparison of genomic diversity and structure of sable antelope (Hippotragus niger) in zoos, conservation centers, and private ranches in North America. ''Evol Appl''. 2020 Sep; '''13''' (8):2143-2154
Detection of copy number variation and selection signatures on the X chromosome in Chinese indigenous sheep with different types of tail. Description: Zhu, Caiye, et al. Detection of copy number variation and selection signatures on the X chromosome in Chinese indigenous sheep with different types of tail. ''Asian-Australas J Anim Sci''. 2020 Sep; '''33''' (9):1378-1386
Effect of recent and ancient inbreeding on production and fertility traits in Canadian Holsteins. Description: Makanjuola, Bayode O, et al. Effect of recent and ancient inbreeding on production and fertility traits in Canadian Holsteins. ''BMC Genomics''. 2020 Sep 1; '''21''' (1):605
Epigenome-wide association study of DNA methylation and adult asthma in the Agricultural Lung Health Study. Description: Hoang, Thanh T, et al. Epigenome-wide association study of DNA methylation and adult asthma in the Agricultural Lung Health Study. ''Eur Respir J''. 2020 Sep; '''56''' (3):
Excess of singleton loss-of-function variants in Parkinson's disease contributes to genetic risk. Description: Bobbili, Dheeraj Reddy, et al. Excess of singleton loss-of-function variants in Parkinson's disease contributes to genetic risk. ''J Med Genet''. 2020 Sep; '''57''' (9):617-623
Extensive Ethnolinguistic Diversity in Vietnam Reflects Multiple Sources of Genetic Diversity. Description: Liu, Dang, et al. Extensive Ethnolinguistic Diversity in Vietnam Reflects Multiple Sources of Genetic Diversity. ''Mol Biol Evol''. 2020 Sep 1; '''37''' (9):2503-2519
Genetic analysis of the modern Australian labradoodle dog breed reveals an excess of the poodle genome. Description: Ali, Muhammad Basil, et al. Genetic analysis of the modern Australian labradoodle dog breed reveals an excess of the poodle genome. ''PLoS Genet''. 2020 Sep; '''16''' (9):e1008956
Genetic determinants of the humoral immune response in MS. Description: Gasperi, Christiane, et al. Genetic determinants of the humoral immune response in MS. ''Neurol Neuroimmunol Neuroinflamm''. 2020 Sep; '''7''' (5):
Genome-wide insights into introgression and its consequences for genome-wide heterozygosity in the Mytilus species complex across Europe. Description: Vendrami, David L J, et al. Genome-wide insights into introgression and its consequences for genome-wide heterozygosity in the Mytilus species complex across Europe. ''Evol Appl''. 2020 Sep; '''13''' (8):2130-2142
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing. Description: Corominas, Jordi, et al. Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing. ''Mol Psychiatry''. 2020 Sep; '''25''' (9):2047-2057
Identification of de novo mutations in prenatal neurodevelopment-associated genes in schizophrenia in two Han Chinese patient-sibling family-based cohorts. Description: Jiang, Shan, et al. Identification of de novo mutations in prenatal neurodevelopment-associated genes in schizophrenia in two Han Chinese patient-sibling family-based cohorts. ''Transl Psychiatry''. 2020 Sep 1; '''10''' (1):307
Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity. Description: Matalonga, Leslie, et al. Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity. ''J Mol Diagn''. 2020 Sep; '''22''' (9):1205-1215
Parallel Genetic Origin of Foot Feathering in Birds. Description: Bortoluzzi, Chiara, et al. Parallel Genetic Origin of Foot Feathering in Birds. ''Mol Biol Evol''. 2020 Sep 1; '''37''' (9):2465-2476
Phenotypic and Molecular Characterization of Risk Loci Associated With Asthma and Lung Function. Description: Karaca, Mehmet, et al. Phenotypic and Molecular Characterization of Risk Loci Associated With Asthma and Lung Function. ''Allergy Asthma Immunol Res''. 2020 Sep; '''12''' (5):806-820
Shared genetic background between children and adults with attention deficit/hyperactivity disorder. Description: Rovira, Paula, et al. Shared genetic background between children and adults with attention deficit/hyperactivity disorder. ''Neuropsychopharmacology''. 2020 Sep; '''45''' (10):1617-1626
The Phenotypic Consequences of Genetic Divergence between Admixed Latin American Populations: Antioquia and Choco, Colombia. Description: Chande, Aroon T, et al. The Phenotypic Consequences of Genetic Divergence between Admixed Latin American Populations: Antioquia and Choco, Colombia. ''Genome Biol Evol''. 2020 Sep 1; '''12''' (9):1516-1527
The relationship between circulating lipids and breast cancer risk: A Mendelian randomization study. Description: Johnson, Kelsey E, et al. The relationship between circulating lipids and breast cancer risk: A Mendelian randomization study. ''PLoS Med''. 2020 Sep; '''17''' (9):e1003302
Whole genome sequencing of elite athletes. Description: Boulygina, Eugenia A, et al. Whole genome sequencing of elite athletes. ''Biol Sport''. 2020 Sep; '''37''' (3):295-304
A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog. Description: Vernau, Karen M, et al. A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog. ''Genes (Basel)''. 2020 Sep 2; '''11''' (9):
Analysis of chromatin organization and gene expression in T cells identifies functional genes for rheumatoid arthritis. Description: Yang, Jing, et al. Analysis of chromatin organization and gene expression in T cells identifies functional genes for rheumatoid arthritis. ''Nat Commun''. 2020 Sep 2; '''11''' (1):4402
Reconstruction of the Largest Pedigree Network for Pear Cultivars and Evaluation of the Genetic Diversity of the USDA-ARS National Pyrus Collection. Description: Montanari, Sara, et al. Reconstruction of the Largest Pedigree Network for Pear Cultivars and Evaluation of the Genetic Diversity of the USDA-ARS National Pyrus Collection. ''G3 (Bethesda)''. 2020 Sep 2; '''10''' (9):3285-3297
Co-expression analysis reveals interpretable gene modules controlled by trans-acting genetic variants. Description: Kolberg, Liis, et al. Co-expression analysis reveals interpretable gene modules controlled by trans-acting genetic variants. ''Elife''. 2020 Sep 3; '''9''':
Genome diversity of Chinese indigenous chicken and the selective signatures in Chinese gamecock chicken. Description: Luo, Wei, et al. Genome diversity of Chinese indigenous chicken and the selective signatures in Chinese gamecock chicken. ''Sci Rep''. 2020 Sep 3; '''10''' (1):14532
Genome-wide association study for circulating fibroblast growth factor 21 and 23. Description: Chuang, Gwo-Tsann, et al. Genome-wide association study for circulating fibroblast growth factor 21 and 23. ''Sci Rep''. 2020 Sep 3; '''10''' (1):14578
High Levels of Genetic Diversity within Nilo-Saharan Populations: Implications for Human Adaptation. Description: Mulindwa, Julius, et al. High Levels of Genetic Diversity within Nilo-Saharan Populations: Implications for Human Adaptation. ''Am J Hum Genet''. 2020 Sep 3; '''107''' (3):473-486
Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs. Description: Chen, Xiao-Feng, et al. Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs. ''JCI Insight''. 2020 Sep 3; '''5''' (17):
Refining the genetic structure and relationships of European cattle breeds through meta-analysis of worldwide genomic SNP data, focusing on Italian cattle. Description: Mastrangelo, Salvatore, et al. Refining the genetic structure and relationships of European cattle breeds through meta-analysis of worldwide genomic SNP data, focusing on Italian cattle. ''Sci Rep''. 2020 Sep 3; '''10''' (1):14522
The Polygenic and Monogenic Basis of Blood Traits and Diseases. Description: Vuckovic, Dragana, et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. ''Cell''. 2020 Sep 3; '''182''' (5):1214-1231.e11
TNF genetic polymorphism (rs1799964) may modify the effect of the dietary inflammatory index on gastric cancer in a case-control study. Description: Kim, Jeeeun, et al. TNF genetic polymorphism (rs1799964) may modify the effect of the dietary inflammatory index on gastric cancer in a case-control study. ''Sci Rep''. 2020 Sep 3; '''10''' (1):14590
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. Description: Saw, Jacqueline, et al. Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. ''Nat Commun''. 2020 Sep 4; '''11''' (1):4432
Genomic Regions 10q22.2, 17q21.31, and 2p23.1 Can Contribute to a Lower Lung Function in African Descent Populations. Description: Fonseca, Hellen, et al. Genomic Regions 10q22.2, 17q21.31, and 2p23.1 Can Contribute to a Lower Lung Function in African Descent Populations. ''Genes (Basel)''. 2020 Sep 4; '''11''' (9):
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Description: Rashkin, Sara R, et al. Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. ''Nat Commun''. 2020 Sep 4; '''11''' (1):4423
Signatures of selection reveal candidate genes involved in economic traits and cold acclimation in five Swedish cattle breeds. Description: Ghoreishifar, Seyed Mohammad, et al. Signatures of selection reveal candidate genes involved in economic traits and cold acclimation in five Swedish cattle breeds. ''Genet Sel Evol''. 2020 Sep 4; '''52''' (1):52
Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorder. Description: Wongpaiboonwattana, Wikrom, et al. Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorder. ''Medicine (Baltimore)''. 2020 Sep 4; '''99''' (36):e21946
Vitamin D Receptor Polymorphisms in Sex-Frailty Paradox. Description: Arosio, Beatrice, et al. Vitamin D Receptor Polymorphisms in Sex-Frailty Paradox. ''Nutrients''. 2020 Sep 5; '''12''' (9):
A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs. Description: Hitti-Malin, Rebekkah J, et al. A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs. ''BMC Genet''. 2020 Sep 7; '''21''' (1):100
Identification of loci controlling mineral element concentration in soybean seeds. Description: Malle, Sidiki, et al. Identification of loci controlling mineral element concentration in soybean seeds. ''BMC Plant Biol''. 2020 Sep 7; '''20''' (1):419
MassARRAY-based single nucleotide polymorphism analysis in breast cancer of north Indian population. Description: Bakshi, Divya, et al. MassARRAY-based single nucleotide polymorphism analysis in breast cancer of north Indian population. ''BMC Cancer''. 2020 Sep 7; '''20''' (1):861
Population sequencing enhances understanding of tea plant evolution. Description: Wang, Xinchao, et al. Population sequencing enhances understanding of tea plant evolution. ''Nat Commun''. 2020 Sep 7; '''11''' (1):4447
An Increased Burden of Highly Active Retrotransposition Competent L1s Is Associated with Parkinson's Disease Risk and Progression in the PPMI Cohort. Description: Pfaff, Abigail L, et al. An Increased Burden of Highly Active Retrotransposition Competent L1s Is Associated with Parkinson's Disease Risk and Progression in the PPMI Cohort. ''Int J Mol Sci''. 2020 Sep 8; '''21''' (18):
Fonio millet genome unlocks African orphan crop diversity for agriculture in a changing climate. Description: Abrouk, Michael, et al. Fonio millet genome unlocks African orphan crop diversity for agriculture in a changing climate. ''Nat Commun''. 2020 Sep 8; '''11''' (1):4488
Human genetic determinants of the gut microbiome and their associations with health and disease: a phenome-wide association study. Description: Groot, Hilde E, et al. Human genetic determinants of the gut microbiome and their associations with health and disease: a phenome-wide association study. ''Sci Rep''. 2020 Sep 8; '''10''' (1):14771
Selection Signatures Analysis Reveals Genes Associated with High-Altitude Adaptation in Tibetan Goats from Nagqu, Tibet. Description: Jin, Meilin, et al. Selection Signatures Analysis Reveals Genes Associated with High-Altitude Adaptation in Tibetan Goats from Nagqu, Tibet. ''Animals (Basel)''. 2020 Sep 8; '''10''' (9):
Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort. Description: Grama, Steluta, et al. Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort. ''Transl Psychiatry''. 2020 Sep 9; '''10''' (1):309
Single-Step Genomic Evaluation for Meat Quality Traits, Sensory Characteristics, and Fatty-Acid Composition in Duroc Pigs. Description: Lopez, Bryan Irvine, et al. Single-Step Genomic Evaluation for Meat Quality Traits, Sensory Characteristics, and Fatty-Acid Composition in Duroc Pigs. ''Genes (Basel)''. 2020 Sep 9; '''11''' (9):
Assessment of genetic risk for improved clinical-neuropathological correlations. Description: Spencer, Barbara E, et al. Assessment of genetic risk for improved clinical-neuropathological correlations. ''Acta Neuropathol Commun''. 2020 Sep 10; '''8''' (1):160
Optimizing the genetic prediction of the eye and hair color for North Eurasian populations. Description: Balanovska, Elena, et al. Optimizing the genetic prediction of the eye and hair color for North Eurasian populations. ''BMC Genomics''. 2020 Sep 10; '''21''' (Suppl 7):527
Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study. Description: Pechlivanis, Sonali, et al. Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study. ''BMC Med Genet''. 2020 Sep 10; '''21''' (1):178
Diversity analysis of 80,000 wheat accessions reveals consequences and opportunities of selection footprints. Description: Sansaloni, Carolina, et al. Diversity analysis of 80,000 wheat accessions reveals consequences and opportunities of selection footprints. ''Nat Commun''. 2020 Sep 11; '''11''' (1):4572
Dutch population structure across space, time and GWAS design. Description: Byrne, Ross P, et al. Dutch population structure across space, time and GWAS design. ''Nat Commun''. 2020 Sep 11; '''11''' (1):4556
Genome-wide detection of signatures of selection in indicine and Brazilian locally adapted taurine cattle breeds using whole-genome re-sequencing data. Description: Peripolli, Elisa, et al. Genome-wide detection of signatures of selection in indicine and Brazilian locally adapted taurine cattle breeds using whole-genome re-sequencing data. ''BMC Genomics''. 2020 Sep 11; '''21''' (1):624
Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx. Description: Gay, Nicole R, et al. Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx. ''Genome Biol''. 2020 Sep 11; '''21''' (1):233
The Macrophage Migration Inhibitory Factor (MIF) Promoter Polymorphisms (rs3063368, rs755622) Predict Acute Kidney Injury and Death after Cardiac Surgery. Description: Averdunk, Luisa, et al. The Macrophage Migration Inhibitory Factor (MIF) Promoter Polymorphisms (rs3063368, rs755622) Predict Acute Kidney Injury and Death after Cardiac Surgery. ''J Clin Med''. 2020 Sep 11; '''9''' (9):
Using High-Density SNP Array to Reveal Selection Signatures Related to Prolificacy in Chinese and Kazakhstan Sheep Breeds. Description: Wang, Yi, et al. Using High-Density SNP Array to Reveal Selection Signatures Related to Prolificacy in Chinese and Kazakhstan Sheep Breeds. ''Animals (Basel)''. 2020 Sep 11; '''10''' (9):
Impacts of CR1 genetic variants on cerebrospinal fluid and neuroimaging biomarkers in alzheimer's disease. Description: Zhu, Xi-Chen, et al. Impacts of CR1 genetic variants on cerebrospinal fluid and neuroimaging biomarkers in alzheimer's disease. ''BMC Med Genet''. 2020 Sep 12; '''21''' (1):181
Interactions between genetics and environment shape Camelina seed oil composition. Description: Brock, Jordan R, et al. Interactions between genetics and environment shape Camelina seed oil composition. ''BMC Plant Biol''. 2020 Sep 14; '''20''' (1):423
Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide association study. Description: Sugino, Shigekazu, et al. Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide association study. ''Hum Genomics''. 2020 Sep 14; '''14''' (1):31
Phenotype-specific differences in polygenicity and effect size distribution across functional annotation categories revealed by AI-MiXeR. Description: Shadrin, Alexey A, et al. Phenotype-specific differences in polygenicity and effect size distribution across functional annotation categories revealed by AI-MiXeR. ''Bioinformatics''. 2020 Sep 15; '''36''' (18):4749-4756
A shared genetic contribution to breast cancer and schizophrenia. Description: Lu, Donghao, et al. A shared genetic contribution to breast cancer and schizophrenia. ''Nat Commun''. 2020 Sep 15; '''11''' (1):4637
SNPs in the interleukin-12 signaling pathway are associated with breast cancer risk in Puerto Rican women. Description: Nunez-Marrero, Angel, et al. SNPs in the interleukin-12 signaling pathway are associated with breast cancer risk in Puerto Rican women. ''Oncotarget''. 2020 Sep 15; '''11''' (37):3420-3431
Removing reference bias and improving indel calling in ancient DNA data analysis by mapping to a sequence variation graph. Description: Martiniano, Rui, et al. Removing reference bias and improving indel calling in ancient DNA data analysis by mapping to a sequence variation graph. ''Genome Biol''. 2020 Sep 17; '''21''' (1):250
An integrated personal and population-based Egyptian genome reference. Description: Wohlers, Inken, et al. An integrated personal and population-based Egyptian genome reference. ''Nat Commun''. 2020 Sep 18; '''11''' (1):4719
Dissecting clinical heterogeneity of bipolar disorder using multiple polygenic risk scores. Description: Coombes, Brandon J, et al. Dissecting clinical heterogeneity of bipolar disorder using multiple polygenic risk scores. ''Transl Psychiatry''. 2020 Sep 18; '''10''' (1):314
DNA methylation across the genome in aged human skeletal muscle tissue and muscle-derived cells: the role of HOX genes and physical activity. Description: Turner, D C, et al. DNA methylation across the genome in aged human skeletal muscle tissue and muscle-derived cells: the role of HOX genes and physical activity. ''Sci Rep''. 2020 Sep 21; '''10''' (1):15360
Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing. Description: Crooks, Lucy, et al. Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing. ''BMC Genet''. 2020 Sep 21; '''21''' (1):111
Identifying Risk Genes and Interpreting Pathogenesis for Parkinson's Disease by a Multiomics Analysis. Description: Cheng, Wen-Wen, et al. Identifying Risk Genes and Interpreting Pathogenesis for Parkinson's Disease by a Multiomics Analysis. ''Genes (Basel)''. 2020 Sep 21; '''11''' (9):
Integrated lipidomics and proteomics network analysis highlights lipid and immunity pathways associated with Alzheimer's disease. Description: Xu, Jin, et al. Integrated lipidomics and proteomics network analysis highlights lipid and immunity pathways associated with Alzheimer's disease. ''Transl Neurodegener''. 2020 Sep 21; '''9''' (1):36
Polygenic risk for autism spectrum disorder affects left amygdala activity and negative emotion in schizophrenia. Description: Qin, Yue, et al. Polygenic risk for autism spectrum disorder affects left amygdala activity and negative emotion in schizophrenia. ''Transl Psychiatry''. 2020 Sep 21; '''10''' (1):322
Interaction between adverse childhood experiences and polygenic risk in patients with bipolar disorder. Description: Park, Young-Min, et al. Interaction between adverse childhood experiences and polygenic risk in patients with bipolar disorder. ''Transl Psychiatry''. 2020 Sep 22; '''10''' (1):326
Resequencing of 1,143 indica rice accessions reveals important genetic variations and different heterosis patterns. Description: Lv, Qiming, et al. Resequencing of 1,143 indica rice accessions reveals important genetic variations and different heterosis patterns. ''Nat Commun''. 2020 Sep 22; '''11''' (1):4778
The genetic basis of natural antibody titers of young healthy pigs and relationships with disease resilience. Description: Chen, Yulu, et al. The genetic basis of natural antibody titers of young healthy pigs and relationships with disease resilience. ''BMC Genomics''. 2020 Sep 22; '''21''' (1):648
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis. Description: Nakamura, Ryoichi, et al. A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis. ''Commun Biol''. 2020 Sep 23; '''3''' (1):526
Participation of HHIP Gene Variants in COPD Susceptibility, Lung Function, and Serum and Sputum Protein Levels in Women Exposed to Biomass-Burning Smoke. Description: Ortega-Martinez, Alejandro, et al. Participation of HHIP Gene Variants in COPD Susceptibility, Lung Function, and Serum and Sputum Protein Levels in Women Exposed to Biomass-Burning Smoke. ''Diagnostics (Basel)''. 2020 Sep 23; '''10''' (10):
The conservation value of admixed phenotypes in a critically endangered species complex. Description: Sadanandan, Keren R, et al. The conservation value of admixed phenotypes in a critically endangered species complex. ''Sci Rep''. 2020 Sep 23; '''10''' (1):15549
Genetics of Arthrogryposis and Macroglossia in Piemontese Cattle Breed. Description: Di Stasio, Liliana, et al. Genetics of Arthrogryposis and Macroglossia in Piemontese Cattle Breed. ''Animals (Basel)''. 2020 Sep 24; '''10''' (10):
Genome-wide association studies of ionomic and agronomic traits in USDA mini core collection of rice and comparative analyses of different mapping methods. Description: Liu, Shuai, et al. Genome-wide association studies of ionomic and agronomic traits in USDA mini core collection of rice and comparative analyses of different mapping methods. ''BMC Plant Biol''. 2020 Sep 24; '''20''' (1):441
DNA-based genealogy reconstruction of Nebbiolo, Barbera and other ancient grapevine cultivars from northwestern Italy. Description: Raimondi, Stefano, et al. DNA-based genealogy reconstruction of Nebbiolo, Barbera and other ancient grapevine cultivars from northwestern Italy. ''Sci Rep''. 2020 Sep 25; '''10''' (1):15782
Epigenomics and transcriptomics of systemic sclerosis CD4+ T cells reveal long-range dysregulation of key inflammatory pathways mediated by disease-associated susceptibility loci. Description: Li, Tianlu, et al. Epigenomics and transcriptomics of systemic sclerosis CD4+ T cells reveal long-range dysregulation of key inflammatory pathways mediated by disease-associated susceptibility loci. ''Genome Med''. 2020 Sep 25; '''12''' (1):81
Angiotensin-converting enzyme 2 (ACE2) levels in relation to risk factors for COVID-19 in two large cohorts of patients with atrial fibrillation. Description: Wallentin, Lars, et al. Angiotensin-converting enzyme 2 (ACE2) levels in relation to risk factors for COVID-19 in two large cohorts of patients with atrial fibrillation. ''Eur Heart J''. 2020 Sep 27;
Variants of WNT7A and GPR124 are associated with hemorrhagic transformation following intravenous thrombolysis in ischemic stroke. Description: Ta, Song, et al. Variants of WNT7A and GPR124 are associated with hemorrhagic transformation following intravenous thrombolysis in ischemic stroke. ''CNS Neurosci Ther''. 2020 Sep 29;
Deleterious AGXT Missense Variant Associated with Type 1 Primary Hyperoxaluria (PH1) in Zwartbles Sheep. Description: Letko, Anna, et al. Deleterious AGXT Missense Variant Associated with Type 1 Primary Hyperoxaluria (PH1) in Zwartbles Sheep. ''Genes (Basel)''. 2020 Sep 29; '''11''' (10):
Development of a SNP linkage map and genome-wide association study for resistance to Aeromonas hydrophila in pacu (Piaractus mesopotamicus). Description: Mastrochirico-Filho, Vito A, et al. Development of a SNP linkage map and genome-wide association study for resistance to Aeromonas hydrophila in pacu (Piaractus mesopotamicus). ''BMC Genomics''. 2020 Sep 29; '''21''' (1):672
Immune response and endocytosis pathways are associated with the resilience against Alzheimer's disease. Description: Tesi, Niccolo, et al. Immune response and endocytosis pathways are associated with the resilience against Alzheimer's disease. ''Transl Psychiatry''. 2020 Sep 29; '''10''' (1):332
New Guinea highland wild dogs are the original New Guinea singing dogs. Description: Surbakti, Suriani, et al. New Guinea highland wild dogs are the original New Guinea singing dogs. ''Proc Natl Acad Sci U S A''. 2020 Sep 29; '''117''' (39):24369-24376
Selection signatures of Fuzhong Buffalo based on whole-genome sequences. Description: Sun, Ting, et al. Selection signatures of Fuzhong Buffalo based on whole-genome sequences. ''BMC Genomics''. 2020 Sep 29; '''21''' (1):674
The effects of common variants in MDM2 and GNRH2 genes on the risk and survival of osteosarcoma in Han populations from Northwest China. Description: Feng, Weilou, et al. The effects of common variants in MDM2 and GNRH2 genes on the risk and survival of osteosarcoma in Han populations from Northwest China. ''Sci Rep''. 2020 Sep 29; '''10''' (1):15939
Use of gene expression and whole-genome sequence information to improve the accuracy of genomic prediction for carcass traits in Hanwoo cattle. Description: de Las Heras-Saldana, Sara, et al. Use of gene expression and whole-genome sequence information to improve the accuracy of genomic prediction for carcass traits in Hanwoo cattle. ''Genet Sel Evol''. 2020 Sep 29; '''52''' (1):54
Genetic basis of falling risk susceptibility in the UK Biobank Study. Description: Trajanoska, Katerina, et al. Genetic basis of falling risk susceptibility in the UK Biobank Study. ''Commun Biol''. 2020 Sep 30; '''3''' (1):543
Integrative genomics analysis identifies five promising genes implicated in insomnia risk based on multiple omics datasets. Description: Sun, Haozhen, et al. Integrative genomics analysis identifies five promising genes implicated in insomnia risk based on multiple omics datasets. ''Biosci Rep''. 2020 Sep 30; '''40''' (9):
The shaping of immunological responses through natural selection after the Roma Diaspora. Description: Dobon, Begona, et al. The shaping of immunological responses through natural selection after the Roma Diaspora. ''Sci Rep''. 2020 Sep 30; '''10''' (1):16134
A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank. Description: Qian, Junyang, et al. A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank. ''PLoS Genet''. 2020 Oct; '''16''' (10):e1009141
An integrated multi-omics approach identifies epigenetic alterations associated with Alzheimer's disease. Description: Nativio, Raffaella, et al. An integrated multi-omics approach identifies epigenetic alterations associated with Alzheimer's disease. ''Nat Genet''. 2020 Oct; '''52''' (10):1024-1035
Estimating indirect parental genetic effects on offspring phenotypes using virtual parental genotypes derived from sibling and half sibling pairs. Description: Hwang, Liang-Dar, et al. Estimating indirect parental genetic effects on offspring phenotypes using virtual parental genotypes derived from sibling and half sibling pairs. ''PLoS Genet''. 2020 Oct; '''16''' (10):e1009154
Function of multiple sclerosis-protective HLA class I alleles revealed by genome-wide protein-quantitative trait loci mapping of interferon signalling. Description: Lundtoft, Christian, et al. Function of multiple sclerosis-protective HLA class I alleles revealed by genome-wide protein-quantitative trait loci mapping of interferon signalling. ''PLoS Genet''. 2020 Oct; '''16''' (10):e1009199
High-depth African genomes inform human migration and health. Description: Choudhury, Ananyo, et al. High-depth African genomes inform human migration and health. ''Nature''. 2020 Oct; '''586''' (7831):741-748
Improved Reference Genome Uncovers Novel Sex-Linked Regions in the Guppy (Poecilia reticulata). Description: Fraser, Bonnie A, et al. Improved Reference Genome Uncovers Novel Sex-Linked Regions in the Guppy (Poecilia reticulata). ''Genome Biol Evol''. 2020 Oct 1; '''12''' (10):1789-1805
Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Description: Bick, Alexander G, et al. Inherited causes of clonal haematopoiesis in 97,691 whole genomes. ''Nature''. 2020 Oct; '''586''' (7831):763-768
Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. Description: Shinohara, Tamao, et al. Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. ''J Cell Mol Med''. 2020 Oct 1;
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells. Description: Bao, Erik L, et al. Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells. ''Nature''. 2020 Oct; '''586''' (7831):769-775
Medium-coverage DNA sequencing in the design of the genetic association study. Description: Xu, Chao, et al. Medium-coverage DNA sequencing in the design of the genetic association study. ''Eur J Hum Genet''. 2020 Oct; '''28''' (10):1459-1466
Meta-analysis of transcriptomic variation in T-cell populations reveals both variable and consistent signatures of gene expression and splicing. Description: Radens, Caleb M, et al. Meta-analysis of transcriptomic variation in T-cell populations reveals both variable and consistent signatures of gene expression and splicing. ''RNA''. 2020 Oct; '''26''' (10):1320-1333
Sex differences in human adipose tissue gene expression and genetic regulation involve adipogenesis. Description: Anderson, Warren D, et al. Sex differences in human adipose tissue gene expression and genetic regulation involve adipogenesis. ''Genome Res''. 2020 Oct; '''30''' (10):1379-1392
A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness. Description: Dauber, Andrew, et al. A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness. ''J Clin Endocrinol Metab''. 2020 Oct 1; '''105''' (10):
ALDH2 genotype modulates the association between alcohol consumption and AST/ALT ratio among middle-aged Japanese men: a genome-wide G x E interaction analysis. Description: Sutoh, Yoichi, et al. ALDH2 genotype modulates the association between alcohol consumption and AST/ALT ratio among middle-aged Japanese men: a genome-wide G x E interaction analysis. ''Sci Rep''. 2020 Oct 1; '''10''' (1):16227
Association between APOE e4 and white matter hyperintensity volume, but not total brain volume or white matter integrity. Description: Lyall, Donald M, et al. Association between APOE e4 and white matter hyperintensity volume, but not total brain volume or white matter integrity. ''Brain Imaging Behav''. 2020 Oct; '''14''' (5):1468-1476
Association of genetic variants in migraineurs with and without restless legs syndrome. Description: Lin, Guan-Yu, et al. Association of genetic variants in migraineurs with and without restless legs syndrome. ''Ann Clin Transl Neurol''. 2020 Oct; '''7''' (10):1942-1950
Association of the RPA3-UMAD1 locus with interstitial lung diseases complicated with rheumatoid arthritis in Japanese. Description: Shirai, Yuya, et al. Association of the RPA3-UMAD1 locus with interstitial lung diseases complicated with rheumatoid arthritis in Japanese. ''Ann Rheum Dis''. 2020 Oct; '''79''' (10):1305-1309
Association of Uncommon, Noncoding Variants in the APOE Region With Risk of Alzheimer Disease in Adults of European Ancestry. Description: Blue, Elizabeth E, et al. Association of Uncommon, Noncoding Variants in the APOE Region With Risk of Alzheimer Disease in Adults of European Ancestry. ''JAMA Netw Open''. 2020 Oct 1; '''3''' (10):e2017666
A study of associations between CUBN, HNF1A, and LIPC gene polymorphisms and coronary artery disease. Description: Park, Han Sung, et al. A study of associations between CUBN, HNF1A, and LIPC gene polymorphisms and coronary artery disease. ''Sci Rep''. 2020 Oct 1; '''10''' (1):16294
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Description: Li, Xinyue, et al. Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. ''PLoS Genet''. 2020 Oct; '''16''' (10):e1009089
AVPR1A main effect and OXTR-by-environment interplay in individual differences in depression level. Description: Kazantseva, A, et al. AVPR1A main effect and OXTR-by-environment interplay in individual differences in depression level. ''Heliyon''. 2020 Oct; '''6''' (10):e05240
Candidate gene mapping identifies genomic variations in the fire blight susceptibility genes HIPM and DIPM across the Malus germplasm. Description: Tegtmeier, Richard, et al. Candidate gene mapping identifies genomic variations in the fire blight susceptibility genes HIPM and DIPM across the Malus germplasm. ''Sci Rep''. 2020 Oct 1; '''10''' (1):16317
Colorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibility. Description: Arnau-Collell, Coral, et al. Colorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibility. ''J Med Genet''. 2020 Oct; '''57''' (10):677-682
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Description: Bigdeli, Tim B, et al. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. ''Mol Psychiatry''. 2020 Oct; '''25''' (10):2455-2467
Effect of maternal preconceptional and pregnancy micronutrient interventions on children's DNA methylation: Findings from the EMPHASIS study. Description: Saffari, Ayden, et al. Effect of maternal preconceptional and pregnancy micronutrient interventions on children's DNA methylation: Findings from the EMPHASIS study. ''Am J Clin Nutr''. 2020 Oct 1; '''112''' (4):1099-1113
*Fine Mapping of the Major Histocompatibility Complex Region and Association of the HLA-B52:01 Allele With Cervical Cancer in Japanese Women.** Description: Masuda, Tatsuo, et al. Fine Mapping of the Major Histocompatibility Complex Region and Association of the HLA-B*52:01 Allele With Cervical Cancer in Japanese Women. ''JAMA Netw Open''. 2020 Oct 1; '''3''' (10):e2023248
Genetic Associations of Chronotype in the Finnish General Population. Description: Maukonen, Mirkka, et al. Genetic Associations of Chronotype in the Finnish General Population. ''J Biol Rhythms''. 2020 Oct; '''35''' (5):501-511
Genetic risk scores and hallucinations in patients with Parkinson disease. Description: Kusters, Cynthia D J, et al. Genetic risk scores and hallucinations in patients with Parkinson disease. ''Neurol Genet''. 2020 Oct; '''6''' (5):e492
Genome-wide insights of Ethiopian indigenous sheep populations reveal the population structure related to tail morphology and phylogeography. Description: Amane, Agraw, et al. Genome-wide insights of Ethiopian indigenous sheep populations reveal the population structure related to tail morphology and phylogeography. ''Genes Genomics''. 2020 Oct; '''42''' (10):1169-1178
Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia. Description: Tang, Man-Hung Eric, et al. Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia. ''Neurol Genet''. 2020 Oct; '''6''' (5):e508
Mendelian randomization while jointly modeling cis genetics identifies causal relationships between gene expression and lipids. Description: van der Graaf, Adriaan, et al. Mendelian randomization while jointly modeling cis genetics identifies causal relationships between gene expression and lipids. ''Nat Commun''. 2020 Oct 1; '''11''' (1):4930
Novel Mutations and Genes That Impact on Growth in Short Stature of Undefined Aetiology: The EPIGROW Study. Description: Perchard, Reena, et al. Novel Mutations and Genes That Impact on Growth in Short Stature of Undefined Aetiology: The EPIGROW Study. ''J Endocr Soc''. 2020 Oct 1; '''4''' (10):bvaa105
Parkinson's disease determinants, prediction and gene-environment interactions in the UK Biobank. Description: Jacobs, Benjamin Meir, et al. Parkinson's disease determinants, prediction and gene-environment interactions in the UK Biobank. ''J Neurol Neurosurg Psychiatry''. 2020 Oct; '''91''' (10):1046-1054
Profiles of histidine-rich glycoprotein associate with age and risk of all-cause mortality. Description: Hong, Mun-Gwan, et al. Profiles of histidine-rich glycoprotein associate with age and risk of all-cause mortality. ''Life Sci Alliance''. 2020 Oct; '''3''' (10):
Similar burden of pathogenic coding variants in exceptionally long-lived individuals and individuals without exceptional longevity. Description: Gutman, Danielle, et al. Similar burden of pathogenic coding variants in exceptionally long-lived individuals and individuals without exceptional longevity. ''Aging Cell''. 2020 Oct; '''19''' (10):e13216
The association of single nucleotide polymorphisms (SNPs) with breast density and breast cancer survival: the Malmo Diet and Cancer Study. Description: Sartor, Hanna, et al. The association of single nucleotide polymorphisms (SNPs) with breast density and breast cancer survival: the Malmo Diet and Cancer Study. ''Acta Radiol''. 2020 Oct; '''61''' (10):1326-1334
The FAM171A2 gene is a key regulator of progranulin expression and modifies the risk of multiple neurodegenerative diseases. Description: Xu, Wei, et al. The FAM171A2 gene is a key regulator of progranulin expression and modifies the risk of multiple neurodegenerative diseases. ''Sci Adv''. 2020 Oct; '''6''' (43):
Two-Sample Mendelian Randomization Study of Lipid levels and Ischemic Heart Disease. Description: Lee, Su Hyun, et al. Two-Sample Mendelian Randomization Study of Lipid levels and Ischemic Heart Disease. ''Korean Circ J''. 2020 Oct; '''50''' (10):940-948
Type 1 diabetes in Africa: an immunogenetic study in the Amhara of North-West Ethiopia. Description: Balcha, Shitaye A, et al. Type 1 diabetes in Africa: an immunogenetic study in the Amhara of North-West Ethiopia. ''Diabetologia''. 2020 Oct; '''63''' (10):2158-2168
Uncovering the complex genetics of human character. Description: Zwir, Igor, et al. Uncovering the complex genetics of human character. ''Mol Psychiatry''. 2020 Oct; '''25''' (10):2295-2312
Uncovering the complex genetics of human temperament. Description: Zwir, Igor, et al. Uncovering the complex genetics of human temperament. ''Mol Psychiatry''. 2020 Oct; '''25''' (10):2275-2294
Whole genome sequencing of Plasmodium vivax isolates reveals frequent sequence and structural polymorphisms in erythrocyte binding genes. Description: Ford, Anthony, et al. Whole genome sequencing of Plasmodium vivax isolates reveals frequent sequence and structural polymorphisms in erythrocyte binding genes. ''PLoS Negl Trop Dis''. 2020 Oct; '''14''' (10):e0008234
Wide variation in the suboptimal distribution of photosynthetic capacity in relation to light across genotypes of wheat. Description: Salter, William T, et al. Wide variation in the suboptimal distribution of photosynthetic capacity in relation to light across genotypes of wheat. ''AoB Plants''. 2020 Oct; '''12''' (5):plaa039
Accuracies of Genomic Prediction for Growth Traits at Weaning and Yearling Ages in Yak. Description: Ge, Fei, et al. Accuracies of Genomic Prediction for Growth Traits at Weaning and Yearling Ages in Yak. ''Animals (Basel)''. 2020 Oct 2; '''10''' (10):
Detection of Selection Signatures Underlying Production and Adaptive Traits Based on Whole-Genome Sequencing of Six Donkey Populations. Description: Zhou, Zihui, et al. Detection of Selection Signatures Underlying Production and Adaptive Traits Based on Whole-Genome Sequencing of Six Donkey Populations. ''Animals (Basel)''. 2020 Oct 7; '''10''' (10):
The impact of training on data from genetically-related lines on the accuracy of genomic predictions for feed efficiency traits in pigs. Description: Aliakbari, Amir, et al. The impact of training on data from genetically-related lines on the accuracy of genomic predictions for feed efficiency traits in pigs. ''Genet Sel Evol''. 2020 Oct 7; '''52''' (1):57
Bacterial genome-wide association study of hyper-virulent pneumococcal serotype 1 identifies genetic variation associated with neurotropism. Description: Chaguza, Chrispin, et al. Bacterial genome-wide association study of hyper-virulent pneumococcal serotype 1 identifies genetic variation associated with neurotropism. ''Commun Biol''. 2020 Oct 8; '''3''' (1):559
Origin and adaptation to high altitude of Tibetan semi-wild wheat. Description: Guo, Weilong, et al. Origin and adaptation to high altitude of Tibetan semi-wild wheat. ''Nat Commun''. 2020 Oct 8; '''11''' (1):5085
The interplay between host genetics and the gut microbiome reveals common and distinct microbiome features for complex human diseases. Description: Xu, Fengzhe, et al. The interplay between host genetics and the gut microbiome reveals common and distinct microbiome features for complex human diseases. ''Microbiome''. 2020 Oct 8; '''8''' (1):145
Genetic variants in MIR17HG affect the susceptibility and prognosis of glioma in a Chinese Han population. Description: Feng, Jigao, et al. Genetic variants in MIR17HG affect the susceptibility and prognosis of glioma in a Chinese Han population. ''BMC Cancer''. 2020 Oct 9; '''20''' (1):976
Genome-wide analysis of expression QTL (eQTL) and allele-specific expression (ASE) in pig muscle identifies candidate genes for meat quality traits. Description: Liu, Yan, et al. Genome-wide analysis of expression QTL (eQTL) and allele-specific expression (ASE) in pig muscle identifies candidate genes for meat quality traits. ''Genet Sel Evol''. 2020 Oct 9; '''52''' (1):59
Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk. Description: Sieh, Weiva, et al. Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk. ''Nat Commun''. 2020 Oct 9; '''11''' (1):5116
Integrative genomic analysis reveals mechanisms of immune evasion in P. falciparum malaria. Description: Dieng, Mame Massar, et al. Integrative genomic analysis reveals mechanisms of immune evasion in P. falciparum malaria. ''Nat Commun''. 2020 Oct 9; '''11''' (1):5093
Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans. Description: Nakatsuka, Nathan, et al. Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans. ''Sci Rep''. 2020 Oct 9; '''10''' (1):16902
Bayesian Analysis of the Association between Casein Complex Haplotype Variants and Milk Yield, Composition, and Curve Shape Parameters in Murciano-Granadina Goats. Description: Inostroza, Maria Gabriela Pizarro, et al. Bayesian Analysis of the Association between Casein Complex Haplotype Variants and Milk Yield, Composition, and Curve Shape Parameters in Murciano-Granadina Goats. ''Animals (Basel)''. 2020 Oct 10; '''10''' (10):
Multiplex melanoma families are enriched for polygenic risk. Description: Law, Matthew H, et al. Multiplex melanoma families are enriched for polygenic risk. ''Hum Mol Genet''. 2020 Oct 10; '''29''' (17):2976-2985
Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions. Description: Sieberts, Solveig K, et al. Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions. ''Sci Data''. 2020 Oct 12; '''7''' (1):340
The influence of CYP1A1 and CYP1A2 polymorphisms on stroke risk in the Chinese population. Description: Mao, Yan, et al. The influence of CYP1A1 and CYP1A2 polymorphisms on stroke risk in the Chinese population. ''Lipids Health Dis''. 2020 Oct 12; '''19''' (1):221
Integrative genomics analysis identifies promising SNPs and genes implicated in tuberculosis risk based on multiple omics datasets. Description: Xu, Mengqiu, et al. Integrative genomics analysis identifies promising SNPs and genes implicated in tuberculosis risk based on multiple omics datasets. ''Aging (Albany NY)''. 2020 Oct 13; '''12''' (19):19173-19220
Population structure and pharmacogenomic risk stratification in the United States. Description: Nagar, Shashwat Deepali, et al. Population structure and pharmacogenomic risk stratification in the United States. ''BMC Biol''. 2020 Oct 13; '''18''' (1):140
Whole genome sequencing data of multiple individuals of Pakistani descent. Description: Khan, Shahid Y, et al. Whole genome sequencing data of multiple individuals of Pakistani descent. ''Sci Data''. 2020 Oct 13; '''7''' (1):350
Genomic diversity and population structure of the Leonberger dog breed. Description: Letko, Anna, et al. Genomic diversity and population structure of the Leonberger dog breed. ''Genet Sel Evol''. 2020 Oct 14; '''52''' (1):61
The Variant rs1784042 of the SIDT2 Gene is Associated with Metabolic Syndrome through Low HDL-c Levels in a Mexican Population. Description: Leon-Reyes, Guadalupe, et al. The Variant rs1784042 of the SIDT2 Gene is Associated with Metabolic Syndrome through Low HDL-c Levels in a Mexican Population. ''Genes (Basel)''. 2020 Oct 14; '''11''' (10):
Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjects. Description: Turpin, Williams, et al. Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjects. ''BMC Med Genet''. 2020 Oct 15; '''21''' (1):204
Genetic Variability in Local and Imported Germplasm Chicken Populations as Revealed by Analyzing Runs of Homozygosity. Description: Dementieva, Natalia V, et al. Genetic Variability in Local and Imported Germplasm Chicken Populations as Revealed by Analyzing Runs of Homozygosity. ''Animals (Basel)''. 2020 Oct 15; '''10''' (10):
Little evidence for associations between the Big Five personality traits and variability in brain gray or white matter. Description: Avinun, Reut, et al. Little evidence for associations between the Big Five personality traits and variability in brain gray or white matter. ''Neuroimage''. 2020 Oct 15; '''220''': 117092
Pleiotropic ZIP8 A391T implicates abnormal manganese homeostasis in complex human disease. Description: Sunuwar, Laxmi, et al. Pleiotropic ZIP8 A391T implicates abnormal manganese homeostasis in complex human disease. ''JCI Insight''. 2020 Oct 15; '''5''' (20):
The association of genetic polymorphisms with nonalcoholic fatty liver disease in a longitudinal study. Description: Chung, Goh Eun, et al. The association of genetic polymorphisms with nonalcoholic fatty liver disease in a longitudinal study. ''BMC Gastroenterol''. 2020 Oct 15; '''20''' (1):344
SLC19A3 Loss-of-Function Variant in Yorkshire Terriers with Leigh-Like Subacute Necrotizing Encephalopathy. Description: Drogemuller, Michaela, et al. SLC19A3 Loss-of-Function Variant in Yorkshire Terriers with Leigh-Like Subacute Necrotizing Encephalopathy. ''Genes (Basel)''. 2020 Oct 16; '''11''' (10):
A Genomic Study of Myxomatous Mitral Valve Disease in Cavalier King Charles Spaniels. Description: Bionda, Arianna, et al. A Genomic Study of Myxomatous Mitral Valve Disease in Cavalier King Charles Spaniels. ''Animals (Basel)''. 2020 Oct 16; '''10''' (10):
Integrated genomics analysis highlights important SNPs and genes implicated in moderate-to-severe asthma based on GWAS and eQTL datasets. Description: Dong, Zhouzhou, et al. Integrated genomics analysis highlights important SNPs and genes implicated in moderate-to-severe asthma based on GWAS and eQTL datasets. ''BMC Pulm Med''. 2020 Oct 16; '''20''' (1):270
Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity. Description: Newell, Felicity, et al. Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity. ''Nat Commun''. 2020 Oct 16; '''11''' (1):5259
Intensified Use of Reproductive Technologies and Reduced Dimensions of Breeding Schemes Put Genetic Diversity at Risk in Dairy Cattle Breeds. Description: Doublet, Anna-Charlotte, et al. Intensified Use of Reproductive Technologies and Reduced Dimensions of Breeding Schemes Put Genetic Diversity at Risk in Dairy Cattle Breeds. ''Animals (Basel)''. 2020 Oct 17; '''10''' (10):
Landscape Genomics of a Widely Distributed Snake, Dolichophis caspius (Gmelin, 1789) across Eastern Europe and Western Asia. Description: Mahtani-Williams, Sarita, et al. Landscape Genomics of a Widely Distributed Snake, Dolichophis caspius (Gmelin, 1789) across Eastern Europe and Western Asia. ''Genes (Basel)''. 2020 Oct 17; '''11''' (10):
A Genome-Wide Association Study Identifies the Association between the 12q24 Locus and Black Tea Consumption in Japanese Populations. Description: Furukawa, Kyohei, et al. A Genome-Wide Association Study Identifies the Association between the 12q24 Locus and Black Tea Consumption in Japanese Populations. ''Nutrients''. 2020 Oct 18; '''12''' (10):
Natural variation in Arabidopsis thaliana rosette area unveils new genes involved in plant development. Description: Gonzalez, Ruben, et al. Natural variation in Arabidopsis thaliana rosette area unveils new genes involved in plant development. ''Sci Rep''. 2020 Oct 19; '''10''' (1):17600
Genetic determinism of spontaneous masculinisation in XX female rainbow trout: new insights using medium throughput genotyping and whole-genome sequencing. Description: Fraslin, Clemence, et al. Genetic determinism of spontaneous masculinisation in XX female rainbow trout: new insights using medium throughput genotyping and whole-genome sequencing. ''Sci Rep''. 2020 Oct 19; '''10''' (1):17693
The Candidate Genes Underlying a Stably Expressed QTL for Low Temperature Germinability in Rice (Oryza sativa L.). Description: Yang, Tifeng, et al. The Candidate Genes Underlying a Stably Expressed QTL for Low Temperature Germinability in Rice (Oryza sativa L.). ''Rice (N Y)''. 2020 Oct 19; '''13''' (1):74
Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals. Description: Xu, Ke, et al. Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals. ''Nat Commun''. 2020 Oct 20; '''11''' (1):5302
Epistatic evidence for gender-dependant slow neurotransmission signalling in substance use disorders: PPP1R12B versus PPP1R1B. Description: Liu, Kefu, et al. Epistatic evidence for gender-dependant slow neurotransmission signalling in substance use disorders: PPP1R12B versus PPP1R1B. ''EBioMedicine''. 2020 Oct 21; '''61''': 103066
Expression Quantitative Trait Locus Mapping in Pulmonary Arterial Hypertension. Description: Ulrich, Anna, et al. Expression Quantitative Trait Locus Mapping in Pulmonary Arterial Hypertension. ''Genes (Basel)''. 2020 Oct 22; '''11''' (11):
Genetic Variants Associated with Non-Alcoholic Fatty Liver Disease Do Not Associate with Measures of Sub-Clinical Atherosclerosis: Results from the IMPROVE Study. Description: Castaldo, Luigi, et al. Genetic Variants Associated with Non-Alcoholic Fatty Liver Disease Do Not Associate with Measures of Sub-Clinical Atherosclerosis: Results from the IMPROVE Study. ''Genes (Basel)''. 2020 Oct 22; '''11''' (11):
Analyzing a putative enhancer of optic disc morphology. Description: Babenko, Vladimir, et al. Analyzing a putative enhancer of optic disc morphology. ''BMC Genet''. 2020 Oct 22; '''21''' (Suppl 1):73
Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy. Description: Strickland, Samantha L, et al. Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy. ''Acta Neuropathol Commun''. 2020 Oct 22; '''8''' (1):172
CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption. Description: Chen, I-Chun, et al. CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption. ''Sci Rep''. 2020 Oct 22; '''10''' (1):18118
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Description: Trevino, Cristina E, et al. Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. ''Sci Rep''. 2020 Oct 22; '''10''' (1):18051
Positive selection in admixed populations from Ethiopia. Description: Walsh, Sandra, et al. Positive selection in admixed populations from Ethiopia. ''BMC Genet''. 2020 Oct 22; '''21''' (Suppl 1):108
The story of the lost twins: decoding the genetic identities of the Kumhar and Kurcha populations from the Indian subcontinent. Description: Das, Ranajit, et al. The story of the lost twins: decoding the genetic identities of the Kumhar and Kurcha populations from the Indian subcontinent. ''BMC Genet''. 2020 Oct 22; '''21''' (Suppl 1):117
Autoantibodies against type I IFNs in patients with life-threatening COVID-19. Description: Bastard, Paul, et al. Autoantibodies against type I IFNs in patients with life-threatening COVID-19. ''Science''. 2020 Oct 23; '''370''' (6515):
Genomic Characterization of a Set of Iberian Peninsula Bovine Local Breeds at Risk of Extinction: Morenas Gallegas. Description: Garcia-Atance, Maria Asuncion, et al. Genomic Characterization of a Set of Iberian Peninsula Bovine Local Breeds at Risk of Extinction: Morenas Gallegas. ''Animals (Basel)''. 2020 Oct 23; '''10''' (11):
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19. Description: Zhang, Qian, et al. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19. ''Science''. 2020 Oct 23; '''370''' (6515):
The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study. Description: Pei, Yu-Fang, et al. The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study. ''Commun Biol''. 2020 Oct 23; '''3''' (1):608
Association of an APBA3 Missense Variant with Risk of Premature Ovarian Failure in the Korean Female Population. Description: Park, JeongMan, et al. Association of an APBA3 Missense Variant with Risk of Premature Ovarian Failure in the Korean Female Population. ''J Pers Med''. 2020 Oct 26; '''10''' (4):
Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort. Description: Moen, Gunn-Helen, et al. Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort. ''Nat Commun''. 2020 Oct 26; '''11''' (1):5404
Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake. Description: Jee, Donghyun, et al. Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake. ''Nutrients''. 2020 Oct 26; '''12''' (11):
A large deletion on CFA28 omitting ACSL5 gene is associated with intestinal lipid malabsorption in the Australian Kelpie dog breed. Description: O'Brien, Mitchell J, et al. A large deletion on CFA28 omitting ACSL5 gene is associated with intestinal lipid malabsorption in the Australian Kelpie dog breed. ''Sci Rep''. 2020 Oct 26; '''10''' (1):18223
Genomic evidence for recurrent genetic admixture during the domestication of Mediterranean olive trees (Olea europaea L.). Description: Julca, Irene, et al. Genomic evidence for recurrent genetic admixture during the domestication of Mediterranean olive trees (Olea europaea L.). ''BMC Biol''. 2020 Oct 26; '''18''' (1):148
Modeling of variables in cellular infection reveals CXCL10 levels are regulated by human genetic variation and the Chlamydia-encoded CPAF protease. Description: Schott, Benjamin H, et al. Modeling of variables in cellular infection reveals CXCL10 levels are regulated by human genetic variation and the Chlamydia-encoded CPAF protease. ''Sci Rep''. 2020 Oct 26; '''10''' (1):18269
Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics. Description: Iacoangeli, Alfredo, et al. Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics. ''Cell Rep''. 2020 Oct 27; '''33''' (4):108323
Identification of novel susceptibility loci for non-syndromic cleft lip with or without cleft palate. Description: Ma, Lan, et al. Identification of novel susceptibility loci for non-syndromic cleft lip with or without cleft palate. ''J Cell Mol Med''. 2020 Oct 27;
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Description: Klarin, Derek, et al. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. ''Circulation''. 2020 Oct 27; '''142''' (17):1633-1646
Genetic polymorphisms of PGF and TNFAIP2 genes related to cervical cancer risk among Uygur females from China. Description: Ainiwaer, Zumurelaiti, et al. Genetic polymorphisms of PGF and TNFAIP2 genes related to cervical cancer risk among Uygur females from China. ''BMC Med Genet''. 2020 Oct 27; '''21''' (1):212
Genome-wide association studies and whole-genome prediction reveal the genetic architecture of KRN in maize. Description: An, Yixin, et al. Genome-wide association studies and whole-genome prediction reveal the genetic architecture of KRN in maize. ''BMC Plant Biol''. 2020 Oct 27; '''20''' (1):490
The landscape of host genetic factors involved in immune response to common viral infections. Description: Kachuri, Linda, et al. The landscape of host genetic factors involved in immune response to common viral infections. ''Genome Med''. 2020 Oct 27; '''12''' (1):93
Comparative Genome Sequence Analyses of Geographic Samples of Aspergillus fumigatus-Relevance for Amphotericin B Resistance. Description: Fan, Yuying, et al. Comparative Genome Sequence Analyses of Geographic Samples of Aspergillus fumigatus-Relevance for Amphotericin B Resistance. ''Microorganisms''. 2020 Oct 28; '''8''' (11):
Genomic Diversity in Sporadic Breast Cancer in a Latin American Population. Description: Brignoni, Lucia, et al. Genomic Diversity in Sporadic Breast Cancer in a Latin American Population. ''Genes (Basel)''. 2020 Oct 28; '''11''' (11):
Genotype by environment interaction for gene expression in Drosophila melanogaster. Description: Huang, Wen, et al. Genotype by environment interaction for gene expression in Drosophila melanogaster. ''Nat Commun''. 2020 Oct 28; '''11''' (1):5451
Recurrent evolution of high virulence in isolated populations of a DNA virus. Description: Hill, Tom, et al. Recurrent evolution of high virulence in isolated populations of a DNA virus. ''Elife''. 2020 Oct 28; '''9''':
Genetic architecture of cardiometabolic risks in people living with HIV. Description: Chang, Haoxiang, et al. Genetic architecture of cardiometabolic risks in people living with HIV. ''BMC Med''. 2020 Oct 28; '''18''' (1):288
Genetic parameters and associated genomic regions for global immunocompetence and other health-related traits in pigs. Description: Ballester, Maria, et al. Genetic parameters and associated genomic regions for global immunocompetence and other health-related traits in pigs. ''Sci Rep''. 2020 Oct 28; '''10''' (1):18462
Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma. Description: Zhang, Chenan, et al. Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma. ''Acta Neuropathol Commun''. 2020 Oct 28; '''8''' (1):173
Inbreeding depression across the genome of Dutch Holstein Friesian dairy cattle. Description: Doekes, Harmen P, et al. Inbreeding depression across the genome of Dutch Holstein Friesian dairy cattle. ''Genet Sel Evol''. 2020 Oct 28; '''52''' (1):64
Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations. Description: Cismaru, Anca Liliana, et al. Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations. ''Genes (Basel)''. 2020 Oct 29; '''11''' (11):
Polymorphisms in Processing and Antigen Presentation-Related Genes and Their Association with Host Susceptibility to Influenza A/H1N1 2009 Pandemic in a Mexican Mestizo Population. Description: Ponce-Gallegos, Marco Antonio, et al. Polymorphisms in Processing and Antigen Presentation-Related Genes and Their Association with Host Susceptibility to Influenza A/H1N1 2009 Pandemic in a Mexican Mestizo Population. ''Viruses''. 2020 Oct 29; '''12''' (11):
Diet Quality and Food Prices Modify Associations between Genetic Susceptibility to Obesity and Adiposity Outcomes. Description: Han, Hannah Yang, et al. Diet Quality and Food Prices Modify Associations between Genetic Susceptibility to Obesity and Adiposity Outcomes. ''Nutrients''. 2020 Oct 30; '''12''' (11):
A new efficient method to detect genetic interactions for lung cancer GWAS. Description: Luyapan, Jennifer, et al. A new efficient method to detect genetic interactions for lung cancer GWAS. ''BMC Med Genomics''. 2020 Oct 30; '''13''' (1):162
Genome-wide genotyping elucidates the geographical diversification and dispersal of the polyploid and clonally propagated yam (Dioscorea alata). Description: Sharif, Bilal Muhammad, et al. Genome-wide genotyping elucidates the geographical diversification and dispersal of the polyploid and clonally propagated yam (Dioscorea alata). ''Ann Bot''. 2020 Oct 30; '''126''' (6):1029-1038
Genome-Wide Association Studies Reveal Susceptibility Loci for Digital Dermatitis in Holstein Cattle. Description: Lai, Ellen, et al. Genome-Wide Association Studies Reveal Susceptibility Loci for Digital Dermatitis in Holstein Cattle. ''Animals (Basel)''. 2020 Oct 31; '''10''' (11):
A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population. Description: Tcheandjieu, Catherine, et al. A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population. ''PLoS Genet''. 2020 Nov; '''16''' (11):e1008802
A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis. Description: Zhou, Dan, et al. A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis. ''Nat Genet''. 2020 Nov; '''52''' (11):1239-1246
Body mass index and risk of dying from a bloodstream infection: A Mendelian randomization study. Description: Rogne, Tormod, et al. Body mass index and risk of dying from a bloodstream infection: A Mendelian randomization study. ''PLoS Med''. 2020 Nov; '''17''' (11):e1003413
Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms. Description: Howe, Laurence J, et al. Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms. ''Genet Epidemiol''. 2020 Nov; '''44''' (8):924-933
Genetic factors for susceptibility to and manifestations of neuromyelitis optica. Description: Matsushita, Takuya, et al. Genetic factors for susceptibility to and manifestations of neuromyelitis optica. ''Ann Clin Transl Neurol''. 2020 Nov; '''7''' (11):2082-2093
Genetic variation in CARD8, a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 diabetes mellitus. Description: Tsetsos, Fotis, et al. Genetic variation in CARD8, a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 diabetes mellitus. ''Diab Vasc Dis Res''. 2020 Nov-Dec; '''17''' (6):1479164120970892
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. Description: Wang, Yunpeng, et al. Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. ''PLoS Genet''. 2020 Nov; '''16''' (11):e1009163
Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium. Description: Verma, Shefali Setia, et al. Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium. ''Clin Pharmacol Ther''. 2020 Nov; '''108''' (5):1067-1077
Genomic Characterization of the Istrian Shorthaired Hound. Description: Djurkin Kusec, Ivona, et al. Genomic Characterization of the Istrian Shorthaired Hound. ''Animals (Basel)''. 2020 Nov 1; '''10''' (11):
LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks. Description: Goldstein, Jeffery A, et al. LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks. ''PLoS Genet''. 2020 Nov; '''16''' (11):e1009077
Mimicry and mitonuclear discordance in nudibranchs: New insights from exon capture phylogenomics. Description: Layton, Kara K S, et al. Mimicry and mitonuclear discordance in nudibranchs: New insights from exon capture phylogenomics. ''Ecol Evol''. 2020 Nov; '''10''' (21):11966-11982
Natural variation in the sequestosome-related gene, sqst-5, underlies zinc homeostasis in Caenorhabditis elegans. Description: Evans, Kathryn S, et al. Natural variation in the sequestosome-related gene, sqst-5, underlies zinc homeostasis in Caenorhabditis elegans. ''PLoS Genet''. 2020 Nov; '''16''' (11):e1008986
Pharmacogenetics of TNF inhibitor response in rheumatoid arthritis utilizing the two-component disease activity score. Description: Gilani, Syed Sa, et al. Pharmacogenetics of TNF inhibitor response in rheumatoid arthritis utilizing the two-component disease activity score. ''Pharmacogenomics''. 2020 Nov; '''21''' (16):1151-1156
PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records. Description: Zheng, Neil S, et al. PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records. ''J Am Med Inform Assoc''. 2020 Nov 1; '''27''' (11):1675-1687
Pregnancy does not modify the risk of MS in genetically susceptible women. Description: Adams, Cameron J, et al. Pregnancy does not modify the risk of MS in genetically susceptible women. ''Neurol Neuroimmunol Neuroinflamm''. 2020 Nov; '''7''' (6):
Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution. Description: Maggiolini, Flavia Angela Maria, et al. Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution. ''Genome Res''. 2020 Nov; '''30''' (11):1680-1693
The Parkinson's Disease Genome-Wide Association Study Locus Browser. Description: Grenn, Francis P, et al. The Parkinson's Disease Genome-Wide Association Study Locus Browser. ''Mov Disord''. 2020 Nov; '''35''' (11):2056-2067
Variants c.677 C>T, c.1298 A>C in MTHFR, and c.66 A>G in MTRR Affect the Occurrence of Recurrent Pregnancy Loss in Chinese Women. Description: Zhang, Yan, et al. Variants c.677 C>T, c.1298 A>C in MTHFR, and c.66 A>G in MTRR Affect the Occurrence of Recurrent Pregnancy Loss in Chinese Women. ''Genet Test Mol Biomarkers''. 2020 Nov; '''24''' (11):717-722
Effect of BDNF Val66Met on hippocampal subfields volumes and compensatory interaction with APOE-epsilon4 in middle-age cognitively unimpaired individuals from the ALFA study. Description: Vilor-Tejedor, Natalia, et al. Effect of BDNF Val66Met on hippocampal subfields volumes and compensatory interaction with APOE-epsilon4 in middle-age cognitively unimpaired individuals from the ALFA study. ''Brain Struct Funct''. 2020 Nov; '''225''' (8):2331-2345
Large-Scale Analyses Provide No Evidence for Gene-Gene Interactions Influencing Type 2 Diabetes Risk. Description: Nag, Abhishek, et al. Large-Scale Analyses Provide No Evidence for Gene-Gene Interactions Influencing Type 2 Diabetes Risk. ''Diabetes''. 2020 Nov; '''69''' (11):2518-2522
SFTPC genetic polymorphisms are associated with tuberculosis susceptibility and clinical phenotype in a Western Chinese Han population. Description: Zhao, Jun-Wei, et al. SFTPC genetic polymorphisms are associated with tuberculosis susceptibility and clinical phenotype in a Western Chinese Han population. ''Exp Ther Med''. 2020 Nov; '''20''' (5):100
Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans. Description: Chang, Xiao, et al. Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans. ''Transl Psychiatry''. 2020 Nov 2; '''10''' (1):370
An Improved Oil Palm Genome Assembly as a Valuable Resource for Crop Improvement and Comparative Genomics in the Arecoideae Subfamily. Description: Ong, Ai-Ling, et al. An Improved Oil Palm Genome Assembly as a Valuable Resource for Crop Improvement and Comparative Genomics in the Arecoideae Subfamily. ''Plants (Basel)''. 2020 Nov 3; '''9''' (11):
Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Mullerian hormone levels in women. Description: Verdiesen, Renee Mg, et al. Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Mullerian hormone levels in women. ''medRxiv''. 2020 Nov 3;
Multi-ancestry genetic study in 5,876 patients identifies an association between excitotoxic genes and early outcomes after acute ischemic stroke. Description: Ibanez, Laura, et al. Multi-ancestry genetic study in 5,876 patients identifies an association between excitotoxic genes and early outcomes after acute ischemic stroke. ''medRxiv''. 2020 Nov 3;
Multiple waves of freshwater colonization of the three-spined stickleback in the Japanese Archipelago. Description: Kakioka, Ryo, et al. Multiple waves of freshwater colonization of the three-spined stickleback in the Japanese Archipelago. ''BMC Evol Biol''. 2020 Nov 3; '''20''' (1):143
Phenotype prediction and characterization of 25 pharmacogenes in Thais from whole genome sequencing for clinical implementation. Description: Mauleekoonphairoj, John, et al. Phenotype prediction and characterization of 25 pharmacogenes in Thais from whole genome sequencing for clinical implementation. ''Sci Rep''. 2020 Nov 3; '''10''' (1):18969
Genetics and geography of leukocyte telomere length in sub-Saharan Africans. Description: Hunt, Steven C, et al. Genetics and geography of leukocyte telomere length in sub-Saharan Africans. ''Hum Mol Genet''. 2020 Nov 4; '''29''' (18):3014-3020
Genome wide association study of passive immunity and disease traits in beef-suckler and dairy calves on Irish farms. Description: Johnston, Dayle, et al. Genome wide association study of passive immunity and disease traits in beef-suckler and dairy calves on Irish farms. ''Sci Rep''. 2020 Nov 4; '''10''' (1):18998
Metabolite signatures of diverse Camellia sinensis tea populations. Description: Yu, Xiaomin, et al. Metabolite signatures of diverse Camellia sinensis tea populations. ''Nat Commun''. 2020 Nov 4; '''11''' (1):5586
The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor. Description: Brandao, Andreia, et al. The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor. ''Cancers (Basel)''. 2020 Nov 4; '''12''' (11):
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Description: Andlauer, Till F M, et al. Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. ''BMC Med''. 2020 Nov 4; '''18''' (1):298
Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. Description: Fritsche, Lars G, et al. Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. ''Am J Hum Genet''. 2020 Nov 5; '''107''' (5):815-836
Clustering of Alzheimer's and Parkinson's disease based on genetic burden of shared molecular mechanisms. Description: Emon, Mohammad Asif, et al. Clustering of Alzheimer's and Parkinson's disease based on genetic burden of shared molecular mechanisms. ''Sci Rep''. 2020 Nov 5; '''10''' (1):19097
Genetic and non-genetic factors associated with the phenotype of exceptional longevity & normal cognition. Description: Han, Bin, et al. Genetic and non-genetic factors associated with the phenotype of exceptional longevity & normal cognition. ''Sci Rep''. 2020 Nov 5; '''10''' (1):19140
Genetic profiling of Vietnamese population from large-scale genomic analysis of non-invasive prenatal testing data. Description: Tran, Ngoc Hieu, et al. Genetic profiling of Vietnamese population from large-scale genomic analysis of non-invasive prenatal testing data. ''Sci Rep''. 2020 Nov 5; '''10''' (1):19142
Genomic Prediction Informed by Biological Processes Expands Our Understanding of the Genetic Architecture Underlying Free Amino Acid Traits in Dry Arabidopsis Seeds. Description: Turner-Hissong, Sarah D, et al. Genomic Prediction Informed by Biological Processes Expands Our Understanding of the Genetic Architecture Underlying Free Amino Acid Traits in Dry Arabidopsis Seeds. ''G3 (Bethesda)''. 2020 Nov 5; '''10''' (11):4227-4239
GWAS-Based Identification of New Loci for Milk Yield, Fat, and Protein in Holstein Cattle. Description: Liu, Liyuan, et al. GWAS-Based Identification of New Loci for Milk Yield, Fat, and Protein in Holstein Cattle. ''Animals (Basel)''. 2020 Nov 5; '''10''' (11):
Identification of Genetic Susceptibility Factors Associated with Canine Gastric Dilatation-Volvulus. Description: Piras, Ignazio S, et al. Identification of Genetic Susceptibility Factors Associated with Canine Gastric Dilatation-Volvulus. ''Genes (Basel)''. 2020 Nov 5; '''11''' (11):
Mapping the genetic basis of diabetes mellitus in the Australian Burmese cat (Felis catus). Description: Samaha, Georgina, et al. Mapping the genetic basis of diabetes mellitus in the Australian Burmese cat (Felis catus). ''Sci Rep''. 2020 Nov 5; '''10''' (1):19194
Polygenic Scores for Height in Admixed Populations. Description: Bitarello, Barbara D, et al. Polygenic Scores for Height in Admixed Populations. ''G3 (Bethesda)''. 2020 Nov 5; '''10''' (11):4027-4036
Translational study of the whole transcriptome in rats and genetic polymorphisms in humans identifies LRP1B and VPS13A as key genes involved in tolerance to cocaine-induced motor disturbances. Description: Vorspan, Florence, et al. Translational study of the whole transcriptome in rats and genetic polymorphisms in humans identifies LRP1B and VPS13A as key genes involved in tolerance to cocaine-induced motor disturbances. ''Transl Psychiatry''. 2020 Nov 6; '''10''' (1):381
Detecting potential causal relationship between multiple risk factors and Alzheimer's disease using multivariable Mendelian randomization. Description: Zhang, Qiang, et al. Detecting potential causal relationship between multiple risk factors and Alzheimer's disease using multivariable Mendelian randomization. ''Aging (Albany NY)''. 2020 Nov 7; '''12''' (21):21747-21757
Genome Wide Epistasis Study of On-Statin Cardiovascular Events with Iterative Feature Reduction and Selection. Description: Adams, Solomon M, et al. Genome Wide Epistasis Study of On-Statin Cardiovascular Events with Iterative Feature Reduction and Selection. ''J Pers Med''. 2020 Nov 7; '''10''' (4):
Identification of Candidate Genes and Pathways Associated with Obesity-Related Traits in Canines via Gene-Set Enrichment and Pathway-Based GWAS Analysis. Description: Sheet, Sunirmal, et al. Identification of Candidate Genes and Pathways Associated with Obesity-Related Traits in Canines via Gene-Set Enrichment and Pathway-Based GWAS Analysis. ''Animals (Basel)''. 2020 Nov 9; '''10''' (11):
Identification of candidate genetic variants and altered protein expression in neural stem and mature neural cells support altered microtubule function to be an essential component in bipolar disorder. Description: Truve, Katarina, et al. Identification of candidate genetic variants and altered protein expression in neural stem and mature neural cells support altered microtubule function to be an essential component in bipolar disorder. ''Transl Psychiatry''. 2020 Nov 9; '''10''' (1):390
Trans-Ancestral Fine-Mapping and Epigenetic Annotation as Tools to Delineate Functionally Relevant Risk Alleles at IKZF1 and IKZF3 in Systemic Lupus Erythematosus. Description: Vyse, Timothy J, et al. Trans-Ancestral Fine-Mapping and Epigenetic Annotation as Tools to Delineate Functionally Relevant Risk Alleles at IKZF1 and IKZF3 in Systemic Lupus Erythematosus. ''Int J Mol Sci''. 2020 Nov 9; '''21''' (21):
Ancient genomes reveal tropical bovid species in the Tibetan Plateau contributed to the prevalence of hunting game until the late Neolithic. Description: Chen, Ningbo, et al. Ancient genomes reveal tropical bovid species in the Tibetan Plateau contributed to the prevalence of hunting game until the late Neolithic. ''Proc Natl Acad Sci U S A''. 2020 Nov 10; '''117''' (45):28150-28159
Exploring the Role of Contactins across Psychological, Psychiatric and Cardiometabolic Traits within UK Biobank. Description: Morris, Julia, et al. Exploring the Role of Contactins across Psychological, Psychiatric and Cardiometabolic Traits within UK Biobank. ''Genes (Basel)''. 2020 Nov 10; '''11''' (11):
GWAS unveils features between early- and late-flowering pearl millets. Description: Diack, Oumar, et al. GWAS unveils features between early- and late-flowering pearl millets. ''BMC Genomics''. 2020 Nov 10; '''21''' (1):777
Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study. Description: Kendall, Kimberley M, et al. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study. ''BJPsych Open''. 2020 Nov 10; '''6''' (6):e139
Investigating the accuracy of imputing autosomal variants in Nellore cattle using the ARS-UCD1.2 assembly of the bovine genome. Description: Hermisdorff, Isis da Costa, et al. Investigating the accuracy of imputing autosomal variants in Nellore cattle using the ARS-UCD1.2 assembly of the bovine genome. ''BMC Genomics''. 2020 Nov 10; '''21''' (1):772
Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles. Description: Herrera-Rivero, Marisol, et al. Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles. ''BMC Dermatol''. 2020 Nov 10; '''20''' (1):16
Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer's disease created by integrative analysis of multi-omics data. Description: Shigemizu, Daichi, et al. Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer's disease created by integrative analysis of multi-omics data. ''Alzheimers Res Ther''. 2020 Nov 10; '''12''' (1):145
Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies. Description: Salmaninejad, Arash, et al. Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies. ''Sci Rep''. 2020 Nov 10; '''10''' (1):19413
A 50-kb deletion disrupting the RSPO2 gene is associated with tetradysmelia in Holstein Friesian cattle. Description: Becker, Doreen, et al. A 50-kb deletion disrupting the RSPO2 gene is associated with tetradysmelia in Holstein Friesian cattle. ''Genet Sel Evol''. 2020 Nov 11; '''52''' (1):68
A multi-breed GWAS for morphometric traits in four Beninese indigenous cattle breeds reveals loci associated with conformation, carcass and adaptive traits. Description: Vanvanhossou, Seyi Fridaius Ulrich, et al. A multi-breed GWAS for morphometric traits in four Beninese indigenous cattle breeds reveals loci associated with conformation, carcass and adaptive traits. ''BMC Genomics''. 2020 Nov 11; '''21''' (1):783
A SINE-VNTR-Alu in the LRIG2 Promoter Is Associated with Gene Expression at the Locus. Description: Hall, Ashley, et al. A SINE-VNTR-Alu in the LRIG2 Promoter Is Associated with Gene Expression at the Locus. ''Int J Mol Sci''. 2020 Nov 11; '''21''' (22):
Impact of Single-Nucleotide Polymorphisms of CTLA-4, CD80 and CD86 on the Effectiveness of Abatacept in Patients with Rheumatoid Arthritis. Description: Marquez Pete, Noelia, et al. Impact of Single-Nucleotide Polymorphisms of CTLA-4, CD80 and CD86 on the Effectiveness of Abatacept in Patients with Rheumatoid Arthritis. ''J Pers Med''. 2020 Nov 11; '''10''' (4):
Novel Genomic Regions Associated with Intramuscular Fatty Acid Composition in Rabbits. Description: Laghouaouta, Houda, et al. Novel Genomic Regions Associated with Intramuscular Fatty Acid Composition in Rabbits. ''Animals (Basel)''. 2020 Nov 11; '''10''' (11):
Key role for lipids in cognitive symptoms of schizophrenia. Description: Maas, Dorien A, et al. Key role for lipids in cognitive symptoms of schizophrenia. ''Transl Psychiatry''. 2020 Nov 12; '''10''' (1):399
Autozygosity influences cardiometabolic disease-associated traits in the AWI-Gen sub-Saharan African study. Description: Ceballos, Francisco C, et al. Autozygosity influences cardiometabolic disease-associated traits in the AWI-Gen sub-Saharan African study. ''Nat Commun''. 2020 Nov 13; '''11''' (1):5754
European landrace diversity for common bean biofortification: a genome-wide association study. Description: Caproni, Leonardo, et al. European landrace diversity for common bean biofortification: a genome-wide association study. ''Sci Rep''. 2020 Nov 13; '''10''' (1):19775
Frequency and methylation status of selected retrotransposition competent L1 loci in amyotrophic lateral sclerosis. Description: Savage, Abigail L, et al. Frequency and methylation status of selected retrotransposition competent L1 loci in amyotrophic lateral sclerosis. ''Mol Brain''. 2020 Nov 13; '''13''' (1):154
Functional investigation of the coronary artery disease gene SVEP1. Description: Winkler, Michael J, et al. Functional investigation of the coronary artery disease gene SVEP1. ''Basic Res Cardiol''. 2020 Nov 13; '''115''' (6):67
Insertion variants missing in the human reference genome are widespread among human populations. Description: Lee, Young-Gun, et al. Insertion variants missing in the human reference genome are widespread among human populations. ''BMC Biol''. 2020 Nov 13; '''18''' (1):167
MPG and NPRL3 Polymorphisms are Associated with Ischemic Stroke Susceptibility and Post-Stroke Mortality. Description: Ryu, Chang Soo, et al. MPG and NPRL3 Polymorphisms are Associated with Ischemic Stroke Susceptibility and Post-Stroke Mortality. ''Diagnostics (Basel)''. 2020 Nov 13; '''10''' (11):
Demographic history mediates the effect of stratification on polygenic scores. Description: Zaidi, Arslan A, et al. Demographic history mediates the effect of stratification on polygenic scores. ''Elife''. 2020 Nov 17; '''9''':
Examining the independent and joint effects of genomic and exposomic liabilities for schizophrenia across the psychosis spectrum. Description: Pries, L-K, et al. Examining the independent and joint effects of genomic and exposomic liabilities for schizophrenia across the psychosis spectrum. ''Epidemiol Psychiatr Sci''. 2020 Nov 17; '''29''': e182
Genomic analysis of worldwide sheep breeds reveals PDGFD as a major target of fat-tail selection in sheep. Description: Dong, Kunzhe, et al. Genomic analysis of worldwide sheep breeds reveals PDGFD as a major target of fat-tail selection in sheep. ''BMC Genomics''. 2020 Nov 17; '''21''' (1):800
Genomic selection for heterobothriosis resistance concurrent with body size in the tiger pufferfish, Takifugu rubripes. Description: Lin, Zijie, et al. Genomic selection for heterobothriosis resistance concurrent with body size in the tiger pufferfish, Takifugu rubripes. ''Sci Rep''. 2020 Nov 17; '''10''' (1):19976
Polygenetic-Risk Scores Related to Crystallin Metabolism Are Associated with Age-Related Cataract Formation and Interact with Hyperglycemia, Hypertension, Western-Style Diet, and Na Intake. Description: Jee, Donghyun, et al. Polygenetic-Risk Scores Related to Crystallin Metabolism Are Associated with Age-Related Cataract Formation and Interact with Hyperglycemia, Hypertension, Western-Style Diet, and Na Intake. ''Nutrients''. 2020 Nov 17; '''12''' (11):
DCC gene network in the prefrontal cortex is associated with total brain volume in childhood. Description: Morgunova, Alice, et al. DCC gene network in the prefrontal cortex is associated with total brain volume in childhood. ''J Psychiatry Neurosci''. 2020 Nov 18; '''46''' (1):E154-E163
Effects of STIP1 and GLCCI1 polymorphisms on the risk of childhood asthma and inhaled corticosteroid response in Chinese asthmatic children. Description: Huang, Juan, et al. Effects of STIP1 and GLCCI1 polymorphisms on the risk of childhood asthma and inhaled corticosteroid response in Chinese asthmatic children. ''BMC Pulm Med''. 2020 Nov 18; '''20''' (1):303
Evidences for a role of two Y-specific genes in sex determination in Populus deltoides. Description: Xue, Liangjiao, et al. Evidences for a role of two Y-specific genes in sex determination in Populus deltoides. ''Nat Commun''. 2020 Nov 18; '''11''' (1):5893
Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Description: Ishida, Sachiko, et al. Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. ''Commun Biol''. 2020 Nov 18; '''3''' (1):686
Mapping of Diabetes Susceptibility Loci in a Domestic Cat Breed with an Unusually High Incidence of Diabetes Mellitus. Description: Balmer, Lois, et al. Mapping of Diabetes Susceptibility Loci in a Domestic Cat Breed with an Unusually High Incidence of Diabetes Mellitus. ''Genes (Basel)''. 2020 Nov 19; '''11''' (11):
Migration of Sogatella furcifera between the Greater Mekong Subregion and northern China revealed by mtDNA and SNP. Description: Yang, Nan, et al. Migration of Sogatella furcifera between the Greater Mekong Subregion and northern China revealed by mtDNA and SNP. ''BMC Evol Biol''. 2020 Nov 19; '''20''' (1):154
PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia. Description: Monroe, Tanner O, et al. PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia. ''Nat Commun''. 2020 Nov 19; '''11''' (1):5903
Polymorphisms in the airway epithelium related genes CDHR3 and EMSY are associated with asthma susceptibility. Description: Zhang, Miaomiao, et al. Polymorphisms in the airway epithelium related genes CDHR3 and EMSY are associated with asthma susceptibility. ''BMC Pulm Med''. 2020 Nov 19; '''20''' (1):305
Female-specific effects of the catechol-O-methyl transferase Val(158)Met gene polymorphism on working memory-related brain function. Description: Fan, Jialing, et al. Female-specific effects of the catechol-O-methyl transferase Val(158)Met gene polymorphism on working memory-related brain function. ''Aging (Albany NY)''. 2020 Nov 22; '''12''' (23):23900-23916
Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Description: Hong, Shengjun, et al. Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. ''Transl Psychiatry''. 2020 Nov 22; '''10''' (1):403
Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection. Description: Adebamowo, Sally N, et al. Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection. ''BMC Med Genet''. 2020 Nov 23; '''21''' (1):231
Genotype imputation and variability in polygenic risk score estimation. Description: Chen, Shang-Fu, et al. Genotype imputation and variability in polygenic risk score estimation. ''Genome Med''. 2020 Nov 23; '''12''' (1):100
Variation under domestication in animal models: the case of the Mexican axolotl. Description: Torres-Sanchez, Maria. Variation under domestication in animal models: the case of the Mexican axolotl. ''BMC Genomics''. 2020 Nov 23; '''21''' (1):827
Chromosomal genome of Triplophysa bleekeri provides insights into its evolution and environmental adaptation. Description: Yuan, Dengyue, et al. Chromosomal genome of Triplophysa bleekeri provides insights into its evolution and environmental adaptation. ''Gigascience''. 2020 Nov 24; '''9''' (11):
Novel polygenic risk score as a translational tool linking depression-related changes in the corticolimbic transcriptome with neural face processing and anhedonic symptoms. Description: Mareckova, Klara, et al. Novel polygenic risk score as a translational tool linking depression-related changes in the corticolimbic transcriptome with neural face processing and anhedonic symptoms. ''Transl Psychiatry''. 2020 Nov 24; '''10''' (1):410
Determinants of vitamin D status in Kenyan calves. Description: Callaby, Rebecca, et al. Determinants of vitamin D status in Kenyan calves. ''Sci Rep''. 2020 Nov 25; '''10''' (1):20590
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Description: Steinthorsdottir, Valgerdur, et al. Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. ''Nat Commun''. 2020 Nov 25; '''11''' (1):5976
Genome-Wide Association Study of Root System Development at Seedling Stage in Rice. Description: Zhang, Hongjia, et al. Genome-Wide Association Study of Root System Development at Seedling Stage in Rice. ''Genes (Basel)''. 2020 Nov 25; '''11''' (12):
Genetic characterization of Addison's disease in Bearded Collies. Description: Gershony, Liza C, et al. Genetic characterization of Addison's disease in Bearded Collies. ''BMC Genomics''. 2020 Nov 26; '''21''' (1):833
Genome-Wide Association Studies for the Concentration of Albumin in Colostrum and Serum in Chinese Holstein. Description: Lin, Shan, et al. Genome-Wide Association Studies for the Concentration of Albumin in Colostrum and Serum in Chinese Holstein. ''Animals (Basel)''. 2020 Nov 26; '''10''' (12):
A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy. Description: Letko, Anna, et al. A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy. ''Genes (Basel)''. 2020 Nov 27; '''11''' (12):
Identification of Novel Loci and Candidate Genes for Cucumber Downy Mildew Resistance Using GWAS. Description: Liu, Xiaoping, et al. Identification of Novel Loci and Candidate Genes for Cucumber Downy Mildew Resistance Using GWAS. ''Plants (Basel)''. 2020 Nov 27; '''9''' (12):
Population genetic analysis of the Plasmodium falciparum circumsporozoite protein in two distinct ecological regions in Ghana. Description: Amegashie, Elikplim A, et al. Population genetic analysis of the Plasmodium falciparum circumsporozoite protein in two distinct ecological regions in Ghana. ''Malar J''. 2020 Nov 27; '''19''' (1):437
The Identification of Runs of Homozygosity Gives a Focus on the Genetic Diversity and Adaptation of the "Charolais de Cuba" Cattle. Description: Rodriguez-Valera, Yoel, et al. The Identification of Runs of Homozygosity Gives a Focus on the Genetic Diversity and Adaptation of the "Charolais de Cuba" Cattle. ''Animals (Basel)''. 2020 Nov 27; '''10''' (12):
Genome-Wide Association Analysis Identifies Resistance Loci for Bacterial Leaf Streak Resistance in Rice (Oryza sativa L.). Description: Sattayachiti, Wannapa, et al. Genome-Wide Association Analysis Identifies Resistance Loci for Bacterial Leaf Streak Resistance in Rice (Oryza sativa L.). ''Plants (Basel)''. 2020 Nov 29; '''9''' (12):
Application of genome-wide insertion/deletion markers on genetic structure analysis and identity signature of Malus accessions. Description: Wang, Xuan, et al. Application of genome-wide insertion/deletion markers on genetic structure analysis and identity signature of Malus accessions. ''BMC Plant Biol''. 2020 Nov 30; '''20''' (1):540
Epigenome-wide meta-analysis of DNA methylation differences in prefrontal cortex implicates the immune processes in Alzheimer's disease. Description: Zhang, Lanyu, et al. Epigenome-wide meta-analysis of DNA methylation differences in prefrontal cortex implicates the immune processes in Alzheimer's disease. ''Nat Commun''. 2020 Nov 30; '''11''' (1):6114
Genome-wide association analysis of the strength of the MAMP-elicited defense response and resistance to target leaf spot in sorghum. Description: Samira, Rozalynne, et al. Genome-wide association analysis of the strength of the MAMP-elicited defense response and resistance to target leaf spot in sorghum. ''Sci Rep''. 2020 Nov 30; '''10''' (1):20817
Polygenic scores for schizophrenia and general cognitive ability: associations with six cognitive domains, premorbid intelligence, and cognitive composite score in individuals with a psychotic disorder and in healthy controls. Description: Engen, Magnus Johan, et al. Polygenic scores for schizophrenia and general cognitive ability: associations with six cognitive domains, premorbid intelligence, and cognitive composite score in individuals with a psychotic disorder and in healthy controls. ''Transl Psychiatry''. 2020 Nov 30; '''10''' (1):416
Analysis of genomic distributions of SARS-CoV-2 reveals a dominant strain type with strong allelic associations. Description: Yang, Hsin-Chou, et al. Analysis of genomic distributions of SARS-CoV-2 reveals a dominant strain type with strong allelic associations. ''Proc Natl Acad Sci U S A''. 2020 Dec 1; '''117''' (48):30679-30686
A polygenic score for age-at-first-birth predicts disinhibition. Description: Richmond-Rakerd, Leah S, et al. A polygenic score for age-at-first-birth predicts disinhibition. ''J Child Psychol Psychiatry''. 2020 Dec; '''61''' (12):1349-1359
Assessing the Role of Long Noncoding RNA in Nucleus Accumbens in Subjects With Alcohol Dependence. Description: Drake, John, et al. Assessing the Role of Long Noncoding RNA in Nucleus Accumbens in Subjects With Alcohol Dependence. ''Alcohol Clin Exp Res''. 2020 Dec; '''44''' (12):2468-2480
Associations among circulating sphingolipids, beta-cell function, and risk of developing type 2 diabetes: A population-based cohort study in China. Description: Yun, Huan, et al. Associations among circulating sphingolipids, beta-cell function, and risk of developing type 2 diabetes: A population-based cohort study in China. ''PLoS Med''. 2020 Dec; '''17''' (12):e1003451
Associations between genetic variants of KIF5B, FMN1, and MGAT3 in the cadherin pathway and pancreatic cancer risk. Description: Zhao, Lingling, et al. Associations between genetic variants of KIF5B, FMN1, and MGAT3 in the cadherin pathway and pancreatic cancer risk. ''Cancer Med''. 2020 Dec; '''9''' (24):9620-9631
Association study between genetic variants in retinol metabolism pathway genes and prostate cancer risk. Description: Cao, Dongliang, et al. Association study between genetic variants in retinol metabolism pathway genes and prostate cancer risk. ''Cancer Med''. 2020 Dec; '''9''' (24):9462-9470
Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion. Description: McMacken, Grace, et al. Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion. ''J Neurol''. 2020 Dec; '''267''' (12):3643-3649
Candidate Genetic Modifiers for RPGR Retinal Degeneration. Description: Appelbaum, Tatyana, et al. Candidate Genetic Modifiers for RPGR Retinal Degeneration. ''Invest Ophthalmol Vis Sci''. 2020 Dec 1; '''61''' (14):20
Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population. Description: Hao, Shaofeng, et al. Comparison of machine learning tools for the prediction of AMD based on genetic, age, and diabetes-related variables in the Chinese population. ''Regen Ther''. 2020 Dec; '''15''': 180-186
Differentiation, evolution and utilization of natural alleles for cold adaptability at the reproductive stage in rice. Description: Guo, Haifeng, et al. Differentiation, evolution and utilization of natural alleles for cold adaptability at the reproductive stage in rice. ''Plant Biotechnol J''. 2020 Dec; '''18''' (12):2491-2503
Education, biological ageing, all-cause and cause-specific mortality and morbidity: UK biobank cohort study. Description: Chadeau-Hyam, Marc, et al. Education, biological ageing, all-cause and cause-specific mortality and morbidity: UK biobank cohort study. ''EClinicalMedicine''. 2020 Dec; '''29-30''': 100658
Examining the effect of smoking on suicidal ideation and attempts: triangulation of epidemiological approaches. Description: Harrison, Ruth, et al. Examining the effect of smoking on suicidal ideation and attempts: triangulation of epidemiological approaches. ''Br J Psychiatry''. 2020 Dec; '''217''' (6):701-707
Genetic associations with temporal shifts in obesity and severe obesity during the obesity epidemic in Norway: A longitudinal population-based cohort (the HUNT Study). Description: Brandkvist, Maria, et al. Genetic associations with temporal shifts in obesity and severe obesity during the obesity epidemic in Norway: A longitudinal population-based cohort (the HUNT Study). ''PLoS Med''. 2020 Dec; '''17''' (12):e1003452
Genetic variants as predictors of toxicity and response in patients with non-small cell lung cancer undergoing first-line platinum-based chemotherapy: Design of the multicenter PGxLUNG study. Description: de Jong, Corine, et al. Genetic variants as predictors of toxicity and response in patients with non-small cell lung cancer undergoing first-line platinum-based chemotherapy: Design of the multicenter PGxLUNG study. ''Thorac Cancer''. 2020 Dec; '''11''' (12):3634-3640
Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment. Description: Rasmussen, Eva Rye, et al. Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment. ''Pharmacogenomics J''. 2020 Dec; '''20''' (6):770-783
Genomic and Phenotypic Divergence in Wild Barley Driven by Microgeographic Adaptation. Description: Bian, Jianxin, et al. Genomic and Phenotypic Divergence in Wild Barley Driven by Microgeographic Adaptation. ''Adv Sci (Weinh)''. 2020 Dec; '''7''' (24):2000709
Identification of Novel Genetic Variants Related to Trabecular Bone Score in Community-Dwelling Older Adults. Description: Kong, Sung Hye, et al. Identification of Novel Genetic Variants Related to Trabecular Bone Score in Community-Dwelling Older Adults. ''Endocrinol Metab (Seoul)''. 2020 Dec; '''35''' (4):801-810
Investigation of gene-gene interactions of clock genes for chronotype in a healthy Korean population. Description: Park, Mira, et al. Investigation of gene-gene interactions of clock genes for chronotype in a healthy Korean population. ''Genomics Inform''. 2020 Dec; '''18''' (4):e38
MICA polymorphisms associated with antithyroid drug-induced agranulocytosis in the Chinese Han population. Description: Gong, Xiaojuan, et al. MICA polymorphisms associated with antithyroid drug-induced agranulocytosis in the Chinese Han population. ''Immun Inflamm Dis''. 2020 Dec; '''8''' (4):695-703
Mood-Stabilizing Antiepileptic Treatment Response in Bipolar Disorder: A Genome-Wide Association Study. Description: Ho, Ada Man-Choi, et al. Mood-Stabilizing Antiepileptic Treatment Response in Bipolar Disorder: A Genome-Wide Association Study. ''Clin Pharmacol Ther''. 2020 Dec; '''108''' (6):1233-1242
Pharmacogenetics of hypoglycemia associated with sulfonylurea therapy in usual clinical care. Description: Mitchell, Sabrina L, et al. Pharmacogenetics of hypoglycemia associated with sulfonylurea therapy in usual clinical care. ''Pharmacogenomics J''. 2020 Dec; '''20''' (6):831-839
Phenomics-based GWAS analysis reveals the genetic architecture for drought resistance in cotton. Description: Li, Baoqi, et al. Phenomics-based GWAS analysis reveals the genetic architecture for drought resistance in cotton. ''Plant Biotechnol J''. 2020 Dec; '''18''' (12):2533-2544
Physiological and genetic convergence supports hypoxia resistance in high-altitude songbirds. Description: Xiong, Ying, et al. Physiological and genetic convergence supports hypoxia resistance in high-altitude songbirds. ''PLoS Genet''. 2020 Dec; '''16''' (12):e1009270
Polymorphisms in mitochondrial ribosomal protein S5 (MRPS5) are associated with leprosy risk in Chinese. Description: Xing, Yan, et al. Polymorphisms in mitochondrial ribosomal protein S5 (MRPS5) are associated with leprosy risk in Chinese. ''PLoS Negl Trop Dis''. 2020 Dec; '''14''' (12):e0008883
Population genomic data in spider mites point to a role for local adaptation in shaping range shifts. Description: Chen, Lei, et al. Population genomic data in spider mites point to a role for local adaptation in shaping range shifts. ''Evol Appl''. 2020 Dec; '''13''' (10):2821-2835
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene. Description: Cooper-Knock, Johnathan, et al. Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene. ''Cell Rep''. 2020 Dec 1; '''33''' (9):108456
Resequencing of 297 melon accessions reveals the genomic history of improvement and loci related to fruit traits in melon. Description: Liu, Shi, et al. Resequencing of 297 melon accessions reveals the genomic history of improvement and loci related to fruit traits in melon. ''Plant Biotechnol J''. 2020 Dec; '''18''' (12):2545-2558
Steelhead (Oncorhynchus mykiss) lineages and sexes show variable patterns of association of adult migration timing and age-at-maturity traits with two genomic regions. Description: Willis, Stuart C, et al. Steelhead (Oncorhynchus mykiss) lineages and sexes show variable patterns of association of adult migration timing and age-at-maturity traits with two genomic regions. ''Evol Appl''. 2020 Dec; '''13''' (10):2836-2856
The Nucleosome Remodeling and Deacetylase Complex Has an Asymmetric, Dynamic, and Modular Architecture. Description: Low, Jason K K, et al. The Nucleosome Remodeling and Deacetylase Complex Has an Asymmetric, Dynamic, and Modular Architecture. ''Cell Rep''. 2020 Dec 1; '''33''' (9):108450
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD. Description: Straniero, Letizia, et al. The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD. ''Neurol Genet''. 2020 Dec; '''6''' (6):e523
COVID-19 genetic risk variants are associated with expression of multiple genes in diverse immune cell types. Description: Schmiedel, Benjamin J, et al. COVID-19 genetic risk variants are associated with expression of multiple genes in diverse immune cell types. ''bioRxiv''. 2020 Dec 2;
Distinct nucleotide patterns among three subgenomes of bread wheat and their potential origins during domestication after allopolyploidization. Description: Zhao, Yan, et al. Distinct nucleotide patterns among three subgenomes of bread wheat and their potential origins during domestication after allopolyploidization. ''BMC Biol''. 2020 Dec 2; '''18''' (1):188
Genetic Basis of Tiller Dynamics of Rice Revealed by Genome-Wide Association Studies. Description: Zhao, Shuyu, et al. Genetic Basis of Tiller Dynamics of Rice Revealed by Genome-Wide Association Studies. ''Plants (Basel)''. 2020 Dec 2; '''9''' (12):
Identification of Novel Genomic Associations and Gene Candidates for Grain Starch Content in Sorghum. Description: Sapkota, Sirjan, et al. Identification of Novel Genomic Associations and Gene Candidates for Grain Starch Content in Sorghum. ''Genes (Basel)''. 2020 Dec 2; '''11''' (12):
Moose genomes reveal past glacial demography and the origin of modern lineages. Description: Dussex, Nicolas, et al. Moose genomes reveal past glacial demography and the origin of modern lineages. ''BMC Genomics''. 2020 Dec 2; '''21''' (1):854
A Multi-omic Integrative Scheme Characterizes Tissues of Action at Loci Associated with Type 2 Diabetes. Description: Torres, Jason M, et al. A Multi-omic Integrative Scheme Characterizes Tissues of Action at Loci Associated with Type 2 Diabetes. ''Am J Hum Genet''. 2020 Dec 3; '''107''' (6):1011-1028
CCDC66 frameshift variant associated with a new form of early-onset progressive retinal atrophy in Portuguese Water Dogs. Description: Murgiano, Leonardo, et al. CCDC66 frameshift variant associated with a new form of early-onset progressive retinal atrophy in Portuguese Water Dogs. ''Sci Rep''. 2020 Dec 3; '''10''' (1):21162
Genetic Analysis of Walnut (Juglans regia L.) Pellicle Pigment Variation Through a Novel, High-Throughput Phenotyping Platform. Description: Sideli, Gina M, et al. Genetic Analysis of Walnut (Juglans regia L.) Pellicle Pigment Variation Through a Novel, High-Throughput Phenotyping Platform. ''G3 (Bethesda)''. 2020 Dec 3; '''10''' (12):4411-4424
Insights into Genetic Diversity, Runs of Homozygosity and Heterozygosity-Rich Regions in Maremmana Semi-Feral Cattle Using Pedigree and Genomic Data. Description: Biscarini, Filippo, et al. Insights into Genetic Diversity, Runs of Homozygosity and Heterozygosity-Rich Regions in Maremmana Semi-Feral Cattle Using Pedigree and Genomic Data. ''Animals (Basel)''. 2020 Dec 3; '''10''' (12):
Machine learning suggests polygenic risk for cognitive dysfunction in amyotrophic lateral sclerosis. Description: Placek, Katerina, et al. Machine learning suggests polygenic risk for cognitive dysfunction in amyotrophic lateral sclerosis. ''EMBO Mol Med''. 2020 Dec 3; e12595
MassArray analysis of genomic susceptibility variants in ovarian cancer. Description: Verma, Sonali, et al. MassArray analysis of genomic susceptibility variants in ovarian cancer. ''Sci Rep''. 2020 Dec 3; '''10''' (1):21101
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus. Description: Yin, Xianyong, et al. Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus. ''Ann Rheum Dis''. 2020 Dec 3;
Runs of Homozygosity in Modern Chicken Revealed by Sequence Data. Description: Talebi, Reza, et al. Runs of Homozygosity in Modern Chicken Revealed by Sequence Data. ''G3 (Bethesda)''. 2020 Dec 3; '''10''' (12):4615-4623
SHROOM3, the gene associated with chronic kidney disease, affects the podocyte structure. Description: Matsuura, Ryo, et al. SHROOM3, the gene associated with chronic kidney disease, affects the podocyte structure. ''Sci Rep''. 2020 Dec 3; '''10''' (1):21103
COG5 variants lead to complex early onset retinal degeneration, upregulation of PERK and DNA damage. Description: Tabbarah, Sami, et al. COG5 variants lead to complex early onset retinal degeneration, upregulation of PERK and DNA damage. ''Sci Rep''. 2020 Dec 4; '''10''' (1):21269
Ecological adaptation in Atlantic herring is associated with large shifts in allele frequencies at hundreds of loci. Description: Han, Fan, et al. Ecological adaptation in Atlantic herring is associated with large shifts in allele frequencies at hundreds of loci. ''Elife''. 2020 Dec 4; '''9''':
Global Autozygosity Is Associated with Cancer Risk, Mutational Signature and Prognosis. Description: Jiang, Limin, et al. Global Autozygosity Is Associated with Cancer Risk, Mutational Signature and Prognosis. ''Cancers (Basel)''. 2020 Dec 4; '''12''' (12):
Coexpression Clusters and Allele-Specific Expression in Metabolism-Based Herbicide Resistance. Description: Giacomini, Darci A, et al. Coexpression Clusters and Allele-Specific Expression in Metabolism-Based Herbicide Resistance. ''Genome Biol Evol''. 2020 Dec 6; '''12''' (12):2267-2278
Digging into the Genomic Past of Swiss Honey Bees by Whole-Genome Sequencing Museum Specimens. Description: Parejo, Melanie, et al. Digging into the Genomic Past of Swiss Honey Bees by Whole-Genome Sequencing Museum Specimens. ''Genome Biol Evol''. 2020 Dec 6; '''12''' (12):2535-2551
Genomic Copy Number Variation Study of Nine Macaca Species Provides New Insights into Their Genetic Divergence, Adaptation, and Biomedical Application. Description: Li, Jing, et al. Genomic Copy Number Variation Study of Nine Macaca Species Provides New Insights into Their Genetic Divergence, Adaptation, and Biomedical Application. ''Genome Biol Evol''. 2020 Dec 6; '''12''' (12):2211-2230
Shared Signature of Recent Positive Selection on the TSBP1-BTNL2-HLA-DRA Genes in Five Native Populations from North Borneo. Description: Hoh, Boon-Peng, et al. Shared Signature of Recent Positive Selection on the TSBP1-BTNL2-HLA-DRA Genes in Five Native Populations from North Borneo. ''Genome Biol Evol''. 2020 Dec 6; '''12''' (12):2245-2257
A systems biology framework integrating GWAS and RNA-seq to shed light on the molecular basis of sperm quality in swine. Description: Godia, Marta, et al. A systems biology framework integrating GWAS and RNA-seq to shed light on the molecular basis of sperm quality in swine. ''Genet Sel Evol''. 2020 Dec 8; '''52''' (1):72
Cerebral small vessel disease genomics and its implications across the lifespan. Description: Sargurupremraj, Muralidharan, et al. Cerebral small vessel disease genomics and its implications across the lifespan. ''Nat Commun''. 2020 Dec 8; '''11''' (1):6285
Donkey genomes provide new insights into domestication and selection for coat color. Description: Wang, Changfa, et al. Donkey genomes provide new insights into domestication and selection for coat color. ''Nat Commun''. 2020 Dec 8; '''11''' (1):6014
In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease. Description: Cahill, Megan E, et al. In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease. ''Vaccines (Basel)''. 2020 Dec 8; '''8''' (4):
Integrative analyses identify susceptibility genes underlying COVID-19 hospitalization. Description: Pathak, Gita A, et al. Integrative analyses identify susceptibility genes underlying COVID-19 hospitalization. ''medRxiv''. 2020 Dec 8;
Genome-Wide Analysis Revealed Homozygosity and Demographic History of Five Chinese Sheep Breeds Adapted to Different Environments. Description: Abied, Adam, et al. Genome-Wide Analysis Revealed Homozygosity and Demographic History of Five Chinese Sheep Breeds Adapted to Different Environments. ''Genes (Basel)''. 2020 Dec 9; '''11''' (12):
Phenome-wide and genome-wide analyses of quality of life in schizophrenia. Description: Pazoki, Raha, et al. Phenome-wide and genome-wide analyses of quality of life in schizophrenia. ''BJPsych Open''. 2020 Dec 9; '''7''' (1):e13
The SNP rs7865618 of 9p21.3 locus emerges as the most promising marker of coronary artery disease in the southern Indian population. Description: Manjula, Gorre, et al. The SNP rs7865618 of 9p21.3 locus emerges as the most promising marker of coronary artery disease in the southern Indian population. ''Sci Rep''. 2020 Dec 9; '''10''' (1):21511
Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility. Description: Vahidnezhad, Hassan, et al. Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility. ''Sci Rep''. 2020 Dec 10; '''10''' (1):21622
Whole-genome sequencing analysis of the cardiometabolic proteome. Description: Gilly, Arthur, et al. Whole-genome sequencing analysis of the cardiometabolic proteome. ''Nat Commun''. 2020 Dec 10; '''11''' (1):6336
Nasopharyngeal carcinoma MHC region deep sequencing identifies HLA and novel non-HLA TRIM31 and TRIM39 loci. Description: Ning, Lvwen, et al. Nasopharyngeal carcinoma MHC region deep sequencing identifies HLA and novel non-HLA TRIM31 and TRIM39 loci. ''Commun Biol''. 2020 Dec 11; '''3''' (1):759
*HLA-DRB107:01 and 08:02 Alleles Confer a Protective Effect Against ACPA-Positive Rheumatoid Arthritis in a Latin American Admixed Population.* Description: Castro-Santos, Patricia, et al. HLA-DRB107:01 and 08:02 Alleles Confer a Protective Effect Against ACPA-Positive Rheumatoid Arthritis in a Latin American Admixed Population. ''Biology (Basel)''. 2020 Dec 14; '''9''' (12):
Male recombination map of the autosomal genome in German Holstein. Description: Qanbari, Saber, et al. Male recombination map of the autosomal genome in German Holstein. ''Genet Sel Evol''. 2020 Dec 14; '''52''' (1):73
The role of polygenic risk and susceptibility genes in breast cancer over the course of life. Description: Mars, Nina, et al. The role of polygenic risk and susceptibility genes in breast cancer over the course of life. ''Nat Commun''. 2020 Dec 14; '''11''' (1):6383
Evolutionary Genomics of Structural Variation in Asian Rice (Oryza sativa) Domestication. Description: Kou, Yixuan, et al. Evolutionary Genomics of Structural Variation in Asian Rice (Oryza sativa) Domestication. ''Mol Biol Evol''. 2020 Dec 16; '''37''' (12):3507-3524
FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses. Description: Ahluwalia, Tarunveer S, et al. FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses. ''Nat Commun''. 2020 Dec 16; '''11''' (1):6398
Genetic architecture of host proteins involved in SARS-CoV-2 infection. Description: Pietzner, Maik, et al. Genetic architecture of host proteins involved in SARS-CoV-2 infection. ''Nat Commun''. 2020 Dec 16; '''11''' (1):6397
Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients. Description: Maltby, Vicki E, et al. Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients. ''Sci Rep''. 2020 Dec 17; '''10''' (1):22217
Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza. Description: Schachler, Kathrin, et al. Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza. ''Sci Rep''. 2020 Dec 17; '''10''' (1):22142
An ultra-high density SNP-based linkage map for enhancing the pikeperch (Sander lucioperca) genome assembly to chromosome-scale. Description: de Los Rios-Perez, Lidia, et al. An ultra-high density SNP-based linkage map for enhancing the pikeperch (Sander lucioperca) genome assembly to chromosome-scale. ''Sci Rep''. 2020 Dec 18; '''10''' (1):22335
Functional annotation of genetic associations by transcriptome-wide association analysis provides insights into neutrophil development regulation. Description: Yao, Yao, et al. Functional annotation of genetic associations by transcriptome-wide association analysis provides insights into neutrophil development regulation. ''Commun Biol''. 2020 Dec 18; '''3''' (1):790
Genomic signatures of recombination in a natural population of the bdelloid rotifer Adineta vaga. Description: Vakhrusheva, Olga A, et al. Genomic signatures of recombination in a natural population of the bdelloid rotifer Adineta vaga. ''Nat Commun''. 2020 Dec 18; '''11''' (1):6421
An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility. Description: Wang, Liuyang, et al. An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility. ''medRxiv''. 2020 Dec 22;
Impact of Genetic Factors on the Age of Onset for Type 2 Diabetes Mellitus in Addition to the Conventional Risk Factors. Description: Piko, Peter, et al. Impact of Genetic Factors on the Age of Onset for Type 2 Diabetes Mellitus in Addition to the Conventional Risk Factors. ''J Pers Med''. 2020 Dec 22; '''11''' (1):
A Bioinformatics Pipeline to Identify a Subset of SNPs for Genomics-Assisted Potato Breeding. Description: Selga, Catja, et al. A Bioinformatics Pipeline to Identify a Subset of SNPs for Genomics-Assisted Potato Breeding. ''Plants (Basel)''. 2020 Dec 24; '''10''' (1):
Apremilast Pharmacogenomics in Russian Patients with Moderate-to-Severe and Severe Psoriasis. Description: Verbenko, Dmitry A, et al. Apremilast Pharmacogenomics in Russian Patients with Moderate-to-Severe and Severe Psoriasis. ''J Pers Med''. 2020 Dec 29; '''11''' (1):
Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment. Description: Cervan-Martin, Miriam, et al. Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment. ''J Pers Med''. 2020 Dec 29; '''11''' (1):
Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer's disease. Description: Meng, Xianglian, et al. Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer's disease. ''BMC Genomics''. 2020 Dec 29; '''21''' (Suppl 11):896
Analysis of NOS Gene Polymorphisms in Relation to Cluster Headache and Predisposing Factors in Sweden. Description: Ran, Caroline, et al. Analysis of NOS Gene Polymorphisms in Relation to Cluster Headache and Predisposing Factors in Sweden. ''Brain Sci''. 2020 Dec 31; '''11''' (1):
Adaptive Gene Content and Allele Distribution Variations in the Wild and Domesticated Populations of Saccharomyces cerevisiae. Description: Han, Da-Yong, et al. Adaptive Gene Content and Allele Distribution Variations in the Wild and Domesticated Populations of Saccharomyces cerevisiae. ''Front Microbiol''. 2021; '''12''': 631250
Admixed Populations Improve Power for Variant Discovery and Portability in Genome-Wide Association Studies. Description: Lin, Meng, et al. Admixed Populations Improve Power for Variant Discovery and Portability in Genome-Wide Association Studies. ''Front Genet''. 2021; '''12''': 673167
A Functional Polymorphism in Accessible Chromatin Region Confers Risk of Non-Small Cell Lung Cancer in Chinese Population. Description: Long, Jieyi, et al. A Functional Polymorphism in Accessible Chromatin Region Confers Risk of Non-Small Cell Lung Cancer in Chinese Population. ''Front Oncol''. 2021; '''11''': 698993
A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population. Description: Zhang, Yue-Miao, et al. A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population. ''Front Immunol''. 2021; '''12''': 600598
A Genome-Wide Association Study and Polygenic Risk Score Analysis of Posttraumatic Stress Disorder and Metabolic Syndrome in a South African Population. Description: Swart, Patricia C, et al. A Genome-Wide Association Study and Polygenic Risk Score Analysis of Posttraumatic Stress Disorder and Metabolic Syndrome in a South African Population. ''Front Neurosci''. 2021; '''15''': 677800
A Genome-Wide Association Study Identifies Novel Risk Loci for Sarcopenia in a Taiwanese Population. Description: Wu, Shou-En, et al. A Genome-Wide Association Study Identifies Novel Risk Loci for Sarcopenia in a Taiwanese Population. ''J Inflamm Res''. 2021; '''14''': 5969-5980
A genome-wide association study of childhood adiposity and blood lipids. Description: O'Nunain, Katie, et al. A genome-wide association study of childhood adiposity and blood lipids. ''Wellcome Open Res''. 2021; '''6''': 303
A genome-wide association study on meat consumption in a Japanese population: the Japan Multi-Institutional Collaborative Cohort study. Description: Nakamura, Yasuyuki, et al. A genome-wide association study on meat consumption in a Japanese population: the Japan Multi-Institutional Collaborative Cohort study. ''J Nutr Sci''. 2021; '''10''': e61
A Germline Variant at 8q24 Contributes to the Serum p2PSA Level in a Chinese Prostate Biopsy Cohort. Description: Lin, Xiaoling, et al. A Germline Variant at 8q24 Contributes to the Serum p2PSA Level in a Chinese Prostate Biopsy Cohort. ''Front Oncol''. 2021; '''11''': 753920
A large-scale genomic association analysis identifies the candidate causal genes conferring stripe rust resistance under multiple field environments. Description: Wu, Jianhui, et al. A large-scale genomic association analysis identifies the candidate causal genes conferring stripe rust resistance under multiple field environments. ''Plant Biotechnol J''. 2021 Jan; '''19''' (1):177-191
Alcohol use and cardiometabolic risk in the UK Biobank: A Mendelian randomization study. Description: Lankester, Joanna, et al. Alcohol use and cardiometabolic risk in the UK Biobank: A Mendelian randomization study. ''PLoS One''. 2021; '''16''' (8):e0255801
A Missense Mutation in the MYBPH Gene Is Associated With Abdominal Fat Traits in Meat-Type Chickens. Description: Trevisoli, Priscila Anchieta, et al. A Missense Mutation in the MYBPH Gene Is Associated With Abdominal Fat Traits in Meat-Type Chickens. ''Front Genet''. 2021; '''12''': 698163
Analysis of Genetic and Non-genetic Predictors of Levodopa Induced Dyskinesia in Parkinson's Disease. Description: Tirozzi, Alfonsina, et al. Analysis of Genetic and Non-genetic Predictors of Levodopa Induced Dyskinesia in Parkinson's Disease. ''Front Pharmacol''. 2021; '''12''': 640603
Analysis of Structural Variants Reveal Novel Selective Regions in the Genome of Meishan Pigs by Whole Genome Sequencing. Description: Du, Heng, et al. Analysis of Structural Variants Reveal Novel Selective Regions in the Genome of Meishan Pigs by Whole Genome Sequencing. ''Front Genet''. 2021; '''12''': 550676
Analysis of the Segregation Distortion of FcRAN1 Genotypes Based on Whole-Genome Resequencing of Fig (Ficus carica L.) Breeding Parents. Description: Ikegami, Hidetoshi, et al. Analysis of the Segregation Distortion of FcRAN1 Genotypes Based on Whole-Genome Resequencing of Fig (Ficus carica L.) Breeding Parents. ''Front Plant Sci''. 2021; '''12''': 647599
Ancestral Spectrum Analysis With Population-Specific Variants. Description: Shi, Gang, et al. Ancestral Spectrum Analysis With Population-Specific Variants. ''Front Genet''. 2021; '''12''': 724638
An Efficient Score Test Integrated with Empirical Bayes for Genome-Wide Association Studies. Description: Xiao, Jing, et al. An Efficient Score Test Integrated with Empirical Bayes for Genome-Wide Association Studies. ''Front Genet''. 2021; '''12''': 742752
An Improved Genome-Wide Polygenic Score Model for Predicting the Risk of Type 2 Diabetes. Description: Liu, Wei, et al. An Improved Genome-Wide Polygenic Score Model for Predicting the Risk of Type 2 Diabetes. ''Front Genet''. 2021; '''12''': 632385
An Integrative Analysis of Transcriptome and GWAS Data to Identify Potential Candidate Genes Influencing Meat Quality Traits in Pigs. Description: Liu, Xianxian, et al. An Integrative Analysis of Transcriptome and GWAS Data to Identify Potential Candidate Genes Influencing Meat Quality Traits in Pigs. ''Front Genet''. 2021; '''12''': 748070
APOE and MAPT Are Associated With Dementia in Neuropathologically Confirmed Parkinson's Disease. Description: Tunold, Jon-Anders, et al. APOE and MAPT Are Associated With Dementia in Neuropathologically Confirmed Parkinson's Disease. ''Front Neurol''. 2021; '''12''': 631145
A population scale analysis of rare SNCA variation in the UK Biobank. Description: Blauwendraat, Cornelis, et al. A population scale analysis of rare SNCA variation in the UK Biobank. ''Neurobiol Dis''. 2021 Jan; '''148''': 105182
A Population-Specific Major Allele Reference Genome From The United Arab Emirates Population. Description: Daw Elbait, Gihan, et al. A Population-Specific Major Allele Reference Genome From The United Arab Emirates Population. ''Front Genet''. 2021; '''12''': 660428
A Single-Step Genome Wide Association Study on Body Size Traits Using Imputation-Based Whole-Genome Sequence Data in Yorkshire Pigs. Description: Liu, Huatao, et al. A Single-Step Genome Wide Association Study on Body Size Traits Using Imputation-Based Whole-Genome Sequence Data in Yorkshire Pigs. ''Front Genet''. 2021; '''12''': 629049
Assessing Genomic Diversity and Productivity Signatures in Dianzhong Cattle by Whole-Genome Scanning. Description: Zhang, Xianfu, et al. Assessing Genomic Diversity and Productivity Signatures in Dianzhong Cattle by Whole-Genome Scanning. ''Front Genet''. 2021; '''12''': 719215
Assessment of Causal Direction Between Gut Microbiota and Inflammatory Bowel Disease: A Mendelian Randomization Analysis. Description: Zhang, Zi-Jia, et al. Assessment of Causal Direction Between Gut Microbiota and Inflammatory Bowel Disease: A Mendelian Randomization Analysis. ''Front Genet''. 2021; '''12''': 631061
Association Analysis of Candidate Variants in Admixed Brazilian Patients With Genetic Generalized Epilepsies. Description: Kaibara, Felipe S, et al. Association Analysis of Candidate Variants in Admixed Brazilian Patients With Genetic Generalized Epilepsies. ''Front Genet''. 2021; '''12''': 672304
Association Analysis of LEP Signaling Pathway with Type 2 Diabetes Mellitus in Chinese Han Population from South China. Description: Yu, Haibing, et al. Association Analysis of LEP Signaling Pathway with Type 2 Diabetes Mellitus in Chinese Han Population from South China. ''Biomed Res Int''. 2021; '''2021''': 5517364
Association Analysis of Variants of DSCAM and BACE2 With Hirschsprung Disease Susceptibility in Han Chinese and Functional Evaluation in Zebrafish. Description: Lu, Yan-Jiao, et al. Association Analysis of Variants of DSCAM and BACE2 With Hirschsprung Disease Susceptibility in Han Chinese and Functional Evaluation in Zebrafish. ''Front Cell Dev Biol''. 2021; '''9''': 641152
Association Between Environmental Factors and Asthma Using Mendelian Randomization: Increased Effect of Body Mass Index on Adult-Onset Moderate-to-Severe Asthma Subtypes. Description: Ha, Tae-Woong, et al. Association Between Environmental Factors and Asthma Using Mendelian Randomization: Increased Effect of Body Mass Index on Adult-Onset Moderate-to-Severe Asthma Subtypes. ''Front Genet''. 2021; '''12''': 639905
Association Between Human Leukocyte Antigen Class I and II Diversity and Non-virus-associated Solid Tumors. Description: Liu, Zhiwei, et al. Association Between Human Leukocyte Antigen Class I and II Diversity and Non-virus-associated Solid Tumors. ''Front Genet''. 2021; '''12''': 675860
Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children. Description: Buda, Piotr, et al. Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children. ''Front Pediatr''. 2021; '''9''': 624798
Association Between Variants in Calcineurin Inhibitor Pharmacokinetic and Pharmacodynamic Genes and Renal Dysfunction in Adult Heart Transplant Recipients. Description: Oreschak, Kris, et al. Association Between Variants in Calcineurin Inhibitor Pharmacokinetic and Pharmacodynamic Genes and Renal Dysfunction in Adult Heart Transplant Recipients. ''Front Genet''. 2021; '''12''': 658983
Association of ABCG2 rs2231142 Allele and BMI With Hyperuricemia in an East Asian Population. Description: Chen, Yen-Ju, et al. Association of ABCG2 rs2231142 Allele and BMI With Hyperuricemia in an East Asian Population. ''Front Genet''. 2021; '''12''': 709887
Association of CDKN2A/CDKN2B Gene Polymorphisms with Increased Susceptibility to Intracranial Aneurysm in a Chinese Han Population. Description: Cui, Xiaopeng, et al. Association of CDKN2A/CDKN2B Gene Polymorphisms with Increased Susceptibility to Intracranial Aneurysm in a Chinese Han Population. ''Neuropsychiatr Dis Treat''. 2021; '''17''': 1443-1449
Association of Extracellular Signal-Regulated Kinase Genes With Myopia: A Longitudinal Study of Chinese Children. Description: Xiao, Haishao, et al. Association of Extracellular Signal-Regulated Kinase Genes With Myopia: A Longitudinal Study of Chinese Children. ''Front Genet''. 2021; '''12''': 654869
Association of GTF2I, NFKB1, and TYK2 Regional Polymorphisms With Systemic Sclerosis in a Chinese Han Population. Description: Liu, Chenxi, et al. Association of GTF2I, NFKB1, and TYK2 Regional Polymorphisms With Systemic Sclerosis in a Chinese Han Population. ''Front Immunol''. 2021; '''12''': 640083
Association of Metabolic Syndrome with Aerobic Exercise and LPL rs3779788 Polymorphism in Taiwan Biobank Individuals. Description: Hsu, Chun-Sheng, et al. Association of Metabolic Syndrome with Aerobic Exercise and LPL rs3779788 Polymorphism in Taiwan Biobank Individuals. ''Diabetes Metab Syndr Obes''. 2021; '''14''': 3997-4004
Association of Polygenetic Risk Scores Related to Immunity and Inflammation with Hyperthyroidism Risk and Interactions between the Polygenetic Scores and Dietary Factors in a Large Cohort. Description: Song, Mi Young, et al. Association of Polygenetic Risk Scores Related to Immunity and Inflammation with Hyperthyroidism Risk and Interactions between the Polygenetic Scores and Dietary Factors in a Large Cohort. ''J Thyroid Res''. 2021; '''2021''': 7664641
Association of the functionally significant polymorphisms of the MMP9 gene with H. pylori-positive gastric ulcer in the Caucasian population of Central Russia. Description: Dvornyk, Volodymyr, et al. Association of the functionally significant polymorphisms of the MMP9 gene with H. pylori-positive gastric ulcer in the Caucasian population of Central Russia. ''PLoS One''. 2021; '''16''' (9):e0257060
Associations Among Parental Caregiving Quality, Cannabinoid Receptor 1 Expression-Based Polygenic Scores, and Infant-Parent Attachment: Evidence for Differential Genetic Susceptibility? Description: Potter-Dickey, Amelia, et al. Associations Among Parental Caregiving Quality, Cannabinoid Receptor 1 Expression-Based Polygenic Scores, and Infant-Parent Attachment: Evidence for Differential Genetic Susceptibility? ''Front Neurosci''. 2021; '''15''': 704392
Associations Between CYP17A1 and SERPINA6/A1 Polymorphisms, and Cardiometabolic Risk Factors in Black South Africans. Description: Dlamini, Siphiwe N, et al. Associations Between CYP17A1 and SERPINA6/A1 Polymorphisms, and Cardiometabolic Risk Factors in Black South Africans. ''Front Genet''. 2021; '''12''': 687335
Associations of Mitochondrial Variants With Lipidomic Traits in a Chinese Cohort With Coronary Artery Disease. Description: Wang, Zixian, et al. Associations of Mitochondrial Variants With Lipidomic Traits in a Chinese Cohort With Coronary Artery Disease. ''Front Genet''. 2021; '''12''': 630359
A Survey of Compound Heterozygous Variants in Pediatric Cancers and Structural Birth Defects. Description: Miller, Dustin B, et al. A Survey of Compound Heterozygous Variants in Pediatric Cancers and Structural Birth Defects. ''Front Genet''. 2021; '''12''': 640242
Biologically Enhanced Genome-Wide Association Study Provides Further Evidence for Candidate Loci and Discovers Novel Loci That Influence Risk of Anterior Cruciate Ligament Rupture in a Dog Model. Description: Baker, Lauren A, et al. Biologically Enhanced Genome-Wide Association Study Provides Further Evidence for Candidate Loci and Discovers Novel Loci That Influence Risk of Anterior Cruciate Ligament Rupture in a Dog Model. ''Front Genet''. 2021; '''12''': 593515
Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins. Description: Li, Zhaoying, et al. Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins. ''PLoS One''. 2021; '''16''' (2):e0246436
Cannabis Use in People With Obsessive-Compulsive Symptomatology: Results From a Mexican Epidemiological Sample. Description: Nicolini, Humberto, et al. Cannabis Use in People With Obsessive-Compulsive Symptomatology: Results From a Mexican Epidemiological Sample. ''Front Psychiatry''. 2021; '''12''': 664228
Can public online databases serve as a source of phenotypic information for Cannabis genetic association studies? Description: Aardema, Matthew L, et al. Can public online databases serve as a source of phenotypic information for Cannabis genetic association studies? ''PLoS One''. 2021; '''16''' (2):e0247607
Cataloging Human PRDM9 Allelic Variation Using Long-Read Sequencing Reveals PRDM9 Population Specificity and Two Distinct Groupings of Related Alleles. Description: Alleva, Benjamin, et al. Cataloging Human PRDM9 Allelic Variation Using Long-Read Sequencing Reveals PRDM9 Population Specificity and Two Distinct Groupings of Related Alleles. ''Front Cell Dev Biol''. 2021; '''9''': 675286
Causal association of cognitive reserve on Alzheimer's disease with putative sex difference. Description: Wang, Hao, et al. Causal association of cognitive reserve on Alzheimer's disease with putative sex difference. ''Alzheimers Dement (Amst)''. 2021; '''13''' (1):e12270
Causal linkage between adult height and kidney function: An integrated population-scale observational analysis and Mendelian randomization study. Description: Park, Sehoon, et al. Causal linkage between adult height and kidney function: An integrated population-scale observational analysis and Mendelian randomization study. ''PLoS One''. 2021; '''16''' (7):e0254649
CD28 Genetic Variants Increase Susceptibility to Diabetic Kidney Disease in Chinese Patients with Type 2 Diabetes: A Cross-Sectional Case Control Study. Description: Li, Yangyang, et al. CD28 Genetic Variants Increase Susceptibility to Diabetic Kidney Disease in Chinese Patients with Type 2 Diabetes: A Cross-Sectional Case Control Study. ''Mediators Inflamm''. 2021; '''2021''': 5521050
CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Description: Yang, Ming Ming, et al. CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. ''Front Immunol''. 2021; '''12''': 608723
Characterization of a Cohort of Patients With LIG4 Deficiency Reveals the Founder Effect of p.R278L, Unique to the Chinese Population. Description: Luo, Xianze, et al. Characterization of a Cohort of Patients With LIG4 Deficiency Reveals the Founder Effect of p.R278L, Unique to the Chinese Population. ''Front Immunol''. 2021; '''12''': 695993
Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease. Description: Torrealba-Acosta, Gabriel, et al. Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease. ''Front Neurol''. 2021; '''12''': 656342
Clinical Significance of Variants in the TTN Gene in a Large Cohort of Patients With Sporadic Dilated Cardiomyopathy. Description: Xiao, Lei, et al. Clinical Significance of Variants in the TTN Gene in a Large Cohort of Patients With Sporadic Dilated Cardiomyopathy. ''Front Cardiovasc Med''. 2021; '''8''': 657689
Clustering patterns mirror the geographical distribution and genetic history of Lemnos and Lesvos sheep populations. Description: Kominakis, Antonios, et al. Clustering patterns mirror the geographical distribution and genetic history of Lemnos and Lesvos sheep populations. ''PLoS One''. 2021; '''16''' (3):e0247787
Collection, genotyping and virus elimination of cassava landraces from Tanzania and documentation of farmer knowledge. Description: Ferguson, M E, et al. Collection, genotyping and virus elimination of cassava landraces from Tanzania and documentation of farmer knowledge. ''PLoS One''. 2021; '''16''' (8):e0255326
Combined Low-/High-Density Modern and Ancient Genome-Wide Data Document Genomic Admixture History of High-Altitude East Asians. Description: Liu, Yan, et al. Combined Low-/High-Density Modern and Ancient Genome-Wide Data Document Genomic Admixture History of High-Altitude East Asians. ''Front Genet''. 2021; '''12''': 582357
Common genetic variants associated with obesity in an African-American and Hispanic/Latino population. Description: Chalazan, Brandon, et al. Common genetic variants associated with obesity in an African-American and Hispanic/Latino population. ''PLoS One''. 2021; '''16''' (5):e0250697
Common Variants in NUS1 and GP2 Genes Contributed to the Risk of Gestational Diabetes Mellitus. Description: Zhang, Tianxiao, et al. Common Variants in NUS1 and GP2 Genes Contributed to the Risk of Gestational Diabetes Mellitus. ''Front Endocrinol (Lausanne)''. 2021; '''12''': 685524
Comparative host transcriptome in response to pathogenic fungi identifies common and species-specific transcriptional antifungal host response pathways. Description: Bruno, Mariolina, et al. Comparative host transcriptome in response to pathogenic fungi identifies common and species-specific transcriptional antifungal host response pathways. ''Comput Struct Biotechnol J''. 2021; '''19''': 647-663
Comparative Signatures of Selection Analyses Identify Loci Under Positive Selection in the Murrah Buffalo of India. Description: Tyagi, Shiv K, et al. Comparative Signatures of Selection Analyses Identify Loci Under Positive Selection in the Murrah Buffalo of India. ''Front Genet''. 2021; '''12''': 673697
Comparing a Mixed Model Approach to Traditional Stability Estimators for Mapping Genotype by Environment Interactions and Yield Stability in Soybean [Glycine max (L.) Merr.]. Description: Happ, Mary M, et al. Comparing a Mixed Model Approach to Traditional Stability Estimators for Mapping Genotype by Environment Interactions and Yield Stability in Soybean [Glycine max (L.) Merr.]. ''Front Plant Sci''. 2021; '''12''': 630175
Comparing Genetic and Socioenvironmental Contributions to Ethnic Differences in C-Reactive Protein. Description: Nagar, Shashwat Deepali, et al. Comparing Genetic and Socioenvironmental Contributions to Ethnic Differences in C-Reactive Protein. ''Front Genet''. 2021; '''12''': 738485
Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy. Description: Letko, Anna, et al. Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy. ''Mol Genet Genomics''. 2021 Jan; '''296''' (1):235-242
Comprehensive Insights Into Forensic Features and Genetic Background of Chinese Northwest Hui Group Using Six Distinct Categories of 231 Molecular Markers. Description: Chen, Chong, et al. Comprehensive Insights Into Forensic Features and Genetic Background of Chinese Northwest Hui Group Using Six Distinct Categories of 231 Molecular Markers. ''Front Genet''. 2021; '''12''': 705753
Conservation Genomics of Wild Red Sage (Salvia miltiorrhiza) and Its Endangered Relatives in China: Population Structure and Interspecific Relationships Revealed From 2b-RAD Data. Description: Zhou, Xuan, et al. Conservation Genomics of Wild Red Sage (Salvia miltiorrhiza) and Its Endangered Relatives in China: Population Structure and Interspecific Relationships Revealed From 2b-RAD Data. ''Front Genet''. 2021; '''12''': 688323
Construction and Clinical Translation of Causal Pan-Cancer Gene Score Across Cancer Types. Description: Tao, Shiyue, et al. Construction and Clinical Translation of Causal Pan-Cancer Gene Score Across Cancer Types. ''Front Genet''. 2021; '''12''': 784775
Construction of a SNP Fingerprinting Database and Population Genetic Analysis of Cigar Tobacco Germplasm Resources in China. Description: Wang, Yanyan, et al. Construction of a SNP Fingerprinting Database and Population Genetic Analysis of Cigar Tobacco Germplasm Resources in China. ''Front Plant Sci''. 2021; '''12''': 618133
Coordinated Expressional Landscape of the Human Placental miRNome and Transcriptome. Description: Inno, Rain, et al. Coordinated Expressional Landscape of the Human Placental miRNome and Transcriptome. ''Front Cell Dev Biol''. 2021; '''9''': 697947
Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project. Description: Lee, Wan-Ping, et al. Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project. ''Front Genet''. 2021; '''12''': 752390
Deep sequencing of DNA from urine of kidney allograft recipients to estimate donor/recipient-specific DNA fractions. Description: Belkadi, Aziz, et al. Deep sequencing of DNA from urine of kidney allograft recipients to estimate donor/recipient-specific DNA fractions. ''PLoS One''. 2021; '''16''' (4):e0249930
Defining functional variants associated with Alzheimer's disease in the induced immune response. Description: Harwood, Janet C, et al. Defining functional variants associated with Alzheimer's disease in the induced immune response. ''Brain Commun''. 2021; '''3''' (2):fcab083
Delineation of Mitochondrial DNA Variants From Exome Sequencing Data and Association of Haplogroups With Obesity in Kuwait. Description: Dashti, Mohammed, et al. Delineation of Mitochondrial DNA Variants From Exome Sequencing Data and Association of Haplogroups With Obesity in Kuwait. ''Front Genet''. 2021; '''12''': 626260
De novo identification and targeted sequencing of SSRs efficiently fingerprints Sorghum bicolor sub-population identity. Description: Baggett, John P, et al. De novo identification and targeted sequencing of SSRs efficiently fingerprints Sorghum bicolor sub-population identity. ''PLoS One''. 2021; '''16''' (3):e0248213
Detection of genomic regions associated malformations in newborn piglets: a machine-learning approach. Description: Bakoev, Siroj, et al. Detection of genomic regions associated malformations in newborn piglets: a machine-learning approach. ''PeerJ''. 2021; '''9''': e11580
Detection of six novel de novo mutations in individuals with low resilience to psychological stress. Description: Azadmarzabadi, Esfandiar, et al. Detection of six novel de novo mutations in individuals with low resilience to psychological stress. ''PLoS One''. 2021; '''16''' (9):e0256285
Differential Genomic Profile in TERT, DSP, and FAM13A Between COPD Patients With Emphysema, IPF, and CPFE Syndrome. Description: Guzman-Vargas, Javier, et al. Differential Genomic Profile in TERT, DSP, and FAM13A Between COPD Patients With Emphysema, IPF, and CPFE Syndrome. ''Front Med (Lausanne)''. 2021; '''8''': 725144
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Description: Livingstone, Katherine M, et al. Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. ''Front Endocrinol (Lausanne)''. 2021; '''12''': 692677
Discovery of Novel Genetic Risk Loci for Acute Central Serous Chorioretinopathy and Genetic Pleiotropic Effect With Age-Related Macular Degeneration. Description: Feng, Lei, et al. Discovery of Novel Genetic Risk Loci for Acute Central Serous Chorioretinopathy and Genetic Pleiotropic Effect With Age-Related Macular Degeneration. ''Front Cell Dev Biol''. 2021; '''9''': 696885
Discovery of Novel Host Molecular Factors Underlying HBV/HCV Infection. Description: Huang, Xubo, et al. Discovery of Novel Host Molecular Factors Underlying HBV/HCV Infection. ''Front Cell Dev Biol''. 2021; '''9''': 690882
DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations. Description: Niazi, Yasmeen, et al. DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations. ''Front Genet''. 2021; '''12''': 691947
Duo Shared Genomic Segment analysis identifies a genome-wide significant risk locus at 18q21.33 in myeloma pedigrees. Description: Griffin Waller, Rosalie, et al. Duo Shared Genomic Segment analysis identifies a genome-wide significant risk locus at 18q21.33 in myeloma pedigrees. ''J Transl Genet Genom''. 2021; '''5''' (2):112-123
Effect of Cytochrome P450 Family 2 Subfamily R Member 1 Variants on the Predisposition of Coronary Heart Disease in the Chinese Han Population. Description: Wang, Qi, et al. Effect of Cytochrome P450 Family 2 Subfamily R Member 1 Variants on the Predisposition of Coronary Heart Disease in the Chinese Han Population. ''Front Cardiovasc Med''. 2021; '''8''': 652729
Endocannabinoid Gene x Gene Interaction Association to Alcohol Use Disorder in Two Adolescent Cohorts. Description: Elkrief, Laurent, et al. Endocannabinoid Gene x Gene Interaction Association to Alcohol Use Disorder in Two Adolescent Cohorts. ''Front Psychiatry''. 2021; '''12''': 645746
Enhanced Identification of Novel Potential Variants for Appendicular Lean Mass by Leveraging Pleiotropy With Bone Mineral Density. Description: Peng, Cheng, et al. Enhanced Identification of Novel Potential Variants for Appendicular Lean Mass by Leveraging Pleiotropy With Bone Mineral Density. ''Front Immunol''. 2021; '''12''': 643894
Environmental and Genetic Determinants of Major Chronic Disease in Beijing-Tianjin-Hebei Region: Protocol for a Community-Based Cohort Study. Description: Liu, Kuo, et al. Environmental and Genetic Determinants of Major Chronic Disease in Beijing-Tianjin-Hebei Region: Protocol for a Community-Based Cohort Study. ''Front Public Health''. 2021; '''9''': 659701
Epigenetic Markers Are Associated With Differences in Isocyanate Biomarker Levels in Exposed Spray-Painters. Description: Taylor, Laura W, et al. Epigenetic Markers Are Associated With Differences in Isocyanate Biomarker Levels in Exposed Spray-Painters. ''Front Genet''. 2021; '''12''': 700636
Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort. Description: Koomar, Tanner, et al. Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort. ''Front Psychiatry''. 2021; '''12''': 668297
Estimation of linkage disequilibrium levels and allele frequency distribution in crossbred Vrindavani cattle using 50K SNP data. Description: Singh, Akansha, et al. Estimation of linkage disequilibrium levels and allele frequency distribution in crossbred Vrindavani cattle using 50K SNP data. ''PLoS One''. 2021; '''16''' (11):e0259572
Evaluating Causal Relationship Between Metabolites and Six Cardiovascular Diseases Based on GWAS Summary Statistics. Description: Qiao, Jiahao, et al. Evaluating Causal Relationship Between Metabolites and Six Cardiovascular Diseases Based on GWAS Summary Statistics. ''Front Genet''. 2021; '''12''': 746677
Evaluation of Septoria Nodorum Blotch (SNB) Resistance in Glumes of Wheat (Triticum aestivum L.) and the Genetic Relationship With Foliar Disease Response. Description: Francki, Michael G, et al. Evaluation of Septoria Nodorum Blotch (SNB) Resistance in Glumes of Wheat (Triticum aestivum L.) and the Genetic Relationship With Foliar Disease Response. ''Front Genet''. 2021; '''12''': 681768
Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants. Description: Namjou, Bahram, et al. Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants. ''Int J Obes (Lond)''. 2021 Jan; '''45''' (1):155-169
Every Night and Every Morn: Effect of Variation in CLOCK Gene on Depression Depends on Exposure to Early and Recent Stress. Description: Gyorik, Dorka, et al. Every Night and Every Morn: Effect of Variation in CLOCK Gene on Depression Depends on Exposure to Early and Recent Stress. ''Front Psychiatry''. 2021; '''12''': 687487
Evolution of inbreeding: a gaze into five Italian beef cattle breeds history. Description: Rovelli, Giacomo, et al. Evolution of inbreeding: a gaze into five Italian beef cattle breeds history. ''PeerJ''. 2021; '''9''': e12049
Examining Individual and Synergistic Contributions of PTSD and Genetics to Blood Pressure: A Trans-Ethnic Meta-Analysis. Description: Sumner, Jennifer A, et al. Examining Individual and Synergistic Contributions of PTSD and Genetics to Blood Pressure: A Trans-Ethnic Meta-Analysis. ''Front Neurosci''. 2021; '''15''': 678503
Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression. Description: Martin, Joanna, et al. Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression. ''PLoS One''. 2021; '''16''' (9):e0248254
Exceptional long-term sperm storage by a female vertebrate. Description: Levine, Brenna A, et al. Exceptional long-term sperm storage by a female vertebrate. ''PLoS One''. 2021; '''16''' (6):e0252049
Exploring a Region on Chromosome 8p23.1 Displaying Positive Selection Signals in Brazilian Admixed Populations: Additional Insights Into Predisposition to Obesity and Related Disorders. Description: Secolin, Rodrigo, et al. Exploring a Region on Chromosome 8p23.1 Displaying Positive Selection Signals in Brazilian Admixed Populations: Additional Insights Into Predisposition to Obesity and Related Disorders. ''Front Genet''. 2021; '''12''': 636542
Fifteen Years of the Australian Imaging, Biomarkers and Lifestyle (AIBL) Study: Progress and Observations from 2,359 Older Adults Spanning the Spectrum from Cognitive Normality to Alzheimer's Disease. Description: Fowler, Christopher, et al. Fifteen Years of the Australian Imaging, Biomarkers and Lifestyle (AIBL) Study: Progress and Observations from 2,359 Older Adults Spanning the Spectrum from Cognitive Normality to Alzheimer's Disease. ''J Alzheimers Dis Rep''. 2021; '''5''' (1):443-468
Five genetic variants explain over 70% of hair coat pheomelanin intensity variation in purebred and mixed breed domestic dogs. Description: Slavney, Andrea J, et al. Five genetic variants explain over 70% of hair coat pheomelanin intensity variation in purebred and mixed breed domestic dogs. ''PLoS One''. 2021; '''16''' (5):e0250579
Functional Variants Surrounding Endothelin 2 Are Associated With Mycobacterium avium Subspecies paratuberculosis Infection. Description: Kiser, Jennifer N, et al. Functional Variants Surrounding Endothelin 2 Are Associated With Mycobacterium avium Subspecies paratuberculosis Infection. ''Front Vet Sci''. 2021; '''8''': 625323
GAS6/Axl Signaling Modulates Blood-Brain Barrier Function Following Intravenous Thrombolysis in Acute Ischemic Stroke. Description: Guo, Zhen-Ni, et al. GAS6/Axl Signaling Modulates Blood-Brain Barrier Function Following Intravenous Thrombolysis in Acute Ischemic Stroke. ''Front Immunol''. 2021; '''12''': 742359
Gene Banks as Reservoirs to Detect Recent Selection: The Example of the Asturiana de los Valles Bovine Breed. Description: Boitard, Simon, et al. Gene Banks as Reservoirs to Detect Recent Selection: The Example of the Asturiana de los Valles Bovine Breed. ''Front Genet''. 2021; '''12''': 575405
Gene-Based Tests of a Genome-Wide Association Study Dataset Highlight Novel Multiple Sclerosis Risk Genes. Description: Li, He, et al. Gene-Based Tests of a Genome-Wide Association Study Dataset Highlight Novel Multiple Sclerosis Risk Genes. ''Front Neurosci''. 2021; '''15''': 614528
Gene-environment interaction in molar-incisor hypomineralization. Description: Bezamat, Mariana, et al. Gene-environment interaction in molar-incisor hypomineralization. ''PLoS One''. 2021; '''16''' (1):e0241898
Gene Expression Analysis in Three Posttraumatic Stress Disorder Cohorts Implicates Inflammation and Innate Immunity Pathways and Uncovers Shared Genetic Risk With Major Depressive Disorder. Description: Garrett, Melanie E, et al. Gene Expression Analysis in Three Posttraumatic Stress Disorder Cohorts Implicates Inflammation and Innate Immunity Pathways and Uncovers Shared Genetic Risk With Major Depressive Disorder. ''Front Neurosci''. 2021; '''15''': 678548
Genes involved in immune, gene translation and chromatin organization pathways associated with Mycoplasma ovipneumoniae presence in nasal secretions of domestic sheep. Description: Mousel, Michelle R, et al. Genes involved in immune, gene translation and chromatin organization pathways associated with Mycoplasma ovipneumoniae presence in nasal secretions of domestic sheep. ''PLoS One''. 2021; '''16''' (7):e0247209
Genetically-determined body mass index and the risk of atrial fibrillation progression in men and women. Description: Siland, J E, et al. Genetically-determined body mass index and the risk of atrial fibrillation progression in men and women. ''PLoS One''. 2021; '''16''' (2):e0246907
Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Description: Chong, Amanda H W, et al. Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. ''Front Immunol''. 2021; '''12''': 727457
Genetic ancestry, admixture, and population structure in rural Dominica. Description: Keith, Monica H, et al. Genetic ancestry, admixture, and population structure in rural Dominica. ''PLoS One''. 2021; '''16''' (11):e0258735
Genetic and Functional Evaluation of the Role of FOXO1 in Antituberculosis Drug-Induced Hepatotoxicity. Description: Zhang, Jingwei, et al. Genetic and Functional Evaluation of the Role of FOXO1 in Antituberculosis Drug-Induced Hepatotoxicity. ''Evid Based Complement Alternat Med''. 2021; '''2021''': 3185874
Genetic Association of Interleukin 33/ST2 Polymorphisms With Behcet's Uveitis. Description: Pei, Minghang, et al. Genetic Association of Interleukin 33/ST2 Polymorphisms With Behcet's Uveitis. ''Front Immunol''. 2021; '''12''': 589639
Genetic associations of fatigue and other symptoms following breast cancer treatment: A prospective study. Description: Cameron, B, et al. Genetic associations of fatigue and other symptoms following breast cancer treatment: A prospective study. ''Brain Behav Immun Health''. 2021 Jan; '''10''': 100189
Genetic Dissection of Grain Yield Component Traits Under High Nighttime Temperature Stress in a Rice Diversity Panel. Description: Kumar, Anuj, et al. Genetic Dissection of Grain Yield Component Traits Under High Nighttime Temperature Stress in a Rice Diversity Panel. ''Front Plant Sci''. 2021; '''12''': 712167
Genetic Dissection Uncovers Genome-Wide Marker-Trait Associations for Plant Growth, Yield, and Yield-Related Traits Under Varying Nitrogen Levels in Nested Synthetic Wheat Introgression Libraries. Description: Sandhu, Nitika, et al. Genetic Dissection Uncovers Genome-Wide Marker-Trait Associations for Plant Growth, Yield, and Yield-Related Traits Under Varying Nitrogen Levels in Nested Synthetic Wheat Introgression Libraries. ''Front Plant Sci''. 2021; '''12''': 738710
Genetic Diversity and Demographic History of the Shaggy Soft-Haired Mouse Abrothrix hirta (Cricetidae; Abrotrichini). Description: Valdez, Lourdes, et al. Genetic Diversity and Demographic History of the Shaggy Soft-Haired Mouse Abrothrix hirta (Cricetidae; Abrotrichini). ''Front Genet''. 2021; '''12''': 642504
Genetic diversity and population history of eight Italian beef cattle breeds using measures of autozygosity. Description: Fabbri, Maria Chiara, et al. Genetic diversity and population history of eight Italian beef cattle breeds using measures of autozygosity. ''PLoS One''. 2021; '''16''' (10):e0248087
Genetic diversity and population structure of sheep (Ovis aries) in Sichuan, China. Description: Zhou, Mingliang, et al. Genetic diversity and population structure of sheep (Ovis aries) in Sichuan, China. ''PLoS One''. 2021; '''16''' (9):e0257974
Genetic Diversity and Signatures of Selection for Thermal Stress in Cattle and Other Two Bos Species Adapted to Divergent Climatic Conditions. Description: Freitas, Pedro H F, et al. Genetic Diversity and Signatures of Selection for Thermal Stress in Cattle and Other Two Bos Species Adapted to Divergent Climatic Conditions. ''Front Genet''. 2021; '''12''': 604823
Genetic diversity and the application of runs of homozygosity-based methods for inbreeding estimation in German White-headed Mutton sheep. Description: Addo, Sowah, et al. Genetic diversity and the application of runs of homozygosity-based methods for inbreeding estimation in German White-headed Mutton sheep. ''PLoS One''. 2021; '''16''' (5):e0250608
Genetic Link Determining the Maternal-Fetal Circulation of Vitamin D. Description: Sampathkumar, Aparna, et al. Genetic Link Determining the Maternal-Fetal Circulation of Vitamin D. ''Front Genet''. 2021; '''12''': 721488
Genetic Loci and Physiologic Pathways Involved in Gestational Diabetes Mellitus Implicated Through Clustering. Description: Powe, Camille E, et al. Genetic Loci and Physiologic Pathways Involved in Gestational Diabetes Mellitus Implicated Through Clustering. ''Diabetes''. 2021 Jan; '''70''' (1):268-281
Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene. Description: Ma, Suk-Ling, et al. Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene. ''Front Neurosci''. 2021; '''15''': 649588
Genetic Parameters and Genome-Wide Association Studies of Eight Longevity Traits Representing Either Full or Partial Lifespan in Chinese Holsteins. Description: Zhang, Hailiang, et al. Genetic Parameters and Genome-Wide Association Studies of Eight Longevity Traits Representing Either Full or Partial Lifespan in Chinese Holsteins. ''Front Genet''. 2021; '''12''': 634986
Genetic risk for Alzheimer's disease, cognition, and mild behavioral impairment in healthy older adults. Description: Creese, Byron, et al. Genetic risk for Alzheimer's disease, cognition, and mild behavioral impairment in healthy older adults. ''Alzheimers Dement (Amst)''. 2021; '''13''' (1):e12164
Genetics and Functional Mechanisms of STAT3 Polymorphisms in Human Tuberculosis. Description: Wang, Feifei, et al. Genetics and Functional Mechanisms of STAT3 Polymorphisms in Human Tuberculosis. ''Front Cell Infect Microbiol''. 2021; '''11''': 669394
Genome-Scale Phylogenetic and Population Genetic Studies Provide Insight Into Introgression and Adaptive Evolution of Takifugu Species in East Asia. Description: Liu, Bo, et al. Genome-Scale Phylogenetic and Population Genetic Studies Provide Insight Into Introgression and Adaptive Evolution of Takifugu Species in East Asia. ''Front Genet''. 2021; '''12''': 625600
Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndrome. Description: Qaiser, Farah, et al. Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndrome. ''Brain Commun''. 2021; '''3''' (3):fcab207
Genome-Wide Analyses Reveal the Genetic Architecture and Candidate Genes of Indicine, Taurine, Synthetic Crossbreds, and Locally Adapted Cattle in Brazil. Description: Verardo, Lucas Lima, et al. Genome-Wide Analyses Reveal the Genetic Architecture and Candidate Genes of Indicine, Taurine, Synthetic Crossbreds, and Locally Adapted Cattle in Brazil. ''Front Genet''. 2021; '''12''': 702822
Genome-wide analysis of genetic diversity and artificial selection in Large White pigs in Russia. Description: Bakoev, Siroj, et al. Genome-wide analysis of genetic diversity and artificial selection in Large White pigs in Russia. ''PeerJ''. 2021; '''9''': e11595
Genome-Wide Analysis Reveals Selection Signatures Involved in Meat Traits and Local Adaptation in Semi-Feral Maremmana Cattle. Description: Ben-Jemaa, Slim, et al. Genome-Wide Analysis Reveals Selection Signatures Involved in Meat Traits and Local Adaptation in Semi-Feral Maremmana Cattle. ''Front Genet''. 2021; '''12''': 675569
Genome-Wide Assessment of Runs of Homozygosity and Estimates of Genomic Inbreeding in a Chinese Composite Pig Breed. Description: Xu, Zhong, et al. Genome-Wide Assessment of Runs of Homozygosity and Estimates of Genomic Inbreeding in a Chinese Composite Pig Breed. ''Front Genet''. 2021; '''12''': 720081
Genome-wide association analysis of Mexican bread wheat landraces for resistance to yellow and stem rust. Description: Vikram, Prashant, et al. Genome-wide association analysis of Mexican bread wheat landraces for resistance to yellow and stem rust. ''PLoS One''. 2021; '''16''' (1):e0246015
Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome. Description: Cai, Ruikun, et al. Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome. ''Front Cell Dev Biol''. 2021; '''9''': 643644
Genome-Wide Association Mapping of Late Blight Tolerance Trait in Potato (Solanum tuberosum L.). Description: Wang, Fang, et al. Genome-Wide Association Mapping of Late Blight Tolerance Trait in Potato (Solanum tuberosum L.). ''Front Genet''. 2021; '''12''': 714575
Genome Wide Association Mapping of Root Traits in the Andean Genepool of Common Bean (Phaseolus vulgaris L.) Grown With and Without Aluminum Toxicity. Description: Ambachew, Daniel, et al. Genome Wide Association Mapping of Root Traits in the Andean Genepool of Common Bean (Phaseolus vulgaris L.) Grown With and Without Aluminum Toxicity. ''Front Plant Sci''. 2021; '''12''': 628687
Genome-Wide Association Studies for Growth Curves in Meat Rabbits Through the Single-Step Nonlinear Mixed Model. Description: Liao, Yonglan, et al. Genome-Wide Association Studies for Growth Curves in Meat Rabbits Through the Single-Step Nonlinear Mixed Model. ''Front Genet''. 2021; '''12''': 750939
Genome-Wide Association Studies for the Detection of Genetic Variants Associated With Daptomycin and Ceftaroline Resistance in Staphylococcus aureus. Description: Weber, Robert E, et al. Genome-Wide Association Studies for the Detection of Genetic Variants Associated With Daptomycin and Ceftaroline Resistance in Staphylococcus aureus. ''Front Microbiol''. 2021; '''12''': 639660
Genome-Wide Association Studies in Indian Buffalo Revealed Genomic Regions for Lactation and Fertility. Description: Vohra, Vikas, et al. Genome-Wide Association Studies in Indian Buffalo Revealed Genomic Regions for Lactation and Fertility. ''Front Genet''. 2021; '''12''': 696109
Genome-Wide Association Studies Reveal Neurological Genes for Dog Herding, Predation, Temperament, and Trainability Traits. Description: Shan, Shuwen, et al. Genome-Wide Association Studies Reveal Neurological Genes for Dog Herding, Predation, Temperament, and Trainability Traits. ''Front Vet Sci''. 2021; '''8''': 693290
Genome-Wide Association Studies Reveal Susceptibility Loci for Noninfectious Claw Lesions in Holstein Dairy Cattle. Description: Lai, Ellen, et al. Genome-Wide Association Studies Reveal Susceptibility Loci for Noninfectious Claw Lesions in Holstein Dairy Cattle. ''Front Genet''. 2021; '''12''': 657375
Genome-Wide Association Study for Body Length, Body Height, and Total Teat Number in Large White Pigs. Description: Hong, Yifeng, et al. Genome-Wide Association Study for Body Length, Body Height, and Total Teat Number in Large White Pigs. ''Front Genet''. 2021; '''12''': 650370
Genome-wide association study identifies 7q11.22 and 7q36.3 associated with noise-induced hearing loss among Chinese population. Description: Niu, Yuguang, et al. Genome-wide association study identifies 7q11.22 and 7q36.3 associated with noise-induced hearing loss among Chinese population. ''J Cell Mol Med''. 2021 Jan; '''25''' (1):411-420
Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. Description: Nishizawa, Daisuke, et al. Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. ''Mol Pain''. 2021 Jan-Dec; '''17''': 1744806921999924
Genome-Wide Association Study Identifies New Candidate Markers for Somatic Cells Score in a Local Dairy Sheep. Description: Sutera, Anna Maria, et al. Genome-Wide Association Study Identifies New Candidate Markers for Somatic Cells Score in a Local Dairy Sheep. ''Front Genet''. 2021; '''12''': 643531
Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients. Description: Weng, Saizheng, et al. Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients. ''PLoS One''. 2021; '''16''' (4):e0249997
Genome-Wide Association Study of Brown Rot (Monilinia spp.) Tolerance in Peach. Description: Fu, Wanfang, et al. Genome-Wide Association Study of Brown Rot (Monilinia spp.) Tolerance in Peach. ''Front Plant Sci''. 2021; '''12''': 635914
Genome-Wide Association Study of Growth Performance and Immune Response to Newcastle Disease Virus of Indigenous Chicken in Rwanda. Description: Habimana, Richard, et al. Genome-Wide Association Study of Growth Performance and Immune Response to Newcastle Disease Virus of Indigenous Chicken in Rwanda. ''Front Genet''. 2021; '''12''': 723980
Genome-Wide Association Study of Meat Quality Traits in a Three-Way Crossbred Commercial Pig Population. Description: Gao, Guangxiong, et al. Genome-Wide Association Study of Meat Quality Traits in a Three-Way Crossbred Commercial Pig Population. ''Front Genet''. 2021; '''12''': 614087
Genome-Wide Association Study of Motor Coordination. Description: Mountford, Hayley S, et al. Genome-Wide Association Study of Motor Coordination. ''Front Hum Neurosci''. 2021; '''15''': 669902
Genome-wide association study of pancreatic fat: The Multiethnic Cohort Adiposity Phenotype Study. Description: Streicher, Samantha A, et al. Genome-wide association study of pancreatic fat: The Multiethnic Cohort Adiposity Phenotype Study. ''PLoS One''. 2021; '''16''' (7):e0249615
Genome-Wide Association Study of Seed Folate Content in Common Bean. Description: Martin, C Joe, et al. Genome-Wide Association Study of Seed Folate Content in Common Bean. ''Front Plant Sci''. 2021; '''12''': 696423
Genome-wide association study of trypanosome prevalence and morphometric traits in purebred and crossbred Baoule cattle of Burkina Faso. Description: Yougbare, Bernadette, et al. Genome-wide association study of trypanosome prevalence and morphometric traits in purebred and crossbred Baoule cattle of Burkina Faso. ''PLoS One''. 2021; '''16''' (8):e0255089
Genome-Wide Association Study to Map Genomic Regions Related to the Initiation Time of Four Growth Stage Traits in Soybean. Description: Yan, Wenliang, et al. Genome-Wide Association Study to Map Genomic Regions Related to the Initiation Time of Four Growth Stage Traits in Soybean. ''Front Genet''. 2021; '''12''': 715529
Genome-Wide Association Study Using Whole-Genome Sequencing Identifies a Genomic Region on Chromosome 6 Associated With Comb Traits in Nandan-Yao Chicken. Description: Yang, Zhuliang, et al. Genome-Wide Association Study Using Whole-Genome Sequencing Identifies a Genomic Region on Chromosome 6 Associated With Comb Traits in Nandan-Yao Chicken. ''Front Genet''. 2021; '''12''': 682501
Genome-Wide Detection of Copy Number Variations and Their Association With Distinct Phenotypes in the World's Sheep. Description: Salehian-Dehkordi, Hosein, et al. Genome-Wide Detection of Copy Number Variations and Their Association With Distinct Phenotypes in the World's Sheep. ''Front Genet''. 2021; '''12''': 670582
Genome-Wide Detection of Runs of Homozygosity in Laiwu Pigs Revealed by Sequencing Data. Description: Fang, Yifei, et al. Genome-Wide Detection of Runs of Homozygosity in Laiwu Pigs Revealed by Sequencing Data. ''Front Genet''. 2021; '''12''': 629966
Genome-Wide Evidence for Complex Hybridization and Demographic History in a Group of Cycas From China. Description: Tao, Yueqi, et al. Genome-Wide Evidence for Complex Hybridization and Demographic History in a Group of Cycas From China. ''Front Genet''. 2021; '''12''': 717200
Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population. Description: Read, Robert W, et al. Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population. ''Front Genet''. 2021; '''12''': 639418
Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy. Description: Song, Meng, et al. Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy. ''Front Neurosci''. 2021; '''15''': 722592
Genome-Wide Scanning for Signatures of Selection Revealed the Putative Genomic Regions and Candidate Genes Controlling Milk Composition and Coat Color Traits in Sahiwal Cattle. Description: Illa, Satish Kumar, et al. Genome-Wide Scanning for Signatures of Selection Revealed the Putative Genomic Regions and Candidate Genes Controlling Milk Composition and Coat Color Traits in Sahiwal Cattle. ''Front Genet''. 2021; '''12''': 699422
Genomic Adaptive Evolution of Sand Rice (Agriophyllum squarrosum) and Its Implications for Desert Ecosystem Restoration. Description: Qian, Chaoju, et al. Genomic Adaptive Evolution of Sand Rice (Agriophyllum squarrosum) and Its Implications for Desert Ecosystem Restoration. ''Front Genet''. 2021; '''12''': 656061
Genomic Analyses Revealed the Genetic Difference and Potential Selection Genes of Growth Traits in Two Duroc Lines. Description: Li, Desen, et al. Genomic Analyses Revealed the Genetic Difference and Potential Selection Genes of Growth Traits in Two Duroc Lines. ''Front Vet Sci''. 2021; '''8''': 725367
Genomic analyses reveal the genetic basis of early maturity and identification of loci and candidate genes in upland cotton (Gossypium hirsutum L.). Description: Li, Libei, et al. Genomic analyses reveal the genetic basis of early maturity and identification of loci and candidate genes in upland cotton (Gossypium hirsutum L.). ''Plant Biotechnol J''. 2021 Jan; '''19''' (1):109-123
Genomic Analysis Reveals Human-Mediated Introgression From European Commercial Pigs to Henan Indigenous Pigs. Description: Wang, Kejun, et al. Genomic Analysis Reveals Human-Mediated Introgression From European Commercial Pigs to Henan Indigenous Pigs. ''Front Genet''. 2021; '''12''': 705803
Genomic comparisons of Persian Kurdish, Persian Arabian and American Thoroughbred horse populations. Description: Yousefi-Mashouf, Navid, et al. Genomic comparisons of Persian Kurdish, Persian Arabian and American Thoroughbred horse populations. ''PLoS One''. 2021; '''16''' (2):e0247123
Genomic consequences of apple improvement. Description: Migicovsky, Zoe, et al. Genomic consequences of apple improvement. ''Hortic Res''. 2021 Jan 1; '''8''' (1):9
Genomic diversity of 39 samples of Pyropia species grown in Japan. Description: Nagano, Yukio, et al. Genomic diversity of 39 samples of Pyropia species grown in Japan. ''PLoS One''. 2021; '''16''' (6):e0252207
Genomic Evidence That Governmentally Produced Cannabis sativa Poorly Represents Genetic Variation Available in State Markets. Description: Vergara, Daniela, et al. Genomic Evidence That Governmentally Produced Cannabis sativa Poorly Represents Genetic Variation Available in State Markets. ''Front Plant Sci''. 2021; '''12''': 668315
Genomic Insight Into the Population Admixture History of Tungusic-Speaking Manchu People in Northeast China. Description: Zhang, Xianpeng, et al. Genomic Insight Into the Population Admixture History of Tungusic-Speaking Manchu People in Northeast China. ''Front Genet''. 2021; '''12''': 754492
Genomic Insights Into the Admixture History of Mongolic- and Tungusic-Speaking Populations From Southwestern East Asia. Description: Chen, Jing, et al. Genomic Insights Into the Admixture History of Mongolic- and Tungusic-Speaking Populations From Southwestern East Asia. ''Front Genet''. 2021; '''12''': 685285
Genomic Loci Affecting Milk Production in German Black Pied Cattle (DSN). Description: Korkuc, Paula, et al. Genomic Loci Affecting Milk Production in German Black Pied Cattle (DSN). ''Front Genet''. 2021; '''12''': 640039
Genomic Prediction of Grain Yield in a Barley MAGIC Population Modeling Genotype per Environment Interaction. Description: Puglisi, Damiano, et al. Genomic Prediction of Grain Yield in a Barley MAGIC Population Modeling Genotype per Environment Interaction. ''Front Plant Sci''. 2021; '''12''': 664148
Genomic Prediction of Two Complex Orthopedic Traits Across Multiple Pure and Mixed Breed Dogs. Description: Jiang, Liping, et al. Genomic Prediction of Two Complex Orthopedic Traits Across Multiple Pure and Mixed Breed Dogs. ''Front Genet''. 2021; '''12''': 666740
Genomic Prediction Using LD-Based Haplotypes Inferred From High-Density Chip and Imputed Sequence Variants in Chinese Simmental Beef Cattle. Description: Li, Hongwei, et al. Genomic Prediction Using LD-Based Haplotypes Inferred From High-Density Chip and Imputed Sequence Variants in Chinese Simmental Beef Cattle. ''Front Genet''. 2021; '''12''': 665382
Genomic Regions Related to White/Black Tail Feather Color in Dwarf Chickens Identified Using a Genome-Wide Association Study. Description: Nie, Changsheng, et al. Genomic Regions Related to White/Black Tail Feather Color in Dwarf Chickens Identified Using a Genome-Wide Association Study. ''Front Genet''. 2021; '''12''': 566047
Genomic Selection and Genome-wide Association Study for Feed-Efficiency Traits in a Farmed Nile Tilapia (Oreochromis niloticus) Population. Description: Barria, Agustin, et al. Genomic Selection and Genome-wide Association Study for Feed-Efficiency Traits in a Farmed Nile Tilapia (Oreochromis niloticus) Population. ''Front Genet''. 2021; '''12''': 737906
Genotyping and Whole-Genome Resequencing of Welsh Sheep Breeds Reveal Candidate Genes and Variants for Adaptation to Local Environment and Socioeconomic Traits. Description: Sweet-Jones, James, et al. Genotyping and Whole-Genome Resequencing of Welsh Sheep Breeds Reveal Candidate Genes and Variants for Adaptation to Local Environment and Socioeconomic Traits. ''Front Genet''. 2021; '''12''': 612492
Genotyping-by-Sequencing of the regional Pacific abalone (Haliotis discus) genomes reveals population structures and patterns of gene flow. Description: Nam, Bo-Hye, et al. Genotyping-by-Sequencing of the regional Pacific abalone (Haliotis discus) genomes reveals population structures and patterns of gene flow. ''PLoS One''. 2021; '''16''' (4):e0247815
GWAS-Top Polymorphisms Associated With Late-Onset Alzheimer Disease in Brazil: Pointing Out Possible New Culprits Among Non-Coding RNAs. Description: Kretzschmar, Gabriela Canalli, et al. GWAS-Top Polymorphisms Associated With Late-Onset Alzheimer Disease in Brazil: Pointing Out Possible New Culprits Among Non-Coding RNAs. ''Front Mol Biosci''. 2021; '''8''': 632314
Haplotype Variations and Evolutionary Analysis of the Granule-Bound Starch Synthase I Gene in the Korean World Rice Collection. Description: Maung, Thant Zin, et al. Haplotype Variations and Evolutionary Analysis of the Granule-Bound Starch Synthase I Gene in the Korean World Rice Collection. ''Front Plant Sci''. 2021; '''12''': 707237
Heterotic Patterns of Temperate and Tropical Maize by Ear Photometry. Description: Tolley, Seth A, et al. Heterotic Patterns of Temperate and Tropical Maize by Ear Photometry. ''Front Plant Sci''. 2021; '''12''': 616975
HIF-1alpha Pulmonary Phenotype Wide Association Study Unveils a Link to Inflammatory Airway Conditions. Description: Kelchtermans, Jelte, et al. HIF-1alpha Pulmonary Phenotype Wide Association Study Unveils a Link to Inflammatory Airway Conditions. ''Front Genet''. 2021; '''12''': 756645
High levels of connectivity over large distances in the diadematid sea urchin Centrostephanus sylviae. Description: Veliz, David, et al. High levels of connectivity over large distances in the diadematid sea urchin Centrostephanus sylviae. ''PLoS One''. 2021; '''16''' (11):e0259595
Hopping or Jumping on the Cliffs: The Unusual Phylogeographical and Demographic Structure of an Extremely Narrow Endemic Mediterranean Plant. Description: Strumia, Sandro, et al. Hopping or Jumping on the Cliffs: The Unusual Phylogeographical and Demographic Structure of an Extremely Narrow Endemic Mediterranean Plant. ''Front Plant Sci''. 2021; '''12''': 737111
Human beta-Defensin 2 Mutations Are Associated With Asthma and Atopy in Children and Its Application Prevents Atopic Asthma in a Mouse Model. Description: Borchers, Natascha S, et al. Human beta-Defensin 2 Mutations Are Associated With Asthma and Atopy in Children and Its Application Prevents Atopic Asthma in a Mouse Model. ''Front Immunol''. 2021; '''12''': 636061
Human genomics of the humoral immune response against polyomaviruses. Description: Hodel, F, et al. Human genomics of the humoral immune response against polyomaviruses. ''Virus Evol''. 2021; '''7''' (2):veab058
Hypomethylation mediates genetic association with the major histocompatibility complex genes in Sjogren's syndrome. Description: Chi, Calvin, et al. Hypomethylation mediates genetic association with the major histocompatibility complex genes in Sjogren's syndrome. ''PLoS One''. 2021; '''16''' (4):e0248429
Identification of candidate genes on the basis of SNP by time-lagged heat stress interactions for milk production traits in German Holstein cattle. Description: Halli, Kathrin, et al. Identification of candidate genes on the basis of SNP by time-lagged heat stress interactions for milk production traits in German Holstein cattle. ''PLoS One''. 2021; '''16''' (10):e0258216
Identification of High-Confidence Structural Variants in Domesticated Rainbow Trout Using Whole-Genome Sequencing. Description: Liu, Sixin, et al. Identification of High-Confidence Structural Variants in Domesticated Rainbow Trout Using Whole-Genome Sequencing. ''Front Genet''. 2021; '''12''': 639355
Identification of New miRNA-mRNA Networks in the Development of Non-syndromic Cleft Lip With or Without Cleft Palate. Description: Fu, Chengyi, et al. Identification of New miRNA-mRNA Networks in the Development of Non-syndromic Cleft Lip With or Without Cleft Palate. ''Front Cell Dev Biol''. 2021; '''9''': 631057
Identification of Novel Quantitative Trait Nucleotides and Candidate Genes for Bacterial Wilt Resistance in Tobacco (Nicotiana tabacum L.) Using Genotyping-by-Sequencing and Multi-Locus Genome-Wide Association Studies. Description: Lai, Ruiqiang, et al. Identification of Novel Quantitative Trait Nucleotides and Candidate Genes for Bacterial Wilt Resistance in Tobacco (Nicotiana tabacum L.) Using Genotyping-by-Sequencing and Multi-Locus Genome-Wide Association Studies. ''Front Plant Sci''. 2021; '''12''': 744175
Identification of Potential Genomic Alterations and the circRNA-miRNA-mRNA Regulatory Network in Primary and Recurrent Synovial Sarcomas. Description: Yao, Qing, et al. Identification of Potential Genomic Alterations and the circRNA-miRNA-mRNA Regulatory Network in Primary and Recurrent Synovial Sarcomas. ''Front Mol Biosci''. 2021; '''8''': 707151
Identifying Imaging Genetics Biomarkers of Alzheimer's Disease by Multi-Task Sparse Canonical Correlation Analysis and Regression. Description: Ke, Fengchun, et al. Identifying Imaging Genetics Biomarkers of Alzheimer's Disease by Multi-Task Sparse Canonical Correlation Analysis and Regression. ''Front Genet''. 2021; '''12''': 706986
Immune-Related Genetic Overlap Between Regional Gray Matter Reductions and Psychiatric Symptoms in Adolescents, and Gene-Set Validation in a Translational Model. Description: Penninck, Lukas, et al. Immune-Related Genetic Overlap Between Regional Gray Matter Reductions and Psychiatric Symptoms in Adolescents, and Gene-Set Validation in a Translational Model. ''Front Syst Neurosci''. 2021; '''15''': 725413
Impact of COL6A4P2 gene polymorphisms on the risk of lung cancer: A case-control study. Description: Dang, Xiaodong, et al. Impact of COL6A4P2 gene polymorphisms on the risk of lung cancer: A case-control study. ''PLoS One''. 2021; '''16''' (5):e0252082
Impact of variant-level batch effects on identification of genetic risk factors in large sequencing studies. Description: Wickland, Daniel P, et al. Impact of variant-level batch effects on identification of genetic risk factors in large sequencing studies. ''PLoS One''. 2021; '''16''' (4):e0249305
Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study. Description: Peng, Linna, et al. Impacts of LOC105371267 Variants on Breast Cancer Susceptibility in Northern Chinese Han Females: A Population-Based Case-Control Study. ''J Oncol''. 2021; '''2021''': 4990695
Incomplete lineage sorting and ancient admixture, and speciation without morphological change in ghost-worm cryptic species. Description: Cerca, Jose, et al. Incomplete lineage sorting and ancient admixture, and speciation without morphological change in ghost-worm cryptic species. ''PeerJ''. 2021; '''9''': e10896
Inflamed Mind: Multiple Genetic Variants of IL6 Influence Suicide Risk Phenotypes in Interaction With Early and Recent Adversities in a Linkage Disequilibrium-Based Clumping Analysis. Description: Bokor, Janos, et al. Inflamed Mind: Multiple Genetic Variants of IL6 Influence Suicide Risk Phenotypes in Interaction With Early and Recent Adversities in a Linkage Disequilibrium-Based Clumping Analysis. ''Front Psychiatry''. 2021; '''12''': 746206
Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability. Description: Matzaraki, Vasiliki, et al. Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability. ''Front Immunol''. 2021; '''12''': 662171
Insight on the Genetics of Atrial Fibrillation in Puerto Rican Hispanics. Description: Gonzalez-Cordero, Ariel F, et al. Insight on the Genetics of Atrial Fibrillation in Puerto Rican Hispanics. ''Stroke Res Treat''. 2021; '''2021''': 8819896
Insights into the genetic architecture of the human face. Description: White, Julie D, et al. Insights into the genetic architecture of the human face. ''Nat Genet''. 2021 Jan; '''53''' (1):45-53
Integrated Bayesian Approaches Shed Light on the Dissemination Routes of the Eurasian Grapevine Germplasm. Description: Mercati, Francesco, et al. Integrated Bayesian Approaches Shed Light on the Dissemination Routes of the Eurasian Grapevine Germplasm. ''Front Plant Sci''. 2021; '''12''': 692661
Integrating Genome-Wide Association Analysis With Transcriptome Sequencing to Identify Candidate Genes Related to Blooming Time in Prunus mume. Description: Zhang, Man, et al. Integrating Genome-Wide Association Analysis With Transcriptome Sequencing to Identify Candidate Genes Related to Blooming Time in Prunus mume. ''Front Plant Sci''. 2021; '''12''': 690841
Integrative genomic phylogeography reveals signs of mitonuclear incompatibility in a natural hybrid goby population. Description: Hirase, Shotaro, et al. Integrative genomic phylogeography reveals signs of mitonuclear incompatibility in a natural hybrid goby population. ''Evolution''. 2021 Jan; '''75''' (1):176-194
Interaction of Alzheimer's Disease-Associated Genetic Risk with Indicators of Socioeconomic Position on Mild Cognitive Impairment in the Heinz Nixdorf Recall Study. Description: Frank, Mirjam, et al. Interaction of Alzheimer's Disease-Associated Genetic Risk with Indicators of Socioeconomic Position on Mild Cognitive Impairment in the Heinz Nixdorf Recall Study. ''J Alzheimers Dis''. 2021; '''82''' (4):1715-1725
Interaction of developmental factors and ordinary stressful life events on brain structure in adults. Description: Ringwald, Kai G, et al. Interaction of developmental factors and ordinary stressful life events on brain structure in adults. ''Neuroimage Clin''. 2021; '''30''': 102683
Interactions Between Adiponectin-Pathway Polymorphisms and Obesity on Postmenopausal Breast Cancer Risk Among African American Women: The WHI SHARe Study. Description: Nam, Gina E, et al. Interactions Between Adiponectin-Pathway Polymorphisms and Obesity on Postmenopausal Breast Cancer Risk Among African American Women: The WHI SHARe Study. ''Front Oncol''. 2021; '''11''': 698198
Interactive Association Between CYP2C9 rs2860905 Polymorphism and Atrial Fibrillation on Ischemic Stroke in Taiwan Biobank Participants. Description: Peng, Jui-Wen, et al. Interactive Association Between CYP2C9 rs2860905 Polymorphism and Atrial Fibrillation on Ischemic Stroke in Taiwan Biobank Participants. ''Pharmgenomics Pers Med''. 2021; '''14''': 1087-1092
Interactive Association Between Intronic Polymorphism (rs10506151) of the LRRK2 Gene and Type 2 Diabetes on Neurodegenerative Diseases. Description: Huang, Mei-Hsuen, et al. Interactive Association Between Intronic Polymorphism (rs10506151) of the LRRK2 Gene and Type 2 Diabetes on Neurodegenerative Diseases. ''Pharmgenomics Pers Med''. 2021; '''14''': 839-847
Intercellular Adhesion Molecule-1 Gene Polymorphisms and Susceptibility to Cervical Cancer in the Northern Chinese Han Population. Description: Feng, Yanan, et al. Intercellular Adhesion Molecule-1 Gene Polymorphisms and Susceptibility to Cervical Cancer in the Northern Chinese Han Population. ''Front Genet''. 2021; '''12''': 668539
Interspecific Sample Prioritization Can Improve QTL Detection With Tree-Based Predictive Models. Description: Shin, Min-Gyoung, et al. Interspecific Sample Prioritization Can Improve QTL Detection With Tree-Based Predictive Models. ''Front Genet''. 2021; '''12''': 684882
Investigating the Features of PDO Green Hams during Salting: Insights for New Markers and Genomic Regions in Commercial Hybrid Pigs. Description: Zappaterra, Martina, et al. Investigating the Features of PDO Green Hams during Salting: Insights for New Markers and Genomic Regions in Commercial Hybrid Pigs. ''Animals (Basel)''. 2021 Jan 1; '''11''' (1):
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction. Description: Demange, Perline A, et al. Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction. ''Nat Genet''. 2021 Jan; '''53''' (1):35-44
Investigation of Causal Effect of Type 2 Diabetes Mellitus on Lung Cancer: A Mendelian Randomization Study. Description: Hong, Tongtong, et al. Investigation of Causal Effect of Type 2 Diabetes Mellitus on Lung Cancer: A Mendelian Randomization Study. ''Front Genet''. 2021; '''12''': 673687
Joint Analysis of Genetic Correlation, Mendelian Randomization and Colocalization Highlights the Bi-Directional Causal Association Between Hypothyroidism and Primary Biliary Cirrhosis. Description: Wang, Yanjun, et al. Joint Analysis of Genetic Correlation, Mendelian Randomization and Colocalization Highlights the Bi-Directional Causal Association Between Hypothyroidism and Primary Biliary Cirrhosis. ''Front Genet''. 2021; '''12''': 753352
Joint Analysis of Genome-Wide Association Data Reveals No Genetic Correlations Between Low Back Pain and Neurodegenerative Diseases. Description: Wu, Pengfei, et al. Joint Analysis of Genome-Wide Association Data Reveals No Genetic Correlations Between Low Back Pain and Neurodegenerative Diseases. ''Front Genet''. 2021; '''12''': 744299
Keep Garfagnina alive. An integrated study on patterns of homozygosity, genomic inbreeding, admixture and breed traceability of the Italian Garfagnina goat breed. Description: Dadousis, Christos, et al. Keep Garfagnina alive. An integrated study on patterns of homozygosity, genomic inbreeding, admixture and breed traceability of the Italian Garfagnina goat breed. ''PLoS One''. 2021; '''16''' (1):e0232436
Large Multicohort Study Reveals a Prostate Cancer Susceptibility Allele at 5p15 Regulating TERT via Androgen Signaling-Orchestrated Chromatin Binding of E2F1 and MYC. Description: Dong, Xiaoming, et al. Large Multicohort Study Reveals a Prostate Cancer Susceptibility Allele at 5p15 Regulating TERT via Androgen Signaling-Orchestrated Chromatin Binding of E2F1 and MYC. ''Front Oncol''. 2021; '''11''': 754206
Leisure Activities, APOE epsilon4, and Cognitive Decline: A Longitudinal Cohort Study. Description: Zhang, Yun, et al. Leisure Activities, APOE epsilon4, and Cognitive Decline: A Longitudinal Cohort Study. ''Front Aging Neurosci''. 2021; '''13''': 736201
Leptin Gene and Leptin Receptor Gene Polymorphisms in Alcohol Use Disorder: Findings Related to Psychopathology. Description: Browning, Brittney D, et al. Leptin Gene and Leptin Receptor Gene Polymorphisms in Alcohol Use Disorder: Findings Related to Psychopathology. ''Front Psychiatry''. 2021; '''12''': 723059
Liver and Kidney Function Biomarkers, Blood Cell Traits and Risk of Severe COVID-19: A Mendelian Randomization Study. Description: Wang, Kai, et al. Liver and Kidney Function Biomarkers, Blood Cell Traits and Risk of Severe COVID-19: A Mendelian Randomization Study. ''Front Genet''. 2021; '''12''': 647303
Local Ancestry Adjusted Allelic Association Analysis Robustly Captures Tuberculosis Susceptibility Loci. Description: Swart, Yolandi, et al. Local Ancestry Adjusted Allelic Association Analysis Robustly Captures Tuberculosis Susceptibility Loci. ''Front Genet''. 2021; '''12''': 716558
Local Ancestry to Identify Selection in Response to Trypanosome Infection in Baoule x Zebu Crossbred Cattle in Burkina Faso. Description: Yougbare, Bernadette, et al. Local Ancestry to Identify Selection in Response to Trypanosome Infection in Baoule x Zebu Crossbred Cattle in Burkina Faso. ''Front Genet''. 2021; '''12''': 670390
LRRC3B Polymorphisms Contributed to Breast Cancer Susceptibility in Chinese Han Population. Description: Wang, Yuxin. LRRC3B Polymorphisms Contributed to Breast Cancer Susceptibility in Chinese Han Population. ''Front Oncol''. 2021; '''11''': 657168
LRRK2 Gene Variants Associated With a Higher Risk for Alcohol Dependence in Multiethnic Populations. Description: Oliveira, Pablo Rafael Silveira, et al. LRRK2 Gene Variants Associated With a Higher Risk for Alcohol Dependence in Multiethnic Populations. ''Front Psychiatry''. 2021; '''12''': 665257
LTA4H rs2660845 association with montelukast response in early and late-onset asthma. Description: Maroteau, Cyrielle, et al. LTA4H rs2660845 association with montelukast response in early and late-onset asthma. ''PLoS One''. 2021; '''16''' (9):e0257396
MEF2C Common Genetic Variation Is Associated With Different Aspects of Cognition in Non-Hispanic White and Caribbean Hispanic Non-demented Older Adults. Description: Sunderaraman, Preeti, et al. MEF2C Common Genetic Variation Is Associated With Different Aspects of Cognition in Non-Hispanic White and Caribbean Hispanic Non-demented Older Adults. ''Front Genet''. 2021; '''12''': 642327
Mendelian randomization study shows no causal effects of serum urate levels on the risk of MS. Description: Harroud, Adil, et al. Mendelian randomization study shows no causal effects of serum urate levels on the risk of MS. ''Neurol Neuroimmunol Neuroinflamm''. 2021 Jan; '''8''' (1):
MicroRNA Variants and HLA-miRNA Interactions are Novel Rheumatoid Arthritis Susceptibility Factors. Description: Guo, Shicheng, et al. MicroRNA Variants and HLA-miRNA Interactions are Novel Rheumatoid Arthritis Susceptibility Factors. ''Front Genet''. 2021; '''12''': 747274
Mitochondrial introgression by ancient admixture between two distant lacustrine fishes in Sulawesi Island. Description: Horoiwa, Mizuki, et al. Mitochondrial introgression by ancient admixture between two distant lacustrine fishes in Sulawesi Island. ''PLoS One''. 2021; '''16''' (6):e0245316
Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing. Description: Sandling, Johanna K, et al. Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing. ''Ann Rheum Dis''. 2021 Jan; '''80''' (1):109-117
Molecular Phylogenesis and Spatiotemporal Spread of SARS-CoV-2 in Southeast Asia. Description: Zhu, Mingjian, et al. Molecular Phylogenesis and Spatiotemporal Spread of SARS-CoV-2 in Southeast Asia. ''Front Public Health''. 2021; '''9''': 685315
Multidimensional Approach Assessing the Role of Interleukin 1 Beta in Mesial Temporal Lobe Epilepsy. Description: Santos, Renato O, et al. Multidimensional Approach Assessing the Role of Interleukin 1 Beta in Mesial Temporal Lobe Epilepsy. ''Front Neurol''. 2021; '''12''': 690847
Multi-Level Analyses of Genome-Wide Association Study to Reveal Significant Risk Genes and Pathways in Neuromyelitis Optica Spectrum Disorder. Description: Li, Ting, et al. Multi-Level Analyses of Genome-Wide Association Study to Reveal Significant Risk Genes and Pathways in Neuromyelitis Optica Spectrum Disorder. ''Front Genet''. 2021; '''12''': 690537
Multi-Locus Genome-Wide Association Studies Reveal Fruit Quality Hotspots in Peach Genome. Description: da Silva Linge, Cassia, et al. Multi-Locus Genome-Wide Association Studies Reveal Fruit Quality Hotspots in Peach Genome. ''Front Plant Sci''. 2021; '''12''': 644799
Multi-Locus Genome-Wide Association Study and Genomic Selection of Kernel Moisture Content at the Harvest Stage in Maize. Description: Zhou, Guangfei, et al. Multi-Locus Genome-Wide Association Study and Genomic Selection of Kernel Moisture Content at the Harvest Stage in Maize. ''Front Plant Sci''. 2021; '''12''': 697688
Multisite schizophrenia classification by integrating structural magnetic resonance imaging data with polygenic risk score. Description: Hu, Ke, et al. Multisite schizophrenia classification by integrating structural magnetic resonance imaging data with polygenic risk score. ''Neuroimage Clin''. 2021; '''32''': 102860
Multivariate genome-wide association study of leaf shape in a Populus deltoides and P. simonii F1 pedigree. Description: Yang, Wenguo, et al. Multivariate genome-wide association study of leaf shape in a Populus deltoides and P. simonii F1 pedigree. ''PLoS One''. 2021; '''16''' (10):e0259278
Mutational Landscape of the Proglucagon-Derived Peptides. Description: Lindquist, Peter, et al. Mutational Landscape of the Proglucagon-Derived Peptides. ''Front Endocrinol (Lausanne)''. 2021; '''12''': 698511
Novel Design of Imputation-Enabled SNP Arrays for Breeding and Research Applications Supporting Multi-Species Hybridization. Description: Keeble-Gagnere, Gabriel, et al. Novel Design of Imputation-Enabled SNP Arrays for Breeding and Research Applications Supporting Multi-Species Hybridization. ''Front Plant Sci''. 2021; '''12''': 756877
Novel Genomic Regions of Fusarium Wilt Resistance in Bottle Gourd [Lagenaria siceraria (Mol.) Standl.] Discovered in Genome-Wide Association Study. Description: Li, Yanwei, et al. Novel Genomic Regions of Fusarium Wilt Resistance in Bottle Gourd [Lagenaria siceraria (Mol.) Standl.] Discovered in Genome-Wide Association Study. ''Front Plant Sci''. 2021; '''12''': 650157
Novel QTLs for salinity tolerance revealed by genome-wide association studies of biomass, chlorophyll and tissue ion content in 176 rice landraces from Bangladesh. Description: Alam, Md Nafis Ul, et al. Novel QTLs for salinity tolerance revealed by genome-wide association studies of biomass, chlorophyll and tissue ion content in 176 rice landraces from Bangladesh. ''PLoS One''. 2021; '''16''' (11):e0259456
Optimization of Genomic Selection to Improve Disease Resistance in Two Marine Fishes, the European Sea Bass (Dicentrarchus labrax) and the Gilthead Sea Bream (Sparus aurata). Description: Griot, Ronan, et al. Optimization of Genomic Selection to Improve Disease Resistance in Two Marine Fishes, the European Sea Bass (Dicentrarchus labrax) and the Gilthead Sea Bream (Sparus aurata). ''Front Genet''. 2021; '''12''': 665920
OptM: estimating the optimal number of migration edges on population trees using Treemix. Description: Fitak, Robert R. OptM: estimating the optimal number of migration edges on population trees using Treemix. ''Biol Methods Protoc''. 2021; '''6''' (1):bpab017
P2RX7 gene variation mediates the effect of childhood adversity and recent stress on the severity of depressive symptoms. Description: Kristof, Zsuliet, et al. P2RX7 gene variation mediates the effect of childhood adversity and recent stress on the severity of depressive symptoms. ''PLoS One''. 2021; '''16''' (6):e0252766
Patterns of allele frequency differences among domestic cat breeds assessed by a 63K SNP array. Description: Alhaddad, Hasan, et al. Patterns of allele frequency differences among domestic cat breeds assessed by a 63K SNP array. ''PLoS One''. 2021; '''16''' (2):e0247092
PCSK9 genetic variants and cognitive abilities: a large-scale Mendelian randomization study. Description: Lyall, Donald M, et al. PCSK9 genetic variants and cognitive abilities: a large-scale Mendelian randomization study. ''Arch Med Sci''. 2021; '''17''' (1):241-244
Peopling History of the Tibetan Plateau and Multiple Waves of Admixture of Tibetans Inferred From Both Ancient and Modern Genome-Wide Data. Description: He, Guanglin, et al. Peopling History of the Tibetan Plateau and Multiple Waves of Admixture of Tibetans Inferred From Both Ancient and Modern Genome-Wide Data. ''Front Genet''. 2021; '''12''': 725243
PFN1 Gene Polymorphisms and the Bone Mineral Density Response to Alendronate Therapy in Postmenopausal Chinese Women with Low Bone Mass. Description: Zhao, Jiao, et al. PFN1 Gene Polymorphisms and the Bone Mineral Density Response to Alendronate Therapy in Postmenopausal Chinese Women with Low Bone Mass. ''Pharmgenomics Pers Med''. 2021; '''14''': 1669-1678
Pharmacogenetics of tenofovir and emtricitabine penetration into cerebrospinal fluid. Description: Decloedt, Eric H, et al. Pharmacogenetics of tenofovir and emtricitabine penetration into cerebrospinal fluid. ''South Afr J HIV Med''. 2021; '''22''' (1):1206
Phenotypic Evaluation and Genetic Analysis of Seedling Emergence in a Global Collection of Wheat Genotypes (Triticum aestivum L.) Under Limited Water Availability. Description: Francki, Michael G, et al. Phenotypic Evaluation and Genetic Analysis of Seedling Emergence in a Global Collection of Wheat Genotypes (Triticum aestivum L.) Under Limited Water Availability. ''Front Plant Sci''. 2021; '''12''': 796176
PLCE1 Polymorphisms Are Associated With Gastric Cancer Risk: The Changes in Protein Spatial Structure May Play a Potential Role. Description: Hu, Xi'e, et al. PLCE1 Polymorphisms Are Associated With Gastric Cancer Risk: The Changes in Protein Spatial Structure May Play a Potential Role. ''Front Genet''. 2021; '''12''': 714915
Polygenic Risk for Insomnia in Adolescents of Diverse Ancestry. Description: Ma, Tengfei, et al. Polygenic Risk for Insomnia in Adolescents of Diverse Ancestry. ''Front Genet''. 2021; '''12''': 654717
Polygenic Risk for Major Depression Interacts with Parental Criticism in Predicting Adolescent Depressive Symptom Development. Description: Nelemans, Stefanie A, et al. Polygenic Risk for Major Depression Interacts with Parental Criticism in Predicting Adolescent Depressive Symptom Development. ''J Youth Adolesc''. 2021 Jan; '''50''' (1):159-176
Polygenic risk scores for Alzheimer's disease are related to dementia risk in APOE varepsilon4 negatives. Description: Najar, Jenna, et al. Polygenic risk scores for Alzheimer's disease are related to dementia risk in APOE varepsilon4 negatives. ''Alzheimers Dement (Amst)''. 2021; '''13''' (1):e12142
Polygenic risk scores in cardiovascular risk prediction: A cohort study and modelling analyses. Description: Sun, Luanluan, et al. Polygenic risk scores in cardiovascular risk prediction: A cohort study and modelling analyses. ''PLoS Med''. 2021 Jan; '''18''' (1):e1003498
Polygenic risk score validation using Korean genomes of 265 early-onset acute myocardial infarction patients and 636 healthy controls. Description: Bhak, Youngjune, et al. Polygenic risk score validation using Korean genomes of 265 early-onset acute myocardial infarction patients and 636 healthy controls. ''PLoS One''. 2021; '''16''' (2):e0246538
Polygenic Scores and Parental Predictors: An Adult Height Study Based on the United Kingdom Biobank and the Framingham Heart Study. Description: You, Chong, et al. Polygenic Scores and Parental Predictors: An Adult Height Study Based on the United Kingdom Biobank and the Framingham Heart Study. ''Front Genet''. 2021; '''12''': 669441
Polygenic scores for smoking and educational attainment have independent influences on academic success and adjustment in adolescence and educational attainment in adulthood. Description: Hicks, Brian M, et al. Polygenic scores for smoking and educational attainment have independent influences on academic success and adjustment in adolescence and educational attainment in adulthood. ''PLoS One''. 2021; '''16''' (8):e0255348
Polymorphisms and Circulating Plasma Protein Levels of Immune Checkpoints (CTLA-4 and PD-1) Are Associated With Posner-Schlossman Syndrome in Southern Chinese. Description: Huang, Xiaosheng, et al. Polymorphisms and Circulating Plasma Protein Levels of Immune Checkpoints (CTLA-4 and PD-1) Are Associated With Posner-Schlossman Syndrome in Southern Chinese. ''Front Immunol''. 2021; '''12''': 607966
Polymorphisms and gene expression in the almond IGT family are not correlated to variability in growth habit in major commercial almond cultivars. Description: Montesinos, Alvaro, et al. Polymorphisms and gene expression in the almond IGT family are not correlated to variability in growth habit in major commercial almond cultivars. ''PLoS One''. 2021; '''16''' (10):e0252001
Polymorphisms in Genes of Lipid Metabolism Are Associated with Type 2 Diabetes Mellitus and Periodontitis, as Comorbidities, and with the Subjects' Periodontal, Glycemic, and Lipid Profiles. Description: Nicchio, Ingra G, et al. Polymorphisms in Genes of Lipid Metabolism Are Associated with Type 2 Diabetes Mellitus and Periodontitis, as Comorbidities, and with the Subjects' Periodontal, Glycemic, and Lipid Profiles. ''J Diabetes Res''. 2021; '''2021''': 1049307
Population Genomics of the "Arcanum" Species Group in Wild Tomatoes: Evidence for Separate Origins of Two Self-Compatible Lineages. Description: Florez-Rueda, Ana M, et al. Population Genomics of the "Arcanum" Species Group in Wild Tomatoes: Evidence for Separate Origins of Two Self-Compatible Lineages. ''Front Plant Sci''. 2021; '''12''': 624442
Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents. Description: Smajlagic, Dinka, et al. Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents. ''Eur J Hum Genet''. 2021 Jan; '''29''' (1):205-215
Population structure of indigenous inhabitants of Arabia. Description: Mineta, Katsuhiko, et al. Population structure of indigenous inhabitants of Arabia. ''PLoS Genet''. 2021 Jan; '''17''' (1):e1009210
Potential Impact of DPYD Variation on Fluoropyrimidine Drug Response in sub-Saharan African Populations. Description: da Rocha, Jorge E B, et al. Potential Impact of DPYD Variation on Fluoropyrimidine Drug Response in sub-Saharan African Populations. ''Front Genet''. 2021; '''12''': 626954
Potential Novel Genes for Late-Onset Alzheimer's Disease in East-Asian Descent Identified by APOE-Stratified Genome-Wide Association Study. Description: Kang, Sarang, et al. Potential Novel Genes for Late-Onset Alzheimer's Disease in East-Asian Descent Identified by APOE-Stratified Genome-Wide Association Study. ''J Alzheimers Dis''. 2021; '''82''' (4):1451-1460
Predicting Complex Traits and Exposures From Polygenic Scores and Blood and Buccal DNA Methylation Profiles. Description: Odintsova, Veronika V, et al. Predicting Complex Traits and Exposures From Polygenic Scores and Blood and Buccal DNA Methylation Profiles. ''Front Psychiatry''. 2021; '''12''': 688464
Predicting Fusarium Head Blight Resistance for Advanced Trials in a Soft Red Winter Wheat Breeding Program With Genomic Selection. Description: Larkin, Dylan L, et al. Predicting Fusarium Head Blight Resistance for Advanced Trials in a Soft Red Winter Wheat Breeding Program With Genomic Selection. ''Front Plant Sci''. 2021; '''12''': 715314
Pre-emptive Breeding Against Karnal Bunt Infection in Common Wheat: Combining Genomic and Agronomic Information to Identify Suitable Parents. Description: Emebiri, Livinus, et al. Pre-emptive Breeding Against Karnal Bunt Infection in Common Wheat: Combining Genomic and Agronomic Information to Identify Suitable Parents. ''Front Plant Sci''. 2021; '''12''': 675859
PRICKLE1 x FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Description: Liu, Dongjing, et al. PRICKLE1 x FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. ''Front Genet''. 2021; '''12''': 674642
Programmed Death Ligand 2 Gene Polymorphisms Are Associated With Lung Adenocarcinoma Risk in Female Never-Smokers. Description: Liang, Sheng-Kai, et al. Programmed Death Ligand 2 Gene Polymorphisms Are Associated With Lung Adenocarcinoma Risk in Female Never-Smokers. ''Front Oncol''. 2021; '''11''': 753788
QTL Mapping for Leaf Area of Tea Plants (Camellia sinensis) Based on a High-Quality Genetic Map Constructed by Whole Genome Resequencing. Description: An, Yanlin, et al. QTL Mapping for Leaf Area of Tea Plants (Camellia sinensis) Based on a High-Quality Genetic Map Constructed by Whole Genome Resequencing. ''Front Plant Sci''. 2021; '''12''': 705285
RAB40C Gene Polymorphisms Were Associated with Alcohol-Induced Osteonecrosis of the Femoral Head. Description: Liu, Chang, et al. RAB40C Gene Polymorphisms Were Associated with Alcohol-Induced Osteonecrosis of the Femoral Head. ''Int J Gen Med''. 2021; '''14''': 3583-3591
Recessive/dominant model: Alternative choice in case-control-based genome-wide association studies. Description: Liu, Han-Ming, et al. Recessive/dominant model: Alternative choice in case-control-based genome-wide association studies. ''PLoS One''. 2021; '''16''' (7):e0254947
Relationship Between KCNQ1 Polymorphism and Type 2 Diabetes Risk in Northwestern China. Description: Xu, Jing, et al. Relationship Between KCNQ1 Polymorphism and Type 2 Diabetes Risk in Northwestern China. ''Pharmgenomics Pers Med''. 2021; '''14''': 1731-1751
Replication of European hypertension associations in a case-control study of 9,534 African Americans. Description: Kaur, Harpreet, et al. Replication of European hypertension associations in a case-control study of 9,534 African Americans. ''PLoS One''. 2021; '''16''' (11):e0259962
Risk and Protective Factors of Lifetime Cocaine-Associated Chest Pain. Description: Clergue-Duval, Virgile, et al. Risk and Protective Factors of Lifetime Cocaine-Associated Chest Pain. ''Front Psychiatry''. 2021; '''12''': 704276
Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG Endophenotypes. Description: Macedo, Ana, et al. Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG Endophenotypes. ''J Alzheimers Dis''. 2021; '''80''' (1):209-223
R-locus for roaned coat is associated with a tandem duplication in an intronic region of USH2A in dogs and also contributes to Dalmatian spotting. Description: Kawakami, Takeshi, et al. R-locus for roaned coat is associated with a tandem duplication in an intronic region of USH2A in dogs and also contributes to Dalmatian spotting. ''PLoS One''. 2021; '''16''' (3):e0248233
Robust Performance of Potentially Functional SNPs in Machine Learning Models for the Prediction of Atorvastatin-Induced Myalgia. Description: Ooi, Brandon N S, et al. Robust Performance of Potentially Functional SNPs in Machine Learning Models for the Prediction of Atorvastatin-Induced Myalgia. ''Front Pharmacol''. 2021; '''12''': 605764
Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis. Description: Pagliari, Maria Teresa, et al. Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis. ''PLoS One''. 2021; '''16''' (10):e0258675
Search for Selection Signatures Related to Trypanosomosis Tolerance in African Goats. Description: Serranito, Bruno, et al. Search for Selection Signatures Related to Trypanosomosis Tolerance in African Goats. ''Front Genet''. 2021; '''12''': 715732
Selective Sweeps Uncovering the Genetic Basis of Horn and Adaptability Traits on Fine-Wool Sheep in China. Description: Guo, Tingting, et al. Selective Sweeps Uncovering the Genetic Basis of Horn and Adaptability Traits on Fine-Wool Sheep in China. ''Front Genet''. 2021; '''12''': 604235
Shared genomic segment analysis in a large high-risk chronic lymphocytic leukemia pedigree implicates CXCR4 in inherited risk. Description: Feusier, Julie E, et al. Shared genomic segment analysis in a large high-risk chronic lymphocytic leukemia pedigree implicates CXCR4 in inherited risk. ''J Transl Genet Genom''. 2021; '''5''': 189-199
Significant East Asian Affinity of the Sichuan Hui Genomic Structure Suggests the Predominance of the Cultural Diffusion Model in the Genetic Formation Process. Description: Liu, Yan, et al. Significant East Asian Affinity of the Sichuan Hui Genomic Structure Suggests the Predominance of the Cultural Diffusion Model in the Genetic Formation Process. ''Front Genet''. 2021; '''12''': 626710
Similar Genetic Architecture of Alzheimer's Disease and Differential APOE Effect Between Sexes. Description: Wang, Hao, et al. Similar Genetic Architecture of Alzheimer's Disease and Differential APOE Effect Between Sexes. ''Front Aging Neurosci''. 2021; '''13''': 674318
Single-cell molecular profiling of all three components of the HPA axis reveals adrenal ABCB1 as a regulator of stress adaptation. Description: Lopez, Juan Pablo, et al. Single-cell molecular profiling of all three components of the HPA axis reveals adrenal ABCB1 as a regulator of stress adaptation. ''Sci Adv''. 2021 Jan; '''7''' (5):
Single-Nucleotide Polymorphisms in the 3' Untranslated Region of CORIN Associated With Cardiovascular Diseases in a Chinese Han Population: A Case-Control Study. Description: Zhao, Yichang, et al. Single-Nucleotide Polymorphisms in the 3' Untranslated Region of CORIN Associated With Cardiovascular Diseases in a Chinese Han Population: A Case-Control Study. ''Front Cardiovasc Med''. 2021; '''8''': 625072
Single-Nucleotide Polymorphisms Related to Leprosy Risk and Clinical Phenotypes Among Chinese Population. Description: Long, Si-Yu, et al. Single-Nucleotide Polymorphisms Related to Leprosy Risk and Clinical Phenotypes Among Chinese Population. ''Pharmgenomics Pers Med''. 2021; '''14''': 813-821
SNAP-25 Single Nucleotide Polymorphisms, Brain Morphology and Intelligence in Children With Borderline Intellectual Functioning: A Mediation Analysis. Description: Blasi, Valeria, et al. SNAP-25 Single Nucleotide Polymorphisms, Brain Morphology and Intelligence in Children With Borderline Intellectual Functioning: A Mediation Analysis. ''Front Neurosci''. 2021; '''15''': 715048
SNP-Based Genotyping Provides Insight Into the West Asian Origin of Russian Local Goats. Description: Deniskova, Tatiana E, et al. SNP-Based Genotyping Provides Insight Into the West Asian Origin of Russian Local Goats. ''Front Genet''. 2021; '''12''': 708740
Sortilin as a Biomarker for Cardiovascular Disease Revisited. Description: Moller, Peter Loof, et al. Sortilin as a Biomarker for Cardiovascular Disease Revisited. ''Front Cardiovasc Med''. 2021; '''8''': 652584
Strong Genetic Structure Observed in Primulina danxiaensis, a Small Herb Endemic to Mount Danxia With Extremely Small Populations. Description: Chen, Sufang, et al. Strong Genetic Structure Observed in Primulina danxiaensis, a Small Herb Endemic to Mount Danxia With Extremely Small Populations. ''Front Genet''. 2021; '''12''': 722149
System-Level Analysis of Alzheimer's Disease Prioritizes Candidate Genes for Neurodegeneration. Description: Brabec, Jeffrey L, et al. System-Level Analysis of Alzheimer's Disease Prioritizes Candidate Genes for Neurodegeneration. ''Front Genet''. 2021; '''12''': 625246
Systems Biology Guided Gene Enrichment Approaches Improve Prediction of Chronic Post-surgical Pain After Spine Fusion. Description: Chidambaran, Vidya, et al. Systems Biology Guided Gene Enrichment Approaches Improve Prediction of Chronic Post-surgical Pain After Spine Fusion. ''Front Genet''. 2021; '''12''': 594250
Targeted capture sequencing identifies genetic variations of GRK4 and RDH8 in Han Chinese with essential hypertension in Xinjiang. Description: Jiang, Wenxi, et al. Targeted capture sequencing identifies genetic variations of GRK4 and RDH8 in Han Chinese with essential hypertension in Xinjiang. ''PLoS One''. 2021; '''16''' (7):e0255311
Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region. Description: Ramensky, Vasily E, et al. Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region. ''Front Genet''. 2021; '''12''': 709419
The ADCYAP1R1 Gene Is Correlated With Posttraumatic Stress Disorder Symptoms Through Diverse Epistases in a Traumatized Chinese Population. Description: Wang, Li, et al. The ADCYAP1R1 Gene Is Correlated With Posttraumatic Stress Disorder Symptoms Through Diverse Epistases in a Traumatized Chinese Population. ''Front Psychiatry''. 2021; '''12''': 665599
The Association Between Single-Nucleotide Polymorphisms of Co-Stimulatory Genes Within Non-HLA Region and the Prognosis of Leukemia Patients With Hematopoietic Stem Cell Transplantation. Description: Chen, Ding-Ping, et al. The Association Between Single-Nucleotide Polymorphisms of Co-Stimulatory Genes Within Non-HLA Region and the Prognosis of Leukemia Patients With Hematopoietic Stem Cell Transplantation. ''Front Immunol''. 2021; '''12''': 730507
The Association between the rs312457 Genotype of the SLC16a13 Gene and Diabetes Mellitus in a Chinese Population. Description: Zheng, Hui, et al. The Association between the rs312457 Genotype of the SLC16a13 Gene and Diabetes Mellitus in a Chinese Population. ''Comput Math Methods Med''. 2021; '''2021''': 9918055
The Effects of Genetic Background for Diurnal Preference on Sleep Development in Early Childhood. Description: Morales-Munoz, Isabel, et al. The Effects of Genetic Background for Diurnal Preference on Sleep Development in Early Childhood. ''Nat Sci Sleep''. 2021; '''13''': 219-228
The genetic and epigenetic profile of serum S100beta in the Lothian Birth Cohort 1936 and its relationship to Alzheimer's disease. Description: A Gadd, Danni, et al. The genetic and epigenetic profile of serum S100beta in the Lothian Birth Cohort 1936 and its relationship to Alzheimer's disease. ''Wellcome Open Res''. 2021; '''6''': 306
The GWAS Analysis of Body Size and Population Verification of Related SNPs in Hu Sheep. Description: Jiang, Junfang, et al. The GWAS Analysis of Body Size and Population Verification of Related SNPs in Hu Sheep. ''Front Genet''. 2021; '''12''': 642552
The Higher Prevalence of Venous Thromboembolism in the Hungarian Roma Population Could Be Due to Elevated Genetic Risk and Stronger Gene-Environmental Interactions. Description: Natae, Shewaye Fituma, et al. The Higher Prevalence of Venous Thromboembolism in the Hungarian Roma Population Could Be Due to Elevated Genetic Risk and Stronger Gene-Environmental Interactions. ''Front Cardiovasc Med''. 2021; '''8''': 647416
The Impact of Ethnicity and Genetic Ancestry on Disease Prevalence and Risk in Colombia. Description: Chande, Aroon T, et al. The Impact of Ethnicity and Genetic Ancestry on Disease Prevalence and Risk in Colombia. ''Front Genet''. 2021; '''12''': 690366
The Relevance of Regenerating Gene 1a Polymorphisms to Radiation Sensitivity and Survival of Nasopharyngeal Carcinoma Receiving Radiotherapy in a Southern Chinese Population. Description: Xing, Hai-Jie, et al. The Relevance of Regenerating Gene 1a Polymorphisms to Radiation Sensitivity and Survival of Nasopharyngeal Carcinoma Receiving Radiotherapy in a Southern Chinese Population. ''Pharmgenomics Pers Med''. 2021; '''14''': 1403-1413
Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey. Description: Zhao, Changheng, et al. Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey. ''Front Genet''. 2021; '''12''': 728764
Tracing the Distribution of European Lactase Persistence Genotypes Along the Americas. Description: Guimaraes Alves, Ana Cecilia, et al. Tracing the Distribution of European Lactase Persistence Genotypes Along the Americas. ''Front Genet''. 2021; '''12''': 671079
UGT1A1 rs4148323 A Allele is Associated With Increased 2-Hydroxy Atorvastatin Formation and Higher Death Risk in Chinese Patients With Coronary Artery Disease. Description: Lei, He-Ping, et al. UGT1A1 rs4148323 A Allele is Associated With Increased 2-Hydroxy Atorvastatin Formation and Higher Death Risk in Chinese Patients With Coronary Artery Disease. ''Front Pharmacol''. 2021; '''12''': 586973
UKB.COVID19: an R package for UK Biobank COVID-19 data processing and analysis. Description: Wang, Longfei, et al. UKB.COVID19: an R package for UK Biobank COVID-19 data processing and analysis. ''F1000Res''. 2021; '''10''': 830
Understanding interactions between risk factors, and assessing the utility of the additive and multiplicative models through simulations. Description: Diaz-Gallo, Lina-Marcela, et al. Understanding interactions between risk factors, and assessing the utility of the additive and multiplicative models through simulations. ''PLoS One''. 2021; '''16''' (4):e0250282
Urbanization reduces gene flow but not genetic diversity of stream salamander populations in the New York City metropolitan area. Description: Fusco, Nicole A, et al. Urbanization reduces gene flow but not genetic diversity of stream salamander populations in the New York City metropolitan area. ''Evol Appl''. 2021 Jan; '''14''' (1):99-116
Use of Deep-Learning Genomics to Discriminate Healthy Individuals from Those with Alzheimer's Disease or Mild Cognitive Impairment. Description: Li, Lanlan, et al. Use of Deep-Learning Genomics to Discriminate Healthy Individuals from Those with Alzheimer's Disease or Mild Cognitive Impairment. ''Behav Neurol''. 2021; '''2021''': 3359103
Using a Two-Sample Mendelian Randomization Method in Assessing the Causal Relationships Between Human Blood Metabolites and Heart Failure. Description: Wang, Zixian, et al. Using a Two-Sample Mendelian Randomization Method in Assessing the Causal Relationships Between Human Blood Metabolites and Heart Failure. ''Front Cardiovasc Med''. 2021; '''8''': 695480
Using genetic relatedness to understand heterogeneous distributions of urban rat-associated pathogens. Description: Byers, Kaylee A, et al. Using genetic relatedness to understand heterogeneous distributions of urban rat-associated pathogens. ''Evol Appl''. 2021 Jan; '''14''' (1):198-209
Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a. Description: Lin, Shang-Kuan, et al. Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a. ''Virus Evol''. 2021; '''7''' (2):veab065
Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility. Description: van Blokland, Irene V, et al. Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility. ''PLoS One''. 2021; '''16''' (8):e0255402
Variable Effects of PD-Risk Associated SNPs and Variants in Parkinsonism-Associated Genes on Disease Phenotype in a Community-Based Cohort. Description: Markopoulou, Katerina, et al. Variable Effects of PD-Risk Associated SNPs and Variants in Parkinsonism-Associated Genes on Disease Phenotype in a Community-Based Cohort. ''Front Neurol''. 2021; '''12''': 662278
Variation of Genomic Sites Associated with Severe Covid-19 Across Populations: Global and National Patterns. Description: Balanovsky, Oleg, et al. Variation of Genomic Sites Associated with Severe Covid-19 Across Populations: Global and National Patterns. ''Pharmgenomics Pers Med''. 2021; '''14''': 1391-1402
Very early onset eosinophilic esophagitis is common, responds to standard therapy, and demonstrates enrichment for CAPN14 genetic variants. Description: Lyles, John L, et al. Very early onset eosinophilic esophagitis is common, responds to standard therapy, and demonstrates enrichment for CAPN14 genetic variants. ''J Allergy Clin Immunol''. 2021 Jan; '''147''' (1):244-254.e6
Vicariance followed by secondary gene flow in a young gazelle species complex. Description: Garcia-Erill, Genis, et al. Vicariance followed by secondary gene flow in a young gazelle species complex. ''Mol Ecol''. 2021 Jan; '''30''' (2):528-544
Weak Association Between the Glutamate Decarboxylase 1 Gene (GAD1) and Schizophrenia in Han Chinese Population. Description: Zhang, Luwen, et al. Weak Association Between the Glutamate Decarboxylase 1 Gene (GAD1) and Schizophrenia in Han Chinese Population. ''Front Neurosci''. 2021; '''15''': 677153
Whole-Blood Mitochondrial DNA Copies Are Associated With the Prognosis of Acute Respiratory Distress Syndrome After Sepsis. Description: Hernandez-Beeftink, Tamara, et al. Whole-Blood Mitochondrial DNA Copies Are Associated With the Prognosis of Acute Respiratory Distress Syndrome After Sepsis. ''Front Immunol''. 2021; '''12''': 737369
Whole-Exome Sequencing Analysis of Human Semen Quality in Russian Multiethnic Population. Description: Kolmykov, Semyon, et al. Whole-Exome Sequencing Analysis of Human Semen Quality in Russian Multiethnic Population. ''Front Genet''. 2021; '''12''': 662846
Whole-Genome Diversification Analysis of the Hornbeam Species Reveals Speciation and Adaptation Among Closely Related Species. Description: Zheng, Zeyu, et al. Whole-Genome Diversification Analysis of the Hornbeam Species Reveals Speciation and Adaptation Among Closely Related Species. ''Front Plant Sci''. 2021; '''12''': 581704
Whole-Genome Resequencing to Study Brucellosis Susceptibility in Sheep. Description: Li, Xiaolong, et al. Whole-Genome Resequencing to Study Brucellosis Susceptibility in Sheep. ''Front Genet''. 2021; '''12''': 653927
Whole-Genome SNP Characterisation Provides Insight for Sustainable Use of Local South African Livestock Populations. Description: van Marle-Koster, Este, et al. Whole-Genome SNP Characterisation Provides Insight for Sustainable Use of Local South African Livestock Populations. ''Front Genet''. 2021; '''12''': 714194
Whole genome variation in 27 Mexican indigenous populations, demographic and biomedical insights. Description: Aguilar-Ordonez, Israel, et al. Whole genome variation in 27 Mexican indigenous populations, demographic and biomedical insights. ''PLoS One''. 2021; '''16''' (4):e0249773
Widespread genetic connectivity of feral pigeons across the Northeastern megacity. Description: Carlen, Elizabeth, et al. Widespread genetic connectivity of feral pigeons across the Northeastern megacity. ''Evol Appl''. 2021 Jan; '''14''' (1):150-162
WNT3A rs752107(C > T) Polymorphism Is Associated With an Increased Risk of Essential Hypertension and Related Cardiovascular Diseases. Description: Ren, Huan, et al. WNT3A rs752107(C > T) Polymorphism Is Associated With an Increased Risk of Essential Hypertension and Related Cardiovascular Diseases. ''Front Cardiovasc Med''. 2021; '''8''': 675222
WSB1 and IL21R Genetic Variants Are Involved in Th2 Immune Responses to Ascaris lumbricoides. Description: Carneiro, Valdirene Leao, et al. WSB1 and IL21R Genetic Variants Are Involved in Th2 Immune Responses to Ascaris lumbricoides. ''Front Immunol''. 2021; '''12''': 622051
A publicly available repository of ROH islands reveals signatures of selection in different livestock and pet species. Description: Gorssen, Wim, et al. A publicly available repository of ROH islands reveals signatures of selection in different livestock and pet species. ''Genet Sel Evol''. 2021 Jan 4; '''53''' (1):2
Association of Serum Mannose With Acute Respiratory Distress Syndrome Risk and Survival. Description: Wei, Yongyue, et al. Association of Serum Mannose With Acute Respiratory Distress Syndrome Risk and Survival. ''JAMA Netw Open''. 2021 Jan 4; '''4''' (1):e2034569
Common health conditions in childhood and adolescence, school absence, and educational attainment: Mendelian randomization study. Description: Hughes, Amanda, et al. Common health conditions in childhood and adolescence, school absence, and educational attainment: Mendelian randomization study. ''NPJ Sci Learn''. 2021 Jan 4; '''6''' (1):1
Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis. Description: Thakur, Nanamika, et al. Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis. ''BMC Med Genomics''. 2021 Jan 4; '''14''' (1):1
Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual. Description: Cousminer, Diana L, et al. Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual. ''Genome Biol''. 2021 Jan 4; '''22''' (1):1
Rapid parallel adaptation despite gene flow in silent crickets. Description: Zhang, Xiao, et al. Rapid parallel adaptation despite gene flow in silent crickets. ''Nat Commun''. 2021 Jan 4; '''12''' (1):50
Spatiotemporal Genetic Diversity of Lions Reveals the Influence of Habitat Fragmentation across Africa. Description: Curry, Caitlin J, et al. Spatiotemporal Genetic Diversity of Lions Reveals the Influence of Habitat Fragmentation across Africa. ''Mol Biol Evol''. 2021 Jan 4; '''38''' (1):48-57
The patterns of deleterious mutations during the domestication of soybean. Description: Kim, Myung-Shin, et al. The patterns of deleterious mutations during the domestication of soybean. ''Nat Commun''. 2021 Jan 4; '''12''' (1):97
Accuracy of Imputation of Microsatellite Markers from a 50K SNP Chip in Spanish Assaf Sheep. Description: Marina, Hector, et al. Accuracy of Imputation of Microsatellite Markers from a 50K SNP Chip in Spanish Assaf Sheep. ''Animals (Basel)''. 2021 Jan 5; '''11''' (1):
Ancient DNA from Guam and the peopling of the Pacific. Description: Pugach, Irina, et al. Ancient DNA from Guam and the peopling of the Pacific. ''Proc Natl Acad Sci U S A''. 2021 Jan 5; '''118''' (1):
Heritable Gut Microbiome Associated with Salmonella enterica Serovar Pullorum Infection in Chickens. Description: Ding, Jinmei, et al. Heritable Gut Microbiome Associated with Salmonella enterica Serovar Pullorum Infection in Chickens. ''mSystems''. 2021 Jan 5; '''6''' (1):
Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer. Description: Usui, Yoshiaki, et al. Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer. ''J Epidemiol''. 2021 Jan 5; '''31''' (1):12-20
Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity. Description: Ostkamp, Patrick, et al. Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity. ''Proc Natl Acad Sci U S A''. 2021 Jan 5; '''118''' (1):
The evolution of skin pigmentation-associated variation in West Eurasia. Description: Ju, Dan, et al. The evolution of skin pigmentation-associated variation in West Eurasia. ''Proc Natl Acad Sci U S A''. 2021 Jan 5; '''118''' (1):
A meta-analysis of genome-wide association studies for average daily gain and lean meat percentage in two Duroc pig populations. Description: Zhou, Shenping, et al. A meta-analysis of genome-wide association studies for average daily gain and lean meat percentage in two Duroc pig populations. ''BMC Genomics''. 2021 Jan 6; '''22''' (1):12
Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Description: Liang, Xiao, et al. Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. ''Mol Brain''. 2021 Jan 6; '''14''' (1):3
Genome-wide association study reveals a patatin-like lipase relating to the reduction of seed oil content in Brassica napus. Description: Wang, Haoyi, et al. Genome-wide association study reveals a patatin-like lipase relating to the reduction of seed oil content in Brassica napus. ''BMC Plant Biol''. 2021 Jan 6; '''21''' (1):6
Germline variants are associated with increased primary melanoma tumor thickness at diagnosis. Description: Mangantig, Ernest, et al. Germline variants are associated with increased primary melanoma tumor thickness at diagnosis. ''Hum Mol Genet''. 2021 Jan 6; '''29''' (21):3578-3587
Multi-Omics Approach Reveals miR-SNPs Affecting Muscle Fatty Acids Profile in Nelore Cattle. Description: Cardoso, Taina Figueiredo, et al. Multi-Omics Approach Reveals miR-SNPs Affecting Muscle Fatty Acids Profile in Nelore Cattle. ''Genes (Basel)''. 2021 Jan 6; '''12''' (1):
Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype. Description: Qaiser, Farah, et al. Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype. ''Orphanet J Rare Dis''. 2021 Jan 6; '''16''' (1):6
Runs of homozygosity analysis of South African sheep breeds from various production systems investigated using OvineSNP50k data. Description: Dzomba, E F, et al. Runs of homozygosity analysis of South African sheep breeds from various production systems investigated using OvineSNP50k data. ''BMC Genomics''. 2021 Jan 6; '''22''' (1):7
A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank Cohort. Description: Younes, Nadin, et al. A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank Cohort. ''J Pers Med''. 2021 Jan 7; '''11''' (1):
Combination of Genome-Wide Polymorphisms and Copy Number Variations of Pharmacogenes in Koreans. Description: Han, Nayoung, et al. Combination of Genome-Wide Polymorphisms and Copy Number Variations of Pharmacogenes in Koreans. ''J Pers Med''. 2021 Jan 7; '''11''' (1):
Distinguishing pedigree relationships via multi-way identity by descent sharing and sex-specific genetic maps. Description: Qiao, Ying, et al. Distinguishing pedigree relationships via multi-way identity by descent sharing and sex-specific genetic maps. ''Am J Hum Genet''. 2021 Jan 7; '''108''' (1):68-83
Genetic pre-screening for glaucoma in population-based epidemiology: protocol for a double-blind prospective screening study within Lifelines (EyeLife). Description: Neustaeter, Anna, et al. Genetic pre-screening for glaucoma in population-based epidemiology: protocol for a double-blind prospective screening study within Lifelines (EyeLife). ''BMC Ophthalmol''. 2021 Jan 7; '''21''' (1):18
Genome-wide association study of yield and related traits in common wheat under salt-stress conditions. Description: Hu, Pan, et al. Genome-wide association study of yield and related traits in common wheat under salt-stress conditions. ''BMC Plant Biol''. 2021 Jan 7; '''21''' (1):27
Genomic imbalances in the placenta are associated with poor fetal growth. Description: Del Gobbo, Giulia F, et al. Genomic imbalances in the placenta are associated with poor fetal growth. ''Mol Med''. 2021 Jan 7; '''27''' (1):3
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. Description: Ortiz-Fernandez, Lourdes, et al. Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. ''Am J Hum Genet''. 2021 Jan 7; '''108''' (1):84-99
Rare and de novo coding variants in chromodomain genes in Chiari I malformation. Description: Sadler, Brooke, et al. Rare and de novo coding variants in chromodomain genes in Chiari I malformation. ''Am J Hum Genet''. 2021 Jan 7; '''108''' (1):100-114
Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D. Description: Mickelson, James R, et al. Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D. ''Skelet Muscle''. 2021 Jan 7; '''11''' (1):2
Testing Sex-Biased Admixture Origin of Macaque Species Using Autosomal and X-Chromosomal Genomic Sequences. Description: Osada, Naoki, et al. Testing Sex-Biased Admixture Origin of Macaque Species Using Autosomal and X-Chromosomal Genomic Sequences. ''Genome Biol Evol''. 2021 Jan 7; '''13''' (1):
A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa. Description: Romdhane, Lilia, et al. A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa. ''NPJ Genom Med''. 2021 Jan 8; '''6''' (1):3
Association between polygenic risk score of Alzheimer's disease and plasma phosphorylated tau in individuals from the Alzheimer's Disease Neuroimaging Initiative. Description: Zettergren, Anna, et al. Association between polygenic risk score of Alzheimer's disease and plasma phosphorylated tau in individuals from the Alzheimer's Disease Neuroimaging Initiative. ''Alzheimers Res Ther''. 2021 Jan 8; '''13''' (1):17
ATACdb: a comprehensive human chromatin accessibility database. Description: Wang, Fan, et al. ATACdb: a comprehensive human chromatin accessibility database. ''Nucleic Acids Res''. 2021 Jan 8; '''49''' (D1):D55-D64
RMVar: an updated database of functional variants involved in RNA modifications. Description: Luo, Xiaotong, et al. RMVar: an updated database of functional variants involved in RNA modifications. ''Nucleic Acids Res''. 2021 Jan 8; '''49''' (D1):D1405-D1412
SLE non-coding genetic risk variant determines the epigenetic dysfunction of an immune cell specific enhancer that controls disease-critical microRNA expression. Description: Hou, Guojun, et al. SLE non-coding genetic risk variant determines the epigenetic dysfunction of an immune cell specific enhancer that controls disease-critical microRNA expression. ''Nat Commun''. 2021 Jan 8; '''12''' (1):135
The minor C-allele of the rs2014355 variant in ACADS gene is associated with exercise-induced increase in HDL cholesterol levels in Taiwanese adults. Description: Yang, Tzi-Peng, et al. The minor C-allele of the rs2014355 variant in ACADS gene is associated with exercise-induced increase in HDL cholesterol levels in Taiwanese adults. ''Medicine (Baltimore)''. 2021 Jan 8; '''100''' (1):e23838
VARAdb: a comprehensive variation annotation database for human. Description: Pan, Qi, et al. VARAdb: a comprehensive variation annotation database for human. ''Nucleic Acids Res''. 2021 Jan 8; '''49''' (D1):D1431-D1444
Assessing genomic diversity and signatures of selection in Jiaxian Red cattle using whole-genome sequencing data. Description: Xia, Xiaoting, et al. Assessing genomic diversity and signatures of selection in Jiaxian Red cattle using whole-genome sequencing data. ''BMC Genomics''. 2021 Jan 9; '''22''' (1):43
The severity of the pathogen-induced acute sickness response is affected by polymorphisms in genes of the NLRP3 inflammasome pathway. Description: Valencia, Braulio M, et al. The severity of the pathogen-induced acute sickness response is affected by polymorphisms in genes of the NLRP3 inflammasome pathway. ''Brain Behav Immun''. 2021 Jan 9;
Almond diversity and homozygosity define structure, kinship, inbreeding, and linkage disequilibrium in cultivated germplasm, and reveal genomic associations with nut and seed weight. Description: Pavan, Stefano, et al. Almond diversity and homozygosity define structure, kinship, inbreeding, and linkage disequilibrium in cultivated germplasm, and reveal genomic associations with nut and seed weight. ''Hortic Res''. 2021 Jan 10; '''8''' (1):15
Common variants in MAEA gene contributed the susceptibility to osteoporosis in Han Chinese postmenopausal women. Description: Cai, Xuan, et al. Common variants in MAEA gene contributed the susceptibility to osteoporosis in Han Chinese postmenopausal women. ''J Orthop Surg Res''. 2021 Jan 10; '''16''' (1):38
A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization. Description: Ong, Jue-Sheng, et al. A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization. ''Nat Commun''. 2021 Jan 11; '''12''' (1):246
Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families. Description: Guzman-Parra, Jose, et al. Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families. ''Transl Psychiatry''. 2021 Jan 11; '''11''' (1):31
Construction and integration of three de novo Japanese human genome assemblies toward a population-specific reference. Description: Takayama, Jun, et al. Construction and integration of three de novo Japanese human genome assemblies toward a population-specific reference. ''Nat Commun''. 2021 Jan 11; '''12''' (1):226
Exploring the biological role of postzygotic and germinal de novo mutations in ASD. Description: Alonso-Gonzalez, A, et al. Exploring the biological role of postzygotic and germinal de novo mutations in ASD. ''Sci Rep''. 2021 Jan 11; '''11''' (1):319
Genomes of Pleistocene Siberian Wolves Uncover Multiple Extinct Wolf Lineages. Description: Ramos-Madrigal, Jazmin, et al. Genomes of Pleistocene Siberian Wolves Uncover Multiple Extinct Wolf Lineages. ''Curr Biol''. 2021 Jan 11; '''31''' (1):198-206.e8
Multi-environment gene interactions linked to the interplay between polysubstance dependence and suicidality. Description: Polimanti, Renato, et al. Multi-environment gene interactions linked to the interplay between polysubstance dependence and suicidality. ''Transl Psychiatry''. 2021 Jan 11; '''11''' (1):34
Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia. Description: Ustinova, Monta, et al. Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia. ''BMC Med Genomics''. 2021 Jan 11; '''14''' (1):18
Population Structure Assessed Using Microsatellite and SNP Data: An Empirical Comparison in West African Cattle. Description: Alvarez, Isabel, et al. Population Structure Assessed Using Microsatellite and SNP Data: An Empirical Comparison in West African Cattle. ''Animals (Basel)''. 2021 Jan 11; '''11''' (1):
Systematic evaluation of the effects of genetic variants on PIWI-interacting RNA expression across 33 cancer types. Description: Xin, Junyi, et al. Systematic evaluation of the effects of genetic variants on PIWI-interacting RNA expression across 33 cancer types. ''Nucleic Acids Res''. 2021 Jan 11; '''49''' (1):90-97
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Description: Panyard, Daniel J, et al. Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. ''Commun Biol''. 2021 Jan 12; '''4''' (1):63
Explore the genetics of weedy traits using rice 3K database. Description: Lin, Yu-Lan, et al. Explore the genetics of weedy traits using rice 3K database. ''Bot Stud''. 2021 Jan 12; '''62''' (1):2
Functional impact of allelic variations/haplotypes of TNF-alpha on reproductive tract infections in Indian women. Description: Sharma, Vineeta, et al. Functional impact of allelic variations/haplotypes of TNF-alpha on reproductive tract infections in Indian women. ''Sci Rep''. 2021 Jan 12; '''11''' (1):627
Quantitative trait loci and transcriptome signatures associated with avian heritable resistance to Campylobacter. Description: Psifidi, Androniki, et al. Quantitative trait loci and transcriptome signatures associated with avian heritable resistance to Campylobacter. ''Sci Rep''. 2021 Jan 12; '''11''' (1):1623
Resequencing of global Tartary buckwheat accessions reveals multiple domestication events and key loci associated with agronomic traits. Description: Zhang, Kaixuan, et al. Resequencing of global Tartary buckwheat accessions reveals multiple domestication events and key loci associated with agronomic traits. ''Genome Biol''. 2021 Jan 12; '''22''' (1):23
TCF7L2 polymorphisms, nut consumption, and the risk of metabolic syndrome: a prospective population based study. Description: Hosseinpour-Niazi, Somayeh, et al. TCF7L2 polymorphisms, nut consumption, and the risk of metabolic syndrome: a prospective population based study. ''Nutr Metab (Lond)''. 2021 Jan 12; '''18''' (1):10
The overlap of genetic susceptibility to schizophrenia and cardiometabolic disease can be used to identify metabolically different groups of individuals. Description: Strawbridge, Rona J, et al. The overlap of genetic susceptibility to schizophrenia and cardiometabolic disease can be used to identify metabolically different groups of individuals. ''Sci Rep''. 2021 Jan 12; '''11''' (1):632
Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Description: Dennis, Jessica K, et al. Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. ''Genome Med''. 2021 Jan 13; '''13''' (1):6
Genome diversity in Ukraine. Description: Oleksyk, Taras K, et al. Genome diversity in Ukraine. ''Gigascience''. 2021 Jan 13; '''10''' (1):
Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks. Description: Amar, David, et al. Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks. ''Nat Commun''. 2021 Jan 13; '''12''' (1):350
Identification of ancestry proportions in admixed groups across the Americas using clinical pharmacogenomic SNP panels. Description: Debortoli, Guilherme, et al. Identification of ancestry proportions in admixed groups across the Americas using clinical pharmacogenomic SNP panels. ''Sci Rep''. 2021 Jan 13; '''11''' (1):1007
Mitochondrial haplogroup J associated with higher risk of obesity in the Qatari population. Description: Dashti, Mohammed, et al. Mitochondrial haplogroup J associated with higher risk of obesity in the Qatari population. ''Sci Rep''. 2021 Jan 13; '''11''' (1):1091
Genome-Wide Association Analysis of Growth Curve Parameters in Chinese Simmental Beef Cattle. Description: Duan, Xinghai, et al. Genome-Wide Association Analysis of Growth Curve Parameters in Chinese Simmental Beef Cattle. ''Animals (Basel)''. 2021 Jan 15; '''11''' (1):
Quantitative MRI phenotypes capture biological heterogeneity in multiple sclerosis patients. Description: Smets, Ide, et al. Quantitative MRI phenotypes capture biological heterogeneity in multiple sclerosis patients. ''Sci Rep''. 2021 Jan 15; '''11''' (1):1573
The technology behind TB DEPOT: a novel public analytics platform integrating tuberculosis clinical, genomic, and radiological data for visual and statistical exploration. Description: Long, Alyssa, et al. The technology behind TB DEPOT: a novel public analytics platform integrating tuberculosis clinical, genomic, and radiological data for visual and statistical exploration. ''J Am Med Inform Assoc''. 2021 Jan 15; '''28''' (1):71-79
Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research. Description: Daga, Sergio, et al. Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research. ''Eur J Hum Genet''. 2021 Jan 17;
Litter Size of Sheep (Ovis aries): Inbreeding Depression and Homozygous Regions. Description: Tao, Lin, et al. Litter Size of Sheep (Ovis aries): Inbreeding Depression and Homozygous Regions. ''Genes (Basel)''. 2021 Jan 18; '''12''' (1):
Revisiting the evolutionary history of domestic and wild ducks based on genomic analyses. Description: Guo, Xing, et al. Revisiting the evolutionary history of domestic and wild ducks based on genomic analyses. ''Zool Res''. 2021 Jan 18; '''42''' (1):43-50
Synaptic processes and immune-related pathways implicated in Tourette syndrome. Description: Tsetsos, Fotis, et al. Synaptic processes and immune-related pathways implicated in Tourette syndrome. ''Transl Psychiatry''. 2021 Jan 18; '''11''' (1):56
Age by Single Nucleotide Polymorphism Interactions on Bronchodilator Response in Asthmatics. Description: Voorhies, Kirsten, et al. Age by Single Nucleotide Polymorphism Interactions on Bronchodilator Response in Asthmatics. ''J Pers Med''. 2021 Jan 19; '''11''' (1):
Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children. Description: Zhang, Hong, et al. Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children. ''BMC Med Genomics''. 2021 Jan 19; '''14''' (1):21
Detection of QTNs for kernel moisture concentration and kernel dehydration rate before physiological maturity in maize using multi-locus GWAS. Description: Li, Shufang, et al. Detection of QTNs for kernel moisture concentration and kernel dehydration rate before physiological maturity in maize using multi-locus GWAS. ''Sci Rep''. 2021 Jan 19; '''11''' (1):1764
Identification of Target Chicken Populations by Machine Learning Models Using the Minimum Number of SNPs. Description: Seo, Dongwon, et al. Identification of Target Chicken Populations by Machine Learning Models Using the Minimum Number of SNPs. ''Animals (Basel)''. 2021 Jan 19; '''11''' (1):
Weighted Single-Step GWAS Identified Candidate Genes Associated with Growth Traits in a Duroc Pig Population. Description: Ruan, Donglin, et al. Weighted Single-Step GWAS Identified Candidate Genes Associated with Growth Traits in a Duroc Pig Population. ''Genes (Basel)''. 2021 Jan 19; '''12''' (1):
Causal effect between total cholesterol and HDL cholesterol as risk factors for chronic kidney disease: a mendelian randomization study. Description: Miao, Liu, et al. Causal effect between total cholesterol and HDL cholesterol as risk factors for chronic kidney disease: a mendelian randomization study. ''BMC Nephrol''. 2021 Jan 20; '''22''' (1):35
Effects of in IL-1B/IL-1RN variants on the susceptibility to head and neck cancer in a chinese Han population. Description: Yin, Yanhai, et al. Effects of in IL-1B/IL-1RN variants on the susceptibility to head and neck cancer in a chinese Han population. ''Cancer Cell Int''. 2021 Jan 20; '''21''' (1):59
Gene expression pattern analysis using dual-color RT-MLPA and integrative genome-wide association studies of eQTL for tuberculosis suscepitibility. Description: Ai, Jing-Wen, et al. Gene expression pattern analysis using dual-color RT-MLPA and integrative genome-wide association studies of eQTL for tuberculosis suscepitibility. ''Respir Res''. 2021 Jan 20; '''22''' (1):23
An across-breed validation study of 46 genetic markers in canine hip dysplasia. Description: Mikkola, Lea, et al. An across-breed validation study of 46 genetic markers in canine hip dysplasia. ''BMC Genomics''. 2021 Jan 21; '''22''' (1):68
Clustering suicidal phenotypes and genetic associations with brain-derived neurotrophic factor in patients with substance use disorders. Description: Icick, Romain, et al. Clustering suicidal phenotypes and genetic associations with brain-derived neurotrophic factor in patients with substance use disorders. ''Transl Psychiatry''. 2021 Jan 21; '''11''' (1):72
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Description: Yao, Xueming, et al. Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. ''Transl Psychiatry''. 2021 Jan 21; '''11''' (1):69
NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Description: da Silva, Rodrigo Salazar, et al. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. ''Hum Mol Genet''. 2021 Jan 21; '''29''' (22):3691-3705
AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data. Description: Quinodoz, Mathieu, et al. AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data. ''Nat Commun''. 2021 Jan 22; '''12''' (1):518
Functional Haplotype of LIPC Induces Triglyceride-Mediated Suppression of HDL-C Levels According to Genome-Wide Association Studies. Description: Liao, Yu-Huang, et al. Functional Haplotype of LIPC Induces Triglyceride-Mediated Suppression of HDL-C Levels According to Genome-Wide Association Studies. ''Genes (Basel)''. 2021 Jan 22; '''12''' (2):
Interaction between ERAP Alleles and HLA Class I Types Support a Role of Antigen Presentation in Hodgkin Lymphoma Development. Description: Jiang, Peijia, et al. Interaction between ERAP Alleles and HLA Class I Types Support a Role of Antigen Presentation in Hodgkin Lymphoma Development. ''Cancers (Basel)''. 2021 Jan 22; '''13''' (3):
Multi-omics analyses of cognitive traits and psychiatric disorders highlights brain-dependent mechanisms. Description: Korologou-Linden, Roxanna, et al. Multi-omics analyses of cognitive traits and psychiatric disorders highlights brain-dependent mechanisms. ''Hum Mol Genet''. 2021 Jan 22; '''32''' (6):885-96
A Truncated Singleton NLR Causes Hybrid Necrosis in Arabidopsis thaliana. Description: Barragan, Ana Cristina, et al. A Truncated Singleton NLR Causes Hybrid Necrosis in Arabidopsis thaliana. ''Mol Biol Evol''. 2021 Jan 23; '''38''' (2):557-574
Genome-wide study of a Neolithic Wartberg grave community reveals distinct HLA variation and hunter-gatherer ancestry. Description: Immel, Alexander, et al. Genome-wide study of a Neolithic Wartberg grave community reveals distinct HLA variation and hunter-gatherer ancestry. ''Commun Biol''. 2021 Jan 25; '''4''' (1):113
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Description: Demontis, Ditte, et al. Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. ''Nat Commun''. 2021 Jan 25; '''12''' (1):576
Shedding Light on the African Enigma: In Vitro Testing of Homo sapiens-Helicobacter pylori Coevolution. Description: Cavadas, Bruno, et al. Shedding Light on the African Enigma: In Vitro Testing of Homo sapiens-Helicobacter pylori Coevolution. ''Microorganisms''. 2021 Jan 25; '''9''' (2):
Population genomics reveal rapid genetic differentiation in a recently invasive population of Rattus norvegicus. Description: Chen, Yi, et al. Population genomics reveal rapid genetic differentiation in a recently invasive population of Rattus norvegicus. ''Front Zool''. 2021 Jan 26; '''18''' (1):6
Understanding the genetic architecture of the metabolically unhealthy normal weight and metabolically healthy obese phenotypes in a Korean population. Description: Park, Jae-Min, et al. Understanding the genetic architecture of the metabolically unhealthy normal weight and metabolically healthy obese phenotypes in a Korean population. ''Sci Rep''. 2021 Jan 26; '''11''' (1):2279
Genetic Background and Inbreeding Depression in Romosinuano Cattle Breed in Mexico. Description: Hidalgo, Jorge, et al. Genetic Background and Inbreeding Depression in Romosinuano Cattle Breed in Mexico. ''Animals (Basel)''. 2021 Jan 28; '''11''' (2):
Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia. Description: Lin, Wei-Yu, et al. Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia. ''Nat Commun''. 2021 Jan 28; '''12''' (1):665
Genome-wide comparative analyses reveal selection signatures underlying adaptation and production in Tibetan and Poll Dorset sheep. Description: Zhang, Yingyue, et al. Genome-wide comparative analyses reveal selection signatures underlying adaptation and production in Tibetan and Poll Dorset sheep. ''Sci Rep''. 2021 Jan 28; '''11''' (1):2466
Highly elevated polygenic risk scores are better predictors of myocardial infarction risk early in life than later. Description: Isgut, Monica, et al. Highly elevated polygenic risk scores are better predictors of myocardial infarction risk early in life than later. ''Genome Med''. 2021 Jan 28; '''13''' (1):13
Uncovering the genetic mechanisms regulating panicle architecture in rice with GPWAS and GWAS. Description: Zhong, Hua, et al. Uncovering the genetic mechanisms regulating panicle architecture in rice with GPWAS and GWAS. ''BMC Genomics''. 2021 Jan 28; '''22''' (1):86
A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa. Description: Nishiguchi, Koji M, et al. A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa. ''Commun Biol''. 2021 Jan 29; '''4''' (1):140
Genomic predictions for fillet yield and firmness in rainbow trout using reduced-density SNP panels. Description: Al-Tobasei, Rafet, et al. Genomic predictions for fillet yield and firmness in rainbow trout using reduced-density SNP panels. ''BMC Genomics''. 2021 Jan 30; '''22''' (1):92
The spectrum of association in HLA region with rheumatoid arthritis in a diverse Asian population: evidence from the MyEIRA case-control study. Description: Tan, Lay Kim, et al. The spectrum of association in HLA region with rheumatoid arthritis in a diverse Asian population: evidence from the MyEIRA case-control study. ''Arthritis Res Ther''. 2021 Jan 30; '''23''' (1):46
Phenotypic and Genomic Analysis of Cystic Hygroma in Pigs. Description: Letko, Anna, et al. Phenotypic and Genomic Analysis of Cystic Hygroma in Pigs. ''Genes (Basel)''. 2021 Jan 31; '''12''' (2):
A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype. Description: Mirshahi, Uyenlinh L, et al. A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype. ''JAMA Netw Open''. 2021 Feb 1; '''4''' (2):e210112
A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Description: Bonfante, Betty, et al. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. ''Sci Adv''. 2021 Feb; '''7''' (6):
A Large-Scale, Stratified Genetic Analysis of the Major Histocompatibility Complex Region in Early- and Late-Onset Psoriasis in China. Description: Zhou, Yi, et al. A Large-Scale, Stratified Genetic Analysis of the Major Histocompatibility Complex Region in Early- and Late-Onset Psoriasis in China. ''Ann Dermatol''. 2021 Feb; '''33''' (1):61-67
Ancient and recent introgression shape the evolutionary history of pollinator adaptation and speciation in a model monkeyflower radiation (Mimulus section Erythranthe). Description: Nelson, Thomas C, et al. Ancient and recent introgression shape the evolutionary history of pollinator adaptation and speciation in a model monkeyflower radiation (Mimulus section Erythranthe). ''PLoS Genet''. 2021 Feb; '''17''' (2):e1009095
Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children. Description: Wu, Qi, et al. Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children. ''J Gene Med''. 2021 Feb; '''23''' (2):e3301
Collagen type XVIII alpha 1 chain (COL18A1) variants affect the risk of anti-tuberculosis drug-induced hepatotoxicity: A prospective study. Description: Cheng, Yuhui, et al. Collagen type XVIII alpha 1 chain (COL18A1) variants affect the risk of anti-tuberculosis drug-induced hepatotoxicity: A prospective study. ''J Clin Lab Anal''. 2021 Feb; '''35''' (2):e23630
Evaluating the effects of cardiometabolic exposures on circulating proteins which may contribute to severe SARS-CoV-2. Description: Richardson, Tom G, et al. Evaluating the effects of cardiometabolic exposures on circulating proteins which may contribute to severe SARS-CoV-2. ''EBioMedicine''. 2021 Feb; '''64''': 103228
Expansion of frozen hybrids in the guppy ectoparasite, Gyrodactylus turnbulli. Description: Konczal, Mateusz, et al. Expansion of frozen hybrids in the guppy ectoparasite, Gyrodactylus turnbulli. ''Mol Ecol''. 2021 Feb; '''30''' (4):1005-1016
Genetic and clinical basis for two distinct subtypes of primary Sjogren's syndrome. Description: Thorlacius, Guethny Ella, et al. Genetic and clinical basis for two distinct subtypes of primary Sjogren's syndrome. ''Rheumatology (Oxford)''. 2021 Feb 1; '''60''' (2):837-848
Genetic loci associated with skin pigmentation in African Americans and their effects on vitamin D deficiency. Description: Batai, Ken, et al. Genetic loci associated with skin pigmentation in African Americans and their effects on vitamin D deficiency. ''PLoS Genet''. 2021 Feb; '''17''' (2):e1009319
Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis. Description: Zysman-Colman, Zofia N, et al. Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis. ''Pediatr Res''. 2021 Feb; '''89''' (3):653-659
Genetics of 35 blood and urine biomarkers in the UK Biobank. Description: Sinnott-Armstrong, Nasa, et al. Genetics of 35 blood and urine biomarkers in the UK Biobank. ''Nat Genet''. 2021 Feb; '''53''' (2):185-194
Genome-wide analysis reveals the patterns of genetic diversity and population structure of 8 Italian local chicken breeds. Description: Cendron, F, et al. Genome-wide analysis reveals the patterns of genetic diversity and population structure of 8 Italian local chicken breeds. ''Poult Sci''. 2021 Feb; '''100''' (2):441-451
Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Description: Stein, Murray B, et al. Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. ''Nat Genet''. 2021 Feb; '''53''' (2):174-184
Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease. Description: Tan, Manuela M X, et al. Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease. ''Mov Disord''. 2021 Feb; '''36''' (2):424-433
Genome-wide association study of serum prostate-specific antigen levels based on 1000 Genomes imputed data in Japanese: the Japan Multi-Institutional Collaborative Cohort Study. Description: Hishida, Asahi, et al. Genome-wide association study of serum prostate-specific antigen levels based on 1000 Genomes imputed data in Japanese: the Japan Multi-Institutional Collaborative Cohort Study. ''Nagoya J Med Sci''. 2021 Feb; '''83''' (1):183-194
Genome-wide association study reveals the genetic determinism of growth traits in a Gushi-Anka F2 chicken population. Description: Zhang, Yanhua, et al. Genome-wide association study reveals the genetic determinism of growth traits in a Gushi-Anka F2 chicken population. ''Heredity (Edinb)''. 2021 Feb; '''126''' (2):293-307
Genomic adaptations to cereal-based diets contribute to mitigate metabolic risk in some human populations of East Asian ancestry. Description: Landini, Arianna, et al. Genomic adaptations to cereal-based diets contribute to mitigate metabolic risk in some human populations of East Asian ancestry. ''Evol Appl''. 2021 Feb; '''14''' (2):297-313
Genomic evidence supports the introgression between two sympatric stickleback species inhabiting the White Sea basin. Description: Nedoluzhko, Artem, et al. Genomic evidence supports the introgression between two sympatric stickleback species inhabiting the White Sea basin. ''Heliyon''. 2021 Feb; '''7''' (2):e06160
Identification and analysis of splicing quantitative trait loci across multiple tissues in the human genome. Description: Garrido-Martin, Diego, et al. Identification and analysis of splicing quantitative trait loci across multiple tissues in the human genome. ''Nat Commun''. 2021 Feb 1; '''12''' (1):727
Insecticide resistance and genetic structure of Aedes aegypti populations from Rio de Janeiro State, Brazil. Description: Rahman, Rafi Ur, et al. Insecticide resistance and genetic structure of Aedes aegypti populations from Rio de Janeiro State, Brazil. ''PLoS Negl Trop Dis''. 2021 Feb; '''15''' (2):e0008492
Large mosaic copy number variations confer autism risk. Description: Sherman, Maxwell A, et al. Large mosaic copy number variations confer autism risk. ''Nat Neurosci''. 2021 Feb; '''24''' (2):197-203
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network. Description: Palmer, Melody R, et al. Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network. ''Genet Epidemiol''. 2021 Feb; '''45''' (1):4-15
Population collapse in Congo rainforest from 400 CE urges reassessment of the Bantu Expansion. Description: Seidensticker, Dirk, et al. Population collapse in Congo rainforest from 400 CE urges reassessment of the Bantu Expansion. ''Sci Adv''. 2021 Feb; '''7''' (7):
Sex Differences in the Risk of Coronary Heart Disease Associated With Type 2 Diabetes: A Mendelian Randomization Analysis. Description: Peters, Tricia M, et al. Sex Differences in the Risk of Coronary Heart Disease Associated With Type 2 Diabetes: A Mendelian Randomization Analysis. ''Diabetes Care''. 2021 Feb; '''44''' (2):556-562
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Description: Tadros, Rafik, et al. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. ''Nat Genet''. 2021 Feb; '''53''' (2):128-134
The association of HLA-C and ERAP1 polymorphisms in early and late onset psoriasis and psoriatic arthritis patients of Hungary. Description: Kepiro, Laszlo, et al. The association of HLA-C and ERAP1 polymorphisms in early and late onset psoriasis and psoriatic arthritis patients of Hungary. ''Postepy Dermatol Alergol''. 2021 Feb; '''38''' (2):43-51
The developmental genetic architecture of vocabulary skills during the first three years of life: Capturing emerging associations with later-life reading and cognition. Description: Verhoef, Ellen, et al. The developmental genetic architecture of vocabulary skills during the first three years of life: Capturing emerging associations with later-life reading and cognition. ''PLoS Genet''. 2021 Feb; '''17''' (2):e1009144
The influence of adult hip shape genetic variants on adolescent hip shape: Findings from a population-based DXA study. Description: Frysz, Monika, et al. The influence of adult hip shape genetic variants on adolescent hip shape: Findings from a population-based DXA study. ''Bone''. 2021 Feb; '''143''': 115792
The influence of X chromosome variants on trait neuroticism. Description: Luciano, Michelle, et al. The influence of X chromosome variants on trait neuroticism. ''Mol Psychiatry''. 2021 Feb; '''26''' (2):483-491
The population genetics of nonmigratory Allen's Hummingbird (Selasphorus sasin sedentarius) following a recent mainland colonization. Description: Myers, Brian M, et al. The population genetics of nonmigratory Allen's Hummingbird (Selasphorus sasin sedentarius) following a recent mainland colonization. ''Ecol Evol''. 2021 Feb; '''11''' (4):1850-1865
The Role of Genetic Ancestry as a Risk Factor for Primary Open-angle Glaucoma in African Americans. Description: Cole, Brian S, et al. The Role of Genetic Ancestry as a Risk Factor for Primary Open-angle Glaucoma in African Americans. ''Invest Ophthalmol Vis Sci''. 2021 Feb 1; '''62''' (2):28
Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder. Description: Huang, Kunling, et al. Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder. ''PLoS Genet''. 2021 Feb; '''17''' (2):e1009309
Urate, Blood Pressure, and Cardiovascular Disease: Evidence From Mendelian Randomization and Meta-Analysis of Clinical Trials. Description: Gill, Dipender, et al. Urate, Blood Pressure, and Cardiovascular Disease: Evidence From Mendelian Randomization and Meta-Analysis of Clinical Trials. ''Hypertension''. 2021 Feb; '''77''' (2):383-392
Variant Spectrum of Formin Homology 2 Domain-Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy. Description: Wu, Guixin, et al. Variant Spectrum of Formin Homology 2 Domain-Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy. ''J Am Heart Assoc''. 2021 Feb; '''10''' (5):e018236
Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBD. Description: Hu, Shixian, et al. Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBD. ''Gut''. 2021 Feb; '''70''' (2):285-296
Whole-genome SNP markers reveal conservation status, signatures of selection, and introgression in Chinese Laiwu pigs. Description: Wang, Xiaopeng, et al. Whole-genome SNP markers reveal conservation status, signatures of selection, and introgression in Chinese Laiwu pigs. ''Evol Appl''. 2021 Feb; '''14''' (2):383-398
Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretion. Description: Hu, Ming, et al. Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretion. ''Cell Rep''. 2021 Feb 2; '''34''' (5):108703
Dynamics of a Dual SARS-CoV-2 Lineage Co-Infection on a Prolonged Viral Shedding COVID-19 Case: Insights into Clinical Severity and Disease Duration. Description: Pedro, Nicole, et al. Dynamics of a Dual SARS-CoV-2 Lineage Co-Infection on a Prolonged Viral Shedding COVID-19 Case: Insights into Clinical Severity and Disease Duration. ''Microorganisms''. 2021 Feb 2; '''9''' (2):
Effect of metabolic genetic variants on long-term disease comorbidity in patients with type 2 diabetes. Description: Abedian, Shifteh, et al. Effect of metabolic genetic variants on long-term disease comorbidity in patients with type 2 diabetes. ''Sci Rep''. 2021 Feb 2; '''11''' (1):2794
Genome-wide association study of high-sensitivity C-reactive protein, D-dimer, and interleukin-6 levels in multiethnic HIV+ cohorts. Description: Sherman, Brad T, et al. Genome-wide association study of high-sensitivity C-reactive protein, D-dimer, and interleukin-6 levels in multiethnic HIV+ cohorts. ''AIDS''. 2021 Feb 2; '''35''' (2):193-204
Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder. Description: Burton, Christie L, et al. Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder. ''Transl Psychiatry''. 2021 Feb 2; '''11''' (1):91
Genomic scans for selective sweeps through haplotype homozygosity and allelic fixation in 14 indigenous sheep breeds from Middle East and South Asia. Description: Eydivandi, Sirous, et al. Genomic scans for selective sweeps through haplotype homozygosity and allelic fixation in 14 indigenous sheep breeds from Middle East and South Asia. ''Sci Rep''. 2021 Feb 2; '''11''' (1):2834
RMR-Related MAP2K6 Gene Variation on the Risk of Overweight/Obesity in Children: A 3-Year Panel Study. Description: Lee, Myoungsook, et al. RMR-Related MAP2K6 Gene Variation on the Risk of Overweight/Obesity in Children: A 3-Year Panel Study. ''J Pers Med''. 2021 Feb 2; '''11''' (2):
Genome-Wide Epigenetic Signatures of Adaptive Developmental Plasticity in the Andes. Description: Childebayeva, Ainash, et al. Genome-Wide Epigenetic Signatures of Adaptive Developmental Plasticity in the Andes. ''Genome Biol Evol''. 2021 Feb 3; '''13''' (2):
Genomic variation, population history and within-archipelago adaptation between island bird populations. Description: Martin, Claudia A, et al. Genomic variation, population history and within-archipelago adaptation between island bird populations. ''R Soc Open Sci''. 2021 Feb 3; '''8''' (2):201146
Associations between human leukocyte antigens and renal function. Description: Lowe, Marcus, et al. Associations between human leukocyte antigens and renal function. ''Sci Rep''. 2021 Feb 4; '''11''' (1):3158
Autozygosity mapping and time-to-spontaneous delivery in Norwegian parent-offspring trios. Description: Sole-Navais, Pol, et al. Autozygosity mapping and time-to-spontaneous delivery in Norwegian parent-offspring trios. ''Hum Mol Genet''. 2021 Feb 4; '''29''' (23):3845-3858
Genetic history of Calabrian Greeks reveals ancient events and long term isolation in the Aspromonte area of Southern Italy. Description: Sarno, Stefania, et al. Genetic history of Calabrian Greeks reveals ancient events and long term isolation in the Aspromonte area of Southern Italy. ''Sci Rep''. 2021 Feb 4; '''11''' (1):3045
Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis. Description: Galata, Gabriella, et al. Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis. ''Am J Hum Genet''. 2021 Feb 4; '''108''' (2):284-294
Identifying Wild Versus Cultivated Gene-Alleles Conferring Seed Coat Color and Days to Flowering in Soybean. Description: Liu, Cheng, et al. Identifying Wild Versus Cultivated Gene-Alleles Conferring Seed Coat Color and Days to Flowering in Soybean. ''Int J Mol Sci''. 2021 Feb 4; '''22''' (4):
Integrative Genomic-Epigenomic Analysis of Clozapine-Treated Patients with Refractory Psychosis. Description: Mayen-Lobo, Yerye Gibran, et al. Integrative Genomic-Epigenomic Analysis of Clozapine-Treated Patients with Refractory Psychosis. ''Pharmaceuticals (Basel)''. 2021 Feb 4; '''14''' (2):
Multi-omic and multi-species meta-analyses of nicotine consumption. Description: Palmer, Rohan H C, et al. Multi-omic and multi-species meta-analyses of nicotine consumption. ''Transl Psychiatry''. 2021 Feb 4; '''11''' (1):98
Multi-trait transcriptome-wide association studies with probabilistic Mendelian randomization. Description: Liu, Lu, et al. Multi-trait transcriptome-wide association studies with probabilistic Mendelian randomization. ''Am J Hum Genet''. 2021 Feb 4; '''108''' (2):240-256
Clinical and Genetic Risk Factors of Recurrent Nonalcoholic Fatty Liver Disease After Liver Transplantation. Description: Satapathy, Sanjaya K, et al. Clinical and Genetic Risk Factors of Recurrent Nonalcoholic Fatty Liver Disease After Liver Transplantation. ''Clin Transl Gastroenterol''. 2021 Feb 5; '''12''' (2):e00302
Dyshomeostatic modulation of Ca(2+)-activated K(+) channels in a human neuronal model of KCNQ2 encephalopathy. Description: Simkin, Dina, et al. Dyshomeostatic modulation of Ca(2+)-activated K(+) channels in a human neuronal model of KCNQ2 encephalopathy. ''Elife''. 2021 Feb 5; '''10''':
Genome-wide genetic links between amyotrophic lateral sclerosis and autoimmune diseases. Description: Li, Chun Yu, et al. Genome-wide genetic links between amyotrophic lateral sclerosis and autoimmune diseases. ''BMC Med''. 2021 Feb 5; '''19''' (1):27
Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Description: Glanville, Kylie P, et al. Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. ''BJPsych Open''. 2021 Feb 5; '''7''' (2):e44
SARS-CoV-2 mutation 614G creates an elastase cleavage site enhancing its spread in high AAT-deficient regions. Description: Bhattacharyya, Chandrika, et al. SARS-CoV-2 mutation 614G creates an elastase cleavage site enhancing its spread in high AAT-deficient regions. ''Infect Genet Evol''. 2021 Feb 5; '''90''': 104760
Identification of QTL regions and candidate genes for growth and feed efficiency in broilers. Description: Li, Wei, et al. Identification of QTL regions and candidate genes for growth and feed efficiency in broilers. ''Genet Sel Evol''. 2021 Feb 6; '''53''' (1):13
Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects. Description: Coltell, Oscar, et al. Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects. ''Nutrients''. 2021 Feb 7; '''13''' (2):
Development of a Clinical and Genetic Prediction Model for Early Intestinal Resection in Patients with Crohn's Disease: Results from the IMPACT Study. Description: Kang, Eun Ae, et al. Development of a Clinical and Genetic Prediction Model for Early Intestinal Resection in Patients with Crohn's Disease: Results from the IMPACT Study. ''J Clin Med''. 2021 Feb 7; '''10''' (4):
Genetic variation among 481 diverse soybean accessions, inferred from genomic re-sequencing. Description: Valliyodan, Babu, et al. Genetic variation among 481 diverse soybean accessions, inferred from genomic re-sequencing. ''Sci Data''. 2021 Feb 8; '''8''' (1):50
Genome-wide fine-mapping identifies pleiotropic and functional variants that predict many traits across global cattle populations. Description: Xiang, Ruidong, et al. Genome-wide fine-mapping identifies pleiotropic and functional variants that predict many traits across global cattle populations. ''Nat Commun''. 2021 Feb 8; '''12''' (1):860
Investigation of ancestral alleles in the Bovinae subfamily. Description: Naji, Maulana M, et al. Investigation of ancestral alleles in the Bovinae subfamily. ''BMC Genomics''. 2021 Feb 8; '''22''' (1):108
Replication of HLA class II locus association with susceptibility to podoconiosis in three Ethiopian ethnic groups. Description: Gebresilase, Tewodros, et al. Replication of HLA class II locus association with susceptibility to podoconiosis in three Ethiopian ethnic groups. ''Sci Rep''. 2021 Feb 8; '''11''' (1):3285
A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Description: Liu, Xiaomin, et al. A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. ''Cell Discov''. 2021 Feb 9; '''7''' (1):9
Causal relationships between genetically determined metabolites and human intelligence: a Mendelian randomization study. Description: Yang, Jian, et al. Causal relationships between genetically determined metabolites and human intelligence: a Mendelian randomization study. ''Mol Brain''. 2021 Feb 9; '''14''' (1):29
Dissecting dynamics and differences of selective pressures in the evolution of human pigmentation. Description: Huang, Xin, et al. Dissecting dynamics and differences of selective pressures in the evolution of human pigmentation. ''Biol Open''. 2021 Feb 9; '''10''' (2):
Ethnic-specific association of amylase gene copy number with adiposity traits in a large Middle Eastern biobank. Description: Rossi, Niccolo', et al. Ethnic-specific association of amylase gene copy number with adiposity traits in a large Middle Eastern biobank. ''NPJ Genom Med''. 2021 Feb 9; '''6''' (1):8
Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank. Description: Yap, Chloe X, et al. Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank. ''Mol Autism''. 2021 Feb 10; '''12''' (1):12
A novel canine reference genome resolves genomic architecture and uncovers transcript complexity. Description: Wang, Chao, et al. A novel canine reference genome resolves genomic architecture and uncovers transcript complexity. ''Commun Biol''. 2021 Feb 10; '''4''' (1):185
Common Myelin Regulatory Factor Gene Variants Predisposing to Excellence in Sports. Description: Peplonska, Beata, et al. Common Myelin Regulatory Factor Gene Variants Predisposing to Excellence in Sports. ''Genes (Basel)''. 2021 Feb 11; '''12''' (2):
Genome-wide association study in hexaploid wheat identifies novel genomic regions associated with resistance to root lesion nematode (Pratylenchus thornei). Description: Kumar, Deepak, et al. Genome-wide association study in hexaploid wheat identifies novel genomic regions associated with resistance to root lesion nematode (Pratylenchus thornei). ''Sci Rep''. 2021 Feb 11; '''11''' (1):3572
GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility. Description: Eriksson, Daniel, et al. GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility. ''Nat Commun''. 2021 Feb 11; '''12''' (1):959
Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts. Description: Graff, Rebecca E, et al. Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts. ''Nat Commun''. 2021 Feb 12; '''12''' (1):970
Inclusion of genetic variants in an ensemble of gradient boosting decision trees does not improve the prediction of citalopram treatment response. Description: Shumake, Jason, et al. Inclusion of genetic variants in an ensemble of gradient boosting decision trees does not improve the prediction of citalopram treatment response. ''Sci Rep''. 2021 Feb 12; '''11''' (1):3780
Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia. Description: Cruz-Bautista, Ivette, et al. Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia. ''Lipids Health Dis''. 2021 Feb 15; '''20''' (1):14
Genetic Effects on Transcriptome Profiles in Colon Epithelium Provide Functional Insights for Genetic Risk Loci. Description: Diez-Obrero, Virginia, et al. Genetic Effects on Transcriptome Profiles in Colon Epithelium Provide Functional Insights for Genetic Risk Loci. ''Cell Mol Gastroenterol Hepatol''. 2021 Feb 16; '''12''' (1):181-197
Personalized genealogical history of UK individuals inferred from biobank-scale IBD segments. Description: Naseri, Ardalan, et al. Personalized genealogical history of UK individuals inferred from biobank-scale IBD segments. ''BMC Biol''. 2021 Feb 16; '''19''' (1):32
Pharmacogenomic Profile and Adverse Drug Reactions in a Prospective Therapeutic Cohort of Chagas Disease Patients Treated with Benznidazole. Description: Franco, Lucas A M, et al. Pharmacogenomic Profile and Adverse Drug Reactions in a Prospective Therapeutic Cohort of Chagas Disease Patients Treated with Benznidazole. ''Int J Mol Sci''. 2021 Feb 16; '''22''' (4):
Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals. Description: Kemper, Kathryn E, et al. Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals. ''Nat Commun''. 2021 Feb 16; '''12''' (1):1050
Genetic diversity and population structure of early and extra-early maturing maize germplasm adapted to sub-Saharan Africa. Description: Badu-Apraku, Baffour, et al. Genetic diversity and population structure of early and extra-early maturing maize germplasm adapted to sub-Saharan Africa. ''BMC Plant Biol''. 2021 Feb 17; '''21''' (1):96
Genome sequences reveal global dispersal routes and suggest convergent genetic adaptations in seahorse evolution. Description: Li, Chunyan, et al. Genome sequences reveal global dispersal routes and suggest convergent genetic adaptations in seahorse evolution. ''Nat Commun''. 2021 Feb 17; '''12''' (1):1094
A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy. Description: Skuladottir, Astros Th, et al. A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy. ''Sci Rep''. 2021 Feb 18; '''11''' (1):4188
GCKR common functional polymorphisms are associated with metabolic syndrome and its components: a 10-year retrospective cohort study in Iranian adults. Description: Zahedi, Asiyeh Sadat, et al. GCKR common functional polymorphisms are associated with metabolic syndrome and its components: a 10-year retrospective cohort study in Iranian adults. ''Diabetol Metab Syndr''. 2021 Feb 18; '''13''' (1):20
Inflammation status modulates the effect of host genetic variation on intestinal gene expression in inflammatory bowel disease. Description: Hu, Shixian, et al. Inflammation status modulates the effect of host genetic variation on intestinal gene expression in inflammatory bowel disease. ''Nat Commun''. 2021 Feb 18; '''12''' (1):1122
Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Description: Gouveia, Mateus H, et al. Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. ''Sci Rep''. 2021 Feb 18; '''11''' (1):4075
Development of a 76k Alpaca (Vicugna pacos) Single Nucleotide Polymorphisms (SNPs) Microarray. Description: Calderon, Marcos, et al. Development of a 76k Alpaca (Vicugna pacos) Single Nucleotide Polymorphisms (SNPs) Microarray. ''Genes (Basel)''. 2021 Feb 19; '''12''' (2):
Development of genome-wide polygenic risk scores for lipid traits and clinical applications for dyslipidemia, subclinical atherosclerosis, and diabetes cardiovascular complications among East Asians. Description: Tam, Claudia H T, et al. Development of genome-wide polygenic risk scores for lipid traits and clinical applications for dyslipidemia, subclinical atherosclerosis, and diabetes cardiovascular complications among East Asians. ''Genome Med''. 2021 Feb 19; '''13''' (1):29
Gastric Cancer Risk Prediction Using an Epidemiological Risk Assessment Model and Polygenic Risk Score. Description: Park, Boyoung, et al. Gastric Cancer Risk Prediction Using an Epidemiological Risk Assessment Model and Polygenic Risk Score. ''Cancers (Basel)''. 2021 Feb 19; '''13''' (4):
Genome-wide association study identified candidate genes for seed size and seed composition improvement in M. truncatula. Description: Chen, Zhijuan, et al. Genome-wide association study identified candidate genes for seed size and seed composition improvement in M. truncatula. ''Sci Rep''. 2021 Feb 19; '''11''' (1):4224
Menopause, Ultraviolet Exposure, and Low Water Intake Potentially Interact with the Genetic Variants Related to Collagen Metabolism Involved in Skin Wrinkle Risk in Middle-Aged Women. Description: Park, Sunmin, et al. Menopause, Ultraviolet Exposure, and Low Water Intake Potentially Interact with the Genetic Variants Related to Collagen Metabolism Involved in Skin Wrinkle Risk in Middle-Aged Women. ''Int J Environ Res Public Health''. 2021 Feb 19; '''18''' (4):
Multi-omics highlights ABO plasma protein as a causal risk factor for COVID-19. Description: Hernandez Cordero, Ana I, et al. Multi-omics highlights ABO plasma protein as a causal risk factor for COVID-19. ''Hum Genet''. 2021 Feb 19;
Widespread signatures of natural selection across human complex traits and functional genomic categories. Description: Zeng, Jian, et al. Widespread signatures of natural selection across human complex traits and functional genomic categories. ''Nat Commun''. 2021 Feb 19; '''12''' (1):1164
Single nucleotide polymorphisms from candidate genes associated with nematode resistance and resilience in Corriedale and Pampinta sheep in Argentina. Description: Raschia, Maria Agustina, et al. Single nucleotide polymorphisms from candidate genes associated with nematode resistance and resilience in Corriedale and Pampinta sheep in Argentina. ''Gene''. 2021 Feb 20; '''770''': 145345
Evidence for Two Main Domestication Trajectories in Saccharomyces cerevisiae Linked to Distinct Bread-Making Processes. Description: Bigey, Frederic, et al. Evidence for Two Main Domestication Trajectories in Saccharomyces cerevisiae Linked to Distinct Bread-Making Processes. ''Curr Biol''. 2021 Feb 22; '''31''' (4):722-732.e5
The 'Tommy Atkins' mango genome reveals candidate genes for fruit quality. Description: Bally, Ian S E, et al. The 'Tommy Atkins' mango genome reveals candidate genes for fruit quality. ''BMC Plant Biol''. 2021 Feb 22; '''21''' (1):108
cfDNA deconvolution via NIPT of a pregnant woman after bone marrow transplant and donor egg IVF. Description: Zhu, Jianjiang, et al. cfDNA deconvolution via NIPT of a pregnant woman after bone marrow transplant and donor egg IVF. ''Hum Genomics''. 2021 Feb 23; '''15''' (1):14
Genomic Regions Associated with Variation in Pigmentation Loss in Saddle Tan Beagles. Description: Nord, Mia E, et al. Genomic Regions Associated with Variation in Pigmentation Loss in Saddle Tan Beagles. ''Genes (Basel)''. 2021 Feb 23; '''12''' (2):
Prioritizing variants of uncertain significance for reclassification using a rule-based algorithm in inherited retinal dystrophies. Description: Iancu, Ionut-Florin, et al. Prioritizing variants of uncertain significance for reclassification using a rule-based algorithm in inherited retinal dystrophies. ''NPJ Genom Med''. 2021 Feb 23; '''6''' (1):18
Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Description: Thareja, Gaurav, et al. Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. ''Nat Commun''. 2021 Feb 23; '''12''' (1):1250
Revealing the role of the human blood plasma proteome in obesity using genetic drivers. Description: Zaghlool, Shaza B, et al. Revealing the role of the human blood plasma proteome in obesity using genetic drivers. ''Nat Commun''. 2021 Feb 24; '''12''' (1):1279
A case of retinitis pigmentosa homozygous for a rare CNGA1 causal variant. Description: Saito, Kohei, et al. A case of retinitis pigmentosa homozygous for a rare CNGA1 causal variant. ''Sci Rep''. 2021 Feb 25; '''11''' (1):4681
Exploring the genetic architecture of feed efficiency traits in chickens. Description: Marchesi, Jorge Augusto Petroli, et al. Exploring the genetic architecture of feed efficiency traits in chickens. ''Sci Rep''. 2021 Feb 25; '''11''' (1):4622
The influence of human genetic variation on Epstein-Barr virus sequence diversity. Description: Rueger, Sina, et al. The influence of human genetic variation on Epstein-Barr virus sequence diversity. ''Sci Rep''. 2021 Feb 25; '''11''' (1):4586
Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes. Description: Park, Jong-Ho, et al. Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes. ''Sci Rep''. 2021 Feb 25; '''11''' (1):4552
A molecular quantitative trait locus map for osteoarthritis. Description: Steinberg, Julia, et al. A molecular quantitative trait locus map for osteoarthritis. ''Nat Commun''. 2021 Feb 26; '''12''' (1):1309
On the use of whole-genome sequence data for across-breed genomic prediction and fine-scale mapping of QTL. Description: Meuwissen, Theo, et al. On the use of whole-genome sequence data for across-breed genomic prediction and fine-scale mapping of QTL. ''Genet Sel Evol''. 2021 Feb 26; '''53''' (1):19
A genome-wide association study identifying the SNPs predictive of rapid joint destruction in patients with rheumatoid arthritis. Description: Hayashi, Shinya, et al. A genome-wide association study identifying the SNPs predictive of rapid joint destruction in patients with rheumatoid arthritis. ''Biomed Rep''. 2021 Mar; '''14''' (3):31
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. Description: Hardcastle, Alison J, et al. A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. ''Commun Biol''. 2021 Mar 1; '''4''' (1):266
Ancient genomic time transect from the Central Asian Steppe unravels the history of the Scythians. Description: Gnecchi-Ruscone, Guido Alberto, et al. Ancient genomic time transect from the Central Asian Steppe unravels the history of the Scythians. ''Sci Adv''. 2021 Mar; '''7''' (13):
An evaluation of inbreeding measures using a whole-genome sequenced cattle pedigree. Description: Alemu, Setegn Worku, et al. An evaluation of inbreeding measures using a whole-genome sequenced cattle pedigree. ''Heredity (Edinb)''. 2021 Mar; '''126''' (3):410-423
A polygenic resilience score moderates the genetic risk for schizophrenia. Description: Hess, Jonathan L, et al. A polygenic resilience score moderates the genetic risk for schizophrenia. ''Mol Psychiatry''. 2021 Mar; '''26''' (3):800-815
Association of genetic variants of TMEM135 and PEX5 in the peroxisome pathway with cutaneous melanoma-specific survival. Description: Wang, Haijiao, et al. Association of genetic variants of TMEM135 and PEX5 in the peroxisome pathway with cutaneous melanoma-specific survival. ''Ann Transl Med''. 2021 Mar; '''9''' (5):396
Association of Single Nucleotide Polymorphisms on Locus 18q21.1 in the Etiology of Nonsyndromic Cleft Lip Palate (NSCLP) in Indian Multiplex Families. Description: Neela, Praveen Kumar, et al. Association of Single Nucleotide Polymorphisms on Locus 18q21.1 in the Etiology of Nonsyndromic Cleft Lip Palate (NSCLP) in Indian Multiplex Families. ''Glob Med Genet''. 2021 Mar; '''8''' (1):24-31
BIN1 rs744373 SNP and COVID-19 mortality. Description: Lehrer, Steven, et al. BIN1 rs744373 SNP and COVID-19 mortality. ''World Acad Sci J''. 2021 Mar-Apr; '''3''' (2):
Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer. Description: Climente-Gonzalez, Hector, et al. Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer. ''PLoS Comput Biol''. 2021 Mar; '''17''' (3):e1008819
Changes in the fine-scale genetic structure of Finland through the 20th century. Description: Kerminen, Sini, et al. Changes in the fine-scale genetic structure of Finland through the 20th century. ''PLoS Genet''. 2021 Mar; '''17''' (3):e1009347
Contribution of Polygenic Risk to Hypertension Among Long-Term Survivors of Childhood Cancer. Description: Sapkota, Yadav, et al. Contribution of Polygenic Risk to Hypertension Among Long-Term Survivors of Childhood Cancer. ''JACC CardioOncol''. 2021 Mar; '''3''' (1):76-84
Do ADHD-impulsivity and BMI have shared polygenic and neural correlates? Description: Barker, Edward D, et al. Do ADHD-impulsivity and BMI have shared polygenic and neural correlates? ''Mol Psychiatry''. 2021 Mar; '''26''' (3):1019-1028
Elevated Polygenic Burden for Autism Spectrum Disorder Is Associated With the Broad Autism Phenotype in Mothers of Individuals With Autism Spectrum Disorder. Description: Nayar, Kritika, et al. Elevated Polygenic Burden for Autism Spectrum Disorder Is Associated With the Broad Autism Phenotype in Mothers of Individuals With Autism Spectrum Disorder. ''Biol Psychiatry''. 2021 Mar 1; '''89''' (5):476-485
Enhancer-Gene Interaction Analyses Identified the Epidermal Growth Factor Receptor as a Susceptibility Gene for Type 2 Diabetes Mellitus. Description: Yang, Yang, et al. Enhancer-Gene Interaction Analyses Identified the Epidermal Growth Factor Receptor as a Susceptibility Gene for Type 2 Diabetes Mellitus. ''Diabetes Metab J''. 2021 Mar; '''45''' (2):241-250
Exome Chip Analysis of 14,026 Koreans Reveals Known and Newly Discovered Genetic Loci Associated with Type 2 Diabetes Mellitus. Description: Cho, Seong Beom, et al. Exome Chip Analysis of 14,026 Koreans Reveals Known and Newly Discovered Genetic Loci Associated with Type 2 Diabetes Mellitus. ''Diabetes Metab J''. 2021 Mar; '''45''' (2):231-240
Functional annotation of lung cancerassociated genetic variants by cell typespecific epigenome and long-range chromatin interactome. Description: Lee, Andrew J, et al. Functional annotation of lung cancerassociated genetic variants by cell typespecific epigenome and long-range chromatin interactome. ''Genomics Inform''. 2021 Mar; '''19''' (1):e3
Genetic architecture and key genes controlling the diversity of oil composition in rice grains. Description: Zhou, Hao, et al. Genetic architecture and key genes controlling the diversity of oil composition in rice grains. ''Mol Plant''. 2021 Mar 1; '''14''' (3):456-469
Genome- and transcriptome-wide association studies provide insights into the genetic basis of natural variation of seed oil content in Brassica napus. Description: Tang, Shan, et al. Genome- and transcriptome-wide association studies provide insights into the genetic basis of natural variation of seed oil content in Brassica napus. ''Mol Plant''. 2021 Mar 1; '''14''' (3):470-487
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Description: Chia, Ruth, et al. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. ''Nat Genet''. 2021 Mar; '''53''' (3):294-303
Genome-wide association analysis identified molecular markers associated with important tea flavor-related metabolites. Description: Fang, Kaixing, et al. Genome-wide association analysis identified molecular markers associated with important tea flavor-related metabolites. ''Hortic Res''. 2021 Mar 1; '''8''' (1):42
Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations. Description: Quistrebert, Jocelyn, et al. Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations. ''PLoS Genet''. 2021 Mar; '''17''' (3):e1009392
Genomic association with pathogen carriage in bighorn sheep (Ovis canadensis). Description: Martin, Alynn M, et al. Genomic association with pathogen carriage in bighorn sheep (Ovis canadensis). ''Ecol Evol''. 2021 Mar; '''11''' (6):2488-2502
High prevalence of TP53 loss and whole-genome doubling in early-onset colorectal cancer. Description: Kim, Jeong Eun, et al. High prevalence of TP53 loss and whole-genome doubling in early-onset colorectal cancer. ''Exp Mol Med''. 2021 Mar; '''53''' (3):446-456
Human Leukocyte Antigen Class II associations in late-onset Myasthenia Gravis. Description: Spagni, Gregorio, et al. Human Leukocyte Antigen Class II associations in late-onset Myasthenia Gravis. ''Ann Clin Transl Neurol''. 2021 Mar; '''8''' (3):656-665
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. Description: Bonder, Marc Jan, et al. Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. ''Nat Genet''. 2021 Mar; '''53''' (3):313-321
IgA Levels Are Associated with Coronary Artery Lesions in Kawasaki Disease. Description: Kim, Jae Jung, et al. IgA Levels Are Associated with Coronary Artery Lesions in Kawasaki Disease. ''Korean Circ J''. 2021 Mar; '''51''' (3):267-278
Immune checkpoint-related serum proteins and genetic variants predict outcomes of localized prostate cancer, a cohort study. Description: Wang, Qinchuan, et al. Immune checkpoint-related serum proteins and genetic variants predict outcomes of localized prostate cancer, a cohort study. ''Cancer Immunol Immunother''. 2021 Mar; '''70''' (3):701-712
Implications of Polymorphisms in the BCKDK and GATA-4 Gene Regions on Stable Warfarin Dose in African Americans. Description: Bargal, Salma A, et al. Implications of Polymorphisms in the BCKDK and GATA-4 Gene Regions on Stable Warfarin Dose in African Americans. ''Clin Transl Sci''. 2021 Mar; '''14''' (2):492-496
Innate and Adaptive Gene Single Nucleotide Polymorphisms Associated With Susceptibility of Severe Inflammatory Complications in Acanthamoeba Keratitis. Description: Carnt, Nicole A, et al. Innate and Adaptive Gene Single Nucleotide Polymorphisms Associated With Susceptibility of Severe Inflammatory Complications in Acanthamoeba Keratitis. ''Invest Ophthalmol Vis Sci''. 2021 Mar 1; '''62''' (3):33
Integrated genetic analyses revealed novel human longevity loci and reduced risks of multiple diseases in a cohort study of 15,651 Chinese individuals. Description: Liu, Xiaomin, et al. Integrated genetic analyses revealed novel human longevity loci and reduced risks of multiple diseases in a cohort study of 15,651 Chinese individuals. ''Aging Cell''. 2021 Mar; '''20''' (3):e13323
Lung expression of genes putatively involved in SARS-CoV-2 infection is modulated in cis by germline variants. Description: Cotroneo, Chiara E, et al. Lung expression of genes putatively involved in SARS-CoV-2 infection is modulated in cis by germline variants. ''Eur J Hum Genet''. 2021 Mar 1;
MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies. Description: Bhattacharya, Arjun, et al. MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies. ''PLoS Genet''. 2021 Mar; '''17''' (3):e1009398
Natural variation in the regulation of neurodevelopmental genes modifies flight performance in Drosophila. Description: Spierer, Adam N, et al. Natural variation in the regulation of neurodevelopmental genes modifies flight performance in Drosophila. ''PLoS Genet''. 2021 Mar; '''17''' (3):e1008887
Population genomic structure of Eurasian and African foxtail millet landrace accessions inferred from genotyping-by-sequencing. Description: Hunt, Harriet V, et al. Population genomic structure of Eurasian and African foxtail millet landrace accessions inferred from genotyping-by-sequencing. ''Plant Genome''. 2021 Mar; '''14''' (1):e20081
Selection and introgression facilitated the adaptation of Chinese native endangered cattle in extreme environments. Description: Liu, Xinfeng, et al. Selection and introgression facilitated the adaptation of Chinese native endangered cattle in extreme environments. ''Evol Appl''. 2021 Mar; '''14''' (3):860-873
The ADCY9 genetic variants are associated with glioma susceptibility and patient prognosis. Description: Zhang, Gang, et al. The ADCY9 genetic variants are associated with glioma susceptibility and patient prognosis. ''Genomics''. 2021 Mar; '''113''' (2):706-716
The Effect of Common Variants in SLC44A2 on the Contribution to the Risk of Deep Cein Thrombosis after Orthopedic Surgery. Description: Zhi, Liqiang, et al. The Effect of Common Variants in SLC44A2 on the Contribution to the Risk of Deep Cein Thrombosis after Orthopedic Surgery. ''J Atheroscler Thromb''. 2021 Mar 1; '''28''' (3):293-303
The structure and diversity of strain-level variation in vaginal bacteria. Description: Tortelli, Brett A, et al. The structure and diversity of strain-level variation in vaginal bacteria. ''Microb Genom''. 2021 Mar; '''7''' (3):
Treatment response to low-dose ketamine infusion for treatment-resistant depression: A gene-based genome-wide association study. Description: Chen, Mu-Hong, et al. Treatment response to low-dose ketamine infusion for treatment-resistant depression: A gene-based genome-wide association study. ''Genomics''. 2021 Mar; '''113''' (2):507-514
Two novel loci underlie natural differences in Caenorhabditis elegans abamectin responses. Description: Evans, Kathryn S, et al. Two novel loci underlie natural differences in Caenorhabditis elegans abamectin responses. ''PLoS Pathog''. 2021 Mar; '''17''' (3):e1009297
Using historical genome-wide DNA to unravel the confused taxonomy in a songbird lineage that is extinct in the wild. Description: Baveja, Pratibha, et al. Using historical genome-wide DNA to unravel the confused taxonomy in a songbird lineage that is extinct in the wild. ''Evol Appl''. 2021 Mar; '''14''' (3):698-709
Whole-genome analyses provide no evidence for dog introgression in Fennoscandian wolf populations. Description: Smeds, Linnea, et al. Whole-genome analyses provide no evidence for dog introgression in Fennoscandian wolf populations. ''Evol Appl''. 2021 Mar; '''14''' (3):721-734
Whole-genome resequencing reveals diversity and selective signals in Longlin goat. Description: Chen, Qiuming, et al. Whole-genome resequencing reveals diversity and selective signals in Longlin goat. ''Gene''. 2021 Mar 1; '''771''': 145371
Whole-Genome Sequence Data Suggest Environmental Adaptation of Ethiopian Sheep Populations. Description: Wiener, Pamela, et al. Whole-Genome Sequence Data Suggest Environmental Adaptation of Ethiopian Sheep Populations. ''Genome Biol Evol''. 2021 Mar 1; '''13''' (3):
Fine-mapping of two differentiated thyroid carcinoma susceptibility loci at 2q35 and 8p12 in Europeans, Melanesians and Polynesians. Description: Guibon, Julie, et al. Fine-mapping of two differentiated thyroid carcinoma susceptibility loci at 2q35 and 8p12 in Europeans, Melanesians and Polynesians. ''Oncotarget''. 2021 Mar 2; '''12''' (5):493-506
Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder. Description: Bonelli, Roberto, et al. Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder. ''Commun Biol''. 2021 Mar 2; '''4''' (1):274
Identification of genetic loci affecting body mass index through interaction with multiple environmental factors using structured linear mixed model. Description: Jung, Hae-Un, et al. Identification of genetic loci affecting body mass index through interaction with multiple environmental factors using structured linear mixed model. ''Sci Rep''. 2021 Mar 2; '''11''' (1):5001
Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk. Description: Shigemizu, Daichi, et al. Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk. ''Transl Psychiatry''. 2021 Mar 3; '''11''' (1):151
Resequencing and SNP discovery of Amur ide (Leuciscus waleckii) provides insights into local adaptations to extreme environments. Description: Wang, Shuangyi, et al. Resequencing and SNP discovery of Amur ide (Leuciscus waleckii) provides insights into local adaptations to extreme environments. ''Sci Rep''. 2021 Mar 3; '''11''' (1):5064
Genome-wide epistasis analysis for Alzheimer's disease and implications for genetic risk prediction. Description: Wang, Hui, et al. Genome-wide epistasis analysis for Alzheimer's disease and implications for genetic risk prediction. ''Alzheimers Res Ther''. 2021 Mar 4; '''13''' (1):55
Integrative analysis of liver-specific non-coding regulatory SNPs associated with the risk of coronary artery disease. Description: Selvarajan, Ilakya, et al. Integrative analysis of liver-specific non-coding regulatory SNPs associated with the risk of coronary artery disease. ''Am J Hum Genet''. 2021 Mar 4; '''108''' (3):411-430
Polymorphisms of the matrix metalloproteinase genes are associated with essential hypertension in a Caucasian population of Central Russia. Description: Moskalenko, Maria, et al. Polymorphisms of the matrix metalloproteinase genes are associated with essential hypertension in a Caucasian population of Central Russia. ''Sci Rep''. 2021 Mar 4; '''11''' (1):5224
Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. Description: Somineni, Hari K, et al. Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. ''Am J Hum Genet''. 2021 Mar 4; '''108''' (3):431-445
Differential Effect of Polymorphisms on Body Mass Index Across the Life Course of Japanese: The Japan Multi-Institutional Collaborative Cohort Study. Description: Iwase, Madoka, et al. Differential Effect of Polymorphisms on Body Mass Index Across the Life Course of Japanese: The Japan Multi-Institutional Collaborative Cohort Study. ''J Epidemiol''. 2021 Mar 5; '''31''' (3):172-179
Shared genetic etiology between Parkinson's disease and blood levels of specific lipids. Description: Xicoy, Helena, et al. Shared genetic etiology between Parkinson's disease and blood levels of specific lipids. ''NPJ Parkinsons Dis''. 2021 Mar 5; '''7''' (1):23
Single cell eQTL analysis identifies cell type-specific genetic control of gene expression in fibroblasts and reprogrammed induced pluripotent stem cells. Description: Neavin, Drew, et al. Single cell eQTL analysis identifies cell type-specific genetic control of gene expression in fibroblasts and reprogrammed induced pluripotent stem cells. ''Genome Biol''. 2021 Mar 5; '''22''' (1):76
The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Description: Tilot, Amanda K, et al. The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. ''Cereb Cortex''. 2021 Mar 5; '''31''' (4):1873-1887
Variants in NEB and RIF1 genes on chr2q23 are associated with skeletal muscle index in Koreans: genome-wide association study. Description: Yoon, Kyung Jae, et al. Variants in NEB and RIF1 genes on chr2q23 are associated with skeletal muscle index in Koreans: genome-wide association study. ''Sci Rep''. 2021 Mar 5; '''11''' (1):2333
Assessing the genetic background and genomic relatedness of red cattle populations originating from Northern Europe. Description: Schmidtmann, Christin, et al. Assessing the genetic background and genomic relatedness of red cattle populations originating from Northern Europe. ''Genet Sel Evol''. 2021 Mar 6; '''53''' (1):23
Genome-wide association studies of plant architecture-related traits and 100-seed weight in soybean landraces. Description: Zhang, Xiaoli, et al. Genome-wide association studies of plant architecture-related traits and 100-seed weight in soybean landraces. ''BMC Genom Data''. 2021 Mar 6; '''22''' (1):10
Association of Leptin Receptor Gene Polymorphisms with Keloids in the Chinese Han Population. Description: Liu, Jing, et al. Association of Leptin Receptor Gene Polymorphisms with Keloids in the Chinese Han Population. ''Med Sci Monit''. 2021 Mar 7; '''27''': e928503
Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk. Description: Ngo, Debby, et al. Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk. ''JCI Insight''. 2021 Mar 8; '''6''' (5):
Testing Implications of the Omnigenic Model for the Genetic Analysis of Loci Identified through Genome-wide Association. Description: Zhang, Wenyu, et al. Testing Implications of the Omnigenic Model for the Genetic Analysis of Loci Identified through Genome-wide Association. ''Curr Biol''. 2021 Mar 8; '''31''' (5):1092-1098.e6
A General Model to Explain Repeated Turnovers of Sex Determination in the Salicaceae. Description: Yang, Wenlu, et al. A General Model to Explain Repeated Turnovers of Sex Determination in the Salicaceae. ''Mol Biol Evol''. 2021 Mar 9; '''38''' (3):968-980
Detection of breeding signatures in wheat using a linkage disequilibrium-corrected mapping approach. Description: Dadshani, Said, et al. Detection of breeding signatures in wheat using a linkage disequilibrium-corrected mapping approach. ''Sci Rep''. 2021 Mar 9; '''11''' (1):5527
Genetic disruption of serine biosynthesis is a key driver of macular telangiectasia type 2 aetiology and progression. Description: Bonelli, Roberto, et al. Genetic disruption of serine biosynthesis is a key driver of macular telangiectasia type 2 aetiology and progression. ''Genome Med''. 2021 Mar 9; '''13''' (1):39
Genomic Analysis Revealed a Convergent Evolution of LINE-1 in Coat Color: A Case Study in Water Buffaloes (Bubalus bubalis). Description: Liang, Dong, et al. Genomic Analysis Revealed a Convergent Evolution of LINE-1 in Coat Color: A Case Study in Water Buffaloes (Bubalus bubalis). ''Mol Biol Evol''. 2021 Mar 9; '''38''' (3):1122-1136
Historical Introgression from Wild Relatives Enhanced Climatic Adaptation and Resistance to Pneumonia in Sheep. Description: Cao, Yin-Hong, et al. Historical Introgression from Wild Relatives Enhanced Climatic Adaptation and Resistance to Pneumonia in Sheep. ''Mol Biol Evol''. 2021 Mar 9; '''38''' (3):838-855
Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder. Description: Mufti, Kheireddin, et al. Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder. ''Neurology''. 2021 Mar 9; '''96''' (10):e1402-e1412
Omics data integration identifies ELOVL7 and MMD gene regions as novel loci for adalimumab response in patients with Crohn's disease. Description: Gorenjak, Mario, et al. Omics data integration identifies ELOVL7 and MMD gene regions as novel loci for adalimumab response in patients with Crohn's disease. ''Sci Rep''. 2021 Mar 9; '''11''' (1):5449
Population Genomics Reveals Incipient Speciation, Introgression, and Adaptation in the African Mona Monkey (Cercopithecus mona). Description: Ayoola, Adeola Oluwakemi, et al. Population Genomics Reveals Incipient Speciation, Introgression, and Adaptation in the African Mona Monkey (Cercopithecus mona). ''Mol Biol Evol''. 2021 Mar 9; '''38''' (3):876-890
A novel nonsense variant of the AGXT identified in a Chinese family: special variant research in the Chinese reference genome. Description: Xu, Chang Bao, et al. A novel nonsense variant of the AGXT identified in a Chinese family: special variant research in the Chinese reference genome. ''BMC Nephrol''. 2021 Mar 10; '''22''' (1):83
Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease. Description: Horowitz, Julie E, et al. Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease. ''Sci Rep''. 2021 Mar 10; '''11''' (1):5595
GWAS findings improved genomic prediction accuracy of lipid profile traits: Tehran Cardiometabolic Genetic Study. Description: Akbarzadeh, Mahdi, et al. GWAS findings improved genomic prediction accuracy of lipid profile traits: Tehran Cardiometabolic Genetic Study. ''Sci Rep''. 2021 Mar 11; '''11''' (1):5780
Imputation accuracy to whole-genome sequence in Nellore cattle. Description: Fernandes Junior, Gerardo A, et al. Imputation accuracy to whole-genome sequence in Nellore cattle. ''Genet Sel Evol''. 2021 Mar 12; '''53''' (1):27
Population genomic and historical analysis suggests a global invasion by bridgehead processes in Mimulus guttatus. Description: Vallejo-Marin, Mario, et al. Population genomic and historical analysis suggests a global invasion by bridgehead processes in Mimulus guttatus. ''Commun Biol''. 2021 Mar 12; '''4''' (1):327
Whole genome comparisons reveal panmixia among fall armyworm (Spodoptera frugiperda) from diverse locations. Description: Schlum, Katrina A, et al. Whole genome comparisons reveal panmixia among fall armyworm (Spodoptera frugiperda) from diverse locations. ''BMC Genomics''. 2021 Mar 12; '''22''' (1):179
Interaction of Sirtuin 1 (SIRT1) candidate longevity gene and particulate matter (PM2.5) on all-cause mortality: a longitudinal cohort study in China. Description: Yao, Yao, et al. Interaction of Sirtuin 1 (SIRT1) candidate longevity gene and particulate matter (PM2.5) on all-cause mortality: a longitudinal cohort study in China. ''Environ Health''. 2021 Mar 14; '''20''' (1):25
Genetic association and causal inference converge on hyperglycaemia as a modifiable factor to improve lung function. Description: Reay, William R, et al. Genetic association and causal inference converge on hyperglycaemia as a modifiable factor to improve lung function. ''Elife''. 2021 Mar 15; '''10''':
Predicting alcohol use disorder remission: a longitudinal multimodal multi-featured machine learning approach. Description: Kinreich, Sivan, et al. Predicting alcohol use disorder remission: a longitudinal multimodal multi-featured machine learning approach. ''Transl Psychiatry''. 2021 Mar 15; '''11''' (1):166
Associations Between Cytochrome P450 (CYP) Gene Single-Nucleotide Polymorphisms and Second-to-Fourth Digit Ratio in Chinese University Students. Description: Zhang, Jing, et al. Associations Between Cytochrome P450 (CYP) Gene Single-Nucleotide Polymorphisms and Second-to-Fourth Digit Ratio in Chinese University Students. ''Med Sci Monit''. 2021 Mar 16; '''27''': e930591
Transcriptome-wide association study reveals two genes that influence mismatch negativity. Description: Bhat, Anjali, et al. Transcriptome-wide association study reveals two genes that influence mismatch negativity. ''Cell Rep''. 2021 Mar 16; '''34''' (11):108868
A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21. Description: Toma, Claudio, et al. A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21. ''J Psychiatry Neurosci''. 2021 Mar 17; '''46''' (2):E247-E257
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients. Description: Stranneheim, Henrik, et al. Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients. ''Genome Med''. 2021 Mar 17; '''13''' (1):40
Estimating the effective sample size in association studies of quantitative traits. Description: Ziyatdinov, Andrey, et al. Estimating the effective sample size in association studies of quantitative traits. ''G3 (Bethesda)''. 2021 Mar 18;
Evaluation of genetic diversity and management of disease in Border Collie dogs. Description: Soh, Pamela Xing Yi, et al. Evaluation of genetic diversity and management of disease in Border Collie dogs. ''Sci Rep''. 2021 Mar 18; '''11''' (1):6243
Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. Description: Zeng, Zheng, et al. Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. ''BMC Med Genomics''. 2021 Mar 18; '''14''' (1):84
Using multivariate endophenotypes to identify psychophysiological mechanisms associated with polygenic scores for substance use, schizophrenia, and education attainment. Description: Harper, Jeremy, et al. Using multivariate endophenotypes to identify psychophysiological mechanisms associated with polygenic scores for substance use, schizophrenia, and education attainment. ''Psychol Med''. 2021 Mar 18; 1-11
Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population. Description: Wu, Zhongwei, et al. Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population. ''Medicine (Baltimore)''. 2021 Mar 19; '''100''' (11):e24818
Examining the association between exposome score for schizophrenia and functioning in schizophrenia, siblings, and healthy controls: Results from the EUGEI study. Description: Erzin, Gamze, et al. Examining the association between exposome score for schizophrenia and functioning in schizophrenia, siblings, and healthy controls: Results from the EUGEI study. ''Eur Psychiatry''. 2021 Mar 19; '''64''' (1):e25
Integration of summary data from GWAS and eQTL studies identified novel risk genes for coronary artery disease. Description: Zhong, Yigang, et al. Integration of summary data from GWAS and eQTL studies identified novel risk genes for coronary artery disease. ''Medicine (Baltimore)''. 2021 Mar 19; '''100''' (11):e24769
Population genomics and haplotype analysis in spelt and bread wheat identifies a gene regulating glume color. Description: Abrouk, Michael, et al. Population genomics and haplotype analysis in spelt and bread wheat identifies a gene regulating glume color. ''Commun Biol''. 2021 Mar 19; '''4''' (1):375
Genome-wide gene-environment interactions in neuroticism: an exploratory study across 25 environments. Description: Werme, Josefin, et al. Genome-wide gene-environment interactions in neuroticism: an exploratory study across 25 environments. ''Transl Psychiatry''. 2021 Mar 22; '''11''' (1):180
Genome-wide long non-coding RNA association study on Han Chinese women identifies lncHSAT164 as a novel susceptibility gene for breast cancer. Description: Xu, Jing-Kai, et al. Genome-wide long non-coding RNA association study on Han Chinese women identifies lncHSAT164 as a novel susceptibility gene for breast cancer. ''Chin Med J (Engl)''. 2021 Mar 22; '''134''' (10):1138-1145
Coping with brain amyloid: genetic heterogeneity and cognitive resilience to Alzheimer's pathophysiology. Description: Ramanan, Vijay K, et al. Coping with brain amyloid: genetic heterogeneity and cognitive resilience to Alzheimer's pathophysiology. ''Acta Neuropathol Commun''. 2021 Mar 23; '''9''' (1):48
A Missense Mutation in the KLF7 Gene Is a Potential Candidate Variant for Congenital Deafness in Australian Stumpy Tail Cattle Dogs. Description: Xu, Fangzheng, et al. A Missense Mutation in the KLF7 Gene Is a Potential Candidate Variant for Congenital Deafness in Australian Stumpy Tail Cattle Dogs. ''Genes (Basel)''. 2021 Mar 24; '''12''' (4):
Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals. Description: Martinez-Magana, Jose Jaime, et al. Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals. ''Sci Rep''. 2021 Mar 24; '''11''' (1):6771
Uncovering genomic regions controlling plant architectural traits in hexaploid wheat using different GWAS models. Description: Muhammad, Ali, et al. Uncovering genomic regions controlling plant architectural traits in hexaploid wheat using different GWAS models. ''Sci Rep''. 2021 Mar 24; '''11''' (1):6767
Association of Polygenetic Risk Scores Related to Cell Differentiation and Inflammation with Thyroid Cancer Risk and Genetic Interaction with Dietary Intake. Description: Song, Sang Shin, et al. Association of Polygenetic Risk Scores Related to Cell Differentiation and Inflammation with Thyroid Cancer Risk and Genetic Interaction with Dietary Intake. ''Cancers (Basel)''. 2021 Mar 25; '''13''' (7):
CPNE3 moderates the association between anxiety and working memory. Description: Chen, Chunhui, et al. CPNE3 moderates the association between anxiety and working memory. ''Sci Rep''. 2021 Mar 25; '''11''' (1):6891
New susceptibility alleles associated with severe coronary artery stenosis in the Lebanese population. Description: Wakim, Victor, et al. New susceptibility alleles associated with severe coronary artery stenosis in the Lebanese population. ''BMC Med Genomics''. 2021 Mar 25; '''14''' (1):90
Genome-Wide Analyses Reveal Genetic Convergence of Prolificacy between Goats and Sheep. Description: Tao, Lin, et al. Genome-Wide Analyses Reveal Genetic Convergence of Prolificacy between Goats and Sheep. ''Genes (Basel)''. 2021 Mar 26; '''12''' (4):
Genotyping by Sequencing Reveals Genetic Relatedness of Southwestern U.S. Blue Maize Landraces. Description: Nankar, Amol N, et al. Genotyping by Sequencing Reveals Genetic Relatedness of Southwestern U.S. Blue Maize Landraces. ''Int J Mol Sci''. 2021 Mar 26; '''22''' (7):
Phenome-wide investigation of the causal associations between childhood BMI and adult trait outcomes: a two-sample Mendelian randomization study. Description: Dong, Shan-Shan, et al. Phenome-wide investigation of the causal associations between childhood BMI and adult trait outcomes: a two-sample Mendelian randomization study. ''Genome Med''. 2021 Mar 26; '''13''' (1):48
Polygenic risk scores for major psychiatric and neurodevelopmental disorders contribute to sleep disturbance in childhood: Adolescent Brain Cognitive Development (ABCD) Study. Description: Ohi, Kazutaka, et al. Polygenic risk scores for major psychiatric and neurodevelopmental disorders contribute to sleep disturbance in childhood: Adolescent Brain Cognitive Development (ABCD) Study. ''Transl Psychiatry''. 2021 Mar 26; '''11''' (1):187
Candidate Genes for the High-Altitude Adaptations of Two Mountain Pine Taxa. Description: Zaborowska, Julia, et al. Candidate Genes for the High-Altitude Adaptations of Two Mountain Pine Taxa. ''Int J Mol Sci''. 2021 Mar 27; '''22''' (7):
Genetic Factors Associated with COPD Depend on the Ancestral Caucasian/Amerindian Component in the Mexican Population. Description: Perez-Rubio, Gloria, et al. Genetic Factors Associated with COPD Depend on the Ancestral Caucasian/Amerindian Component in the Mexican Population. ''Diagnostics (Basel)''. 2021 Mar 27; '''11''' (4):
Genetic factors influencing a neurobiological substrate for psychiatric disorders. Description: Andlauer, Till F M, et al. Genetic factors influencing a neurobiological substrate for psychiatric disorders. ''Transl Psychiatry''. 2021 Mar 29; '''11''' (1):192
Insights into the demographic history of Asia from common ancestry and admixture in the genomic landscape of present-day Austroasiatic speakers. Description: Tagore, Debashree, et al. Insights into the demographic history of Asia from common ancestry and admixture in the genomic landscape of present-day Austroasiatic speakers. ''BMC Biol''. 2021 Mar 29; '''19''' (1):61
The Effect of FGF21 and Its Genetic Variants on Food and Drug Cravings, Adipokines and Metabolic Traits. Description: Epperlein, Sarah, et al. The Effect of FGF21 and Its Genetic Variants on Food and Drug Cravings, Adipokines and Metabolic Traits. ''Biomedicines''. 2021 Mar 29; '''9''' (4):
Genetic variants in the cholesterol biosynthesis pathway genes and risk of prostate cancer. Description: Cheng, Yifei, et al. Genetic variants in the cholesterol biosynthesis pathway genes and risk of prostate cancer. ''Gene''. 2021 Mar 30; '''774''': 145432
Model-based assessment of replicability for genome-wide association meta-analysis. Description: McGuire, Daniel, et al. Model-based assessment of replicability for genome-wide association meta-analysis. ''Nat Commun''. 2021 Mar 30; '''12''' (1):1964
Multiple migrations to the Philippines during the last 50,000 years. Description: Larena, Maximilian, et al. Multiple migrations to the Philippines during the last 50,000 years. ''Proc Natl Acad Sci U S A''. 2021 Mar 30; '''118''' (13):
Prediction of steroid resistance and steroid dependence in nephrotic syndrome children. Description: Zaorska, Katarzyna, et al. Prediction of steroid resistance and steroid dependence in nephrotic syndrome children. ''J Transl Med''. 2021 Mar 30; '''19''' (1):130
Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood. Description: Pfeiffer, J R, et al. Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood. ''Clin Epigenetics''. 2021 Mar 31; '''13''' (1):68
Dietary Habit Is Associated with Depression and Intelligence: An Observational and Genome-Wide Environmental Interaction Analysis in the UK Biobank Cohort. Description: Cheng, Bolun, et al. Dietary Habit Is Associated with Depression and Intelligence: An Observational and Genome-Wide Environmental Interaction Analysis in the UK Biobank Cohort. ''Nutrients''. 2021 Mar 31; '''13''' (4):
Genetic influences on externalizing psychopathology overlap with cognitive functioning and show developmental variation. Description: Mollon, Josephine, et al. Genetic influences on externalizing psychopathology overlap with cognitive functioning and show developmental variation. ''Eur Psychiatry''. 2021 Mar 31; '''64''' (1):e29
Alignment of single-cell RNA-seq samples without overcorrection using kernel density matching. Description: Chen, Mengjie, et al. Alignment of single-cell RNA-seq samples without overcorrection using kernel density matching. ''Genome Res''. 2021 Apr; '''31''' (4):698-712
Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders. Description: Rao, Xi, et al. Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders. ''Mol Psychiatry''. 2021 Apr; '''26''' (4):1142-1151
ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease. Description: Helkkula, Pyry, et al. ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease. ''PLoS Genet''. 2021 Apr; '''17''' (4):e1009501
Archaeogenomic distinctiveness of the Isthmo-Colombian area. Description: Capodiferro, Marco Rosario, et al. Archaeogenomic distinctiveness of the Isthmo-Colombian area. ''Cell''. 2021 Apr 1; '''184''' (7):1706-1723.e24
A Single-Nucleotide Mutation in a GLUTAMATE RECEPTOR-LIKE Gene Confers Resistance to Fusarium Wilt in Gossypium hirsutum. Description: Liu, Shiming, et al. A Single-Nucleotide Mutation in a GLUTAMATE RECEPTOR-LIKE Gene Confers Resistance to Fusarium Wilt in Gossypium hirsutum. ''Adv Sci (Weinh)''. 2021 Apr; '''8''' (7):2002723
Assessment of LIN28A variants in Parkinson's disease in large European cohorts. Description: Diez-Fairen, Monica, et al. Assessment of LIN28A variants in Parkinson's disease in large European cohorts. ''Neurobiol Aging''. 2021 Apr; '''100''': 118.e1-118.e3
Association of MACROD2 gene variants with obesity and physical activity in a Korean population. Description: Kim, Hye-Rim, et al. Association of MACROD2 gene variants with obesity and physical activity in a Korean population. ''Mol Genet Genomic Med''. 2021 Apr; '''9''' (4):e1635
Association of Nucleotide Variants of GRHL3, IRF6, NAT2, SDC2, BCL3, and PVRL1 Genes with Nonsyndromic Cleft Lip With/Without Cleft Palate in Multigenerational Families: A Retrospective Study. Description: Neela, Praveen Kumar, et al. Association of Nucleotide Variants of GRHL3, IRF6, NAT2, SDC2, BCL3, and PVRL1 Genes with Nonsyndromic Cleft Lip With/Without Cleft Palate in Multigenerational Families: A Retrospective Study. ''Contemp Clin Dent''. 2021 Apr-Jun; '''12''' (2):138-142
Association of regular aerobic exercises and neuromuscular junction variants with incidence of frailty: an analysis of the Chinese Longitudinal Health and Longevity Survey. Description: Zhang, Yu-Jie, et al. Association of regular aerobic exercises and neuromuscular junction variants with incidence of frailty: an analysis of the Chinese Longitudinal Health and Longevity Survey. ''J Cachexia Sarcopenia Muscle''. 2021 Apr; '''12''' (2):350-357
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Description: Andlauer, Till F M, et al. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. ''Mol Psychiatry''. 2021 Apr; '''26''' (4):1286-1298
Characterization of alcohol polygenic risk scores in the context of mental health outcomes: Within-individual and intergenerational analyses in the Avon Longitudinal Study of Parents and Children. Description: Easey, Kayleigh E, et al. Characterization of alcohol polygenic risk scores in the context of mental health outcomes: Within-individual and intergenerational analyses in the Avon Longitudinal Study of Parents and Children. ''Drug Alcohol Depend''. 2021 Apr 1; '''221''': 108654
Childhood maltreatment and cognitive functioning: the role of depression, parental education, and polygenic predisposition. Description: Goltermann, Janik, et al. Childhood maltreatment and cognitive functioning: the role of depression, parental education, and polygenic predisposition. ''Neuropsychopharmacology''. 2021 Apr; '''46''' (5):891-899
Comparisons of Polyexposure, Polygenic, and Clinical Risk Scores in Risk Prediction of Type 2 Diabetes. Description: He, Yixuan, et al. Comparisons of Polyexposure, Polygenic, and Clinical Risk Scores in Risk Prediction of Type 2 Diabetes. ''Diabetes Care''. 2021 Apr; '''44''' (4):935-943
Comprehensive analysis of the major histocompatibility complex in systemic sclerosis identifies differential HLA associations by clinical and serological subtypes. Description: Acosta-Herrera, Marialbert, et al. Comprehensive analysis of the major histocompatibility complex in systemic sclerosis identifies differential HLA associations by clinical and serological subtypes. ''Ann Rheum Dis''. 2021 Apr 1;
Diet quality indices, genetic risk and risk of cardiovascular disease and mortality: a longitudinal analysis of 77 004 UK Biobank participants. Description: Livingstone, Katherine M, et al. Diet quality indices, genetic risk and risk of cardiovascular disease and mortality: a longitudinal analysis of 77 004 UK Biobank participants. ''BMJ Open''. 2021 Apr 1; '''11''' (4):e045362
Episodes of gene flow and selection during the evolutionary history of domesticated barley. Description: Civan, Peter, et al. Episodes of gene flow and selection during the evolutionary history of domesticated barley. ''BMC Genomics''. 2021 Apr 1; '''22''' (1):227
Evaluating the association between single nucleotide polymorphisms in the stonin 2 (STON2) gene and keratoconus in a Han Chinese population. Description: Zhang, Jing, et al. Evaluating the association between single nucleotide polymorphisms in the stonin 2 (STON2) gene and keratoconus in a Han Chinese population. ''Ann Transl Med''. 2021 Apr; '''9''' (8):616
Genetic analyses of lodging resistance and yield provide insights into post-Green-Revolution breeding in rice. Description: Guo, Zilong, et al. Genetic analyses of lodging resistance and yield provide insights into post-Green-Revolution breeding in rice. ''Plant Biotechnol J''. 2021 Apr; '''19''' (4):814-829
Genetic predisposition to alcohol dependence: The combined role of polygenic risk to general psychopathology and to high alcohol consumption. Description: Facal, Fernando, et al. Genetic predisposition to alcohol dependence: The combined role of polygenic risk to general psychopathology and to high alcohol consumption. ''Drug Alcohol Depend''. 2021 Apr 1; '''221''': 108556
Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study. Description: Bowden, Sarah J, et al. Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study. ''Lancet Oncol''. 2021 Apr; '''22''' (4):548-557
Genetic Variations in Thiamin Transferase SLC35F3 and the Risk of Hypertension in Koreans. Description: Seo, Ja-Young, et al. Genetic Variations in Thiamin Transferase SLC35F3 and the Risk of Hypertension in Koreans. ''Clin Nutr Res''. 2021 Apr; '''10''' (2):140-149
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes. Description: Alfradique-Dunham, Isabel, et al. Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes. ''Neurol Genet''. 2021 Apr; '''7''' (2):e557
Genome-wide association study of cardiovascular disease in testicular cancer patients treated with platinum-based chemotherapy. Description: Steggink, Lars C, et al. Genome-wide association study of cardiovascular disease in testicular cancer patients treated with platinum-based chemotherapy. ''Pharmacogenomics J''. 2021 Apr; '''21''' (2):152-164
Heterogeneity of a dwarf phenotype in Dutch traditional chicken breeds revealed by genomic analyses. Description: Wu, Zhou, et al. Heterogeneity of a dwarf phenotype in Dutch traditional chicken breeds revealed by genomic analyses. ''Evol Appl''. 2021 Apr; '''14''' (4):1095-1108
High-throughput genotype-based population structure analysis of selected buffalo breeds. Description: Thakor, Prakash B, et al. High-throughput genotype-based population structure analysis of selected buffalo breeds. ''Transl Anim Sci''. 2021 Apr; '''5''' (2):txab033
Identification of common predisposing loci to hematopoietic cancers in four dog breeds. Description: Hedan, Benoit, et al. Identification of common predisposing loci to hematopoietic cancers in four dog breeds. ''PLoS Genet''. 2021 Apr; '''17''' (4):e1009395
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Description: Peyrot, Wouter J, et al. Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. ''Nat Genet''. 2021 Apr; '''53''' (4):445-454
Investigating regions of shared genetic variation in attention deficit/hyperactivity disorder and major depressive disorder: a GWAS meta-analysis. Description: Powell, Victoria, et al. Investigating regions of shared genetic variation in attention deficit/hyperactivity disorder and major depressive disorder: a GWAS meta-analysis. ''Sci Rep''. 2021 Apr 1; '''11''' (1):7353
MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneity. Description: Zhu, Anqi, et al. MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneity. ''PLoS Genet''. 2021 Apr; '''17''' (4):e1009455
Muscle allele-specific expression QTLs may affect meat quality traits in Bos indicus. Description: Bruscadin, Jennifer Jessica, et al. Muscle allele-specific expression QTLs may affect meat quality traits in Bos indicus. ''Sci Rep''. 2021 Apr 1; '''11''' (1):7321
Phenotypically independent profiles relevant to mental health are genetically correlated. Description: Roelfs, Daniel, et al. Phenotypically independent profiles relevant to mental health are genetically correlated. ''Transl Psychiatry''. 2021 Apr 1; '''11''' (1):202
Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank. Description: Fawcett, Katherine A, et al. Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank. ''ERJ Open Res''. 2021 Apr; '''7''' (2):
Polygenic Risk Scores Augment Stroke Subtyping. Description: Li, Jiang, et al. Polygenic Risk Scores Augment Stroke Subtyping. ''Neurol Genet''. 2021 Apr; '''7''' (2):e560
Population genomic evidence of Plasmodium vivax Southeast Asian origin. Description: Daron, Josquin, et al. Population genomic evidence of Plasmodium vivax Southeast Asian origin. ''Sci Adv''. 2021 Apr; '''7''' (18):
Rare, Protein-Altering Variants in AS3MT and Arsenic Metabolism Efficiency: A Multi-Population Association Study. Description: Delgado, Dayana A, et al. Rare, Protein-Altering Variants in AS3MT and Arsenic Metabolism Efficiency: A Multi-Population Association Study. ''Environ Health Perspect''. 2021 Apr; '''129''' (4):47007
Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD. Description: Wegermann, Kara, et al. Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD. ''Hepatol Commun''. 2021 Apr; '''5''' (4):598-607
Sex-stratified genome-wide association study of multisite chronic pain in UK Biobank. Description: Johnston, Keira J A, et al. Sex-stratified genome-wide association study of multisite chronic pain in UK Biobank. ''PLoS Genet''. 2021 Apr; '''17''' (4):e1009428
Single nucleotide polymorphisms associated with methotrexate-induced nausea in juvenile idiopathic arthritis. Description: Kyvsgaard, Nini, et al. Single nucleotide polymorphisms associated with methotrexate-induced nausea in juvenile idiopathic arthritis. ''Pediatr Rheumatol Online J''. 2021 Apr 1; '''19''' (1):51
The burden of rare damaging variants in hereditary atypical parkinsonism genes is increased in patients with Parkinson's disease. Description: Kim, Yun Joong, et al. The burden of rare damaging variants in hereditary atypical parkinsonism genes is increased in patients with Parkinson's disease. ''Neurobiol Aging''. 2021 Apr; '''100''': 118.e5-118.e13
The Effect of SMN Gene Dosage on ALS Risk and Disease Severity. Description: Moisse, Matthieu, et al. The Effect of SMN Gene Dosage on ALS Risk and Disease Severity. ''Ann Neurol''. 2021 Apr; '''89''' (4):686-697
The genomics of rapid climatic adaptation and parallel evolution in North American house mice. Description: Ferris, Kathleen G, et al. The genomics of rapid climatic adaptation and parallel evolution in North American house mice. ''PLoS Genet''. 2021 Apr; '''17''' (4):e1009495
Virus-derived variation in diverse human genomes. Description: Kojima, Shohei, et al. Virus-derived variation in diverse human genomes. ''PLoS Genet''. 2021 Apr; '''17''' (4):e1009324
Identification of novel functional CpG-SNPs associated with Type 2 diabetes and birth weight. Description: Liu, Rui-Ke, et al. Identification of novel functional CpG-SNPs associated with Type 2 diabetes and birth weight. ''Aging (Albany NY)''. 2021 Apr 4; '''13''' (7):10619-10658
Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine. Description: Bastard, Paul, et al. Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine. ''J Exp Med''. 2021 Apr 5; '''218''' (4):
Exome-wide scan identifies significant association of rs4788084 in IL27 promoter with increase in hepatic fat content among Indians. Description: Chatterjee, Ankita, et al. Exome-wide scan identifies significant association of rs4788084 in IL27 promoter with increase in hepatic fat content among Indians. ''Gene''. 2021 Apr 5; '''775''': 145431
Obelisc: an identical-by-descent mapping tool based on SNP streak. Description: Sonehara, Kyuto, et al. Obelisc: an identical-by-descent mapping tool based on SNP streak. ''Bioinformatics''. 2021 Apr 5; '''36''' (24):5567-5570
Genetic Regulation of Biomarkers as Stress Proxies in Dairy Cows. Description: Milanesi, Marco, et al. Genetic Regulation of Biomarkers as Stress Proxies in Dairy Cows. ''Genes (Basel)''. 2021 Apr 6; '''12''' (4):
Genome survey and high-resolution genetic map provide valuable genetic resources for Fenneropenaeus chinensis. Description: Meng, Xianhong, et al. Genome survey and high-resolution genetic map provide valuable genetic resources for Fenneropenaeus chinensis. ''Sci Rep''. 2021 Apr 6; '''11''' (1):7533
Genomic Context Differs Between Human Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy. Description: Puckelwartz, Megan J, et al. Genomic Context Differs Between Human Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy. ''J Am Heart Assoc''. 2021 Apr 6; '''10''' (7):e019944
Genetic substructure and complex demographic history of South African Bantu speakers. Description: Sengupta, Dhriti, et al. Genetic substructure and complex demographic history of South African Bantu speakers. ''Nat Commun''. 2021 Apr 7; '''12''' (1):2080
Interactions of genetic variants and prenatal stress in relation to the risk for recurrent respiratory infections in children. Description: Korhonen, Laura S, et al. Interactions of genetic variants and prenatal stress in relation to the risk for recurrent respiratory infections in children. ''Sci Rep''. 2021 Apr 7; '''11''' (1):7589
Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality. Description: Alghamdi, Jahad, et al. Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality. ''Genomics''. 2021 Apr 7; '''113''' (4):1733-1741
Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19. Description: Klaric, Lucija, et al. Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19. ''medRxiv''. 2021 Apr 7;
The impact of late-career job loss and genetic risk on body mass index: Evidence from variance polygenic scores. Description: Schmitz, Lauren L, et al. The impact of late-career job loss and genetic risk on body mass index: Evidence from variance polygenic scores. ''Sci Rep''. 2021 Apr 7; '''11''' (1):7647
The OSMR Gene Is Involved in Hirschsprung Associated Enterocolitis Susceptibility through an Altered Downstream Signaling. Description: Bachetti, Tiziana, et al. The OSMR Gene Is Involved in Hirschsprung Associated Enterocolitis Susceptibility through an Altered Downstream Signaling. ''Int J Mol Sci''. 2021 Apr 7; '''22''' (8):
Association of TGFB -509C>T promoter polymorphism with primary angle closure glaucoma in a North Indian Punjabi cohort. Description: Thakur, Nanamika, et al. Association of TGFB -509C>T promoter polymorphism with primary angle closure glaucoma in a North Indian Punjabi cohort. ''BMC Ophthalmol''. 2021 Apr 8; '''21''' (1):165
Effects of polygenic risk for major mental disorders and cross-disorder on cortical complexity. Description: Schmitt, Simon, et al. Effects of polygenic risk for major mental disorders and cross-disorder on cortical complexity. ''Psychol Med''. 2021 Apr 8; '''52''' (16):1-12
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Description: Curtis, Sarah W, et al. The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. ''HGG Adv''. 2021 Apr 8; '''2''' (2):
Transcriptome prediction performance across machine learning models and diverse ancestries. Description: Okoro, Paul C, et al. Transcriptome prediction performance across machine learning models and diverse ancestries. ''HGG Adv''. 2021 Apr 8; '''2''' (2):
A G316A Polymorphism in the Ornithine Decarboxylase Gene Promoter Modulates MYCN-Driven Childhood Neuroblastoma. Description: Gamble, Laura D, et al. A G316A Polymorphism in the Ornithine Decarboxylase Gene Promoter Modulates MYCN-Driven Childhood Neuroblastoma. ''Cancers (Basel)''. 2021 Apr 9; '''13''' (8):
Association of ST6GAL1 and CYP19A1 polymorphisms in the 3'-UTR with astrocytoma risk and prognosis in a Chinese Han population. Description: Wang, Tuo, et al. Association of ST6GAL1 and CYP19A1 polymorphisms in the 3'-UTR with astrocytoma risk and prognosis in a Chinese Han population. ''BMC Cancer''. 2021 Apr 9; '''21''' (1):391
Distinct clinical phenotypes for Crohn's disease derived from patient surveys. Description: Liu, Tianyun, et al. Distinct clinical phenotypes for Crohn's disease derived from patient surveys. ''BMC Gastroenterol''. 2021 Apr 9; '''21''' (1):160
A combined RAD-Seq and WGS approach reveals the genomic basis of yellow color variation in bumble bee Bombus terrestris. Description: Rahman, Sarthok Rasique, et al. A combined RAD-Seq and WGS approach reveals the genomic basis of yellow color variation in bumble bee Bombus terrestris. ''Sci Rep''. 2021 Apr 12; '''11''' (1):7996
Cardiometabolic risks of SARS-CoV-2 hospitalization using Mendelian Randomization. Description: Lorincz-Comi, Noah, et al. Cardiometabolic risks of SARS-CoV-2 hospitalization using Mendelian Randomization. ''Sci Rep''. 2021 Apr 12; '''11''' (1):7848
HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry. Description: Konte, Bettina, et al. HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry. ''Transl Psychiatry''. 2021 Apr 12; '''11''' (1):214
Intake of food rich in saturated fat in relation to subclinical atherosclerosis and potential modulating effects from single genetic variants. Description: Laguzzi, Federica, et al. Intake of food rich in saturated fat in relation to subclinical atherosclerosis and potential modulating effects from single genetic variants. ''Sci Rep''. 2021 Apr 12; '''11''' (1):7866
Multiomics integrative analysis identifies APOE allele-specific blood biomarkers associated to Alzheimer's disease etiopathogenesis. Description: Madrid, Laura, et al. Multiomics integrative analysis identifies APOE allele-specific blood biomarkers associated to Alzheimer's disease etiopathogenesis. ''Aging (Albany NY)''. 2021 Apr 12; '''13''' (7):9277-9329
Prediction of Alzheimer's disease using multi-variants from a Chinese genome-wide association study. Description: Jia, Longfei, et al. Prediction of Alzheimer's disease using multi-variants from a Chinese genome-wide association study. ''Brain''. 2021 Apr 12; '''144''' (3):924-937
A model and test for coordinated polygenic epistasis in complex traits. Description: Sheppard, Brooke, et al. A model and test for coordinated polygenic epistasis in complex traits. ''Proc Natl Acad Sci U S A''. 2021 Apr 13; '''118''' (15):
Analysis of whole-genome re-sequencing data of ducks reveals a diverse demographic history and extensive gene flow between Southeast/South Asian and Chinese populations. Description: Jiang, Fan, et al. Analysis of whole-genome re-sequencing data of ducks reveals a diverse demographic history and extensive gene flow between Southeast/South Asian and Chinese populations. ''Genet Sel Evol''. 2021 Apr 13; '''53''' (1):35
A New Catalog of Structural Variants in 1,301 A. thaliana Lines from Africa, Eurasia, and North America Reveals a Signature of Balancing Selection at Defense Response Genes. Description: Goktay, Mehmet, et al. A New Catalog of Structural Variants in 1,301 A. thaliana Lines from Africa, Eurasia, and North America Reveals a Signature of Balancing Selection at Defense Response Genes. ''Mol Biol Evol''. 2021 Apr 13; '''38''' (4):1498-1511
A Two-Locus System with Strong Epistasis Underlies Rapid Parasite-Mediated Evolution of Host Resistance. Description: Ameline, Camille, et al. A Two-Locus System with Strong Epistasis Underlies Rapid Parasite-Mediated Evolution of Host Resistance. ''Mol Biol Evol''. 2021 Apr 13; '''38''' (4):1512-1528
Comparative analysis of chloroplast genomes of cultivars and wild species of sweetpotato (Ipomoea batatas [L.] Lam). Description: Xiao, Shizhuo, et al. Comparative analysis of chloroplast genomes of cultivars and wild species of sweetpotato (Ipomoea batatas [L.] Lam). ''BMC Genomics''. 2021 Apr 13; '''22''' (1):262
Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis. Description: Heng, Anna Hwee Sing, et al. Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis. ''BMC Med Genomics''. 2021 Apr 13; '''14''' (1):103
Machine learning, transcriptome, and genotyping chip analyses provide insights into SNP markers identifying flower color in Platycodon grandiflorus. Description: Yu, Go-Eun, et al. Machine learning, transcriptome, and genotyping chip analyses provide insights into SNP markers identifying flower color in Platycodon grandiflorus. ''Sci Rep''. 2021 Apr 13; '''11''' (1):8019
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. Description: Shang, Ning, et al. Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. ''NPJ Digit Med''. 2021 Apr 13; '''4''' (1):70
Genetic diversity in global chicken breeds in relation to their genetic distances to wild populations. Description: Malomane, Dorcus Kholofelo, et al. Genetic diversity in global chicken breeds in relation to their genetic distances to wild populations. ''Genet Sel Evol''. 2021 Apr 14; '''53''' (1):36
Complex pleiotropic genetic architecture of evolved heat stress and oxidative stress resistance in the nematode Caenorhabditis remanei. Description: O'Connor, Christine H, et al. Complex pleiotropic genetic architecture of evolved heat stress and oxidative stress resistance in the nematode Caenorhabditis remanei. ''G3 (Bethesda)''. 2021 Apr 15; '''11''' (4):
Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility. Description: Lonjou, Christine, et al. Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility. ''Int J Cancer''. 2021 Apr 15; '''148''' (8):1895-1909
Genetic characterization of a Sorghum bicolor multiparent mapping population emphasizing carbon-partitioning dynamics. Description: Boatwright, J Lucas, et al. Genetic characterization of a Sorghum bicolor multiparent mapping population emphasizing carbon-partitioning dynamics. ''G3 (Bethesda)''. 2021 Apr 15; '''11''' (4):
Genetic scores for adult subcortical volumes associate with subcortical volumes during infancy and childhood. Description: Lamballais, Sander, et al. Genetic scores for adult subcortical volumes associate with subcortical volumes during infancy and childhood. ''Hum Brain Mapp''. 2021 Apr 15; '''42''' (6):1583-1593
High-resolution genome-wide association study pinpoints metal transporter and chelator genes involved in the genetic control of element levels in maize grain. Description: Wu, Di, et al. High-resolution genome-wide association study pinpoints metal transporter and chelator genes involved in the genetic control of element levels in maize grain. ''G3 (Bethesda)''. 2021 Apr 15; '''11''' (4):
Risk of gout among Taiwanese adults with ALDH-2 rs671 polymorphism according to BMI and alcohol intake. Description: Liu, Yu-Ruey, et al. Risk of gout among Taiwanese adults with ALDH-2 rs671 polymorphism according to BMI and alcohol intake. ''Arthritis Res Ther''. 2021 Apr 15; '''23''' (1):115
Deletion of CTCF sites in the SHH locus alters enhancer-promoter interactions and leads to acheiropodia. Description: Ushiki, Aki, et al. Deletion of CTCF sites in the SHH locus alters enhancer-promoter interactions and leads to acheiropodia. ''Nat Commun''. 2021 Apr 16; '''12''' (1):2282
Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease. Description: Watt, Stephen, et al. Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease. ''Nat Commun''. 2021 Apr 16; '''12''' (1):2298
Identification of Novel Loci and Candidate Genes for Resistance to Powdery Mildew in a Resequenced Cucumber Germplasm. Description: Liu, Xiaoping, et al. Identification of Novel Loci and Candidate Genes for Resistance to Powdery Mildew in a Resequenced Cucumber Germplasm. ''Genes (Basel)''. 2021 Apr 16; '''12''' (4):
Genome-Wide Association Study Demonstrates the Role Played by the CD226 Gene in Rasa Aragonesa Sheep Reproductive Seasonality. Description: Lakhssassi, Kenza, et al. Genome-Wide Association Study Demonstrates the Role Played by the CD226 Gene in Rasa Aragonesa Sheep Reproductive Seasonality. ''Animals (Basel)''. 2021 Apr 19; '''11''' (4):
Genome-Wide Association Study of Local Thai Indica Rice Seedlings Exposed to Excessive Iron. Description: Kaewcheenchai, Reunreudee, et al. Genome-Wide Association Study of Local Thai Indica Rice Seedlings Exposed to Excessive Iron. ''Plants (Basel)''. 2021 Apr 19; '''10''' (4):
Germline variants at SOHLH2 influence multiple myeloma risk. Description: Duran-Lozano, Laura, et al. Germline variants at SOHLH2 influence multiple myeloma risk. ''Blood Cancer J''. 2021 Apr 19; '''11''' (4):76
The mitochondrial genomes of the human pathogens Coccidioides immitis and C. posadasii. Description: de Melo Teixeira, Marcus, et al. The mitochondrial genomes of the human pathogens Coccidioides immitis and C. posadasii. ''G3 (Bethesda)''. 2021 Apr 19;
Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants. Description: Pinsach-Abuin, Mel Lina, et al. Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants. ''Cell Rep Med''. 2021 Apr 20; '''2''' (4):100250
Association among extracellular superoxide dismutase genotype, plasma concentration, and comorbidity in the very old and centenarians. Description: Sasaki, Takashi, et al. Association among extracellular superoxide dismutase genotype, plasma concentration, and comorbidity in the very old and centenarians. ''Sci Rep''. 2021 Apr 20; '''11''' (1):8539
Association between genetic variants of the norepinephrine transporter gene (SLC6A2) and bipolar I disorder. Description: Kim, Sun-Young, et al. Association between genetic variants of the norepinephrine transporter gene (SLC6A2) and bipolar I disorder. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2021 Apr 20; '''107''': 110227
Genetic diversity of the North African population revealed by the typing of SNPs in the DRD2/ANKK1 genomic region. Description: Mestiri, Souhir, et al. Genetic diversity of the North African population revealed by the typing of SNPs in the DRD2/ANKK1 genomic region. ''Gene''. 2021 Apr 20; '''777''': 145466
Genome-Wide Association Study Reveals the QTLs for Seed Storability in World Rice Core Collections. Description: Wu, Fangxi, et al. Genome-Wide Association Study Reveals the QTLs for Seed Storability in World Rice Core Collections. ''Plants (Basel)''. 2021 Apr 20; '''10''' (4):
Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis. Description: Ojavee, Sven E, et al. Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis. ''Nat Commun''. 2021 Apr 20; '''12''' (1):2337
Genomic insights into the origin, domestication and genetic basis of agronomic traits of castor bean. Description: Xu, Wei, et al. Genomic insights into the origin, domestication and genetic basis of agronomic traits of castor bean. ''Genome Biol''. 2021 Apr 20; '''22''' (1):113
HATK: HLA analysis toolkit. Description: Choi, Wanson, et al. HATK: HLA analysis toolkit. ''Bioinformatics''. 2021 Apr 20; '''37''' (3):416-418
NOD1 rs2075820 (p.E266K) polymorphism is associated with gastric cancer among individuals infected with cagPAI-positive H. pylori. Description: Gonzalez-Hormazabal, Patricio, et al. NOD1 rs2075820 (p.E266K) polymorphism is associated with gastric cancer among individuals infected with cagPAI-positive H. pylori. ''Biol Res''. 2021 Apr 20; '''54''' (1):13
SNPs with intermediate minor allele frequencies facilitate accurate breed assignment of Indian Tharparkar cattle. Description: Kumar, Harshit, et al. SNPs with intermediate minor allele frequencies facilitate accurate breed assignment of Indian Tharparkar cattle. ''Gene''. 2021 Apr 20; '''777''': 145473
The impact of identity by descent on fitness and disease in dogs. Description: Mooney, Jazlyn A, et al. The impact of identity by descent on fitness and disease in dogs. ''Proc Natl Acad Sci U S A''. 2021 Apr 20; '''118''' (16):
The polymorphisms of FGFR2 and MGAT5 affect the susceptibility to COPD in the Chinese people. Description: Li, Xiaobo, et al. The polymorphisms of FGFR2 and MGAT5 affect the susceptibility to COPD in the Chinese people. ''BMC Pulm Med''. 2021 Apr 20; '''21''' (1):129
ABO blood groups, COVID-19 infection and mortality. Description: Lehrer, Steven, et al. ABO blood groups, COVID-19 infection and mortality. ''Blood Cells Mol Dis''. 2021 Apr 21; '''89''': 102571
Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs. Description: Noskova, Adela, et al. Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs. ''BMC Genomics''. 2021 Apr 21; '''22''' (1):290
Development of an Australian Bread Wheat Nested Association Mapping Population, a New Genetic Diversity Resource for Breeding under Dry and Hot Climates. Description: Chidzanga, Charity, et al. Development of an Australian Bread Wheat Nested Association Mapping Population, a New Genetic Diversity Resource for Breeding under Dry and Hot Climates. ''Int J Mol Sci''. 2021 Apr 21; '''22''' (9):
Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium. Description: Kasela, Silva, et al. Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium. ''Genome Med''. 2021 Apr 21; '''13''' (1):66
Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits. Description: Rizzardi, Lindsay F, et al. Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits. ''Genome Biol''. 2021 Apr 22; '''22''' (1):116
Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia. Description: Hao, Qing, et al. Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia. ''Aging (Albany NY)''. 2021 Apr 23; '''13''' (9):12456-12465
Cotton pan-genome retrieves the lost sequences and genes during domestication and selection. Description: Li, Jianying, et al. Cotton pan-genome retrieves the lost sequences and genes during domestication and selection. ''Genome Biol''. 2021 Apr 23; '''22''' (1):119
Homocysteine, B vitamins, and cardiovascular disease: a Mendelian randomization study. Description: Yuan, Shuai, et al. Homocysteine, B vitamins, and cardiovascular disease: a Mendelian randomization study. ''BMC Med''. 2021 Apr 23; '''19''' (1):97
The impact of non-additive genetic associations on age-related complex diseases. Description: Guindo-Martinez, Marta, et al. The impact of non-additive genetic associations on age-related complex diseases. ''Nat Commun''. 2021 Apr 23; '''12''' (1):2436
Enriched-GWAS and Transcriptome Analysis to Refine and Characterize a Major QTL for Anaerobic Germination Tolerance in Rice. Description: Tnani, Hedia, et al. Enriched-GWAS and Transcriptome Analysis to Refine and Characterize a Major QTL for Anaerobic Germination Tolerance in Rice. ''Int J Mol Sci''. 2021 Apr 24; '''22''' (9):
A Mendelian randomization study of the role of lipoprotein subfractions in coronary artery disease. Description: Zhao, Qingyuan, et al. A Mendelian randomization study of the role of lipoprotein subfractions in coronary artery disease. ''Elife''. 2021 Apr 26; '''10''':
A Nonsense Variant in Hephaestin Like 1 (HEPHL1) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle. Description: Kuca, Thibaud, et al. A Nonsense Variant in Hephaestin Like 1 (HEPHL1) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle. ''Genes (Basel)''. 2021 Apr 26; '''12''' (5):
Gene network and biological pathways associated with susceptibility to differentiated thyroid carcinoma. Description: Kulkarni, Om, et al. Gene network and biological pathways associated with susceptibility to differentiated thyroid carcinoma. ''Sci Rep''. 2021 Apr 26; '''11''' (1):8932
Association between CCN1 gene polymorphism and acute coronary syndrome in Chinese Han and Uygur populations. Description: Li, Yan-Hong, et al. Association between CCN1 gene polymorphism and acute coronary syndrome in Chinese Han and Uygur populations. ''Hereditas''. 2021 Apr 27; '''158''' (1):16
Genome wide association study identifies four loci for early onset schizophrenia. Description: Guo, Suqin, et al. Genome wide association study identifies four loci for early onset schizophrenia. ''Transl Psychiatry''. 2021 Apr 27; '''11''' (1):248
Genome-wide association study of circulating interleukin 6 levels identifies novel loci. Description: Ahluwalia, Tarunveer S, et al. Genome-wide association study of circulating interleukin 6 levels identifies novel loci. ''Hum Mol Genet''. 2021 Apr 27; '''30''' (5):393-409
Causal Effects of Serum Levels of n-3 or n-6 Polyunsaturated Fatty Acids on Coronary Artery Disease: Mendelian Randomization Study. Description: Park, Sehoon, et al. Causal Effects of Serum Levels of n-3 or n-6 Polyunsaturated Fatty Acids on Coronary Artery Disease: Mendelian Randomization Study. ''Nutrients''. 2021 Apr 28; '''13''' (5):
Differential expressions of anthocyanin synthesis genes underlie flower color divergence in a sympatric Rhododendron sanguineum complex. Description: Ye, Lin-Jiang, et al. Differential expressions of anthocyanin synthesis genes underlie flower color divergence in a sympatric Rhododendron sanguineum complex. ''BMC Plant Biol''. 2021 Apr 28; '''21''' (1):204
Variants at the ASIP locus contribute to coat color darkening in Nellore cattle. Description: Trigo, Beatriz B, et al. Variants at the ASIP locus contribute to coat color darkening in Nellore cattle. ''Genet Sel Evol''. 2021 Apr 28; '''53''' (1):40
Characteristics of epigenetic aging across gestational and perinatal tissues. Description: Dieckmann, Linda, et al. Characteristics of epigenetic aging across gestational and perinatal tissues. ''Clin Epigenetics''. 2021 Apr 29; '''13''' (1):97
Genome-wide insights on gastrointestinal nematode resistance in autochthonous Tunisian sheep. Description: Ahbara, A M, et al. Genome-wide insights on gastrointestinal nematode resistance in autochthonous Tunisian sheep. ''Sci Rep''. 2021 Apr 29; '''11''' (1):9250
Investigating Olfactory Gene Variation and Odour Identification in Older Adults. Description: Raj, Siddharth, et al. Investigating Olfactory Gene Variation and Odour Identification in Older Adults. ''Genes (Basel)''. 2021 Apr 29; '''12''' (5):
Investigation of triple-negative breast cancer risk alleles in an International African-enriched cohort. Description: Martini, Rachel, et al. Investigation of triple-negative breast cancer risk alleles in an International African-enriched cohort. ''Sci Rep''. 2021 Apr 29; '''11''' (1):9247
KLK3 SNP-SNP interactions for prediction of prostate cancer aggressiveness. Description: Lin, Hui-Yi, et al. KLK3 SNP-SNP interactions for prediction of prostate cancer aggressiveness. ''Sci Rep''. 2021 Apr 29; '''11''' (1):9264
The association of heat shock protein genetic polymorphisms with age-related hearing impairment in Taiwan. Description: Chang, Ning-Chia, et al. The association of heat shock protein genetic polymorphisms with age-related hearing impairment in Taiwan. ''J Otolaryngol Head Neck Surg''. 2021 Apr 29; '''50''' (1):31
The impact of cell type and context-dependent regulatory variants on human immune traits. Description: Mu, Zepeng, et al. The impact of cell type and context-dependent regulatory variants on human immune traits. ''Genome Biol''. 2021 Apr 29; '''22''' (1):122
Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes. Description: Torres, Guillermo G, et al. Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes. ''J Gerontol A Biol Sci Med Sci''. 2021 Apr 30; '''76''' (5):786-795
Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS). Description: Najd Hassan Bonab, Leila, et al. Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS). ''Gene''. 2021 Apr 30; '''778''': 145485
MARS: leveraging allelic heterogeneity to increase power of association testing. Description: Hormozdiari, Farhad, et al. MARS: leveraging allelic heterogeneity to increase power of association testing. ''Genome Biol''. 2021 Apr 30; '''22''' (1):128
Polygenic Risk Score of Longevity Predicts Longer Survival Across an Age Continuum. Description: Tesi, Niccolo', et al. Polygenic Risk Score of Longevity Predicts Longer Survival Across an Age Continuum. ''J Gerontol A Biol Sci Med Sci''. 2021 Apr 30; '''76''' (5):750-759
3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Description: Hoskens, Hanne, et al. 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. ''PLoS Genet''. 2021 May; '''17''' (5):e1009528
A genome-wide association study for prolificacy in three Polish sheep breeds. Description: Smolucha, Grzegorz, et al. A genome-wide association study for prolificacy in three Polish sheep breeds. ''J Appl Genet''. 2021 May; '''62''' (2):323-326
Ancestry specific associations of a genetic risk score, dietary patterns and metabolic syndrome: a longitudinal ARIC study. Description: Hardy, Dale S, et al. Ancestry specific associations of a genetic risk score, dietary patterns and metabolic syndrome: a longitudinal ARIC study. ''BMC Med Genomics''. 2021 May 1; '''14''' (1):118
An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training-induced muscle fiber hypertrophy in younger men. Description: Vann, Christopher G, et al. An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training-induced muscle fiber hypertrophy in younger men. ''FASEB J''. 2021 May; '''35''' (5):e21587
Association between the Arylalkylamine N-Acetyltransferase (AANAT) Gene and Seasonality in Patients with Bipolar Disorder. Description: Yang, So Yung, et al. Association between the Arylalkylamine N-Acetyltransferase (AANAT) Gene and Seasonality in Patients with Bipolar Disorder. ''Psychiatry Investig''. 2021 May; '''18''' (5):453-462
Association of the CD2AP locus with cognitive functioning among middle-aged individuals with a family history of Alzheimer's disease. Description: Manzali, Sigalit Batia, et al. Association of the CD2AP locus with cognitive functioning among middle-aged individuals with a family history of Alzheimer's disease. ''Neurobiol Aging''. 2021 May; '''101''': 50-56
Beta-lactam-induced immediate hypersensitivity reactions: A genome-wide association study of a deeply phenotyped cohort. Description: Nicoletti, Paola, et al. Beta-lactam-induced immediate hypersensitivity reactions: A genome-wide association study of a deeply phenotyped cohort. ''J Allergy Clin Immunol''. 2021 May; '''147''' (5):1830-1837.e15
Childhood trauma, life-time self-harm, and suicidal behaviour and ideation are associated with polygenic scores for autism. Description: Warrier, Varun, et al. Childhood trauma, life-time self-harm, and suicidal behaviour and ideation are associated with polygenic scores for autism. ''Mol Psychiatry''. 2021 May; '''26''' (5):1670-1684
Chronic migraine: Genetics or environment? Description: Chalmer, Mona Ameri, et al. Chronic migraine: Genetics or environment? ''Eur J Neurol''. 2021 May; '''28''' (5):1726-1736
Clinical and Genetic Findings in 28 American Cocker Spaniels with Aural Ceruminous Gland Hyperplasia and Ectasia. Description: Kaimio, Mirja, et al. Clinical and Genetic Findings in 28 American Cocker Spaniels with Aural Ceruminous Gland Hyperplasia and Ectasia. ''J Comp Pathol''. 2021 May; '''185''': 30-44
Comprehensive genotyping of a Brazilian cassava (Manihot esculenta Crantz) germplasm bank: insights into diversification and domestication. Description: Ogbonna, Alex C, et al. Comprehensive genotyping of a Brazilian cassava (Manihot esculenta Crantz) germplasm bank: insights into diversification and domestication. ''Theor Appl Genet''. 2021 May; '''134''' (5):1343-1362
Design and evaluation of a custom 50K Infinium SNP array for egg-type chickens. Description: Liu, Zhuang, et al. Design and evaluation of a custom 50K Infinium SNP array for egg-type chickens. ''Poult Sci''. 2021 May; '''100''' (5):101044
Dissecting the role of Amerindian genetic ancestry and the ApoE epsilon4 allele on Alzheimer disease in an admixed Peruvian population. Description: Marca-Ysabel, Maria Victoria, et al. Dissecting the role of Amerindian genetic ancestry and the ApoE epsilon4 allele on Alzheimer disease in an admixed Peruvian population. ''Neurobiol Aging''. 2021 May; '''101''': 298.e11-298.e15
DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population. Description: Niazi, Yasmeen, et al. DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population. ''DNA Repair (Amst)''. 2021 May; '''101''': 103079
Evaluation of polygenic prediction methodology within a reference-standardized framework. Description: Pain, Oliver, et al. Evaluation of polygenic prediction methodology within a reference-standardized framework. ''PLoS Genet''. 2021 May; '''17''' (5):e1009021
First genome-wide association study on rocuronium dose requirements shows association with SLCO1A2. Description: Ahlstrom, Sirkku, et al. First genome-wide association study on rocuronium dose requirements shows association with SLCO1A2. ''Br J Anaesth''. 2021 May; '''126''' (5):949-957
Gene-environment correlations and causal effects of childhood maltreatment on physical and mental health: a genetically informed approach. Description: Warrier, Varun, et al. Gene-environment correlations and causal effects of childhood maltreatment on physical and mental health: a genetically informed approach. ''Lancet Psychiatry''. 2021 May; '''8''' (5):373-386
Genetic characteristics of Korean Jeju Black cattle with high density single nucleotide polymorphisms. Description: Alam, M Zahangir, et al. Genetic characteristics of Korean Jeju Black cattle with high density single nucleotide polymorphisms. ''Anim Biosci''. 2021 May; '''34''' (5):789-800
Genetic predictors of gene expression associated with psychiatric comorbidity in patients with inflammatory bowel disease - A pilot study. Description: Bruinooge, Allan, et al. Genetic predictors of gene expression associated with psychiatric comorbidity in patients with inflammatory bowel disease - A pilot study. ''Genomics''. 2021 May; '''113''' (3):919-932
Genetic predisposition, Abeta misfolding in blood plasma, and Alzheimer's disease. Description: Stocker, Hannah, et al. Genetic predisposition, Abeta misfolding in blood plasma, and Alzheimer's disease. ''Transl Psychiatry''. 2021 May 1; '''11''' (1):261
Genetic variants in glutamate-, Abeta-, and tau-related pathways determine polygenic risk for Alzheimer's disease. Description: Lawingco, Ted, et al. Genetic variants in glutamate-, Abeta-, and tau-related pathways determine polygenic risk for Alzheimer's disease. ''Neurobiol Aging''. 2021 May; '''101''': 299.e13-299.e21
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images. Description: Currant, Hannah, et al. Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images. ''PLoS Genet''. 2021 May; '''17''' (5):e1009497
Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis. Description: Vandebergh, Marijne, et al. Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis. ''Ann Neurol''. 2021 May; '''89''' (5):884-894
Genome-wide association coupled gene to gene interaction studies unveil novel epistatic targets among major effect loci impacting rice grain chalkiness. Description: Misra, Gopal, et al. Genome-wide association coupled gene to gene interaction studies unveil novel epistatic targets among major effect loci impacting rice grain chalkiness. ''Plant Biotechnol J''. 2021 May; '''19''' (5):910-925
Genome-wide association studies for agronomical traits in winter rice accessions of Assam. Description: Verma, Rahul K, et al. Genome-wide association studies for agronomical traits in winter rice accessions of Assam. ''Genomics''. 2021 May; '''113''' (3):1037-1047
Genomic inbreeding and population structure of northern pike (Esox lucius) in Xinjiang, China. Description: Luan, Peixian, et al. Genomic inbreeding and population structure of northern pike (Esox lucius) in Xinjiang, China. ''Ecol Evol''. 2021 May; '''11''' (10):5657-5668
Genomic scans for selection signatures revealed candidate genes for adaptation and production traits in a variety of cattle breeds. Description: Saravanan, K A, et al. Genomic scans for selection signatures revealed candidate genes for adaptation and production traits in a variety of cattle breeds. ''Genomics''. 2021 May; '''113''' (3):955-963
Genomics of response to porcine reproductive and respiratory syndrome virus in purebred and crossbred sows: antibody response and performance following natural infection vs. vaccination. Description: Sanglard, Leticia P, et al. Genomics of response to porcine reproductive and respiratory syndrome virus in purebred and crossbred sows: antibody response and performance following natural infection vs. vaccination. ''J Anim Sci''. 2021 May 1; '''99''' (5):
GLIS1, a potential candidate gene affect fat deposition in sheep tail. Description: Luo, Rongsong, et al. GLIS1, a potential candidate gene affect fat deposition in sheep tail. ''Mol Biol Rep''. 2021 May; '''48''' (5):4925-4931
Glucocorticoid signaling in pancreatic islets modulates gene regulatory programs and genetic risk of type 2 diabetes. Description: Aylward, Anthony, et al. Glucocorticoid signaling in pancreatic islets modulates gene regulatory programs and genetic risk of type 2 diabetes. ''PLoS Genet''. 2021 May; '''17''' (5):e1009531
Introgression, admixture, and selection facilitate genetic adaptation to high-altitude environments in cattle. Description: Wang, Xiuge, et al. Introgression, admixture, and selection facilitate genetic adaptation to high-altitude environments in cattle. ''Genomics''. 2021 May; '''113''' (3):1491-1503
Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation. Description: Vahidnezhad, Hassan, et al. Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation. ''Matrix Biol''. 2021 May; '''99''': 43-57
Latent trait modeling of tau neuropathology in progressive supranuclear palsy. Description: Kouri, Naomi, et al. Latent trait modeling of tau neuropathology in progressive supranuclear palsy. ''Acta Neuropathol''. 2021 May; '''141''' (5):667-680
Local environment-driven adaptive evolution in a marine invasive ascidian (Molgula manhattensis). Description: Chen, Yiyong, et al. Local environment-driven adaptive evolution in a marine invasive ascidian (Molgula manhattensis). ''Ecol Evol''. 2021 May; '''11''' (9):4252-4266
One size does not fit all. Genomics differentiates among anorexia nervosa, bulimia nervosa, and binge-eating disorder. Description: Hubel, Christopher, et al. One size does not fit all. Genomics differentiates among anorexia nervosa, bulimia nervosa, and binge-eating disorder. ''Int J Eat Disord''. 2021 May; '''54''' (5):785-793
Pedigree reconstruction and distant pairwise relatedness estimation from genome sequence data: A demonstration in a population of rhesus macaques (Macaca mulatta). Description: Petty, Lauren E, et al. Pedigree reconstruction and distant pairwise relatedness estimation from genome sequence data: A demonstration in a population of rhesus macaques (Macaca mulatta). ''Mol Ecol Resour''. 2021 May; '''21''' (4):1333-1346
Population structure, inbreeding and admixture in local cattle populations managed by community-based breeding programs in Burkina Faso. Description: Ouedraogo, Dominique, et al. Population structure, inbreeding and admixture in local cattle populations managed by community-based breeding programs in Burkina Faso. ''J Anim Breed Genet''. 2021 May; '''138''' (3):379-388
Prioritization of Osteoporosis-Associated Genome-wide Association Study (GWAS) Single-Nucleotide Polymorphisms (SNPs) Using Epigenomics and Transcriptomics. Description: Zhang, Xiao, et al. Prioritization of Osteoporosis-Associated Genome-wide Association Study (GWAS) Single-Nucleotide Polymorphisms (SNPs) Using Epigenomics and Transcriptomics. ''JBMR Plus''. 2021 May; '''5''' (5):e10481
Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine. Description: Juang, Jyh-Ming Jimmy, et al. Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine. ''J Adv Res''. 2021 May; '''30''': 147-158
Socioeconomic Deprivation Index Is Associated With Psychiatric Disorders: An Observational and Genome-wide Gene-by-Environment Interaction Analysis in the UK Biobank Cohort. Description: Ye, Jing, et al. Socioeconomic Deprivation Index Is Associated With Psychiatric Disorders: An Observational and Genome-wide Gene-by-Environment Interaction Analysis in the UK Biobank Cohort. ''Biol Psychiatry''. 2021 May 1; '''89''' (9):888-895
The genomic signal of local environmental adaptation in Aedes aegypti mosquitoes. Description: Bennett, Kelly L, et al. The genomic signal of local environmental adaptation in Aedes aegypti mosquitoes. ''Evol Appl''. 2021 May; '''14''' (5):1301-1313
The genomics of childhood eating behaviours. Description: Herle, Moritz, et al. The genomics of childhood eating behaviours. ''Nat Hum Behav''. 2021 May; '''5''' (5):625-630
The Parkinson's Disease DNA Variant Browser. Description: Kim, Jonggeol J, et al. The Parkinson's Disease DNA Variant Browser. ''Mov Disord''. 2021 May; '''36''' (5):1250-1258
The pattern of runs of homozygosity and genomic inbreeding in world-wide sheep populations. Description: Nosrati, Maryam, et al. The pattern of runs of homozygosity and genomic inbreeding in world-wide sheep populations. ''Genomics''. 2021 May; '''113''' (3):1407-1415
Parathyroid Hormone Gene and Genes Involved in the Maintenance of Vitamin D Levels Association with Mandibular Retrognathism. Description: Kuchler, Erika Calvano, et al. Parathyroid Hormone Gene and Genes Involved in the Maintenance of Vitamin D Levels Association with Mandibular Retrognathism. ''J Pers Med''. 2021 May 2; '''11''' (5):
A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study. Description: Yoshimura, Keito, et al. A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study. ''Sci Rep''. 2021 May 3; '''11''' (1):9446
Low frequency variants associated with leukocyte telomere length in the Singapore Chinese population. Description: Chang, Xuling, et al. Low frequency variants associated with leukocyte telomere length in the Singapore Chinese population. ''Commun Biol''. 2021 May 3; '''4''' (1):519
Next generation plasma proteome profiling to monitor health and disease. Description: Zhong, Wen, et al. Next generation plasma proteome profiling to monitor health and disease. ''Nat Commun''. 2021 May 3; '''12''' (1):2493
Chloroplast genomes in Populus (Salicaceae): comparisons from an intensively sampled genus reveal dynamic patterns of evolution. Description: Zhou, Jiawei, et al. Chloroplast genomes in Populus (Salicaceae): comparisons from an intensively sampled genus reveal dynamic patterns of evolution. ''Sci Rep''. 2021 May 4; '''11''' (1):9471
Fine-Scale Genetic Structure and Demographic History in the Miyako Islands of the Ryukyu Archipelago. Description: Matsunami, Masatoshi, et al. Fine-Scale Genetic Structure and Demographic History in the Miyako Islands of the Ryukyu Archipelago. ''Mol Biol Evol''. 2021 May 4; '''38''' (5):2045-2056
Maintenance of Adaptive Dynamics and No Detectable Load in a Range-Edge Outcrossing Plant Population. Description: Takou, Margarita, et al. Maintenance of Adaptive Dynamics and No Detectable Load in a Range-Edge Outcrossing Plant Population. ''Mol Biol Evol''. 2021 May 4; '''38''' (5):1820-1836
Multi-tissue neocortical transcriptome-wide association study implicates 8 genes across 6 genomic loci in Alzheimer's disease. Description: Gockley, Jake, et al. Multi-tissue neocortical transcriptome-wide association study implicates 8 genes across 6 genomic loci in Alzheimer's disease. ''Genome Med''. 2021 May 4; '''13''' (1):76
Variability in porcine microRNA genes and its association with mRNA expression and lipid phenotypes. Description: Marmol-Sanchez, Emilio, et al. Variability in porcine microRNA genes and its association with mRNA expression and lipid phenotypes. ''Genet Sel Evol''. 2021 May 4; '''53''' (1):43
Whole-genome sequencing analysis of semi-supercentenarians. Description: Garagnani, Paolo, et al. Whole-genome sequencing analysis of semi-supercentenarians. ''Elife''. 2021 May 4; '''10''':
Genomic patterns of structural variation among diverse genotypes of Sorghum bicolor and a potential role for deletions in local adaptation. Description: Songsomboon, Kittikun, et al. Genomic patterns of structural variation among diverse genotypes of Sorghum bicolor and a potential role for deletions in local adaptation. ''G3 (Bethesda)''. 2021 May 5;
Detection of selection signatures in farmed coho salmon (Oncorhynchus kisutch) using dense genome-wide information. Description: Lopez, M E, et al. Detection of selection signatures in farmed coho salmon (Oncorhynchus kisutch) using dense genome-wide information. ''Sci Rep''. 2021 May 6; '''11''' (1):9685
Genetic and environmental modulation of transposition shapes the evolutionary potential of Arabidopsis thaliana. Description: Baduel, Pierre, et al. Genetic and environmental modulation of transposition shapes the evolutionary potential of Arabidopsis thaliana. ''Genome Biol''. 2021 May 6; '''22''' (1):138
Limited haplotype diversity underlies polygenic trait architecture across 70 years of wheat breeding. Description: Scott, Michael F, et al. Limited haplotype diversity underlies polygenic trait architecture across 70 years of wheat breeding. ''Genome Biol''. 2021 May 6; '''22''' (1):137
Tejaas: reverse regression increases power for detecting trans-eQTLs. Description: Banerjee, Saikat, et al. Tejaas: reverse regression increases power for detecting trans-eQTLs. ''Genome Biol''. 2021 May 6; '''22''' (1):142
Genomic Variation and Recent Population Histories of Spotted (Strix occidentalis) and Barred (Strix varia) Owls. Description: Fujito, Naoko T, et al. Genomic Variation and Recent Population Histories of Spotted (Strix occidentalis) and Barred (Strix varia) Owls. ''Genome Biol Evol''. 2021 May 7; '''13''' (5):
Increased hypospadias risk by GREM1 rs3743104[G] in the southern Han Chinese population. Description: Deng, Fuming, et al. Increased hypospadias risk by GREM1 rs3743104[G] in the southern Han Chinese population. ''Aging (Albany NY)''. 2021 May 7; '''13''' (10):13898-13908
Large genetic diversity and strong positive selection in F-box and GPCR genes among the wild isolates of Caenorhabditis elegans. Description: Ma, Fuqiang, et al. Large genetic diversity and strong positive selection in F-box and GPCR genes among the wild isolates of Caenorhabditis elegans. ''Genome Biol Evol''. 2021 May 7; '''13''' (5):
The Genetic Variation of Lactase Persistence Alleles in Sudan and South Sudan. Description: Hollfelder, Nina, et al. The Genetic Variation of Lactase Persistence Alleles in Sudan and South Sudan. ''Genome Biol Evol''. 2021 May 7; '''13''' (5):
Genome-wide association study reveals novel loci associated with feeding behavior in Pekin ducks. Description: Li, Guang-Sheng, et al. Genome-wide association study reveals novel loci associated with feeding behavior in Pekin ducks. ''BMC Genomics''. 2021 May 8; '''22''' (1):334
Genome-wide detection of CNV regions and their potential association with growth and fatness traits in Duroc pigs. Description: Qiu, Yibin, et al. Genome-wide detection of CNV regions and their potential association with growth and fatness traits in Duroc pigs. ''BMC Genomics''. 2021 May 8; '''22''' (1):332
Tracing genetic signatures of bat-to-human coronaviruses and early transmission of North American SARS-CoV-2. Description: Ou, Xumin, et al. Tracing genetic signatures of bat-to-human coronaviruses and early transmission of North American SARS-CoV-2. ''Transbound Emerg Dis''. 2021 May 9;
A novel family of secreted insect proteins linked to plant gall development. Description: Korgaonkar, Aishwarya, et al. A novel family of secreted insect proteins linked to plant gall development. ''Curr Biol''. 2021 May 10; '''31''' (9):1836-1849.e12
Clinical Markers of Chronic Hypoxemia in Respiratory Patients Residing at Moderate Altitude. Description: Fernandez-Plata, Rosario, et al. Clinical Markers of Chronic Hypoxemia in Respiratory Patients Residing at Moderate Altitude. ''Life (Basel)''. 2021 May 10; '''11''' (5):
High genetic diversity and low differentiation reflect the ecological versatility of the African leopard. Description: Pecnerova, Patricia, et al. High genetic diversity and low differentiation reflect the ecological versatility of the African leopard. ''Curr Biol''. 2021 May 10; '''31''' (9):1862-1871.e5
Fast and pervasive transcriptomic resilience and acclimation of extremely heat-tolerant coral holobionts from the northern Red Sea. Description: Savary, Romain, et al. Fast and pervasive transcriptomic resilience and acclimation of extremely heat-tolerant coral holobionts from the northern Red Sea. ''Proc Natl Acad Sci U S A''. 2021 May 11; '''118''' (19):
Exploring genetic resistance to infectious salmon anaemia virus in Atlantic salmon by genome-wide association and RNA sequencing. Description: Gervais, O, et al. Exploring genetic resistance to infectious salmon anaemia virus in Atlantic salmon by genome-wide association and RNA sequencing. ''BMC Genomics''. 2021 May 13; '''22''' (1):345
Genetic and Metabolic Determinants of Plasma Levels of ANGPTL8. Description: Oldoni, Federico, et al. Genetic and Metabolic Determinants of Plasma Levels of ANGPTL8. ''J Clin Endocrinol Metab''. 2021 May 13; '''106''' (6):1649-1667
Genetic Variants of Alcohol Metabolizing Enzymes and Alcohol-Related Liver Cirrhosis Risk. Description: Ayuso, Pedro, et al. Genetic Variants of Alcohol Metabolizing Enzymes and Alcohol-Related Liver Cirrhosis Risk. ''J Pers Med''. 2021 May 13; '''11''' (5):
Genome wide association study of response to interval and continuous exercise training: the Predict-HIIT study. Description: Williams, Camilla J, et al. Genome wide association study of response to interval and continuous exercise training: the Predict-HIIT study. ''J Biomed Sci''. 2021 May 13; '''28''' (1):37
Natural variation in fecundity is correlated with species-wide levels of divergence in Caenorhabditis elegans. Description: Zhang, Gaotian, et al. Natural variation in fecundity is correlated with species-wide levels of divergence in Caenorhabditis elegans. ''G3 (Bethesda)''. 2021 May 13;
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease. Description: de Goede, Olivia M, et al. Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease. ''Cell''. 2021 May 13; '''184''' (10):2633-2648.e19
The genomic history of the Aegean palatial civilizations. Description: Clemente, Florian, et al. The genomic history of the Aegean palatial civilizations. ''Cell''. 2021 May 13; '''184''' (10):2565-2586.e21
CLOCK Gene Variation Is Associated with the Incidence of Metabolic Syndrome Modulated by Monounsaturated Fatty Acids. Description: Shin, Dayeon, et al. CLOCK Gene Variation Is Associated with the Incidence of Metabolic Syndrome Modulated by Monounsaturated Fatty Acids. ''J Pers Med''. 2021 May 14; '''11''' (5):
Deploying viscosity and starch polymer properties to predict cooking and eating quality models: A novel breeding tool to predict texture. Description: Buenafe, Reuben James Q, et al. Deploying viscosity and starch polymer properties to predict cooking and eating quality models: A novel breeding tool to predict texture. ''Carbohydr Polym''. 2021 May 15; '''260''': 117766
Genome wide association study for the identification of genes associated with tail fat deposition in Chinese sheep breeds. Description: Zhu, Caiye, et al. Genome wide association study for the identification of genes associated with tail fat deposition in Chinese sheep breeds. ''Biol Open''. 2021 May 15; '''10''' (5):
A multi-omics study links TNS3 and SEPT7 to long-term former smoking NSCLC survival. Description: Shen, Sipeng, et al. A multi-omics study links TNS3 and SEPT7 to long-term former smoking NSCLC survival. ''NPJ Precis Oncol''. 2021 May 17; '''5''' (1):39
ANGPTL3 Variants Associate with Lower Levels of Irisin and C-Peptide in a Cohort of Arab Individuals. Description: Alanbaei, Muath, et al. ANGPTL3 Variants Associate with Lower Levels of Irisin and C-Peptide in a Cohort of Arab Individuals. ''Genes (Basel)''. 2021 May 17; '''12''' (5):
ddRAD sequencing: an emerging technology added to the biosecurity toolbox for tracing the origin of brown marmorated stink bug, Halyomorpha halys (Hemiptera: Pentatomidae). Description: Yan, Juncong, et al. ddRAD sequencing: an emerging technology added to the biosecurity toolbox for tracing the origin of brown marmorated stink bug, Halyomorpha halys (Hemiptera: Pentatomidae). ''BMC Genomics''. 2021 May 17; '''22''' (1):355
Host Genome-Wide Association Study of Infant Susceptibility to Shigella-Associated Diarrhea. Description: Duchen, Dylan, et al. Host Genome-Wide Association Study of Infant Susceptibility to Shigella-Associated Diarrhea. ''Infect Immun''. 2021 May 17; '''89''' (6):
Imputed gene expression risk scores: a functionally informed component of polygenic risk. Description: Pain, Oliver, et al. Imputed gene expression risk scores: a functionally informed component of polygenic risk. ''Hum Mol Genet''. 2021 May 17; '''30''' (8):727-738
Sources of Resistance to Common Bacterial Blight and Charcoal Rot Disease for the Production of Mesoamerican Common Beans in the Southern United States. Description: Ambachew, Daniel, et al. Sources of Resistance to Common Bacterial Blight and Charcoal Rot Disease for the Production of Mesoamerican Common Beans in the Southern United States. ''Plants (Basel)''. 2021 May 17; '''10''' (5):
Polygenic Panels Predicting the Susceptibility of Multiple Upper Aerodigestive Tract Cancer in Oral Cancer Patients. Description: Chien, Huei-Tzu, et al. Polygenic Panels Predicting the Susceptibility of Multiple Upper Aerodigestive Tract Cancer in Oral Cancer Patients. ''J Pers Med''. 2021 May 18; '''11''' (5):
The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Description: Elvsashagen, Torbjorn, et al. The genetic architecture of the human thalamus and its overlap with ten common brain disorders. ''Nat Commun''. 2021 May 18; '''12''' (1):2909
Adaptive Admixture of HLA Class I Allotypes Enhanced Genetically Determined Strength of Natural Killer Cells in East Asians. Description: Deng, Zhihui, et al. Adaptive Admixture of HLA Class I Allotypes Enhanced Genetically Determined Strength of Natural Killer Cells in East Asians. ''Mol Biol Evol''. 2021 May 19; '''38''' (6):2582-2596
Investigating the impact of reference assembly choice on genomic analyses in a cattle breed. Description: Lloret-Villas, Audald, et al. Investigating the impact of reference assembly choice on genomic analyses in a cattle breed. ''BMC Genomics''. 2021 May 19; '''22''' (1):363
Novel Alzheimer's disease risk variants identified based on whole-genome sequencing of APOE epsilon4 carriers. Description: Park, Jong-Ho, et al. Novel Alzheimer's disease risk variants identified based on whole-genome sequencing of APOE epsilon4 carriers. ''Transl Psychiatry''. 2021 May 19; '''11''' (1):296
Recent Evolutionary History of Tigers Highlights Contrasting Roles of Genetic Drift and Selection. Description: Armstrong, Ellie E, et al. Recent Evolutionary History of Tigers Highlights Contrasting Roles of Genetic Drift and Selection. ''Mol Biol Evol''. 2021 May 19; '''38''' (6):2366-2379
ADIPOQ and LEP variants on asthma and atopy: Genetic association modified by overweight. Description: Santos Coelho, Raisa, et al. ADIPOQ and LEP variants on asthma and atopy: Genetic association modified by overweight. ''Gene''. 2021 May 20; '''781''': 145540
Continent-wide genomic signatures of adaptation to urbanisation in a songbird across Europe. Description: Salmon, Pablo, et al. Continent-wide genomic signatures of adaptation to urbanisation in a songbird across Europe. ''Nat Commun''. 2021 May 20; '''12''' (1):2983
Genetic architecture and lifetime dynamics of inbreeding depression in a wild mammal. Description: Stoffel, M A, et al. Genetic architecture and lifetime dynamics of inbreeding depression in a wild mammal. ''Nat Commun''. 2021 May 20; '''12''' (1):2972
Genome-wide association study of early-onset bipolar I disorder in the Han Taiwanese population. Description: Wu, Lawrence Shih-Hsin, et al. Genome-wide association study of early-onset bipolar I disorder in the Han Taiwanese population. ''Transl Psychiatry''. 2021 May 20; '''11''' (1):301
NGSremix: A software tool for estimating pairwise relatedness between admixed individuals from next-generation sequencing data. Description: Nohr, Anne Krogh, et al. NGSremix: A software tool for estimating pairwise relatedness between admixed individuals from next-generation sequencing data. ''G3 (Bethesda)''. 2021 May 20;
Replication of GWAS significant loci in a sub-Saharan African Cohort with early childhood caries: a pilot study. Description: Olatosi, Olubukola O, et al. Replication of GWAS significant loci in a sub-Saharan African Cohort with early childhood caries: a pilot study. ''BMC Oral Health''. 2021 May 20; '''21''' (1):274
The impact of chromosomal fusions on 3D genome folding and recombination in the germ line. Description: Vara, Covadonga, et al. The impact of chromosomal fusions on 3D genome folding and recombination in the germ line. ''Nat Commun''. 2021 May 20; '''12''' (1):2981
Gene variants and expression changes of SIRT1 and SIRT6 in peripheral blood are associated with Parkinson's disease. Description: Maszlag-Torok, Rita, et al. Gene variants and expression changes of SIRT1 and SIRT6 in peripheral blood are associated with Parkinson's disease. ''Sci Rep''. 2021 May 21; '''11''' (1):10677
Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease. Description: Reddy, Joseph S, et al. Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease. ''Acta Neuropathol Commun''. 2021 May 21; '''9''' (1):93
Predicting Conversion from MCI to AD Combining Multi-Modality Data and Based on Molecular Subtype. Description: Li, Hai-Tao, et al. Predicting Conversion from MCI to AD Combining Multi-Modality Data and Based on Molecular Subtype. ''Brain Sci''. 2021 May 21; '''11''' (6):
A Non-APOE Polygenic Risk Score for Alzheimer's Disease Is Associated With Cerebrospinal Fluid Neurofilament Light in a Representative Sample of Cognitively Unimpaired 70-Year Olds. Description: Skoog, Ingmar, et al. A Non-APOE Polygenic Risk Score for Alzheimer's Disease Is Associated With Cerebrospinal Fluid Neurofilament Light in a Representative Sample of Cognitively Unimpaired 70-Year Olds. ''J Gerontol A Biol Sci Med Sci''. 2021 May 22; '''76''' (6):983-990
Association between MANBA Gene Variants and Chronic Kidney Disease in a Korean Population. Description: Kim, Hye-Rim, et al. Association between MANBA Gene Variants and Chronic Kidney Disease in a Korean Population. ''J Clin Med''. 2021 May 23; '''10''' (11):
Genome-Wide Patterns of Homozygosity Reveal the Conservation Status in Five Italian Goat Populations. Description: Mastrangelo, Salvatore, et al. Genome-Wide Patterns of Homozygosity Reveal the Conservation Status in Five Italian Goat Populations. ''Animals (Basel)''. 2021 May 23; '''11''' (6):
Innate and Adaptive Immune Genes Associated with MERS-CoV Infection in Dromedaries. Description: Lado, Sara, et al. Innate and Adaptive Immune Genes Associated with MERS-CoV Infection in Dromedaries. ''Cells''. 2021 May 23; '''10''' (6):
ALDH2 p.E504K Variation and Sex Are Major Factors Associated with Current and Quitting Alcohol Drinking in Japanese Oldest Old. Description: Sasaki, Takashi, et al. ALDH2 p.E504K Variation and Sex Are Major Factors Associated with Current and Quitting Alcohol Drinking in Japanese Oldest Old. ''Genes (Basel)''. 2021 May 24; '''12''' (6):
Genome-Wide Association Studies of Somatic Cell Count in the Assaf Breed. Description: Oner, Yasemin, et al. Genome-Wide Association Studies of Somatic Cell Count in the Assaf Breed. ''Animals (Basel)''. 2021 May 24; '''11''' (6):
The genetic history of Greenlandic-European contact. Description: The genetic history of Greenlandic-European contact. ''''. 2021 May 24; '''31''' (10):2214-2219.e4
Whole-genome re-sequencing data to infer historical demography and speciation processes in land snails: the study of two Candidula sister species. Description: Chueca, Luis J, et al. Whole-genome re-sequencing data to infer historical demography and speciation processes in land snails: the study of two Candidula sister species. ''Philos Trans R Soc Lond B Biol Sci''. 2021 May 24; '''376''' (1825):20200156
Genetics of symptom remission in outpatients with COVID-19. Description: Dube, Marie-Pierre, et al. Genetics of symptom remission in outpatients with COVID-19. ''Sci Rep''. 2021 May 25; '''11''' (1):10847
Genome-wide association analysis reveals that EDNRB2 causes a dose-dependent loss of pigmentation in ducks. Description: Xi, Yang, et al. Genome-wide association analysis reveals that EDNRB2 causes a dose-dependent loss of pigmentation in ducks. ''BMC Genomics''. 2021 May 25; '''22''' (1):381
Reference SVA insertion polymorphisms are associated with Parkinson's Disease progression and differential gene expression. Description: Pfaff, Abigail L, et al. Reference SVA insertion polymorphisms are associated with Parkinson's Disease progression and differential gene expression. ''NPJ Parkinsons Dis''. 2021 May 25; '''7''' (1):44
A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3. Description: Vattathil, Selina M, et al. A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3. ''Genes (Basel)''. 2021 May 26; '''12''' (6):
Genetic analysis of three maize husk traits by QTL mapping in a maize-teosinte population. Description: Zhang, Xiaolei, et al. Genetic analysis of three maize husk traits by QTL mapping in a maize-teosinte population. ''BMC Genomics''. 2021 May 26; '''22''' (1):386
The climatic and genetic heritage of Italian goat breeds with genomic SNP data. Description: Cortellari, Matteo, et al. The climatic and genetic heritage of Italian goat breeds with genomic SNP data. ''Sci Rep''. 2021 May 26; '''11''' (1):10986
The origin of island populations of the African malaria mosquito, Anopheles coluzzii. Description: Campos, Melina, et al. The origin of island populations of the African malaria mosquito, Anopheles coluzzii. ''Commun Biol''. 2021 May 26; '''4''' (1):630
ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance. Description: Kagami, Masayo, et al. ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance. ''Clin Epigenetics''. 2021 May 26; '''13''' (1):119
Application of Genomic Data for Reliability Improvement of Pig Breeding Value Estimates. Description: Melnikova, Ekaterina, et al. Application of Genomic Data for Reliability Improvement of Pig Breeding Value Estimates. ''Animals (Basel)''. 2021 May 27; '''11''' (6):
Dynamic landscape of immune cell-specific gene regulation in immune-mediated diseases. Description: Ota, Mineto, et al. Dynamic landscape of immune cell-specific gene regulation in immune-mediated diseases. ''Cell''. 2021 May 27; '''184''' (11):3006-3021.e17
Genetic Predisposition to Alzheimer's Disease Is Associated with Enlargement of Perivascular Spaces in Centrum Semiovale Region. Description: Ciampa, Iacopo, et al. Genetic Predisposition to Alzheimer's Disease Is Associated with Enlargement of Perivascular Spaces in Centrum Semiovale Region. ''Genes (Basel)''. 2021 May 27; '''12''' (6):
Whole-genome resequencing of large yellow croaker (Larimichthys crocea) reveals the population structure and signatures of environmental adaptation. Description: Kon, Tetsuo, et al. Whole-genome resequencing of large yellow croaker (Larimichthys crocea) reveals the population structure and signatures of environmental adaptation. ''Sci Rep''. 2021 May 27; '''11''' (1):11235
Czechoslovakian Wolfdog Genomic Divergence from Its Ancestors Canis lupus, German Shepherd Dog, and Different Sheepdogs of European Origin. Description: Moravcikova, Nina, et al. Czechoslovakian Wolfdog Genomic Divergence from Its Ancestors Canis lupus, German Shepherd Dog, and Different Sheepdogs of European Origin. ''Genes (Basel)''. 2021 May 28; '''12''' (6):
Genetically determined hypoalbuminemia as a risk factor for hypertension: instrumental variable analysis. Description: Choi, Jong Wook, et al. Genetically determined hypoalbuminemia as a risk factor for hypertension: instrumental variable analysis. ''Sci Rep''. 2021 May 28; '''11''' (1):11290
Genetic evaluation of the variants using MassARRAY in non-small cell lung cancer among North Indians. Description: Bhat, Gh Rasool, et al. Genetic evaluation of the variants using MassARRAY in non-small cell lung cancer among North Indians. ''Sci Rep''. 2021 May 28; '''11''' (1):11291
The Genes of Freedom: Genome-Wide Insights into Marronage, Admixture and Ethnogenesis in the Gulf of Guinea. Description: Almeida, Joao, et al. The Genes of Freedom: Genome-Wide Insights into Marronage, Admixture and Ethnogenesis in the Gulf of Guinea. ''Genes (Basel)''. 2021 May 28; '''12''' (6):
Association of ADH1B polymorphism and alcohol consumption with increased risk of intracerebral hemorrhagic stroke. Description: Lin, Chun-Hsiang, et al. Association of ADH1B polymorphism and alcohol consumption with increased risk of intracerebral hemorrhagic stroke. ''J Transl Med''. 2021 May 29; '''19''' (1):227
Single-Step Genome Wide Association Study Identifies QTL Signals for Untrimmed and Trimmed Thigh Weight in Italian Crossbred Pigs for Dry-Cured Ham Production. Description: Palombo, Valentino, et al. Single-Step Genome Wide Association Study Identifies QTL Signals for Untrimmed and Trimmed Thigh Weight in Italian Crossbred Pigs for Dry-Cured Ham Production. ''Animals (Basel)''. 2021 May 29; '''11''' (6):
Variants in the Obesity-Linked FTO gene locus modulates psychopathological features of patients with Anorexia Nervosa. Description: Gonzalez, Luz M, et al. Variants in the Obesity-Linked FTO gene locus modulates psychopathological features of patients with Anorexia Nervosa. ''Gene''. 2021 May 30; '''783''': 145572
Analysis of selection signatures on the Z chromosome of bidirectional selection broiler lines for the assessment of abdominal fat content. Description: Wang, Tao, et al. Analysis of selection signatures on the Z chromosome of bidirectional selection broiler lines for the assessment of abdominal fat content. ''BMC Genom Data''. 2021 May 31; '''22''' (1):18
Genomic Regions and Candidate Genes Linked to Capped Hock in Pig. Description: Getmantseva, Lyubov, et al. Genomic Regions and Candidate Genes Linked to Capped Hock in Pig. ''Life (Basel)''. 2021 May 31; '''11''' (6):
Prostate cancer risk variants of the HOXB genetic locus. Description: Dupont, William D, et al. Prostate cancer risk variants of the HOXB genetic locus. ''Sci Rep''. 2021 May 31; '''11''' (1):11385
Association of HLA-DQA2 and HLA-B With Moyamoya Disease in the Chinese Han Population. Description: Wan, Jiang, et al. Association of HLA-DQA2 and HLA-B With Moyamoya Disease in the Chinese Han Population. ''Neurol Genet''. 2021 Jun; '''7''' (3):e592
A structural brain network of genetic vulnerability to psychiatric illness. Description: Taquet, Maxime, et al. A structural brain network of genetic vulnerability to psychiatric illness. ''Mol Psychiatry''. 2021 Jun; '''26''' (6):2089-2100
A Type 2 Diabetes Subtype Responsive to ACCORD Intensive Glycemia Treatment. Description: Mariam, Arshiya, et al. A Type 2 Diabetes Subtype Responsive to ACCORD Intensive Glycemia Treatment. ''Diabetes Care''. 2021 Jun; '''44''' (6):1410-1418
Brain predictive coding processes are associated to COMT gene Val158Met polymorphism. Description: Bonetti, L, et al. Brain predictive coding processes are associated to COMT gene Val158Met polymorphism. ''Neuroimage''. 2021 Jun; '''233''': 117954
Causal inference for heritable phenotypic risk factors using heterogeneous genetic instruments. Description: Wang, Jingshu, et al. Causal inference for heritable phenotypic risk factors using heterogeneous genetic instruments. ''PLoS Genet''. 2021 Jun; '''17''' (6):e1009575
Common genetic variation in circadian clock genes are associated with cardiovascular risk factors in an African American and Hispanic/Latino cohort. Description: Salazar, Pablo, et al. Common genetic variation in circadian clock genes are associated with cardiovascular risk factors in an African American and Hispanic/Latino cohort. ''Int J Cardiol Heart Vasc''. 2021 Jun; '''34''': 100808
Deep transcriptome sequencing of subgenual anterior cingulate cortex reveals cross-diagnostic and diagnosis-specific RNA expression changes in major psychiatric disorders. Description: Akula, Nirmala, et al. Deep transcriptome sequencing of subgenual anterior cingulate cortex reveals cross-diagnostic and diagnosis-specific RNA expression changes in major psychiatric disorders. ''Neuropsychopharmacology''. 2021 Jun; '''46''' (7):1364-1372
Differences Between Familial and Sporadic Celiac Disease. Description: Airaksinen, Laura, et al. Differences Between Familial and Sporadic Celiac Disease. ''Dig Dis Sci''. 2021 Jun; '''66''' (6):1981-1988
Effect of APOE and a polygenic risk score on incident dementia and cognitive decline in a healthy older population. Description: Riaz, Moeen, et al. Effect of APOE and a polygenic risk score on incident dementia and cognitive decline in a healthy older population. ''Aging Cell''. 2021 Jun; '''20''' (6):e13384
Genetic Interactions with Intrauterine Diabetes Exposure in Relation to Obesity: The EPOCH and Project Viva Studies. Description: Stanislawski, Maggie A, et al. Genetic Interactions with Intrauterine Diabetes Exposure in Relation to Obesity: The EPOCH and Project Viva Studies. ''Pediatr Rep''. 2021 Jun 1; '''13''' (2):279-288
Genetic sensitivity analysis: Adjusting for genetic confounding in epidemiological associations. Description: Pingault, Jean-Baptiste, et al. Genetic sensitivity analysis: Adjusting for genetic confounding in epidemiological associations. ''PLoS Genet''. 2021 Jun; '''17''' (6):e1009590
Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene. Description: Gonda, Xenia, et al. Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene. ''Transl Psychiatry''. 2021 Jun 1; '''11''' (1):337
Genome-wide association study identifies susceptibility loci of brain atrophy to NFIA and ST18 in Alzheimer's disease. Description: Kim, Bo-Hyun, et al. Genome-wide association study identifies susceptibility loci of brain atrophy to NFIA and ST18 in Alzheimer's disease. ''Neurobiol Aging''. 2021 Jun; '''102''': 200.e1-200.e11
Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. Description: Okada, Daigo, et al. Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. ''J Hum Genet''. 2021 Jun; '''66''' (6):557-567
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Description: Mullins, Niamh, et al. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. ''Nat Genet''. 2021 Jun; '''53''' (6):817-829
Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease. Description: Liu, Ganqiang, et al. Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease. ''Nat Genet''. 2021 Jun; '''53''' (6):787-793
Genomic analysis of diet composition finds novel loci and associations with health and lifestyle. Description: Meddens, S Fleur W, et al. Genomic analysis of diet composition finds novel loci and associations with health and lifestyle. ''Mol Psychiatry''. 2021 Jun; '''26''' (6):2056-2069
GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size. Description: Asif, Huma, et al. GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size. ''Mol Psychiatry''. 2021 Jun; '''26''' (6):2048-2055
High-throughput framework for genetic analyses of adverse drug reactions using electronic health records. Description: Zheng, Neil S, et al. High-throughput framework for genetic analyses of adverse drug reactions using electronic health records. ''PLoS Genet''. 2021 Jun; '''17''' (6):e1009593
High-throughput phenotyping methods for quantifying hair fiber morphology. Description: Lasisi, Tina, et al. High-throughput phenotyping methods for quantifying hair fiber morphology. ''Sci Rep''. 2021 Jun 1; '''11''' (1):11535
Identification of the PmWEEP locus controlling weeping traits in Prunus mume through an integrated genome-wide association study and quantitative trait locus mapping. Description: Zhuo, Xiaokang, et al. Identification of the PmWEEP locus controlling weeping traits in Prunus mume through an integrated genome-wide association study and quantitative trait locus mapping. ''Hortic Res''. 2021 Jun 1; '''8''' (1):131
Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes. Description: Cerqueira, Juliana X M, et al. Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes. ''J Hum Genet''. 2021 Jun; '''66''' (6):613-623
Integrative analysis of genetic and clinical risk factors for bone loss in a Korean population. Description: Lee, Ji Hyun, et al. Integrative analysis of genetic and clinical risk factors for bone loss in a Korean population. ''Bone''. 2021 Jun; '''147''': 115910
Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Description: Glanville, Kylie P, et al. Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. ''Biol Psychiatry Glob Open Sci''. 2021 Jun; '''1''' (1):48-58
Joint contributions of the gut microbiota and host genetics to feed efficiency in chickens. Description: Wen, Chaoliang, et al. Joint contributions of the gut microbiota and host genetics to feed efficiency in chickens. ''Microbiome''. 2021 Jun 1; '''9''' (1):126
Level and change in bone microarchitectural parameters and their relationship with previous fracture and established bone mineral density loci. Description: Fuggle, Nicholas R, et al. Level and change in bone microarchitectural parameters and their relationship with previous fracture and established bone mineral density loci. ''Bone''. 2021 Jun; '''147''': 115937
Leveraging genomics to understand threats to migratory birds. Description: Larison, Brenda, et al. Leveraging genomics to understand threats to migratory birds. ''Evol Appl''. 2021 Jun; '''14''' (6):1646-1658
Long tracks of homozygosity predict the severity of alcohol use disorders in an American Indian population. Description: Peng, Qian, et al. Long tracks of homozygosity predict the severity of alcohol use disorders in an American Indian population. ''Mol Psychiatry''. 2021 Jun; '''26''' (6):2200-2211
Multimodally profiling memory T cells from a tuberculosis cohort identifies cell state associations with demographics, environment and disease. Description: Nathan, Aparna, et al. Multimodally profiling memory T cells from a tuberculosis cohort identifies cell state associations with demographics, environment and disease. ''Nat Immunol''. 2021 Jun; '''22''' (6):781-793
Mutation load decreases with haplotype age in wild Soay sheep. Description: Stoffel, Martin A, et al. Mutation load decreases with haplotype age in wild Soay sheep. ''Evol Lett''. 2021 Jun; '''5''' (3):187-195
Natural selection contributes to the myopia epidemic. Description: Long, Erping, et al. Natural selection contributes to the myopia epidemic. ''Natl Sci Rev''. 2021 Jun; '''8''' (6):
NLRP1 variant M1184V decreases inflammasome activation in the context of DPP9 inhibition and asthma severity. Description: Moecking, Jonas, et al. NLRP1 variant M1184V decreases inflammasome activation in the context of DPP9 inhibition and asthma severity. ''J Allergy Clin Immunol''. 2021 Jun; '''147''' (6):2134-2145.e20
Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia. Description: Mol, Merel O, et al. Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia. ''Neurol Genet''. 2021 Jun; '''7''' (3):e596
Population genomics reveals historical and ongoing recombination in the Fusarium oxysporum species complex. Description: McTaggart, A R, et al. Population genomics reveals historical and ongoing recombination in the Fusarium oxysporum species complex. ''Stud Mycol''. 2021 Jun; '''99''': 100132
Predictive nomogram for leprosy using genetic and epidemiological risk factors in Southwestern China: Case-control and prospective analyses. Description: Long, Si-Yu, et al. Predictive nomogram for leprosy using genetic and epidemiological risk factors in Southwestern China: Case-control and prospective analyses. ''EBioMedicine''. 2021 Jun; '''68''': 103408
Relationship Between Blood Pressure and Incident Cardiovascular Disease: Linear and Nonlinear Mendelian Randomization Analyses. Description: Malik, Rainer, et al. Relationship Between Blood Pressure and Incident Cardiovascular Disease: Linear and Nonlinear Mendelian Randomization Analyses. ''Hypertension''. 2021 Jun; '''77''' (6):2004-2013
Shared heritability of human face and brain shape. Description: Naqvi, Sahin, et al. Shared heritability of human face and brain shape. ''Nat Genet''. 2021 Jun; '''53''' (6):830-839
Sparse deep neural networks on imaging genetics for schizophrenia case-control classification. Description: Chen, Jiayu, et al. Sparse deep neural networks on imaging genetics for schizophrenia case-control classification. ''Hum Brain Mapp''. 2021 Jun 1; '''42''' (8):2556-2568
Speciation along a latitudinal gradient: The origin of the Neotropical cycad sister pair Dioon sonorense-D. vovidesii (Zamiaceae). Description: Gutierrez-Ortega, Jose Said, et al. Speciation along a latitudinal gradient: The origin of the Neotropical cycad sister pair Dioon sonorense-D. vovidesii (Zamiaceae). ''Ecol Evol''. 2021 Jun; '''11''' (11):6962-6976
The assembly of caprine Y chromosome sequence reveals a unique paternal phylogenetic pattern and improves our understanding of the origin of domestic goat. Description: Xiao, Changyi, et al. The assembly of caprine Y chromosome sequence reveals a unique paternal phylogenetic pattern and improves our understanding of the origin of domestic goat. ''Ecol Evol''. 2021 Jun; '''11''' (12):7779-7795
The interaction of resource use and gene flow on the phenotypic divergence of benthic and pelagic morphs of Icelandic Arctic charr (Salvelinus alpinus). Description: Brachmann, Matthew K, et al. The interaction of resource use and gene flow on the phenotypic divergence of benthic and pelagic morphs of Icelandic Arctic charr (Salvelinus alpinus). ''Ecol Evol''. 2021 Jun; '''11''' (12):7315-7334
Three genes associated with anterior and posterior cruciate ligament injury : a genome-wide association analysis. Description: Kim, Stuart K, et al. Three genes associated with anterior and posterior cruciate ligament injury : a genome-wide association analysis. ''Bone Jt Open''. 2021 Jun; '''2''' (6):414-421
Up-regulated long noncoding RNA AC007128.1 and its genetic polymorphisms associated with Tuberculosis susceptibility. Description: Yan, Hong, et al. Up-regulated long noncoding RNA AC007128.1 and its genetic polymorphisms associated with Tuberculosis susceptibility. ''Ann Transl Med''. 2021 Jun; '''9''' (12):1018
Variation in the SERPINA6/SERPINA1 locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease. Description: Crawford, Andrew A, et al. Variation in the SERPINA6/SERPINA1 locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease. ''J Hum Genet''. 2021 Jun; '''66''' (6):625-636
Variations and expression features of CYP2D6 contribute to schizophrenia risk. Description: Ma, Liang, et al. Variations and expression features of CYP2D6 contribute to schizophrenia risk. ''Mol Psychiatry''. 2021 Jun; '''26''' (6):2605-2615
Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome. Description: Borda, Victor, et al. Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome. ''PLoS Negl Trop Dis''. 2021 Jun; '''15''' (6):e0009507
Whole genome sequencing of 10K patients with acute ischaemic stroke or transient ischaemic attack: design, methods and baseline patient characteristics. Description: Cheng, Si, et al. Whole genome sequencing of 10K patients with acute ischaemic stroke or transient ischaemic attack: design, methods and baseline patient characteristics. ''Stroke Vasc Neurol''. 2021 Jun; '''6''' (2):291-297
X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis. Description: Asselta, Rosanna, et al. X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis. ''Gastroenterology''. 2021 Jun; '''160''' (7):2483-2495.e26
Change by challenge: A common genetic basis behind childhood cognitive development and cognitive training. Description: Sauce, Bruno, et al. Change by challenge: A common genetic basis behind childhood cognitive development and cognitive training. ''NPJ Sci Learn''. 2021 Jun 2; '''6''' (1):16
On the origin and diversification of Podolian cattle breeds: testing scenarios of European colonization using genome-wide SNP data. Description: Senczuk, Gabriele, et al. On the origin and diversification of Podolian cattle breeds: testing scenarios of European colonization using genome-wide SNP data. ''Genet Sel Evol''. 2021 Jun 2; '''53''' (1):48
Genetic risk of clozapine-induced leukopenia and neutropenia: a genome-wide association study. Description: Chen, Jianhua, et al. Genetic risk of clozapine-induced leukopenia and neutropenia: a genome-wide association study. ''Transl Psychiatry''. 2021 Jun 3; '''11''' (1):343
Genome-wide association study on blood pressure traits in the Iranian population suggests ZBED9 as a new locus for hypertension. Description: Kolifarhood, Goodarz, et al. Genome-wide association study on blood pressure traits in the Iranian population suggests ZBED9 as a new locus for hypertension. ''Sci Rep''. 2021 Jun 3; '''11''' (1):11699
Genotyping-by-Sequencing-Based Genome-Wide Association Studies of Fusarium Wilt Resistance in Radishes (Raphanus sativus L.). Description: Lee, O New, et al. Genotyping-by-Sequencing-Based Genome-Wide Association Studies of Fusarium Wilt Resistance in Radishes (Raphanus sativus L.). ''Genes (Basel)''. 2021 Jun 3; '''12''' (6):
Wolfberry genomes and the evolution of Lycium (Solanaceae). Description: Cao, You-Long, et al. Wolfberry genomes and the evolution of Lycium (Solanaceae). ''Commun Biol''. 2021 Jun 3; '''4''' (1):671
Genome-Wide Association Analysis for Triazole Resistance in Aspergillus fumigatus. Description: Fan, Yuying, et al. Genome-Wide Association Analysis for Triazole Resistance in Aspergillus fumigatus. ''Pathogens''. 2021 Jun 4; '''10''' (6):
Mutations in bdcA and valS Correlate with Quinolone Resistance in Wastewater Escherichia coli. Description: Malekian, Negin, et al. Mutations in bdcA and valS Correlate with Quinolone Resistance in Wastewater Escherichia coli. ''Int J Mol Sci''. 2021 Jun 4; '''22''' (11):
Shared Genetic Etiology between Alzheimer's Disease and Blood Levels of Specific Cytokines and Growth Factors. Description: van der Linden, Robert J, et al. Shared Genetic Etiology between Alzheimer's Disease and Blood Levels of Specific Cytokines and Growth Factors. ''Genes (Basel)''. 2021 Jun 5; '''12''' (6):
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Description: de Rojas, Itziar, et al. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. ''Nat Commun''. 2021 Jun 7; '''12''' (1):3417
Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents. Description: Fuzo, Carlos Alessandro, et al. Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents. ''Sci Rep''. 2021 Jun 7; '''11''' (1):11992
An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of alpha-synuclein. Description: Kara, Eleanna, et al. An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of alpha-synuclein. ''Cell Rep''. 2021 Jun 8; '''35''' (10):109189
Genome-wide copy number variation analysis of hepatitis B infection in a Japanese population. Description: Kikuchi, Masataka, et al. Genome-wide copy number variation analysis of hepatitis B infection in a Japanese population. ''Hum Genome Var''. 2021 Jun 8; '''8''' (1):22
Genomic Analyses of Unveil Helmeted Guinea Fowl (Numida meleagris) Domestication in West Africa. Description: Shen, Quan-Kuan, et al. Genomic Analyses of Unveil Helmeted Guinea Fowl (Numida meleagris) Domestication in West Africa. ''Genome Biol Evol''. 2021 Jun 8; '''13''' (6):
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. Description: Goodrich, Julia K, et al. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. ''Nat Commun''. 2021 Jun 9; '''12''' (1):3505
Genetic and morphological estimates of androgen exposure predict social deficits in multiple neurodevelopmental disorder cohorts. Description: McKenna, Brooke G, et al. Genetic and morphological estimates of androgen exposure predict social deficits in multiple neurodevelopmental disorder cohorts. ''Mol Autism''. 2021 Jun 9; '''12''' (1):43
Genome-wide association analysis of adaptation to oxygen stress in Nile tilapia (Oreochromis niloticus). Description: Yu, Xiaofei, et al. Genome-wide association analysis of adaptation to oxygen stress in Nile tilapia (Oreochromis niloticus). ''BMC Genomics''. 2021 Jun 9; '''22''' (1):426
Identification of Novel Mutations in Colorectal Cancer Patients Using AmpliSeq Comprehensive Cancer Panel. Description: Almuzzaini, Bader, et al. Identification of Novel Mutations in Colorectal Cancer Patients Using AmpliSeq Comprehensive Cancer Panel. ''J Pers Med''. 2021 Jun 9; '''11''' (6):
Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders. Description: Mosley, Trenell J, et al. Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders. ''BMC Med Genomics''. 2021 Jun 9; '''14''' (1):154
A new molecular classification to drive precision treatment strategies in primary Sjogren's syndrome. Description: Soret, Perrine, et al. A new molecular classification to drive precision treatment strategies in primary Sjogren's syndrome. ''Nat Commun''. 2021 Jun 10; '''12''' (1):3523
Genetic Susceptibility to Periodontal Disease in Down Syndrome: A Case-Control Study. Description: Fernandez, Maria, et al. Genetic Susceptibility to Periodontal Disease in Down Syndrome: A Case-Control Study. ''Int J Mol Sci''. 2021 Jun 10; '''22''' (12):
Mapping methylation quantitative trait loci in cardiac tissues nominates risk loci and biological pathways in congenital heart disease. Description: Li, Ming, et al. Mapping methylation quantitative trait loci in cardiac tissues nominates risk loci and biological pathways in congenital heart disease. ''BMC Genom Data''. 2021 Jun 10; '''22''' (1):20
Resequencing of 672 Native Rice Accessions to Explore Genetic Diversity and Trait Associations in Vietnam. Description: Higgins, Janet, et al. Resequencing of 672 Native Rice Accessions to Explore Genetic Diversity and Trait Associations in Vietnam. ''Rice (N Y)''. 2021 Jun 10; '''14''' (1):52
The deep population history of northern East Asia from the Late Pleistocene to the Holocene. Description: Mao, Xiaowei, et al. The deep population history of northern East Asia from the Late Pleistocene to the Holocene. ''Cell''. 2021 Jun 10; '''184''' (12):3256-3266.e13
An epigenetic pathway in rice connects genetic variation to anaerobic germination and seedling establishment. Description: Castano-Duque, Lina, et al. An epigenetic pathway in rice connects genetic variation to anaerobic germination and seedling establishment. ''Plant Physiol''. 2021 Jun 11; '''186''' (2):1042-1059
Effects of the association between APOE rs405509 polymorphisms and gene-environment interactions on hand grip strength among middle-aged and elderly people in a rural population in southern China. Description: He, Haoyu, et al. Effects of the association between APOE rs405509 polymorphisms and gene-environment interactions on hand grip strength among middle-aged and elderly people in a rural population in southern China. ''J Orthop Surg Res''. 2021 Jun 11; '''16''' (1):372
Evidence of the interplay of genetics and culture in Ethiopia. Description: Lopez, Saioa, et al. Evidence of the interplay of genetics and culture in Ethiopia. ''Nat Commun''. 2021 Jun 11; '''12''' (1):3581
Genomic, Habitat, and Leaf Shape Analyses Reveal a Possible Cryptic Species and Vulnerability to Climate Change in a Threatened Daisy. Description: Blyth, Colette, et al. Genomic, Habitat, and Leaf Shape Analyses Reveal a Possible Cryptic Species and Vulnerability to Climate Change in a Threatened Daisy. ''Life (Basel)''. 2021 Jun 11; '''11''' (6):
The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations. Description: Singh, Prajjval Pratap, et al. The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations. ''Sci Rep''. 2021 Jun 11; '''11''' (1):12346
Expression Quantitative Trait Loci (eQTLs) Associated with Retrotransposons Demonstrate their Modulatory Effect on the Transcriptome. Description: Koks, Sulev, et al. Expression Quantitative Trait Loci (eQTLs) Associated with Retrotransposons Demonstrate their Modulatory Effect on the Transcriptome. ''Int J Mol Sci''. 2021 Jun 12; '''22''' (12):
Leveraging breeding programs and genomic data in Norway spruce (Picea abies L. Karst) for GWAS analysis. Description: Chen, Zhi-Qiang, et al. Leveraging breeding programs and genomic data in Norway spruce (Picea abies L. Karst) for GWAS analysis. ''Genome Biol''. 2021 Jun 13; '''22''' (1):179
Identification of genomic regions affecting production traits in pigs divergently selected for feed efficiency. Description: Delpuech, Emilie, et al. Identification of genomic regions affecting production traits in pigs divergently selected for feed efficiency. ''Genet Sel Evol''. 2021 Jun 14; '''53''' (1):49
Population-scale peach genome analyses unravel selection patterns and biochemical basis underlying fruit flavor. Description: Yu, Yang, et al. Population-scale peach genome analyses unravel selection patterns and biochemical basis underlying fruit flavor. ''Nat Commun''. 2021 Jun 14; '''12''' (1):3604
Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Description: Liu, Yi, et al. Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. ''Elife''. 2021 Jun 15; '''10''':
Genome-wide scan reveals genetic divergence in Italian Holstein cows bred within PDO cheese production chains. Description: Ablondi, Michela, et al. Genome-wide scan reveals genetic divergence in Italian Holstein cows bred within PDO cheese production chains. ''Sci Rep''. 2021 Jun 15; '''11''' (1):12601
Genomic basis for drought resistance in European beech forests threatened by climate change. Description: Pfenninger, Markus, et al. Genomic basis for drought resistance in European beech forests threatened by climate change. ''Elife''. 2021 Jun 16; '''10''':
Primary Ovarian Insufficiency in Women With Addison's Disease. Description: Vogt, Elinor C, et al. Primary Ovarian Insufficiency in Women With Addison's Disease. ''J Clin Endocrinol Metab''. 2021 Jun 16; '''106''' (7):e2656-e2663
The genomes of precision edited cloned calves show no evidence for off-target events or increased de novo mutagenesis. Description: Jivanji, Swati, et al. The genomes of precision edited cloned calves show no evidence for off-target events or increased de novo mutagenesis. ''BMC Genomics''. 2021 Jun 17; '''22''' (1):457
Unique Polymorphisms at BCL11A, HBS1L-MYB and HBB Loci Associated with HbF in Kuwaiti Patients with Sickle Cell Disease. Description: Akbulut-Jeradi, Nagihan, et al. Unique Polymorphisms at BCL11A, HBS1L-MYB and HBB Loci Associated with HbF in Kuwaiti Patients with Sickle Cell Disease. ''J Pers Med''. 2021 Jun 17; '''11''' (6):
Identification of Gene Associated with Sweetness in Corn (Zea mays L.) by Genome-Wide Association Study (GWAS) and Development of a Functional SNP Marker for Predicting Sweet Corn. Description: Ruanjaichon, Vinitchan, et al. Identification of Gene Associated with Sweetness in Corn (Zea mays L.) by Genome-Wide Association Study (GWAS) and Development of a Functional SNP Marker for Predicting Sweet Corn. ''Plants (Basel)''. 2021 Jun 18; '''10''' (6):
Influence of the FCGR2A rs1801274 and FCGR3A rs396991 Polymorphisms on Response to Abatacept in Patients with Rheumatoid Arthritis. Description: Marquez Pete, Noelia, et al. Influence of the FCGR2A rs1801274 and FCGR3A rs396991 Polymorphisms on Response to Abatacept in Patients with Rheumatoid Arthritis. ''J Pers Med''. 2021 Jun 18; '''11''' (6):
Ancient genomes reveal structural shifts after the arrival of Steppe-related ancestry in the Italian Peninsula. Description: Saupe, Tina, et al. Ancient genomes reveal structural shifts after the arrival of Steppe-related ancestry in the Italian Peninsula. ''Curr Biol''. 2021 Jun 21; '''31''' (12):2576-2591.e12
Genetic and behavioral adaptation of Candida parapsilosis to the microbiome of hospitalized infants revealed by in situ genomics, transcriptomics, and proteomics. Description: West, Patrick T, et al. Genetic and behavioral adaptation of Candida parapsilosis to the microbiome of hospitalized infants revealed by in situ genomics, transcriptomics, and proteomics. ''Microbiome''. 2021 Jun 21; '''9''' (1):142
Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment. Description: Wielscher, Matthias, et al. Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment. ''Genome Med''. 2021 Jun 21; '''13''' (1):104
Identification of sixteen novel candidate genes for late onset Parkinson's disease. Description: Gialluisi, Alessandro, et al. Identification of sixteen novel candidate genes for late onset Parkinson's disease. ''Mol Neurodegener''. 2021 Jun 21; '''16''' (1):35
Identifying novel genetic variants for brain amyloid deposition: a genome-wide association study in the Korean population. Description: Kim, Hang-Rai, et al. Identifying novel genetic variants for brain amyloid deposition: a genome-wide association study in the Korean population. ''Alzheimers Res Ther''. 2021 Jun 21; '''13''' (1):117
Genetic Risk Scores Identify Genetic Aetiology of Inflammatory Bowel Disease Phenotypes. Description: Voskuil, M D, et al. Genetic Risk Scores Identify Genetic Aetiology of Inflammatory Bowel Disease Phenotypes. ''J Crohns Colitis''. 2021 Jun 22; '''15''' (6):930-937
The Plasmodium falciparum Rh5 invasion protein complex reveals an excess of rare variant mutations. Description: Ndwiga, Leonard, et al. The Plasmodium falciparum Rh5 invasion protein complex reveals an excess of rare variant mutations. ''Malar J''. 2021 Jun 23; '''20''' (1):278
Genome-scale comparative analysis for host resistance against sea lice between Atlantic salmon and rainbow trout. Description: Caceres, Pablo, et al. Genome-scale comparative analysis for host resistance against sea lice between Atlantic salmon and rainbow trout. ''Sci Rep''. 2021 Jun 24; '''11''' (1):13231
Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. Description: Wang, Mengqiao, et al. Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. ''Genes (Basel)''. 2021 Jun 24; '''12''' (7):
Optimizing expression quantitative trait locus mapping workflows for single-cell studies. Description: Cuomo, Anna S E, et al. Optimizing expression quantitative trait locus mapping workflows for single-cell studies. ''Genome Biol''. 2021 Jun 24; '''22''' (1):188
Prediction of Probable Major Depressive Disorder in the Taiwan Biobank: An Integrated Machine Learning and Genome-Wide Analysis Approach. Description: Lin, Eugene, et al. Prediction of Probable Major Depressive Disorder in the Taiwan Biobank: An Integrated Machine Learning and Genome-Wide Analysis Approach. ''J Pers Med''. 2021 Jun 24; '''11''' (7):
Extensive Genome-Wide Phylogenetic Discordance Is Due to Incomplete Lineage Sorting and Not Ongoing Introgression in a Rapidly Radiated Bryophyte Genus. Description: Meleshko, Olena, et al. Extensive Genome-Wide Phylogenetic Discordance Is Due to Incomplete Lineage Sorting and Not Ongoing Introgression in a Rapidly Radiated Bryophyte Genus. ''Mol Biol Evol''. 2021 Jun 25; '''38''' (7):2750-2766
Genome-wide association analyses identify genotype-by-environment interactions of growth traits in Simmental cattle. Description: Braz, Camila U, et al. Genome-wide association analyses identify genotype-by-environment interactions of growth traits in Simmental cattle. ''Sci Rep''. 2021 Jun 25; '''11''' (1):13335
Genome-Wide Association Study of the Genetic Basis of Effective Tiller Number in Rice. Description: Ren, Mengmeng, et al. Genome-Wide Association Study of the Genetic Basis of Effective Tiller Number in Rice. ''Rice (N Y)''. 2021 Jun 25; '''14''' (1):56
Genomics of Gulf War Illness in U.S. Veterans Who Served during the 1990-1991 Persian Gulf War: Methods and Rationale for Veterans Affairs Cooperative Study #2006. Description: Radhakrishnan, Krishnan, et al. Genomics of Gulf War Illness in U.S. Veterans Who Served during the 1990-1991 Persian Gulf War: Methods and Rationale for Veterans Affairs Cooperative Study #2006. ''Brain Sci''. 2021 Jun 25; '''11''' (7):
Population genomics of apricots unravels domestication history and adaptive events. Description: Groppi, Alexis, et al. Population genomics of apricots unravels domestication history and adaptive events. ''Nat Commun''. 2021 Jun 25; '''12''' (1):3956
Validation of the Prediction Accuracy for 13 Traits in Chinese Simmental Beef Cattle Using a Preselected Low-Density SNP Panel. Description: Xu, Ling, et al. Validation of the Prediction Accuracy for 13 Traits in Chinese Simmental Beef Cattle Using a Preselected Low-Density SNP Panel. ''Animals (Basel)''. 2021 Jun 25; '''11''' (7):
High resolution mapping and candidate gene identification of downy mildew race 16 resistance in spinach. Description: Bhattarai, Gehendra, et al. High resolution mapping and candidate gene identification of downy mildew race 16 resistance in spinach. ''BMC Genomics''. 2021 Jun 26; '''22''' (1):478
Association between STAT4 gene polymorphism and type 2 diabetes risk in Chinese Han population. Description: Cui, Jiaqi, et al. Association between STAT4 gene polymorphism and type 2 diabetes risk in Chinese Han population. ''BMC Med Genomics''. 2021 Jun 27; '''14''' (1):169
Genome-Wide Association Study on Reproduction-Related Body-Shape Traits of Chinese Holstein Cows. Description: Lu, Xubin, et al. Genome-Wide Association Study on Reproduction-Related Body-Shape Traits of Chinese Holstein Cows. ''Animals (Basel)''. 2021 Jun 28; '''11''' (7):
New neural network classification method for individuals ancestry prediction from SNPs data. Description: Soumare, H, et al. New neural network classification method for individuals ancestry prediction from SNPs data. ''BioData Min''. 2021 Jun 28; '''14''' (1):30
The genetic organization of longitudinal subcortical volumetric change is stable throughout the lifespan. Description: Fjell, Anders Martin, et al. The genetic organization of longitudinal subcortical volumetric change is stable throughout the lifespan. ''Elife''. 2021 Jun 28; '''10''':
BIGwas: Single-command quality control and association testing for multi-cohort and biobank-scale GWAS/PheWAS data. Description: Kassens, Jan Christian, et al. BIGwas: Single-command quality control and association testing for multi-cohort and biobank-scale GWAS/PheWAS data. ''Gigascience''. 2021 Jun 29; '''10''' (6):
Chromosome anchoring in Senegalese sole (Solea senegalensis) reveals sex-associated markers and genome rearrangements in flatfish. Description: Guerrero-Cozar, Israel, et al. Chromosome anchoring in Senegalese sole (Solea senegalensis) reveals sex-associated markers and genome rearrangements in flatfish. ''Sci Rep''. 2021 Jun 29; '''11''' (1):13460
Copper Imbalance in Alzheimer's Disease: Meta-Analysis of Serum, Plasma, and Brain Specimens, and Replication Study Evaluating ATP7B Gene Variants. Description: Squitti, Rosanna, et al. Copper Imbalance in Alzheimer's Disease: Meta-Analysis of Serum, Plasma, and Brain Specimens, and Replication Study Evaluating ATP7B Gene Variants. ''Biomolecules''. 2021 Jun 29; '''11''' (7):
Deleterious Mutations in the TPO Gene Associated with Familial Thyroid Follicular Cell Carcinoma in Dutch German Longhaired Pointers. Description: Yu, Yun, et al. Deleterious Mutations in the TPO Gene Associated with Familial Thyroid Follicular Cell Carcinoma in Dutch German Longhaired Pointers. ''Genes (Basel)''. 2021 Jun 29; '''12''' (7):
Functionally significant polymorphisms of the MMP-9 gene are associated with peptic ulcer disease in the Caucasian population of Central Russia. Description: Minyaylo, Oksana, et al. Functionally significant polymorphisms of the MMP-9 gene are associated with peptic ulcer disease in the Caucasian population of Central Russia. ''Sci Rep''. 2021 Jun 29; '''11''' (1):13515
Genome-Wide Association Study for Ultraviolet-B Resistance in Soybean (Glycine max L.). Description: Lee, Taeklim, et al. Genome-Wide Association Study for Ultraviolet-B Resistance in Soybean (Glycine max L.). ''Plants (Basel)''. 2021 Jun 29; '''10''' (7):
Investigating inbreeding in the turkey (Meleagris gallopavo) genome. Description: Adams, Sarah M, et al. Investigating inbreeding in the turkey (Meleagris gallopavo) genome. ''Poult Sci''. 2021 Jun 29; '''100''' (11):101366
Protocol for a pharmacogenomic study on individualised antipsychotic drug treatment for patients with schizophrenia. Description: Su, Yi, et al. Protocol for a pharmacogenomic study on individualised antipsychotic drug treatment for patients with schizophrenia. ''BJPsych Open''. 2021 Jun 29; '''7''' (4):e121
Integration of a single-step genome-wide association study with a multi-tissue transcriptome analysis provides novel insights into the genetic basis of wool and weight traits in sheep. Description: Zhao, Bingru, et al. Integration of a single-step genome-wide association study with a multi-tissue transcriptome analysis provides novel insights into the genetic basis of wool and weight traits in sheep. ''Genet Sel Evol''. 2021 Jun 30; '''53''' (1):56
Relationship between polymorphism of receptor SCARB2 gene and clinical severity of enterovirus-71 associated hand-foot-mouth disease. Description: Wang, Xia, et al. Relationship between polymorphism of receptor SCARB2 gene and clinical severity of enterovirus-71 associated hand-foot-mouth disease. ''Virol J''. 2021 Jun 30; '''18''' (1):132
Signatures of Selection and Genomic Diversity of Muskellunge (Esox masquinongy) from Two Populations in North America. Description: Chinchilla-Vargas, Josue, et al. Signatures of Selection and Genomic Diversity of Muskellunge (Esox masquinongy) from Two Populations in North America. ''Genes (Basel)''. 2021 Jun 30; '''12''' (7):
A Causal Web between Chronotype and Metabolic Health Traits. Description: Williams, John A, et al. A Causal Web between Chronotype and Metabolic Health Traits. ''Genes (Basel)''. 2021 Jul 1; '''12''' (7):
Accelerated discovery of functional genomic variation in pigs. Description: Derks, Martijn F L, et al. Accelerated discovery of functional genomic variation in pigs. ''Genomics''. 2021 Jul; '''113''' (4):2229-2239
A fast and robust Bayesian nonparametric method for prediction of complex traits using summary statistics. Description: Zhou, Geyu, et al. A fast and robust Bayesian nonparametric method for prediction of complex traits using summary statistics. ''PLoS Genet''. 2021 Jul; '''17''' (7):e1009697
A multi-phenotype genome-wide association study of clades causing tuberculosis in a Ghanaian- and South African cohort. Description: Muller, Stephanie J, et al. A multi-phenotype genome-wide association study of clades causing tuberculosis in a Ghanaian- and South African cohort. ''Genomics''. 2021 Jul; '''113''' (4):1802-1815
An atlas of mitochondrial DNA genotype-phenotype associations in the UK Biobank. Description: Yonova-Doing, Ekaterina, et al. An atlas of mitochondrial DNA genotype-phenotype associations in the UK Biobank. ''Nat Genet''. 2021 Jul; '''53''' (7):982-993
A next generation sequencing combined genome-wide association study identifies novel tuberculosis susceptibility loci in Chinese population. Description: Li, Mo, et al. A next generation sequencing combined genome-wide association study identifies novel tuberculosis susceptibility loci in Chinese population. ''Genomics''. 2021 Jul; '''113''' (4):2377-2384
ARHGEF26 enhances Salmonella invasion and inflammation in cells and mice. Description: Bourgeois, Jeffrey S, et al. ARHGEF26 enhances Salmonella invasion and inflammation in cells and mice. ''PLoS Pathog''. 2021 Jul; '''17''' (7):e1009713
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy. Description: Wolking, Stefan, et al. Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy. ''Ann Clin Transl Neurol''. 2021 Jul; '''8''' (7):1376-1387
Association between TFEB gene polymorphism, gene-environment interaction, and fatty liver disease: A case-control study in China. Description: Mo, Chunbao, et al. Association between TFEB gene polymorphism, gene-environment interaction, and fatty liver disease: A case-control study in China. ''Sci Prog''. 2021 Jul-Sep; '''104''' (3):368504211043766
A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Description: Veturi, Yogasudha, et al. A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. ''Nat Genet''. 2021 Jul; '''53''' (7):972-981
Automated AI labeling of optic nerve head enables insights into cross-ancestry glaucoma risk and genetic discovery in >280,000 images from UKB and CLSA. Description: Han, Xikun, et al. Automated AI labeling of optic nerve head enables insights into cross-ancestry glaucoma risk and genetic discovery in >280,000 images from UKB and CLSA. ''Am J Hum Genet''. 2021 Jul 1; '''108''' (7):1204-1216
A variant in the 3'-untranslated region of the MC2R gene decreases the risk of schizophrenia in a female Han Chinese population. Description: Tang, Liang, et al. A variant in the 3'-untranslated region of the MC2R gene decreases the risk of schizophrenia in a female Han Chinese population. ''J Int Med Res''. 2021 Jul; '''49''' (7):3000605211029504
Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Description: Levey, Daniel F, et al. Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. ''Nat Neurosci''. 2021 Jul; '''24''' (7):954-963
Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation. Description: Liang, Dan, et al. Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation. ''Nat Neurosci''. 2021 Jul; '''24''' (7):941-953
Detection of Phenotype-Related Mutations of COVID-19 via the Whole Genomic Data. Description: Lv, Jinxiong, et al. Detection of Phenotype-Related Mutations of COVID-19 via the Whole Genomic Data. ''IEEE/ACM Trans Comput Biol Bioinform''. 2021 Jul-Aug; '''18''' (4):1242-1249
Development and testing of a combined species SNP array for the European seabass (Dicentrarchus labrax) and gilthead seabream (Sparus aurata). Description: Penaloza, C, et al. Development and testing of a combined species SNP array for the European seabass (Dicentrarchus labrax) and gilthead seabream (Sparus aurata). ''Genomics''. 2021 Jul; '''113''' (4):2096-2107
Development of a 38 K single nucleotide polymorphism array and application in genomic selection for resistance against Vibrio harveyi in Chinese tongue sole, Cynoglossus semilaevis. Description: Lu, Sheng, et al. Development of a 38 K single nucleotide polymorphism array and application in genomic selection for resistance against Vibrio harveyi in Chinese tongue sole, Cynoglossus semilaevis. ''Genomics''. 2021 Jul; '''113''' (4):1838-1844
Divergent improvement of two cultivated allotetraploid cotton species. Description: Fang, Lei, et al. Divergent improvement of two cultivated allotetraploid cotton species. ''Plant Biotechnol J''. 2021 Jul; '''19''' (7):1325-1336
Ethiopian indigenous goats offer insights into past and recent demographic dynamics and local adaptation in sub-Saharan African goats. Description: Tarekegn, Getinet M, et al. Ethiopian indigenous goats offer insights into past and recent demographic dynamics and local adaptation in sub-Saharan African goats. ''Evol Appl''. 2021 Jul; '''14''' (7):1716-1731
Ethnic Identity and Genome Wide Runs of Homozygosity. Description: Fieder, Martin, et al. Ethnic Identity and Genome Wide Runs of Homozygosity. ''Behav Genet''. 2021 Jul; '''51''' (4):405-413
Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes. Description: Robertson, Catherine C, et al. Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes. ''Nat Genet''. 2021 Jul; '''53''' (7):962-971
Gene-Environment Interactions in Multiple Sclerosis: A UK Biobank Study. Description: Jacobs, Benjamin Meir, et al. Gene-Environment Interactions in Multiple Sclerosis: A UK Biobank Study. ''Neurol Neuroimmunol Neuroinflamm''. 2021 Jul; '''8''' (4):
Genetic inference of the mating system of free-ranging domestic dogs. Description: Natoli, Eugenia, et al. Genetic inference of the mating system of free-ranging domestic dogs. ''Behav Ecol''. 2021 Jul-Aug; '''32''' (4):646-656
Genetic Susceptibility for Low Testosterone in Men and Its Implications in Biology and Screening: Data from the UK Biobank. Description: Fantus, Richard J, et al. Genetic Susceptibility for Low Testosterone in Men and Its Implications in Biology and Screening: Data from the UK Biobank. ''Eur Urol Open Sci''. 2021 Jul; '''29''': 36-46
Genome-wide association mapping of sodium and potassium concentration in rice grains and shoots under alternate wetting and drying and continuously flooded irrigation. Description: Chen, Caijin, et al. Genome-wide association mapping of sodium and potassium concentration in rice grains and shoots under alternate wetting and drying and continuously flooded irrigation. ''Theor Appl Genet''. 2021 Jul; '''134''' (7):2315-2334
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease. Description: Lai, Dongbing, et al. Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease. ''Ann Neurol''. 2021 Jul; '''90''' (1):76-88
Genome-Wide Association Study of Korean Asthmatics: A Comparison With UK Asthmatics. Description: An, Jin, et al. Genome-Wide Association Study of Korean Asthmatics: A Comparison With UK Asthmatics. ''Allergy Asthma Immunol Res''. 2021 Jul; '''13''' (4):609-622
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Description: Gialluisi, Alessandro, et al. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. ''Mol Psychiatry''. 2021 Jul; '''26''' (7):3004-3017
Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida. Description: Wolujewicz, Paul, et al. Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida. ''Genet Med''. 2021 Jul; '''23''' (7):1211-1218
High-density single nucleotide polymorphism chip-based conservation genetic analysis of indigenous pig breeds from Shandong Province, China. Description: Wang, Yanping, et al. High-density single nucleotide polymorphism chip-based conservation genetic analysis of indigenous pig breeds from Shandong Province, China. ''Anim Biosci''. 2021 Jul; '''34''' (7):1123-1133
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. Description: Audain, Enrique, et al. Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. ''PLoS Genet''. 2021 Jul; '''17''' (7):e1009679
Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology. Description: Alipanahi, Babak, et al. Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology. ''Am J Hum Genet''. 2021 Jul 1; '''108''' (7):1217-1230
LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease. Description: Sosero, Yuri L, et al. LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease. ''Neurobiol Aging''. 2021 Jul; '''103''': 142.e1-142.e5
Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2. Description: Simpson, Claire L, et al. Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2. ''Invest Ophthalmol Vis Sci''. 2021 Jul 1; '''62''' (9):16
New Polygenic Risk Score to Predict High Myopia in Singapore Chinese Children. Description: Lanca, Carla, et al. New Polygenic Risk Score to Predict High Myopia in Singapore Chinese Children. ''Transl Vis Sci Technol''. 2021 Jul 1; '''10''' (8):26
Next-Generation HLA Sequence Analysis Uncovers Shared Risk Alleles Between Clinically Distinct Forms of Childhood Uveitis. Description: Wennink, Roos A W, et al. Next-Generation HLA Sequence Analysis Uncovers Shared Risk Alleles Between Clinically Distinct Forms of Childhood Uveitis. ''Invest Ophthalmol Vis Sci''. 2021 Jul 1; '''62''' (9):19
On the potential of Angiosperms353 for population genomic studies. Description: Slimp, Madeline, et al. On the potential of Angiosperms353 for population genomic studies. ''Appl Plant Sci''. 2021 Jul; '''9''' (7):
OsTPR boosts the superior grains through increase in upper secondary rachis branches without incurring a grain quality penalty. Description: Pasion, Erstelle A, et al. OsTPR boosts the superior grains through increase in upper secondary rachis branches without incurring a grain quality penalty. ''Plant Biotechnol J''. 2021 Jul; '''19''' (7):1396-1411
Pharmacogenomic landscape of COVID-19 therapies from Indian population genomes. Description: Sahana, S, et al. Pharmacogenomic landscape of COVID-19 therapies from Indian population genomes. ''Pharmacogenomics''. 2021 Jul; '''22''' (10):603-618
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios. Description: Ray, Debashree, et al. Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios. ''PLoS Genet''. 2021 Jul; '''17''' (7):e1009584
Polymorphisms in TYMS for Prediction of Capecitabine-Induced Hand-Foot Syndrome in Chinese Patients with Colorectal Cancer. Description: Dong, Si-Qi, et al. Polymorphisms in TYMS for Prediction of Capecitabine-Induced Hand-Foot Syndrome in Chinese Patients with Colorectal Cancer. ''Cancer Res Treat''. 2021 Jul; '''53''' (3):724-732
Population genomics and phylogeography of the boll weevil, Anthonomus grandis Boheman (Coleoptera: Curculionidae), in the United States, northern Mexico, and Argentina. Description: Raszick, Tyler J, et al. Population genomics and phylogeography of the boll weevil, Anthonomus grandis Boheman (Coleoptera: Curculionidae), in the United States, northern Mexico, and Argentina. ''Evol Appl''. 2021 Jul; '''14''' (7):1778-1793
Population matched (pm) germline allelic variants of immunoglobulin (IG) loci: Relevance in infectious diseases and vaccination studies in human populations. Description: Khatri, Indu, et al. Population matched (pm) germline allelic variants of immunoglobulin (IG) loci: Relevance in infectious diseases and vaccination studies in human populations. ''Genes Immun''. 2021 Jul; '''22''' (3):172-186
Powerful detection of polygenic selection and evidence of environmental adaptation in US beef cattle. Description: Rowan, Troy N, et al. Powerful detection of polygenic selection and evidence of environmental adaptation in US beef cattle. ''PLoS Genet''. 2021 Jul; '''17''' (7):e1009652
Preadult polytoxicomania-strong environmental underpinnings and first genetic hints. Description: Steixner-Kumar, Agnes A, et al. Preadult polytoxicomania-strong environmental underpinnings and first genetic hints. ''Mol Psychiatry''. 2021 Jul; '''26''' (7):3211-3222
Risk factors mediating the effect of body mass index and waist-to-hip ratio on cardiovascular outcomes: Mendelian randomization analysis. Description: Gill, Dipender, et al. Risk factors mediating the effect of body mass index and waist-to-hip ratio on cardiovascular outcomes: Mendelian randomization analysis. ''Int J Obes (Lond)''. 2021 Jul; '''45''' (7):1428-1438
Selection and evaluation of bi-allelic autosomal SNP markers for paternity testing in Koreans. Description: Bae, Soyeon, et al. Selection and evaluation of bi-allelic autosomal SNP markers for paternity testing in Koreans. ''Int J Legal Med''. 2021 Jul; '''135''' (4):1369-1374
Single nucleotide polymorphism-based analysis of the genetic structure of Liangshan pig population. Description: Liu, Bin, et al. Single nucleotide polymorphism-based analysis of the genetic structure of Liangshan pig population. ''Anim Biosci''. 2021 Jul; '''34''' (7):1105-1115
Synergistic effect of genetic polymorphisms in TLR6 and TLR10 genes on the risk of pulmonary tuberculosis in a Moldavian population. Description: Varzari, Alexander, et al. Synergistic effect of genetic polymorphisms in TLR6 and TLR10 genes on the risk of pulmonary tuberculosis in a Moldavian population. ''Innate Immun''. 2021 Jul; '''27''' (5):365-376
The chromosome-level reference genome assembly for Dendrobium officinale and its utility of functional genomics research and molecular breeding study. Description: Niu, Zhitao, et al. The chromosome-level reference genome assembly for Dendrobium officinale and its utility of functional genomics research and molecular breeding study. ''Acta Pharm Sin B''. 2021 Jul; '''11''' (7):2080-2092
The effect of common variants in GDF5 gene on the susceptibility to chronic postsurgical pain. Description: Yan, Shaoyao, et al. The effect of common variants in GDF5 gene on the susceptibility to chronic postsurgical pain. ''J Orthop Surg Res''. 2021 Jul 1; '''16''' (1):420
The genome of the Pyrenean desman and the effects of bottlenecks and inbreeding on the genomic landscape of an endangered species. Description: Escoda, Lidia, et al. The genome of the Pyrenean desman and the effects of bottlenecks and inbreeding on the genomic landscape of an endangered species. ''Evol Appl''. 2021 Jul; '''14''' (7):1898-1913
Variants in BANK1 are associated with lupus nephritis of European ancestry. Description: Bolin, Karin, et al. Variants in BANK1 are associated with lupus nephritis of European ancestry. ''Genes Immun''. 2021 Jul; '''22''' (3):194-202
Whole genome sequencing reveals high differentiation, low levels of genetic diversity and short runs of homozygosity among Swedish wels catfish. Description: Jensen, Axel, et al. Whole genome sequencing reveals high differentiation, low levels of genetic diversity and short runs of homozygosity among Swedish wels catfish. ''Heredity (Edinb)''. 2021 Jul; '''127''' (1):79-91
Development and validation of a clinical and genetic model for predicting risk of severe COVID-19. Description: Dite, Gillian S, et al. Development and validation of a clinical and genetic model for predicting risk of severe COVID-19. ''Epidemiol Infect''. 2021 Jul 2; '''149''': e162
FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression. Description: Puan, Kia Joo, et al. FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression. ''Commun Biol''. 2021 Jul 2; '''4''' (1):832
Genetic basis and network underlying synergistic roots and shoots biomass accumulation revealed by genome-wide association studies in rice. Description: Zhao, Yan, et al. Genetic basis and network underlying synergistic roots and shoots biomass accumulation revealed by genome-wide association studies in rice. ''Sci Rep''. 2021 Jul 2; '''11''' (1):13769
The genetic basis of adaptation in phenology in an introduced population of Black Cottonwood (Populus trichocarpa, Torr. & Gray). Description: Apuli, Rami-Petteri, et al. The genetic basis of adaptation in phenology in an introduced population of Black Cottonwood (Populus trichocarpa, Torr. & Gray). ''BMC Plant Biol''. 2021 Jul 2; '''21''' (1):317
Admixture mapping reveals the association between Native American ancestry at 3q13.11 and reduced risk of Alzheimer's disease in Caribbean Hispanics. Description: Horimoto, Andrea R V R, et al. Admixture mapping reveals the association between Native American ancestry at 3q13.11 and reduced risk of Alzheimer's disease in Caribbean Hispanics. ''Alzheimers Res Ther''. 2021 Jul 3; '''13''' (1):122
A major QTL at the LHCGR/FSHR locus for multiple birth in Holstein cattle. Description: Widmer, Sarah, et al. A major QTL at the LHCGR/FSHR locus for multiple birth in Holstein cattle. ''Genet Sel Evol''. 2021 Jul 3; '''53''' (1):57
A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle. Description: Jacinto, Joana G P, et al. A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle. ''Genes (Basel)''. 2021 Jul 4; '''12''' (7):
GWAS Hits for Bilateral Convergent Strabismus with Exophthalmos in Holstein Cattle Using Imputed Sequence Level Genotypes. Description: Bogeholz, Anke, et al. GWAS Hits for Bilateral Convergent Strabismus with Exophthalmos in Holstein Cattle Using Imputed Sequence Level Genotypes. ''Genes (Basel)''. 2021 Jul 4; '''12''' (7):
Genotyping and lipid profiling of 601 cultivated sunflower lines reveals novel genetic determinants of oil fatty acid content. Description: Chernova, Alina I, et al. Genotyping and lipid profiling of 601 cultivated sunflower lines reveals novel genetic determinants of oil fatty acid content. ''BMC Genomics''. 2021 Jul 5; '''22''' (1):505
Parentage Analysis in Giant Grouper (Epinephelus lanceolatus) Using Microsatellite and SNP Markers from Genotyping-by-Sequencing Data. Description: Weng, Zhuoying, et al. Parentage Analysis in Giant Grouper (Epinephelus lanceolatus) Using Microsatellite and SNP Markers from Genotyping-by-Sequencing Data. ''Genes (Basel)''. 2021 Jul 5; '''12''' (7):
Calcium-Sensing Receptor Polymorphisms at rs1801725 Are Associated with Increased Risk of Secondary Malignancies. Description: Actkins, Ky'Era V, et al. Calcium-Sensing Receptor Polymorphisms at rs1801725 Are Associated with Increased Risk of Secondary Malignancies. ''J Pers Med''. 2021 Jul 6; '''11''' (7):
Joint disease-specificity at the regulatory base-pair level. Description: Muthuirulan, Pushpanathan, et al. Joint disease-specificity at the regulatory base-pair level. ''Nat Commun''. 2021 Jul 6; '''12''' (1):4161
Pseudoexfoliation and Cataract Syndrome Associated with Genetic and Epidemiological Factors in a Mayan Cohort of Guatemala. Description: Hicks, Patrice M, et al. Pseudoexfoliation and Cataract Syndrome Associated with Genetic and Epidemiological Factors in a Mayan Cohort of Guatemala. ''Int J Environ Res Public Health''. 2021 Jul 6; '''18''' (14):
Rampant Genome-Wide Admixture across the Heliconius Radiation. Description: Kozak, Krzysztof M, et al. Rampant Genome-Wide Admixture across the Heliconius Radiation. ''Genome Biol Evol''. 2021 Jul 6; '''13''' (7):
The association between polymorphisms near TMEM18 and the risk of obesity: a meta-analysis. Description: Koj, Natalia, et al. The association between polymorphisms near TMEM18 and the risk of obesity: a meta-analysis. ''BMC Med Genomics''. 2021 Jul 6; '''14''' (1):179
Genetic evidence for a causative effect of airflow obstruction on left ventricular filling: a Mendelian randomisation study. Description: Harbaum, Lars, et al. Genetic evidence for a causative effect of airflow obstruction on left ventricular filling: a Mendelian randomisation study. ''Respir Res''. 2021 Jul 7; '''22''' (1):199
Global patterns in genomic diversity underpinning the evolution of insecticide resistance in the aphid crop pest Myzus persicae. Description: Singh, Kumar Saurabh, et al. Global patterns in genomic diversity underpinning the evolution of insecticide resistance in the aphid crop pest Myzus persicae. ''Commun Biol''. 2021 Jul 7; '''4''' (1):847
HSD17B7 gene in self-renewal and oncogenicity of keratinocytes from Black versus White populations. Description: Xu, Xiaoying, et al. HSD17B7 gene in self-renewal and oncogenicity of keratinocytes from Black versus White populations. ''EMBO Mol Med''. 2021 Jul 7; '''13''' (7):e14133
LINC01414/LINC00824 genetic polymorphisms in association with the susceptibility of chronic obstructive pulmonary disease. Description: Zhou, Xiaoman, et al. LINC01414/LINC00824 genetic polymorphisms in association with the susceptibility of chronic obstructive pulmonary disease. ''BMC Pulm Med''. 2021 Jul 7; '''21''' (1):213
The first insight into the genetic structure of the population of modern Serbia. Description: Drljaca, Tamara, et al. The first insight into the genetic structure of the population of modern Serbia. ''Sci Rep''. 2021 Jul 7; '''11''' (1):13995
Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study. Description: Dominguez-Baleon, Carmen, et al. Understanding the effect of smoking and drinking behavior on Parkinson's disease risk: a Mendelian randomization study. ''Sci Rep''. 2021 Jul 7; '''11''' (1):13980
A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits. Description: Bolormaa, Sunduimijid, et al. A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits. ''Genet Sel Evol''. 2021 Jul 8; '''53''' (1):58
Common deletion variants causing protocadherin-alpha deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. Description: Teekakirikul, Polakit, et al. Common deletion variants causing protocadherin-alpha deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. ''HGG Adv''. 2021 Jul 8; '''2''' (3):
Genetic Screening to Identify Candidate Resistance Alleles to Cry1F Corn in Fall Armyworm Using Targeted Sequencing. Description: Schlum, Katrina, et al. Genetic Screening to Identify Candidate Resistance Alleles to Cry1F Corn in Fall Armyworm Using Targeted Sequencing. ''Insects''. 2021 Jul 8; '''12''' (7):
Human population history at the crossroads of East and Southeast Asia since 11,000 years ago. Description: Wang, Tianyi, et al. Human population history at the crossroads of East and Southeast Asia since 11,000 years ago. ''Cell''. 2021 Jul 8; '''184''' (14):3829-3841.e21
The Associations between COMT and MAO-B Genetic Variants with Negative Symptoms in Patients with Schizophrenia. Description: Madzarac, Zoran, et al. The Associations between COMT and MAO-B Genetic Variants with Negative Symptoms in Patients with Schizophrenia. ''Curr Issues Mol Biol''. 2021 Jul 8; '''43''' (2):618-636
Effect of NEUROG3 polymorphism rs144643855 on regional spontaneous brain activity in major depressive disorder. Description: Hou, Zhuoliang, et al. Effect of NEUROG3 polymorphism rs144643855 on regional spontaneous brain activity in major depressive disorder. ''Behav Brain Res''. 2021 Jul 9; '''409''': 113310
Gene-gene and gene-environment interactions on cord blood total IgE in Chinese Han children. Description: Hua, Li, et al. Gene-gene and gene-environment interactions on cord blood total IgE in Chinese Han children. ''Allergy Asthma Clin Immunol''. 2021 Jul 9; '''17''' (1):69
A genome-wide association study of the longitudinal course of executive functions. Description: Wendel, Bernadette, et al. A genome-wide association study of the longitudinal course of executive functions. ''Transl Psychiatry''. 2021 Jul 10; '''11''' (1):386
Epigenetic rewiring of skeletal muscle enhancers after exercise training supports a role in whole-body function and human health. Description: Williams, Kristine, et al. Epigenetic rewiring of skeletal muscle enhancers after exercise training supports a role in whole-body function and human health. ''Mol Metab''. 2021 Jul 10; '''53''': 101290
Genome-wide diversity in the California condor tracks its prehistoric abundance and decline. Description: Robinson, Jacqueline A, et al. Genome-wide diversity in the California condor tracks its prehistoric abundance and decline. ''Curr Biol''. 2021 Jul 12; '''31''' (13):2939-2946.e5
Profiling variable-number tandem repeat variation across populations using repeat-pangenome graphs. Description: Lu, Tsung-Yu, et al. Profiling variable-number tandem repeat variation across populations using repeat-pangenome graphs. ''Nat Commun''. 2021 Jul 12; '''12''' (1):4250
An FGA Frameshift Variant Associated with Afibrinogenemia in Dachshunds. Description: Mischke, Reinhard, et al. An FGA Frameshift Variant Associated with Afibrinogenemia in Dachshunds. ''Genes (Basel)''. 2021 Jul 13; '''12''' (7):
Genetic regulation of OAS1 nonsense-mediated decay underlies association with risk of severe COVID-19. Description: Banday, A Rouf, et al. Genetic regulation of OAS1 nonsense-mediated decay underlies association with risk of severe COVID-19. ''medRxiv''. 2021 Jul 13;
Grid search approach to discriminate between old and recent inbreeding using phenotypic, pedigree and genomic information. Description: Sumreddee, Pattarapol, et al. Grid search approach to discriminate between old and recent inbreeding using phenotypic, pedigree and genomic information. ''BMC Genomics''. 2021 Jul 13; '''22''' (1):538
Investigating the genetic architecture of disease resilience in pigs by genome-wide association studies of complete blood count traits collected from a natural disease challenge model. Description: Bai, Xuechun, et al. Investigating the genetic architecture of disease resilience in pigs by genome-wide association studies of complete blood count traits collected from a natural disease challenge model. ''BMC Genomics''. 2021 Jul 13; '''22''' (1):535
Selection for environmental variance of litter size in rabbits involves genes in pathways controlling animal resilience. Description: Casto-Rebollo, Cristina, et al. Selection for environmental variance of litter size in rabbits involves genes in pathways controlling animal resilience. ''Genet Sel Evol''. 2021 Jul 13; '''53''' (1):59
Genomic Risk Prediction for Breast Cancer in Older Women. Description: Lacaze, Paul, et al. Genomic Risk Prediction for Breast Cancer in Older Women. ''Cancers (Basel)''. 2021 Jul 14; '''13''' (14):
Haplotype-resolved germline and somatic alterations in renal medullary carcinomas. Description: Tan, Kar-Tong, et al. Haplotype-resolved germline and somatic alterations in renal medullary carcinomas. ''Genome Med''. 2021 Jul 14; '''13''' (1):114
TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study. Description: Meijer, A J M, et al. TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study. ''NPJ Precis Oncol''. 2021 Jul 14; '''5''' (1):64
Haplotype Analysis of BADH1 by Next-Generation Sequencing Reveals Association with Salt Tolerance in Rice during Domestication. Description: Min, Myeong-Hyeon, et al. Haplotype Analysis of BADH1 by Next-Generation Sequencing Reveals Association with Salt Tolerance in Rice during Domestication. ''Int J Mol Sci''. 2021 Jul 15; '''22''' (14):
The conserved ASTN2/BRINP1 locus at 9q33.1-33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain. Description: Pol-Fuster, Josep, et al. The conserved ASTN2/BRINP1 locus at 9q33.1-33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain. ''Sci Rep''. 2021 Jul 15; '''11''' (1):14529
The Role of FER rs4957796 in the Risk of Developing and Dying from a Bloodstream Infection: A 23-Year Follow-up of the Population-based Nord-Trondelag Health Study. Description: Rogne, Tormod, et al. The Role of FER rs4957796 in the Risk of Developing and Dying from a Bloodstream Infection: A 23-Year Follow-up of the Population-based Nord-Trondelag Health Study. ''Clin Infect Dis''. 2021 Jul 15; '''73''' (2):e297-e303
Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. Description: Stanzick, Kira J, et al. Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. ''Nat Commun''. 2021 Jul 16; '''12''' (1):4350
Interaction between ALDH2 rs671 and life habits affects the risk of hypertension in Koreans: A STROBE observational study. Description: Kim, Sung-Soo, et al. Interaction between ALDH2 rs671 and life habits affects the risk of hypertension in Koreans: A STROBE observational study. ''Medicine (Baltimore)''. 2021 Jul 16; '''100''' (28):e26664
A combined GWAS approach reveals key loci for socially-affected traits in Yorkshire pigs. Description: Wu, Pingxian, et al. A combined GWAS approach reveals key loci for socially-affected traits in Yorkshire pigs. ''Commun Biol''. 2021 Jul 20; '''4''' (1):891
An association study in the Taiwan Biobank elicits three novel candidates for cognitive aging in old adults: NCAM1, TTC12 and ZBTB20. Description: Lin, Eugene, et al. An association study in the Taiwan Biobank elicits three novel candidates for cognitive aging in old adults: NCAM1, TTC12 and ZBTB20. ''Aging (Albany NY)''. 2021 Jul 20; '''13''' (14):18769-18788
Contextualizing genetic risk score for disease screening and rare variant discovery. Description: Zhou, Dan, et al. Contextualizing genetic risk score for disease screening and rare variant discovery. ''Nat Commun''. 2021 Jul 20; '''12''' (1):4418
Genome-wide association screening and verification of potential genes associated with root architectural traits in maize (Zea mays L.) at multiple seedling stages. Description: Moussa, Abdourazak Alio, et al. Genome-wide association screening and verification of potential genes associated with root architectural traits in maize (Zea mays L.) at multiple seedling stages. ''BMC Genomics''. 2021 Jul 20; '''22''' (1):558
Genomic heterogeneity affects the response to Daylight Saving Time. Description: Tyler, Jonathan, et al. Genomic heterogeneity affects the response to Daylight Saving Time. ''Sci Rep''. 2021 Jul 20; '''11''' (1):14792
Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Description: Brandes, Nadav, et al. Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. ''Sci Rep''. 2021 Jul 21; '''11''' (1):14901
Single Nucleotide Polymorphism Induces Divergent Dynamic Patterns in CYP3A5: A Microsecond Scale Biomolecular Simulation of Variants Identified in Sub-Saharan African Populations. Description: Othman, Houcemeddine, et al. Single Nucleotide Polymorphism Induces Divergent Dynamic Patterns in CYP3A5: A Microsecond Scale Biomolecular Simulation of Variants Identified in Sub-Saharan African Populations. ''Int J Mol Sci''. 2021 Jul 21; '''22''' (15):
New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis. Description: Choquet, Helene, et al. New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis. ''Commun Biol''. 2021 Jul 22; '''4''' (1):864
Quantifying the contribution of Neanderthal introgression to the heritability of complex traits. Description: McArthur, Evonne, et al. Quantifying the contribution of Neanderthal introgression to the heritability of complex traits. ''Nat Commun''. 2021 Jul 22; '''12''' (1):4481
Altered splicing associated with the pathology of inflammatory bowel disease. Description: Berger, Kiera, et al. Altered splicing associated with the pathology of inflammatory bowel disease. ''Hum Genomics''. 2021 Jul 23; '''15''' (1):47
Identification of 22 susceptibility loci associated with testicular germ cell tumors. Description: Pluta, John, et al. Identification of 22 susceptibility loci associated with testicular germ cell tumors. ''Nat Commun''. 2021 Jul 23; '''12''' (1):4487
Identifying individuals with high risk of Alzheimer's disease using polygenic risk scores. Description: Leonenko, Ganna, et al. Identifying individuals with high risk of Alzheimer's disease using polygenic risk scores. ''Nat Commun''. 2021 Jul 23; '''12''' (1):4506
Long-range linkage disequilibrium in French beef cattle breeds. Description: El Hou, Abdelmajid, et al. Long-range linkage disequilibrium in French beef cattle breeds. ''Genet Sel Evol''. 2021 Jul 23; '''53''' (1):63
Polygenic Risk Scores Differentiating Schizophrenia From Bipolar Disorder Are Associated With Premorbid Intelligence in Schizophrenia Patients and Healthy Subjects. Description: Ohi, Kazutaka, et al. Polygenic Risk Scores Differentiating Schizophrenia From Bipolar Disorder Are Associated With Premorbid Intelligence in Schizophrenia Patients and Healthy Subjects. ''Int J Neuropsychopharmacol''. 2021 Jul 23; '''24''' (7):562-569
Cooperative Communication with Humans Evolved to Emerge Early in Domestic Dogs. Description: Salomons, Hannah, et al. Cooperative Communication with Humans Evolved to Emerge Early in Domestic Dogs. ''Curr Biol''. 2021 Jul 26; '''31''' (14):3137-3144.e11
A Bidirectional Mendelian Randomization Study to evaluate the causal role of reduced blood vitamin D levels with type 2 diabetes risk in South Asians and Europeans. Description: Bejar, Cynthia A, et al. A Bidirectional Mendelian Randomization Study to evaluate the causal role of reduced blood vitamin D levels with type 2 diabetes risk in South Asians and Europeans. ''Nutr J''. 2021 Jul 27; '''20''' (1):71
Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Description: Benchek, Penelope, et al. Association between genes regulating neural pathways for quantitative traits of speech and language disorders. ''NPJ Genom Med''. 2021 Jul 27; '''6''' (1):64
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms. Description: Ward, Lucas D, et al. GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms. ''Nat Commun''. 2021 Jul 27; '''12''' (1):4571
Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization. Description: Pathak, Gita A, et al. Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization. ''Nat Commun''. 2021 Jul 27; '''12''' (1):4569
Large-scale ratcheting in a bacterial DEAH/RHA-type RNA helicase that modulates antibiotics susceptibility. Description: Grass, Lena M, et al. Large-scale ratcheting in a bacterial DEAH/RHA-type RNA helicase that modulates antibiotics susceptibility. ''Proc Natl Acad Sci U S A''. 2021 Jul 27; '''118''' (30):
The trans-omics landscape of COVID-19. Description: Wu, Peng, et al. The trans-omics landscape of COVID-19. ''Nat Commun''. 2021 Jul 27; '''12''' (1):4543
A neurogenetic analysis of female autism. Description: Jack, Allison, et al. A neurogenetic analysis of female autism. ''Brain''. 2021 Jul 28; '''144''' (6):1911-1926
A SNP assay for assessing diversity in immune genes in the honey bee (Apis mellifera L.). Description: Henriques, Dora, et al. A SNP assay for assessing diversity in immune genes in the honey bee (Apis mellifera L.). ''Sci Rep''. 2021 Jul 28; '''11''' (1):15317
Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. Description: Fatumo, Segun, et al. Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. ''Hum Mol Genet''. 2021 Jul 28; '''30''' (16):1559-1568
Genome-Wide Association Study Using Whole-Genome Sequence Data for Fertility, Health Indicator, and Endoparasite Infection Traits in German Black Pied Cattle. Description: Wolf, Manuel J, et al. Genome-Wide Association Study Using Whole-Genome Sequence Data for Fertility, Health Indicator, and Endoparasite Infection Traits in German Black Pied Cattle. ''Genes (Basel)''. 2021 Jul 28; '''12''' (8):
Identification of ROBO2 as a Potential Locus Associated with Inhaled Corticosteroid Response in Childhood Asthma. Description: Hernandez-Pacheco, Natalia, et al. Identification of ROBO2 as a Potential Locus Associated with Inhaled Corticosteroid Response in Childhood Asthma. ''J Pers Med''. 2021 Jul 28; '''11''' (8):
Brassica rapa Domestication: Untangling Wild and Feral Forms and Convergence of Crop Morphotypes. Description: McAlvay, Alex C, et al. Brassica rapa Domestication: Untangling Wild and Feral Forms and Convergence of Crop Morphotypes. ''Mol Biol Evol''. 2021 Jul 29; '''38''' (8):3358-3372
Demographic History, Adaptation, and NRAP Convergent Evolution at Amino Acid Residue 100 in the World Northernmost Cattle from Siberia. Description: Buggiotti, Laura, et al. Demographic History, Adaptation, and NRAP Convergent Evolution at Amino Acid Residue 100 in the World Northernmost Cattle from Siberia. ''Mol Biol Evol''. 2021 Jul 29; '''38''' (8):3093-3110
Genome-Wide Association Study Identifies 12 Loci Associated with Body Weight at Age 8 Weeks in Korean Native Chickens. Description: Cha, Jihye, et al. Genome-Wide Association Study Identifies 12 Loci Associated with Body Weight at Age 8 Weeks in Korean Native Chickens. ''Genes (Basel)''. 2021 Jul 29; '''12''' (8):
Identification of pleiotropy at the gene level between psychiatric disorders and related traits. Description: Polushina, Tatiana, et al. Identification of pleiotropy at the gene level between psychiatric disorders and related traits. ''Transl Psychiatry''. 2021 Jul 29; '''11''' (1):410
Migration through a Major Andean Ecogeographic Disruption as a Driver of Genetic and Phenotypic Diversity in a Wild Tomato Species. Description: Landis, Jacob B, et al. Migration through a Major Andean Ecogeographic Disruption as a Driver of Genetic and Phenotypic Diversity in a Wild Tomato Species. ''Mol Biol Evol''. 2021 Jul 29; '''38''' (8):3202-3219
Reconstructing the Human Genetic History of Mainland Southeast Asia: Insights from Genome-Wide Data from Thailand and Laos. Description: Kutanan, Wibhu, et al. Reconstructing the Human Genetic History of Mainland Southeast Asia: Insights from Genome-Wide Data from Thailand and Laos. ''Mol Biol Evol''. 2021 Jul 29; '''38''' (8):3459-3477
Fast and flexible estimation of effective migration surfaces. Description: Marcus, Joseph, et al. Fast and flexible estimation of effective migration surfaces. ''Elife''. 2021 Jul 30; '''10''':
Genetic Association of the Functional WDR4 Gene in Male Fertility. Description: Wang, Yu-Jia, et al. Genetic Association of the Functional WDR4 Gene in Male Fertility. ''J Pers Med''. 2021 Jul 30; '''11''' (8):
Genetic association study of childhood aggression across raters, instruments, and age. Description: Ip, Hill F, et al. Genetic association study of childhood aggression across raters, instruments, and age. ''Transl Psychiatry''. 2021 Jul 30; '''11''' (1):413
Genome-Wide Association Study Identifies Candidate Genes Associated with Feet and Leg Conformation Traits in Chinese Holstein Cattle. Description: Abdalla, Ismail Mohamed, et al. Genome-Wide Association Study Identifies Candidate Genes Associated with Feet and Leg Conformation Traits in Chinese Holstein Cattle. ''Animals (Basel)''. 2021 Jul 30; '''11''' (8):
Genome-Wide Association Study in Rice Revealed a Novel Gene in Determining Plant Height and Stem Development, by Encoding a WRKY Transcription Factor. Description: Wei, Xiaoshuang, et al. Genome-Wide Association Study in Rice Revealed a Novel Gene in Determining Plant Height and Stem Development, by Encoding a WRKY Transcription Factor. ''Int J Mol Sci''. 2021 Jul 30; '''22''' (15):
Minor Allele Frequencies and Molecular Pathways Differences for SNPs Associated with Amyotrophic Lateral Sclerosis in Subjects Participating in the UKBB and 1000 Genomes Project. Description: D'Antona, Salvatore, et al. Minor Allele Frequencies and Molecular Pathways Differences for SNPs Associated with Amyotrophic Lateral Sclerosis in Subjects Participating in the UKBB and 1000 Genomes Project. ''J Clin Med''. 2021 Jul 30; '''10''' (15):
Genetic Variation in the ASTN2 Locus in Cardiovascular, Metabolic and Psychiatric Traits: Evidence for Pleiotropy Rather Than Shared Biology. Description: Burt, Olivia, et al. Genetic Variation in the ASTN2 Locus in Cardiovascular, Metabolic and Psychiatric Traits: Evidence for Pleiotropy Rather Than Shared Biology. ''Genes (Basel)''. 2021 Jul 31; '''12''' (8):
Non-Lynch Familial and Early-Onset Colorectal Cancer Explained by Accumulation of Low-Risk Genetic Variants. Description: Mur, Pilar, et al. Non-Lynch Familial and Early-Onset Colorectal Cancer Explained by Accumulation of Low-Risk Genetic Variants. ''Cancers (Basel)''. 2021 Jul 31; '''13''' (15):
A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataract. Description: Jones, Johanna L, et al. A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataract. ''Eur J Hum Genet''. 2021 Aug; '''29''' (8):1206-1215
Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource. Description: Iwaki, Hirotaka, et al. Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource. ''Mov Disord''. 2021 Aug; '''36''' (8):1795-1804
Association study of taste preference: Analysis in the Lithuanian population. Description: Kavaliauskiene, Ingrida, et al. Association study of taste preference: Analysis in the Lithuanian population. ''Food Sci Nutr''. 2021 Aug; '''9''' (8):4310-4321
A Y-linked anti-Mullerian hormone type-II receptor is the sex-determining gene in ayu, Plecoglossus altivelis. Description: Nakamoto, Masatoshi, et al. A Y-linked anti-Mullerian hormone type-II receptor is the sex-determining gene in ayu, Plecoglossus altivelis. ''PLoS Genet''. 2021 Aug; '''17''' (8):e1009705
Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs. Description: Christen, Matthias, et al. Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs. ''PLoS Genet''. 2021 Aug; '''17''' (8):e1009716
Effects of increased body mass index on employment status: a Mendelian randomisation study. Description: Campbell, Desmond D, et al. Effects of increased body mass index on employment status: a Mendelian randomisation study. ''Int J Obes (Lond)''. 2021 Aug; '''45''' (8):1790-1801
Gene-based mapping of trehalose biosynthetic pathway genes reveals association with source- and sink-related yield traits in a spring wheat panel. Description: Lyra, Danilo H, et al. Gene-based mapping of trehalose biosynthetic pathway genes reveals association with source- and sink-related yield traits in a spring wheat panel. ''Food Energy Secur''. 2021 Aug; '''10''' (3):e292
Genetic architecture of root and shoot ionomes in rice (Oryza sativa L.). Description: Cobb, Joshua N, et al. Genetic architecture of root and shoot ionomes in rice (Oryza sativa L.). ''Theor Appl Genet''. 2021 Aug; '''134''' (8):2613-2637
Genetic landscape of Gullah African Americans. Description: Zimmerman, Kip D, et al. Genetic landscape of Gullah African Americans. ''Am J Phys Anthropol''. 2021 Aug; '''175''' (4):905-919
Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache. Description: Harder, Aster V E, et al. Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache. ''Ann Neurol''. 2021 Aug; '''90''' (2):203-216
Genetic variation near CXCL12 is associated with susceptibility to HIV-related non-Hodgkin lymphoma. Description: Thorball, Christian W, et al. Genetic variation near CXCL12 is associated with susceptibility to HIV-related non-Hodgkin lymphoma. ''Haematologica''. 2021 Aug 1; '''106''' (8):2233-2241
Genetic variation of rs12918566 affects GRIN2A expression and is associated with spontaneous movement response during sevoflurane anesthesia induction. Description: Chen, Ming-Hua, et al. Genetic variation of rs12918566 affects GRIN2A expression and is associated with spontaneous movement response during sevoflurane anesthesia induction. ''Brain Behav''. 2021 Aug; '''11''' (8):e02165
Genome of a middle Holocene hunter-gatherer from Wallacea. Description: Carlhoff, Selina, et al. Genome of a middle Holocene hunter-gatherer from Wallacea. ''Nature''. 2021 Aug; '''596''' (7873):543-547
Genome-wide association studies of exacerbations in children using long-acting beta2-agonists. Description: Slob, Elise M A, et al. Genome-wide association studies of exacerbations in children using long-acting beta2-agonists. ''Pediatr Allergy Immunol''. 2021 Aug; '''32''' (6):1197-1207
Genotype imputation in case-only studies of gene-environment interaction: validity and power. Description: Aleknonyte-Resch, Milda, et al. Genotype imputation in case-only studies of gene-environment interaction: validity and power. ''Hum Genet''. 2021 Aug; '''140''' (8):1217-1228
*Heterozygosity of the Alpha 1-Antitrypsin PiZ Allele and Risk of Liver Disease.** Description: Hakim, Aaron, et al. Heterozygosity of the Alpha 1-Antitrypsin Pi*Z Allele and Risk of Liver Disease. ''Hepatol Commun''. 2021 Aug; '''5''' (8):1348-1361
HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schonlein purpura nephritis in Finnish pediatric population: a genome-wide association study. Description: Koskela, Mikael, et al. HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schonlein purpura nephritis in Finnish pediatric population: a genome-wide association study. ''Pediatr Nephrol''. 2021 Aug; '''36''' (8):2311-2318
Identification of quantitative trait loci associated with calmness and gentleness in honey bees using whole-genome sequences. Description: Guichard, M, et al. Identification of quantitative trait loci associated with calmness and gentleness in honey bees using whole-genome sequences. ''Anim Genet''. 2021 Aug; '''52''' (4):472-481
Identifying genetic risk variants associated with noise-induced hearing loss based on a novel strategy for evaluating individual susceptibility. Description: Jiang, Zhuang, et al. Identifying genetic risk variants associated with noise-induced hearing loss based on a novel strategy for evaluating individual susceptibility. ''Hear Res''. 2021 Aug; '''407''': 108281
Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus. Description: Rajabli, Farid, et al. Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus. ''Neurobiol Aging''. 2021 Aug; '''104''': 115.e1-115.e7
Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors -results of the Heinz Nixdorf Recall Study. Description: Pechlivanis, Sonali, et al. Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors -results of the Heinz Nixdorf Recall Study. ''Naunyn Schmiedebergs Arch Pharmacol''. 2021 Aug; '''394''' (8):1713-1725
Physical activity attenuates postprandial hyperglycaemia in homozygous TBC1D4 loss-of-function mutation carriers. Description: Schnurr, Theresia M, et al. Physical activity attenuates postprandial hyperglycaemia in homozygous TBC1D4 loss-of-function mutation carriers. ''Diabetologia''. 2021 Aug; '''64''' (8):1795-1804
Polygenic Scores for Cognitive Abilities and Their Association with Different Aspects of General Intelligence-A Deep Phenotyping Approach. Description: Genc, Erhan, et al. Polygenic Scores for Cognitive Abilities and Their Association with Different Aspects of General Intelligence-A Deep Phenotyping Approach. ''Mol Neurobiol''. 2021 Aug; '''58''' (8):4145-4156
Putative pathogen-selected polymorphisms in the PKLR gene are associated with mycobacterial susceptibility in Brazilian and African populations. Description: Bezerra, Ohanna Cavalcanti de Lima, et al. Putative pathogen-selected polymorphisms in the PKLR gene are associated with mycobacterial susceptibility in Brazilian and African populations. ''PLoS Negl Trop Dis''. 2021 Aug; '''15''' (8):e0009434
Regional heritability mapping identifies several novel loci (STAT4, ULK4, and KCNH5) for primary biliary cholangitis in the Japanese population. Description: Gervais, Olivier, et al. Regional heritability mapping identifies several novel loci (STAT4, ULK4, and KCNH5) for primary biliary cholangitis in the Japanese population. ''Eur J Hum Genet''. 2021 Aug; '''29''' (8):1282-1291
rMVP: A Memory-efficient, Visualization-enhanced, and Parallel-accelerated Tool for Genome-wide Association Study. Description: Yin, Lilin, et al. rMVP: A Memory-efficient, Visualization-enhanced, and Parallel-accelerated Tool for Genome-wide Association Study. ''Genomics Proteomics Bioinformatics''. 2021 Aug; '''19''' (4):619-628
Single-marker and haplotype-based genome-wide association studies for the number of teats in two heavy pig breeds. Description: Bovo, S, et al. Single-marker and haplotype-based genome-wide association studies for the number of teats in two heavy pig breeds. ''Anim Genet''. 2021 Aug; '''52''' (4):440-450
STAT3 polymorphisms in North Africa and its implication in breast cancer. Description: Ziadi, Wafa, et al. STAT3 polymorphisms in North Africa and its implication in breast cancer. ''Mol Genet Genomic Med''. 2021 Aug; '''9''' (8):e1744
Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal hernias: genetics in inguinal hernias. Description: Hikino, Keiko, et al. Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal hernias: genetics in inguinal hernias. ''EBioMedicine''. 2021 Aug; '''70''': 103532
The different fates of two Asian horseshoe crab species with different dispersal abilities. Description: Tang, Qian, et al. The different fates of two Asian horseshoe crab species with different dispersal abilities. ''Evol Appl''. 2021 Aug; '''14''' (8):2124-2133
The genetics and evolution of eye color in domestic pigeons (Columba livia). Description: Si, Si, et al. The genetics and evolution of eye color in domestic pigeons (Columba livia). ''PLoS Genet''. 2021 Aug; '''17''' (8):e1009770
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family. Description: Carrion-Castillo, Amaia, et al. Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family. ''Hum Genet''. 2021 Aug; '''140''' (8):1183-1200
Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry. Description: Liu, Cong, et al. Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry. ''JAMA Netw Open''. 2021 Aug 2; '''4''' (8):e2119084
GSAP regulates lipid homeostasis and mitochondrial function associated with Alzheimer's disease. Description: Xu, Peng, et al. GSAP regulates lipid homeostasis and mitochondrial function associated with Alzheimer's disease. ''J Exp Med''. 2021 Aug 2; '''218''' (8):
Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes. Description: Pan, David Z, et al. Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes. ''Genome Med''. 2021 Aug 2; '''13''' (1):123
Isotype-specific Antibody Responses to Mycobacterium avium paratuberculosis Antigens Are Associated With the Use of Biologic Therapy in Inflammatory Bowel Disease. Description: van der Sloot, Kimberley W J, et al. Isotype-specific Antibody Responses to Mycobacterium avium paratuberculosis Antigens Are Associated With the Use of Biologic Therapy in Inflammatory Bowel Disease. ''J Crohns Colitis''. 2021 Aug 2; '''15''' (8):1253-1263
The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene. Description: Bagheri, Minoo, et al. The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene. ''Sci Rep''. 2021 Aug 2; '''11''' (1):15652
Endomembrane targeting of human OAS1 p46 augments antiviral activity. Description: Soveg, Frank W, et al. Endomembrane targeting of human OAS1 p46 augments antiviral activity. ''Elife''. 2021 Aug 3; '''10''':
Identification and Validation of Marketing Weight-Related SNP Markers Using SLAF Sequencing in Male Yangzhou Geese. Description: Melak, Sherif, et al. Identification and Validation of Marketing Weight-Related SNP Markers Using SLAF Sequencing in Male Yangzhou Geese. ''Genes (Basel)''. 2021 Aug 3; '''12''' (8):
Protective Role of Genetic Variants in HSP90 Genes-Complex in COPD Secondary to Biomass-Burning Smoke Exposure and Non-Severe COPD Forms in Tobacco Smoking Subjects. Description: Ambrocio-Ortiz, Enrique, et al. Protective Role of Genetic Variants in HSP90 Genes-Complex in COPD Secondary to Biomass-Burning Smoke Exposure and Non-Severe COPD Forms in Tobacco Smoking Subjects. ''Curr Issues Mol Biol''. 2021 Aug 3; '''43''' (2):887-899
TWAS results are complementary to and less affected by linkage disequilibrium than GWAS. Description: Li, Delin, et al. TWAS results are complementary to and less affected by linkage disequilibrium than GWAS. ''Plant Physiol''. 2021 Aug 3; '''186''' (4):1800-1811
Genome-wide association studies for production, respiratory disease, and immune-related traits in Landrace pigs. Description: Uemoto, Yoshinobu, et al. Genome-wide association studies for production, respiratory disease, and immune-related traits in Landrace pigs. ''Sci Rep''. 2021 Aug 4; '''11''' (1):15823
Genome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucoma. Description: Lo Faro, Valeria, et al. Genome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucoma. ''BMC Genomics''. 2021 Aug 4; '''22''' (1):590
The role of age at menarche and age at menopause in Alzheimer's disease: evidence from a bidirectional mendelian randomization study. Description: Li, Mingli, et al. The role of age at menarche and age at menopause in Alzheimer's disease: evidence from a bidirectional mendelian randomization study. ''Aging (Albany NY)''. 2021 Aug 4; '''13''' (15):19722-19749
Ancient viral genomes reveal introduction of human pathogenic viruses into Mexico during the transatlantic slave trade. Description: Guzman-Solis, Axel A, et al. Ancient viral genomes reveal introduction of human pathogenic viruses into Mexico during the transatlantic slave trade. ''Elife''. 2021 Aug 5; '''10''':
Estimates of genomic inbreeding and identification of candidate regions that differ between Chinese indigenous sheep breeds. Description: Liu, Jiaxin, et al. Estimates of genomic inbreeding and identification of candidate regions that differ between Chinese indigenous sheep breeds. ''J Anim Sci Biotechnol''. 2021 Aug 5; '''12''' (1):95
Fast and accurate exhaustive higher-order epistasis search with BitEpi. Description: Bayat, Arash, et al. Fast and accurate exhaustive higher-order epistasis search with BitEpi. ''Sci Rep''. 2021 Aug 5; '''11''' (1):15923
*Genome-wide association study reveals an association between the HLA-DPB1( )02:01:02 allele and wheat-dependent exercise-induced anaphylaxis.** Description: Fukunaga, Koya, et al. Genome-wide association study reveals an association between the HLA-DPB1( *)02:01:02 allele and wheat-dependent exercise-induced anaphylaxis. ''Am J Hum Genet''. 2021 Aug 5; '''108''' (8):1540-1548
Genomic partitioning of inbreeding depression in humans. Description: Yengo, Loic, et al. Genomic partitioning of inbreeding depression in humans. ''Am J Hum Genet''. 2021 Aug 5; '''108''' (8):1488-1501
NNT mediates redox-dependent pigmentation via a UVB- and MITF-independent mechanism. Description: Allouche, Jennifer, et al. NNT mediates redox-dependent pigmentation via a UVB- and MITF-independent mechanism. ''Cell''. 2021 Aug 5; '''184''' (16):4268-4283.e20
Understanding the impact of SNPs associated with autism spectrum disorder on biological pathways in the human fetal and adult cortex. Description: Golovina, E, et al. Understanding the impact of SNPs associated with autism spectrum disorder on biological pathways in the human fetal and adult cortex. ''Sci Rep''. 2021 Aug 5; '''11''' (1):15867
Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia. Description: Li, Quanlin, et al. Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia. ''Am J Hum Genet''. 2021 Aug 5; '''108''' (8):1478-1487
Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management. Description: Samaha, Georgina, et al. Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management. ''BMC Genomics''. 2021 Aug 6; '''22''' (1):601
Identification and allele mining of new candidate genes underlying rice grain weight and grain shape by genome-wide association study. Description: Niu, Yanan, et al. Identification and allele mining of new candidate genes underlying rice grain weight and grain shape by genome-wide association study. ''BMC Genomics''. 2021 Aug 6; '''22''' (1):602
Whole-genome sequencing of Schistosoma mansoni reveals extensive diversity with limited selection despite mass drug administration. Description: Berger, Duncan J, et al. Whole-genome sequencing of Schistosoma mansoni reveals extensive diversity with limited selection despite mass drug administration. ''Nat Commun''. 2021 Aug 6; '''12''' (1):4776
Relationships between apparent cortical thickness and working memory across the lifespan - Effects of genetics and socioeconomic status. Description: Krogsrud, Stine K, et al. Relationships between apparent cortical thickness and working memory across the lifespan - Effects of genetics and socioeconomic status. ''Dev Cogn Neurosci''. 2021 Aug 8; '''51''': 100997
Protocol for a case-control study investigating the clinical phenotypes and genetic regulation of endometriosis in Indian women: the ECGRI study. Description: Gajbhiye, Rahul K, et al. Protocol for a case-control study investigating the clinical phenotypes and genetic regulation of endometriosis in Indian women: the ECGRI study. ''BMJ Open''. 2021 Aug 9; '''11''' (8):e050844
A case-control study on correlation between the single nucleotide polymorphism of CLEC4E and the susceptibility to tuberculosis among Han people in Western China. Description: Zhou, Wenjing, et al. A case-control study on correlation between the single nucleotide polymorphism of CLEC4E and the susceptibility to tuberculosis among Han people in Western China. ''BMC Infect Dis''. 2021 Aug 10; '''21''' (1):788
A microRNA panel compared to environmental and polygenic scores for colorectal cancer risk prediction. Description: Raut, Janhavi R, et al. A microRNA panel compared to environmental and polygenic scores for colorectal cancer risk prediction. ''Nat Commun''. 2021 Aug 10; '''12''' (1):4811
Identification of candidate genomic regions for chicken egg number traits based on genome-wide association study. Description: Zhao, Xiurong, et al. Identification of candidate genomic regions for chicken egg number traits based on genome-wide association study. ''BMC Genomics''. 2021 Aug 10; '''22''' (1):610
In silico characterisation of putative Plasmodium falciparum vaccine candidates in African malaria populations. Description: Ajibola, O, et al. In silico characterisation of putative Plasmodium falciparum vaccine candidates in African malaria populations. ''Sci Rep''. 2021 Aug 10; '''11''' (1):16215
Multi-locus genome-wide association studies for five yield-related traits in rice. Description: Zhong, Hua, et al. Multi-locus genome-wide association studies for five yield-related traits in rice. ''BMC Plant Biol''. 2021 Aug 10; '''21''' (1):364
Possible Protective Effect of LOXL1 Variant in the Cohort of Chernobyl Catastrophe Clean-Up Workers. Description: Zukauskaite, Gabriele, et al. Possible Protective Effect of LOXL1 Variant in the Cohort of Chernobyl Catastrophe Clean-Up Workers. ''Genes (Basel)''. 2021 Aug 10; '''12''' (8):
Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan. Description: Tsai, Chia-Kuang, et al. Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan. ''J Headache Pain''. 2021 Aug 11; '''22''' (1):89
Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia. Description: Liu, Jiewei, et al. Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia. ''BMC Med''. 2021 Aug 12; '''19''' (1):177
GLIS1 regulates trabecular meshwork function and intraocular pressure and is associated with glaucoma in humans. Description: Nair, K Saidas, et al. GLIS1 regulates trabecular meshwork function and intraocular pressure and is associated with glaucoma in humans. ''Nat Commun''. 2021 Aug 12; '''12''' (1):4877
Unraveling the Genetic Diversity and Population Structure of Bangladeshi Indigenous Cattle Populations Using 50K SNP Markers. Description: Bhuiyan, Mohammad Shamsul Alam, et al. Unraveling the Genetic Diversity and Population Structure of Bangladeshi Indigenous Cattle Populations Using 50K SNP Markers. ''Animals (Basel)''. 2021 Aug 12; '''11''' (8):
Artificial image objects for classification of schizophrenia with GWAS-selected SNVs and convolutional neural network. Description: Chen, Xiangning, et al. Artificial image objects for classification of schizophrenia with GWAS-selected SNVs and convolutional neural network. ''Patterns (N Y)''. 2021 Aug 13; '''2''' (8):100303
Loci and natural alleles for cadmium-mediated growth responses revealed by a genome wide association study and transcriptome analysis in rice. Description: Yu, Jianping, et al. Loci and natural alleles for cadmium-mediated growth responses revealed by a genome wide association study and transcriptome analysis in rice. ''BMC Plant Biol''. 2021 Aug 13; '''21''' (1):374
Association between hypertension and coffee drinking based on CYP1A2 rs762551 single nucleotide polymorphism in Taiwanese. Description: Hou, Chien-Chou, et al. Association between hypertension and coffee drinking based on CYP1A2 rs762551 single nucleotide polymorphism in Taiwanese. ''Nutr Metab (Lond)''. 2021 Aug 14; '''18''' (1):78
A genetic sum score of effect alleles associated with serum lipid concentrations interacts with educational attainment. Description: Emmel, Carina, et al. A genetic sum score of effect alleles associated with serum lipid concentrations interacts with educational attainment. ''Sci Rep''. 2021 Aug 16; '''11''' (1):16541
Genome-wide association study of individual sugar content in fruit of Japanese pear (Pyrus spp.). Description: Nishio, Sogo, et al. Genome-wide association study of individual sugar content in fruit of Japanese pear (Pyrus spp.). ''BMC Plant Biol''. 2021 Aug 16; '''21''' (1):378
A genome-wide association study of quantitative computed tomographic emphysema in Korean populations. Description: Sin, Sooim, et al. A genome-wide association study of quantitative computed tomographic emphysema in Korean populations. ''Sci Rep''. 2021 Aug 17; '''11''' (1):16692
Genetic diversity analysis of Korean peanut germplasm using 48 K SNPs 'Axiom_Arachis' Array and its application for cultivar differentiation. Description: Nabi, Rizwana Begum Syed, et al. Genetic diversity analysis of Korean peanut germplasm using 48 K SNPs 'Axiom_Arachis' Array and its application for cultivar differentiation. ''Sci Rep''. 2021 Aug 17; '''11''' (1):16630
New loci and neuronal pathways for resilience to heat stress in cattle. Description: Cheruiyot, Evans K, et al. New loci and neuronal pathways for resilience to heat stress in cattle. ''Sci Rep''. 2021 Aug 17; '''11''' (1):16619
The ABCC4 gene is associated with pyometra in golden retriever dogs. Description: Arendt, Maja, et al. The ABCC4 gene is associated with pyometra in golden retriever dogs. ''Sci Rep''. 2021 Aug 17; '''11''' (1):16647
Dietary carbohydrates interacts with AMY1 polymorphisms to influence the incidence of type 2 diabetes in Korean adults. Description: Shin, Dayeon, et al. Dietary carbohydrates interacts with AMY1 polymorphisms to influence the incidence of type 2 diabetes in Korean adults. ''Sci Rep''. 2021 Aug 18; '''11''' (1):16788
Exploring human-genome gut-microbiome interaction in Parkinson's disease. Description: Wallen, Zachary D, et al. Exploring human-genome gut-microbiome interaction in Parkinson's disease. ''NPJ Parkinsons Dis''. 2021 Aug 18; '''7''' (1):74
Reconstructing genetic histories and social organisation in Neolithic and Bronze Age Croatia. Description: Freilich, Suzanne, et al. Reconstructing genetic histories and social organisation in Neolithic and Bronze Age Croatia. ''Sci Rep''. 2021 Aug 18; '''11''' (1):16729
Association between Polygenetic Risk Scores of Low Immunity and Interactions between These Scores and Moderate Fat Intake in a Large Cohort. Description: Park, Sunmin, et al. Association between Polygenetic Risk Scores of Low Immunity and Interactions between These Scores and Moderate Fat Intake in a Large Cohort. ''Nutrients''. 2021 Aug 19; '''13''' (8):
Novel Sources of Pre-Harvest Sprouting Resistance for Japonica Rice Improvement. Description: Lee, Jae-Sung, et al. Novel Sources of Pre-Harvest Sprouting Resistance for Japonica Rice Improvement. ''Plants (Basel)''. 2021 Aug 19; '''10''' (8):
Whole Genome Sequencing Reveals Multiple Linked Genetic Variants on Canine Chromosome 12 Associated with Risk for Symmetrical Lupoid Onychodystrophy (SLO) in the Bearded Collie. Description: Gershony, Liza C, et al. Whole Genome Sequencing Reveals Multiple Linked Genetic Variants on Canine Chromosome 12 Associated with Risk for Symmetrical Lupoid Onychodystrophy (SLO) in the Bearded Collie. ''Genes (Basel)''. 2021 Aug 19; '''12''' (8):
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19. Description: Asano, Takaki, et al. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19. ''Sci Immunol''. 2021 Aug 19; '''6''' (62):
A Genome-Wide Association Study on Liver Stiffness Changes during Hepatitis C Virus Infection Cure. Description: Corma-Gomez, Anais, et al. A Genome-Wide Association Study on Liver Stiffness Changes during Hepatitis C Virus Infection Cure. ''Diagnostics (Basel)''. 2021 Aug 20; '''11''' (8):
Genome-Wide Association Study Reveals the Genetic Basis of Chilling Tolerance in Rice at the Reproductive Stage. Description: Jeong, Byeong Yong, et al. Genome-Wide Association Study Reveals the Genetic Basis of Chilling Tolerance in Rice at the Reproductive Stage. ''Plants (Basel)''. 2021 Aug 20; '''10''' (8):
Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios. Description: Wu, Xi, et al. Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios. ''iScience''. 2021 Aug 20; '''24''' (8):102894
Population Genomics Reveals Gene Flow and Adaptive Signature in Invasive Weed Mikania micrantha. Description: Ruan, Xiaoxian, et al. Population Genomics Reveals Gene Flow and Adaptive Signature in Invasive Weed Mikania micrantha. ''Genes (Basel)''. 2021 Aug 20; '''12''' (8):
Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. Description: Cheng, Shiqiang, et al. Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. ''Transl Psychiatry''. 2021 Aug 20; '''11''' (1):431
Genetic diversity and main functional composition of Lingzhi strains from main producing areas in China. Description: Liu, Yuan-Chao, et al. Genetic diversity and main functional composition of Lingzhi strains from main producing areas in China. ''AMB Express''. 2021 Aug 21; '''11''' (1):119
Risk Factors, Clinical Features, and Polygenic Risk Scores in Schizophrenia and Schizoaffective Disorder Depressive-Type. Description: Dennison, Charlotte A, et al. Risk Factors, Clinical Features, and Polygenic Risk Scores in Schizophrenia and Schizoaffective Disorder Depressive-Type. ''Schizophr Bull''. 2021 Aug 21; '''47''' (5):1375-1384
Analysis of Homozygous-by-Descent (HBD) Segments for Purebred and Crossbred Pigs in Russia. Description: Bakoev, Siroj, et al. Analysis of Homozygous-by-Descent (HBD) Segments for Purebred and Crossbred Pigs in Russia. ''Life (Basel)''. 2021 Aug 22; '''11''' (8):
Gene Polymorphisms of the Renin-Angiotensin System and Bleeding Complications of Warfarin: Genetic-Based Machine Learning Models. Description: Kim, Joo-Hee, et al. Gene Polymorphisms of the Renin-Angiotensin System and Bleeding Complications of Warfarin: Genetic-Based Machine Learning Models. ''Pharmaceuticals (Basel)''. 2021 Aug 22; '''14''' (8):
Genetic Origins and Sex-Biased Admixture of the Huis. Description: Ma, Xixian, et al. Genetic Origins and Sex-Biased Admixture of the Huis. ''Mol Biol Evol''. 2021 Aug 23; '''38''' (9):3804-3819
Genome-scale sequencing and analysis of human, wolf, and bison DNA from 25,000-year-old sediment. Description: Gelabert, Pere, et al. Genome-scale sequencing and analysis of human, wolf, and bison DNA from 25,000-year-old sediment. ''Curr Biol''. 2021 Aug 23; '''31''' (16):3564-3574.e9
Locally Adaptive Inversions Modulate Genetic Variation at Different Geographic Scales in a Seaweed Fly. Description: Merot, Claire, et al. Locally Adaptive Inversions Modulate Genetic Variation at Different Geographic Scales in a Seaweed Fly. ''Mol Biol Evol''. 2021 Aug 23; '''38''' (9):3953-3971
PER Gene Family Polymorphisms in Relation to Cluster Headache and Circadian Rhythm in Sweden. Description: Jennysdotter Olofsgard, Felicia, et al. PER Gene Family Polymorphisms in Relation to Cluster Headache and Circadian Rhythm in Sweden. ''Brain Sci''. 2021 Aug 23; '''11''' (8):
Evidence for opposing selective forces operating on human-specific duplicated TCAF genes in Neanderthals and humans. Description: Hsieh, PingHsun, et al. Evidence for opposing selective forces operating on human-specific duplicated TCAF genes in Neanderthals and humans. ''Nat Commun''. 2021 Aug 25; '''12''' (1):5118
The Association of Renal Function and Plasma Metals Modified by EGFR and TNF-alpha Gene Polymorphisms in Metal Industrial Workers and General Population. Description: Chen, Tzu-Hua, et al. The Association of Renal Function and Plasma Metals Modified by EGFR and TNF-alpha Gene Polymorphisms in Metal Industrial Workers and General Population. ''Int J Environ Res Public Health''. 2021 Aug 25; '''18''' (17):
Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation. Description: Czamara, Darina, et al. Betamethasone administration during pregnancy is associated with placental epigenetic changes with implications for inflammation. ''Clin Epigenetics''. 2021 Aug 26; '''13''' (1):165
Catenin Alpha 2 May Be a Biomarker or Potential Drug Target in Psychiatric Disorders with Perseverative Negative Thinking. Description: Eszlari, Nora, et al. Catenin Alpha 2 May Be a Biomarker or Potential Drug Target in Psychiatric Disorders with Perseverative Negative Thinking. ''Pharmaceuticals (Basel)''. 2021 Aug 26; '''14''' (9):
Genetic Architecture and Genome-Wide Adaptive Signatures Underlying Stem Lenticel Traits in Populus tomentosa. Description: Li, Peng, et al. Genetic Architecture and Genome-Wide Adaptive Signatures Underlying Stem Lenticel Traits in Populus tomentosa. ''Int J Mol Sci''. 2021 Aug 26; '''22''' (17):
GWAS and Post-GWAS High-Resolution Mapping Analyses Identify Strong Novel Candidate Genes Influencing the Fatty Acid Composition of the Longissimus dorsi Muscle in Pigs. Description: Lee, Jae-Bong, et al. GWAS and Post-GWAS High-Resolution Mapping Analyses Identify Strong Novel Candidate Genes Influencing the Fatty Acid Composition of the Longissimus dorsi Muscle in Pigs. ''Genes (Basel)''. 2021 Aug 26; '''12''' (9):
Genetic Dissection of Phosphorus Use Efficiency in a Maize Association Population under Two P Levels in the Field. Description: Li, Dongdong, et al. Genetic Dissection of Phosphorus Use Efficiency in a Maize Association Population under Two P Levels in the Field. ''Int J Mol Sci''. 2021 Aug 27; '''22''' (17):
Genome-Wide Association Study Based on Random Regression Model Reveals Candidate Genes Associated with Longitudinal Data in Chinese Simmental Beef Cattle. Description: Du, Lili, et al. Genome-Wide Association Study Based on Random Regression Model Reveals Candidate Genes Associated with Longitudinal Data in Chinese Simmental Beef Cattle. ''Animals (Basel)''. 2021 Aug 27; '''11''' (9):
The Association between 5-Hydroxytryptamine Receptor 1B rs13212041 Polymorphism and Trait Anxiety in Chinese Han College Subjects. Description: Ruan, Xiaofei, et al. The Association between 5-Hydroxytryptamine Receptor 1B rs13212041 Polymorphism and Trait Anxiety in Chinese Han College Subjects. ''Life (Basel)''. 2021 Aug 27; '''11''' (9):
Genetic Diversity and Identification of Homozygosity-Rich Genomic Regions in Seven Italian Heritage Turkey (Meleagris gallopavo) Breeds. Description: Bernini, Francesca, et al. Genetic Diversity and Identification of Homozygosity-Rich Genomic Regions in Seven Italian Heritage Turkey (Meleagris gallopavo) Breeds. ''Genes (Basel)''. 2021 Aug 28; '''12''' (9):
Hypertensive Patients Exhibit Enhanced Thrombospondin-1 Levels at High-Altitude. Description: Sharma, Kavita, et al. Hypertensive Patients Exhibit Enhanced Thrombospondin-1 Levels at High-Altitude. ''Life (Basel)''. 2021 Aug 29; '''11''' (9):
Whole-genome sequencing of endangered Zhoushan cattle suggests its origin and the association of MC1R with black coat colour. Description: Jiang, Lihua, et al. Whole-genome sequencing of endangered Zhoushan cattle suggests its origin and the association of MC1R with black coat colour. ''Sci Rep''. 2021 Aug 30; '''11''' (1):17359
Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Description: Fan, Wei, et al. Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. ''mSystems''. 2021 Aug 31; '''6''' (4):e0015821
Reciprocal adaptation of rice and Xanthomonas oryzae pv. oryzae: cross-species 2D GWAS reveals the underlying genetics. Description: Zhang, Fan, et al. Reciprocal adaptation of rice and Xanthomonas oryzae pv. oryzae: cross-species 2D GWAS reveals the underlying genetics. ''Plant Cell''. 2021 Aug 31; '''33''' (8):2538-2561
Trans-ethnic genome-wide association study of severe COVID-19. Description: Wu, Peng, et al. Trans-ethnic genome-wide association study of severe COVID-19. ''Commun Biol''. 2021 Aug 31; '''4''' (1):1034
Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments. Description: Vojgani, Elaheh, et al. Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments. ''Theor Appl Genet''. 2021 Sep; '''134''' (9):2913-2930
Accounting for genetic architecture for body weight improves accuracy of predicting breeding values in a commercial line of broilers. Description: Rome, Helene, et al. Accounting for genetic architecture for body weight improves accuracy of predicting breeding values in a commercial line of broilers. ''J Anim Breed Genet''. 2021 Sep; '''138''' (5):528-540
Adult-onset diabetes in Middle Eastern immigrants to Sweden: Novel subgroups and diabetic complications-The All New Diabetes in Scania cohort diabetic complications and ethnicity. Description: Bennet, Louise, et al. Adult-onset diabetes in Middle Eastern immigrants to Sweden: Novel subgroups and diabetic complications-The All New Diabetes in Scania cohort diabetic complications and ethnicity. ''Diabetes Metab Res Rev''. 2021 Sep; '''37''' (6):e3419
A globally diverse reference alignment and panel for imputation of mitochondrial DNA variants. Description: McInerney, Tim W, et al. A globally diverse reference alignment and panel for imputation of mitochondrial DNA variants. ''BMC Bioinformatics''. 2021 Sep 1; '''22''' (1):417
A major quantitative trait locus affecting resistance to Tilapia lake virus in farmed Nile tilapia (Oreochromis niloticus). Description: Barria, Agustin, et al. A major quantitative trait locus affecting resistance to Tilapia lake virus in farmed Nile tilapia (Oreochromis niloticus). ''Heredity (Edinb)''. 2021 Sep; '''127''' (3):334-343
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs. Description: Cordell, Heather J, et al. An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs. ''J Hepatol''. 2021 Sep; '''75''' (3):572-581
Association between LINC-PINT and LINC00599 gene polymorphism and the risk of steroid-induced osteonecrosis of the femoral head in the population of northern China. Description: Sun, Menghu, et al. Association between LINC-PINT and LINC00599 gene polymorphism and the risk of steroid-induced osteonecrosis of the femoral head in the population of northern China. ''Steroids''. 2021 Sep; '''173''': 108886
Careful feature selection is key in classification of Alzheimer's disease patients based on whole-genome sequencing data. Description: Osipowicz, Marlena, et al. Careful feature selection is key in classification of Alzheimer's disease patients based on whole-genome sequencing data. ''NAR Genom Bioinform''. 2021 Sep; '''3''' (3):lqab069
Continuity of Genetic Risk for Aggressive Behavior Across the Life-Course. Description: van der Laan, Camiel M, et al. Continuity of Genetic Risk for Aggressive Behavior Across the Life-Course. ''Behav Genet''. 2021 Sep; '''51''' (5):592-606
Deciphering variation of 239 elite japonica rice genomes for whole genome sequences-enabled breeding. Description: Liu, Chuanxue, et al. Deciphering variation of 239 elite japonica rice genomes for whole genome sequences-enabled breeding. ''Genomics''. 2021 Sep; '''113''' (5):3083-3091
Detection of genomic regions underlying milk production traits in Valle del Belice dairy sheep using regional heritability mapping. Description: Sutera, Anna Maria, et al. Detection of genomic regions underlying milk production traits in Valle del Belice dairy sheep using regional heritability mapping. ''J Anim Breed Genet''. 2021 Sep; '''138''' (5):552-561
Detection of selection signatures in the genome of a farmed population of anadromous rainbow trout (Oncorhynchus mykiss). Description: Cadiz, Maria I, et al. Detection of selection signatures in the genome of a farmed population of anadromous rainbow trout (Oncorhynchus mykiss). ''Genomics''. 2021 Sep; '''113''' (5):3395-3404
Donor genetic variants as risk factors for thrombosis after liver transplantation: A genome-wide association study. Description: Li, Yanni, et al. Donor genetic variants as risk factors for thrombosis after liver transplantation: A genome-wide association study. ''Am J Transplant''. 2021 Sep; '''21''' (9):3133-3147
Epigenetic prediction of major depressive disorder. Description: Barbu, Miruna C, et al. Epigenetic prediction of major depressive disorder. ''Mol Psychiatry''. 2021 Sep; '''26''' (9):5112-5123
Family based and case-control designs reveal an association of TFAP2A in nonsyndromic cleft lip only among Vietnamese population. Description: Nguyen, Duc Minh, et al. Family based and case-control designs reveal an association of TFAP2A in nonsyndromic cleft lip only among Vietnamese population. ''Mol Genet Genomic Med''. 2021 Sep; '''9''' (9):e1754
Genetic association and differential expression of HLAComplexGroup lncRNAs in pemphigus. Description: Salviano-Silva, Amanda, et al. Genetic association and differential expression of HLAComplexGroup lncRNAs in pemphigus. ''J Autoimmun''. 2021 Sep; '''123''': 102705
Genetic association scan of 32 osteoarthritis susceptibility genes identified TP63 associated with an endemic osteoarthritis, Kashin-Beck disease. Description: Cheng, Bolun, et al. Genetic association scan of 32 osteoarthritis susceptibility genes identified TP63 associated with an endemic osteoarthritis, Kashin-Beck disease. ''Bone''. 2021 Sep; '''150''': 115997
Genetic dissection of complex traits using hierarchical biological knowledge. Description: Tanaka, Hidenori, et al. Genetic dissection of complex traits using hierarchical biological knowledge. ''PLoS Comput Biol''. 2021 Sep; '''17''' (9):e1009373
Genetic polymorphisms at 19q13.33 are associated with [-2]proPSA (p2PSA) levels and provide additional predictive value to prostate health index for prostate cancer. Description: Huang, Da, et al. Genetic polymorphisms at 19q13.33 are associated with [-2]proPSA (p2PSA) levels and provide additional predictive value to prostate health index for prostate cancer. ''Prostate''. 2021 Sep; '''81''' (13):971-982
Genome-wide haplotype association study in imaging genetics using whole-brain sulcal openings of 16,304 UK Biobank subjects. Description: Karkar, Slim, et al. Genome-wide haplotype association study in imaging genetics using whole-brain sulcal openings of 16,304 UK Biobank subjects. ''Eur J Hum Genet''. 2021 Sep; '''29''' (9):1424-1437
Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation. Description: Min, Josine L, et al. Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation. ''Nat Genet''. 2021 Sep; '''53''' (9):1311-1321
HLA class I genes modulate disease risk and age at onset together with DR-DQ in Chinese patients with insulin-requiring type 1 diabetes. Description: Jiang, Ziyu, et al. HLA class I genes modulate disease risk and age at onset together with DR-DQ in Chinese patients with insulin-requiring type 1 diabetes. ''Diabetologia''. 2021 Sep; '''64''' (9):2026-2036
Identification and functional analysis of the perforin-1 like gene in disease resistance in half smooth tongue sole (Cynoglossus semilaevis). Description: Fu, Xiaoqin, et al. Identification and functional analysis of the perforin-1 like gene in disease resistance in half smooth tongue sole (Cynoglossus semilaevis). ''Dev Comp Immunol''. 2021 Sep; '''122''': 104135
Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism. Description: Lam, Wai-Yee, et al. Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism. ''EBioMedicine''. 2021 Sep; '''71''': 103530
Immunogenetic aspects of idiopathic recurrent miscarriage in the Kazakh population. Description: Svyatova, Gulnara, et al. Immunogenetic aspects of idiopathic recurrent miscarriage in the Kazakh population. ''J Med Life''. 2021 Sep-Oct; '''14''' (5):676-682
Influence of Maternal Lifestyle and Diet on Perinatal DNA Methylation Signatures Associated With Childhood Arterial Stiffness at 8 to 9 Years. Description: Murray, Robert, et al. Influence of Maternal Lifestyle and Diet on Perinatal DNA Methylation Signatures Associated With Childhood Arterial Stiffness at 8 to 9 Years. ''Hypertension''. 2021 Sep; '''78''' (3):787-800
Integration of selection signatures and multi-trait GWAS reveals polygenic genetic architecture of carcass traits in beef cattle. Description: Niu, Qunhao, et al. Integration of selection signatures and multi-trait GWAS reveals polygenic genetic architecture of carcass traits in beef cattle. ''Genomics''. 2021 Sep; '''113''' (5):3325-3336
Interaction between the STAT4 rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus. Description: Reid, Sarah, et al. Interaction between the STAT4 rs11889341(T) risk allele and smoking confers increased risk of myocardial infarction and nephritis in patients with systemic lupus erythematosus. ''Ann Rheum Dis''. 2021 Sep; '''80''' (9):1183-1189
Introgression contributes to distribution of structural variations in cattle. Description: Upadhyay, Maulik, et al. Introgression contributes to distribution of structural variations in cattle. ''Genomics''. 2021 Sep; '''113''' (5):3092-3102
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Description: Vosa, Urmo, et al. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. ''Nat Genet''. 2021 Sep; '''53''' (9):1300-1310
On cross-ancestry cancer polygenic risk scores. Description: Fritsche, Lars G, et al. On cross-ancestry cancer polygenic risk scores. ''PLoS Genet''. 2021 Sep; '''17''' (9):e1009670
Phylogeographic analysis delimits three evolutionary significant units of least chipmunks in North America and identifies unique genetic diversity within the imperiled Penasco population. Description: Puckett, Emily E, et al. Phylogeographic analysis delimits three evolutionary significant units of least chipmunks in North America and identifies unique genetic diversity within the imperiled Penasco population. ''Ecol Evol''. 2021 Sep; '''11''' (17):12114-12128
Polygenic Risk and the Course of Attention-Deficit/Hyperactivity Disorder From Childhood to Young Adulthood: Findings From a Nationally Representative Cohort. Description: Agnew-Blais, Jessica C, et al. Polygenic Risk and the Course of Attention-Deficit/Hyperactivity Disorder From Childhood to Young Adulthood: Findings From a Nationally Representative Cohort. ''J Am Acad Child Adolesc Psychiatry''. 2021 Sep; '''60''' (9):1147-1156
Postictal Psychosis in Epilepsy: A Clinicogenetic Study. Description: Braatz, Vera, et al. Postictal Psychosis in Epilepsy: A Clinicogenetic Study. ''Ann Neurol''. 2021 Sep; '''90''' (3):464-476
Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences. Description: Zhan, Lingyu, et al. Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences. ''PLoS Genet''. 2021 Sep; '''17''' (9):e1009772
Strong isolation by distance among local populations of an endangered butterfly species (Euphydryas aurinia). Description: Pertoldi, Cino, et al. Strong isolation by distance among local populations of an endangered butterfly species (Euphydryas aurinia). ''Ecol Evol''. 2021 Sep; '''11''' (18):12790-12800
Testing and estimation of X-chromosome SNP effects: Impact of model assumptions. Description: Song, Yilin, et al. Testing and estimation of X-chromosome SNP effects: Impact of model assumptions. ''Genet Epidemiol''. 2021 Sep; '''45''' (6):577-592
The Association of Human Leukocyte Antigen and COVID-19 in Southern China. Description: Yu, Xueping, et al. The Association of Human Leukocyte Antigen and COVID-19 in Southern China. ''Open Forum Infect Dis''. 2021 Sep; '''8''' (9):ofab410
The associations of CNR1 SNPs and haplotypes with vulnerability and treatment response phenotypes in Han Chinese with major depressive disorder: A case-control association study. Description: Yang, Chenghao, et al. The associations of CNR1 SNPs and haplotypes with vulnerability and treatment response phenotypes in Han Chinese with major depressive disorder: A case-control association study. ''Mol Genet Genomic Med''. 2021 Sep; '''9''' (9):e1752
The genetic consequences of dog breed formation-Accumulation of deleterious genetic variation and fixation of mutations associated with myxomatous mitral valve disease in cavalier King Charles spaniels. Description: Axelsson, Erik, et al. The genetic consequences of dog breed formation-Accumulation of deleterious genetic variation and fixation of mutations associated with myxomatous mitral valve disease in cavalier King Charles spaniels. ''PLoS Genet''. 2021 Sep; '''17''' (9):e1009726
Using genetics to detangle the relationships between red cell distribution width and cardiovascular diseases: a unique role for body mass index. Description: Thayer, Timothy E, et al. Using genetics to detangle the relationships between red cell distribution width and cardiovascular diseases: a unique role for body mass index. ''Open Heart''. 2021 Sep; '''8''' (2):
Whole-Genome Sequencing of a 900-Year-Old Human Skeleton Supports Two Past Migration Events from the Russian Far East to Northern Japan. Description: Sato, Takehiro, et al. Whole-Genome Sequencing of a 900-Year-Old Human Skeleton Supports Two Past Migration Events from the Russian Far East to Northern Japan. ''Genome Biol Evol''. 2021 Sep 1; '''13''' (9):
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. Description: Prokopenko, Dmitry, et al. Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. ''Alzheimers Dement''. 2021 Sep; '''17''' (9):1509-1527
A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR. Description: Xu, Mai, et al. A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR. ''Am J Hum Genet''. 2021 Sep 2; '''108''' (9):1611-1630
Brain-trait-associated variants impact cell-type-specific gene regulation during neurogenesis. Description: Aygun, Nil, et al. Brain-trait-associated variants impact cell-type-specific gene regulation during neurogenesis. ''Am J Hum Genet''. 2021 Sep 2; '''108''' (9):1647-1668
Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms. Description: Zhang, Tongwu, et al. Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms. ''Am J Hum Genet''. 2021 Sep 2; '''108''' (9):1631-1646
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Description: Boer, Cindy G, et al. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. ''Cell''. 2021 Sep 2; '''184''' (18):4784-4818.e17
Developmental and temporal characteristics of clonal sperm mosaicism. Description: Yang, Xiaoxu, et al. Developmental and temporal characteristics of clonal sperm mosaicism. ''Cell''. 2021 Sep 2; '''184''' (18):4772-4783.e15
Functional characterization of T2D-associated SNP effects on baseline and ER stress-responsive beta cell transcriptional activation. Description: Khetan, Shubham, et al. Functional characterization of T2D-associated SNP effects on baseline and ER stress-responsive beta cell transcriptional activation. ''Nat Commun''. 2021 Sep 2; '''12''' (1):5242
Genome-wide association studies for canine hip dysplasia in single and multiple populations - implications and potential novel risk loci. Description: Wang, Shizhi, et al. Genome-wide association studies for canine hip dysplasia in single and multiple populations - implications and potential novel risk loci. ''BMC Genomics''. 2021 Sep 2; '''22''' (1):636
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions. Description: Reus, Lianne M, et al. Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions. ''Transl Psychiatry''. 2021 Sep 2; '''11''' (1):451
Genome-wide sequencing-based identification of methylation quantitative trait loci and their role in schizophrenia risk. Description: Perzel Mandell, Kira A, et al. Genome-wide sequencing-based identification of methylation quantitative trait loci and their role in schizophrenia risk. ''Nat Commun''. 2021 Sep 2; '''12''' (1):5251
Is BRD7 associated with spermatogenesis impairment and male infertility in humans? A case-control study in a Han Chinese population. Description: He, Tianrong, et al. Is BRD7 associated with spermatogenesis impairment and male infertility in humans? A case-control study in a Han Chinese population. ''Basic Clin Androl''. 2021 Sep 2; '''31''' (1):19
The genomic history of the Middle East. Description: Almarri, Mohamed A, et al. The genomic history of the Middle East. ''Cell''. 2021 Sep 2; '''184''' (18):4612-4625.e14
Dynamics of sex chromosome evolution in a rapid radiation of cichlid fishes. Description: El Taher, Athimed, et al. Dynamics of sex chromosome evolution in a rapid radiation of cichlid fishes. ''Sci Adv''. 2021 Sep 3; '''7''' (36):eabe8215
Assessing the effect of interaction between C-reactive protein and gut microbiome on the risks of anxiety and depression. Description: Chen, Yujing, et al. Assessing the effect of interaction between C-reactive protein and gut microbiome on the risks of anxiety and depression. ''Mol Brain''. 2021 Sep 4; '''14''' (1):133
Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent. Description: Upadhyai, Priyanka, et al. Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent. ''Life (Basel)''. 2021 Sep 5; '''11''' (9):
Eagle for better genome-wide association mapping. Description: George, Andrew W, et al. Eagle for better genome-wide association mapping. ''G3 (Bethesda)''. 2021 Sep 6; '''11''' (9):
Genome-wide association studies of mineral and phytic acid concentrations in pea (Pisum sativum L.) to evaluate biofortification potential. Description: Powers, Sarah, et al. Genome-wide association studies of mineral and phytic acid concentrations in pea (Pisum sativum L.) to evaluate biofortification potential. ''G3 (Bethesda)''. 2021 Sep 6; '''11''' (9):
Genome-wide association study identifies new loci associated with noise-induced tinnitus in Chinese populations. Description: Xie, Chengyong, et al. Genome-wide association study identifies new loci associated with noise-induced tinnitus in Chinese populations. ''BMC Genom Data''. 2021 Sep 6; '''22''' (1):31
Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats. Description: Ding, Yuting, et al. Mitonuclear mismatch alters nuclear gene expression in naturally introgressed Rhinolophus bats. ''Front Zool''. 2021 Sep 6; '''18''' (1):42
PUMAS: fine-tuning polygenic risk scores with GWAS summary statistics. Description: Zhao, Zijie, et al. PUMAS: fine-tuning polygenic risk scores with GWAS summary statistics. ''Genome Biol''. 2021 Sep 6; '''22''' (1):257
Regional Heritability Mapping of Quantitative Trait Loci Controlling Traits Related to Growth and Productivity in Popcorn (Zea mays L.). Description: Mafra, Gabrielle Sousa, et al. Regional Heritability Mapping of Quantitative Trait Loci Controlling Traits Related to Growth and Productivity in Popcorn (Zea mays L.). ''Plants (Basel)''. 2021 Sep 6; '''10''' (9):
RNA polymerase mapping in plants identifies intergenic regulatory elements enriched in causal variants. Description: Lozano, Roberto, et al. RNA polymerase mapping in plants identifies intergenic regulatory elements enriched in causal variants. ''G3 (Bethesda)''. 2021 Sep 6;
Unveiling Comparative Genomic Trajectories of Selection and Key Candidate Genes in Egg-Type Russian White and Meat-Type White Cornish Chickens. Description: Abdelmanova, Alexandra S, et al. Unveiling Comparative Genomic Trajectories of Selection and Key Candidate Genes in Egg-Type Russian White and Meat-Type White Cornish Chickens. ''Biology (Basel)''. 2021 Sep 6; '''10''' (9):
Base excision repair causes age-dependent accumulation of single-stranded DNA breaks that contribute to Parkinson disease pathology. Description: SenGupta, Tanima, et al. Base excision repair causes age-dependent accumulation of single-stranded DNA breaks that contribute to Parkinson disease pathology. ''Cell Rep''. 2021 Sep 7; '''36''' (10):109668
Evolution of cytokine production capacity in ancient and modern European populations. Description: Dominguez-Andres, Jorge, et al. Evolution of cytokine production capacity in ancient and modern European populations. ''Elife''. 2021 Sep 7; '''10''':
SUPERGNOVA: local genetic correlation analysis reveals heterogeneous etiologic sharing of complex traits. Description: Zhang, Yiliang, et al. SUPERGNOVA: local genetic correlation analysis reveals heterogeneous etiologic sharing of complex traits. ''Genome Biol''. 2021 Sep 7; '''22''' (1):262
A genome-wide association analysis for body weight at 35 days measured on 137,343 broiler chickens. Description: Dadousis, Christos, et al. A genome-wide association analysis for body weight at 35 days measured on 137,343 broiler chickens. ''Genet Sel Evol''. 2021 Sep 8; '''53''' (1):70
HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders. Description: Le Clerc, Sigrid, et al. HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders. ''Sci Rep''. 2021 Sep 8; '''11''' (1):17823
A genome-wide scan to identify signatures of selection in two Iranian indigenous chicken ecotypes. Description: Rostamzadeh Mahdabi, Elaheh, et al. A genome-wide scan to identify signatures of selection in two Iranian indigenous chicken ecotypes. ''Genet Sel Evol''. 2021 Sep 9; '''53''' (1):72
Landscape genetics and the genetic legacy of Upper Paleolithic and Mesolithic hunter-gatherers in the modern Caucasus. Description: Gavashelishvili, Alexander, et al. Landscape genetics and the genetic legacy of Upper Paleolithic and Mesolithic hunter-gatherers in the modern Caucasus. ''Sci Rep''. 2021 Sep 9; '''11''' (1):17985
SNPs in Sheep: Characterization of Lithuanian Sheep Populations. Description: Sveistiene, Ruta, et al. SNPs in Sheep: Characterization of Lithuanian Sheep Populations. ''Animals (Basel)''. 2021 Sep 9; '''11''' (9):
Lack of association of FKBP5 SNPs and haplotypes with susceptibility and treatment response phenotypes in Han Chinese with major depressive disorder: A pilot case-control study (STROBE). Description: Yang, Chenghao, et al. Lack of association of FKBP5 SNPs and haplotypes with susceptibility and treatment response phenotypes in Han Chinese with major depressive disorder: A pilot case-control study (STROBE). ''Medicine (Baltimore)''. 2021 Sep 10; '''100''' (36):e26983
Sweepstake reproductive success and collective dispersal produce chaotic genetic patchiness in a broadcast spawner. Description: Vendrami, David L J, et al. Sweepstake reproductive success and collective dispersal produce chaotic genetic patchiness in a broadcast spawner. ''Sci Adv''. 2021 Sep 10; '''7''' (37):eabj4713
Biomolecular insights into North African-related ancestry, mobility and diet in eleventh-century Al-Andalus. Description: Silva, Marina, et al. Biomolecular insights into North African-related ancestry, mobility and diet in eleventh-century Al-Andalus. ''Sci Rep''. 2021 Sep 13; '''11''' (1):18121
Genetic predisposition to tinnitus in the UK Biobank population. Description: Urbanek, Madeleine E, et al. Genetic predisposition to tinnitus in the UK Biobank population. ''Sci Rep''. 2021 Sep 13; '''11''' (1):18150
Human inbreeding has decreased in time through the Holocene. Description: Ceballos, Francisco C, et al. Human inbreeding has decreased in time through the Holocene. ''Curr Biol''. 2021 Sep 13; '''31''' (17):3925-3934.e8
Integrating a genome-wide association study with transcriptomic data to predict candidate genes and favourable haplotypes influencing Brassica napus seed phytate. Description: Liu, Haijiang, et al. Integrating a genome-wide association study with transcriptomic data to predict candidate genes and favourable haplotypes influencing Brassica napus seed phytate. ''DNA Res''. 2021 Sep 13; '''28''' (5):
Genetic basis and adaptation trajectory of soybean from its temperate origin to tropics. Description: Dong, Lidong, et al. Genetic basis and adaptation trajectory of soybean from its temperate origin to tropics. ''Nat Commun''. 2021 Sep 14; '''12''' (1):5445
Genome-wide association study reveals the genetic architecture of root hair length in maize. Description: Liu, Lin, et al. Genome-wide association study reveals the genetic architecture of root hair length in maize. ''BMC Genomics''. 2021 Sep 14; '''22''' (1):664
Identifying the lungs as a susceptible site for allele-specific regulatory changes associated with type 1 diabetes risk. Description: Ho, Daniel, et al. Identifying the lungs as a susceptible site for allele-specific regulatory changes associated with type 1 diabetes risk. ''Commun Biol''. 2021 Sep 14; '''4''' (1):1072
Analysis of 427 genomes reveals moso bamboo population structure and genetic basis of property traits. Description: Zhao, Hansheng, et al. Analysis of 427 genomes reveals moso bamboo population structure and genetic basis of property traits. ''Nat Commun''. 2021 Sep 15; '''12''' (1):5466
Analysis of genes (TMEM106B, GRN, ABCC9, KCNMB2, and APOE) implicated in risk for LATE-NC and hippocampal sclerosis provides pathogenetic insights: a retrospective genetic association study. Description: Dugan, Adam J, et al. Analysis of genes (TMEM106B, GRN, ABCC9, KCNMB2, and APOE) implicated in risk for LATE-NC and hippocampal sclerosis provides pathogenetic insights: a retrospective genetic association study. ''Acta Neuropathol Commun''. 2021 Sep 15; '''9''' (1):152
Association Study among Comethylation Modules, Genetic Polymorphisms and Clinical Features in Mexican Teenagers with Eating Disorders: Preliminary Results. Description: Nolasco-Rosales, German Alberto, et al. Association Study among Comethylation Modules, Genetic Polymorphisms and Clinical Features in Mexican Teenagers with Eating Disorders: Preliminary Results. ''Nutrients''. 2021 Sep 15; '''13''' (9):
Brain-derived neurotrophic factor gene variants and obesity in former smokers. Description: Yang, Shan-Shan, et al. Brain-derived neurotrophic factor gene variants and obesity in former smokers. ''BMC Genomics''. 2021 Sep 15; '''22''' (1):668
Detection and Visualization of Heterozygosity-Rich Regions and Runs of Homozygosity in Worldwide Sheep Populations. Description: Selli, Alana, et al. Detection and Visualization of Heterozygosity-Rich Regions and Runs of Homozygosity in Worldwide Sheep Populations. ''Animals (Basel)''. 2021 Sep 15; '''11''' (9):
Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight. Description: Beck, Jeffrey J, et al. Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight. ''Hum Mol Genet''. 2021 Sep 15; '''30''' (19):1894-1905
An association study in the Taiwan Biobank elicits the GABAA receptor genes GABRB3, GABRA5, and GABRG3 as candidate loci for sleep duration in the Taiwanese population. Description: Hou, Sheue-Jane, et al. An association study in the Taiwan Biobank elicits the GABAA receptor genes GABRB3, GABRA5, and GABRG3 as candidate loci for sleep duration in the Taiwanese population. ''BMC Med Genomics''. 2021 Sep 16; '''14''' (1):223
Local adaptation and archaic introgression shape global diversity at human structural variant loci. Description: Yan, Stephanie M, et al. Local adaptation and archaic introgression shape global diversity at human structural variant loci. ''Elife''. 2021 Sep 16; '''10''':
MIDESP: Mutual Information-Based Detection of Epistatic SNP Pairs for Qualitative and Quantitative Phenotypes. Description: Heinrich, Felix, et al. MIDESP: Mutual Information-Based Detection of Epistatic SNP Pairs for Qualitative and Quantitative Phenotypes. ''Biology (Basel)''. 2021 Sep 16; '''10''' (9):
The Relationship between Metabolic Syndrome and Plasma Metals Modified by EGFR and TNF-alpha Gene Polymorphisms. Description: Chen, Tzu-Hua, et al. The Relationship between Metabolic Syndrome and Plasma Metals Modified by EGFR and TNF-alpha Gene Polymorphisms. ''Toxics''. 2021 Sep 16; '''9''' (9):
Ancient genomics reveals tripartite origins of Japanese populations. Description: Cooke, Niall P, et al. Ancient genomics reveals tripartite origins of Japanese populations. ''Sci Adv''. 2021 Sep 17; '''7''' (38):eabh2419
Environmental Influences Measured by Epigenetic Clock and Vulnerability Components at Birth Impact Clinical ASD Heterogeneity. Description: Neri de Souza Reis, Viviane, et al. Environmental Influences Measured by Epigenetic Clock and Vulnerability Components at Birth Impact Clinical ASD Heterogeneity. ''Genes (Basel)''. 2021 Sep 17; '''12''' (9):
Phylogeographic reconstruction of the marbled crayfish origin. Description: Gutekunst, Julian, et al. Phylogeographic reconstruction of the marbled crayfish origin. ''Commun Biol''. 2021 Sep 17; '''4''' (1):1096
Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy. Description: Buono, Russell J, et al. Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy. ''Genes (Basel)''. 2021 Sep 18; '''12''' (9):
Whole-genome resequencing of Japanese whiting ( Sillago japonica) provide insights into local adaptations. Description: Han, Zhi-Qiang, et al. Whole-genome resequencing of Japanese whiting ( Sillago japonica) provide insights into local adaptations. ''Zool Res''. 2021 Sep 18; '''42''' (5):548-561
Inferred Ancestral Origin of Cancer Cell Lines Associates with Differential Drug Response. Description: Nguyen, Phong B H, et al. Inferred Ancestral Origin of Cancer Cell Lines Associates with Differential Drug Response. ''Int J Mol Sci''. 2021 Sep 20; '''22''' (18):
APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups. Description: Goyal, Shiwali, et al. APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups. ''Lipids Health Dis''. 2021 Sep 21; '''20''' (1):113
Fine mapping of the HLA locus in Parkinson's disease in Europeans. Description: Yu, Eric, et al. Fine mapping of the HLA locus in Parkinson's disease in Europeans. ''NPJ Parkinsons Dis''. 2021 Sep 21; '''7''' (1):84
Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort. Description: Zainul Abidin, Fatin N, et al. Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort. ''Neuroimage Clin''. 2021 Sep 21; '''32''': 102823
Haplotype divergence supports long-term asexuality in the oribatid mite Oppiella nova. Description: Brandt, Alexander, et al. Haplotype divergence supports long-term asexuality in the oribatid mite Oppiella nova. ''Proc Natl Acad Sci U S A''. 2021 Sep 21; '''118''' (38):
Runs of homozygosity analysis reveals consensus homozygous regions affecting production traits in Chinese Simmental beef cattle. Description: Zhao, Guoyao, et al. Runs of homozygosity analysis reveals consensus homozygous regions affecting production traits in Chinese Simmental beef cattle. ''BMC Genomics''. 2021 Sep 21; '''22''' (1):678
Admixture with indigenous people helps local adaptation: admixture-enabled selection in Polynesians. Description: Isshiki, Mariko, et al. Admixture with indigenous people helps local adaptation: admixture-enabled selection in Polynesians. ''BMC Ecol Evol''. 2021 Sep 22; '''21''' (1):179
Expression quantitative trait loci for ETV4 and MEOX1 are associated with adult asthma in Japanese populations. Description: Yatagai, Yohei, et al. Expression quantitative trait loci for ETV4 and MEOX1 are associated with adult asthma in Japanese populations. ''Sci Rep''. 2021 Sep 22; '''11''' (1):18791
Polymorphic estrogen receptor binding site causes Cd2-dependent sex bias in the susceptibility to autoimmune diseases. Description: Fernandez Lahore, Gonzalo, et al. Polymorphic estrogen receptor binding site causes Cd2-dependent sex bias in the susceptibility to autoimmune diseases. ''Nat Commun''. 2021 Sep 22; '''12''' (1):5565
Analyses of child cardiometabolic phenotype following assisted reproductive technologies using a pragmatic trial emulation approach. Description: Huang, Jonathan Yinhao, et al. Analyses of child cardiometabolic phenotype following assisted reproductive technologies using a pragmatic trial emulation approach. ''Nat Commun''. 2021 Sep 23; '''12''' (1):5613
Association of female reproductive tract microbiota with egg production in layer chickens. Description: Su, Yuan, et al. Association of female reproductive tract microbiota with egg production in layer chickens. ''Gigascience''. 2021 Sep 23; '''10''' (9):
Common host variation drives malaria parasite fitness in healthy human red cells. Description: Ebel, Emily R, et al. Common host variation drives malaria parasite fitness in healthy human red cells. ''Elife''. 2021 Sep 23; '''10''':
Genome Evolution of Filamentous Cyanobacterium Nostoc Species: From Facultative Symbiosis to Free Living. Description: Huo, Da, et al. Genome Evolution of Filamentous Cyanobacterium Nostoc Species: From Facultative Symbiosis to Free Living. ''Microorganisms''. 2021 Sep 23; '''9''' (10):
Microglial-expressed genetic risk variants, cognitive function and brain volume in patients with schizophrenia and healthy controls. Description: Corley, Emma, et al. Microglial-expressed genetic risk variants, cognitive function and brain volume in patients with schizophrenia and healthy controls. ''Transl Psychiatry''. 2021 Sep 23; '''11''' (1):490
Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings. Description: Lybech, Line K M, et al. Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings. ''Genes (Basel)''. 2021 Sep 23; '''12''' (10):
Genetic risk model for in-stent restenosis of second-and third-generation drug-eluting stents. Description: Liu, Yen-Wen, et al. Genetic risk model for in-stent restenosis of second-and third-generation drug-eluting stents. ''iScience''. 2021 Sep 24; '''24''' (9):103082
Genome-Wide Association Studies for Milk Somatic Cell Score in Romanian Dairy Cattle. Description: Ilie, Daniela Elena, et al. Genome-Wide Association Studies for Milk Somatic Cell Score in Romanian Dairy Cattle. ''Genes (Basel)''. 2021 Sep 24; '''12''' (10):
Investigating the shared genetic architecture between multiple sclerosis and inflammatory bowel diseases. Description: Yang, Yuanhao, et al. Investigating the shared genetic architecture between multiple sclerosis and inflammatory bowel diseases. ''Nat Commun''. 2021 Sep 24; '''12''' (1):5641
PRKG2 Splice Site Variant in Dogo Argentino Dogs with Disproportionate Dwarfism. Description: Rudd Garces, Gabriela, et al. PRKG2 Splice Site Variant in Dogo Argentino Dogs with Disproportionate Dwarfism. ''Genes (Basel)''. 2021 Sep 24; '''12''' (10):
A Novel QTL and a Candidate Gene Are Associated with the Progressive Motility of Franches-Montagnes Stallion Spermatozoa after Thaw. Description: Gmel, Annik Imogen, et al. A Novel QTL and a Candidate Gene Are Associated with the Progressive Motility of Franches-Montagnes Stallion Spermatozoa after Thaw. ''Genes (Basel)''. 2021 Sep 25; '''12''' (10):
MIA3 Splice Defect in Cane Corso Dogs with Dental-Skeletal-Retinal Anomaly (DSRA). Description: Christen, Matthias, et al. MIA3 Splice Defect in Cane Corso Dogs with Dental-Skeletal-Retinal Anomaly (DSRA). ''Genes (Basel)''. 2021 Sep 25; '''12''' (10):
Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci. Description: Pappas, Chris M, et al. Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci. ''Hum Genomics''. 2021 Sep 25; '''15''' (1):60
Revealing the coexistence of differentiation and communication in an endemic hare, Lepus yarkandensis (Mammalia, Leporidae) using specific-length amplified fragment sequencing. Description: Ababaikeri, Buweihailiqiemu, et al. Revealing the coexistence of differentiation and communication in an endemic hare, Lepus yarkandensis (Mammalia, Leporidae) using specific-length amplified fragment sequencing. ''Front Zool''. 2021 Sep 26; '''18''' (1):50
A candidate chromosome inversion in Arctic charr (Salvelinus alpinus) identified by population genetic analysis techniques. Description: Hale, Matthew C, et al. A candidate chromosome inversion in Arctic charr (Salvelinus alpinus) identified by population genetic analysis techniques. ''G3 (Bethesda)''. 2021 Sep 27; '''11''' (10):
Admixture mapping reveals loci for carcass mass in red deer x sika hybrids in Kintyre, Scotland. Description: McFarlane, S Eryn, et al. Admixture mapping reveals loci for carcass mass in red deer x sika hybrids in Kintyre, Scotland. ''G3 (Bethesda)''. 2021 Sep 27; '''11''' (10):
Broad Concordance in the Spatial Distribution of Adaptive and Neutral Genetic Variation across an Elevational Gradient in Deer Mice. Description: Schweizer, Rena M, et al. Broad Concordance in the Spatial Distribution of Adaptive and Neutral Genetic Variation across an Elevational Gradient in Deer Mice. ''Mol Biol Evol''. 2021 Sep 27; '''38''' (10):4286-4300
Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People. Description: Lo, Yun-Hua, et al. Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People. ''Mol Biol Evol''. 2021 Sep 27; '''38''' (10):4149-4165
MHC class IIa haplotypes derived by high-throughput SNP screening in an isolated sheep population. Description: Dicks, Kara L, et al. MHC class IIa haplotypes derived by high-throughput SNP screening in an isolated sheep population. ''G3 (Bethesda)''. 2021 Sep 27; '''11''' (10):
Molecular Clocks and Archeogenomics of a Late Period Egyptian Date Palm Leaf Reveal Introgression from Wild Relatives and Add Timestamps on the Domestication. Description: Perez-Escobar, Oscar A, et al. Molecular Clocks and Archeogenomics of a Late Period Egyptian Date Palm Leaf Reveal Introgression from Wild Relatives and Add Timestamps on the Domestication. ''Mol Biol Evol''. 2021 Sep 27; '''38''' (10):4475-4492
Museomics Dissects the Genetic Basis for Adaptive Seasonal Coloration in the Least Weasel. Description: Miranda, Ines, et al. Museomics Dissects the Genetic Basis for Adaptive Seasonal Coloration in the Least Weasel. ''Mol Biol Evol''. 2021 Sep 27; '''38''' (10):4388-4402
Patterns and Causes of Signed Linkage Disequilibria in Flies and Plants. Description: Sandler, George, et al. Patterns and Causes of Signed Linkage Disequilibria in Flies and Plants. ''Mol Biol Evol''. 2021 Sep 27; '''38''' (10):4310-4321
The Evolutionary History of Wild, Domesticated, and Feral Brassica oleracea (Brassicaceae). Description: Mabry, Makenzie E, et al. The Evolutionary History of Wild, Domesticated, and Feral Brassica oleracea (Brassicaceae). ''Mol Biol Evol''. 2021 Sep 27; '''38''' (10):4419-4434
Whole-genome variation of transposable element insertions in a maize diversity panel. Description: Qiu, Yinjie, et al. Whole-genome variation of transposable element insertions in a maize diversity panel. ''G3 (Bethesda)''. 2021 Sep 27; '''11''' (10):
A high-resolution genome-wide association study of the grain ionome and agronomic traits in rice Oryza sativa subsp. indica. Description: Cu, Suong T, et al. A high-resolution genome-wide association study of the grain ionome and agronomic traits in rice Oryza sativa subsp. indica. ''Sci Rep''. 2021 Sep 28; '''11''' (1):19230
Identical twins carry a persistent epigenetic signature of early genome programming. Description: van Dongen, Jenny, et al. Identical twins carry a persistent epigenetic signature of early genome programming. ''Nat Commun''. 2021 Sep 28; '''12''' (1):5618
Associations between ALDH Genetic Variants, Alcohol Consumption, and the Risk of Nasopharyngeal Carcinoma in an East Asian Population. Description: Liao, Wen-Ling, et al. Associations between ALDH Genetic Variants, Alcohol Consumption, and the Risk of Nasopharyngeal Carcinoma in an East Asian Population. ''Genes (Basel)''. 2021 Sep 29; '''12''' (10):
Development of a multi-species SNP array for serrasalmid fish Colossoma macropomum and Piaractus mesopotamicus. Description: Mastrochirico-Filho, Vito A, et al. Development of a multi-species SNP array for serrasalmid fish Colossoma macropomum and Piaractus mesopotamicus. ''Sci Rep''. 2021 Sep 29; '''11''' (1):19289
Fur colour in the Arctic fox: genetic architecture and consequences for fitness. Description: Tietgen, Lukas, et al. Fur colour in the Arctic fox: genetic architecture and consequences for fitness. ''Proc Biol Sci''. 2021 Sep 29; '''288''' (1959):20211452
Carrot Consumption Frequency Associated with Reduced BMI and Obesity through the SNP Intermediary rs4445711. Description: Fujihara, Kazuya, et al. Carrot Consumption Frequency Associated with Reduced BMI and Obesity through the SNP Intermediary rs4445711. ''Nutrients''. 2021 Sep 30; '''13''' (10):
Cortical thickness is differently associated with ALDH2 rs671 polymorphism according to level of amyloid deposition. Description: Cho, Yong Hyuk, et al. Cortical thickness is differently associated with ALDH2 rs671 polymorphism according to level of amyloid deposition. ''Sci Rep''. 2021 Sep 30; '''11''' (1):19529
Development of SNP Set for the Marker-Assisted Selection of Guar (Cyamopsis tetragonoloba (L.) Taub.) Based on a Custom Reference Genome Assembly. Description: Grigoreva, Elizaveta, et al. Development of SNP Set for the Marker-Assisted Selection of Guar (Cyamopsis tetragonoloba (L.) Taub.) Based on a Custom Reference Genome Assembly. ''Plants (Basel)''. 2021 Sep 30; '''10''' (10):
Genomic risk prediction of coronary artery disease in women with breast cancer: a prospective cohort study. Description: Liou, Lathan, et al. Genomic risk prediction of coronary artery disease in women with breast cancer: a prospective cohort study. ''Breast Cancer Res''. 2021 Sep 30; '''23''' (1):94
GWAS identifies an ortholog of the rice D11 gene as a candidate gene for grain size in an international collection of hexaploid wheat. Description: Tekeu, Honore, et al. GWAS identifies an ortholog of the rice D11 gene as a candidate gene for grain size in an international collection of hexaploid wheat. ''Sci Rep''. 2021 Sep 30; '''11''' (1):19483
Metabolic profiling of maternal serum of women at high-risk of spontaneous preterm birth using NMR and MGWAS approach. Description: Gupta, Juhi K, et al. Metabolic profiling of maternal serum of women at high-risk of spontaneous preterm birth using NMR and MGWAS approach. ''Biosci Rep''. 2021 Sep 30; '''41''' (9):
Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease. Description: Tran, Ngan K, et al. Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease. ''Sci Rep''. 2021 Sep 30; '''11''' (1):19425
Pleiotropic Effects of Functional MUC1 Variants on Cardiometabolic, Renal, and Hematological Traits in the Taiwanese Population. Description: Teng, Ming-Sheng, et al. Pleiotropic Effects of Functional MUC1 Variants on Cardiometabolic, Renal, and Hematological Traits in the Taiwanese Population. ''Int J Mol Sci''. 2021 Sep 30; '''22''' (19):
Regional TMPRSS2 V197M Allele Frequencies Are Correlated with COVID-19 Case Fatality Rates. Description: Jeon, Sungwon, et al. Regional TMPRSS2 V197M Allele Frequencies Are Correlated with COVID-19 Case Fatality Rates. ''Mol Cells''. 2021 Sep 30; '''44''' (9):680-687
A panel of rhythm gene polymorphisms is involved in susceptibility to type 2 diabetes mellitus and bipolar disorder. Description: Min, Wenjiao, et al. A panel of rhythm gene polymorphisms is involved in susceptibility to type 2 diabetes mellitus and bipolar disorder. ''Ann Transl Med''. 2021 Oct; '''9''' (20):1555
A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay. Description: Gotkine, Marc, et al. A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay. ''Neurobiol Aging''. 2021 Oct; '''106''': 351.e1-351.e6
Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children. Description: Lan, Chaoting, et al. Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children. ''J Cell Mol Med''. 2021 Oct; '''25''' (20):9609-9616
Associations between major psychiatric disorder polygenic risk scores and blood-based markers in UK biobank. Description: Sewell, Michael D E, et al. Associations between major psychiatric disorder polygenic risk scores and blood-based markers in UK biobank. ''Brain Behav Immun''. 2021 Oct; '''97''': 32-41
Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia. Description: Legge, Sophie E, et al. Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia. ''JAMA Psychiatry''. 2021 Oct 1; '''78''' (10):1143-1151
Associations of Nutrient Intake Changes During Childhood with Adolescent Hepatic Fat: The Exploring Perinatal Outcomes Among CHildren Study. Description: Cohen, Catherine C, et al. Associations of Nutrient Intake Changes During Childhood with Adolescent Hepatic Fat: The Exploring Perinatal Outcomes Among CHildren Study. ''J Pediatr''. 2021 Oct; '''237''': 50-58.e3
Cannabis labelling is associated with genetic variation in terpene synthase genes. Description: Watts, Sophie, et al. Cannabis labelling is associated with genetic variation in terpene synthase genes. ''Nat Plants''. 2021 Oct; '''7''' (10):1330-1334
Chromatin accessibility and gene expression during adipocyte differentiation identify context-dependent effects at cardiometabolic GWAS loci. Description: Perrin, Hannah J, et al. Chromatin accessibility and gene expression during adipocyte differentiation identify context-dependent effects at cardiometabolic GWAS loci. ''PLoS Genet''. 2021 Oct; '''17''' (10):e1009865
Concerted genomic and epigenomic changes accompany stabilization of Arabidopsis allopolyploids. Description: Jiang, Xinyu, et al. Concerted genomic and epigenomic changes accompany stabilization of Arabidopsis allopolyploids. ''Nat Ecol Evol''. 2021 Oct; '''5''' (10):1382-1393
Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates. Description: Goudswaard, Lucy J, et al. Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates. ''Int J Obes (Lond)''. 2021 Oct; '''45''' (10):2221-2229
Estimation of regional polygenicity from GWAS provides insights into the genetic architecture of complex traits. Description: Johnson, Ruth, et al. Estimation of regional polygenicity from GWAS provides insights into the genetic architecture of complex traits. ''PLoS Comput Biol''. 2021 Oct; '''17''' (10):e1009483
Factors associated with orthodontic pain. Description: Lin, Wei, et al. Factors associated with orthodontic pain. ''J Oral Rehabil''. 2021 Oct; '''48''' (10):1135-1143
Fine-scale population structure in five rural populations from the Spanish Eastern Pyrenees using high-coverage whole-genome sequence data. Description: Maceda, Iago, et al. Fine-scale population structure in five rural populations from the Spanish Eastern Pyrenees using high-coverage whole-genome sequence data. ''Eur J Hum Genet''. 2021 Oct; '''29''' (10):1557-1565
Generation of multiple human iPSC lines from peripheral blood mononuclear cells of two SLC2A3 deletion and two SLC2A3 duplication carriers. Description: Ziegler, Georg C, et al. Generation of multiple human iPSC lines from peripheral blood mononuclear cells of two SLC2A3 deletion and two SLC2A3 duplication carriers. ''Stem Cell Res''. 2021 Oct; '''56''': 102526
Genetic drift from the out-of-Africa bottleneck leads to biased estimation of genetic architecture and selection. Description: Ashraf, Bilal, et al. Genetic drift from the out-of-Africa bottleneck leads to biased estimation of genetic architecture and selection. ''Eur J Hum Genet''. 2021 Oct; '''29''' (10):1549-1556
Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. Description: DeMichele-Sweet, Mary Ann A, et al. Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. ''Mol Psychiatry''. 2021 Oct; '''26''' (10):5797-5811
Genome-wide association studies reveals polygenic genetic architecture of litter traits in Duroc pigs. Description: Ding, Rongrong, et al. Genome-wide association studies reveals polygenic genetic architecture of litter traits in Duroc pigs. ''Theriogenology''. 2021 Oct 1; '''173''': 269-278
Genome-wide family-based study in torus palatinus affected individuals. Description: Bezamat, Mariana, et al. Genome-wide family-based study in torus palatinus affected individuals. ''Arch Oral Biol''. 2021 Oct; '''130''': 105221
GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels. Description: Casares-Marfil, Desire, et al. GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels. ''PLoS Negl Trop Dis''. 2021 Oct; '''15''' (10):e0009874
Improving the resolution of canine genome-wide association studies using genotype imputation: A study of two breeds. Description: Jenkins, Christopher A, et al. Improving the resolution of canine genome-wide association studies using genotype imputation: A study of two breeds. ''Anim Genet''. 2021 Oct; '''52''' (5):703-713
Integrating Genomic and Transcriptomic Data to Reveal Genetic Mechanisms Underlying Piao Chicken Rumpless Trait. Description: Wang, Yun-Mei, et al. Integrating Genomic and Transcriptomic Data to Reveal Genetic Mechanisms Underlying Piao Chicken Rumpless Trait. ''Genomics Proteomics Bioinformatics''. 2021 Oct; '''19''' (5):787-799
Leveraging auxiliary data from arbitrary distributions to boost GWAS discovery with Flexible cFDR. Description: Hutchinson, Anna, et al. Leveraging auxiliary data from arbitrary distributions to boost GWAS discovery with Flexible cFDR. ''PLoS Genet''. 2021 Oct; '''17''' (10):e1009853
Maternal and offspring genetic risk score analyses of fetal alcohol exposure and attention-deficit hyperactivity disorder risk in offspring. Description: Haan, Elis, et al. Maternal and offspring genetic risk score analyses of fetal alcohol exposure and attention-deficit hyperactivity disorder risk in offspring. ''Alcohol Clin Exp Res''. 2021 Oct; '''45''' (10):2090-2102
Multi-Omics Analysis Reveals the Mechanism Underlying the Edaphic Adaptation in Wild Barley at Evolution Slope (Tabigha). Description: Cai, Shengguan, et al. Multi-Omics Analysis Reveals the Mechanism Underlying the Edaphic Adaptation in Wild Barley at Evolution Slope (Tabigha). ''Adv Sci (Weinh)''. 2021 Oct; '''8''' (20):e2101374
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. Description: Karlsson Linner, Richard, et al. Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. ''Nat Neurosci''. 2021 Oct; '''24''' (10):1367-1376
Polygenic basis and biomedical consequences of telomere length variation. Description: Codd, Veryan, et al. Polygenic basis and biomedical consequences of telomere length variation. ''Nat Genet''. 2021 Oct; '''53''' (10):1425-1433
Population-level deep sequencing reveals the interplay of clonal and sexual reproduction in the fungal wheat pathogen Zymoseptoria tritici. Description: Singh, Nikhil Kumar, et al. Population-level deep sequencing reveals the interplay of clonal and sexual reproduction in the fungal wheat pathogen Zymoseptoria tritici. ''Microb Genom''. 2021 Oct; '''7''' (10):
Prediction of clinical diagnosis of Alzheimer's disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOE status in a community-based cohort prospectively followed over 17 years. Description: Stocker, H, et al. Prediction of clinical diagnosis of Alzheimer's disease, vascular, mixed, and all-cause dementia by a polygenic risk score and APOE status in a community-based cohort prospectively followed over 17 years. ''Mol Psychiatry''. 2021 Oct; '''26''' (10):5812-5822
SLC17A3 rs9379800 and Ischemic Stroke Susceptibility at the Northern Region of Malaysia. Description: Ching, Shu Chai, et al. SLC17A3 rs9379800 and Ischemic Stroke Susceptibility at the Northern Region of Malaysia. ''J Stroke Cerebrovasc Dis''. 2021 Oct; '''30''' (10):105908
SORL1 mutation in a Greek family with Parkinson's disease and dementia. Description: Xiromerisiou, Georgia, et al. SORL1 mutation in a Greek family with Parkinson's disease and dementia. ''Ann Clin Transl Neurol''. 2021 Oct; '''8''' (10):1961-1969
Systematic assessment of variability in the proteome of iPSC derivatives. Description: Beekhuis-Hoekstra, Stephanie D, et al. Systematic assessment of variability in the proteome of iPSC derivatives. ''Stem Cell Res''. 2021 Oct; '''56''': 102512
The association between polygenic scores for attention-deficit/hyperactivity disorder and school performance: The role of attention-deficit/hyperactivity disorder symptoms, polygenic scores for educational attainment, and shared familial factors. Description: Jangmo, Andreas, et al. The association between polygenic scores for attention-deficit/hyperactivity disorder and school performance: The role of attention-deficit/hyperactivity disorder symptoms, polygenic scores for educational attainment, and shared familial factors. ''JCPP Adv''. 2021 Oct; '''1''' (3):e12030
Through 40,000 years of human presence in Southern Europe: the Italian case study. Description: Aneli, Serena, et al. Through 40,000 years of human presence in Southern Europe: the Italian case study. ''Hum Genet''. 2021 Oct; '''140''' (10):1417-1431
Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13. Description: Acharya, Anushree, et al. Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13. ''J Hum Genet''. 2021 Oct; '''66''' (10):1009-1018
X-treme loss of sequence diversity linked to neo-X chromosomes in filarial nematodes. Description: Mattick, John, et al. X-treme loss of sequence diversity linked to neo-X chromosomes in filarial nematodes. ''PLoS Negl Trop Dis''. 2021 Oct; '''15''' (10):e0009838
Functional Haplotypes and Evolutionary Insight into the Granule-Bound Starch Synthase II (GBSSII) Gene in Korean Rice Accessions (KRICE_CORE). Description: Maung, Thant Zin, et al. Functional Haplotypes and Evolutionary Insight into the Granule-Bound Starch Synthase II (GBSSII) Gene in Korean Rice Accessions (KRICE_CORE). ''Foods''. 2021 Oct 3; '''10''' (10):
Genetic Variants Associated With Human Eye Size Are Distinct From Those Conferring Susceptibility to Myopia. Description: Plotnikov, Denis, et al. Genetic Variants Associated With Human Eye Size Are Distinct From Those Conferring Susceptibility to Myopia. ''Invest Ophthalmol Vis Sci''. 2021 Oct 4; '''62''' (13):24
Analysis of selection signatures reveals important insights into the adaptability of high-altitude Indian sheep breed Changthangi. Description: Ahmad, Sheikh Firdous, et al. Analysis of selection signatures reveals important insights into the adaptability of high-altitude Indian sheep breed Changthangi. ''Gene''. 2021 Oct 5; '''799''': 145809
BMI1 is associated with CS8F amyloid-beta and rates of cognitive decline in Alzheimer's disease. Description: Kim, Jun Pyo, et al. BMI1 is associated with CS8F amyloid-beta and rates of cognitive decline in Alzheimer's disease. ''Alzheimers Res Ther''. 2021 Oct 5; '''13''' (1):164
Genome-wide association studies of yield-related traits in high-latitude japonica rice. Description: Zhang, Guomin, et al. Genome-wide association studies of yield-related traits in high-latitude japonica rice. ''BMC Genom Data''. 2021 Oct 5; '''22''' (1):39
Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories. Description: Lali, Ricky, et al. Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories. ''Nat Commun''. 2021 Oct 6; '''12''' (1):5852
Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer's disease. Description: Kumar, Atul, et al. Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer's disease. ''Sci Rep''. 2021 Oct 6; '''11''' (1):19853
How rare and common risk variation jointly affect liability for autism spectrum disorder. Description: Klei, Lambertus, et al. How rare and common risk variation jointly affect liability for autism spectrum disorder. ''Mol Autism''. 2021 Oct 6; '''12''' (1):66
The Mediation Effects of Aluminum in Plasma and Dipeptidyl Peptidase Like Protein 6 (DPP6) Polymorphism on Renal Function via Genome-Wide Typing Association. Description: Chen, Ting-Hao, et al. The Mediation Effects of Aluminum in Plasma and Dipeptidyl Peptidase Like Protein 6 (DPP6) Polymorphism on Renal Function via Genome-Wide Typing Association. ''Int J Environ Res Public Health''. 2021 Oct 6; '''18''' (19):
A 584 bp deletion in CTRB2 inhibits chymotrypsin B2 activity and secretion and confers risk of pancreatic cancer. Description: Jermusyk, Ashley, et al. A 584 bp deletion in CTRB2 inhibits chymotrypsin B2 activity and secretion and confers risk of pancreatic cancer. ''Am J Hum Genet''. 2021 Oct 7; '''108''' (10):1852-1865
A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene. Description: Magusali, Naciye, et al. A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene. ''Brain''. 2021 Oct 7;
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo. Description: Skuladottir, Astros Th, et al. A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo. ''Commun Biol''. 2021 Oct 7; '''4''' (1):1148
Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data. Description: Ongaro, Linda, et al. Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data. ''Genes (Basel)''. 2021 Oct 7; '''12''' (10):
Fc receptor-like 1, 3, and 6 variants are associated with rheumatoid arthritis risk in the Chinese Han population. Description: Yang, Yonghui, et al. Fc receptor-like 1, 3, and 6 variants are associated with rheumatoid arthritis risk in the Chinese Han population. ''Genes Environ''. 2021 Oct 7; '''43''' (1):42
Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Description: Kachuri, Linda, et al. Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. ''Am J Hum Genet''. 2021 Oct 7; '''108''' (10):1823-1835
Genome-Wide Association Study on Adiponectin-Mediated Suppression of HDL-C Levels in Taiwanese Individuals Identifies Functional Haplotypes in CDH13. Description: Er, Leay-Kiaw, et al. Genome-Wide Association Study on Adiponectin-Mediated Suppression of HDL-C Levels in Taiwanese Individuals Identifies Functional Haplotypes in CDH13. ''Genes (Basel)''. 2021 Oct 7; '''12''' (10):
Genome-wide association study revealed genetic variations of ABA sensitivity controlled by multiple stress-related genes in rice. Description: Peng, Lei, et al. Genome-wide association study revealed genetic variations of ABA sensitivity controlled by multiple stress-related genes in rice. ''Stress Biol''. 2021 Oct 7; '''1''' (1):10
Hepatitis B virus persistent infection-related single nucleotide polymorphisms in HLA regions are associated with viral load in hepatoma families. Description: Hsieh, Ai-Ru, et al. Hepatitis B virus persistent infection-related single nucleotide polymorphisms in HLA regions are associated with viral load in hepatoma families. ''World J Gastroenterol''. 2021 Oct 7; '''27''' (37):6262-6276
rs41291957 controls miR-143 and miR-145 expression and impacts coronary artery disease risk. Description: Hall, Ignacio Fernando, et al. rs41291957 controls miR-143 and miR-145 expression and impacts coronary artery disease risk. ''EMBO Mol Med''. 2021 Oct 7; '''13''' (10):e14060
The genome of Shorea leprosula (Dipterocarpaceae) highlights the ecological relevance of drought in aseasonal tropical rainforests. Description: Ng, Kevin Kit Siong, et al. The genome of Shorea leprosula (Dipterocarpaceae) highlights the ecological relevance of drought in aseasonal tropical rainforests. ''Commun Biol''. 2021 Oct 7; '''4''' (1):1166
Population genomics provides insights into the population structure and temperature-driven adaptation of Collichthys lucidus. Description: Zhao, Linlin, et al. Population genomics provides insights into the population structure and temperature-driven adaptation of Collichthys lucidus. ''BMC Genomics''. 2021 Oct 8; '''22''' (1):729
Rare single nucleotide variants in COL5A1 promoter do not play a major role in keratoconus susceptibility associated with rs1536482. Description: Skorodumova, Liubov O, et al. Rare single nucleotide variants in COL5A1 promoter do not play a major role in keratoconus susceptibility associated with rs1536482. ''BMC Ophthalmol''. 2021 Oct 8; '''21''' (1):357
Influence of polygenic risk scores for schizophrenia and resilience on the cognition of individuals at-risk for psychosis. Description: He, Qin, et al. Influence of polygenic risk scores for schizophrenia and resilience on the cognition of individuals at-risk for psychosis. ''Transl Psychiatry''. 2021 Oct 9; '''11''' (1):518
Shortened leukocyte telomere length in young adults who use methamphetamine. Description: Lin, Yen-Feng, et al. Shortened leukocyte telomere length in young adults who use methamphetamine. ''Transl Psychiatry''. 2021 Oct 9; '''11''' (1):519
COVID-19: Impact on linguistic and genetic isolates of India. Description: Singh, Prajjval Pratap, et al. COVID-19: Impact on linguistic and genetic isolates of India. ''Genes Immun''. 2021 Oct 11;
Philippine Ayta possess the highest level of Denisovan ancestry in the world. Description: Larena, Maximilian, et al. Philippine Ayta possess the highest level of Denisovan ancestry in the world. ''Curr Biol''. 2021 Oct 11; '''31''' (19):4219-4230.e10
Relationships of Ischemic Stroke Occurrence and Outcome with Gene Variants Encoding Enzymes of Tryptophan Metabolism. Description: Boros, Fanni Annamaria, et al. Relationships of Ischemic Stroke Occurrence and Outcome with Gene Variants Encoding Enzymes of Tryptophan Metabolism. ''Biomedicines''. 2021 Oct 11; '''9''' (10):
Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals. Description: Koch, Elise, et al. Sex-specific effects of polygenic risk for schizophrenia on lifespan cognitive functioning in healthy individuals. ''Transl Psychiatry''. 2021 Oct 11; '''11''' (1):520
The genetic impact of an Ebola outbreak on a wild gorilla population. Description: Fontsere, Claudia, et al. The genetic impact of an Ebola outbreak on a wild gorilla population. ''BMC Genomics''. 2021 Oct 11; '''22''' (1):735
Truly privacy-preserving federated analytics for precision medicine with multiparty homomorphic encryption. Description: Froelicher, David, et al. Truly privacy-preserving federated analytics for precision medicine with multiparty homomorphic encryption. ''Nat Commun''. 2021 Oct 11; '''12''' (1):5910
Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer. Description: Ferreiro-Iglesias, Aida, et al. Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer. ''Nat Commun''. 2021 Oct 12; '''12''' (1):5945
The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas. Description: Garcia-Ortiz, Humberto, et al. The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas. ''Nat Commun''. 2021 Oct 12; '''12''' (1):5942
Thousands of Qatari genomes inform human migration history and improve imputation of Arab haplotypes. Description: Razali, Rozaimi Mohamad, et al. Thousands of Qatari genomes inform human migration history and improve imputation of Arab haplotypes. ''Nat Commun''. 2021 Oct 12; '''12''' (1):5929
TIGER: The gene expression regulatory variation landscape of human pancreatic islets. Description: Alonso, Lorena, et al. TIGER: The gene expression regulatory variation landscape of human pancreatic islets. ''Cell Rep''. 2021 Oct 12; '''37''' (2):109807
Utility of polygenic embryo screening for disease depends on the selection strategy. Description: Lencz, Todd, et al. Utility of polygenic embryo screening for disease depends on the selection strategy. ''Elife''. 2021 Oct 12; '''10''':
Accelerating the Development of Heat Tolerant Tomato Hybrids through a Multi-Traits Evaluation of Parental Lines Combining Phenotypic and Genotypic Analysis. Description: Olivieri, Fabrizio, et al. Accelerating the Development of Heat Tolerant Tomato Hybrids through a Multi-Traits Evaluation of Parental Lines Combining Phenotypic and Genotypic Analysis. ''Plants (Basel)''. 2021 Oct 13; '''10''' (10):
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients. Description: Barizzone, Nadia, et al. An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients. ''Genes (Basel)''. 2021 Oct 13; '''12''' (10):
Causal associations of intelligence with schizophrenia and bipolar disorder: A Mendelian randomization analysis. Description: Ohi, Kazutaka, et al. Causal associations of intelligence with schizophrenia and bipolar disorder: A Mendelian randomization analysis. ''Eur Psychiatry''. 2021 Oct 13; '''64''' (1):e61
Genetic propensity for obesity, socioeconomic position, and trajectories of body mass index in older adults. Description: Tommerup, Kristiane, et al. Genetic propensity for obesity, socioeconomic position, and trajectories of body mass index in older adults. ''Sci Rep''. 2021 Oct 13; '''11''' (1):20276
Genomic prediction for testes weight of the tiger pufferfish, Takifugu rubripes, using medium to low density SNPs. Description: Hosoya, Sho, et al. Genomic prediction for testes weight of the tiger pufferfish, Takifugu rubripes, using medium to low density SNPs. ''Sci Rep''. 2021 Oct 13; '''11''' (1):20372
Associations between SNPs in Intestinal Cholesterol Absorption and Endogenous Cholesterol Synthesis Genes with Cholesterol Metabolism. Description: Schroor, Maite M, et al. Associations between SNPs in Intestinal Cholesterol Absorption and Endogenous Cholesterol Synthesis Genes with Cholesterol Metabolism. ''Biomedicines''. 2021 Oct 14; '''9''' (10):
Genetic Analyses of Amphotericin B Susceptibility in Aspergillus fumigatus. Description: Fan, Yuying, et al. Genetic Analyses of Amphotericin B Susceptibility in Aspergillus fumigatus. ''J Fungi (Basel)''. 2021 Oct 14; '''7''' (10):
Genome-wide scans for signatures of selection in Mangalarga Marchador horses using high-throughput SNP genotyping. Description: Santos, Wellington B, et al. Genome-wide scans for signatures of selection in Mangalarga Marchador horses using high-throughput SNP genotyping. ''BMC Genomics''. 2021 Oct 14; '''22''' (1):737
Leptin Receptor (rs1137101) and Brain-Derived Neurotrophic Factor (rs925946) Gene Variants Are Associated with Obesity in the Early- but Not in the Late-Onset Population of Hungarian Psoriatic Patients. Description: Szentkereszty-Kovacs, Zita, et al. Leptin Receptor (rs1137101) and Brain-Derived Neurotrophic Factor (rs925946) Gene Variants Are Associated with Obesity in the Early- but Not in the Late-Onset Population of Hungarian Psoriatic Patients. ''Life (Basel)''. 2021 Oct 14; '''11''' (10):
More Than a Moggy; A Population Genetics Analysis of the United Kingdom's Non-Pedigree Cats. Description: Irving McGrath, Jennifer, et al. More Than a Moggy; A Population Genetics Analysis of the United Kingdom's Non-Pedigree Cats. ''Genes (Basel)''. 2021 Oct 14; '''12''' (10):
Association of COMT Polymorphisms with Multiple Physical Activity-Related Injuries among University Students in China. Description: Chen, Shangmin, et al. Association of COMT Polymorphisms with Multiple Physical Activity-Related Injuries among University Students in China. ''Int J Environ Res Public Health''. 2021 Oct 15; '''18''' (20):
Diabetic kidney disease: Are the reported associations with single-nucleotide polymorphisms disease-specific? Description: Saracyn, Marek, et al. Diabetic kidney disease: Are the reported associations with single-nucleotide polymorphisms disease-specific? ''World J Diabetes''. 2021 Oct 15; '''12''' (10):1765-1777
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Description: Georges, Adrien, et al. Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. ''Nat Commun''. 2021 Oct 15; '''12''' (1):6031
Genome-wide association study revealed novel candidate gene loci associated with soluble E-selectin levels in a Taiwanese population. Description: Teng, Ming-Sheng, et al. Genome-wide association study revealed novel candidate gene loci associated with soluble E-selectin levels in a Taiwanese population. ''Atherosclerosis''. 2021 Oct 15; '''337''': 18-26
Genome-wide selection signatures detection in Shanghai Holstein cattle population identified genes related to adaption, health and reproduction traits. Description: Liu, Dengying, et al. Genome-wide selection signatures detection in Shanghai Holstein cattle population identified genes related to adaption, health and reproduction traits. ''BMC Genomics''. 2021 Oct 15; '''22''' (1):747
ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score. Description: Oh, Jong Jin, et al. ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score. ''Cancers (Basel)''. 2021 Oct 17; '''13''' (20):
A genetic determinant of VEGF-A levels is associated with telomere attrition. Description: Gorenjak, Vesna, et al. A genetic determinant of VEGF-A levels is associated with telomere attrition. ''Aging (Albany NY)''. 2021 Oct 18; '''13''' (20):23517-23526
Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion. Description: Jensen, Matthew, et al. Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion. ''Genome Med''. 2021 Oct 18; '''13''' (1):163
Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets. Description: Marquez-Luna, Carla, et al. Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets. ''Nat Commun''. 2021 Oct 18; '''12''' (1):6052
Associations between Genetic Variants in the Vitamin D Metabolism Pathway and Severity of COVID-19 among UAE Residents. Description: Al-Anouti, Fatme, et al. Associations between Genetic Variants in the Vitamin D Metabolism Pathway and Severity of COVID-19 among UAE Residents. ''Nutrients''. 2021 Oct 20; '''13''' (11):
Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia. Description: Bartram, Thies, et al. Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia. ''J Clin Med''. 2021 Oct 20; '''10''' (21):
Impact of BMI and waist circumference on epigenome-wide DNA methylation and identification of epigenetic biomarkers in blood: an EWAS in multi-ethnic Asian individuals. Description: Chen, Yuqing, et al. Impact of BMI and waist circumference on epigenome-wide DNA methylation and identification of epigenetic biomarkers in blood: an EWAS in multi-ethnic Asian individuals. ''Clin Epigenetics''. 2021 Oct 20; '''13''' (1):195
MIR17HG genetic variations affect the susceptibility of IgA nephropathy in Chinese Han people. Description: Yang, Kai, et al. MIR17HG genetic variations affect the susceptibility of IgA nephropathy in Chinese Han people. ''Gene''. 2021 Oct 20; '''800''': 145838
Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients. Description: Heinrich, Maria, et al. Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients. ''BMC Med Genomics''. 2021 Oct 21; '''14''' (1):248
Genome-wide Association Study of Estradiol Levels and the Causal Effect of Estradiol on Bone Mineral Density. Description: Schmitz, Daniel, et al. Genome-wide Association Study of Estradiol Levels and the Causal Effect of Estradiol on Bone Mineral Density. ''J Clin Endocrinol Metab''. 2021 Oct 21; '''106''' (11):e4471-e4486
Multi-tissue transcriptome-wide association study identifies eight candidate genes and tissue-specific gene expression underlying endometrial cancer susceptibility. Description: Kho, Pik Fang, et al. Multi-tissue transcriptome-wide association study identifies eight candidate genes and tissue-specific gene expression underlying endometrial cancer susceptibility. ''Commun Biol''. 2021 Oct 21; '''4''' (1):1211
Genome wide association mapping for agronomic, fruit quality, and root architectural traits in tomato under organic farming conditions. Description: Tripodi, Pasquale, et al. Genome wide association mapping for agronomic, fruit quality, and root architectural traits in tomato under organic farming conditions. ''BMC Plant Biol''. 2021 Oct 22; '''21''' (1):481
African Gene Flow Reduces Beta-Ionone Anosmia/Hyposmia Prevalence in Admixed Malagasy Populations. Description: Razafindrazaka, Harilanto, et al. African Gene Flow Reduces Beta-Ionone Anosmia/Hyposmia Prevalence in Admixed Malagasy Populations. ''Brain Sci''. 2021 Oct 25; '''11''' (11):
Equine vitiligo-like depigmentation in grey horses is related to genes involved in immune response and tumor metastasis. Description: Druml, Thomas, et al. Equine vitiligo-like depigmentation in grey horses is related to genes involved in immune response and tumor metastasis. ''BMC Vet Res''. 2021 Oct 25; '''17''' (1):336
Impact of Genetic Polymorphisms on the Metabolic Pathway of Vitamin D and Survival in Non-Small Cell Lung Cancer. Description: Pineda Lancheros, Laura Elena, et al. Impact of Genetic Polymorphisms on the Metabolic Pathway of Vitamin D and Survival in Non-Small Cell Lung Cancer. ''Nutrients''. 2021 Oct 25; '''13''' (11):
Interactions between Polygenic Risk Scores, Dietary Pattern, and Menarche Age with the Obesity Risk in a Large Hospital-Based Cohort. Description: Park, Sunmin, et al. Interactions between Polygenic Risk Scores, Dietary Pattern, and Menarche Age with the Obesity Risk in a Large Hospital-Based Cohort. ''Nutrients''. 2021 Oct 25; '''13''' (11):
PDX1 and MC4R genetic polymorphisms are associated with type 2 diabetes mellitus risk in the Chinese Han population. Description: Wang, Ning, et al. PDX1 and MC4R genetic polymorphisms are associated with type 2 diabetes mellitus risk in the Chinese Han population. ''BMC Med Genomics''. 2021 Oct 25; '''14''' (1):249
Susceptibility of Field-Collected Nyssorhynchus darlingi to Plasmodium spp. in Western Amazonian Brazil. Description: Alonso, Diego Peres, et al. Susceptibility of Field-Collected Nyssorhynchus darlingi to Plasmodium spp. in Western Amazonian Brazil. ''Genes (Basel)''. 2021 Oct 25; '''12''' (11):
Whole-exome analysis in Tunisian Imazighen and Arabs shows the impact of demography in functional variation. Description: Lucas-Sanchez, Marcel, et al. Whole-exome analysis in Tunisian Imazighen and Arabs shows the impact of demography in functional variation. ''Sci Rep''. 2021 Oct 26; '''11''' (1):21125
A genome variation map provides insights into the genetics of walnut adaptation and agronomic traits. Description: Ji, Feiyang, et al. A genome variation map provides insights into the genetics of walnut adaptation and agronomic traits. ''Genome Biol''. 2021 Oct 27; '''22''' (1):300
Genetic Continuity of Bronze Age Ancestry with Increased Steppe-Related Ancestry in Late Iron Age Uzbekistan. Description: Kumar, Vikas, et al. Genetic Continuity of Bronze Age Ancestry with Increased Steppe-Related Ancestry in Late Iron Age Uzbekistan. ''Mol Biol Evol''. 2021 Oct 27; '''38''' (11):4908-4917
Genome Analysis Traces Regional Dispersal of Rice in Taiwan and Southeast Asia. Description: Alam, Ornob, et al. Genome Analysis Traces Regional Dispersal of Rice in Taiwan and Southeast Asia. ''Mol Biol Evol''. 2021 Oct 27; '''38''' (11):4832-4846
Genomewide association study and genomic prediction for growth traits in yellow-plumage chicken using genotyping-by-sequencing. Description: Yang, Ruifei, et al. Genomewide association study and genomic prediction for growth traits in yellow-plumage chicken using genotyping-by-sequencing. ''Genet Sel Evol''. 2021 Oct 27; '''53''' (1):82
Genome-Wide SNPs Clarify a Complex Radiation and Support Recognition of an Additional Cat Species. Description: Trindade, Fernanda J, et al. Genome-Wide SNPs Clarify a Complex Radiation and Support Recognition of an Additional Cat Species. ''Mol Biol Evol''. 2021 Oct 27; '''38''' (11):4987-4991
Genomic Evidence for Speciation with Gene Flow in Broadcast Spawning Marine Invertebrates. Description: Hirase, Shotaro, et al. Genomic Evidence for Speciation with Gene Flow in Broadcast Spawning Marine Invertebrates. ''Mol Biol Evol''. 2021 Oct 27; '''38''' (11):4683-4699
Highly Replicated Evolution of Parapatric Ecotypes. Description: James, Maddie E, et al. Highly Replicated Evolution of Parapatric Ecotypes. ''Mol Biol Evol''. 2021 Oct 27; '''38''' (11):4805-4821
Human-Mediated Admixture and Selection Shape the Diversity on the Modern Swine (Sus scrofa) Y Chromosomes. Description: Ai, Huashui, et al. Human-Mediated Admixture and Selection Shape the Diversity on the Modern Swine (Sus scrofa) Y Chromosomes. ''Mol Biol Evol''. 2021 Oct 27; '''38''' (11):5051-5065
Investigating the Role of Leukocyte Telomere Length in Treatment-Resistant Depression and in Response to Electroconvulsive Therapy. Description: Pisanu, Claudia, et al. Investigating the Role of Leukocyte Telomere Length in Treatment-Resistant Depression and in Response to Electroconvulsive Therapy. ''J Pers Med''. 2021 Oct 27; '''11''' (11):
Papua New Guinean Genomes Reveal the Complex Settlement of North Sahul. Description: Brucato, Nicolas, et al. Papua New Guinean Genomes Reveal the Complex Settlement of North Sahul. ''Mol Biol Evol''. 2021 Oct 27; '''38''' (11):5107-5121
Genome-Wide Landscape of North-Eastern European Populations: A View from Lithuania. Description: Urnikyte, Alina, et al. Genome-Wide Landscape of North-Eastern European Populations: A View from Lithuania. ''Genes (Basel)''. 2021 Oct 28; '''12''' (11):
Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Description: Pott, Janne, et al. Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. ''Metabolites''. 2021 Oct 28; '''11''' (11):
Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Description: Lin, Wei-Yu, et al. Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. ''Nat Commun''. 2021 Oct 29; '''12''' (1):6233
Genomic Signatures of Domestication Selection in the Australasian Snapper (Chrysophrys auratus). Description: Baesjou, Jean-Paul, et al. Genomic Signatures of Domestication Selection in the Australasian Snapper (Chrysophrys auratus). ''Genes (Basel)''. 2021 Oct 29; '''12''' (11):
Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Description: Vysotskiy, Mikhail, et al. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. ''Genome Med''. 2021 Oct 29; '''13''' (1):172
Discovery of new genetic loci for male sexual orientation in Han population. Description: Hu, Shao-Hua, et al. Discovery of new genetic loci for male sexual orientation in Han population. ''Cell Discov''. 2021 Oct 31; '''7''' (1):103
A chickpea genetic variation map based on the sequencing of 3,366 genomes. Description: Varshney, Rajeev K, et al. A chickpea genetic variation map based on the sequencing of 3,366 genomes. ''Nature''. 2021 Nov; '''599''' (7886):622-627
A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle. Description: Jacinto, Joana G P, et al. A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle. ''Mol Genet Genomics''. 2021 Nov; '''296''' (6):1313-1322
A knockout mutation associated with juvenile paroxysmal dyskinesia in Markiesje dogs indicates SOD1 pleiotropy. Description: Mandigers, P J J, et al. A knockout mutation associated with juvenile paroxysmal dyskinesia in Markiesje dogs indicates SOD1 pleiotropy. ''Hum Genet''. 2021 Nov; '''140''' (11):1547-1552
A missense variant in IFT122 associated with a canine model of retinitis pigmentosa. Description: Kaukonen, Maria, et al. A missense variant in IFT122 associated with a canine model of retinitis pigmentosa. ''Hum Genet''. 2021 Nov; '''140''' (11):1569-1579
Analysis of PTRHD1 common and rare variants in European patients with Parkinson's disease. Description: Sosero, Yuri L, et al. Analysis of PTRHD1 common and rare variants in European patients with Parkinson's disease. ''Neurobiol Aging''. 2021 Nov; '''107''': 178-180
An assessment of the effect of the genotype on postoperative venous thromboembolism risk in 140,831 surgical patients. Description: A Christensen, Mathias, et al. An assessment of the effect of the genotype on postoperative venous thromboembolism risk in 140,831 surgical patients. ''Ann Med Surg (Lond)''. 2021 Nov; '''71''': 102938
Anti-Microbial Antibody Response is Associated With Future Onset of Crohn's Disease Independent of Biomarkers of Altered Gut Barrier Function, Subclinical Inflammation, and Genetic Risk. Description: Lee, Sun-Ho, et al. Anti-Microbial Antibody Response is Associated With Future Onset of Crohn's Disease Independent of Biomarkers of Altered Gut Barrier Function, Subclinical Inflammation, and Genetic Risk. ''Gastroenterology''. 2021 Nov; '''161''' (5):1540-1551
Assessing the levels of intraspecific admixture and interspecific hybridization in Iberian wild goats (Capra pyrenaica). Description: Cardoso, Taina Figueiredo, et al. Assessing the levels of intraspecific admixture and interspecific hybridization in Iberian wild goats (Capra pyrenaica). ''Evol Appl''. 2021 Nov; '''14''' (11):2618-2634
Association between HLA alleles and Epstein-Barr virus Zta-IgA serological status in healthy males from southern China. Description: Yuan, Lei-Lei, et al. Association between HLA alleles and Epstein-Barr virus Zta-IgA serological status in healthy males from southern China. ''J Gene Med''. 2021 Nov; '''23''' (11):e3375
Associations between the CADM2 gene, substance use, risky sexual behavior, and self-control: A phenome-wide association study. Description: Arends, Rachel M, et al. Associations between the CADM2 gene, substance use, risky sexual behavior, and self-control: A phenome-wide association study. ''Addict Biol''. 2021 Nov; '''26''' (6):e13015
Assortative mating and within-spouse pair comparisons. Description: Howe, Laurence J, et al. Assortative mating and within-spouse pair comparisons. ''PLoS Genet''. 2021 Nov; '''17''' (11):e1009883
Causal Associations Between Blood Lipids and COVID-19 Risk: A Two-Sample Mendelian Randomization Study. Description: Zhang, Kun, et al. Causal Associations Between Blood Lipids and COVID-19 Risk: A Two-Sample Mendelian Randomization Study. ''Arterioscler Thromb Vasc Biol''. 2021 Nov; '''41''' (11):2802-2810
Childhood adversity correlates with stable changes in DNA methylation trajectories in children and converges with epigenetic signatures of prenatal stress. Description: Martins, Jade, et al. Childhood adversity correlates with stable changes in DNA methylation trajectories in children and converges with epigenetic signatures of prenatal stress. ''Neurobiol Stress''. 2021 Nov; '''15''': 100336
Comparative genomics suggests local adaptations in the invasive small hive beetle. Description: Liu, Yuanzhen, et al. Comparative genomics suggests local adaptations in the invasive small hive beetle. ''Ecol Evol''. 2021 Nov; '''11''' (22):15780-15791
Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas. Description: Ongaro, Linda, et al. Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas. ''Hum Mol Genet''. 2021 Nov 1; '''30''' (22):2123-2134
Contributions of PTSD polygenic risk and environmental stress to suicidality in preadolescents. Description: Daskalakis, Nikolaos P, et al. Contributions of PTSD polygenic risk and environmental stress to suicidality in preadolescents. ''Neurobiol Stress''. 2021 Nov; '''15''': 100411
ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers. Description: Gelfman, Sahar, et al. ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers. ''Invest Ophthalmol Vis Sci''. 2021 Nov 1; '''62''' (14):3
Examining the bidirectional association between emotion recognition and social autistic traits using observational and genetic analyses. Description: Reed, Zoe E, et al. Examining the bidirectional association between emotion recognition and social autistic traits using observational and genetic analyses. ''J Child Psychol Psychiatry''. 2021 Nov; '''62''' (11):1330-1338
Fine mapping of the major histocompatibility complex (MHC) in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) suggests involvement of both HLA class I and class II loci. Description: Hajdarevic, Riad, et al. Fine mapping of the major histocompatibility complex (MHC) in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) suggests involvement of both HLA class I and class II loci. ''Brain Behav Immun''. 2021 Nov; '''98''': 101-109
Genome-wide association findings from the brains for dementia research cohort. Description: Young, Joshua, et al. Genome-wide association findings from the brains for dementia research cohort. ''Neurobiol Aging''. 2021 Nov; '''107''': 159-167
Genome-wide Association Study Identifies 2 New Loci Associated With Anti-NMDAR Encephalitis. Description: Tietz, Anja K, et al. Genome-wide Association Study Identifies 2 New Loci Associated With Anti-NMDAR Encephalitis. ''Neurol Neuroimmunol Neuroinflamm''. 2021 Nov; '''8''' (6):
Genome-wide DNA arrays profiling unravels the genetic structure of Iranian sheep and pattern of admixture with worldwide coarse-wool sheep breeds. Description: Moosanezhad Khabisi, Mozhdeh, et al. Genome-wide DNA arrays profiling unravels the genetic structure of Iranian sheep and pattern of admixture with worldwide coarse-wool sheep breeds. ''Genomics''. 2021 Nov; '''113''' (6):3501-3511
Genome-Wide Linkage and Association Study of Childhood Gender Nonconformity in Males. Description: Sanders, Alan R, et al. Genome-Wide Linkage and Association Study of Childhood Gender Nonconformity in Males. ''Arch Sex Behav''. 2021 Nov; '''50''' (8):3377-3383
Genome-wide SNP identification in Fraxinus linking genetic characteristics to tolerance of Agrilus planipennis. Description: Hale, Cecelia E, et al. Genome-wide SNP identification in Fraxinus linking genetic characteristics to tolerance of Agrilus planipennis. ''Ecol Evol''. 2021 Nov; '''11''' (21):14775-14788
Gut microbiota is associated with bone mineral density : an observational and genome-wide environmental interaction analysis in the UK Biobank cohort. Description: Cheng, Bolun, et al. Gut microbiota is associated with bone mineral density : an observational and genome-wide environmental interaction analysis in the UK Biobank cohort. ''Bone Joint Res''. 2021 Nov; '''10''' (11):734-741
Identifying a novel biological mechanism for alcohol addiction associated with circRNA networks acting as potential miRNA sponges. Description: Vornholt, Eric, et al. Identifying a novel biological mechanism for alcohol addiction associated with circRNA networks acting as potential miRNA sponges. ''Addict Biol''. 2021 Nov; '''26''' (6):e13071
Identifying Genomic Regions Targeted During Eggplant Domestication Using Transcriptome Data. Description: Page, Anna M L, et al. Identifying Genomic Regions Targeted During Eggplant Domestication Using Transcriptome Data. ''J Hered''. 2021 Nov 1; '''112''' (6):519-525
In-frame deletion in canine PITRM1 is associated with a severe early-onset epilepsy, mitochondrial dysfunction and neurodegeneration. Description: Hytonen, Marjo K, et al. In-frame deletion in canine PITRM1 is associated with a severe early-onset epilepsy, mitochondrial dysfunction and neurodegeneration. ''Hum Genet''. 2021 Nov; '''140''' (11):1593-1609
Integrative analysis of genomic and epigenomic data reveal underlying superenhancer-mediated microRNA regulatory network for human bone mineral density. Description: Bai, Wei-Yang, et al. Integrative analysis of genomic and epigenomic data reveal underlying superenhancer-mediated microRNA regulatory network for human bone mineral density. ''Hum Mol Genet''. 2021 Nov 1; '''30''' (22):2177-2189
Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases. Description: Ritchie, Scott C, et al. Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases. ''Nat Metab''. 2021 Nov; '''3''' (11):1476-1483
Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection. Description: Heilbronner, Urs, et al. Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection. ''BJPsych Open''. 2021 Nov; '''7''' (6):e188
Intronic variant in POU1F1 associated with canine pituitary dwarfism. Description: Kyostila, Kaisa, et al. Intronic variant in POU1F1 associated with canine pituitary dwarfism. ''Hum Genet''. 2021 Nov; '''140''' (11):1553-1562
Investigation of gene-environment interactions in relation to tic severity. Description: Abdulkadir, Mohamed, et al. Investigation of gene-environment interactions in relation to tic severity. ''J Neural Transm (Vienna)''. 2021 Nov; '''128''' (11):1757-1765
Local adaptations of Mediterranean sheep and goats through an integrative approach. Description: Serranito, Bruno, et al. Local adaptations of Mediterranean sheep and goats through an integrative approach. ''Sci Rep''. 2021 Nov 1; '''11''' (1):21363
Maternal and child genetic liability for smoking and caffeine consumption and child mental health: an intergenerational genetic risk score analysis in the ALSPAC cohort. Description: Schellhas, Laura, et al. Maternal and child genetic liability for smoking and caffeine consumption and child mental health: an intergenerational genetic risk score analysis in the ALSPAC cohort. ''Addiction''. 2021 Nov; '''116''' (11):3153-3166
Mendelian randomisation highlights hypothyroidism as a causal determinant of idiopathic pulmonary fibrosis. Description: Zhang, Yanan, et al. Mendelian randomisation highlights hypothyroidism as a causal determinant of idiopathic pulmonary fibrosis. ''EBioMedicine''. 2021 Nov; '''73''': 103669
Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations. Description: Emde, Anne-Katrin, et al. Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations. ''BMC Genomics''. 2021 Nov 1; '''22''' (1):666
Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss. Description: Hytonen, Marjo K, et al. Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss. ''Hum Genet''. 2021 Nov; '''140''' (11):1611-1618
Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation. Description: Shelton, G Diane, et al. Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation. ''Neuromuscul Disord''. 2021 Nov; '''31''' (11):1169-1178
Pharmacogenetic Predictors of Cannabidiol Response and Tolerability in Treatment-Resistant Epilepsy. Description: Davis, Brittney H, et al. Pharmacogenetic Predictors of Cannabidiol Response and Tolerability in Treatment-Resistant Epilepsy. ''Clin Pharmacol Ther''. 2021 Nov; '''110''' (5):1368-1380
Pharmacogenomic polygenic risk score for clopidogrel responsiveness among Caribbean Hispanics: A candidate gene approach. Description: Duconge, Jorge, et al. Pharmacogenomic polygenic risk score for clopidogrel responsiveness among Caribbean Hispanics: A candidate gene approach. ''Clin Transl Sci''. 2021 Nov; '''14''' (6):2254-2266
Prediction of heterosis in the recent rapeseed (Brassica napus) polyploid by pairing parental nucleotide sequences. Description: Wang, Qian, et al. Prediction of heterosis in the recent rapeseed (Brassica napus) polyploid by pairing parental nucleotide sequences. ''PLoS Genet''. 2021 Nov; '''17''' (11):e1009879
Prefrontal cortex VAMP1 gene network moderates the effect of the early environment on cognitive flexibility in children. Description: Dalmaz, Carla, et al. Prefrontal cortex VAMP1 gene network moderates the effect of the early environment on cognitive flexibility in children. ''Neurobiol Learn Mem''. 2021 Nov; '''185''': 107509
Searching for improvements in predicting human eye colour from DNA. Description: Kukla-Bartoszek, Magdalena, et al. Searching for improvements in predicting human eye colour from DNA. ''Int J Legal Med''. 2021 Nov; '''135''' (6):2175-2187
Targeted re-sequencing and genome-wide association analysis for wood property traits in breeding population of Eucalyptus tereticornis x E. grandis. Description: Ghosh Dasgupta, Modhumita, et al. Targeted re-sequencing and genome-wide association analysis for wood property traits in breeding population of Eucalyptus tereticornis x E. grandis. ''Genomics''. 2021 Nov; '''113''' (6):4276-4292
T cell composition and polygenic multiple sclerosis risk: A population-based study in children. Description: de Mol, Casper L, et al. T cell composition and polygenic multiple sclerosis risk: A population-based study in children. ''Eur J Neurol''. 2021 Nov; '''28''' (11):3731-3741
The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark. Description: Leinoe, Eva, et al. The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark. ''J Thromb Haemost''. 2021 Nov; '''19''' (11):2884-2892
The genetic structure of Norway. Description: Mattingsdal, Morten, et al. The genetic structure of Norway. ''Eur J Hum Genet''. 2021 Nov; '''29''' (11):1710-1718
The genomic origins of the Bronze Age Tarim Basin mummies. Description: Zhang, Fan, et al. The genomic origins of the Bronze Age Tarim Basin mummies. ''Nature''. 2021 Nov; '''599''' (7884):256-261
The impact of common genetic variants in cognitive decline in the first seven years of Parkinson's disease: A longitudinal observational study. Description: Chung, Janete, et al. The impact of common genetic variants in cognitive decline in the first seven years of Parkinson's disease: A longitudinal observational study. ''Neurosci Lett''. 2021 Nov 1; '''764''': 136243
The role of frontotemporal dementia associated genes in patients with Alzheimer's disease. Description: Xiao, Xuewen, et al. The role of frontotemporal dementia associated genes in patients with Alzheimer's disease. ''Neurobiol Aging''. 2021 Nov; '''107''': 153-158
An integrative analysis of genomic and exposomic data for complex traits and phenotypic prediction. Description: Zhou, Xuan, et al. An integrative analysis of genomic and exposomic data for complex traits and phenotypic prediction. ''Sci Rep''. 2021 Nov 2; '''11''' (1):21495
Genetic variations for the eggshell crystal structure revealed by genome-wide association study in chickens. Description: Li, Quanlin, et al. Genetic variations for the eggshell crystal structure revealed by genome-wide association study in chickens. ''BMC Genomics''. 2021 Nov 2; '''22''' (1):786
Insight into the Candidate Genes and Enriched Pathways Associated with Height, Length, Length to Height Ratio and Body-Weight of Korean Indigenous Breed, Jindo Dog Using Gene Set Enrichment-Based GWAS Analysis. Description: Sheet, Sunirmal, et al. Insight into the Candidate Genes and Enriched Pathways Associated with Height, Length, Length to Height Ratio and Body-Weight of Korean Indigenous Breed, Jindo Dog Using Gene Set Enrichment-Based GWAS Analysis. ''Animals (Basel)''. 2021 Nov 2; '''11''' (11):
Machine learning-enabled phenotyping for GWAS and TWAS of WUE traits in 869 field-grown sorghum accessions. Description: Ferguson, John N, et al. Machine learning-enabled phenotyping for GWAS and TWAS of WUE traits in 869 field-grown sorghum accessions. ''Plant Physiol''. 2021 Nov 3; '''187''' (3):1481-1500
Role of Sex on the Genetic Susceptibility to Childhood Asthma in Latinos and African Americans. Description: Espuela-Ortiz, Antonio, et al. Role of Sex on the Genetic Susceptibility to Childhood Asthma in Latinos and African Americans. ''J Pers Med''. 2021 Nov 3; '''11''' (11):
A large Canadian cohort provides insights into the genetic architecture of human hair colour. Description: Lona-Durazo, Frida, et al. A large Canadian cohort provides insights into the genetic architecture of human hair colour. ''Commun Biol''. 2021 Nov 4; '''4''' (1):1253
Genetic overlap and causality between blood metabolites and migraine. Description: Tanha, Hamzeh M, et al. Genetic overlap and causality between blood metabolites and migraine. ''Am J Hum Genet''. 2021 Nov 4; '''108''' (11):2086-2098
High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height. Description: Wang, Shouchuang, et al. High-quality reference genome sequences of two coconut cultivars provide insights into evolution of monocot chromosomes and differentiation of fiber content and plant height. ''Genome Biol''. 2021 Nov 4; '''22''' (1):304
Deep learning model reveals potential risk genes for ADHD, especially Ephrin receptor gene EPHA5. Description: Liu, Lu, et al. Deep learning model reveals potential risk genes for ADHD, especially Ephrin receptor gene EPHA5. ''Brief Bioinform''. 2021 Nov 5; '''22''' (6):
Frequency of allele variations in the CFTR gene in a Mexican population. Description: Cantu-Reyna, Consuelo, et al. Frequency of allele variations in the CFTR gene in a Mexican population. ''BMC Med Genomics''. 2021 Nov 5; '''14''' (1):262
Genetic Diversity in Chimpanzee Transcriptomics Does Not Represent Wild Populations. Description: Shukla, Navya, et al. Genetic Diversity in Chimpanzee Transcriptomics Does Not Represent Wild Populations. ''Genome Biol Evol''. 2021 Nov 5; '''13''' (11):
Exploring the size of reference population for expected accuracy of genomic prediction using simulated and real data in Japanese Black cattle. Description: Takeda, Masayuki, et al. Exploring the size of reference population for expected accuracy of genomic prediction using simulated and real data in Japanese Black cattle. ''BMC Genomics''. 2021 Nov 6; '''22''' (1):799
Interaction of Alcohol Consumption and ABCG2 rs2231142 Variant Contributes to Hyperuricemia in a Taiwanese Population. Description: Chen, I-Chieh, et al. Interaction of Alcohol Consumption and ABCG2 rs2231142 Variant Contributes to Hyperuricemia in a Taiwanese Population. ''J Pers Med''. 2021 Nov 7; '''11''' (11):
Calling large indels in 1047 Arabidopsis with IndelEnsembler. Description: Liu, Dong-Xu, et al. Calling large indels in 1047 Arabidopsis with IndelEnsembler. ''Nucleic Acids Res''. 2021 Nov 8; '''49''' (19):10879-10894
Characterisation of insomnia as an environmental risk factor for asthma via Mendelian randomization and gene environment interaction. Description: Kim, Dong Jun, et al. Characterisation of insomnia as an environmental risk factor for asthma via Mendelian randomization and gene environment interaction. ''Sci Rep''. 2021 Nov 8; '''11''' (1):21813
Confirming the TMEM232 gene associated with atopic dermatitis through targeted capture sequencing. Description: Zheng, Jie, et al. Confirming the TMEM232 gene associated with atopic dermatitis through targeted capture sequencing. ''Sci Rep''. 2021 Nov 8; '''11''' (1):21830
Polygenic risk score across distinct colorectal cancer screening outcomes: from premalignant polyps to colorectal cancer. Description: Obon-Santacana, Mireia, et al. Polygenic risk score across distinct colorectal cancer screening outcomes: from premalignant polyps to colorectal cancer. ''BMC Med''. 2021 Nov 8; '''19''' (1):261
CD46 Genetic Variability and HIV-1 Infection Susceptibility. Description: Serrano-Risquez, Carmen, et al. CD46 Genetic Variability and HIV-1 Infection Susceptibility. ''Cells''. 2021 Nov 9; '''10''' (11):
Evolutionary history and pan-genome dynamics of strawberry (Fragaria spp.). Description: Qiao, Qin, et al. Evolutionary history and pan-genome dynamics of strawberry (Fragaria spp.). ''Proc Natl Acad Sci U S A''. 2021 Nov 9; '''118''' (45):
Genome analyses revealed genetic admixture and selection signatures in Bos indicus. Description: Dixit, S P, et al. Genome analyses revealed genetic admixture and selection signatures in Bos indicus. ''Sci Rep''. 2021 Nov 9; '''11''' (1):21924
Genome-Wide Polygenic Risk Score for Predicting High Risk Glaucoma Individuals of Han Chinese Ancestry. Description: Hsiao, Yu-Jer, et al. Genome-Wide Polygenic Risk Score for Predicting High Risk Glaucoma Individuals of Han Chinese Ancestry. ''J Pers Med''. 2021 Nov 9; '''11''' (11):
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity. Description: Cappadona, Claudio, et al. MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity. ''J Pers Med''. 2021 Nov 9; '''11''' (11):
The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Description: Hanscombe, Ken B, et al. The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. ''Genome Med''. 2021 Nov 9; '''13''' (1):180
Elevated circulating follistatin associates with an increased risk of type 2 diabetes. Description: Wu, Chuanyan, et al. Elevated circulating follistatin associates with an increased risk of type 2 diabetes. ''Nat Commun''. 2021 Nov 10; '''12''' (1):6486
Individual variations in 'brain age' relate to early-life factors more than to longitudinal brain change. Description: Vidal-Pineiro, Didac, et al. Individual variations in 'brain age' relate to early-life factors more than to longitudinal brain change. ''Elife''. 2021 Nov 10; '''10''':
Interaction of Polygenetic Variants for Gestational Diabetes Mellitus Risk with Breastfeeding and Korean Balanced Diet to Influence Type 2 Diabetes Risk in Later Life in a Large Hospital-Based Cohort. Description: Park, Sunmin. Interaction of Polygenetic Variants for Gestational Diabetes Mellitus Risk with Breastfeeding and Korean Balanced Diet to Influence Type 2 Diabetes Risk in Later Life in a Large Hospital-Based Cohort. ''J Pers Med''. 2021 Nov 10; '''11''' (11):
The Influence of FUT2 and FUT3 Polymorphisms and Nasopharyngeal Microbiome on Respiratory Infections in Breastfed Bangladeshi Infants from the Microbiota and Health Study. Description: Binia, Aristea, et al. The Influence of FUT2 and FUT3 Polymorphisms and Nasopharyngeal Microbiome on Respiratory Infections in Breastfed Bangladeshi Infants from the Microbiota and Health Study. ''mSphere''. 2021 Nov 10; e0068621
Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder. Description: Mattioli, Francesca, et al. Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder. ''NPJ Genom Med''. 2021 Nov 11; '''6''' (1):94
Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy. Description: Verhoef, Ellen, et al. Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy. ''Nat Commun''. 2021 Nov 11; '''12''' (1):6534
Genome-wide association study of hospitalized COVID-19 patients in the United Arab Emirates. Description: Mousa, Mira, et al. Genome-wide association study of hospitalized COVID-19 patients in the United Arab Emirates. ''EBioMedicine''. 2021 Nov 11; '''74''': 103695
Natural hybridization among three Rhododendron species (Ericaceae) revealed by morphological and genomic evidence. Description: Zheng, Wei, et al. Natural hybridization among three Rhododendron species (Ericaceae) revealed by morphological and genomic evidence. ''BMC Plant Biol''. 2021 Nov 11; '''21''' (1):529
Archaeogenetic analysis of Neolithic sheep from Anatolia suggests a complex demographic history since domestication. Description: Yurtman, Erinc, et al. Archaeogenetic analysis of Neolithic sheep from Anatolia suggests a complex demographic history since domestication. ''Commun Biol''. 2021 Nov 12; '''4''' (1):1279
Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity. Description: Li, Ao, et al. Genome of the estuarine oyster provides insights into climate impact and adaptive plasticity. ''Commun Biol''. 2021 Nov 12; '''4''' (1):1287
Identification of yield-related genes through genome-wide association: case study of weeping forsythia, an emerging medicinal crop. Description: Li, Yong, et al. Identification of yield-related genes through genome-wide association: case study of weeping forsythia, an emerging medicinal crop. ''Genes Genomics''. 2021 Nov 12;
Self-reported sleep relates to microstructural hippocampal decline in ss-amyloid positive Adults beyond genetic risk. Description: Grydeland, Hakon, et al. Self-reported sleep relates to microstructural hippocampal decline in ss-amyloid positive Adults beyond genetic risk. ''Sleep''. 2021 Nov 12; '''44''' (11):
Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants. Description: Nudel, Ron, et al. Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants. ''J Neurodev Disord''. 2021 Nov 13; '''13''' (1):54
Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator. Description: Yamada, Mitsuhiro, et al. Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator. ''Commun Biol''. 2021 Nov 15; '''4''' (1):1288
Multiple stages of evolutionary change in anthrax toxin receptor expression in humans. Description: Choate, Lauren A, et al. Multiple stages of evolutionary change in anthrax toxin receptor expression in humans. ''Nat Commun''. 2021 Nov 15; '''12''' (1):6590
A Genome-Wide Association Study of a Korean Population Identifies Genetic Susceptibility to Hypertension Based on Sex-Specific Differences. Description: Cho, Seong-Beom, et al. A Genome-Wide Association Study of a Korean Population Identifies Genetic Susceptibility to Hypertension Based on Sex-Specific Differences. ''Genes (Basel)''. 2021 Nov 16; '''12''' (11):
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages. Description: Park, Jun Young, et al. A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages. ''Transl Psychiatry''. 2021 Nov 16; '''11''' (1):590
Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart Failure. Description: Paranjpe, Ishan, et al. Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart Failure. ''J Am Heart Assoc''. 2021 Nov 16; '''10''' (22):e021916
IRF7 and RNH1 are modifying factors of HIV-1 reservoirs: a genome-wide association analysis. Description: Zhang, Zhenhua, et al. IRF7 and RNH1 are modifying factors of HIV-1 reservoirs: a genome-wide association analysis. ''BMC Med''. 2021 Nov 16; '''19''' (1):282
Linked supergenes underlie split sex ratio and social organization in an ant. Description: Lagunas-Robles, German, et al. Linked supergenes underlie split sex ratio and social organization in an ant. ''Proc Natl Acad Sci U S A''. 2021 Nov 16; '''118''' (46):
NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population. Description: Zhang, Peng, et al. NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population. ''Cell Rep''. 2021 Nov 16; '''37''' (7):110017
The genetic susceptibility profile of type 2 diabetes and reflection of its possible role related to reproductive dysfunctions in the southern Indian population of Hyderabad. Description: Irgam, Kumuda, et al. The genetic susceptibility profile of type 2 diabetes and reflection of its possible role related to reproductive dysfunctions in the southern Indian population of Hyderabad. ''BMC Med Genomics''. 2021 Nov 16; '''14''' (1):272
Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood. Description: Elam, Kit K, et al. Age varying polygenic effects on alcohol use in African Americans and European Americans from adolescence to adulthood. ''Sci Rep''. 2021 Nov 17; '''11''' (1):22425
Association of a Total Cholesterol Polygenic Score with Cholesterol Levels and Pathological Biomarkers across the Alzheimer's Disease Spectrum. Description: Nilsson, Nathalie I V, et al. Association of a Total Cholesterol Polygenic Score with Cholesterol Levels and Pathological Biomarkers across the Alzheimer's Disease Spectrum. ''Genes (Basel)''. 2021 Nov 17; '''12''' (11):
Honey bee genetics shape the strain-level structure of gut microbiota in social transmission. Description: Wu, Jiaqiang, et al. Honey bee genetics shape the strain-level structure of gut microbiota in social transmission. ''Microbiome''. 2021 Nov 17; '''9''' (1):225
CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle. Description: Hafliger, Irene M, et al. CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle. ''Int J Mol Sci''. 2021 Nov 18; '''22''' (22):
Genome-wide association study (GWAS) of leaf wax components of apple. Description: Cao, Fuguo, et al. Genome-wide association study (GWAS) of leaf wax components of apple. ''Stress Biol''. 2021 Nov 18; '''1''' (1):13
Genome-wide scan for selective footprints and genes related to cold tolerance in Chantecler chickens. Description: Xu, Nai-Yi, et al. Genome-wide scan for selective footprints and genes related to cold tolerance in Chantecler chickens. ''Zool Res''. 2021 Nov 18; '''42''' (6):710-720
Idefix: identifying accidental sample mix-ups in biobanks using polygenic scores. Description: Warmerdam, Robert, et al. Idefix: identifying accidental sample mix-ups in biobanks using polygenic scores. ''Bioinformatics''. 2021 Nov 18;
Polygenic Risk Scores for Prediction of Gastric Cancer Based on Bioinformatics Screening and Validation of Functional lncRNA SNPs. Description: Duan, Fujiao, et al. Polygenic Risk Scores for Prediction of Gastric Cancer Based on Bioinformatics Screening and Validation of Functional lncRNA SNPs. ''Clin Transl Gastroenterol''. 2021 Nov 18; '''12''' (11):e00430
Whole-genome sequence analysis unveils different origins of European and Asiatic mouflon and domestication-related genes in sheep. Description: Chen, Ze-Hui, et al. Whole-genome sequence analysis unveils different origins of European and Asiatic mouflon and domestication-related genes in sheep. ''Commun Biol''. 2021 Nov 18; '''4''' (1):1307
Ancient genome analyses shed light on kinship organization and mating practice of Late Neolithic society in China. Description: Ning, Chao, et al. Ancient genome analyses shed light on kinship organization and mating practice of Late Neolithic society in China. ''iScience''. 2021 Nov 19; '''24''' (11):103352
A Polygenic Risk Score Predicts Incident Prostate Cancer Risk in Older Men but Does Not Select for Clinically Significant Disease. Description: Bakshi, Andrew, et al. A Polygenic Risk Score Predicts Incident Prostate Cancer Risk in Older Men but Does Not Select for Clinically Significant Disease. ''Cancers (Basel)''. 2021 Nov 19; '''13''' (22):
Epstein-Barr virus nuclear antigen 2 extensively rewires the human chromatin landscape at autoimmune risk loci. Description: Hong, Ted, et al. Epstein-Barr virus nuclear antigen 2 extensively rewires the human chromatin landscape at autoimmune risk loci. ''Genome Res''. 2021 Nov 19;
Genomewide Association Analyses of Lactation Persistency and Milk Production Traits in Holstein Cattle Based on Imputed Whole-Genome Sequence Data. Description: Pedrosa, Victor B, et al. Genomewide Association Analyses of Lactation Persistency and Milk Production Traits in Holstein Cattle Based on Imputed Whole-Genome Sequence Data. ''Genes (Basel)''. 2021 Nov 19; '''12''' (11):
Genomic transformation and social organization during the Copper Age-Bronze Age transition in southern Iberia. Description: Villalba-Mouco, Vanessa, et al. Genomic transformation and social organization during the Copper Age-Bronze Age transition in southern Iberia. ''Sci Adv''. 2021 Nov 19; '''7''' (47):eabi7038
Pervasive hybridization with local wild relatives in Western European grapevine varieties. Description: Freitas, Sara, et al. Pervasive hybridization with local wild relatives in Western European grapevine varieties. ''Sci Adv''. 2021 Nov 19; '''7''' (47):eabi8584
Selection shapes the landscape of functional variation in wild house mice. Description: Lawal, Raman Akinyanju, et al. Selection shapes the landscape of functional variation in wild house mice. ''BMC Biol''. 2021 Nov 19; '''19''' (1):239
Selective Sweeps and Polygenic Adaptation Drive Local Adaptation along Moisture and Temperature Gradients in Natural Populations of Coast Redwood and Giant Sequoia. Description: De La Torre, Amanda R, et al. Selective Sweeps and Polygenic Adaptation Drive Local Adaptation along Moisture and Temperature Gradients in Natural Populations of Coast Redwood and Giant Sequoia. ''Genes (Basel)''. 2021 Nov 19; '''12''' (11):
Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2. Description: Fan, Yanbo, et al. Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2. ''iScience''. 2021 Nov 19; '''24''' (11):103196
Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation Study. Description: Zazuli, Zulfan, et al. Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation Study. ''J Pers Med''. 2021 Nov 20; '''11''' (11):
Association of single nucleotide polymorphisms with insulin secretion, insulin sensitivity, and diabetes in women with a history of gestational diabetes mellitus. Description: Prasad, Rashmi B, et al. Association of single nucleotide polymorphisms with insulin secretion, insulin sensitivity, and diabetes in women with a history of gestational diabetes mellitus. ''BMC Med Genomics''. 2021 Nov 20; '''14''' (1):274
Genome-wide association analysis uncovers the genetic architecture of tradeoff between flowering date and yield components in sesame. Description: Sabag, Idan, et al. Genome-wide association analysis uncovers the genetic architecture of tradeoff between flowering date and yield components in sesame. ''BMC Plant Biol''. 2021 Nov 22; '''21''' (1):549
Identification and replication of novel genetic variants of ABO gene to reduce the incidence of diseases and promote longevity by modulating lipid homeostasis. Description: Ni, Xiaolin, et al. Identification and replication of novel genetic variants of ABO gene to reduce the incidence of diseases and promote longevity by modulating lipid homeostasis. ''Aging (Albany NY)''. 2021 Nov 22; '''13''' (22):24655-24674
Identification of quantitative trait nucleotides and candidate genes for tuber yield and mosaic virus tolerance in an elite population of white guinea yam (Dioscorea rotundata) using genome-wide association scan. Description: Agre, Paterne A, et al. Identification of quantitative trait nucleotides and candidate genes for tuber yield and mosaic virus tolerance in an elite population of white guinea yam (Dioscorea rotundata) using genome-wide association scan. ''BMC Plant Biol''. 2021 Nov 22; '''21''' (1):552
Poking COVID-19: Insights on Genomic Constraints among Immune-Related Genes between Qatari and Italian Populations. Description: Mbarek, Hamdi, et al. Poking COVID-19: Insights on Genomic Constraints among Immune-Related Genes between Qatari and Italian Populations. ''Genes (Basel)''. 2021 Nov 22; '''12''' (11):
Genotyping-in-Thousands by sequencing of archival fish scales reveals maintenance of genetic variation following a severe demographic contraction in kokanee salmon. Description: Setzke, Christopher, et al. Genotyping-in-Thousands by sequencing of archival fish scales reveals maintenance of genetic variation following a severe demographic contraction in kokanee salmon. ''Sci Rep''. 2021 Nov 23; '''11''' (1):22798
Autism-related dietary preferences mediate autism-gut microbiome associations. Description: Yap, Chloe X, et al. Autism-related dietary preferences mediate autism-gut microbiome associations. ''Cell''. 2021 Nov 24; '''184''' (24):5916-5931.e17
Molecular and phenotypic profiling of colorectal cancer patients in West Africa reveals biological insights. Description: Alatise, Olusegun Isaac, et al. Molecular and phenotypic profiling of colorectal cancer patients in West Africa reveals biological insights. ''Nat Commun''. 2021 Nov 24; '''12''' (1):6821
Synergistic insights into human health from aptamer- and antibody-based proteomic profiling. Description: Pietzner, Maik, et al. Synergistic insights into human health from aptamer- and antibody-based proteomic profiling. ''Nat Commun''. 2021 Nov 24; '''12''' (1):6822
A supergene underlies linked variation in color and morphology in a Holarctic songbird. Description: Funk, Erik R, et al. A supergene underlies linked variation in color and morphology in a Holarctic songbird. ''Nat Commun''. 2021 Nov 25; '''12''' (1):6833
Admixture mapping analysis reveals differential genetic ancestry associated with Chagas disease susceptibility in the Colombian population. Description: Casares-Marfil, Desire, et al. Admixture mapping analysis reveals differential genetic ancestry associated with Chagas disease susceptibility in the Colombian population. ''Hum Mol Genet''. 2021 Nov 30; '''30''' (24):2503-2512
Ancient autozygous segments subject to positive selection suggest adaptive immune responses in West African cattle. Description: Goyache, Felix, et al. Ancient autozygous segments subject to positive selection suggest adaptive immune responses in West African cattle. ''Gene''. 2021 Nov 30; '''803''': 145899
Genetic Differences between Physical Injury Patients With and Without Post-traumatic Syndrome: Focus on Secondary Findings and Potential Variants Revealed by Whole Exome Sequencing. Description: Kang, Hee-Ju, et al. Genetic Differences between Physical Injury Patients With and Without Post-traumatic Syndrome: Focus on Secondary Findings and Potential Variants Revealed by Whole Exome Sequencing. ''Clin Psychopharmacol Neurosci''. 2021 Nov 30; '''19''' (4):683-694
Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders. Description: van Duijvenboden, Stefan, et al. Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders. ''Hum Mol Genet''. 2021 Nov 30; '''30''' (24):2513-2523
Investigation of C-reactive protein and AIM2 methylation as a marker for PTSD in Australian Vietnam veterans. Description: McD Young, Ross, et al. Investigation of C-reactive protein and AIM2 methylation as a marker for PTSD in Australian Vietnam veterans. ''Gene''. 2021 Nov 30; '''803''': 145898
Accelerated cardiovascular risk after viral clearance in hepatitis C patients with the NAMPT-rs61330082 TT genotype: An 8-year prospective cohort study. Description: Chang, Ming-Ling, et al. Accelerated cardiovascular risk after viral clearance in hepatitis C patients with the NAMPT-rs61330082 TT genotype: An 8-year prospective cohort study. ''Virulence''. 2021 Dec; '''12''' (1):270-280
A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens. Description: Liu, Wei, et al. A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens. ''BMC Med''. 2021 Dec 1; '''19''' (1):302
A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer. Description: Yu, Yajun, et al. A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer. ''Mol Oncol''. 2021 Dec; '''15''' (12):3329-3347
A host-based whole genome sequencing study reveals novel risk loci associated with severity of influenza A(H1N1)pdm09 infection. Description: Li, Mo, et al. A host-based whole genome sequencing study reveals novel risk loci associated with severity of influenza A(H1N1)pdm09 infection. ''Emerg Microbes Infect''. 2021 Dec; '''10''' (1):123-131
Assessing the potential correlation of polymorphisms in the IL6R with relative IL6 elevation in severely ill COVID-19 patients'. Description: Smieszek, Sandra P, et al. Assessing the potential correlation of polymorphisms in the IL6R with relative IL6 elevation in severely ill COVID-19 patients'. ''Cytokine''. 2021 Dec; '''148''': 155662
Association analysis of pulmonary tuberculosis and vitamin D Receptor Gene Polymorphisms of Han population in Western China. Description: Xu, Shaohua, et al. Association analysis of pulmonary tuberculosis and vitamin D Receptor Gene Polymorphisms of Han population in Western China. ''Microb Pathog''. 2021 Dec; '''161''' (Pt A):105190
Associations of corin genetic polymorphisms with salt sensitivity, blood pressure changes, and hypertension incidence in Chinese adults. Description: Zou, Ting, et al. Associations of corin genetic polymorphisms with salt sensitivity, blood pressure changes, and hypertension incidence in Chinese adults. ''J Clin Hypertens (Greenwich)''. 2021 Dec; '''23''' (12):2115-2123
A transcriptome-wide association study to detect novel genes for volumetric bone mineral density. Description: Liu, Anqi, et al. A transcriptome-wide association study to detect novel genes for volumetric bone mineral density. ''Bone''. 2021 Dec; '''153''': 116106
BDNF-Met polymorphism and amyloid-beta in relation to cognitive decline in cognitively normal elderly: the SCIENCe project. Description: van den Bosch, Karlijn A, et al. BDNF-Met polymorphism and amyloid-beta in relation to cognitive decline in cognitively normal elderly: the SCIENCe project. ''Neurobiol Aging''. 2021 Dec; '''108''': 146-154
Candidates for Balancing Selection in Leishmania donovani Complex Parasites. Description: Grace, Cooper Alastair, et al. Candidates for Balancing Selection in Leishmania donovani Complex Parasites. ''Genome Biol Evol''. 2021 Dec 1; '''13''' (12):
Deep resequencing identifies candidate functional genes in leprosy GWAS loci. Description: Fava, Vinicius M, et al. Deep resequencing identifies candidate functional genes in leprosy GWAS loci. ''PLoS Negl Trop Dis''. 2021 Dec; '''15''' (12):e0010029
Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree. Description: Halvorsen, Matthew, et al. Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree. ''Mol Psychiatry''. 2021 Dec; '''26''' (12):7522-7529
Exome sequencing identifies a disease variant of the mitochondrial ATP-Mg/Pi carrier SLC25A25 in two families with kidney stones. Description: Jabalameli, M Reza, et al. Exome sequencing identifies a disease variant of the mitochondrial ATP-Mg/Pi carrier SLC25A25 in two families with kidney stones. ''Mol Genet Genomic Med''. 2021 Dec; '''9''' (12):e1749
Exploring the genetic heterogeneity in major depression across diagnostic criteria. Description: Jermy, Bradley S, et al. Exploring the genetic heterogeneity in major depression across diagnostic criteria. ''Mol Psychiatry''. 2021 Dec; '''26''' (12):7337-7345
Genetic diversity and structure of Rhododendron meddianum, a plant species with extremely small populations. Description: Zhang, Xiu-Jiao, et al. Genetic diversity and structure of Rhododendron meddianum, a plant species with extremely small populations. ''Plant Divers''. 2021 Dec; '''43''' (6):472-479
Genetic variant in microRNA-146a gene is associated with risk of rheumatoid arthritis. Description: Zhang, Lin-Lin, et al. Genetic variant in microRNA-146a gene is associated with risk of rheumatoid arthritis. ''Ann Med''. 2021 Dec; '''53''' (1):824-829
Genetic variants in Hippo pathway genes are associated with house dust mite-induced allergic rhinitis in a Chinese population. Description: Chen, Min, et al. Genetic variants in Hippo pathway genes are associated with house dust mite-induced allergic rhinitis in a Chinese population. ''Clin Transl Allergy''. 2021 Dec; '''11''' (10):e12077
Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease. Description: Lakshman Kumar, Preeti, et al. Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease. ''J Cachexia Sarcopenia Muscle''. 2021 Dec; '''12''' (6):1803-1817
Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration. Description: Bourgeois, Stephane, et al. Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration. ''EBioMedicine''. 2021 Dec; '''74''': 103728
Genome-wide association study of asthma, total IgE, and lung function in a cohort of Peruvian children. Description: Akenroye, Ayobami T, et al. Genome-wide association study of asthma, total IgE, and lung function in a cohort of Peruvian children. ''J Allergy Clin Immunol''. 2021 Dec; '''148''' (6):1493-1504
Genome-wide scan for runs of homozygosity identifies candidate genes in Wannan Black pigs. Description: Wu, Xudong, et al. Genome-wide scan for runs of homozygosity identifies candidate genes in Wannan Black pigs. ''Anim Biosci''. 2021 Dec; '''34''' (12):1895-1902
Human gut microbiome impacts skeletal muscle mass via gut microbial synthesis of the short-chain fatty acid butyrate among healthy menopausal women. Description: Lv, Wan-Qiang, et al. Human gut microbiome impacts skeletal muscle mass via gut microbial synthesis of the short-chain fatty acid butyrate among healthy menopausal women. ''J Cachexia Sarcopenia Muscle''. 2021 Dec; '''12''' (6):1860-1870
Hybridization Dynamics and Extensive Introgression in the Daphnia longispina Species Complex: New Insights from a High-Quality Daphnia galeata Reference Genome. Description: Nickel, Jana, et al. Hybridization Dynamics and Extensive Introgression in the Daphnia longispina Species Complex: New Insights from a High-Quality Daphnia galeata Reference Genome. ''Genome Biol Evol''. 2021 Dec 1; '''13''' (12):
Identification of rare coding variants associated with Kawasaki disease by whole exome sequencing. Description: Kim, Jae-Jung, et al. Identification of rare coding variants associated with Kawasaki disease by whole exome sequencing. ''Genomics Inform''. 2021 Dec; '''19''' (4):e38
Integration of whole genome sequencing and transcriptomics reveals a complex picture of the reestablishment of insecticide resistance in the major malaria vector Anopheles coluzzii. Description: Ingham, Victoria A, et al. Integration of whole genome sequencing and transcriptomics reveals a complex picture of the reestablishment of insecticide resistance in the major malaria vector Anopheles coluzzii. ''PLoS Genet''. 2021 Dec; '''17''' (12):e1009970
Interaction between Genetic Risk Scores for reduced pulmonary function and smoking, asthma and endotoxin. Description: Sikdar, Sinjini, et al. Interaction between Genetic Risk Scores for reduced pulmonary function and smoking, asthma and endotoxin. ''Thorax''. 2021 Dec; '''76''' (12):1219-1226
Low genome-wide divergence between two lizard populations with high adaptive phenotypic differentiation. Description: Llanos-Garrido, Alejandro, et al. Low genome-wide divergence between two lizard populations with high adaptive phenotypic differentiation. ''Ecol Evol''. 2021 Dec; '''11''' (24):18055-18065
Mapping the human genetic architecture of COVID-19. Description: Mapping the human genetic architecture of COVID-19. ''Nature''. 2021 Dec; '''600''' (7889):472-477
Maternal trichloroethylene exposure and metabolic gene polymorphisms may interact during fetal cardiovascular malformation. Description: Liu, Zhen, et al. Maternal trichloroethylene exposure and metabolic gene polymorphisms may interact during fetal cardiovascular malformation. ''Reprod Toxicol''. 2021 Dec; '''106''': 1-8
Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease. Description: Ponte, Belen, et al. Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease. ''Kidney Int''. 2021 Dec; '''100''' (6):1282-1291
Mitochondrial pathway polygenic risk scores are associated with Alzheimer's Disease. Description: Paliwal, Devashi, et al. Mitochondrial pathway polygenic risk scores are associated with Alzheimer's Disease. ''Neurobiol Aging''. 2021 Dec; '''108''': 213-222
Mito-nuclear discordance at a mimicry color transition zone in bumble bee Bombus melanopygus. Description: Wham, Briana E, et al. Mito-nuclear discordance at a mimicry color transition zone in bumble bee Bombus melanopygus. ''Ecol Evol''. 2021 Dec; '''11''' (24):18151-18168
Neurexin 1 variants as risk factors for suicide death. Description: William, Nancy, et al. Neurexin 1 variants as risk factors for suicide death. ''Mol Psychiatry''. 2021 Dec; '''26''' (12):7436-7445
New genetic variants associated with major adverse cardiovascular events in patients with acute coronary syndromes and treated with clopidogrel and aspirin. Description: Liu, Xiaomin, et al. New genetic variants associated with major adverse cardiovascular events in patients with acute coronary syndromes and treated with clopidogrel and aspirin. ''Pharmacogenomics J''. 2021 Dec; '''21''' (6):664-672
Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease. Description: Sipeky, Csilla, et al. Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease. ''Prostate Cancer Prostatic Dis''. 2021 Dec; '''24''' (4):1158-1166
Phenotypic and genotypic parallel evolution in parapatric ecotypes of Senecio. Description: James, Maddie E, et al. Phenotypic and genotypic parallel evolution in parapatric ecotypes of Senecio. ''Evolution''. 2021 Dec; '''75''' (12):3115-3131
Polymorphisms analysis for association between ADIPO signaling pathway and genetic susceptibility to T2DM in Chinese han population. Description: Yu, Haibing, et al. Polymorphisms analysis for association between ADIPO signaling pathway and genetic susceptibility to T2DM in Chinese han population. ''Adipocyte''. 2021 Dec; '''10''' (1):463-474
Population-specific diversity of the immunoglobulin constant heavy G chain (IGHG) genes. Description: Bashirova, Arman A, et al. Population-specific diversity of the immunoglobulin constant heavy G chain (IGHG) genes. ''Genes Immun''. 2021 Dec; '''22''' (7-8):327-334
Population structure, genomic diversity and demographic history of Komodo dragons inferred from whole-genome sequencing. Description: Iannucci, Alessio, et al. Population structure, genomic diversity and demographic history of Komodo dragons inferred from whole-genome sequencing. ''Mol Ecol''. 2021 Dec; '''30''' (23):6309-6324
Rare protein-coding variants implicate genes involved in risk of suicide death. Description: DiBlasi, Emily, et al. Rare protein-coding variants implicate genes involved in risk of suicide death. ''Am J Med Genet B Neuropsychiatr Genet''. 2021 Dec; '''186''' (8):508-520
The Euscaphis japonica genome and the evolution of malvids. Description: Sun, Wei-Hong, et al. The Euscaphis japonica genome and the evolution of malvids. ''Plant J''. 2021 Dec; '''108''' (5):1382-1399
The role of vascular dementia associated genes in patients with Alzheimer's disease: A large case-control study in the Chinese population. Description: Xiao, Xuewen, et al. The role of vascular dementia associated genes in patients with Alzheimer's disease: A large case-control study in the Chinese population. ''CNS Neurosci Ther''. 2021 Dec; '''27''' (12):1531-1539
Tsukushi and TSKU genotype in obesity and related metabolic disorders. Description: Li, Y, et al. Tsukushi and TSKU genotype in obesity and related metabolic disorders. ''J Endocrinol Invest''. 2021 Dec; '''44''' (12):2645-2654
Unveiling Genetic Variants Underlying Vitamin D Deficiency in Multiple Korean Cohorts by a Genome-Wide Association Study. Description: Kim, Ye An, et al. Unveiling Genetic Variants Underlying Vitamin D Deficiency in Multiple Korean Cohorts by a Genome-Wide Association Study. ''Endocrinol Metab (Seoul)''. 2021 Dec; '''36''' (6):1189-1200
Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology. Description: Shadrin, Alexey A, et al. Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology. ''Neuroimage''. 2021 Dec 1; '''244''': 118603
Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. Description: Shaw, Douglas M, et al. Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. ''Am J Hum Genet''. 2021 Dec 2; '''108''' (12):2271-2283
The effect of inbreeding, body size and morphology on health in dog breeds. Description: Bannasch, Danika, et al. The effect of inbreeding, body size and morphology on health in dog breeds. ''Canine Med Genet''. 2021 Dec 2; '''8''' (1):12
Phenotyping stomatal closure by thermal imaging for GWAS and TWAS of water use efficiency-related genes. Description: Pignon, Charles P, et al. Phenotyping stomatal closure by thermal imaging for GWAS and TWAS of water use efficiency-related genes. ''Plant Physiol''. 2021 Dec 4; '''187''' (4):2544-2562
Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Description: Liu, Xiaomin, et al. Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. ''Cell Discov''. 2021 Dec 7; '''7''' (1):117
Environment-driven reprogramming of gamete DNA methylation occurs during maturation and is transmitted intergenerationally in Atlantic Salmon. Description: Wellband, Kyle, et al. Environment-driven reprogramming of gamete DNA methylation occurs during maturation and is transmitted intergenerationally in Atlantic Salmon. ''G3 (Bethesda)''. 2021 Dec 8; '''11''' (12):
Identification of Novel Genomic Variations in Susceptibility to Nonsyndromic Cleft Lip and Palate Patients. Description: Avasthi, Kapil Kumar, et al. Identification of Novel Genomic Variations in Susceptibility to Nonsyndromic Cleft Lip and Palate Patients. ''Pediatr Rep''. 2021 Dec 8; '''13''' (4):650-657
Smooth-threshold multivariate genetic prediction incorporating gene-environment interactions. Description: Ueki, Masao, et al. Smooth-threshold multivariate genetic prediction incorporating gene-environment interactions. ''G3 (Bethesda)''. 2021 Dec 8; '''11''' (12):
Depressive symptoms and neuroticism-related traits are the main factors associated with wellbeing independent of the history of lifetime depression in the UK Biobank. Description: Fabbri, Chiara, et al. Depressive symptoms and neuroticism-related traits are the main factors associated with wellbeing independent of the history of lifetime depression in the UK Biobank. ''Psychol Med''. 2021 Dec 9; '''53''' (7):1-9
Genome Fractionation and Loss of Heterozygosity in Hybrids and Polyploids: Mechanisms, Consequences for Selection, and Link to Gene Function. Description: Janko, Karel, et al. Genome Fractionation and Loss of Heterozygosity in Hybrids and Polyploids: Mechanisms, Consequences for Selection, and Link to Gene Function. ''Mol Biol Evol''. 2021 Dec 9; '''38''' (12):5255-5274
Multiple Sources of Introduction of North American Arabidopsis thaliana from across Eurasia. Description: Shirsekar, Gautam, et al. Multiple Sources of Introduction of North American Arabidopsis thaliana from across Eurasia. ''Mol Biol Evol''. 2021 Dec 9; '''38''' (12):5328-5344
Functional rare variant in a C/EBP beta binding site in NINJ2 gene increases the risk of coronary artery disease. Description: Wang, Pengyun, et al. Functional rare variant in a C/EBP beta binding site in NINJ2 gene increases the risk of coronary artery disease. ''Aging (Albany NY)''. 2021 Dec 12; '''13''' (23):25393-25407
The effects of MIR137HG genetic polymorphisms on the susceptibility of alcohol-induced osteonecrosis of the femoral head in a Chinese male population. Description: Guo, Yongchang, et al. The effects of MIR137HG genetic polymorphisms on the susceptibility of alcohol-induced osteonecrosis of the femoral head in a Chinese male population. ''Gene''. 2021 Dec 15; '''804''': 145902
The neurobiological basis of divergent thinking: Insight from gene co-expression network-based analysis. Description: Zhang, Shun, et al. The neurobiological basis of divergent thinking: Insight from gene co-expression network-based analysis. ''Neuroimage''. 2021 Dec 15; '''245''': 118762
Analytical protocol to identify local ancestry-associated molecular features in cancer. Description: Carrot-Zhang, Jian, et al. Analytical protocol to identify local ancestry-associated molecular features in cancer. ''STAR Protoc''. 2021 Dec 17; '''2''' (4):100766
Evolutionary history of the extinct Sardinian dhole. Description: Ciucani, Marta Maria, et al. Evolutionary history of the extinct Sardinian dhole. ''Curr Biol''. 2021 Dec 20; '''31''' (24):5571-5579.e6
The influence of FAAH genetic variation on physiological, cognitive, and neural signatures of fear acquisition and extinction learning in women with PTSD. Description: Crombie, Kevin M, et al. The influence of FAAH genetic variation on physiological, cognitive, and neural signatures of fear acquisition and extinction learning in women with PTSD. ''Neuroimage Clin''. 2021 Dec 20; '''33''': 102922
Crimean-Congo Hemorrhagic Fever Virus Past Infections Are Associated with Two Innate Immune Response Candidate Genes in Dromedaries. Description: Lado, Sara, et al. Crimean-Congo Hemorrhagic Fever Virus Past Infections Are Associated with Two Innate Immune Response Candidate Genes in Dromedaries. ''Cells''. 2021 Dec 21; '''11''' (1):
Invasion genomics uncover contrasting scenarios of genetic diversity in a widespread marine invader. Description: Jaspers, Cornelia, et al. Invasion genomics uncover contrasting scenarios of genetic diversity in a widespread marine invader. ''Proc Natl Acad Sci U S A''. 2021 Dec 21; '''118''' (51):
The genomes of 204 Vitis vinifera accessions reveal the origin of European wine grapes. Description: Magris, Gabriele, et al. The genomes of 204 Vitis vinifera accessions reveal the origin of European wine grapes. ''Nat Commun''. 2021 Dec 21; '''12''' (1):7240
Identification of Potential Pleiotropic Genes for Immune and Skeletal Diseases Using Multivariate MetaCCA Analysis. Description: He, Pei, et al. Identification of Potential Pleiotropic Genes for Immune and Skeletal Diseases Using Multivariate MetaCCA Analysis. ''Curr Genomics''. 2021 Dec 31; '''22''' (8):596-606
A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis. Description: Affolter, Verena K, et al. A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis. ''PLoS One''. 2022; '''17''' (10):e0275367
A dietary carbohydrate - gut Parasutterella - human fatty acid biosynthesis metabolic axis in obesity and type 2 diabetes. Description: Henneke, Lea, et al. A dietary carbohydrate - gut Parasutterella - human fatty acid biosynthesis metabolic axis in obesity and type 2 diabetes. ''Gut Microbes''. 2022 Jan-Dec; '''14''' (1):2057778
A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women. Description: Yoo, Hye-Young, et al. A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women. ''Clin Cosmet Investig Dermatol''. 2022; '''15''': 433-445
A Genome-Wide Association Study on Abdominal Adiposity-Related Traits in Adult Korean Men. Description: Kim, Hyun-Jin, et al. A Genome-Wide Association Study on Abdominal Adiposity-Related Traits in Adult Korean Men. ''Obes Facts''. 2022; '''15''' (4):590-599
A high-density genome-wide association with absolute blood monocyte count in domestic sheep identifies novel loci. Description: Oliveira, Ryan D, et al. A high-density genome-wide association with absolute blood monocyte count in domestic sheep identifies novel loci. ''PLoS One''. 2022; '''17''' (5):e0266748
Algorithmic identification of atypical diabetes in electronic health record (EHR) systems. Description: Cromer, Sara J, et al. Algorithmic identification of atypical diabetes in electronic health record (EHR) systems. ''PLoS One''. 2022; '''17''' (12):e0278759
An alien in Marseille: investigations on a single Aedes aegypti mosquito likely introduced by a merchant ship from tropical Africa to Europe. Description: Jeannin, Charles, et al. An alien in Marseille: investigations on a single Aedes aegypti mosquito likely introduced by a merchant ship from tropical Africa to Europe. ''Parasite''. 2022; '''29''': 42
A novel pathogenesis concept of biliary atresia approached by combined molecular strategies. Description: Laochareonsuk, Wison, et al. A novel pathogenesis concept of biliary atresia approached by combined molecular strategies. ''PLoS One''. 2022; '''17''' (11):e0277334
APOE and KLF14 genetic variants are sex-specific for low high-density lipoprotein cholesterol identified by a genome-wide association study. Description: Lee, Ying-Hui, et al. APOE and KLF14 genetic variants are sex-specific for low high-density lipoprotein cholesterol identified by a genome-wide association study. ''Genet Mol Biol''. 2022; '''45''' (1):e20210280
APOE, TOMM40, and sex interactions on neural network connectivity. Description: Li, Tianqi, et al. APOE, TOMM40, and sex interactions on neural network connectivity. ''Neurobiol Aging''. 2022 Jan; '''109''': 158-165
Association of Estrogen-Related Polygenetic Risk Scores with Breast Cancer and Interactions with Alcohol Intake, Early Menarche, and Nulligravida. Description: Song, Sang Shin, et al. Association of Estrogen-Related Polygenetic Risk Scores with Breast Cancer and Interactions with Alcohol Intake, Early Menarche, and Nulligravida. ''Asian Pac J Cancer Prev''. 2022 Jan 1; '''23''' (1):13-24
Association of SPI1 Haplotypes with Altered SPI1 Gene Expression and Alzheimer's Disease Risk. Description: Cao, Han, et al. Association of SPI1 Haplotypes with Altered SPI1 Gene Expression and Alzheimer's Disease Risk. ''J Alzheimers Dis''. 2022; '''86''' (4):1861-1873
Associations of human leukocyte antigen with neutralizing antibody titers in a tetravalent dengue vaccine phase 2 efficacy trial in Thailand. Description: Thomas, Rasmi, et al. Associations of human leukocyte antigen with neutralizing antibody titers in a tetravalent dengue vaccine phase 2 efficacy trial in Thailand. ''Hum Immunol''. 2022 Jan; '''83''' (1):53-60
Associations of maternal blood pressure-raising polygenic risk scores with fetal weight. Description: Workalemahu, Tsegaselassie, et al. Associations of maternal blood pressure-raising polygenic risk scores with fetal weight. ''J Hum Hypertens''. 2022 Jan; '''36''' (1):69-76
Automated Machine Learning: A Case Study of Genomic "Image-Based" Prediction in Maize Hybrids. Description: Galli, Giovanni, et al. Automated Machine Learning: A Case Study of Genomic "Image-Based" Prediction in Maize Hybrids. ''Front Plant Sci''. 2022; '''13''': 845524
DArTSeq SNP-based genetic diversity and population structure studies among taro [(Colocasia esculenta (L.) Schott] accessions sourced from Nigeria and Vanuatu. Description: Fufa, Tilahun Wondimu, et al. DArTSeq SNP-based genetic diversity and population structure studies among taro [(Colocasia esculenta (L.) Schott] accessions sourced from Nigeria and Vanuatu. ''PLoS One''. 2022; '''17''' (11):e0269302
Effects of aerobic and resistance exercise on glycosylated hemoglobin (HbA1c) concentrations in non-diabetic Taiwanese individuals based on the waist-hip ratio. Description: Chou, Ying-Hsiang, et al. Effects of aerobic and resistance exercise on glycosylated hemoglobin (HbA1c) concentrations in non-diabetic Taiwanese individuals based on the waist-hip ratio. ''PLoS One''. 2022; '''17''' (5):e0267387
Evaluating the role of ARSA in Chinese patients with Parkinson's disease. Description: Pan, Hong-Xu, et al. Evaluating the role of ARSA in Chinese patients with Parkinson's disease. ''Neurobiol Aging''. 2022 Jan; '''109''': 269-272
Exploring the genetic correlation between obesity-related traits and regional brain volumes: Evidence from UK Biobank cohort. Description: Pan, Xingchen, et al. Exploring the genetic correlation between obesity-related traits and regional brain volumes: Evidence from UK Biobank cohort. ''Neuroimage Clin''. 2022; '''33''': 102870
Four Systemic Lupus Erythematosus Subgroups, Defined by Autoantibodies Status, Differ Regarding HLA-DRB1 Genotype Associations and Immunological and Clinical Manifestations. Description: Diaz-Gallo, Lina-Marcela, et al. Four Systemic Lupus Erythematosus Subgroups, Defined by Autoantibodies Status, Differ Regarding HLA-DRB1 Genotype Associations and Immunological and Clinical Manifestations. ''ACR Open Rheumatol''. 2022 Jan; '''4''' (1):27-39
Functional coding haplotypes and machine-learning feature elimination identifies predictors of Methotrexate Response in Rheumatoid Arthritis patients. Description: Lim, Ashley J W, et al. Functional coding haplotypes and machine-learning feature elimination identifies predictors of Methotrexate Response in Rheumatoid Arthritis patients. ''EBioMedicine''. 2022 Jan; '''75''': 103800
Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies. Description: Lopes, Katia de Paiva, et al. Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies. ''Nat Genet''. 2022 Jan; '''54''' (1):4-17
Genome-wide association study-based prediction of atrial fibrillation using artificial intelligence. Description: Kwon, Oh-Seok, et al. Genome-wide association study-based prediction of atrial fibrillation using artificial intelligence. ''Open Heart''. 2022 Jan; '''9''' (1):
Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Description: Wong, Henry Sung-Ching, et al. Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. ''PLoS Genet''. 2022 Jan; '''18''' (1):e1009952
Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Description: Harper, Jordan D, et al. Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. ''J Alzheimers Dis''. 2022; '''88''' (2):787-798
Genome-wide clonal variability in European pear "Rocha" using high-throughput sequencing. Description: Serra, Octavio, et al. Genome-wide clonal variability in European pear "Rocha" using high-throughput sequencing. ''Hortic Res''. 2022; '''9''': uhac111
Genomic insights in ascending aortic size and distensibility. Description: Benjamins, Jan Walter, et al. Genomic insights in ascending aortic size and distensibility. ''EBioMedicine''. 2022 Jan; '''75''': 103783
Global Genome Diversity and Recombination in Mycoplasma pneumoniae. Description: Hsieh, Yu-Chia, et al. Global Genome Diversity and Recombination in Mycoplasma pneumoniae. ''Emerg Infect Dis''. 2022 Jan; '''28''' (1):111-117
Hereditary variants of unknown significance in African American women with breast cancer. Description: McDonald, J Tyson, et al. Hereditary variants of unknown significance in African American women with breast cancer. ''PLoS One''. 2022; '''17''' (10):e0273835
Imputation provides an opportunity to study filaggrin ( FLG) null mutations in large population cohorts that lack bespoke genotyping. Description: Paternoster, Lavinia, et al. Imputation provides an opportunity to study filaggrin ( FLG) null mutations in large population cohorts that lack bespoke genotyping. ''Wellcome Open Res''. 2022; '''7''': 36
Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control Cohort. Description: Brolin, Kajsa, et al. Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control Cohort. ''J Parkinsons Dis''. 2022; '''12''' (1):153-171
Is there an association of genetic polymorphisms of the catechol-O-methyltransferase gene (rs165656 and rs174675) and the 5-hydroxytryptamine receptor 2A gene (rs4941573 and rs6313) with sleep bruxism in individuals with obstructive sleep apnea? Description: Duarte, Joyce, et al. Is there an association of genetic polymorphisms of the catechol-O-methyltransferase gene (rs165656 and rs174675) and the 5-hydroxytryptamine receptor 2A gene (rs4941573 and rs6313) with sleep bruxism in individuals with obstructive sleep apnea? ''Arch Oral Biol''. 2022 Jan; '''133''': 105315
Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs. Description: Blades, Matthew, et al. Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs. ''PLoS One''. 2022; '''17''' (5):e0267604
Large uncertainty in individual polygenic risk score estimation impacts PRS-based risk stratification. Description: Ding, Yi, et al. Large uncertainty in individual polygenic risk score estimation impacts PRS-based risk stratification. ''Nat Genet''. 2022 Jan; '''54''' (1):30-39
Leveraging large multi-center cohorts of Alzheimer disease endophenotypes to understand the role of Klotho heterozygosity on disease risk. Description: Ali, Muhammad, et al. Leveraging large multi-center cohorts of Alzheimer disease endophenotypes to understand the role of Klotho heterozygosity on disease risk. ''PLoS One''. 2022; '''17''' (5):e0267298
NAToRA, a relatedness-pruning method to minimize the loss of dataset size in genetic and omics analyses. Description: Leal, Thiago Peixoto, et al. NAToRA, a relatedness-pruning method to minimize the loss of dataset size in genetic and omics analyses. ''Comput Struct Biotechnol J''. 2022; '''20''': 1821-1828
Patterns of genomic divergence in sympatric and allopatric speciation of three Mihoutao (Actinidia) species. Description: Liu, Yongbo, et al. Patterns of genomic divergence in sympatric and allopatric speciation of three Mihoutao (Actinidia) species. ''Hortic Res''. 2022; '''9''': uhac054
Polymorphisms of the BCL2 gene associated with susceptibility to tuberculosis. Description: He, Juan, et al. Polymorphisms of the BCL2 gene associated with susceptibility to tuberculosis. ''Rev Inst Med Trop Sao Paulo''. 2022; '''64''': e59
Prediction of clinically significant prostate cancer using polygenic risk models in Asians. Description: Song, Sang Hun, et al. Prediction of clinically significant prostate cancer using polygenic risk models in Asians. ''Investig Clin Urol''. 2022 Jan; '''63''' (1):42-52
Rank-invariant estimation of inbreeding coefficients. Description: Zhang, Qian S, et al. Rank-invariant estimation of inbreeding coefficients. ''Heredity (Edinb)''. 2022 Jan; '''128''' (1):1-10
Rare variants in previously identified linkage regions associated with carotid plaque in Dominican Republic families. Description: Dueker, Nicole D, et al. Rare variants in previously identified linkage regions associated with carotid plaque in Dominican Republic families. ''PLoS One''. 2022; '''17''' (1):e0250799
RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts. Description: Brolin, Kajsa, et al. RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts. ''Neurobiol Aging''. 2022 Jan; '''109''': 264-268
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Description: Blokland, Gabriella A M, et al. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. ''Biol Psychiatry''. 2022 Jan 1; '''91''' (1):102-117
Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. Description: Ahmed, Waheed Ul-Rahman, et al. Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. ''PLoS One''. 2022; '''17''' (12):e0272261
Single-nucleotide polymorphisms of the SLC17A9 and P2RY12 genes are significantly associated with phantom tooth pain. Description: Soeda, Moe, et al. Single-nucleotide polymorphisms of the SLC17A9 and P2RY12 genes are significantly associated with phantom tooth pain. ''Mol Pain''. 2022 Jan-Dec; '''18''': 17448069221089592
Subgroups of patients with young-onset type 2 diabetes in India reveal insulin deficiency as a major driver. Description: Prasad, Rashmi B, et al. Subgroups of patients with young-onset type 2 diabetes in India reveal insulin deficiency as a major driver. ''Diabetologia''. 2022 Jan; '''65''' (1):65-78
The Genetic Architecture of Nitrogen Use Efficiency in Switchgrass (Panicum virgatum L.). Description: Shrestha, Vivek, et al. The Genetic Architecture of Nitrogen Use Efficiency in Switchgrass (Panicum virgatum L.). ''Front Plant Sci''. 2022; '''13''': 893610
The role of circulating galectin-1 in type 2 diabetes and chronic kidney disease: evidence from cross-sectional, longitudinal and Mendelian randomisation analyses. Description: Drake, Isabel, et al. The role of circulating galectin-1 in type 2 diabetes and chronic kidney disease: evidence from cross-sectional, longitudinal and Mendelian randomisation analyses. ''Diabetologia''. 2022 Jan; '''65''' (1):128-139
Two divergent haplotypes from a highly heterozygous lychee genome suggest independent domestication events for early and late-maturing cultivars. Description: Hu, Guibing, et al. Two divergent haplotypes from a highly heterozygous lychee genome suggest independent domestication events for early and late-maturing cultivars. ''Nat Genet''. 2022 Jan; '''54''' (1):73-83
Type 2 Diabetes, PNPLA3 rs738409 Polymorphism, and the Risk of Liver Cirrhosis: Analysis of Taiwan Biobank. Description: Hsueh, Kuan-Chun, et al. Type 2 Diabetes, PNPLA3 rs738409 Polymorphism, and the Risk of Liver Cirrhosis: Analysis of Taiwan Biobank. ''Front Genet''. 2022; '''13''': 822700
Unexpected post-glacial colonisation route explains the white colour of barn owls (Tyto alba) from the British Isles. Description: Machado, Ana Paula, et al. Unexpected post-glacial colonisation route explains the white colour of barn owls (Tyto alba) from the British Isles. ''Mol Ecol''. 2022 Jan; '''31''' (2):482-497
Association between single nucleotide polymorphism of rs1937 in TFAM gene and longevity among the elderly Chinese population: based on the CLHLS study. Description: Chen, Qing, et al. Association between single nucleotide polymorphism of rs1937 in TFAM gene and longevity among the elderly Chinese population: based on the CLHLS study. ''BMC Geriatr''. 2022 Jan 3; '''22''' (1):16
Evaluation of the phenotypic and genomic background of variability based on litter size of Large White pigs. Description: Sell-Kubiak, Ewa, et al. Evaluation of the phenotypic and genomic background of variability based on litter size of Large White pigs. ''Genet Sel Evol''. 2022 Jan 3; '''54''' (1):1
Accuracies of genomic predictions for disease resistance of striped catfish to Edwardsiella ictaluri using artificial intelligence algorithms. Description: Vu, Nguyen Thanh, et al. Accuracies of genomic predictions for disease resistance of striped catfish to Edwardsiella ictaluri using artificial intelligence algorithms. ''G3 (Bethesda)''. 2022 Jan 4; '''12''' (1):
Analysis of independent cohorts of outbred CFW mice reveals novel loci for behavioral and physiological traits and identifies factors determining reproducibility. Description: Zou, Jennifer, et al. Analysis of independent cohorts of outbred CFW mice reveals novel loci for behavioral and physiological traits and identifies factors determining reproducibility. ''G3 (Bethesda)''. 2022 Jan 4; '''12''' (1):
A chromosome-scale genome assembly for the holly (Ilex polyneura) provides insights into genomic adaptations to elevation in Southwest China. Description: Yao, Xin, et al. A chromosome-scale genome assembly for the holly (Ilex polyneura) provides insights into genomic adaptations to elevation in Southwest China. ''Hortic Res''. 2022 Jan 5; '''9''':
Genetic association of TMPRSS2 rs2070788 polymorphism with COVID-19 case fatality rate among Indian populations. Description: Pandey, Rudra Kumar, et al. Genetic association of TMPRSS2 rs2070788 polymorphism with COVID-19 case fatality rate among Indian populations. ''Infect Genet Evol''. 2022 Jan 5; '''98''': 105206
Fast estimation of genetic correlation for biobank-scale data. Description: Wu, Yue, et al. Fast estimation of genetic correlation for biobank-scale data. ''Am J Hum Genet''. 2022 Jan 6; '''109''' (1):24-32
Genetic architecture of gene regulation in Indonesian populations identifies QTLs associated with global and local ancestries. Description: Natri, Heini M, et al. Genetic architecture of gene regulation in Indonesian populations identifies QTLs associated with global and local ancestries. ''Am J Hum Genet''. 2022 Jan 6; '''109''' (1):50-65
Genome-wide association study identifies SNPs for growth performance and serum indicators in Valgus-varus deformity broilers (Gallus gallus) using ddGBS sequencing. Description: Guo, Yaping, et al. Genome-wide association study identifies SNPs for growth performance and serum indicators in Valgus-varus deformity broilers (Gallus gallus) using ddGBS sequencing. ''BMC Genomics''. 2022 Jan 6; '''23''' (1):26
Limb development genes underlie variation in human fingerprint patterns. Description: Li, Jinxi, et al. Limb development genes underlie variation in human fingerprint patterns. ''Cell''. 2022 Jan 6; '''185''' (1):95-112.e18
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. Description: Hindy, George, et al. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. ''Am J Hum Genet''. 2022 Jan 6; '''109''' (1):81-96
Ancient Demographics Determine the Effectiveness of Genetic Purging in Endangered Lizards. Description: Xie, Hong-Xin, et al. Ancient Demographics Determine the Effectiveness of Genetic Purging in Endangered Lizards. ''Mol Biol Evol''. 2022 Jan 7; '''39''' (1):
Dietary, Cultural, and Pathogens-Related Selective Pressures Shaped Differential Adaptive Evolution among Native Mexican Populations. Description: Ojeda-Granados, Claudia, et al. Dietary, Cultural, and Pathogens-Related Selective Pressures Shaped Differential Adaptive Evolution among Native Mexican Populations. ''Mol Biol Evol''. 2022 Jan 7; '''39''' (1):
Genome-wide association study identifies tumor anatomical site-specific risk variants for colorectal cancer survival. Description: Labadie, Julia D, et al. Genome-wide association study identifies tumor anatomical site-specific risk variants for colorectal cancer survival. ''Sci Rep''. 2022 Jan 7; '''12''' (1):127
Genomic Signatures of Sexual Selection on Pollen-Expressed Genes in Arabis alpina. Description: Gutierrez-Valencia, Juanita, et al. Genomic Signatures of Sexual Selection on Pollen-Expressed Genes in Arabis alpina. ''Mol Biol Evol''. 2022 Jan 7; '''39''' (1):
Homogeneity of Arabian Peninsula dromedary camel populations with signals of geographic distinction based on whole genome sequence data. Description: Bahbahani, Hussain, et al. Homogeneity of Arabian Peninsula dromedary camel populations with signals of geographic distinction based on whole genome sequence data. ''Sci Rep''. 2022 Jan 7; '''12''' (1):130
Insights into opium poppy (Papaver spp.) genetic diversity from genotyping-by-sequencing analysis. Description: Hong, Uyen Vu Thuy, et al. Insights into opium poppy (Papaver spp.) genetic diversity from genotyping-by-sequencing analysis. ''Sci Rep''. 2022 Jan 7; '''12''' (1):111
Island Biogeography Revisited: Museomics Reveals Affinities of Shelf Island Birds Determined by Bathymetry and Paleo-Rivers, Not by Distance to Mainland. Description: Garg, Kritika M, et al. Island Biogeography Revisited: Museomics Reveals Affinities of Shelf Island Birds Determined by Bathymetry and Paleo-Rivers, Not by Distance to Mainland. ''Mol Biol Evol''. 2022 Jan 7; '''39''' (1):
Landscape and Climatic Variations Shaped Secondary Contacts amid Barn Owls of the Western Palearctic. Description: Cumer, Tristan, et al. Landscape and Climatic Variations Shaped Secondary Contacts amid Barn Owls of the Western Palearctic. ''Mol Biol Evol''. 2022 Jan 7; '''39''' (1):
Polygenic risk, familial liability and stress reactivity in psychosis: an experience sampling study. Description: Schick, Anita, et al. Polygenic risk, familial liability and stress reactivity in psychosis: an experience sampling study. ''Psychol Med''. 2022 Jan 7; '''53''' (7):1-10
Population Genomics of Wall Lizards Reflects the Dynamic History of the Mediterranean Basin. Description: Yang, Weizhao, et al. Population Genomics of Wall Lizards Reflects the Dynamic History of the Mediterranean Basin. ''Mol Biol Evol''. 2022 Jan 7; '''39''' (1):
Population Histories and Genomic Diversity of South American Natives. Description: Castro E Silva, Marcos Araujo, et al. Population Histories and Genomic Diversity of South American Natives. ''Mol Biol Evol''. 2022 Jan 7; '''39''' (1):
TcoFBase: a comprehensive database for decoding the regulatory transcription co-factors in human and mouse. Description: Zhang, Yuexin, et al. TcoFBase: a comprehensive database for decoding the regulatory transcription co-factors in human and mouse. ''Nucleic Acids Res''. 2022 Jan 7; '''50''' (D1):D391-D401
A data-adaptive Bayesian regression approach for polygenic risk prediction. Description: Song, Shuang, et al. A data-adaptive Bayesian regression approach for polygenic risk prediction. ''Bioinformatics''. 2022 Jan 10;
Diverse effect of MC4R risk alleles on obesity-related traits over a lifetime: Evidence from a well-designed cohort study. Description: Moazzam-Jazi, Maryam, et al. Diverse effect of MC4R risk alleles on obesity-related traits over a lifetime: Evidence from a well-designed cohort study. ''Gene''. 2022 Jan 10; '''807''': 145950
Effective identification of varieties by nucleotide polymorphisms and its application for essentially derived variety identification in rice. Description: Yuan, Xiong, et al. Effective identification of varieties by nucleotide polymorphisms and its application for essentially derived variety identification in rice. ''BMC Bioinformatics''. 2022 Jan 10; '''23''' (1):30
Genome-wide association studies for immunoglobulin concentrations in colostrum and serum in Chinese Holstein. Description: Lin, Shan, et al. Genome-wide association studies for immunoglobulin concentrations in colostrum and serum in Chinese Holstein. ''BMC Genomics''. 2022 Jan 10; '''23''' (1):41
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Description: Scholz, Markus, et al. Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. ''Nat Commun''. 2022 Jan 10; '''13''' (1):143
Polygenic contribution to the relationship of loneliness and social isolation with schizophrenia. Description: Andreu-Bernabeu, Alvaro, et al. Polygenic contribution to the relationship of loneliness and social isolation with schizophrenia. ''Nat Commun''. 2022 Jan 10; '''13''' (1):51
The genome of oil-Camellia and population genomics analysis provide insights into seed oil domestication. Description: Lin, Ping, et al. The genome of oil-Camellia and population genomics analysis provide insights into seed oil domestication. ''Genome Biol''. 2022 Jan 10; '''23''' (1):14
Associations between genetic loci, environment factors and mental disorders: a genome-wide survival analysis using the UK Biobank data. Description: Meng, Peilin, et al. Associations between genetic loci, environment factors and mental disorders: a genome-wide survival analysis using the UK Biobank data. ''Transl Psychiatry''. 2022 Jan 11; '''12''' (1):17
DeepNull models non-linear covariate effects to improve phenotypic prediction and association power. Description: McCaw, Zachary R, et al. DeepNull models non-linear covariate effects to improve phenotypic prediction and association power. ''Nat Commun''. 2022 Jan 11; '''13''' (1):241
Germline HLA landscape does not predict efficacy of pembrolizumab monotherapy across solid tumor types. Description: Chhibber, Aparna, et al. Germline HLA landscape does not predict efficacy of pembrolizumab monotherapy across solid tumor types. ''Immunity''. 2022 Jan 11; '''55''' (1):56-64.e4
Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Description: Hysi, Pirro G, et al. Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. ''Metabolites''. 2022 Jan 11; '''12''' (1):
Signatures of selection in recently domesticated macadamia. Description: Lin, Jishan, et al. Signatures of selection in recently domesticated macadamia. ''Nat Commun''. 2022 Jan 11; '''13''' (1):242
Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank. Description: Dashti, Hassan S, et al. Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank. ''BMC Med''. 2022 Jan 12; '''20''' (1):5
The formation of avian montane diversity across barriers and along elevational gradients. Description: Pujolar, Jose Martin, et al. The formation of avian montane diversity across barriers and along elevational gradients. ''Nat Commun''. 2022 Jan 12; '''13''' (1):268
Genetic Factors Associated with Prostate Cancer Conversion from Active Surveillance to Treatment. Description: Jiang, Yu, et al. Genetic Factors Associated with Prostate Cancer Conversion from Active Surveillance to Treatment. ''HGG Adv''. 2022 Jan 13; '''3''' (1):
GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia. Description: Chong, Michael, et al. GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia. ''Elife''. 2022 Jan 13; '''11''':
Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide. Description: Stuart, Philip E, et al. Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide. ''HGG Adv''. 2022 Jan 13; '''3''' (1):
Signatures of selection underpinning rapid coral adaptation to the world's warmest reefs. Description: Smith, Edward G, et al. Signatures of selection underpinning rapid coral adaptation to the world's warmest reefs. ''Sci Adv''. 2022 Jan 14; '''8''' (2):eabl7287
Transcriptome and Metabolite Insights into Domestication Process of Cultivated Barley in China. Description: Zhou, Yu, et al. Transcriptome and Metabolite Insights into Domestication Process of Cultivated Barley in China. ''Plants (Basel)''. 2022 Jan 14; '''11''' (2):
Association of genetic variants in autophagy-lysosome pathway genes with susceptibility and survival to prostate cancer. Description: Zhu, Qiuyuan, et al. Association of genetic variants in autophagy-lysosome pathway genes with susceptibility and survival to prostate cancer. ''Gene''. 2022 Jan 15; '''808''': 145953
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis. Description: Mascia, E, et al. Burden of rare coding variants in an Italian cohort of familial multiple sclerosis. ''J Neuroimmunol''. 2022 Jan 15; '''362''': 577760
Genomic interrogation of a MAGIC population highlights genetic factors controlling fiber quality traits in cotton. Description: Wang, Maojun, et al. Genomic interrogation of a MAGIC population highlights genetic factors controlling fiber quality traits in cotton. ''Commun Biol''. 2022 Jan 17; '''5''' (1):60
Genome-wide association study identifies quantitative trait loci affecting cattle temperament. Description: Shen, Jia-Fei, et al. Genome-wide association study identifies quantitative trait loci affecting cattle temperament. ''Zool Res''. 2022 Jan 18; '''43''' (1):14-25
Mendelian randomisation analyses of UK Biobank and published data suggest that increased adiposity lowers risk of breast and prostate cancer. Description: Amin, Hasnat A, et al. Mendelian randomisation analyses of UK Biobank and published data suggest that increased adiposity lowers risk of breast and prostate cancer. ''Sci Rep''. 2022 Jan 18; '''12''' (1):909
Multiple haplotype-based analyses provide genetic and evolutionary insights into tomato fruit weight and composition. Description: Zhao, Jiantao, et al. Multiple haplotype-based analyses provide genetic and evolutionary insights into tomato fruit weight and composition. ''Hortic Res''. 2022 Jan 18;
A common variant in 11q23.3 associated with hyperlipidemia is mediated by the binding and regulation of GATA4. Description: Chou, Wen-Cheng, et al. A common variant in 11q23.3 associated with hyperlipidemia is mediated by the binding and regulation of GATA4. ''NPJ Genom Med''. 2022 Jan 19; '''7''' (1):4
Genome and transcriptome profiling of spontaneous preterm birth phenotypes. Description: Gupta, Juhi K, et al. Genome and transcriptome profiling of spontaneous preterm birth phenotypes. ''Sci Rep''. 2022 Jan 19; '''12''' (1):1003
Genomic population structure and local adaptation of the wild strawberry Fragaria nilgerrensis. Description: Hu, Yuxi, et al. Genomic population structure and local adaptation of the wild strawberry Fragaria nilgerrensis. ''Hortic Res''. 2022 Jan 19;
Variation of Positive Predictive Values of Fecal Immunochemical Tests by Polygenic Risk Score in a Large Screening Cohort. Description: Niedermaier, Tobias, et al. Variation of Positive Predictive Values of Fecal Immunochemical Tests by Polygenic Risk Score in a Large Screening Cohort. ''Clin Transl Gastroenterol''. 2022 Jan 19; '''13''' (3):e00458
Prediction of conserved and variable heat and cold stress response in maize using cis-regulatory information. Description: Zhou, Peng, et al. Prediction of conserved and variable heat and cold stress response in maize using cis-regulatory information. ''Plant Cell''. 2022 Jan 20; '''34''' (1):514-534
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. Description: Skoric-Milosavljevic, Doris, et al. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. ''Circ Res''. 2022 Jan 21; '''130''' (2):166-180
Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia. Description: Vassos, Evangelos, et al. Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia. ''Schizophr Bull''. 2022 Jan 21; '''48''' (1):20-26
Tissue-specific multi-omics analysis of atrial fibrillation. Description: Assum, Ines, et al. Tissue-specific multi-omics analysis of atrial fibrillation. ''Nat Commun''. 2022 Jan 21; '''13''' (1):441
A single-nucleotide mutation within the TBX3 enhancer increased body size in Chinese horses. Description: Liu, Xuexue, et al. A single-nucleotide mutation within the TBX3 enhancer increased body size in Chinese horses. ''Curr Biol''. 2022 Jan 24; '''32''' (2):480-487.e6
Massive genome inversion drives coexistence of divergent morphs in common quails. Description: Sanchez-Donoso, Ines, et al. Massive genome inversion drives coexistence of divergent morphs in common quails. ''Curr Biol''. 2022 Jan 24; '''32''' (2):462-469.e6
A genome-wide association study of serum proteins reveals shared loci with common diseases. Description: Gudjonsson, Alexander, et al. A genome-wide association study of serum proteins reveals shared loci with common diseases. ''Nat Commun''. 2022 Jan 25; '''13''' (1):480
GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion. Description: Kasai, Mariko, et al. GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion. ''Sci Rep''. 2022 Jan 25; '''12''' (1):1332
Variability in newborn telomere length is explained by inheritance and intrauterine environment. Description: Chen, Li, et al. Variability in newborn telomere length is explained by inheritance and intrauterine environment. ''BMC Med''. 2022 Jan 25; '''20''' (1):20
Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations. Description: Sadler, Brooke, et al. Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations. ''Blood Adv''. 2022 Jan 25; '''6''' (2):420-428
An unbiased test reveals no enrichment of sexually antagonistic polymorphisms on the human X chromosome. Description: Ruzicka, Filip, et al. An unbiased test reveals no enrichment of sexually antagonistic polymorphisms on the human X chromosome. ''Proc Biol Sci''. 2022 Jan 26; '''289''' (1967):20212314
Immune marker levels in severe mental disorders: associations with polygenic risk scores of related mental phenotypes and psoriasis. Description: Werner, Maren Caroline Frogner, et al. Immune marker levels in severe mental disorders: associations with polygenic risk scores of related mental phenotypes and psoriasis. ''Transl Psychiatry''. 2022 Jan 26; '''12''' (1):38
Polygenic risk and causal inference of psychiatric comorbidity in inflammatory bowel disease among patients with European ancestry. Description: Li, Yao, et al. Polygenic risk and causal inference of psychiatric comorbidity in inflammatory bowel disease among patients with European ancestry. ''J Transl Med''. 2022 Jan 27; '''20''' (1):43
Population structure analysis to explore genetic diversity and geographical distribution characteristics of cultivated-type tea plant in Guizhou Plateau. Description: Zhao, Zhifei, et al. Population structure analysis to explore genetic diversity and geographical distribution characteristics of cultivated-type tea plant in Guizhou Plateau. ''BMC Plant Biol''. 2022 Jan 27; '''22''' (1):55
Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Description: Lee, Brian, et al. Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. ''BMC Genomics''. 2022 Jan 28; '''23''' (1):85
Sex, age, and ethnic dependency of lipoprotein variants as the risk factors of ischemic heart disease: a detailed study on the different age-classes and genders in Tehran Cardiometabolic Genetic Study (TCGS). Description: Lanjanian, Hossein, et al. Sex, age, and ethnic dependency of lipoprotein variants as the risk factors of ischemic heart disease: a detailed study on the different age-classes and genders in Tehran Cardiometabolic Genetic Study (TCGS). ''Biol Sex Differ''. 2022 Jan 28; '''13''' (1):4
A framework for research into continental ancestry groups of the UK Biobank. Description: Constantinescu, Andrei-Emil, et al. A framework for research into continental ancestry groups of the UK Biobank. ''Hum Genomics''. 2022 Jan 29; '''16''' (1):3
Genetic characterization evaluation of a novel multiple system containing 57 deletion/insertion polymorphic loci with short amplicons in Hunan Han population and its intercontinental populations analyses. Description: Fang, Yating, et al. Genetic characterization evaluation of a novel multiple system containing 57 deletion/insertion polymorphic loci with short amplicons in Hunan Han population and its intercontinental populations analyses. ''Gene''. 2022 Jan 30; '''809''': 146006
Genetic variants in splicing factor genes and susceptibility to bladder cancer. Description: Wang, Xi, et al. Genetic variants in splicing factor genes and susceptibility to bladder cancer. ''Gene''. 2022 Jan 30; '''809''': 146022
Multilocus evaluation of genetic predictors of multiple sclerosis. Description: Timasheva, Yanina, et al. Multilocus evaluation of genetic predictors of multiple sclerosis. ''Gene''. 2022 Jan 30; '''809''': 146008
Gene-gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer. Description: Rosenberger, Albert, et al. Gene-gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer. ''Eur J Med Res''. 2022 Jan 31; '''27''' (1):14
Genome-wide run of homozygosity analysis reveals candidate genomic regions associated with environmental adaptations of Tibetan native chickens. Description: Yuan, Jingwei, et al. Genome-wide run of homozygosity analysis reveals candidate genomic regions associated with environmental adaptations of Tibetan native chickens. ''BMC Genomics''. 2022 Jan 31; '''23''' (1):91
Investigating the effect of sexual behaviour on oropharyngeal cancer risk: a methodological assessment of Mendelian randomization. Description: Gormley, Mark, et al. Investigating the effect of sexual behaviour on oropharyngeal cancer risk: a methodological assessment of Mendelian randomization. ''BMC Med''. 2022 Jan 31; '''20''' (1):40
Allele imputation for the killer cell immunoglobulin-like receptor KIR3DL1/S1. Description: Harrison, Genelle F, et al. Allele imputation for the killer cell immunoglobulin-like receptor KIR3DL1/S1. ''PLoS Comput Biol''. 2022 Feb; '''18''' (2):e1009059
Associations between AGT, MTHFR, and VEGF gene polymorphisms and preeclampsia in the Chinese population. Description: Ding, Guifeng, et al. Associations between AGT, MTHFR, and VEGF gene polymorphisms and preeclampsia in the Chinese population. ''Placenta''. 2022 Feb; '''118''': 38-45
Associations of circulating C-reactive proteins, APOE epsilon4, and brain markers for Alzheimer's disease in healthy samples across the lifespan. Description: Wang, Yunpeng, et al. Associations of circulating C-reactive proteins, APOE epsilon4, and brain markers for Alzheimer's disease in healthy samples across the lifespan. ''Brain Behav Immun''. 2022 Feb; '''100''': 243-253
A transcriptome-based association study of growth, wood quality, and oleoresin traits in a slash pine breeding population. Description: Ding, Xianyin, et al. A transcriptome-based association study of growth, wood quality, and oleoresin traits in a slash pine breeding population. ''PLoS Genet''. 2022 Feb; '''18''' (2):e1010017
Clinical Relevance of Gastroesophageal Cancer Associated SNPs for Oncologic Outcome After Curative Surgery. Description: Jung, Jin-On, et al. Clinical Relevance of Gastroesophageal Cancer Associated SNPs for Oncologic Outcome After Curative Surgery. ''Ann Surg Oncol''. 2022 Feb; '''29''' (2):1453-1462
CREBRF missense variant rs373863828 has both direct and indirect effects on type 2 diabetes and fasting glucose in Polynesian peoples living in Samoa and Aotearoa New Zealand. Description: Russell, Emily M, et al. CREBRF missense variant rs373863828 has both direct and indirect effects on type 2 diabetes and fasting glucose in Polynesian peoples living in Samoa and Aotearoa New Zealand. ''BMJ Open Diabetes Res Care''. 2022 Feb; '''10''' (1):
Detection of candidate gene networks involved in resistance to Sclerotinia sclerotiorum in soybean. Description: Zhang, Yu, et al. Detection of candidate gene networks involved in resistance to Sclerotinia sclerotiorum in soybean. ''J Appl Genet''. 2022 Feb; '''63''' (1):1-14
Exploring the causal effect of maternal pregnancy adiposity on offspring adiposity: Mendelian randomisation using polygenic risk scores. Description: Bond, Tom A, et al. Exploring the causal effect of maternal pregnancy adiposity on offspring adiposity: Mendelian randomisation using polygenic risk scores. ''BMC Med''. 2022 Feb 1; '''20''' (1):34
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy. Description: Spielmann, Nadine, et al. Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy. ''Nat Cardiovasc Res''. 2022 Feb; '''1''' (2):157-173
Genetic association analysis between IL9 and coronary artery disease in a Chinese Han population. Description: Zha, Lingfeng, et al. Genetic association analysis between IL9 and coronary artery disease in a Chinese Han population. ''Cytokine''. 2022 Feb; '''150''': 155761
Genetic polymorphisms in ADRB2 and ADRB1 are associated with differential survival in heart failure patients taking beta-blockers. Description: Guerra, Leonardo A, et al. Genetic polymorphisms in ADRB2 and ADRB1 are associated with differential survival in heart failure patients taking beta-blockers. ''Pharmacogenomics J''. 2022 Feb; '''22''' (1):62-68
Genetic risk for the polycystic ovary syndrome, bone mineral density and fractures in women and men: A UK Biobank Mendelian randomisation study. Description: Deshmukh, Harshal, et al. Genetic risk for the polycystic ovary syndrome, bone mineral density and fractures in women and men: A UK Biobank Mendelian randomisation study. ''Bone''. 2022 Feb; '''155''': 116285
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. Description: Hautakangas, Heidi, et al. Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. ''Nat Genet''. 2022 Feb; '''54''' (2):152-160
Genomewide association analysis of warfarin dose requirements in Middle Eastern and North African populations. Description: El Rouby, Nihal, et al. Genomewide association analysis of warfarin dose requirements in Middle Eastern and North African populations. ''Clin Transl Sci''. 2022 Feb; '''15''' (2):558-566
Genome-wide association of individual vulnerability with alcohol-associated liver disease: A Korean genome and epidemiology study. Description: Kim, Kwang Yoon, et al. Genome-wide association of individual vulnerability with alcohol-associated liver disease: A Korean genome and epidemiology study. ''Hepatology''. 2022 Feb; '''75''' (2):391-402
Genomic predictors of testosterone levels are associated with muscle fiber size and strength. Description: Guilherme, Joao Paulo L F, et al. Genomic predictors of testosterone levels are associated with muscle fiber size and strength. ''Eur J Appl Physiol''. 2022 Feb; '''122''' (2):415-423
Identification of genomic loci regulating grain iron content in aus rice under two irrigation management systems. Description: Talukdar, Partha, et al. Identification of genomic loci regulating grain iron content in aus rice under two irrigation management systems. ''Food Energy Secur''. 2022 Feb; '''11''' (1):e329
Intraspecific independent evolution of floral spur length in response to local flower visitor size in Japanese Aquilegia in different mountain regions. Description: Toji, Tsubasa, et al. Intraspecific independent evolution of floral spur length in response to local flower visitor size in Japanese Aquilegia in different mountain regions. ''Ecol Evol''. 2022 Feb; '''12''' (3):e8668
Large-scale deep multi-layer analysis of Alzheimer's disease brain reveals strong proteomic disease-related changes not observed at the RNA level. Description: Johnson, Erik C B, et al. Large-scale deep multi-layer analysis of Alzheimer's disease brain reveals strong proteomic disease-related changes not observed at the RNA level. ''Nat Neurosci''. 2022 Feb; '''25''' (2):213-225
Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease. Description: Jiang, Li, et al. Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease. ''Neurobiol Aging''. 2022 Feb; '''110''': 106-112
Mapping of novel loci involved in lung and colon tumor susceptibility by the use of genetically selected mouse strains. Description: Borrego, Andrea, et al. Mapping of novel loci involved in lung and colon tumor susceptibility by the use of genetically selected mouse strains. ''Genes Immun''. 2022 Feb; '''23''' (1):23-32
Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19. Description: Huffman, Jennifer E, et al. Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19. ''Nat Genet''. 2022 Feb; '''54''' (2):125-127
Novel role for caspase recruitment domain family member 14 and its genetic variant rs11652075 in skin filaggrin homeostasis. Description: DeVore, Stanley B, et al. Novel role for caspase recruitment domain family member 14 and its genetic variant rs11652075 in skin filaggrin homeostasis. ''J Allergy Clin Immunol''. 2022 Feb; '''149''' (2):708-717
Potential role for immune-related genes in autism spectrum disorders: Evidence from genome-wide association meta-analysis of autistic traits. Description: Arenella, Martina, et al. Potential role for immune-related genes in autism spectrum disorders: Evidence from genome-wide association meta-analysis of autistic traits. ''Autism''. 2022 Feb; '''26''' (2):361-372
Regulatory Variant rs2535629 in ITIH3 Intron Confers Schizophrenia Risk By Regulating CTCF Binding and SFMBT1 Expression. Description: Li, Yifan, et al. Regulatory Variant rs2535629 in ITIH3 Intron Confers Schizophrenia Risk By Regulating CTCF Binding and SFMBT1 Expression. ''Adv Sci (Weinh)''. 2022 Feb; '''9''' (6):e2104786
Resequencing 250 Soybean Accessions: New Insights into Genes Associated with Agronomic Traits and Genetic Networks. Description: Yang, Chunming, et al. Resequencing 250 Soybean Accessions: New Insights into Genes Associated with Agronomic Traits and Genetic Networks. ''Genomics Proteomics Bioinformatics''. 2022 Feb; '''20''' (1):29-41
Resequencing of 301 ramie accessions identifies genetic loci and breeding selection for fibre yield traits. Description: Zeng, Zheng, et al. Resequencing of 301 ramie accessions identifies genetic loci and breeding selection for fibre yield traits. ''Plant Biotechnol J''. 2022 Feb; '''20''' (2):323-334
The DNA methylome of cervical cells can predict the presence of ovarian cancer. Description: Barrett, James E, et al. The DNA methylome of cervical cells can predict the presence of ovarian cancer. ''Nat Commun''. 2022 Feb 1; '''13''' (1):448
The polymorphisms of extracellular matrix-remodeling genes are associated with pelvic organ prolapse. Description: Li, Lei, et al. The polymorphisms of extracellular matrix-remodeling genes are associated with pelvic organ prolapse. ''Int Urogynecol J''. 2022 Feb; '''33''' (2):267-274
The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples. Description: Barrett, James E, et al. The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples. ''Nat Commun''. 2022 Feb 1; '''13''' (1):449
Approximate Bayesian Computation Untangles Signatures of Contemporary and Historical Hybridization between Two Endangered Species. Description: Dittberner, Hannes, et al. Approximate Bayesian Computation Untangles Signatures of Contemporary and Historical Hybridization between Two Endangered Species. ''Mol Biol Evol''. 2022 Feb 3; '''39''' (2):
Assortative mating biases marker-based heritability estimators. Description: Border, Richard, et al. Assortative mating biases marker-based heritability estimators. ''Nat Commun''. 2022 Feb 3; '''13''' (1):660
Chromosomal Fusions Facilitate Adaptation to Divergent Environments in Threespine Stickleback. Description: Liu, Zuyao, et al. Chromosomal Fusions Facilitate Adaptation to Divergent Environments in Threespine Stickleback. ''Mol Biol Evol''. 2022 Feb 3; '''39''' (2):
Demographic History and Natural Selection Shape Patterns of Deleterious Mutation Load and Barriers to Introgression across Populus Genome. Description: Liu, Shuyu, et al. Demographic History and Natural Selection Shape Patterns of Deleterious Mutation Load and Barriers to Introgression across Populus Genome. ''Mol Biol Evol''. 2022 Feb 3; '''39''' (2):
Dissecting the genetic architecture of suicide attempt and repeated attempts in Korean patients with bipolar disorder using polygenic risk scores. Description: Lee, Dongbin, et al. Dissecting the genetic architecture of suicide attempt and repeated attempts in Korean patients with bipolar disorder using polygenic risk scores. ''Int J Bipolar Disord''. 2022 Feb 3; '''10''' (1):3
Dissecting the molecular basis of human interneuron migration in forebrain assembloids from Timothy syndrome. Description: Birey, Fikri, et al. Dissecting the molecular basis of human interneuron migration in forebrain assembloids from Timothy syndrome. ''Cell Stem Cell''. 2022 Feb 3; '''29''' (2):248-264.e7
First genome-wide association study investigating blood pressure and renal traits in domestic cats. Description: Jepson, R E, et al. First genome-wide association study investigating blood pressure and renal traits in domestic cats. ''Sci Rep''. 2022 Feb 3; '''12''' (1):1899
Genetic Connections and Convergent Evolution of Tropical Indigenous Peoples in Asia. Description: Deng, Lian, et al. Genetic Connections and Convergent Evolution of Tropical Indigenous Peoples in Asia. ''Mol Biol Evol''. 2022 Feb 3; '''39''' (2):
Genomic insights into the evolution of Echinochloa species as weed and orphan crop. Description: Wu, Dongya, et al. Genomic insights into the evolution of Echinochloa species as weed and orphan crop. ''Nat Commun''. 2022 Feb 3; '''13''' (1):689
Graph-based pan-genome reveals structural and sequence variations related to agronomic traits and domestication in cucumber. Description: Li, Hongbo, et al. Graph-based pan-genome reveals structural and sequence variations related to agronomic traits and domestication in cucumber. ''Nat Commun''. 2022 Feb 3; '''13''' (1):682
Harnessing tissue-specific genetic variation to dissect putative causal pathways between body mass index and cardiometabolic phenotypes. Description: Leyden, Genevieve M, et al. Harnessing tissue-specific genetic variation to dissect putative causal pathways between body mass index and cardiometabolic phenotypes. ''Am J Hum Genet''. 2022 Feb 3; '''109''' (2):240-252
The Genetic Origin of Daunians and the Pan-Mediterranean Southern Italian Iron Age Context. Description: Aneli, Serena, et al. The Genetic Origin of Daunians and the Pan-Mediterranean Southern Italian Iron Age Context. ''Mol Biol Evol''. 2022 Feb 3; '''39''' (2):
Tracing the Origin and Evolutionary Fate of Recent Gene Retrocopies in Natural Populations of the House Mouse. Description: Zhang, Wenyu, et al. Tracing the Origin and Evolutionary Fate of Recent Gene Retrocopies in Natural Populations of the House Mouse. ''Mol Biol Evol''. 2022 Feb 3; '''39''' (2):
Whole-Genome Resequencing of Worldwide Wild and Domestic Sheep Elucidates Genetic Diversity, Introgression, and Agronomically Important Loci. Description: Lv, Feng-Hua, et al. Whole-Genome Resequencing of Worldwide Wild and Domestic Sheep Elucidates Genetic Diversity, Introgression, and Agronomically Important Loci. ''Mol Biol Evol''. 2022 Feb 3; '''39''' (2):
ABHD5 frameshift deletion in Golden Retrievers with ichthyosis. Description: Kiener, Sarah, et al. ABHD5 frameshift deletion in Golden Retrievers with ichthyosis. ''G3 (Bethesda)''. 2022 Feb 4; '''12''' (2):
Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping. Description: Belloy, Michael E, et al. Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping. ''Alzheimers Res Ther''. 2022 Feb 4; '''14''' (1):22
Comparison of mixed model based approaches for correcting for population substructure with application to extreme phenotype sampling. Description: Onifade, Maryam, et al. Comparison of mixed model based approaches for correcting for population substructure with application to extreme phenotype sampling. ''BMC Genomics''. 2022 Feb 4; '''23''' (1):98
Development of the Wheat Practical Haplotype Graph database as a resource for genotyping data storage and genotype imputation. Description: Jordan, Katherine W, et al. Development of the Wheat Practical Haplotype Graph database as a resource for genotyping data storage and genotype imputation. ''G3 (Bethesda)''. 2022 Feb 4; '''12''' (2):
Interpretable network-guided epistasis detection. Description: Duroux, Diane, et al. Interpretable network-guided epistasis detection. ''Gigascience''. 2022 Feb 4; '''11''':
The highly continuous reference genome of a leaf-chimeric red pineapple (Ananas comosus var. bracteatus f. tricolor) provides insights into elaboration of leaf color. Description: Feng, Lijun, et al. The highly continuous reference genome of a leaf-chimeric red pineapple (Ananas comosus var. bracteatus f. tricolor) provides insights into elaboration of leaf color. ''G3 (Bethesda)''. 2022 Feb 4; '''12''' (2):
The rs1458038 variant near FGF5 is associated with poor response to calcium channel blockers among Filipinos. Description: Punzalan, Felix Eduardo R, et al. The rs1458038 variant near FGF5 is associated with poor response to calcium channel blockers among Filipinos. ''Medicine (Baltimore)''. 2022 Feb 4; '''101''' (5):e28703
Trend, population structure, and trait mapping from 15 years of national varietal trials of UK winter wheat. Description: Shorinola, Oluwaseyi, et al. Trend, population structure, and trait mapping from 15 years of national varietal trials of UK winter wheat. ''G3 (Bethesda)''. 2022 Feb 4; '''12''' (2):
Epigenetically-regulated RPN2 gene influences lymphocyte activation and is involved in pathogenesis of rheumatoid arthritis. Description: He, Pei, et al. Epigenetically-regulated RPN2 gene influences lymphocyte activation and is involved in pathogenesis of rheumatoid arthritis. ''Gene''. 2022 Feb 5; '''810''': 146059
Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. Description: Mitchell, Brittany L, et al. Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. ''Nat Commun''. 2022 Feb 7; '''13''' (1):702
Integration of genomics, transcriptomics and metabolomics identifies candidate loci underlying fruit weight in loquat. Description: Peng, Ze, et al. Integration of genomics, transcriptomics and metabolomics identifies candidate loci underlying fruit weight in loquat. ''Hortic Res''. 2022 Feb 7;
ATAD3B and SKIL polymorphisms associated with antipsychotic-induced QTc interval change in patients with schizophrenia: a genome-wide association study. Description: Lu, Zhe, et al. ATAD3B and SKIL polymorphisms associated with antipsychotic-induced QTc interval change in patients with schizophrenia: a genome-wide association study. ''Transl Psychiatry''. 2022 Feb 8; '''12''' (1):56
Transcriptome-wide changes in gene expression, splicing, and lncRNAs in response to a live attenuated dengue virus vaccine. Description: Kim, Eun-Young, et al. Transcriptome-wide changes in gene expression, splicing, and lncRNAs in response to a live attenuated dengue virus vaccine. ''Cell Rep''. 2022 Feb 8; '''38''' (6):110341
Antioxidative Defense Genes and Brain Structure in Youth Bipolar Disorder. Description: Zou, Yi, et al. Antioxidative Defense Genes and Brain Structure in Youth Bipolar Disorder. ''Int J Neuropsychopharmacol''. 2022 Feb 11; '''25''' (2):89-98
Genomic correlation, shared loci, and causal relationship between obesity and polycystic ovary syndrome: a large-scale genome-wide cross-trait analysis. Description: Liu, Qianwen, et al. Genomic correlation, shared loci, and causal relationship between obesity and polycystic ovary syndrome: a large-scale genome-wide cross-trait analysis. ''BMC Med''. 2022 Feb 11; '''20''' (1):66
Genomic variants affecting homoeologous gene expression dosage contribute to agronomic trait variation in allopolyploid wheat. Description: He, Fei, et al. Genomic variants affecting homoeologous gene expression dosage contribute to agronomic trait variation in allopolyploid wheat. ''Nat Commun''. 2022 Feb 11; '''13''' (1):826
Somatic mutational profiles and germline polygenic risk scores in human cancer. Description: Liu, Yuxi, et al. Somatic mutational profiles and germline polygenic risk scores in human cancer. ''Genome Med''. 2022 Feb 11; '''14''' (1):14
Gene-Interaction-Sensitive enrichment analysis in congenital heart disease. Description: Woodward, Alexa A, et al. Gene-Interaction-Sensitive enrichment analysis in congenital heart disease. ''BioData Min''. 2022 Feb 12; '''15''' (1):4
Interaction between a diabetes-related methylation site (TXNIP cg19693031) and variant (GLUT1 rs841853) on fasting blood glucose levels among non-diabetics. Description: Tsai, Hao-Hung, et al. Interaction between a diabetes-related methylation site (TXNIP cg19693031) and variant (GLUT1 rs841853) on fasting blood glucose levels among non-diabetics. ''J Transl Med''. 2022 Feb 14; '''20''' (1):87
A population study of clinically actionable genetic variation affecting drug response from the Middle East. Description: Jithesh, Puthen Veettil, et al. A population study of clinically actionable genetic variation affecting drug response from the Middle East. ''NPJ Genom Med''. 2022 Feb 15; '''7''' (1):10
Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants. Description: Chen, Rui, et al. Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants. ''BMC Med''. 2022 Feb 16; '''20''' (1):68
Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism. Description: Zhu, Yihui, et al. Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism. ''Genome Biol''. 2022 Feb 16; '''23''' (1):46
Polygenic association with severity and long-term outcome in eating disorder cases. Description: Johansson, Therese, et al. Polygenic association with severity and long-term outcome in eating disorder cases. ''Transl Psychiatry''. 2022 Feb 16; '''12''' (1):61
Epigenome-wide association study of posttraumatic stress disorder identifies novel loci in U.S. military veterans. Description: Montalvo-Ortiz, Janitza L, et al. Epigenome-wide association study of posttraumatic stress disorder identifies novel loci in U.S. military veterans. ''Transl Psychiatry''. 2022 Feb 17; '''12''' (1):65
Integrating single-cell sequencing data with GWAS summary statistics reveals CD16+monocytes and memory CD8+T cells involved in severe COVID-19. Description: Ma, Yunlong, et al. Integrating single-cell sequencing data with GWAS summary statistics reveals CD16+monocytes and memory CD8+T cells involved in severe COVID-19. ''Genome Med''. 2022 Feb 17; '''14''' (1):16
Population genomics of Zea species identifies selection signatures during maize domestication and adaptation. Description: Xu, Gen, et al. Population genomics of Zea species identifies selection signatures during maize domestication and adaptation. ''BMC Plant Biol''. 2022 Feb 18; '''22''' (1):72
Functionally prioritised whole-genome sequence variants improve the accuracy of genomic prediction for heat tolerance. Description: Cheruiyot, Evans K, et al. Functionally prioritised whole-genome sequence variants improve the accuracy of genomic prediction for heat tolerance. ''Genet Sel Evol''. 2022 Feb 19; '''54''' (1):17
Genomic insights into longan evolution from a chromosome-level genome assembly and population genomics of longan accessions. Description: Wang, Jing, et al. Genomic insights into longan evolution from a chromosome-level genome assembly and population genomics of longan accessions. ''Hortic Res''. 2022 Feb 19;
GWAS and genomic prediction of milk urea nitrogen in Australian and New Zealand dairy cattle. Description: van den Berg, Irene, et al. GWAS and genomic prediction of milk urea nitrogen in Australian and New Zealand dairy cattle. ''Genet Sel Evol''. 2022 Feb 19; '''54''' (1):15
Quantitative multidimensional phenotypes improve genetic analysis of laterality traits. Description: Schmitz, Judith, et al. Quantitative multidimensional phenotypes improve genetic analysis of laterality traits. ''Transl Psychiatry''. 2022 Feb 19; '''12''' (1):68
Rare coding variants in RCN3 are associated with blood pressure. Description: He, Karen Y, et al. Rare coding variants in RCN3 are associated with blood pressure. ''BMC Genomics''. 2022 Feb 19; '''23''' (1):148
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants. Description: Tuncay, Islam Oguz, et al. Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants. ''NPJ Genom Med''. 2022 Feb 21; '''7''' (1):13
Environmentally sensitive hotspots in the methylome of the early human embryo. Description: Silver, Matt J, et al. Environmentally sensitive hotspots in the methylome of the early human embryo. ''Elife''. 2022 Feb 21; '''11''':
Genomic characterization of the world's longest selection experiment in mouse reveals the complexity of polygenic traits. Description: Palma-Vera, Sergio E, et al. Genomic characterization of the world's longest selection experiment in mouse reveals the complexity of polygenic traits. ''BMC Biol''. 2022 Feb 21; '''20''' (1):52
The Medaka Inbred Kiyosu-Karlsruhe (MIKK) panel. Description: Fitzgerald, Tomas, et al. The Medaka Inbred Kiyosu-Karlsruhe (MIKK) panel. ''Genome Biol''. 2022 Feb 21; '''23''' (1):59
Polympact: exploring functional relations among common human genetic variants. Description: Valentini, Samuel, et al. Polympact: exploring functional relations among common human genetic variants. ''Nucleic Acids Res''. 2022 Feb 22; '''50''' (3):1335-1350
Association of social isolation, loneliness and genetic risk with incidence of dementia: UK Biobank Cohort Study. Description: Elovainio, Marko, et al. Association of social isolation, loneliness and genetic risk with incidence of dementia: UK Biobank Cohort Study. ''BMJ Open''. 2022 Feb 23; '''12''' (2):e053936
Combined use of Oxford Nanopore and Illumina sequencing yields insights into soybean structural variation biology. Description: Lemay, Marc-Andre, et al. Combined use of Oxford Nanopore and Illumina sequencing yields insights into soybean structural variation biology. ''BMC Biol''. 2022 Feb 23; '''20''' (1):53
High polygenic predisposition for ADHD and a greater risk of all-cause mortality: a large population-based longitudinal study. Description: Ajnakina, Olesya, et al. High polygenic predisposition for ADHD and a greater risk of all-cause mortality: a large population-based longitudinal study. ''BMC Med''. 2022 Feb 23; '''20''' (1):62
Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes. Description: Tamlander, Max, et al. Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes. ''Commun Biol''. 2022 Feb 23; '''5''' (1):158
MIG-seq is an effective method for high-throughput genotyping in wheat (Triticum spp.). Description: Nishimura, Kazusa, et al. MIG-seq is an effective method for high-throughput genotyping in wheat (Triticum spp.). ''DNA Res''. 2022 Feb 27; '''29''' (2):
Genome variation in tick infestation and cryptic divergence in Tunisian indigenous sheep. Description: Ahbara, Abulgasim M, et al. Genome variation in tick infestation and cryptic divergence in Tunisian indigenous sheep. ''BMC Genomics''. 2022 Feb 28; '''23''' (1):167
Natural and human-driven selection of a single non-coding body size variant in ancient and modern canids. Description: Plassais, Jocelyn, et al. Natural and human-driven selection of a single non-coding body size variant in ancient and modern canids. ''Curr Biol''. 2022 Feb 28; '''32''' (4):889-897.e9
A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci. Description: Chang, Xiao, et al. A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci. ''J Allergy Clin Immunol''. 2022 Mar; '''149''' (3):988-998
Amygdala and anterior cingulate transcriptomes from individuals with bipolar disorder reveal downregulated neuroimmune and synaptic pathways. Description: Zandi, Peter P, et al. Amygdala and anterior cingulate transcriptomes from individuals with bipolar disorder reveal downregulated neuroimmune and synaptic pathways. ''Nat Neurosci''. 2022 Mar; '''25''' (3):381-389
An integrative genomics approach identifies KDM4 as a modulator of trained immunity. Description: Moorlag, Simone J C F M, et al. An integrative genomics approach identifies KDM4 as a modulator of trained immunity. ''Eur J Immunol''. 2022 Mar; '''52''' (3):431-446
Antipsychotic medication-mediated cognitive change in schizophrenia and polygenic score for cognitive ability. Description: Blackman, Rachael K, et al. Antipsychotic medication-mediated cognitive change in schizophrenia and polygenic score for cognitive ability. ''Schizophr Res Cogn''. 2022 Mar; '''27''': 100223
Association between WWOX/MAF variants and dementia-related neuropathologic endophenotypes. Description: Dugan, Adam J, et al. Association between WWOX/MAF variants and dementia-related neuropathologic endophenotypes. ''Neurobiol Aging''. 2022 Mar; '''111''': 95-106
Association of FAAH p.Pro129Thr and COMT p.Ala72Ser with schizophrenia and comorbid substance use through next-generation sequencing: an exploratory analysis. Description: Martinez-Magana, Jose J, et al. Association of FAAH p.Pro129Thr and COMT p.Ala72Ser with schizophrenia and comorbid substance use through next-generation sequencing: an exploratory analysis. ''Braz J Psychiatry''. 2022 Mar-Abr; '''44''' (2):164-170
Association of Habitual Alcohol Intake With Risk of Cardiovascular Disease. Description: Biddinger, Kiran J, et al. Association of Habitual Alcohol Intake With Risk of Cardiovascular Disease. ''JAMA Netw Open''. 2022 Mar 1; '''5''' (3):e223849
A tool for translating polygenic scores onto the absolute scale using summary statistics. Description: Pain, Oliver, et al. A tool for translating polygenic scores onto the absolute scale using summary statistics. ''Eur J Hum Genet''. 2022 Mar; '''30''' (3):339-348
Comparative genomics and selection analysis of Yeonsan Ogye black chicken with whole-genome sequencing. Description: Cho, Youngbeom, et al. Comparative genomics and selection analysis of Yeonsan Ogye black chicken with whole-genome sequencing. ''Genomics''. 2022 Mar; '''114''' (2):110298
Different genes may be involved in distal and local sensitization: A genome-wide gene-based association study and meta-analysis. Description: Kouraki, Afroditi, et al. Different genes may be involved in distal and local sensitization: A genome-wide gene-based association study and meta-analysis. ''Eur J Pain''. 2022 Mar; '''26''' (3):740-753
Evaluation of the EMPAR study population on the basis of metabolic phenotypes of selected pharmacogenes. Description: Fracowiak, Jochen, et al. Evaluation of the EMPAR study population on the basis of metabolic phenotypes of selected pharmacogenes. ''Pharmacogenomics J''. 2022 Mar; '''22''' (2):136-144
Expanding the environmental scope: an environment-wide association study for mental well-being. Description: van de Weijer, Margot P, et al. Expanding the environmental scope: an environment-wide association study for mental well-being. ''J Expo Sci Environ Epidemiol''. 2022 Mar; '''32''' (2):195-204
From Mendel laws to whole genetic association study to decipher the swine mulefoot phenotype. Description: Facioli, Fernanda Luiza, et al. From Mendel laws to whole genetic association study to decipher the swine mulefoot phenotype. ''Res Vet Sci''. 2022 Mar; '''143''': 58-65
Functional noncoding SNPs in human endothelial cells fine-map vascular trait associations. Description: Toropainen, Anu, et al. Functional noncoding SNPs in human endothelial cells fine-map vascular trait associations. ''Genome Res''. 2022 Mar; '''32''' (3):409-424
Genetic Risk for Smoking: Disentangling Interplay Between Genes and Socioeconomic Status. Description: Pasman, Joelle A, et al. Genetic Risk for Smoking: Disentangling Interplay Between Genes and Socioeconomic Status. ''Behav Genet''. 2022 Mar; '''52''' (2):92-107
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A. Description: Spena, Silvia, et al. Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A. ''Haemophilia''. 2022 Mar; '''28''' (2):270-277
Genomic consequences of colonisation, migration and genetic drift in barn owl insular populations of the eastern Mediterranean. Description: Machado, Ana Paula, et al. Genomic consequences of colonisation, migration and genetic drift in barn owl insular populations of the eastern Mediterranean. ''Mol Ecol''. 2022 Mar; '''31''' (5):1375-1388
Genomic regions controlling yield-related traits in spring wheat: a mini review and a case study for rainfed environments in Australia and China. Description: Liu, Hui, et al. Genomic regions controlling yield-related traits in spring wheat: a mini review and a case study for rainfed environments in Australia and China. ''Genomics''. 2022 Mar; '''114''' (2):110268
Genotyping by sequencing suggests overwintering of Peronospora destructor in southwestern Quebec, Canada. Description: Van der Heyden, Herve, et al. Genotyping by sequencing suggests overwintering of Peronospora destructor in southwestern Quebec, Canada. ''Mol Plant Pathol''. 2022 Mar; '''23''' (3):339-354
GWAS in people of Middle Eastern descent reveals a locus protective of kidney function-a cross-sectional study. Description: Mohamed, Siham A, et al. GWAS in people of Middle Eastern descent reveals a locus protective of kidney function-a cross-sectional study. ''BMC Med''. 2022 Mar 1; '''20''' (1):76
Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse-Brief Report. Description: Richardson, Tom G, et al. Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse-Brief Report. ''Arterioscler Thromb Vasc Biol''. 2022 Mar; '''42''' (3):362-365
Imbalanced segregation of recombinant haplotypes in hybrid populations reveals inter- and intrachromosomal Dobzhansky-Muller incompatibilities. Description: Li, Juan, et al. Imbalanced segregation of recombinant haplotypes in hybrid populations reveals inter- and intrachromosomal Dobzhansky-Muller incompatibilities. ''PLoS Genet''. 2022 Mar; '''18''' (3):e1010120
Increased risk of Graves ophthalmopathy in patients with increasing TRAb after radioiodine treatment and the impact of CTLA4 on TRAb titres. Description: Shahida, Bushra, et al. Increased risk of Graves ophthalmopathy in patients with increasing TRAb after radioiodine treatment and the impact of CTLA4 on TRAb titres. ''Endocrine''. 2022 Mar; '''75''' (3):856-864
Interactions between dietary patterns and genetic factors in relation to incident dementia among 70-year-olds. Description: Samuelsson, Jessica, et al. Interactions between dietary patterns and genetic factors in relation to incident dementia among 70-year-olds. ''Eur J Nutr''. 2022 Mar; '''61''' (2):871-884
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia. Description: Pardinas, Antonio F, et al. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia. ''JAMA Psychiatry''. 2022 Mar 1; '''79''' (3):260-269
Meta-analysis of genome-wide association studies for litter size in sheep. Description: Gholizadeh, Mohsen, et al. Meta-analysis of genome-wide association studies for litter size in sheep. ''Theriogenology''. 2022 Mar 1; '''180''': 103-112
Morphometric Analysis of Structural MRI Using Schizophrenia Meta-analytic Priors Distinguish Patients from Controls in Two Independent Samples and in a Sample of Individuals With High Polygenic Risk. Description: Lancaster, Thomas M, et al. Morphometric Analysis of Structural MRI Using Schizophrenia Meta-analytic Priors Distinguish Patients from Controls in Two Independent Samples and in a Sample of Individuals With High Polygenic Risk. ''Schizophr Bull''. 2022 Mar 1; '''48''' (2):524-532
Multiple genetic variations of chronic rhinosinusitis with nasal polyps are associated with respiratory parameters in men with obstructive sleep apnea. Description: Zhang, Qianqian, et al. Multiple genetic variations of chronic rhinosinusitis with nasal polyps are associated with respiratory parameters in men with obstructive sleep apnea. ''Sleep Breath''. 2022 Mar; '''26''' (1):57-65
Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer's disease in a Chinese population: a case-control study. Description: Wen, Ya-Fei, et al. Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer's disease in a Chinese population: a case-control study. ''Neural Regen Res''. 2022 Mar; '''17''' (3):682-689
New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genes. Description: Mestiri, Souhir, et al. New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genes. ''Mol Genet Genomic Med''. 2022 Mar; '''10''' (3):e1871
Novel open reading frames in human accelerated regions and transposable elements reveal new leads to understand schizophrenia and bipolar disorder. Description: Erady, Chaitanya, et al. Novel open reading frames in human accelerated regions and transposable elements reveal new leads to understand schizophrenia and bipolar disorder. ''Mol Psychiatry''. 2022 Mar; '''27''' (3):1455-1468
Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank. Description: Wang, Louise, et al. Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank. ''Genet Med''. 2022 Mar; '''24''' (3):601-609
Polygenic scores for handedness and their association with asymmetries in brain structure. Description: Ocklenburg, Sebastian, et al. Polygenic scores for handedness and their association with asymmetries in brain structure. ''Brain Struct Funct''. 2022 Mar; '''227''' (2):515-527
Population differentiation and epidemic tracking of Bursaphelenchus xylophilus in China based on chromosome-level assembly and whole-genome sequencing data. Description: Ding, Xiaolei, et al. Population differentiation and epidemic tracking of Bursaphelenchus xylophilus in China based on chromosome-level assembly and whole-genome sequencing data. ''Pest Manag Sci''. 2022 Mar; '''78''' (3):1213-1226
Signatures of selection in Nelore cattle revealed by whole-genome sequencing data. Description: Maiorano, Amanda Marchi, et al. Signatures of selection in Nelore cattle revealed by whole-genome sequencing data. ''Genomics''. 2022 Mar; '''114''' (2):110304
The association of genetic alterations with response rate in newly diagnosed chronic myeloid leukemia patients. Description: Park, Hyunkyung, et al. The association of genetic alterations with response rate in newly diagnosed chronic myeloid leukemia patients. ''Leuk Res''. 2022 Mar; '''114''': 106791
The evolutionary pathways for local adaptation in mountain hares. Description: Giska, Iwona, et al. The evolutionary pathways for local adaptation in mountain hares. ''Mol Ecol''. 2022 Mar; '''31''' (5):1487-1503
The impact of prehistoric human dispersals on the presence of tobacco-related oral cancer in Northeast India. Description: Kundu, Sharbadeb, et al. The impact of prehistoric human dispersals on the presence of tobacco-related oral cancer in Northeast India. ''Gene''. 2022 Mar 1; '''813''': 146098
Unraveling a fine-scale high genetic heterogeneity and recent continental connections of an Arabian Peninsula population. Description: Eaaswarkhanth, Muthukrishnan, et al. Unraveling a fine-scale high genetic heterogeneity and recent continental connections of an Arabian Peninsula population. ''Eur J Hum Genet''. 2022 Mar; '''30''' (3):307-319
Fine-Scale Genetic Structure in the United Arab Emirates Reflects Endogamous and Consanguineous Culture, Population History, and Geography. Description: Elliott, Katherine S, et al. Fine-Scale Genetic Structure in the United Arab Emirates Reflects Endogamous and Consanguineous Culture, Population History, and Geography. ''Mol Biol Evol''. 2022 Mar 2; '''39''' (3):
Phylogeny, diversification, and biogeography of a hemiclonal hybrid system of native Australian freshwater fishes (Gobiiformes: Gobioidei: Eleotridae: Hypseleotris). Description: Thacker, Christine E, et al. Phylogeny, diversification, and biogeography of a hemiclonal hybrid system of native Australian freshwater fishes (Gobiiformes: Gobioidei: Eleotridae: Hypseleotris). ''BMC Ecol Evol''. 2022 Mar 2; '''22''' (1):22
Accounting for age of onset and family history improves power in genome-wide association studies. Description: Pedersen, Emil M, et al. Accounting for age of onset and family history improves power in genome-wide association studies. ''Am J Hum Genet''. 2022 Mar 3; '''109''' (3):417-432
A functional genomics approach in Tanzanian population identifies distinct genetic regulators of cytokine production compared to European population. Description: Boahen, Collins K, et al. A functional genomics approach in Tanzanian population identifies distinct genetic regulators of cytokine production compared to European population. ''Am J Hum Genet''. 2022 Mar 3; '''109''' (3):471-485
GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating alpha-Klotho levels. Description: Gergei, Ingrid, et al. GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating alpha-Klotho levels. ''Hum Mol Genet''. 2022 Mar 3; '''31''' (5):792-802
Innovative computational approaches shed light on genetic mechanisms underlying cognitive impairment among children born extremely preterm. Description: Liu, Weifang, et al. Innovative computational approaches shed light on genetic mechanisms underlying cognitive impairment among children born extremely preterm. ''J Neurodev Disord''. 2022 Mar 3; '''14''' (1):16
Unveiling genetic variants for age-related sarcopenia by conducting a genome-wide association study on Korean cohorts. Description: Jin, Heejin, et al. Unveiling genetic variants for age-related sarcopenia by conducting a genome-wide association study on Korean cohorts. ''Sci Rep''. 2022 Mar 3; '''12''' (1):3501
Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation. Description: Merkle, Florian T, et al. Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation. ''Cell Stem Cell''. 2022 Mar 3; '''29''' (3):472-486.e7
Analysis of genotype-by-environment interactions in a maize mapping population. Description: Hudson, Asher I, et al. Analysis of genotype-by-environment interactions in a maize mapping population. ''G3 (Bethesda)''. 2022 Mar 4; '''12''' (3):
Combining genetic resources and elite material populations to improve the accuracy of genomic prediction in apple. Description: Cazenave, Xabi, et al. Combining genetic resources and elite material populations to improve the accuracy of genomic prediction in apple. ''G3 (Bethesda)''. 2022 Mar 4; '''12''' (3):
ddRAD Sequencing Identifies Pesticide Resistance-Related Loci and Reveals New Insights into Genetic Structure of Bactericera cockerelli as a Plant Pathogen Vector. Description: Kiani, Mahnaz, et al. ddRAD Sequencing Identifies Pesticide Resistance-Related Loci and Reveals New Insights into Genetic Structure of Bactericera cockerelli as a Plant Pathogen Vector. ''Insects''. 2022 Mar 4; '''13''' (3):
Enhancer promoter interactome and Mendelian randomization identify network of druggable vascular genes in coronary artery disease. Description: Chignon, Arnaud, et al. Enhancer promoter interactome and Mendelian randomization identify network of druggable vascular genes in coronary artery disease. ''Hum Genomics''. 2022 Mar 4; '''16''' (1):8
Genomic prediction of growth in a commercially, recreationally, and culturally important marine resource, the Australian snapper (Chrysophrys auratus). Description: Sandoval-Castillo, Jonathan, et al. Genomic prediction of growth in a commercially, recreationally, and culturally important marine resource, the Australian snapper (Chrysophrys auratus). ''G3 (Bethesda)''. 2022 Mar 4; '''12''' (3):
Likelihood-based Mendelian randomization analysis with automated instrument selection and horizontal pleiotropic modeling. Description: Yuan, Zhongshang, et al. Likelihood-based Mendelian randomization analysis with automated instrument selection and horizontal pleiotropic modeling. ''Sci Adv''. 2022 Mar 4; '''8''' (9):eabl5744
Modeling allelic diversity of multiparent mapping populations affects detection of quantitative trait loci. Description: Odell, Sarah G, et al. Modeling allelic diversity of multiparent mapping populations affects detection of quantitative trait loci. ''G3 (Bethesda)''. 2022 Mar 4; '''12''' (3):
Whole-genome sequencing of 1,171 elderly admixed individuals from Sao Paulo, Brazil. Description: Naslavsky, Michel S, et al. Whole-genome sequencing of 1,171 elderly admixed individuals from Sao Paulo, Brazil. ''Nat Commun''. 2022 Mar 4; '''13''' (1):1004
Genomic footprints of sorghum domestication and breeding selection for multiple end uses. Description: Wu, Xiaoyuan, et al. Genomic footprints of sorghum domestication and breeding selection for multiple end uses. ''Mol Plant''. 2022 Mar 7; '''15''' (3):537-551
Population genomic analysis reveals domestication of cultivated rye from weedy rye. Description: Sun, Yanqing, et al. Population genomic analysis reveals domestication of cultivated rye from weedy rye. ''Mol Plant''. 2022 Mar 7; '''15''' (3):552-561
Schizophrenia risk loci from xMHC region were associated with antipsychotic response in chronic schizophrenic patients with persistent positive symptom. Description: Li, Jiang, et al. Schizophrenia risk loci from xMHC region were associated with antipsychotic response in chronic schizophrenic patients with persistent positive symptom. ''Transl Psychiatry''. 2022 Mar 7; '''12''' (1):92
The spinach YY genome reveals sex chromosome evolution, domestication, and introgression history of the species. Description: Ma, Xiaokai, et al. The spinach YY genome reveals sex chromosome evolution, domestication, and introgression history of the species. ''Genome Biol''. 2022 Mar 7; '''23''' (1):75
Wheat breeding history reveals synergistic selection of pleiotropic genomic sites for plant architecture and grain yield. Description: Li, Aili, et al. Wheat breeding history reveals synergistic selection of pleiotropic genomic sites for plant architecture and grain yield. ''Mol Plant''. 2022 Mar 7; '''15''' (3):504-519
Ancient genomes from the Himalayas illuminate the genetic history of Tibetans and their Tibeto-Burman speaking neighbors. Description: Liu, Chi-Chun, et al. Ancient genomes from the Himalayas illuminate the genetic history of Tibetans and their Tibeto-Burman speaking neighbors. ''Nat Commun''. 2022 Mar 8; '''13''' (1):1203
A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects. Description: Acosta-Uribe, Juliana, et al. A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects. ''Genome Med''. 2022 Mar 8; '''14''' (1):27
Distinct biological ages of organs and systems identified from a multi-omics study. Description: Nie, Chao, et al. Distinct biological ages of organs and systems identified from a multi-omics study. ''Cell Rep''. 2022 Mar 8; '''38''' (10):110459
Examining facial emotion recognition as an intermediate phenotype for psychosis: Findings from the EUGEI study. Description: Fusar-Poli, Laura, et al. Examining facial emotion recognition as an intermediate phenotype for psychosis: Findings from the EUGEI study. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2022 Mar 8; '''113''': 110440
Impact of polygenic risk for coronary artery disease and cardiovascular medication burden on cognitive impairment in psychotic disorders. Description: Zhang, Lusi, et al. Impact of polygenic risk for coronary artery disease and cardiovascular medication burden on cognitive impairment in psychotic disorders. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2022 Mar 8; '''113''': 110464
A large and diverse autosomal haplotype is associated with sex-linked colour polymorphism in the guppy. Description: Paris, Josephine R, et al. A large and diverse autosomal haplotype is associated with sex-linked colour polymorphism in the guppy. ''Nat Commun''. 2022 Mar 9; '''13''' (1):1233
A machine learning-assisted model for renal urate underexcretion with genetic and clinical variables among Chinese men with gout. Description: Sun, Mingshu, et al. A machine learning-assisted model for renal urate underexcretion with genetic and clinical variables among Chinese men with gout. ''Arthritis Res Ther''. 2022 Mar 9; '''24''' (1):67
An enhancer variant at 16q22.1 predisposes to hepatocellular carcinoma via regulating PRMT7 expression. Description: Shen, Ting, et al. An enhancer variant at 16q22.1 predisposes to hepatocellular carcinoma via regulating PRMT7 expression. ''Nat Commun''. 2022 Mar 9; '''13''' (1):1232
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus. Description: Stacey, David, et al. Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus. ''Nat Commun''. 2022 Mar 9; '''13''' (1):1222
Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Description: Caron, Barthelemy, et al. Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. ''Genome Med''. 2022 Mar 9; '''14''' (1):28
Genomic patterns of homozygosity and inbreeding depression in Murciano-Granadina goats. Description: Luigi-Sierra, Maria Gracia, et al. Genomic patterns of homozygosity and inbreeding depression in Murciano-Granadina goats. ''J Anim Sci Biotechnol''. 2022 Mar 10; '''13''' (1):35
Genome-wide pharmacogenetics of anti-drug antibody response to bococizumab highlights key residues in HLA DRB1 and DQB1. Description: Chasman, Daniel I, et al. Genome-wide pharmacogenetics of anti-drug antibody response to bococizumab highlights key residues in HLA DRB1 and DQB1. ''Sci Rep''. 2022 Mar 11; '''12''' (1):4266
Genomic consequences of domestication of the Siamese fighting fish. Description: Kwon, Young Mi, et al. Genomic consequences of domestication of the Siamese fighting fish. ''Sci Adv''. 2022 Mar 11; '''8''' (10):eabm4950
Understanding signatures of positive natural selection in human zinc transporter genes. Description: Roca-Umbert, Ana, et al. Understanding signatures of positive natural selection in human zinc transporter genes. ''Sci Rep''. 2022 Mar 12; '''12''' (1):4320
MIR17HG polymorphisms contribute to high-altitude pulmonary edema susceptibility in the Chinese population. Description: Si, Lining, et al. MIR17HG polymorphisms contribute to high-altitude pulmonary edema susceptibility in the Chinese population. ''Sci Rep''. 2022 Mar 14; '''12''' (1):4346
The Effect of Phenotype and Genotype on the Plasma Proteome in Patients with Inflammatory Bowel Disease. Description: Bourgonje, Arno R, et al. The Effect of Phenotype and Genotype on the Plasma Proteome in Patients with Inflammatory Bowel Disease. ''J Crohns Colitis''. 2022 Mar 14; '''16''' (3):414-429
A genetic risk score of alleles related to MGUS interacts with socioeconomic position in a population-based cohort. Description: Baak, Lisa, et al. A genetic risk score of alleles related to MGUS interacts with socioeconomic position in a population-based cohort. ''Sci Rep''. 2022 Mar 15; '''12''' (1):4409
Genetic diversity and population structure of an African yam bean (Sphenostylis stenocarpa) collection from IITA GenBank. Description: Shitta, Ndenum Suzzy, et al. Genetic diversity and population structure of an African yam bean (Sphenostylis stenocarpa) collection from IITA GenBank. ''Sci Rep''. 2022 Mar 15; '''12''' (1):4437
Interrogating Associations Between Polygenic Liabilities and Electroconvulsive Therapy Effectiveness. Description: Luykx, Jurjen J, et al. Interrogating Associations Between Polygenic Liabilities and Electroconvulsive Therapy Effectiveness. ''Biol Psychiatry''. 2022 Mar 15; '''91''' (6):531-539
Target-oriented prioritization: targeted selection strategy by integrating organismal and molecular traits through predictive analytics in breeding. Description: Yang, Wenyu, et al. Target-oriented prioritization: targeted selection strategy by integrating organismal and molecular traits through predictive analytics in breeding. ''Genome Biol''. 2022 Mar 15; '''23''' (1):80
Characterization of runs of homozygosity, heterozygosity-enriched regions, and population structure in cattle populations selected for different breeding goals. Description: Mulim, Henrique Alberto, et al. Characterization of runs of homozygosity, heterozygosity-enriched regions, and population structure in cattle populations selected for different breeding goals. ''BMC Genomics''. 2022 Mar 16; '''23''' (1):209
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis. Description: Zhang, Sai, et al. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis. ''Neuron''. 2022 Mar 16; '''110''' (6):992-1008.e11
Study protocol to quantify the genetic architecture of sonographic cervical length and its relationship to spontaneous preterm birth. Description: Wolf, Hope M, et al. Study protocol to quantify the genetic architecture of sonographic cervical length and its relationship to spontaneous preterm birth. ''BMJ Open''. 2022 Mar 17; '''12''' (3):e053631
Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood. Description: Ruiz-Arenas, Carlos, et al. Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood. ''Elife''. 2022 Mar 18; '''11''':
Parallel reduction in flowering time from de novo mutations enable evolutionary rescue in colonizing lineages. Description: Fulgione, Andrea, et al. Parallel reduction in flowering time from de novo mutations enable evolutionary rescue in colonizing lineages. ''Nat Commun''. 2022 Mar 18; '''13''' (1):1461
Population genomics reveals that natural variation in PRDM16 contributes to cold tolerance in domestic cattle. Description: Yan, Chun-Long, et al. Population genomics reveals that natural variation in PRDM16 contributes to cold tolerance in domestic cattle. ''Zool Res''. 2022 Mar 18; '''43''' (2):275-284
Taller height and risk of coronary heart disease and cancer: A within-sibship Mendelian randomization study. Description: Howe, Laurence J, et al. Taller height and risk of coronary heart disease and cancer: A within-sibship Mendelian randomization study. ''Elife''. 2022 Mar 18; '''11''':
The interplay of additivity, dominance, and epistasis on fitness in a diploid yeast cross. Description: Matsui, Takeshi, et al. The interplay of additivity, dominance, and epistasis on fitness in a diploid yeast cross. ''Nat Commun''. 2022 Mar 18; '''13''' (1):1463
Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese. Description: Chau, Jeffrey Fong Ting, et al. Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese. ''NPJ Genom Med''. 2022 Mar 21; '''7''' (1):23
GCAT\|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing. Description: Valls-Margarit, Jordi, et al. GCAT\|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing. ''Nucleic Acids Res''. 2022 Mar 21; '''50''' (5):2464-2479
Inbreeding, Native American ancestry and child mortality: linking human selection and paediatric medicine. Description: Koenigstein, Fabienne, et al. Inbreeding, Native American ancestry and child mortality: linking human selection and paediatric medicine. ''Hum Mol Genet''. 2022 Mar 21; '''31''' (6):975-984
Genetic diversity and signatures of selection for heat tolerance and immune response in Iranian native chickens. Description: Asadollahpour Nanaei, Hojjat, et al. Genetic diversity and signatures of selection for heat tolerance and immune response in Iranian native chickens. ''BMC Genomics''. 2022 Mar 22; '''23''' (1):224
Genetics, leadership position, and well-being: An investigation with a large-scale GWAS. Description: Song, Zhaoli, et al. Genetics, leadership position, and well-being: An investigation with a large-scale GWAS. ''Proc Natl Acad Sci U S A''. 2022 Mar 22; '''119''' (12):e2114271119
Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer. Description: Dong, Qian, et al. Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer. ''Genome Med''. 2022 Mar 22; '''14''' (1):32
GWAS on birth year infant mortality rates provides evidence of recent natural selection. Description: Wu, Yuchang, et al. GWAS on birth year infant mortality rates provides evidence of recent natural selection. ''Proc Natl Acad Sci U S A''. 2022 Mar 22; '''119''' (12):e2117312119
The influence of childhood asthma on adult height: evidence from the UK Biobank. Description: Chen, Wenwen, et al. The influence of childhood asthma on adult height: evidence from the UK Biobank. ''BMC Med''. 2022 Mar 22; '''20''' (1):94
Genetic regulation of post-translational modification of two distinct proteins. Description: Landini, Arianna, et al. Genetic regulation of post-translational modification of two distinct proteins. ''Nat Commun''. 2022 Mar 24; '''13''' (1):1586
Artemisinin resistance in the malaria parasite, Plasmodium falciparum, originates from its initial transcriptional response. Description: Zhu, Lei, et al. Artemisinin resistance in the malaria parasite, Plasmodium falciparum, originates from its initial transcriptional response. ''Commun Biol''. 2022 Mar 28; '''5''' (1):274
Estimation of the bidirectional relationship between schizophrenia and inflammatory bowel disease using the mendelian randomization approach. Description: Qian, Li, et al. Estimation of the bidirectional relationship between schizophrenia and inflammatory bowel disease using the mendelian randomization approach. ''Schizophrenia (Heidelb)''. 2022 Mar 28; '''8''' (1):31
ggComp enables dissection of germplasm resources and construction of a multiscale germplasm network in wheat. Description: Yang, Zhengzhao, et al. ggComp enables dissection of germplasm resources and construction of a multiscale germplasm network in wheat. ''Plant Physiol''. 2022 Mar 28; '''188''' (4):1950-1965
In-depth analysis reveals complex molecular aetiology in a cohort of idiopathic cerebral palsy. Description: Li, Na, et al. In-depth analysis reveals complex molecular aetiology in a cohort of idiopathic cerebral palsy. ''Brain''. 2022 Mar 29; '''145''' (1):119-141
Identification of important genomic footprints using eight different selection signature statistics in domestic cattle breeds. Description: Rajawat, Divya, et al. Identification of important genomic footprints using eight different selection signature statistics in domestic cattle breeds. ''Gene''. 2022 Mar 30; '''816''': 146165
A functional variant of SHARPIN confers increased risk of late-onset Alzheimer's disease. Description: Asanomi, Yuya, et al. A functional variant of SHARPIN confers increased risk of late-onset Alzheimer's disease. ''J Hum Genet''. 2022 Apr; '''67''' (4):203-208
A general framework for predicting the transcriptomic consequences of non-coding variation and small molecules. Description: Abdalla, Moustafa, et al. A general framework for predicting the transcriptomic consequences of non-coding variation and small molecules. ''PLoS Comput Biol''. 2022 Apr; '''18''' (4):e1010028
A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Description: Schack, Line M H, et al. A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. ''Br J Cancer''. 2022 Apr; '''126''' (7):1082-1090
A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. Description: Kimbrel, Nathan A, et al. A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. ''Mol Psychiatry''. 2022 Apr; '''27''' (4):2264-2272
Association of Genetic Ancestry and Molecular Signatures with Cancer Survival Disparities: A Pan-Cancer Analysis. Description: Lee, Kara Keun, et al. Association of Genetic Ancestry and Molecular Signatures with Cancer Survival Disparities: A Pan-Cancer Analysis. ''Cancer Res''. 2022 Apr 1; '''82''' (7):1222-1233
Association of Genetic Variants Linked to Late-Onset Alzheimer Disease With Cognitive Test Performance by Midlife. Description: Zimmerman, Scott C, et al. Association of Genetic Variants Linked to Late-Onset Alzheimer Disease With Cognitive Test Performance by Midlife. ''JAMA Netw Open''. 2022 Apr 1; '''5''' (4):e225491
Association of MTOR and PDGFRA gene polymorphisms with different degrees of myopia severity. Description: Li, Xuan, et al. Association of MTOR and PDGFRA gene polymorphisms with different degrees of myopia severity. ''Exp Eye Res''. 2022 Apr; '''217''': 108962
Association of rs3027178 polymorphism in the circadian clock gene PER1 with susceptibility to Alzheimer's disease and longevity in an Italian population. Description: Bacalini, Maria Giulia, et al. Association of rs3027178 polymorphism in the circadian clock gene PER1 with susceptibility to Alzheimer's disease and longevity in an Italian population. ''Geroscience''. 2022 Apr; '''44''' (2):881-896
A study using single-locus and multi-locus genome-wide association study to identify genes associated with teat number in Hu sheep. Description: Zhao, Yuhetian, et al. A study using single-locus and multi-locus genome-wide association study to identify genes associated with teat number in Hu sheep. ''Anim Genet''. 2022 Apr; '''53''' (2):203-211
Comparative genomics and signatures of selection in North Atlantic eels. Description: Pujolar, Jose Martin, et al. Comparative genomics and signatures of selection in North Atlantic eels. ''Mar Genomics''. 2022 Apr; '''62''': 100933
Elevated plasma levels of CXCL16 in severe COVID-19 patients. Description: Smieszek, Sandra P, et al. Elevated plasma levels of CXCL16 in severe COVID-19 patients. ''Cytokine''. 2022 Apr; '''152''': 155810
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. Description: Maihofer, Adam X, et al. Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. ''Biol Psychiatry''. 2022 Apr 1; '''91''' (7):626-636
Genetic risk of hyperuricemia in hypertensive patients associated with antihypertensive drug therapy: A longitudinal study. Description: Chen, Yu, et al. Genetic risk of hyperuricemia in hypertensive patients associated with antihypertensive drug therapy: A longitudinal study. ''Clin Genet''. 2022 Apr; '''101''' (4):411-420
Genetic Variants Associated with Adverse Events after Angiotensin-Converting Enzyme Inhibitor Use: Replication after GWAS-Based Discovery. Description: Lee, Chan Joo, et al. Genetic Variants Associated with Adverse Events after Angiotensin-Converting Enzyme Inhibitor Use: Replication after GWAS-Based Discovery. ''Yonsei Med J''. 2022 Apr; '''63''' (4):342-348
Genome sequencing and transcriptome analyses provide insights into the origin and domestication of water caltrop (Trapa spp., Lythraceae). Description: Lu, Rui-Sen, et al. Genome sequencing and transcriptome analyses provide insights into the origin and domestication of water caltrop (Trapa spp., Lythraceae). ''Plant Biotechnol J''. 2022 Apr; '''20''' (4):761-776
Genome-wide association studies dissect the G x E interaction for agronomic traits in a worldwide collection of safflowers (Carthamus tinctorius L.). Description: Zhao, Huanhuan, et al. Genome-wide association studies dissect the G x E interaction for agronomic traits in a worldwide collection of safflowers (Carthamus tinctorius L.). ''Mol Breed''. 2022 Apr; '''42''' (4):24
Genomic analysis of a parasite invasion: Colonization of the Americas by the blood fluke Schistosoma mansoni. Description: Platt, Roy N 2nd, et al. Genomic analysis of a parasite invasion: Colonization of the Americas by the blood fluke Schistosoma mansoni. ''Mol Ecol''. 2022 Apr; '''31''' (8):2242-2263
Genomic and GWAS analyses demonstrate phylogenomic relationships of Gossypium barbadense in China and selection for fibre length, lint percentage and Fusarium wilt resistance. Description: Zhao, Nan, et al. Genomic and GWAS analyses demonstrate phylogenomic relationships of Gossypium barbadense in China and selection for fibre length, lint percentage and Fusarium wilt resistance. ''Plant Biotechnol J''. 2022 Apr; '''20''' (4):691-710
Global flyway evolution in red knots Calidris canutus and genetic evidence for a Nearctic refugium. Description: Conklin, Jesse R, et al. Global flyway evolution in red knots Calidris canutus and genetic evidence for a Nearctic refugium. ''Mol Ecol''. 2022 Apr; '''31''' (7):2124-2139
Haplotype mapping uncovers unexplored variation in wild and domesticated soybean at the major protein locus cqProt-003. Description: Marsh, Jacob I, et al. Haplotype mapping uncovers unexplored variation in wild and domesticated soybean at the major protein locus cqProt-003. ''Theor Appl Genet''. 2022 Apr; '''135''' (4):1443-1455
HLA autoimmune risk alleles restrict the hypervariable region of T cell receptors. Description: Ishigaki, Kazuyoshi, et al. HLA autoimmune risk alleles restrict the hypervariable region of T cell receptors. ''Nat Genet''. 2022 Apr; '''54''' (4):393-402
Integrating whole-genome sequencing with multi-omic data reveals the impact of structural variants on gene regulation in the human brain. Description: Vialle, Ricardo A, et al. Integrating whole-genome sequencing with multi-omic data reveals the impact of structural variants on gene regulation in the human brain. ''Nat Neurosci''. 2022 Apr; '''25''' (4):504-514
Introgressive hybridisation between domestic pigs (Sus scrofa domesticus) and endemic Corsican wild boars (S. s. meridionalis): effects of human-mediated interventions. Description: Schleimer, Anna, et al. Introgressive hybridisation between domestic pigs (Sus scrofa domesticus) and endemic Corsican wild boars (S. s. meridionalis): effects of human-mediated interventions. ''Heredity (Edinb)''. 2022 Apr; '''128''' (4):279-290
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores. Description: Weissbrod, Omer, et al. Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores. ''Nat Genet''. 2022 Apr; '''54''' (4):450-458
New insights into the genetic etiology of Alzheimer's disease and related dementias. Description: Bellenguez, Celine, et al. New insights into the genetic etiology of Alzheimer's disease and related dementias. ''Nat Genet''. 2022 Apr; '''54''' (4):412-436
Non-synonymous alterations in AKR7A3 and ABCA6 correlate with bleeding in aged patients treated with rivaroxaban. Description: Zhao, Ming, et al. Non-synonymous alterations in AKR7A3 and ABCA6 correlate with bleeding in aged patients treated with rivaroxaban. ''Clin Transl Sci''. 2022 Apr; '''15''' (4):923-929
Oxytocin receptor genotype moderates the association between maternal prenatal stress and infant early self-regulation. Description: Kajanoja, Jani, et al. Oxytocin receptor genotype moderates the association between maternal prenatal stress and infant early self-regulation. ''Psychoneuroendocrinology''. 2022 Apr; '''138''': 105669
PD-L1 overexpression correlates with JAK2-V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms. Description: Milosevic Feenstra, Jelena D, et al. PD-L1 overexpression correlates with JAK2-V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms. ''Am J Hematol''. 2022 Apr; '''97''' (4):390-400
Pharmacogenomic landscape of Indian population using whole genomes. Description: Sahana, S, et al. Pharmacogenomic landscape of Indian population using whole genomes. ''Clin Transl Sci''. 2022 Apr; '''15''' (4):866-877
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. Description: Okbay, Aysu, et al. Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. ''Nat Genet''. 2022 Apr; '''54''' (4):437-449
Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications. Description: Mullan, Kerry A, et al. Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications. ''Epilepsia''. 2022 Apr; '''63''' (4):936-949
Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity. Description: Daniel, Laura L, et al. Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity. ''Clin Transl Sci''. 2022 Apr; '''15''' (4):859-865
Secondary analyses for genome-wide association studies using expression quantitative trait loci. Description: Ngwa, Julius S, et al. Secondary analyses for genome-wide association studies using expression quantitative trait loci. ''Genet Epidemiol''. 2022 Apr; '''46''' (3-4):170-181
Supergene origin and maintenance in Atlantic cod. Description: Matschiner, Michael, et al. Supergene origin and maintenance in Atlantic cod. ''Nat Ecol Evol''. 2022 Apr; '''6''' (4):469-481
The Cycas genome and the early evolution of seed plants. Description: Liu, Yang, et al. The Cycas genome and the early evolution of seed plants. ''Nat Plants''. 2022 Apr; '''8''' (4):389-401
The genetic architecture of language functional connectivity. Description: Mekki, Yasmina, et al. The genetic architecture of language functional connectivity. ''Neuroimage''. 2022 Apr 1; '''249''': 118795
The relationship between temperament, polygenic score for intelligence and cognition: A population-based study of middle-aged adults. Description: Tolli, Pekka, et al. The relationship between temperament, polygenic score for intelligence and cognition: A population-based study of middle-aged adults. ''Genes Brain Behav''. 2022 Apr; '''21''' (4):e12798
Transcript levels in plasma contribute substantial predictive value as potential Alzheimer's disease biomarkers in African Americans. Description: Reddy, Joseph S, et al. Transcript levels in plasma contribute substantial predictive value as potential Alzheimer's disease biomarkers in African Americans. ''EBioMedicine''. 2022 Apr; '''78''': 103929
Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Description: Yeung, Ming Wai, et al. Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. ''Arterioscler Thromb Vasc Biol''. 2022 Apr; '''42''' (4):484-501
Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder. Description: Wendt, Frank R, et al. Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder. ''Mol Psychiatry''. 2022 Apr; '''27''' (4):2206-2215
A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk. Description: Chang, Diana, et al. A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk. ''Sci Rep''. 2022 Apr 2; '''12''' (1):5574
A large deletion at the cortex locus eliminates butterfly wing patterning. Description: Hanly, Joseph J, et al. A large deletion at the cortex locus eliminates butterfly wing patterning. ''G3 (Bethesda)''. 2022 Apr 4; '''12''' (4):
DNA methylation in peripheral tissues and left-handedness. Description: Odintsova, Veronika V, et al. DNA methylation in peripheral tissues and left-handedness. ''Sci Rep''. 2022 Apr 4; '''12''' (1):5606
Genetic and environment effects on structural neuroimaging endophenotype for bipolar disorder: a novel molecular approach. Description: Hu, Bo, et al. Genetic and environment effects on structural neuroimaging endophenotype for bipolar disorder: a novel molecular approach. ''Transl Psychiatry''. 2022 Apr 4; '''12''' (1):137
Genetic mapping of loci involved in oil tocopherol composition control in Russian sunflower (Helianthus annuus L.) lines. Description: Gubaev, Rim, et al. Genetic mapping of loci involved in oil tocopherol composition control in Russian sunflower (Helianthus annuus L.) lines. ''G3 (Bethesda)''. 2022 Apr 4; '''12''' (4):
gJLS2: an R package for generalized joint location and scale analysis in X-inclusive genome-wide association studies. Description: Deng, Wei Q, et al. gJLS2: an R package for generalized joint location and scale analysis in X-inclusive genome-wide association studies. ''G3 (Bethesda)''. 2022 Apr 4; '''12''' (4):
Methylation quantitative trait loci are largely consistent across disease states in Crohn's disease. Description: Venkateswaran, Suresh, et al. Methylation quantitative trait loci are largely consistent across disease states in Crohn's disease. ''G3 (Bethesda)''. 2022 Apr 4; '''12''' (4):
Recovery of mitogenomes from whole genome sequences to infer maternal diversity in 1883 modern taurine and indicine cattle. Description: Dorji, Jigme, et al. Recovery of mitogenomes from whole genome sequences to infer maternal diversity in 1883 modern taurine and indicine cattle. ''Sci Rep''. 2022 Apr 4; '''12''' (1):5582
A chromosome-level genome of the human blood fluke Schistosoma japonicum identifies the genomic basis of host-switching. Description: Luo, Fang, et al. A chromosome-level genome of the human blood fluke Schistosoma japonicum identifies the genomic basis of host-switching. ''Cell Rep''. 2022 Apr 5; '''39''' (1):110638
Identification of host-pathogen-disease relationships using a scalable multiplex serology platform in UK Biobank. Description: Mentzer, Alexander J, et al. Identification of host-pathogen-disease relationships using a scalable multiplex serology platform in UK Biobank. ''Nat Commun''. 2022 Apr 5; '''13''' (1):1818
Mapping anorexia nervosa genes to clinical phenotypes. Description: Johnson, Jessica S, et al. Mapping anorexia nervosa genes to clinical phenotypes. ''Psychol Med''. 2022 Apr 5; '''53''' (6):1-15
Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders. Description: Okhuijsen-Pfeifer, C, et al. Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders. ''Transl Psychiatry''. 2022 Apr 7; '''12''' (1):145
Global population genomic signature of Spodoptera frugiperda (fall armyworm) supports complex introduction events across the Old World. Description: Tay, Wee Tek, et al. Global population genomic signature of Spodoptera frugiperda (fall armyworm) supports complex introduction events across the Old World. ''Commun Biol''. 2022 Apr 7; '''5''' (1):297
Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes. Description: Burch, Kathryn S, et al. Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes. ''Am J Hum Genet''. 2022 Apr 7; '''109''' (4):692-709
RAREsim: A simulation method for very rare genetic variants. Description: Null, Megan, et al. RAREsim: A simulation method for very rare genetic variants. ''Am J Hum Genet''. 2022 Apr 7; '''109''' (4):680-691
The genomic signatures of natural selection in admixed human populations. Description: Cuadros-Espinoza, Sebastian, et al. The genomic signatures of natural selection in admixed human populations. ''Am J Hum Genet''. 2022 Apr 7; '''109''' (4):710-726
The individual and global impact of copy-number variants on complex human traits. Description: Auwerx, Chiara, et al. The individual and global impact of copy-number variants on complex human traits. ''Am J Hum Genet''. 2022 Apr 7; '''109''' (4):647-668
Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease. Description: Gong, Jiafen, et al. Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease. ''NPJ Genom Med''. 2022 Apr 8; '''7''' (1):28
Species Persistence with Hybridization in Toad-Headed Lizards Driven by Divergent Selection and Low Recombination. Description: Gao, Wei, et al. Species Persistence with Hybridization in Toad-Headed Lizards Driven by Divergent Selection and Low Recombination. ''Mol Biol Evol''. 2022 Apr 10; '''39''' (4):
Unveiling the Genetic History of the Maniq, a Primary Hunter-Gatherer Society. Description: Gollner, Tobias, et al. Unveiling the Genetic History of the Maniq, a Primary Hunter-Gatherer Society. ''Genome Biol Evol''. 2022 Apr 10; '''14''' (4):
Canalization of the Polygenic Risk for Common Diseases and Traits in the UK Biobank Cohort. Description: Nagpal, Sini, et al. Canalization of the Polygenic Risk for Common Diseases and Traits in the UK Biobank Cohort. ''Mol Biol Evol''. 2022 Apr 11; '''39''' (4):
Disentangling Signatures of Selection Before and After European Colonization in Latin Americans. Description: Mendoza-Revilla, Javier, et al. Disentangling Signatures of Selection Before and After European Colonization in Latin Americans. ''Mol Biol Evol''. 2022 Apr 11; '''39''' (4):
The role of ADHD genetic risk in mid-to-late life somatic health conditions. Description: Garcia-Argibay, Miguel, et al. The role of ADHD genetic risk in mid-to-late life somatic health conditions. ''Transl Psychiatry''. 2022 Apr 11; '''12''' (1):152
A generalist-specialist trade-off between switchgrass cytotypes impacts climate adaptation and geographic range. Description: Napier, Joseph D, et al. A generalist-specialist trade-off between switchgrass cytotypes impacts climate adaptation and geographic range. ''Proc Natl Acad Sci U S A''. 2022 Apr 12; '''119''' (15):e2118879119
An integrative skeletal and paleogenomic analysis of stature variation suggests relatively reduced health for early European farmers. Description: Marciniak, Stephanie, et al. An integrative skeletal and paleogenomic analysis of stature variation suggests relatively reduced health for early European farmers. ''Proc Natl Acad Sci U S A''. 2022 Apr 12; '''119''' (15):e2106743119
A polygenic risk score for nasopharyngeal carcinoma shows potential for risk stratification and personalized screening. Description: He, Yong-Qiao, et al. A polygenic risk score for nasopharyngeal carcinoma shows potential for risk stratification and personalized screening. ''Nat Commun''. 2022 Apr 12; '''13''' (1):1966
A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia. Description: Miyagawa, Taku, et al. A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia. ''NPJ Genom Med''. 2022 Apr 12; '''7''' (1):29
Bovine host genome acts on rumen microbiome function linked to methane emissions. Description: Martinez-Alvaro, Marina, et al. Bovine host genome acts on rumen microbiome function linked to methane emissions. ''Commun Biol''. 2022 Apr 12; '''5''' (1):350
High genomic diversity in the endangered East Greenland Svalbard Barents Sea stock of bowhead whales (Balaena mysticetus). Description: Cerca, Jose, et al. High genomic diversity in the endangered East Greenland Svalbard Barents Sea stock of bowhead whales (Balaena mysticetus). ''Sci Rep''. 2022 Apr 12; '''12''' (1):6118
Ancient genomes reveal origin and rapid trans-Eurasian migration of 7(th) century Avar elites. Description: Gnecchi-Ruscone, Guido Alberto, et al. Ancient genomes reveal origin and rapid trans-Eurasian migration of 7(th) century Avar elites. ''Cell''. 2022 Apr 14; '''185''' (8):1402-1413.e21
Chromosome evolution and the genetic basis of agronomically important traits in greater yam. Description: Bredeson, Jessen V, et al. Chromosome evolution and the genetic basis of agronomically important traits in greater yam. ''Nat Commun''. 2022 Apr 14; '''13''' (1):2001
A Regional Burden of Sequence-Level Variation in the 22q11.2 Region Influences Schizophrenia Risk and Educational Attainment. Description: Breetvelt, Elemi J, et al. A Regional Burden of Sequence-Level Variation in the 22q11.2 Region Influences Schizophrenia Risk and Educational Attainment. ''Biol Psychiatry''. 2022 Apr 15; '''91''' (8):718-726
Polymorphisms of the filaggrin gene are associated with atopic dermatitis in the Caucasian population of Central Russia. Description: Churnosov, Mikhail, et al. Polymorphisms of the filaggrin gene are associated with atopic dermatitis in the Caucasian population of Central Russia. ''Gene''. 2022 Apr 15; '''818''': 146219
Comparative genomics of disease and carriage serotype 1 pneumococci. Description: Chaguza, Chrispin, et al. Comparative genomics of disease and carriage serotype 1 pneumococci. ''Genome Biol Evol''. 2022 Apr 19;
Long-term artificial selection of Hanwoo (Korean) cattle left genetic signatures for the breeding traits and has altered the genomic structure. Description: Seo, Dongwon, et al. Long-term artificial selection of Hanwoo (Korean) cattle left genetic signatures for the breeding traits and has altered the genomic structure. ''Sci Rep''. 2022 Apr 19; '''12''' (1):6438
Mapping the Cord Blood Transcriptome of Pregnancies Affected by Early Maternal Anemia to Identify Signatures of Fetal Programming. Description: Hatem, Gad, et al. Mapping the Cord Blood Transcriptome of Pregnancies Affected by Early Maternal Anemia to Identify Signatures of Fetal Programming. ''J Clin Endocrinol Metab''. 2022 Apr 19; '''107''' (5):1303-1316
Therapeutic Targets for Heart Failure Identified Using Proteomics and Mendelian Randomization. Description: Henry, Albert, et al. Therapeutic Targets for Heart Failure Identified Using Proteomics and Mendelian Randomization. ''Circulation''. 2022 Apr 19; '''145''' (16):1205-1217
Genetic Susceptibility to Enteric Fever in Experimentally Challenged Human Volunteers. Description: Barton, Amber, et al. Genetic Susceptibility to Enteric Fever in Experimentally Challenged Human Volunteers. ''Infect Immun''. 2022 Apr 21; '''90''' (4):e0038921
Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways. Description: Kim, Yuhree, et al. Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways. ''Commun Biol''. 2022 Apr 21; '''5''' (1):386
Genetic analysis of over half a million people characterises C-reactive protein loci. Description: Said, Saredo, et al. Genetic analysis of over half a million people characterises C-reactive protein loci. ''Nat Commun''. 2022 Apr 22; '''13''' (1):2198
Genetic susceptibility to patient-reported xerostomia among long-term oropharyngeal cancer survivors. Description: Aggarwal, Puja, et al. Genetic susceptibility to patient-reported xerostomia among long-term oropharyngeal cancer survivors. ''Sci Rep''. 2022 Apr 22; '''12''' (1):6662
PAGEANT: personal access to genome and analysis of natural traits. Description: Huang, Jie, et al. PAGEANT: personal access to genome and analysis of natural traits. ''Nucleic Acids Res''. 2022 Apr 22; '''50''' (7):e39
A functionally divergent SOC1 homolog improves soybean yield and latitudinal adaptation. Description: Kou, Kun, et al. A functionally divergent SOC1 homolog improves soybean yield and latitudinal adaptation. ''Curr Biol''. 2022 Apr 25; '''32''' (8):1728-1742.e6
Genetic variation in ALDH4A1 is associated with muscle health over the lifespan and across species. Description: Villa, Osvaldo, et al. Genetic variation in ALDH4A1 is associated with muscle health over the lifespan and across species. ''Elife''. 2022 Apr 26; '''11''':
The Tibetan-Yi region is both a corridor and a barrier for human gene flow. Description: Zhang, Zhe, et al. The Tibetan-Yi region is both a corridor and a barrier for human gene flow. ''Cell Rep''. 2022 Apr 26; '''39''' (4):110720
Epistatic selection on a selfish Segregation Distorter supergene - drive, recombination, and genetic load. Description: Navarro-Dominguez, Beatriz, et al. Epistatic selection on a selfish Segregation Distorter supergene - drive, recombination, and genetic load. ''Elife''. 2022 Apr 29; '''11''':
A high-quality reference genome for Fraxinus pennsylvanica for ash species restoration and research. Description: Huff, Matt, et al. A high-quality reference genome for Fraxinus pennsylvanica for ash species restoration and research. ''Mol Ecol Resour''. 2022 May; '''22''' (4):1284-1302
Apolipoprotein B is a novel marker for early tau pathology in Alzheimer's disease. Description: Picard, Cynthia, et al. Apolipoprotein B is a novel marker for early tau pathology in Alzheimer's disease. ''Alzheimers Dement''. 2022 May; '''18''' (5):875-887
Chromosome-level Thlaspi arvense genome provides new tools for translational research and for a newly domesticated cash cover crop of the cooler climates. Description: Nunn, Adam, et al. Chromosome-level Thlaspi arvense genome provides new tools for translational research and for a newly domesticated cash cover crop of the cooler climates. ''Plant Biotechnol J''. 2022 May; '''20''' (5):944-963
Coalescent-based species delimitation in North American pinyon pines using low-copy nuclear genes and plastomes. Description: Montes, Jose-Ruben, et al. Coalescent-based species delimitation in North American pinyon pines using low-copy nuclear genes and plastomes. ''Am J Bot''. 2022 May; '''109''' (5):706-726
Combining population genomics with demographic analyses highlights habitat patchiness and larval dispersal as determinants of connectivity in coastal fish species. Description: Knutsen, Halvor, et al. Combining population genomics with demographic analyses highlights habitat patchiness and larval dispersal as determinants of connectivity in coastal fish species. ''Mol Ecol''. 2022 May; '''31''' (9):2562-2577
De novo chromosome-level genome of a semi-dwarf cultivar of Prunus persica identifies the aquaporin PpTIP2 as responsible for temperature-sensitive semi-dwarf trait and PpB3-1 for flower type and size. Description: Lian, Xiaodong, et al. De novo chromosome-level genome of a semi-dwarf cultivar of Prunus persica identifies the aquaporin PpTIP2 as responsible for temperature-sensitive semi-dwarf trait and PpB3-1 for flower type and size. ''Plant Biotechnol J''. 2022 May; '''20''' (5):886-902
Detection of candidate genes affecting milk production traits in sheep using whole-genome sequencing analysis. Description: Rezvannejad, Elham, et al. Detection of candidate genes affecting milk production traits in sheep using whole-genome sequencing analysis. ''Vet Med Sci''. 2022 May; '''8''' (3):1197-1204
Development of a clinical polygenic risk score assay and reporting workflow. Description: Hao, Limin, et al. Development of a clinical polygenic risk score assay and reporting workflow. ''Nat Med''. 2022 May; '''28''' (5):1006-1013
Eating disorder symptoms and their associations with anthropometric and psychiatric polygenic scores. Description: Abdulkadir, Mohamed, et al. Eating disorder symptoms and their associations with anthropometric and psychiatric polygenic scores. ''Eur Eat Disord Rev''. 2022 May; '''30''' (3):221-236
Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis. Description: Eapen, Amy A, et al. Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis. ''PLoS Genet''. 2022 May; '''18''' (5):e1009973
Extensive sampling of Saccharomyces cerevisiae in Taiwan reveals ecology and evolution of predomesticated lineages. Description: Lee, Tracy Jiaye, et al. Extensive sampling of Saccharomyces cerevisiae in Taiwan reveals ecology and evolution of predomesticated lineages. ''Genome Res''. 2022 May; '''32''' (5):864-877
Gene interaction analysis of psoriasis in Chinese Han population. Description: Xu, Qiongqiong, et al. Gene interaction analysis of psoriasis in Chinese Han population. ''Mol Genet Genomic Med''. 2022 May; '''10''' (5):e1858
Genetic and genomic characterization followed by single-step genomic evaluation of withers height in German Warmblood horses. Description: Vosgerau, Sarah, et al. Genetic and genomic characterization followed by single-step genomic evaluation of withers height in German Warmblood horses. ''J Appl Genet''. 2022 May; '''63''' (2):369-378
Genetic association study in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) identifies several potential risk loci. Description: Hajdarevic, Riad, et al. Genetic association study in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) identifies several potential risk loci. ''Brain Behav Immun''. 2022 May; '''102''': 362-369
Genome-wide association study reveals the genetic basis of growth trait in yellow catfish with sexual size dimorphism. Description: Huang, Peipei, et al. Genome-wide association study reveals the genetic basis of growth trait in yellow catfish with sexual size dimorphism. ''Genomics''. 2022 May; '''114''' (3):110380
HLA-DR polymorphism in SARS-CoV-2 infection and susceptibility to symptomatic COVID-19. Description: Astbury, Stuart, et al. HLA-DR polymorphism in SARS-CoV-2 infection and susceptibility to symptomatic COVID-19. ''Immunology''. 2022 May; '''166''' (1):68-77
HLA variants associated with azathioprine-induced pancreatitis in patients with Crohn's disease. Description: As, Joel, et al. HLA variants associated with azathioprine-induced pancreatitis in patients with Crohn's disease. ''Clin Transl Sci''. 2022 May; '''15''' (5):1249-1256
Identification of PDXDC1 as a novel pleiotropic susceptibility locus shared between lumbar spine bone mineral density and birth weight. Description: Song, Yu-Qian, et al. Identification of PDXDC1 as a novel pleiotropic susceptibility locus shared between lumbar spine bone mineral density and birth weight. ''J Mol Med (Berl)''. 2022 May; '''100''' (5):723-734
Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder. Description: Hakkinen, Katja, et al. Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder. ''Pharmacogenomics J''. 2022 May; '''22''' (3):166-172
Improving polygenic prediction in ancestrally diverse populations. Description: Ruan, Yunfeng, et al. Improving polygenic prediction in ancestrally diverse populations. ''Nat Genet''. 2022 May; '''54''' (5):573-580
Metabolomic profiling revealed altered lipid metabolite levels in childhood food allergy. Description: Jang, Haerin, et al. Metabolomic profiling revealed altered lipid metabolite levels in childhood food allergy. ''J Allergy Clin Immunol''. 2022 May; '''149''' (5):1722-1731.e9
Prediabetes blunts DPP4 genetic control of postprandial glycaemia and insulin secretion. Description: Patarrao, Rita S, et al. Prediabetes blunts DPP4 genetic control of postprandial glycaemia and insulin secretion. ''Diabetologia''. 2022 May; '''65''' (5):861-871
Predicting Pancreatic Cancer in the UK Biobank Cohort Using Polygenic Risk Scores and Diabetes Mellitus. Description: Sharma, Shreya, et al. Predicting Pancreatic Cancer in the UK Biobank Cohort Using Polygenic Risk Scores and Diabetes Mellitus. ''Gastroenterology''. 2022 May; '''162''' (6):1665-1674.e2
Prediction of incident atherosclerotic cardiovascular disease with polygenic risk of metabolic disease: Analysis of 3 prospective cohort studies in Korea. Description: Song, Han, et al. Prediction of incident atherosclerotic cardiovascular disease with polygenic risk of metabolic disease: Analysis of 3 prospective cohort studies in Korea. ''Atherosclerosis''. 2022 May; '''348''': 16-24
Sex-dimorphic gene effects on survival outcomes in people with coronary artery disease. Description: Dungan, Jennifer R, et al. Sex-dimorphic gene effects on survival outcomes in people with coronary artery disease. ''Am Heart J Plus''. 2022 May; '''17''':
Sex-heterogeneous SNPs disproportionately influence gene expression and health. Description: Traglia, Michela, et al. Sex-heterogeneous SNPs disproportionately influence gene expression and health. ''PLoS Genet''. 2022 May; '''18''' (5):e1010147
Shared genetic etiology and antagonistic relationship of plasma renin activity and systolic blood pressure in a Korean cohorts. Description: Jung, Jaehoon, et al. Shared genetic etiology and antagonistic relationship of plasma renin activity and systolic blood pressure in a Korean cohorts. ''Genomics''. 2022 May; '''114''' (3):110334
Signatures of selection are present in the genome of two close autochthonous cattle breeds raised in the North of Italy and mainly distinguished for their coat colours. Description: Bertolini, Francesca, et al. Signatures of selection are present in the genome of two close autochthonous cattle breeds raised in the North of Italy and mainly distinguished for their coat colours. ''J Anim Breed Genet''. 2022 May; '''139''' (3):307-319
Single nucleotide polymorphisms in FOXP1 and RORA of the lymphocyte activation-related pathway affect survival of lung cancer patients. Description: Du, Hailei, et al. Single nucleotide polymorphisms in FOXP1 and RORA of the lymphocyte activation-related pathway affect survival of lung cancer patients. ''Transl Lung Cancer Res''. 2022 May; '''11''' (5):890-901
The genomic landscape of blood groups in Indigenous Australians in remote communities. Description: Jadhao, Sudhir, et al. The genomic landscape of blood groups in Indigenous Australians in remote communities. ''Transfusion''. 2022 May; '''62''' (5):1110-1120
UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. Description: Lin, Nan, et al. UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. ''Pharmacogenomics J''. 2022 May; '''22''' (3):160-165
Whole-genome sequencing identifies rare missense variants of WNT16 and ERVW-1 causing the systemic lupus erythematosus. Description: Chen, Jianhai, et al. Whole-genome sequencing identifies rare missense variants of WNT16 and ERVW-1 causing the systemic lupus erythematosus. ''Genomics''. 2022 May; '''114''' (3):110332
Whole-genome sequencing reveals novel ethnicity-specific rare variants associated with Alzheimer's disease. Description: Shigemizu, Daichi, et al. Whole-genome sequencing reveals novel ethnicity-specific rare variants associated with Alzheimer's disease. ''Mol Psychiatry''. 2022 May; '''27''' (5):2554-2562
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Description: Howe, Laurence J, et al. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. ''Nat Genet''. 2022 May; '''54''' (5):581-592
The Genomics of Colorectal Cancer in Populations with African and European Ancestry. Description: Myer, Parvathi A, et al. The Genomics of Colorectal Cancer in Populations with African and European Ancestry. ''Cancer Discov''. 2022 May 2; '''12''' (5):1282-1293
DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases. Description: Wielscher, Matthias, et al. DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases. ''Nat Commun''. 2022 May 3; '''13''' (1):2408
Insights into Mus musculus Population Structure across Eurasia Revealed by Whole-Genome Analysis. Description: Fujiwara, Kazumichi, et al. Insights into Mus musculus Population Structure across Eurasia Revealed by Whole-Genome Analysis. ''Genome Biol Evol''. 2022 May 3; '''14''' (5):
Mutation Load in Sunflower Inversions Is Negatively Correlated with Inversion Heterozygosity. Description: Huang, Kaichi, et al. Mutation Load in Sunflower Inversions Is Negatively Correlated with Inversion Heterozygosity. ''Mol Biol Evol''. 2022 May 3; '''39''' (5):
Palaeogenomic analysis of black rat (Rattus rattus) reveals multiple European introductions associated with human economic history. Description: Yu, He, et al. Palaeogenomic analysis of black rat (Rattus rattus) reveals multiple European introductions associated with human economic history. ''Nat Commun''. 2022 May 3; '''13''' (1):2399
Concurrent outcomes from multiple approaches of epistasis analysis for human body mass index associated loci provide insights into obesity biology. Description: D'Silva, Sheldon, et al. Concurrent outcomes from multiple approaches of epistasis analysis for human body mass index associated loci provide insights into obesity biology. ''Sci Rep''. 2022 May 4; '''12''' (1):7306
Genetic architecture of orbital telorism. Description: Knol, Maria J, et al. Genetic architecture of orbital telorism. ''Hum Mol Genet''. 2022 May 4; '''31''' (9):1531-1543
Genomes from Verteba cave suggest diversity within the Trypillians in Ukraine. Description: Gelabert, Pere, et al. Genomes from Verteba cave suggest diversity within the Trypillians in Ukraine. ''Sci Rep''. 2022 May 4; '''12''' (1):7242
Genome wide association study on development and evolution of glutinous rice. Description: Jiang, Conghui, et al. Genome wide association study on development and evolution of glutinous rice. ''BMC Genom Data''. 2022 May 4; '''23''' (1):33
Genome-wide association study reveals the genetic architecture for calcium accumulation in grains of hexaploid wheat (Triticum aestivum L.). Description: Shi, Xia, et al. Genome-wide association study reveals the genetic architecture for calcium accumulation in grains of hexaploid wheat (Triticum aestivum L.). ''BMC Plant Biol''. 2022 May 4; '''22''' (1):229
Combining fMRI and DISC1 gene haplotypes to understand working memory-related brain activity in schizophrenia. Description: Guardiola-Ripoll, Maria, et al. Combining fMRI and DISC1 gene haplotypes to understand working memory-related brain activity in schizophrenia. ''Sci Rep''. 2022 May 5; '''12''' (1):7351
Distribution of TAS2R38 bitter taste receptor phenotype and haplotypes among COVID-19 patients. Description: Risso, D, et al. Distribution of TAS2R38 bitter taste receptor phenotype and haplotypes among COVID-19 patients. ''Sci Rep''. 2022 May 5; '''12''' (1):7381
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals. Description: D'Alterio, Giuseppe, et al. Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals. ''Genet Med''. 2022 May 5;
Leveraging LD eigenvalue regression to improve the estimation of SNP heritability and confounding inflation. Description: Song, Shuang, et al. Leveraging LD eigenvalue regression to improve the estimation of SNP heritability and confounding inflation. ''Am J Hum Genet''. 2022 May 5; '''109''' (5):802-811
Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk. Description: Schaid, Daniel J, et al. Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk. ''Am J Hum Genet''. 2022 May 5; '''109''' (5):900-908
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program. Description: Hu, Xiaowei, et al. Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program. ''Am J Hum Genet''. 2022 May 5; '''109''' (5):857-870
Population genetics and microevolution of clinical Candida glabrata reveals recombinant sequence types and hyper-variation within mitochondrial genomes, virulence genes, and drug targets. Description: Helmstetter, Nicolas, et al. Population genetics and microevolution of clinical Candida glabrata reveals recombinant sequence types and hyper-variation within mitochondrial genomes, virulence genes, and drug targets. ''Genetics''. 2022 May 5; '''221''' (1):
Exploring transposable element-based markers to identify allelic variations underlying agronomic traits in rice. Description: Yan, Haidong, et al. Exploring transposable element-based markers to identify allelic variations underlying agronomic traits in rice. ''Plant Commun''. 2022 May 9; '''3''' (3):100270
Genomic insights on the contribution of introgressions from Xian/Indica to the genetic improvement of Geng/Japonica rice cultivars. Description: Cui, Di, et al. Genomic insights on the contribution of introgressions from Xian/Indica to the genetic improvement of Geng/Japonica rice cultivars. ''Plant Commun''. 2022 May 9; '''3''' (3):100325
Using genomic prediction to detect microevolutionary change of a quantitative trait. Description: Hunter, D C, et al. Using genomic prediction to detect microevolutionary change of a quantitative trait. ''Proc Biol Sci''. 2022 May 11; '''289''' (1974):20220330
Exploring the association between birthweight and breast cancer using summary statistics from a perspective of genetic correlation, mediation, and causality. Description: Zhang, Meng, et al. Exploring the association between birthweight and breast cancer using summary statistics from a perspective of genetic correlation, mediation, and causality. ''J Transl Med''. 2022 May 14; '''20''' (1):227
Analysis of human leukocyte antigen associations in human papillomavirus-positive and -negative head and neck cancer: Comparison with cervical cancer. Description: Ekanayake Weeramange, Chameera, et al. Analysis of human leukocyte antigen associations in human papillomavirus-positive and -negative head and neck cancer: Comparison with cervical cancer. ''Cancer''. 2022 May 15; '''128''' (10):1937-1947
A genome-wide association study for melatonin secretion. Description: Liu, Pi-Hua, et al. A genome-wide association study for melatonin secretion. ''Sci Rep''. 2022 May 16; '''12''' (1):8025
The Effects of Common Genetic Variation in 96 Genes Involved in Thyroid Hormone Regulation on TSH and FT4 Concentrations. Description: Sterenborg, Rosalie B T M, et al. The Effects of Common Genetic Variation in 96 Genes Involved in Thyroid Hormone Regulation on TSH and FT4 Concentrations. ''J Clin Endocrinol Metab''. 2022 May 17; '''107''' (6):e2276-e2283
Using machine learning to improve the accuracy of genomic prediction of reproduction traits in pigs. Description: Wang, Xue, et al. Using machine learning to improve the accuracy of genomic prediction of reproduction traits in pigs. ''J Anim Sci Biotechnol''. 2022 May 17; '''13''' (1):60
Phosphonate coating of commercial iron oxide nanoparticles for nanowarming cryopreserved samples. Description: Pasek-Allen, Jacqueline L, et al. Phosphonate coating of commercial iron oxide nanoparticles for nanowarming cryopreserved samples. ''J Mater Chem B''. 2022 May 18; '''10''' (19):3734-3746
Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci. Description: Laaksonen, Jaakko, et al. Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci. ''Hum Mol Genet''. 2022 May 19; '''31''' (10):1720-1732
A systematic comparison of FOSL1, FOSL2 and BATF-mediated transcriptional regulation during early human Th17 differentiation. Description: Shetty, Ankitha, et al. A systematic comparison of FOSL1, FOSL2 and BATF-mediated transcriptional regulation during early human Th17 differentiation. ''Nucleic Acids Res''. 2022 May 20; '''50''' (9):4938-4958
A two-step adaptive walk rewires nutrient transport in a challenging edaphic environment. Description: Tergemina, Emmanuel, et al. A two-step adaptive walk rewires nutrient transport in a challenging edaphic environment. ''Sci Adv''. 2022 May 20; '''8''' (20):eabm9385
Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank. Description: Fawcett, Katherine A, et al. Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank. ''BMC Med Genomics''. 2022 May 21; '''15''' (1):119
Association of APOE-Independent Alzheimer Disease Polygenic Risk Score With Brain Amyloid Deposition in Asymptomatic Older Adults. Description: Xicota, Laura, et al. Association of APOE-Independent Alzheimer Disease Polygenic Risk Score With Brain Amyloid Deposition in Asymptomatic Older Adults. ''Neurology''. 2022 May 23;
An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations. Description: Quiat, Daniel, et al. An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations. ''Proc Natl Acad Sci U S A''. 2022 May 24; '''119''' (21):e2203928119
High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases. Description: Hiz Kurul, Semra, et al. High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases. ''Brain''. 2022 May 24; '''145''' (4):1507-1518
Population interconnectivity over the past 120,000 years explains distribution and diversity of Central African hunter-gatherers. Description: Padilla-Iglesias, Cecilia, et al. Population interconnectivity over the past 120,000 years explains distribution and diversity of Central African hunter-gatherers. ''Proc Natl Acad Sci U S A''. 2022 May 24; '''119''' (21):e2113936119
Genome-wide identification of copy number variation and association with fat deposition in thin and fat-tailed sheep breeds. Description: Taghizadeh, Shadan, et al. Genome-wide identification of copy number variation and association with fat deposition in thin and fat-tailed sheep breeds. ''Sci Rep''. 2022 May 25; '''12''' (1):8834
Chromosome-level genome assembly and characterization of Sophora Japonica. Description: Lei, Weixiao, et al. Chromosome-level genome assembly and characterization of Sophora Japonica. ''DNA Res''. 2022 May 27; '''29''' (3):
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery. Description: Oliver, Karen L, et al. Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery. ''EBioMedicine''. 2022 May 27; '''81''': 104079
An update of the salmon louse (Lepeophtheirus salmonis) reference genome assembly. Description: Joshi, Jay, et al. An update of the salmon louse (Lepeophtheirus salmonis) reference genome assembly. ''G3 (Bethesda)''. 2022 May 30; '''12''' (6):
Association of variations in the Fanconi anemia complementation group and prognosis in Non-small cell lung cancer patients with Platinum-based chemotherapy. Description: Mo, Jun-Luan, et al. Association of variations in the Fanconi anemia complementation group and prognosis in Non-small cell lung cancer patients with Platinum-based chemotherapy. ''Gene''. 2022 May 30; '''825''': 146398
Ratios of Acetaminophen Metabolites Identify New Loci of Pharmacogenetic Relevance in a Genome-Wide Association Study. Description: Thareja, Gaurav, et al. Ratios of Acetaminophen Metabolites Identify New Loci of Pharmacogenetic Relevance in a Genome-Wide Association Study. ''Metabolites''. 2022 May 30; '''12''' (6):
A genome-wide functional genomics approach uncovers genetic determinants of immune phenotypes in type 1 diabetes. Description: Chu, Xiaojing, et al. A genome-wide functional genomics approach uncovers genetic determinants of immune phenotypes in type 1 diabetes. ''Elife''. 2022 May 31; '''11''':
beta-Amyloid-Dependent and -Independent Genetic Pathways Regulating CSF Tau Biomarkers in Alzheimer Disease. Description: Kumar, Atul, et al. beta-Amyloid-Dependent and -Independent Genetic Pathways Regulating CSF Tau Biomarkers in Alzheimer Disease. ''Neurology''. 2022 May 31;
ABO genotype alters the gut microbiota by regulating GalNAc levels in pigs. Description: Yang, Hui, et al. ABO genotype alters the gut microbiota by regulating GalNAc levels in pigs. ''Nature''. 2022 Jun; '''606''' (7913):358-367
Admixture Mapping of Alzheimer's disease in Caribbean Hispanics identifies a new locus on 22q13.1. Description: Kizil, Caghan, et al. Admixture Mapping of Alzheimer's disease in Caribbean Hispanics identifies a new locus on 22q13.1. ''Mol Psychiatry''. 2022 Jun; '''27''' (6):2813-2820
A multivariant recall-by-genotype study of the metabolomic signature of BMI. Description: Fang, Si, et al. A multivariant recall-by-genotype study of the metabolomic signature of BMI. ''Obesity (Silver Spring)''. 2022 Jun; '''30''' (6):1298-1310
Analysis of the genomic landscapes of Barbadian and Nigerian women with triple negative breast cancer. Description: Hercules, Shawn M, et al. Analysis of the genomic landscapes of Barbadian and Nigerian women with triple negative breast cancer. ''Cancer Causes Control''. 2022 Jun; '''33''' (6):831-841
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam. Description: Campbell, Ciaran, et al. A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam. ''Epilepsia''. 2022 Jun; '''63''' (6):1563-1570
Association between genetic and socioenvironmental risk for schizophrenia during upbringing in a UK longitudinal cohort. Description: Newbury, J B, et al. Association between genetic and socioenvironmental risk for schizophrenia during upbringing in a UK longitudinal cohort. ''Psychol Med''. 2022 Jun; '''52''' (8):1527-1537
Association between IKBKAP polymorphisms and Hirschsprung's disease susceptibility in Chinese children. Description: Wang, Ning, et al. Association between IKBKAP polymorphisms and Hirschsprung's disease susceptibility in Chinese children. ''Transl Pediatr''. 2022 Jun; '''11''' (6):789-796
Association of Inherited Mutations in DNA Repair Genes with Localized Prostate Cancer. Description: Lee, Daniel J, et al. Association of Inherited Mutations in DNA Repair Genes with Localized Prostate Cancer. ''Eur Urol''. 2022 Jun; '''81''' (6):559-567
Effects of depression on employment and social outcomes: a Mendelian randomisation study. Description: Campbell, Desmond, et al. Effects of depression on employment and social outcomes: a Mendelian randomisation study. ''J Epidemiol Community Health''. 2022 Jun; '''76''' (6):563-571
EPIC: Inferring relevant cell types for complex traits by integrating genome-wide association studies and single-cell RNA sequencing. Description: Wang, Rujin, et al. EPIC: Inferring relevant cell types for complex traits by integrating genome-wide association studies and single-cell RNA sequencing. ''PLoS Genet''. 2022 Jun; '''18''' (6):e1010251
Ethnic differences in the frequency of beta-amyloid deposition in cognitively normal individuals. Description: Kim, Jaeho, et al. Ethnic differences in the frequency of beta-amyloid deposition in cognitively normal individuals. ''Neurobiol Aging''. 2022 Jun; '''114''': 27-37
Further evidence from common garden rearing experiments of heritable traits separating lean and siscowet lake charr (Salvelinus namaycush) ecotypes. Description: Euclide, Peter T, et al. Further evidence from common garden rearing experiments of heritable traits separating lean and siscowet lake charr (Salvelinus namaycush) ecotypes. ''Mol Ecol''. 2022 Jun; '''31''' (12):3432-3450
Gene-lifestyle interactions in the genomics of human complex traits. Description: Laville, Vincent, et al. Gene-lifestyle interactions in the genomics of human complex traits. ''Eur J Hum Genet''. 2022 Jun; '''30''' (6):730-739
Genetic variants associated with low-density lipoprotein cholesterol and systolic blood pressure and the risk of recurrent cardiovascular disease in patients with established vascular disease. Description: Groenland, Eline H, et al. Genetic variants associated with low-density lipoprotein cholesterol and systolic blood pressure and the risk of recurrent cardiovascular disease in patients with established vascular disease. ''Atherosclerosis''. 2022 Jun; '''350''': 102-108
Genome-wide association analysis reveals new insights into the genetic architecture of defensive, agro-morphological and quality-related traits in cassava. Description: Rabbi, Ismail Yusuf, et al. Genome-wide association analysis reveals new insights into the genetic architecture of defensive, agro-morphological and quality-related traits in cassava. ''Plant Mol Biol''. 2022 Jun; '''109''' (3):195-213
Genome-Wide Association Study Identifies Genetic Loci Associated With Fat Cell Number and Overlap With Genetic Risk Loci for Type 2 Diabetes. Description: Kulyte, Agne, et al. Genome-Wide Association Study Identifies Genetic Loci Associated With Fat Cell Number and Overlap With Genetic Risk Loci for Type 2 Diabetes. ''Diabetes''. 2022 Jun 1; '''71''' (6):1350-1362
Genome-wide association study of 7661 Chinese Han individuals and fine-mapping major histocompatibility complex identifies HLA-DRB1 as associated with IgA vasculitis. Description: Xia, Liang, et al. Genome-wide association study of 7661 Chinese Han individuals and fine-mapping major histocompatibility complex identifies HLA-DRB1 as associated with IgA vasculitis. ''J Clin Lab Anal''. 2022 Jun; '''36''' (6):e24457
Genomic analysis defines clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancer. Description: Lips, Esther H, et al. Genomic analysis defines clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancer. ''Nat Genet''. 2022 Jun; '''54''' (6):850-860
Genomic associations with poxvirus across divergent island populations in Berthelot's pipit. Description: Sheppard, Eleanor C, et al. Genomic associations with poxvirus across divergent island populations in Berthelot's pipit. ''Mol Ecol''. 2022 Jun; '''31''' (11):3154-3173
Genomic changes underlying repeated niche shifts in an adaptive radiation. Description: Marques, David A, et al. Genomic changes underlying repeated niche shifts in an adaptive radiation. ''Evolution''. 2022 Jun; '''76''' (6):1301-1319
Geographic Origin and Vertical Transmission of Leishmania infantum Parasites in Hunting Hounds, United States. Description: Franssen, Susanne U, et al. Geographic Origin and Vertical Transmission of Leishmania infantum Parasites in Hunting Hounds, United States. ''Emerg Infect Dis''. 2022 Jun; '''28''' (6):1211-1223
Graph pangenome captures missing heritability and empowers tomato breeding. Description: Zhou, Yao, et al. Graph pangenome captures missing heritability and empowers tomato breeding. ''Nature''. 2022 Jun; '''606''' (7914):527-534
High Blood Pressure and Intraocular Pressure: A Mendelian Randomization Study. Description: Plotnikov, Denis, et al. High Blood Pressure and Intraocular Pressure: A Mendelian Randomization Study. ''Invest Ophthalmol Vis Sci''. 2022 Jun 1; '''63''' (6):29
Identification of ST1 reveals a selection involving hitchhiking of seed morphology and oil content during soybean domestication. Description: Li, Jun, et al. Identification of ST1 reveals a selection involving hitchhiking of seed morphology and oil content during soybean domestication. ''Plant Biotechnol J''. 2022 Jun; '''20''' (6):1110-1121
Imputed expression of schizophrenia-associated genes and cognitive measures in patients with schizophrenia. Description: Fabbri, Chiara, et al. Imputed expression of schizophrenia-associated genes and cognitive measures in patients with schizophrenia. ''Mol Genet Genomic Med''. 2022 Jun; '''10''' (6):e1942
Longer screen time utilization is associated with the polygenic risk for Attention-deficit/hyperactivity disorder with mediation by brain white matter microstructure. Description: Yang, Anyi, et al. Longer screen time utilization is associated with the polygenic risk for Attention-deficit/hyperactivity disorder with mediation by brain white matter microstructure. ''EBioMedicine''. 2022 Jun; '''80''': 104039
Multi-ancestry genome-wide association study of asthma exacerbations. Description: Herrera-Luis, Esther, et al. Multi-ancestry genome-wide association study of asthma exacerbations. ''Pediatr Allergy Immunol''. 2022 Jun; '''33''' (6):e13802
Reconstructing the history of founder events using genome-wide patterns of allele sharing across individuals. Description: Tournebize, Remi, et al. Reconstructing the history of founder events using genome-wide patterns of allele sharing across individuals. ''PLoS Genet''. 2022 Jun; '''18''' (6):e1010243
Seaweed and Iodine Intakes and SLC5A5 rs77277498 in Relation to Thyroid Cancer. Description: Hoang, Tung, et al. Seaweed and Iodine Intakes and SLC5A5 rs77277498 in Relation to Thyroid Cancer. ''Endocrinol Metab (Seoul)''. 2022 Jun; '''37''' (3):513-523
The HDAC9-associated risk locus promotes coronary artery disease by governing TWIST1. Description: Ma, Lijiang, et al. The HDAC9-associated risk locus promotes coronary artery disease by governing TWIST1. ''PLoS Genet''. 2022 Jun; '''18''' (6):e1010261
Transferability of genetic risk scores in African populations. Description: Kamiza, Abram B, et al. Transferability of genetic risk scores in African populations. ''Nat Med''. 2022 Jun; '''28''' (6):1163-1166
Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Description: Nieves-Colon, Maria A, et al. Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. ''Am J Hum Genet''. 2022 Jun 2; '''109''' (6):1117-1139
Evolutionary Conservation Genomics Reveals Recent Speciation and Local Adaptation in Threatened Takins. Description: Yang, Lin, et al. Evolutionary Conservation Genomics Reveals Recent Speciation and Local Adaptation in Threatened Takins. ''Mol Biol Evol''. 2022 Jun 2; '''39''' (6):
Genetic architecture of microRNA expression and its link to complex diseases in the Japanese population. Description: Sonehara, Kyuto, et al. Genetic architecture of microRNA expression and its link to complex diseases in the Japanese population. ''Hum Mol Genet''. 2022 Jun 4; '''31''' (11):1806-1820
Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia. Description: Guggenheim, Jeremy A, et al. Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia. ''Hum Mol Genet''. 2022 Jun 4; '''31''' (11):1909-1919
First report on genome wide association study in western Indian population reveals host genetic factors for COVID-19 severity and outcome. Description: Pandit, Ramesh, et al. First report on genome wide association study in western Indian population reveals host genetic factors for COVID-19 severity and outcome. ''Genomics''. 2022 Jun 6; '''114''' (4):110399
How methodological changes have influenced our understanding of population structure in threatened species: insights from tiger populations across India. Description: Aylward, Megan, et al. How methodological changes have influenced our understanding of population structure in threatened species: insights from tiger populations across India. ''Philos Trans R Soc Lond B Biol Sci''. 2022 Jun 6; '''377''' (1852):20200418
Life-threatening viral disease in a novel form of autosomal recessive IFNAR2 deficiency in the Arctic. Description: Duncan, Christopher J A, et al. Life-threatening viral disease in a novel form of autosomal recessive IFNAR2 deficiency in the Arctic. ''J Exp Med''. 2022 Jun 6; '''219''' (6):
The genetic legacy of the Manila galleon trade in Mexico. Description: Rodriguez-Rodriguez, Juan Esteban, et al. The genetic legacy of the Manila galleon trade in Mexico. ''Philos Trans R Soc Lond B Biol Sci''. 2022 Jun 6; '''377''' (1852):20200419
The role of common genetic variation in presumed monogenic epilepsies. Description: Campbell, Ciaran, et al. The role of common genetic variation in presumed monogenic epilepsies. ''EBioMedicine''. 2022 Jun 6; '''81''': 104098
Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol. Description: Shi, Mingjian, et al. Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol. ''J Am Heart Assoc''. 2022 Jun 7; '''11''' (11):e024388
Integrative PheWAS analysis in risk categorization of major depressive disorder and identifying their associations with genetic variants using a latent topic model approach. Description: Meng, Xiangfei, et al. Integrative PheWAS analysis in risk categorization of major depressive disorder and identifying their associations with genetic variants using a latent topic model approach. ''Transl Psychiatry''. 2022 Jun 8; '''12''' (1):240
Limited association between infections, autoimmune disease and genetic risk and immune activation in severe mental disorders. Description: Werner, Maren Caroline Frogner, et al. Limited association between infections, autoimmune disease and genetic risk and immune activation in severe mental disorders. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2022 Jun 8; '''116''': 110511
Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilities. Description: Mallard, Travis T, et al. Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilities. ''Cell Genom''. 2022 Jun 8; '''2''' (6):
Link between cognitive polygenic risk scores and clinical progression after a first-psychotic episode. Description: Segura, Alex G, et al. Link between cognitive polygenic risk scores and clinical progression after a first-psychotic episode. ''Psychol Med''. 2022 Jun 9; '''53''' (10):1-14
Educational attainment as a modifier for the effect of polygenic scores for cardiovascular risk factors: cross-sectional and prospective analysis of UK Biobank. Description: Carter, Alice R, et al. Educational attainment as a modifier for the effect of polygenic scores for cardiovascular risk factors: cross-sectional and prospective analysis of UK Biobank. ''Int J Epidemiol''. 2022 Jun 13; '''51''' (3):885-897
Meprin A1 subunit beta gene polymorphism is associated with the length of post-partum anestrus interval in Murrah buffaloes. Description: Kumar, Thota Venkata Chaitanya, et al. Meprin A1 subunit beta gene polymorphism is associated with the length of post-partum anestrus interval in Murrah buffaloes. ''Gene''. 2022 Jun 15; '''827''': 146456
Ancient Maltese genomes and the genetic geography of Neolithic Europe. Description: Ariano, Bruno, et al. Ancient Maltese genomes and the genetic geography of Neolithic Europe. ''Curr Biol''. 2022 Jun 20; '''32''' (12):2668-2680.e6
Variants in proinflammatory genes IL1RL1, IL1B and IRF4 are associated with overweight in a pediatric Brazilian population. Description: Melo, Ana Paula Castro, et al. Variants in proinflammatory genes IL1RL1, IL1B and IRF4 are associated with overweight in a pediatric Brazilian population. ''Gene''. 2022 Jun 20; '''828''': 146478
Corin Missense Variants, Blood Pressure, and Hypertension in 11 322 Black Individuals: Insights From REGARDS and the Jackson Heart Study. Description: Parcha, Vibhu, et al. Corin Missense Variants, Blood Pressure, and Hypertension in 11 322 Black Individuals: Insights From REGARDS and the Jackson Heart Study. ''J Am Heart Assoc''. 2022 Jun 21; '''11''' (12):e025582
Revealing the recent demographic history of Europe via haplotype sharing in the UK Biobank. Description: Gilbert, Edmund, et al. Revealing the recent demographic history of Europe via haplotype sharing in the UK Biobank. ''Proc Natl Acad Sci U S A''. 2022 Jun 21; '''119''' (25):e2119281119
Genome-wide association studies in non-anxiety individuals identified novel risk loci for depression. Description: Cheng, Bolun, et al. Genome-wide association studies in non-anxiety individuals identified novel risk loci for depression. ''Eur Psychiatry''. 2022 Jun 22; '''65''' (1):e38
Expression of the GZMB Gene Polymorphism, SNP rs8192917, in 990 Han Chinese Patients with Postoperative Keloids. Description: Wen, Xiulin, et al. Expression of the GZMB Gene Polymorphism, SNP rs8192917, in 990 Han Chinese Patients with Postoperative Keloids. ''Med Sci Monit''. 2022 Jun 23; '''28''': e936963
PolarMorphism enables discovery of shared genetic variants across multiple traits from GWAS summary statistics. Description: von Berg, Joanna, et al. PolarMorphism enables discovery of shared genetic variants across multiple traits from GWAS summary statistics. ''Bioinformatics''. 2022 Jun 24; '''38''' (Suppl 1):i212-i219
Protoplast fusion in Bacillus species produces frequent, unbiased, genome-wide homologous recombination. Description: Vasileva, Delyana P, et al. Protoplast fusion in Bacillus species produces frequent, unbiased, genome-wide homologous recombination. ''Nucleic Acids Res''. 2022 Jun 24; '''50''' (11):6211-6223
Functional associations between polymorphic regions of the human 3'IgH locus and COVID-19 disease. Description: Colucci, Mattia, et al. Functional associations between polymorphic regions of the human 3'IgH locus and COVID-19 disease. ''Gene''. 2022 Jun 27; '''838''': 146698
Interaction between maternal killer immunoglobulin-like receptors and offspring HLAs and susceptibility of childhood ALL. Description: Feng, Qianxi, et al. Interaction between maternal killer immunoglobulin-like receptors and offspring HLAs and susceptibility of childhood ALL. ''Blood Adv''. 2022 Jun 28; '''6''' (12):3756-3766
Microbiome-associated human genetic variants impact phenome-wide disease risk. Description: Markowitz, Robert H George, et al. Microbiome-associated human genetic variants impact phenome-wide disease risk. ''Proc Natl Acad Sci U S A''. 2022 Jun 28; '''119''' (26):e2200551119
Racial and ethnic differences in clonal hematopoiesis, tumor markers, and outcomes of patients with multiple myeloma. Description: Peres, Lauren C, et al. Racial and ethnic differences in clonal hematopoiesis, tumor markers, and outcomes of patients with multiple myeloma. ''Blood Adv''. 2022 Jun 28; '''6''' (12):3767-3778
Inbreeding depression and the probability of racing in the Thoroughbred horse. Description: Hill, Emmeline W, et al. Inbreeding depression and the probability of racing in the Thoroughbred horse. ''Proc Biol Sci''. 2022 Jun 29; '''289''' (1977):20220487
A Genome-Wide Association Study Reveals Two Genetic Markers for Chondromalacia. Description: Kim, Stuart K, et al. A Genome-Wide Association Study Reveals Two Genetic Markers for Chondromalacia. ''Cartilage''. 2022 Jul-Sep; '''13''' (3):19476035221121790
Alcohol consumption, blood DNA methylation and breast cancer: a Mendelian randomisation study. Description: Zhou, Xuan, et al. Alcohol consumption, blood DNA methylation and breast cancer: a Mendelian randomisation study. ''Eur J Epidemiol''. 2022 Jul; '''37''' (7):701-712
Alcohol consumption, DNA methylation and colorectal cancer risk: Results from pooled cohort studies and Mendelian randomization analysis. Description: Zhou, Xuan, et al. Alcohol consumption, DNA methylation and colorectal cancer risk: Results from pooled cohort studies and Mendelian randomization analysis. ''Int J Cancer''. 2022 Jul 1; '''151''' (1):83-94
A locus at 19q13.31 significantly reduces the ApoE epsilon4 risk for Alzheimer's Disease in African Ancestry. Description: Rajabli, Farid, et al. A locus at 19q13.31 significantly reduces the ApoE epsilon4 risk for Alzheimer's Disease in African Ancestry. ''PLoS Genet''. 2022 Jul; '''18''' (7):e1009977
Ancient genomes from the last three millennia support multiple human dispersals into Wallacea. Description: Oliveira, Sandra, et al. Ancient genomes from the last three millennia support multiple human dispersals into Wallacea. ''Nat Ecol Evol''. 2022 Jul; '''6''' (7):1024-1034
An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-epsilon4 in female patients with Alzheimer's disease. Description: Jiang, Yuanbing, et al. An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-epsilon4 in female patients with Alzheimer's disease. ''Nat Aging''. 2022 Jul; '''2''' (7):616-634
Assessment of burden and segregation profiles of CNVs in patients with epilepsy. Description: Moreau, Claudia, et al. Assessment of burden and segregation profiles of CNVs in patients with epilepsy. ''Ann Clin Transl Neurol''. 2022 Jul; '''9''' (7):1050-1058
Benchmarking statistical methods for analyzing parent-child dyads in genetic association studies. Description: Ray, Debashree, et al. Benchmarking statistical methods for analyzing parent-child dyads in genetic association studies. ''Genet Epidemiol''. 2022 Jul; '''46''' (5-6):266-284
Depressive symptom trajectories and polygenic risk scores in individuals with an immune-mediated inflammatory disease. Description: Kowalec, Kaarina, et al. Depressive symptom trajectories and polygenic risk scores in individuals with an immune-mediated inflammatory disease. ''Gen Hosp Psychiatry''. 2022 Jul-Aug; '''77''': 21-28
Evaluating the Potential of Polygenic Risk Score to Improve Colorectal Cancer Screening. Description: Arnau-Collell, Coral, et al. Evaluating the Potential of Polygenic Risk Score to Improve Colorectal Cancer Screening. ''Cancer Epidemiol Biomarkers Prev''. 2022 Jul 1; '''31''' (7):1305-1312
Exploring polygenic-environment and residual-environment interactions for depressive symptoms within the UK Biobank. Description: Gillett, Alexandra C, et al. Exploring polygenic-environment and residual-environment interactions for depressive symptoms within the UK Biobank. ''Genet Epidemiol''. 2022 Jul; '''46''' (5-6):219-233
Genetic evidence for the most common risk factors for chronic axonal polyneuropathy in the general population. Description: Taams, Noor E, et al. Genetic evidence for the most common risk factors for chronic axonal polyneuropathy in the general population. ''Eur J Neurol''. 2022 Jul; '''29''' (7):2066-2073
Genetic Evidence Supporting a Causal Role of Depression in Alzheimer's Disease. Description: Harerimana, Nadia V, et al. Genetic Evidence Supporting a Causal Role of Depression in Alzheimer's Disease. ''Biol Psychiatry''. 2022 Jul 1; '''92''' (1):25-33
Genetic variants associated with acamprosate treatment response in alcohol use disorder patients: A multiple omics study. Description: Ho, Ming-Fen, et al. Genetic variants associated with acamprosate treatment response in alcohol use disorder patients: A multiple omics study. ''Br J Pharmacol''. 2022 Jul; '''179''' (13):3330-3345
Genome-wide linkage analysis combined with genome sequencing in large families with intracranial aneurysms. Description: Bakker, Mark K, et al. Genome-wide linkage analysis combined with genome sequencing in large families with intracranial aneurysms. ''Eur J Hum Genet''. 2022 Jul; '''30''' (7):833-840
Genome-wide scan for selection signatures and genes related to heat tolerance in domestic chickens in the tropical and temperate regions in Asia. Description: Guo, Xing, et al. Genome-wide scan for selection signatures and genes related to heat tolerance in domestic chickens in the tropical and temperate regions in Asia. ''Poult Sci''. 2022 Jul; '''101''' (7):101821
Genomic and transcriptomic analysis unveils population evolution and development of pesticide resistance in fall armyworm Spodoptera frugiperda. Description: Gui, Furong, et al. Genomic and transcriptomic analysis unveils population evolution and development of pesticide resistance in fall armyworm Spodoptera frugiperda. ''Protein Cell''. 2022 Jul; '''13''' (7):513-531
Genomic insights into recent species divergence in Nicotiana benthamiana and natural variation in Rdr1 gene controlling viral susceptibility. Description: Cauz-Santos, Luiz A, et al. Genomic insights into recent species divergence in Nicotiana benthamiana and natural variation in Rdr1 gene controlling viral susceptibility. ''Plant J''. 2022 Jul; '''111''' (1):7-18
Genomic signatures for drylands adaptation at gene-rich regions in African zebu cattle. Description: Tijjani, Abdulfatai, et al. Genomic signatures for drylands adaptation at gene-rich regions in African zebu cattle. ''Genomics''. 2022 Jul; '''114''' (4):110423
Grey wolf genomic history reveals a dual ancestry of dogs. Description: Bergstrom, Anders, et al. Grey wolf genomic history reveals a dual ancestry of dogs. ''Nature''. 2022 Jul; '''607''' (7918):313-320
Integrating genomics and transcriptomics to identify candidate genes for subcutaneous fat deposition in beef cattle. Description: Du, Lili, et al. Integrating genomics and transcriptomics to identify candidate genes for subcutaneous fat deposition in beef cattle. ''Genomics''. 2022 Jul; '''114''' (4):110406
Integrative analysis of omics summary data reveals putative mechanisms linked to different cell populations in systemic lupus erythematosus. Description: Cui, Mintian, et al. Integrative analysis of omics summary data reveals putative mechanisms linked to different cell populations in systemic lupus erythematosus. ''Genomics''. 2022 Jul; '''114''' (4):110435
Molecular and archaeological evidence on the geographical origin of domestication for Camelina sativa. Description: Brock, Jordan R, et al. Molecular and archaeological evidence on the geographical origin of domestication for Camelina sativa. ''Am J Bot''. 2022 Jul; '''109''' (7):1177-1190
Multiple introductions and overwintering shape the progressive invasion of Aedes albopictus beyond the Alps. Description: Vavassori, Laura, et al. Multiple introductions and overwintering shape the progressive invasion of Aedes albopictus beyond the Alps. ''Ecol Evol''. 2022 Jul; '''12''' (7):e9138
Network-based meta-analysis and the candidate gene association studies reveal novel ethnicity-specific variants in MFSD3 and MRPL43 associated with dementia with Lewy bodies. Description: Shigemizu, Daichi, et al. Network-based meta-analysis and the candidate gene association studies reveal novel ethnicity-specific variants in MFSD3 and MRPL43 associated with dementia with Lewy bodies. ''Am J Med Genet B Neuropsychiatr Genet''. 2022 Jul; '''189''' (5):139-150
Parental inflammatory bowel disease and autism in children. Description: Sadik, Aws, et al. Parental inflammatory bowel disease and autism in children. ''Nat Med''. 2022 Jul; '''28''' (7):1406-1411
Pharmacogenomics of cisplatin-induced neurotoxicities: Hearing loss, tinnitus, and peripheral sensory neuropathy. Description: Zhang, Xindi, et al. Pharmacogenomics of cisplatin-induced neurotoxicities: Hearing loss, tinnitus, and peripheral sensory neuropathy. ''Cancer Med''. 2022 Jul; '''11''' (14):2801-2816
Polygenic and socioeconomic risk for high body mass index: 69 years of follow-up across life. Description: Bann, David, et al. Polygenic and socioeconomic risk for high body mass index: 69 years of follow-up across life. ''PLoS Genet''. 2022 Jul; '''18''' (7):e1010233
Reviving ghost alleles: Genetically admixed coyotes along the American Gulf Coast are critical for saving the endangered red wolf. Description: vonHoldt, Bridgett M, et al. Reviving ghost alleles: Genetically admixed coyotes along the American Gulf Coast are critical for saving the endangered red wolf. ''Sci Adv''. 2022 Jul; '''8''' (26):eabn7731
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility. Description: Silvennoinen, Katri, et al. SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility. ''Acta Neuropathol''. 2022 Jul; '''144''' (1):107-127
Smoking and infertility: multivariable regression and Mendelian randomization analyses in the Norwegian Mother, Father and Child Cohort Study. Description: Hernaez, Alvaro, et al. Smoking and infertility: multivariable regression and Mendelian randomization analyses in the Norwegian Mother, Father and Child Cohort Study. ''Fertil Steril''. 2022 Jul; '''118''' (1):180-190
Whole-genome sequencing reveals host factors underlying critical COVID-19. Description: Kousathanas, Athanasios, et al. Whole-genome sequencing reveals host factors underlying critical COVID-19. ''Nature''. 2022 Jul; '''607''' (7917):97-103
Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS. Description: Juyal, Garima, et al. Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS. ''J Ayurveda Integr Med''. 2022 Jul 3; '''13''' (3):100578
Genetic determinants of fungi-induced ROS production are associated with the risk of invasive pulmonary aspergillosis. Description: Matzaraki, Vasiliki, et al. Genetic determinants of fungi-induced ROS production are associated with the risk of invasive pulmonary aspergillosis. ''Redox Biol''. 2022 Jul 4; '''55''': 102391
An efficient method to identify, date, and describe admixture events using haplotype information. Description: Wangkumhang, Pongsakorn, et al. An efficient method to identify, date, and describe admixture events using haplotype information. ''Genome Res''. 2022 Jul 6;
Demographic history differences between Hispanics and Brazilians imprint haplotype features. Description: da Cruz, Pedro Rodrigues Sousa, et al. Demographic history differences between Hispanics and Brazilians imprint haplotype features. ''G3 (Bethesda)''. 2022 Jul 6; '''12''' (7):
Estimate of inbreeding depression on growth and reproductive traits in a Large White pig population. Description: Zhang, Yu, et al. Estimate of inbreeding depression on growth and reproductive traits in a Large White pig population. ''G3 (Bethesda)''. 2022 Jul 6; '''12''' (7):
Haplotype and population structure inference using neural networks in whole-genome sequencing data. Description: Meisner, Jonas, et al. Haplotype and population structure inference using neural networks in whole-genome sequencing data. ''Genome Res''. 2022 Jul 6; '''32''' (8):1542-52
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. Description: Choquet, Helene, et al. Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. ''Hum Mol Genet''. 2022 Jul 7; '''31''' (13):2279-2293
A spectrum of recessiveness among Mendelian disease variants in UK Biobank. Description: Barton, Alison R, et al. A spectrum of recessiveness among Mendelian disease variants in UK Biobank. ''Am J Hum Genet''. 2022 Jul 7; '''109''' (7):1298-1307
Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis. Description: Alcina, Antonio, et al. Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis. ''Hum Mol Genet''. 2022 Jul 7; '''31''' (13):2155-2163
The impact of anorexia nervosa and BMI polygenic risk on childhood growth: A 20-year longitudinal population-based study. Description: Abdulkadir, Mohamed, et al. The impact of anorexia nervosa and BMI polygenic risk on childhood growth: A 20-year longitudinal population-based study. ''Am J Hum Genet''. 2022 Jul 7; '''109''' (7):1242-1254
Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Description: Osterman, Michael D, et al. Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. ''Invest Ophthalmol Vis Sci''. 2022 Jul 8; '''63''' (8):17
Analysis of Genetic Diversity in the American Standardbred Horse Utilizing Short Tandem Repeats and Single Nucleotide Polymorphisms. Description: Esdaile, Elizabeth, et al. Analysis of Genetic Diversity in the American Standardbred Horse Utilizing Short Tandem Repeats and Single Nucleotide Polymorphisms. ''J Hered''. 2022 Jul 9; '''113''' (3):238-247
Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease. Description: Huang, Xiaoli, et al. Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease. ''BMC Med Genomics''. 2022 Jul 13; '''15''' (1):158
Higher native Peruvian genetic ancestry proportion is associated with tuberculosis progression risk. Description: Asgari, Samira, et al. Higher native Peruvian genetic ancestry proportion is associated with tuberculosis progression risk. ''Cell Genom''. 2022 Jul 13; '''2''' (7):
Serotonin 5-HT(2A) receptor polymorphisms are associated with irritability and aggression in conduct disorder. Description: Nedic Erjavec, Gordana, et al. Serotonin 5-HT(2A) receptor polymorphisms are associated with irritability and aggression in conduct disorder. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2022 Jul 13; '''117''': 110542
Your height affects your health: genetic determinants and health-related outcomes in Taiwan. Description: Chiou, Jian-Shiun, et al. Your height affects your health: genetic determinants and health-related outcomes in Taiwan. ''BMC Med''. 2022 Jul 13; '''20''' (1):250
A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels. Description: Schubert, Maria, et al. A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels. ''J Clin Endocrinol Metab''. 2022 Jul 14; '''107''' (8):2350-2361
Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental health. Description: Tissink, Elleke, et al. Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental health. ''Commun Biol''. 2022 Jul 16; '''5''' (1):710
Extensive simulations assess the performance of genome-wide association mapping in various Saccharomyces cerevisiae subpopulations. Description: Peter, Jackson, et al. Extensive simulations assess the performance of genome-wide association mapping in various Saccharomyces cerevisiae subpopulations. ''Philos Trans R Soc Lond B Biol Sci''. 2022 Jul 18; '''377''' (1855):20200514
Association between COVID-19 and telomere length: A bidirectional Mendelian randomization study. Description: Huang, Danqi, et al. Association between COVID-19 and telomere length: A bidirectional Mendelian randomization study. ''J Med Virol''. 2022 Jul 19;
ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia. Description: Karnes, Jason H, et al. ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia. ''Blood''. 2022 Jul 21; '''140''' (3):274-284
Association with HLA-DRbeta1 position 37 distinguishes juvenile dermatomyositis from adult-onset myositis. Description: Deakin, Claire T, et al. Association with HLA-DRbeta1 position 37 distinguishes juvenile dermatomyositis from adult-onset myositis. ''Hum Mol Genet''. 2022 Jul 21; '''31''' (14):2471-2481
BIRC6 modifies risk of invasive bacterial infection in Kenyan children. Description: Gilchrist, James J, et al. BIRC6 modifies risk of invasive bacterial infection in Kenyan children. ''Elife''. 2022 Jul 22; '''11''':
Genome-Wide Association Study Identified a Quantitative Trait Locus and Two Candidate Genes on Sus scrofa Chromosome 2 Affecting Vulvar Traits of Suhuai Pigs. Description: Yin, Yanzhen, et al. Genome-Wide Association Study Identified a Quantitative Trait Locus and Two Candidate Genes on Sus scrofa Chromosome 2 Affecting Vulvar Traits of Suhuai Pigs. ''Genes (Basel)''. 2022 Jul 22; '''13''' (8):
Population Genomics of New Zealand Pouched Lamprey (kanakana; piharau; Geotria australis). Description: Miller, Allison K, et al. Population Genomics of New Zealand Pouched Lamprey (kanakana; piharau; Geotria australis). ''J Hered''. 2022 Jul 23; '''113''' (4):380-397
Cognitive Capacity Genome-Wide Polygenic Scores Identify Individuals with Slower Cognitive Decline in Aging. Description: Joo, Yoonjung Yoonie, et al. Cognitive Capacity Genome-Wide Polygenic Scores Identify Individuals with Slower Cognitive Decline in Aging. ''Genes (Basel)''. 2022 Jul 24; '''13''' (8):
Source Identification and Genome-Wide Association Analysis of Crown Rot Resistance in Wheat. Description: Pu, Lefan, et al. Source Identification and Genome-Wide Association Analysis of Crown Rot Resistance in Wheat. ''Plants (Basel)''. 2022 Jul 24; '''11''' (15):
Systems Genetic Identification of Mitochondrion-Associated Alzheimer's Disease Genes and Implications for Disease Risk Prediction. Description: Xu, Xuan, et al. Systems Genetic Identification of Mitochondrion-Associated Alzheimer's Disease Genes and Implications for Disease Risk Prediction. ''Biomedicines''. 2022 Jul 24; '''10''' (8):
A Genome-Wide Search for Candidate Genes of Meat Production in Jalgin Merino Considering Known Productivity Genes. Description: Krivoruchko, Alexander, et al. A Genome-Wide Search for Candidate Genes of Meat Production in Jalgin Merino Considering Known Productivity Genes. ''Genes (Basel)''. 2022 Jul 26; '''13''' (8):
Genome-Wide Association Analysis for Chronic Superficial Keratitis in the Australian Racing Greyhound. Description: Karamatic, Steven, et al. Genome-Wide Association Analysis for Chronic Superficial Keratitis in the Australian Racing Greyhound. ''Genes (Basel)''. 2022 Jul 26; '''13''' (8):
Incipient Sympatric Speciation and Evolution of Soil Bacteria Revealed by Metagenomic and Structured Non-Coding RNAs Analysis. Description: Mukherjee, Sumit, et al. Incipient Sympatric Speciation and Evolution of Soil Bacteria Revealed by Metagenomic and Structured Non-Coding RNAs Analysis. ''Biology (Basel)''. 2022 Jul 26; '''11''' (8):
Shared mechanisms across the major psychiatric and neurodegenerative diseases. Description: Wingo, Thomas S, et al. Shared mechanisms across the major psychiatric and neurodegenerative diseases. ''Nat Commun''. 2022 Jul 26; '''13''' (1):4314
Transcriptomic and proteomic retinal pigment epithelium signatures of age-related macular degeneration. Description: Senabouth, Anne, et al. Transcriptomic and proteomic retinal pigment epithelium signatures of age-related macular degeneration. ''Nat Commun''. 2022 Jul 26; '''13''' (1):4233
Brain Proteome-Wide Association Study Identifies Candidate Genes that Regulate Protein Abundance Associated with Post-Traumatic Stress Disorder. Description: Zhang, Zhen, et al. Brain Proteome-Wide Association Study Identifies Candidate Genes that Regulate Protein Abundance Associated with Post-Traumatic Stress Disorder. ''Genes (Basel)''. 2022 Jul 27; '''13''' (8):
Comparing personalized brain-based and genetic risk scores for major depressive disorder in large population samples of adults and adolescents. Description: Thng, Gladi, et al. Comparing personalized brain-based and genetic risk scores for major depressive disorder in large population samples of adults and adolescents. ''Eur Psychiatry''. 2022 Jul 28; '''65''' (1):e44
Conserved QTL and chromosomal inversion affect resistance to columnaris disease in 2 rainbow trout (Oncorhyncus mykiss) populations. Description: Calboli, Federico C F, et al. Conserved QTL and chromosomal inversion affect resistance to columnaris disease in 2 rainbow trout (Oncorhyncus mykiss) populations. ''G3 (Bethesda)''. 2022 Jul 29; '''12''' (8):
Combining GWAS and TWAS to identify candidate causal genes for tocochromanol levels in maize grain. Description: Wu, Di, et al. Combining GWAS and TWAS to identify candidate causal genes for tocochromanol levels in maize grain. ''Genetics''. 2022 Jul 30; '''221''' (4):
A gene-based capture assay for surveying patterns of genetic diversity and insecticide resistance in a worldwide group of invasive mosquitoes. Description: Aardema, Matthew L, et al. A gene-based capture assay for surveying patterns of genetic diversity and insecticide resistance in a worldwide group of invasive mosquitoes. ''PLoS Negl Trop Dis''. 2022 Aug; '''16''' (8):e0010689
A polygenic architecture with habitat-dependent effects underlies ecological differentiation in Silene. Description: Gramlich, Susanne, et al. A polygenic architecture with habitat-dependent effects underlies ecological differentiation in Silene. ''New Phytol''. 2022 Aug; '''235''' (4):1641-1652
Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma. Description: Chen, Cheng, et al. Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma. ''JAMA Netw Open''. 2022 Aug 1; '''5''' (8):e2225647
Auxilin is a novel susceptibility gene for congenital heart block which directly impacts fetal heart function. Description: Meisgen, Sabrina, et al. Auxilin is a novel susceptibility gene for congenital heart block which directly impacts fetal heart function. ''Ann Rheum Dis''. 2022 Aug; '''81''' (8):1151-1161
Deep structure, long-distance migration and admixture in the colour polymorphic land snail Cepaea nemoralis. Description: Ramos-Gonzalez, Daniel, et al. Deep structure, long-distance migration and admixture in the colour polymorphic land snail Cepaea nemoralis. ''J Evol Biol''. 2022 Aug; '''35''' (8):1110-1125
Epigenetic control of ataxin-1 in multiple sclerosis. Description: Ma, Qin, et al. Epigenetic control of ataxin-1 in multiple sclerosis. ''Ann Clin Transl Neurol''. 2022 Aug; '''9''' (8):1186-1194
Genetic Association of Attention-Deficit/Hyperactivity Disorder and Major Depression With Suicidal Ideation and Attempts in Children: The Adolescent Brain Cognitive Development Study. Description: Lee, Phil H, et al. Genetic Association of Attention-Deficit/Hyperactivity Disorder and Major Depression With Suicidal Ideation and Attempts in Children: The Adolescent Brain Cognitive Development Study. ''Biol Psychiatry''. 2022 Aug 1; '''92''' (3):236-245
Genetic evidence for a potential causal relationship between insomnia symptoms and suicidal behavior: a Mendelian randomization study. Description: Nassan, Malik, et al. Genetic evidence for a potential causal relationship between insomnia symptoms and suicidal behavior: a Mendelian randomization study. ''Neuropsychopharmacology''. 2022 Aug; '''47''' (9):1672-1679
Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries. Description: Banday, A Rouf, et al. Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries. ''Nat Genet''. 2022 Aug; '''54''' (8):1103-1116
Genetic risk of type 2 diabetes modifies the effects of a lifestyle intervention aimed at the prevention of gestational and postpartum diabetes. Description: Huvinen, Emilia, et al. Genetic risk of type 2 diabetes modifies the effects of a lifestyle intervention aimed at the prevention of gestational and postpartum diabetes. ''Diabetologia''. 2022 Aug; '''65''' (8):1291-1301
Genetics are not likely to offer clinically useful predictions for elevated liver enzyme levels in patients using low dose methotrexate. Description: Cui, Jing, et al. Genetics are not likely to offer clinically useful predictions for elevated liver enzyme levels in patients using low dose methotrexate. ''Semin Arthritis Rheum''. 2022 Aug; '''55''': 152036
Genome-Wide 3'-UTR Single Nucleotide Polymorphism Association Study Identifies Significant Prostate Cancer Risk-Associated Functional Loci at 8p21.2 in Chinese Population. Description: Zhang, Ning, et al. Genome-Wide 3'-UTR Single Nucleotide Polymorphism Association Study Identifies Significant Prostate Cancer Risk-Associated Functional Loci at 8p21.2 in Chinese Population. ''Adv Sci (Weinh)''. 2022 Aug; '''9''' (23):e2201420
Genome-wide analysis of Schistosoma mansoni reveals limited population structure and possible praziquantel drug selection pressure within Ugandan hot-spot communities. Description: Vianney, Tushabe John, et al. Genome-wide analysis of Schistosoma mansoni reveals limited population structure and possible praziquantel drug selection pressure within Ugandan hot-spot communities. ''PLoS Negl Trop Dis''. 2022 Aug; '''16''' (8):e0010188
Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank. Description: Xue, Zhengbo, et al. Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank. ''EBioMedicine''. 2022 Aug; '''82''': 104161
Genomic erosion in a demographically recovered bird species during conservation rescue. Description: Jackson, Hazel A, et al. Genomic erosion in a demographically recovered bird species during conservation rescue. ''Conserv Biol''. 2022 Aug; '''36''' (4):e13918
Genomic evidence of contemporary hybridization between Schistosoma species. Description: Berger, Duncan J, et al. Genomic evidence of contemporary hybridization between Schistosoma species. ''PLoS Pathog''. 2022 Aug; '''18''' (8):e1010706
Host genotype interacts with aerial spore communities and influences the needle mycobiome of Norway spruce. Description: Redondo, Miguel A, et al. Host genotype interacts with aerial spore communities and influences the needle mycobiome of Norway spruce. ''Environ Microbiol''. 2022 Aug; '''24''' (8):3640-3654
Human adaptation to arsenic in Bolivians living in the Andes. Description: De Loma, Jessica, et al. Human adaptation to arsenic in Bolivians living in the Andes. ''Chemosphere''. 2022 Aug; '''301''': 134764
Identification of genetic variants of the IL-22 gene in association with an altered risk of COPD susceptibility. Description: Wang, Yan, et al. Identification of genetic variants of the IL-22 gene in association with an altered risk of COPD susceptibility. ''Clin Respir J''. 2022 Aug; '''16''' (8):537-545
Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis. Description: Li, Jin, et al. Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis. ''Arthritis Rheumatol''. 2022 Aug; '''74''' (8):1420-1429
Identification of QTLs for wheat heading time across multiple-environments. Description: Benaouda, Salma, et al. Identification of QTLs for wheat heading time across multiple-environments. ''Theor Appl Genet''. 2022 Aug; '''135''' (8):2833-2848
Integrating GWAS and TWAS to elucidate the genetic architecture of maize leaf cuticular conductance. Description: Lin, Meng, et al. Integrating GWAS and TWAS to elucidate the genetic architecture of maize leaf cuticular conductance. ''Plant Physiol''. 2022 Aug 1; '''189''' (4):2144-2158
Mapping of promoter usage QTL using RNA-seq data reveals their contributions to complex traits. Description: Kubota, Naoto, et al. Mapping of promoter usage QTL using RNA-seq data reveals their contributions to complex traits. ''PLoS Comput Biol''. 2022 Aug; '''18''' (8):e1010436
Multi-omics analyses of 398 foxtail millet accessions reveal genomic regions associated with domestication, metabolite traits, and anti-inflammatory effects. Description: Li, Xukai, et al. Multi-omics analyses of 398 foxtail millet accessions reveal genomic regions associated with domestication, metabolite traits, and anti-inflammatory effects. ''Mol Plant''. 2022 Aug 1; '''15''' (8):1367-1383
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors. Description: Liu, Hui, et al. Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors. ''Ann Neurol''. 2022 Aug; '''92''' (2):270-278
Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia. Description: Zhang, Qian, et al. Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia. ''J Exp Med''. 2022 Aug 1; '''219''' (8):
Separating the effects of childhood and adult body size on inflammatory arthritis: a Mendelian randomisation study. Description: Zhao, Sizheng Steven, et al. Separating the effects of childhood and adult body size on inflammatory arthritis: a Mendelian randomisation study. ''RMD Open''. 2022 Aug; '''8''' (2):
Sorghum Association Panel whole-genome sequencing establishes cornerstone resource for dissecting genomic diversity. Description: Boatwright, J Lucas, et al. Sorghum Association Panel whole-genome sequencing establishes cornerstone resource for dissecting genomic diversity. ''Plant J''. 2022 Aug; '''111''' (3):888-904
Spatial multi-omic map of human myocardial infarction. Description: Kuppe, Christoph, et al. Spatial multi-omic map of human myocardial infarction. ''Nature''. 2022 Aug; '''608''' (7924):766-777
Splenic clearance of rigid erythrocytes as an inherited mechanism for splenomegaly and natural resistance to malaria. Description: Henry, Benoit, et al. Splenic clearance of rigid erythrocytes as an inherited mechanism for splenomegaly and natural resistance to malaria. ''EBioMedicine''. 2022 Aug; '''82''': 104167
Variants in the Niemann-pick type C genes are not associated with Alzheimer's disease: a large case-control study in the Chinese population. Description: Xiao, Xuewen, et al. Variants in the Niemann-pick type C genes are not associated with Alzheimer's disease: a large case-control study in the Chinese population. ''Neurobiol Aging''. 2022 Aug; '''116''': 49-54
Variation in cardiovascular disease risk factors among older adults in the Hunter Community Study cohort: A comparison of diet quality versus polygenic risk score. Description: Reay, William R, et al. Variation in cardiovascular disease risk factors among older adults in the Hunter Community Study cohort: A comparison of diet quality versus polygenic risk score. ''J Hum Nutr Diet''. 2022 Aug; '''35''' (4):675-688
Association between Ancestry-Specific 6q25 Variants and Breast Cancer Subtypes in Peruvian Women. Description: Zavala, Valentina A, et al. Association between Ancestry-Specific 6q25 Variants and Breast Cancer Subtypes in Peruvian Women. ''Cancer Epidemiol Biomarkers Prev''. 2022 Aug 2; '''31''' (8):1602-1609
Improving GWAS discovery and genomic prediction accuracy in biobank data. Description: Orliac, Etienne J, et al. Improving GWAS discovery and genomic prediction accuracy in biobank data. ''Proc Natl Acad Sci U S A''. 2022 Aug 2; '''119''' (31):e2121279119
Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans. Description: Lemmela, Susanna, et al. Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans. ''Elife''. 2022 Aug 2; '''11''':
A Phylogeny-aware GWAS Framework to Correct for Heritable Pathogen Effects on Infectious Disease Traits. Description: Nadeau, Sarah, et al. A Phylogeny-aware GWAS Framework to Correct for Heritable Pathogen Effects on Infectious Disease Traits. ''Mol Biol Evol''. 2022 Aug 3; '''39''' (8):
Assessing Human Genome-wide Variation in the Massim Region of Papua New Guinea and Implications for the Kula Trading Tradition. Description: Liu, Dang, et al. Assessing Human Genome-wide Variation in the Massim Region of Papua New Guinea and Implications for the Kula Trading Tradition. ''Mol Biol Evol''. 2022 Aug 3; '''39''' (8):
Identification and functional characterization of a novel susceptibility locus for small vessel vasculitis with MPO-ANCA. Description: Dahlqvist, Johanna, et al. Identification and functional characterization of a novel susceptibility locus for small vessel vasculitis with MPO-ANCA. ''Rheumatology (Oxford)''. 2022 Aug 3; '''61''' (8):3461-3470
Uncovering Signals of Positive Selection in Peruvian Populations from Three Ecological Regions. Description: Caro-Consuegra, Rocio, et al. Uncovering Signals of Positive Selection in Peruvian Populations from Three Ecological Regions. ''Mol Biol Evol''. 2022 Aug 3; '''39''' (8):
Multi-ancestry fine-mapping improves precision to identify causal genes in transcriptome-wide association studies. Description: Lu, Zeyun, et al. Multi-ancestry fine-mapping improves precision to identify causal genes in transcriptome-wide association studies. ''Am J Hum Genet''. 2022 Aug 4; '''109''' (8):1388-1404
Simultaneous inference of parental admixture proportions and admixture times from unphased local ancestry calls. Description: Avadhanam, Siddharth, et al. Simultaneous inference of parental admixture proportions and admixture times from unphased local ancestry calls. ''Am J Hum Genet''. 2022 Aug 4; '''109''' (8):1405-1420
A single nucleotide polymorphism of the thyrotropin releasing hormone degrading ectoenzyme (TRHDE) gene is associated with post-partum anestrus in Murrah buffalo. Description: Verma, Surya Kant, et al. A single nucleotide polymorphism of the thyrotropin releasing hormone degrading ectoenzyme (TRHDE) gene is associated with post-partum anestrus in Murrah buffalo. ''Gene''. 2022 Aug 5; '''834''': 146580
A cognitive neurogenetic approach to uncovering the structure of executive functions. Description: Feng, Junjiao, et al. A cognitive neurogenetic approach to uncovering the structure of executive functions. ''Nat Commun''. 2022 Aug 6; '''13''' (1):4588
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden. Description: Gabriel, Aurelie A G, et al. Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden. ''J Natl Cancer Inst''. 2022 Aug 8; '''114''' (8):1159-1166
Northeastern Asian and Jomon-related genetic structure in the Three Kingdoms period of Gimhae, Korea. Description: Gelabert, Pere, et al. Northeastern Asian and Jomon-related genetic structure in the Three Kingdoms period of Gimhae, Korea. ''Curr Biol''. 2022 Aug 8; '''32''' (15):3232-3244.e6
Using whole-genome sequencing to characterize clinically significant blood groups among healthy older Australians. Description: Jadhao, Sudhir, et al. Using whole-genome sequencing to characterize clinically significant blood groups among healthy older Australians. ''Blood Adv''. 2022 Aug 9; '''6''' (15):4593-4604
Genomic analyses of wild argali, domestic sheep, and their hybrids provide insights into chromosome evolution, phenotypic variation, and germplasm innovation. Description: Li, Xin, et al. Genomic analyses of wild argali, domestic sheep, and their hybrids provide insights into chromosome evolution, phenotypic variation, and germplasm innovation. ''Genome Res''. 2022 Aug 10; '''32''' (9):1669-84
Association of T-box gene polymorphisms with the risk of Wolff-Parkinson-White syndrome in a Han Chinese population. Description: Han, Bing, et al. Association of T-box gene polymorphisms with the risk of Wolff-Parkinson-White syndrome in a Han Chinese population. ''Medicine (Baltimore)''. 2022 Aug 12; '''101''' (32):e30046
Boosting Schizophrenia Genetics by Utilizing Genetic Overlap With Brain Morphology. Description: van der Meer, Dennis, et al. Boosting Schizophrenia Genetics by Utilizing Genetic Overlap With Brain Morphology. ''Biol Psychiatry''. 2022 Aug 15; '''92''' (4):291-298
Breeding Dairy Cattle for Female Fertility and Production in the Age of Genomics. Description: Weller, Joel Ira, et al. Breeding Dairy Cattle for Female Fertility and Production in the Age of Genomics. ''Vet Sci''. 2022 Aug 15; '''9''' (8):
Infection Polygenic Factors Account for a Small Proportion of the Relationship Between Infections and Mental Disorders. Description: Shorter, John R, et al. Infection Polygenic Factors Account for a Small Proportion of the Relationship Between Infections and Mental Disorders. ''Biol Psychiatry''. 2022 Aug 15; '''92''' (4):283-290
The sexual brain, genes, and cognition: A machine-predicted brain sex score explains individual differences in cognitive intelligence and genetic influence in young children. Description: Kim, Kakyeong, et al. The sexual brain, genes, and cognition: A machine-predicted brain sex score explains individual differences in cognitive intelligence and genetic influence in young children. ''Hum Brain Mapp''. 2022 Aug 15; '''43''' (12):3857-3872
Assembly of a pangenome for global cattle reveals missing sequences and novel structural variations, providing new insights into their diversity and evolutionary history. Description: Zhou, Yang, et al. Assembly of a pangenome for global cattle reveals missing sequences and novel structural variations, providing new insights into their diversity and evolutionary history. ''Genome Res''. 2022 Aug 17; '''32''' (8):1585-601
Genome-wide association study and functional follow-up identify 14q12 as a candidate risk locus for cervical cancer. Description: Ramachandran, Dhanya, et al. Genome-wide association study and functional follow-up identify 14q12 as a candidate risk locus for cervical cancer. ''Hum Mol Genet''. 2022 Aug 17; '''31''' (15):2483-2497
Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity. Description: Zhang, Sai, et al. Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity. ''Cell Syst''. 2022 Aug 17; '''13''' (8):598-614.e6
Sodium-calcium exchanger-3 regulates pain "wind-up": From human psychophysics to spinal mechanisms. Description: Trendafilova, Teodora, et al. Sodium-calcium exchanger-3 regulates pain "wind-up": From human psychophysics to spinal mechanisms. ''Neuron''. 2022 Aug 17; '''110''' (16):2571-2587.e13
The evolution and diversification of oakleaf butterflies. Description: Wang, Shuting, et al. The evolution and diversification of oakleaf butterflies. ''Cell''. 2022 Aug 18; '''185''' (17):3138-3152.e20
Comparative genomics uncovers the evolutionary history, demography, and molecular adaptations of South American canids. Description: Chavez, Daniel E, et al. Comparative genomics uncovers the evolutionary history, demography, and molecular adaptations of South American canids. ''Proc Natl Acad Sci U S A''. 2022 Aug 23; '''119''' (34):e2205986119
Deep learning predicts DNA methylation regulatory variants in the human brain and elucidates the genetics of psychiatric disorders. Description: Zhou, Jiyun, et al. Deep learning predicts DNA methylation regulatory variants in the human brain and elucidates the genetics of psychiatric disorders. ''Proc Natl Acad Sci U S A''. 2022 Aug 23; '''119''' (34):e2206069119
Genetic assortative mating for schizophrenia and bipolar disorder. Description: Jefsen, Oskar Hougaard, et al. Genetic assortative mating for schizophrenia and bipolar disorder. ''Eur Psychiatry''. 2022 Aug 23; '''65''' (1):e53
Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk. Description: Li, Yafang, et al. Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk. ''Hum Mol Genet''. 2022 Aug 23; '''31''' (16):2831-2843
Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. Description: Castaneda-Garcia, Carolina, et al. Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. ''Hum Mol Genet''. 2022 Aug 25; '''31''' (17):2845-2856
Organization of gene programs revealed by unsupervised analysis of diverse gene-trait associations. Description: Mizikovsky, Dalia, et al. Organization of gene programs revealed by unsupervised analysis of diverse gene-trait associations. ''Nucleic Acids Res''. 2022 Aug 26; '''50''' (15):e87
Uncovering the genomic basis of an extraordinary plant invasion. Description: Bieker, Vanessa C, et al. Uncovering the genomic basis of an extraordinary plant invasion. ''Sci Adv''. 2022 Aug 26; '''8''' (34):eabo5115
A single introduction of wild rabbits triggered the biological invasion of Australia. Description: Alves, Joel M, et al. A single introduction of wild rabbits triggered the biological invasion of Australia. ''Proc Natl Acad Sci U S A''. 2022 Aug 30; '''119''' (35):e2122734119
EfGD: the Erianthus fulvus genome database. Description: Qian, Zhenfeng, et al. EfGD: the Erianthus fulvus genome database. ''Database (Oxford)''. 2022 Aug 31; '''2022''':
Alcohol use disorder is associated with DNA methylation-based shortening of telomere length and regulated by TESPA1: implications for aging. Description: Jung, Jeesun, et al. Alcohol use disorder is associated with DNA methylation-based shortening of telomere length and regulated by TESPA1: implications for aging. ''Mol Psychiatry''. 2022 Sep; '''27''' (9):3875-3884
A multi-tissue atlas of regulatory variants in cattle. Description: Liu, Shuli, et al. A multi-tissue atlas of regulatory variants in cattle. ''Nat Genet''. 2022 Sep; '''54''' (9):1438-1447
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex. Description: Antaki, Danny, et al. A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex. ''Nat Genet''. 2022 Sep; '''54''' (9):1284-1292
Are polymorphisms affecting serum urate, renal urate handling and alcohol intake associated with co-morbidities in gout cases? A case-control study using data from the UK Biobank. Description: Sandoval-Plata, Gabriela, et al. Are polymorphisms affecting serum urate, renal urate handling and alcohol intake associated with co-morbidities in gout cases? A case-control study using data from the UK Biobank. ''Rheumatol Int''. 2022 Sep; '''42''' (9):1617-1622
Association of autism diagnosis and polygenic scores with eating disorder severity. Description: Zhang, Ruyue, et al. Association of autism diagnosis and polygenic scores with eating disorder severity. ''Eur Eat Disord Rev''. 2022 Sep; '''30''' (5):442-458
A suggested shared aetiology of dementia - a colocalization study. Description: Yu, Xinzhu, et al. A suggested shared aetiology of dementia - a colocalization study. ''Neurobiol Aging''. 2022 Sep; '''117''': 71-82
Changes in Ploidy Drive Reproduction Transition and Genomic Diversity in a Polyploid Fish Complex. Description: Lu, Meng, et al. Changes in Ploidy Drive Reproduction Transition and Genomic Diversity in a Polyploid Fish Complex. ''Mol Biol Evol''. 2022 Sep 1; '''39''' (9):
Comparative genome anatomy reveals evolutionary insights into a unique amphitriploid fish. Description: Wang, Yang, et al. Comparative genome anatomy reveals evolutionary insights into a unique amphitriploid fish. ''Nat Ecol Evol''. 2022 Sep; '''6''' (9):1354-1366
Effects of Pharmacokinetic Gene Variation on Therapeutic Drug Levels and Antidepressant Treatment Response. Description: Scherf-Clavel, Maike, et al. Effects of Pharmacokinetic Gene Variation on Therapeutic Drug Levels and Antidepressant Treatment Response. ''Pharmacopsychiatry''. 2022 Sep; '''55''' (5):246-254
Expression of CD70 Modulates Nitric Oxide and Redox Status in Endothelial Cells. Description: Pandey, Arvind K, et al. Expression of CD70 Modulates Nitric Oxide and Redox Status in Endothelial Cells. ''Arterioscler Thromb Vasc Biol''. 2022 Sep; '''42''' (9):1169-1185
Gene-environment correlations across geographic regions affect genome-wide association studies. Description: Abdellaoui, Abdel, et al. Gene-environment correlations across geographic regions affect genome-wide association studies. ''Nat Genet''. 2022 Sep; '''54''' (9):1345-1354
Genetic correlates of phenotypic heterogeneity in autism. Description: Warrier, Varun, et al. Genetic correlates of phenotypic heterogeneity in autism. ''Nat Genet''. 2022 Sep; '''54''' (9):1293-1304
Genetic structure correlates with ethnolinguistic diversity in eastern and southern Africa. Description: Atkinson, Elizabeth G, et al. Genetic structure correlates with ethnolinguistic diversity in eastern and southern Africa. ''Am J Hum Genet''. 2022 Sep 1; '''109''' (9):1667-1679
Genome-wide association study for circulating FGF21 in patients with alcohol use disorder: Molecular links between the SNHG16 locus and catecholamine metabolism. Description: Ho, Ming-Fen, et al. Genome-wide association study for circulating FGF21 in patients with alcohol use disorder: Molecular links between the SNHG16 locus and catecholamine metabolism. ''Mol Metab''. 2022 Sep; '''63''': 101534
Genome-wide association study of leprosy in Malawi and Mali. Description: Gilchrist, James J, et al. Genome-wide association study of leprosy in Malawi and Mali. ''PLoS Pathog''. 2022 Sep; '''18''' (9):e1010312
Genome-wide meta-analysis of alcohol use disorder in East Asians. Description: Zhou, Hang, et al. Genome-wide meta-analysis of alcohol use disorder in East Asians. ''Neuropsychopharmacology''. 2022 Sep; '''47''' (10):1791-1797
Genome-wide study of early and severe childhood asthma identifies interaction between CDHR3 and GSDMB. Description: Eliasen, Anders U, et al. Genome-wide study of early and severe childhood asthma identifies interaction between CDHR3 and GSDMB. ''J Allergy Clin Immunol''. 2022 Sep; '''150''' (3):622-630
Genome-wide survey on three local horse populations with a focus on runs of homozygosity pattern. Description: Criscione, Andrea, et al. Genome-wide survey on three local horse populations with a focus on runs of homozygosity pattern. ''J Anim Breed Genet''. 2022 Sep; '''139''' (5):540-555
Genomic Risk Score for Advanced Osteoarthritis in Older Adults. Description: Lacaze, Paul, et al. Genomic Risk Score for Advanced Osteoarthritis in Older Adults. ''Arthritis Rheumatol''. 2022 Sep; '''74''' (9):1480-1487
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios. Description: Byrska-Bishop, Marta, et al. High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios. ''Cell''. 2022 Sep 1; '''185''' (18):3426-3440.e19
Increased Risk of Preeclampsia in Women With a Genetic Predisposition to Elevated Blood Pressure. Description: Kivioja, Anna, et al. Increased Risk of Preeclampsia in Women With a Genetic Predisposition to Elevated Blood Pressure. ''Hypertension''. 2022 Sep; '''79''' (9):2008-2015
Independent phenotypic plasticity axes define distinct obesity sub-types. Description: Yang, Chih-Hsiang, et al. Independent phenotypic plasticity axes define distinct obesity sub-types. ''Nat Metab''. 2022 Sep; '''4''' (9):1150-1165
Inferring intelligence of ancient people based on modern genomic studies. Description: Dauyey, Kaisar, et al. Inferring intelligence of ancient people based on modern genomic studies. ''J Hum Genet''. 2022 Sep; '''67''' (9):527-532
Lung- and liver-dominant phenotypes of Korean eight constitution medicine have different profiles of genotype associated with each organ function. Description: Kim, Changkeun, et al. Lung- and liver-dominant phenotypes of Korean eight constitution medicine have different profiles of genotype associated with each organ function. ''Physiol Rep''. 2022 Sep; '''10''' (17):e15459
Multi-locus genome-wide association studies reveal novel alleles for flowering time under vernalisation and extended photoperiod in a barley MAGIC population. Description: Dang, Viet Hoang, et al. Multi-locus genome-wide association studies reveal novel alleles for flowering time under vernalisation and extended photoperiod in a barley MAGIC population. ''Theor Appl Genet''. 2022 Sep; '''135''' (9):3087-3102
Natural adaptation and human selection of northeast African sheep genomes. Description: Ahbara, Abulgasim M, et al. Natural adaptation and human selection of northeast African sheep genomes. ''Genomics''. 2022 Sep; '''114''' (5):110448
Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort. Description: Loesch, Douglas P, et al. Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort. ''Parkinsonism Relat Disord''. 2022 Sep; '''102''': 7-15
Polygenic signals of sex differences in selection in humans from the UK Biobank. Description: Ruzicka, Filip, et al. Polygenic signals of sex differences in selection in humans from the UK Biobank. ''PLoS Biol''. 2022 Sep; '''20''' (9):e3001768
Rs9891446 in NTN1 is associated with right-side cleft lip in Han Chinese population. Description: Tao, Hong-Xu, et al. Rs9891446 in NTN1 is associated with right-side cleft lip in Han Chinese population. ''Arch Oral Biol''. 2022 Sep; '''141''': 105485
The Apportionment of Pharmacogenomic Variation: Race, Ethnicity, and Adverse Drug Reactions. Description: Jordan, I King, et al. The Apportionment of Pharmacogenomic Variation: Race, Ethnicity, and Adverse Drug Reactions. ''Med Res Arch''. 2022 Sep; '''10''' (9):
The Genetic Echo of the Tarim Mummies in Modern Central Asians. Description: Dai, Shan-Shan, et al. The Genetic Echo of the Tarim Mummies in Modern Central Asians. ''Mol Biol Evol''. 2022 Sep 1; '''39''' (9):
The potential effects of HECTD4 variants on fasting glucose and triglyceride levels in relation to prevalence of type 2 diabetes based on alcohol intake. Description: Lee, Yoo Jeong, et al. The potential effects of HECTD4 variants on fasting glucose and triglyceride levels in relation to prevalence of type 2 diabetes based on alcohol intake. ''Arch Toxicol''. 2022 Sep; '''96''' (9):2487-2499
*The UGT1A922 genotype identifies a high-risk group for irinotecan toxicity among gastric cancer patients.** Description: Lee, Choong-Kun, et al. The UGT1A9*22 genotype identifies a high-risk group for irinotecan toxicity among gastric cancer patients. ''Genomics Inform''. 2022 Sep; '''20''' (3):e29
Uncovering natural variation in root system architecture and growth dynamics using a robotics-assisted phenomics platform. Description: LaRue, Therese, et al. Uncovering natural variation in root system architecture and growth dynamics using a robotics-assisted phenomics platform. ''Elife''. 2022 Sep 1; '''11''':
Whole-genome resequencing reveals domestication and signatures of selection in Ujimqin, Sunit, and Wu Ranke Mongolian sheep breeds. Description: Wang, Hanning, et al. Whole-genome resequencing reveals domestication and signatures of selection in Ujimqin, Sunit, and Wu Ranke Mongolian sheep breeds. ''Anim Biosci''. 2022 Sep; '''35''' (9):1303-1313
Investigating Genetic Determinants of Plasma Inositol Status in Adult Humans. Description: Weston, Eleanor, et al. Investigating Genetic Determinants of Plasma Inositol Status in Adult Humans. ''J Nutr''. 2022 Sep 2; '''152''' (11):2333-42
A genome-wide association study of important reproduction traits in large white pigs. Description: Chang Wu, Zheng, et al. A genome-wide association study of important reproduction traits in large white pigs. ''Gene''. 2022 Sep 5; '''838''': 146702
Autologous K63 deubiquitylation within the BRCA1-A complex licenses DNA damage recognition. Description: Jiang, Qinqin, et al. Autologous K63 deubiquitylation within the BRCA1-A complex licenses DNA damage recognition. ''J Cell Biol''. 2022 Sep 5; '''221''' (9):
Impact of FOXP3 gene polymorphisms and gene-environment interactions in asthma and atopy in a Brazilian population. Description: Marques, Cintia Rodrigues, et al. Impact of FOXP3 gene polymorphisms and gene-environment interactions in asthma and atopy in a Brazilian population. ''Gene''. 2022 Sep 5; '''838''': 146706
Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Description: Smith, Courtney J, et al. Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. ''Elife''. 2022 Sep 8; '''11''':
PAM-altering SNP-based allele-specific CRISPR-Cas9 therapeutic strategies for Huntington's disease. Description: Shin, Jun Wan, et al. PAM-altering SNP-based allele-specific CRISPR-Cas9 therapeutic strategies for Huntington's disease. ''Mol Ther Methods Clin Dev''. 2022 Sep 8; '''26''': 547-561
Evaluation of the causal relationship between smoking and schizophrenia in East Asia. Description: Su, Mei-Hsin, et al. Evaluation of the causal relationship between smoking and schizophrenia in East Asia. ''Schizophrenia (Heidelb)''. 2022 Sep 9; '''8''' (1):72
Socioeconomic and genomic roots of verbal ability from current evidence. Description: Guo, Guang, et al. Socioeconomic and genomic roots of verbal ability from current evidence. ''NPJ Sci Learn''. 2022 Sep 9; '''7''' (1):22
Integrative multi-omics database (iMOMdb) of Asian pregnant women. Description: Pan, Hong, et al. Integrative multi-omics database (iMOMdb) of Asian pregnant women. ''Hum Mol Genet''. 2022 Sep 10; '''31''' (18):3051-3067
Analysis of genome and methylation changes in Chinese indigenous chickens over time provides insight into species conservation. Description: Zeng, Tao, et al. Analysis of genome and methylation changes in Chinese indigenous chickens over time provides insight into species conservation. ''Commun Biol''. 2022 Sep 12; '''5''' (1):952
Whole-genome resequencing of the wheat A subgenome progenitor Triticum urartu provides insights into its demographic history and geographic adaptation. Description: Wang, Xin, et al. Whole-genome resequencing of the wheat A subgenome progenitor Triticum urartu provides insights into its demographic history and geographic adaptation. ''Plant Commun''. 2022 Sep 12; '''3''' (5):100345
Genome-wide association analysis of 101 accessions dissects the genetic basis of shell thickness for genetic improvement in Persian walnut (Juglans regia L.). Description: Wang, Jiangtao, et al. Genome-wide association analysis of 101 accessions dissects the genetic basis of shell thickness for genetic improvement in Persian walnut (Juglans regia L.). ''BMC Plant Biol''. 2022 Sep 13; '''22''' (1):436
Genetic variation in ST6GAL1 is a determinant of capecitabine and oxaliplatin induced hand-foot syndrome. Description: Watts, Katie, et al. Genetic variation in ST6GAL1 is a determinant of capecitabine and oxaliplatin induced hand-foot syndrome. ''Int J Cancer''. 2022 Sep 15; '''151''' (6):957-966
Identification of candidate sex-specific genomic regions in male and female Asian arowana genomes. Description: Mu, Xidong, et al. Identification of candidate sex-specific genomic regions in male and female Asian arowana genomes. ''Gigascience''. 2022 Sep 15; '''11''':
Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves. Description: Chan, Melanie M Y, et al. Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves. ''Elife''. 2022 Sep 20; '''11''':
Transcriptome-wide summary data-based Mendelian randomization analysis reveals 38 novel genes associated with severe COVID-19. Description: Krishnamoorthy, Suhas, et al. Transcriptome-wide summary data-based Mendelian randomization analysis reveals 38 novel genes associated with severe COVID-19. ''J Med Virol''. 2022 Sep 20;
Genome-Wide Association Study Reveals Candidate Genes for Root-Related Traits in Rice. Description: Xiang, Jun, et al. Genome-Wide Association Study Reveals Candidate Genes for Root-Related Traits in Rice. ''Curr Issues Mol Biol''. 2022 Sep 21; '''44''' (10):4386-4405
Patterns of genetic variation and QTLs controlling grain traits in a collection of global wheat germplasm revealed by high-quality SNP markers. Description: Chou, Chia-Hui, et al. Patterns of genetic variation and QTLs controlling grain traits in a collection of global wheat germplasm revealed by high-quality SNP markers. ''BMC Plant Biol''. 2022 Sep 22; '''22''' (1):455
Association of Alzheimer's disease polygenic risk scores with amyloid accumulation in cognitively intact older adults. Description: Luckett, Emma S, et al. Association of Alzheimer's disease polygenic risk scores with amyloid accumulation in cognitively intact older adults. ''Alzheimers Res Ther''. 2022 Sep 23; '''14''' (1):138
Whole genome resequencing reveals the genetic contribution of Kazakh and Swiss Brown cattle to a population of Xinjiang Brown cattle. Description: Chen, Qiuming, et al. Whole genome resequencing reveals the genetic contribution of Kazakh and Swiss Brown cattle to a population of Xinjiang Brown cattle. ''Gene''. 2022 Sep 25; '''839''': 146725
Genetic Dissection of Epistatic Interactions Contributing Yield-Related Agronomic Traits in Rice Using the Compressed Mixed Model. Description: Li, Ling, et al. Genetic Dissection of Epistatic Interactions Contributing Yield-Related Agronomic Traits in Rice Using the Compressed Mixed Model. ''Plants (Basel)''. 2022 Sep 26; '''11''' (19):
Developing CIRdb as a catalog of natural genetic variation in the Canary Islanders. Description: Diaz-de Usera, Ana, et al. Developing CIRdb as a catalog of natural genetic variation in the Canary Islanders. ''Sci Rep''. 2022 Sep 27; '''12''' (1):16132
Dense phenotyping from electronic health records enables machine learning-based prediction of preterm birth. Description: Abraham, Abin, et al. Dense phenotyping from electronic health records enables machine learning-based prediction of preterm birth. ''BMC Med''. 2022 Sep 28; '''20''' (1):333
Effects of psychosis-associated genetic markers on brain volumetry: a systematic review of replicated findings and an independent validation. Description: Vouga Ribeiro, Nuno, et al. Effects of psychosis-associated genetic markers on brain volumetry: a systematic review of replicated findings and an independent validation. ''Psychol Med''. 2022 Sep 28; '''52''' (16):1-16
Genetic structure and geneflow of Malus across the Korean Peninsula using genotyping-by-sequencing. Description: Ha, Young-Ho, et al. Genetic structure and geneflow of Malus across the Korean Peninsula using genotyping-by-sequencing. ''Sci Rep''. 2022 Sep 28; '''12''' (1):16262
Alzheimer's disease related single nucleotide polymorphisms and correlation with intracerebral hemorrhage incidence. Description: Sawyer, Russell P, et al. Alzheimer's disease related single nucleotide polymorphisms and correlation with intracerebral hemorrhage incidence. ''Medicine (Baltimore)''. 2022 Sep 30; '''101''' (39):e30782
Selection signature analyses and genome-wide association reveal genomic hotspot regions that reflect differences between breeds of horse with contrasting risk of degenerative suspensory ligament desmitis. Description: Momen, Mehdi, et al. Selection signature analyses and genome-wide association reveal genomic hotspot regions that reflect differences between breeds of horse with contrasting risk of degenerative suspensory ligament desmitis. ''G3 (Bethesda)''. 2022 Sep 30; '''12''' (10):
Sex-biased admixture and assortative mating shape genetic variation and influence demographic inference in admixed Cabo Verdeans. Description: Korunes, Katharine L, et al. Sex-biased admixture and assortative mating shape genetic variation and influence demographic inference in admixed Cabo Verdeans. ''G3 (Bethesda)''. 2022 Sep 30; '''12''' (10):
SNP discovery and association study for growth, fatness and meat quality traits in Iberian crossbred pigs. Description: Ovilo, C, et al. SNP discovery and association study for growth, fatness and meat quality traits in Iberian crossbred pigs. ''Sci Rep''. 2022 Sep 30; '''12''' (1):16361
A Prism Vote method for individualized risk prediction of traits in genotype data of Multi-population. Description: Xia, Xiaoxuan, et al. A Prism Vote method for individualized risk prediction of traits in genotype data of Multi-population. ''PLoS Genet''. 2022 Oct; '''18''' (10):e1010443
A saturated map of common genetic variants associated with human height. Description: Yengo, Loic, et al. A saturated map of common genetic variants associated with human height. ''Nature''. 2022 Oct; '''610''' (7933):704-712
Associated regions for multiple birth in Brown Swiss and Original Braunvieh cattle on chromosomes 15 and 11. Description: Widmer, Sarah, et al. Associated regions for multiple birth in Brown Swiss and Original Braunvieh cattle on chromosomes 15 and 11. ''Anim Genet''. 2022 Oct; '''53''' (5):557-569
Association of polygenic risk for schizophrenia with fast sleep spindle density depends on pro-cognitive variants. Description: Schilling, Claudia, et al. Association of polygenic risk for schizophrenia with fast sleep spindle density depends on pro-cognitive variants. ''Eur Arch Psychiatry Clin Neurosci''. 2022 Oct; '''272''' (7):1193-1203
Association of third molar agenesis and microdontia with genetic polymorphisms in vitamin-D-related genes. Description: Herrmann, Susann, et al. Association of third molar agenesis and microdontia with genetic polymorphisms in vitamin-D-related genes. ''Ann Anat''. 2022 Oct; '''244''': 151972
Associations of genetic variations in NEDD4L with salt sensitivity, blood pressure changes and hypertension incidence in Chinese adults. Description: Niu, Ze-Jiaxin, et al. Associations of genetic variations in NEDD4L with salt sensitivity, blood pressure changes and hypertension incidence in Chinese adults. ''J Clin Hypertens (Greenwich)''. 2022 Oct; '''24''' (10):1381-1389
Clinical and Genetic Risk Factors for Acute Incident Venous Thromboembolism in Ambulatory Patients With COVID-19. Description: Xie, JunQing, et al. Clinical and Genetic Risk Factors for Acute Incident Venous Thromboembolism in Ambulatory Patients With COVID-19. ''JAMA Intern Med''. 2022 Oct 1; '''182''' (10):1063-1070
Cohort profile: the Food Chain Plus (FoCus) cohort. Description: Geisler, Corinna, et al. Cohort profile: the Food Chain Plus (FoCus) cohort. ''Eur J Epidemiol''. 2022 Oct; '''37''' (10):1087-1105
Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility. Description: Cervan-Martin, Miriam, et al. Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility. ''Andrology''. 2022 Oct; '''10''' (7):1339-1350
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy. Description: Hopfner, Franziska, et al. Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy. ''Mov Disord''. 2022 Oct; '''37''' (10):2110-2121
Complex population history affects admixture analyses in nine-spined sticklebacks. Description: Feng, Xueyun, et al. Complex population history affects admixture analyses in nine-spined sticklebacks. ''Mol Ecol''. 2022 Oct; '''31''' (20):5386-5401
Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome. Description: Alver, Maris, et al. Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome. ''Mol Psychiatry''. 2022 Oct; '''27''' (10):4191-4200
COX7A2L genetic variants determine cardiorespiratory fitness in mice and human. Description: Benegiamo, Giorgia, et al. COX7A2L genetic variants determine cardiorespiratory fitness in mice and human. ''Nat Metab''. 2022 Oct; '''4''' (10):1336-1351
Deregulation of complement components C4A and CSMD1 peripheral expression in first-episode psychosis and links to cognitive ability. Description: Hatzimanolis, Alex, et al. Deregulation of complement components C4A and CSMD1 peripheral expression in first-episode psychosis and links to cognitive ability. ''Eur Arch Psychiatry Clin Neurosci''. 2022 Oct; '''272''' (7):1219-1228
Diverse environmental perturbations reveal the evolution and context-dependency of genetic effects on gene expression levels. Description: Lea, Amanda J, et al. Diverse environmental perturbations reveal the evolution and context-dependency of genetic effects on gene expression levels. ''Genome Res''. 2022 Oct; '''32''' (10):1826-1839
Dynamics of Methylation of CpG Sites Associated With Systemic Lupus Erythematosus Subtypes in a Longitudinal Cohort. Description: Lanata, Cristina M, et al. Dynamics of Methylation of CpG Sites Associated With Systemic Lupus Erythematosus Subtypes in a Longitudinal Cohort. ''Arthritis Rheumatol''. 2022 Oct; '''74''' (10):1676-1686
Functional characterization of enhancer activity during a long terminal repeat's evolution. Description: Du, Alan Y, et al. Functional characterization of enhancer activity during a long terminal repeat's evolution. ''Genome Res''. 2022 Oct; '''32''' (10):1840-1851
Generation of a chromosome-level genome assembly for Pacific halibut (Hippoglossus stenolepis) and characterization of its sex-determining genomic region. Description: Jasonowicz, Andrew J, et al. Generation of a chromosome-level genome assembly for Pacific halibut (Hippoglossus stenolepis) and characterization of its sex-determining genomic region. ''Mol Ecol Resour''. 2022 Oct; '''22''' (7):2685-2700
Genetic and environmental drivers of large-scale epigenetic variation in Thlaspi arvense. Description: Galanti, Dario, et al. Genetic and environmental drivers of large-scale epigenetic variation in Thlaspi arvense. ''PLoS Genet''. 2022 Oct; '''18''' (10):e1010452
Genetic Liabilities Differentiating Bipolar Disorder, Schizophrenia, and Major Depressive Disorder, and Phenotypic Heterogeneity in Bipolar Disorder. Description: Richards, Alexander L, et al. Genetic Liabilities Differentiating Bipolar Disorder, Schizophrenia, and Major Depressive Disorder, and Phenotypic Heterogeneity in Bipolar Disorder. ''JAMA Psychiatry''. 2022 Oct 1; '''79''' (10):1032-1039
Genetic parameters and genome-wide association study of digital cushion thickness in Holstein cows. Description: Barden, Matthew, et al. Genetic parameters and genome-wide association study of digital cushion thickness in Holstein cows. ''J Dairy Sci''. 2022 Oct; '''105''' (10):8237-8256
Genome Reporting for Healthy Populations-Pipeline for Genomic Screening from the GENCOV COVID-19 Study. Description: Frangione, Erika, et al. Genome Reporting for Healthy Populations-Pipeline for Genomic Screening from the GENCOV COVID-19 Study. ''Curr Protoc''. 2022 Oct; '''2''' (10):e534
Genome-wide association study identifies kallikrein 5 in type 2 inflammation-low asthma. Description: Jackman, Janet K, et al. Genome-wide association study identifies kallikrein 5 in type 2 inflammation-low asthma. ''J Allergy Clin Immunol''. 2022 Oct; '''150''' (4):972-978.e7
Genomic Architecture of Yield Performance of an Elite Rice Hybrid Revealed by its Derived Recombinant Inbred Line and Their Backcross Hybrid Populations. Description: Zhang, Fan, et al. Genomic Architecture of Yield Performance of an Elite Rice Hybrid Revealed by its Derived Recombinant Inbred Line and Their Backcross Hybrid Populations. ''Rice (N Y)''. 2022 Oct 1; '''15''' (1):49
Genomics-informed delineation of conservation units in a desert amphibian. Description: Forester, Brenna R, et al. Genomics-informed delineation of conservation units in a desert amphibian. ''Mol Ecol''. 2022 Oct; '''31''' (20):5249-5269
Genomics reveal population structure, evolutionary history, and signatures of selection in the northern bottlenose whale, Hyperoodon ampullatus. Description: de Greef, Evelien, et al. Genomics reveal population structure, evolutionary history, and signatures of selection in the northern bottlenose whale, Hyperoodon ampullatus. ''Mol Ecol''. 2022 Oct; '''31''' (19):4919-4931
How interactions between ADHD and schools affect educational achievement: a family-based genetically sensitive study. Description: Cheesman, Rosa, et al. How interactions between ADHD and schools affect educational achievement: a family-based genetically sensitive study. ''J Child Psychol Psychiatry''. 2022 Oct; '''63''' (10):1174-1185
Immune system-wide Mendelian randomization and triangulation analyses support autoimmunity as a modifiable component in dementia-causing diseases. Description: Lindbohm, Joni V, et al. Immune system-wide Mendelian randomization and triangulation analyses support autoimmunity as a modifiable component in dementia-causing diseases. ''Nat Aging''. 2022 Oct; '''2''' (10):956-972
Improved pea reference genome and pan-genome highlight genomic features and evolutionary characteristics. Description: Yang, Tao, et al. Improved pea reference genome and pan-genome highlight genomic features and evolutionary characteristics. ''Nat Genet''. 2022 Oct; '''54''' (10):1553-1563
Including diverse and admixed populations in genetic epidemiology research. Description: Caliebe, Amke, et al. Including diverse and admixed populations in genetic epidemiology research. ''Genet Epidemiol''. 2022 Oct; '''46''' (7):347-371
Integrative analysis of genomic and exposomic influences on youth mental health. Description: Choi, Karmel W, et al. Integrative analysis of genomic and exposomic influences on youth mental health. ''J Child Psychol Psychiatry''. 2022 Oct; '''63''' (10):1196-1205
Landscape genomics of the American lobster (Homarus americanus). Description: Dorant, Yann, et al. Landscape genomics of the American lobster (Homarus americanus). ''Mol Ecol''. 2022 Oct; '''31''' (20):5182-5200
Mother's and children's ADHD genetic risk, household chaos and children's ADHD symptoms: A gene-environment correlation study. Description: Agnew-Blais, Jessica C, et al. Mother's and children's ADHD genetic risk, household chaos and children's ADHD symptoms: A gene-environment correlation study. ''J Child Psychol Psychiatry''. 2022 Oct; '''63''' (10):1153-1163
Natural and anthropogenic landscape factors shape functional connectivity of an ecological specialist in urban Southern California. Description: Wenner, Sarah M, et al. Natural and anthropogenic landscape factors shape functional connectivity of an ecological specialist in urban Southern California. ''Mol Ecol''. 2022 Oct; '''31''' (20):5214-5230
Natural variation in C. elegans short tandem repeats. Description: Zhang, Gaotian, et al. Natural variation in C. elegans short tandem repeats. ''Genome Res''. 2022 Oct; '''32''' (10):1852-1861
Paraben exposures and their interactions with ESR1/2 genetic polymorphisms on hypertension. Description: Zhou, Shuang, et al. Paraben exposures and their interactions with ESR1/2 genetic polymorphisms on hypertension. ''Environ Res''. 2022 Oct; '''213''': 113651
Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Description: Dube, Marie-Pierre, et al. Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. ''ESC Heart Fail''. 2022 Oct; '''9''' (5):2997-3008
Polygenic scores for schizophrenia and major depression are associated with psychosocial risk factors in children: evidence of gene-environment correlation. Description: Machlitt-Northen, Sandra, et al. Polygenic scores for schizophrenia and major depression are associated with psychosocial risk factors in children: evidence of gene-environment correlation. ''J Child Psychol Psychiatry''. 2022 Oct; '''63''' (10):1140-1152
Prioritized candidate causal haplotype blocks in plant genome-wide association studies. Description: Wu, Xing, et al. Prioritized candidate causal haplotype blocks in plant genome-wide association studies. ''PLoS Genet''. 2022 Oct; '''18''' (10):e1010437
Sodium-glucose cotransporter 1 inhibition and gout: Mendelian randomisation study. Description: Zhao, Sizheng Steven, et al. Sodium-glucose cotransporter 1 inhibition and gout: Mendelian randomisation study. ''Semin Arthritis Rheum''. 2022 Oct; '''56''': 152058
Suicidal ideation during adolescence: The roles of aggregate genetic liability for suicide attempts and negative life events in the past year. Description: Lannoy, Severine, et al. Suicidal ideation during adolescence: The roles of aggregate genetic liability for suicide attempts and negative life events in the past year. ''J Child Psychol Psychiatry''. 2022 Oct; '''63''' (10):1164-1173
The autotetraploid potato genome provides insights into highly heterozygous species. Description: Wang, Fang, et al. The autotetraploid potato genome provides insights into highly heterozygous species. ''Plant Biotechnol J''. 2022 Oct; '''20''' (10):1996-2005
The genetic architecture of blood pressure variability: A genome-wide association study of 9370 participants from UK Biobank. Description: Jia, Pingping, et al. The genetic architecture of blood pressure variability: A genome-wide association study of 9370 participants from UK Biobank. ''J Clin Hypertens (Greenwich)''. 2022 Oct; '''24''' (10):1370-1380
The western redcedar genome reveals low genetic diversity in a self-compatible conifer. Description: Shalev, Tal J, et al. The western redcedar genome reveals low genetic diversity in a self-compatible conifer. ''Genome Res''. 2022 Oct; '''32''' (10):1952-1964
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis. Description: Ewans, Lisa J, et al. Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis. ''Eur J Hum Genet''. 2022 Oct; '''30''' (10):1121-1131
Genome-Wide Investigation of Maximum Habitual Alcohol Intake in US Veterans in Relation to Alcohol Consumption Traits and Alcohol Use Disorder. Description: Deak, Joseph D, et al. Genome-Wide Investigation of Maximum Habitual Alcohol Intake in US Veterans in Relation to Alcohol Consumption Traits and Alcohol Use Disorder. ''JAMA Netw Open''. 2022 Oct 3; '''5''' (10):e2238880
Both indirect maternal and direct fetal genetic effects reflect the observational relationship between higher birth weight and lower adult bone mass. Description: Xia, Jiang-Wei, et al. Both indirect maternal and direct fetal genetic effects reflect the observational relationship between higher birth weight and lower adult bone mass. ''BMC Med''. 2022 Oct 4; '''20''' (1):361
Functional genomics analysis reveals the evolutionary adaptation and demographic history of pygmy lorises. Description: Li, Ming-Li, et al. Functional genomics analysis reveals the evolutionary adaptation and demographic history of pygmy lorises. ''Proc Natl Acad Sci U S A''. 2022 Oct 4; '''119''' (40):e2123030119
Genetic adaptation of skin pigmentation in highland Tibetans. Description: Yang, Zhaohui, et al. Genetic adaptation of skin pigmentation in highland Tibetans. ''Proc Natl Acad Sci U S A''. 2022 Oct 4; '''119''' (40):e2200421119
Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population. Description: Shi, Mengyao, et al. Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population. ''J Am Heart Assoc''. 2022 Oct 4; '''11''' (19):e025245
Pharmacogenetic Variation and Its Clinical Relevance in a Latin American Rural Population. Description: Olloquequi, Jordi, et al. Pharmacogenetic Variation and Its Clinical Relevance in a Latin American Rural Population. ''Int J Mol Sci''. 2022 Oct 4; '''23''' (19):
Using neuroimaging genomics to investigate the evolution of human brain structure. Description: Alagoz, Gokberk, et al. Using neuroimaging genomics to investigate the evolution of human brain structure. ''Proc Natl Acad Sci U S A''. 2022 Oct 4; '''119''' (40):e2200638119
Candidate Modifier Genes for the Penetrance of Leber's Hereditary Optic Neuropathy. Description: Cheng, Hui-Chen, et al. Candidate Modifier Genes for the Penetrance of Leber's Hereditary Optic Neuropathy. ''Int J Mol Sci''. 2022 Oct 6; '''23''' (19):
Lifestage Sex-Specific Genetic Effects on Metabolic Disorders in an Adult Population in Korea: The Korean Genome and Epidemiology Study. Description: Kim, Young-Sang, et al. Lifestage Sex-Specific Genetic Effects on Metabolic Disorders in an Adult Population in Korea: The Korean Genome and Epidemiology Study. ''Int J Mol Sci''. 2022 Oct 6; '''23''' (19):
Demographic and Selection Histories of Populations Across the Sahel/Savannah Belt. Description: Fortes-Lima, Cesar, et al. Demographic and Selection Histories of Populations Across the Sahel/Savannah Belt. ''Mol Biol Evol''. 2022 Oct 7; '''39''' (10):
Tracing Bai-Yue Ancestry in Aboriginal Li People on Hainan Island. Description: Chen, Hao, et al. Tracing Bai-Yue Ancestry in Aboriginal Li People on Hainan Island. ''Mol Biol Evol''. 2022 Oct 7; '''39''' (10):
Familial Linkage and Association of the NR3C1 Gene with Type 2 Diabetes and Depression Comorbidity. Description: Amin, Mutaz, et al. Familial Linkage and Association of the NR3C1 Gene with Type 2 Diabetes and Depression Comorbidity. ''Int J Mol Sci''. 2022 Oct 8; '''23''' (19):
Genome-wide association mapping reveals genes underlying population-level metabolome diversity in a fungal crop pathogen. Description: Singh, Nikhil Kumar, et al. Genome-wide association mapping reveals genes underlying population-level metabolome diversity in a fungal crop pathogen. ''BMC Biol''. 2022 Oct 8; '''20''' (1):224
Multi-Omic analyses characterize the ceramide/sphingomyelin pathway as a therapeutic target in Alzheimer's disease. Description: Baloni, Priyanka, et al. Multi-Omic analyses characterize the ceramide/sphingomyelin pathway as a therapeutic target in Alzheimer's disease. ''Commun Biol''. 2022 Oct 8; '''5''' (1):1074
Evolutionary responses of a reef-building coral to climate change at the end of the last glacial maximum. Description: Zhang, Jia, et al. Evolutionary responses of a reef-building coral to climate change at the end of the last glacial maximum. ''Mol Biol Evol''. 2022 Oct 11; '''39''' (10):
The diverse genetic origins of a Classical period Greek army. Description: Reitsema, Laurie J, et al. The diverse genetic origins of a Classical period Greek army. ''Proc Natl Acad Sci U S A''. 2022 Oct 11; '''119''' (41):e2205272119
Parasite Genotype Is a Major Predictor of Mortality from Visceral Leishmaniasis. Description: Grace, Cooper Alastair, et al. Parasite Genotype Is a Major Predictor of Mortality from Visceral Leishmaniasis. ''mBio''. 2022 Oct 12; '''13''' (6):e0206822
Characterisation of ethnic differences in DNA methylation between UK-resident South Asians and Europeans. Description: Elliott, Hannah R, et al. Characterisation of ethnic differences in DNA methylation between UK-resident South Asians and Europeans. ''Clin Epigenetics''. 2022 Oct 15; '''14''' (1):130
Mapping of Candidate Genes in Response to Low Nitrogen in Rice Seedlings. Description: Li, Jia, et al. Mapping of Candidate Genes in Response to Low Nitrogen in Rice Seedlings. ''Rice (N Y)''. 2022 Oct 15; '''15''' (1):51
Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study. Description: Nethander, Maria, et al. Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study. ''Cell Rep Med''. 2022 Oct 18; '''3''' (10):100776
Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Description: Moitinho-Silva, Lucas, et al. Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. ''Nat Commun''. 2022 Oct 19; '''13''' (1):6204
Extensive genome introgression between domestic ferret and European polecat during population recovery in Great Britain. Description: Etherington, Graham J, et al. Extensive genome introgression between domestic ferret and European polecat during population recovery in Great Britain. ''J Hered''. 2022 Oct 21; '''113''' (5):500-515
Genomes from a medieval mass burial show Ashkenazi-associated hereditary diseases pre-date the 12th century. Description: Brace, Selina, et al. Genomes from a medieval mass burial show Ashkenazi-associated hereditary diseases pre-date the 12th century. ''Curr Biol''. 2022 Oct 24; '''32''' (20):4350-4359.e6
Genome-Wide Association Studies Revealed Significant QTLs and Candidate Genes Associated with Backfat and Loin Muscle Area in Pigs Using Imputation-Based Whole Genome Sequencing Data. Description: Li, Jie, et al. Genome-Wide Association Studies Revealed Significant QTLs and Candidate Genes Associated with Backfat and Loin Muscle Area in Pigs Using Imputation-Based Whole Genome Sequencing Data. ''Animals (Basel)''. 2022 Oct 24; '''12''' (21):
Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification. Description: Wang, Nan, et al. Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification. ''Proc Natl Acad Sci U S A''. 2022 Oct 25; '''119''' (43):e2206076119
The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration. Description: Rossi, Giacomina, et al. The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration. ''Int J Mol Sci''. 2022 Oct 25; '''23''' (21):
Genomic and Molecular Identification of Genes Contributing to the Caspofungin Paradoxical Effect in Aspergillus fumigatus. Description: Zhao, Shu, et al. Genomic and Molecular Identification of Genes Contributing to the Caspofungin Paradoxical Effect in Aspergillus fumigatus. ''Microbiol Spectr''. 2022 Oct 26; '''10''' (5):e0051922
Heritable and Nonheritable Rumen Bacteria Are Associated with Different Characters of Lactation Performance of Dairy Cows. Description: Zang, Xin-Wei, et al. Heritable and Nonheritable Rumen Bacteria Are Associated with Different Characters of Lactation Performance of Dairy Cows. ''mSystems''. 2022 Oct 26; '''7''' (5):e0042222
A Polynesian-specific copy number variant encompassing the MICA gene associates with gout. Description: Wang, Ke, et al. A Polynesian-specific copy number variant encompassing the MICA gene associates with gout. ''Hum Mol Genet''. 2022 Oct 28; '''31''' (21):3757-3768
Genomic Signatures Reveal Breeding Effects of Lulai Pigs. Description: Cao, Rui, et al. Genomic Signatures Reveal Breeding Effects of Lulai Pigs. ''Genes (Basel)''. 2022 Oct 28; '''13''' (11):
Pharmacokinetic and pharmacogenetic associations with dolutegravir neuropsychiatric adverse events in an African population. Description: Griesel, Rulan, et al. Pharmacokinetic and pharmacogenetic associations with dolutegravir neuropsychiatric adverse events in an African population. ''J Antimicrob Chemother''. 2022 Oct 28; '''77''' (11):3110-3117
Genome-Wide Association Study of Exercise-Induced Fat Loss Efficiency. Description: Bojarczuk, Aleksandra, et al. Genome-Wide Association Study of Exercise-Induced Fat Loss Efficiency. ''Genes (Basel)''. 2022 Oct 29; '''13''' (11):
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder. Description: Chan, Ada J S, et al. Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder. ''Nat Commun''. 2022 Oct 29; '''13''' (1):6463
Geographical Patterns of Genetic Variation in Locoto Chile (Capsicum pubescens) in the Americas Inferred by Genome-Wide Data Analysis. Description: Palombo, Nahuel E, et al. Geographical Patterns of Genetic Variation in Locoto Chile (Capsicum pubescens) in the Americas Inferred by Genome-Wide Data Analysis. ''Plants (Basel)''. 2022 Oct 29; '''11''' (21):
Polygenic heterogeneity in antidepressant treatment and placebo response. Description: Nohr, Anne Krogh, et al. Polygenic heterogeneity in antidepressant treatment and placebo response. ''Transl Psychiatry''. 2022 Oct 29; '''12''' (1):456
Genome-Wide Association Mapping Identifies New Candidate Genes for Cold Stress and Chilling Acclimation at Seedling Stage in Rice (Oryza sativa L.). Description: Li, Jianguo, et al. Genome-Wide Association Mapping Identifies New Candidate Genes for Cold Stress and Chilling Acclimation at Seedling Stage in Rice (Oryza sativa L.). ''Int J Mol Sci''. 2022 Oct 30; '''23''' (21):
Genome-Wide Association Study of Growth Traits in a Four-Way Crossbred Pig Population. Description: Wang, Huiyu, et al. Genome-Wide Association Study of Growth Traits in a Four-Way Crossbred Pig Population. ''Genes (Basel)''. 2022 Oct 31; '''13''' (11):
Assessing the contribution of genetic nurture to refractive error. Description: Guggenheim, Jeremy A, et al. Assessing the contribution of genetic nurture to refractive error. ''Eur J Hum Genet''. 2022 Nov; '''30''' (11):1226-1232
Association between IL1RL1 gene polymorphisms and allergic rhinitis risk in the Chinese Han population. Description: Li, Zhengqing, et al. Association between IL1RL1 gene polymorphisms and allergic rhinitis risk in the Chinese Han population. ''J Clin Lab Anal''. 2022 Nov; '''36''' (11):e24747
Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits. Description: O'Leary, Aet, et al. Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits. ''Mol Psychiatry''. 2022 Nov; '''27''' (11):4464-4473
Circulating Soluble CD163, Associations With Cardiovascular Outcomes and Mortality, and Identification of Genetic Variants in Older Individuals: The Cardiovascular Health Study. Description: Durda, Peter, et al. Circulating Soluble CD163, Associations With Cardiovascular Outcomes and Mortality, and Identification of Genetic Variants in Older Individuals: The Cardiovascular Health Study. ''J Am Heart Assoc''. 2022 Nov; '''11''' (21):e024374
Common genetic variants associated with melanoma risk or naevus count in patients with wildtype MC1R melanoma. Description: Calbet-Llopart, Neus, et al. Common genetic variants associated with melanoma risk or naevus count in patients with wildtype MC1R melanoma. ''Br J Dermatol''. 2022 Nov; '''187''' (5):753-764
Complex population structure and haplotype patterns in the Western European honey bee from sequencing a large panel of haploid drones. Description: Wragg, David, et al. Complex population structure and haplotype patterns in the Western European honey bee from sequencing a large panel of haploid drones. ''Mol Ecol Resour''. 2022 Nov; '''22''' (8):3068-3086
Educational attainment polygenic scores, socioeconomic factors, and cortical structure in children and adolescents. Description: Merz, Emily C, et al. Educational attainment polygenic scores, socioeconomic factors, and cortical structure in children and adolescents. ''Hum Brain Mapp''. 2022 Nov; '''43''' (16):4886-4900
Exploring the association of interleukin polymorphisms with aggression and internalizing behaviors in children and adolescents. Description: Pouget, Jennie G, et al. Exploring the association of interleukin polymorphisms with aggression and internalizing behaviors in children and adolescents. ''Brain Behav''. 2022 Nov; '''12''' (11):e2753
Genomewide association study identifies a novel variant associated with tacrolimus trough concentration in Chinese renal transplant recipients. Description: Yang, Siyao, et al. Genomewide association study identifies a novel variant associated with tacrolimus trough concentration in Chinese renal transplant recipients. ''Clin Transl Sci''. 2022 Nov; '''15''' (11):2640-2651
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Description: Jansen, Iris E, et al. Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. ''Acta Neuropathol''. 2022 Nov; '''144''' (5):821-842
Genomic basis of insularity and ecological divergence in barn owls (Tyto alba) of the Canary Islands. Description: Cumer, Tristan, et al. Genomic basis of insularity and ecological divergence in barn owls (Tyto alba) of the Canary Islands. ''Heredity (Edinb)''. 2022 Nov; '''129''' (5):281-294
GWAS of Reproductive Traits in Large White Pigs on Chip and Imputed Whole-Genome Sequencing Data. Description: Wang, Xiaoqing, et al. GWAS of Reproductive Traits in Large White Pigs on Chip and Imputed Whole-Genome Sequencing Data. ''Int J Mol Sci''. 2022 Nov 1; '''23''' (21):
Host genetic determinants drive compartment-specific assembly of tea plant microbiomes. Description: Tan, Xiangfeng, et al. Host genetic determinants drive compartment-specific assembly of tea plant microbiomes. ''Plant Biotechnol J''. 2022 Nov; '''20''' (11):2174-2186
Implementation of NUDT15 Genotyping to Prevent Azathioprine-Induced Leukopenia for Patients With Autoimmune Disorders in Chinese Population. Description: Wang, Chuang-Wei, et al. Implementation of NUDT15 Genotyping to Prevent Azathioprine-Induced Leukopenia for Patients With Autoimmune Disorders in Chinese Population. ''Clin Pharmacol Ther''. 2022 Nov; '''112''' (5):1079-1087
Mer-tyrosine kinase: a novel susceptibility gene for SLE related end-stage renal disease. Description: Yavuz, Sule, et al. Mer-tyrosine kinase: a novel susceptibility gene for SLE related end-stage renal disease. ''Lupus Sci Med''. 2022 Nov; '''9''' (1):
Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities. Description: Katsumata, Yuriko, et al. Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities. ''Neurobiol Dis''. 2022 Nov; '''174''': 105880
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes. Description: Wei, Wei, et al. Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes. ''Nature''. 2022 Nov; '''611''' (7934):105-114
Pharmacogenetics of Dolutegravir Plasma Exposure Among Southern Africans With Human Immunodeficiency Virus. Description: Cindi, Zinhle, et al. Pharmacogenetics of Dolutegravir Plasma Exposure Among Southern Africans With Human Immunodeficiency Virus. ''J Infect Dis''. 2022 Nov 1; '''226''' (9):1616-1625
Population genomics of a predatory mammal reveals patterns of decline and impacts of exposure to toxic toads. Description: von Takach, Brenton, et al. Population genomics of a predatory mammal reveals patterns of decline and impacts of exposure to toxic toads. ''Mol Ecol''. 2022 Nov; '''31''' (21):5468-5486
Rare and common genetic determinants of metabolic individuality and their effects on human health. Description: Surendran, Praveen, et al. Rare and common genetic determinants of metabolic individuality and their effects on human health. ''Nat Med''. 2022 Nov; '''28''' (11):2321-2332
Secondary contact rather than coexistence-Erebia butterflies in the Alps. Description: Augustijnen, Hannah, et al. Secondary contact rather than coexistence-Erebia butterflies in the Alps. ''Evolution''. 2022 Nov; '''76''' (11):2669-2686
Species' attributes predict the relative magnitude of ecological and genetic recovery following mass mortality. Description: Schiebelhut, Lauren M, et al. Species' attributes predict the relative magnitude of ecological and genetic recovery following mass mortality. ''Mol Ecol''. 2022 Nov; '''31''' (22):5714-5728
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Description: Weiner, Daniel J, et al. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. ''Nat Genet''. 2022 Nov; '''54''' (11):1630-1639
The pan-genome of Aspergillus fumigatus provides a high-resolution view of its population structure revealing high levels of lineage-specific diversity driven by recombination. Description: Lofgren, Lotus A, et al. The pan-genome of Aspergillus fumigatus provides a high-resolution view of its population structure revealing high levels of lineage-specific diversity driven by recombination. ''PLoS Biol''. 2022 Nov; '''20''' (11):e3001890
The role of genetic predisposition in cardiovascular risk after cancer diagnosis: a matched cohort study of the UK Biobank. Description: Yang, Huazhen, et al. The role of genetic predisposition in cardiovascular risk after cancer diagnosis: a matched cohort study of the UK Biobank. ''Br J Cancer''. 2022 Nov; '''127''' (9):1650-1659
The Roles of MTRR and MTHFR Gene Polymorphisms in Colorectal Cancer Survival. Description: Wang, Yu, et al. The Roles of MTRR and MTHFR Gene Polymorphisms in Colorectal Cancer Survival. ''Nutrients''. 2022 Nov 1; '''14''' (21):
African Ancestry-Associated Gene Expression Profiles in Triple-Negative Breast Cancer Underlie Altered Tumor Biology and Clinical Outcome in Women of African Descent. Description: Martini, Rachel, et al. African Ancestry-Associated Gene Expression Profiles in Triple-Negative Breast Cancer Underlie Altered Tumor Biology and Clinical Outcome in Women of African Descent. ''Cancer Discov''. 2022 Nov 2; '''12''' (11):2530-2551
Elucidating the Genetic Relationships on the Original Old Sicilian Triticum Spp. Collection by SNP Genotyping. Description: Fiore, Maria Carola, et al. Elucidating the Genetic Relationships on the Original Old Sicilian Triticum Spp. Collection by SNP Genotyping. ''Int J Mol Sci''. 2022 Nov 2; '''23''' (21):
Immune and Genomic Analysis of Boxer Dog Breed and Its Relationship with Leishmania infantum Infection. Description: Alvarez, Luis, et al. Immune and Genomic Analysis of Boxer Dog Breed and Its Relationship with Leishmania infantum Infection. ''Vet Sci''. 2022 Nov 2; '''9''' (11):
Waxy is an important factor for grain fissure resistance and head rice yield as revealed by a genome-wide association study. Description: Deng, Zhuyun, et al. Waxy is an important factor for grain fissure resistance and head rice yield as revealed by a genome-wide association study. ''J Exp Bot''. 2022 Nov 2; '''73''' (19):6942-6954
Balancing at the Borderline of a Breed: A Case Study of the Hungarian Short-Haired Vizsla Dog Breed, Definition of the Breed Profile Using Simple SNP-Based Methods. Description: Varga, Laszlo, et al. Balancing at the Borderline of a Breed: A Case Study of the Hungarian Short-Haired Vizsla Dog Breed, Definition of the Breed Profile Using Simple SNP-Based Methods. ''Genes (Basel)''. 2022 Nov 3; '''13''' (11):
Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Description: Lee, Chia-Jung, et al. Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. ''Commun Biol''. 2022 Nov 3; '''5''' (1):1175
Population Structure and Selection Signatures Underlying Domestication Inferred from Genome-Wide Copy Number Variations in Chinese Indigenous Pigs. Description: Zhang, Wei, et al. Population Structure and Selection Signatures Underlying Domestication Inferred from Genome-Wide Copy Number Variations in Chinese Indigenous Pigs. ''Genes (Basel)''. 2022 Nov 3; '''13''' (11):
Widespread Gene Expression Divergence in Butterfly Sensory Tissues Plays a Fundamental Role During Reproductive Isolation and Speciation. Description: Wu, Ningning, et al. Widespread Gene Expression Divergence in Butterfly Sensory Tissues Plays a Fundamental Role During Reproductive Isolation and Speciation. ''Mol Biol Evol''. 2022 Nov 3; '''39''' (11):
A genomic snapshot of demographic and cultural dynamism in Upper Mesopotamia during the Neolithic Transition. Description: Altinisik, N Ezgi, et al. A genomic snapshot of demographic and cultural dynamism in Upper Mesopotamia during the Neolithic Transition. ''Sci Adv''. 2022 Nov 4; '''8''' (44):eabo3609
An SNN retrocopy insertion upstream of GPR22 is associated with dark red coat color in Poodles. Description: Batcher, Kevin, et al. An SNN retrocopy insertion upstream of GPR22 is associated with dark red coat color in Poodles. ''G3 (Bethesda)''. 2022 Nov 4; '''12''' (11):
Effect of Single Nucleotide Polymorphisms in the Vitamin D Metabolic Pathway on Susceptibility to Non-Small-Cell Lung Cancer. Description: Pineda Lancheros, Laura Elena, et al. Effect of Single Nucleotide Polymorphisms in the Vitamin D Metabolic Pathway on Susceptibility to Non-Small-Cell Lung Cancer. ''Nutrients''. 2022 Nov 4; '''14''' (21):
Genome screening, reporting, and genetic counseling for healthy populations. Description: Casalino, Selina, et al. Genome screening, reporting, and genetic counseling for healthy populations. ''Hum Genet''. 2022 Nov 4; 1-12
Analysis of clinically relevant variants from ancestrally diverse Asian genomes. Description: Chan, Sock Hoai, et al. Analysis of clinically relevant variants from ancestrally diverse Asian genomes. ''Nat Commun''. 2022 Nov 5; '''13''' (1):6694
Assessing the Relationship Between High-sensitivity C-reactive Protein and Kidney Function Employing Mendelian Randomization in the Japanese Community-based J-MICC Study. Description: Fujii, Ryosuke, et al. Assessing the Relationship Between High-sensitivity C-reactive Protein and Kidney Function Employing Mendelian Randomization in the Japanese Community-based J-MICC Study. ''J Epidemiol''. 2022 Nov 5; '''32''' (11):483-488
Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK. Description: Piga, Noemi-Nicole, et al. Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK. ''Sci Rep''. 2022 Nov 5; '''12''' (1):18828
New Genomic Regions Identified for Resistance to Spot Blotch and Terminal Heat Stress in an Interspecific Population of Triticum aestivum and T. spelta. Description: Navathe, Sudhir, et al. New Genomic Regions Identified for Resistance to Spot Blotch and Terminal Heat Stress in an Interspecific Population of Triticum aestivum and T. spelta. ''Plants (Basel)''. 2022 Nov 5; '''11''' (21):
Parent-of-Origin inference for biobanks. Description: Hofmeister, Robin J, et al. Parent-of-Origin inference for biobanks. ''Nat Commun''. 2022 Nov 5; '''13''' (1):6668
Interspecific Gene Flow and Selective Sweeps in Picea wilsonii, P. neoveitchii and P. likiangensis. Description: Liu, Yifu, et al. Interspecific Gene Flow and Selective Sweeps in Picea wilsonii, P. neoveitchii and P. likiangensis. ''Plants (Basel)''. 2022 Nov 6; '''11''' (21):
Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland. Description: Clark, Jeremy S C, et al. Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland. ''Sci Rep''. 2022 Nov 7; '''12''' (1):18923
Chromosome-level genome and population genomics reveal evolutionary characteristics and conservation status of Chinese indigenous geese. Description: Ouyang, Jing, et al. Chromosome-level genome and population genomics reveal evolutionary characteristics and conservation status of Chinese indigenous geese. ''Commun Biol''. 2022 Nov 7; '''5''' (1):1191
Denisovan and Neanderthal archaic introgression differentially impacted the genetics of complex traits in modern populations. Description: Koller, Dora, et al. Denisovan and Neanderthal archaic introgression differentially impacted the genetics of complex traits in modern populations. ''BMC Biol''. 2022 Nov 7; '''20''' (1):249
Genetically predicted telomere length and Alzheimer's disease endophenotypes: a Mendelian randomization study. Description: Rodriguez-Fernandez, Blanca, et al. Genetically predicted telomere length and Alzheimer's disease endophenotypes: a Mendelian randomization study. ''Alzheimers Res Ther''. 2022 Nov 7; '''14''' (1):167
Integrating Genome-Wide Association Study with RNA-Sequencing Reveals HDAC9 as a Candidate GeneInfluencing Loin Muscle Area in Beijing Black Pigs. Description: Hou, Renda, et al. Integrating Genome-Wide Association Study with RNA-Sequencing Reveals HDAC9 as a Candidate GeneInfluencing Loin Muscle Area in Beijing Black Pigs. ''Biology (Basel)''. 2022 Nov 8; '''11''' (11):
Ocular morphologic traits in the American Cocker Spaniel may confer primary angle closure glaucoma susceptibility. Description: Park, Sangwan, et al. Ocular morphologic traits in the American Cocker Spaniel may confer primary angle closure glaucoma susceptibility. ''Sci Rep''. 2022 Nov 8; '''12''' (1):18980
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Description: Mingardo, Enrico, et al. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. ''Commun Biol''. 2022 Nov 9; '''5''' (1):1203
Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles. Description: Oraki Kohshour, Mojtaba, et al. Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles. ''Transl Psychiatry''. 2022 Nov 9; '''12''' (1):471
Prophage-encoded immune evasion factors are critical for Staphylococcus aureus host infection, switching, and adaptation. Description: Chaguza, Chrispin, et al. Prophage-encoded immune evasion factors are critical for Staphylococcus aureus host infection, switching, and adaptation. ''Cell Genom''. 2022 Nov 9; '''2''' (11):
Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish. Description: Tian, David, et al. Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish. ''Proc Biol Sci''. 2022 Nov 9; '''289''' (1986):20221561
Single-cell genome-wide association reveals that a nonsynonymous variant in ERAP1 confers increased susceptibility to influenza virus. Description: Schott, Benjamin H, et al. Single-cell genome-wide association reveals that a nonsynonymous variant in ERAP1 confers increased susceptibility to influenza virus. ''Cell Genom''. 2022 Nov 9; '''2''' (11):
Genomic trajectories of a near-extinction event in the Chatham Island black robin. Description: von Seth, Johanna, et al. Genomic trajectories of a near-extinction event in the Chatham Island black robin. ''BMC Genomics''. 2022 Nov 10; '''23''' (1):747
Genomic Variation across a Clinical Cryptococcus Population Linked to Disease Outcome. Description: Sephton-Clark, Poppy, et al. Genomic Variation across a Clinical Cryptococcus Population Linked to Disease Outcome. ''mBio''. 2022 Nov 10; '''13''' (6):e0262622
Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Description: Cervan-Martin, Miriam, et al. Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. ''Commun Biol''. 2022 Nov 10; '''5''' (1):1220
Novel genes and sex differences in COVID-19 severity. Description: Cruz, Raquel, et al. Novel genes and sex differences in COVID-19 severity. ''Hum Mol Genet''. 2022 Nov 10; '''31''' (22):3789-3806
Host-plant adaptation as a driver of incipient speciation in the fall armyworm (Spodoptera frugiperda). Description: Fiteni, Estelle, et al. Host-plant adaptation as a driver of incipient speciation in the fall armyworm (Spodoptera frugiperda). ''BMC Ecol Evol''. 2022 Nov 11; '''22''' (1):133
Improving Genomic Prediction with Machine Learning Incorporating TPE for Hyperparameters Optimization. Description: Liang, Mang, et al. Improving Genomic Prediction with Machine Learning Incorporating TPE for Hyperparameters Optimization. ''Biology (Basel)''. 2022 Nov 11; '''11''' (11):
Repeated out-of-Africa expansions of Helicobacter pylori driven by replacement of deleterious mutations. Description: Thorpe, Harry A, et al. Repeated out-of-Africa expansions of Helicobacter pylori driven by replacement of deleterious mutations. ''Nat Commun''. 2022 Nov 11; '''13''' (1):6842
The impact of ABCB1 and CES1 polymorphisms on the safety of dabigatran in patients with non-valvular atrial fibrillation. Description: Zhu, Zhu, et al. The impact of ABCB1 and CES1 polymorphisms on the safety of dabigatran in patients with non-valvular atrial fibrillation. ''BMC Cardiovasc Disord''. 2022 Nov 11; '''22''' (1):481
APOE E4 is associated with impaired self-declared cognition but not disease risk or age of onset in Nigerians with Parkinson's disease. Description: Okubadejo, Njideka U, et al. APOE E4 is associated with impaired self-declared cognition but not disease risk or age of onset in Nigerians with Parkinson's disease. ''NPJ Parkinsons Dis''. 2022 Nov 12; '''8''' (1):155
Gene-gene interaction detection with deep learning. Description: Cui, Tianyu, et al. Gene-gene interaction detection with deep learning. ''Commun Biol''. 2022 Nov 12; '''5''' (1):1238
Genome-wide SNPs in the spiny lobster Panulirus homarus reveal a hybrid origin for its subspecies. Description: Farhadi, Ahmad, et al. Genome-wide SNPs in the spiny lobster Panulirus homarus reveal a hybrid origin for its subspecies. ''BMC Genomics''. 2022 Nov 12; '''23''' (1):750
Evolution of different rice ecotypes and genetic basis of flooding adaptability in Deepwater rice by GWAS. Description: Wang, Xueqiang, et al. Evolution of different rice ecotypes and genetic basis of flooding adaptability in Deepwater rice by GWAS. ''BMC Plant Biol''. 2022 Nov 14; '''22''' (1):526
Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Description: Koskeridis, Fotios, et al. Pleiotropic genetic architecture and novel loci for C-reactive protein levels. ''Nat Commun''. 2022 Nov 14; '''13''' (1):6939
Polygenic risk scores for schizophrenia and major depression are associated with socio-economic indicators of adversity in two British community samples. Description: Machlitt-Northen, Sandra, et al. Polygenic risk scores for schizophrenia and major depression are associated with socio-economic indicators of adversity in two British community samples. ''Transl Psychiatry''. 2022 Nov 14; '''12''' (1):477
Characterisation of retrotransposon insertion polymorphisms in whole genome sequencing data from individuals with amyotrophic lateral sclerosis. Description: Savage, Abigail L, et al. Characterisation of retrotransposon insertion polymorphisms in whole genome sequencing data from individuals with amyotrophic lateral sclerosis. ''Gene''. 2022 Nov 15; '''843''': 146799
Genomic Consequences of Fragmentation in the Endangered Fennoscandian Arctic Fox (Vulpes lagopus). Description: Cockerill, Christopher A, et al. Genomic Consequences of Fragmentation in the Endangered Fennoscandian Arctic Fox (Vulpes lagopus). ''Genes (Basel)''. 2022 Nov 15; '''13''' (11):
Genome-Wide Association Studies for Flesh Color and Intramuscular Fat in (Duroc x Landrace x Large White) Crossbred Commercial Pigs. Description: Li, Hao, et al. Genome-Wide Association Studies for Flesh Color and Intramuscular Fat in (Duroc x Landrace x Large White) Crossbred Commercial Pigs. ''Genes (Basel)''. 2022 Nov 16; '''13''' (11):
Investigation of Genetic Variants Associated with Tryptophan Metabolite Levels via Serotonin and Kynurenine Pathways in Patients with Bipolar Disorder. Description: Pisanu, Claudia, et al. Investigation of Genetic Variants Associated with Tryptophan Metabolite Levels via Serotonin and Kynurenine Pathways in Patients with Bipolar Disorder. ''Metabolites''. 2022 Nov 17; '''12''' (11):
Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes. Description: Nag, Abhishek, et al. Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes. ''Sci Adv''. 2022 Nov 18; '''8''' (46):eadd5430
Identification of New Genes and Genetic Variant Loci Associated with Breast Muscle Development in the Mini-Cobb F2 Chicken Population Using a Genome-Wide Association Study. Description: He, Yang, et al. Identification of New Genes and Genetic Variant Loci Associated with Breast Muscle Development in the Mini-Cobb F2 Chicken Population Using a Genome-Wide Association Study. ''Genes (Basel)''. 2022 Nov 18; '''13''' (11):
Identifying Genetic Variants and Metabolites Associated with Rapid Estimated Glomerular Filtration Rate Decline in Korea Based on Genome-Metabolomic Integrative Analysis. Description: Lee, Sangjun, et al. Identifying Genetic Variants and Metabolites Associated with Rapid Estimated Glomerular Filtration Rate Decline in Korea Based on Genome-Metabolomic Integrative Analysis. ''Metabolites''. 2022 Nov 19; '''12''' (11):
The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Description: van der Meer, Dennis, et al. The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. ''Commun Biol''. 2022 Nov 19; '''5''' (1):1271
Genome-wide analysis-based single nucleotide polymorphism marker sets to identify diverse genotypes in cabbage cultivars (Brassica oleracea var. capitata). Description: Jo, Jinkwan, et al. Genome-wide analysis-based single nucleotide polymorphism marker sets to identify diverse genotypes in cabbage cultivars (Brassica oleracea var. capitata). ''Sci Rep''. 2022 Nov 21; '''12''' (1):20030
A global analysis of matches and mismatches between human genetic and linguistic histories. Description: Barbieri, Chiara, et al. A global analysis of matches and mismatches between human genetic and linguistic histories. ''Proc Natl Acad Sci U S A''. 2022 Nov 22; '''119''' (47):e2122084119
Impact of cultural and genetic structure on food choices along the Silk Road. Description: Aneli, Serena, et al. Impact of cultural and genetic structure on food choices along the Silk Road. ''Proc Natl Acad Sci U S A''. 2022 Nov 22; '''119''' (47):e2209311119
The genetic risk of gestational diabetes in South Asian women. Description: Lamri, Amel, et al. The genetic risk of gestational diabetes in South Asian women. ''Elife''. 2022 Nov 22; '''11''':
Sex-related differences in single nucleotide polymorphisms associated with dyslipidemia in a Korean population. Description: Lee, Gyeonghee, et al. Sex-related differences in single nucleotide polymorphisms associated with dyslipidemia in a Korean population. ''Lipids Health Dis''. 2022 Nov 23; '''21''' (1):124
Identification of 4 New Loci Associated With Primary Hyperparathyroidism (PHPT) and a Polygenic Risk Score for PHPT. Description: Soto-Pedre, Enrique, et al. Identification of 4 New Loci Associated With Primary Hyperparathyroidism (PHPT) and a Polygenic Risk Score for PHPT. ''J Clin Endocrinol Metab''. 2022 Nov 25; '''107''' (12):3302-3308
Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Description: Degenhardt, Frauke, et al. Detailed stratified GWAS analysis for severe COVID-19 in four European populations. ''Hum Mol Genet''. 2022 Nov 28; '''31''' (23):3945-3966
Immunological and genomic characterization of Ibizan Hound dogs in an endemic Leishmania infantum region. Description: Alvarez, Luis, et al. Immunological and genomic characterization of Ibizan Hound dogs in an endemic Leishmania infantum region. ''Parasit Vectors''. 2022 Nov 28; '''15''' (1):445
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. Description: Price, Kaitlyn M, et al. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. ''Transl Psychiatry''. 2022 Nov 29; '''12''' (1):495
Pain predict genetics: protocol for a prospective observational study of clinical and genetic factors to predict the development of postoperative pain. Description: Li, Song, et al. Pain predict genetics: protocol for a prospective observational study of clinical and genetic factors to predict the development of postoperative pain. ''BMJ Open''. 2022 Nov 29; '''12''' (11):e066134
The APOE locus is linked to decline in general cognitive function: 20-years follow-up in the Doetinchem Cohort Study. Description: Rietman, M Liset, et al. The APOE locus is linked to decline in general cognitive function: 20-years follow-up in the Doetinchem Cohort Study. ''Transl Psychiatry''. 2022 Nov 29; '''12''' (1):496
A genome-wide association study identifies a novel association between SDC3 and apparent treatment-resistant hypertension. Description: Xiao, Xiao, et al. A genome-wide association study identifies a novel association between SDC3 and apparent treatment-resistant hypertension. ''BMC Med''. 2022 Nov 30; '''20''' (1):463
Meta-analysis of genome-wide association studies uncovers shared candidate genes across breeds for pig fatness trait. Description: Zeng, Haonan, et al. Meta-analysis of genome-wide association studies uncovers shared candidate genes across breeds for pig fatness trait. ''BMC Genomics''. 2022 Nov 30; '''23''' (1):786
Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma. Description: Gao, Xiaoyi Raymond, et al. Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma. ''Nat Commun''. 2022 Nov 30; '''13''' (1):7376
Admixture has obscured signals of historical hard sweeps in humans. Description: Souilmi, Yassine, et al. Admixture has obscured signals of historical hard sweeps in humans. ''Nat Ecol Evol''. 2022 Dec; '''6''' (12):2003-2015
A high-density integrated map for grapevine based on three mapping populations genotyped by the Vitis18K SNP chip. Description: Vervalle, Jessica A, et al. A high-density integrated map for grapevine based on three mapping populations genotyped by the Vitis18K SNP chip. ''Theor Appl Genet''. 2022 Dec; '''135''' (12):4371-4390
Alzheimer's genetic risk effects on cerebral blood flow across the lifespan are proximal to gene expression. Description: Chandler, Hannah, et al. Alzheimer's genetic risk effects on cerebral blood flow across the lifespan are proximal to gene expression. ''Neurobiol Aging''. 2022 Dec; '''120''': 1-9
Chromosome-level Genomes Reveal the Genetic Basis of Descending Dysploidy and Sex Determination in Morus Plants. Description: Xia, Zhongqiang, et al. Chromosome-level Genomes Reveal the Genetic Basis of Descending Dysploidy and Sex Determination in Morus Plants. ''Genomics Proteomics Bioinformatics''. 2022 Dec; '''20''' (6):1119-1137
Clonal relationship and alcohol consumption-associated mutational signature in synchronous hypopharyngeal tumours and oesophageal squamous cell carcinoma. Description: Ko, Josephine Mun-Yee, et al. Clonal relationship and alcohol consumption-associated mutational signature in synchronous hypopharyngeal tumours and oesophageal squamous cell carcinoma. ''Br J Cancer''. 2022 Dec; '''127''' (12):2166-2174
Comparative analysis of genomic inbreeding parameters and runs of homozygosity islands in several fancy and meat rabbit breeds. Description: Ballan, Mohamad, et al. Comparative analysis of genomic inbreeding parameters and runs of homozygosity islands in several fancy and meat rabbit breeds. ''Anim Genet''. 2022 Dec; '''53''' (6):849-862
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Description: Aragam, Krishna G, et al. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. ''Nat Genet''. 2022 Dec; '''54''' (12):1803-1815
Gene set enrichment analysis of pathophysiological pathways highlights oxidative stress in psychosis. Description: Pistis, Giorgio, et al. Gene set enrichment analysis of pathophysiological pathways highlights oxidative stress in psychosis. ''Mol Psychiatry''. 2022 Dec; '''27''' (12):5135-5143
Genetic analysis of the PCSK9 locus in psychological, psychiatric, metabolic and cardiovascular traits in UK Biobank. Description: Hay, Rachel, et al. Genetic analysis of the PCSK9 locus in psychological, psychiatric, metabolic and cardiovascular traits in UK Biobank. ''Eur J Hum Genet''. 2022 Dec; '''30''' (12):1380-1390
Genetic diversity fuels gene discovery for tobacco and alcohol use. Description: Saunders, Gretchen R B, et al. Genetic diversity fuels gene discovery for tobacco and alcohol use. ''Nature''. 2022 Dec; '''612''' (7941):720-724
Genetics of randomly bred cats support the cradle of cat domestication being in the Near East. Description: Nilson, Sara M, et al. Genetics of randomly bred cats support the cradle of cat domestication being in the Near East. ''Heredity (Edinb)''. 2022 Dec; '''129''' (6):346-355
Genetic variations in relation to bleeding and pharmacodynamics of dabigatran in Chinese patients with nonvalvular atrial fibrillation: A nationwide multicentre prospective cohort study. Description: Xiang, Qian, et al. Genetic variations in relation to bleeding and pharmacodynamics of dabigatran in Chinese patients with nonvalvular atrial fibrillation: A nationwide multicentre prospective cohort study. ''Clin Transl Med''. 2022 Dec; '''12''' (12):e1104
Genome-wide association study for frozen-thawed sperm motility in stallions across various horse breeds. Description: Nikitkina, Elena V, et al. Genome-wide association study for frozen-thawed sperm motility in stallions across various horse breeds. ''Anim Biosci''. 2022 Dec; '''35''' (12):1827-1838
Identity-by-descent analysis of a large Tourette's syndrome pedigree from Costa Rica implicates genes involved in neuronal development and signal transduction. Description: Ryan, Niamh, et al. Identity-by-descent analysis of a large Tourette's syndrome pedigree from Costa Rica implicates genes involved in neuronal development and signal transduction. ''Mol Psychiatry''. 2022 Dec; '''27''' (12):5020-5027
IFNL4 genotype influences the rate of HIV-1 seroconversion in men who have sex with men. Description: Meza, Giovanna, et al. IFNL4 genotype influences the rate of HIV-1 seroconversion in men who have sex with men. ''Virulence''. 2022 Dec; '''13''' (1):757-763
Improving the computation efficiency of polygenic risk score modeling: faster in Julia. Description: Faucon, Annika, et al. Improving the computation efficiency of polygenic risk score modeling: faster in Julia. ''Life Sci Alliance''. 2022 Dec; '''5''' (12):
Investigating the phenotypic and genetic associations between personality traits and suicidal behavior across major mental health diagnoses. Description: Kalman, Janos L, et al. Investigating the phenotypic and genetic associations between personality traits and suicidal behavior across major mental health diagnoses. ''Eur Arch Psychiatry Clin Neurosci''. 2022 Dec; '''272''' (8):1611-1620
Leveraging interindividual variability of regulatory activity for refining genetic regulation of gene expression in schizophrenia. Description: Alver, Maris, et al. Leveraging interindividual variability of regulatory activity for refining genetic regulation of gene expression in schizophrenia. ''Mol Psychiatry''. 2022 Dec; '''27''' (12):5177-5185
Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits. Description: Chun, Sung, et al. Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits. ''PLoS Genet''. 2022 Dec; '''18''' (12):e1010557
Long-range chromosomal interactions increase and mark repressed gene expression during adipogenesis. Description: Garske, Kristina M, et al. Long-range chromosomal interactions increase and mark repressed gene expression during adipogenesis. ''Epigenetics''. 2022 Dec; '''17''' (13):1849-1862
MicroRNA binding site variation is enriched in psychiatric disorders. Description: Geaghan, Michael P, et al. MicroRNA binding site variation is enriched in psychiatric disorders. ''Hum Mutat''. 2022 Dec; '''43''' (12):2153-2169
New insights into the novel sequences of the chicken pan-genome by liquid chip. Description: Wang, Fei, et al. New insights into the novel sequences of the chicken pan-genome by liquid chip. ''J Anim Sci''. 2022 Dec 1; '''100''' (12):
Pan-tumor landscape of fibroblast growth factor receptor 1-4 genomic alterations. Description: Murugesan, K, et al. Pan-tumor landscape of fibroblast growth factor receptor 1-4 genomic alterations. ''ESMO Open''. 2022 Dec; '''7''' (6):100641
Rare copy number variation in posttraumatic stress disorder. Description: Maihofer, Adam X, et al. Rare copy number variation in posttraumatic stress disorder. ''Mol Psychiatry''. 2022 Dec; '''27''' (12):5062-5069
Replacement of microsatellite markers by imputed medium-density SNP arrays for parentage control in German warmblood horses. Description: Nolte, Wietje, et al. Replacement of microsatellite markers by imputed medium-density SNP arrays for parentage control in German warmblood horses. ''J Appl Genet''. 2022 Dec; '''63''' (4):783-792
Resolving drug selection and migration in an inbred South American Plasmodium falciparum population with identity-by-descent analysis. Description: Carrasquilla, Manuela, et al. Resolving drug selection and migration in an inbred South American Plasmodium falciparum population with identity-by-descent analysis. ''PLoS Pathog''. 2022 Dec; '''18''' (12):e1010993
Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case-control study and meta-analysis. Description: Moazzam-Jazi, Maryam, et al. Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case-control study and meta-analysis. ''Sci Rep''. 2022 Dec 1; '''12''' (1):20709
Rs7537605 polymorphism in VAV3 gene and rs28665122 polymorphism in SEPS gene are not associated with Hashimoto's thyroiditis in North-East Algerian population. Description: Kherrour, Warda, et al. Rs7537605 polymorphism in VAV3 gene and rs28665122 polymorphism in SEPS gene are not associated with Hashimoto's thyroiditis in North-East Algerian population. ''Afr Health Sci''. 2022 Dec; '''22''' (4):252-260
Single nucleotide polymorphism-based analysis of the genetic structure of the Min pig conserved population. Description: Meng, Fanbing, et al. Single nucleotide polymorphism-based analysis of the genetic structure of the Min pig conserved population. ''Anim Biosci''. 2022 Dec; '''35''' (12):1839-1849
Transferability of Alzheimer Disease Polygenic Risk Score Across Populations and Its Association With Alzheimer Disease-Related Phenotypes. Description: Jung, Sang-Hyuk, et al. Transferability of Alzheimer Disease Polygenic Risk Score Across Populations and Its Association With Alzheimer Disease-Related Phenotypes. ''JAMA Netw Open''. 2022 Dec 1; '''5''' (12):e2247162
Whole genome population structure of North Atlantic kelp confirms high-latitude glacial refugia. Description: Bringloe, Trevor T, et al. Whole genome population structure of North Atlantic kelp confirms high-latitude glacial refugia. ''Mol Ecol''. 2022 Dec; '''31''' (24):6473-6488
Comparative Genomics Provides Etiologic and Biological Insight into Melanoma Subtypes. Description: Newell, Felicity, et al. Comparative Genomics Provides Etiologic and Biological Insight into Melanoma Subtypes. ''Cancer Discov''. 2022 Dec 2; '''12''' (12):2856-2879
Effects of Pre-Pregnancy Overweight/Obesity on the Pattern of Association of Hypertension Susceptibility Genes with Preeclampsia. Description: Abramova, Maria, et al. Effects of Pre-Pregnancy Overweight/Obesity on the Pattern of Association of Hypertension Susceptibility Genes with Preeclampsia. ''Life (Basel)''. 2022 Dec 3; '''12''' (12):
Markhor-derived Introgression of a Genomic Region Encompassing PAPSS2 Confers High-altitude Adaptability in Tibetan Goats. Description: Li, Chao, et al. Markhor-derived Introgression of a Genomic Region Encompassing PAPSS2 Confers High-altitude Adaptability in Tibetan Goats. ''Mol Biol Evol''. 2022 Dec 5; '''39''' (12):
The evolutionary process of invasion in the fall armyworm (Spodoptera frugiperda). Description: Yainna, Sudeeptha, et al. The evolutionary process of invasion in the fall armyworm (Spodoptera frugiperda). ''Sci Rep''. 2022 Dec 6; '''12''' (1):21063
Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population. Description: Escher, Luciana Maia, et al. Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population. ''Sci Rep''. 2022 Dec 8; '''12''' (1):21240
Disease patterns of coronary heart disease and type 2 diabetes harbored distinct and shared genetic architecture. Description: Xiao, Han, et al. Disease patterns of coronary heart disease and type 2 diabetes harbored distinct and shared genetic architecture. ''Cardiovasc Diabetol''. 2022 Dec 9; '''21''' (1):276
Methodological challenges in the genomic analysis of an endangered mammal population with low genetic diversity. Description: Escoda, Lidia, et al. Methodological challenges in the genomic analysis of an endangered mammal population with low genetic diversity. ''Sci Rep''. 2022 Dec 10; '''12''' (1):21390
Genome-wide association study reveals ethnicity-specific SNPs associated with ankylosing spondylitis in the Taiwanese population. Description: Ko, Ching-Lung, et al. Genome-wide association study reveals ethnicity-specific SNPs associated with ankylosing spondylitis in the Taiwanese population. ''J Transl Med''. 2022 Dec 12; '''20''' (1):589
Phenome-wide association study of loci harboring de novo tandem repeat mutations in UK Biobank exomes. Description: Wendt, Frank R, et al. Phenome-wide association study of loci harboring de novo tandem repeat mutations in UK Biobank exomes. ''Nat Commun''. 2022 Dec 12; '''13''' (1):7682
The role of Neanderthal introgression in liver cancer. Description: Taravella Oill, Angela M, et al. The role of Neanderthal introgression in liver cancer. ''BMC Med Genomics''. 2022 Dec 12; '''15''' (1):255
Meta-analysis fine-mapping is often miscalibrated at single-variant resolution. Description: Kanai, Masahiro, et al. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution. ''Cell Genom''. 2022 Dec 14; '''2''' (12):
Rare Amyloid Precursor Protein Point Mutations Recapitulate Worldwide Migration and Admixture in Healthy Individuals: Implications for the Study of Neurodegeneration. Description: Abondio, Paolo, et al. Rare Amyloid Precursor Protein Point Mutations Recapitulate Worldwide Migration and Admixture in Healthy Individuals: Implications for the Study of Neurodegeneration. ''Int J Mol Sci''. 2022 Dec 14; '''23''' (24):
The missing link between genetic association and regulatory function. Description: Connally, Noah J, et al. The missing link between genetic association and regulatory function. ''Elife''. 2022 Dec 14; '''11''':
Chromosome-level genome sequence of the Genetically Improved Farmed Tilapia (GIFT, Oreochromis niloticus) highlights regions of introgression with O. mossambicus. Description: Etherington, G J, et al. Chromosome-level genome sequence of the Genetically Improved Farmed Tilapia (GIFT, Oreochromis niloticus) highlights regions of introgression with O. mossambicus. ''BMC Genomics''. 2022 Dec 15; '''23''' (1):832
Genome-wide identification of SNPs associated with body weight in yak. Description: Jiang, Hui, et al. Genome-wide identification of SNPs associated with body weight in yak. ''BMC Genomics''. 2022 Dec 15; '''23''' (1):833
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis. Description: Hindy, George, et al. Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis. ''J Clin Invest''. 2022 Dec 15; '''132''' (24):
Comparative Silk Transcriptomics Illuminates Distinctive Impact of Artificial Selection in Silkworm Modern Breeding. Description: Zhu, Kesen, et al. Comparative Silk Transcriptomics Illuminates Distinctive Impact of Artificial Selection in Silkworm Modern Breeding. ''Insects''. 2022 Dec 16; '''13''' (12):
Analysis of merged transcriptomic and genomic datasets to identify genes and pathways underlying residual feed intake in growing pigs. Description: Ibragimov, Emil, et al. Analysis of merged transcriptomic and genomic datasets to identify genes and pathways underlying residual feed intake in growing pigs. ''Sci Rep''. 2022 Dec 19; '''12''' (1):21946
Genome-wide association study identifies novel loci associated with skin autofluorescence in individuals without diabetes. Description: Vollenbrock, Charlotte E, et al. Genome-wide association study identifies novel loci associated with skin autofluorescence in individuals without diabetes. ''BMC Genomics''. 2022 Dec 19; '''23''' (1):840
A population-based study of precision health assessments using multi-omics network-derived biological functional modules. Description: Zhang, Wei, et al. A population-based study of precision health assessments using multi-omics network-derived biological functional modules. ''Cell Rep Med''. 2022 Dec 20; '''3''' (12):100847
Polygenic risk for schizophrenia as a moderator of associations between childhood trauma and schizotypy. Description: Tonini, Emiliana, et al. Polygenic risk for schizophrenia as a moderator of associations between childhood trauma and schizotypy. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2022 Dec 20; '''119''': 110612
A genome-wide association study implicates the pleiotropic effect of NMUR2 on asthma and COPD. Description: Do, Ah Ra, et al. A genome-wide association study implicates the pleiotropic effect of NMUR2 on asthma and COPD. ''Sci Rep''. 2022 Dec 21; '''12''' (1):22073
Genomic Assembly of Clinical Candida glabrata (Nakaseomyces glabrata) Isolates Reveals within-Species Structural Plasticity and Association with In Vitro Antifungal Susceptibility. Description: Stefanini, Irene, et al. Genomic Assembly of Clinical Candida glabrata (Nakaseomyces glabrata) Isolates Reveals within-Species Structural Plasticity and Association with In Vitro Antifungal Susceptibility. ''Microbiol Spectr''. 2022 Dec 21; '''10''' (6):e0182722
Selection Signatures in Italian Livestock Guardian and Herding Shepherd Dogs. Description: Bionda, Arianna, et al. Selection Signatures in Italian Livestock Guardian and Herding Shepherd Dogs. ''Vet Sci''. 2022 Dec 21; '''10''' (1):
Demographic and Genome Wide Association Analyses According to Muscle Mass Using Data of the Korean Genome and Epidemiology Study. Description: Gim, Jeong-An, et al. Demographic and Genome Wide Association Analyses According to Muscle Mass Using Data of the Korean Genome and Epidemiology Study. ''J Korean Med Sci''. 2022 Dec 26; '''37''' (50):e346
Chromosome-level genome assembly of goose provides insight into the adaptation and growth of local goose breeds. Description: Zhao, Qiqi, et al. Chromosome-level genome assembly of goose provides insight into the adaptation and growth of local goose breeds. ''Gigascience''. 2022 Dec 28; '''12''':
EraSOR: a software tool to eliminate inflation caused by sample overlap in polygenic score analyses. Description: Choi, Shing Wan, et al. EraSOR: a software tool to eliminate inflation caused by sample overlap in polygenic score analyses. ''Gigascience''. 2022 Dec 28; '''12''':
Genome resequencing reveals independent domestication and breeding improvement of naked oat. Description: Nan, Jinsheng, et al. Genome resequencing reveals independent domestication and breeding improvement of naked oat. ''Gigascience''. 2022 Dec 28; '''12''':
xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments. Description: Farek, Jesse, et al. xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments. ''Gigascience''. 2022 Dec 28; '''12''':
Portability of Polygenic Risk Scores for Sleep Duration, Insomnia and Chronotype in 33,493 Individuals. Description: Perkio, Anna, et al. Portability of Polygenic Risk Scores for Sleep Duration, Insomnia and Chronotype in 33,493 Individuals. ''Clocks Sleep''. 2022 Dec 30; '''5''' (1):10-20
Deep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes. Description: Libiseller-Egger, Julian, et al. Deep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes. ''Sci Rep''. 2022 Dec 31; '''12''' (1):22625
A combined clinical and genetic model for predicting risk of ovarian cancer. Description: Dite, Gillian S, et al. A combined clinical and genetic model for predicting risk of ovarian cancer. ''Eur J Cancer Prev''. 2023 Jan 1; '''32''' (1):57-64
Adolescent anxiety and pain problems: A joint, genome-wide investigation and pathway-based analysis. Description: Mascheretti, Sara, et al. Adolescent anxiety and pain problems: A joint, genome-wide investigation and pathway-based analysis. ''PLoS One''. 2023; '''18''' (5):e0285263
Age and sex differences in the association between APOE genotype and Alzheimer's disease in a Taiwan Chinese population. Description: Huang, Ling-Chun, et al. Age and sex differences in the association between APOE genotype and Alzheimer's disease in a Taiwan Chinese population. ''Front Aging Neurosci''. 2023; '''15''': 1246592
A genome-wide and candidate gene association study of preterm birth in Korean pregnant women. Description: Hur, Young Min, et al. A genome-wide and candidate gene association study of preterm birth in Korean pregnant women. ''PLoS One''. 2023; '''18''' (11):e0294948
A genome-wide association study (GWAS) of the personality constructs in CPAI-2 in Taiwanese Hakka populations. Description: Kao, Pei-Ying, et al. A genome-wide association study (GWAS) of the personality constructs in CPAI-2 in Taiwanese Hakka populations. ''PLoS One''. 2023; '''18''' (2):e0281903
A HST1-like gene controls tiller angle through regulating endogenous auxin in common wheat. Description: Zhao, Lei, et al. A HST1-like gene controls tiller angle through regulating endogenous auxin in common wheat. ''Plant Biotechnol J''. 2023 Jan; '''21''' (1):122-135
A multi-trait GWAS-based genetic association network controlling soybean architecture and seed traits. Description: Niu, Mengrou, et al. A multi-trait GWAS-based genetic association network controlling soybean architecture and seed traits. ''Front Plant Sci''. 2023; '''14''': 1302359
Analysis of ancestry-specific polygenic risk score and diet composition in type 2 diabetes. Description: Hardy, Dale S, et al. Analysis of ancestry-specific polygenic risk score and diet composition in type 2 diabetes. ''PLoS One''. 2023; '''18''' (5):e0285827
Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population. Description: Shen, Yiran, et al. Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population. ''PLoS One''. 2023; '''18''' (1):e0276700
Androgen receptor polyQ alleles and COVID-19 severity in men: A replication study. Description: Lopez-Rodriguez, Rosario, et al. Androgen receptor polyQ alleles and COVID-19 severity in men: A replication study. ''Andrology''. 2023 Jan; '''11''' (1):24-31
A novel integrative multi-omics approach to unravel the genetic determinants of rare diseases with application in sinusoidal obstruction syndrome. Description: Waespe, Nicolas, et al. A novel integrative multi-omics approach to unravel the genetic determinants of rare diseases with application in sinusoidal obstruction syndrome. ''PLoS One''. 2023; '''18''' (4):e0281892
A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort. Description: Bui, Audrey, et al. A partitioned 88-loci psoriasis genetic risk score reveals HLA and non-HLA contributions to clinical phenotypes in a Newfoundland psoriasis cohort. ''Front Genet''. 2023; '''14''': 1141010
Application of an Improved 2-Dimensional High-Throughput Soybean Root Phenotyping Platform to Identify Novel Genetic Variants Regulating Root Architecture Traits. Description: Chandnani, Rahul, et al. Application of an Improved 2-Dimensional High-Throughput Soybean Root Phenotyping Platform to Identify Novel Genetic Variants Regulating Root Architecture Traits. ''Plant Phenomics''. 2023; '''5''': 0097
Assessing genetic diversity and defining signatures of positive selection on the genome of dromedary camels from the southeast of the Arabian Peninsula. Description: Al Abri, Mohammad, et al. Assessing genetic diversity and defining signatures of positive selection on the genome of dromedary camels from the southeast of the Arabian Peninsula. ''Front Vet Sci''. 2023; '''10''': 1296610
Assessing the associations between known genetic variants and substance use in people with HIV in the United States. Description: Haas, Cameron B, et al. Assessing the associations between known genetic variants and substance use in people with HIV in the United States. ''PLoS One''. 2023; '''18''' (10):e0292068
Assessing the prediction of type 2 diabetes risk using polygenic and clinical risk scores in South Asian study populations. Description: Rout, Madhusmita, et al. Assessing the prediction of type 2 diabetes risk using polygenic and clinical risk scores in South Asian study populations. ''Ther Adv Endocrinol Metab''. 2023; '''14''': 20420188231220120
Association between an inflammatory biomarker score and future dementia diagnosis in the population-based UK Biobank cohort of 500,000 people. Description: Mekli, Krisztina, et al. Association between an inflammatory biomarker score and future dementia diagnosis in the population-based UK Biobank cohort of 500,000 people. ''PLoS One''. 2023; '''18''' (7):e0288045
Association of the fibronectin type III domain-containing protein 5 rs1746661 single nucleotide polymorphism with reduced brain glucose metabolism in elderly humans. Description: Lima-Filho, Ricardo A S, et al. Association of the fibronectin type III domain-containing protein 5 rs1746661 single nucleotide polymorphism with reduced brain glucose metabolism in elderly humans. ''Brain Commun''. 2023; '''5''' (4):fcad216
Associations between genetic variants in sphingolipid metabolism pathway genes and hepatitis B virus-related hepatocellular carcinoma survival. Description: Jiang, Binbin, et al. Associations between genetic variants in sphingolipid metabolism pathway genes and hepatitis B virus-related hepatocellular carcinoma survival. ''Front Oncol''. 2023; '''13''': 1252158
Augmenting Granzyme B-Expressing NK Cells by Invariant NKT Ligand-Loaded APCs in Patients with Postoperative Early Stage Non-Small Cell Lung Cancer: Results of a Randomized Phase II Study. Description: Iyoda, Tomonori, et al. Augmenting Granzyme B-Expressing NK Cells by Invariant NKT Ligand-Loaded APCs in Patients with Postoperative Early Stage Non-Small Cell Lung Cancer: Results of a Randomized Phase II Study. ''Immunohorizons''. 2023 Jan 1; '''7''' (1):1-16
Better safe than sorry-Whole-genome sequencing indicates that missense variants are significant in susceptibility to COVID-19. Description: Slomian, Dawid, et al. Better safe than sorry-Whole-genome sequencing indicates that missense variants are significant in susceptibility to COVID-19. ''PLoS One''. 2023; '''18''' (1):e0279356
Causal relationship between levels of myeloperoxidase and obstructive sleep apnea: a bidirectional two-sample Mendelian randomization study. Description: Tang, Weihua, et al. Causal relationship between levels of myeloperoxidase and obstructive sleep apnea: a bidirectional two-sample Mendelian randomization study. ''Front Neurol''. 2023; '''14''': 1305580
Comparing feature selection and machine learning approaches for predicting CYP2D6 methylation from genetic variation. Description: Fong, Wei Jing, et al. Comparing feature selection and machine learning approaches for predicting CYP2D6 methylation from genetic variation. ''Front Neuroinform''. 2023; '''17''': 1244336
COVID-19 and cognitive performance: a Mendelian randomization study. Description: Tang, Ching-Man, et al. COVID-19 and cognitive performance: a Mendelian randomization study. ''Front Public Health''. 2023; '''11''': 1185957
Cytokine gene polymorphism and parasite susceptibility in free-living rodents: Importance of non-coding variants. Description: Kloch, Agnieszka, et al. Cytokine gene polymorphism and parasite susceptibility in free-living rodents: Importance of non-coding variants. ''PLoS One''. 2023; '''18''' (1):e0258009
DNA extraction from clotted blood in genotyping quality. Description: Stanzick, Kira J, et al. DNA extraction from clotted blood in genotyping quality. ''Biotechniques''. 2023 Jan; '''74''' (1):23-29
Effect of structural variation in the promoter region of RsMYB1.1 on the skin color of radish taproot. Description: Kim, Jiin, et al. Effect of structural variation in the promoter region of RsMYB1.1 on the skin color of radish taproot. ''Front Plant Sci''. 2023; '''14''': 1327009
Effects of gene-lifestyle interactions on obesity based on a multi-locus risk score: A cross-sectional analysis. Description: Nakamura, Sho, et al. Effects of gene-lifestyle interactions on obesity based on a multi-locus risk score: A cross-sectional analysis. ''PLoS One''. 2023; '''18''' (2):e0279169
Eurasian back-migration into Northeast Africa was a complex and multifaceted process. Description: Hammaren, Rickard, et al. Eurasian back-migration into Northeast Africa was a complex and multifaceted process. ''PLoS One''. 2023; '''18''' (11):e0290423
Examination of runs of homozygosity in relation to height in an endogamous Namibian population. Description: Swinford, Natalie, et al. Examination of runs of homozygosity in relation to height in an endogamous Namibian population. ''Am J Biol Anthropol''. 2023 Jan; '''180''' (1):207-215
Examining interactions between polygenic scores and interpersonal trauma exposure on alcohol consumption and use disorder in an ancestrally diverse college cohort. Description: Sheerin, Christina M, et al. Examining interactions between polygenic scores and interpersonal trauma exposure on alcohol consumption and use disorder in an ancestrally diverse college cohort. ''Front Genet''. 2023; '''14''': 1274381
Exploring domestication pattern in lotus: insights from dispensable genome assembly. Description: Qi, Huanhuan, et al. Exploring domestication pattern in lotus: insights from dispensable genome assembly. ''Front Plant Sci''. 2023; '''14''': 1294033
FairPRS: adjusting for admixed populations in polygenic risk scores using invariant risk minimization. Description: Machado Reyes, Diego, et al. FairPRS: adjusting for admixed populations in polygenic risk scores using invariant risk minimization. ''Pac Symp Biocomput''. 2023; '''28''': 198-208
First genome-wide data from Italian European beech (Fagus sylvatica L.): Strong and ancient differentiation between Alps and Apennines. Description: Marchesini, Alexis, et al. First genome-wide data from Italian European beech (Fagus sylvatica L.): Strong and ancient differentiation between Alps and Apennines. ''PLoS One''. 2023; '''18''' (7):e0288986
From a different angle: genetic diversity underlies differentiation of waterlogging-induced epinasty in tomato. Description: Geldhof, Batist, et al. From a different angle: genetic diversity underlies differentiation of waterlogging-induced epinasty in tomato. ''Front Plant Sci''. 2023; '''14''': 1178778
From chip to SNP: Rapid development and evaluation of a targeted capture genotyping-by-sequencing approach to support research and management of a plaguing rodent. Description: Oh, Kevin P, et al. From chip to SNP: Rapid development and evaluation of a targeted capture genotyping-by-sequencing approach to support research and management of a plaguing rodent. ''PLoS One''. 2023; '''18''' (8):e0288701
Gene and pathway based burden analyses in familial lymphoid cancer cases: Rare variants in immune pathway genes. Description: Ralli, Sneha, et al. Gene and pathway based burden analyses in familial lymphoid cancer cases: Rare variants in immune pathway genes. ''PLoS One''. 2023; '''18''' (6):e0287602
Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort. Description: Hui, Daniel, et al. Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort. ''PLoS Genet''. 2023 Jan; '''19''' (1):e1010584
Gene-diet interaction analysis using novel weighted food scores discovers the adipocytokine signaling pathway associated with the development of type 2 diabetes. Description: Apio, Catherine, et al. Gene-diet interaction analysis using novel weighted food scores discovers the adipocytokine signaling pathway associated with the development of type 2 diabetes. ''Front Endocrinol (Lausanne)''. 2023; '''14''': 1165744
Gene-environment interaction study on the polygenic risk score for neuroticism, childhood adversity, and parental bonding. Description: Klingenberg, Boris, et al. Gene-environment interaction study on the polygenic risk score for neuroticism, childhood adversity, and parental bonding. ''Personal Neurosci''. 2023; '''6''': e5
Genetically determined alcohol consumption and cancer risk in Korea. Description: Jung, Keum Ji, et al. Genetically determined alcohol consumption and cancer risk in Korea. ''Epidemiol Health''. 2023; '''45''': e2023077
Genetic and biomarker modulation of arterial stiffness change in the SardiNIA population cohort. Description: Asefa, Nigus G, et al. Genetic and biomarker modulation of arterial stiffness change in the SardiNIA population cohort. ''Front Epidemiol''. 2023; '''3''': 1295209
Genetic architecture and polygenic risk score prediction of degenerative suspensory ligament desmitis (DSLD) in the Peruvian Horse. Description: Momen, Mehdi, et al. Genetic architecture and polygenic risk score prediction of degenerative suspensory ligament desmitis (DSLD) in the Peruvian Horse. ''Front Genet''. 2023; '''14''': 1201628
Genetic difference between two Schistosoma japonicum isolates with contrasting cercarial shedding patterns revealed by whole genome sequencing. Description: Sun, Hui-Ying, et al. Genetic difference between two Schistosoma japonicum isolates with contrasting cercarial shedding patterns revealed by whole genome sequencing. ''Parasite''. 2023; '''30''': 59
Genetic diversity and breed-informative SNPs identification in domestic pig populations using coding SNPs. Description: Hayah, Ichrak, et al. Genetic diversity and breed-informative SNPs identification in domestic pig populations using coding SNPs. ''Front Genet''. 2023; '''14''': 1229741
Genetic footprints of assortative mating in the Japanese population. Description: Yamamoto, Kenichi, et al. Genetic footprints of assortative mating in the Japanese population. ''Nat Hum Behav''. 2023 Jan; '''7''' (1):65-73
Genetic interactions of schizophrenia using gene-based statistical epistasis exclusively identify nervous system-related pathways and key hub genes. Description: Genetic interactions of schizophrenia using gene-based statistical epistasis exclusively identify nervous system-related pathways and key hub genes. ''''. 2023; '''14''': 1301150
Genetic landscape of Parkinson's disease and related diseases in Luxembourg. Description: Landoulsi, Zied, et al. Genetic landscape of Parkinson's disease and related diseases in Luxembourg. ''Front Aging Neurosci''. 2023; '''15''': 1282174
Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Description: Kiiskinen, Tuomo, et al. Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. ''Nat Med''. 2023 Jan; '''29''' (1):209-218
Genetic predisposition to lung adenocarcinoma outcome is a feature already present in patients' noninvolved lung tissue. Description: Minnai, Francesca, et al. Genetic predisposition to lung adenocarcinoma outcome is a feature already present in patients' noninvolved lung tissue. ''Cancer Sci''. 2023 Jan; '''114''' (1):281-294
Genetic risk, metabolic syndrome, and gastrointestinal cancer risk: A prospective cohort study. Description: Liu, Yaqian, et al. Genetic risk, metabolic syndrome, and gastrointestinal cancer risk: A prospective cohort study. ''Cancer Med''. 2023 Jan; '''12''' (1):597-605
Genetic variants in RNA m(5) C modification genes associated with survival and chemotherapy efficacy of colorectal cancer. Description: Chen, Silu, et al. Genetic variants in RNA m(5) C modification genes associated with survival and chemotherapy efficacy of colorectal cancer. ''Cancer Med''. 2023 Jan; '''12''' (2):1376-1388
Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage. Description: Gaastra, Ben, et al. Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage. ''Eur J Neurol''. 2023 Jan; '''30''' (1):116-124
Genome and chromosome wide association studies for growth traits in Simmental and Simbrah cattle. Description: Calderon-Chagoya, Rene, et al. Genome and chromosome wide association studies for growth traits in Simmental and Simbrah cattle. ''Anim Biosci''. 2023 Jan; '''36''' (1):19-28
Genome- and Exome-Wide Association Studies Revealed Candidate Genes Associated with DaTscan Imaging Features. Description: Yaghoobi, Arash, et al. Genome- and Exome-Wide Association Studies Revealed Candidate Genes Associated with DaTscan Imaging Features. ''Parkinsons Dis''. 2023; '''2023''': 2893662
Genome architecture and diverged selection shaping pattern of genomic differentiation in wild barley. Description: Zhang, Wenying, et al. Genome architecture and diverged selection shaping pattern of genomic differentiation in wild barley. ''Plant Biotechnol J''. 2023 Jan; '''21''' (1):46-62
Genome-wide analysis highlights genetic admixture in exotic germplasm resources of Eucalyptus and unexpected ancestral genomic composition of interspecific hybrids. Description: de Oliveira, Danyllo Amaral, et al. Genome-wide analysis highlights genetic admixture in exotic germplasm resources of Eucalyptus and unexpected ancestral genomic composition of interspecific hybrids. ''PLoS One''. 2023; '''18''' (8):e0289536
Genome-wide association study of abdominal MRI-measured visceral fat: The multiethnic cohort adiposity phenotype study. Description: Streicher, Samantha A, et al. Genome-wide association study of abdominal MRI-measured visceral fat: The multiethnic cohort adiposity phenotype study. ''PLoS One''. 2023; '''18''' (1):e0279932
Genome-wide association study of early liveweight traits in fat-tailed Akkaraman lambs. Description: Cinar, Mehmet Ulas, et al. Genome-wide association study of early liveweight traits in fat-tailed Akkaraman lambs. ''PLoS One''. 2023; '''18''' (11):e0291805
Genome-wide association study of lipase and esterase in wholegrain wheat flour (Triticum aestivum L.). Description: Wei, Chun Yue, et al. Genome-wide association study of lipase and esterase in wholegrain wheat flour (Triticum aestivum L.). ''PLoS One''. 2023; '''18''' (3):e0282510
Genome-wide association with footrot in hair and wool sheep. Description: Cinar, Mehmet Ulas, et al. Genome-wide association with footrot in hair and wool sheep. ''Front Genet''. 2023; '''14''': 1297444
Genome-wide genetic architecture for plant maturity and drought tolerance in diploid potatoes. Description: Fofana, Bourlaye, et al. Genome-wide genetic architecture for plant maturity and drought tolerance in diploid potatoes. ''Front Genet''. 2023; '''14''': 1306519
Genome-wide single nucleotide polymorphism (SNP) data reveal potential candidate genes for litter traits in a Yorkshire pig population. Description: Zhang, Yu, et al. Genome-wide single nucleotide polymorphism (SNP) data reveal potential candidate genes for litter traits in a Yorkshire pig population. ''Arch Anim Breed''. 2023; '''66''' (4):357-368
Genome-wide study of linkage disequilibrium, population structure, and inbreeding in Iranian indigenous sheep breeds. Description: Barani, S, et al. Genome-wide study of linkage disequilibrium, population structure, and inbreeding in Iranian indigenous sheep breeds. ''PLoS One''. 2023; '''18''' (6):e0286463
Genomic and demographic processes differentially influence genetic variation across the human X chromosome. Description: Cotter, Daniel J, et al. Genomic and demographic processes differentially influence genetic variation across the human X chromosome. ''PLoS One''. 2023; '''18''' (11):e0287609
Genomic diversity and population structure of teosinte (Zea spp.) and its conservation implications. Description: Rivera-Rodriguez, Diana Maria, et al. Genomic diversity and population structure of teosinte (Zea spp.) and its conservation implications. ''PLoS One''. 2023; '''18''' (10):e0291944
Genomic inbreeding measures applied to a population of mice divergently selected for birth weight environmental variance. Description: Ojeda-Marin, Candela, et al. Genomic inbreeding measures applied to a population of mice divergently selected for birth weight environmental variance. ''Front Genet''. 2023; '''14''': 1303748
Genomic investigation of the Chinese alligator reveals wild-extinct genetic diversity and genomic consequences of their continuous decline. Description: Yang, Shangchen, et al. Genomic investigation of the Chinese alligator reveals wild-extinct genetic diversity and genomic consequences of their continuous decline. ''Mol Ecol Resour''. 2023 Jan; '''23''' (1):294-311
Genomic prediction of rice mesocotyl length indicative of directing seeding suitability using a half-sib hybrid population. Description: Chen, Liang, et al. Genomic prediction of rice mesocotyl length indicative of directing seeding suitability using a half-sib hybrid population. ''PLoS One''. 2023; '''18''' (4):e0283989
Genomic prediction using information across years with epistatic models and dimension reduction via haplotype blocks. Description: Vojgani, Elaheh, et al. Genomic prediction using information across years with epistatic models and dimension reduction via haplotype blocks. ''PLoS One''. 2023; '''18''' (3):e0282288
Genomic screening of allelic and genotypic transmission ratio distortion in horse. Description: Laseca, Nora, et al. Genomic screening of allelic and genotypic transmission ratio distortion in horse. ''PLoS One''. 2023; '''18''' (8):e0289066
GSEL: a fast, flexible python package for detecting signatures of diverse evolutionary forces on genomic regions. Description: Abraham, Abin, et al. GSEL: a fast, flexible python package for detecting signatures of diverse evolutionary forces on genomic regions. ''Bioinformatics''. 2023 Jan 1; '''39''' (1):
Hierarchical association of COPD to principal genetic components of biological systems. Description: Carlin, Daniel E, et al. Hierarchical association of COPD to principal genetic components of biological systems. ''PLoS One''. 2023; '''18''' (5):e0286064
High polygenic risk score is a risk factor associated with colorectal cancer based on data from the UK Biobank. Description: Yang, Mei, et al. High polygenic risk score is a risk factor associated with colorectal cancer based on data from the UK Biobank. ''PLoS One''. 2023; '''18''' (11):e0295155
Homocysteine levels, genetic background, and cognitive impairment in Parkinson's disease. Description: Perinan, Maria Teresa, et al. Homocysteine levels, genetic background, and cognitive impairment in Parkinson's disease. ''J Neurol''. 2023 Jan; '''270''' (1):477-485
Human leukocyte antigen alleles associate with COVID-19 vaccine immunogenicity and risk of breakthrough infection. Description: Mentzer, Alexander J, et al. Human leukocyte antigen alleles associate with COVID-19 vaccine immunogenicity and risk of breakthrough infection. ''Nat Med''. 2023 Jan; '''29''' (1):147-157
Identification of copy number variations in the genome of Dairy Gir cattle. Description: Braga, Larissa G, et al. Identification of copy number variations in the genome of Dairy Gir cattle. ''PLoS One''. 2023; '''18''' (4):e0284085
Identification of loci associated with water use efficiency and symbiotic nitrogen fixation in soybean. Description: Arifuzzaman, Muhammad, et al. Identification of loci associated with water use efficiency and symbiotic nitrogen fixation in soybean. ''Front Plant Sci''. 2023; '''14''': 1271849
Identification of novel genetic variants, including PIM1 and LINC01491, with ICD-10 based diagnosis of pulmonary arterial hypertension in the UK Biobank cohort. Description: Pu, Alex, et al. Identification of novel genetic variants, including PIM1 and LINC01491, with ICD-10 based diagnosis of pulmonary arterial hypertension in the UK Biobank cohort. ''Front Drug Discov (Lausanne)''. 2023; '''3''':
Identification of potentially pathogenic variants for autism spectrum disorders using gene-burden analysis. Description: Rihar, Nika, et al. Identification of potentially pathogenic variants for autism spectrum disorders using gene-burden analysis. ''PLoS One''. 2023; '''18''' (5):e0273957
Identification of the shared genetic architecture underlying seven autoimmune diseases with GWAS summary statistics. Description: Wang, Yuping, et al. Identification of the shared genetic architecture underlying seven autoimmune diseases with GWAS summary statistics. ''Front Immunol''. 2023; '''14''': 1303675
Identifying genetically redundant accessions in the world's largest cassava collection. Description: Carvajal-Yepes, Monica, et al. Identifying genetically redundant accessions in the world's largest cassava collection. ''Front Plant Sci''. 2023; '''14''': 1338377
Identity-by-descent analysis of CMTX3 links three families through a common founder. Description: Henden, Lyndal, et al. Identity-by-descent analysis of CMTX3 links three families through a common founder. ''J Hum Genet''. 2023 Jan; '''68''' (1):47-49
Integrative polygenic analysis of the protective effects of fatty acid metabolism on disease as modified by obesity. Description: Astore, Courtney, et al. Integrative polygenic analysis of the protective effects of fatty acid metabolism on disease as modified by obesity. ''Front Nutr''. 2023; '''10''': 1308622
Intravesical BCG in patients with non-muscle invasive bladder cancer induces trained immunity and decreases respiratory infections. Description: van Puffelen, Jelmer H, et al. Intravesical BCG in patients with non-muscle invasive bladder cancer induces trained immunity and decreases respiratory infections. ''J Immunother Cancer''. 2023 Jan; '''11''' (1):
Investigating the genetic basis of maize ear characteristics: a comprehensive genome-wide study utilizing high-throughput phenotypic measurement method and system. Description: Wang, Jinglu, et al. Investigating the genetic basis of maize ear characteristics: a comprehensive genome-wide study utilizing high-throughput phenotypic measurement method and system. ''Front Plant Sci''. 2023; '''14''': 1248446
Is there hybridization between diploid and tetraploid Euphrasia in a secondary contact zone? Description: Brown, Max R, et al. Is there hybridization between diploid and tetraploid Euphrasia in a secondary contact zone? ''Am J Bot''. 2023 Jan; '''110''' (1):e16100
Kazakh national dog breed Tazy: What do we know? Description: Perfilyeva, Anastassiya, et al. Kazakh national dog breed Tazy: What do we know? ''PLoS One''. 2023; '''18''' (3):e0282041
Large registry-based analysis of genetic predisposition to tuberculosis identifies genetic risk factors at HLA. Description: Tervi, Anniina, et al. Large registry-based analysis of genetic predisposition to tuberculosis identifies genetic risk factors at HLA. ''Hum Mol Genet''. 2023 Jan 1; '''32''' (1):161-171
Leveraging Multi-Ancestry Polygenic Risk Scores for Body Mass Index to Predict Antiretroviral Therapy-Induced Weight Gain. Description: Keat, Karl, et al. Leveraging Multi-Ancestry Polygenic Risk Scores for Body Mass Index to Predict Antiretroviral Therapy-Induced Weight Gain. ''Pac Symp Biocomput''. 2023; '''28''': 233-244
Mapping yield and yield-related traits using diverse common bean germplasm. Description: Reinprecht, Yarmilla, et al. Mapping yield and yield-related traits using diverse common bean germplasm. ''Front Genet''. 2023; '''14''': 1246904
Membranous nephropathy in the UK Biobank. Description: Hamilton, Patrick, et al. Membranous nephropathy in the UK Biobank. ''PLoS One''. 2023; '''18''' (4):e0281795
Mendelian randomization to evaluate the causal relationship between liver enzymes and the risk of six specific bone and joint-related diseases. Description: Huang, Guiwu, et al. Mendelian randomization to evaluate the causal relationship between liver enzymes and the risk of six specific bone and joint-related diseases. ''Front Immunol''. 2023; '''14''': 1195553
Molecular genetic characterization and meat-use functional gene identification in Jianshui yellow-brown ducks through combined resequencing and transcriptome analysis. Description: Li, Xinpeng, et al. Molecular genetic characterization and meat-use functional gene identification in Jianshui yellow-brown ducks through combined resequencing and transcriptome analysis. ''Front Vet Sci''. 2023; '''10''': 1269904
Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings. Description: Dapas, Matthew, et al. Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings. ''PLoS Genet''. 2023 Jan; '''19''' (1):e1010594
Multi-omic modeling of antidepressant response implicates dynamic immune and inflammatory changes in individuals who respond to treatment. Description: Fuh, Shih-Chieh, et al. Multi-omic modeling of antidepressant response implicates dynamic immune and inflammatory changes in individuals who respond to treatment. ''PLoS One''. 2023; '''18''' (5):e0285123
Multi-tissue transcriptome analysis to identify candidate genes associated with weight regulation in Hanwoo cattle. Description: Jang, Subin, et al. Multi-tissue transcriptome analysis to identify candidate genes associated with weight regulation in Hanwoo cattle. ''Front Genet''. 2023; '''14''': 1304638
No association between genetically predicted C-reactive protein levels and colorectal cancer survival in Korean: two-sample Mendelian randomization analysis. Description: Choi, Chang Kyun, et al. No association between genetically predicted C-reactive protein levels and colorectal cancer survival in Korean: two-sample Mendelian randomization analysis. ''Epidemiol Health''. 2023; '''45''': e2023039
Novel HLA allele associations with susceptibility, staging, symptomatic state, autoimmune hepatitis and hepatocellular carcinoma events for primary biliary cholangitis in the Japanese population. Description: Khor, Seik-Soon, et al. Novel HLA allele associations with susceptibility, staging, symptomatic state, autoimmune hepatitis and hepatocellular carcinoma events for primary biliary cholangitis in the Japanese population. ''Front Immunol''. 2023; '''14''': 1151502
Observational and genetic analyses clarify the relationship between type 2 diabetes mellitus and gallstone disease. Description: Yan, Peijing, et al. Observational and genetic analyses clarify the relationship between type 2 diabetes mellitus and gallstone disease. ''Front Endocrinol (Lausanne)''. 2023; '''14''': 1337071
Parent-reported child appetite moderates relationships between child genetic obesity risk and parental feeding practices. Description: Jansen, Elena, et al. Parent-reported child appetite moderates relationships between child genetic obesity risk and parental feeding practices. ''Front Nutr''. 2023; '''10''': 1174441
Pedigree-based QTL analysis of flower size traits in two multi-parental diploid rose populations. Description: Rawandoozi, Zena, et al. Pedigree-based QTL analysis of flower size traits in two multi-parental diploid rose populations. ''Front Plant Sci''. 2023; '''14''': 1226713
Pharmacogenomics of intravenous immunoglobulin response in Kawasaki disease. Description: Shrestha, Sadeep, et al. Pharmacogenomics of intravenous immunoglobulin response in Kawasaki disease. ''Front Immunol''. 2023; '''14''': 1287094
Phenotypic evolution in durum wheat (Triticum durum Desf.) based on SNPs, morphological traits, UPOV descriptors and kernel-related traits. Description: Marzario, Stefania, et al. Phenotypic evolution in durum wheat (Triticum durum Desf.) based on SNPs, morphological traits, UPOV descriptors and kernel-related traits. ''Front Plant Sci''. 2023; '''14''': 1206560
Polygenic resilience score may be sensitive to preclinical Alzheimer's disease changes. Description: Eissman, Jaclyn M, et al. Polygenic resilience score may be sensitive to preclinical Alzheimer's disease changes. ''Pac Symp Biocomput''. 2023; '''28''': 449-460
Population structure of wild soybean (Glycine soja) based on SLAF-seq have implications for its conservation. Description: Meng, Jing, et al. Population structure of wild soybean (Glycine soja) based on SLAF-seq have implications for its conservation. ''PeerJ''. 2023; '''11''': e16415
Position of Hungarian Merino among other Merinos, within-breed genetic similarity network and markers associated with daily weight gain. Description: Zsolnai, Attila, et al. Position of Hungarian Merino among other Merinos, within-breed genetic similarity network and markers associated with daily weight gain. ''Anim Biosci''. 2023 Jan; '''36''' (1):10-18
Potential disease biomarkers for diabetic retinopathy identified through Mendelian randomization analysis. Description: Zou, Xuyan, et al. Potential disease biomarkers for diabetic retinopathy identified through Mendelian randomization analysis. ''Front Endocrinol (Lausanne)''. 2023; '''14''': 1339374
Predicting type 2 diabetes risk before and after solid organ transplantation using polygenic scores in a Danish cohort. Description: Dos Santos, Quenia, et al. Predicting type 2 diabetes risk before and after solid organ transplantation using polygenic scores in a Danish cohort. ''Front Mol Biosci''. 2023; '''10''': 1282412
PTPN13 rs989902 and CHEK2 rs738722 are associated with esophageal cancer. Description: Tu, Ruisha, et al. PTPN13 rs989902 and CHEK2 rs738722 are associated with esophageal cancer. ''Ann Med''. 2023; '''55''' (2):2281659
Rare CIDEC coding variants enriched in age-related macular degeneration patients with small low-luminance deficit cause lipid droplet and fat storage defects. Description: Kim, Sehyun, et al. Rare CIDEC coding variants enriched in age-related macular degeneration patients with small low-luminance deficit cause lipid droplet and fat storage defects. ''PLoS One''. 2023; '''18''' (4):e0280484
Reassessing the genetic variability of Tectona grandis through high-throughput genotyping: Insights on its narrow genetic base. Description: Dos Anjos, Isabela Vera, et al. Reassessing the genetic variability of Tectona grandis through high-throughput genotyping: Insights on its narrow genetic base. ''PLoS One''. 2023; '''18''' (10):e0285518
Reduced representation approaches produce similar results to whole genome sequencing for some common phylogeographic analyses. Description: Duckett, Drew J, et al. Reduced representation approaches produce similar results to whole genome sequencing for some common phylogeographic analyses. ''PLoS One''. 2023; '''18''' (11):e0291941
Rewiring of the seed metabolome during Tartary buckwheat domestication. Description: Zhao, Hui, et al. Rewiring of the seed metabolome during Tartary buckwheat domestication. ''Plant Biotechnol J''. 2023 Jan; '''21''' (1):150-164
Sequencing-based fine-mapping and in silico functional characterization of the 10q24.32 arsenic metabolism efficiency locus across multiple arsenic-exposed populations. Description: Chernoff, Meytal Batya, et al. Sequencing-based fine-mapping and in silico functional characterization of the 10q24.32 arsenic metabolism efficiency locus across multiple arsenic-exposed populations. ''PLoS Genet''. 2023 Jan; '''19''' (1):e1010588
Single-nucleotide polymorphisms link gout with health-related lifestyle factors in Korean cohorts. Description: Jeon, Hye Kyung, et al. Single-nucleotide polymorphisms link gout with health-related lifestyle factors in Korean cohorts. ''PLoS One''. 2023; '''18''' (12):e0295038
Single nucleotide variants in the IL33 and IL1RL1 (ST2) genes are associated with periodontitis and with Aggregatibacter actinomycetemcomitans in the dental plaque biofilm: A putative role in understanding the host immune response in periodontitis. Description: Trindade, Soraya C, et al. Single nucleotide variants in the IL33 and IL1RL1 (ST2) genes are associated with periodontitis and with Aggregatibacter actinomycetemcomitans in the dental plaque biofilm: A putative role in understanding the host immune response in periodontitis. ''PLoS One''. 2023; '''18''' (3):e0283179
The associations of APP, PSEN1, and PSEN2 genes with Alzheimer's disease: A large case-control study in Chinese population. Description: Xiao, Xuewen, et al. The associations of APP, PSEN1, and PSEN2 genes with Alzheimer's disease: A large case-control study in Chinese population. ''CNS Neurosci Ther''. 2023 Jan; '''29''' (1):122-128
The Dissection of Nitrogen Response Traits Using Drone Phenotyping and Dynamic Phenotypic Analysis to Explore N Responsiveness and Associated Genetic Loci in Wheat. Description: Ding, Guohui, et al. The Dissection of Nitrogen Response Traits Using Drone Phenotyping and Dynamic Phenotypic Analysis to Explore N Responsiveness and Associated Genetic Loci in Wheat. ''Plant Phenomics''. 2023; '''5''': 0128
The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes. Description: Dallali, Hamza, et al. The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes. ''Front Endocrinol (Lausanne)''. 2023; '''14''': 1293124
*The HLA-B57:01 allele corresponds to a very large MHC haploblock likely explaining its massive effect for HIV-1 elite control.** Description: Rahmouni, Myriam, et al. The HLA-B*57:01 allele corresponds to a very large MHC haploblock likely explaining its massive effect for HIV-1 elite control. ''Front Immunol''. 2023; '''14''': 1305856
The impact of COVID-19 on pulmonary, neurological, and cardiac outcomes: evidence from a Mendelian randomization study. Description: Shenoy, Pooja U, et al. The impact of COVID-19 on pulmonary, neurological, and cardiac outcomes: evidence from a Mendelian randomization study. ''Front Public Health''. 2023; '''11''': 1303183
The Interindividual Variability of Phytofluene Bioavailability is Associated with a Combination of Single Nucleotide Polymorphisms. Description: Zumaraga, Mark Pretzel, et al. The Interindividual Variability of Phytofluene Bioavailability is Associated with a Combination of Single Nucleotide Polymorphisms. ''Mol Nutr Food Res''. 2023 Jan; '''67''' (2):e2200580
The investigation of WNT6 and WNT10A single nucleotide polymorphisms as potential biomarkers for dental pulp calcification in orthodontic patients. Description: Ramirez, Iago, et al. The investigation of WNT6 and WNT10A single nucleotide polymorphisms as potential biomarkers for dental pulp calcification in orthodontic patients. ''PLoS One''. 2023; '''18''' (8):e0288782
The LHX2-OTX2 transcriptional regulatory module controls retinal pigmented epithelium differentiation and underlies genetic risk for age-related macular degeneration. Description: Cohen-Gulkar, Mazal, et al. The LHX2-OTX2 transcriptional regulatory module controls retinal pigmented epithelium differentiation and underlies genetic risk for age-related macular degeneration. ''PLoS Biol''. 2023 Jan; '''21''' (1):e3001924
The performance of genome sequencing as a first-tier test for neurodevelopmental disorders. Description: van der Sanden, Bart P G H, et al. The performance of genome sequencing as a first-tier test for neurodevelopmental disorders. ''Eur J Hum Genet''. 2023 Jan; '''31''' (1):81-88
*The rare DRB104:08-DQ8 haplotype is the main HLA class II genetic driver and discriminative factor of Early-onset Type 1 diabetes in the Portuguese population.** Description: Caramalho, Iris, et al. The rare DRB1*04:08-DQ8 haplotype is the main HLA class II genetic driver and discriminative factor of Early-onset Type 1 diabetes in the Portuguese population. ''Front Immunol''. 2023; '''14''': 1299609
The Role of Global and Local Ancestry on Clopidogrel Response in African Americans. Description: Yang, Guang, et al. The Role of Global and Local Ancestry on Clopidogrel Response in African Americans. ''Pac Symp Biocomput''. 2023; '''28''': 221-232
Time-ordering japonica/geng genomes analysis indicates the importance of large structural variants in rice breeding. Description: Wang, Yu, et al. Time-ordering japonica/geng genomes analysis indicates the importance of large structural variants in rice breeding. ''Plant Biotechnol J''. 2023 Jan; '''21''' (1):202-218
Two distinct Fusarium graminearum populations colonized European wheat in the past two decades. Description: Kulik, Tomasz, et al. Two distinct Fusarium graminearum populations colonized European wheat in the past two decades. ''PLoS One''. 2023; '''18''' (12):e0296302
Type 2 diabetes mellitus and the risk of male infertility: a Mendelian randomization study. Description: Zhu, Xiao-Bin, et al. Type 2 diabetes mellitus and the risk of male infertility: a Mendelian randomization study. ''Front Endocrinol (Lausanne)''. 2023; '''14''': 1279058
Uncovering a causal connection between the Lachnoclostridium genus in fecal microbiota and non-alcoholic fatty liver disease: a two-sample Mendelian randomization analysis. Description: Dai, Wanhui, et al. Uncovering a causal connection between the Lachnoclostridium genus in fecal microbiota and non-alcoholic fatty liver disease: a two-sample Mendelian randomization analysis. ''Front Microbiol''. 2023; '''14''': 1276790
Uncovering the candidate genes related to sheep body weight using multi-trait genome-wide association analysis. Description: Li, Yunna, et al. Uncovering the candidate genes related to sheep body weight using multi-trait genome-wide association analysis. ''Front Vet Sci''. 2023; '''10''': 1206383
Unraveling the role of non-coding rare variants in epilepsy. Description: Girard, Alexandre, et al. Unraveling the role of non-coding rare variants in epilepsy. ''PLoS One''. 2023; '''18''' (9):e0291935
Whole exome sequencing reveals genetic landscape associated with left ventricular outflow tract obstruction in Chinese Han population. Description: Geng, Zilong, et al. Whole exome sequencing reveals genetic landscape associated with left ventricular outflow tract obstruction in Chinese Han population. ''Front Genet''. 2023; '''14''': 1267368
Whole genome sequencing reveals population diversity and variation in HIV-1 specific host genes. Description: Thami, Prisca K, et al. Whole genome sequencing reveals population diversity and variation in HIV-1 specific host genes. ''Front Genet''. 2023; '''14''': 1290624
Maize cytolines as models to study the impact of different cytoplasms on gene expression under heat stress conditions. Description: Ardelean, Ioana V, et al. Maize cytolines as models to study the impact of different cytoplasms on gene expression under heat stress conditions. ''BMC Plant Biol''. 2023 Jan 2; '''23''' (1):4
Convergent changes in melanocortin receptor 1 gene are associated with black-headed coat color in sheep. Description: Zhou, Qian, et al. Convergent changes in melanocortin receptor 1 gene are associated with black-headed coat color in sheep. ''J Anim Sci''. 2023 Jan 3; '''101''':
Design and characterization of a high-resolution multiple-SNP capture array by target sequencing for sheep. Description: Guo, Yingwei, et al. Design and characterization of a high-resolution multiple-SNP capture array by target sequencing for sheep. ''J Anim Sci''. 2023 Jan 3; '''101''':
Epidemiologic and Genetic Associations of Endometriosis With Depression, Anxiety, and Eating Disorders. Description: Koller, Dora, et al. Epidemiologic and Genetic Associations of Endometriosis With Depression, Anxiety, and Eating Disorders. ''JAMA Netw Open''. 2023 Jan 3; '''6''' (1):e2251214
Genome-wide sequencing identifies a thermal-tolerance related synonymous mutation in the mussel, Mytilisepta virgata. Description: Tan, Yue, et al. Genome-wide sequencing identifies a thermal-tolerance related synonymous mutation in the mussel, Mytilisepta virgata. ''Commun Biol''. 2023 Jan 3; '''6''' (1):5
Natural selection of immune and metabolic genes associated with health in two lowland Bolivian populations. Description: Lea, Amanda J, et al. Natural selection of immune and metabolic genes associated with health in two lowland Bolivian populations. ''Proc Natl Acad Sci U S A''. 2023 Jan 3; '''120''' (1):e2207544120
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error. Description: Musolf, Anthony M, et al. Rare variant analyses across multiethnic cohorts identify novel genes for refractive error. ''Commun Biol''. 2023 Jan 3; '''6''' (1):6
The genetic architecture of the human skeletal form. Description: Kun, Eucharist, et al. The genetic architecture of the human skeletal form. ''bioRxiv''. 2023 Jan 3;
The role of inbreeding depression on productive performance in the Italian Holstein breed. Description: Ablondi, Michela, et al. The role of inbreeding depression on productive performance in the Italian Holstein breed. ''J Anim Sci''. 2023 Jan 3; '''101''':
Associations of PART1 and DEFB1 polymorphisms with Dental Caries in twelve-year-old children in Southern China: a cross-sectional study. Description: Ma, Fei, et al. Associations of PART1 and DEFB1 polymorphisms with Dental Caries in twelve-year-old children in Southern China: a cross-sectional study. ''BMC Pediatr''. 2023 Jan 4; '''23''' (1):6
Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation. Description: Hanlon, Meredith T, et al. Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation. ''BMC Plant Biol''. 2023 Jan 4; '''23''' (1):6
Genomic Consequences of and Demographic Response to Pervasive Hybridization Over Time in Climate-Sensitive Pikas. Description: Ge, Deyan, et al. Genomic Consequences of and Demographic Response to Pervasive Hybridization Over Time in Climate-Sensitive Pikas. ''Mol Biol Evol''. 2023 Jan 4; '''40''' (1):
Independent Evolution of Sex Chromosomes and Male Pregnancy-Related Genes in Two Seahorse Species. Description: Long, Xin, et al. Independent Evolution of Sex Chromosomes and Male Pregnancy-Related Genes in Two Seahorse Species. ''Mol Biol Evol''. 2023 Jan 4; '''40''' (1):
Insights into the Genomic and Phenotypic Landscape of the Oleaginous Yeast Yarrowia lipolytica. Description: Bigey, Frederic, et al. Insights into the Genomic and Phenotypic Landscape of the Oleaginous Yeast Yarrowia lipolytica. ''J Fungi (Basel)''. 2023 Jan 4; '''9''' (1):
Integrating Common Risk Factors with Polygenic Scores Improves the Prediction of Type 2 Diabetes. Description: Timasheva, Yanina, et al. Integrating Common Risk Factors with Polygenic Scores Improves the Prediction of Type 2 Diabetes. ''Int J Mol Sci''. 2023 Jan 4; '''24''' (2):
Large-Scale Chromosomal Changes Lead to Genome-Level Expression Alterations, Environmental Adaptation, and Speciation in the Gayal (Bos frontalis). Description: Li, Yan, et al. Large-Scale Chromosomal Changes Lead to Genome-Level Expression Alterations, Environmental Adaptation, and Speciation in the Gayal (Bos frontalis). ''Mol Biol Evol''. 2023 Jan 4; '''40''' (1):
Rs11726196 Single-Nucleotide Polymorphism of the Transient Receptor Potential Canonical 3 (TRPC3) Gene Is Associated with Chronic Pain. Description: Aoki, Yoshinori, et al. Rs11726196 Single-Nucleotide Polymorphism of the Transient Receptor Potential Canonical 3 (TRPC3) Gene Is Associated with Chronic Pain. ''Int J Mol Sci''. 2023 Jan 5; '''24''' (2):
Animal-SNPAtlas: a comprehensive SNP database for multiple animals. Description: Gao, Yingjie, et al. Animal-SNPAtlas: a comprehensive SNP database for multiple animals. ''Nucleic Acids Res''. 2023 Jan 6; '''51''' (D1):D816-D826
Association of Polygenic Variants Involved in Immunity and Inflammation with Duodenal Ulcer Risk and Their Interaction with Irregular Eating Habits. Description: Park, Sunmin, et al. Association of Polygenic Variants Involved in Immunity and Inflammation with Duodenal Ulcer Risk and Their Interaction with Irregular Eating Habits. ''Nutrients''. 2023 Jan 6; '''15''' (2):
Combining Clinical and Genetic Data to Predict Response to Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients: A Precision Medicine Approach. Description: Ferre, Laura, et al. Combining Clinical and Genetic Data to Predict Response to Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients: A Precision Medicine Approach. ''J Pers Med''. 2023 Jan 6; '''13''' (1):
CottonMD: a multi-omics database for cotton biological study. Description: Yang, Zhiquan, et al. CottonMD: a multi-omics database for cotton biological study. ''Nucleic Acids Res''. 2023 Jan 6; '''51''' (D1):D1446-D1456
Evaluating and implementing block jackknife resampling Mendelian randomization to mitigate bias induced by overlapping samples. Description: Fang, Si, et al. Evaluating and implementing block jackknife resampling Mendelian randomization to mitigate bias induced by overlapping samples. ''Hum Mol Genet''. 2023 Jan 6; '''32''' (2):192-203
GWAS Atlas: an updated knowledgebase integrating more curated associations in plants and animals. Description: Liu, Xiaonan, et al. GWAS Atlas: an updated knowledgebase integrating more curated associations in plants and animals. ''Nucleic Acids Res''. 2023 Jan 6; '''51''' (D1):D969-D976
Host Genetic Variants Linked to COVID-19 Neurological Complications and Susceptibility in Young Adults-A Preliminary Analysis. Description: Kazantseva, Anastasiya, et al. Host Genetic Variants Linked to COVID-19 Neurological Complications and Susceptibility in Young Adults-A Preliminary Analysis. ''J Pers Med''. 2023 Jan 6; '''13''' (1):
RMDisease V2.0: an updated database of genetic variants that affect RNA modifications with disease and trait implication. Description: Song, Bowen, et al. RMDisease V2.0: an updated database of genetic variants that affect RNA modifications with disease and trait implication. ''Nucleic Acids Res''. 2023 Jan 6; '''51''' (D1):D1388-D1396
A two-stage genome-wide association study identifies novel germline genetic variations in CACNA2D3 associated with radiotherapy response in nasopharyngeal carcinoma. Description: Yu, Lu-Lu, et al. A two-stage genome-wide association study identifies novel germline genetic variations in CACNA2D3 associated with radiotherapy response in nasopharyngeal carcinoma. ''J Transl Med''. 2023 Jan 9; '''21''' (1):11
Characterization of Danube Swabian population samples on a high-resolution genome-wide basis. Description: Banfai, Zsolt, et al. Characterization of Danube Swabian population samples on a high-resolution genome-wide basis. ''BMC Genomics''. 2023 Jan 9; '''24''' (1):9
Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity. Description: Rajagopal, Veera M, et al. Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity. ''Sci Rep''. 2023 Jan 9; '''13''' (1):429
Spatial and temporal heterogeneity in human mobility patterns in Holocene Southwest Asia and the East Mediterranean. Description: Koptekin, Dilek, et al. Spatial and temporal heterogeneity in human mobility patterns in Holocene Southwest Asia and the East Mediterranean. ''Curr Biol''. 2023 Jan 9; '''33''' (1):41-57.e15
Identification of genetic variants associated with diabetic kidney disease in multiple Korean cohorts via a genome-wide association study mega-analysis. Description: Jin, Heejin, et al. Identification of genetic variants associated with diabetic kidney disease in multiple Korean cohorts via a genome-wide association study mega-analysis. ''BMC Med''. 2023 Jan 11; '''21''' (1):16
MicroRNA-eQTLs in the developing human neocortex link miR-4707-3p expression to brain size. Description: Lafferty, Michael J, et al. MicroRNA-eQTLs in the developing human neocortex link miR-4707-3p expression to brain size. ''Elife''. 2023 Jan 11; '''12''':
Molecular Landscape of Tourette's Disorder. Description: Widomska, Joanna, et al. Molecular Landscape of Tourette's Disorder. ''Int J Mol Sci''. 2023 Jan 11; '''24''' (2):
Population Genomic Analyses Suggest a Hybrid Origin, Cryptic Sexuality, and Decay of Genes Regulating Seed Development for the Putatively Strictly Asexual Kingdonia uniflora (Circaeasteraceae, Ranunculales). Description: Sun, Yanxia, et al. Population Genomic Analyses Suggest a Hybrid Origin, Cryptic Sexuality, and Decay of Genes Regulating Seed Development for the Putatively Strictly Asexual Kingdonia uniflora (Circaeasteraceae, Ranunculales). ''Int J Mol Sci''. 2023 Jan 11; '''24''' (2):
Role of SNPs located in the exon 9 of ATAPA1 gene on goose egg production. Description: Ouyang, Qingyuan, et al. Role of SNPs located in the exon 9 of ATAPA1 gene on goose egg production. ''Poult Sci''. 2023 Jan 11; '''102''' (4):102488
Complex multiple introductions drive fall armyworm invasions into Asia and Australia. Description: Rane, Rahul, et al. Complex multiple introductions drive fall armyworm invasions into Asia and Australia. ''Sci Rep''. 2023 Jan 12; '''13''' (1):660
GWAS Explorer: an open-source tool to explore, visualize, and access GWAS summary statistics in the PLCO Atlas. Description: Machiela, Mitchell J, et al. GWAS Explorer: an open-source tool to explore, visualize, and access GWAS summary statistics in the PLCO Atlas. ''Sci Data''. 2023 Jan 12; '''10''' (1):25
The association of genetic variation in CACNA1C with resting-state functional connectivity in youth bipolar disorder. Description: Jiang, Xinyue, et al. The association of genetic variation in CACNA1C with resting-state functional connectivity in youth bipolar disorder. ''Int J Bipolar Disord''. 2023 Jan 13; '''11''' (1):3
A pleiotropic variant in DNAJB4 is associated with multiple myeloma risk. Description: Dicanio, Marco, et al. A pleiotropic variant in DNAJB4 is associated with multiple myeloma risk. ''Int J Cancer''. 2023 Jan 15; '''152''' (2):239-248
Effects of Interaction between SLC35F3 and Carbohydrate Intake on the Incidence of Metabolic Syndrome in Korean Middle-Aged Adults. Description: Park, Haeun, et al. Effects of Interaction between SLC35F3 and Carbohydrate Intake on the Incidence of Metabolic Syndrome in Korean Middle-Aged Adults. ''Nutrients''. 2023 Jan 16; '''15''' (2):
Whole-genome resequencing reveals genetic differences and the genetic basis of parapodium number in Russian and Chinese Apostichopus japonicus. Description: Guo, Chao, et al. Whole-genome resequencing reveals genetic differences and the genetic basis of parapodium number in Russian and Chinese Apostichopus japonicus. ''BMC Genomics''. 2023 Jan 16; '''24''' (1):25
Community-engaged ancient DNA project reveals diverse origins of 18th-century African descendants in Charleston, South Carolina. Description: Fleskes, Raquel E, et al. Community-engaged ancient DNA project reveals diverse origins of 18th-century African descendants in Charleston, South Carolina. ''Proc Natl Acad Sci U S A''. 2023 Jan 17; '''120''' (3):e2201620120
Genome-wide parallelism underlies contemporary adaptation in urban lizards. Description: Winchell, Kristin M, et al. Genome-wide parallelism underlies contemporary adaptation in urban lizards. ''Proc Natl Acad Sci U S A''. 2023 Jan 17; '''120''' (3):e2216789120
SNPs Sets in Codifying Genes for Xenobiotics-Processing Enzymes Are Associated with COPD Secondary to Biomass-Burning Smoke. Description: Ambrocio-Ortiz, Enrique, et al. SNPs Sets in Codifying Genes for Xenobiotics-Processing Enzymes Are Associated with COPD Secondary to Biomass-Burning Smoke. ''Curr Issues Mol Biol''. 2023 Jan 17; '''45''' (2):799-819
Chicken chromatin accessibility atlas accelerates epigenetic annotation of birds and gene fine-mapping associated with growth traits. Description: Zhu, Xiao-Ning, et al. Chicken chromatin accessibility atlas accelerates epigenetic annotation of birds and gene fine-mapping associated with growth traits. ''Zool Res''. 2023 Jan 18; '''44''' (1):53-62
Genomic analysis of indigenous goats in Southwest Asia reveals evidence of ancient adaptive introgression related to desert climate. Description: Asadollahpour Nanaei, Hojjat, et al. Genomic analysis of indigenous goats in Southwest Asia reveals evidence of ancient adaptive introgression related to desert climate. ''Zool Res''. 2023 Jan 18; '''44''' (1):20-29
Whole-genome resequencing reveals recent signatures of selection in five populations of largemouth bass ( Micropterus salmoides). Description: Sun, Cheng-Fei, et al. Whole-genome resequencing reveals recent signatures of selection in five populations of largemouth bass ( Micropterus salmoides). ''Zool Res''. 2023 Jan 18; '''44''' (1):78-89
A comprehensive investigation into the genetic relationship between music engagement and mental health. Description: Wesseldijk, Laura W, et al. A comprehensive investigation into the genetic relationship between music engagement and mental health. ''Transl Psychiatry''. 2023 Jan 19; '''13''' (1):15
Highly differentiated loci resolve phylogenetic relationships in the Bean Goose complex. Description: Ottenburghs, Jente, et al. Highly differentiated loci resolve phylogenetic relationships in the Bean Goose complex. ''BMC Ecol Evol''. 2023 Jan 19; '''23''' (1):2
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Description: Gupta, Rahul, et al. Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. ''medRxiv''. 2023 Jan 19;
Selection signatures for local and regional adaptation in Chinese Mongolian horse breeds reveal candidate genes for hoof health. Description: Han, Haige, et al. Selection signatures for local and regional adaptation in Chinese Mongolian horse breeds reveal candidate genes for hoof health. ''BMC Genomics''. 2023 Jan 19; '''24''' (1):35
Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Description: Megat, Salim, et al. Integrative genetic analysis illuminates ALS heritability and identifies risk genes. ''Nat Commun''. 2023 Jan 20; '''14''' (1):342
Excitatory/inhibitory imbalance in autism: the role of glutamate and GABA gene-sets in symptoms and cortical brain structure. Description: Hollestein, Viola, et al. Excitatory/inhibitory imbalance in autism: the role of glutamate and GABA gene-sets in symptoms and cortical brain structure. ''Transl Psychiatry''. 2023 Jan 21; '''13''' (1):18
Assessing HLA imputation accuracy in a West African population. Description: Nanjala, Ruth, et al. Assessing HLA imputation accuracy in a West African population. ''bioRxiv''. 2023 Jan 23;
MiXcan: a framework for cell-type-aware transcriptome-wide association studies with an application to breast cancer. Description: Song, Xiaoyu, et al. MiXcan: a framework for cell-type-aware transcriptome-wide association studies with an application to breast cancer. ''Nat Commun''. 2023 Jan 23; '''14''' (1):377
Polygenic risk for mental disorders as predictors of posttraumatic stress disorder after mild traumatic brain injury. Description: Stein, Murray B, et al. Polygenic risk for mental disorders as predictors of posttraumatic stress disorder after mild traumatic brain injury. ''Transl Psychiatry''. 2023 Jan 25; '''13''' (1):24
Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks. Description: Appadurai, Vivek, et al. Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks. ''Commun Biol''. 2023 Jan 26; '''6''' (1):101
Estimation and implications of the genetic architecture of fasting and non-fasting blood glucose. Description: Qiao, Zhen, et al. Estimation and implications of the genetic architecture of fasting and non-fasting blood glucose. ''Nat Commun''. 2023 Jan 27; '''14''' (1):451
Investigation of genetic variants and causal biomarkers associated with brain aging. Description: Kim, Jangho, et al. Investigation of genetic variants and causal biomarkers associated with brain aging. ''Sci Rep''. 2023 Jan 27; '''13''' (1):1526
TLR4 and MD2 variation among horses with differential TNFalpha baseline concentrations and response to intravenous lipopolysaccharide infusion. Description: Mukhopadhyay, Abhijit, et al. TLR4 and MD2 variation among horses with differential TNFalpha baseline concentrations and response to intravenous lipopolysaccharide infusion. ''Sci Rep''. 2023 Jan 27; '''13''' (1):1486
Whole exome sequencing and replication for breast cancer among Hispanic/Latino women identifies FANCM as a susceptibility gene for estrogen-receptor-negative breast cancer. Description: Nierenberg, Jovia L, et al. Whole exome sequencing and replication for breast cancer among Hispanic/Latino women identifies FANCM as a susceptibility gene for estrogen-receptor-negative breast cancer. ''medRxiv''. 2023 Jan 28;
Analysis of dog breed diversity using a composite selection index. Description: Hsu, Wei-Tse, et al. Analysis of dog breed diversity using a composite selection index. ''Sci Rep''. 2023 Jan 30; '''13''' (1):1674
Multi-ancestry study of the genetics of problematic alcohol use in >1 million individuals. Description: Zhou, Hang, et al. Multi-ancestry study of the genetics of problematic alcohol use in >1 million individuals. ''medRxiv''. 2023 Jan 30;
Polymorphisms in TRIB2 and CAPRIN2 Genes Contribute to the Susceptibility to High Myopia-Induced Cataract in Han Chinese Population. Description: Ma, Bo, et al. Polymorphisms in TRIB2 and CAPRIN2 Genes Contribute to the Susceptibility to High Myopia-Induced Cataract in Han Chinese Population. ''Med Sci Monit''. 2023 Jan 30; '''29''': e937702
A chromosome-level reference genome and pangenome for barn swallow population genomics. Description: Secomandi, Simona, et al. A chromosome-level reference genome and pangenome for barn swallow population genomics. ''Cell Rep''. 2023 Jan 31; '''42''' (1):111992
Can Intelligence Affect Alcohol-, Smoking-, and Physical Activity-Related Behaviors? A Mendelian Randomization Study. Description: Li, Hansen, et al. Can Intelligence Affect Alcohol-, Smoking-, and Physical Activity-Related Behaviors? A Mendelian Randomization Study. ''J Intell''. 2023 Jan 31; '''11''' (2):
A genome-wide association study identifies a new variant associated with word reading fluency in Chinese children. Description: Wang, Zhengjun, et al. A genome-wide association study identifies a new variant associated with word reading fluency in Chinese children. ''Genes Brain Behav''. 2023 Feb; '''22''' (1):e12833
A Guide for Selection of Genetic Instruments in Mendelian Randomization Studies of Type 2 Diabetes and HbA1c: Toward an Integrated Approach. Description: Garfield, Victoria, et al. A Guide for Selection of Genetic Instruments in Mendelian Randomization Studies of Type 2 Diabetes and HbA1c: Toward an Integrated Approach. ''Diabetes''. 2023 Feb 1; '''72''' (2):175-183
Association between a single nucleotide polymorphism in the R3HCC1 gene and irinotecan toxicity. Description: Kanesada, Kou, et al. Association between a single nucleotide polymorphism in the R3HCC1 gene and irinotecan toxicity. ''Cancer Med''. 2023 Feb; '''12''' (4):4294-4305
Association of high-sensitivity C-reactive protein and diabetic nephropathy in patients with type 2 diabetes: a Mendelian randomization study. Description: Lin, Cheng-Chieh, et al. Association of high-sensitivity C-reactive protein and diabetic nephropathy in patients with type 2 diabetes: a Mendelian randomization study. ''BMJ Open Diabetes Res Care''. 2023 Feb; '''11''' (1):
Chromosome-scale genomes reveal genomic consequences of inbreeding in the South China tiger: A comparative study with the Amur tiger. Description: Zhang, Le, et al. Chromosome-scale genomes reveal genomic consequences of inbreeding in the South China tiger: A comparative study with the Amur tiger. ''Mol Ecol Resour''. 2023 Feb; '''23''' (2):330-347
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction. Description: Miyazawa, Kazuo, et al. Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction. ''Nat Genet''. 2023 Feb; '''55''' (2):187-197
Effect of Pathway-specific Polygenic Risk Scores for Alzheimer's Disease (AD) on Rate of Change in Cognitive Function and AD-related Biomarkers among Asymptomatic Individuals. Description: Xu, Yuexuan, et al. Effect of Pathway-specific Polygenic Risk Scores for Alzheimer's Disease (AD) on Rate of Change in Cognitive Function and AD-related Biomarkers among Asymptomatic Individuals. ''medRxiv''. 2023 Feb 1;
Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study. Description: Buch, Stephan, et al. Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study. ''Gut''. 2023 Feb; '''72''' (2):381-391
Genome-wide association analysis of nine reproduction and morphological traits in three goat breeds from Southern China. Description: Sun, Xiaoyan, et al. Genome-wide association analysis of nine reproduction and morphological traits in three goat breeds from Southern China. ''Anim Biosci''. 2023 Feb; '''36''' (2):191-199
Genome-wide association study meta-analysis of suicide death and suicidal behavior. Description: Li, Qingqin S, et al. Genome-wide association study meta-analysis of suicide death and suicidal behavior. ''Mol Psychiatry''. 2023 Feb; '''28''' (2):891-900
GWAS on retinal vasculometry phenotypes. Description: Jiang, Xiaofan, et al. GWAS on retinal vasculometry phenotypes. ''PLoS Genet''. 2023 Feb; '''19''' (2):e1010583
High polygenic risk score for exceptional longevity is associated with a healthy metabolic profile. Description: Revelas, Mary, et al. High polygenic risk score for exceptional longevity is associated with a healthy metabolic profile. ''Geroscience''. 2023 Feb; '''45''' (1):399-413
Impairment of kidney function and kidney cancer: A bidirectional Mendelian randomization study. Description: Lin, Yifei, et al. Impairment of kidney function and kidney cancer: A bidirectional Mendelian randomization study. ''Cancer Med''. 2023 Feb; '''12''' (3):3610-3622
Landscape of pathogenic mutations in premature ovarian insufficiency. Description: Ke, Hanni, et al. Landscape of pathogenic mutations in premature ovarian insufficiency. ''Nat Med''. 2023 Feb; '''29''' (2):483-492
Lost genome segments associate with trait diversity during rice domestication. Description: Zheng, Xiaoming, et al. Lost genome segments associate with trait diversity during rice domestication. ''BMC Biol''. 2023 Feb 1; '''21''' (1):20
Metabolic pathways enriched according to ERG status are associated with biochemical recurrence in Hispanic/Latino patients with prostate cancer. Description: Acosta-Vega, Natalia L, et al. Metabolic pathways enriched according to ERG status are associated with biochemical recurrence in Hispanic/Latino patients with prostate cancer. ''Cancer Med''. 2023 Feb; '''12''' (4):4306-4320
MRBEE: A novel bias-corrected multivariable Mendelian Randomization method. Description: Zhu, Xiaofeng, et al. MRBEE: A novel bias-corrected multivariable Mendelian Randomization method. ''Res Sq''. 2023 Feb 1;
Multiple sclerosis risk variants influence the peripheral B-cell compartment early in life in the general population. Description: de Mol, Casper L, et al. Multiple sclerosis risk variants influence the peripheral B-cell compartment early in life in the general population. ''Eur J Neurol''. 2023 Feb; '''30''' (2):434-442
Newly identified sex chromosomes in the Sphagnum (peat moss) genome alter carbon sequestration and ecosystem dynamics. Description: Healey, Adam L, et al. Newly identified sex chromosomes in the Sphagnum (peat moss) genome alter carbon sequestration and ecosystem dynamics. ''Nat Plants''. 2023 Feb; '''9''' (2):238-254
PD-L1 gene amplification and focality: relationship with protein expression. Description: Jardim, Denis Leonardo, et al. PD-L1 gene amplification and focality: relationship with protein expression. ''J Immunother Cancer''. 2023 Feb; '''11''' (2):
Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity. Description: Yoshiji, Satoshi, et al. Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity. ''Nat Metab''. 2023 Feb; '''5''' (2):248-264
PRSet: Pathway-based polygenic risk score analyses and software. Description: Choi, Shing Wan, et al. PRSet: Pathway-based polygenic risk score analyses and software. ''PLoS Genet''. 2023 Feb; '''19''' (2):e1010624
Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation. Description: Currant, Hannah, et al. Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation. ''PLoS Genet''. 2023 Feb; '''19''' (2):e1010587
Testing for association between exonic glucagon-like peptide 1 receptor mutation with physical and brain health traits in UK Biobank. Description: Ward, Joey, et al. Testing for association between exonic glucagon-like peptide 1 receptor mutation with physical and brain health traits in UK Biobank. ''Diabetes Obes Metab''. 2023 Feb; '''25''' (2):623-627
The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study. Description: Taylor, Kurt, et al. The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study. ''BMC Med''. 2023 Feb 1; '''21''' (1):35
The genomic analysis of current-day North African populations reveals the existence of trans-Saharan migrations with different origins and dates. Description: Lucas-Sanchez, Marcel, et al. The genomic analysis of current-day North African populations reveals the existence of trans-Saharan migrations with different origins and dates. ''Hum Genet''. 2023 Feb; '''142''' (2):305-320
The gut microbiome and child mental health: A population-based study. Description: Kraaij, Robert, et al. The gut microbiome and child mental health: A population-based study. ''Brain Behav Immun''. 2023 Feb; '''108''': 188-196
TTLL11 gene is associated with sustained attention performance and brain networks: A genome-wide association study of a healthy Chinese sample. Description: Liu, Hejun, et al. TTLL11 gene is associated with sustained attention performance and brain networks: A genome-wide association study of a healthy Chinese sample. ''Genes Brain Behav''. 2023 Feb; '''22''' (1):e12835
Unraveling the genetics underlying micronutrient signatures of diversity panel present in brown rice through genome-ionome linkages. Description: Pasion, Erstelle A, et al. Unraveling the genetics underlying micronutrient signatures of diversity panel present in brown rice through genome-ionome linkages. ''Plant J''. 2023 Feb; '''113''' (4):749-771
Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study. Description: Moen, Gunn-Helen, et al. Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study. ''Behav Genet''. 2023 Feb; '''53''' (1):40-52
Whole-genome sequencing identifies potential candidate genes for egg production traits in laying ducks (Anas platyrhynchos). Description: Sun, Yanfa, et al. Whole-genome sequencing identifies potential candidate genes for egg production traits in laying ducks (Anas platyrhynchos). ''Sci Rep''. 2023 Feb 1; '''13''' (1):1821
X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study. Description: Hayden, Lystra P, et al. X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study. ''Respir Res''. 2023 Feb 1; '''24''' (1):38
Functional interpretation, cataloging, and analysis of 1,341 glucose-6-phosphate dehydrogenase variants. Description: Geck, Renee C, et al. Functional interpretation, cataloging, and analysis of 1,341 glucose-6-phosphate dehydrogenase variants. ''Am J Hum Genet''. 2023 Feb 2; '''110''' (2):228-239
The impact of 22q11.2 copy-number variants on human traits in the general population. Description: Zamariolli, Malu, et al. The impact of 22q11.2 copy-number variants on human traits in the general population. ''Am J Hum Genet''. 2023 Feb 2; '''110''' (2):300-313
Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. Description: Ko, Seyoon, et al. Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. ''Am J Hum Genet''. 2023 Feb 2; '''110''' (2):314-325
Association of time spent in outdoor light and genetic risk with the incidence of depression. Description: Lin, Jing, et al. Association of time spent in outdoor light and genetic risk with the incidence of depression. ''Transl Psychiatry''. 2023 Feb 3; '''13''' (1):40
Deciphering the Genetic Basis of Silkworm Cocoon Colors Provides New Insights into Biological Coloration and Phenotypic Diversification. Description: Lu, Yaru, et al. Deciphering the Genetic Basis of Silkworm Cocoon Colors Provides New Insights into Biological Coloration and Phenotypic Diversification. ''Mol Biol Evol''. 2023 Feb 3; '''40''' (2):
Development of Nuclear DNA Markers for Applications in Genetic Diversity Study of Oil Palm-Pollinating Weevil Populations. Description: Mohd Rodzik, Fairuz Farhana, et al. Development of Nuclear DNA Markers for Applications in Genetic Diversity Study of Oil Palm-Pollinating Weevil Populations. ''Insects''. 2023 Feb 3; '''14''' (2):
Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals. Description: Akiyama, Masato, et al. Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals. ''Commun Biol''. 2023 Feb 3; '''6''' (1):143
Genomic Insights into the Population History of the Resande or Swedish Travelers. Description: Vila-Valls, Laura, et al. Genomic Insights into the Population History of the Resande or Swedish Travelers. ''Genome Biol Evol''. 2023 Feb 3; '''15''' (2):
Immunogenetic Determinants of Susceptibility to Head and Neck Cancer in the Million Veteran Program Cohort. Description: Liu, Yanhong, et al. Immunogenetic Determinants of Susceptibility to Head and Neck Cancer in the Million Veteran Program Cohort. ''Cancer Res''. 2023 Feb 3; '''83''' (3):386-397
Prognostic evaluation of polygenic risk score underlying pan-cancer analysis: evidence from two large-scale cohorts. Description: Xin, Junyi, et al. Prognostic evaluation of polygenic risk score underlying pan-cancer analysis: evidence from two large-scale cohorts. ''EBioMedicine''. 2023 Feb 3; '''89''': 104454
Structural variation across 138,134 samples in the TOPMed consortium. Description: Jun, Goo, et al. Structural variation across 138,134 samples in the TOPMed consortium. ''Res Sq''. 2023 Feb 3;
Oxytocin vs. placebo effects on intrusive memory consolidation using a trauma film paradigm: a randomized, controlled experimental study in healthy women. Description: Maslahati, Tolou, et al. Oxytocin vs. placebo effects on intrusive memory consolidation using a trauma film paradigm: a randomized, controlled experimental study in healthy women. ''Transl Psychiatry''. 2023 Feb 4; '''13''' (1):42
Prehistoric human migration between Sundaland and South Asia was driven by sea-level rise. Description: Kim, Hie Lim, et al. Prehistoric human migration between Sundaland and South Asia was driven by sea-level rise. ''Commun Biol''. 2023 Feb 4; '''6''' (1):150
Association between Single Nucleotide Polymorphisms Related to Vitamin D Metabolism and the Risk of Developing Asthma. Description: Rojo-Tolosa, Susana, et al. Association between Single Nucleotide Polymorphisms Related to Vitamin D Metabolism and the Risk of Developing Asthma. ''Nutrients''. 2023 Feb 5; '''15''' (4):
Consolidation of metabolomic, proteomic, and GWAS data in connective model of schizophrenia. Description: Kopylov, Arthur T, et al. Consolidation of metabolomic, proteomic, and GWAS data in connective model of schizophrenia. ''Sci Rep''. 2023 Feb 6; '''13''' (1):2139
Discovering novel clues of natural selection on four worldwide goat breeds. Description: Manunza, Arianna, et al. Discovering novel clues of natural selection on four worldwide goat breeds. ''Sci Rep''. 2023 Feb 6; '''13''' (1):2110
Range-wide whole-genome resequencing of the brown bear reveals drivers of intraspecies divergence. Description: de Jong, Menno J, et al. Range-wide whole-genome resequencing of the brown bear reveals drivers of intraspecies divergence. ''Commun Biol''. 2023 Feb 6; '''6''' (1):153
Establishing a Prediction Model for the Efficacy of Platinum-Based Chemotherapy in NSCLC Based on a Two Cohorts GWAS Study. Description: Xiao, Qi, et al. Establishing a Prediction Model for the Efficacy of Platinum-Based Chemotherapy in NSCLC Based on a Two Cohorts GWAS Study. ''J Clin Med''. 2023 Feb 7; '''12''' (4):
Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion. Description: Hawkes, Gareth, et al. Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion. ''medRxiv''. 2023 Feb 7;
Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Description: Pike, Mindy M, et al. Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. ''J Am Heart Assoc''. 2023 Feb 7; '''12''' (3):e027993
Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus. Description: Khunsriraksakul, Chachrit, et al. Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus. ''Nat Commun''. 2023 Feb 7; '''14''' (1):668
Population genetic analysis of Plasmodium knowlesi reveals differential selection and exchange events between Borneo and Peninsular sub-populations. Description: Turkiewicz, Anna, et al. Population genetic analysis of Plasmodium knowlesi reveals differential selection and exchange events between Borneo and Peninsular sub-populations. ''Sci Rep''. 2023 Feb 7; '''13''' (1):2142
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementia. Description: Wightman, Douglas P, et al. Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementia. ''Sci Rep''. 2023 Feb 7; '''13''' (1):2179
Resurrection genomics provides molecular and phenotypic evidence of rapid adaptation to salinization in a keystone aquatic species. Description: Wersebe, Matthew J, et al. Resurrection genomics provides molecular and phenotypic evidence of rapid adaptation to salinization in a keystone aquatic species. ''Proc Natl Acad Sci U S A''. 2023 Feb 7; '''120''' (6):e2217276120
Contributions of rare and common variation to early-onset and atypical dementia risk. Description: Wright, Carter A, et al. Contributions of rare and common variation to early-onset and atypical dementia risk. ''medRxiv''. 2023 Feb 8;
The Combined Effect of Polygenic Risk Score and Prostate Health Index in Chinese Men Undergoing Prostate Biopsy. Description: Ruan, Xiaohao, et al. The Combined Effect of Polygenic Risk Score and Prostate Health Index in Chinese Men Undergoing Prostate Biopsy. ''J Clin Med''. 2023 Feb 8; '''12''' (4):
Whole-body adipose tissue multi-omic analyses in sheep reveal molecular mechanisms underlying local adaptation to extreme environments. Description: Xu, Ya-Xi, et al. Whole-body adipose tissue multi-omic analyses in sheep reveal molecular mechanisms underlying local adaptation to extreme environments. ''Commun Biol''. 2023 Feb 8; '''6''' (1):159
Genetic population structures of common scavenging species near hydrothermal vents in the Okinawa Trough. Description: Kise, Hiroki, et al. Genetic population structures of common scavenging species near hydrothermal vents in the Okinawa Trough. ''Sci Rep''. 2023 Feb 9; '''13''' (1):2348
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. Description: Pan, Hongxu, et al. Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. ''NPJ Parkinsons Dis''. 2023 Feb 9; '''9''' (1):22
Insights into the domestication of avocado and potential genetic contributors to heterodichogamy. Description: Solares, Edwin, et al. Insights into the domestication of avocado and potential genetic contributors to heterodichogamy. ''G3 (Bethesda)''. 2023 Feb 9; '''13''' (2):
The demographic history of house mice (Mus musculus domesticus) in eastern North America. Description: Agwamba, Kennedy D, et al. The demographic history of house mice (Mus musculus domesticus) in eastern North America. ''G3 (Bethesda)''. 2023 Feb 9; '''13''' (2):
Genomic architecture of migration timing in a long-distance migratory songbird. Description: de Greef, Evelien, et al. Genomic architecture of migration timing in a long-distance migratory songbird. ''Sci Rep''. 2023 Feb 10; '''13''' (1):2437
Identification and analysis of individuals who deviate from their genetically-predicted phenotype. Description: Hawkes, Gareth, et al. Identification and analysis of individuals who deviate from their genetically-predicted phenotype. ''bioRxiv''. 2023 Feb 10;
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children. Description: Lee, Danyel, et al. Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children. ''Science''. 2023 Feb 10; '''379''' (6632):eabo3627
Interleukin 6 and interferon gamma haplotypes are related to cytokine serum levels in dogs in an endemic Leishmania infantum region. Description: Alvarez, Luis, et al. Interleukin 6 and interferon gamma haplotypes are related to cytokine serum levels in dogs in an endemic Leishmania infantum region. ''Infect Dis Poverty''. 2023 Feb 10; '''12''' (1):9
Maternal Donor and Genetic Variation of Lagerstroemia indica Cultivars. Description: Guo, Chang, et al. Maternal Donor and Genetic Variation of Lagerstroemia indica Cultivars. ''Int J Mol Sci''. 2023 Feb 10; '''24''' (4):
Time-varying effects are common in genetic control of gestational duration. Description: Juodakis, Julius, et al. Time-varying effects are common in genetic control of gestational duration. ''medRxiv''. 2023 Feb 10;
BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data. Description: Ma, Shiyang, et al. BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data. ''Genome Biol''. 2023 Feb 13; '''24''' (1):24
Gene-Nutrient Interactions in Obesity: COBLL1 Genetic Variants Interact with Dietary Fat Intake to Modulate the Incidence of Obesity. Description: Kwak, Junkyung, et al. Gene-Nutrient Interactions in Obesity: COBLL1 Genetic Variants Interact with Dietary Fat Intake to Modulate the Incidence of Obesity. ''Int J Mol Sci''. 2023 Feb 13; '''24''' (4):
Origins, timing and introgression of domestic geese revealed by whole genome data. Description: Wen, Junhui, et al. Origins, timing and introgression of domestic geese revealed by whole genome data. ''J Anim Sci Biotechnol''. 2023 Feb 13; '''14''' (1):26
Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Description: Stevenson-Hoare, Joshua, et al. Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. ''Brain''. 2023 Feb 13; '''146''' (2):690-699
An Oxylipin-Related Nutrient Pattern and Risk of Type 1 Diabetes in the Diabetes Autoimmunity Study in the Young (DAISY). Description: Buckner, Teresa, et al. An Oxylipin-Related Nutrient Pattern and Risk of Type 1 Diabetes in the Diabetes Autoimmunity Study in the Young (DAISY). ''Nutrients''. 2023 Feb 14; '''15''' (4):
Emergence of Antifungal Resistant Subclades in the Global Predominant Phylogenetic Population of Candida albicans. Description: Gong, Jie, et al. Emergence of Antifungal Resistant Subclades in the Global Predominant Phylogenetic Population of Candida albicans. ''Microbiol Spectr''. 2023 Feb 14; '''11''' (1):e0380722
Robust Bioinformatics Approaches Result in the First Polygenic Risk Score for BMI in Greek Adults. Description: Kafyra, Maria, et al. Robust Bioinformatics Approaches Result in the First Polygenic Risk Score for BMI in Greek Adults. ''J Pers Med''. 2023 Feb 14; '''13''' (2):
Assessing the interaction effects of brain structure longitudinal changes and life environmental factors on depression and anxiety. Description: Yang, Xuena, et al. Assessing the interaction effects of brain structure longitudinal changes and life environmental factors on depression and anxiety. ''Hum Brain Mapp''. 2023 Feb 15; '''44''' (3):1227-1238
Neanderthal Introgression Shaped Human Circadian Traits. Description: Velazquez-Arcelay, Keila, et al. Neanderthal Introgression Shaped Human Circadian Traits. ''bioRxiv''. 2023 Feb 15;
Association of Plant-Based and High-Protein Diets with a Lower Obesity Risk Defined by Fat Mass in Middle-Aged and Elderly Persons with a High Genetic Risk of Obesity. Description: Daily, James W, et al. Association of Plant-Based and High-Protein Diets with a Lower Obesity Risk Defined by Fat Mass in Middle-Aged and Elderly Persons with a High Genetic Risk of Obesity. ''Nutrients''. 2023 Feb 20; '''15''' (4):
Development of antidrug antibodies against adalimumab maps to variation within the HLA-DR peptide-binding groove. Description: Tsakok, Teresa, et al. Development of antidrug antibodies against adalimumab maps to variation within the HLA-DR peptide-binding groove. ''JCI Insight''. 2023 Feb 22; '''8''' (4):
Genetic variation supports a causal role for valproate in prevention of ischemic stroke. Description: Mayerhofer, Ernst, et al. Genetic variation supports a causal role for valproate in prevention of ischemic stroke. ''medRxiv''. 2023 Feb 22;
Germline VWF/MPRIP and somatoplasm FGA variants synergically confer susceptibility to non-traumatic osteonecrosis of the femoral head. Description: Wang, Dawei, et al. Germline VWF/MPRIP and somatoplasm FGA variants synergically confer susceptibility to non-traumatic osteonecrosis of the femoral head. ''Sci Rep''. 2023 Feb 22; '''13''' (1):3112
Uncovering the complex genetic architecture of human plasma lipidome using machine learning methods. Description: Lehtimaki, Miikael, et al. Uncovering the complex genetic architecture of human plasma lipidome using machine learning methods. ''Sci Rep''. 2023 Feb 22; '''13''' (1):3078
Distilling functional variations for human UGT2B4 upstream region based on selection signals and implications for phenotypes of Neanderthal and Denisovan. Description: Wang, Pin-Yi, et al. Distilling functional variations for human UGT2B4 upstream region based on selection signals and implications for phenotypes of Neanderthal and Denisovan. ''Sci Rep''. 2023 Feb 23; '''13''' (1):3134
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome. Description: Jain, Pritesh, et al. Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome. ''Transl Psychiatry''. 2023 Feb 23; '''13''' (1):69
A thousand-genome panel retraces the global spread and adaptation of a major fungal crop pathogen. Description: Feurtey, Alice, et al. A thousand-genome panel retraces the global spread and adaptation of a major fungal crop pathogen. ''Nat Commun''. 2023 Feb 24; '''14''' (1):1059
Disentangling clustering configuration intricacies for divergently selected chicken breeds. Description: Vakhrameev, Anatoly B, et al. Disentangling clustering configuration intricacies for divergently selected chicken breeds. ''Sci Rep''. 2023 Feb 27; '''13''' (1):3319
An oligogenic architecture underlying ecological and reproductive divergence in sympatric populations. Description: Brisevac, Dusica, et al. An oligogenic architecture underlying ecological and reproductive divergence in sympatric populations. ''Elife''. 2023 Feb 28; '''12''':
Contributions of NR1H3 genetic polymorphisms to susceptibility and effects of narrowband UVB phototherapy to nonsegmental vitiligo. Description: Xu, Meifeng, et al. Contributions of NR1H3 genetic polymorphisms to susceptibility and effects of narrowband UVB phototherapy to nonsegmental vitiligo. ''Sci Rep''. 2023 Feb 28; '''13''' (1):3384
correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes. Description: Nyerki, Emil, et al. correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes. ''Genome Biol''. 2023 Feb 28; '''24''' (1):38
Estimating human mobility in Holocene Western Eurasia with large-scale ancient genomic data. Description: Schmid, Clemens, et al. Estimating human mobility in Holocene Western Eurasia with large-scale ancient genomic data. ''Proc Natl Acad Sci U S A''. 2023 Feb 28; '''120''' (9):e2218375120
Polygenic adaptation from standing genetic variation allows rapid ecotype formation. Description: Fuhrmann, Nico, et al. Polygenic adaptation from standing genetic variation allows rapid ecotype formation. ''Elife''. 2023 Feb 28; '''12''':
Polygenic risk scores enhance prediction of body mass index increase in individuals with a first episode of psychosis. Description: Muntane, Gerard, et al. Polygenic risk scores enhance prediction of body mass index increase in individuals with a first episode of psychosis. ''Eur Psychiatry''. 2023 Feb 28; '''66''' (1):e28
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data. Description: Liu, Zipeng, et al. Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data. ''Nat Commun''. 2023 Feb 28; '''14''' (1):1131
A critical role of brain network architecture in a continuum model of autism spectrum disorders spanning from healthy individuals with genetic liability to individuals with ASD. Description: Khundrakpam, Budhachandra, et al. A critical role of brain network architecture in a continuum model of autism spectrum disorders spanning from healthy individuals with genetic liability to individuals with ASD. ''Mol Psychiatry''. 2023 Mar; '''28''' (3):1210-1218
A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies. Description: Strippel, Christine, et al. A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies. ''Brain''. 2023 Mar 1; '''146''' (3):977-990
Allele-dependent interaction of LRRK2 and NOD2 in leprosy. Description: Dallmann-Sauer, Monica, et al. Allele-dependent interaction of LRRK2 and NOD2 in leprosy. ''PLoS Pathog''. 2023 Mar; '''19''' (3):e1011260
Association between psoriatic disease and lifestyle factors and comorbidities: cross-sectional analysis and Mendelian randomization. Description: Zhao, Sizheng Steven, et al. Association between psoriatic disease and lifestyle factors and comorbidities: cross-sectional analysis and Mendelian randomization. ''Rheumatology (Oxford)''. 2023 Mar 1; '''62''' (3):1272-1285
Associations of atrial natriuretic peptide with measures of insulin and adipose depots. Description: Couch, Catharine A, et al. Associations of atrial natriuretic peptide with measures of insulin and adipose depots. ''Physiol Rep''. 2023 Mar; '''11''' (5):e15625
Fine mapping and accurate prediction of complex traits using Bayesian Variable Selection models applied to biobank-size data. Description: de Los Campos, Gustavo, et al. Fine mapping and accurate prediction of complex traits using Bayesian Variable Selection models applied to biobank-size data. ''Eur J Hum Genet''. 2023 Mar; '''31''' (3):313-320
Genetic basis of resistance to southern corn leaf blight in the maize multi-parent population and diversity panel. Description: Chen, Gengshen, et al. Genetic basis of resistance to southern corn leaf blight in the maize multi-parent population and diversity panel. ''Plant Biotechnol J''. 2023 Mar; '''21''' (3):506-520
Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder. Description: Hahn, Tim, et al. Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder. ''Mol Psychiatry''. 2023 Mar; '''28''' (3):1057-1063
Genome-Wide Association Study on Longitudinal Change in Fasting Plasma Glucose in Korean Population. Description: Jin, Heejin, et al. Genome-Wide Association Study on Longitudinal Change in Fasting Plasma Glucose in Korean Population. ''Diabetes Metab J''. 2023 Mar; '''47''' (2):255-266
Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humans. Description: Hamanaka, Kohei, et al. Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humans. ''Genome Res''. 2023 Mar; '''33''' (3):435-447
Growth rates of human induced pluripotent stem cells and neural stem cells from attention-deficit hyperactivity disorder patients: a preliminary study. Description: Yde Ohki, Cristine Marie, et al. Growth rates of human induced pluripotent stem cells and neural stem cells from attention-deficit hyperactivity disorder patients: a preliminary study. ''J Neural Transm (Vienna)''. 2023 Mar; '''130''' (3):243-252
Haptools: a toolkit for admixture and haplotype analysis. Description: Massarat, Arya R, et al. Haptools: a toolkit for admixture and haplotype analysis. ''Bioinformatics''. 2023 Mar 1; '''39''' (3):
Heritability and gene functions associated with sclerotia formation of Rhizoctonia solani AG-7 using whole genome sequencing and genome-wide association study. Description: Lin, Yu-Cheng, et al. Heritability and gene functions associated with sclerotia formation of Rhizoctonia solani AG-7 using whole genome sequencing and genome-wide association study. ''Microb Genom''. 2023 Mar; '''9''' (3):
Host variation in type I interferon signaling genes (MX1), C-C chemokine receptor type 5 gene, and major histocompatibility complex class I alleles in treated HIV+ noncontrollers predict viral reservoir size. Description: Siegel, David A, et al. Host variation in type I interferon signaling genes (MX1), C-C chemokine receptor type 5 gene, and major histocompatibility complex class I alleles in treated HIV+ noncontrollers predict viral reservoir size. ''AIDS''. 2023 Mar 1; '''37''' (3):477-488
Mapping mitonuclear epistasis using a novel recombinant yeast population. Description: Nguyen, Tuc H M, et al. Mapping mitonuclear epistasis using a novel recombinant yeast population. ''PLoS Genet''. 2023 Mar; '''19''' (3):e1010401
Polygenic indices for cognition in healthy aging; the role of brain measures. Description: Tsapanou, A, et al. Polygenic indices for cognition in healthy aging; the role of brain measures. ''Neuroimage Rep''. 2023 Mar; '''3''' (1):
Polygenic risk scores for schizophrenia are associated with oculomotor endophenotypes. Description: Coors, Annabell, et al. Polygenic risk scores for schizophrenia are associated with oculomotor endophenotypes. ''Psychol Med''. 2023 Mar; '''53''' (4):1611-1619
Population structure and hybridisation in a population of Hawaiian feral chickens. Description: Martin Cerezo, Maria Luisa, et al. Population structure and hybridisation in a population of Hawaiian feral chickens. ''Heredity (Edinb)''. 2023 Mar; '''130''' (3):154-162
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Description: Liu, Dongjing, et al. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. ''Nat Genet''. 2023 Mar; '''55''' (3):369-376
Selective whole-genome amplification reveals population genetics of Leishmania braziliensis directly from patient skin biopsies. Description: Pilling, Olivia A, et al. Selective whole-genome amplification reveals population genetics of Leishmania braziliensis directly from patient skin biopsies. ''PLoS Pathog''. 2023 Mar; '''19''' (3):e1011230
Spatial genetic structure of European wild boar, with inferences on late-Pleistocene and Holocene demographic history. Description: de Jong, Joost F, et al. Spatial genetic structure of European wild boar, with inferences on late-Pleistocene and Holocene demographic history. ''Heredity (Edinb)''. 2023 Mar; '''130''' (3):135-144
The giant diploid faba genome unlocks variation in a global protein crop. Description: Jayakodi, Murukarthick, et al. The giant diploid faba genome unlocks variation in a global protein crop. ''Nature''. 2023 Mar; '''615''' (7953):652-659
Tuberculosis severity associates with variants and eQTLs related to vascular biology and infection-induced inflammation. Description: McHenry, Michael L, et al. Tuberculosis severity associates with variants and eQTLs related to vascular biology and infection-induced inflammation. ''PLoS Genet''. 2023 Mar; '''19''' (3):e1010387
Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip. Description: Dembic, Maja, et al. Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip. ''Mol Genet Genomics''. 2023 Mar; '''298''' (2):329-342
Whole-genome sequencing reveals an association between small genomic deletions and an increased risk of developing Parkinson's disease. Description: Oh, Ji-Hye, et al. Whole-genome sequencing reveals an association between small genomic deletions and an increased risk of developing Parkinson's disease. ''Exp Mol Med''. 2023 Mar; '''55''' (3):555-564
A lack of population structure characterizes the invasive Lonicera japonica in West Virginia and across eastern North America. Description: Barrett, Craig F, et al. A lack of population structure characterizes the invasive Lonicera japonica in West Virginia and across eastern North America. ''bioRxiv''. 2023 Mar 2;
Allelic variation of TaWD40-4B.1 contributes to drought tolerance by modulating catalase activity in wheat. Description: Tian, Geng, et al. Allelic variation of TaWD40-4B.1 contributes to drought tolerance by modulating catalase activity in wheat. ''Nat Commun''. 2023 Mar 2; '''14''' (1):1200
Analysis of structural variation among inbred mouse strains. Description: Arslan, Ahmed, et al. Analysis of structural variation among inbred mouse strains. ''BMC Genomics''. 2023 Mar 2; '''24''' (1):97
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance. Description: Jacquemin, Valerie, et al. Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance. ''Hum Genomics''. 2023 Mar 2; '''17''' (1):16
Effect of tissue-grouped regulatory variants associated to type 2 diabetes in related secondary outcomes. Description: Hemerich, Daiane, et al. Effect of tissue-grouped regulatory variants associated to type 2 diabetes in related secondary outcomes. ''Sci Rep''. 2023 Mar 2; '''13''' (1):3579
Genome-wide association study of 17 serum biochemical indicators in a chicken F(2) resource population. Description: Song, Haijie, et al. Genome-wide association study of 17 serum biochemical indicators in a chicken F(2) resource population. ''BMC Genomics''. 2023 Mar 2; '''24''' (1):98
Mega-scale Bayesian regression methods for genome-wide prediction and association studies with thousands of traits. Description: Qu, Jiayi, et al. Mega-scale Bayesian regression methods for genome-wide prediction and association studies with thousands of traits. ''Genetics''. 2023 Mar 2; '''223''' (3):
Polygenic risk of Social-isolation and its influence on social behavior, psychosis, depression and autism spectrum disorder. Description: Socrates, Adam, et al. Polygenic risk of Social-isolation and its influence on social behavior, psychosis, depression and autism spectrum disorder. ''Res Sq''. 2023 Mar 2;
Whole-genome sequencing of cryopreserved resources from French Large White pigs at two distinct sampling times reveals strong signatures of convergent and divergent selection between the dam and sire lines. Description: Boitard, Simon, et al. Whole-genome sequencing of cryopreserved resources from French Large White pigs at two distinct sampling times reveals strong signatures of convergent and divergent selection between the dam and sire lines. ''Genet Sel Evol''. 2023 Mar 2; '''55''' (1):13
Population Structure, Demographic History, and Adaptation of Giant Honeybees in China Revealed by Population Genomic Data. Description: Cao, Lianfei, et al. Population Structure, Demographic History, and Adaptation of Giant Honeybees in China Revealed by Population Genomic Data. ''Genome Biol Evol''. 2023 Mar 3; '''15''' (3):
The dogs of Chernobyl: Demographic insights into populations inhabiting the nuclear exclusion zone. Description: Spatola, Gabriella J, et al. The dogs of Chernobyl: Demographic insights into populations inhabiting the nuclear exclusion zone. ''Sci Adv''. 2023 Mar 3; '''9''' (9):eade2537
The Legacy of Infectious Disease Exposure on the Genomic Diversity of Indigenous Southern Mexicans. Description: Garcia, Obed A, et al. The Legacy of Infectious Disease Exposure on the Genomic Diversity of Indigenous Southern Mexicans. ''Genome Biol Evol''. 2023 Mar 3; '''15''' (3):
Association of laxatives use with incident dementia and modifying effect of genetic susceptibility: a population-based cohort study with propensity score matching. Description: Feng, Jiangtao, et al. Association of laxatives use with incident dementia and modifying effect of genetic susceptibility: a population-based cohort study with propensity score matching. ''BMC Geriatr''. 2023 Mar 4; '''23''' (1):122
Chromosome Fissions and Fusions Act as Barriers to Gene Flow between Brenthis Fritillary Butterflies. Description: Mackintosh, Alexander, et al. Chromosome Fissions and Fusions Act as Barriers to Gene Flow between Brenthis Fritillary Butterflies. ''Mol Biol Evol''. 2023 Mar 4; '''40''' (3):
Comparative Genomic and Transcriptomic Analyses Reveal the Impacts of Genetic Admixture in Kazaks, Uyghurs, and Huis. Description: Pan, Yuwen, et al. Comparative Genomic and Transcriptomic Analyses Reveal the Impacts of Genetic Admixture in Kazaks, Uyghurs, and Huis. ''Mol Biol Evol''. 2023 Mar 4; '''40''' (3):
Contrasting Patterns of Single Nucleotide Polymorphisms and Structural Variation Across Multiple Invasions. Description: Stuart, Katarina C, et al. Contrasting Patterns of Single Nucleotide Polymorphisms and Structural Variation Across Multiple Invasions. ''Mol Biol Evol''. 2023 Mar 4; '''40''' (3):
Genomic Basis of Adaptation to a Novel Precipitation Regime. Description: Elfarargi, Ahmed F, et al. Genomic Basis of Adaptation to a Novel Precipitation Regime. ''Mol Biol Evol''. 2023 Mar 4; '''40''' (3):
HaploBlocks: Efficient Detection of Positive Selection in Large Population Genomic Datasets. Description: Kirsch-Gerweck, Benedikt, et al. HaploBlocks: Efficient Detection of Positive Selection in Large Population Genomic Datasets. ''Mol Biol Evol''. 2023 Mar 4; '''40''' (3):
Limited Song Mixing Without Genomic Gene Flow in a Contact Zone Between Two Songbird Species. Description: Wu, Lei, et al. Limited Song Mixing Without Genomic Gene Flow in a Contact Zone Between Two Songbird Species. ''Mol Biol Evol''. 2023 Mar 4; '''40''' (3):
Recombination Variation Shapes Phylogeny and Introgression in Wild Diploid Strawberries. Description: Feng, Chao, et al. Recombination Variation Shapes Phylogeny and Introgression in Wild Diploid Strawberries. ''Mol Biol Evol''. 2023 Mar 4; '''40''' (3):
The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data. Description: Leonard, Hampton L, et al. The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data. ''NPJ Parkinsons Dis''. 2023 Mar 4; '''9''' (1):33
Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence. Description: Hassanin, Emadeldin, et al. Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence. ''BMC Med Genomics''. 2023 Mar 5; '''16''' (1):42
Associations of polygenic risk scores with posttraumatic stress symptom trajectories following combat deployment. Description: Campbell-Sills, Laura, et al. Associations of polygenic risk scores with posttraumatic stress symptom trajectories following combat deployment. ''Psychol Med''. 2023 Mar 6; '''53''' (14):1-10
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Description: Thareja, Gaurav, et al. Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. ''Hum Mol Genet''. 2023 Mar 6; '''32''' (6):907-916
A global phylogenomic analysis of the shiitake genus Lentinula. Description: Sierra-Patev, Sean, et al. A global phylogenomic analysis of the shiitake genus Lentinula. ''Proc Natl Acad Sci U S A''. 2023 Mar 7; '''120''' (10):e2214076120
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. Description: Xiao, Brenda, et al. Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. ''J Am Heart Assoc''. 2023 Mar 7; '''12''' (5):e026561
OTTERS: a powerful TWAS framework leveraging summary-level reference data. Description: Dai, Qile, et al. OTTERS: a powerful TWAS framework leveraging summary-level reference data. ''Nat Commun''. 2023 Mar 7; '''14''' (1):1271
Cold-induced vasodilation response in a Japanese cohort: insights from cold-water immersion and genome-wide association studies. Description: Yasukochi, Yoshiki, et al. Cold-induced vasodilation response in a Japanese cohort: insights from cold-water immersion and genome-wide association studies. ''J Physiol Anthropol''. 2023 Mar 8; '''42''' (1):2
Potentially causal associations between placental DNA methylation and schizophrenia and other neuropsychiatric disorders. Description: Cilleros-Portet, Ariadna, et al. Potentially causal associations between placental DNA methylation and schizophrenia and other neuropsychiatric disorders. ''medRxiv''. 2023 Mar 8;
Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring. Description: Campos, Adrian I, et al. Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring. ''Sleep''. 2023 Mar 9; '''46''' (3):
Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations. Description: Auwerx, Chiara, et al. Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations. ''Elife''. 2023 Mar 9; '''12''':
Extensive sequence duplication in Arabidopsis revealed by pseudo-heterozygosity. Description: Jaegle, Benjamin, et al. Extensive sequence duplication in Arabidopsis revealed by pseudo-heterozygosity. ''Genome Biol''. 2023 Mar 9; '''24''' (1):44
Genetic mapping and molecular mechanism behind color variation in the Asian vine snake. Description: Tang, Chen-Yang, et al. Genetic mapping and molecular mechanism behind color variation in the Asian vine snake. ''Genome Biol''. 2023 Mar 9; '''24''' (1):46
Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank. Description: Wuttke, Matthias, et al. Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank. ''Nat Commun''. 2023 Mar 9; '''14''' (1):1287
No evidence for sex chromosomes in natural populations of the cichlid fish Astatotilapia burtoni. Description: Lichilin, Nicolas, et al. No evidence for sex chromosomes in natural populations of the cichlid fish Astatotilapia burtoni. ''G3 (Bethesda)''. 2023 Mar 9; '''13''' (3):
Population genetic analysis of the microsporidium Ordospora colligata reveals the role of natural selection and phylogeography on its extremely compact and reduced genome. Description: Angst, Pascal, et al. Population genetic analysis of the microsporidium Ordospora colligata reveals the role of natural selection and phylogeography on its extremely compact and reduced genome. ''G3 (Bethesda)''. 2023 Mar 9; '''13''' (3):
Healthy Diet, Polygenic Risk Score, and Upper Gastrointestinal Cancer Risk: A Prospective Study from UK Biobank. Description: Liu, Wenmin, et al. Healthy Diet, Polygenic Risk Score, and Upper Gastrointestinal Cancer Risk: A Prospective Study from UK Biobank. ''Nutrients''. 2023 Mar 10; '''15''' (6):
Identifying metabolic features of colorectal cancer liability using Mendelian randomization. Description: Bull, Caroline J, et al. Identifying metabolic features of colorectal cancer liability using Mendelian randomization. ''medRxiv''. 2023 Mar 10;
The genetic architecture of human amygdala volumes and their overlap with common brain disorders. Description: Ou, Ya-Nan, et al. The genetic architecture of human amygdala volumes and their overlap with common brain disorders. ''Transl Psychiatry''. 2023 Mar 11; '''13''' (1):90
Association of rare variants in ARSA with Parkinson's disease. Description: Senkevich, Konstantin, et al. Association of rare variants in ARSA with Parkinson's disease. ''medRxiv''. 2023 Mar 13;
The genetic architecture of pain intensity in a sample of 598,339 U.S. veterans. Description: Toikumo, Sylvanus, et al. The genetic architecture of pain intensity in a sample of 598,339 U.S. veterans. ''medRxiv''. 2023 Mar 13;
Identification of candidate genomic regions for egg yolk moisture content based on a genome-wide association study. Description: Zhang, Ruiqi, et al. Identification of candidate genomic regions for egg yolk moisture content based on a genome-wide association study. ''BMC Genomics''. 2023 Mar 14; '''24''' (1):110
Inferring biological kinship in ancient datasets: comparing the response of ancient DNA-specific software packages to low coverage data. Description: Marsh, William A, et al. Inferring biological kinship in ancient datasets: comparing the response of ancient DNA-specific software packages to low coverage data. ''BMC Genomics''. 2023 Mar 14; '''24''' (1):111
Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Description: Makowski, Carolina, et al. Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. ''Proc Natl Acad Sci U S A''. 2023 Mar 14; '''120''' (11):e2214834120
Lifetime cannabis use and childhood trauma associated with CNR1 genetic variants increase the risk of psychosis: findings from the STREAM study. Description: Loureiro, Camila Marcelino, et al. Lifetime cannabis use and childhood trauma associated with CNR1 genetic variants increase the risk of psychosis: findings from the STREAM study. ''Braz J Psychiatry''. 2023 Mar 14; '''45''' (3):226-35
Epistatic Features and Machine Learning Improve Alzheimer's Risk Prediction Over Polygenic Risk Scores. Description: Hermes, Stephen, et al. Epistatic Features and Machine Learning Improve Alzheimer's Risk Prediction Over Polygenic Risk Scores. ''medRxiv''. 2023 Mar 15;
Genetic diversity and signatures of selection in BoHuai goat revealed by whole-genome sequencing. Description: Yao, Zhi, et al. Genetic diversity and signatures of selection in BoHuai goat revealed by whole-genome sequencing. ''BMC Genomics''. 2023 Mar 15; '''24''' (1):116
Heritable Risk and Protective Genetic Components of Glaucoma Medication Non-Adherence. Description: Barr, Julie L, et al. Heritable Risk and Protective Genetic Components of Glaucoma Medication Non-Adherence. ''Int J Mol Sci''. 2023 Mar 15; '''24''' (6):
Human genetic history on the Tibetan Plateau in the past 5100 years. Description: Wang, Hongru, et al. Human genetic history on the Tibetan Plateau in the past 5100 years. ''Sci Adv''. 2023 Mar 15; '''9''' (11):eadd5582
Population Structure and Genetic Diversity Analysis of "Yufen 1" H Line Chickens Using Whole-Genome Resequencing. Description: Liu, Cong, et al. Population Structure and Genetic Diversity Analysis of "Yufen 1" H Line Chickens Using Whole-Genome Resequencing. ''Life (Basel)''. 2023 Mar 15; '''13''' (3):
The Association of the Polymorphisms in the FUT8-Related Locus with the Plasma Glycosylation in Post-Traumatic Stress Disorder. Description: Tudor, Lucija, et al. The Association of the Polymorphisms in the FUT8-Related Locus with the Plasma Glycosylation in Post-Traumatic Stress Disorder. ''Int J Mol Sci''. 2023 Mar 16; '''24''' (6):
Analysis of Systemic Epigenetic Alterations in Inflammatory Bowel Disease: Defining Geographical, Genetic and Immune-Inflammatory influences on the Circulating Methylome. Description: Kalla, Rahul, et al. Analysis of Systemic Epigenetic Alterations in Inflammatory Bowel Disease: Defining Geographical, Genetic and Immune-Inflammatory influences on the Circulating Methylome. ''J Crohns Colitis''. 2023 Mar 18; '''17''' (2):170-184
An Extremes of Phenotype Approach Confirms Significant Genetic Heterogeneity in Patients with Ulcerative Colitis. Description: Mortlock, Sally, et al. An Extremes of Phenotype Approach Confirms Significant Genetic Heterogeneity in Patients with Ulcerative Colitis. ''J Crohns Colitis''. 2023 Mar 18; '''17''' (2):277-288
Do environmental effects indexed by parental genetic variation influence common psychiatric symptoms in childhood? Description: Jami, Eshim S, et al. Do environmental effects indexed by parental genetic variation influence common psychiatric symptoms in childhood? ''Transl Psychiatry''. 2023 Mar 18; '''13''' (1):94
Intercross population study reveals that co-mutation of mitfa genes in two subgenomes induces red skin color in common carp ( Cyprinus carpio wuyuanensis). Description: Li, Bi-Jun, et al. Intercross population study reveals that co-mutation of mitfa genes in two subgenomes induces red skin color in common carp ( Cyprinus carpio wuyuanensis). ''Zool Res''. 2023 Mar 18; '''44''' (2):276-286
Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish. Description: Lynch, Megan T, et al. Associations of genome-wide and regional autozygosity with 96 complex traits in old order Amish. ''BMC Genomics''. 2023 Mar 20; '''24''' (1):134
Mapping the dynamic genetic regulatory architecture of HLA genes at single-cell resolution. Description: Kang, Joyce B, et al. Mapping the dynamic genetic regulatory architecture of HLA genes at single-cell resolution. ''medRxiv''. 2023 Mar 20;
Systematic Selection Signature Analysis of Chinese Gamecocks Based on Genomic and Transcriptomic Data. Description: Ren, Xufang, et al. Systematic Selection Signature Analysis of Chinese Gamecocks Based on Genomic and Transcriptomic Data. ''Int J Mol Sci''. 2023 Mar 20; '''24''' (6):
The lingering effects of Neanderthal introgression on human complex traits. Description: Wei, Xinzhu, et al. The lingering effects of Neanderthal introgression on human complex traits. ''Elife''. 2023 Mar 20; '''12''':
Investigating Vitamin D Receptor Genetic Markers in a Cluster Headache Meta-Analysis. Description: Jennysdotter Olofsgard, Felicia, et al. Investigating Vitamin D Receptor Genetic Markers in a Cluster Headache Meta-Analysis. ''Int J Mol Sci''. 2023 Mar 21; '''24''' (6):
A genome-wide association study identifies a possible role for cannabinoid signalling in the pathogenesis of diabetic kidney disease. Description: Osman, Wael, et al. A genome-wide association study identifies a possible role for cannabinoid signalling in the pathogenesis of diabetic kidney disease. ''Sci Rep''. 2023 Mar 22; '''13''' (1):4661
Inflammation and Blood-Brain Barrier in Depression: Interaction of CLDN5 and IL6 Gene Variants in Stress-Induced Depression. Description: Gal, Zsofia, et al. Inflammation and Blood-Brain Barrier in Depression: Interaction of CLDN5 and IL6 Gene Variants in Stress-Induced Depression. ''Int J Neuropsychopharmacol''. 2023 Mar 22; '''26''' (3):189-197
Intergenerational effects of parental educational attainment on parenting and childhood educational outcomes: Evidence from MoBa using within-family Mendelian randomization. Description: Havdahl, Alexandra, et al. Intergenerational effects of parental educational attainment on parenting and childhood educational outcomes: Evidence from MoBa using within-family Mendelian randomization. ''medRxiv''. 2023 Mar 22;
Single Nucleotide Polymorphisms in the Vitamin D Metabolic Pathway and Their Relationship with High Blood Pressure Risk. Description: Rojo-Tolosa, Susana, et al. Single Nucleotide Polymorphisms in the Vitamin D Metabolic Pathway and Their Relationship with High Blood Pressure Risk. ''Int J Mol Sci''. 2023 Mar 22; '''24''' (6):
GWAS of grain color and tannin content in Chinese sorghum based on whole-genome sequencing. Description: Zhang, Liyi, et al. GWAS of grain color and tannin content in Chinese sorghum based on whole-genome sequencing. ''Theor Appl Genet''. 2023 Mar 23; '''136''' (4):77
Association of blood pressure with incident diabetic microvascular complications among diabetic patients: Longitudinal findings from the UK Biobank. Description: Li, Cong, et al. Association of blood pressure with incident diabetic microvascular complications among diabetic patients: Longitudinal findings from the UK Biobank. ''J Glob Health''. 2023 Mar 24; '''13''': 04027
Susceptibility to Colorectal Cancer Based on HSD17B4 rs721673 and rs721675 Polymorphisms and Alcohol Intake among Taiwan Biobank Participants: A Retrospective Case Control Study Using the Nationwide Claims Data. Description: Lin, Tzu-Chiao, et al. Susceptibility to Colorectal Cancer Based on HSD17B4 rs721673 and rs721675 Polymorphisms and Alcohol Intake among Taiwan Biobank Participants: A Retrospective Case Control Study Using the Nationwide Claims Data. ''J Pers Med''. 2023 Mar 24; '''13''' (4):
A common variant rs2054564 in ADAMST17 is associated with susceptibility to lumbar spondylosis. Description: Taniguchi, Yuki, et al. A common variant rs2054564 in ADAMST17 is associated with susceptibility to lumbar spondylosis. ''Sci Rep''. 2023 Mar 25; '''13''' (1):4900
Gene-environment interaction explains a part of missing heritability in human body mass index. Description: Jung, Hae-Un, et al. Gene-environment interaction explains a part of missing heritability in human body mass index. ''Commun Biol''. 2023 Mar 25; '''6''' (1):324
Large haploblocks underlie rapid adaptation in the invasive weed Ambrosia artemisiifolia. Description: Battlay, Paul, et al. Large haploblocks underlie rapid adaptation in the invasive weed Ambrosia artemisiifolia. ''Nat Commun''. 2023 Mar 27; '''14''' (1):1717
Polygenic risk scores for the prediction of common cancers in East Asians: A population-based prospective cohort study. Description: Ho, Peh Joo, et al. Polygenic risk scores for the prediction of common cancers in East Asians: A population-based prospective cohort study. ''Elife''. 2023 Mar 27; '''12''':
Rare genetic variants in SEC24D modify orofacial cleft phenotypes. Description: Curtis, Sarah W, et al. Rare genetic variants in SEC24D modify orofacial cleft phenotypes. ''medRxiv''. 2023 Mar 27;
Genomic prediction in pigs using data from a commercial crossbred population: insights from the Duroc x (Landrace x Yorkshire) three-way crossbreeding system. Description: Liu, Siyi, et al. Genomic prediction in pigs using data from a commercial crossbred population: insights from the Duroc x (Landrace x Yorkshire) three-way crossbreeding system. ''Genet Sel Evol''. 2023 Mar 28; '''55''' (1):21
Multiple founding paternal lineages inferred from the newly-developed 639-plex Y-SNP panel suggested the complex admixture and migration history of Chinese people. Description: He, Guanglin, et al. Multiple founding paternal lineages inferred from the newly-developed 639-plex Y-SNP panel suggested the complex admixture and migration history of Chinese people. ''Hum Genomics''. 2023 Mar 28; '''17''' (1):29
Multi-ancestry meta-analysis of tobacco use disorders based on electronic health record data prioritizes novel candidate risk genes and reveals associations with numerous health outcomes. Description: Toikumo, Sylvanus, et al. Multi-ancestry meta-analysis of tobacco use disorders based on electronic health record data prioritizes novel candidate risk genes and reveals associations with numerous health outcomes. ''medRxiv''. 2023 Mar 29;
Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits. Description: Park, Joshua K, et al. Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits. ''Elife''. 2023 Mar 29; '''12''':
In silico prioritisation of microRNA-associated common variants in multiple sclerosis. Description: Fashina, Ifeolutembi A, et al. In silico prioritisation of microRNA-associated common variants in multiple sclerosis. ''Hum Genomics''. 2023 Mar 30; '''17''' (1):31
Integration of epigenetic and genetic profiles identifies multiple sclerosis disease-critical cell types and genes. Description: Ma, Qin, et al. Integration of epigenetic and genetic profiles identifies multiple sclerosis disease-critical cell types and genes. ''Commun Biol''. 2023 Mar 30; '''6''' (1):342
Genetic correlations between Alzheimer's disease and gut microbiome genera. Description: Cammann, Davis, et al. Genetic correlations between Alzheimer's disease and gut microbiome genera. ''Sci Rep''. 2023 Mar 31; '''13''' (1):5258
Genetic variants and haplotypes in fibulin-5 (FBLN5) are associated with pseudoexfoliation glaucoma but not with pseudoexfoliation syndrome. Description: Kapuganti, Ramani Shyam, et al. Genetic variants and haplotypes in fibulin-5 (FBLN5) are associated with pseudoexfoliation glaucoma but not with pseudoexfoliation syndrome. ''Biosci Rep''. 2023 Mar 31; '''43''' (3):
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. Description: Suzuki, Ken, et al. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. ''medRxiv''. 2023 Mar 31;
A genome-wide association study identified new variants associated with mathematical abilities in Chinese children. Description: Zhang, Liming, et al. A genome-wide association study identified new variants associated with mathematical abilities in Chinese children. ''Genes Brain Behav''. 2023 Apr; '''22''' (2):e12843
Brain structure and allelic associations in Alzheimer's disease. Description: Moon, Seok Woo, et al. Brain structure and allelic associations in Alzheimer's disease. ''CNS Neurosci Ther''. 2023 Apr; '''29''' (4):1034-1048
Causal linkage of tobacco smoking with ageing: Mendelian randomization analysis towards telomere attrition and sarcopenia. Description: Park, Sehoon, et al. Causal linkage of tobacco smoking with ageing: Mendelian randomization analysis towards telomere attrition and sarcopenia. ''J Cachexia Sarcopenia Muscle''. 2023 Apr; '''14''' (2):955-963
CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome. Description: Pinnaro, Catherina T, et al. CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome. ''Hum Genet''. 2023 Apr; '''142''' (4):523-530
Gene polymorphisms associated with heterogeneity and senescence characteristics of sarcopenia in chronic obstructive pulmonary disease. Description: Attaway, Amy H, et al. Gene polymorphisms associated with heterogeneity and senescence characteristics of sarcopenia in chronic obstructive pulmonary disease. ''J Cachexia Sarcopenia Muscle''. 2023 Apr; '''14''' (2):1083-1095
Genetic effects on the timing of parturition and links to fetal birth weight. Description: Sole-Navais, Pol, et al. Genetic effects on the timing of parturition and links to fetal birth weight. ''Nat Genet''. 2023 Apr; '''55''' (4):559-567
Genomic analysis of two phlebotomine sand fly vectors of Leishmania from the New and Old World. Description: Labbe, Frederic, et al. Genomic analysis of two phlebotomine sand fly vectors of Leishmania from the New and Old World. ''PLoS Negl Trop Dis''. 2023 Apr; '''17''' (4):e0010862
Multiple-model GWAS identifies optimal allelic combinations of quantitative trait loci for malic acid in tomato. Description: Gai, Wenxian, et al. Multiple-model GWAS identifies optimal allelic combinations of quantitative trait loci for malic acid in tomato. ''Hortic Res''. 2023 Apr; '''10''' (4):uhad021
Pharmacogenetic actionability and medication prescribing in people with cystic fibrosis. Description: Anderson, Justin D, et al. Pharmacogenetic actionability and medication prescribing in people with cystic fibrosis. ''Clin Transl Sci''. 2023 Apr; '''16''' (4):662-672
Polygenic scores for psychiatric disorders in a diverse postmortem brain tissue cohort. Description: Duncan, Laramie, et al. Polygenic scores for psychiatric disorders in a diverse postmortem brain tissue cohort. ''Neuropsychopharmacology''. 2023 Apr; '''48''' (5):764-772
PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation. Description: Truong, Brittany T, et al. PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation. ''Dis Model Mech''. 2023 Apr 1; '''16''' (4):
Selection, recombination and population history effects on runs of homozygosity (ROH) in wild red deer (Cervus elaphus). Description: Hewett, Anna M, et al. Selection, recombination and population history effects on runs of homozygosity (ROH) in wild red deer (Cervus elaphus). ''Heredity (Edinb)''. 2023 Apr; '''130''' (4):242-250
Spatiotemporal fluctuations of population structure in the Americas revealed by a meta-analysis of the first decade of archaeogenomes. Description: Dos Santos, Andre Luiz Campelo, et al. Spatiotemporal fluctuations of population structure in the Americas revealed by a meta-analysis of the first decade of archaeogenomes. ''Am J Biol Anthropol''. 2023 Apr; '''180''' (4):703-714
The Genetic Architectures of Functional and Structural Connectivity Properties within Cerebral Resting-State Networks. Description: Tissink, Elleke, et al. The Genetic Architectures of Functional and Structural Connectivity Properties within Cerebral Resting-State Networks. ''eNeuro''. 2023 Apr; '''10''' (4):
The genome sequence and demographic history of Przewalskia tangutica (Solanaceae), an endangered alpine plant on the Qinghai-Tibet Plateau. Description: Wu, Ying, et al. The genome sequence and demographic history of Przewalskia tangutica (Solanaceae), an endangered alpine plant on the Qinghai-Tibet Plateau. ''DNA Res''. 2023 Apr 1; '''30''' (2):
Multi-Polymorphism Analysis Reveals Joint Effects in Males With Chronic Central Serous Chorioretinopathy. Description: Chen, Zhen Ji, et al. Multi-Polymorphism Analysis Reveals Joint Effects in Males With Chronic Central Serous Chorioretinopathy. ''Invest Ophthalmol Vis Sci''. 2023 Apr 3; '''64''' (4):19
Multivariate genome-wide association analysis by iterative hard thresholding. Description: Chu, Benjamin B, et al. Multivariate genome-wide association analysis by iterative hard thresholding. ''Bioinformatics''. 2023 Apr 3; '''39''' (4):
Reference genomes of channel catfish and blue catfish reveal multiple pericentric chromosome inversions. Description: Waldbieser, Geoffrey C, et al. Reference genomes of channel catfish and blue catfish reveal multiple pericentric chromosome inversions. ''BMC Biol''. 2023 Apr 3; '''21''' (1):67
Genome-wide association study in 404,302 individuals identifies 7 significant loci for reaction time variability. Description: Wootton, Olivia, et al. Genome-wide association study in 404,302 individuals identifies 7 significant loci for reaction time variability. ''medRxiv''. 2023 Apr 4;
Unprocessed Red Meat and Processed Meat Consumption, Plasma Metabolome, and Risk of Ischemic Heart Disease: A Prospective Cohort Study of UK Biobank. Description: Dong, Xue, et al. Unprocessed Red Meat and Processed Meat Consumption, Plasma Metabolome, and Risk of Ischemic Heart Disease: A Prospective Cohort Study of UK Biobank. ''J Am Heart Assoc''. 2023 Apr 4; '''12''' (7):e027934
Connectome and regulatory hubs of CAGE highly active enhancers. Description: Briend, Mewen, et al. Connectome and regulatory hubs of CAGE highly active enhancers. ''Sci Rep''. 2023 Apr 5; '''13''' (1):5594
High-density single nucleotide polymorphism markers reveal the population structure of 2 local chicken genetic resources. Description: Tolone, Marco, et al. High-density single nucleotide polymorphism markers reveal the population structure of 2 local chicken genetic resources. ''Poult Sci''. 2023 Apr 5; '''102''' (7):102692
Insight into the evolutionary and domesticated history of the most widely cultivated mushroom Agaricus bisporus via mitogenome sequences of 361 global strains. Description: Zhang, Ming-Zhe, et al. Insight into the evolutionary and domesticated history of the most widely cultivated mushroom Agaricus bisporus via mitogenome sequences of 361 global strains. ''BMC Genomics''. 2023 Apr 5; '''24''' (1):182
Population-Based Impact of Smoking, Drinking, and Genetic Factors on HDL-cholesterol Levels in J-MICC Study Participants. Description: Nindita, Yora, et al. Population-Based Impact of Smoking, Drinking, and Genetic Factors on HDL-cholesterol Levels in J-MICC Study Participants. ''J Epidemiol''. 2023 Apr 5; '''33''' (4):193-200
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Description: Matuozzo, Daniela, et al. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. ''Genome Med''. 2023 Apr 5; '''15''' (1):22
The functional change of the P2X7R containing the Ala(348) to Thr polymorphism is associated with the pathogenesis of gout. Description: Li, Man-Yun, et al. The functional change of the P2X7R containing the Ala(348) to Thr polymorphism is associated with the pathogenesis of gout. ''Sci Rep''. 2023 Apr 5; '''13''' (1):5603
Deep learning-based polygenic risk analysis for Alzheimer's disease prediction. Description: Zhou, Xiaopu, et al. Deep learning-based polygenic risk analysis for Alzheimer's disease prediction. ''Commun Med (Lond)''. 2023 Apr 6; '''3''' (1):49
Extensive crop-wild hybridization during Brassica evolution and selection during the domestication and diversification of Brassica crops. Description: Saban, Jasmine M, et al. Extensive crop-wild hybridization during Brassica evolution and selection during the domestication and diversification of Brassica crops. ''Genetics''. 2023 Apr 6; '''223''' (4):
Genomic adaptation to extreme climate conditions in beef cattle as a consequence of cross-breeding program. Description: Tian, Rugang, et al. Genomic adaptation to extreme climate conditions in beef cattle as a consequence of cross-breeding program. ''BMC Genomics''. 2023 Apr 6; '''24''' (1):186
Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Description: Png, Grace, et al. Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. ''Hum Mol Genet''. 2023 Apr 6; '''32''' (8):1266-1275
Multiomics of human aortic endothelial cells reveals cell subtypes with heterogeneous responses to canonical endothelial-to-mesenchymal perturbations. Description: Adelus, Maria L, et al. Multiomics of human aortic endothelial cells reveals cell subtypes with heterogeneous responses to canonical endothelial-to-mesenchymal perturbations. ''bioRxiv''. 2023 Apr 6;
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate. Description: Robinson, Kelsey, et al. Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate. ''medRxiv''. 2023 Apr 6;
Analysis of the Combined Effect of rs699 and rs5051 on Angiotensinogen Expression and Hypertension. Description: Powell, Nicholas R, et al. Analysis of the Combined Effect of rs699 and rs5051 on Angiotensinogen Expression and Hypertension. ''bioRxiv''. 2023 Apr 8;
Effects of epigenetic age acceleration on kidney function: a Mendelian randomization study. Description: Pan, Yang, et al. Effects of epigenetic age acceleration on kidney function: a Mendelian randomization study. ''Clin Epigenetics''. 2023 Apr 8; '''15''' (1):61
Independently evolved pollution resistance in four killifish populations is largely explained by few variants of large effect. Description: Miller, Jeffrey T, et al. Independently evolved pollution resistance in four killifish populations is largely explained by few variants of large effect. ''bioRxiv''. 2023 Apr 8;
The Queensland Twin Adolescent Brain Project, a longitudinal study of adolescent brain development. Description: Strike, Lachlan T, et al. The Queensland Twin Adolescent Brain Project, a longitudinal study of adolescent brain development. ''Sci Data''. 2023 Apr 8; '''10''' (1):195
Tree-based QTL mapping with expected local genetic relatedness matrices. Description: Link, Vivian, et al. Tree-based QTL mapping with expected local genetic relatedness matrices. ''bioRxiv''. 2023 Apr 8;
Analysis of rare Parkinson's disease variants in millions of people. Description: Pitz, Vanessa, et al. Analysis of rare Parkinson's disease variants in millions of people. ''Res Sq''. 2023 Apr 10;
Automated quantitative trait locus analysis (AutoQTL). Description: Freda, Philip J, et al. Automated quantitative trait locus analysis (AutoQTL). ''BioData Min''. 2023 Apr 10; '''16''' (1):14
Bacterial community modifies host genetics effect on early childhood caries. Description: Blostein, Freida, et al. Bacterial community modifies host genetics effect on early childhood caries. ''medRxiv''. 2023 Apr 10;
Hunter-gatherer admixture facilitated natural selection in Neolithic European farmers. Description: Davy, Tom, et al. Hunter-gatherer admixture facilitated natural selection in Neolithic European farmers. ''Curr Biol''. 2023 Apr 10; '''33''' (7):1365-1371.e3
Identification of Genetic Markers Linked to The Activity of Indoleamine 2,3-Dioxygenase and Kidney Function. Description: Kim, Hye-Rim, et al. Identification of Genetic Markers Linked to The Activity of Indoleamine 2,3-Dioxygenase and Kidney Function. ''Metabolites''. 2023 Apr 10; '''13''' (4):
A polygenic basis for birth weight in a wild population of red deer (Cervus elaphus). Description: Gauzere, Julie, et al. A polygenic basis for birth weight in a wild population of red deer (Cervus elaphus). ''G3 (Bethesda)''. 2023 Apr 11; '''13''' (4):
Genetic susceptibility for autoimmune diseases and white blood cell count. Description: Vaitinadin, Nataraja Sarma, et al. Genetic susceptibility for autoimmune diseases and white blood cell count. ''Sci Rep''. 2023 Apr 11; '''13''' (1):5852
Identification of breed-specific genomic variants in Colombian Creole pig breeds by whole-genome sequencing. Description: Suarez-Mesa, Rafael, et al. Identification of breed-specific genomic variants in Colombian Creole pig breeds by whole-genome sequencing. ''Trop Anim Health Prod''. 2023 Apr 11; '''55''' (3):154
Population-size history inferences from the coho salmon (Oncorhynchus kisutch) genome. Description: Rondeau, Eric B, et al. Population-size history inferences from the coho salmon (Oncorhynchus kisutch) genome. ''G3 (Bethesda)''. 2023 Apr 11; '''13''' (4):
Protein coding variation in the J:ARC and J:DO outbred laboratory mouse stocks provides a molecular basis for distinct research applications. Description: Cornes, Belinda K, et al. Protein coding variation in the J:ARC and J:DO outbred laboratory mouse stocks provides a molecular basis for distinct research applications. ''G3 (Bethesda)''. 2023 Apr 11; '''13''' (4):
Application of Mendelian randomization to explore the causal role of the human gut microbiome in colorectal cancer. Description: Hatcher, Charlie, et al. Application of Mendelian randomization to explore the causal role of the human gut microbiome in colorectal cancer. ''Sci Rep''. 2023 Apr 12; '''13''' (1):5968
Characterization of genome-wide STR variation in 6487 human genomes. Description: Shi, Yirong, et al. Characterization of genome-wide STR variation in 6487 human genomes. ''Nat Commun''. 2023 Apr 12; '''14''' (1):2092
Exploring the causal role of the immune response to varicella-zoster virus on multiple traits: a phenome-wide Mendelian randomization study. Description: Yu, Xinzhu, et al. Exploring the causal role of the immune response to varicella-zoster virus on multiple traits: a phenome-wide Mendelian randomization study. ''BMC Med''. 2023 Apr 12; '''21''' (1):143
ME-Bayes SL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups. Description: Jin, Jin, et al. ME-Bayes SL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups. ''bioRxiv''. 2023 Apr 13;
Preliminary Investigation of Essentially Derived Variety of Tea Tree and Development of SNP Markers. Description: Li, Li, et al. Preliminary Investigation of Essentially Derived Variety of Tea Tree and Development of SNP Markers. ''Plants (Basel)''. 2023 Apr 13; '''12''' (8):
A genome-wide scan to identify signatures of selection in Lueyang black -bone chicken. Description: Xue, Zhen, et al. A genome-wide scan to identify signatures of selection in Lueyang black -bone chicken. ''Poult Sci''. 2023 Apr 14; '''102''' (7):102721
Polymorphisms of CARD9 Gene Predict Disease Progression and Renal Survival of Immunoglobulin A Nephropathy. Description: He, Chunhong, et al. Polymorphisms of CARD9 Gene Predict Disease Progression and Renal Survival of Immunoglobulin A Nephropathy. ''Kidney Blood Press Res''. 2023 Apr 14; '''48''' (1):436-44
SOX17 Deficiency Mediates Pulmonary Hypertension: At the Crossroads of Sex, Metabolism, and Genetics. Description: Sangam, Shreya, et al. SOX17 Deficiency Mediates Pulmonary Hypertension: At the Crossroads of Sex, Metabolism, and Genetics. ''Am J Respir Crit Care Med''. 2023 Apr 15; '''207''' (8):1055-1069
CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis. Description: Nuzhat, Nafisa, et al. CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis. ''J Clin Invest''. 2023 Apr 17; '''133''' (8):
Longitudinal fundus imaging and its genome-wide association analysis provide evidence for a human retinal aging clock. Description: Ahadi, Sara, et al. Longitudinal fundus imaging and its genome-wide association analysis provide evidence for a human retinal aging clock. ''Elife''. 2023 Apr 17; '''12''':
The causal role of intestinal microbiome in development of pre-eclampsia. Description: Xiong, Zhihui, et al. The causal role of intestinal microbiome in development of pre-eclampsia. ''Funct Integr Genomics''. 2023 Apr 17; '''23''' (2):127
Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics. Description: Chan, Tsz Fung, et al. Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics. ''bioRxiv''. 2023 Apr 18;
Population dynamics and drug resistance mutations in Plasmodium falciparum on the Bijagos Archipelago, Guinea-Bissau. Description: Moss, Sophie, et al. Population dynamics and drug resistance mutations in Plasmodium falciparum on the Bijagos Archipelago, Guinea-Bissau. ''Sci Rep''. 2023 Apr 18; '''13''' (1):6311
Population genomic analysis provides evidence of the past success and future potential of South China tiger captive conservation. Description: Wang, Chen, et al. Population genomic analysis provides evidence of the past success and future potential of South China tiger captive conservation. ''BMC Biol''. 2023 Apr 18; '''21''' (1):64
A Comprehensive Analysis of 21 Actionable Pharmacogenes in the Spanish Population: From Genetic Characterisation to Clinical Impact. Description: Nunez-Torres, Rocio, et al. A Comprehensive Analysis of 21 Actionable Pharmacogenes in the Spanish Population: From Genetic Characterisation to Clinical Impact. ''Pharmaceutics''. 2023 Apr 19; '''15''' (4):
Genetic analysis of global faba bean diversity, agronomic traits and selection signatures. Description: Skovbjerg, Cathrine Kiel, et al. Genetic analysis of global faba bean diversity, agronomic traits and selection signatures. ''Theor Appl Genet''. 2023 Apr 19; '''136''' (5):114
Genetic regulatory and biological implications of the 10q24.32 schizophrenia risk locus. Description: Wang, Junyang, et al. Genetic regulatory and biological implications of the 10q24.32 schizophrenia risk locus. ''Brain''. 2023 Apr 19; '''146''' (4):1403-1419
Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population. Description: Zhang, Zhu, et al. Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population. ''BMC Med''. 2023 Apr 19; '''21''' (1):153
Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs. Description: Han, Seong Kyu, et al. Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs. ''Nat Commun''. 2023 Apr 19; '''14''' (1):2229
Using allele scores to identify confounding by reverse causation: studies of alcohol consumption as an exemplar. Description: Sallis, Hannah M, et al. Using allele scores to identify confounding by reverse causation: studies of alcohol consumption as an exemplar. ''Int J Epidemiol''. 2023 Apr 19; '''52''' (2):536-544
Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients. Description: Wu, Yiming, et al. Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients. ''Nat Commun''. 2023 Apr 20; '''14''' (1):2256
The ACE rs1799752 Variant Is Associated with COVID-19 Severity but Is Independent of Serum ACE Activity in Hospitalized and Recovered Patients. Description: Fricke-Galindo, Ingrid, et al. The ACE rs1799752 Variant Is Associated with COVID-19 Severity but Is Independent of Serum ACE Activity in Hospitalized and Recovered Patients. ''Int J Mol Sci''. 2023 Apr 21; '''24''' (8):
Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation. Description: He, Xinmiao, et al. Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation. ''Vet Sci''. 2023 Apr 23; '''10''' (5):
Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome. Description: Lancaster, Megan C, et al. Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome. ''medRxiv''. 2023 Apr 25;
Leveraging IgG N-glycosylation to infer the causality between T2D and hypertension. Description: Wang, Haotian, et al. Leveraging IgG N-glycosylation to infer the causality between T2D and hypertension. ''Diabetol Metab Syndr''. 2023 Apr 25; '''15''' (1):80
The adaptive evolution of cancer driver genes. Description: Gu, Langyu, et al. The adaptive evolution of cancer driver genes. ''BMC Genomics''. 2023 Apr 25; '''24''' (1):215
Genetic structure of an endangered species Ormosia henryi in southern China, and implications for conservation. Description: Zhou, Chengchuan, et al. Genetic structure of an endangered species Ormosia henryi in southern China, and implications for conservation. ''BMC Plant Biol''. 2023 Apr 26; '''23''' (1):220
Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer disease. Description: Ali, Muhammad, et al. Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer disease. ''Acta Neuropathol Commun''. 2023 Apr 26; '''11''' (1):68
When One's Not Enough: Colony Pool-Seq Outperforms Individual-Based Methods for Assessing Introgression in Apis mellifera mellifera. Description: Buswell, Victoria G, et al. When One's Not Enough: Colony Pool-Seq Outperforms Individual-Based Methods for Assessing Introgression in Apis mellifera mellifera. ''Insects''. 2023 Apr 27; '''14''' (5):
The Newfoundland and Labrador mosaic founder population descends from an Irish and British diaspora from 300 years ago. Description: Gilbert, Edmund, et al. The Newfoundland and Labrador mosaic founder population descends from an Irish and British diaspora from 300 years ago. ''Commun Biol''. 2023 Apr 28; '''6''' (1):469
Investigating the association between glycaemic traits and colorectal cancer in the Japanese population using Mendelian randomisation. Description: Hanyuda, Akiko, et al. Investigating the association between glycaemic traits and colorectal cancer in the Japanese population using Mendelian randomisation. ''Sci Rep''. 2023 Apr 29; '''13''' (1):7052
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Description: Barry, Alexandra, et al. Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. ''Nat Commun''. 2023 Apr 29; '''14''' (1):2481
Unsupervised representation learning improves genomic discovery for lung function and respiratory disease prediction. Description: Yun, Taedong, et al. Unsupervised representation learning improves genomic discovery for lung function and respiratory disease prediction. ''medRxiv''. 2023 Apr 29;
A benchmark study on current GWAS models in admixed populations. Description: Yang, Zikun, et al. A benchmark study on current GWAS models in admixed populations. ''bioRxiv''. 2023 Apr 30;
Association between vascular ultrasound features and DNA sequencing in breast cancer: a preliminary study. Description: Han, Mi-Ryung, et al. Association between vascular ultrasound features and DNA sequencing in breast cancer: a preliminary study. ''Discov Oncol''. 2023 Apr 30; '''14''' (1):52
A candidate locus in the renalase gene and susceptibility to blood pressure responses to the dietary salt. Description: A candidate locus in the renalase gene and susceptibility to blood pressure responses to the dietary salt. ''''. 2023 May 1; '''41''' (5):723-732
A novel candidate gene CLN8 regulates fat deposition in avian. Description: Li, Xiaoqin, et al. A novel candidate gene CLN8 regulates fat deposition in avian. ''J Anim Sci Biotechnol''. 2023 May 1; '''14''' (1):70
APOL1 and the risk of adverse renal outcomes in patients of African ancestry with systemic lupus erythematosus. Description: Chung, Cecilia P, et al. APOL1 and the risk of adverse renal outcomes in patients of African ancestry with systemic lupus erythematosus. ''Lupus''. 2023 May; '''32''' (6):763-770
A secreted protease-like protein in Zymoseptoria tritici is responsible for avirulence on Stb9 resistance gene in wheat. Description: Amezrou, Reda, et al. A secreted protease-like protein in Zymoseptoria tritici is responsible for avirulence on Stb9 resistance gene in wheat. ''PLoS Pathog''. 2023 May; '''19''' (5):e1011376
Association between inflammation and cognition: Triangulation of evidence using a population-based cohort and Mendelian randomization analyses. Description: Slaney, Chloe, et al. Association between inflammation and cognition: Triangulation of evidence using a population-based cohort and Mendelian randomization analyses. ''Brain Behav Immun''. 2023 May; '''110''': 30-42
Defining the key intrahepatic gene networks in HCV infection driven by sex. Description: Marchi, Emanuele, et al. Defining the key intrahepatic gene networks in HCV infection driven by sex. ''Gut''. 2023 May; '''72''' (5):984-994
Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia. Description: Rammos, Alexandros, et al. Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia. ''Mol Psychiatry''. 2023 May; '''28''' (5):2081-2087
Genetic factors associated with serum amylase in a Japanese population: combined analysis of copy-number and single-nucleotide variants. Description: Nayema, Zannatun, et al. Genetic factors associated with serum amylase in a Japanese population: combined analysis of copy-number and single-nucleotide variants. ''J Hum Genet''. 2023 May; '''68''' (5):313-319
Genetic variants influenced the risk of bleeding and pharmacodynamics of rivaroxaban in patients with nonvalvular atrial fibrillation: A multicentre prospective cohort study. Description: Xiang, Qian, et al. Genetic variants influenced the risk of bleeding and pharmacodynamics of rivaroxaban in patients with nonvalvular atrial fibrillation: A multicentre prospective cohort study. ''Clin Transl Med''. 2023 May; '''13''' (5):e1263
Highly complete long-read genomes reveal pangenomic variation underlying yeast phenotypic diversity. Description: Weller, Cory A, et al. Highly complete long-read genomes reveal pangenomic variation underlying yeast phenotypic diversity. ''Genome Res''. 2023 May; '''33''' (5):729-740
High-resolution structural variants catalogue in a large-scale whole genome sequenced bovine family cohort data. Description: Lee, Young-Lim, et al. High-resolution structural variants catalogue in a large-scale whole genome sequenced bovine family cohort data. ''BMC Genomics''. 2023 May 1; '''24''' (1):225
Identification of TaGL1-B1 gene controlling grain length through regulation of jasmonic acid in common wheat. Description: Niaz, Mohsin, et al. Identification of TaGL1-B1 gene controlling grain length through regulation of jasmonic acid in common wheat. ''Plant Biotechnol J''. 2023 May; '''21''' (5):979-989
Incidence of LADA and Type 2 Diabetes in Relation to Tobacco Use and Genetic Susceptibility to Type 2 Diabetes and Related Traits: Findings From a Swedish Case-Control Study and the Norwegian HUNT Study. Description: Edstorp, Jessica, et al. Incidence of LADA and Type 2 Diabetes in Relation to Tobacco Use and Genetic Susceptibility to Type 2 Diabetes and Related Traits: Findings From a Swedish Case-Control Study and the Norwegian HUNT Study. ''Diabetes Care''. 2023 May 1; '''46''' (5):1028-1036
Multisite Pain and Myocardial Infarction and Stroke: A Prospective Cohort and Mendelian Randomization Analysis. Description: Tian, Jing, et al. Multisite Pain and Myocardial Infarction and Stroke: A Prospective Cohort and Mendelian Randomization Analysis. ''JACC Adv''. 2023 May; '''2''' (3):100295
On the holobiont 'predictome' of immunocompetence in pigs. Description: Calle-Garcia, Joan, et al. On the holobiont 'predictome' of immunocompetence in pigs. ''Genet Sel Evol''. 2023 May 1; '''55''' (1):29
Partner choice, confounding and trait convergence all contribute to phenotypic partner similarity. Description: Sjaarda, Jennifer, et al. Partner choice, confounding and trait convergence all contribute to phenotypic partner similarity. ''Nat Hum Behav''. 2023 May; '''7''' (5):776-789
Population genomics and conservation management of the threatened black-footed tree-rat (Mesembriomys gouldii) in northern Australia. Description: von Takach, Brenton, et al. Population genomics and conservation management of the threatened black-footed tree-rat (Mesembriomys gouldii) in northern Australia. ''Heredity (Edinb)''. 2023 May; '''130''' (5):278-288
Recombination between heterologous human acrocentric chromosomes. Description: Guarracino, Andrea, et al. Recombination between heterologous human acrocentric chromosomes. ''Nature''. 2023 May; '''617''' (7960):335-343
Recurrent 17q12 microduplications contribute to renal disease but not diabetes. Description: Cannon, Stuart, et al. Recurrent 17q12 microduplications contribute to renal disease but not diabetes. ''J Med Genet''. 2023 May; '''60''' (5):491-497
Super-pangenome analyses highlight genomic diversity and structural variation across wild and cultivated tomato species. Description: Li, Ning, et al. Super-pangenome analyses highlight genomic diversity and structural variation across wild and cultivated tomato species. ''Nat Genet''. 2023 May; '''55''' (5):852-860
Whole genome analyses reveal novel genes associated with chicken adaptation to tropical and frigid environments. Description: Shi, Shourong, et al. Whole genome analyses reveal novel genes associated with chicken adaptation to tropical and frigid environments. ''J Adv Res''. 2023 May; '''47''': 13-25
Association between the LRP1B and APOE loci and the development of Parkinson's disease dementia. Description: Real, Raquel, et al. Association between the LRP1B and APOE loci and the development of Parkinson's disease dementia. ''Brain''. 2023 May 2; '''146''' (5):1873-1887
Conservation management strategy impacts inbreeding and mutation load in scimitar-horned oryx. Description: Humble, Emily, et al. Conservation management strategy impacts inbreeding and mutation load in scimitar-horned oryx. ''Proc Natl Acad Sci U S A''. 2023 May 2; '''120''' (18):e2210756120
Extensive intra- and inter-genetic admixture of Chinese gamecock and other indigenous chicken breeds revealed by genomic data. Description: Ren, Xufang, et al. Extensive intra- and inter-genetic admixture of Chinese gamecock and other indigenous chicken breeds revealed by genomic data. ''Poult Sci''. 2023 May 2; '''102''' (7):102766
Population Genomic Evidence of Adaptive Response during the Invasion History of Plasmodium falciparum in the Americas. Description: Lefebvre, Margaux J M, et al. Population Genomic Evidence of Adaptive Response during the Invasion History of Plasmodium falciparum in the Americas. ''Mol Biol Evol''. 2023 May 2; '''40''' (5):
Genome-wide assessment and mapping of inbreeding depression identifies candidate genes associated with semen traits in Holstein bulls. Description: Ghoreishifar, Mohammad, et al. Genome-wide assessment and mapping of inbreeding depression identifies candidate genes associated with semen traits in Holstein bulls. ''BMC Genomics''. 2023 May 3; '''24''' (1):230
Genomic variability and population structure of six Colombian cattle breeds. Description: Martinez, Rodrigo, et al. Genomic variability and population structure of six Colombian cattle breeds. ''Trop Anim Health Prod''. 2023 May 3; '''55''' (3):185
Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulation. Description: Peachey, Neal, et al. Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulation. ''Res Sq''. 2023 May 3;
Selection-driven trait loss in independently evolved cavefish populations. Description: Moran, Rachel L, et al. Selection-driven trait loss in independently evolved cavefish populations. ''Nat Commun''. 2023 May 3; '''14''' (1):2557
Dissecting the polygenic basis of atherosclerosis via disease-associated cell state signatures. Description: Ord, Tiit, et al. Dissecting the polygenic basis of atherosclerosis via disease-associated cell state signatures. ''Am J Hum Genet''. 2023 May 4; '''110''' (5):722-740
Genetic heritage of the Baphuthi highlights an over-ethnicized notion of "Bushman" in the Maloti-Drakensberg, southern Africa. Description: Daniels, Ryan Joseph, et al. Genetic heritage of the Baphuthi highlights an over-ethnicized notion of "Bushman" in the Maloti-Drakensberg, southern Africa. ''Am J Hum Genet''. 2023 May 4; '''110''' (5):880-894
Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis. Description: Miyahara, Kazusa, et al. Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis. ''Transl Psychiatry''. 2023 May 4; '''13''' (1):144
Investigating the relationship between depression and breast cancer: observational and genetic analyses. Description: Wu, Xueyao, et al. Investigating the relationship between depression and breast cancer: observational and genetic analyses. ''BMC Med''. 2023 May 4; '''21''' (1):170
Whole-genome sequencing identifies interferon-induced protein IFI6/IFI27-like as a strong candidate gene for VNN resistance in European sea bass. Description: Delpuech, Emilie, et al. Whole-genome sequencing identifies interferon-induced protein IFI6/IFI27-like as a strong candidate gene for VNN resistance in European sea bass. ''Genet Sel Evol''. 2023 May 4; '''55''' (1):30
Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis. Description: Yarmolinsky, James, et al. Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis. ''medRxiv''. 2023 May 5;
Evaluation of the Performance of the RECODe Equation with the Addition of Polygenic Risk Scores for Adverse Cardiovascular Outcomes in Individuals with Type II Diabetes. Description: Tsao, Noah L, et al. Evaluation of the Performance of the RECODe Equation with the Addition of Polygenic Risk Scores for Adverse Cardiovascular Outcomes in Individuals with Type II Diabetes. ''medRxiv''. 2023 May 5;
Genetic dissection of behavioral traits related to successful training of drug detection dogs. Description: Matsumoto, Yuki, et al. Genetic dissection of behavioral traits related to successful training of drug detection dogs. ''Sci Rep''. 2023 May 5; '''13''' (1):7326
netMUG: a novel network-guided multi-view clustering workflow for dissecting genetic and facial heterogeneity. Description: Li, Zuqi, et al. netMUG: a novel network-guided multi-view clustering workflow for dissecting genetic and facial heterogeneity. ''bioRxiv''. 2023 May 5;
Predicting environmental and ecological drivers of human population structure. Description: Pless, Evlyn, et al. Predicting environmental and ecological drivers of human population structure. ''Mol Biol Evol''. 2023 May 5; '''40''' (5):
Strategies to improve genomic predictions for 35 duck carcass traits in an F(2) population. Description: Cai, Wentao, et al. Strategies to improve genomic predictions for 35 duck carcass traits in an F(2) population. ''J Anim Sci Biotechnol''. 2023 May 6; '''14''' (1):74
Automatic landmarking identifies new loci associated with face morphology and implicates Neanderthal introgression in human nasal shape. Description: Li, Qing, et al. Automatic landmarking identifies new loci associated with face morphology and implicates Neanderthal introgression in human nasal shape. ''Commun Biol''. 2023 May 8; '''6''' (1):481
Fast integration and accumulation of beneficial breeding alleles through an AB-NAMIC strategy in wheat. Description: Jiao, Chengzhi, et al. Fast integration and accumulation of beneficial breeding alleles through an AB-NAMIC strategy in wheat. ''Plant Commun''. 2023 May 8; '''4''' (3):100549
HIBLUP: an integration of statistical models on the BLUP framework for efficient genetic evaluation using big genomic data. Description: Yin, Lilin, et al. HIBLUP: an integration of statistical models on the BLUP framework for efficient genetic evaluation using big genomic data. ''Nucleic Acids Res''. 2023 May 8; '''51''' (8):3501-3512
Pistachio genomes provide insights into nut tree domestication and ZW sex chromosome evolution. Description: Kafkas, Salih, et al. Pistachio genomes provide insights into nut tree domestication and ZW sex chromosome evolution. ''Plant Commun''. 2023 May 8; '''4''' (3):100497
Influence of TPH2 and HTR1A polymorphisms on lifelong premature ejaculation risk among the chinese Han population. Description: Wang, Fei, et al. Influence of TPH2 and HTR1A polymorphisms on lifelong premature ejaculation risk among the chinese Han population. ''BMC Urol''. 2023 May 9; '''23''' (1):86
A deep catalog of protein-coding variation in 985,830 individuals. Description: Sun, Kathie Y, et al. A deep catalog of protein-coding variation in 985,830 individuals. ''bioRxiv''. 2023 May 10;
Exploring the genetic correlation of cardiovascular diseases and mood disorders in the UK Biobank. Description: Chen, Chi-Jen, et al. Exploring the genetic correlation of cardiovascular diseases and mood disorders in the UK Biobank. ''Epidemiol Psychiatr Sci''. 2023 May 10; '''32''': e31
Genetic basis of STEM occupational choice and regional economic performance: a UK biobank genome-wide association study. Description: Zhu, Chen, et al. Genetic basis of STEM occupational choice and regional economic performance: a UK biobank genome-wide association study. ''Hum Genomics''. 2023 May 10; '''17''' (1):40
Gene-x-environment analysis supports protective effects of eveningness chronotype on self-reported and actigraphy-derived sleep duration among those who always work night shifts in the UK Biobank. Description: Akimova, Evelina T, et al. Gene-x-environment analysis supports protective effects of eveningness chronotype on self-reported and actigraphy-derived sleep duration among those who always work night shifts in the UK Biobank. ''Sleep''. 2023 May 10; '''46''' (5):
Improving the accuracy of genomic prediction for meat quality traits using whole genome sequence data in pigs. Description: Zhuang, Zhanwei, et al. Improving the accuracy of genomic prediction for meat quality traits using whole genome sequence data in pigs. ''J Anim Sci Biotechnol''. 2023 May 10; '''14''' (1):67
Polygenic risk affects the penetrance of monogenic kidney disease. Description: Khan, Atlas, et al. Polygenic risk affects the penetrance of monogenic kidney disease. ''medRxiv''. 2023 May 10;
A comprehensive analysis of copy number variations in diverse apple populations. Description: Xu, Jinsheng, et al. A comprehensive analysis of copy number variations in diverse apple populations. ''BMC Genomics''. 2023 May 11; '''24''' (1):256
Sex differences in the polygenic architecture of hearing problems in adults. Description: De Angelis, Flavio, et al. Sex differences in the polygenic architecture of hearing problems in adults. ''Genome Med''. 2023 May 11; '''15''' (1):36
The eQTL colocalization and transcriptome-wide association study identify potentially causal genes responsible for economic traits in Simmental beef cattle. Description: Cai, Wentao, et al. The eQTL colocalization and transcriptome-wide association study identify potentially causal genes responsible for economic traits in Simmental beef cattle. ''J Anim Sci Biotechnol''. 2023 May 11; '''14''' (1):78
The size and composition of haplotype reference panels impact the accuracy of imputation from low-pass sequencing in cattle. Description: Lloret-Villas, Audald, et al. The size and composition of haplotype reference panels impact the accuracy of imputation from low-pass sequencing in cattle. ''Genet Sel Evol''. 2023 May 11; '''55''' (1):33
Germline modifiers of the tumor immune microenvironment implicate drivers of cancer risk and immunotherapy response. Description: Pagadala, Meghana, et al. Germline modifiers of the tumor immune microenvironment implicate drivers of cancer risk and immunotherapy response. ''Nat Commun''. 2023 May 12; '''14''' (1):2744
Oryza CLIMtools: An Online Portal for Investigating Genome-Environment Associations in Rice. Description: Ferrero-Serrano, Angel, et al. Oryza CLIMtools: An Online Portal for Investigating Genome-Environment Associations in Rice. ''bioRxiv''. 2023 May 12;
Variation along P2RX7 interacts with early traumas on severity of anxiety suggesting a role for neuroinflammation. Description: Kristof, Zsuliet, et al. Variation along P2RX7 interacts with early traumas on severity of anxiety suggesting a role for neuroinflammation. ''Sci Rep''. 2023 May 12; '''13''' (1):7757
Association between CLOCK Gene Polymorphisms and Insomnia Risk According to Food Groups: A KoGES Longitudinal Study. Description: Lee, Sunghee. Association between CLOCK Gene Polymorphisms and Insomnia Risk According to Food Groups: A KoGES Longitudinal Study. ''Nutrients''. 2023 May 13; '''15''' (10):
Functional variants identify sex-specific genes and pathways in Alzheimer's Disease. Description: Bourquard, Thomas, et al. Functional variants identify sex-specific genes and pathways in Alzheimer's Disease. ''Nat Commun''. 2023 May 13; '''14''' (1):2765
Development and testing of a polygenic risk score for breast cancer aggressiveness. Description: Shieh, Yiwey, et al. Development and testing of a polygenic risk score for breast cancer aggressiveness. ''NPJ Precis Oncol''. 2023 May 15; '''7''' (1):42
Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes. Description: Villaplana-Velasco, Ana, et al. Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes. ''Commun Biol''. 2023 May 15; '''6''' (1):523
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes. Description: McAllan, Liam, et al. Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes. ''Nat Commun''. 2023 May 15; '''14''' (1):2784
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy. Description: Ollila, Hanna M, et al. Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy. ''Nat Commun''. 2023 May 15; '''14''' (1):2709
Predictive network analysis identifies JMJD6 and other potential key drivers in Alzheimer's disease. Description: Merchant, Julie P, et al. Predictive network analysis identifies JMJD6 and other potential key drivers in Alzheimer's disease. ''Commun Biol''. 2023 May 15; '''6''' (1):503
Prioritization of potential causative genes for schizophrenia in placenta. Description: Ursini, Gianluca, et al. Prioritization of potential causative genes for schizophrenia in placenta. ''Nat Commun''. 2023 May 15; '''14''' (1):2613
Disentangling the genetic overlap and causal relationships between primary open-angle glaucoma, brain morphology and four major neurodegenerative disorders. Description: Diaz-Torres, Santiago, et al. Disentangling the genetic overlap and causal relationships between primary open-angle glaucoma, brain morphology and four major neurodegenerative disorders. ''EBioMedicine''. 2023 May 16; '''92''': 104615
Genetic Diversity and Breeding Signatures for Regional Indica Rice Improvement in Guangdong of Southern China. Description: Hang, Yu, et al. Genetic Diversity and Breeding Signatures for Regional Indica Rice Improvement in Guangdong of Southern China. ''Rice (N Y)''. 2023 May 16; '''16''' (1):25
Genetic prediction of colitis in non-small cell lung cancer patients on immune checkpoint inhibitor therapy. Description: Middha, Pooja, et al. Genetic prediction of colitis in non-small cell lung cancer patients on immune checkpoint inhibitor therapy. ''medRxiv''. 2023 May 16;
Population structure analysis to explore genetic diversity and geographical distribution characteristics of wild tea plant in Guizhou Plateau. Description: He, Limin, et al. Population structure analysis to explore genetic diversity and geographical distribution characteristics of wild tea plant in Guizhou Plateau. ''BMC Plant Biol''. 2023 May 16; '''23''' (1):255
Insights into human health from phenome- and genome-wide analyses of UK Biobank retinal optical coherence tomography phenotypes. Description: Zekavat, Seyedeh Maryam, et al. Insights into human health from phenome- and genome-wide analyses of UK Biobank retinal optical coherence tomography phenotypes. ''medRxiv''. 2023 May 17;
Defining honeybee subspecies in an evolutionary context warrants strategized conservation. Description: Qiu, Lifei, et al. Defining honeybee subspecies in an evolutionary context warrants strategized conservation. ''Zool Res''. 2023 May 18; '''44''' (3):483-493
Genetic and epidemiological analyses of infection load and its relationship with psychiatric disorders. Description: Nudel, Ron, et al. Genetic and epidemiological analyses of infection load and its relationship with psychiatric disorders. ''Epidemiol Infect''. 2023 May 18; '''151''': e93
Association of NAFLD with FGF21 Polygenic Hazard Score, and Its Interaction with Protein Intake Level in Korean Adults. Description: Lee, Hae Jin, et al. Association of NAFLD with FGF21 Polygenic Hazard Score, and Its Interaction with Protein Intake Level in Korean Adults. ''Nutrients''. 2023 May 19; '''15''' (10):
Environment as a limiting factor of the historical global spread of mungbean. Description: Ong, Pei-Wen, et al. Environment as a limiting factor of the historical global spread of mungbean. ''Elife''. 2023 May 19; '''12''':
Restriction site-associated DNA sequencing technologies as an alternative to low-density SNP chips for genomic selection: a simulation study in layer chickens. Description: Herry, Florian, et al. Restriction site-associated DNA sequencing technologies as an alternative to low-density SNP chips for genomic selection: a simulation study in layer chickens. ''BMC Genomics''. 2023 May 19; '''24''' (1):271
Identifying signatures of positive selection in human populations from North Africa. Description: Caro-Consuegra, Rocio, et al. Identifying signatures of positive selection in human populations from North Africa. ''Sci Rep''. 2023 May 20; '''13''' (1):8166
Graph construction method impacts variation representation and analyses in a bovine super-pangenome. Description: Leonard, Alexander S, et al. Graph construction method impacts variation representation and analyses in a bovine super-pangenome. ''Genome Biol''. 2023 May 22; '''24''' (1):124
Profiling the immune epigenome across global cattle breeds. Description: Powell, Jessica, et al. Profiling the immune epigenome across global cattle breeds. ''Genome Biol''. 2023 May 22; '''24''' (1):127
Circulating S100B levels at birth and risk of six major neuropsychiatric or neurological disorders: a two-sample Mendelian Randomization Study. Description: Pan, Mengyu, et al. Circulating S100B levels at birth and risk of six major neuropsychiatric or neurological disorders: a two-sample Mendelian Randomization Study. ''Transl Psychiatry''. 2023 May 24; '''13''' (1):174
Harmonization of CSF and imaging biomarkers for Alzheimer's disease biomarkers: need and practical applications for genetics studies and preclinical classification. Description: Timsina, Jigyasha, et al. Harmonization of CSF and imaging biomarkers for Alzheimer's disease biomarkers: need and practical applications for genetics studies and preclinical classification. ''bioRxiv''. 2023 May 24;
Regulation of inflammation and protection against invasive pneumococcal infection by the long pentraxin PTX3. Description: Porte, Remi, et al. Regulation of inflammation and protection against invasive pneumococcal infection by the long pentraxin PTX3. ''Elife''. 2023 May 24; '''12''':
The MC1R r allele does not increase melanoma risk in MITF E318K carriers. Description: Wallingford, Courtney K, et al. The MC1R r allele does not increase melanoma risk in MITF E318K carriers. ''Br J Dermatol''. 2023 May 24; '''188''' (6):770-776
A Multi-Omic Mosaic Model of Acetaminophen Induced Alanine Aminotransferase Elevation. Description: Monte, Andrew A, et al. A Multi-Omic Mosaic Model of Acetaminophen Induced Alanine Aminotransferase Elevation. ''J Med Toxicol''. 2023 May 25; 1-7
A genomic data archive from the Network for Pancreatic Organ donors with Diabetes. Description: Perry, Daniel J, et al. A genomic data archive from the Network for Pancreatic Organ donors with Diabetes. ''Sci Data''. 2023 May 26; '''10''' (1):323
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population. Description: Shi, Jianxin, et al. Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population. ''Nat Commun''. 2023 May 26; '''14''' (1):3043
The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. Description: Ou, Ya-Nan, et al. The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. ''Transl Psychiatry''. 2023 May 26; '''13''' (1):180
Evolutionarily recent retrotransposons contribute to schizophrenia. Description: Modenini, Giorgia, et al. Evolutionarily recent retrotransposons contribute to schizophrenia. ''Transl Psychiatry''. 2023 May 27; '''13''' (1):181
Association of neurotransmitter pathway polygenic risk with specific symptom profiles in psychosis. Description: Warren, Tracy L, et al. Association of neurotransmitter pathway polygenic risk with specific symptom profiles in psychosis. ''medRxiv''. 2023 May 28;
SOX7: Novel Autistic Gene Identified by Analysis of Multi-Omics Data. Description: Gonzales, Samantha, et al. SOX7: Novel Autistic Gene Identified by Analysis of Multi-Omics Data. ''bioRxiv''. 2023 May 28;
Biomarker and genomic analyses reveal molecular signatures of non-cardioembolic ischemic stroke. Description: Ding, Lingling, et al. Biomarker and genomic analyses reveal molecular signatures of non-cardioembolic ischemic stroke. ''Signal Transduct Target Ther''. 2023 May 30; '''8''' (1):222
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. Description: Martinez-Carrasco, Alejandro, et al. Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. ''medRxiv''. 2023 May 30;
Inferring cell-type-specific causal gene regulatory networks during human neurogenesis. Description: Aygun, Nil, et al. Inferring cell-type-specific causal gene regulatory networks during human neurogenesis. ''Genome Biol''. 2023 May 30; '''24''' (1):130
Multigenic resistance to Xylella fastidiosa in wild grapes (Vitis sps.) and its implications within a changing climate. Description: Morales-Cruz, Abraham, et al. Multigenic resistance to Xylella fastidiosa in wild grapes (Vitis sps.) and its implications within a changing climate. ''Commun Biol''. 2023 May 30; '''6''' (1):580
The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Description: Xia, Charley, et al. The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. ''Nat Commun''. 2023 May 30; '''14''' (1):3146
The shared genetic architecture of smoking behaviours and psychiatric disorders: evidence from a population-based longitudinal study in England. Description: Ajnakina, Olesya, et al. The shared genetic architecture of smoking behaviours and psychiatric disorders: evidence from a population-based longitudinal study in England. ''BMC Genom Data''. 2023 May 30; '''24''' (1):31
The SWine IMputation (SWIM) haplotype reference panel enables nucleotide resolution genetic mapping in pigs. Description: Ding, Rongrong, et al. The SWine IMputation (SWIM) haplotype reference panel enables nucleotide resolution genetic mapping in pigs. ''Commun Biol''. 2023 May 30; '''6''' (1):577
Association of Polymorphisms in ZFHX1B and PAX6 With Anisometropia in Chinese Children: The Hong Kong Children Eye Genetics Study. Description: Wang, Yu Yao, et al. Association of Polymorphisms in ZFHX1B and PAX6 With Anisometropia in Chinese Children: The Hong Kong Children Eye Genetics Study. ''Invest Ophthalmol Vis Sci''. 2023 Jun 1; '''64''' (7):6
Autosomal recessive hyposegmentation of granulocytes in Australian Shepherd Dogs indicates a role for LMBR1L in myeloid leukocytes. Description: Lourdes Frehner, Bianca, et al. Autosomal recessive hyposegmentation of granulocytes in Australian Shepherd Dogs indicates a role for LMBR1L in myeloid leukocytes. ''PLoS Genet''. 2023 Jun; '''19''' (6):e1010805
Breed identification using breed-informative SNPs and machine learning based on whole genome sequence data and SNP chip data. Description: Zhao, Changheng, et al. Breed identification using breed-informative SNPs and machine learning based on whole genome sequence data and SNP chip data. ''J Anim Sci Biotechnol''. 2023 Jun 1; '''14''' (1):85
Childhood, adolescent, and adulthood adiposity are associated with risk of PCOS: a Mendelian randomization study with meta-analysis. Description: Dobbie, Laurence J, et al. Childhood, adolescent, and adulthood adiposity are associated with risk of PCOS: a Mendelian randomization study with meta-analysis. ''Hum Reprod''. 2023 Jun 1; '''38''' (6):1168-1182
Clinical and genome-wide association analysis of chemoradiation-induced hearing loss in nasopharyngeal carcinoma. Description: He, Yong-Qiao, et al. Clinical and genome-wide association analysis of chemoradiation-induced hearing loss in nasopharyngeal carcinoma. ''Hum Genet''. 2023 Jun; '''142''' (6):759-772
Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits. Description: Vysotskiy, Mikhail, et al. Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits. ''PLoS Genet''. 2023 Jun; '''19''' (6):e1010780
Cross-tissue omics analysis discovers ten adipose genes encoding secreted proteins in obesity-related non-alcoholic fatty liver disease. Description: Darci-Maher, Nicholas, et al. Cross-tissue omics analysis discovers ten adipose genes encoding secreted proteins in obesity-related non-alcoholic fatty liver disease. ''EBioMedicine''. 2023 Jun; '''92''': 104620
Cumulative genetic score of KIAA0319 affects reading ability in Chinese children: moderation by parental education and mediation by rapid automatized naming. Description: Zhao, Jingjing, et al. Cumulative genetic score of KIAA0319 affects reading ability in Chinese children: moderation by parental education and mediation by rapid automatized naming. ''Behav Brain Funct''. 2023 Jun 1; '''19''' (1):10
Design and validation of a high-density single nucleotide polymorphism array for the Eastern oyster (Crassostrea virginica). Description: Xuereb, Amanda, et al. Design and validation of a high-density single nucleotide polymorphism array for the Eastern oyster (Crassostrea virginica). ''G3 (Bethesda)''. 2023 Jun 1; '''13''' (6):
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. Description: Yu Chen, Hao, et al. Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. ''Eur Heart J''. 2023 Jun 1; '''44''' (21):1927-1939
Effects of urban living environments on mental health in adults. Description: Xu, Jiayuan, et al. Effects of urban living environments on mental health in adults. ''Nat Med''. 2023 Jun; '''29''' (6):1456-1467
EGFR and MMP-9 are associated with neointimal hyperplasia in systemic-to-pulmonary shunts in children with complex cyanotic heart disease. Description: Kottmann, Philip, et al. EGFR and MMP-9 are associated with neointimal hyperplasia in systemic-to-pulmonary shunts in children with complex cyanotic heart disease. ''Mamm Genome''. 2023 Jun; '''34''' (2):285-297
Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture. Description: Kachuri, Linda, et al. Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture. ''Nat Genet''. 2023 Jun; '''55''' (6):952-963
Genes encoding agrin (AGRN) and neurotrypsin (PRSS12) are associated with muscle mass, strength and plasma C-terminal agrin fragment concentration. Description: Pratt, Jedd, et al. Genes encoding agrin (AGRN) and neurotrypsin (PRSS12) are associated with muscle mass, strength and plasma C-terminal agrin fragment concentration. ''Geroscience''. 2023 Jun; '''45''' (3):1289-1302
Genetically adjusted PSA levels for prostate cancer screening. Description: Kachuri, Linda, et al. Genetically adjusted PSA levels for prostate cancer screening. ''Nat Med''. 2023 Jun; '''29''' (6):1412-1423
Genetic analysis of infectious bronchitis virus (IBV) in vaccinated poultry populations over a period of 10 years. Description: Vermeulen, Cornelis J, et al. Genetic analysis of infectious bronchitis virus (IBV) in vaccinated poultry populations over a period of 10 years. ''Avian Pathol''. 2023 Jun; '''52''' (3):157-167
Genetic patterning for child psychopathology is distinct from that for adults and implicates fetal cerebellar development. Description: Hughes, Dylan E, et al. Genetic patterning for child psychopathology is distinct from that for adults and implicates fetal cerebellar development. ''Nat Neurosci''. 2023 Jun; '''26''' (6):959-969
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Description: Schlosser, Pascal, et al. Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. ''Nat Genet''. 2023 Jun; '''55''' (6):995-1008
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation. Description: Adlam, David, et al. Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation. ''Nat Genet''. 2023 Jun; '''55''' (6):964-972
Genome-wide association study of chronic sputum production implicates loci involved in mucus production and infection. Description: Packer, Richard J, et al. Genome-wide association study of chronic sputum production implicates loci involved in mucus production and infection. ''Eur Respir J''. 2023 Jun; '''61''' (6):
Genome-wide association study of osteonecrosis of the jaw in Danish patients receiving antiresorptive therapy for osteoporosis: A case-control study. Description: Pedersen, Alma B, et al. Genome-wide association study of osteonecrosis of the jaw in Danish patients receiving antiresorptive therapy for osteoporosis: A case-control study. ''Bone Rep''. 2023 Jun; '''18''': 101648
Genomic conservation of crop wild relatives: A case study of citrus. Description: Wang, Nan, et al. Genomic conservation of crop wild relatives: A case study of citrus. ''PLoS Genet''. 2023 Jun; '''19''' (6):e1010811
Genomic Insights into Adaptation to Karst Limestone and Incipient Speciation in East Asian Platycarya spp. (Juglandaceae). Description: Cao, Yu, et al. Genomic Insights into Adaptation to Karst Limestone and Incipient Speciation in East Asian Platycarya spp. (Juglandaceae). ''Mol Biol Evol''. 2023 Jun 1; '''40''' (6):
Hidden Genetic Regulation of Human Complex Traits via Brain Isoforms. Description: Pan, Lu, et al. Hidden Genetic Regulation of Human Complex Traits via Brain Isoforms. ''Phenomics''. 2023 Jun; '''3''' (3):217-227
Host Genetic Factors, Comorbidities and the Risk of Severe COVID-19. Description: Zhu, Dongliang, et al. Host Genetic Factors, Comorbidities and the Risk of Severe COVID-19. ''J Epidemiol Glob Health''. 2023 Jun; '''13''' (2):279-291
Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis. Description: Sjaarda, Jennifer, et al. Identification of four novel loci associated with psychotropic drug-induced weight gain in a Swiss psychiatric longitudinal study: A GWAS analysis. ''Mol Psychiatry''. 2023 Jun; '''28''' (6):2320-2327
Identification of new risk loci shared across systemic vasculitides points towards potential target genes for drug repurposing. Description: Ortiz-Fernandez, Lourdes, et al. Identification of new risk loci shared across systemic vasculitides points towards potential target genes for drug repurposing. ''Ann Rheum Dis''. 2023 Jun; '''82''' (6):837-847
Identification of Novel Associations and Localization of Signals in Idiopathic Inflammatory Myopathies Using Genome-Wide Imputation. Description: Rothwell, Simon, et al. Identification of Novel Associations and Localization of Signals in Idiopathic Inflammatory Myopathies Using Genome-Wide Imputation. ''Arthritis Rheumatol''. 2023 Jun; '''75''' (6):1021-1027
Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Description: Rudman, Najda, et al. Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. ''Diabetologia''. 2023 Jun; '''66''' (6):1071-1083
Interactions between genetic variants and environmental risk factors are associated with the severity of pelvic organ prolapse. Description: Li, Lei, et al. Interactions between genetic variants and environmental risk factors are associated with the severity of pelvic organ prolapse. ''Menopause''. 2023 Jun 1; '''30''' (6):621-628
Leveraging genetic overlap between irritability and psychiatric disorders to identify genetic variants of major psychiatric disorders. Description: Jung, Kyeongmin, et al. Leveraging genetic overlap between irritability and psychiatric disorders to identify genetic variants of major psychiatric disorders. ''Exp Mol Med''. 2023 Jun; '''55''' (6):1193-1202
Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals. Description: Agren, Richard, et al. Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals. ''Mol Biol Evol''. 2023 Jun 1; '''40''' (6):
Mapping genetic effects on cell type-specific chromatin accessibility and annotating complex immune trait variants using single nucleus ATAC-seq in peripheral blood. Description: Benaglio, Paola, et al. Mapping genetic effects on cell type-specific chromatin accessibility and annotating complex immune trait variants using single nucleus ATAC-seq in peripheral blood. ''PLoS Genet''. 2023 Jun; '''19''' (6):e1010759
Northwest African Neolithic initiated by migrants from Iberia and Levant. Description: Simoes, Luciana G, et al. Northwest African Neolithic initiated by migrants from Iberia and Levant. ''Nature''. 2023 Jun; '''618''' (7965):550-556
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data. Description: Tomofuji, Yoshihiko, et al. Reconstruction of the personal information from human genome reads in gut metagenome sequencing data. ''Nat Microbiol''. 2023 Jun; '''8''' (6):1079-1094
Shared genetic architecture between attention-deficit/hyperactivity disorder and lifespan. Description: Vilar-Ribo, Laura, et al. Shared genetic architecture between attention-deficit/hyperactivity disorder and lifespan. ''Neuropsychopharmacology''. 2023 Jun; '''48''' (7):981-990
Structural architecture and brain network efficiency link polygenic scores to intelligence. Description: Genc, Erhan, et al. Structural architecture and brain network efficiency link polygenic scores to intelligence. ''Hum Brain Mapp''. 2023 Jun 1; '''44''' (8):3359-3376
TaTPP-7A positively feedback regulates grain filling and wheat grain yield through T6P-SnRK1 signalling pathway and sugar-ABA interaction. Description: Liu, Hongxia, et al. TaTPP-7A positively feedback regulates grain filling and wheat grain yield through T6P-SnRK1 signalling pathway and sugar-ABA interaction. ''Plant Biotechnol J''. 2023 Jun; '''21''' (6):1159-1175
The First Crested Duck Genome Reveals Clues to Genetic Compensation and Crest Cushion Formation. Description: Chang, Guobin, et al. The First Crested Duck Genome Reveals Clues to Genetic Compensation and Crest Cushion Formation. ''Genomics Proteomics Bioinformatics''. 2023 Jun; '''21''' (3):483-500
The impact of rare protein coding genetic variation on adult cognitive function. Description: Chen, Chia-Yen, et al. The impact of rare protein coding genetic variation on adult cognitive function. ''Nat Genet''. 2023 Jun; '''55''' (6):927-938
The Role of Introgression During the Radiation of Endemic Fishes Adapted to Living at Extreme Altitudes in the Tibetan Plateau. Description: Qian, Yuting, et al. The Role of Introgression During the Radiation of Endemic Fishes Adapted to Living at Extreme Altitudes in the Tibetan Plateau. ''Mol Biol Evol''. 2023 Jun 1; '''40''' (6):
Modeling the longitudinal changes of ancestry diversity in the Million Veteran Program. Description: Wendt, Frank R, et al. Modeling the longitudinal changes of ancestry diversity in the Million Veteran Program. ''Hum Genomics''. 2023 Jun 2; '''17''' (1):46
Polymorphisms of the GCLC Gene Are Novel Genetic Markers for Susceptibility to Psoriasis Associated with Alcohol Abuse and Cigarette Smoking. Description: Efanova, Ekaterina, et al. Polymorphisms of the GCLC Gene Are Novel Genetic Markers for Susceptibility to Psoriasis Associated with Alcohol Abuse and Cigarette Smoking. ''Life (Basel)''. 2023 Jun 2; '''13''' (6):
Fetally-encoded GDF15 and maternal GDF15 sensitivity are major determinants of nausea and vomiting in human pregnancy. Description: Fejzo, M, et al. Fetally-encoded GDF15 and maternal GDF15 sensitivity are major determinants of nausea and vomiting in human pregnancy. ''bioRxiv''. 2023 Jun 4;
Cell-type-specific Alzheimer's disease polygenic risk scores are associated with distinct disease processes in Alzheimer's disease. Description: Yang, Hyun-Sik, et al. Cell-type-specific Alzheimer's disease polygenic risk scores are associated with distinct disease processes in Alzheimer's disease. ''medRxiv''. 2023 Jun 5;
Comprehensive analysis of geographic and breed-purpose influences on genetic diversity and inherited disease risk in the Doberman dog breed. Description: Wade, Claire M, et al. Comprehensive analysis of geographic and breed-purpose influences on genetic diversity and inherited disease risk in the Doberman dog breed. ''Canine Med Genet''. 2023 Jun 5; '''10''' (1):7
Pathogen-specific innate immune response patterns are distinctly affected by genetic diversity. Description: Hader, Antje, et al. Pathogen-specific innate immune response patterns are distinctly affected by genetic diversity. ''Nat Commun''. 2023 Jun 5; '''14''' (1):3239
The genetics of a "femaleness/maleness" score in cardiometabolic traits in the UK biobank. Description: Vosberg, Daniel E, et al. The genetics of a "femaleness/maleness" score in cardiometabolic traits in the UK biobank. ''Sci Rep''. 2023 Jun 5; '''13''' (1):9109
Associations between polymorphisms in leptin and leptin receptor genes and colorectal cancer survival. Description: Du, Meizhi, et al. Associations between polymorphisms in leptin and leptin receptor genes and colorectal cancer survival. ''Cancer Biol Med''. 2023 Jun 6; '''20''' (6):438-51
Lifestyle, genetic risk and incidence of cancer: a prospective cohort study of 13 cancer types. Description: Byrne, Stephanie, et al. Lifestyle, genetic risk and incidence of cancer: a prospective cohort study of 13 cancer types. ''Int J Epidemiol''. 2023 Jun 6; '''52''' (3):817-826
Pueraria montana Population Structure and Genetic Diversity Based on Chloroplast Genome Data. Description: Sun, Jiahui, et al. Pueraria montana Population Structure and Genetic Diversity Based on Chloroplast Genome Data. ''Plants (Basel)''. 2023 Jun 6; '''12''' (12):
Allelic and genotypic frequencies of SNP related to beef and carcass quality in Romosinuano cattle in Mexico. Description: Rocha, Ricardo Martinez, et al. Allelic and genotypic frequencies of SNP related to beef and carcass quality in Romosinuano cattle in Mexico. ''Trop Anim Health Prod''. 2023 Jun 7; '''55''' (4):233
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism. Description: Iglesias, Maria Jesus, et al. Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism. ''Nat Commun''. 2023 Jun 7; '''14''' (1):3280
Sparse Phenotyping and Haplotype-Based Models for Genomic Prediction in Rice. Description: He, Sang, et al. Sparse Phenotyping and Haplotype-Based Models for Genomic Prediction in Rice. ''Rice (N Y)''. 2023 Jun 7; '''16''' (1):27
Multiancestry sex-stratified genomic associations with HIV viral load and controller status from the ICGH. Description: Vergara, Candelaria, et al. Multiancestry sex-stratified genomic associations with HIV viral load and controller status from the ICGH. ''JCI Insight''. 2023 Jun 8; '''8''' (11):
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity. Description: Wall, Jeffrey D, et al. South Asian medical cohorts reveal strong founder effects and high rates of homozygosity. ''Nat Commun''. 2023 Jun 8; '''14''' (1):3377
ddRAD sequencing based genotyping of six indigenous dairy cattle breeds of India to infer existing genetic diversity and population structure. Description: Masharing, Nampher, et al. ddRAD sequencing based genotyping of six indigenous dairy cattle breeds of India to infer existing genetic diversity and population structure. ''Sci Rep''. 2023 Jun 9; '''13''' (1):9379
Six-year trajectories and associated factors of positive and negative symptoms in schizophrenia patients, siblings, and controls: Genetic Risk and Outcome of Psychosis (GROUP) study. Description: Habtewold, Tesfa Dejenie, et al. Six-year trajectories and associated factors of positive and negative symptoms in schizophrenia patients, siblings, and controls: Genetic Risk and Outcome of Psychosis (GROUP) study. ''Sci Rep''. 2023 Jun 9; '''13''' (1):9391
Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects. Description: Ayers, Katie L, et al. Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects. ''Nat Commun''. 2023 Jun 9; '''14''' (1):3403
Development and Replication of a Genome-Wide Polygenic Risk Score for Chronic Back Pain. Description: Tsepilov, Yakov A, et al. Development and Replication of a Genome-Wide Polygenic Risk Score for Chronic Back Pain. ''J Pers Med''. 2023 Jun 10; '''13''' (6):
Rare genetic variants impact muscle strength. Description: Huang, Yunfeng, et al. Rare genetic variants impact muscle strength. ''Nat Commun''. 2023 Jun 10; '''14''' (1):3449
Apolipoprotein E moderates the association between Non- APOE Polygenic Risk Score for Alzheimer's Disease and Aging on Preclinical Cognitive Function. Description: Xu, Yuexuan, et al. Apolipoprotein E moderates the association between Non- APOE Polygenic Risk Score for Alzheimer's Disease and Aging on Preclinical Cognitive Function. ''medRxiv''. 2023 Jun 12;
Evaluating Genomic Polygenic Risk Scores for Childhood Acute Lymphoblastic Leukemia in Latinos. Description: Jeon, Soyoung, et al. Evaluating Genomic Polygenic Risk Scores for Childhood Acute Lymphoblastic Leukemia in Latinos. ''medRxiv''. 2023 Jun 12;
Systems genetics identifies miRNA-mediated regulation of host response in COVID-19. Description: Gjorgjieva, T, et al. Systems genetics identifies miRNA-mediated regulation of host response in COVID-19. ''Hum Genomics''. 2023 Jun 12; '''17''' (1):49
Vitamin D Status, Cdx2 Genotype, and Colorectal Cancer Survival: Population-Based Patient Cohort. Description: Gwenzi, Tafirenyika, et al. Vitamin D Status, Cdx2 Genotype, and Colorectal Cancer Survival: Population-Based Patient Cohort. ''Nutrients''. 2023 Jun 12; '''15''' (12):
Common genetic variants contribute to heritability of age at onset of schizophrenia. Description: Sada-Fuente, Ester, et al. Common genetic variants contribute to heritability of age at onset of schizophrenia. ''Transl Psychiatry''. 2023 Jun 13; '''13''' (1):201
Evaluating significance of European-associated index SNPs in the East Asian population for 31 complex phenotypes. Description: Qiao, Jiahao, et al. Evaluating significance of European-associated index SNPs in the East Asian population for 31 complex phenotypes. ''BMC Genomics''. 2023 Jun 13; '''24''' (1):324
Genome-wide association study of preterm birth and gestational age in a Japanese population. Description: Hasegawa, Keita, et al. Genome-wide association study of preterm birth and gestational age in a Japanese population. ''Hum Genome Var''. 2023 Jun 13; '''10''' (1):19
SAMHD1 single nucleotide polymorphisms impact outcome in children with newly diagnosed acute myeloid leukemia. Description: Marrero, Richard J, et al. SAMHD1 single nucleotide polymorphisms impact outcome in children with newly diagnosed acute myeloid leukemia. ''Blood Adv''. 2023 Jun 13; '''7''' (11):2538-2550
Genetic diversity and selection signatures in a gene bank panel of maize inbred lines from Southeast Europe compared with two West European panels. Description: Galic, Vlatko, et al. Genetic diversity and selection signatures in a gene bank panel of maize inbred lines from Southeast Europe compared with two West European panels. ''BMC Plant Biol''. 2023 Jun 14; '''23''' (1):315
Genomic evidence reveals high genetic diversity in a narrowly distributed species and natural hybridization risk with a widespread species in the genus Geodorum. Description: Zhu, Xianliang, et al. Genomic evidence reveals high genetic diversity in a narrowly distributed species and natural hybridization risk with a widespread species in the genus Geodorum. ''BMC Plant Biol''. 2023 Jun 14; '''23''' (1):317
Dynamic effective connectivity among large-scale brain networks mediates risk of anxiety. Description: Dynamic effective connectivity among large-scale brain networks mediates risk of anxiety. ''''. 2023 Jun 15; '''44''' (9):3730-3743
Genome-Wide Association Study of Seed Morphology Traits in Senegalese Sorghum Cultivars. Description: Ahn, Ezekiel, et al. Genome-Wide Association Study of Seed Morphology Traits in Senegalese Sorghum Cultivars. ''Plants (Basel)''. 2023 Jun 16; '''12''' (12):
Expanding the application of haplotype-based genomic predictions to the wild: A case of antibody response against Teladorsagia circumcincta in Soay sheep. Description: Vahedi, Seyed Milad, et al. Expanding the application of haplotype-based genomic predictions to the wild: A case of antibody response against Teladorsagia circumcincta in Soay sheep. ''BMC Genomics''. 2023 Jun 17; '''24''' (1):335
Global patterns of genomic and phenotypic variation in the invasive harlequin ladybird. Description: Li, Hongran, et al. Global patterns of genomic and phenotypic variation in the invasive harlequin ladybird. ''BMC Biol''. 2023 Jun 19; '''21''' (1):141
Haplotype-Based Genome-Wide Association Analysis Using Exome Capture Assay and Digital Phenotyping Identifies Genetic Loci Underlying Salt Tolerance Mechanisms in Wheat. Description: Pasam, Raj K, et al. Haplotype-Based Genome-Wide Association Analysis Using Exome Capture Assay and Digital Phenotyping Identifies Genetic Loci Underlying Salt Tolerance Mechanisms in Wheat. ''Plants (Basel)''. 2023 Jun 19; '''12''' (12):
UBAP2 plays a role in bone homeostasis through the regulation of osteoblastogenesis and osteoclastogenesis. Description: Kim, Jeonghyun, et al. UBAP2 plays a role in bone homeostasis through the regulation of osteoblastogenesis and osteoclastogenesis. ''Nat Commun''. 2023 Jun 20; '''14''' (1):3668
Mitochondria-wide association study observed significant interactions of mitochondrial respiratory and the inflammatory in the development of anxiety and depression. Description: Liu, Li, et al. Mitochondria-wide association study observed significant interactions of mitochondrial respiratory and the inflammatory in the development of anxiety and depression. ''Transl Psychiatry''. 2023 Jun 21; '''13''' (1):216
Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy. Description: Khan, Zia, et al. Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy. ''Genome Med''. 2023 Jun 21; '''15''' (1):45
Genetically-regulated pathway-polygenic risk score (GRPa-PRS): A risk stratification method to identify genetically regulated pathways in polygenic diseases. Description: Li, Xiaoyang, et al. Genetically-regulated pathway-polygenic risk score (GRPa-PRS): A risk stratification method to identify genetically regulated pathways in polygenic diseases. ''medRxiv''. 2023 Jun 27;
Modeling of mitochondrial genetic polymorphisms reveals induction of heteroplasmy by pleiotropic disease locus 10398A>G. Description: Smullen, Molly, et al. Modeling of mitochondrial genetic polymorphisms reveals induction of heteroplasmy by pleiotropic disease locus 10398A>G. ''Sci Rep''. 2023 Jun 27; '''13''' (1):10405
Natural genetic variation in the pheromone production of C. elegans. Description: Lee, Daehan, et al. Natural genetic variation in the pheromone production of C. elegans. ''Proc Natl Acad Sci U S A''. 2023 Jun 27; '''120''' (26):e2221150120
Genetic variants in epoxyeicosatrienoic acid processing and degradation pathways are associated with gestational diabetes mellitus. Description: Lai, Siyu, et al. Genetic variants in epoxyeicosatrienoic acid processing and degradation pathways are associated with gestational diabetes mellitus. ''Nutr J''. 2023 Jun 28; '''22''' (1):31
Classification and deep-learning-based prediction of Alzheimer disease subtypes by using genomic data. Description: Shigemizu, Daichi, et al. Classification and deep-learning-based prediction of Alzheimer disease subtypes by using genomic data. ''Transl Psychiatry''. 2023 Jun 29; '''13''' (1):232
Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program. Description: Verma, Anurag, et al. Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program. ''medRxiv''. 2023 Jun 29;
Evaluation of the selection of key individuals for genotype imputation in Chinese yellow-feathered chicken. Description: Zheng, Ming, et al. Evaluation of the selection of key individuals for genotype imputation in Chinese yellow-feathered chicken. ''Poult Sci''. 2023 Jun 29; '''102''' (10):102901
Fast and flexible joint fine-mapping of multiple traits via the Sum of Single Effects model. Description: Zou, Yuxin, et al. Fast and flexible joint fine-mapping of multiple traits via the Sum of Single Effects model. ''bioRxiv''. 2023 Jun 29;
Genetic dissection of 26 meat cut, meat quality and carcass traits in four pig populations. Description: Xie, Lei, et al. Genetic dissection of 26 meat cut, meat quality and carcass traits in four pig populations. ''Genet Sel Evol''. 2023 Jun 29; '''55''' (1):43
Genome-wide case-only analysis of gene-gene interactions with known Parkinson's disease risk variants reveals link between LRRK2 and SYT10. Description: Aleknonyte-Resch, Milda, et al. Genome-wide case-only analysis of gene-gene interactions with known Parkinson's disease risk variants reveals link between LRRK2 and SYT10. ''NPJ Parkinsons Dis''. 2023 Jun 29; '''9''' (1):102
Lacustrine speciation associated with chromosomal inversion in a lineage of riverine fishes. Description: MacGuigan, Daniel J, et al. Lacustrine speciation associated with chromosomal inversion in a lineage of riverine fishes. ''Evolution''. 2023 Jun 29; '''77''' (7):1505-1521
Targeting hepatitis B vaccine escape using immunogenetics in Bangladeshi infants. Description: Butler-Laporte, Guillaume, et al. Targeting hepatitis B vaccine escape using immunogenetics in Bangladeshi infants. ''medRxiv''. 2023 Jun 29;
An analytical framework for decoding cell type-specific genetic variation of gene regulation. Description: Xiao, Yanyu, et al. An analytical framework for decoding cell type-specific genetic variation of gene regulation. ''Nat Commun''. 2023 Jun 30; '''14''' (1):3884
Associations between polygenic risk score and covid-19 susceptibility and severity across ethnic groups: UK Biobank analysis. Description: Farooqi, Raabia, et al. Associations between polygenic risk score and covid-19 susceptibility and severity across ethnic groups: UK Biobank analysis. ''BMC Med Genomics''. 2023 Jun 30; '''16''' (1):150
Exploratory genome-wide analyses of cortical inhibition, facilitation, and plasticity in late-life depression. Description: Wathra, Rafae A, et al. Exploratory genome-wide analyses of cortical inhibition, facilitation, and plasticity in late-life depression. ''Transl Psychiatry''. 2023 Jun 30; '''13''' (1):234
A graph-based genome and pan-genome variation of the model plant Setaria. Description: He, Qiang, et al. A graph-based genome and pan-genome variation of the model plant Setaria. ''Nat Genet''. 2023 Jul; '''55''' (7):1232-1242
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease. Description: Patel, Aniruddh P, et al. A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease. ''Nat Med''. 2023 Jul; '''29''' (7):1793-1803
A statistical framework to identify cell types whose genetically regulated proportions are associated with complex diseases. Description: Liu, Wei, et al. A statistical framework to identify cell types whose genetically regulated proportions are associated with complex diseases. ''PLoS Genet''. 2023 Jul; '''19''' (7):e1010825
Behavioural deficits of autism spectrum disorder and associations with different gene clusters: a study with the whole-genome transmission disequilibrium test. Description: Guo, Qi, et al. Behavioural deficits of autism spectrum disorder and associations with different gene clusters: a study with the whole-genome transmission disequilibrium test. ''BMJ Paediatr Open''. 2023 Jul; '''7''' (1):
Combined genome-wide association study of 136 quantitative ear morphology traits in multiple populations reveal 8 novel loci. Description: Li, Yi, et al. Combined genome-wide association study of 136 quantitative ear morphology traits in multiple populations reveal 8 novel loci. ''PLoS Genet''. 2023 Jul; '''19''' (7):e1010786
Comprehensive genomic analyses of Vigna unguiculata provide insights into population differentiation and the genetic basis of key agricultural traits. Description: Pan, Lei, et al. Comprehensive genomic analyses of Vigna unguiculata provide insights into population differentiation and the genetic basis of key agricultural traits. ''Plant Biotechnol J''. 2023 Jul; '''21''' (7):1426-1439
Development of a Single-nucleotide Polymorphism Genotyping Assay for the Rapid Detection of Vancomycin-intermediate Resistance in Staphylococcus aureus Epidemic Lineage ST5. Description: Kim, Jung Wook, et al. Development of a Single-nucleotide Polymorphism Genotyping Assay for the Rapid Detection of Vancomycin-intermediate Resistance in Staphylococcus aureus Epidemic Lineage ST5. ''Ann Lab Med''. 2023 Jul 1; '''43''' (4):355-363
Does maternal genetic liability to folate deficiency influence the risk of antiseizure medication-associated language impairment and autistic traits in children of women with epilepsy? Description: Nilsen Husebye, Elisabeth Synnove, et al. Does maternal genetic liability to folate deficiency influence the risk of antiseizure medication-associated language impairment and autistic traits in children of women with epilepsy? ''Am J Clin Nutr''. 2023 Jul; '''118''' (1):303-313
Genetic architecture of brain age and its causal relations with brain and mental disorders. Description: Leonardsen, Esten H, et al. Genetic architecture of brain age and its causal relations with brain and mental disorders. ''Mol Psychiatry''. 2023 Jul; '''28''' (7):3111-3120
Genetic impacts on nigral iron deposition in Parkinson's disease: A preliminary quantitative susceptibility mapping study. Description: Wu, Jingjing, et al. Genetic impacts on nigral iron deposition in Parkinson's disease: A preliminary quantitative susceptibility mapping study. ''CNS Neurosci Ther''. 2023 Jul; '''29''' (7):1776-1784
Genetic variations in HMGCR and PCSK9 and kidney function: a Mendelian randomization study. Description: Park, Sehoon, et al. Genetic variations in HMGCR and PCSK9 and kidney function: a Mendelian randomization study. ''Kidney Res Clin Pract''. 2023 Jul; '''42''' (4):460-472
Genome-wide Association Study for AKI. Description: Bhatraju, Pavan K, et al. Genome-wide Association Study for AKI. ''Kidney360''. 2023 Jul 1; '''4''' (7):870-880
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci. Description: Han, Xikun, et al. Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci. ''Nat Genet''. 2023 Jul; '''55''' (7):1116-1125
LncRNA BCLET variant confers bladder cancer susceptibility through alternative splicing of MSANTD2 exon 1. Description: Liu, Hanting, et al. LncRNA BCLET variant confers bladder cancer susceptibility through alternative splicing of MSANTD2 exon 1. ''Cancer Med''. 2023 Jul; '''12''' (13):14440-14451
MLX plays a key role in lipid and glucose metabolism in humans: Evidence from in vitro and in vivo studies. Description: Nagarajan, Shilpa R, et al. MLX plays a key role in lipid and glucose metabolism in humans: Evidence from in vitro and in vivo studies. ''Metabolism''. 2023 Jul; '''144''': 155563
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease. Description: Lake, Julie, et al. Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease. ''Mol Psychiatry''. 2023 Jul; '''28''' (7):3121-3132
Pharmacogenetics of tenofovir renal toxicity in HIV-positive Southern Africans. Description: Mateza, Somila, et al. Pharmacogenetics of tenofovir renal toxicity in HIV-positive Southern Africans. ''Pharmacogenet Genomics''. 2023 Jul 1; '''33''' (5):91-100
Phenotypic effects of genetic variants associated with autism. Description: Rolland, Thomas, et al. Phenotypic effects of genetic variants associated with autism. ''Nat Med''. 2023 Jul; '''29''' (7):1671-1680
Rare coding variants in CHRNB2 reduce the likelihood of smoking. Description: Rajagopal, Veera M, et al. Rare coding variants in CHRNB2 reduce the likelihood of smoking. ''Nat Genet''. 2023 Jul; '''55''' (7):1138-1148
Repurposing antidiabetic drugs for rheumatoid arthritis: results from a two-sample Mendelian randomization study. Description: Qin, Chenxi, et al. Repurposing antidiabetic drugs for rheumatoid arthritis: results from a two-sample Mendelian randomization study. ''Eur J Epidemiol''. 2023 Jul; '''38''' (7):809-819
Sleep disturbances in ADHD: investigating the contribution of polygenic liability for ADHD and sleep-related phenotypes. Description: Lewis, Katie J S, et al. Sleep disturbances in ADHD: investigating the contribution of polygenic liability for ADHD and sleep-related phenotypes. ''Eur Child Adolesc Psychiatry''. 2023 Jul; '''32''' (7):1253-1261
The genetic polymorphisms of immune-related genes contribute to the susceptibility and survival of lymphoma. Description: Gu, Chaoyang, et al. The genetic polymorphisms of immune-related genes contribute to the susceptibility and survival of lymphoma. ''Cancer Med''. 2023 Jul; '''12''' (14):14960-14978
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. Description: Lassen, Frederik H, et al. Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. ''medRxiv''. 2023 Jul 3;
Genome-wide association analysis identifies a susceptibility locus for sporadic vestibular schwannoma at 9p21. Description: Sadler, Katherine V, et al. Genome-wide association analysis identifies a susceptibility locus for sporadic vestibular schwannoma at 9p21. ''Brain''. 2023 Jul 3; '''146''' (7):2861-2868
Homozygosity mapping in the Kazakh national dog breed Tazy. Description: Perfilyeva, Anastassiya, et al. Homozygosity mapping in the Kazakh national dog breed Tazy. ''Sci Rep''. 2023 Jul 3; '''13''' (1):10735
Impact of genetic variations in the WNT family members and RUNX2 on dental and skeletal maturation: a cross-sectional study. Description: Bitencourt Reis, Caio Luiz, et al. Impact of genetic variations in the WNT family members and RUNX2 on dental and skeletal maturation: a cross-sectional study. ''Head Face Med''. 2023 Jul 3; '''19''' (1):26
Physical Activity, Sedentary Behavior, and Type 2 Diabetes: Mendelian Randomization Analysis. Description: Yuan, Shuai, et al. Physical Activity, Sedentary Behavior, and Type 2 Diabetes: Mendelian Randomization Analysis. ''J Endocr Soc''. 2023 Jul 3; '''7''' (8):bvad090
The 2020 derecho revealed limited overlap between maize genes associated with root lodging and root system architecture. Description: Zheng, Zihao, et al. The 2020 derecho revealed limited overlap between maize genes associated with root lodging and root system architecture. ''Plant Physiol''. 2023 Jul 3; '''192''' (3):2394-2403
Whole-genome Analyses Reveal Past Population Fluctuations and Low Genetic Diversities of the North Pacific Albatrosses. Description: Huynh, Stella, et al. Whole-genome Analyses Reveal Past Population Fluctuations and Low Genetic Diversities of the North Pacific Albatrosses. ''Mol Biol Evol''. 2023 Jul 3; '''40''' (7):
Characterization of large-scale genomic differences in the first complete human genome. Description: Yang, Xiangyu, et al. Characterization of large-scale genomic differences in the first complete human genome. ''Genome Biol''. 2023 Jul 4; '''24''' (1):157
Genome-Wide Association Study of Xian Rice Grain Shape and Weight in Different Environments. Description: Wang, Nansheng, et al. Genome-Wide Association Study of Xian Rice Grain Shape and Weight in Different Environments. ''Plants (Basel)''. 2023 Jul 4; '''12''' (13):
Hiding in plain sight: Genome-wide recombination and a dynamic accessory genome drive diversity in Fusarium oxysporum f.sp. ciceris. Description: Fayyaz, Amna, et al. Hiding in plain sight: Genome-wide recombination and a dynamic accessory genome drive diversity in Fusarium oxysporum f.sp. ciceris. ''Proc Natl Acad Sci U S A''. 2023 Jul 4; '''120''' (27):e2220570120
High-Altitude Andean H194R HIF2A Allele Is a Hypomorphic Allele. Description: Jorgensen, Kelsey, et al. High-Altitude Andean H194R HIF2A Allele Is a Hypomorphic Allele. ''Mol Biol Evol''. 2023 Jul 5; '''40''' (7):
Uncovering the Genomic Basis of Infection Through Co-genomic Sequencing of Hosts and Parasites. Description: Dexter, Eric, et al. Uncovering the Genomic Basis of Infection Through Co-genomic Sequencing of Hosts and Parasites. ''Mol Biol Evol''. 2023 Jul 5; '''40''' (7):
A human leukocyte antigen imputation study uncovers possible genetic interplay between gut inflammatory processes and autism spectrum disorders. Description: Lombardi, Laura, et al. A human leukocyte antigen imputation study uncovers possible genetic interplay between gut inflammatory processes and autism spectrum disorders. ''Transl Psychiatry''. 2023 Jul 6; '''13''' (1):244
Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26. Description: Alpen, Karen, et al. Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26. ''Neuro Oncol''. 2023 Jul 6; '''25''' (7):1355-1365
Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility. Description: Talwar, James V, et al. Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility. ''Am J Hum Genet''. 2023 Jul 6; '''110''' (7):1138-1161
Genetic risk assessment of lethal prostate cancer using polygenic risk score and hereditary cancer susceptibility genes. Description: Ruan, Xiaohao, et al. Genetic risk assessment of lethal prostate cancer using polygenic risk score and hereditary cancer susceptibility genes. ''J Transl Med''. 2023 Jul 6; '''21''' (1):446
Deep integrative models for large-scale human genomics. Description: Sigurdsson, Arnor I, et al. Deep integrative models for large-scale human genomics. ''Nucleic Acids Res''. 2023 Jul 7; '''51''' (12):e67
Impact of Lung-Related Polygenic Risk Scores on Chronic Obstructive Pulmonary Disease Risk and Their Interaction with w-3 Fatty Acid Intake in Middle-Aged and Elderly Individuals. Description: Kim, Ki-Song, et al. Impact of Lung-Related Polygenic Risk Scores on Chronic Obstructive Pulmonary Disease Risk and Their Interaction with w-3 Fatty Acid Intake in Middle-Aged and Elderly Individuals. ''Nutrients''. 2023 Jul 7; '''15''' (13):
Optimal strategies for learning multi-ancestry polygenic scores vary across traits. Description: Lehmann, Brieuc, et al. Optimal strategies for learning multi-ancestry polygenic scores vary across traits. ''Nat Commun''. 2023 Jul 7; '''14''' (1):4023
A 3' UTR Deletion Is a Leading Candidate Causal Variant at the TMEM106B Locus Reducing Risk for FTLD-TDP. Description: Chemparathy, Augustine, et al. A 3' UTR Deletion Is a Leading Candidate Causal Variant at the TMEM106B Locus Reducing Risk for FTLD-TDP. ''medRxiv''. 2023 Jul 8;
Immune-Neuroendocrine Patterning and Response to Stress. A latent profile analysis in the English Longitudinal Study of Ageing. Description: Hamilton, Odessa S, et al. Immune-Neuroendocrine Patterning and Response to Stress. A latent profile analysis in the English Longitudinal Study of Ageing. ''medRxiv''. 2023 Jul 8;
A protocol for applying low-coverage whole-genome sequencing data in structural variation studies. Description: Liu, Qi, et al. A protocol for applying low-coverage whole-genome sequencing data in structural variation studies. ''STAR Protoc''. 2023 Jul 10; '''4''' (3):102433
Genomic analysis, trajectory tracking, and field surveys reveal sources and long-distance dispersal routes of wheat stripe rust pathogen in China. Description: Li, Yuxiang, et al. Genomic analysis, trajectory tracking, and field surveys reveal sources and long-distance dispersal routes of wheat stripe rust pathogen in China. ''Plant Commun''. 2023 Jul 10; '''4''' (4):100563
Genomic clines across the species boundary between a hybrid pine and its progenitor in the eastern Tibetan Plateau. Description: Guo, Jing-Fang, et al. Genomic clines across the species boundary between a hybrid pine and its progenitor in the eastern Tibetan Plateau. ''Plant Commun''. 2023 Jul 10; '''4''' (4):100574
Genetic background to attention deficit and hyperactivity disorder and attention deficit and hyperactivity disorder symptoms at the age of 5 years: the role of sleep duration. Description: Morales-Munoz, Isabel, et al. Genetic background to attention deficit and hyperactivity disorder and attention deficit and hyperactivity disorder symptoms at the age of 5 years: the role of sleep duration. ''Sleep''. 2023 Jul 11; '''46''' (7):
Race, Ethnicity, and Pharmacogenomic Variation in the United States and the United Kingdom. Description: Sharma, Shivam, et al. Race, Ethnicity, and Pharmacogenomic Variation in the United States and the United Kingdom. ''Pharmaceutics''. 2023 Jul 11; '''15''' (7):
Genome-Wide SNP and Indel Discovery in Abaca (Musa textilis Nee) and among Other Musa spp. for Abaca Genetic Resources Management. Description: Barbosa, Cris Francis C, et al. Genome-Wide SNP and Indel Discovery in Abaca (Musa textilis Nee) and among Other Musa spp. for Abaca Genetic Resources Management. ''Curr Issues Mol Biol''. 2023 Jul 12; '''45''' (7):5776-5797
Reduced Vrk2 expression is associated with higher risk of depression in humans and mediates depressive-like behaviors in mice. Description: Yin, Mei-Yu, et al. Reduced Vrk2 expression is associated with higher risk of depression in humans and mediates depressive-like behaviors in mice. ''BMC Med''. 2023 Jul 14; '''21''' (1):256
A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth. Description: Wang, Li, et al. A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth. ''BMC Med''. 2023 Jul 17; '''21''' (1):258
A high-quality genome assembly highlights the evolutionary history of the great bustard (Otis tarda, Otidiformes). Description: Luo, Haoran, et al. A high-quality genome assembly highlights the evolutionary history of the great bustard (Otis tarda, Otidiformes). ''Commun Biol''. 2023 Jul 18; '''6''' (1):746
Ancient dolphin genomes reveal rapid repeated adaptation to coastal waters. Description: Louis, Marie, et al. Ancient dolphin genomes reveal rapid repeated adaptation to coastal waters. ''Nat Commun''. 2023 Jul 18; '''14''' (1):4020
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. Description: Zhao, Yingjie, et al. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. ''NPJ Genom Med''. 2023 Jul 18; '''8''' (1):17
Genetic insights into ossification of the posterior longitudinal ligament of the spine. Description: Koike, Yoshinao, et al. Genetic insights into ossification of the posterior longitudinal ligament of the spine. ''Elife''. 2023 Jul 18; '''12''':
Genome-wide association study identifies risk loci within the major histocompatibility complex region for Hunner-type interstitial cystitis. Description: Akiyama, Yoshiyuki, et al. Genome-wide association study identifies risk loci within the major histocompatibility complex region for Hunner-type interstitial cystitis. ''Cell Rep Med''. 2023 Jul 18; '''4''' (7):101114
Identification of Markers Associated with Wheat Dwarf Virus (WDV) Tolerance/Resistance in Barley (Hordeum vulgare ssp. vulgare) Using Genome-Wide Association Studies. Description: Soleimani, Behnaz, et al. Identification of Markers Associated with Wheat Dwarf Virus (WDV) Tolerance/Resistance in Barley (Hordeum vulgare ssp. vulgare) Using Genome-Wide Association Studies. ''Viruses''. 2023 Jul 18; '''15''' (7):
Integrating genetics and metabolomics from multi-ethnic and multi-fluid data reveals putative mechanisms for age-related macular degeneration. Description: Han, Xikun, et al. Integrating genetics and metabolomics from multi-ethnic and multi-fluid data reveals putative mechanisms for age-related macular degeneration. ''Cell Rep Med''. 2023 Jul 18; '''4''' (7):101085
Biobank-scale methods and projections for sparse polygenic prediction from machine learning. Description: Raben, Timothy G, et al. Biobank-scale methods and projections for sparse polygenic prediction from machine learning. ''Sci Rep''. 2023 Jul 19; '''13''' (1):11662
A Genome-Wide Association Study Reveals Region Associated with Seed Protein Content in Cowpea. Description: Chen, Yilin, et al. A Genome-Wide Association Study Reveals Region Associated with Seed Protein Content in Cowpea. ''Plants (Basel)''. 2023 Jul 20; '''12''' (14):
APOE - epsilon 4 and BIN1 increase risk of Alzheimer's disease pathology but not specifically of Lewy body pathology. Description: Talyansky, Seth, et al. APOE - epsilon 4 and BIN1 increase risk of Alzheimer's disease pathology but not specifically of Lewy body pathology. ''medRxiv''. 2023 Jul 20;
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals. Description: Montanucci, Ludovica, et al. Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals. ''Nat Commun''. 2023 Jul 20; '''14''' (1):4392
The Genetic Architecture of Vitamin D Deficiency among an Elderly Lebanese Middle Eastern Population: An Exome-Wide Association Study. Description: Hendi, Nagham Nafiz, et al. The Genetic Architecture of Vitamin D Deficiency among an Elderly Lebanese Middle Eastern Population: An Exome-Wide Association Study. ''Nutrients''. 2023 Jul 20; '''15''' (14):
Major chromosome 5H haplotype switch structures the European two-rowed spring barley germplasm of the past 190 years. Description: Wonneberger, Ronja, et al. Major chromosome 5H haplotype switch structures the European two-rowed spring barley germplasm of the past 190 years. ''Theor Appl Genet''. 2023 Jul 21; '''136''' (8):174
Mitochondrial genetic variants associated with bipolar disorder and Schizophrenia in a Japanese population. Description: Tachi, Ryobu, et al. Mitochondrial genetic variants associated with bipolar disorder and Schizophrenia in a Japanese population. ''Int J Bipolar Disord''. 2023 Jul 21; '''11''' (1):26
APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer's Disease pathology. Description: Chemparathy, Augustine, et al. APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer's Disease pathology. ''medRxiv''. 2023 Jul 24;
Association study of human leukocyte antigen (HLA) variants and idiopathic pulmonary fibrosis. Description: Guillen-Guio, Beatriz, et al. Association study of human leukocyte antigen (HLA) variants and idiopathic pulmonary fibrosis. ''medRxiv''. 2023 Jul 24;
Bioarchaeological and paleogenomic profiling of the unusual Neolithic burial from Grotta di Pietra Sant'Angelo (Calabria, Italy). Description: Fontani, Francesco, et al. Bioarchaeological and paleogenomic profiling of the unusual Neolithic burial from Grotta di Pietra Sant'Angelo (Calabria, Italy). ''Sci Rep''. 2023 Jul 24; '''13''' (1):11978
Blood epigenome-wide association studies of suicide attempt in adults with bipolar disorder. Description: Mirza, Salahudeen, et al. Blood epigenome-wide association studies of suicide attempt in adults with bipolar disorder. ''medRxiv''. 2023 Jul 24;
Genomic analysis and prediction of genomic values for distichiasis in Staffordshire bull terriers. Description: Jorgensen, Dina, et al. Genomic analysis and prediction of genomic values for distichiasis in Staffordshire bull terriers. ''Canine Med Genet''. 2023 Jul 24; '''10''' (1):9
Identification of Genetic Loci for Rice Seedling Mesocotyl Elongation in Both Natural and Artificial Segregating Populations. Description: Feng, Fangjun, et al. Identification of Genetic Loci for Rice Seedling Mesocotyl Elongation in Both Natural and Artificial Segregating Populations. ''Plants (Basel)''. 2023 Jul 24; '''12''' (14):
Using social interaction models for genetic analysis of skin damage in gilts. Description: Leite, Natalia Galoro, et al. Using social interaction models for genetic analysis of skin damage in gilts. ''Genet Sel Evol''. 2023 Jul 24; '''55''' (1):52
Assessment of bidirectional relationships between brain imaging-derived phenotypes and stroke: a Mendelian randomization study. Description: Yu, Ke, et al. Assessment of bidirectional relationships between brain imaging-derived phenotypes and stroke: a Mendelian randomization study. ''BMC Med''. 2023 Jul 25; '''21''' (1):271
Genome-wide association study identified six loci associated with adverse drug reactions to aripiprazole in schizophrenia patients. Description: Wang, Xueping, et al. Genome-wide association study identified six loci associated with adverse drug reactions to aripiprazole in schizophrenia patients. ''Schizophrenia (Heidelb)''. 2023 Jul 25; '''9''' (1):44
Identification of loci involved in childhood visual acuity and associations with cognitive skills and educational attainment. Description: Schmitz, Judith, et al. Identification of loci involved in childhood visual acuity and associations with cognitive skills and educational attainment. ''NPJ Sci Learn''. 2023 Jul 25; '''8''' (1):25
Leukocytes carrying Clonal Hematopoiesis of Indeterminate Potential (CHIP) Mutations invade Human Atherosclerotic Plaques. Description: von Scheidt, Moritz, et al. Leukocytes carrying Clonal Hematopoiesis of Indeterminate Potential (CHIP) Mutations invade Human Atherosclerotic Plaques. ''medRxiv''. 2023 Jul 26;
Whole genome sequencing reveals signals of adaptive admixture in Creole cattle. Description: Ben-Jemaa, Slim, et al. Whole genome sequencing reveals signals of adaptive admixture in Creole cattle. ''Sci Rep''. 2023 Jul 27; '''13''' (1):12155
The role and risks of selective adaptation in extreme coral habitats. Description: Scucchia, Federica, et al. The role and risks of selective adaptation in extreme coral habitats. ''Nat Commun''. 2023 Jul 28; '''14''' (1):4475
Alzheimer's polygenic risk scores, APOE, Alzheimer's disease risk, and dementia-related blood biomarker levels in a population-based cohort study followed over 17 years. Description: Stocker, Hannah, et al. Alzheimer's polygenic risk scores, APOE, Alzheimer's disease risk, and dementia-related blood biomarker levels in a population-based cohort study followed over 17 years. ''Alzheimers Res Ther''. 2023 Jul 29; '''15''' (1):129
Assessing causal relationship between circulating cytokines and age-related neurodegenerative diseases: a bidirectional two-sample Mendelian randomization analysis. Description: Yin, Zihan, et al. Assessing causal relationship between circulating cytokines and age-related neurodegenerative diseases: a bidirectional two-sample Mendelian randomization analysis. ''Sci Rep''. 2023 Jul 29; '''13''' (1):12325
A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population. Description: Mauleekoonphairoj, John, et al. A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population. ''Sci Rep''. 2023 Jul 31; '''13''' (1):12360
Chromosome-level genome assembly and population genomics of Robinia pseudoacacia reveal the genetic basis for its wide cultivation. Description: Wang, Zefu, et al. Chromosome-level genome assembly and population genomics of Robinia pseudoacacia reveal the genetic basis for its wide cultivation. ''Commun Biol''. 2023 Jul 31; '''6''' (1):797
Genetic impacts on DNA methylation help elucidate regulatory genomic processes. Description: Villicana, Sergio, et al. Genetic impacts on DNA methylation help elucidate regulatory genomic processes. ''Genome Biol''. 2023 Jul 31; '''24''' (1):176
Population transcriptogenomics highlights impaired metabolism and small population sizes in tree frogs living in the Chernobyl Exclusion Zone. Description: Car, Clement, et al. Population transcriptogenomics highlights impaired metabolism and small population sizes in tree frogs living in the Chernobyl Exclusion Zone. ''BMC Biol''. 2023 Jul 31; '''21''' (1):164
Abdominal obesity is a more important causal risk factor for pancreatic cancer than overall obesity. Description: Maina, Jared G, et al. Abdominal obesity is a more important causal risk factor for pancreatic cancer than overall obesity. ''Eur J Hum Genet''. 2023 Aug; '''31''' (8):962-966
Accurate detection of shared genetic architecture from GWAS summary statistics in the small-sample context. Description: Willis, Thomas W, et al. Accurate detection of shared genetic architecture from GWAS summary statistics in the small-sample context. ''PLoS Genet''. 2023 Aug; '''19''' (8):e1010852
A Genetic Locus within the FMN1/GREM1 Gene Region Interacts with Body Mass Index in Colorectal Cancer Risk. Description: Aglago, Elom K, et al. A Genetic Locus within the FMN1/GREM1 Gene Region Interacts with Body Mass Index in Colorectal Cancer Risk. ''Cancer Res''. 2023 Aug 1; '''83''' (15):2572-2583
An HBV susceptibility variant of KNG1 modulates the therapeutic effects of interferons alpha and lambda1 in HBV infection by promoting MAVS lysosomal degradation. Description: Zhang, Bin, et al. An HBV susceptibility variant of KNG1 modulates the therapeutic effects of interferons alpha and lambda1 in HBV infection by promoting MAVS lysosomal degradation. ''EBioMedicine''. 2023 Aug; '''94''': 104694
A novel de novo TP63 mutation in whole-exome sequencing of a Syrian family with Oral cleft and ectrodactyly. Description: Simpson, Claire L, et al. A novel de novo TP63 mutation in whole-exome sequencing of a Syrian family with Oral cleft and ectrodactyly. ''Mol Genet Genomic Med''. 2023 Aug; '''11''' (8):e2179
A Pilot Genome-Wide Association Study Identifies Novel Markers of Metabolic Syndrome in Patients with Psoriasis. Description: Oh, Seung-Min, et al. A Pilot Genome-Wide Association Study Identifies Novel Markers of Metabolic Syndrome in Patients with Psoriasis. ''Ann Dermatol''. 2023 Aug; '''35''' (4):285-292
A single-cell atlas of in vitro multiculture systems uncovers the in vivo lineage trajectory and cell state in the human lung. Description: Lee, Woochan, et al. A single-cell atlas of in vitro multiculture systems uncovers the in vivo lineage trajectory and cell state in the human lung. ''Exp Mol Med''. 2023 Aug; '''55''' (8):1831-1842
Association of single nucleotide polymorphisms with dyslipidemia and risk of metabolic disorders in the State of Qatar. Description: Al-Sharshani, Dalal, et al. Association of single nucleotide polymorphisms with dyslipidemia and risk of metabolic disorders in the State of Qatar. ''Mol Genet Genomic Med''. 2023 Aug; '''11''' (8):e2178
Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Description: Islam, Md Rafiqul, et al. Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. ''Hum Genet''. 2023 Aug; '''142''' (8):1149-1172
Estimation of genetic parameters for pork belly traits. Description: Lee, Seung-Hoon, et al. Estimation of genetic parameters for pork belly traits. ''Anim Biosci''. 2023 Aug; '''36''' (8):1156-1166
Exome-wide association study of treatment-resistant depression suggests novel treatment targets. Description: Shah, Shrey B, et al. Exome-wide association study of treatment-resistant depression suggests novel treatment targets. ''Sci Rep''. 2023 Aug 1; '''13''' (1):12467
Genes of Predisposition to Childhood Beta-Cell Acute Lymphoblastic Leukemia in the Kazakh Population. Description: Svyatova, Gulnara, et al. Genes of Predisposition to Childhood Beta-Cell Acute Lymphoblastic Leukemia in the Kazakh Population. ''Asian Pac J Cancer Prev''. 2023 Aug 1; '''24''' (8):2653-2666
Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis. Description: Yarmolinsky, James, et al. Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis. ''Diabetologia''. 2023 Aug; '''66''' (8):1481-1500
Genetic diversity and signatures of selection in four indigenous horse breeds of Iran. Description: Mousavi, Seyedeh Fatemeh, et al. Genetic diversity and signatures of selection in four indigenous horse breeds of Iran. ''Heredity (Edinb)''. 2023 Aug; '''131''' (2):96-108
Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood. Description: Hawkes, Gareth, et al. Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood. ''Diabetologia''. 2023 Aug; '''66''' (8):1472-1480
Genetics of Pulmonary Pressure and Right Ventricle Stress Identify Diabetes as a Causal Risk Factor. Description: Bagheri, Minoo, et al. Genetics of Pulmonary Pressure and Right Ventricle Stress Identify Diabetes as a Causal Risk Factor. ''J Am Heart Assoc''. 2023 Aug; '''12''' (15):e029190
Genetic structure and characteristics of Tibetan chickens. Description: Li, Shijun, et al. Genetic structure and characteristics of Tibetan chickens. ''Poult Sci''. 2023 Aug; '''102''' (8):102767
Genome-wide association study revealed the genomic regions associated with skin pigmentation in an Ogye x White Leghorn F2 chicken population. Description: Cha, Jihye, et al. Genome-wide association study revealed the genomic regions associated with skin pigmentation in an Ogye x White Leghorn F2 chicken population. ''Poult Sci''. 2023 Aug; '''102''' (8):102720
Genome-wide by environment interaction studies of maternal smoking and educational score in UK biobank. Description: Huang, Huimei, et al. Genome-wide by environment interaction studies of maternal smoking and educational score in UK biobank. ''Psychiatr Genet''. 2023 Aug 1; '''33''' (4):152-159
Genomic diversity landscapes in outcrossing and selfing Caenorhabditis nematodes. Description: Teterina, Anastasia A, et al. Genomic diversity landscapes in outcrossing and selfing Caenorhabditis nematodes. ''PLoS Genet''. 2023 Aug; '''19''' (8):e1010879
Genomic Resequencing Unravels the Genetic Basis of Domestication, Expansion, and Trait Improvement in Morus Atropurpurea. Description: Dai, Fanwei, et al. Genomic Resequencing Unravels the Genetic Basis of Domestication, Expansion, and Trait Improvement in Morus Atropurpurea. ''Adv Sci (Weinh)''. 2023 Aug; '''10''' (24):e2300039
GSTM1 and GSTT1 polymorphisms associated with pain in a chemotherapy-induced peripheral neuropathy cohort. Description: Dunn, Paul J, et al. GSTM1 and GSTT1 polymorphisms associated with pain in a chemotherapy-induced peripheral neuropathy cohort. ''J Cancer Res Clin Oncol''. 2023 Aug; '''149''' (10):7405-7412
Identifying genetic loci that are associated with changes in gene expression in PTSD in a South African cohort. Description: Swart, Patricia C, et al. Identifying genetic loci that are associated with changes in gene expression in PTSD in a South African cohort. ''J Neurochem''. 2023 Aug; '''166''' (4):705-719
Low and high serum IgG associates with respiratory infections in a young and working age population. Description: Holma, Pia, et al. Low and high serum IgG associates with respiratory infections in a young and working age population. ''EBioMedicine''. 2023 Aug; '''94''': 104712
Migraine, chronic kidney disease and kidney function: observational and genetic analyses. Description: Zhang, Wenqiang, et al. Migraine, chronic kidney disease and kidney function: observational and genetic analyses. ''Hum Genet''. 2023 Aug; '''142''' (8):1185-1200
Multi-ancestry GWAS analysis identifies two novel loci associated with diabetic eye disease and highlights APOL1 as a high risk locus in patients with diabetic macular edema. Description: Stockwell, Amy D, et al. Multi-ancestry GWAS analysis identifies two novel loci associated with diabetic eye disease and highlights APOL1 as a high risk locus in patients with diabetic macular edema. ''PLoS Genet''. 2023 Aug; '''19''' (8):e1010609
Polygenic contributions to performance on the Balloon Analogue Risk Task. Description: Nurmi, E L, et al. Polygenic contributions to performance on the Balloon Analogue Risk Task. ''Mol Psychiatry''. 2023 Aug; '''28''' (8):3524-3530
Polygenicity of Comorbid Depression in Multiple Sclerosis. Description: Kowalec, Kaarina, et al. Polygenicity of Comorbid Depression in Multiple Sclerosis. ''Neurology''. 2023 Aug 1; '''101''' (5):e522-e532
Profiling the Somatic Mutational Landscape of Breast Tumors from Hispanic/Latina Women Reveals Conserved and Unique Characteristics. Description: Ding, Yuan Chun, et al. Profiling the Somatic Mutational Landscape of Breast Tumors from Hispanic/Latina Women Reveals Conserved and Unique Characteristics. ''Cancer Res''. 2023 Aug 1; '''83''' (15):2600-2613
Studying the genetics of participation using footprints left on the ascertained genotypes. Description: Benonisdottir, Stefania, et al. Studying the genetics of participation using footprints left on the ascertained genotypes. ''Nat Genet''. 2023 Aug; '''55''' (8):1413-1420
Transcriptomic risk scores for attention deficit/hyperactivity disorder. Description: Cabana-Dominguez, Judit, et al. Transcriptomic risk scores for attention deficit/hyperactivity disorder. ''Mol Psychiatry''. 2023 Aug; '''28''' (8):3493-3502
Genetic insights into resting heart rate and its role in cardiovascular disease. Description: van de Vegte, Yordi J, et al. Genetic insights into resting heart rate and its role in cardiovascular disease. ''Nat Commun''. 2023 Aug 2; '''14''' (1):4646
Genomic insight into domestication of rubber tree. Description: Chao, Jinquan, et al. Genomic insight into domestication of rubber tree. ''Nat Commun''. 2023 Aug 2; '''14''' (1):4651
Linear and Nonlinear Associations Between Vitamin D and Grip Strength: A Mendelian Randomization Study in UK Biobank. Description: Pinto Pereira, Snehal M, et al. Linear and Nonlinear Associations Between Vitamin D and Grip Strength: A Mendelian Randomization Study in UK Biobank. ''J Gerontol A Biol Sci Med Sci''. 2023 Aug 2; '''78''' (8):1483-1488
A syntelog-based pan-genome provides insights into rice domestication and de-domestication. Description: Wu, Dongya, et al. A syntelog-based pan-genome provides insights into rice domestication and de-domestication. ''Genome Biol''. 2023 Aug 3; '''24''' (1):179
Genetic Architecture of Flowering Time Differs Between Populations With Contrasting Demographic and Selective Histories. Description: Neto, Celia, et al. Genetic Architecture of Flowering Time Differs Between Populations With Contrasting Demographic and Selective Histories. ''Mol Biol Evol''. 2023 Aug 3; '''40''' (8):
Genetic Incompatibilities and Evolutionary Rescue by Wild Relatives Shaped Grain Amaranth Domestication. Description: Goncalves-Dias, Jose, et al. Genetic Incompatibilities and Evolutionary Rescue by Wild Relatives Shaped Grain Amaranth Domestication. ''Mol Biol Evol''. 2023 Aug 3; '''40''' (8):
Local ancestry and selection in admixed Sanjiang cattle. Description: Lyu, Yang, et al. Local ancestry and selection in admixed Sanjiang cattle. ''Stress Biol''. 2023 Aug 3; '''3''' (1):30
Multiple Origins and Genomic Basis of Complex Traits in Sighthounds. Description: Li, Wu-Lue, et al. Multiple Origins and Genomic Basis of Complex Traits in Sighthounds. ''Mol Biol Evol''. 2023 Aug 3; '''40''' (8):
Unraveling Prevalence and Effects of Deleterious Mutations in Maize Elite Lines across Decades of Modern Breeding. Description: Sun, Shichao, et al. Unraveling Prevalence and Effects of Deleterious Mutations in Maize Elite Lines across Decades of Modern Breeding. ''Mol Biol Evol''. 2023 Aug 3; '''40''' (8):
A multi-omics analysis identifies molecular features associated with fertility in heifers (Bos taurus). Description: Marrella, Mackenzie A, et al. A multi-omics analysis identifies molecular features associated with fertility in heifers (Bos taurus). ''Sci Rep''. 2023 Aug 4; '''13''' (1):12664
Improving Genetic Association Studies with a Novel Methodology that Unveils the Hidden Complexity of All-Cause Heart Failure. Description: Gregg, John T, et al. Improving Genetic Association Studies with a Novel Methodology that Unveils the Hidden Complexity of All-Cause Heart Failure. ''medRxiv''. 2023 Aug 4;
Interpreting SNP heritability in admixed populations. Description: Huang, Jinguo, et al. Interpreting SNP heritability in admixed populations. ''bioRxiv''. 2023 Aug 4;
The meaning of wild: Genetic and adaptive consequences from large-scale releases of domestic mallards. Description: Lavretsky, Philip, et al. The meaning of wild: Genetic and adaptive consequences from large-scale releases of domestic mallards. ''Commun Biol''. 2023 Aug 5; '''6''' (1):819
History of the terrestrial isopod genus Ligidium in Japan based on phylogeographic analysis. Description: Harigai, Wakana, et al. History of the terrestrial isopod genus Ligidium in Japan based on phylogeographic analysis. ''BMC Ecol Evol''. 2023 Aug 7; '''23''' (1):38
Megafaunal extinctions, not climate change, may explain Holocene genetic diversity declines in Numenius shorebirds. Description: Tan, Hui Zhen, et al. Megafaunal extinctions, not climate change, may explain Holocene genetic diversity declines in Numenius shorebirds. ''Elife''. 2023 Aug 7; '''12''':
Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases. Description: Carland, Corinne, et al. Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases. ''Clin Proteomics''. 2023 Aug 7; '''20''' (1):31
Association of LINC-PINT polymorphisms with lumbar disc herniation risk among Chinese Han population: a case control study. Description: Wu, Yimin, et al. Association of LINC-PINT polymorphisms with lumbar disc herniation risk among Chinese Han population: a case control study. ''J Orthop Surg Res''. 2023 Aug 8; '''18''' (1):585
Gene expression changes in sickle cell reticulocytes and their clinical associations. Description: Zhang, Xu, et al. Gene expression changes in sickle cell reticulocytes and their clinical associations. ''Sci Rep''. 2023 Aug 8; '''13''' (1):12864
Genome wide association analysis of cuticle deposition in laying hens. Description: Wang, Zhang, et al. Genome wide association analysis of cuticle deposition in laying hens. ''Poult Sci''. 2023 Aug 8; '''102''' (10):102990
Advancing diagnosis and management of liver disease in adults through exome sequencing. Description: Zheng, Melanie, et al. Advancing diagnosis and management of liver disease in adults through exome sequencing. ''EBioMedicine''. 2023 Aug 9; '''95''': 104747
Contribution of an Asian-prevalent HLA haplotype to the risk of HBV-related hepatocellular carcinoma. Description: Kawamura, Atsushi, et al. Contribution of an Asian-prevalent HLA haplotype to the risk of HBV-related hepatocellular carcinoma. ''Sci Rep''. 2023 Aug 9; '''13''' (1):12944
Cystatin C is glucocorticoid responsive, directs recruitment of Trem2+ macrophages, and predicts failure of cancer immunotherapy. Description: Kleeman, Sam O, et al. Cystatin C is glucocorticoid responsive, directs recruitment of Trem2+ macrophages, and predicts failure of cancer immunotherapy. ''Cell Genom''. 2023 Aug 9; '''3''' (8):100347
Genetic continuity, isolation, and gene flow in Stone Age Central and Eastern Europe. Description: Mattila, Tiina M, et al. Genetic continuity, isolation, and gene flow in Stone Age Central and Eastern Europe. ''Commun Biol''. 2023 Aug 9; '''6''' (1):793
Genotyping and population characteristics of the China Kadoorie Biobank. Description: Walters, Robin G, et al. Genotyping and population characteristics of the China Kadoorie Biobank. ''Cell Genom''. 2023 Aug 9; '''3''' (8):100361
Impact of pathogen genetics on clinical phenotypes in a population of Talaromyces marneffei from Vietnam. Description: Sephton-Clark, Poppy, et al. Impact of pathogen genetics on clinical phenotypes in a population of Talaromyces marneffei from Vietnam. ''Genetics''. 2023 Aug 9; '''224''' (4):
Insights from a chum salmon (Oncorhynchus keta) genome assembly regarding whole-genome duplication and nucleotide variation influencing gene function. Description: Rondeau, Eric B, et al. Insights from a chum salmon (Oncorhynchus keta) genome assembly regarding whole-genome duplication and nucleotide variation influencing gene function. ''G3 (Bethesda)''. 2023 Aug 9; '''13''' (8):
Linkage and association of variants in the dopamine receptor 2 gene (DRD2) with polycystic ovary syndrome. Description: Amin, Mutaz, et al. Linkage and association of variants in the dopamine receptor 2 gene (DRD2) with polycystic ovary syndrome. ''J Ovarian Res''. 2023 Aug 10; '''16''' (1):158
A genome-wide by PM(10) exposure interaction study for blood pressure in Korean adults. Description: Kim, Hyun-Jin, et al. A genome-wide by PM(10) exposure interaction study for blood pressure in Korean adults. ''Sci Rep''. 2023 Aug 11; '''13''' (1):13060
Potential of low-density genotype imputation for cost-efficient genomic selection for resistance to Flavobacterium columnare in rainbow trout (Oncorhynchus mykiss). Description: Fraslin, Clemence, et al. Potential of low-density genotype imputation for cost-efficient genomic selection for resistance to Flavobacterium columnare in rainbow trout (Oncorhynchus mykiss). ''Genet Sel Evol''. 2023 Aug 14; '''55''' (1):59
Association between vmPFC gray matter volume and smoking initiation in adolescents. Description: Xiang, Shitong, et al. Association between vmPFC gray matter volume and smoking initiation in adolescents. ''Nat Commun''. 2023 Aug 15; '''14''' (1):4684
Causal role of immune cells in schizophrenia: Mendelian randomization (MR) study. Description: Wang, Chengdong, et al. Causal role of immune cells in schizophrenia: Mendelian randomization (MR) study. ''BMC Psychiatry''. 2023 Aug 15; '''23''' (1):590
The genomic history of the indigenous people of the Canary Islands. Description: Serrano, Javier G, et al. The genomic history of the indigenous people of the Canary Islands. ''Nat Commun''. 2023 Aug 15; '''14''' (1):4641
Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease. Description: Georgakis, Marios K, et al. Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease. ''medRxiv''. 2023 Aug 16;
Polygenic Risk Score Improves Prediction of Primary Open Angle Glaucoma Onset in the Ocular Hypertension Treatment Study. Description: Singh, Rishabh K, et al. Polygenic Risk Score Improves Prediction of Primary Open Angle Glaucoma Onset in the Ocular Hypertension Treatment Study. ''medRxiv''. 2023 Aug 16;
Genetic characterisation of the Connemara pony and the Warmblood horse using a within-breed clustering approach. Description: Lindsay-McGee, Victoria, et al. Genetic characterisation of the Connemara pony and the Warmblood horse using a within-breed clustering approach. ''Genet Sel Evol''. 2023 Aug 17; '''55''' (1):60
Genome-Wide Association Studies Using 3VmrMLM Model Provide New Insights into Branched-Chain Amino Acid Contents in Rice Grains. Description: Sui, Yao, et al. Genome-Wide Association Studies Using 3VmrMLM Model Provide New Insights into Branched-Chain Amino Acid Contents in Rice Grains. ''Plants (Basel)''. 2023 Aug 17; '''12''' (16):
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Description: Akbari, Parsa, et al. A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. ''Nat Commun''. 2023 Aug 18; '''14''' (1):5023
Genetic-based dissection of resistance to bacterial leaf streak in rice by GWAS. Description: Zhu, Xiaoyang, et al. Genetic-based dissection of resistance to bacterial leaf streak in rice by GWAS. ''BMC Plant Biol''. 2023 Aug 18; '''23''' (1):396
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics. Description: Mosley, Jonathan D, et al. Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics. ''medRxiv''. 2023 Aug 21;
Deep learning based phenotyping of medical images improves power for gene discovery of complex disease. Description: Flynn, Brianna I, et al. Deep learning based phenotyping of medical images improves power for gene discovery of complex disease. ''NPJ Digit Med''. 2023 Aug 21; '''6''' (1):155
Environmental and genetic predictors of human cardiovascular ageing. Description: Shah, Mit, et al. Environmental and genetic predictors of human cardiovascular ageing. ''Nat Commun''. 2023 Aug 21; '''14''' (1):4941
Genome-wide scan for runs of homozygosity in South American Camelids. Description: Pallotti, Stefano, et al. Genome-wide scan for runs of homozygosity in South American Camelids. ''BMC Genomics''. 2023 Aug 21; '''24''' (1):470
LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry. Description: Katsumata, Yuriko, et al. LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry. ''J Neuropathol Exp Neurol''. 2023 Aug 21; '''82''' (9):760-768
Noncoding genetic variation in ISPD distinguishes gamecocks from nongame chickens. Description: Bendesky, Andres, et al. Noncoding genetic variation in ISPD distinguishes gamecocks from nongame chickens. ''bioRxiv''. 2023 Aug 21;
Comparative Analysis Reveals Different Evolutionary Fates and Biological Functions in Wheat Duplicated Genes (Triticum aestivum L.). Description: Cui, Licao, et al. Comparative Analysis Reveals Different Evolutionary Fates and Biological Functions in Wheat Duplicated Genes (Triticum aestivum L.). ''Plants (Basel)''. 2023 Aug 22; '''12''' (17):
Genetic Variation and Sensory Perception of a Pediatric Formulation of Ibuprofen: Can a Medicine Taste Too Good for Some? Description: Mennella, Julie A, et al. Genetic Variation and Sensory Perception of a Pediatric Formulation of Ibuprofen: Can a Medicine Taste Too Good for Some? ''Int J Mol Sci''. 2023 Aug 22; '''24''' (17):
Multiomics Data Analysis Identified CpG Sites That Mediate the Impact of Smoking on Cardiometabolic Traits. Description: Nikpay, Majid. Multiomics Data Analysis Identified CpG Sites That Mediate the Impact of Smoking on Cardiometabolic Traits. ''Epigenomes''. 2023 Aug 22; '''7''' (3):
Multivariate Genome-Wide Association Study of Concentrations of Seven Elements in Seeds Reveals Four New Loci in Russian Wheat Lines. Description: Potapova, Nadezhda A, et al. Multivariate Genome-Wide Association Study of Concentrations of Seven Elements in Seeds Reveals Four New Loci in Russian Wheat Lines. ''Plants (Basel)''. 2023 Aug 22; '''12''' (17):
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2. Description: Littleton, Sheridan H, et al. Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2. ''bioRxiv''. 2023 Aug 22;
A Case-Only Genome-Wide Interaction Study of Smoking and Bladder Cancer Risk: Results from the COBLAnCE Cohort. Description: Karimi, Maryam, et al. A Case-Only Genome-Wide Interaction Study of Smoking and Bladder Cancer Risk: Results from the COBLAnCE Cohort. ''Cancers (Basel)''. 2023 Aug 23; '''15''' (17):
Accurate haplotype construction and detection of selection signatures enabled by high quality pig genome sequences. Description: Tong, Xinkai, et al. Accurate haplotype construction and detection of selection signatures enabled by high quality pig genome sequences. ''Nat Commun''. 2023 Aug 23; '''14''' (1):5126
Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects. Description: Ito, Shuji, et al. Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects. ''Nat Commun''. 2023 Aug 23; '''14''' (1):4863
Neuroimaging-AI Endophenotypes of Brain Diseases in the General Population: Towards a Dimensional System of Vulnerability. Description: Wen, Junhao, et al. Neuroimaging-AI Endophenotypes of Brain Diseases in the General Population: Towards a Dimensional System of Vulnerability. ''medRxiv''. 2023 Aug 24;
Reference LINE-1 insertion polymorphisms correlate with Parkinson's disease progression and differential transcript expression in the PPMI cohort. Description: Frohlich, Alexander, et al. Reference LINE-1 insertion polymorphisms correlate with Parkinson's disease progression and differential transcript expression in the PPMI cohort. ''Sci Rep''. 2023 Aug 24; '''13''' (1):13857
Understanding the underlying genetic mechanisms for age at first calving, inter-calving period and scrotal circumference in Bonsmara cattle. Description: Reding, Jason J, et al. Understanding the underlying genetic mechanisms for age at first calving, inter-calving period and scrotal circumference in Bonsmara cattle. ''BMC Genomics''. 2023 Aug 24; '''24''' (1):480
A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets. Description: Di Scipio, Matteo, et al. A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets. ''Nat Commun''. 2023 Aug 25; '''14''' (1):5196
DNA methylation at the suppressor of cytokine signaling 3 (SOCS3) gene influences height in childhood. Description: Issarapu, Prachand, et al. DNA methylation at the suppressor of cytokine signaling 3 (SOCS3) gene influences height in childhood. ''Nat Commun''. 2023 Aug 25; '''14''' (1):5200
The combined effect of lifestyle factors and polygenic scores on age at onset in Parkinson's disease. Description: Gabbert, Carolin, et al. The combined effect of lifestyle factors and polygenic scores on age at onset in Parkinson's disease. ''medRxiv''. 2023 Aug 25;
Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments. Description: Alibutud, Rohan, et al. Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments. ''Int J Mol Sci''. 2023 Aug 26; '''24''' (17):
A high-resolution genotype-phenotype map identifies the TaSPL17 controlling grain number and size in wheat. Description: Liu, Yangyang, et al. A high-resolution genotype-phenotype map identifies the TaSPL17 controlling grain number and size in wheat. ''Genome Biol''. 2023 Aug 28; '''24''' (1):196
Genome-Wide Association Study to Identify QTL for Carcass Traits in Korean Hanwoo Cattle. Description: Alam, Mohammad Zahangir, et al. Genome-Wide Association Study to Identify QTL for Carcass Traits in Korean Hanwoo Cattle. ''Animals (Basel)''. 2023 Aug 28; '''13''' (17):
ApoE gene polymorphisms and metals and their interactions with cognitive function. Description: Ye, Zeyan, et al. ApoE gene polymorphisms and metals and their interactions with cognitive function. ''BMC Med Genomics''. 2023 Aug 29; '''16''' (1):206
Genome-wide association studies of human and rat BMI converge on synapse, epigenome, and hormone signaling networks. Description: Wright, Sarah N, et al. Genome-wide association studies of human and rat BMI converge on synapse, epigenome, and hormone signaling networks. ''Cell Rep''. 2023 Aug 29; '''42''' (8):112873
Identifying the mediating role of socioeconomic status on the relationship between schizophrenia and major depressive disorder: a Mendelian randomisation analysis. Description: Xu, Qiang, et al. Identifying the mediating role of socioeconomic status on the relationship between schizophrenia and major depressive disorder: a Mendelian randomisation analysis. ''Schizophrenia (Heidelb)''. 2023 Aug 29; '''9''' (1):53
A polygenic risk score for Alzheimer's disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. Description: Sofer, Tamar, et al. A polygenic risk score for Alzheimer's disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. ''Alzheimers Res Ther''. 2023 Aug 30; '''15''' (1):146
Associations of cardiometabolic polygenic risk scores with cardiovascular disease in African Americans. Description: Tsegaselassie, Workalemahu, et al. Associations of cardiometabolic polygenic risk scores with cardiovascular disease in African Americans. ''Res Sq''. 2023 Aug 30;
Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes. Description: Llucia-Carol, Laia, et al. Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes. ''Int J Mol Sci''. 2023 Aug 30; '''24''' (17):
GWLD: an R package for genome-wide linkage disequilibrium analysis. Description: Zhang, Rong, et al. GWLD: an R package for genome-wide linkage disequilibrium analysis. ''G3 (Bethesda)''. 2023 Aug 30; '''13''' (9):
Universal Genome-Wide Association Studies: Powerful Joint Ancestry and Association Testing. Description: Shriner, Daniel, et al. Universal Genome-Wide Association Studies: Powerful Joint Ancestry and Association Testing. ''HGG Adv''. 2023 Aug 30; '''4''' (4):100235
Using Drosophila to identify naturally occurring genetic modifiers of amyloid beta 42- and tau-induced toxicity. Description: Yang, Ming, et al. Using Drosophila to identify naturally occurring genetic modifiers of amyloid beta 42- and tau-induced toxicity. ''G3 (Bethesda)''. 2023 Aug 30; '''13''' (9):
Whole-genome sequencing reveals adaptations of hairy-footed jerboas (Dipus, Dipodidae) to diverse desert environments. Description: Peng, Xingwen, et al. Whole-genome sequencing reveals adaptations of hairy-footed jerboas (Dipus, Dipodidae) to diverse desert environments. ''BMC Biol''. 2023 Aug 30; '''21''' (1):182
Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials. Description: Loomis, Stephanie J, et al. Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials. ''Sci Rep''. 2023 Aug 31; '''13''' (1):14313
Genomic Characterization and Initial Insight into Mastitis-Associated SNP Profiles of Local Latvian Bos taurus Breeds. Description: Gudra, Dita, et al. Genomic Characterization and Initial Insight into Mastitis-Associated SNP Profiles of Local Latvian Bos taurus Breeds. ''Animals (Basel)''. 2023 Aug 31; '''13''' (17):
Neurogenetic mechanisms of risk for ADHD: Examining associations of polygenic scores and brain volumes in a population cohort. Description: He, Quanfa, et al. Neurogenetic mechanisms of risk for ADHD: Examining associations of polygenic scores and brain volumes in a population cohort. ''J Neurodev Disord''. 2023 Aug 31; '''15''' (1):30
Young SINEs in pig genomes impact gene regulation, genetic diversity, and complex traits. Description: Zhao, Pengju, et al. Young SINEs in pig genomes impact gene regulation, genetic diversity, and complex traits. ''Commun Biol''. 2023 Aug 31; '''6''' (1):894
A common variant SNP rs1937810 in the MPP7 gene contributes to the susceptibility of breast cancer in the Chinese Han population. Description: Li, Rong, et al. A common variant SNP rs1937810 in the MPP7 gene contributes to the susceptibility of breast cancer in the Chinese Han population. ''Mol Genet Genomic Med''. 2023 Sep; '''11''' (9):e2198
Anthropogenic hybridization and its influence on the adaptive potential of the Sardinian wild boar (Sus scrofa meridionalis). Description: Fabbri, Giulia, et al. Anthropogenic hybridization and its influence on the adaptive potential of the Sardinian wild boar (Sus scrofa meridionalis). ''J Appl Genet''. 2023 Sep; '''64''' (3):521-530
Association of mitochondrial DNA variation with high myopia in a Han Chinese population. Description: Xing, Shilai, et al. Association of mitochondrial DNA variation with high myopia in a Han Chinese population. ''Mol Genet Genomics''. 2023 Sep; '''298''' (5):1059-1071
Bayesian bi-level variable selection for genome-wide survival study. Description: Lee, Eunjee, et al. Bayesian bi-level variable selection for genome-wide survival study. ''Genomics Inform''. 2023 Sep; '''21''' (3):e28
Causal associations of sarcopenia-related traits with cardiometabolic disease and Alzheimer's disease and the mediating role of insulin resistance: A Mendelian randomization study. Description: Ye, Chaojie, et al. Causal associations of sarcopenia-related traits with cardiometabolic disease and Alzheimer's disease and the mediating role of insulin resistance: A Mendelian randomization study. ''Aging Cell''. 2023 Sep; '''22''' (9):e13923
Circulating metabolites modulated by diet are associated with depression. Description: van der Spek, Ashley, et al. Circulating metabolites modulated by diet are associated with depression. ''Mol Psychiatry''. 2023 Sep; '''28''' (9):3874-3887
Common and disorder-specific cortical thickness alterations in internalizing, externalizing and thought disorders during early adolescence: an Adolescent Brain and Cognitive Development study. Description: Yu, Gechang, et al. Common and disorder-specific cortical thickness alterations in internalizing, externalizing and thought disorders during early adolescence: an Adolescent Brain and Cognitive Development study. ''J Psychiatry Neurosci''. 2023 Sep-Oct; '''48''' (5):E345-E356
De Novo Mutation Rates in Sticklebacks. Description: Zhang, Chaowei, et al. De Novo Mutation Rates in Sticklebacks. ''Mol Biol Evol''. 2023 Sep 1; '''40''' (9):
Dissecting human population variation in single-cell responses to SARS-CoV-2. Description: Aquino, Yann, et al. Dissecting human population variation in single-cell responses to SARS-CoV-2. ''Nature''. 2023 Sep; '''621''' (7977):120-128
Evolution of Human Brain Left-Right Asymmetry: Old Genes with New Functions. Description: Wang, Jianguo, et al. Evolution of Human Brain Left-Right Asymmetry: Old Genes with New Functions. ''Mol Biol Evol''. 2023 Sep 1; '''40''' (9):
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk. Description: Wilcox, Naomi, et al. Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk. ''Nat Genet''. 2023 Sep; '''55''' (9):1435-1439
Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes. Description: Warrier, Varun, et al. Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes. ''Nat Genet''. 2023 Sep; '''55''' (9):1483-1493
Genetics of cell-type-specific post-transcriptional gene regulation during human neurogenesis. Description: Aygun, Nil, et al. Genetics of cell-type-specific post-transcriptional gene regulation during human neurogenesis. ''bioRxiv''. 2023 Sep 1;
Genetic variants associated with SARS-CoV-2 infection also affect lung function and asthma severity. Description: Silva, Milca de Jesus, et al. Genetic variants associated with SARS-CoV-2 infection also affect lung function and asthma severity. ''Heliyon''. 2023 Sep; '''9''' (9):e19235
Genome assembly and resequencing analyses provide new insights into the evolution, domestication and ornamental traits of crape myrtle. Description: Zhou, Yang, et al. Genome assembly and resequencing analyses provide new insights into the evolution, domestication and ornamental traits of crape myrtle. ''Hortic Res''. 2023 Sep; '''10''' (9):uhad146
Genome-wide association and replication studies for handedness in a Korean community-based cohort. Description: Song, Youhyun, et al. Genome-wide association and replication studies for handedness in a Korean community-based cohort. ''Brain Behav''. 2023 Sep; '''13''' (9):e3121
Genome-wide association study of abnormal elevation of ALT in patients exposed to atabecestat. Description: Li, Qingqin S, et al. Genome-wide association study of abnormal elevation of ALT in patients exposed to atabecestat. ''BMC Genomics''. 2023 Sep 1; '''24''' (1):513
Genomic analysis reveals complex population structure within the smooth newt, Lissotriton vulgaris, in Central Europe. Description: Herczeg, David, et al. Genomic analysis reveals complex population structure within the smooth newt, Lissotriton vulgaris, in Central Europe. ''Ecol Evol''. 2023 Sep; '''13''' (9):e10478
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Description: GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. ''Nat Genet''. 2023 Sep; '''55''' (9):1471-1482
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. Description: Lagou, Vasiliki, et al. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. ''Nat Genet''. 2023 Sep; '''55''' (9):1448-1461
Historic Sampling of a Vanishing Beast: Population Structure and Diversity in the Black Rhinoceros. Description: Sanchez-Barreiro, Fatima, et al. Historic Sampling of a Vanishing Beast: Population Structure and Diversity in the Black Rhinoceros. ''Mol Biol Evol''. 2023 Sep 1; '''40''' (9):
HLA in isolated REM sleep behavior disorder and Lewy body dementia. Description: Yu, Eric, et al. HLA in isolated REM sleep behavior disorder and Lewy body dementia. ''Ann Clin Transl Neurol''. 2023 Sep; '''10''' (9):1682-1687
Increased glutamate in type 2 diabetes in the Korean population is associated with increased plasminogen levels. Description: Lee, Hyo Jung, et al. Increased glutamate in type 2 diabetes in the Korean population is associated with increased plasminogen levels. ''J Diabetes''. 2023 Sep; '''15''' (9):777-786
Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients. Description: Al-Jumaan, Mohammed, et al. Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients. ''Genome Med''. 2023 Sep 1; '''15''' (1):65
Interploidy Introgression Shaped Adaptation during the Origin and Domestication History of Brassica napus. Description: Wang, Tianpeng, et al. Interploidy Introgression Shaped Adaptation during the Origin and Domestication History of Brassica napus. ''Mol Biol Evol''. 2023 Sep 1; '''40''' (9):
Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson's disease. Description: Zhou, Yangjie, et al. Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson's disease. ''NPJ Parkinsons Dis''. 2023 Sep 1; '''9''' (1):129
Natural variation and genetic loci underlying resistance to grain shattering in standing crop of modern wheat. Description: Emebiri, Livinus, et al. Natural variation and genetic loci underlying resistance to grain shattering in standing crop of modern wheat. ''Mol Genet Genomics''. 2023 Sep; '''298''' (5):1211-1224
Ocular and neural genes jointly regulate the visuospatial working memory in ADHD children. Description: Zhao, Yilu, et al. Ocular and neural genes jointly regulate the visuospatial working memory in ADHD children. ''Behav Brain Funct''. 2023 Sep 1; '''19''' (1):14
On the Origins of Phenotypic Parallelism in Benthic and Limnetic Stickleback. Description: Dean, Laura L, et al. On the Origins of Phenotypic Parallelism in Benthic and Limnetic Stickleback. ''Mol Biol Evol''. 2023 Sep 1; '''40''' (9):
Population history modulates the fitness effects of Copy Number Variation in the Roma. Description: Antinucci, Marco, et al. Population history modulates the fitness effects of Copy Number Variation in the Roma. ''Hum Genet''. 2023 Sep; '''142''' (9):1327-1343
Reassessing the association of MUC5B with survival in idiopathic pulmonary fibrosis. Description: Cai, Siyang, et al. Reassessing the association of MUC5B with survival in idiopathic pulmonary fibrosis. ''Ann Hum Genet''. 2023 Sep; '''87''' (5):248-253
Recombulator-X: A fast and user-friendly tool for estimating X chromosome recombination rates in forensic genetics. Description: Aneli, Serena, et al. Recombulator-X: A fast and user-friendly tool for estimating X chromosome recombination rates in forensic genetics. ''PLoS Comput Biol''. 2023 Sep; '''19''' (9):e1011474
Region-specific reversal of epidermal planar polarity in the rosette fancy mouse. Description: Cetera, Maureen, et al. Region-specific reversal of epidermal planar polarity in the rosette fancy mouse. ''Development''. 2023 Sep 1; '''150''' (17):
Review and further developments in statistical corrections for Winner's Curse in genetic association studies. Description: Forde, Amanda, et al. Review and further developments in statistical corrections for Winner's Curse in genetic association studies. ''PLoS Genet''. 2023 Sep; '''19''' (9):e1010546
Sex- and APOE-specific genetic risk factors for late-onset Alzheimer's disease: Evidence from gene-gene interaction of longevity-related loci. Description: Dato, Serena, et al. Sex- and APOE-specific genetic risk factors for late-onset Alzheimer's disease: Evidence from gene-gene interaction of longevity-related loci. ''Aging Cell''. 2023 Sep; '''22''' (9):e13938
Sex differences in brain protein expression and disease. Description: Wingo, Aliza P, et al. Sex differences in brain protein expression and disease. ''Nat Med''. 2023 Sep; '''29''' (9):2224-2232
Single-nucleotide polymorphism at alcohol dehydrogenase 1B: A susceptible gene marker in oro-/hypopharyngeal cancers from genome-wide association study. Description: Chien, Hui-Tzu, et al. Single-nucleotide polymorphism at alcohol dehydrogenase 1B: A susceptible gene marker in oro-/hypopharyngeal cancers from genome-wide association study. ''Cancer Med''. 2023 Sep; '''12''' (18):19174-19187
*SLCO1B15 is protective against non-senile cataracts in cohort prescribed statins: analysis in a British-South Asian cohort.** Description: Magavern, Emma F, et al. SLCO1B1*5 is protective against non-senile cataracts in cohort prescribed statins: analysis in a British-South Asian cohort. ''Pharmacogenomics J''. 2023 Sep; '''23''' (5):134-139
Solanum americanum genome-assisted discovery of immune receptors that detect potato late blight pathogen effectors. Description: Lin, Xiao, et al. Solanum americanum genome-assisted discovery of immune receptors that detect potato late blight pathogen effectors. ''Nat Genet''. 2023 Sep; '''55''' (9):1579-1588
Stratified genetic analysis reveals sex differences in MPO-ANCA-associated vasculitis. Description: Ekman, Diana, et al. Stratified genetic analysis reveals sex differences in MPO-ANCA-associated vasculitis. ''Rheumatology (Oxford)''. 2023 Sep 1; '''62''' (9):3213-3218
The effects of AQP4 rs162009 on resting-state brain activity in Parkinson's disease. Description: Jiang, Mengze, et al. The effects of AQP4 rs162009 on resting-state brain activity in Parkinson's disease. ''CNS Neurosci Ther''. 2023 Sep; '''29''' (9):2645-2655
The Genomic Basis of Adaptation to High Elevations in Africanized Honey Bees. Description: Everitt, Turid, et al. The Genomic Basis of Adaptation to High Elevations in Africanized Honey Bees. ''Genome Biol Evol''. 2023 Sep 1; '''15''' (9):
TMEM132D and VIPR2 Polymorphisms as Genetic Risk Loci for Retinal Detachment: A Genome-Wide Association Study and Polygenic Risk Score Analysis. Description: Chuang, Hao-Kai, et al. TMEM132D and VIPR2 Polymorphisms as Genetic Risk Loci for Retinal Detachment: A Genome-Wide Association Study and Polygenic Risk Score Analysis. ''Invest Ophthalmol Vis Sci''. 2023 Sep 1; '''64''' (12):17
Variant-based heritability assessment of dexmedetomidine and fentanyl clearance in pediatric patients. Description: Shannon, Morgan L, et al. Variant-based heritability assessment of dexmedetomidine and fentanyl clearance in pediatric patients. ''Clin Transl Sci''. 2023 Sep; '''16''' (9):1628-1638
Variations in Genes Encoding Human Papillomavirus Binding Receptors and Susceptibility to Cervical Precancer. Description: Mukherjee, Amrita, et al. Variations in Genes Encoding Human Papillomavirus Binding Receptors and Susceptibility to Cervical Precancer. ''Cancer Epidemiol Biomarkers Prev''. 2023 Sep 1; '''32''' (9):1190-1197
X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease. Description: Leal, Thiago P, et al. X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease. ''Mov Disord''. 2023 Sep; '''38''' (9):1625-1635
Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies. Description: Park, Jun Young, et al. Machine learning-based quantification for disease uncertainty increases the statistical power of genetic association studies. ''Bioinformatics''. 2023 Sep 2; '''39''' (9):
Genetic dissection and genomic prediction for pork cuts and carcass morphology traits in pig. Description: Xie, Lei, et al. Genetic dissection and genomic prediction for pork cuts and carcass morphology traits in pig. ''J Anim Sci Biotechnol''. 2023 Sep 3; '''14''' (1):116
Interactions between Polygenetic Variants and Lifestyle Factors in Hypothyroidism: A Hospital-Based Cohort Study. Description: Kim, Da Sol, et al. Interactions between Polygenetic Variants and Lifestyle Factors in Hypothyroidism: A Hospital-Based Cohort Study. ''Nutrients''. 2023 Sep 3; '''15''' (17):
Comparative and population genomics of buckwheat species reveal key determinants of flavor and fertility. Description: Zhang, Kaixuan, et al. Comparative and population genomics of buckwheat species reveal key determinants of flavor and fertility. ''Mol Plant''. 2023 Sep 4; '''16''' (9):1427-1444
Genetic Diversity, Population Structure, and Environmental Adaptation Signatures of Chinese Coastal Hard-Shell Mussel Mytilus coruscus Revealed by Whole-Genome Sequencing. Description: Guo, Feng, et al. Genetic Diversity, Population Structure, and Environmental Adaptation Signatures of Chinese Coastal Hard-Shell Mussel Mytilus coruscus Revealed by Whole-Genome Sequencing. ''Int J Mol Sci''. 2023 Sep 4; '''24''' (17):
Genomic Basis of Adaptive Divergence in Leg Length between Ground- and Tree-Dwelling Species within a Bird Family. Description: Huang, Miaomiao, et al. Genomic Basis of Adaptive Divergence in Leg Length between Ground- and Tree-Dwelling Species within a Bird Family. ''Genome Biol Evol''. 2023 Sep 4; '''15''' (9):
Improved pearl millet genomes representing the global heterotic pool offer a framework for molecular breeding applications. Description: Ramu, Punna, et al. Improved pearl millet genomes representing the global heterotic pool offer a framework for molecular breeding applications. ''Commun Biol''. 2023 Sep 4; '''6''' (1):902
The effects of SCARB2 and SELPLG gene polymorphisms on EV71 infection in hand, foot and mouth disease. Description: Duan, Feng Yuan, et al. The effects of SCARB2 and SELPLG gene polymorphisms on EV71 infection in hand, foot and mouth disease. ''Biomol Biomed''. 2023 Sep 4; '''23''' (5):815-824
Association of PTGER4 and PRKAA1 genetic polymorphisms with gastric cancer. Description: Yu, Shuyong, et al. Association of PTGER4 and PRKAA1 genetic polymorphisms with gastric cancer. ''BMC Med Genomics''. 2023 Sep 5; '''16''' (1):209
Evolution and distribution of rabies viruses from a panorama view. Description: Li, Gen, et al. Evolution and distribution of rabies viruses from a panorama view. ''Microbiol Spectr''. 2023 Sep 5; '''11''' (5):e0525722
Obesity Prediction in Young Adults from the Jerusalem Perinatal Study: Contribution of Polygenic Risk and Early Life Exposures. Description: Hochner, Hagit, et al. Obesity Prediction in Young Adults from the Jerusalem Perinatal Study: Contribution of Polygenic Risk and Early Life Exposures. ''medRxiv''. 2023 Sep 6;
An eQTL-based Approach Reveals Candidate L1 Transcriptional Regulators in Lymphoblastoid Cells. Description: Bravo, Juan I, et al. An eQTL-based Approach Reveals Candidate L1 Transcriptional Regulators in Lymphoblastoid Cells. ''bioRxiv''. 2023 Sep 7;
Genomes of cultivated and wild Capsicum species provide insights into pepper domestication and population differentiation. Description: Liu, Feng, et al. Genomes of cultivated and wild Capsicum species provide insights into pepper domestication and population differentiation. ''Nat Commun''. 2023 Sep 7; '''14''' (1):5487
Long-term longitudinal analysis of 4,187 participants reveals new insights into determinants of incident clonal hematopoiesis. Description: Uddin, Md Mesbah, et al. Long-term longitudinal analysis of 4,187 participants reveals new insights into determinants of incident clonal hematopoiesis. ''medRxiv''. 2023 Sep 7;
Epigenetic variations are more substantial than genetic variations in rapid adaptation of oyster to Pacific oyster mortality syndrome. Description: Gawra, Janan, et al. Epigenetic variations are more substantial than genetic variations in rapid adaptation of oyster to Pacific oyster mortality syndrome. ''Sci Adv''. 2023 Sep 8; '''9''' (36):eadh8990
Human immune phenotyping reveals accelerated aging in type 1 diabetes. Description: Shapiro, Melanie R, et al. Human immune phenotyping reveals accelerated aging in type 1 diabetes. ''JCI Insight''. 2023 Sep 8; '''8''' (17):
A near-complete genome assembly of the allotetrapolyploid Cenchrus fungigraminus (JUJUNCAO) provides insights into its evolution and C4 photosynthesis. Description: Zheng, Huakun, et al. A near-complete genome assembly of the allotetrapolyploid Cenchrus fungigraminus (JUJUNCAO) provides insights into its evolution and C4 photosynthesis. ''Plant Commun''. 2023 Sep 11; '''4''' (5):100633
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes. Description: Fan, Qiao, et al. Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes. ''Nat Commun''. 2023 Sep 11; '''14''' (1):5574
Dietary approach to stop hypertension and healthy eating index 2015, modify the association between FTO polymorphisms and obesity phenotypes. Description: Hosseini-Esfahani, Firoozeh, et al. Dietary approach to stop hypertension and healthy eating index 2015, modify the association between FTO polymorphisms and obesity phenotypes. ''BMC Res Notes''. 2023 Sep 11; '''16''' (1):204
Impact of CD40 gene polymorphisms on the risk of cervical squamous cell carcinoma: a case-control study. Description: Zhu, Manning, et al. Impact of CD40 gene polymorphisms on the risk of cervical squamous cell carcinoma: a case-control study. ''BMC Cancer''. 2023 Sep 11; '''23''' (1):845
Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families. Description: Hebbar, Prashantha, et al. Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families. ''Sci Rep''. 2023 Sep 11; '''13''' (1):14978
APOE-epsilon4 and BIN1 increase risk of Alzheimer's disease pathology but not specifically of Lewy body pathology. Description: Talyansky, Seth, et al. APOE-epsilon4 and BIN1 increase risk of Alzheimer's disease pathology but not specifically of Lewy body pathology. ''Acta Neuropathol Commun''. 2023 Sep 12; '''11''' (1):149
Genome and whole-genome resequencing of Cinnamomum camphora elucidate its dominance in subtropical urban landscapes. Description: Li, Danqing, et al. Genome and whole-genome resequencing of Cinnamomum camphora elucidate its dominance in subtropical urban landscapes. ''BMC Biol''. 2023 Sep 12; '''21''' (1):192
Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy. Description: Garrett, Melanie E, et al. Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy. ''Blood Adv''. 2023 Sep 12; '''7''' (17):4782-4793
Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy. Description: Sanga, Shamita, et al. Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy. ''Sci Rep''. 2023 Sep 12; '''13''' (1):15095
The genomic footprint of whaling and isolation in fin whale populations. Description: Nigenda-Morales, Sergio F, et al. The genomic footprint of whaling and isolation in fin whale populations. ''Nat Commun''. 2023 Sep 12; '''14''' (1):5465
Identifying latent genetic interactions in genome-wide association studies using multiple traits. Description: Bass, Andrew J, et al. Identifying latent genetic interactions in genome-wide association studies using multiple traits. ''bioRxiv''. 2023 Sep 13;
Impact of gallstone disease on the risk of stroke and coronary artery disease: evidence from prospective observational studies and genetic analyses. Description: Zhang, Li, et al. Impact of gallstone disease on the risk of stroke and coronary artery disease: evidence from prospective observational studies and genetic analyses. ''BMC Med''. 2023 Sep 13; '''21''' (1):353
After the Infection: A Survey of Pathogens and Non-communicable Human Disease. Description: Lape, Michael, et al. After the Infection: A Survey of Pathogens and Non-communicable Human Disease. ''medRxiv''. 2023 Sep 14;
Analysis of polygenic selection in purebred and crossbred pig genomes using generation proxy selection mapping. Description: Grohmann, Caleb J, et al. Analysis of polygenic selection in purebred and crossbred pig genomes using generation proxy selection mapping. ''Genet Sel Evol''. 2023 Sep 14; '''55''' (1):62
Genetic variation in glutamatergic genes moderates the effects of childhood adversity on brain volume and IQ in treatment-resistant schizophrenia. Description: Mohamed Saini, Suriati, et al. Genetic variation in glutamatergic genes moderates the effects of childhood adversity on brain volume and IQ in treatment-resistant schizophrenia. ''Schizophrenia (Heidelb)''. 2023 Sep 14; '''9''' (1):59
Genetic Variations in TrkB.T1 Isoform and Their Association with Somatic and Psychological Symptoms in Individuals with IBS. Description: Hong, H, et al. Genetic Variations in TrkB.T1 Isoform and Their Association with Somatic and Psychological Symptoms in Individuals with IBS. ''medRxiv''. 2023 Sep 14;
Interaction between genetic susceptibility to obesity and food intake on BMI in Finnish school-aged children. Description: Viljakainen, Heli, et al. Interaction between genetic susceptibility to obesity and food intake on BMI in Finnish school-aged children. ''Sci Rep''. 2023 Sep 14; '''13''' (1):15265
Overestimated prediction using polygenic prediction derived from summary statistics. Description: Park, David Keetae, et al. Overestimated prediction using polygenic prediction derived from summary statistics. ''BMC Genom Data''. 2023 Sep 14; '''24''' (1):52
Dense residential areas promote gene flow in dengue vector mosquito Aedes albopictus. Description: Yeo, Huiqing, et al. Dense residential areas promote gene flow in dengue vector mosquito Aedes albopictus. ''iScience''. 2023 Sep 15; '''26''' (9):107577
Genome-wide association study identifies several loci for HEV seropositivity. Description: Smatti, Maria K, et al. Genome-wide association study identifies several loci for HEV seropositivity. ''iScience''. 2023 Sep 15; '''26''' (9):107586
Genome-Wide Association Study of Starch Properties in Local Thai Rice. Description: Praphasanobol, Parama, et al. Genome-Wide Association Study of Starch Properties in Local Thai Rice. ''Plants (Basel)''. 2023 Sep 17; '''12''' (18):
Association analysis of agronomic traits and construction of genetic networks by resequencing of 306 sugar beet (Beta vulgaris L.) lines. Description: Wang, Liang, et al. Association analysis of agronomic traits and construction of genetic networks by resequencing of 306 sugar beet (Beta vulgaris L.) lines. ''Sci Rep''. 2023 Sep 18; '''13''' (1):15422
Associations between telomere attrition, genetic variants in telomere maintenance genes, and non-small cell lung cancer risk in the Jammu and Kashmir population of North India. Description: Bhat, Gh Rasool, et al. Associations between telomere attrition, genetic variants in telomere maintenance genes, and non-small cell lung cancer risk in the Jammu and Kashmir population of North India. ''BMC Cancer''. 2023 Sep 18; '''23''' (1):874
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human. Description: Niskanen, Julia E, et al. Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human. ''Genome Med''. 2023 Sep 18; '''15''' (1):73
Population genetics of marmosets in Asian primate research centers and loci associated with epileptic risk revealed by whole-genome sequencing. Description: Yang, XiangYu, et al. Population genetics of marmosets in Asian primate research centers and loci associated with epileptic risk revealed by whole-genome sequencing. ''Zool Res''. 2023 Sep 18; '''44''' (5):837-847
Potential selection for lipid kinase activity and spermatogenesis in Henan native pig breeds and growth shaping by introgression of European genes. Description: Qiao, Ruimin, et al. Potential selection for lipid kinase activity and spermatogenesis in Henan native pig breeds and growth shaping by introgression of European genes. ''Genet Sel Evol''. 2023 Sep 18; '''55''' (1):64
Structural variation and introgression from wild populations in East Asian cattle genomes confer adaptation to local environment. Description: Xia, Xiaoting, et al. Structural variation and introgression from wild populations in East Asian cattle genomes confer adaptation to local environment. ''Genome Biol''. 2023 Sep 18; '''24''' (1):211
Evolutionary origin of genomic structural variations in domestic yaks. Description: Liu, Xinfeng, et al. Evolutionary origin of genomic structural variations in domestic yaks. ''Nat Commun''. 2023 Sep 19; '''14''' (1):5617
Lymphoma in Border Collies: Genome-Wide Association and Pedigree Analysis. Description: Soh, Pamela Xing Yi, et al. Lymphoma in Border Collies: Genome-Wide Association and Pedigree Analysis. ''Vet Sci''. 2023 Sep 19; '''10''' (9):
Pathway-Specific Polygenic Scores Improve Cross-Ancestry Prediction of Psychosis and Clinical Outcomes. Description: Tubbs, Justin D, et al. Pathway-Specific Polygenic Scores Improve Cross-Ancestry Prediction of Psychosis and Clinical Outcomes. ''medRxiv''. 2023 Sep 19;
Dopamine pathway and Parkinson's risk variants are associated with levodopa-induced dyskinesia. Description: Sosero, Yuri L, et al. Dopamine pathway and Parkinson's risk variants are associated with levodopa-induced dyskinesia. ''medRxiv''. 2023 Sep 20;
Genomic consequences of isolation and inbreeding in an island dingo population. Description: Leon-Apodaca, Ana V, et al. Genomic consequences of isolation and inbreeding in an island dingo population. ''bioRxiv''. 2023 Sep 20;
Analysis of population structure and genetic diversity in low-variance Saimaa ringed seals using low-coverage whole-genome sequence data. Description: Olkkonen, Emmi, et al. Analysis of population structure and genetic diversity in low-variance Saimaa ringed seals using low-coverage whole-genome sequence data. ''STAR Protoc''. 2023 Sep 21; '''4''' (4):102567
Genetic diversity and ancestry of the Khmuic-speaking ethnic groups in Thailand: a genome-wide perspective. Description: Kampuansai, Jatupol, et al. Genetic diversity and ancestry of the Khmuic-speaking ethnic groups in Thailand: a genome-wide perspective. ''Sci Rep''. 2023 Sep 21; '''13''' (1):15710
A de novo evolved gene contributes to rice grain shape difference between indica and japonica. Description: Chen, Rujia, et al. A de novo evolved gene contributes to rice grain shape difference between indica and japonica. ''Nat Commun''. 2023 Sep 22; '''14''' (1):5906
Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss. Description: Henne, Sabrina Katrin, et al. Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss. ''Nat Commun''. 2023 Sep 22; '''14''' (1):5492
Ancestry-attenuated effects of socioeconomic deprivation on type 2 diabetes disparities in the All of Us cohort. Description: Lam, Vincent, et al. Ancestry-attenuated effects of socioeconomic deprivation on type 2 diabetes disparities in the All of Us cohort. ''Res Sq''. 2023 Sep 22;
Genetic Variants in Carbohydrate Digestive Enzyme and Transport Genes Associated with Risk of Irritable Bowel Syndrome. Description: Hong, Hyejeong, et al. Genetic Variants in Carbohydrate Digestive Enzyme and Transport Genes Associated with Risk of Irritable Bowel Syndrome. ''medRxiv''. 2023 Sep 22;
Distinct explanations underlie gene-environment interactions in the UK Biobank. Description: Durvasula, Arun, et al. Distinct explanations underlie gene-environment interactions in the UK Biobank. ''medRxiv''. 2023 Sep 23;
Angular limb deformity associated with TSPAN18, NRG3 and NOVA2 in Rambouillet rams. Description: Becker, Gabrielle M, et al. Angular limb deformity associated with TSPAN18, NRG3 and NOVA2 in Rambouillet rams. ''Sci Rep''. 2023 Sep 25; '''13''' (1):16059
Genome-wide enhancer-gene regulatory maps link causal variants to target genes underlying human cancer risk. Description: Ying, Pingting, et al. Genome-wide enhancer-gene regulatory maps link causal variants to target genes underlying human cancer risk. ''Nat Commun''. 2023 Sep 25; '''14''' (1):5958
Host genetic variation at a locus near CHD1L impacts HIV sequence diversity in a South African population. Description: Schulz, Vanessa E, et al. Host genetic variation at a locus near CHD1L impacts HIV sequence diversity in a South African population. ''J Virol''. 2023 Sep 25; '''97''' (10):e0095423
Reliable multiplex generation of pooled induced pluripotent stem cells. Description: Smullen, Molly, et al. Reliable multiplex generation of pooled induced pluripotent stem cells. ''Cell Rep Methods''. 2023 Sep 25; '''3''' (9):100570
Whole-genome sequencing revealed genetic diversity, structure and patterns of selection in Guizhou indigenous chickens. Description: Xu, Dan, et al. Whole-genome sequencing revealed genetic diversity, structure and patterns of selection in Guizhou indigenous chickens. ''BMC Genomics''. 2023 Sep 26; '''24''' (1):570
Consistent changes in muscle metabolism underlie dive performance across multiple lineages of diving ducks. Description: Schell, Elizabeth R, et al. Consistent changes in muscle metabolism underlie dive performance across multiple lineages of diving ducks. ''Proc Biol Sci''. 2023 Sep 27; '''290''' (2007):20231466
DNA methylation at quantitative trait loci (mQTLs) varies with cell type and nonheritable factors and may improve breast cancer risk assessment. Description: Herzog, Chiara, et al. DNA methylation at quantitative trait loci (mQTLs) varies with cell type and nonheritable factors and may improve breast cancer risk assessment. ''NPJ Precis Oncol''. 2023 Sep 27; '''7''' (1):99
Genetic risk score in multiple sclerosis is associated with unique gut microbiome. Description: Elsayed, Noha S, et al. Genetic risk score in multiple sclerosis is associated with unique gut microbiome. ''Sci Rep''. 2023 Sep 27; '''13''' (1):16269
Heterotic grouping of provitamin A-enriched maize inbred lines for increased provitamin A content in hybrids. Description: Maazou, Abdoul-Raouf Sayadi, et al. Heterotic grouping of provitamin A-enriched maize inbred lines for increased provitamin A content in hybrids. ''BMC Genom Data''. 2023 Sep 27; '''24''' (1):57
Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration. Description: Austin-Zimmerman, Isabelle, et al. Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration. ''Nat Commun''. 2023 Sep 28; '''14''' (1):6059
Polygenic risk scores of lithium response and treatment resistance in major depressive disorder. Description: Xiong, Ying, et al. Polygenic risk scores of lithium response and treatment resistance in major depressive disorder. ''Transl Psychiatry''. 2023 Sep 28; '''13''' (1):301
SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy. Description: Roshandel, Delnaz, et al. SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy. ''NPJ Genom Med''. 2023 Sep 28; '''8''' (1):28
Status and physiological significance of circulating adiponectin in the very old and centenarians: an observational study. Description: Sasaki, Takashi, et al. Status and physiological significance of circulating adiponectin in the very old and centenarians: an observational study. ''Elife''. 2023 Sep 28; '''12''':
Diversity and genetic architecture of agro-morphological traits in a core collection of European traditional tomato. Description: Pons, Clara, et al. Diversity and genetic architecture of agro-morphological traits in a core collection of European traditional tomato. ''J Exp Bot''. 2023 Sep 29; '''74''' (18):5896-5916
GDF-15 (a biomarker for metformin) and the risk of COVID-19: A two-sample Mendelian randomization study. Description: Wang, Ya, et al. GDF-15 (a biomarker for metformin) and the risk of COVID-19: A two-sample Mendelian randomization study. ''Medicine (Baltimore)''. 2023 Sep 29; '''102''' (39):e34675
Genome-First Approach of the Prevalence and Cancer Phenotypes of Pathogenic or Likely Pathogenic Germline TP53 Variants. Description: de Andrade, Kelvin C, et al. Genome-First Approach of the Prevalence and Cancer Phenotypes of Pathogenic or Likely Pathogenic Germline TP53 Variants. ''HGG Adv''. 2023 Sep 29; '''5''' (1):100242
Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes. Description: Schroeder, Philip, et al. Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes. ''medRxiv''. 2023 Sep 29;
Genetic variants in melanogenesis proteins TYRP1 and TYR are associated with the golden rhesus macaque phenotype. Description: Peterson, Samuel M, et al. Genetic variants in melanogenesis proteins TYRP1 and TYR are associated with the golden rhesus macaque phenotype. ''G3 (Bethesda)''. 2023 Sep 30; '''13''' (10):
Genome-wide association analysis identifies natural allelic variants associated with panicle architecture variation in African rice, Oryza glaberrima Steud. Description: Ntakirutimana, Fabrice, et al. Genome-wide association analysis identifies natural allelic variants associated with panicle architecture variation in African rice, Oryza glaberrima Steud. ''G3 (Bethesda)''. 2023 Sep 30; '''13''' (10):
RNA viruses, M satellites, chromosomal killer genes, and killer/nonkiller phenotypes in the 100-genomes S. cerevisiae strains. Description: Vijayraghavan, Sriram, et al. RNA viruses, M satellites, chromosomal killer genes, and killer/nonkiller phenotypes in the 100-genomes S. cerevisiae strains. ''G3 (Bethesda)''. 2023 Sep 30; '''13''' (10):
A Genome-Wide Association Study of Outcome After Aneurysmal Subarachnoid Haemorrhage: Discovery Analysis. Description: Gaastra, Ben, et al. A Genome-Wide Association Study of Outcome After Aneurysmal Subarachnoid Haemorrhage: Discovery Analysis. ''Transl Stroke Res''. 2023 Oct; '''14''' (5):681-687
B cell polygenic risk scores associate with anti-dsDNA antibodies and nephritis in systemic lupus erythematosus. Description: Hedenstedt, Anna, et al. B cell polygenic risk scores associate with anti-dsDNA antibodies and nephritis in systemic lupus erythematosus. ''Lupus Sci Med''. 2023 Oct; '''10''' (2):
Characterization analysis of Rongchang pig population based on the Zhongxin-1 Porcine Breeding Array PLUS. Description: Leng, Dong, et al. Characterization analysis of Rongchang pig population based on the Zhongxin-1 Porcine Breeding Array PLUS. ''Anim Biosci''. 2023 Oct; '''36''' (10):1508-1516
Deciphering genetic basis of developmental and agronomic traits by integrating high-throughput optical phenotyping and genome-wide association studies in wheat. Description: Gao, Jie, et al. Deciphering genetic basis of developmental and agronomic traits by integrating high-throughput optical phenotyping and genome-wide association studies in wheat. ''Plant Biotechnol J''. 2023 Oct; '''21''' (10):1966-1977
Direct and Indirect Genetic Effects on Aggression. Description: van der Laan, Camiel M, et al. Direct and Indirect Genetic Effects on Aggression. ''Biol Psychiatry Glob Open Sci''. 2023 Oct; '''3''' (4):958-968
Generation of two induced pluripotent stem cell lines from patients with Down syndrome. Description: Zhu, Wenjuan, et al. Generation of two induced pluripotent stem cell lines from patients with Down syndrome. ''Stem Cell Res''. 2023 Oct; '''72''': 103204
Genetic associations vary across the spectrum of fasting serum insulin: results from the European IDEFICS/I.Family children's cohort. Description: Mehlig, Kirsten, et al. Genetic associations vary across the spectrum of fasting serum insulin: results from the European IDEFICS/I.Family children's cohort. ''Diabetologia''. 2023 Oct; '''66''' (10):1914-1924
Genetic basis of lineage-specific evolution of fruit traits in hexaploid persimmon. Description: Horiuchi, Ayano, et al. Genetic basis of lineage-specific evolution of fruit traits in hexaploid persimmon. ''DNA Res''. 2023 Oct 1; '''30''' (5):
Genetic, environmental, and behavioral correlates of lifetime suicide attempt: Analysis of additive and interactive effects in two cohorts of US Army soldiers. Description: Campbell-Sills, Laura, et al. Genetic, environmental, and behavioral correlates of lifetime suicide attempt: Analysis of additive and interactive effects in two cohorts of US Army soldiers. ''Neuropsychopharmacology''. 2023 Oct; '''48''' (11):1623-1629
Genome-wide analysis identifies novel loci influencing plasma apolipoprotein E concentration and Alzheimer's disease risk. Description: Aslam, M Muaaz, et al. Genome-wide analysis identifies novel loci influencing plasma apolipoprotein E concentration and Alzheimer's disease risk. ''Mol Psychiatry''. 2023 Oct; '''28''' (10):4451-4462
Genome-wide association mapping in a sweet cherry germplasm collection (Prunus avium L.) reveals candidate genes for fruit quality traits. Description: Donkpegan, Armel S L, et al. Genome-wide association mapping in a sweet cherry germplasm collection (Prunus avium L.) reveals candidate genes for fruit quality traits. ''Hortic Res''. 2023 Oct; '''10''' (10):uhad191
Genome-wide meta-analyses identify five new risk loci for nonsyndromic orofacial clefts in the Chinese Han population. Description: Yu, Yafen, et al. Genome-wide meta-analyses identify five new risk loci for nonsyndromic orofacial clefts in the Chinese Han population. ''Mol Genet Genomic Med''. 2023 Oct; '''11''' (10):e2226
Genome-wide single-nucleotide polymorphism data and mitochondrial hypervariable region 1 nucleotide sequence reveal the origin of the Akhal-Teke horse. Description: Kang, Zhoucairang, et al. Genome-wide single-nucleotide polymorphism data and mitochondrial hypervariable region 1 nucleotide sequence reveal the origin of the Akhal-Teke horse. ''Anim Biosci''. 2023 Oct; '''36''' (10):1499-1507
Genomic evidence of sex chromosome aneuploidy and infection-associated genotypes in the tsetse fly Glossina fuscipes, the major vector of African trypanosomiasis in Uganda. Description: Saarman, Norah P, et al. Genomic evidence of sex chromosome aneuploidy and infection-associated genotypes in the tsetse fly Glossina fuscipes, the major vector of African trypanosomiasis in Uganda. ''Infect Genet Evol''. 2023 Oct; '''114''': 105501
Genomic insights into selection for heterozygous alleles and woody traits in Populus tomentosa. Description: Li, Peng, et al. Genomic insights into selection for heterozygous alleles and woody traits in Populus tomentosa. ''Plant Biotechnol J''. 2023 Oct; '''21''' (10):2002-2018
Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Description: Ziyatdinov, Andrey, et al. Genotyping, sequencing and analysis of 140,000 adults from Mexico City. ''Nature''. 2023 Oct; '''622''' (7984):784-793
Investigating genetically stratified subgroups to better understand the etiology of alcohol misuse. Description: Thijssen, Anais B, et al. Investigating genetically stratified subgroups to better understand the etiology of alcohol misuse. ''Mol Psychiatry''. 2023 Oct; '''28''' (10):4225-4233
LncRNA BCCE4 Genetically Enhances the PD-L1/PD-1 Interaction in Smoking-Related Bladder Cancer by Modulating miR-328-3p-USP18 Signaling. Description: Zheng, Rui, et al. LncRNA BCCE4 Genetically Enhances the PD-L1/PD-1 Interaction in Smoking-Related Bladder Cancer by Modulating miR-328-3p-USP18 Signaling. ''Adv Sci (Weinh)''. 2023 Oct; '''10''' (30):e2303473
Metabolic syndrome and cognitive deficits in the Greek cohort of Epirus Health Study. Description: Koutsonida, Myrto, et al. Metabolic syndrome and cognitive deficits in the Greek cohort of Epirus Health Study. ''Neurol Sci''. 2023 Oct; '''44''' (10):3523-3533
Patterns of cytonuclear discordance and divergence between subspecies of the scarlet macaw (Ara macao) in Central America. Description: Aardema, Matthew L, et al. Patterns of cytonuclear discordance and divergence between subspecies of the scarlet macaw (Ara macao) in Central America. ''Genetica''. 2023 Oct; '''151''' (4-5):281-292
Plasma proteomic associations with genetics and health in the UK Biobank. Description: Sun, Benjamin B, et al. Plasma proteomic associations with genetics and health in the UK Biobank. ''Nature''. 2023 Oct; '''622''' (7982):329-338
Population genomics identifies genetic signatures of carrot domestication and improvement and uncovers the origin of high-carotenoid orange carrots. Description: Coe, Kevin, et al. Population genomics identifies genetic signatures of carrot domestication and improvement and uncovers the origin of high-carotenoid orange carrots. ''Nat Plants''. 2023 Oct; '''9''' (10):1643-1658
RBFOX1 and Working Memory: From Genome to Transcriptome Revealed Posttranscriptional Mechanism Separate From Attention-Deficit/Hyperactivity Disorder. Description: Zhong, Yuanxin, et al. RBFOX1 and Working Memory: From Genome to Transcriptome Revealed Posttranscriptional Mechanism Separate From Attention-Deficit/Hyperactivity Disorder. ''Biol Psychiatry Glob Open Sci''. 2023 Oct; '''3''' (4):1042-1052
Refining the genetic risk of breast cancer with rare haplotypes and pattern mining. Description: Letsou, William, et al. Refining the genetic risk of breast cancer with rare haplotypes and pattern mining. ''Life Sci Alliance''. 2023 Oct; '''6''' (10):
Schizophrenia Polygenic Risk During Typical Development Reflects Multiscale Cortical Organization. Description: Kirschner, Matthias, et al. Schizophrenia Polygenic Risk During Typical Development Reflects Multiscale Cortical Organization. ''Biol Psychiatry Glob Open Sci''. 2023 Oct; '''3''' (4):1083-1093
Schizophrenia polygenic risk score and type 2 diabetes onset in older adults with no schizophrenia diagnosis. Description: Shamsutdinova, Diana, et al. Schizophrenia polygenic risk score and type 2 diabetes onset in older adults with no schizophrenia diagnosis. ''Psychiatr Genet''. 2023 Oct 1; '''33''' (5):191-201
Structure and function of rice hybrid genomes reveal genetic basis and optimal performance of heterosis. Description: Gu, Zhoulin, et al. Structure and function of rice hybrid genomes reveal genetic basis and optimal performance of heterosis. ''Nat Genet''. 2023 Oct; '''55''' (10):1745-1756
The complete and fully-phased diploid genome of a male Han Chinese. Description: Yang, Chentao, et al. The complete and fully-phased diploid genome of a male Han Chinese. ''Cell Res''. 2023 Oct; '''33''' (10):745-761
The distribution of dietary choline intake and serum choline levels in Australian women during pregnancy and associated early life factors. Description: Staskova, Lada, et al. The distribution of dietary choline intake and serum choline levels in Australian women during pregnancy and associated early life factors. ''Eur J Nutr''. 2023 Oct; '''62''' (7):2855-2872
The pig pangenome provides insights into the roles of coding structural variations in genetic diversity and adaptation. Description: Li, Zhengcao, et al. The pig pangenome provides insights into the roles of coding structural variations in genetic diversity and adaptation. ''Genome Res''. 2023 Oct; '''33''' (10):1833-1847
Tissue-Specific Oxysterols as Predictors of Antidepressant (Escitalopram) Treatment Response in Patients With Major Depressive Disorder. Description: Sun, Zuoli, et al. Tissue-Specific Oxysterols as Predictors of Antidepressant (Escitalopram) Treatment Response in Patients With Major Depressive Disorder. ''Biol Psychiatry Glob Open Sci''. 2023 Oct; '''3''' (4):663-672
Trans-ancestry meta-analysis of genome wide association studies of inhibitory control. Description: Arnatkeviciute, Aurina, et al. Trans-ancestry meta-analysis of genome wide association studies of inhibitory control. ''Mol Psychiatry''. 2023 Oct; '''28''' (10):4175-4184
Treatment resistance NMDA receptor pathway polygenic score is associated with brain glutamate in schizophrenia. Description: Griffiths, Kira, et al. Treatment resistance NMDA receptor pathway polygenic score is associated with brain glutamate in schizophrenia. ''Schizophr Res''. 2023 Oct; '''260''': 152-159
Youth Team Sports Participation Associates With Reduced Dimensional Psychopathology Through Interaction With Biological Risk Factors. Description: Kunitoki, Keiko, et al. Youth Team Sports Participation Associates With Reduced Dimensional Psychopathology Through Interaction With Biological Risk Factors. ''Biol Psychiatry Glob Open Sci''. 2023 Oct; '''3''' (4):875-883
Discovery of Ancestry-specific Variants Associated with Clopidogrel Response among Caribbean Hispanics. Description: Yang, Guang, et al. Discovery of Ancestry-specific Variants Associated with Clopidogrel Response among Caribbean Hispanics. ''medRxiv''. 2023 Oct 2;
Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records. Description: Ruth, Katherine S, et al. Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records. ''BMC Med Genomics''. 2023 Oct 2; '''16''' (1):231
Metabolomics and machine learning technique revealed that germination enhances the multi-nutritional properties of pigmented rice. Description: Tiozon, Rhowell Jr N, et al. Metabolomics and machine learning technique revealed that germination enhances the multi-nutritional properties of pigmented rice. ''Commun Biol''. 2023 Oct 2; '''6''' (1):1000
The phenotypic and genotypic association of grip strength with frailty, physical performance and functional limitations over time in older adults. Description: Stringa, Najada, et al. The phenotypic and genotypic association of grip strength with frailty, physical performance and functional limitations over time in older adults. ''Age Ageing''. 2023 Oct 2; '''52''' (10):
Wood cookstove use is associated with gastric cancer in Central America and mediated by host genetics. Description: Rifkin, Samara B, et al. Wood cookstove use is associated with gastric cancer in Central America and mediated by host genetics. ''Sci Rep''. 2023 Oct 2; '''13''' (1):16515
Epigenomic response to albuterol treatment in asthma-relevant airway epithelial cells. Description: Perez-Garcia, Javier, et al. Epigenomic response to albuterol treatment in asthma-relevant airway epithelial cells. ''Clin Epigenetics''. 2023 Oct 3; '''15''' (1):156
Genomic analysis reveals a cryptic pangolin species. Description: Gu, Tong-Tong, et al. Genomic analysis reveals a cryptic pangolin species. ''Proc Natl Acad Sci U S A''. 2023 Oct 3; '''120''' (40):e2304096120
Interplay Of Serum Bilirubin and Tobacco Smoking with Lung and Head and Neck Cancers in a Diverse, EHR-linked Los Angeles Biobank. Description: Venkateswaran, Vidhya, et al. Interplay Of Serum Bilirubin and Tobacco Smoking with Lung and Head and Neck Cancers in a Diverse, EHR-linked Los Angeles Biobank. ''medRxiv''. 2023 Oct 3;
Investigating the Impact of Sun/UV Protection and Ease of Skin Tanning on the Risk of Pseudoexfoliation Glaucoma: A Mendelian Randomization Study. Description: Dai, Jinyue, et al. Investigating the Impact of Sun/UV Protection and Ease of Skin Tanning on the Risk of Pseudoexfoliation Glaucoma: A Mendelian Randomization Study. ''Invest Ophthalmol Vis Sci''. 2023 Oct 3; '''64''' (13):4
Uncovering the complex relationship between balding, testosterone and skin cancers in men. Description: Ong, Jue-Sheng, et al. Uncovering the complex relationship between balding, testosterone and skin cancers in men. ''Nat Commun''. 2023 Oct 3; '''14''' (1):5962
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Description: Budu-Aggrey, Ashley, et al. European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. ''Nat Commun''. 2023 Oct 4; '''14''' (1):6172
Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis. Description: Mullin, Benjamin H, et al. Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis. ''Genetics''. 2023 Oct 4; '''225''' (2):
A new Approach to Identify Gene-Environment Interactions and Reveal New Biological Insight in Complex traits. Description: Zhu, Xiaofeng, et al. A new Approach to Identify Gene-Environment Interactions and Reveal New Biological Insight in Complex traits. ''Res Sq''. 2023 Oct 5;
Gender-dependent multiple cross-phenotype association of interferon lambda genetic variants with peripheral blood profiles in healthy individuals. Description: Roy, Debarati Guha, et al. Gender-dependent multiple cross-phenotype association of interferon lambda genetic variants with peripheral blood profiles in healthy individuals. ''Mol Genet Genomic Med''. 2023 Oct 5; '''12''' (1):e2292
Life course effects of genetic susceptibility to higher body size on body fat and lean mass: prospective cohort study. Description: Waterfield, Scott, et al. Life course effects of genetic susceptibility to higher body size on body fat and lean mass: prospective cohort study. ''Int J Epidemiol''. 2023 Oct 5; '''52''' (5):1377-1387
Genetic variants for smoking behaviour and risk of skin cancer. Description: Dusingize, Jean Claude, et al. Genetic variants for smoking behaviour and risk of skin cancer. ''Sci Rep''. 2023 Oct 6; '''13''' (1):16873
Phenotypic but not genetically predicted heart rate variability associated with all-cause mortality. Description: Tegegne, Balewgizie S, et al. Phenotypic but not genetically predicted heart rate variability associated with all-cause mortality. ''Commun Biol''. 2023 Oct 6; '''6''' (1):1013
The pan-genome and local adaptation of Arabidopsis thaliana. Description: Kang, Minghui, et al. The pan-genome and local adaptation of Arabidopsis thaliana. ''Nat Commun''. 2023 Oct 6; '''14''' (1):6259
Variants in the DDX6-CXCR5 autoimmune disease risk locus influence the regulatory network in immune cells and salivary gland. Description: Wiley, Mandi M, et al. Variants in the DDX6-CXCR5 autoimmune disease risk locus influence the regulatory network in immune cells and salivary gland. ''bioRxiv''. 2023 Oct 6;
Ethnicity- and sex-specific genome wide association study on Parkinson's disease. Description: Park, Kye Won, et al. Ethnicity- and sex-specific genome wide association study on Parkinson's disease. ''NPJ Parkinsons Dis''. 2023 Oct 7; '''9''' (1):141
Low levels of small HDL particles predict but do not influence risk of sepsis. Description: Hamilton, Fergus, et al. Low levels of small HDL particles predict but do not influence risk of sepsis. ''Crit Care''. 2023 Oct 9; '''27''' (1):389
Neanderthal introgression in SCN9A impacts mechanical pain sensitivity. Description: Faux, Pierre, et al. Neanderthal introgression in SCN9A impacts mechanical pain sensitivity. ''Commun Biol''. 2023 Oct 10; '''6''' (1):958
Genotype-based "virtual" metabolomics in a clinical biobank identifies novel metabolite-disease associations. Description: Bagheri, Minoo, et al. Genotype-based "virtual" metabolomics in a clinical biobank identifies novel metabolite-disease associations. ''Res Sq''. 2023 Oct 11;
Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study. Description: Ye, Qiang, et al. Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study. ''HGG Adv''. 2023 Oct 12; '''4''' (4):100230
Genome-wide association study reveals candidate genes for traits related to meat quality in Colombian Creole hair sheep. Description: Revelo, Herman Alberto, et al. Genome-wide association study reveals candidate genes for traits related to meat quality in Colombian Creole hair sheep. ''Trop Anim Health Prod''. 2023 Oct 12; '''55''' (6):357
Influence of autozygosity on common disease risk across the phenotypic spectrum. Description: Malawsky, Daniel S, et al. Influence of autozygosity on common disease risk across the phenotypic spectrum. ''Cell''. 2023 Oct 12; '''186''' (21):4514-4527.e14
Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome. Description: Blue, Elizabeth E, et al. Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome. ''HGG Adv''. 2023 Oct 12; '''4''' (4):100232
Revealing polygenic pleiotropy using genetic risk scores for asthma. Description: Dapas, Matthew, et al. Revealing polygenic pleiotropy using genetic risk scores for asthma. ''HGG Adv''. 2023 Oct 12; '''4''' (4):100233
Genomic analysis reveals limited hybridization among three giraffe species in Kenya. Description: Coimbra, Raphael T F, et al. Genomic analysis reveals limited hybridization among three giraffe species in Kenya. ''BMC Biol''. 2023 Oct 13; '''21''' (1):215
Human-specific evolutionary markers linked to foetal neurodevelopment modulate brain surface area in schizophrenia. Description: Guardiola-Ripoll, Maria, et al. Human-specific evolutionary markers linked to foetal neurodevelopment modulate brain surface area in schizophrenia. ''Commun Biol''. 2023 Oct 13; '''6''' (1):1040
Brain-wide genome-wide colocalization study for integrating genetics, transcriptomics and brain morphometry in Alzheimer's disease. Description: Bao, Jingxuan, et al. Brain-wide genome-wide colocalization study for integrating genetics, transcriptomics and brain morphometry in Alzheimer's disease. ''Neuroimage''. 2023 Oct 15; '''280''': 120346
Genomic insights into the comorbidity between type 2 diabetes and schizophrenia. Description: Arruda, Ana Luiza, et al. Genomic insights into the comorbidity between type 2 diabetes and schizophrenia. ''medRxiv''. 2023 Oct 16;
Genome-wide association study for body weight and feed consumption traits in Japanese quail using Bayesian approaches. Description: Alboali, Hassan, et al. Genome-wide association study for body weight and feed consumption traits in Japanese quail using Bayesian approaches. ''Poult Sci''. 2023 Oct 17; '''103''' (1):103208
Novel Alzheimer's disease genes and epistasis identified using machine learning GWAS platform. Description: Lundberg, Mischa, et al. Novel Alzheimer's disease genes and epistasis identified using machine learning GWAS platform. ''Sci Rep''. 2023 Oct 17; '''13''' (1):17662
Range-wide and temporal genomic analyses reveal the consequences of near-extinction in Swedish moose. Description: Dussex, Nicolas, et al. Range-wide and temporal genomic analyses reveal the consequences of near-extinction in Swedish moose. ''Commun Biol''. 2023 Oct 17; '''6''' (1):1035
The admixed brushtail possum genome reveals invasion history in New Zealand and novel imprinted genes. Description: Bond, Donna M, et al. The admixed brushtail possum genome reveals invasion history in New Zealand and novel imprinted genes. ''Nat Commun''. 2023 Oct 17; '''14''' (1):6364
Adaptive divergence and genetic vulnerability of relict species under climate change: a case study of Pterocarya macroptera. Description: Wang, Tian-Rui, et al. Adaptive divergence and genetic vulnerability of relict species under climate change: a case study of Pterocarya macroptera. ''Ann Bot''. 2023 Oct 18; '''132''' (2):241-254
Association of polygenic risk for bipolar disorder with grey matter structure and white matter integrity in youth. Description: Jiang, Xinyue, et al. Association of polygenic risk for bipolar disorder with grey matter structure and white matter integrity in youth. ''Transl Psychiatry''. 2023 Oct 18; '''13''' (1):322
Clinical utility of polygenic scores for cardiometabolic disease in Arabs. Description: Shim, Injeong, et al. Clinical utility of polygenic scores for cardiometabolic disease in Arabs. ''Nat Commun''. 2023 Oct 18; '''14''' (1):6535
Genetic and dietary modulators of the inflammatory response in the gastrointestinal tract of the BXD mouse genetic reference population. Description: Li, Xiaoxu, et al. Genetic and dietary modulators of the inflammatory response in the gastrointestinal tract of the BXD mouse genetic reference population. ''Elife''. 2023 Oct 19; '''12''':
Transcriptional regulation and overexpression of GST cluster enhances pesticide resistance in the cotton bollworm, Helicoverpa armigera (Lepidoptera: Noctuidae). Description: Jin, Minghui, et al. Transcriptional regulation and overexpression of GST cluster enhances pesticide resistance in the cotton bollworm, Helicoverpa armigera (Lepidoptera: Noctuidae). ''Commun Biol''. 2023 Oct 19; '''6''' (1):1064
Genome-wide association analysis of heifer livability and early first calving in Holstein cattle. Description: Gao, Yahui, et al. Genome-wide association analysis of heifer livability and early first calving in Holstein cattle. ''BMC Genomics''. 2023 Oct 21; '''24''' (1):628
The novel IMAGE001 genotyping array as a valuable alternative for genetic diversity screening in chicken: a demonstration in a local chicken breed in Belgium. Description: Meyermans, Roel, et al. The novel IMAGE001 genotyping array as a valuable alternative for genetic diversity screening in chicken: a demonstration in a local chicken breed in Belgium. ''Poult Sci''. 2023 Oct 21; '''103''' (1):103221
Genome-wide analyses identify NEAT1 as genetic modifier of age at onset of amyotrophic lateral sclerosis. Description: Li, Chunyu, et al. Genome-wide analyses identify NEAT1 as genetic modifier of age at onset of amyotrophic lateral sclerosis. ''Mol Neurodegener''. 2023 Oct 23; '''18''' (1):77
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease. Description: Williams, Alexander T, et al. Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease. ''Nat Commun''. 2023 Oct 23; '''14''' (1):6713
Genetic influences on alcohol flushing in East Asian populations. Description: Cho, Yoonsu, et al. Genetic influences on alcohol flushing in East Asian populations. ''BMC Genomics''. 2023 Oct 24; '''24''' (1):638
Identification of asthma-related genes using asthmatic blood eQTLs of Korean patients. Description: Kim, Dong Jun, et al. Identification of asthma-related genes using asthmatic blood eQTLs of Korean patients. ''BMC Med Genomics''. 2023 Oct 24; '''16''' (1):259
Increased homozygosity due to endogamy results in fitness consequences in a human population. Description: Swinford, N A, et al. Increased homozygosity due to endogamy results in fitness consequences in a human population. ''Proc Natl Acad Sci U S A''. 2023 Oct 24; '''120''' (43):e2309552120
Learning gene networks under SNP perturbation using SNP and allele-specific expression data. Description: Yoon, Jun Ho, et al. Learning gene networks under SNP perturbation using SNP and allele-specific expression data. ''bioRxiv''. 2023 Oct 24;
Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve. Description: Carlisle, Steven G, et al. Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve. ''medRxiv''. 2023 Oct 24;
Genome-Wide Association Study of Fiber Diameter in Alpacas. Description: More, Manuel, et al. Genome-Wide Association Study of Fiber Diameter in Alpacas. ''Animals (Basel)''. 2023 Oct 25; '''13''' (21):
Mapping the landscape of lineage-specific dynamic regulation of gene expression using single-cell transcriptomics and application to genetics of complex disease. Description: Abe, Hanna, et al. Mapping the landscape of lineage-specific dynamic regulation of gene expression using single-cell transcriptomics and application to genetics of complex disease. ''medRxiv''. 2023 Oct 25;
Uncovering the history of recombination and population structure in western Canadian stripe rust populations through mating type alleles. Description: Holden, Samuel, et al. Uncovering the history of recombination and population structure in western Canadian stripe rust populations through mating type alleles. ''BMC Biol''. 2023 Oct 25; '''21''' (1):233
Identification of genetic variants associated with anterior cruciate ligament rupture and AKC standard coat color in the Labrador Retriever. Description: Lee, B T, et al. Identification of genetic variants associated with anterior cruciate ligament rupture and AKC standard coat color in the Labrador Retriever. ''BMC Genom Data''. 2023 Oct 26; '''24''' (1):60
Adipose tissue eQTL meta-analysis reveals the contribution of allelic heterogeneity to gene expression regulation and cardiometabolic traits. Description: Brotman, Sarah M, et al. Adipose tissue eQTL meta-analysis reveals the contribution of allelic heterogeneity to gene expression regulation and cardiometabolic traits. ''bioRxiv''. 2023 Oct 27;
CXCL12 regulates coronary artery dominance in diverse populations and links development to disease. Description: Rios Coronado, Pamela E, et al. CXCL12 regulates coronary artery dominance in diverse populations and links development to disease. ''medRxiv''. 2023 Oct 27;
Investigation of the genetic aetiology of Lewy body diseases with and without dementia. Description: Wu, Lesley, et al. Investigation of the genetic aetiology of Lewy body diseases with and without dementia. ''medRxiv''. 2023 Oct 27;
Allostatic load in early adolescence: gene / environment contributions and relevance for mental health. Description: Hoffman, Kevin W, et al. Allostatic load in early adolescence: gene / environment contributions and relevance for mental health. ''medRxiv''. 2023 Oct 28;
Association of Single-Nucleotide Polymorphisms in Capecitabine Bioactivation Pathway with Adjuvant Therapy Safety in Colorectal Cancer Patients. Description: Cura, Yasmin, et al. Association of Single-Nucleotide Polymorphisms in Capecitabine Bioactivation Pathway with Adjuvant Therapy Safety in Colorectal Cancer Patients. ''Pharmaceutics''. 2023 Oct 28; '''15''' (11):
Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. Description: Ferar, Kathleen, et al. Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. ''Sci Rep''. 2023 Oct 28; '''13''' (1):18532
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder. Description: Bacchelli, Elena, et al. Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder. ''Res Sq''. 2023 Oct 28;
Genome-Wide Association Studies of Biluochun Tea Plant Populations in Dongting Mountain and Comprehensive Identification of Candidate Genes Associated with Core Agronomic Traits by Four Analysis Models. Description: Lei, Xiaogang, et al. Genome-Wide Association Studies of Biluochun Tea Plant Populations in Dongting Mountain and Comprehensive Identification of Candidate Genes Associated with Core Agronomic Traits by Four Analysis Models. ''Plants (Basel)''. 2023 Oct 30; '''12''' (21):
Proteomic Network Analysis of Alzheimer's Disease Cerebrospinal Fluid Reveals Alterations Associated with APOE epsilon4 Genotype and Atomoxetine Treatment. Description: Dammer, Eric B, et al. Proteomic Network Analysis of Alzheimer's Disease Cerebrospinal Fluid Reveals Alterations Associated with APOE epsilon4 Genotype and Atomoxetine Treatment. ''medRxiv''. 2023 Oct 30;
Comparative Analysis of Microsatellite and SNP Markers for Genetic Management of Red Deer. Description: Perez-Gonzalez, Javier, et al. Comparative Analysis of Microsatellite and SNP Markers for Genetic Management of Red Deer. ''Animals (Basel)''. 2023 Oct 31; '''13''' (21):
Downregulation of a transcription factor associated with resistance to Bt toxin Vip3Aa in the invasive fall armyworm. Description: Jin, Minghui, et al. Downregulation of a transcription factor associated with resistance to Bt toxin Vip3Aa in the invasive fall armyworm. ''Proc Natl Acad Sci U S A''. 2023 Oct 31; '''120''' (44):e2306932120
Genetic and Lifestyle-Related Factors Influencing Serum Hyper-Propionylcarnitine Concentrations and Their Association with Metabolic Syndrome and Cardiovascular Disease Risk. Description: Lee, Yong-Hwa, et al. Genetic and Lifestyle-Related Factors Influencing Serum Hyper-Propionylcarnitine Concentrations and Their Association with Metabolic Syndrome and Cardiovascular Disease Risk. ''Int J Mol Sci''. 2023 Oct 31; '''24''' (21):
Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Description: Ottensmann, Linda, et al. Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. ''Nat Commun''. 2023 Oct 31; '''14''' (1):6934
Structure-informed clustering for population stratification in association studies. Description: Bose, Aritra, et al. Structure-informed clustering for population stratification in association studies. ''BMC Bioinformatics''. 2023 Oct 31; '''24''' (1):411
A case of forensic genomics in Uganda reveals animal ownership and low exotic genetic introgression in indigenous cattle. Description: Masembe, Charles, et al. A case of forensic genomics in Uganda reveals animal ownership and low exotic genetic introgression in indigenous cattle. ''Vet Med Sci''. 2023 Nov; '''9''' (6):2844-2851
Age-dependent topic modeling of comorbidities in UK Biobank identifies disease subtypes with differential genetic risk. Description: Jiang, Xilin, et al. Age-dependent topic modeling of comorbidities in UK Biobank identifies disease subtypes with differential genetic risk. ''Nat Genet''. 2023 Nov; '''55''' (11):1854-1865
A genome-wide genomic score added to standard recommended stratification tools does not improve the identification of patients with very low bone mineral density. Description: Therkildsen, J, et al. A genome-wide genomic score added to standard recommended stratification tools does not improve the identification of patients with very low bone mineral density. ''Osteoporos Int''. 2023 Nov; '''34''' (11):1893-1906
A haplotype-resolved chromosome-scale genome for Quercus rubra L. provides insights into the genetics of adaptive traits for red oak species. Description: Kapoor, Beant, et al. A haplotype-resolved chromosome-scale genome for Quercus rubra L. provides insights into the genetics of adaptive traits for red oak species. ''G3 (Bethesda)''. 2023 Nov 1; '''13''' (11):
An atlas of genetic determinants of forearm fracture. Description: Nethander, Maria, et al. An atlas of genetic determinants of forearm fracture. ''Nat Genet''. 2023 Nov; '''55''' (11):1820-1830
A SACS deletion variant in Great Pyrenees dogs causes autosomal recessive neuronal degeneration. Description: Ekenstedt, Kari J, et al. A SACS deletion variant in Great Pyrenees dogs causes autosomal recessive neuronal degeneration. ''Hum Genet''. 2023 Nov; '''142''' (11):1587-1601
A TaSnRK1alpha Modulates TaPAP6L-Mediated Wheat Cold Tolerance through Regulating Endogenous Jasmonic Acid. Description: Zhang, Lingran, et al. A TaSnRK1alpha Modulates TaPAP6L-Mediated Wheat Cold Tolerance through Regulating Endogenous Jasmonic Acid. ''Adv Sci (Weinh)''. 2023 Nov; '''10''' (31):e2303478
Causal effects of time-varying body size on selected autoimmune disorders: a life course Mendelian randomisation study. Description: Freuer, Dennis, et al. Causal effects of time-varying body size on selected autoimmune disorders: a life course Mendelian randomisation study. ''RMD Open''. 2023 Nov; '''9''' (4):
Combined reference-free and multi-reference based GWAS uncover cryptic variation underlying rapid adaptation in a fungal plant pathogen. Description: Dutta, Anik, et al. Combined reference-free and multi-reference based GWAS uncover cryptic variation underlying rapid adaptation in a fungal plant pathogen. ''PLoS Pathog''. 2023 Nov; '''19''' (11):e1011801
Comparative population genomics analysis uncovers genomic footprints and genes influencing body weight trait in Chinese indigenous chicken. Description: Wang, Huie, et al. Comparative population genomics analysis uncovers genomic footprints and genes influencing body weight trait in Chinese indigenous chicken. ''Poult Sci''. 2023 Nov; '''102''' (11):103031
Conservation priority and run of homozygosity pattern assessment of global chicken genetic resources. Description: Gao, Chaoqun, et al. Conservation priority and run of homozygosity pattern assessment of global chicken genetic resources. ''Poult Sci''. 2023 Nov; '''102''' (11):103030
Cross-ancestry analyses identify new genetic loci associated with 25-hydroxyvitamin D. Description: Wang, Xiaotong, et al. Cross-ancestry analyses identify new genetic loci associated with 25-hydroxyvitamin D. ''PLoS Genet''. 2023 Nov; '''19''' (11):e1011033
Developmentally specified characterization of the irritability spectrum at early school age: Implications for pragmatic mental health screening. Description: Hirsch, Emily, et al. Developmentally specified characterization of the irritability spectrum at early school age: Implications for pragmatic mental health screening. ''Int J Methods Psychiatr Res''. 2023 Nov; '''32''' (S1):e1985
Evaluating the impact of modeling choices on the performance of integrated genetic and clinical models. Description: Morley, Theodore J, et al. Evaluating the impact of modeling choices on the performance of integrated genetic and clinical models. ''medRxiv''. 2023 Nov 1;
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture. Description: Harris, Rebekah V, et al. Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture. ''Ann Neurol''. 2023 Nov; '''94''' (5):825-835
Frequencies of Diagnostically Significant Polymorphisms of Hereditary Breast Cancer Forms in BRCA1 and BRCA2 Genes in the Kazakh Population. Description: Svyatova, Gulnara, et al. Frequencies of Diagnostically Significant Polymorphisms of Hereditary Breast Cancer Forms in BRCA1 and BRCA2 Genes in the Kazakh Population. ''Asian Pac J Cancer Prev''. 2023 Nov 1; '''24''' (11):3899-3907
Genetic and transcriptomic dissection of host defense to Goss's bacterial wilt and leaf blight of maize. Description: Hao, Yangfan, et al. Genetic and transcriptomic dissection of host defense to Goss's bacterial wilt and leaf blight of maize. ''G3 (Bethesda)''. 2023 Nov 1; '''13''' (11):
Genomes of the cosmopolitan fruit pest Bactrocera dorsalis (Diptera: Tephritidae) reveal its global invasion history and thermal adaptation. Description: Zhang, Yue, et al. Genomes of the cosmopolitan fruit pest Bactrocera dorsalis (Diptera: Tephritidae) reveal its global invasion history and thermal adaptation. ''J Adv Res''. 2023 Nov; '''53''': 61-74
Genome-wide methylation patterns from canine nanopore assemblies. Description: Schall, Peter Z, et al. Genome-wide methylation patterns from canine nanopore assemblies. ''G3 (Bethesda)''. 2023 Nov 1; '''13''' (11):
Investigation of potential genetic factors for growth traits in yellow-feather broilers using weighted single-step genome-wide association study. Description: Fang, Xiang, et al. Investigation of potential genetic factors for growth traits in yellow-feather broilers using weighted single-step genome-wide association study. ''Poult Sci''. 2023 Nov; '''102''' (11):103034
No phenotypic or genotypic evidence for a link between sleep duration and brain atrophy. Description: Fjell, Anders M, et al. No phenotypic or genotypic evidence for a link between sleep duration and brain atrophy. ''Nat Hum Behav''. 2023 Nov; '''7''' (11):2008-2022
Polymorphisms in Cyclooxygenase, Lipoxygenase, and TP53 Genes Predict Colorectal Polyp Risk Reduction by Aspirin in the seAFOod Polyp Prevention Trial. Description: Davies, John R, et al. Polymorphisms in Cyclooxygenase, Lipoxygenase, and TP53 Genes Predict Colorectal Polyp Risk Reduction by Aspirin in the seAFOod Polyp Prevention Trial. ''Cancer Prev Res (Phila)''. 2023 Nov 1; '''16''' (11):621-629
Population genomic analyses suggest recent dispersal events of the pathogen Cercospora zeina into East and Southern African maize cropping systems. Description: Welgemoed, Tanya, et al. Population genomic analyses suggest recent dispersal events of the pathogen Cercospora zeina into East and Southern African maize cropping systems. ''G3 (Bethesda)''. 2023 Nov 1; '''13''' (11):
Population Genomics of the Facultatively Sexual Liverwort Marchantia polymorpha. Description: Sandler, George, et al. Population Genomics of the Facultatively Sexual Liverwort Marchantia polymorpha. ''Genome Biol Evol''. 2023 Nov 1; '''15''' (11):
TNS1 and NRXN1 Genes Interacting With Early-Life Smoking Exposure in Asthma-Plus-Eczema Susceptibility. Description: Margaritte-Jeannin, Patricia, et al. TNS1 and NRXN1 Genes Interacting With Early-Life Smoking Exposure in Asthma-Plus-Eczema Susceptibility. ''Allergy Asthma Immunol Res''. 2023 Nov; '''15''' (6):779-794
Variants of IL6, IL10, FCN2, RNASE3, IL12B and IL17B loci are associated with Schistosoma mansoni worm burden in the Albert Nile region of Uganda. Description: Nyangiri, Oscar Asanya, et al. Variants of IL6, IL10, FCN2, RNASE3, IL12B and IL17B loci are associated with Schistosoma mansoni worm burden in the Albert Nile region of Uganda. ''PLoS Negl Trop Dis''. 2023 Nov; '''17''' (11):e0011796
A proteomic analysis of atrial fibrillation in a prospective longitudinal cohort (AGES-Reykjavik study). Description: Jonmundsson, Thorarinn, et al. A proteomic analysis of atrial fibrillation in a prospective longitudinal cohort (AGES-Reykjavik study). ''Europace''. 2023 Nov 2; '''25''' (11):
Genetic risk factor clustering within and across neurodegenerative diseases. Description: Koretsky, Mathew J, et al. Genetic risk factor clustering within and across neurodegenerative diseases. ''Brain''. 2023 Nov 2; '''146''' (11):4486-4494
Genomic Heterogeneity of Cryptosporidium parvum Isolates From Children in Bangladesh: Implications for Parasite Biology and Human Infection. Description: Carey, Maureen, et al. Genomic Heterogeneity of Cryptosporidium parvum Isolates From Children in Bangladesh: Implications for Parasite Biology and Human Infection. ''J Infect Dis''. 2023 Nov 2; '''228''' (9):1292-1298
The Proinflammatory Role of ANGPTL8 R59W Variant in Modulating Inflammation through NF-kappaB Signaling Pathway under TNFalpha Stimulation. Description: Abu-Farha, Mohamed, et al. The Proinflammatory Role of ANGPTL8 R59W Variant in Modulating Inflammation through NF-kappaB Signaling Pathway under TNFalpha Stimulation. ''Cells''. 2023 Nov 2; '''12''' (21):
The shared genetic architecture and evolution of human language and musical rhythm. Description: Alagoz, Gokberk, et al. The shared genetic architecture and evolution of human language and musical rhythm. ''bioRxiv''. 2023 Nov 2;
Genetic analyses identify evidence for a causal relationship between Ewing sarcoma and hernias. Description: Yang, Tianzhong, et al. Genetic analyses identify evidence for a causal relationship between Ewing sarcoma and hernias. ''HGG Adv''. 2023 Nov 3; '''5''' (1):100254
Genomic signals of local adaptation in Picea crassifolia. Description: Feng, Shuo, et al. Genomic signals of local adaptation in Picea crassifolia. ''BMC Plant Biol''. 2023 Nov 3; '''23''' (1):534
Genomics Reveals Complex Population History and Unexpected Diversity of Eurasian Otters (Lutra lutra) in Britain Relative to Genetic Methods. Description: du Plessis, Sarah J, et al. Genomics Reveals Complex Population History and Unexpected Diversity of Eurasian Otters (Lutra lutra) in Britain Relative to Genetic Methods. ''Mol Biol Evol''. 2023 Nov 3; '''40''' (11):
HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases. Description: Butler-Laporte, Guillaume, et al. HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases. ''Commun Biol''. 2023 Nov 3; '''6''' (1):1113
Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies. Description: van der Voorn, Stephanie M, et al. Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies. ''Int J Mol Sci''. 2023 Nov 3; '''24''' (21):
Redefining the Evolutionary History of the Rock Dove, Columba livia, Using Whole Genome Sequences. Description: Hernandez-Alonso, German, et al. Redefining the Evolutionary History of the Rock Dove, Columba livia, Using Whole Genome Sequences. ''Mol Biol Evol''. 2023 Nov 3; '''40''' (11):
Whole Genome Resequencing Revealed the Genetic Relationship and Selected Regions among Baicheng-You, Beijing-You, and European-Origin Broilers. Description: Yang, Kai, et al. Whole Genome Resequencing Revealed the Genetic Relationship and Selected Regions among Baicheng-You, Beijing-You, and European-Origin Broilers. ''Biology (Basel)''. 2023 Nov 3; '''12''' (11):
Naturally occurring canine laminopathy leading to a dilated and fibrosing cardiomyopathy in the Nova Scotia Duck Tolling Retriever. Description: Bannasch, Danika L, et al. Naturally occurring canine laminopathy leading to a dilated and fibrosing cardiomyopathy in the Nova Scotia Duck Tolling Retriever. ''Sci Rep''. 2023 Nov 4; '''13''' (1):19077
Candidate Genes for IgA Nephropathy in Pediatric Patients: Exome-Wide Association Study. Description: Buianova, Anastasiia A, et al. Candidate Genes for IgA Nephropathy in Pediatric Patients: Exome-Wide Association Study. ''Int J Mol Sci''. 2023 Nov 5; '''24''' (21):
Evolution of a ZW sex chromosome system in willows. Description: Hu, Nan, et al. Evolution of a ZW sex chromosome system in willows. ''Nat Commun''. 2023 Nov 6; '''14''' (1):7144
Integration of risk variants from GWAS with SARS-CoV-2 RNA interactome prioritizes FUBP1 and RAB2A as risk genes for COVID-19. Description: Shi, Weiwen, et al. Integration of risk variants from GWAS with SARS-CoV-2 RNA interactome prioritizes FUBP1 and RAB2A as risk genes for COVID-19. ''Sci Rep''. 2023 Nov 6; '''13''' (1):19194
Genomic formation of Tibeto-Burman speaking populations in Guizhou, Southwest China. Description: Chen, Jinwen, et al. Genomic formation of Tibeto-Burman speaking populations in Guizhou, Southwest China. ''BMC Genomics''. 2023 Nov 7; '''24''' (1):672
Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients. Description: Tang, Wei, et al. Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients. ''Cancer Res Commun''. 2023 Nov 7; '''3''' (11):2244-2255
Unappreciated subcontinental admixture in Europeans and European Americans and implications for genetic epidemiology studies. Description: Gouveia, Mateus H, et al. Unappreciated subcontinental admixture in Europeans and European Americans and implications for genetic epidemiology studies. ''Nat Commun''. 2023 Nov 7; '''14''' (1):6802
Epistasis regulates genetic control of cardiac hypertrophy. Description: Wang, Qianru, et al. Epistasis regulates genetic control of cardiac hypertrophy. ''medRxiv''. 2023 Nov 8;
Genomic Markers Associated with Cytomegalovirus DNAemia in Kidney Transplant Recipients. Description: Shapira, Guy, et al. Genomic Markers Associated with Cytomegalovirus DNAemia in Kidney Transplant Recipients. ''Viruses''. 2023 Nov 8; '''15''' (11):
SIGNET: transcriptome-wide causal inference for gene regulatory networks. Description: Jiang, Zhongli, et al. SIGNET: transcriptome-wide causal inference for gene regulatory networks. ''Sci Rep''. 2023 Nov 8; '''13''' (1):19371
The impact of placental genomic risk for schizophrenia and birth asphyxia on brain development. Description: Wortinger, Laura A, et al. The impact of placental genomic risk for schizophrenia and birth asphyxia on brain development. ''Transl Psychiatry''. 2023 Nov 8; '''13''' (1):343
Exploring the potential of incremental feature selection to improve genomic prediction accuracy. Description: Heinrich, Felix, et al. Exploring the potential of incremental feature selection to improve genomic prediction accuracy. ''Genet Sel Evol''. 2023 Nov 9; '''55''' (1):78
Human MCTS1-dependent translation of JAK2 is essential for IFN-gamma immunity to mycobacteria. Description: Bohlen, Jonathan, et al. Human MCTS1-dependent translation of JAK2 is essential for IFN-gamma immunity to mycobacteria. ''Cell''. 2023 Nov 9; '''186''' (23):5114-5134.e27
The impact of common variants on gene expression in the human brain: from RNA to protein to schizophrenia risk. Description: Liang, Qiuman, et al. The impact of common variants on gene expression in the human brain: from RNA to protein to schizophrenia risk. ''bioRxiv''. 2023 Nov 10;
A phenome-wide approach to identify causal risk factors for deep vein thrombosis. Description: Constantinescu, Andrei-Emil, et al. A phenome-wide approach to identify causal risk factors for deep vein thrombosis. ''BMC Med Genomics''. 2023 Nov 11; '''16''' (1):284
Comparative genomics and genome-wide SNPs of endangered Eld's deer provide breeder selection for inbreeding avoidance. Description: Pumpitakkul, Vichayanee, et al. Comparative genomics and genome-wide SNPs of endangered Eld's deer provide breeder selection for inbreeding avoidance. ''Sci Rep''. 2023 Nov 13; '''13''' (1):19806
Genetic Diversity and Signatures of Selection in the Roughskin Sculpin (Trachidermus fasciatus) Revealed by Whole Genome Sequencing. Description: San, Lize, et al. Genetic Diversity and Signatures of Selection in the Roughskin Sculpin (Trachidermus fasciatus) Revealed by Whole Genome Sequencing. ''Biology (Basel)''. 2023 Nov 13; '''12''' (11):
Alternative polyadenylation-related genetic variants contribute to bladder cancer risk. Description: Liu, Ting, et al. Alternative polyadenylation-related genetic variants contribute to bladder cancer risk. ''J Biomed Res''. 2023 Nov 15; '''37''' (6):405-417
Fatty acid desaturation and lipoxygenase pathways support trained immunity. Description: Ferreira, Anaisa V, et al. Fatty acid desaturation and lipoxygenase pathways support trained immunity. ''Nat Commun''. 2023 Nov 15; '''14''' (1):7385
Identifying genetic variants that influence the abundance of cell states in single-cell data. Description: Rumker, Laurie, et al. Identifying genetic variants that influence the abundance of cell states in single-cell data. ''bioRxiv''. 2023 Nov 15;
The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons. Description: Jones-Tabah, Jace, et al. The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons. ''bioRxiv''. 2023 Nov 15;
Association between polymorphisms of immune response genes and early childhood caries - systematic review, gene-based, gene cluster, and meta-analysis. Description: Aruna, P, et al. Association between polymorphisms of immune response genes and early childhood caries - systematic review, gene-based, gene cluster, and meta-analysis. ''J Genet Eng Biotechnol''. 2023 Nov 16; '''21''' (1):124
Chromosome genome assembly and whole genome sequencing of 110 individuals of Conogethes punctiferalis (Guenee). Description: Gao, Bojia, et al. Chromosome genome assembly and whole genome sequencing of 110 individuals of Conogethes punctiferalis (Guenee). ''Sci Data''. 2023 Nov 16; '''10''' (1):805
Elucidation of the genetic determination of clutch traits in Chinese local chickens of the Laiwu Black breed. Description: Wang, Jie, et al. Elucidation of the genetic determination of clutch traits in Chinese local chickens of the Laiwu Black breed. ''BMC Genomics''. 2023 Nov 16; '''24''' (1):686
New insights into the genetic predisposition of brucellosis and its effect on the gut and vaginal microbiota in goats. Description: Sallam, Ahmed M, et al. New insights into the genetic predisposition of brucellosis and its effect on the gut and vaginal microbiota in goats. ''Sci Rep''. 2023 Nov 16; '''13''' (1):20086
Immunoglobulin-like receptors in chickens: identification, functional characterization, and renaming to cluster homolog of immunoglobulin-like receptors. Description: Sparling, Brandi A, et al. Immunoglobulin-like receptors in chickens: identification, functional characterization, and renaming to cluster homolog of immunoglobulin-like receptors. ''Poult Sci''. 2023 Nov 17; '''103''' (2):103292
New Insights into Polygenic Score-Lifestyle Interactions for Cardiometabolic Risk Factors from Genome-Wide Interaction Analyses. Description: D'Urso, Shannon, et al. New Insights into Polygenic Score-Lifestyle Interactions for Cardiometabolic Risk Factors from Genome-Wide Interaction Analyses. ''Nutrients''. 2023 Nov 17; '''15''' (22):
Comparative genomics of widespread and narrow-range white-bellied rats in the Niviventer niviventer species complex sheds light on invasive rodent success. Description: Wu, Xin-Lai, et al. Comparative genomics of widespread and narrow-range white-bellied rats in the Niviventer niviventer species complex sheds light on invasive rodent success. ''Zool Res''. 2023 Nov 18; '''44''' (6):1052-1063
Can polygenic risk scores help explain disease prevalence differences around the world? A worldwide investigation. Description: Jain, Pritesh R, et al. Can polygenic risk scores help explain disease prevalence differences around the world? A worldwide investigation. ''BMC Genom Data''. 2023 Nov 20; '''24''' (1):70
Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases. Description: Garrison, McKinzie A, et al. Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases. ''Sci Data''. 2023 Nov 20; '''10''' (1):813
Validation of an Integrated Genetic-Epigenetic Test for the Assessment of Coronary Heart Disease. Description: Philibert, Robert, et al. Validation of an Integrated Genetic-Epigenetic Test for the Assessment of Coronary Heart Disease. ''J Am Heart Assoc''. 2023 Nov 20; '''12''' (22):e030934
Case-Control Study of the Association between Single Nucleotide Polymorphisms of Genes Involved in Xenobiotic Detoxification and Antioxidant Protection with the Long-Term Influence of Organochlorine Pesticides on the Population of the Almaty Region. Description: Altynova, Nazym, et al. Case-Control Study of the Association between Single Nucleotide Polymorphisms of Genes Involved in Xenobiotic Detoxification and Antioxidant Protection with the Long-Term Influence of Organochlorine Pesticides on the Population of the Almaty Region. ''Toxics''. 2023 Nov 21; '''11''' (12):
CoreSNP: an efficient pipeline for core marker profile selection from genome-wide SNP datasets in crops. Description: Dou, Tingyu, et al. CoreSNP: an efficient pipeline for core marker profile selection from genome-wide SNP datasets in crops. ''BMC Plant Biol''. 2023 Nov 21; '''23''' (1):580
Genome-wide association analysis unveils candidate genes and loci associated with aplasia cutis congenita in pigs. Description: Zhou, Fuchen, et al. Genome-wide association analysis unveils candidate genes and loci associated with aplasia cutis congenita in pigs. ''BMC Genomics''. 2023 Nov 21; '''24''' (1):701
A comprehensive analysis of genetic risk for metabolic syndrome in the Egyptian population via allele frequency investigation and Missense3D predictions. Description: Bassyouni, Mahmoud, et al. A comprehensive analysis of genetic risk for metabolic syndrome in the Egyptian population via allele frequency investigation and Missense3D predictions. ''Sci Rep''. 2023 Nov 22; '''13''' (1):20517
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis. Description: Yu, Hao, et al. Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis. ''bioRxiv''. 2023 Nov 22;
Circulating extracellular vesicles in human cardiorenal syndrome promote renal injury in a kidney-on-chip system. Description: Chatterjee, Emeli, et al. Circulating extracellular vesicles in human cardiorenal syndrome promote renal injury in a kidney-on-chip system. ''JCI Insight''. 2023 Nov 22; '''8''' (22):
Genetic architecture of individual meiotic crossover rate and distribution in Atlantic Salmon. Description: Brekke, Cathrine, et al. Genetic architecture of individual meiotic crossover rate and distribution in Atlantic Salmon. ''Sci Rep''. 2023 Nov 22; '''13''' (1):20481
Genetic association study of Preterm birth and Gestational age in a population-based case-control study in Peru: Genetics of PTB and GA in pregnant women in Peru. Description: Juvinao-Quintero, Diana L, et al. Genetic association study of Preterm birth and Gestational age in a population-based case-control study in Peru: Genetics of PTB and GA in pregnant women in Peru. ''medRxiv''. 2023 Nov 22;
Genome-wide association study exploring the genetic architecture of eggshell speckles in laying hens. Description: Cheng, Xue, et al. Genome-wide association study exploring the genetic architecture of eggshell speckles in laying hens. ''BMC Genomics''. 2023 Nov 22; '''24''' (1):704
Oryza glumaepatula: A wild relative to improve drought tolerance in cultivated rice. Description: Thathapalli Prakash, Parthiban, et al. Oryza glumaepatula: A wild relative to improve drought tolerance in cultivated rice. ''Plant Physiol''. 2023 Nov 22; '''193''' (4):2381-2397
Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson's study. Description: Pachchek, Sinthuja, et al. Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson's study. ''NPJ Parkinsons Dis''. 2023 Nov 23; '''9''' (1):156
Evaluation of circulating plasma proteins in breast cancer using Mendelian randomisation. Description: Malarstig, Anders, et al. Evaluation of circulating plasma proteins in breast cancer using Mendelian randomisation. ''Nat Commun''. 2023 Nov 24; '''14''' (1):7680
TIE1 and TEK signalling, intraocular pressure, and primary open-angle glaucoma: a Mendelian randomization study. Description: Rajasundaram, Skanda, et al. TIE1 and TEK signalling, intraocular pressure, and primary open-angle glaucoma: a Mendelian randomization study. ''J Transl Med''. 2023 Nov 24; '''21''' (1):847
Genetic diversity and historical demography of underutilised goat breeds in North-Western Europe. Description: Manunza, Arianna, et al. Genetic diversity and historical demography of underutilised goat breeds in North-Western Europe. ''Sci Rep''. 2023 Nov 25; '''13''' (1):20728
Phylogenetic, population structure, and population demographic analyses reveal that Vicia sepium in Japan is native and not introduced. Description: Tamaki, Ichiro, et al. Phylogenetic, population structure, and population demographic analyses reveal that Vicia sepium in Japan is native and not introduced. ''Sci Rep''. 2023 Nov 25; '''13''' (1):20746
A high-resolution haplotype-resolved Reference panel constructed from the China Kadoorie Biobank Study. Description: Yu, Canqing, et al. A high-resolution haplotype-resolved Reference panel constructed from the China Kadoorie Biobank Study. ''Nucleic Acids Res''. 2023 Nov 27; '''51''' (21):11770-11782
A papain-like cysteine protease-released small signal peptide confers wheat resistance to wheat yellow mosaic virus. Description: Liu, Peng, et al. A papain-like cysteine protease-released small signal peptide confers wheat resistance to wheat yellow mosaic virus. ''Nat Commun''. 2023 Nov 27; '''14''' (1):7773
Association between 14 candidate genes, PM2.5, and affective disorders: a study of the Taiwan Biobank. Description: Ma, Kai-Jie, et al. Association between 14 candidate genes, PM2.5, and affective disorders: a study of the Taiwan Biobank. ''BMC Public Health''. 2023 Nov 27; '''23''' (1):2346
A web-based genome-wide association study reveals the susceptibility loci of common adverse events following COVID-19 vaccination in the Japanese population. Description: Nogawa, Shun, et al. A web-based genome-wide association study reveals the susceptibility loci of common adverse events following COVID-19 vaccination in the Japanese population. ''Sci Rep''. 2023 Nov 27; '''13''' (1):20820
BRSK2 in pancreatic beta cells promotes hyperinsulinemia-coupled insulin resistance and its genetic variants are associated with human type 2 diabetes. Description: Xu, Rufeng, et al. BRSK2 in pancreatic beta cells promotes hyperinsulinemia-coupled insulin resistance and its genetic variants are associated with human type 2 diabetes. ''J Mol Cell Biol''. 2023 Nov 27; '''15''' (5):
Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel. Description: Levi, Hagai, et al. Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel. ''J Med Genet''. 2023 Nov 27; '''60''' (12):1186-1197
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events. Description: Heyne, Henrike O, et al. Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events. ''medRxiv''. 2023 Nov 27;
Targeted sequencing of high-density SNPs provides an enhanced tool for forensic applications and genetic landscape exploration in Chinese Korean ethnic group. Description: Lan, Qiong, et al. Targeted sequencing of high-density SNPs provides an enhanced tool for forensic applications and genetic landscape exploration in Chinese Korean ethnic group. ''Hum Genomics''. 2023 Nov 27; '''17''' (1):107
Global genetic diversity, introgression, and evolutionary adaptation of indicine cattle revealed by whole genome sequencing. Description: Chen, Ningbo, et al. Global genetic diversity, introgression, and evolutionary adaptation of indicine cattle revealed by whole genome sequencing. ''Nat Commun''. 2023 Nov 28; '''14''' (1):7803
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability. Description: Schmilovich, Zoe, et al. Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability. ''medRxiv''. 2023 Nov 29;
Psychosis Endophenotypes: A Gene-Set-Specific Polygenic Risk Score Analysis. Description: Wang, Baihan, et al. Psychosis Endophenotypes: A Gene-Set-Specific Polygenic Risk Score Analysis. ''Schizophr Bull''. 2023 Nov 29; '''49''' (6):1625-1636
The impact of genetic risk for schizophrenia on eating disorder clinical presentations. Description: Zhang, Ruyue, et al. The impact of genetic risk for schizophrenia on eating disorder clinical presentations. ''Transl Psychiatry''. 2023 Nov 29; '''13''' (1):366
Y and Mitochondrial Chromosomes in the Heterogeneous Stock Rat Population. Description: Okamoto, Faith, et al. Y and Mitochondrial Chromosomes in the Heterogeneous Stock Rat Population. ''bioRxiv''. 2023 Nov 29;
Association between MC1R gene and coat color segregation in Shanxia long black pig and Lulai black pig. Description: Zheng, Hao, et al. Association between MC1R gene and coat color segregation in Shanxia long black pig and Lulai black pig. ''BMC Genom Data''. 2023 Nov 30; '''24''' (1):74
Genetic insights into the dissolution of dioecy in diploid persimmon Diospyros oleifera Cheng. Description: Sun, Peng, et al. Genetic insights into the dissolution of dioecy in diploid persimmon Diospyros oleifera Cheng. ''BMC Plant Biol''. 2023 Nov 30; '''23''' (1):606
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Description: Gupta, Yask, et al. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. ''Nat Commun''. 2023 Nov 30; '''14''' (1):7836
WITHDRAWN: Genome-wide risk prediction of primary open-angle glaucoma across multiple ancestries. Description: Gharahkhani, Puya, et al. WITHDRAWN: Genome-wide risk prediction of primary open-angle glaucoma across multiple ancestries. ''medRxiv''. 2023 Nov 30;
A Genetic Risk Variant for Multiple Sclerosis Severity is Associated with Brain Atrophy. Description: Gasperi, Christiane, et al. A Genetic Risk Variant for Multiple Sclerosis Severity is Associated with Brain Atrophy. ''Ann Neurol''. 2023 Dec; '''94''' (6):1080-1085
Archaic Introgression Shaped Human Circadian Traits. Description: Velazquez-Arcelay, Keila, et al. Archaic Introgression Shaped Human Circadian Traits. ''Genome Biol Evol''. 2023 Dec 1; '''15''' (12):
Association of biological age with health outcomes and its modifiable factors. Description: Liu, Wei-Shi, et al. Association of biological age with health outcomes and its modifiable factors. ''Aging Cell''. 2023 Dec; '''22''' (12):e13995
Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder. Description: Amare, Azmeraw T, et al. Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder. ''Mol Psychiatry''. 2023 Dec; '''28''' (12):5251-5261
Association of polygenic scores for depression and neuroticism with perceived stress in daily life during a long-lasting stress period. Description: Peter, Hannah L, et al. Association of polygenic scores for depression and neuroticism with perceived stress in daily life during a long-lasting stress period. ''Genes Brain Behav''. 2023 Dec; '''22''' (6):e12872
Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes. Description: Glessner, Joseph T, et al. Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes. ''J Hepatol''. 2023 Dec; '''79''' (6):1385-1395
Causal links of alpha-thalassemia indices and cardiometabolic traits and diabetes: MR study. Description: Hsu, Lung-An, et al. Causal links of alpha-thalassemia indices and cardiometabolic traits and diabetes: MR study. ''Life Sci Alliance''. 2023 Dec; '''6''' (12):
Characteristics of insulin resistance in Korean adults from the perspective of circadian and metabolic sensing genes. Description: Park, Miso S, et al. Characteristics of insulin resistance in Korean adults from the perspective of circadian and metabolic sensing genes. ''Genes Genomics''. 2023 Dec; '''45''' (12):1475-1487
Divergent mechanisms of reduced growth performance in Betula ermanii saplings from high-altitude and low-latitude range edges. Description: Aihara, Takaki, et al. Divergent mechanisms of reduced growth performance in Betula ermanii saplings from high-altitude and low-latitude range edges. ''Heredity (Edinb)''. 2023 Dec; '''131''' (5-6):387-397
DNA hydroxymethylation differences underlie phenotypic divergence of somatic growth in Nile tilapia reared in common garden. Description: Konstantinidis, Ioannis, et al. DNA hydroxymethylation differences underlie phenotypic divergence of somatic growth in Nile tilapia reared in common garden. ''Epigenetics''. 2023 Dec; '''18''' (1):2282323
Evidence of survival bias in the association between APOE-ϵ4 and age of ischemic stroke onset. Description: von Berg, Joanna, et al. Evidence of survival bias in the association between APOE-ϵ4 and age of ischemic stroke onset. ''medRxiv''. 2023 Dec 1;
Examination of eQTL Polymorphisms Associated with Increased Risk of Progressive Complicated Sarcoidosis in European and African Descent Subjects. Description: Casanova, Nancy G, et al. Examination of eQTL Polymorphisms Associated with Increased Risk of Progressive Complicated Sarcoidosis in European and African Descent Subjects. ''Eur J Respir Med''. 2023 Dec; '''5''' (1):359-371
Extensive Phylogenomic Discordance and the Complex Evolutionary History of the Neotropical Cat Genus Leopardus. Description: Lescroart, Jonas, et al. Extensive Phylogenomic Discordance and the Complex Evolutionary History of the Neotropical Cat Genus Leopardus. ''Mol Biol Evol''. 2023 Dec 1; '''40''' (12):
Genetic Affinities and Adaptation of the South-West Coast Populations of India. Description: Kumar, Lomous, et al. Genetic Affinities and Adaptation of the South-West Coast Populations of India. ''Genome Biol Evol''. 2023 Dec 1; '''15''' (12):
Genetic diversity and microevolution in clinical Cryptococcus isolates from Cameroon. Description: Sephton-Clark, Poppy, et al. Genetic diversity and microevolution in clinical Cryptococcus isolates from Cameroon. ''Med Mycol''. 2023 Dec 1; '''61''' (12):
Genetic Load and Adaptive Potential of a Recovered Avian Species that Narrowly Avoided Extinction. Description: Femerling, Georgette, et al. Genetic Load and Adaptive Potential of a Recovered Avian Species that Narrowly Avoided Extinction. ''Mol Biol Evol''. 2023 Dec 1; '''40''' (12):
Genome and haplotype provide insights into the population differentiation and breeding improvement of Gossypium barbadense. Description: Wang, Nian, et al. Genome and haplotype provide insights into the population differentiation and breeding improvement of Gossypium barbadense. ''J Adv Res''. 2023 Dec; '''54''': 15-27
GWAS reveals genomic associations with swine inflammation and necrosis syndrome. Description: Gerhards, Katharina, et al. GWAS reveals genomic associations with swine inflammation and necrosis syndrome. ''Mamm Genome''. 2023 Dec; '''34''' (4):586-601
Haplotype-based inference of recent effective population size in modern and ancient DNA samples. Description: Fournier, Romain, et al. Haplotype-based inference of recent effective population size in modern and ancient DNA samples. ''Nat Commun''. 2023 Dec 1; '''14''' (1):7945
Host genetics and gut microbiota jointly regulate blood biochemical indicators in chickens. Description: Jiang, Xinwei, et al. Host genetics and gut microbiota jointly regulate blood biochemical indicators in chickens. ''Appl Microbiol Biotechnol''. 2023 Dec; '''107''' (24):7601-7620
Indigenous Australian genomes show deep structure and rich novel variation. Description: Silcocks, Matthew, et al. Indigenous Australian genomes show deep structure and rich novel variation. ''Nature''. 2023 Dec; '''624''' (7992):593-601
Influence of Diabetes Family History on the Associations of Combined Genetic and Lifestyle Risks with Diabetes in the Tohoku Medical Megabank Community-Based Cohort Study. Description: Takase, Masato, et al. Influence of Diabetes Family History on the Associations of Combined Genetic and Lifestyle Risks with Diabetes in the Tohoku Medical Megabank Community-Based Cohort Study. ''J Atheroscler Thromb''. 2023 Dec 1; '''30''' (12):1950-1965
Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain. Description: Bhattacharya, Arjun, et al. Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain. ''Nat Genet''. 2023 Dec; '''55''' (12):2117-2128
Landscape genomics reveals adaptive genetic differentiation driven by multiple environmental variables in naked barley on the Qinghai-Tibetan Plateau. Description: Chen, Tongrui, et al. Landscape genomics reveals adaptive genetic differentiation driven by multiple environmental variables in naked barley on the Qinghai-Tibetan Plateau. ''Heredity (Edinb)''. 2023 Dec; '''131''' (5-6):316-326
Long-read RNA-seq atlas of novel microglia isoforms elucidates disease-associated genetic regulation of splicing. Description: Humphrey, Jack, et al. Long-read RNA-seq atlas of novel microglia isoforms elucidates disease-associated genetic regulation of splicing. ''medRxiv''. 2023 Dec 1;
Mapping and Functional Dissection of the Rumpless Trait in Piao Chicken Identifies a Causal Loss of Function Mutation in the Novel Gene Rum. Description: Guo, Ying, et al. Mapping and Functional Dissection of the Rumpless Trait in Piao Chicken Identifies a Causal Loss of Function Mutation in the Novel Gene Rum. ''Mol Biol Evol''. 2023 Dec 1; '''40''' (12):
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications. Description: Levey, Daniel F, et al. Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications. ''Nat Genet''. 2023 Dec; '''55''' (12):2094-2103
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. Description: Zhou, Hang, et al. Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. ''Nat Med''. 2023 Dec; '''29''' (12):3184-3192
Natural polymorphisms in ZmIRX15A affect water-use efficiency by modulating stomatal density in maize. Description: Zhang, Kun, et al. Natural polymorphisms in ZmIRX15A affect water-use efficiency by modulating stomatal density in maize. ''Plant Biotechnol J''. 2023 Dec; '''21''' (12):2560-2573
Pangenome analysis reveals genomic variations associated with domestication traits in broomcorn millet. Description: Chen, Jinfeng, et al. Pangenome analysis reveals genomic variations associated with domestication traits in broomcorn millet. ''Nat Genet''. 2023 Dec; '''55''' (12):2243-2254
Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. Description: Dahl, Andrew, et al. Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. ''Nat Genet''. 2023 Dec; '''55''' (12):2082-2093
Polygenic risk of obesity and BMI trajectories over 36 years: A longitudinal study of adult Finnish twins. Description: Berntzen, Bram J, et al. Polygenic risk of obesity and BMI trajectories over 36 years: A longitudinal study of adult Finnish twins. ''Obesity (Silver Spring)''. 2023 Dec; '''31''' (12):3086-3094
Prediabetic HbA1c and Cortical Atrophy: Underlying Neurobiology. Description: Shin, Jean, et al. Prediabetic HbA1c and Cortical Atrophy: Underlying Neurobiology. ''Diabetes Care''. 2023 Dec 1; '''46''' (12):2267-2272
Prevalence of genetically determined trehalase deficiency in populations of Siberia and Russian Far East. Description: Kozlov, Andrey, et al. Prevalence of genetically determined trehalase deficiency in populations of Siberia and Russian Far East. ''Int J Circumpolar Health''. 2023 Dec; '''82''' (1):2183931
Proteome-wide mendelian randomization identifies causal plasma proteins in venous thromboembolism development. Description: Li, Haobo, et al. Proteome-wide mendelian randomization identifies causal plasma proteins in venous thromboembolism development. ''J Hum Genet''. 2023 Dec; '''68''' (12):805-812
Rare functional variants in the CRP and G6PC genes modify the relationship between obesity and serum C-reactive protein in white British population. Description: Li, Xia, et al. Rare functional variants in the CRP and G6PC genes modify the relationship between obesity and serum C-reactive protein in white British population. ''Mol Genet Genomic Med''. 2023 Dec; '''11''' (12):e2255
Schizophrenia polygenic risk score in psychosis proneness. Description: Mas-Bermejo, Patricia, et al. Schizophrenia polygenic risk score in psychosis proneness. ''Eur Arch Psychiatry Clin Neurosci''. 2023 Dec; '''273''' (8):1665-1675
The polygenic and reactive nature of observed parenting. Description: Runze, Jana, et al. The polygenic and reactive nature of observed parenting. ''Genes Brain Behav''. 2023 Dec; '''22''' (6):e12874
Uncovering associations between pre-existing conditions and COVID-19 Severity: A polygenic risk score approach across three large biobanks. Description: Fritsche, Lars G, et al. Uncovering associations between pre-existing conditions and COVID-19 Severity: A polygenic risk score approach across three large biobanks. ''PLoS Genet''. 2023 Dec; '''19''' (12):e1010907
Accurate and efficient estimation of local heritability using summary statistics and the linkage disequilibrium matrix. Description: Li, Hui, et al. Accurate and efficient estimation of local heritability using summary statistics and the linkage disequilibrium matrix. ''Nat Commun''. 2023 Dec 2; '''14''' (1):7954
Unraveling the Genomic Association for Milk Production Traits and Signatures of Selection of Cattle in a Harsh Tropical Environment. Description: Velayudhan, Silpa Mullakkalparambil, et al. Unraveling the Genomic Association for Milk Production Traits and Signatures of Selection of Cattle in a Harsh Tropical Environment. ''Biology (Basel)''. 2023 Dec 2; '''12''' (12):
Whole genomes from Angola and Mozambique inform about the origins and dispersals of major African migrations. Description: Tallman, Sam, et al. Whole genomes from Angola and Mozambique inform about the origins and dispersals of major African migrations. ''Nat Commun''. 2023 Dec 2; '''14''' (1):7967
Research Note: Development and application of specific molecular identity cards for "Yufen 1" H line chickens. Description: Liu, Cong, et al. Research Note: Development and application of specific molecular identity cards for "Yufen 1" H line chickens. ''Poult Sci''. 2023 Dec 3; '''103''' (2):103343
Genetic discovery and risk prediction for type 1 diabetes in individuals without high-risk HLA-DR3/DR4 haplotypes. Description: McGrail, Carolyn, et al. Genetic discovery and risk prediction for type 1 diabetes in individuals without high-risk HLA-DR3/DR4 haplotypes. ''medRxiv''. 2023 Dec 4;
Mendelian randomization analyses suggest a causal role for circulating GIP and IL-1RA levels in homeostatic model assessment-derived measures of beta-cell function and insulin sensitivity in Africans without type 2 diabetes. Description: Meeks, Karlijn A C, et al. Mendelian randomization analyses suggest a causal role for circulating GIP and IL-1RA levels in homeostatic model assessment-derived measures of beta-cell function and insulin sensitivity in Africans without type 2 diabetes. ''Genome Med''. 2023 Dec 4; '''15''' (1):108
A low-inflammatory diet is associated with a lower incidence of diabetes: role of diabetes-related genetic risk. Description: Yang, Rongrong, et al. A low-inflammatory diet is associated with a lower incidence of diabetes: role of diabetes-related genetic risk. ''BMC Med''. 2023 Dec 5; '''21''' (1):483
Exploring the mechanism of artificial selection signature in Chinese indigenous pigs by leveraging multiple bioinformatics database tools. Description: Feng, Xueyan, et al. Exploring the mechanism of artificial selection signature in Chinese indigenous pigs by leveraging multiple bioinformatics database tools. ''BMC Genomics''. 2023 Dec 5; '''24''' (1):743
Metabolic changes preceding bladder cancer occurrence among Korean men: a nested case-control study from the KCPS-II cohort. Description: Han, Youngmin, et al. Metabolic changes preceding bladder cancer occurrence among Korean men: a nested case-control study from the KCPS-II cohort. ''Cancer Metab''. 2023 Dec 5; '''11''' (1):23
Prostate cancer genetic risk and associated aggressive disease in men of African ancestry. Description: Soh, Pamela X Y, et al. Prostate cancer genetic risk and associated aggressive disease in men of African ancestry. ''Nat Commun''. 2023 Dec 5; '''14''' (1):8037
Association of ESR1 germline variants with TP53 somatic variants in breast tumors in a genome-wide study. Description: Tjader, Nijole P, et al. Association of ESR1 germline variants with TP53 somatic variants in breast tumors in a genome-wide study. ''medRxiv''. 2023 Dec 6;
Genome-wide selective signatures mining the candidate genes for egg laying in goose. Description: Zhao, Hongchang, et al. Genome-wide selective signatures mining the candidate genes for egg laying in goose. ''BMC Genomics''. 2023 Dec 6; '''24''' (1):750
Genomic diversity of wild and cultured Yesso scallop Mizuhopecten yessoensis from Japan and Canada. Description: Sutherland, Ben J G, et al. Genomic diversity of wild and cultured Yesso scallop Mizuhopecten yessoensis from Japan and Canada. ''G3 (Bethesda)''. 2023 Dec 6; '''13''' (12):
Targeting Longevity Gene SLC13A5: A Novel Approach to Prevent Age-Related Bone Fragility and Osteoporosis. Description: Zahn, Grit, et al. Targeting Longevity Gene SLC13A5: A Novel Approach to Prevent Age-Related Bone Fragility and Osteoporosis. ''Metabolites''. 2023 Dec 6; '''13''' (12):
Investigation of genomic and transcriptomic risk factors in clopidogrel response in African Americans. Description: Yang, Guang, et al. Investigation of genomic and transcriptomic risk factors in clopidogrel response in African Americans. ''medRxiv''. 2023 Dec 7;
A multidimensional social risk atlas of depression and anxiety: An observational and genome-wide environmental interaction study. Description: Pan, Chuyu, et al. A multidimensional social risk atlas of depression and anxiety: An observational and genome-wide environmental interaction study. ''J Glob Health''. 2023 Dec 8; '''13''': 04146
Assessing the validity of a self-reported clinical diagnosis of schizophrenia. Description: Woolway, Grace E, et al. Assessing the validity of a self-reported clinical diagnosis of schizophrenia. ''medRxiv''. 2023 Dec 8;
Association of genetic risk and lifestyle with pancreatic cancer and their age dependency: a large prospective cohort study in the UK Biobank. Description: Zeng, Liangtang, et al. Association of genetic risk and lifestyle with pancreatic cancer and their age dependency: a large prospective cohort study in the UK Biobank. ''BMC Med''. 2023 Dec 8; '''21''' (1):489
DNA methylation modulated genetic variant effect on gene transcriptional regulation. Description: Zeng, Yong, et al. DNA methylation modulated genetic variant effect on gene transcriptional regulation. ''Genome Biol''. 2023 Dec 8; '''24''' (1):285
Genetic dissection of maize (Zea maysL.) trace element traits using genome-wide association studies. Description: Zhu, Hang, et al. Genetic dissection of maize (Zea maysL.) trace element traits using genome-wide association studies. ''BMC Plant Biol''. 2023 Dec 8; '''23''' (1):631
Genome- and Transcriptome-wide Association Studies to Discover Candidate Genes for Diverse Root Phenotypes in Cultivated Rice. Description: Wei, Shujun, et al. Genome- and Transcriptome-wide Association Studies to Discover Candidate Genes for Diverse Root Phenotypes in Cultivated Rice. ''Rice (N Y)''. 2023 Dec 8; '''16''' (1):55
Lack of association between HLA and asymptomatic SARS-CoV-2 infection. Description: Marchal, Astrid, et al. Lack of association between HLA and asymptomatic SARS-CoV-2 infection. ''medRxiv''. 2023 Dec 8;
Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts. Description: Al-Ali, Amein K, et al. Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts. ''Sci Rep''. 2023 Dec 10; '''13''' (1):21866
Dispersal from the Qinghai-Tibet plateau by a high-altitude butterfly is associated with rapid expansion and reorganization of its genome. Description: Zhao, Youjie, et al. Dispersal from the Qinghai-Tibet plateau by a high-altitude butterfly is associated with rapid expansion and reorganization of its genome. ''Nat Commun''. 2023 Dec 11; '''14''' (1):8190
Effect of Genetic and Dietary Perturbation of Glycine Metabolism on Atherosclerosis in Humans and Mice. Description: Biswas, Subarna, et al. Effect of Genetic and Dietary Perturbation of Glycine Metabolism on Atherosclerosis in Humans and Mice. ''medRxiv''. 2023 Dec 11;
Polygenic prediction of human longevity on the supposition of pervasive pleiotropy. Description: Jabalameli, M Reza, et al. Polygenic prediction of human longevity on the supposition of pervasive pleiotropy. ''medRxiv''. 2023 Dec 11;
The Population Divergence and Genetic Basis of Local Adaptation of Wild Soybean (Glycine soja) in China. Description: Liu, Xiaodong, et al. The Population Divergence and Genetic Basis of Local Adaptation of Wild Soybean (Glycine soja) in China. ''Plants (Basel)''. 2023 Dec 11; '''12''' (24):
The population-level impact of Enterococcus faecalis genetics on intestinal colonization and extraintestinal infection. Description: Chaguza, Chrispin, et al. The population-level impact of Enterococcus faecalis genetics on intestinal colonization and extraintestinal infection. ''Microbiol Spectr''. 2023 Dec 12; '''11''' (6):e0020123
Analysis of Genetic Diversity in Adzuki Beans (Vigna angularis): Insights into Environmental Adaptation and Early Breeding Strategies for Yield Improvement. Description: Wang, Xiaohan, et al. Analysis of Genetic Diversity in Adzuki Beans (Vigna angularis): Insights into Environmental Adaptation and Early Breeding Strategies for Yield Improvement. ''Plants (Basel)''. 2023 Dec 13; '''12''' (24):
Structural variants involved in high-altitude adaptation detected using single-molecule long-read sequencing. Description: Shi, Jinlong, et al. Structural variants involved in high-altitude adaptation detected using single-molecule long-read sequencing. ''Nat Commun''. 2023 Dec 13; '''14''' (1):8282
Analysis of clinical Candida parapsilosis isolates reveals copy number variation in key fluconazole resistance genes. Description: Bergin, Sean, et al. Analysis of clinical Candida parapsilosis isolates reveals copy number variation in key fluconazole resistance genes. ''bioRxiv''. 2023 Dec 14;
Genomic Analysis of Lymphoma Risk in Bullmastiff Dogs. Description: Mortlock, Sally A, et al. Genomic Analysis of Lymphoma Risk in Bullmastiff Dogs. ''Vet Sci''. 2023 Dec 14; '''10''' (12):
Genomic diversity in functionally relevant genes modifies neurodevelopmental versus neoplastic risks in individuals with germline PTEN variants. Description: Eng, Charis, et al. Genomic diversity in functionally relevant genes modifies neurodevelopmental versus neoplastic risks in individuals with germline PTEN variants. ''Res Sq''. 2023 Dec 14;
Managing genomic diversity in conservation programs of Chinese domestic chickens. Description: Zhang, Mengmeng, et al. Managing genomic diversity in conservation programs of Chinese domestic chickens. ''Genet Sel Evol''. 2023 Dec 14; '''55''' (1):92
Mapping restricted introgression across the genomes of admixed indigenous African cattle breeds. Description: Friedrich, Juliane, et al. Mapping restricted introgression across the genomes of admixed indigenous African cattle breeds. ''Genet Sel Evol''. 2023 Dec 14; '''55''' (1):91
Polygenic risk alters the penetrance of monogenic kidney disease. Description: Khan, Atlas, et al. Polygenic risk alters the penetrance of monogenic kidney disease. ''Nat Commun''. 2023 Dec 14; '''14''' (1):8318
A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes. Description: McEvoy, Alannah, et al. A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes. ''Sci Rep''. 2023 Dec 15; '''13''' (1):22360
Evidence for early domestic yak, taurine cattle, and their hybrids on the Tibetan Plateau. Description: Chen, Ningbo, et al. Evidence for early domestic yak, taurine cattle, and their hybrids on the Tibetan Plateau. ''Sci Adv''. 2023 Dec 15; '''9''' (50):eadi6857
Genetic and observational associations of lung function with gastrointestinal tract diseases: pleiotropic and mendelian randomization analysis. Description: Jiang, Minghui, et al. Genetic and observational associations of lung function with gastrointestinal tract diseases: pleiotropic and mendelian randomization analysis. ''Respir Res''. 2023 Dec 15; '''24''' (1):315
Tandem gene duplications contributed to high-level azole resistance in a rapidly expanding Candida tropicalis population. Description: Fan, Xin, et al. Tandem gene duplications contributed to high-level azole resistance in a rapidly expanding Candida tropicalis population. ''Nat Commun''. 2023 Dec 15; '''14''' (1):8369
A resource of induced pluripotent stem cell (iPSC) lines including clinical, genomic, and cellular data from genetically isolated families with mood and psychotic disorders. Description: Detera-Wadleigh, Sevilla D, et al. A resource of induced pluripotent stem cell (iPSC) lines including clinical, genomic, and cellular data from genetically isolated families with mood and psychotic disorders. ''Transl Psychiatry''. 2023 Dec 16; '''13''' (1):397
TWAS revealed significant causal loci for milk production and its composition in Murrah buffaloes. Description: Chhotaray, Supriya, et al. TWAS revealed significant causal loci for milk production and its composition in Murrah buffaloes. ''Sci Rep''. 2023 Dec 16; '''13''' (1):22401
Ridge regression and deep learning models for genome-wide selection of complex traits in New Mexican Chile peppers. Description: Lozada, Dennis N, et al. Ridge regression and deep learning models for genome-wide selection of complex traits in New Mexican Chile peppers. ''BMC Genom Data''. 2023 Dec 18; '''24''' (1):80
Descriptive Statistics and Genome-Wide Copy Number Analysis of Milk Production Traits of Jiangsu Chinese Holstein Cows. Description: Zhu, Hao, et al. Descriptive Statistics and Genome-Wide Copy Number Analysis of Milk Production Traits of Jiangsu Chinese Holstein Cows. ''Animals (Basel)''. 2023 Dec 19; '''14''' (1):
Genetic Variants at the 9p21.3 Locus Are Associated with Risk for Non-Compressible Artery Disease: Results from the ARTPER Study. Description: Via, Marc, et al. Genetic Variants at the 9p21.3 Locus Are Associated with Risk for Non-Compressible Artery Disease: Results from the ARTPER Study. ''Genes (Basel)''. 2023 Dec 19; '''15''' (1):
Investigation of ABO Gene Variants across More Than 60 Pig Breeds and Populations and Other Suidae Species Using Whole-Genome Sequencing Datasets. Description: Bolner, Matteo, et al. Investigation of ABO Gene Variants across More Than 60 Pig Breeds and Populations and Other Suidae Species Using Whole-Genome Sequencing Datasets. ''Animals (Basel)''. 2023 Dec 19; '''14''' (1):
Genetic Architecture of Abdominal Fat Deposition Revealed by a Genome-Wide Association Study in the Laying Chicken. Description: Guo, Jun, et al. Genetic Architecture of Abdominal Fat Deposition Revealed by a Genome-Wide Association Study in the Laying Chicken. ''Genes (Basel)''. 2023 Dec 20; '''15''' (1):
Genome-Wide Association Analysis of Reproductive Traits in Chinese Holstein Cattle. Description: Liu, Jiashuang, et al. Genome-Wide Association Analysis of Reproductive Traits in Chinese Holstein Cattle. ''Genes (Basel)''. 2023 Dec 20; '''15''' (1):
Genomic analysis identifies risk factors in restless legs syndrome. Description: Akcimen, Fulya, et al. Genomic analysis identifies risk factors in restless legs syndrome. ''medRxiv''. 2023 Dec 20;
Genomic Predictions in Korean Hanwoo Cows: A Comparative Analysis of Genomic BLUP and Bayesian Methods for Reproductive Traits. Description: Haque, Md Azizul, et al. Genomic Predictions in Korean Hanwoo Cows: A Comparative Analysis of Genomic BLUP and Bayesian Methods for Reproductive Traits. ''Animals (Basel)''. 2023 Dec 20; '''14''' (1):
USP7/Maged1-mediated H2A monoubiquitination in the paraventricular thalamus: an epigenetic mechanism involved in cocaine use disorder. Description: Cheron, Julian, et al. USP7/Maged1-mediated H2A monoubiquitination in the paraventricular thalamus: an epigenetic mechanism involved in cocaine use disorder. ''Nat Commun''. 2023 Dec 20; '''14''' (1):8481
Genome-Wide Association Study for Somatic Skeletal Traits in Duroc x (Landrace x Yorkshire) Pigs. Description: Gao, Xin, et al. Genome-Wide Association Study for Somatic Skeletal Traits in Duroc x (Landrace x Yorkshire) Pigs. ''Animals (Basel)''. 2023 Dec 21; '''14''' (1):
Risk of newly developed atrial fibrillation by alcohol consumption differs according to genetic predisposition to alcohol metabolism: a large-scale cohort study with UK Biobank. Description: Park, Chan Soon, et al. Risk of newly developed atrial fibrillation by alcohol consumption differs according to genetic predisposition to alcohol metabolism: a large-scale cohort study with UK Biobank. ''BMC Med''. 2023 Dec 21; '''21''' (1):509
Unraveling the causal genes and transcriptomic determinants of human telomere length. Description: Chang, Ying, et al. Unraveling the causal genes and transcriptomic determinants of human telomere length. ''Nat Commun''. 2023 Dec 21; '''14''' (1):8517
Association Study of a Comprehensive Panel of Neuropeptide-Related Polymorphisms Suggest Potential Roles in Verbal Learning and Memory. Description: Avgan, Nesli, et al. Association Study of a Comprehensive Panel of Neuropeptide-Related Polymorphisms Suggest Potential Roles in Verbal Learning and Memory. ''Genes (Basel)''. 2023 Dec 24; '''15''' (1):
Genome-wide QTL mapping across three tissues highlights several Alzheimer's and Parkinson's disease loci potentially acting via DNA methylation. Description: Ohlei, Olena, et al. Genome-wide QTL mapping across three tissues highlights several Alzheimer's and Parkinson's disease loci potentially acting via DNA methylation. ''medRxiv''. 2023 Dec 24;
Host genetic variants associated with susceptibility and severity of pneumococcal pneumonia in adult patients. Description: Boix-Palop, Lucia, et al. Host genetic variants associated with susceptibility and severity of pneumococcal pneumonia in adult patients. ''Pneumonia (Nathan)''. 2023 Dec 25; '''15''' (1):18
Systematic analysis of Mendelian disease-associated gene variants reveals new classes of cancer-predisposing genes. Description: Song, Seulki, et al. Systematic analysis of Mendelian disease-associated gene variants reveals new classes of cancer-predisposing genes. ''Genome Med''. 2023 Dec 25; '''15''' (1):107
Evaluation of imputation performance of multiple reference panels in a Pakistani population. Description: Xu, Jiayi, et al. Evaluation of imputation performance of multiple reference panels in a Pakistani population. ''medRxiv''. 2023 Dec 26;
Genome-Wide Association Studies Reveal Candidate Genes Associated with Pigmentation Patterns of Single Feathers of Tianfu Nonghua Ducks. Description: Twumasi, Grace, et al. Genome-Wide Association Studies Reveal Candidate Genes Associated with Pigmentation Patterns of Single Feathers of Tianfu Nonghua Ducks. ''Animals (Basel)''. 2023 Dec 26; '''14''' (1):
Genomic loci influence patterns of structural covariance in the human brain. Description: Wen, Junhao, et al. Genomic loci influence patterns of structural covariance in the human brain. ''Proc Natl Acad Sci U S A''. 2023 Dec 26; '''120''' (52):e2300842120
Mapping of the gene network that regulates glycan clock of ageing. Description: Frkatovic-Hodzic, Azra, et al. Mapping of the gene network that regulates glycan clock of ageing. ''Aging (Albany NY)''. 2023 Dec 26; '''15''' (24):14509-14552
Citrullinated and MMP-degraded vimentin is associated with chronic pulmonary diseases and genetic variants in PADI3/PADI4 and CFH in postmenopausal women. Description: Bager, Cecilie Liv, et al. Citrullinated and MMP-degraded vimentin is associated with chronic pulmonary diseases and genetic variants in PADI3/PADI4 and CFH in postmenopausal women. ''Sci Rep''. 2023 Dec 27; '''13''' (1):23039
Efficient estimation for large-scale linkage disequilibrium patterns of the human genome. Description: Huang, Xin, et al. Efficient estimation for large-scale linkage disequilibrium patterns of the human genome. ''Elife''. 2023 Dec 27; '''12''':
Potentially functional genetic variants in ferroptosis-related CREB3 and GALNT14 genes predict survival of hepatitis B virus-related hepatocellular carcinoma. Description: Zhan, Shicheng, et al. Potentially functional genetic variants in ferroptosis-related CREB3 and GALNT14 genes predict survival of hepatitis B virus-related hepatocellular carcinoma. ''Cancer Med''. 2023 Dec 27; '''13''' (1):
Whole-genome sequencing provides novel insights into the evolutionary history and genetic adaptation of reindeer populations in northern Eurasia. Description: Pokharel, Kisun, et al. Whole-genome sequencing provides novel insights into the evolutionary history and genetic adaptation of reindeer populations in northern Eurasia. ''Sci Rep''. 2023 Dec 27; '''13''' (1):23019
A Functional Single-Nucleotide Polymorphism Upstream of the Collagen Type III Gene Is Associated with Catastrophic Fracture Risk in Thoroughbred Horses. Description: Palomino Lago, Esther, et al. A Functional Single-Nucleotide Polymorphism Upstream of the Collagen Type III Gene Is Associated with Catastrophic Fracture Risk in Thoroughbred Horses. ''Animals (Basel)''. 2023 Dec 28; '''14''' (1):
Analysis of the Genetic Diversity in Tea Plant Germplasm in Fujian Province Based on Restriction Site-Associated DNA Sequencing. Description: Jiang, Lele, et al. Analysis of the Genetic Diversity in Tea Plant Germplasm in Fujian Province Based on Restriction Site-Associated DNA Sequencing. ''Plants (Basel)''. 2023 Dec 28; '''13''' (1):
The accuracy of polygenic score models for anthropometric traits and Type II Diabetes in the Native Hawaiian Population. Description: Lo, Ying-Chu, et al. The accuracy of polygenic score models for anthropometric traits and Type II Diabetes in the Native Hawaiian Population. ''medRxiv''. 2023 Dec 28;
Genetic Association and Differential RNA Expression of Histone (De)Acetylation-Related Genes in Pemphigus Foliaceus-A Possible Epigenetic Effect in the Autoimmune Response. Description: Sulzbach Denardin, Maiara, et al. Genetic Association and Differential RNA Expression of Histone (De)Acetylation-Related Genes in Pemphigus Foliaceus-A Possible Epigenetic Effect in the Autoimmune Response. ''Life (Basel)''. 2023 Dec 29; '''14''' (1):
100 ancient genomes show repeated population turnovers in Neolithic Denmark. Description: Allentoft, Morten E, et al. 100 ancient genomes show repeated population turnovers in Neolithic Denmark. ''Nature''. 2024 Jan; '''625''' (7994):329-337
Accuracy of genotype imputation of a low-density SNP array for the Amazon fish Colossoma macropomum. Description: Agudelo, John F G, et al. Accuracy of genotype imputation of a low-density SNP array for the Amazon fish Colossoma macropomum. ''Genet Mol Biol''. 2024; '''47''' (3):e20230364
Accurate identification of Helicoverpa armigera-Helicoverpa zea hybrids using genome admixture analysis: implications for genomic surveillance. Description: Trujillo, Dario, et al. Accurate identification of Helicoverpa armigera-Helicoverpa zea hybrids using genome admixture analysis: implications for genomic surveillance. ''Front Insect Sci''. 2024; '''4''': 1339143
A compendium of genetic regulatory effects across pig tissues. Description: Teng, Jinyan, et al. A compendium of genetic regulatory effects across pig tissues. ''Nat Genet''. 2024 Jan; '''56''' (1):112-123
A Genome-Wide Association Study of Serum Metabolite Profiles in Septic Shock Patients. Description: Daubney, Emily R, et al. A Genome-Wide Association Study of Serum Metabolite Profiles in Septic Shock Patients. ''Crit Care Explor''. 2024 Jan; '''6''' (1):e1030
A genome-wide cross-trait analysis identifies shared loci and causal relationships of obesity and lipidemic traits with psoriasis. Description: Wu, Yuan, et al. A genome-wide cross-trait analysis identifies shared loci and causal relationships of obesity and lipidemic traits with psoriasis. ''Front Immunol''. 2024; '''15''': 1328297
Altered levels of IFN-gamma, IL-4, and IL-5 depend on the TLR4 rs4986790 genotype in COPD smokers but not those exposed to biomass-burning smoke. Description: Gutierrez-Romero, Karla Jazmin, et al. Altered levels of IFN-gamma, IL-4, and IL-5 depend on the TLR4 rs4986790 genotype in COPD smokers but not those exposed to biomass-burning smoke. ''Front Immunol''. 2024; '''15''': 1411408
Alzheimer's disease genetic risk and changes in brain atrophy and white matter hyperintensities in cognitively unimpaired adults. Description: Soldan, Anja, et al. Alzheimer's disease genetic risk and changes in brain atrophy and white matter hyperintensities in cognitively unimpaired adults. ''Brain Commun''. 2024; '''6''' (5):fcae276
Analysis of genome-wide association studies of low-temperature germination in Xian and Geng rice. Description: Li, Kang, et al. Analysis of genome-wide association studies of low-temperature germination in Xian and Geng rice. ''Front Plant Sci''. 2024; '''15''': 1404879
Anthocyanin gene enrichment in the distal region of cotton chromosome A07: mechanisms of reproductive organ coloration. Description: Zheng, Liuchang, et al. Anthocyanin gene enrichment in the distal region of cotton chromosome A07: mechanisms of reproductive organ coloration. ''Front Plant Sci''. 2024; '''15''': 1381071
A polygenic risk score for the QT interval is an independent predictor of drug-induced QT prolongation. Description: Simon, Steven T, et al. A polygenic risk score for the QT interval is an independent predictor of drug-induced QT prolongation. ''PLoS One''. 2024; '''19''' (6):e0303261
Assessment of genetic diversity and population structure of U.S. Polypay sheep from breed origins to future genomic selection. Description: Wilson, Carrie S, et al. Assessment of genetic diversity and population structure of U.S. Polypay sheep from breed origins to future genomic selection. ''Front Genet''. 2024; '''15''': 1436990
Assessment tools for cognitive performance in Parkinson's disease and its genetic contributors. Description: Cao, Ling-Xiao, et al. Assessment tools for cognitive performance in Parkinson's disease and its genetic contributors. ''Front Neurol''. 2024; '''15''': 1413187
Association of birth weight, childhood obesity, and age at menarche with the risk of ovarian dysfunction: A mendelian randomization study. Description: Dang, Chunxiao, et al. Association of birth weight, childhood obesity, and age at menarche with the risk of ovarian dysfunction: A mendelian randomization study. ''PLoS One''. 2024; '''19''' (7):e0306365
Association of Blood MicroRNA Expression and Polymorphisms with Cognitive and Biomarker Changes in Older Adults. Description: Sadlon, A, et al. Association of Blood MicroRNA Expression and Polymorphisms with Cognitive and Biomarker Changes in Older Adults. ''J Prev Alzheimers Dis''. 2024; '''11''' (1):230-240
Association of Sleep Pattern and Genetic Susceptibility with Obstructive Sleep Apnea: A Prospective Analysis of the UK Biobank. Description: Zhou, Rong, et al. Association of Sleep Pattern and Genetic Susceptibility with Obstructive Sleep Apnea: A Prospective Analysis of the UK Biobank. ''Nat Sci Sleep''. 2024; '''16''': 503-515
Associations of genetic variations in the M3 receptor with salt sensitivity, longitudinal changes in blood pressure and the incidence of hypertension in Chinese adults. Description: Zhang, Xi, et al. Associations of genetic variations in the M3 receptor with salt sensitivity, longitudinal changes in blood pressure and the incidence of hypertension in Chinese adults. ''J Clin Hypertens (Greenwich)''. 2024 Jan; '''26''' (1):36-46
Associations of prior pulmonary tuberculosis with the incident COPD: a prospective cohort study. Description: Zeng, Zhilin, et al. Associations of prior pulmonary tuberculosis with the incident COPD: a prospective cohort study. ''Ther Adv Respir Dis''. 2024 Jan-Dec; '''18''': 17534666241239455
Association study of human leukocyte antigen variants and idiopathic pulmonary fibrosis. Description: Guillen-Guio, Beatriz, et al. Association study of human leukocyte antigen variants and idiopathic pulmonary fibrosis. ''ERJ Open Res''. 2024 Jan; '''10''' (1):
Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population. Description: Li, Yang, et al. Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population. ''Front Genet''. 2024; '''15''': 1438375
ATF3 coordinates the survival and proliferation of cardiac macrophages and protects against ischemia-reperfusion injury. Description: Shao, Yihui, et al. ATF3 coordinates the survival and proliferation of cardiac macrophages and protects against ischemia-reperfusion injury. ''Nat Cardiovasc Res''. 2024 Jan; '''3''' (1):28-45
Bioinformatic validation and machine learning-based exploration of purine metabolism-related gene signatures in the context of immunotherapeutic strategies for nonspecific orbital inflammation. Description: Wu, Zixuan, et al. Bioinformatic validation and machine learning-based exploration of purine metabolism-related gene signatures in the context of immunotherapeutic strategies for nonspecific orbital inflammation. ''Front Immunol''. 2024; '''15''': 1318316
BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. Description: Hoggart, Clive J, et al. BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. ''Nat Genet''. 2024 Jan; '''56''' (1):180-186
Building a community-driven bioinformatics platform to facilitate Cannabis sativa multi-omics research. Description: Mansueto, Locedie, et al. Building a community-driven bioinformatics platform to facilitate Cannabis sativa multi-omics research. ''GigaByte''. 2024; '''2024''': gigabyte137
Cathepsin-mediated regulation of alpha-synuclein in Parkinson's disease: a Mendelian randomization study. Description: Lin, Liyu, et al. Cathepsin-mediated regulation of alpha-synuclein in Parkinson's disease: a Mendelian randomization study. ''Front Aging Neurosci''. 2024; '''16''': 1394807
Causal association of blood cell traits with inflammatory bowel diseases: a Mendelian randomization study. Description: Zhang, Fangyuan, et al. Causal association of blood cell traits with inflammatory bowel diseases: a Mendelian randomization study. ''Front Nutr''. 2024; '''11''': 1256832
Causal associations of immune cell phenotypes with migraine: A mendelian randomization study. Description: Chai, Weifang, et al. Causal associations of immune cell phenotypes with migraine: A mendelian randomization study. ''Mol Pain''. 2024 Jan-Dec; '''20''': 17448069241274679
Causal link between hypothyroidism and gastric cancer risk: insights gained through multivariable Mendelian randomization and mediation analysis. Description: Zhang, Tianyue, et al. Causal link between hypothyroidism and gastric cancer risk: insights gained through multivariable Mendelian randomization and mediation analysis. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1388608
Causal relationship between immunophenotypes and mitral valve prolapse: a bidirectional Mendelian randomization study. Description: Wang, Yue, et al. Causal relationship between immunophenotypes and mitral valve prolapse: a bidirectional Mendelian randomization study. ''Front Cardiovasc Med''. 2024; '''11''': 1404284
Causal role of immune cells in uveitis: Mendelian randomization study. Description: Wu, Jiahui, et al. Causal role of immune cells in uveitis: Mendelian randomization study. ''Front Immunol''. 2024; '''15''': 1402074
Characteristics of immune cells and causal relationship with chondromalacia: A two-sample, bidirectional mendelian randomization study. Description: Chai, Weiwei, et al. Characteristics of immune cells and causal relationship with chondromalacia: A two-sample, bidirectional mendelian randomization study. ''Mol Pain''. 2024 Jan-Dec; '''20''': 17448069241289962
Clinical application of sparse canonical correlation analysis to detect genetic associations with cortical thickness in Alzheimer's disease. Description: Kim, Bo-Hyun, et al. Clinical application of sparse canonical correlation analysis to detect genetic associations with cortical thickness in Alzheimer's disease. ''Front Neurosci''. 2024; '''18''': 1428900
Comparison of ddRADseq and EUChip60K SNP genotyping systems for population genetics and genomic selection in Eucalyptus dunnii (Maiden). Description: Aguirre, Natalia Cristina, et al. Comparison of ddRADseq and EUChip60K SNP genotyping systems for population genetics and genomic selection in Eucalyptus dunnii (Maiden). ''Front Genet''. 2024; '''15''': 1361418
Complex genetic architecture of the chicken Growth1 QTL region. Description: Ou, Jen-Hsiang, et al. Complex genetic architecture of the chicken Growth1 QTL region. ''PLoS One''. 2024; '''19''' (5):e0295109
Comprehensive genetic diversity and genome-wide association studies revealed the genetic basis of avocado fruit quality traits. Description: Li, Jin, et al. Comprehensive genetic diversity and genome-wide association studies revealed the genetic basis of avocado fruit quality traits. ''Front Plant Sci''. 2024; '''15''': 1433436
Comprehensive Sex-Stratified Genetic Analysis of 28 Blood Biomarkers and Depression Reveals a Significant Association between Depression and Low Levels of Total Protein in Females. Description: Kiewa, Jacqueline, et al. Comprehensive Sex-Stratified Genetic Analysis of 28 Blood Biomarkers and Depression Reveals a Significant Association between Depression and Low Levels of Total Protein in Females. ''Complex Psychiatry''. 2024 Jan-Dec; '''10''' (1-4):19-34
Comprehensive whole-genome resequencing unveils genetic diversity and selective signatures of the Xiangdong black goat. Description: Liu, Ziao, et al. Comprehensive whole-genome resequencing unveils genetic diversity and selective signatures of the Xiangdong black goat. ''Front Genet''. 2024; '''15''': 1326828
Consumption of sugary beverages, genetic predisposition and the risk of depression: a prospective cohort study. Description: Chen, Yanchun, et al. Consumption of sugary beverages, genetic predisposition and the risk of depression: a prospective cohort study. ''Gen Psychiatr''. 2024; '''37''' (4):e101446
Converging forms: an examination of sub-Arctic, circumarctic, and Central Asian Ranunculus auricomus agg. populations. Description: Bradican, John Paul, et al. Converging forms: an examination of sub-Arctic, circumarctic, and Central Asian Ranunculus auricomus agg. populations. ''Front Plant Sci''. 2024; '''15''': 1415059
Copy number variants selected during pig domestication inferred from whole genome resequencing. Description: Zhang, Wei, et al. Copy number variants selected during pig domestication inferred from whole genome resequencing. ''Front Vet Sci''. 2024; '''11''': 1364267
Deciphering the genetic structure of the Quebec founder population using genealogies. Description: Gagnon, Laurence, et al. Deciphering the genetic structure of the Quebec founder population using genealogies. ''Eur J Hum Genet''. 2024 Jan; '''32''' (1):91-97
De novo genome assembly and population genomics of a shrub tree Barthea barthei (Hance) krass provide insights into the adaptive color variations. Description: Huang, Weicheng, et al. De novo genome assembly and population genomics of a shrub tree Barthea barthei (Hance) krass provide insights into the adaptive color variations. ''Front Plant Sci''. 2024; '''15''': 1365686
Development and application of a 1K functional liquid chip for lactation performance in Bactrian camels. Description: Guo, Lili, et al. Development and application of a 1K functional liquid chip for lactation performance in Bactrian camels. ''Front Vet Sci''. 2024; '''11''': 1359923
Development of a 45K pepper GBTS liquid-phase gene chip and its application in genome-wide association studies. Description: Li, Zixiong, et al. Development of a 45K pepper GBTS liquid-phase gene chip and its application in genome-wide association studies. ''Front Plant Sci''. 2024; '''15''': 1405190
Development of a high-density sub-species-specific targeted SNP assay for Rocky Mountain bighorn sheep (Ovis canadensis canadensis). Description: Deakin, Samuel, et al. Development of a high-density sub-species-specific targeted SNP assay for Rocky Mountain bighorn sheep (Ovis canadensis canadensis). ''PeerJ''. 2024; '''12''': e16946
Dissecting the association between gut microbiota and hypertrophic scarring: a bidirectional Mendelian randomization study. Description: Xue, Kaikai, et al. Dissecting the association between gut microbiota and hypertrophic scarring: a bidirectional Mendelian randomization study. ''Front Microbiol''. 2024; '''15''': 1345717
Efficacy of federated learning on genomic data: a study on the UK Biobank and the 1000 Genomes Project. Description: Kolobkov, Dmitry, et al. Efficacy of federated learning on genomic data: a study on the UK Biobank and the 1000 Genomes Project. ''Front Big Data''. 2024; '''7''': 1266031
Elevated genetic risk for multiple sclerosis emerged in steppe pastoralist populations. Description: Barrie, William, et al. Elevated genetic risk for multiple sclerosis emerged in steppe pastoralist populations. ''Nature''. 2024 Jan; '''625''' (7994):321-328
Epigenetic Age Acceleration and Chronological Age: Associations With Cognitive Performance in Daily Life. Description: Zavala, Daisy V, et al. Epigenetic Age Acceleration and Chronological Age: Associations With Cognitive Performance in Daily Life. ''J Gerontol A Biol Sci Med Sci''. 2024 Jan 1; '''79''' (1):
Epigenetic associations of GPNMB rs199347 variant with alcohol consumption in Parkinson's disease. Description: Chen, Yen-Chung, et al. Epigenetic associations of GPNMB rs199347 variant with alcohol consumption in Parkinson's disease. ''Front Psychiatry''. 2024; '''15''': 1377403
Evaluating the associations between intelligence quotient and multi-tissue proteome from the brain, CSF and plasma. Description: Shi, Sirong, et al. Evaluating the associations between intelligence quotient and multi-tissue proteome from the brain, CSF and plasma. ''Brain Commun''. 2024; '''6''' (4):fcae207
Evaluating the link between immune characteristics and attention deficit hyperactivity disorder through a bi-directional Mendelian randomization study. Description: Jue, Hu, et al. Evaluating the link between immune characteristics and attention deficit hyperactivity disorder through a bi-directional Mendelian randomization study. ''Front Immunol''. 2024; '''15''': 1367418
Evaluation of stripe rust resistance and genome-wide association study in wheat varieties derived from the International Center for Agricultural Research in the Dry Areas. Description: Gao, Zhonghao, et al. Evaluation of stripe rust resistance and genome-wide association study in wheat varieties derived from the International Center for Agricultural Research in the Dry Areas. ''Front Plant Sci''. 2024; '''15''': 1377253
Evidence of survival bias in the association between APOE-capital JE, Ukrainian4 and age at ischemic stroke onset. Description: von Berg, Joanna, et al. Evidence of survival bias in the association between APOE-capital JE, Ukrainian4 and age at ischemic stroke onset. ''Front Genet''. 2024; '''15''': 1392061
Explainable artificial intelligence for genotype-to-phenotype prediction in plant breeding: a case study with a dataset from an almond germplasm collection. Description: Novielli, Pierfrancesco, et al. Explainable artificial intelligence for genotype-to-phenotype prediction in plant breeding: a case study with a dataset from an almond germplasm collection. ''Front Plant Sci''. 2024; '''15''': 1434229
Exploratory focused pharmacogenetic testing reveals novel markers associated with risperidone pharmacokinetics in Saudi children with autism. Description: Shilbayeh, Sireen Abdul Rahim, et al. Exploratory focused pharmacogenetic testing reveals novel markers associated with risperidone pharmacokinetics in Saudi children with autism. ''Front Pharmacol''. 2024; '''15''': 1356763
Exploring genetic diversity and population structure in Cinnamomum cassia (L.) J.Presl germplasm in China through phenotypic, chemical component, and molecular marker analyses. Description: Han, Panpan, et al. Exploring genetic diversity and population structure in Cinnamomum cassia (L.) J.Presl germplasm in China through phenotypic, chemical component, and molecular marker analyses. ''Front Plant Sci''. 2024; '''15''': 1374648
Exploring the causal relationship between immune cell and all-cause heart failure: a Mendelian randomization study. Description: Li, Jixu, et al. Exploring the causal relationship between immune cell and all-cause heart failure: a Mendelian randomization study. ''Front Cardiovasc Med''. 2024; '''11''': 1363200
Exploring the genetic causal relationship between physical activity and migraine in European population based on Mendelian randomization analysis. Description: Exploring the genetic causal relationship between physical activity and migraine in European population based on Mendelian randomization analysis. ''''. 2024; '''15''': 1434433
Exploring the genetic diversity and population structure of aerial yams (Dioscorea bulbifera L.) DArT-seq and agronomic traits. Description: Ekaette, Eunice, et al. Exploring the genetic diversity and population structure of aerial yams (Dioscorea bulbifera L.) DArT-seq and agronomic traits. ''PLoS One''. 2024; '''19''' (8):e0306631
Exploring the impact of computer game playing on cognitive function, Alzheimer's disease risk, and brain-derived neurotrophic factor levels: Basic evidence from Mendelian randomization. Description: Wu, Jinlong, et al. Exploring the impact of computer game playing on cognitive function, Alzheimer's disease risk, and brain-derived neurotrophic factor levels: Basic evidence from Mendelian randomization. ''Digit Health''. 2024 Jan-Dec; '''10''': 20552076241256519
Exploring the Shared Genetic Architecture Between Obstructive Sleep Apnea and Body Mass Index. Description: Zhou, Peng, et al. Exploring the Shared Genetic Architecture Between Obstructive Sleep Apnea and Body Mass Index. ''Nat Sci Sleep''. 2024; '''16''': 711-723
Extensive transcriptome data providing great efficacy in genetic research and adaptive gene discovery: a case study of Elymus sibiricus L. (Poaceae, Triticeae). Description: Xiong, Yanli, et al. Extensive transcriptome data providing great efficacy in genetic research and adaptive gene discovery: a case study of Elymus sibiricus L. (Poaceae, Triticeae). ''Front Plant Sci''. 2024; '''15''': 1457980
First insight of the genome-wide association study and genomic prediction into enteritis disease (Vibrio harveyi) resistance trait in the lined seahorse (Hippocampus erectus). Description: Li, Siping, et al. First insight of the genome-wide association study and genomic prediction into enteritis disease (Vibrio harveyi) resistance trait in the lined seahorse (Hippocampus erectus). ''Front Immunol''. 2024; '''15''': 1474746
Frailty index and risk of delirium in hospitalized patients: a two-sample Mendelian randomization study. Description: Chen, Yu, et al. Frailty index and risk of delirium in hospitalized patients: a two-sample Mendelian randomization study. ''Front Med (Lausanne)''. 2024; '''11''': 1361437
Functional Annotation and Gene Set Analysis of Gastric Cancer Risk Loci in a Korean Population. Description: Pyun, Hyojin, et al. Functional Annotation and Gene Set Analysis of Gastric Cancer Risk Loci in a Korean Population. ''Cancer Res Treat''. 2024 Jan; '''56''' (1):191-198
GDF15 linked to maternal risk of nausea and vomiting during pregnancy. Description: Fejzo, M, et al. GDF15 linked to maternal risk of nausea and vomiting during pregnancy. ''Nature''. 2024 Jan; '''625''' (7996):760-767
Genetic ancestry is related to potential sources of breast cancer health disparities among Colombian women. Description: Rey-Vargas, Laura, et al. Genetic ancestry is related to potential sources of breast cancer health disparities among Colombian women. ''PLoS One''. 2024; '''19''' (6):e0306037
Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry. Description: Brandenburg, Jean-Tristan, et al. Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry. ''Front Genet''. 2024; '''15''': 1372042
Genetic association of the gut microbiota with epigenetic clocks mediated by inflammatory cytokines: a Mendelian randomization analysis. Description: Tian, Siyu, et al. Genetic association of the gut microbiota with epigenetic clocks mediated by inflammatory cytokines: a Mendelian randomization analysis. ''Front Immunol''. 2024; '''15''': 1339722
Genetic basis of local adaptation in the cold-tolerant mangrove Kandelia obovata. Description: Zou, Chuangchao, et al. Genetic basis of local adaptation in the cold-tolerant mangrove Kandelia obovata. ''Front Plant Sci''. 2024; '''15''': 1385210
Genetic characterization of cashmere goat (Capra hircus) populations in Mongolia. Description: Baldan, Sergelen, et al. Genetic characterization of cashmere goat (Capra hircus) populations in Mongolia. ''Front Genet''. 2024; '''15''': 1421529
Genetic dissection of stem and leaf rachis prickles in diploid rose using a pedigree-based QTL analysis. Description: Rawandoozi, Zena J, et al. Genetic dissection of stem and leaf rachis prickles in diploid rose using a pedigree-based QTL analysis. ''Front Plant Sci''. 2024; '''15''': 1356750
Genetic diversity among maize (Zea mays L.) inbred lines adapted to Japanese climates. Description: Mitsuhashi, Shohei. Genetic diversity among maize (Zea mays L.) inbred lines adapted to Japanese climates. ''PLoS One''. 2024; '''19''' (1):e0297549
Genetic diversity of a Silybum marianum (L.) Gaertn. germplasm collection revealed by DNA Diversity Array Technology (DArTseq). Description: Puglisi, Damiano, et al. Genetic diversity of a Silybum marianum (L.) Gaertn. germplasm collection revealed by DNA Diversity Array Technology (DArTseq). ''PLoS One''. 2024; '''19''' (8):e0308368
Genetic drift, historic migration, and limited gene flow contributing to the subpopulation divergence in wild sea beet (Beta vulgaris ssp. maritima (L.) Arcang). Description: Tehseen, Muhammad Massub, et al. Genetic drift, historic migration, and limited gene flow contributing to the subpopulation divergence in wild sea beet (Beta vulgaris ssp. maritima (L.) Arcang). ''PLoS One''. 2024; '''19''' (9):e0308626
Genetic drivers of human plasma metabolites that determine mortality in heart failure patients with reduced ejection fraction. Description: Revathi Venkateswaran, Vandana, et al. Genetic drivers of human plasma metabolites that determine mortality in heart failure patients with reduced ejection fraction. ''Front Cardiovasc Med''. 2024; '''11''': 1409340
Genetic insights into repurposing statins for hyperthyroidism prevention: a drug-target Mendelian randomization study. Description: Huang, Anqi, et al. Genetic insights into repurposing statins for hyperthyroidism prevention: a drug-target Mendelian randomization study. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1331031
Genetic loci associated with tissue-specific resistance to powdery mildew in octoploid strawberry (Fragaria x ananassa). Description: Lynn, Samantha C, et al. Genetic loci associated with tissue-specific resistance to powdery mildew in octoploid strawberry (Fragaria x ananassa). ''Front Plant Sci''. 2024; '''15''': 1376061
Genetic risk for hospitalization of African American patients with severe mental illness reveals HLA loci. Description: Lori, Adriana, et al. Genetic risk for hospitalization of African American patients with severe mental illness reveals HLA loci. ''Front Psychiatry''. 2024; '''15''': 1140376
Genetic signatures of AKT1 variants associated with worse COVID-19 outcomes - a multicentric observational study. Description: de Almeida, Ingrid Marins, et al. Genetic signatures of AKT1 variants associated with worse COVID-19 outcomes - a multicentric observational study. ''Front Immunol''. 2024; '''15''': 1422349
Genetic structure and selective sweeps in Kirghiz sheep using SNP50K bead chip. Description: Li, Xiaopeng, et al. Genetic structure and selective sweeps in Kirghiz sheep using SNP50K bead chip. ''Front Genet''. 2024; '''15''': 1432105
Genetic support of causal association between lipid and glucose metabolism and stress urinary incontinence in women: a bidirectional Mendelian randomization and multivariable-adjusted study. Description: Xiang, Nanyan, et al. Genetic support of causal association between lipid and glucose metabolism and stress urinary incontinence in women: a bidirectional Mendelian randomization and multivariable-adjusted study. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1394252
Genetic variants in hypoxia-inducible factor pathway are associated with colorectal cancer risk and immune infiltration. Description: Guo, Mengfan, et al. Genetic variants in hypoxia-inducible factor pathway are associated with colorectal cancer risk and immune infiltration. ''J Cell Mol Med''. 2024 Jan; '''28''' (1):e18019
Genetic variants in primary cilia-related genes associated with the prognosis of first-line chemotherapy in colorectal cancer. Description: Qiu, Lei, et al. Genetic variants in primary cilia-related genes associated with the prognosis of first-line chemotherapy in colorectal cancer. ''Cancer Med''. 2024 Jan; '''13''' (2):e6996
Genome-wide Analysis Identified SEMA4D, Novel Candidate Gene for Temperature Sensitivity in Patients With Non-Small Cell Lung Cancer. Description: Park, Jung-Hyang, et al. Genome-wide Analysis Identified SEMA4D, Novel Candidate Gene for Temperature Sensitivity in Patients With Non-Small Cell Lung Cancer. ''Integr Cancer Ther''. 2024 Jan-Dec; '''23''': 15347354241233544
Genome-wide analysis of population structure, effective population size and inbreeding in Iranian and exotic horses. Description: Bazvand, B, et al. Genome-wide analysis of population structure, effective population size and inbreeding in Iranian and exotic horses. ''PLoS One''. 2024; '''19''' (3):e0299109
Genome-wide and pan-genomic analysis reveals rich variants of NBS-LRR genes in a newly developed wild rice line from Oryza alta Swallen. Description: Shivute, Fimanekeni Ndaitavela, et al. Genome-wide and pan-genomic analysis reveals rich variants of NBS-LRR genes in a newly developed wild rice line from Oryza alta Swallen. ''Front Plant Sci''. 2024; '''15''': 1345708
Genome-wide association analysis and admixture mapping in a Puerto Rican cohort supports an Alzheimer disease risk locus on chromosome 12. Description: Akgun, Bilcag, et al. Genome-wide association analysis and admixture mapping in a Puerto Rican cohort supports an Alzheimer disease risk locus on chromosome 12. ''Front Aging Neurosci''. 2024; '''16''': 1459796
Genome-wide association analysis identifies a candidate gene controlling seed size and yield in Xanthoceras sorbifolium Bunge. Description: Zhao, Ziquan, et al. Genome-wide association analysis identifies a candidate gene controlling seed size and yield in Xanthoceras sorbifolium Bunge. ''Hortic Res''. 2024 Jan; '''11''' (1):uhad243
Genome-wide association analysis of fleece traits in Northwest Xizang white cashmere goat. Description: Lu, Xiaotian, et al. Genome-wide association analysis of fleece traits in Northwest Xizang white cashmere goat. ''Front Vet Sci''. 2024; '''11''': 1409084
Genome-wide association analysis reveal candidate genes and haplotypes related to root weight in cucumber (Cucumis sativus L.). Description: Dai, Zhuonan, et al. Genome-wide association analysis reveal candidate genes and haplotypes related to root weight in cucumber (Cucumis sativus L.). ''Front Plant Sci''. 2024; '''15''': 1417314
Genome-wide association studies reveal novel QTLs for agronomic traits in soybean. Description: Han, Dongwei, et al. Genome-wide association studies reveal novel QTLs for agronomic traits in soybean. ''Front Plant Sci''. 2024; '''15''': 1375646
Genome-wide association study and genomic prediction for resistance to brown planthopper in rice. Description: Zhou, Cong, et al. Genome-wide association study and genomic prediction for resistance to brown planthopper in rice. ''Front Plant Sci''. 2024; '''15''': 1373081
Genome-wide association study and polygenic score assessment of insulin resistance. Description: Aliyu, Usama, et al. Genome-wide association study and polygenic score assessment of insulin resistance. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1384103
Genome-wide association study for growth traits with 1066 individuals in largemouth bass (Micropterus salmoides). Description: Han, Wei, et al. Genome-wide association study for growth traits with 1066 individuals in largemouth bass (Micropterus salmoides). ''Front Mol Biosci''. 2024; '''11''': 1443522
Genome-Wide Association Study for Test-Day Milk Yield, Proteins, and Composition Traits of Crossbred Dairy Cattle in Ethiopia. Description: Rekik, B, et al. Genome-Wide Association Study for Test-Day Milk Yield, Proteins, and Composition Traits of Crossbred Dairy Cattle in Ethiopia. ''Int J Genomics''. 2024; '''2024''': 1472779
Genome-wide association study for yield-related traits in faba bean (Vicia faba L.). Description: Gutierrez, Natalia, et al. Genome-wide association study for yield-related traits in faba bean (Vicia faba L.). ''Front Plant Sci''. 2024; '''15''': 1328690
Genome-wide association study of preserved ratio impaired spirometry (PRISm). Description: Higbee, Daniel H, et al. Genome-wide association study of preserved ratio impaired spirometry (PRISm). ''Eur Respir J''. 2024 Jan; '''63''' (1):
Genome-wide data reveal bi-direction and asymmetrical hybridization origin of a fern species Microlepia matthewii. Description: Luo, Jun-Jie, et al. Genome-wide data reveal bi-direction and asymmetrical hybridization origin of a fern species Microlepia matthewii. ''Front Plant Sci''. 2024; '''15''': 1392990
Genome-wide meta-analysis of short-tandem repeats for Parkinson's disease risk using genotype imputation. Description: Ohlei, Olena, et al. Genome-wide meta-analysis of short-tandem repeats for Parkinson's disease risk using genotype imputation. ''Brain Commun''. 2024; '''6''' (3):fcae146
Genomic analyses of agronomic traits in tea plants and related Camellia species. Description: Duan, Shengchang, et al. Genomic analyses of agronomic traits in tea plants and related Camellia species. ''Front Plant Sci''. 2024; '''15''': 1449006
Genomic insights into adaptation and inbreeding among Sub-Saharan African cattle from pastoral and agropastoral systems. Description: Akinsola, Oludayo M, et al. Genomic insights into adaptation and inbreeding among Sub-Saharan African cattle from pastoral and agropastoral systems. ''Front Genet''. 2024; '''15''': 1430291
Genomic signals of local adaptation across climatically heterogenous habitats in an invasive tropical fruit fly (Bactrocera tryoni). Description: Parvizi, Elahe, et al. Genomic signals of local adaptation across climatically heterogenous habitats in an invasive tropical fruit fly (Bactrocera tryoni). ''Heredity (Edinb)''. 2024 Jan; '''132''' (1):18-29
Genomic signatures of positive selection in Awarik dromedary camels from southwestern of Saudi Arabia. Description: Almathen, Faisal. Genomic signatures of positive selection in Awarik dromedary camels from southwestern of Saudi Arabia. ''Front Vet Sci''. 2024; '''11''': 1443748
Genotype-associated heritable rumen bacteria can be a stable microbiota passed to the offspring. Description: Zang, Xinwei, et al. Genotype-associated heritable rumen bacteria can be a stable microbiota passed to the offspring. ''ISME Commun''. 2024 Jan; '''4''' (1):ycad020
Genotype-based "virtual" metabolomics in a clinical biobank identifies novel metabolite-disease associations. Description: Bagheri, Minoo, et al. Genotype-based "virtual" metabolomics in a clinical biobank identifies novel metabolite-disease associations. ''Front Genet''. 2024; '''15''': 1392622
Genotypic and phenotypic characterisation of three local chicken ecotypes of Ghana based on principal component analysis and body measurements. Description: Botchway, Princess K, et al. Genotypic and phenotypic characterisation of three local chicken ecotypes of Ghana based on principal component analysis and body measurements. ''PLoS One''. 2024; '''19''' (8):e0308420
Global and local ancestry estimation in a captive baboon colony. Description: Kendall, Christopher, et al. Global and local ancestry estimation in a captive baboon colony. ''PLoS One''. 2024; '''19''' (7):e0305157
Gut microbial diversity moderates polygenic risk of schizophrenia. Description: Zhang, Liyuan, et al. Gut microbial diversity moderates polygenic risk of schizophrenia. ''Front Psychiatry''. 2024; '''15''': 1275719
Gut microbiota and pancreatic cancer risk, and the mediating role of immune cells and inflammatory cytokines: a Mendelian randomization study. Description: Chen, Zhiting, et al. Gut microbiota and pancreatic cancer risk, and the mediating role of immune cells and inflammatory cytokines: a Mendelian randomization study. ''Front Immunol''. 2024; '''15''': 1408770
Gut Subdoligranulum variabile ameliorates rheumatoid arthritis by promoting TSG-6 synthesis from joint cells. Description: Li, Hongfeng, et al. Gut Subdoligranulum variabile ameliorates rheumatoid arthritis by promoting TSG-6 synthesis from joint cells. ''Front Immunol''. 2024; '''15''': 1418717
GWAS and polygenic risk score of severe COVID-19 in Eastern Europe. Description: Kovalenko, Elena, et al. GWAS and polygenic risk score of severe COVID-19 in Eastern Europe. ''Front Med (Lausanne)''. 2024; '''11''': 1409714
GWAS of resistance to three bacterial diseases in the Andean common bean diversity panel. Description: Soler-Garzon, Alvaro, et al. GWAS of resistance to three bacterial diseases in the Andean common bean diversity panel. ''Front Plant Sci''. 2024; '''15''': 1469381
Historical spread routes of wild walnuts in Central Asia shaped by man-made and nature. Description: Li, Xuerong, et al. Historical spread routes of wild walnuts in Central Asia shaped by man-made and nature. ''Front Plant Sci''. 2024; '''15''': 1394409
HLA and KIR genetic association and NK cells in anti-NMDAR encephalitis. Description: Peris Sempere, Vicente, et al. HLA and KIR genetic association and NK cells in anti-NMDAR encephalitis. ''Front Immunol''. 2024; '''15''': 1423149
Host genetic regulation of human gut microbial structural variation. Description: Zhernakova, Daria V, et al. Host genetic regulation of human gut microbial structural variation. ''Nature''. 2024 Jan; '''625''' (7996):813-821
Host response to influenza infections in human blood: association of influenza severity with host genetics and transcriptomic response. Description: Schughart, Klaus, et al. Host response to influenza infections in human blood: association of influenza severity with host genetics and transcriptomic response. ''Front Immunol''. 2024; '''15''': 1385362
Human extracellular matrix (ECM)-like collagen and its bioactivity. Description: Zhou, Hui, et al. Human extracellular matrix (ECM)-like collagen and its bioactivity. ''Regen Biomater''. 2024; '''11''': rbae008
Human visceral leishmaniasis and polymorphisms in interleukin-coding genes: a systematic review. Description: Vieira, Amanda Virginia Batista, et al. Human visceral leishmaniasis and polymorphisms in interleukin-coding genes: a systematic review. ''J Venom Anim Toxins Incl Trop Dis''. 2024; '''30''': e20240018
Hybrid de novo and haplotype-resolved genome assembly of Vechur cattle - elucidating genetic variation. Description: Muthusamy, Poorvishaa V, et al. Hybrid de novo and haplotype-resolved genome assembly of Vechur cattle - elucidating genetic variation. ''Front Genet''. 2024; '''15''': 1338224
IBD sharing patterns as intra-breed admixture indicators in small ruminants. Description: Blondeau Da Silva, Stephane, et al. IBD sharing patterns as intra-breed admixture indicators in small ruminants. ''Heredity (Edinb)''. 2024 Jan; '''132''' (1):30-42
Identification of eight genomic protective alleles for mitochondrial diabetes by Kinship-graph convolutional network. Description: Wang, Jiahao, et al. Identification of eight genomic protective alleles for mitochondrial diabetes by Kinship-graph convolutional network. ''J Diabetes Investig''. 2024 Jan; '''15''' (1):52-62
Identification of Heilongjiang crossbred beef cattle pedigrees and reveals functional genes related to economic traits based on whole-genome SNP data. Description: Li, Shuang, et al. Identification of Heilongjiang crossbred beef cattle pedigrees and reveals functional genes related to economic traits based on whole-genome SNP data. ''Front Genet''. 2024; '''15''': 1435793
Identification of positively selected genes in Mycobacterium tuberculosis from southern Xinjiang Uygur autonomous region of China. Description: Deng, Lele, et al. Identification of positively selected genes in Mycobacterium tuberculosis from southern Xinjiang Uygur autonomous region of China. ''Front Microbiol''. 2024; '''15''': 1290227
Identification of shared genetic risks underlying metabolic syndrome and its related traits in the Korean population. Description: Kim, Jun Young, et al. Identification of shared genetic risks underlying metabolic syndrome and its related traits in the Korean population. ''Front Genet''. 2024; '''15''': 1417262
Identifying therapeutic targets for breast cancer: insights from systematic Mendelian randomization analysis. Description: Yao, Tao, et al. Identifying therapeutic targets for breast cancer: insights from systematic Mendelian randomization analysis. ''Front Oncol''. 2024; '''14''': 1407795
Inflammatory factors and risk of lung adenocarcinoma: a Mendelian randomization study mediated by blood metabolites. Description: Ding, Zheng, et al. Inflammatory factors and risk of lung adenocarcinoma: a Mendelian randomization study mediated by blood metabolites. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1446863
Influence of TMX2-CTNND1 polymorphism on cortical thickness in schizophrenia patients and unaffected siblings: an exploratory study based on target region sequencing. Description: Tan, Wenjian, et al. Influence of TMX2-CTNND1 polymorphism on cortical thickness in schizophrenia patients and unaffected siblings: an exploratory study based on target region sequencing. ''Braz J Psychiatry''. 2024; '''46''': e20233322
Interactions between circulating inflammatory factors and autism spectrum disorder: a bidirectional Mendelian randomization study in European population. Description: Long, Junzi, et al. Interactions between circulating inflammatory factors and autism spectrum disorder: a bidirectional Mendelian randomization study in European population. ''Front Immunol''. 2024; '''15''': 1370276
Investigating causality and shared genetic architecture between body mass index and cognitive function: a genome-wide cross-trait analysis and bi-directional Mendelian randomization study. Description: Chen, Mingyi, et al. Investigating causality and shared genetic architecture between body mass index and cognitive function: a genome-wide cross-trait analysis and bi-directional Mendelian randomization study. ''Front Aging Neurosci''. 2024; '''16''': 1466799
Investigating the shared genetic architecture between frailty and insomnia. Description: Song, Zhiwei, et al. Investigating the shared genetic architecture between frailty and insomnia. ''Front Aging Neurosci''. 2024; '''16''': 1358996
Phylogenomics reveal Populusgonggaensis as a hybrid between P.lasiocarpa and P.cathayana (Salicaceae). Description: Du, Wenyan, et al. Phylogenomics reveal Populusgonggaensis as a hybrid between P.lasiocarpa and P.cathayana (Salicaceae). ''PhytoKeys''. 2024; '''237''': 161-177
Large-scale genomic and transcriptomic analyses elucidate the genetic basis of high meat yield in chickens. Description: Tan, Xiaodong, et al. Large-scale genomic and transcriptomic analyses elucidate the genetic basis of high meat yield in chickens. ''J Adv Res''. 2024 Jan; '''55''': 1-16
Large scale sequence-based screen for recessive variants allows for identification and monitoring of rare deleterious variants in pigs. Description: Boshove, Anne, et al. Large scale sequence-based screen for recessive variants allows for identification and monitoring of rare deleterious variants in pigs. ''PLoS Genet''. 2024 Jan; '''20''' (1):e1011034
Longitudinal method comparison: modeling polygenic risk for post-traumatic stress disorder over time in individuals of African and European ancestry. Description: Passero, Kristin, et al. Longitudinal method comparison: modeling polygenic risk for post-traumatic stress disorder over time in individuals of African and European ancestry. ''Front Genet''. 2024; '''15''': 1203577
Low but highly geographically structured genomic diversity of East Asian Eurasian otters and its conservation implications. Description: Li, Shou-Hsien, et al. Low but highly geographically structured genomic diversity of East Asian Eurasian otters and its conservation implications. ''Evol Appl''. 2024 Jan; '''17''' (1):e13630
Mendelian randomization analysis and validation supports MEGF9 and MLLT11 as potential targets for the treatment of varicocele and male infertility. Description: Cai, Bin, et al. Mendelian randomization analysis and validation supports MEGF9 and MLLT11 as potential targets for the treatment of varicocele and male infertility. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1416384
Mendelian Randomization and Transcriptomic Analysis Reveal the Protective Role of NKT Cells in Sepsis. Description: Liu, Qingxiang, et al. Mendelian Randomization and Transcriptomic Analysis Reveal the Protective Role of NKT Cells in Sepsis. ''J Inflamm Res''. 2024; '''17''': 3159-3171
Mendelian randomization based on immune cells in diabetic nephropathy. Description: Zhou, Ye, et al. Mendelian randomization based on immune cells in diabetic nephropathy. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1460652
Mendelian randomization study of whole blood viscosity and cardiovascular diseases. Description: Bhak, Youngjune, et al. Mendelian randomization study of whole blood viscosity and cardiovascular diseases. ''PLoS One''. 2024; '''19''' (4):e0294095
Metabolic and genetic risk factors associated with pre-diabetes and type 2 diabetes in Thai healthcare employees: A long-term study from the Siriraj Health (SIH) cohort study. Description: Mongkolsucharitkul, Pichanun, et al. Metabolic and genetic risk factors associated with pre-diabetes and type 2 diabetes in Thai healthcare employees: A long-term study from the Siriraj Health (SIH) cohort study. ''PLoS One''. 2024; '''19''' (6):e0303085
MicroRNA binding site variants-new potential markers of primary osteoporosis in men and women. Description: Yalaev, Bulat, et al. MicroRNA binding site variants-new potential markers of primary osteoporosis in men and women. ''Front Genet''. 2024; '''15''': 1470310
Mitochondrial related variants associated with cardiovascular traits. Description: Canadas-Garre, Marisa, et al. Mitochondrial related variants associated with cardiovascular traits. ''Front Physiol''. 2024; '''15''': 1395371
Molecular genetic identification of Wuzhishan ant chicken, a newly discovered resource in China. Description: Gu, Lihong, et al. Molecular genetic identification of Wuzhishan ant chicken, a newly discovered resource in China. ''Front Vet Sci''. 2024; '''11''': 1319854
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. Description: Kim, Jonggeol Jeffrey, et al. Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. ''Nat Genet''. 2024 Jan; '''56''' (1):27-36
Multi-omic prediction of incident type 2 diabetes. Description: Carrasco-Zanini, Julia, et al. Multi-omic prediction of incident type 2 diabetes. ''Diabetologia''. 2024 Jan; '''67''' (1):102-112
Multiple Allergic Rhinitis Single Nucleotide Polymorphism Variants are Associated with Sleep-Breathing Parameters in Men with Obstructive Sleep Apnea: A Large-Scale Study. Description: Zeng, Qiying, et al. Multiple Allergic Rhinitis Single Nucleotide Polymorphism Variants are Associated with Sleep-Breathing Parameters in Men with Obstructive Sleep Apnea: A Large-Scale Study. ''Nat Sci Sleep''. 2024; '''16''': 989-1000
Neural EGFL like 1 as a novel gene for Trabecular Bone Score in older adults: The Bushehr Elderly Health (BEH) program. Description: Bidkhori, Mohammad, et al. Neural EGFL like 1 as a novel gene for Trabecular Bone Score in older adults: The Bushehr Elderly Health (BEH) program. ''PLoS One''. 2024; '''19''' (9):e0309401
New genetic biomarkers predicting 5-aminosalicylate-induced adverse events in patients with inflammatory bowel diseases. Description: Park, Jihye, et al. New genetic biomarkers predicting 5-aminosalicylate-induced adverse events in patients with inflammatory bowel diseases. ''Therap Adv Gastroenterol''. 2024; '''17''': 17562848241227029
Non-causal relationship of polycystic ovarian syndrome with homocysteine and B vitamins: evidence from a two-sample Mendelian randomization. Description: Su, Nianjun, et al. Non-causal relationship of polycystic ovarian syndrome with homocysteine and B vitamins: evidence from a two-sample Mendelian randomization. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1393847
Persistent thinness and anorexia nervosa differ on a genomic level. Description: Hubel, Christopher, et al. Persistent thinness and anorexia nervosa differ on a genomic level. ''Eur J Hum Genet''. 2024 Jan; '''32''' (1):117-124
Perturbational phenotyping of human blood cells reveals genetically determined latent traits associated with subsets of common diseases. Description: Homilius, Max, et al. Perturbational phenotyping of human blood cells reveals genetically determined latent traits associated with subsets of common diseases. ''Nat Genet''. 2024 Jan; '''56''' (1):37-50
Pharmacogenetic landscape of pain management variants among Mediterranean populations. Description: Jmel, Haifa, et al. Pharmacogenetic landscape of pain management variants among Mediterranean populations. ''Front Pharmacol''. 2024; '''15''': 1380613
PIK3CA regulates development of diabetes retinopathy through the PI3K/Akt/mTOR pathway. Description: Guan, Ruijuan, et al. PIK3CA regulates development of diabetes retinopathy through the PI3K/Akt/mTOR pathway. ''PLoS One''. 2024; '''19''' (1):e0295813
Plasma pTau181 and pTau217 predict asymptomatic amyloid accumulation equally well as amyloid PET. Description: De Meyer, Steffi, et al. Plasma pTau181 and pTau217 predict asymptomatic amyloid accumulation equally well as amyloid PET. ''Brain Commun''. 2024; '''6''' (4):fcae162
Polioencephalopathy in Eurasier dogs. Description: Rawson, Faye, et al. Polioencephalopathy in Eurasier dogs. ''J Vet Intern Med''. 2024 Jan-Feb; '''38''' (1):277-284
Polygenic risk associated with Alzheimer's disease and other traits influences genes involved in T cell signaling and activation. Description: Dressman, Dallin, et al. Polygenic risk associated with Alzheimer's disease and other traits influences genes involved in T cell signaling and activation. ''Front Immunol''. 2024; '''15''': 1337831
Polygenic risk score for acute rejection based on donor-recipient non-HLA genotype mismatch. Description: Cao, Rui, et al. Polygenic risk score for acute rejection based on donor-recipient non-HLA genotype mismatch. ''PLoS One''. 2024; '''19''' (5):e0303446
Polygenic risk scores for cardiometabolic traits demonstrate importance of ancestry for predictive precision medicine. Description: Kember, Rachel L, et al. Polygenic risk scores for cardiometabolic traits demonstrate importance of ancestry for predictive precision medicine. ''Pac Symp Biocomput''. 2024; '''29''': 611-626
Polygenic scores and Mendelian randomization identify plasma proteins causally implicated in Alzheimer's disease. Description: Cammann, Davis B, et al. Polygenic scores and Mendelian randomization identify plasma proteins causally implicated in Alzheimer's disease. ''Front Neurosci''. 2024; '''18''': 1404377
Polymorphism rs3733591 of the SLC2A9 gene and metabolic syndrome affect gout risk in Taiwan Biobank subjects. Description: Lin, Chun-Nan, et al. Polymorphism rs3733591 of the SLC2A9 gene and metabolic syndrome affect gout risk in Taiwan Biobank subjects. ''Front Genet''. 2024; '''15''': 1374405
Population genetic structure of Hymenopellis radicata germplasm resources based on genome re-sequencing. Description: Cao, Luping, et al. Population genetic structure of Hymenopellis radicata germplasm resources based on genome re-sequencing. ''Front Microbiol''. 2024; '''15''': 1287641
Population genomic analyses reveal high diversity, recombination and nosocomial transmission among Candida glabrata (Nakaseomyces glabrata) isolates causing invasive infections. Description: Wang, Yue, et al. Population genomic analyses reveal high diversity, recombination and nosocomial transmission among Candida glabrata (Nakaseomyces glabrata) isolates causing invasive infections. ''Microb Genom''. 2024 Jan; '''10''' (1):
Population structure and genetic diversity of mango (Mangifera indica L.) germplasm resources as revealed by single-nucleotide polymorphism markers. Description: Liang, Qingzhi, et al. Population structure and genetic diversity of mango (Mangifera indica L.) germplasm resources as revealed by single-nucleotide polymorphism markers. ''Front Plant Sci''. 2024; '''15''': 1328126
Population structure and selective signature of Kirghiz sheep by Illumina Ovine SNP50 BeadChip. Description: Yang, Ruizhi, et al. Population structure and selective signature of Kirghiz sheep by Illumina Ovine SNP50 BeadChip. ''PeerJ''. 2024; '''12''': e17980
Rare copy number variation in autoimmune Addison's disease. Description: Artaza, Haydee, et al. Rare copy number variation in autoimmune Addison's disease. ''Front Immunol''. 2024; '''15''': 1374499
Refining the genomic profiles of North African sheep breeds through meta-analysis of worldwide genomic SNP data. Description: Baazaoui, Imen, et al. Refining the genomic profiles of North African sheep breeds through meta-analysis of worldwide genomic SNP data. ''Front Vet Sci''. 2024; '''11''': 1339321
Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits. Description: Nicoletti, Paola, et al. Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits. ''Genet Med Open''. 2024; '''2''':
Relationships of B12 and Homocysteine with Outcomes in the SURE-PD, SURE-PD3, and STEADY-PDIII Trials. Description: Christine, Chadwick W, et al. Relationships of B12 and Homocysteine with Outcomes in the SURE-PD, SURE-PD3, and STEADY-PDIII Trials. ''J Parkinsons Dis''. 2024; '''14''' (6):1243-1255
Retinoic acid signaling regulates spatiotemporal specification of human green and red cones. Description: Hadyniak, Sarah E, et al. Retinoic acid signaling regulates spatiotemporal specification of human green and red cones. ''PLoS Biol''. 2024 Jan; '''22''' (1):e3002464
Revealing the genetic complexity of hypothyroidism: integrating complementary association methods. Description: Zucker, Roei, et al. Revealing the genetic complexity of hypothyroidism: integrating complementary association methods. ''Front Genet''. 2024; '''15''': 1409226
RPTOR Is an Alzheimer's Disease Susceptibility Gene Associated with the Risk Factors Body Mass Index and Infectious Encephalitis. Description: Lehrer, Steven, et al. RPTOR Is an Alzheimer's Disease Susceptibility Gene Associated with the Risk Factors Body Mass Index and Infectious Encephalitis. ''J Alzheimers Dis Rep''. 2024; '''8''' (1):715-721
rs12411980 single-nucleotide polymorphism related to PRTFDC1 expression is significantly associated with phantom tooth pain. Description: Araida, Jun, et al. rs12411980 single-nucleotide polymorphism related to PRTFDC1 expression is significantly associated with phantom tooth pain. ''Mol Pain''. 2024 Jan-Dec; '''20''': 17448069241272215
Screening of functional genes for hypoxia adaptation in Tibetan pigs by combined genome resequencing and transcriptome analysis. Description: Ni, Bin, et al. Screening of functional genes for hypoxia adaptation in Tibetan pigs by combined genome resequencing and transcriptome analysis. ''Front Vet Sci''. 2024; '''11''': 1486258
Searching for gene-gene interactions through variance quantitative trait loci of 29 continuous Taiwan Biobank phenotypes. Description: Lin, Wan-Yu. Searching for gene-gene interactions through variance quantitative trait loci of 29 continuous Taiwan Biobank phenotypes. ''Front Genet''. 2024; '''15''': 1357238
Selective signatures in composite MONTANA TROPICAL beef cattle reveal potential genomic regions for tropical adaptation. Description: Santos, Camila Alves Dos, et al. Selective signatures in composite MONTANA TROPICAL beef cattle reveal potential genomic regions for tropical adaptation. ''PLoS One''. 2024; '''19''' (4):e0301937
Self- and informant-reported personality traits and vaccination against COVID-19. Description: Arumae, Kadri, et al. Self- and informant-reported personality traits and vaccination against COVID-19. ''PLoS One''. 2024; '''19''' (3):e0287413
Shared genetic correlations between kidney diseases and sepsis. Description: Zhang, Tianlong, et al. Shared genetic correlations between kidney diseases and sepsis. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1396041
Shared genetic links between hypothyroidism and psychiatric disorders: evidence from a comprehensive genetic analysis. Description: Zhou, Jianlong, et al. Shared genetic links between hypothyroidism and psychiatric disorders: evidence from a comprehensive genetic analysis. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1370019
SMARTER-database: a tool to integrate SNP array datasets for sheep and goat breeds. Description: Cozzi, Paolo, et al. SMARTER-database: a tool to integrate SNP array datasets for sheep and goat breeds. ''GigaByte''. 2024; '''2024''': gigabyte139
Stratifying early-onset emotional disorders: using genetics to assess persistence in young people of European and South Asian ancestry. Description: Dennison, Charlotte A, et al. Stratifying early-onset emotional disorders: using genetics to assess persistence in young people of European and South Asian ancestry. ''J Child Psychol Psychiatry''. 2024 Jan; '''65''' (1):42-51
The causal association between gut microbiota and postpartum depression: a two-sample Mendelian randomization study. Description: Jin, Wenjun, et al. The causal association between gut microbiota and postpartum depression: a two-sample Mendelian randomization study. ''Front Microbiol''. 2024; '''15''': 1415237
The causal relationship between gut microbiota and diabetic neuropathy: a bi-directional two-sample Mendelian randomization study. Description: Xie, Long, et al. The causal relationship between gut microbiota and diabetic neuropathy: a bi-directional two-sample Mendelian randomization study. ''Front Endocrinol (Lausanne)''. 2024; '''15''': 1402014
The effects of psychiatric disorders on the risk of chronic heart failure: a univariable and multivariable Mendelian randomization study. Description: Chen, Yang, et al. The effects of psychiatric disorders on the risk of chronic heart failure: a univariable and multivariable Mendelian randomization study. ''Front Public Health''. 2024; '''12''': 1306150
The genetic landscape of autism spectrum disorder in the Middle Eastern population. Description: Al-Sarraj, Yasser, et al. The genetic landscape of autism spectrum disorder in the Middle Eastern population. ''Front Genet''. 2024; '''15''': 1363849
The genetic legacy of the expansion of Bantu-speaking peoples in Africa. Description: Fortes-Lima, Cesar A, et al. The genetic legacy of the expansion of Bantu-speaking peoples in Africa. ''Nature''. 2024 Jan; '''625''' (7995):540-547
The genomics and evolution of inter-sexual mimicry and female-limited polymorphisms in damselflies. Description: Willink, Beatriz, et al. The genomics and evolution of inter-sexual mimicry and female-limited polymorphisms in damselflies. ''Nat Ecol Evol''. 2024 Jan; '''8''' (1):83-97
The interaction between polygenic risk score and trauma affects the likelihood of post-traumatic stress disorder in female victims of sexual assault. Description: Bugiga, Amanda Victoria Gomes, et al. The interaction between polygenic risk score and trauma affects the likelihood of post-traumatic stress disorder in female victims of sexual assault. ''Braz J Psychiatry''. 2024; '''46''': e20233335
The PREVENT dementia programme: baseline demographic, lifestyle, imaging and cognitive data from a midlife cohort study investigating risk factors for dementia. Description: Ritchie, Craig W, et al. The PREVENT dementia programme: baseline demographic, lifestyle, imaging and cognitive data from a midlife cohort study investigating risk factors for dementia. ''Brain Commun''. 2024; '''6''' (3):fcae189
The Role of Genetic Variations in the FAAH rs324420 Polymorphism and its Interaction with CRHR1 rs110402 and CNR1 rs2180619 in Anxiety and- Trauma Related Symptoms After Military Deployment. Description: Leen, Nadia, et al. The Role of Genetic Variations in the FAAH rs324420 Polymorphism and its Interaction with CRHR1 rs110402 and CNR1 rs2180619 in Anxiety and- Trauma Related Symptoms After Military Deployment. ''Chronic Stress (Thousand Oaks)''. 2024 Jan-Dec; '''8''': 24705470241285828
The role of Immune cells in Alzheimer's disease: a bidirectional Mendelian randomization study. Description: Zhang, Erdong, et al. The role of Immune cells in Alzheimer's disease: a bidirectional Mendelian randomization study. ''Front Aging Neurosci''. 2024; '''16''': 1433691
The Time-Varying Impact of COVID-19 on the Acute Kidney Disorders: A Historical Matched Cohort Study and Mendelian Randomization Analysis. Description: Li, Chunyang, et al. The Time-Varying Impact of COVID-19 on the Acute Kidney Disorders: A Historical Matched Cohort Study and Mendelian Randomization Analysis. ''Health Data Sci''. 2024; '''4''': 0159
Transcriptome data reveals the conservation genetics of Cypripedium forrestii, a plant species with extremely small populations endemic to Yunnan, China. Description: Lin, Liewen, et al. Transcriptome data reveals the conservation genetics of Cypripedium forrestii, a plant species with extremely small populations endemic to Yunnan, China. ''Front Plant Sci''. 2024; '''15''': 1303625
Trio-based exome sequencing and high-resolution HLA typing in families of patients with autoimmune adrenal insufficiency and autoimmune polyglandular syndrome. Description: Buianova, Anastasiia, et al. Trio-based exome sequencing and high-resolution HLA typing in families of patients with autoimmune adrenal insufficiency and autoimmune polyglandular syndrome. ''PLoS One''. 2024; '''19''' (10):e0312335
Unraveling the immunological landscape in acute pancreatitis progression to sepsis: insights from a Mendelian randomization study on immune cell traits. Description: Liu, Wenbin, et al. Unraveling the immunological landscape in acute pancreatitis progression to sepsis: insights from a Mendelian randomization study on immune cell traits. ''Front Immunol''. 2024; '''15''': 1374787
Unveiling a potential threat to forest ecosystems: molecular diagnosis of Alliaria petiolata, a newly introduced alien plant in Korea. Description: Choi, Tae-Young, et al. Unveiling a potential threat to forest ecosystems: molecular diagnosis of Alliaria petiolata, a newly introduced alien plant in Korea. ''Front Plant Sci''. 2024; '''15''': 1395676
Using genetics to investigate the association between lanosterol and cataract. Description: Hashimi, Munisa, et al. Using genetics to investigate the association between lanosterol and cataract. ''Front Genet''. 2024; '''15''': 1231521
Using UAV-Based Temporal Spectral Indices to Dissect Changes in the Stay-Green Trait in Wheat. Description: Yu, Rui, et al. Using UAV-Based Temporal Spectral Indices to Dissect Changes in the Stay-Green Trait in Wheat. ''Plant Phenomics''. 2024; '''6''': 0171
Variant calling and genotyping accuracy of ddRAD-seq: Comparison with 20X WGS in layers. Description: Doublet, Mathilde, et al. Variant calling and genotyping accuracy of ddRAD-seq: Comparison with 20X WGS in layers. ''PLoS One''. 2024; '''19''' (7):e0298565
Whole-genome resequencing reveals genetic diversity, differentiation, and selection signatures of yak breeds/populations in southwestern China. Description: Zhang, Shilin, et al. Whole-genome resequencing reveals genetic diversity, differentiation, and selection signatures of yak breeds/populations in southwestern China. ''Front Genet''. 2024; '''15''': 1382128
Whole-genome scan for selection signature associated with temperature adaptation in Iranian sheep breeds. Description: Patiabadi, Zahra, et al. Whole-genome scan for selection signature associated with temperature adaptation in Iranian sheep breeds. ''PLoS One''. 2024; '''19''' (8):e0309023
Whole genome sequencing identified genomic diversity and candidated genes associated with economic traits in Northeasern Merino in China. Description: Yi, Wenfeng, et al. Whole genome sequencing identified genomic diversity and candidated genes associated with economic traits in Northeasern Merino in China. ''Front Genet''. 2024; '''15''': 1302222
Whole-genome sequencing reveals rare variants associated with gout in Taiwanese males. Description: Tseng, Yu-Ping, et al. Whole-genome sequencing reveals rare variants associated with gout in Taiwanese males. ''Front Genet''. 2024; '''15''': 1423714
Exploring the role of polymorphic interspecies structural variants in reproductive isolation and adaptive divergence in Eucalyptus. Description: Ferguson, Scott, et al. Exploring the role of polymorphic interspecies structural variants in reproductive isolation and adaptive divergence in Eucalyptus. ''Gigascience''. 2024 Jan 2; '''13''':
Genetic dissection of resistance to gray leaf spot by genome-wide association study in a multi-parent maize population. Description: Hu, Can, et al. Genetic dissection of resistance to gray leaf spot by genome-wide association study in a multi-parent maize population. ''BMC Plant Biol''. 2024 Jan 2; '''24''' (1):10
Genomic exploration of the endangered oriental stork, Ciconia boyciana, sheds light on migration adaptation and future conservation. Description: Yang, Shangchen, et al. Genomic exploration of the endangered oriental stork, Ciconia boyciana, sheds light on migration adaptation and future conservation. ''Gigascience''. 2024 Jan 2; '''13''':
Genomic insights into endangerment and conservation of the garlic-fruit tree (Malania oleifera), a plant species with extremely small populations. Description: Shen, Yuanting, et al. Genomic insights into endangerment and conservation of the garlic-fruit tree (Malania oleifera), a plant species with extremely small populations. ''Gigascience''. 2024 Jan 2; '''13''':
GSC: efficient lossless compression of VCF files with fast query. Description: Luo, Xiaolong, et al. GSC: efficient lossless compression of VCF files with fast query. ''Gigascience''. 2024 Jan 2; '''13''':
Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups. Description: Jeon, Sungwon, et al. Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups. ''Gigascience''. 2024 Jan 2; '''13''':
Mechanisms of hepatic steatosis in chickens: integrated analysis of the host genome, molecular phenomics and gut microbiome. Description: Sun, Congjiao, et al. Mechanisms of hepatic steatosis in chickens: integrated analysis of the host genome, molecular phenomics and gut microbiome. ''Gigascience''. 2024 Jan 2; '''13''':
The chromosome-scale genome of Magnolia sinica (Magnoliaceae) provides insights into the conservation of plant species with extremely small populations (PSESP). Description: Cai, Lei, et al. The chromosome-scale genome of Magnolia sinica (Magnoliaceae) provides insights into the conservation of plant species with extremely small populations (PSESP). ''Gigascience''. 2024 Jan 2; '''13''':
*The HLA-DRB109:01-DQB103:03 haplotype is associated with the risk for late-onset Alzheimer's disease in APOE [Formula: see text]4-negative Japanese adults.* Description: Shigemizu, Daichi, et al. The HLA-DRB109:01-DQB103:03 haplotype is associated with the risk for late-onset Alzheimer's disease in APOE [Formula: see text]4-negative Japanese adults. ''NPJ Aging''. 2024 Jan 2; '''10''' (1):3
Whole-genome sequencing of the invasive golden apple snail Pomacea canaliculata from Asia reveals rapid expansion and adaptive evolution. Description: Lu, Yan, et al. Whole-genome sequencing of the invasive golden apple snail Pomacea canaliculata from Asia reveals rapid expansion and adaptive evolution. ''Gigascience''. 2024 Jan 2; '''13''':
A Burden of Rare Copy Number Variants in Obsessive-Compulsive Disorder. Description: Halvorsen, Matthew, et al. A Burden of Rare Copy Number Variants in Obsessive-Compulsive Disorder. ''Res Sq''. 2024 Jan 3;
African bushpigs exhibit porous species boundaries and appeared in Madagascar concurrently with human arrival. Description: Balboa, Renzo F, et al. African bushpigs exhibit porous species boundaries and appeared in Madagascar concurrently with human arrival. ''Nat Commun''. 2024 Jan 3; '''15''' (1):172
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease. Description: Riesmeijer, Sophie A, et al. A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease. ''Nat Commun''. 2024 Jan 3; '''15''' (1):199
Analysis of ddRAD-seq data provides new insights into the genomic structure and patterns of diversity in Italian donkey populations. Description: Criscione, Andrea, et al. Analysis of ddRAD-seq data provides new insights into the genomic structure and patterns of diversity in Italian donkey populations. ''J Anim Sci''. 2024 Jan 3; '''102''':
A Study of the Resistance of Hu Sheep Lambs to Escherichia coli F17 Based on Whole Genome Sequencing. Description: Duan, Yanjun, et al. A Study of the Resistance of Hu Sheep Lambs to Escherichia coli F17 Based on Whole Genome Sequencing. ''Animals (Basel)''. 2024 Jan 3; '''14''' (1):
Effect of genotyping density on the detection of runs of homozygosity and heterozygosity in cattle. Description: Falchi, Laura, et al. Effect of genotyping density on the detection of runs of homozygosity and heterozygosity in cattle. ''J Anim Sci''. 2024 Jan 3; '''102''':
Mutation of the cyclooxygenase 2 gene promoter and anastomotic leakage in colorectal cancer patients: retrospective cohort study. Description: Grahn, Oskar, et al. Mutation of the cyclooxygenase 2 gene promoter and anastomotic leakage in colorectal cancer patients: retrospective cohort study. ''BJS Open''. 2024 Jan 3; '''8''' (1):
Rice Seed Protrusion Quantitative Trait Loci Mapping through Genome-Wide Association Study. Description: Ding, Xiaowen, et al. Rice Seed Protrusion Quantitative Trait Loci Mapping through Genome-Wide Association Study. ''Plants (Basel)''. 2024 Jan 3; '''13''' (1):
The Impact of Recent Demography on Functional Genetic Variation in North African Human Groups. Description: Lucas-Sanchez, Marcel, et al. The Impact of Recent Demography on Functional Genetic Variation in North African Human Groups. ''Mol Biol Evol''. 2024 Jan 3; '''41''' (1):
Unravelling novel and pleiotropic genes for cannon bone circumference and bone mineral density in Yorkshire pigs. Description: Qiu, Zijian, et al. Unravelling novel and pleiotropic genes for cannon bone circumference and bone mineral density in Yorkshire pigs. ''J Anim Sci''. 2024 Jan 3; '''102''':
Whole-genome resequencing reveals the uniqueness of Subei yak. Description: Guo, Shaoke, et al. Whole-genome resequencing reveals the uniqueness of Subei yak. ''J Anim Sci''. 2024 Jan 3; '''102''':
Parental and child genetic burden of glycaemic dysregulation and early-life cognitive development: an Asian and European prospective cohort study. Description: Huang, Jian, et al. Parental and child genetic burden of glycaemic dysregulation and early-life cognitive development: an Asian and European prospective cohort study. ''Transl Psychiatry''. 2024 Jan 4; '''14''' (1):2
The Genetic Selection of HSPD1 and HSPE1 Reduce Inflammation of Liver and Spleen While Restraining the Growth and Development of Skeletal Muscle in Wuzhishan Pigs. Description: Ren, Yuwei, et al. The Genetic Selection of HSPD1 and HSPE1 Reduce Inflammation of Liver and Spleen While Restraining the Growth and Development of Skeletal Muscle in Wuzhishan Pigs. ''Animals (Basel)''. 2024 Jan 4; '''14''' (1):
AGIDB: a versatile database for genotype imputation and variant decoding across species. Description: Zhang, Kaili, et al. AGIDB: a versatile database for genotype imputation and variant decoding across species. ''Nucleic Acids Res''. 2024 Jan 5; '''52''' (D1):D835-D849
CropGS-Hub: a comprehensive database of genotype and phenotype resources for genomic prediction in major crops. Description: Chen, Jiaxin, et al. CropGS-Hub: a comprehensive database of genotype and phenotype resources for genomic prediction in major crops. ''Nucleic Acids Res''. 2024 Jan 5; '''52''' (D1):D1519-D1529
Differential methylation analysis in neuropathologically confirmed dementia with Lewy bodies. Description: Reho, Paolo, et al. Differential methylation analysis in neuropathologically confirmed dementia with Lewy bodies. ''Commun Biol''. 2024 Jan 5; '''7''' (1):35
eRNAbase: a comprehensive database for decoding the regulatory eRNAs in human and mouse. Description: Song, Chao, et al. eRNAbase: a comprehensive database for decoding the regulatory eRNAs in human and mouse. ''Nucleic Acids Res''. 2024 Jan 5; '''52''' (D1):D81-D91
Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity. Description: Mbarek, Hamdi, et al. Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity. ''Hum Reprod''. 2024 Jan 5; '''39''' (1):240-257
*Human leukocyte antigen-DQA104:01 and rs2040406 variants are associated with elevated risk of childhood Burkitt lymphoma.** Description: Liu, Zhiwei, et al. Human leukocyte antigen-DQA1*04:01 and rs2040406 variants are associated with elevated risk of childhood Burkitt lymphoma. ''Commun Biol''. 2024 Jan 5; '''7''' (1):41
m7GHub V2.0: an updated database for decoding the N7-methylguanosine (m7G) epitranscriptome. Description: Wang, Xuan, et al. m7GHub V2.0: an updated database for decoding the N7-methylguanosine (m7G) epitranscriptome. ''Nucleic Acids Res''. 2024 Jan 5; '''52''' (D1):D203-D212
Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma. Description: Choquet, Helene, et al. Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma. ''Commun Biol''. 2024 Jan 5; '''7''' (1):33
Negative Selection on a SOD1 Mutation Limits Canine Degenerative Myelopathy While Avoiding Inbreeding. Description: Ukawa, Hisashi, et al. Negative Selection on a SOD1 Mutation Limits Canine Degenerative Myelopathy While Avoiding Inbreeding. ''Genome Biol Evol''. 2024 Jan 5; '''16''' (1):
Signatures of Co-evolution and Co-regulation in the CYP3A and CYP4F Genes in Humans. Description: Richard-St-Hilaire, Alex, et al. Signatures of Co-evolution and Co-regulation in the CYP3A and CYP4F Genes in Humans. ''Genome Biol Evol''. 2024 Jan 5; '''16''' (1):
High-dimensional phenotyping to define the genetic basis of cellular morphology. Description: Tegtmeyer, Matthew, et al. High-dimensional phenotyping to define the genetic basis of cellular morphology. ''Nat Commun''. 2024 Jan 6; '''15''' (1):347
OXTR polymorphisms associated with severity and treatment responses of schizophrenia. Description: Lv, Xue, et al. OXTR polymorphisms associated with severity and treatment responses of schizophrenia. ''Schizophrenia (Heidelb)''. 2024 Jan 6; '''10''' (1):7
Detection of Runs of Homozygosity and Identification of Candidate Genes in the Whole Genome of Tunchang Pigs. Description: Wang, Ziyi, et al. Detection of Runs of Homozygosity and Identification of Candidate Genes in the Whole Genome of Tunchang Pigs. ''Animals (Basel)''. 2024 Jan 8; '''14''' (2):
MassArray Genotyping as a Selection Tool for Extending the Shelf-Life of Fresh Gilthead Sea Bream and European Seabass. Description: Angelakopoulos, Rafael, et al. MassArray Genotyping as a Selection Tool for Extending the Shelf-Life of Fresh Gilthead Sea Bream and European Seabass. ''Animals (Basel)''. 2024 Jan 8; '''14''' (2):
Rare copy-number variants as modulators of common disease susceptibility. Description: Auwerx, Chiara, et al. Rare copy-number variants as modulators of common disease susceptibility. ''Genome Med''. 2024 Jan 8; '''16''' (1):5
Characterizing epigenetic aging in an adult sickle cell disease cohort. Description: Le, Brandon M, et al. Characterizing epigenetic aging in an adult sickle cell disease cohort. ''Blood Adv''. 2024 Jan 9; '''8''' (1):47-55
Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cell types for glaucoma. Description: Hamel, Andrew R, et al. Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cell types for glaucoma. ''Nat Commun''. 2024 Jan 9; '''15''' (1):396
The Anti-Mullerian Hormone as Endocrine and Molecular Marker Associated with Reproductive Performance in Holstein Dairy Cows Exposed to Heat Stress. Description: Contreras-Mendez, Luis A, et al. The Anti-Mullerian Hormone as Endocrine and Molecular Marker Associated with Reproductive Performance in Holstein Dairy Cows Exposed to Heat Stress. ''Animals (Basel)''. 2024 Jan 9; '''14''' (2):
The genome of the black-footed cat: Revealing a rich natural history and urgent conservation priorities for small felids. Description: Yuan, Jiaqing, et al. The genome of the black-footed cat: Revealing a rich natural history and urgent conservation priorities for small felids. ''Proc Natl Acad Sci U S A''. 2024 Jan 9; '''121''' (2):e2310763120
A cis-regulatory element regulates ERAP2 expression through autoimmune disease risk SNPs. Description: Venema, Wouter J, et al. A cis-regulatory element regulates ERAP2 expression through autoimmune disease risk SNPs. ''Cell Genom''. 2024 Jan 10; '''4''' (1):100460
Embers of the Past: Early Childhood Traumas Interact with Variation in P2RX7 Gene Implicated in Neuroinflammation on Markers of Current Suicide Risk. Description: Kristof, Zsuliet, et al. Embers of the Past: Early Childhood Traumas Interact with Variation in P2RX7 Gene Implicated in Neuroinflammation on Markers of Current Suicide Risk. ''Int J Mol Sci''. 2024 Jan 10; '''25''' (2):
Levels of complement factor H-related 4 protein do not influence susceptibility to age-related macular degeneration or its course of progression. Description: Zouache, M A, et al. Levels of complement factor H-related 4 protein do not influence susceptibility to age-related macular degeneration or its course of progression. ''Nat Commun''. 2024 Jan 10; '''15''' (1):443
Multi-ancestry genetic analysis of gene regulation in coronary arteries prioritizes disease risk loci. Description: Hodonsky, Chani J, et al. Multi-ancestry genetic analysis of gene regulation in coronary arteries prioritizes disease risk loci. ''Cell Genom''. 2024 Jan 10; '''4''' (1):100465
Non-additive genetic components contribute significantly to population-wide gene expression variation. Description: Tsouris, Andreas, et al. Non-additive genetic components contribute significantly to population-wide gene expression variation. ''Cell Genom''. 2024 Jan 10; '''4''' (1):100459
Population clustering of structural brain aging and its association with brain development. Description: Duan, Haojing, et al. Population clustering of structural brain aging and its association with brain development. ''medRxiv''. 2024 Jan 10;
Shared Genetics between Age at Menarche and Type 2 Diabetes Mellitus: Genome-Wide Genetic Correlation Study. Description: Cheng, Yuan-Fang, et al. Shared Genetics between Age at Menarche and Type 2 Diabetes Mellitus: Genome-Wide Genetic Correlation Study. ''Biomedicines''. 2024 Jan 11; '''12''' (1):
A Genome-Wide Association Study for Resistance to Tropical Theileriosis in Two Bovine Portuguese Autochthonous Breeds. Description: Valente, Diana, et al. A Genome-Wide Association Study for Resistance to Tropical Theileriosis in Two Bovine Portuguese Autochthonous Breeds. ''Pathogens''. 2024 Jan 12; '''13''' (1):
Genomic resources for a historical collection of cultivated two-row European spring barley genotypes. Description: Schreiber, Miriam, et al. Genomic resources for a historical collection of cultivated two-row European spring barley genotypes. ''Sci Data''. 2024 Jan 12; '''11''' (1):66
Identification of Signatures of Positive Selection That Have Shaped the Genomic Landscape of South African Pig Populations. Description: Hlongwane, Nompilo L, et al. Identification of Signatures of Positive Selection That Have Shaped the Genomic Landscape of South African Pig Populations. ''Animals (Basel)''. 2024 Jan 12; '''14''' (2):
PASTRY: achieving balanced power for detecting risk and protective minor alleles in meta-analysis of association studies with overlapping subjects. Description: Kim, Emma E, et al. PASTRY: achieving balanced power for detecting risk and protective minor alleles in meta-analysis of association studies with overlapping subjects. ''BMC Bioinformatics''. 2024 Jan 12; '''25''' (1):24
The origins of the Guinness stout yeast. Description: Kerruish, Daniel W M, et al. The origins of the Guinness stout yeast. ''Commun Biol''. 2024 Jan 12; '''7''' (1):68
Exploring Genomics and Microbial Ecology: Analysis of Bidens pilosa L. Genetic Structure and Soil Microbiome Diversity by RAD-Seq and Metabarcoding. Description: Reyes-Ardila, Wendy Lorena, et al. Exploring Genomics and Microbial Ecology: Analysis of Bidens pilosa L. Genetic Structure and Soil Microbiome Diversity by RAD-Seq and Metabarcoding. ''Plants (Basel)''. 2024 Jan 13; '''13''' (2):
Risk of Sperm Disorders and Impaired Fertility in Frozen-Thawed Bull Semen: A Genome-Wide Association Study. Description: Dementieva, Natalia V, et al. Risk of Sperm Disorders and Impaired Fertility in Frozen-Thawed Bull Semen: A Genome-Wide Association Study. ''Animals (Basel)''. 2024 Jan 13; '''14''' (2):
The melatonin receptor genes are linked and associated with the risk of polycystic ovary syndrome. Description: Postolache, Teodor T, et al. The melatonin receptor genes are linked and associated with the risk of polycystic ovary syndrome. ''J Ovarian Res''. 2024 Jan 13; '''17''' (1):17
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. Description: Bisschoff, Michelle, et al. Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. ''Orphanet J Rare Dis''. 2024 Jan 14; '''19''' (1):15
Genetic associations with longevity are on average stronger in females than in males. Description: Zeng, Yi, et al. Genetic associations with longevity are on average stronger in females than in males. ''Heliyon''. 2024 Jan 15; '''10''' (1):e23691
Genome-wide SNP-sex interaction analysis of susceptibility to idiopathic pulmonary fibrosis. Description: Leavy, Olivia C, et al. Genome-wide SNP-sex interaction analysis of susceptibility to idiopathic pulmonary fibrosis. ''medRxiv''. 2024 Jan 15;
Haplotype-aware modeling of cis-regulatory effects highlights the gaps remaining in eQTL data. Description: Ehsan, Nava, et al. Haplotype-aware modeling of cis-regulatory effects highlights the gaps remaining in eQTL data. ''Nat Commun''. 2024 Jan 15; '''15''' (1):522
Large scale plasma proteomics identifies novel proteins and protein networks associated with heart failure development. Description: Shah, Amil M, et al. Large scale plasma proteomics identifies novel proteins and protein networks associated with heart failure development. ''Nat Commun''. 2024 Jan 15; '''15''' (1):528
Multi-ancestry meta-analysis of host genetic susceptibility to tuberculosis identifies shared genetic architecture. Description: Schurz, Haiko, et al. Multi-ancestry meta-analysis of host genetic susceptibility to tuberculosis identifies shared genetic architecture. ''Elife''. 2024 Jan 15; '''13''':
Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men. Description: Janivara, Rohini, et al. Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men. ''bioRxiv''. 2024 Jan 15;
A genome-wide association study of social trust in 33,882 Danish blood donors. Description: Sequeros, Celia Burgos, et al. A genome-wide association study of social trust in 33,882 Danish blood donors. ''Sci Rep''. 2024 Jan 16; '''14''' (1):1402
Effects of uric acid on ischemic diseases, stratified by lipid levels: a drug-target, nonlinear Mendelian randomization study. Description: Kim, Jungeun, et al. Effects of uric acid on ischemic diseases, stratified by lipid levels: a drug-target, nonlinear Mendelian randomization study. ''Sci Rep''. 2024 Jan 16; '''14''' (1):1338
OMICs Signatures Linking Persistent Organic Pollutants to Cardiovascular Disease in the Swedish Mammography Cohort. Description: Schillemans, Tessa, et al. OMICs Signatures Linking Persistent Organic Pollutants to Cardiovascular Disease in the Swedish Mammography Cohort. ''Environ Sci Technol''. 2024 Jan 16; '''58''' (2):1036-1047
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young. Description: Puckelwartz, Megan J, et al. The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young. ''Genome Med''. 2024 Jan 16; '''16''' (1):13
The Impact of IL1B rs1143634 and DEFB1 rs11362 Variants on Periodontitis Risk in Phenylketonuria and Type 1 Diabetes Mellitus Patients in a Latvian Population. Description: Emulina, Darta Elizabete, et al. The Impact of IL1B rs1143634 and DEFB1 rs11362 Variants on Periodontitis Risk in Phenylketonuria and Type 1 Diabetes Mellitus Patients in a Latvian Population. ''Diagnostics (Basel)''. 2024 Jan 16; '''14''' (2):
A genome-wide investigation into the underlying genetic architecture of personality traits and overlap with psychopathology. Description: Gupta, Priya, et al. A genome-wide investigation into the underlying genetic architecture of personality traits and overlap with psychopathology. ''medRxiv''. 2024 Jan 17;
Evaluating the Efficacy of Type 2 Diabetes Polygenic Risk Scores in an Independent European Population. Description: Briviba, Monta, et al. Evaluating the Efficacy of Type 2 Diabetes Polygenic Risk Scores in an Independent European Population. ''Int J Mol Sci''. 2024 Jan 17; '''25''' (2):
Genetic patterns and genome-wide association analysis of eggshell quality traits of egg-type chicken across an extended laying period. Description: Chen, Xiaoman, et al. Genetic patterns and genome-wide association analysis of eggshell quality traits of egg-type chicken across an extended laying period. ''Poult Sci''. 2024 Jan 17; '''103''' (4):103458
Genome-wide association identifies novel ROP risk loci in a multiethnic cohort. Description: Li, Xiaohui, et al. Genome-wide association identifies novel ROP risk loci in a multiethnic cohort. ''Commun Biol''. 2024 Jan 17; '''7''' (1):107
Host genotype, soil composition, and geo-climatic factors shape the fonio seed microbiome. Description: Tabassum, Naheed, et al. Host genotype, soil composition, and geo-climatic factors shape the fonio seed microbiome. ''Microbiome''. 2024 Jan 17; '''12''' (1):11
Diminished social motivation in early psychosis is associated with polygenic liability for low vitamin D. Description: Hatzimanolis, Alex, et al. Diminished social motivation in early psychosis is associated with polygenic liability for low vitamin D. ''Transl Psychiatry''. 2024 Jan 18; '''14''' (1):36
Genetic Diversity, Population Structure and Selection Signature in Begait Goats Revealed by Whole-Genome Sequencing. Description: Gebreselase, Haile Berihulay, et al. Genetic Diversity, Population Structure and Selection Signature in Begait Goats Revealed by Whole-Genome Sequencing. ''Animals (Basel)''. 2024 Jan 18; '''14''' (2):
Genomic insights into Plasmodium vivax population structure and diversity in central Africa. Description: Gartner, Valerie, et al. Genomic insights into Plasmodium vivax population structure and diversity in central Africa. ''Malar J''. 2024 Jan 18; '''23''' (1):27
Investigation of genetic determinants of cognitive change in later life. Description: Mahedy, Liam, et al. Investigation of genetic determinants of cognitive change in later life. ''Transl Psychiatry''. 2024 Jan 18; '''14''' (1):31
Longitudinal single cell atlas identifies complex temporal relationship between type I interferon response and COVID-19 severity. Description: Lin, Quy Xiao Xuan, et al. Longitudinal single cell atlas identifies complex temporal relationship between type I interferon response and COVID-19 severity. ''Nat Commun''. 2024 Jan 18; '''15''' (1):567
Polygenic scores for tobacco use provide insights into systemic health risks in a diverse EHR-linked biobank in Los Angeles. Description: Venkateswaran, Vidhya, et al. Polygenic scores for tobacco use provide insights into systemic health risks in a diverse EHR-linked biobank in Los Angeles. ''Transl Psychiatry''. 2024 Jan 18; '''14''' (1):38
Proteomic associations with forced expiratory volume: a Mendelian randomisation study. Description: Axelsson, Gisli Thor, et al. Proteomic associations with forced expiratory volume: a Mendelian randomisation study. ''Respir Res''. 2024 Jan 18; '''25''' (1):44
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements. Description: Scholz, Markus, et al. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements. ''Nat Commun''. 2024 Jan 18; '''15''' (1):586
Genetic architecture distinguishes tinnitus from hearing loss. Description: Clifford, Royce E, et al. Genetic architecture distinguishes tinnitus from hearing loss. ''Nat Commun''. 2024 Jan 19; '''15''' (1):614
Genetic history of Cambridgeshire before and after the Black Death. Description: Hui, Ruoyun, et al. Genetic history of Cambridgeshire before and after the Black Death. ''Sci Adv''. 2024 Jan 19; '''10''' (3):eadi5903
Genomic insights into the Montseny brook newt (Calotriton arnoldi), a Critically Endangered glacial relict. Description: Talavera, Adrian, et al. Genomic insights into the Montseny brook newt (Calotriton arnoldi), a Critically Endangered glacial relict. ''iScience''. 2024 Jan 19; '''27''' (1):108665
Nuclear environmental DNA resolves fine-scale population genetic structure in an aquatic habitat. Description: Nuclear environmental DNA resolves fine-scale population genetic structure in an aquatic habitat. ''''. 2024 Jan 19; '''27''' (1):108669
The Impact of Different Intensities of Physical Activity on Serum Urate and Gout: A Mendelian Randomization Study. Description: Yang, Tangxun, et al. The Impact of Different Intensities of Physical Activity on Serum Urate and Gout: A Mendelian Randomization Study. ''Metabolites''. 2024 Jan 19; '''14''' (1):
Genomic heterozygosity is associated with a lower risk of osteoarthritis. Description: Gill, Robert, et al. Genomic heterozygosity is associated with a lower risk of osteoarthritis. ''BMC Genomics''. 2024 Jan 20; '''25''' (1):85
SOX9 gene shows association with adolescent idiopathic scoliosis predisposition in Northwest Indians. Description: Singh, Hemender, et al. SOX9 gene shows association with adolescent idiopathic scoliosis predisposition in Northwest Indians. ''Eur J Med Res''. 2024 Jan 20; '''29''' (1):66
Deep learning predicts DNA methylation regulatory variants in specific brain cell types and enhances fine mapping for brain disorders. Description: Zhou, Jiyun, et al. Deep learning predicts DNA methylation regulatory variants in specific brain cell types and enhances fine mapping for brain disorders. ''bioRxiv''. 2024 Jan 21;
Exploratory study of cold hypersensitivity in Japanese women: genetic associations and somatic symptom burden. Description: Wu, Xuefeng, et al. Exploratory study of cold hypersensitivity in Japanese women: genetic associations and somatic symptom burden. ''Sci Rep''. 2024 Jan 22; '''14''' (1):1918
Molecular quantitative trait loci in reproductive tissues impact male fertility in cattle. Description: Mapel, Xena Marie, et al. Molecular quantitative trait loci in reproductive tissues impact male fertility in cattle. ''Nat Commun''. 2024 Jan 22; '''15''' (1):674
Common and specific genetic basis of metabolite-mediated drought responses in rice. Description: Guo, Zilong, et al. Common and specific genetic basis of metabolite-mediated drought responses in rice. ''Stress Biol''. 2024 Jan 23; '''4''' (1):6
Human whole-exome genotype data for Alzheimer's disease. Description: Leung, Yuk Yee, et al. Human whole-exome genotype data for Alzheimer's disease. ''Nat Commun''. 2024 Jan 23; '''15''' (1):684
Genetic background of juniper (Juniperus spp.) consumption predicted by fecal near-infrared spectroscopy in divergently selected goats raised in harsh rangeland environments. Description: Mulim, Henrique A, et al. Genetic background of juniper (Juniperus spp.) consumption predicted by fecal near-infrared spectroscopy in divergently selected goats raised in harsh rangeland environments. ''BMC Genomics''. 2024 Jan 24; '''25''' (1):107
Identification of a common haplotype in carriers of rob(1;29) in 32 Italian cattle breeds. Description: Cortellari, Matteo, et al. Identification of a common haplotype in carriers of rob(1;29) in 32 Italian cattle breeds. ''Sci Rep''. 2024 Jan 24; '''14''' (1):2057
Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number. Description: Koller, Adriana, et al. Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number. ''Sci Rep''. 2024 Jan 24; '''14''' (1):2083
Causal association between allostatic load and accelerated white matter brain aging: findings from the UK Biobank. Description: Feng, Li, et al. Causal association between allostatic load and accelerated white matter brain aging: findings from the UK Biobank. ''medRxiv''. 2024 Jan 26;
Comparative genomic analyses provide new insights into evolutionary history and conservation genomics of gorillas. Description: van der Valk, Tom, et al. Comparative genomic analyses provide new insights into evolutionary history and conservation genomics of gorillas. ''BMC Ecol Evol''. 2024 Jan 26; '''24''' (1):14
Genomic analysis of Nigerian indigenous chickens reveals their genetic diversity and adaptation to heat-stress. Description: Rachman, Mifta P, et al. Genomic analysis of Nigerian indigenous chickens reveals their genetic diversity and adaptation to heat-stress. ''Sci Rep''. 2024 Jan 26; '''14''' (1):2209
Pathogenic/likely pathogenic mutations identified in Vietnamese children diagnosed with autism spectrum disorder using high-resolution SNP genotyping platform. Description: Bui, Duyen T, et al. Pathogenic/likely pathogenic mutations identified in Vietnamese children diagnosed with autism spectrum disorder using high-resolution SNP genotyping platform. ''Sci Rep''. 2024 Jan 29; '''14''' (1):2360
Unraveling the epigenetic code: human kidney DNA methylation and chromatin dynamics in renal disease development. Description: Yan, Yu, et al. Unraveling the epigenetic code: human kidney DNA methylation and chromatin dynamics in renal disease development. ''Nat Commun''. 2024 Jan 29; '''15''' (1):873
A genome-wide association study reveals the relationship between human genetic variation and the nasal microbiome. Description: Liu, Xiaomin, et al. A genome-wide association study reveals the relationship between human genetic variation and the nasal microbiome. ''Commun Biol''. 2024 Jan 30; '''7''' (1):139
Genome-wide association study, population structure, and genetic diversity of the tea plant in Guizhou Plateau. Description: Wang, Yihan, et al. Genome-wide association study, population structure, and genetic diversity of the tea plant in Guizhou Plateau. ''BMC Plant Biol''. 2024 Jan 30; '''24''' (1):79
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications. Description: Sterenborg, Rosalie B T M, et al. Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications. ''Nat Commun''. 2024 Jan 30; '''15''' (1):888
Revealing third-order interactions through the integration of machine learning and entropy methods in genomic studies. Description: Yaldiz, Burcu, et al. Revealing third-order interactions through the integration of machine learning and entropy methods in genomic studies. ''BioData Min''. 2024 Jan 30; '''17''' (1):3
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. Description: Wang, Hui, et al. Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. ''medRxiv''. 2024 Jan 30;
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcgamma receptor region. Description: Ishikawa, Yuki, et al. GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcgamma receptor region. ''Nat Commun''. 2024 Jan 31; '''15''' (1):319
Inbreeding depression is associated with recent homozygous-by-descent segments in Belgian Blue beef cattle. Description: Naji, Maulana Mughitz, et al. Inbreeding depression is associated with recent homozygous-by-descent segments in Belgian Blue beef cattle. ''Genet Sel Evol''. 2024 Jan 31; '''56''' (1):10
Resting heart rate causally affects the brain cortical structure: Mendelian randomization study. Description: Zhong, Yinsheng, et al. Resting heart rate causally affects the brain cortical structure: Mendelian randomization study. ''Cereb Cortex''. 2024 Jan 31; '''34''' (2):
A common NFKB1 variant detected through antibody analysis in UK Biobank predicts risk of infection and allergy. Description: Chong, Amanda Y, et al. A common NFKB1 variant detected through antibody analysis in UK Biobank predicts risk of infection and allergy. ''Am J Hum Genet''. 2024 Feb 1; '''111''' (2):295-308
A naturally occurring variant of SHLP2 is a protective factor in Parkinson's disease. Description: Kim, Su-Jeong, et al. A naturally occurring variant of SHLP2 is a protective factor in Parkinson's disease. ''Mol Psychiatry''. 2024 Feb; '''29''' (2):505-517
Apolipoprotein E moderates the association between non-APOE polygenic risk score for Alzheimer's disease and aging on preclinical cognitive function. Description: Xu, Yuexuan, et al. Apolipoprotein E moderates the association between non-APOE polygenic risk score for Alzheimer's disease and aging on preclinical cognitive function. ''Alzheimers Dement''. 2024 Feb; '''20''' (2):1063-1075
Atopic dermatitis-associated genetic variants regulate LOC100294145 expression implicating interleukin-27 production and type 1 interferon signaling. Description: Teo, Wei Yi, et al. Atopic dermatitis-associated genetic variants regulate LOC100294145 expression implicating interleukin-27 production and type 1 interferon signaling. ''World Allergy Organ J''. 2024 Feb; '''17''' (2):100869
C9orf72 Repeat Expansion Discordance in 6 Multigenerational Kindreds. Description: Ryan, Marie, et al. C9orf72 Repeat Expansion Discordance in 6 Multigenerational Kindreds. ''Neurol Genet''. 2024 Feb; '''10''' (1):e200112
Development and evaluation of a novel single nucleotide polymorphism panel for North American bison. Description: Stroupe, Sam, et al. Development and evaluation of a novel single nucleotide polymorphism panel for North American bison. ''Evol Appl''. 2024 Feb; '''17''' (2):e13658
Divergent Selection in Low Recombination Regions Shapes the Genomic Islands in Two Incipient Shorebird Species. Description: Zhou, Wenjun, et al. Divergent Selection in Low Recombination Regions Shapes the Genomic Islands in Two Incipient Shorebird Species. ''Mol Biol Evol''. 2024 Feb 1; '''41''' (2):
Duck pan-genome reveals two transposon insertions caused bodyweight enlarging and white plumage phenotype formation during evolution. Description: Wang, Kejun, et al. Duck pan-genome reveals two transposon insertions caused bodyweight enlarging and white plumage phenotype formation during evolution. ''Imeta''. 2024 Feb; '''3''' (1):e154
Dynamic Phytomeric Growth Contributes to Local Adaptation in Barley. Description: Huang, Yongyu, et al. Dynamic Phytomeric Growth Contributes to Local Adaptation in Barley. ''Mol Biol Evol''. 2024 Feb 1; '''41''' (2):
Estimating the impact of transmitted and non-transmitted psychiatric and neurodevelopmental polygenic scores on youth emotional problems. Description: Shakeshaft, Amy, et al. Estimating the impact of transmitted and non-transmitted psychiatric and neurodevelopmental polygenic scores on youth emotional problems. ''Mol Psychiatry''. 2024 Feb; '''29''' (2):238-246
Genomic analysis of fruit size and shape traits in apple: unveiling candidate genes through GWAS analysis. Description: Dujak, Christian, et al. Genomic analysis of fruit size and shape traits in apple: unveiling candidate genes through GWAS analysis. ''Hortic Res''. 2024 Feb; '''11''' (2):uhad270
Genomic prediction based on preselected single-nucleotide polymorphisms from genome-wide association study and imputed whole-genome sequence data annotation for growth traits in Duroc pigs. Description: Zhang, Yuling, et al. Genomic prediction based on preselected single-nucleotide polymorphisms from genome-wide association study and imputed whole-genome sequence data annotation for growth traits in Duroc pigs. ''Evol Appl''. 2024 Feb; '''17''' (2):e13651
Identification of candidate genes affecting the tibia quality in Nonghua duck. Description: Lu, Yinjuan, et al. Identification of candidate genes affecting the tibia quality in Nonghua duck. ''Poult Sci''. 2024 Feb 1; '''103''' (4):103515
Longitudinal change in memory performance as a strong endophenotype for Alzheimer's disease. Description: Archer, Derek B, et al. Longitudinal change in memory performance as a strong endophenotype for Alzheimer's disease. ''Alzheimers Dement''. 2024 Feb; '''20''' (2):1268-1283
Marital status and genetic liability independently predict coronary heart disease incidence. Description: Silventoinen, Karri, et al. Marital status and genetic liability independently predict coronary heart disease incidence. ''Scand J Public Health''. 2024 Feb; '''52''' (1):1-4
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Description: Meng, Xiangrui, et al. Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. ''Nat Genet''. 2024 Feb; '''56''' (2):222-233
NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge. Description: Greenfest-Allen, Emily, et al. NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge. ''Alzheimers Dement''. 2024 Feb; '''20''' (2):1123-1136
Polygenetic risk scores and phenotypic constellations of obsessive-compulsive disorder in clozapine-treated schizophrenia. Description: Morgenroth, Carla Lou, et al. Polygenetic risk scores and phenotypic constellations of obsessive-compulsive disorder in clozapine-treated schizophrenia. ''Eur Arch Psychiatry Clin Neurosci''. 2024 Feb; '''274''' (1):181-193
Protective Association of APOC1/rs4420638 with Risk of Obesity: A case-control Study in Portuguese Children. Description: Manco, Licinio, et al. Protective Association of APOC1/rs4420638 with Risk of Obesity: A case-control Study in Portuguese Children. ''Biochem Genet''. 2024 Feb; '''62''' (1):254-263
Sex-specific genetic architecture of late-life memory performance. Description: Eissman, Jaclyn M, et al. Sex-specific genetic architecture of late-life memory performance. ''Alzheimers Dement''. 2024 Feb; '''20''' (2):1250-1267
Signatures of selection in Mulinia lateralis underpinning its rapid adaptation to laboratory conditions. Description: Yang, Zujing, et al. Signatures of selection in Mulinia lateralis underpinning its rapid adaptation to laboratory conditions. ''Evol Appl''. 2024 Feb; '''17''' (2):e13657
Systematic identification of genotype-dependent enhancer variants in eosinophilic esophagitis. Description: Shook, Molly S, et al. Systematic identification of genotype-dependent enhancer variants in eosinophilic esophagitis. ''Am J Hum Genet''. 2024 Feb 1; '''111''' (2):280-294
The Addis Ababa Lions: Whole-Genome Sequencing of a Rare and Precious Population. Description: Barazandeh, Marjan, et al. The Addis Ababa Lions: Whole-Genome Sequencing of a Rare and Precious Population. ''Genome Biol Evol''. 2024 Feb 1; '''16''' (2):
The estimation of additive genetic variance of body size in a wild passerine is sensitive to the method used to estimate relatedness among the individuals. Description: Jablonszky, Monika, et al. The estimation of additive genetic variance of body size in a wild passerine is sensitive to the method used to estimate relatedness among the individuals. ''Ecol Evol''. 2024 Feb; '''14''' (2):e10981
The predictive capacity of polygenic risk scores for disease risk is only moderately influenced by imputation panels tailored to the target population. Description: Levi, Hagai, et al. The predictive capacity of polygenic risk scores for disease risk is only moderately influenced by imputation panels tailored to the target population. ''Bioinformatics''. 2024 Feb 1; '''40''' (2):
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder. Description: Yahia, Ashraf, et al. Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder. ''Hum Genet''. 2024 Feb; '''143''' (2):169-183
Biological basis of extensive pleiotropy between blood traits and cancer risk. Description: Pardo-Cea, Miguel Angel, et al. Biological basis of extensive pleiotropy between blood traits and cancer risk. ''Genome Med''. 2024 Feb 2; '''16''' (1):21
Dysfunction of duplicated pair rice histone acetyltransferases causes segregation distortion and an interspecific reproductive barrier. Description: Liao, Ben, et al. Dysfunction of duplicated pair rice histone acetyltransferases causes segregation distortion and an interspecific reproductive barrier. ''Nat Commun''. 2024 Feb 2; '''15''' (1):996
Evaluation of penalized and machine learning methods for asthma disease prediction in the Korean Genome and Epidemiology Study (KoGES). Description: Choi, Yongjun, et al. Evaluation of penalized and machine learning methods for asthma disease prediction in the Korean Genome and Epidemiology Study (KoGES). ''BMC Bioinformatics''. 2024 Feb 2; '''25''' (1):56
Polymorphisms in transcription factor binding sites and enhancer regions and pancreatic ductal adenocarcinoma risk. Description: Unal, Pelin, et al. Polymorphisms in transcription factor binding sites and enhancer regions and pancreatic ductal adenocarcinoma risk. ''Hum Genomics''. 2024 Feb 2; '''18''' (1):12
Exploring reciprocal causation: bidirectional mendelian randomization study of gut microbiota composition and thyroid cancer. Description: Zhou, Jiating, et al. Exploring reciprocal causation: bidirectional mendelian randomization study of gut microbiota composition and thyroid cancer. ''J Cancer Res Clin Oncol''. 2024 Feb 3; '''150''' (2):75
Genome-wide association analysis of composite sleep health scores in 413,904 individuals. Description: Goodman, Matthew O, et al. Genome-wide association analysis of composite sleep health scores in 413,904 individuals. ''medRxiv''. 2024 Feb 3;
Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. Description: Sun, Quan, et al. Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. ''Nat Commun''. 2024 Feb 3; '''15''' (1):1016
A functional genomic framework to elucidate novel causal non-alcoholic fatty liver disease genes. Description: Saliba-Gustafsson, Peter, et al. A functional genomic framework to elucidate novel causal non-alcoholic fatty liver disease genes. ''medRxiv''. 2024 Feb 4;
APOE epsilon4 and Intracerebral Hemorrhage in Patients With Brain Arteriovenous Malformation. Description: Renedo, Daniela, et al. APOE epsilon4 and Intracerebral Hemorrhage in Patients With Brain Arteriovenous Malformation. ''JAMA Netw Open''. 2024 Feb 5; '''7''' (2):e2355368
BMI and Cardiometabolic Traits in Japanese: A Mendelian Randomization Study. Description: Nagayoshi, Mako, et al. BMI and Cardiometabolic Traits in Japanese: A Mendelian Randomization Study. ''J Epidemiol''. 2024 Feb 5; '''34''' (2):51-62
Genome-Wide Interaction Study of Dietary Intake and Colorectal Cancer Risk in the UK Biobank. Description: Hoang, Tung, et al. Genome-Wide Interaction Study of Dietary Intake and Colorectal Cancer Risk in the UK Biobank. ''JAMA Netw Open''. 2024 Feb 5; '''7''' (2):e240465
Impact of individual level uncertainty of lung cancer polygenic risk score (PRS) on risk stratification. Description: Wang, Xinan, et al. Impact of individual level uncertainty of lung cancer polygenic risk score (PRS) on risk stratification. ''Genome Med''. 2024 Feb 5; '''16''' (1):22
Natural genetic variation in GLK1-mediated photosynthetic acclimation in response to light. Description: Muino, Jose M, et al. Natural genetic variation in GLK1-mediated photosynthetic acclimation in response to light. ''BMC Plant Biol''. 2024 Feb 5; '''24''' (1):87
Novel functional insights into ischemic stroke biology provided by the first genome-wide association study of stroke in indigenous Africans. Description: Akinyemi, Rufus O, et al. Novel functional insights into ischemic stroke biology provided by the first genome-wide association study of stroke in indigenous Africans. ''Genome Med''. 2024 Feb 5; '''16''' (1):25
Role of Transporters and Enzymes in Metabolism and Distribution of 4-Chlorokynurenine (AV-101). Description: Patel, Waseema, et al. Role of Transporters and Enzymes in Metabolism and Distribution of 4-Chlorokynurenine (AV-101). ''Mol Pharm''. 2024 Feb 5; '''21''' (2):550-563
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death. Description: Minnai, Francesca, et al. A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death. ''Sci Rep''. 2024 Feb 6; '''14''' (1):3000
Ancestral alleles defined for 70 million cattle variants using a population-based likelihood ratio test. Description: Dorji, Jigme, et al. Ancestral alleles defined for 70 million cattle variants using a population-based likelihood ratio test. ''Genet Sel Evol''. 2024 Feb 6; '''56''' (1):11
Identify Candidate Genes Associated with the Weight and Egg Quality Traits in Wenshui Green Shell-Laying Chickens by the Copy Number Variation-Based Genome-Wide Association Study. Description: Yang, Suozhou, et al. Identify Candidate Genes Associated with the Weight and Egg Quality Traits in Wenshui Green Shell-Laying Chickens by the Copy Number Variation-Based Genome-Wide Association Study. ''Vet Sci''. 2024 Feb 6; '''11''' (2):
Improving genetic risk modeling of dementia from real-world data in underrepresented populations. Description: Fu, Mingzhou, et al. Improving genetic risk modeling of dementia from real-world data in underrepresented populations. ''medRxiv''. 2024 Feb 6;
A cosmopolitan inversion facilitates seasonal adaptation in overwintering Drosophila. Description: Nunez, Joaquin C B, et al. A cosmopolitan inversion facilitates seasonal adaptation in overwintering Drosophila. ''Genetics''. 2024 Feb 7; '''226''' (2):
Genomic loci involved in sensing environmental cues and metabolism affect seasonal coat shedding in Bos taurus and Bos indicus cattle. Description: Durbin, Harly J, et al. Genomic loci involved in sensing environmental cues and metabolism affect seasonal coat shedding in Bos taurus and Bos indicus cattle. ''G3 (Bethesda)''. 2024 Feb 7; '''14''' (2):
Identification and validation of supervariants reveal novel loci associated with human white matter microstructure. Description: Wang, Shiying, et al. Identification and validation of supervariants reveal novel loci associated with human white matter microstructure. ''Genome Res''. 2024 Feb 7; '''34''' (1):20-33
The main genetic locus associated with the evolution of gamecocks is centered on ISPD. Description: Bendesky, Andres, et al. The main genetic locus associated with the evolution of gamecocks is centered on ISPD. ''G3 (Bethesda)''. 2024 Feb 7; '''14''' (2):
Whole genome sequencing of a family with autosomal dominant features within the oculoauriculovertebral spectrum. Description: Petrin, A L, et al. Whole genome sequencing of a family with autosomal dominant features within the oculoauriculovertebral spectrum. ''medRxiv''. 2024 Feb 7;
Attenuation of HOIL-1L ligase activity promotes systemic autoimmune disorders by augmenting linear ubiquitin signaling. Description: Fuseya, Yasuhiro, et al. Attenuation of HOIL-1L ligase activity promotes systemic autoimmune disorders by augmenting linear ubiquitin signaling. ''JCI Insight''. 2024 Feb 8; '''9''' (3):
Disease clusters subsequent to anxiety and stress-related disorders and their genetic determinants. Description: Han, Xin, et al. Disease clusters subsequent to anxiety and stress-related disorders and their genetic determinants. ''Nat Commun''. 2024 Feb 8; '''15''' (1):1209
Genetics of sleep medication purchases suggests causality from sleep problems to psychiatric traits. Description: Broberg, Martin, et al. Genetics of sleep medication purchases suggests causality from sleep problems to psychiatric traits. ''Sleep''. 2024 Feb 8; '''47''' (2):
Links between the genetic determinants of morning plasma cortisol and body shape: a two-sample Mendelian randomisation study. Description: Christakoudi, Sofia, et al. Links between the genetic determinants of morning plasma cortisol and body shape: a two-sample Mendelian randomisation study. ''Sci Rep''. 2024 Feb 8; '''14''' (1):3230
Estimating blue mussel (Mytilus edulis) connectivity and settlement capacity in mid-latitude fjord regions. Description: Corrochano-Fraile, Ana, et al. Estimating blue mussel (Mytilus edulis) connectivity and settlement capacity in mid-latitude fjord regions. ''Commun Biol''. 2024 Feb 9; '''7''' (1):166
Global diversity, recurrent evolution, and recent selection on amylase structural haplotypes in humans. Description: Bolognini, Davide, et al. Global diversity, recurrent evolution, and recent selection on amylase structural haplotypes in humans. ''bioRxiv''. 2024 Feb 9;
A graph-based pan-genome of Brassica oleracea provides new insights into its domestication and morphotype diversification. Description: Guo, Ning, et al. A graph-based pan-genome of Brassica oleracea provides new insights into its domestication and morphotype diversification. ''Plant Commun''. 2024 Feb 12; '''5''' (2):100791
Novel genetic markers for chronic kidney disease in a geographically isolated population of Indigenous Australians: Individual and multiple phenotype genome-wide association study. Description: Arunachalam, Vignesh, et al. Novel genetic markers for chronic kidney disease in a geographically isolated population of Indigenous Australians: Individual and multiple phenotype genome-wide association study. ''Genome Med''. 2024 Feb 12; '''16''' (1):29
Widespread incomplete lineage sorting and introgression shaped adaptive radiation in the Gossypium genus. Description: Xu, Yanchao, et al. Widespread incomplete lineage sorting and introgression shaped adaptive radiation in the Gossypium genus. ''Plant Commun''. 2024 Feb 12; '''5''' (2):100728
Fine-mapping genomic loci refines bipolar disorder risk genes. Description: Koromina, Maria, et al. Fine-mapping genomic loci refines bipolar disorder risk genes. ''medRxiv''. 2024 Feb 13;
Integration of risk factor polygenic risk score with disease polygenic risk score for disease prediction. Description: Jung, Hyein, et al. Integration of risk factor polygenic risk score with disease polygenic risk score for disease prediction. ''Commun Biol''. 2024 Feb 13; '''7''' (1):180
iSCORE-PD: an isogenic stem cell collection to research Parkinson's Disease. Description: Busquets, Oriol, et al. iSCORE-PD: an isogenic stem cell collection to research Parkinson's Disease. ''bioRxiv''. 2024 Feb 13;
Epiallelic variation of non-coding RNA genes and their phenotypic consequences. Description: Liu, Jie, et al. Epiallelic variation of non-coding RNA genes and their phenotypic consequences. ''Nat Commun''. 2024 Feb 14; '''15''' (1):1375
Natural selection and genetic diversity maintenance in a parasitic wasp during continuous biological control application. Description: Li, Bingyan, et al. Natural selection and genetic diversity maintenance in a parasitic wasp during continuous biological control application. ''Nat Commun''. 2024 Feb 14; '''15''' (1):1379
Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk. Description: Nakamura, Takumi, et al. Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk. ''Cell Genom''. 2024 Feb 14; '''4''' (2):100488
Evolutionary origin and distribution of amino acid mutations associated with resistance to sodium channel modulators in onion thrips, Thrips tabaci. Description: Jouraku, Akiya, et al. Evolutionary origin and distribution of amino acid mutations associated with resistance to sodium channel modulators in onion thrips, Thrips tabaci. ''Sci Rep''. 2024 Feb 15; '''14''' (1):3792
Expression quantitative trait loci analysis in rheumatoid arthritis identifies tissue specific variants associated with severity and outcome. Description: Goldmann, Katriona, et al. Expression quantitative trait loci analysis in rheumatoid arthritis identifies tissue specific variants associated with severity and outcome. ''Ann Rheum Dis''. 2024 Feb 15; '''83''' (3):288-299
Investigating the association between genetically proxied circulating levels of immune checkpoint proteins and cancer survival: protocol for a Mendelian randomisation analysis. Description: Bate, Tessa, et al. Investigating the association between genetically proxied circulating levels of immune checkpoint proteins and cancer survival: protocol for a Mendelian randomisation analysis. ''BMJ Open''. 2024 Feb 15; '''14''' (2):e075981
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis. Description: Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis. ''''. 2024 Feb 15; '''10''' (3):e24975
Polygenic effects on brain functional endophenotype for deficit and non-deficit schizophrenia. Description: Fang, Jin, et al. Polygenic effects on brain functional endophenotype for deficit and non-deficit schizophrenia. ''Schizophrenia (Heidelb)''. 2024 Feb 16; '''10''' (1):18
Proteome-wide Mendelian randomization identifies causal plasma proteins in lung cancer. Description: Li, Hongru, et al. Proteome-wide Mendelian randomization identifies causal plasma proteins in lung cancer. ''iScience''. 2024 Feb 16; '''27''' (2):108985
50,000 years of Evolutionary History of India: Insights from ~2,700 Whole Genome Sequences. Description: Kerdoncuff, Elise, et al. 50,000 years of Evolutionary History of India: Insights from ~2,700 Whole Genome Sequences. ''bioRxiv''. 2024 Feb 17;
Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes. Description: Nakamura, Wataru, et al. Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes. ''NPJ Genom Med''. 2024 Feb 17; '''9''' (1):11
Genome-wide epistasis analysis reveals gene-gene interaction network on an intermediate endophenotype P-tau/Abeta(42) ratio in ADNI cohort. Description: Zhang, Qiushi, et al. Genome-wide epistasis analysis reveals gene-gene interaction network on an intermediate endophenotype P-tau/Abeta(42) ratio in ADNI cohort. ''Sci Rep''. 2024 Feb 17; '''14''' (1):3984
Associations between gut microbiota and three prostate diseases: a bidirectional two-sample Mendelian randomization study. Description: Liu, Xiaoyang, et al. Associations between gut microbiota and three prostate diseases: a bidirectional two-sample Mendelian randomization study. ''Sci Rep''. 2024 Feb 18; '''14''' (1):4019
Shared genomic segments analysis identifies MHC class I and class III molecules as genetic risk factors for juvenile idiopathic arthritis. Description: Avery, Cecile N, et al. Shared genomic segments analysis identifies MHC class I and class III molecules as genetic risk factors for juvenile idiopathic arthritis. ''HGG Adv''. 2024 Feb 18; '''5''' (2):100277
Ancestry Specific Polygenic Risk Score, Dietary Patterns, Physical Activity, and Cardiovascular Disease. Description: Hardy, Dale, et al. Ancestry Specific Polygenic Risk Score, Dietary Patterns, Physical Activity, and Cardiovascular Disease. ''Nutrients''. 2024 Feb 19; '''16''' (4):
Genetic influences on circulating retinol and its relationship to human health. Description: Reay, William R, et al. Genetic influences on circulating retinol and its relationship to human health. ''Nat Commun''. 2024 Feb 19; '''15''' (1):1490
Genetic analysis of the X chromosome in people with Lewy body dementia nominates new risk loci. Description: Bayram, Ece, et al. Genetic analysis of the X chromosome in people with Lewy body dementia nominates new risk loci. ''NPJ Parkinsons Dis''. 2024 Feb 20; '''10''' (1):39
Genetic analysis of transcription factors in dopaminergic neuronal development in Parkinson's disease. Description: Zhao, Yuwen, et al. Genetic analysis of transcription factors in dopaminergic neuronal development in Parkinson's disease. ''Chin Med J (Engl)''. 2024 Feb 20; '''137''' (4):450-456
Host-gut microbiota interactions shape parasite infections in farmed Atlantic salmon. Description: Brealey, Jaelle C, et al. Host-gut microbiota interactions shape parasite infections in farmed Atlantic salmon. ''mSystems''. 2024 Feb 20; '''9''' (2):e0104323
Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation. Description: Lo Faro, Valeria, et al. Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation. ''Cell Rep Med''. 2024 Feb 20; '''5''' (2):101430
Complex European invasion history of Anoplophora glabripennis (Motschulsky): new insights in its population genomic differentiation using genotype-by-sequencing. Description: Haeussermann, Iris, et al. Complex European invasion history of Anoplophora glabripennis (Motschulsky): new insights in its population genomic differentiation using genotype-by-sequencing. ''Sci Rep''. 2024 Feb 21; '''14''' (1):4263
Giant pandas in captivity undergo short-term adaptation in nerve-related pathways. Description: Li, Yan, et al. Giant pandas in captivity undergo short-term adaptation in nerve-related pathways. ''BMC Zool''. 2024 Feb 21; '''9''' (1):4
Genetic Variants Linked to Myocardial Infarction in Individuals with Non-Alcoholic Fatty Liver Disease and Their Potential Interaction with Dietary Patterns. Description: Lee, Sung-Bum, et al. Genetic Variants Linked to Myocardial Infarction in Individuals with Non-Alcoholic Fatty Liver Disease and Their Potential Interaction with Dietary Patterns. ''Nutrients''. 2024 Feb 22; '''16''' (5):
Genome-wide detection of positive and balancing signatures of selection shared by four domesticated rainbow trout populations (Oncorhynchus mykiss). Description: Paul, Katy, et al. Genome-wide detection of positive and balancing signatures of selection shared by four domesticated rainbow trout populations (Oncorhynchus mykiss). ''Genet Sel Evol''. 2024 Feb 22; '''56''' (1):13
HDL levels modulate the impact of type 2 diabetes susceptibility alleles in older adults. Description: Sullivan, Siobhan O ', et al. HDL levels modulate the impact of type 2 diabetes susceptibility alleles in older adults. ''Lipids Health Dis''. 2024 Feb 22; '''23''' (1):56
Shared genetic architecture and causal relationship between sleep behaviors and lifespan. Description: Wu, Yong, et al. Shared genetic architecture and causal relationship between sleep behaviors and lifespan. ''Transl Psychiatry''. 2024 Feb 22; '''14''' (1):108
Coexpression network analysis of the adult brain sheds light on the pathogenic mechanism of DDR1 in schizophrenia and bipolar disorder. Description: Aranda, Selena, et al. Coexpression network analysis of the adult brain sheds light on the pathogenic mechanism of DDR1 in schizophrenia and bipolar disorder. ''Transl Psychiatry''. 2024 Feb 23; '''14''' (1):112
Dipterocarpoidae genomics reveal their demography and adaptations to Asian rainforests. Description: Wang, Rong, et al. Dipterocarpoidae genomics reveal their demography and adaptations to Asian rainforests. ''Nat Commun''. 2024 Feb 23; '''15''' (1):1683
Japanese wolves are most closely related to dogs and share DNA with East Eurasian dogs. Description: Gojobori, Jun, et al. Japanese wolves are most closely related to dogs and share DNA with East Eurasian dogs. ''Nat Commun''. 2024 Feb 23; '''15''' (1):1680
Metabolomic associations of impaired awareness of hypoglycaemia in type 1 diabetes. Description: Varkevisser, R D M, et al. Metabolomic associations of impaired awareness of hypoglycaemia in type 1 diabetes. ''Sci Rep''. 2024 Feb 23; '''14''' (1):4485
A distinct class of pan-cancer susceptibility genes revealed by an alternative polyadenylation transcriptome-wide association study. Description: Chen, Hui, et al. A distinct class of pan-cancer susceptibility genes revealed by an alternative polyadenylation transcriptome-wide association study. ''Nat Commun''. 2024 Feb 26; '''15''' (1):1729
The structure of psychiatric comorbidity without selection and assortative mating. Description: Ayorech, Ziada, et al. The structure of psychiatric comorbidity without selection and assortative mating. ''Transl Psychiatry''. 2024 Feb 26; '''14''' (1):121
Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression. Description: Tian, Ruoyu, et al. Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression. ''Nat Commun''. 2024 Feb 26; '''15''' (1):1755
Dissecting the genetic overlap between three complex phenotypes with trivariate MiXeR. Description: Shadrin, Alexey A, et al. Dissecting the genetic overlap between three complex phenotypes with trivariate MiXeR. ''medRxiv''. 2024 Feb 27;
Genetic variant in a BaP-activated super-enhancer increases prostate cancer risk by promoting AhR-mediated FAM227A expression. Description: Fan, Lulu, et al. Genetic variant in a BaP-activated super-enhancer increases prostate cancer risk by promoting AhR-mediated FAM227A expression. ''J Biomed Res''. 2024 Feb 27; '''38''' (2):149-162
Nightmares share genetic risk factors with sleep and psychiatric traits. Description: Ollila, Hanna M, et al. Nightmares share genetic risk factors with sleep and psychiatric traits. ''Transl Psychiatry''. 2024 Feb 27; '''14''' (1):123
Structural models of genome-wide covariance identify multiple common dimensions in autism. Description: de Hoyos, Lucia, et al. Structural models of genome-wide covariance identify multiple common dimensions in autism. ''Nat Commun''. 2024 Feb 27; '''15''' (1):1770
The SNP rs6859 in NECTIN2 gene is associated with underlying heterogeneous trajectories of cognitive changes in older adults. Description: Rajendrakumar, Aravind Lathika, et al. The SNP rs6859 in NECTIN2 gene is associated with underlying heterogeneous trajectories of cognitive changes in older adults. ''BMC Neurol''. 2024 Feb 27; '''24''' (1):78
Comprehensive whole-genome analyses of the UK Biobank reveal significant sex differences in both genotype missingness and allele frequency on the X chromosome. Description: Chen, Desmond Zeya, et al. Comprehensive whole-genome analyses of the UK Biobank reveal significant sex differences in both genotype missingness and allele frequency on the X chromosome. ''Hum Mol Genet''. 2024 Feb 28; '''33''' (6):543-551
Genetic and environmental factors driving congenital solitary functioning kidney. Description: Groen In 't Woud, Sander, et al. Genetic and environmental factors driving congenital solitary functioning kidney. ''Nephrol Dial Transplant''. 2024 Feb 28; '''39''' (3):463-472
Using clinical and genetic risk factors for risk prediction of 8 cancers in the UK Biobank. Description: Hu, Jiaqi, et al. Using clinical and genetic risk factors for risk prediction of 8 cancers in the UK Biobank. ''JNCI Cancer Spectr''. 2024 Feb 29; '''8''' (2):
A machine-learning method for biobank-scale genetic prediction of blood group antigens. Description: Hyvarinen, Kati, et al. A machine-learning method for biobank-scale genetic prediction of blood group antigens. ''PLoS Comput Biol''. 2024 Mar; '''20''' (3):e1011977
Dissection of figured wood trait in curly birch (Betula pendula Roth var. carelica (Mercklin) Hamet-Ahti) using high-throughput genotyping. Description: Gubaev, Rim, et al. Dissection of figured wood trait in curly birch (Betula pendula Roth var. carelica (Mercklin) Hamet-Ahti) using high-throughput genotyping. ''Sci Rep''. 2024 Mar 1; '''14''' (1):5058
Extreme trait GWAS (Et-GWAS): Unraveling rare variants in the 3,000 rice genome. Description: Gnanapragasam, Niranjani, et al. Extreme trait GWAS (Et-GWAS): Unraveling rare variants in the 3,000 rice genome. ''Life Sci Alliance''. 2024 Mar; '''7''' (3):
Genetically proxied PCSK9 inhibition is associated with reduced psoriatic arthritis risk. Description: Li, Junhong, et al. Genetically proxied PCSK9 inhibition is associated with reduced psoriatic arthritis risk. ''Inflamm Res''. 2024 Mar; '''73''' (3):475-484
Genetic Basis and Evolutionary Forces of Sexually Dimorphic Color Variation in a Toad-Headed Agamid Lizard. Description: Lu, Bin, et al. Genetic Basis and Evolutionary Forces of Sexually Dimorphic Color Variation in a Toad-Headed Agamid Lizard. ''Mol Biol Evol''. 2024 Mar 1; '''41''' (3):
Genetic Basis and Evolution of Structural Color Polymorphism in an Australian Songbird. Description: Sin, Simon Yung Wa, et al. Genetic Basis and Evolution of Structural Color Polymorphism in an Australian Songbird. ''Mol Biol Evol''. 2024 Mar 1; '''41''' (3):
Genetic characterization of the ALFA study: Uncovering genetic profiles in the Alzheimer's continuum. Description: Vilor-Tejedor, Natalia, et al. Genetic characterization of the ALFA study: Uncovering genetic profiles in the Alzheimer's continuum. ''Alzheimers Dement''. 2024 Mar; '''20''' (3):1703-1715
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Description: Suzuki, Ken, et al. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. ''Nature''. 2024 Mar; '''627''' (8003):347-357
Genetic risk score for Alzheimer's disease predicts brain volume differences in mid and late life in UK biobank participants. Description: Buto, Peter T, et al. Genetic risk score for Alzheimer's disease predicts brain volume differences in mid and late life in UK biobank participants. ''Alzheimers Dement''. 2024 Mar; '''20''' (3):1978-1987
Genome and GWAS analysis identified genes significantly related to phenotypic state of Rhododendron bark. Description: Ye, Qiannan, et al. Genome and GWAS analysis identified genes significantly related to phenotypic state of Rhododendron bark. ''Hortic Res''. 2024 Mar; '''11''' (3):uhae008
Genome-wide association studies identify novel loci in rapidly progressive Alzheimer's disease. Description: Wang, Ping, et al. Genome-wide association studies identify novel loci in rapidly progressive Alzheimer's disease. ''Alzheimers Dement''. 2024 Mar; '''20''' (3):2034-2046
Genome-wide association study to reveal new candidate genes using single-step approaches for productive traits of Yorkshire pig in Korea. Description: Park, Jun. Genome-wide association study to reveal new candidate genes using single-step approaches for productive traits of Yorkshire pig in Korea. ''Anim Biosci''. 2024 Mar; '''37''' (3):451-460
Genomic Analyses Capture the Human-Induced Demographic Collapse and Recovery in a Wide-Ranging Cervid. Description: Kessler, Camille, et al. Genomic Analyses Capture the Human-Induced Demographic Collapse and Recovery in a Wide-Ranging Cervid. ''Mol Biol Evol''. 2024 Mar 1; '''41''' (3):
Genomic insights into local adaptation and phenotypic diversity of Wenchang chickens. Description: Gu, Li-Hong, et al. Genomic insights into local adaptation and phenotypic diversity of Wenchang chickens. ''Poult Sci''. 2024 Mar; '''103''' (3):103376
Genomic insights into the population history and adaptive traits of Latin American Criollo cattle. Description: Ward, James A, et al. Genomic insights into the population history and adaptive traits of Latin American Criollo cattle. ''R Soc Open Sci''. 2024 Mar; '''11''' (3):231388
Germline determinants of aberrant signaling pathways in cancer. Description: Dalfovo, Davide, et al. Germline determinants of aberrant signaling pathways in cancer. ''NPJ Precis Oncol''. 2024 Mar 1; '''8''' (1):57
Identification of genomic diversity and selection signatures in Luxi cattle using whole-genome sequencing data. Description: Hu, Mingyue, et al. Identification of genomic diversity and selection signatures in Luxi cattle using whole-genome sequencing data. ''Anim Biosci''. 2024 Mar; '''37''' (3):461-470
Lung Cancer in Ever- and Never-Smokers: Findings from Multi-Population GWAS Studies. Description: Li, Yafang, et al. Lung Cancer in Ever- and Never-Smokers: Findings from Multi-Population GWAS Studies. ''Cancer Epidemiol Biomarkers Prev''. 2024 Mar 1; '''33''' (3):389-399
Natural variation in Fatty Acid 9 is a determinant of fatty acid and protein content. Description: Qi, Zhaoming, et al. Natural variation in Fatty Acid 9 is a determinant of fatty acid and protein content. ''Plant Biotechnol J''. 2024 Mar; '''22''' (3):759-773
Neuroimaging genomics as a window into the evolution of human sulcal organization. Description: Goltermann, Ole, et al. Neuroimaging genomics as a window into the evolution of human sulcal organization. ''Cereb Cortex''. 2024 Mar 1; '''34''' (3):
Optimising machine learning prediction of minimum inhibitory concentrations in Klebsiella pneumoniae. Description: Batisti Biffignandi, Gherard, et al. Optimising machine learning prediction of minimum inhibitory concentrations in Klebsiella pneumoniae. ''Microb Genom''. 2024 Mar; '''10''' (3):
OR11H1 Missense Variant Confers the Susceptibility to Vogt-Koyanagi-Harada Disease by Mediating Gadd45g Expression. Description: Li, Xingran, et al. OR11H1 Missense Variant Confers the Susceptibility to Vogt-Koyanagi-Harada Disease by Mediating Gadd45g Expression. ''Adv Sci (Weinh)''. 2024 Mar; '''11''' (11):e2306563
PAPipe: A Pipeline for Comprehensive Population Genetic Analysis. Description: Park, Nayoung, et al. PAPipe: A Pipeline for Comprehensive Population Genetic Analysis. ''Mol Biol Evol''. 2024 Mar 1; '''41''' (3):
Polygenic Risk Associations with Clinical Characteristics and Recurrence of Dupuytren Disease. Description: Riesmeijer, Sophie A, et al. Polygenic Risk Associations with Clinical Characteristics and Recurrence of Dupuytren Disease. ''Plast Reconstr Surg''. 2024 Mar 1; '''153''' (3):573e-583e
Polygenic Scores Clarify the Relationship Between Mental Health and Gender Diversity. Description: Thomas, Taylor R, et al. Polygenic Scores Clarify the Relationship Between Mental Health and Gender Diversity. ''Biol Psychiatry Glob Open Sci''. 2024 Mar; '''4''' (2):100291
Population genomic evidence of structured and connected Plasmodium vivax populations under host selection in Latin America. Description: Kattenberg, Johanna Helena, et al. Population genomic evidence of structured and connected Plasmodium vivax populations under host selection in Latin America. ''Ecol Evol''. 2024 Mar; '''14''' (3):e11103
Shared genetic architectures of educational attainment in East Asian and European populations. Description: Chen, Tzu-Ting, et al. Shared genetic architectures of educational attainment in East Asian and European populations. ''Nat Hum Behav''. 2024 Mar; '''8''' (3):562-575
Synergistic toxicity with copper contributes to NAT2-associated isoniazid toxicity. Description: Yoon, Jihoon G, et al. Synergistic toxicity with copper contributes to NAT2-associated isoniazid toxicity. ''Exp Mol Med''. 2024 Mar; '''56''' (3):570-582
Targeting postsynaptic glutamate receptor scaffolding proteins PSD-95 and PICK1 for obesity treatment. Description: Fadahunsi, Nicole, et al. Targeting postsynaptic glutamate receptor scaffolding proteins PSD-95 and PICK1 for obesity treatment. ''Sci Adv''. 2024 Mar; '''10''' (9):eadg2636
The chromosome-scale genome and population genomics reveal the adaptative evolution of Populus pruinosa to desertification environment. Description: Sun, Jianhao, et al. The chromosome-scale genome and population genomics reveal the adaptative evolution of Populus pruinosa to desertification environment. ''Hortic Res''. 2024 Mar; '''11''' (3):uhae034
The relationship between extreme inter-individual variation in macrophage gene expression and genetic susceptibility to inflammatory bowel disease. Description: O'Brien, Claire L, et al. The relationship between extreme inter-individual variation in macrophage gene expression and genetic susceptibility to inflammatory bowel disease. ''Hum Genet''. 2024 Mar; '''143''' (3):233-261
Transposable Element Insertions Are Associated with Batesian Mimicry in the Pantropical Butterfly Hypolimnas misippus. Description: Orteu, Anna, et al. Transposable Element Insertions Are Associated with Batesian Mimicry in the Pantropical Butterfly Hypolimnas misippus. ''Mol Biol Evol''. 2024 Mar 1; '''41''' (3):
Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep. Description: Liang, Benmeng, et al. Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep. ''J Adv Res''. 2024 Mar; '''57''': 1-13
Ultimate drivers of forced extra-pair copulations in birds lacking a penis: jackdaws as a case-study. Description: Hooper, Rebecca, et al. Ultimate drivers of forced extra-pair copulations in birds lacking a penis: jackdaws as a case-study. ''R Soc Open Sci''. 2024 Mar; '''11''' (3):231226
Chromosomal Inversions and the Demography of Speciation in Drosophila montana and Drosophila flavomontana. Description: Poikela, Noora, et al. Chromosomal Inversions and the Demography of Speciation in Drosophila montana and Drosophila flavomontana. ''Genome Biol Evol''. 2024 Mar 2; '''16''' (3):
Highly Resolved Genomes of Two Closely Related Lineages of the Rodent Louse Polyplax serrata with Different Host Specificities. Description: Martinu, Jana, et al. Highly Resolved Genomes of Two Closely Related Lineages of the Rodent Louse Polyplax serrata with Different Host Specificities. ''Genome Biol Evol''. 2024 Mar 2; '''16''' (3):
Metabolic syndrome risk in adult coffee drinkers with the rs301 variant of the LPL gene. Description: Hsieh, Pao-Chun, et al. Metabolic syndrome risk in adult coffee drinkers with the rs301 variant of the LPL gene. ''Nutr J''. 2024 Mar 2; '''23''' (1):30
Turnovers of Sex-Determining Mutation in the Golden Pompano and Related Species Provide Insights into Microevolution of Undifferentiated Sex Chromosome. Description: Guo, Liang, et al. Turnovers of Sex-Determining Mutation in the Golden Pompano and Related Species Provide Insights into Microevolution of Undifferentiated Sex Chromosome. ''Genome Biol Evol''. 2024 Mar 2; '''16''' (3):
Establishment and Characterization of an Epstein-Barr Virus-positive Cell Line from a Non-keratinizing Differentiated Primary Nasopharyngeal Carcinoma. Description: Chai, Annie Wai Yeeng, et al. Establishment and Characterization of an Epstein-Barr Virus-positive Cell Line from a Non-keratinizing Differentiated Primary Nasopharyngeal Carcinoma. ''Cancer Res Commun''. 2024 Mar 4; '''4''' (3):645-659
Genetic architecture of the structural connectome. Description: Wainberg, Michael, et al. Genetic architecture of the structural connectome. ''Nat Commun''. 2024 Mar 4; '''15''' (1):1962
Genome-wide diversity, population structure and signatures of inbreeding in the African buffalo in Mozambique. Description: Colangelo, Paolo, et al. Genome-wide diversity, population structure and signatures of inbreeding in the African buffalo in Mozambique. ''BMC Ecol Evol''. 2024 Mar 4; '''24''' (1):29
Long-Term Body Mass Index Variability and Adverse Cardiovascular Outcomes. Description: Almuwaqqat, Zakaria, et al. Long-Term Body Mass Index Variability and Adverse Cardiovascular Outcomes. ''JAMA Netw Open''. 2024 Mar 4; '''7''' (3):e243062
Physical Activity and Incident Obesity Across the Spectrum of Genetic Risk for Obesity. Description: Brittain, Evan L, et al. Physical Activity and Incident Obesity Across the Spectrum of Genetic Risk for Obesity. ''JAMA Netw Open''. 2024 Mar 4; '''7''' (3):e243821
An interactive atlas of genomic, proteomic, and metabolomic biomarkers promotes the potential of proteins to predict complex diseases. Description: Benson, Mikael, et al. An interactive atlas of genomic, proteomic, and metabolomic biomarkers promotes the potential of proteins to predict complex diseases. ''Res Sq''. 2024 Mar 5;
Bidirectional relationship between type 2 diabetes mellitus and coronary artery disease: Prospective cohort study and genetic analyses. Description: Zhang, Wenqiang, et al. Bidirectional relationship between type 2 diabetes mellitus and coronary artery disease: Prospective cohort study and genetic analyses. ''Chin Med J (Engl)''. 2024 Mar 5; '''137''' (5):577-587
Evaluation of the Observational Associations and Shared Genetics Between Glaucoma With Depression and Anxiety. Description: Zhang, Xiayin, et al. Evaluation of the Observational Associations and Shared Genetics Between Glaucoma With Depression and Anxiety. ''Invest Ophthalmol Vis Sci''. 2024 Mar 5; '''65''' (3):12
Genomic ancestry and social dynamics of the last hunter-gatherers of Atlantic France. Description: Simoes, Luciana G, et al. Genomic ancestry and social dynamics of the last hunter-gatherers of Atlantic France. ''Proc Natl Acad Sci U S A''. 2024 Mar 5; '''121''' (10):e2310545121
New insights into the genetic loci related to egg weight and age at first egg traits in broiler breeder. Description: Ma, Xiaochun, et al. New insights into the genetic loci related to egg weight and age at first egg traits in broiler breeder. ''Poult Sci''. 2024 Mar 5; '''103''' (5):103613
Origin and diversity of Capsella bursa-pastoris from the genomic point of view. Description: Penin, Aleksey A, et al. Origin and diversity of Capsella bursa-pastoris from the genomic point of view. ''BMC Biol''. 2024 Mar 5; '''22''' (1):52
Proteomic Associations of Adverse Outcomes in Human Heart Failure. Description: Dib, Marie-Joe, et al. Proteomic Associations of Adverse Outcomes in Human Heart Failure. ''J Am Heart Assoc''. 2024 Mar 5; '''13''' (5):e031154
Assessment of selective breeding effects and selection signatures in Qingyuan partridge chicken and its strains. Description: Kong, Shaofen, et al. Assessment of selective breeding effects and selection signatures in Qingyuan partridge chicken and its strains. ''Poult Sci''. 2024 Mar 6; '''103''' (5):103626
Deleterious phenotypes in wild Arabidopsis arenosa populations are common and linked to runs of homozygosity. Description: Barragan, A Cristina, et al. Deleterious phenotypes in wild Arabidopsis arenosa populations are common and linked to runs of homozygosity. ''G3 (Bethesda)''. 2024 Mar 6; '''14''' (3):
Differentiated adaptative genetic architecture and language-related demographical history in South China inferred from 619 genomes from 56 populations. Description: Sun, Qiuxia, et al. Differentiated adaptative genetic architecture and language-related demographical history in South China inferred from 619 genomes from 56 populations. ''BMC Biol''. 2024 Mar 6; '''22''' (1):55
Microbiome-enabled genomic selection improves prediction accuracy for nitrogen-related traits in maize. Description: Yang, Zhikai, et al. Microbiome-enabled genomic selection improves prediction accuracy for nitrogen-related traits in maize. ''G3 (Bethesda)''. 2024 Mar 6; '''14''' (3):
SNP-based and haplotype-based genome-wide association on drug dependence in Han Chinese. Description: Xu, Hanli, et al. SNP-based and haplotype-based genome-wide association on drug dependence in Han Chinese. ''BMC Genomics''. 2024 Mar 6; '''25''' (1):255
Classification of Schizophrenia, Bipolar Disorder and Major Depressive Disorder with Comorbid Traits and Deep Learning Algorithms. Description: Chen, Xiangning, et al. Classification of Schizophrenia, Bipolar Disorder and Major Depressive Disorder with Comorbid Traits and Deep Learning Algorithms. ''Res Sq''. 2024 Mar 7;
Clustering Schizophrenia Genes by Their Temporal Expression Patterns Aids Functional Interpretation. Description: van der Meer, Dennis, et al. Clustering Schizophrenia Genes by Their Temporal Expression Patterns Aids Functional Interpretation. ''Schizophr Bull''. 2024 Mar 7; '''50''' (2):327-338
Genetic parameter estimation and molecular foundation of chicken egg-laying trait. Description: Chen, Anqi, et al. Genetic parameter estimation and molecular foundation of chicken egg-laying trait. ''Poult Sci''. 2024 Mar 8; '''103''' (6):103627
Invasive fall armyworms are corn strain. Description: Durand, Karine, et al. Invasive fall armyworms are corn strain. ''Sci Rep''. 2024 Mar 8; '''14''' (1):5696
A genome-wide association study based on the China Kadoorie Biobank identifies genetic associations between snoring and cardiometabolic traits. Description: Zhu, Yunqing, et al. A genome-wide association study based on the China Kadoorie Biobank identifies genetic associations between snoring and cardiometabolic traits. ''Commun Biol''. 2024 Mar 9; '''7''' (1):305
Genomic dissection of the correlation between milk yield and various health traits using functional and evolutionary information about imputed sequence variants of 34,497 German Holstein cows. Description: Schneider, Helen, et al. Genomic dissection of the correlation between milk yield and various health traits using functional and evolutionary information about imputed sequence variants of 34,497 German Holstein cows. ''BMC Genomics''. 2024 Mar 9; '''25''' (1):265
Integration of whole-exome sequencing and structural neuroimaging analysis in major depressive disorder: a joint study. Description: Oh, Eun-Young, et al. Integration of whole-exome sequencing and structural neuroimaging analysis in major depressive disorder: a joint study. ''Transl Psychiatry''. 2024 Mar 9; '''14''' (1):141
Multivariate canonical correlation analysis identifies additional genetic variants for chronic kidney disease. Description: Osborne, Amy J, et al. Multivariate canonical correlation analysis identifies additional genetic variants for chronic kidney disease. ''NPJ Syst Biol Appl''. 2024 Mar 9; '''10''' (1):28
Genetic diversity of variants involved in drug response among Tunisian and Italian populations toward personalized medicine. Description: Jmel, Haifa, et al. Genetic diversity of variants involved in drug response among Tunisian and Italian populations toward personalized medicine. ''Sci Rep''. 2024 Mar 10; '''14''' (1):5842
Population genomic analysis unravels the evolutionary roadmap of pericarp color in rice. Description: Xie, Lingjuan, et al. Population genomic analysis unravels the evolutionary roadmap of pericarp color in rice. ''Plant Commun''. 2024 Mar 11; '''5''' (3):100778
Studying the relationship between intelligence quotient and schizophrenia polygenic scores in a family design with first-episode psychosis population. Description: Murillo-Garcia, Nancy, et al. Studying the relationship between intelligence quotient and schizophrenia polygenic scores in a family design with first-episode psychosis population. ''Eur Psychiatry''. 2024 Mar 11; '''67''' (1):e31
Investigating the Association of Polygenic Risk Scores With Thyroid Cancer Susceptibility in a Han Chinese Population. Description: Chen, Yi-Hao, et al. Investigating the Association of Polygenic Risk Scores With Thyroid Cancer Susceptibility in a Han Chinese Population. ''J Endocr Soc''. 2024 Mar 12; '''8''' (5):bvae052
Shared and distinct interactions of type 1 and type 2 Epstein-Barr Nuclear Antigen 2 with the human genome. Description: Viel, Kenyatta C M F, et al. Shared and distinct interactions of type 1 and type 2 Epstein-Barr Nuclear Antigen 2 with the human genome. ''BMC Genomics''. 2024 Mar 12; '''25''' (1):273
Ancient genomes illuminate Eastern Arabian population history and adaptation against malaria. Description: Martiniano, Rui, et al. Ancient genomes illuminate Eastern Arabian population history and adaptation against malaria. ''Cell Genom''. 2024 Mar 13; '''4''' (3):100507
Exploring the contribution of lifestyle to the impact of education on the risk of cancer through Mendelian randomization analysis. Description: Zagkos, Loukas, et al. Exploring the contribution of lifestyle to the impact of education on the risk of cancer through Mendelian randomization analysis. ''Sci Rep''. 2024 Mar 13; '''14''' (1):6074
Genome wide association study in Swedish Labrador retrievers identifies genetic loci associated with hip dysplasia and body weight. Description: Kieler, Ida Nordang, et al. Genome wide association study in Swedish Labrador retrievers identifies genetic loci associated with hip dysplasia and body weight. ''Sci Rep''. 2024 Mar 13; '''14''' (1):6090
Integrative high-throughput enhancer surveying and functional verification divulges a YY2-condensed regulatory axis conferring risk for osteoporosis. Description: Chen, Xiao-Feng, et al. Integrative high-throughput enhancer surveying and functional verification divulges a YY2-condensed regulatory axis conferring risk for osteoporosis. ''Cell Genom''. 2024 Mar 13; '''4''' (3):100501
Polygenic risk score-based phenome-wide association study of head and neck cancer across two large biobanks. Description: Lee, Young Chan, et al. Polygenic risk score-based phenome-wide association study of head and neck cancer across two large biobanks. ''BMC Med''. 2024 Mar 14; '''22''' (1):120
Altered pubertal timing in 7q11.23 copy number variations and associated genetic mechanisms. Description: Wei, Shau-Ming, et al. Altered pubertal timing in 7q11.23 copy number variations and associated genetic mechanisms. ''iScience''. 2024 Mar 15; '''27''' (3):109113
Causal relationship between particulate matter and COVID-19 risk: A mendelian randomization study. Description: Zhu, Jiayi, et al. Causal relationship between particulate matter and COVID-19 risk: A mendelian randomization study. ''Heliyon''. 2024 Mar 15; '''10''' (5):e27083
Genetic and Metabolic Characteristics of Lean Nonalcoholic Fatty Liver Disease in a Korean Health Examinee Cohort. Description: Park, Huiyul, et al. Genetic and Metabolic Characteristics of Lean Nonalcoholic Fatty Liver Disease in a Korean Health Examinee Cohort. ''Gut Liver''. 2024 Mar 15; '''18''' (2):316-327
Including microbiome information in a multi-trait genomic evaluation: a case study on longitudinal growth performance in beef cattle. Description: Martinez-Alvaro, Marina, et al. Including microbiome information in a multi-trait genomic evaluation: a case study on longitudinal growth performance in beef cattle. ''Genet Sel Evol''. 2024 Mar 15; '''56''' (1):19
A framework for conducting time-varying genome-wide association studies: An application to body mass index across childhood in six multiethnic cohorts. Description: Burrows, Kimberley, et al. A framework for conducting time-varying genome-wide association studies: An application to body mass index across childhood in six multiethnic cohorts. ''medRxiv''. 2024 Mar 16;
Is GBA1 T369M not a risk factor for Parkinson's disease in the Swedish population? Description: Brolin, Kajsa Atterling, et al. Is GBA1 T369M not a risk factor for Parkinson's disease in the Swedish population? ''medRxiv''. 2024 Mar 16;
Genetic and Environmental Factors in Autoimmune Thyroid Disease: Exploring Associations with Selenium Levels and Novel Loci in a Latvian Cohort. Description: Upmale-Engela, Sabine, et al. Genetic and Environmental Factors in Autoimmune Thyroid Disease: Exploring Associations with Selenium Levels and Novel Loci in a Latvian Cohort. ''Curr Issues Mol Biol''. 2024 Mar 17; '''46''' (3):2553-2565
Deciphering the population structure and genetic basis of growth traits from whole-genome resequencing of the leopard coral grouper ( Plectropomus leopardus). Description: Wu, Shao-Xuan, et al. Deciphering the population structure and genetic basis of growth traits from whole-genome resequencing of the leopard coral grouper ( Plectropomus leopardus). ''Zool Res''. 2024 Mar 18; '''45''' (2):329-340
Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation. Description: Theriault, Sebastien, et al. Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation. ''Nat Commun''. 2024 Mar 18; '''15''' (1):2407
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. Description: LeMaster, C, et al. Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. ''medRxiv''. 2024 Mar 18;
Iron Status and Risk of Heart Disease, Stroke, and Diabetes: A Mendelian Randomization Study in European Adults. Description: Liu, Yunan, et al. Iron Status and Risk of Heart Disease, Stroke, and Diabetes: A Mendelian Randomization Study in European Adults. ''J Am Heart Assoc''. 2024 Mar 19; '''13''' (6):e031732
The adaptation of bumblebees to extremely high elevation associated with their gut microbiota. Description: Dong, Jiu-Hong, et al. The adaptation of bumblebees to extremely high elevation associated with their gut microbiota. ''mSystems''. 2024 Mar 19; '''9''' (3):e0121923
Transcriptome data analysis provides insights into the conservation of Michelia lacei, a plant species with extremely small populations distributed in Yunnan province, China. Description: Liu, Yang, et al. Transcriptome data analysis provides insights into the conservation of Michelia lacei, a plant species with extremely small populations distributed in Yunnan province, China. ''BMC Plant Biol''. 2024 Mar 19; '''24''' (1):200
Elucidation of the genetic determination of body weight and size in Chinese local chicken breeds by large-scale genomic analyses. Description: Wang, Jie, et al. Elucidation of the genetic determination of body weight and size in Chinese local chicken breeds by large-scale genomic analyses. ''BMC Genomics''. 2024 Mar 20; '''25''' (1):296
Exploring the causal relationship between immune cells and idiopathic pulmonary fibrosis: a bi-directional Mendelian randomization study. Description: He, Zhao, et al. Exploring the causal relationship between immune cells and idiopathic pulmonary fibrosis: a bi-directional Mendelian randomization study. ''BMC Pulm Med''. 2024 Mar 20; '''24''' (1):145
Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum. Description: Venkatesh, Samvida S, et al. Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum. ''medRxiv''. 2024 Mar 20;
Pangenome-genotyped structural variation improves molecular phenotype mapping in cattle. Description: Leonard, Alexander S, et al. Pangenome-genotyped structural variation improves molecular phenotype mapping in cattle. ''Genome Res''. 2024 Mar 20; '''34''' (2):300-309
Structural and genetic diversity in the secreted mucins, MUC5AC and MUC5B. Description: Plender, Elizabeth G, et al. Structural and genetic diversity in the secreted mucins, MUC5AC and MUC5B. ''bioRxiv''. 2024 Mar 20;
Utilizing multimodal AI to improve genetic analyses of cardiovascular traits. Description: Zhou, Yuchen, et al. Utilizing multimodal AI to improve genetic analyses of cardiovascular traits. ''medRxiv''. 2024 Mar 20;
Genomic insights into shank and eggshell color in Italian local chickens. Description: Perini, Francesco, et al. Genomic insights into shank and eggshell color in Italian local chickens. ''Poult Sci''. 2024 Mar 21; '''103''' (6):103677
Human pangenome analysis of sequences missing from the reference genome reveals their widespread evolutionary, phenotypic, and functional roles. Description: Wu, Zhikun, et al. Human pangenome analysis of sequences missing from the reference genome reveals their widespread evolutionary, phenotypic, and functional roles. ''Nucleic Acids Res''. 2024 Mar 21; '''52''' (5):2212-2230
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates. Description: Viggiano, Marta, et al. Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates. ''NPJ Genom Med''. 2024 Mar 22; '''9''' (1):21
Identification and Genetic Dissection of Resistance to Red Crown Rot Disease in a Diverse Soybean Germplasm Population. Description: Antwi-Boasiako, Augustine, et al. Identification and Genetic Dissection of Resistance to Red Crown Rot Disease in a Diverse Soybean Germplasm Population. ''Plants (Basel)''. 2024 Mar 24; '''13''' (7):
Exploring Genetic Diversity within aus Rice Germplasm: Insights into the Variations in Agro-morphological Traits. Description: Sar, Puranjoy, et al. Exploring Genetic Diversity within aus Rice Germplasm: Insights into the Variations in Agro-morphological Traits. ''Rice (N Y)''. 2024 Mar 25; '''17''' (1):20
Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study. Description: Tissink, E P, et al. Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study. ''Nat Commun''. 2024 Mar 26; '''15''' (1):2655
Cross-pollination in seed-blended refuge and selection for Vip3A resistance in a lepidopteran pest as detected by genomic monitoring. Description: Pezzini, Daniela, et al. Cross-pollination in seed-blended refuge and selection for Vip3A resistance in a lepidopteran pest as detected by genomic monitoring. ''Proc Natl Acad Sci U S A''. 2024 Mar 26; '''121''' (13):e2319838121
Deciphering the Genetic Basis of Allelopathy in japonica Rice Cultivated in Temperate Regions Using a Genome-Wide Association Study. Description: Garcia-Romeral, Julia, et al. Deciphering the Genetic Basis of Allelopathy in japonica Rice Cultivated in Temperate Regions Using a Genome-Wide Association Study. ''Rice (N Y)''. 2024 Mar 26; '''17''' (1):22
Polygenic risk score for ulcerative colitis predicts immune checkpoint inhibitor-mediated colitis. Description: Middha, Pooja, et al. Polygenic risk score for ulcerative colitis predicts immune checkpoint inhibitor-mediated colitis. ''Nat Commun''. 2024 Mar 26; '''15''' (1):2568
Unveiling the Genetic Mechanism of Meat Color in Pigs through GWAS, Multi-Tissue, and Single-Cell Transcriptome Signatures Exploration. Description: Liu, Cheng, et al. Unveiling the Genetic Mechanism of Meat Color in Pigs through GWAS, Multi-Tissue, and Single-Cell Transcriptome Signatures Exploration. ''Int J Mol Sci''. 2024 Mar 26; '''25''' (7):
Using rare genetic mutations to revisit structural brain asymmetry. Description: Kopal, Jakub, et al. Using rare genetic mutations to revisit structural brain asymmetry. ''Nat Commun''. 2024 Mar 26; '''15''' (1):2639
A diverse panel of 755 bread wheat accessions harbors untapped genetic diversity in landraces and reveals novel genetic regions conferring powdery mildew resistance. Description: Leber, Rebecca, et al. A diverse panel of 755 bread wheat accessions harbors untapped genetic diversity in landraces and reveals novel genetic regions conferring powdery mildew resistance. ''Theor Appl Genet''. 2024 Mar 27; '''137''' (4):88
A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children. Description: Lin, Yu-Ping, et al. A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children. ''NPJ Sci Learn''. 2024 Mar 27; '''9''' (1):26
New role of fat-free mass in cancer risk linked with genetic predisposition. Description: Harris, Benjamin H L, et al. New role of fat-free mass in cancer risk linked with genetic predisposition. ''Sci Rep''. 2024 Mar 27; '''14''' (1):7270
Systematic immune cell dysregulation and molecular subtypes revealed by single-cell RNA-seq of subjects with type 1 diabetes. Description: Honardoost, Mohammad Amin, et al. Systematic immune cell dysregulation and molecular subtypes revealed by single-cell RNA-seq of subjects with type 1 diabetes. ''Genome Med''. 2024 Mar 27; '''16''' (1):45
Convergent Mutations and Single Nucleotide Variants in Mitochondrial Genomes of Modern Humans and Neanderthals. Description: Ferreira, Renata C, et al. Convergent Mutations and Single Nucleotide Variants in Mitochondrial Genomes of Modern Humans and Neanderthals. ''Int J Mol Sci''. 2024 Mar 28; '''25''' (7):
Genetic control of DNA methylation is largely shared across European and East Asian populations. Description: Hatton, Alesha A, et al. Genetic control of DNA methylation is largely shared across European and East Asian populations. ''Nat Commun''. 2024 Mar 28; '''15''' (1):2713
Lingo: an automated, web-based deep phenotyping platform for language ability. Description: Casten, Lucas G, et al. Lingo: an automated, web-based deep phenotyping platform for language ability. ''medRxiv''. 2024 Mar 29;
Omics-based construction of regulatory variants can be applied to help decipher pig liver-related traits. Description: Ling, Ziqi, et al. Omics-based construction of regulatory variants can be applied to help decipher pig liver-related traits. ''Commun Biol''. 2024 Mar 29; '''7''' (1):381
Three Modes of Viral Adaption by the Heart. Description: Griffiths, Cameron D, et al. Three Modes of Viral Adaption by the Heart. ''bioRxiv''. 2024 Mar 29;
Networks of gut bacteria relate to cardiovascular disease in a multi-ethnic population: the HELIUS study. Description: Warmbrunn, Moritz V, et al. Networks of gut bacteria relate to cardiovascular disease in a multi-ethnic population: the HELIUS study. ''Cardiovasc Res''. 2024 Mar 30; '''120''' (4):372-384
The Evolution, Expression Patterns, and Domestication Selection Analysis of the Annexin Gene Family in the Barley Pan-Genome. Description: Chen, Liqin, et al. The Evolution, Expression Patterns, and Domestication Selection Analysis of the Annexin Gene Family in the Barley Pan-Genome. ''Int J Mol Sci''. 2024 Mar 30; '''25''' (7):
The therapeutic landscape for COVID-19 and post-COVID-19 medications from genetic profiling of the Vietnamese population and a predictive model of drug-drug interaction for comorbid COVID-19 patients. Description: Nguyen, Thien Khac, et al. The therapeutic landscape for COVID-19 and post-COVID-19 medications from genetic profiling of the Vietnamese population and a predictive model of drug-drug interaction for comorbid COVID-19 patients. ''Heliyon''. 2024 Mar 30; '''10''' (6):e27043
Associations of measured and genetically predicted leukocyte telomere length with vascular phenotypes: a population-based study. Description: Liu, Dan, et al. Associations of measured and genetically predicted leukocyte telomere length with vascular phenotypes: a population-based study. ''Geroscience''. 2024 Apr; '''46''' (2):1947-1970
Benchmarking multi-ancestry prostate cancer polygenic risk scores in a real-world cohort. Description: Shah, Yajas, et al. Benchmarking multi-ancestry prostate cancer polygenic risk scores in a real-world cohort. ''PLoS Comput Biol''. 2024 Apr; '''20''' (4):e1011990
Better together against genetic heterogeneity: A sex-combined joint main and interaction analysis of 290 quantitative traits in the UK Biobank. Description: Lin, Boxi, et al. Better together against genetic heterogeneity: A sex-combined joint main and interaction analysis of 290 quantitative traits in the UK Biobank. ''PLoS Genet''. 2024 Apr; '''20''' (4):e1011221
Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samples. Description: Holmgren, Asbjorn, et al. Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samples. ''Mol Psychiatry''. 2024 Apr; '''29''' (4):1128-1138
Clinical and Genetic Analysis of Patients With TK2 Deficiency. Description: Ceballos, Francisco, et al. Clinical and Genetic Analysis of Patients With TK2 Deficiency. ''Neurol Genet''. 2024 Apr; '''10''' (2):e200138
Clinical and genetic determinants of vitamin D receptor expression in cutaneous melanoma patients. Description: De Smedt, Julie, et al. Clinical and genetic determinants of vitamin D receptor expression in cutaneous melanoma patients. ''Melanoma Res''. 2024 Apr 1; '''34''' (2):125-133
Diversity of salt tolerance in Vigna nakashimae, wild related species of the azuki bean (Vigna angularis). Description: Ogiso-Tanaka, Eri, et al. Diversity of salt tolerance in Vigna nakashimae, wild related species of the azuki bean (Vigna angularis). ''Breed Sci''. 2024 Apr; '''74''' (2):166-172
Does Thrombosis Play a Causal Role in Lacunar Stroke and Cerebral Small Vessel Disease? Description: Koohi, Fatemeh, et al. Does Thrombosis Play a Causal Role in Lacunar Stroke and Cerebral Small Vessel Disease? ''Stroke''. 2024 Apr; '''55''' (4):934-942
Epigenome-wide association study of DNA methylation in maternal blood leukocytes with BMI in pregnancy and gestational weight gain. Description: Opsahl, J O, et al. Epigenome-wide association study of DNA methylation in maternal blood leukocytes with BMI in pregnancy and gestational weight gain. ''Int J Obes (Lond)''. 2024 Apr; '''48''' (4):584-593
Evaluation of accuracies of genomic predictions for body conformation traits in Korean Holstein. Description: Haque, Md Azizul, et al. Evaluation of accuracies of genomic predictions for body conformation traits in Korean Holstein. ''Anim Biosci''. 2024 Apr; '''37''' (4):555-566
Genetic associations with dementia-related proteinopathy: Application of item response theory. Description: Katsumata, Yuriko, et al. Genetic associations with dementia-related proteinopathy: Application of item response theory. ''Alzheimers Dement''. 2024 Apr; '''20''' (4):2906-2921
Genetic factors influencing milk and fat yields in tropically adapted dairy cattle: insights from quantitative trait loci analysis and gene associations. Description: Laodim, Thawee, et al. Genetic factors influencing milk and fat yields in tropically adapted dairy cattle: insights from quantitative trait loci analysis and gene associations. ''Anim Biosci''. 2024 Apr; '''37''' (4):576-590
Genome-wide association and Mendelian randomisation analysis among 30,699 Chinese pregnant women identifies novel genetic and molecular risk factors for gestational diabetes and glycaemic traits. Description: Zhen, Jianxin, et al. Genome-wide association and Mendelian randomisation analysis among 30,699 Chinese pregnant women identifies novel genetic and molecular risk factors for gestational diabetes and glycaemic traits. ''Diabetologia''. 2024 Apr; '''67''' (4):703-713
Genome-wide association study of early-onset and late-onset postpartum depression: the IGEDEPP prospective study. Description: Tebeka, Sarah, et al. Genome-wide association study of early-onset and late-onset postpartum depression: the IGEDEPP prospective study. ''Eur Psychiatry''. 2024 Apr 1; '''67''' (1):1-36
Genome-wide Association Study of Susceptibility Loci for Self-Reported Atopic Dermatitis and Allergic Rhinitis in the Korean Population. Description: Kim, Jee Woo, et al. Genome-wide Association Study of Susceptibility Loci for Self-Reported Atopic Dermatitis and Allergic Rhinitis in the Korean Population. ''Ann Dermatol''. 2024 Apr; '''36''' (2):74-80
Genome-wide characterization of circulating metabolic biomarkers. Description: Karjalainen, Minna K, et al. Genome-wide characterization of circulating metabolic biomarkers. ''Nature''. 2024 Apr; '''628''' (8006):130-138
Genome-Wide Polygenic Score for Muscle Strength Predicts Risk for Common Diseases and Lifespan: A Prospective Cohort Study. Description: Herranen, Paivi, et al. Genome-Wide Polygenic Score for Muscle Strength Predicts Risk for Common Diseases and Lifespan: A Prospective Cohort Study. ''J Gerontol A Biol Sci Med Sci''. 2024 Apr 1; '''79''' (4):
Genomic analysis reveals deep population divergence in the water snake Trimerodytes percarinatus (Serpentes, Natricidae). Description: Lyu, Bing, et al. Genomic analysis reveals deep population divergence in the water snake Trimerodytes percarinatus (Serpentes, Natricidae). ''Ecol Evol''. 2024 Apr; '''14''' (4):e11278
Genomic evidence for evolutionary history and local adaptation of two endemic apricots: Prunus hongpingensis and P. zhengheensis. Description: Dai, Xiaokang, et al. Genomic evidence for evolutionary history and local adaptation of two endemic apricots: Prunus hongpingensis and P. zhengheensis. ''Hortic Res''. 2024 Apr; '''11''' (4):uhad215
Genomics of post-bottleneck recovery in the northern elephant seal. Description: Hoelzel, A Rus, et al. Genomics of post-bottleneck recovery in the northern elephant seal. ''Nat Ecol Evol''. 2024 Apr; '''8''' (4):686-694
Hybrid speciation driven by multilocus introgression of ecological traits. Description: Rosser, Neil, et al. Hybrid speciation driven by multilocus introgression of ecological traits. ''Nature''. 2024 Apr; '''628''' (8009):811-817
Integration of polygenic and gut metagenomic risk prediction for common diseases. Description: Liu, Yang, et al. Integration of polygenic and gut metagenomic risk prediction for common diseases. ''Nat Aging''. 2024 Apr; '''4''' (4):584-594
Into the Wild: A novel wild-derived inbred strain resource expands the genomic and phenotypic diversity of laboratory mouse models. Description: Dumont, Beth L, et al. Into the Wild: A novel wild-derived inbred strain resource expands the genomic and phenotypic diversity of laboratory mouse models. ''PLoS Genet''. 2024 Apr; '''20''' (4):e1011228
Levels of the HtrA1 Protein in Serum and Vitreous Humor Are Independent of Genetic Risk for Age-Related Macular Degeneration at the 10q26 Locus. Description: Williams, Brandi L, et al. Levels of the HtrA1 Protein in Serum and Vitreous Humor Are Independent of Genetic Risk for Age-Related Macular Degeneration at the 10q26 Locus. ''Invest Ophthalmol Vis Sci''. 2024 Apr 1; '''65''' (4):34
Mother's smoking habits affects IL10 methylation but not asthma in Ecuadorian children. Description: Ochoa-Aviles, Cristina, et al. Mother's smoking habits affects IL10 methylation but not asthma in Ecuadorian children. ''Mol Genet Genomic Med''. 2024 Apr; '''12''' (4):e2438
Patients with periodontitis might increase the risk of urologic cancers: a bidirectional two-sample Mendelian randomization study. Description: Li, Bojia, et al. Patients with periodontitis might increase the risk of urologic cancers: a bidirectional two-sample Mendelian randomization study. ''Int Urol Nephrol''. 2024 Apr; '''56''' (4):1243-1251
Phylogeography, origin and population structure of the self-fertile emerging plant pathogen Phytophthora pseudosyringae. Description: Mullett, Martin S, et al. Phylogeography, origin and population structure of the self-fertile emerging plant pathogen Phytophthora pseudosyringae. ''Mol Plant Pathol''. 2024 Apr; '''25''' (4):e13450
Population diversity, admixture, and demographic trend of the Sumba Ongole cattle based on genomic data. Description: Sudrajad, Pita, et al. Population diversity, admixture, and demographic trend of the Sumba Ongole cattle based on genomic data. ''Anim Biosci''. 2024 Apr; '''37''' (4):591-599
Population genomics of the white-beaked dolphin (Lagenorhynchus albirostris): Implications for conservation amid climate-driven range shifts. Description: Gose, Marc-Alexander, et al. Population genomics of the white-beaked dolphin (Lagenorhynchus albirostris): Implications for conservation amid climate-driven range shifts. ''Heredity (Edinb)''. 2024 Apr; '''132''' (4):192-201
Significant genomic introgression from grey junglefowl (Gallus sonneratii) to domestic chickens (Gallus gallus domesticus). Description: Zhao, Xiurong, et al. Significant genomic introgression from grey junglefowl (Gallus sonneratii) to domestic chickens (Gallus gallus domesticus). ''J Anim Sci Biotechnol''. 2024 Apr 1; '''15''' (1):45
SPTLC2 variants are associated with early-onset ALS and FTD due to aberrant sphingolipid synthesis. Description: Naruse, Hiroya, et al. SPTLC2 variants are associated with early-onset ALS and FTD due to aberrant sphingolipid synthesis. ''Ann Clin Transl Neurol''. 2024 Apr; '''11''' (4):946-957
The genome and population genomics of allopolyploid Coffea arabica reveal the diversification history of modern coffee cultivars. Description: Salojarvi, Jarkko, et al. The genome and population genomics of allopolyploid Coffea arabica reveal the diversification history of modern coffee cultivars. ''Nat Genet''. 2024 Apr; '''56''' (4):721-731
Using blood transcriptome analysis for Alzheimer's disease diagnosis and patient stratification. Description: Zhong, Huan, et al. Using blood transcriptome analysis for Alzheimer's disease diagnosis and patient stratification. ''Alzheimers Dement''. 2024 Apr; '''20''' (4):2469-2484
Whole genomes show contrasting trends of population size changes and genomic diversity for an Amazonian endemic passerine over the late quaternary. Description: Dalapicolla, Jeronymo, et al. Whole genomes show contrasting trends of population size changes and genomic diversity for an Amazonian endemic passerine over the late quaternary. ''Ecol Evol''. 2024 Apr; '''14''' (4):e11250
Whole genome-wide sequence analysis of long-lived families (Long-Life Family Study) identifies MTUS2 gene associated with late-onset Alzheimer's disease. Description: Xicota, Laura, et al. Whole genome-wide sequence analysis of long-lived families (Long-Life Family Study) identifies MTUS2 gene associated with late-onset Alzheimer's disease. ''Alzheimers Dement''. 2024 Apr; '''20''' (4):2670-2679
Calling Structural Variants with Confidence from Short-Read Data in Wild Bird Populations. Description: David, Gabriel, et al. Calling Structural Variants with Confidence from Short-Read Data in Wild Bird Populations. ''Genome Biol Evol''. 2024 Apr 2; '''16''' (4):
Childhood urbanicity is associated with emotional episodic memory-related striatal function and common variation in NTRK2. Description: Zhang, Xiao, et al. Childhood urbanicity is associated with emotional episodic memory-related striatal function and common variation in NTRK2. ''BMC Med''. 2024 Apr 2; '''22''' (1):146
Exome-wide analysis implicates rare protein-altering variants in human handedness. Description: Schijven, Dick, et al. Exome-wide analysis implicates rare protein-altering variants in human handedness. ''Nat Commun''. 2024 Apr 2; '''15''' (1):2632
Genetic determinants of plasma protein levels in the Estonian population. Description: Kalnapenkis, Anette, et al. Genetic determinants of plasma protein levels in the Estonian population. ''Sci Rep''. 2024 Apr 2; '''14''' (1):7694
Multiple Genomic Landscapes of Recombination and Genomic Divergence in Wild Populations of House Mice-The Role of Chromosomal Fusions and Prdm9. Description: Marin-Garcia, Cristina, et al. Multiple Genomic Landscapes of Recombination and Genomic Divergence in Wild Populations of House Mice-The Role of Chromosomal Fusions and Prdm9. ''Mol Biol Evol''. 2024 Apr 2; '''41''' (4):
Polygenic Scores and Preclinical Cardiovascular Disease in Individuals With HIV: Insights From the REPRIEVE Trial. Description: Zou, Roger S, et al. Polygenic Scores and Preclinical Cardiovascular Disease in Individuals With HIV: Insights From the REPRIEVE Trial. ''J Am Heart Assoc''. 2024 Apr 2; '''13''' (7):e033413
Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia. Description: Lokki, A, et al. Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia. ''Res Sq''. 2024 Apr 2;
scalepopgen: Bioinformatic Workflow Resources Implemented in Nextflow for Comprehensive Population Genomic Analyses. Description: Upadhyay, Maulik, et al. scalepopgen: Bioinformatic Workflow Resources Implemented in Nextflow for Comprehensive Population Genomic Analyses. ''Mol Biol Evol''. 2024 Apr 2; '''41''' (4):
Enhanced resolution profiling in twins reveals differential methylation signatures of type 2 diabetes with links to its complications. Description: Christiansen, Colette, et al. Enhanced resolution profiling in twins reveals differential methylation signatures of type 2 diabetes with links to its complications. ''EBioMedicine''. 2024 Apr 3; '''103''': 105096
Gene expression plasticity facilitates acclimatization of a long-lived Caribbean coral across divergent reef environments. Description: Castillo, Karl D, et al. Gene expression plasticity facilitates acclimatization of a long-lived Caribbean coral across divergent reef environments. ''Sci Rep''. 2024 Apr 3; '''14''' (1):7859
Genetic predisposition to childhood obesity does not influence the risk of developing skin cancer in adulthood. Description: Keatley, Jay, et al. Genetic predisposition to childhood obesity does not influence the risk of developing skin cancer in adulthood. ''Sci Rep''. 2024 Apr 3; '''14''' (1):7854
High-density genetic linkage mapping in Sitka spruce advances the integration of genomic resources in conifers. Description: Tumas, Hayley, et al. High-density genetic linkage mapping in Sitka spruce advances the integration of genomic resources in conifers. ''G3 (Bethesda)''. 2024 Apr 3; '''14''' (4):
Identification of superior and rare haplotypes to optimize branch number in soybean. Description: Yu, Hui, et al. Identification of superior and rare haplotypes to optimize branch number in soybean. ''Theor Appl Genet''. 2024 Apr 3; '''137''' (4):93
Immunogenetics of lithium response and psychiatric phenotypes in patients with bipolar disorder. Description: Herrera-Rivero, Marisol, et al. Immunogenetics of lithium response and psychiatric phenotypes in patients with bipolar disorder. ''Transl Psychiatry''. 2024 Apr 3; '''14''' (1):174
Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations. Description: Pandey, Rudra Kumar, et al. Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations. ''Sci Rep''. 2024 Apr 3; '''14''' (1):7822
Genetic Variation and Composition of Two Commercial Estonian Dairy Cattle Breeds Assessed by SNP Data. Description: Varv, Sirje, et al. Genetic Variation and Composition of Two Commercial Estonian Dairy Cattle Breeds Assessed by SNP Data. ''Animals (Basel)''. 2024 Apr 4; '''14''' (7):
Genomic Prediction of Growth Traits in Yorkshire Pigs of Different Reference Group Sizes Using Different Estimated Breeding Value Models. Description: Yin, Chang, et al. Genomic Prediction of Growth Traits in Yorkshire Pigs of Different Reference Group Sizes Using Different Estimated Breeding Value Models. ''Animals (Basel)''. 2024 Apr 4; '''14''' (7):
Human leukocyte antigen variants associate with BNT162b2 mRNA vaccine response. Description: Esposito, Martina, et al. Human leukocyte antigen variants associate with BNT162b2 mRNA vaccine response. ''Commun Med (Lond)''. 2024 Apr 4; '''4''' (1):63
Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemic. Description: Quinn, Liam, et al. Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemic. ''Am J Hum Genet''. 2024 Apr 4; '''111''' (4):668-679
The HLA region in ANCA-associated vasculitis: characterisation of genetic associations in a Scandinavian patient population. Description: Lundtoft, Christian, et al. The HLA region in ANCA-associated vasculitis: characterisation of genetic associations in a Scandinavian patient population. ''RMD Open''. 2024 Apr 4; '''10''' (2):
Adaptive functions of structural variants in human brain development. Description: Ding, Wanqiu, et al. Adaptive functions of structural variants in human brain development. ''Sci Adv''. 2024 Apr 5; '''10''' (14):eadl4600
Association of Genetic Risk for Age-Related Macular Degeneration with Morphological Features of the Retinal Microvascular Network. Description: Sendecki, Adam, et al. Association of Genetic Risk for Age-Related Macular Degeneration with Morphological Features of the Retinal Microvascular Network. ''Diagnostics (Basel)''. 2024 Apr 5; '''14''' (7):
Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China. Description: Jin, Ye, et al. Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China. ''Ital J Pediatr''. 2024 Apr 5; '''50''' (1):62
Gene specific effects on brain volume and cognition of TMEM106B in frontotemporal lobar degeneration. Description: Vandebergh, Marijne, et al. Gene specific effects on brain volume and cognition of TMEM106B in frontotemporal lobar degeneration. ''medRxiv''. 2024 Apr 5;
Identification of a novel marker and its associated laccase gene for regulating ear length in tropical and subtropical maize lines. Description: Bi, Yaqi, et al. Identification of a novel marker and its associated laccase gene for regulating ear length in tropical and subtropical maize lines. ''Theor Appl Genet''. 2024 Apr 5; '''137''' (4):94
Single-cell 'omic profiles of human aortic endothelial cells in vitro and human atherosclerotic lesions ex vivo reveal heterogeneity of endothelial subtype and response to activating perturbations. Description: Adelus, Maria L, et al. Single-cell 'omic profiles of human aortic endothelial cells in vitro and human atherosclerotic lesions ex vivo reveal heterogeneity of endothelial subtype and response to activating perturbations. ''Elife''. 2024 Apr 5; '''12''':
Variation in the mu-opioid receptor gene (OPRM1) moderates the influence of maternal sensitivity on child attachment. Description: Tchalova, K, et al. Variation in the mu-opioid receptor gene (OPRM1) moderates the influence of maternal sensitivity on child attachment. ''Transl Psychiatry''. 2024 Apr 5; '''14''' (1):181
Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medications. Description: Sadler, Marie C, et al. Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medications. ''medRxiv''. 2024 Apr 7;
A Multivariate Genome-Wide Association Study Reveals Neural Correlates and Common Biological Mechanisms of Psychopathology Spectra. Description: Davis, Christal, et al. A Multivariate Genome-Wide Association Study Reveals Neural Correlates and Common Biological Mechanisms of Psychopathology Spectra. ''Res Sq''. 2024 Apr 8;
Characterizing the polygenic overlap and shared loci between rheumatoid arthritis and cardiovascular diseases. Description: Sun, Xiaohui, et al. Characterizing the polygenic overlap and shared loci between rheumatoid arthritis and cardiovascular diseases. ''BMC Med''. 2024 Apr 8; '''22''' (1):152
Genomic and phenotypic signatures provide insights into the wide adaptation of a global plant invader. Description: Hao, Yan, et al. Genomic and phenotypic signatures provide insights into the wide adaptation of a global plant invader. ''Plant Commun''. 2024 Apr 8; '''5''' (4):100820
Oryza CLIMtools: A genome-environment association resource reveals adaptive roles for heterotrimeric G proteins in the regulation of rice agronomic traits. Description: Ferrero-Serrano, Angel, et al. Oryza CLIMtools: A genome-environment association resource reveals adaptive roles for heterotrimeric G proteins in the regulation of rice agronomic traits. ''Plant Commun''. 2024 Apr 8; '''5''' (4):100813
A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans. Description: Moksnes, Marta R, et al. A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans. ''Commun Biol''. 2024 Apr 9; '''7''' (1):432
Genetic associations of risk behaviours and educational achievement. Description: Arellano Spano, Michelle, et al. Genetic associations of risk behaviours and educational achievement. ''Commun Biol''. 2024 Apr 10; '''7''' (1):435
Genomic wide association study and selective sweep analysis identify genes associated with improved yield under drought in Turkish winter wheat germplasm. Description: Sehgal, Deepmala, et al. Genomic wide association study and selective sweep analysis identify genes associated with improved yield under drought in Turkish winter wheat germplasm. ''Sci Rep''. 2024 Apr 10; '''14''' (1):8431
Risk factors affecting polygenic score performance across diverse cohorts. Description: Hui, Daniel, et al. Risk factors affecting polygenic score performance across diverse cohorts. ''medRxiv''. 2024 Apr 10;
Genome-Wide Genetic Analysis of Dropout in a Controlled Exercise Intervention in Sedentary Adults With Overweight or Obesity and Cardiometabolic Disease. Description: Jiang, Rong, et al. Genome-Wide Genetic Analysis of Dropout in a Controlled Exercise Intervention in Sedentary Adults With Overweight or Obesity and Cardiometabolic Disease. ''Ann Behav Med''. 2024 Apr 11; '''58''' (5):363-374
Next-generation sequencing of host genetics risk factors associated with COVID-19 severity and long-COVID in Colombian population. Description: Angulo-Aguado, Mariana, et al. Next-generation sequencing of host genetics risk factors associated with COVID-19 severity and long-COVID in Colombian population. ''Sci Rep''. 2024 Apr 11; '''14''' (1):8497
Genome-wide analysis to uncover how Pocillopora acuta survives the challenging intertidal environment. Description: Poquita-Du, Rosa Celia, et al. Genome-wide analysis to uncover how Pocillopora acuta survives the challenging intertidal environment. ''Sci Rep''. 2024 Apr 12; '''14''' (1):8538
Introgression and disruption of migration routes have shaped the genetic integrity of wildebeest populations. Description: Liu, Xiaodong, et al. Introgression and disruption of migration routes have shaped the genetic integrity of wildebeest populations. ''Nat Commun''. 2024 Apr 12; '''15''' (1):2921
Population structure and identification of genomic regions associated with productive traits in five Italian beef cattle breeds. Description: Colombi, Daniele, et al. Population structure and identification of genomic regions associated with productive traits in five Italian beef cattle breeds. ''Sci Rep''. 2024 Apr 12; '''14''' (1):8529
Utility of polygenic scores across diverse diseases in a hospital cohort for predictive modeling. Description: Sun, Ting-Hsuan, et al. Utility of polygenic scores across diverse diseases in a hospital cohort for predictive modeling. ''Nat Commun''. 2024 Apr 12; '''15''' (1):3168
Human cytomegalovirus extensively re-organizes the human genome, diminishing TEAD1 transcription factor activity. Description: Sayeed, Khund, et al. Human cytomegalovirus extensively re-organizes the human genome, diminishing TEAD1 transcription factor activity. ''bioRxiv''. 2024 Apr 13;
Mendelian Randomization Analysis Identifies Inverse Causal Relationship between External Eating and Metabolic Phenotypes. Description: Timasheva, Yanina, et al. Mendelian Randomization Analysis Identifies Inverse Causal Relationship between External Eating and Metabolic Phenotypes. ''Nutrients''. 2024 Apr 13; '''16''' (8):
Functional Analysis of G6PD Variants Associated With Low G6PD Activity in the All of Us Research Program. Description: Powell, Nicholas R, et al. Functional Analysis of G6PD Variants Associated With Low G6PD Activity in the All of Us Research Program. ''medRxiv''. 2024 Apr 14;
Comparing the effect of imputation reference panel composition in four distinct Latin American cohorts. Description: French, Jennifer N, et al. Comparing the effect of imputation reference panel composition in four distinct Latin American cohorts. ''bioRxiv''. 2024 Apr 15;
Demuxafy: improvement in droplet assignment by integrating multiple single-cell demultiplexing and doublet detection methods. Description: Neavin, Drew, et al. Demuxafy: improvement in droplet assignment by integrating multiple single-cell demultiplexing and doublet detection methods. ''Genome Biol''. 2024 Apr 15; '''25''' (1):94
Efficient storage and regression computation for population-scale genome sequencing studies. Description: Rivas, Manuel A, et al. Efficient storage and regression computation for population-scale genome sequencing studies. ''bioRxiv''. 2024 Apr 15;
Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders. Description: Wigdor, Emilie M, et al. Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders. ''Sci Rep''. 2024 Apr 15; '''14''' (1):8708
Polygenic risk for suicide attempt is associated with lifetime suicide attempt in US soldiers independent of parental risk. Description: Stein, Murray B, et al. Polygenic risk for suicide attempt is associated with lifetime suicide attempt in US soldiers independent of parental risk. ''J Affect Disord''. 2024 Apr 15; '''351''': 671-682
Polygenic risk score-based phenome-wide association for glaucoma and its impact on disease susceptibility in two large biobanks. Description: Yun, Jae-Seung, et al. Polygenic risk score-based phenome-wide association for glaucoma and its impact on disease susceptibility in two large biobanks. ''J Transl Med''. 2024 Apr 15; '''22''' (1):355
Shared genetic architecture between autoimmune disorders and B-cell acute lymphoblastic leukemia: insights from large-scale genome-wide cross-trait analysis. Description: Yu, Xinghao, et al. Shared genetic architecture between autoimmune disorders and B-cell acute lymphoblastic leukemia: insights from large-scale genome-wide cross-trait analysis. ''BMC Med''. 2024 Apr 15; '''22''' (1):161
sRAGE levels are decreased in plasma and sputum of COPD secondary to biomass-burning smoke and tobacco smoking: Differences according to the rs3134940 AGER variant. Description: Fricke-Galindo, Ingrid, et al. sRAGE levels are decreased in plasma and sputum of COPD secondary to biomass-burning smoke and tobacco smoking: Differences according to the rs3134940 AGER variant. ''Heliyon''. 2024 Apr 15; '''10''' (7):e28675
Human genetic associations of the airway microbiome in chronic obstructive pulmonary disease. Description: Gao, Jingyuan, et al. Human genetic associations of the airway microbiome in chronic obstructive pulmonary disease. ''Respir Res''. 2024 Apr 16; '''25''' (1):165
Investigative power of Genomic Informational Field Theory (GIFT) relative to GWAS for genotype-phenotype mapping. Description: Kyratzi, Panagiota, et al. Investigative power of Genomic Informational Field Theory (GIFT) relative to GWAS for genotype-phenotype mapping. ''bioRxiv''. 2024 Apr 16;
Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease. Description: Kim, Kyung-Hee, et al. Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease. ''Proc Natl Acad Sci U S A''. 2024 Apr 16; '''121''' (16):e2322924121
TOPMed imputed genomics enhances genomic atlas of the human proteome in brain, cerebrospinal fluid, and plasma. Description: Yi, Heng, et al. TOPMed imputed genomics enhances genomic atlas of the human proteome in brain, cerebrospinal fluid, and plasma. ''Sci Data''. 2024 Apr 16; '''11''' (1):387
An early-onset specific polygenic risk score optimizes age-based risk estimate and stratification of prostate cancer: population-based cohort study. Description: Cheng, Yifei, et al. An early-onset specific polygenic risk score optimizes age-based risk estimate and stratification of prostate cancer: population-based cohort study. ''J Transl Med''. 2024 Apr 17; '''22''' (1):366
Genetic susceptibility to schizophrenia through neuroinflammatory pathways is associated with retinal thinning: Findings from the UK-Biobank. Description: Rabe, Finn, et al. Genetic susceptibility to schizophrenia through neuroinflammatory pathways is associated with retinal thinning: Findings from the UK-Biobank. ''medRxiv''. 2024 Apr 17;
Multi-trait GWAS for diverse ancestries: mapping the knowledge gap. Description: Troubat, Lucie, et al. Multi-trait GWAS for diverse ancestries: mapping the knowledge gap. ''BMC Genomics''. 2024 Apr 17; '''25''' (1):375
Pan-azole- and multi-fungicide-resistant Aspergillus fumigatus is widespread in the United States. Description: Celia-Sanchez, B N, et al. Pan-azole- and multi-fungicide-resistant Aspergillus fumigatus is widespread in the United States. ''Appl Environ Microbiol''. 2024 Apr 17; '''90''' (4):e0178223
Exploring the role of apolipoprotein E gene promoter polymorphisms in susceptibility to normal-tension glaucoma in a Korean population. Description: Park, Young Jun, et al. Exploring the role of apolipoprotein E gene promoter polymorphisms in susceptibility to normal-tension glaucoma in a Korean population. ''Sci Rep''. 2024 Apr 18; '''14''' (1):8972
Features Associated with Visible Lamina Cribrosa Pores in Individuals of African Ancestry with Glaucoma: Primary Open-Angle African Ancestry Glaucoma Genetics (POAAGG) Study. Description: Jordan, Jalin A, et al. Features Associated with Visible Lamina Cribrosa Pores in Individuals of African Ancestry with Glaucoma: Primary Open-Angle African Ancestry Glaucoma Genetics (POAAGG) Study. ''Vision (Basel)''. 2024 Apr 18; '''8''' (2):
Genetic and Phenotypic Profiling of Triptan Users in a Swedish Cluster Headache Cohort. Description: Jennysdotter Olofsgard, Felicia, et al. Genetic and Phenotypic Profiling of Triptan Users in a Swedish Cluster Headache Cohort. ''J Mol Neurosci''. 2024 Apr 18; '''74''' (2):45
Genetic architecture of white striping in turkeys (Meleagris gallopavo). Description: Vanderhout, Ryley J, et al. Genetic architecture of white striping in turkeys (Meleagris gallopavo). ''Sci Rep''. 2024 Apr 18; '''14''' (1):9007
Polygenic Risk Score Predicts Earlier-Onset Adult Systemic Lupus Erythematosus and First-Year Renal Diseases in a Taiwanese Cohort. Description: Chen, Yen-Ju, et al. Polygenic Risk Score Predicts Earlier-Onset Adult Systemic Lupus Erythematosus and First-Year Renal Diseases in a Taiwanese Cohort. ''RMD Open''. 2024 Apr 18; '''10''' (2):
Decoding triancestral origins, archaic introgression, and natural selection in the Japanese population by whole-genome sequencing. Description: Liu, Xiaoxi, et al. Decoding triancestral origins, archaic introgression, and natural selection in the Japanese population by whole-genome sequencing. ''Sci Adv''. 2024 Apr 19; '''10''' (16):eadi8419
Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits. Description: Song, Weichen, et al. Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits. ''Elife''. 2024 Apr 19; '''12''':
Role of Inflammation in Depressive and Anxiety Disorders, Affect, and Cognition: Genetic and Non-Genetic Findings in the Lifelines Cohort Study. Description: Giollabhui, Naoise Mac, et al. Role of Inflammation in Depressive and Anxiety Disorders, Affect, and Cognition: Genetic and Non-Genetic Findings in the Lifelines Cohort Study. ''medRxiv''. 2024 Apr 19;
Rome III Criteria Capture Higher Irritable Bowel Syndrome SNP-Heritability and Highlight a Novel Genetic Link with Cardiovascular Traits. Description: Camargo Tavares, Leticia, et al. Rome III Criteria Capture Higher Irritable Bowel Syndrome SNP-Heritability and Highlight a Novel Genetic Link with Cardiovascular Traits. ''Cell Mol Gastroenterol Hepatol''. 2024 Apr 19; '''18''' (2):101345
The Role of PNPLA3_rs738409 Gene Variant, Lifestyle Factors, and Bioactive Compounds in Nonalcoholic Fatty Liver Disease: A Population-Based and Molecular Approach towards Healthy Nutrition. Description: Liu, Meiling, et al. The Role of PNPLA3_rs738409 Gene Variant, Lifestyle Factors, and Bioactive Compounds in Nonalcoholic Fatty Liver Disease: A Population-Based and Molecular Approach towards Healthy Nutrition. ''Nutrients''. 2024 Apr 21; '''16''' (8):
An approach to identify gene-environment interactions and reveal new biological insight in complex traits. Description: Zhu, Xiaofeng, et al. An approach to identify gene-environment interactions and reveal new biological insight in complex traits. ''Nat Commun''. 2024 Apr 22; '''15''' (1):3385
Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder. Description: Khan, Hamid, et al. Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder. ''Sci Rep''. 2024 Apr 22; '''14''' (1):9230
Clinical associations with a polygenic predisposition to benign lower white blood cell counts. Description: Mosley, Jonathan D, et al. Clinical associations with a polygenic predisposition to benign lower white blood cell counts. ''Nat Commun''. 2024 Apr 22; '''15''' (1):3384
Genetic insights into agronomic and morphological traits of drug-type cannabis revealed by genome-wide association studies. Description: de Ronne, Maxime, et al. Genetic insights into agronomic and morphological traits of drug-type cannabis revealed by genome-wide association studies. ''Sci Rep''. 2024 Apr 22; '''14''' (1):9162
A genomic basis of vocal rhythm in birds. Description: Sebastianelli, Matteo, et al. A genomic basis of vocal rhythm in birds. ''Nat Commun''. 2024 Apr 23; '''15''' (1):3095
Identifying the causal relationship between immune factors and osteonecrosis: a two-sample Mendelian randomization study. Description: Wang, Chao, et al. Identifying the causal relationship between immune factors and osteonecrosis: a two-sample Mendelian randomization study. ''Sci Rep''. 2024 Apr 23; '''14''' (1):9371
Comprehensive genome assembly reveals genetic diversity and carcass consumption insights in critically endangered Asian king vultures. Description: Buthasane, Wannapol, et al. Comprehensive genome assembly reveals genetic diversity and carcass consumption insights in critically endangered Asian king vultures. ''Sci Rep''. 2024 Apr 24; '''14''' (1):9455
Integrated genome-wide association and transcriptomic analysis to identify receptor kinase genes to stripe rust resistance in wheat germplasm from southwestern China. Description: Qiao, Liang, et al. Integrated genome-wide association and transcriptomic analysis to identify receptor kinase genes to stripe rust resistance in wheat germplasm from southwestern China. ''BMC Plant Biol''. 2024 Apr 24; '''24''' (1):319
Large-scale cross-ancestry genome-wide meta-analysis of serum urate. Description: Cho, Chamlee, et al. Large-scale cross-ancestry genome-wide meta-analysis of serum urate. ''Nat Commun''. 2024 Apr 24; '''15''' (1):3441
Germline genetic regulation of the colorectal tumor immune microenvironment. Description: Schmit, Stephanie L, et al. Germline genetic regulation of the colorectal tumor immune microenvironment. ''BMC Genomics''. 2024 Apr 25; '''25''' (1):409
Inference of selective forces on house mouse genomes during secondary contact in East Asia. Description: Fujiwara, Kazumichi, et al. Inference of selective forces on house mouse genomes during secondary contact in East Asia. ''Genome Res''. 2024 Apr 25; '''34''' (3):366-375
Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection. Description: Marchal, Astrid, et al. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection. ''HGG Adv''. 2024 Apr 26; '''5''' (3):100300
A cross ancestry genetic study of psychiatric disorders from India. Description: Holla, Bharath, et al. A cross ancestry genetic study of psychiatric disorders from India. ''medRxiv''. 2024 Apr 27;
Phylogenomic analysis of the Lake Kronotskoe species flock of Dolly Varden charr reveals genetic and developmental signatures of sympatric radiation. Description: Woronowicz, Katherine C, et al. Phylogenomic analysis of the Lake Kronotskoe species flock of Dolly Varden charr reveals genetic and developmental signatures of sympatric radiation. ''bioRxiv''. 2024 Apr 27;
Genome- and epigenome-wide association studies identify susceptibility of CpG sites and regions for metabolic syndrome in a Korean population. Description: Lee, Ho-Sun, et al. Genome- and epigenome-wide association studies identify susceptibility of CpG sites and regions for metabolic syndrome in a Korean population. ''Clin Epigenetics''. 2024 Apr 29; '''16''' (1):60
Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus. Description: Elashi, Asma A, et al. Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus. ''BMC Med Genomics''. 2024 Apr 29; '''17''' (1):115
Genome-wide association study of metabolic dysfunction-associated fatty liver disease in a Korean population. Description: Lee, Young, et al. Genome-wide association study of metabolic dysfunction-associated fatty liver disease in a Korean population. ''Sci Rep''. 2024 Apr 29; '''14''' (1):9753
Mitochondrial complex I deficiency stratifies idiopathic Parkinson's disease. Description: Flones, Irene H, et al. Mitochondrial complex I deficiency stratifies idiopathic Parkinson's disease. ''Nat Commun''. 2024 Apr 29; '''15''' (1):3631
Artificial selection footprints in indigenous and commercial chicken genomes. Description: Wu, Siwen, et al. Artificial selection footprints in indigenous and commercial chicken genomes. ''BMC Genomics''. 2024 Apr 30; '''25''' (1):428
Cis-eQTLs in seven duck tissues identify novel candidate genes for growth and carcass traits. Description: Cai, Wentao, et al. Cis-eQTLs in seven duck tissues identify novel candidate genes for growth and carcass traits. ''BMC Genomics''. 2024 Apr 30; '''25''' (1):429
Heterogeneity analysis provides evidence for a genetically homogeneous subtype of bipolar-disorder. Description: McGrouther, Caroline C, et al. Heterogeneity analysis provides evidence for a genetically homogeneous subtype of bipolar-disorder. ''ArXiv''. 2024 Apr 30;
Malaria resistance-related biological adaptation and complex evolutionary footprints inferred from one integrative Tai-Kadai-related genomic resource. Description: Duan, Shuhan, et al. Malaria resistance-related biological adaptation and complex evolutionary footprints inferred from one integrative Tai-Kadai-related genomic resource. ''Heliyon''. 2024 Apr 30; '''10''' (8):e29235
Mapping seasonal migration in a songbird hybrid zone -- heritability, genetic correlations, and genomic patterns linked to speciation. Description: Justen, Hannah C, et al. Mapping seasonal migration in a songbird hybrid zone -- heritability, genetic correlations, and genomic patterns linked to speciation. ''Proc Natl Acad Sci U S A''. 2024 Apr 30; '''121''' (18):e2313442121
The Role of Genomic-Informed Risk Assessments in Predicting Dementia Outcomes. Description: Andrews, Shea J, et al. The Role of Genomic-Informed Risk Assessments in Predicting Dementia Outcomes. ''medRxiv''. 2024 Apr 30;
A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing. Description: Bjornstad, Pal Marius, et al. A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing. ''Eur J Hum Genet''. 2024 May; '''32''' (5):513-520
A comprehensive genome-wide cross-trait analysis of sexual factors and uterine leiomyoma. Description: Wu, Xueyao, et al. A comprehensive genome-wide cross-trait analysis of sexual factors and uterine leiomyoma. ''PLoS Genet''. 2024 May; '''20''' (5):e1011268
A novel approach of kinship determination based on the physical length of genetically shared regions of chromosomes. Description: Cho, Sohee, et al. A novel approach of kinship determination based on the physical length of genetically shared regions of chromosomes. ''Genes Genomics''. 2024 May; '''46''' (5):577-587
A pan-genome of 69 Arabidopsis thaliana accessions reveals a conserved genome structure throughout the global species range. Description: Lian, Qichao, et al. A pan-genome of 69 Arabidopsis thaliana accessions reveals a conserved genome structure throughout the global species range. ''Nat Genet''. 2024 May; '''56''' (5):982-991
A polygenetic risk score combined with environmental factors better predict susceptibility to hepatocellular carcinoma in Chinese population. Description: Zou, Yuanlin, et al. A polygenetic risk score combined with environmental factors better predict susceptibility to hepatocellular carcinoma in Chinese population. ''Cancer Med''. 2024 May; '''13''' (9):e7230
Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study. Description: Xu, Liyan, et al. Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study. ''Invest Ophthalmol Vis Sci''. 2024 May 1; '''65''' (5):29
Comparative assessment of the effective population size and linkage disequilibrium of Karan Fries cattle revealed viable population dynamics. Description: Bhardwaj, Shivam, et al. Comparative assessment of the effective population size and linkage disequilibrium of Karan Fries cattle revealed viable population dynamics. ''Anim Biosci''. 2024 May; '''37''' (5):795-806
Evaluation of genetic differentiation and search for candidate genes for reproductive traits in pigs. Description: Romanets, Elena, et al. Evaluation of genetic differentiation and search for candidate genes for reproductive traits in pigs. ''Anim Biosci''. 2024 May; '''37''' (5):832-838
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability. Description: Urpa, Lea, et al. Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability. ''Eur J Hum Genet''. 2024 May; '''32''' (5):576-583
Genetic evidence for the causal effects of C-reactive protein on self-reported habitual sleep duration. Description: Iakunchykova, Olena, et al. Genetic evidence for the causal effects of C-reactive protein on self-reported habitual sleep duration. ''Brain Behav Immun Health''. 2024 May; '''37''': 100754
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits. Description: Keaton, Jacob M, et al. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits. ''Nat Genet''. 2024 May; '''56''' (5):778-791
Genome-wide association study and fine-mapping on Korean biobank to discover renal trait-associated variants. Description: Lee, Dong-Jin, et al. Genome-wide association study and fine-mapping on Korean biobank to discover renal trait-associated variants. ''Kidney Res Clin Pract''. 2024 May; '''43''' (3):299-312
Genome-wide association study for bone quality of ducks during the laying period. Description: Yang, Qinglan, et al. Genome-wide association study for bone quality of ducks during the laying period. ''Poult Sci''. 2024 May; '''103''' (5):103575
*Genome-Wide Association Study Identifies IFIH1 and HLA-DQB105:02 Loci Associated With Anti-NMDAR Encephalitis.** Description: Liu, Xu, et al. Genome-Wide Association Study Identifies IFIH1 and HLA-DQB1*05:02 Loci Associated With Anti-NMDAR Encephalitis. ''Neurol Neuroimmunol Neuroinflamm''. 2024 May; '''11''' (3):e200221
Genome-wide variants and optimal allelic combinations for citric acid in tomato. Description: Gai, Wenxian, et al. Genome-wide variants and optimal allelic combinations for citric acid in tomato. ''Hortic Res''. 2024 May; '''11''' (5):uhae070
Genomic signatures of strawberry domestication and diversification. Description: Fan, Zhen, et al. Genomic signatures of strawberry domestication and diversification. ''Plant Cell''. 2024 May 1; '''36''' (5):1622-1636
Geographic variation of mutagenic exposures in kidney cancer genomes. Description: Senkin, Sergey, et al. Geographic variation of mutagenic exposures in kidney cancer genomes. ''Nature''. 2024 May; '''629''' (8013):910-918
Haplotype-resolved T2T reference genomes for wild and domesticated accessions shed new insights into the domestication of jujube. Description: Li, Kun, et al. Haplotype-resolved T2T reference genomes for wild and domesticated accessions shed new insights into the domestication of jujube. ''Hortic Res''. 2024 May; '''11''' (5):uhae071
Helicobacter pylori Treatment and Gastric Cancer Risk Among Individuals With High Genetic Risk for Gastric Cancer. Description: Xu, Heng-Min, et al. Helicobacter pylori Treatment and Gastric Cancer Risk Among Individuals With High Genetic Risk for Gastric Cancer. ''JAMA Netw Open''. 2024 May 1; '''7''' (5):e2413708
High-resolution African HLA resource uncovers HLA-DRB1 expression effects underlying vaccine response. Description: Mentzer, Alexander J, et al. High-resolution African HLA resource uncovers HLA-DRB1 expression effects underlying vaccine response. ''Nat Med''. 2024 May; '''30''' (5):1384-1394
Histologic, metabolomic, and transcriptomic differences in fir trees from a peri-urban forest under chronic ozone exposure. Description: Reyes-Galindo, Veronica, et al. Histologic, metabolomic, and transcriptomic differences in fir trees from a peri-urban forest under chronic ozone exposure. ''Ecol Evol''. 2024 May; '''14''' (5):e11343
Identification of an novel genetic variant associated with osteoporosis: insights from the Taiwan Biobank Study. Description: Liaw, Yi-Ching, et al. Identification of an novel genetic variant associated with osteoporosis: insights from the Taiwan Biobank Study. ''JBMR Plus''. 2024 May; '''8''' (5):ziae028
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Description: Ghouse, Jonas, et al. Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. ''Nat Genet''. 2024 May; '''56''' (5):827-837
Investigation of inherited noncoding genetic variation impacting the pharmacogenomics of childhood acute lymphoblastic leukemia treatment. Description: Bhattarai, Kashi Raj, et al. Investigation of inherited noncoding genetic variation impacting the pharmacogenomics of childhood acute lymphoblastic leukemia treatment. ''Nat Commun''. 2024 May 1; '''15''' (1):3681
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. Description: Zheng, Zhili, et al. Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. ''Nat Genet''. 2024 May; '''56''' (5):767-777
Meta-analysis of Epstein-Barr virus genomes in Southern Chinese identifies genetic variants and high risk viral lineage associated with nasopharyngeal carcinoma. Description: Wong, Ka Wo, et al. Meta-analysis of Epstein-Barr virus genomes in Southern Chinese identifies genetic variants and high risk viral lineage associated with nasopharyngeal carcinoma. ''PLoS Pathog''. 2024 May; '''20''' (5):e1012263
Neuroticism polygenic risk predicts conversion from mild cognitive impairment to Alzheimer's disease by impairing inferior parietal surface area. Description: Li, Qiaojun, et al. Neuroticism polygenic risk predicts conversion from mild cognitive impairment to Alzheimer's disease by impairing inferior parietal surface area. ''Hum Brain Mapp''. 2024 May; '''45''' (7):e26709
Non-linear Mendelian randomization: detection of biases using negative controls with a focus on BMI, Vitamin D and LDL cholesterol. Description: Hamilton, Fergus W, et al. Non-linear Mendelian randomization: detection of biases using negative controls with a focus on BMI, Vitamin D and LDL cholesterol. ''Eur J Epidemiol''. 2024 May; '''39''' (5):451-465
On the effect heterogeneity of established disease susceptibility loci for Alzheimer's disease across different genetic ancestries. Description: Lee, Sanghun, et al. On the effect heterogeneity of established disease susceptibility loci for Alzheimer's disease across different genetic ancestries. ''Alzheimers Dement''. 2024 May; '''20''' (5):3397-3405
Physical activity alters the effect of genetic determinants of adiposity on hypertension among individuals of European ancestry in the UKB. Description: Hezekiah, Chukwueloka, et al. Physical activity alters the effect of genetic determinants of adiposity on hypertension among individuals of European ancestry in the UKB. ''Scand J Med Sci Sports''. 2024 May; '''34''' (5):e14636
Predicting Risks of Dry Eye Disease Development Using a Genome-Wide Polygenic Risk Score Model. Description: Hsu, Chih-Chien, et al. Predicting Risks of Dry Eye Disease Development Using a Genome-Wide Polygenic Risk Score Model. ''Transl Vis Sci Technol''. 2024 May 1; '''13''' (5):13
regionalpcs: improved discovery of DNA methylation associations with complex traits. Description: Eulalio, Tiffany, et al. regionalpcs: improved discovery of DNA methylation associations with complex traits. ''bioRxiv''. 2024 May 1;
Socio-economic differences in body mass index: the contribution of genetic factors. Description: Silventoinen, Karri, et al. Socio-economic differences in body mass index: the contribution of genetic factors. ''Int J Obes (Lond)''. 2024 May; '''48''' (5):741-745
The effects of case/control ratio and sample size on genome-wide association studies: A simulation study. Description: Turgut, Ali Osman, et al. The effects of case/control ratio and sample size on genome-wide association studies: A simulation study. ''Vet Med Sci''. 2024 May; '''10''' (3):e1444
The genetic regulation of the gastric transcriptome is associated with metabolic and obesity-related traits and diseases. Description: Koebbe, Laura L, et al. The genetic regulation of the gastric transcriptome is associated with metabolic and obesity-related traits and diseases. ''Physiol Genomics''. 2024 May 1; '''56''' (5):384-396
The phylogenetic relationship and demographic history of rhesus macaques (Macaca mulatta) in subtropical and temperate regions, China. Description: Zhou, Yanyan, et al. The phylogenetic relationship and demographic history of rhesus macaques (Macaca mulatta) in subtropical and temperate regions, China. ''Ecol Evol''. 2024 May; '''14''' (5):e11429
Understanding the genomic heterogeneity of North African Imazighen: from broad to microgeographical perspectives. Description: Vila-Valls, Laura, et al. Understanding the genomic heterogeneity of North African Imazighen: from broad to microgeographical perspectives. ''Sci Rep''. 2024 May 1; '''14''' (1):9979
Expanding the repertoire reveals recurrent, cryptic, and hematopoietic HLA class I minor histocompatibility antigens. Description: Fuchs, Kyra J, et al. Expanding the repertoire reveals recurrent, cryptic, and hematopoietic HLA class I minor histocompatibility antigens. ''Blood''. 2024 May 2; '''143''' (18):1856-1872
Genetic legacy and adaptive signatures: investigating the history, diversity, and selection signatures in Rendena cattle resilient to eighteenth century rinderpest epidemics. Description: Somenzi, Elisa, et al. Genetic legacy and adaptive signatures: investigating the history, diversity, and selection signatures in Rendena cattle resilient to eighteenth century rinderpest epidemics. ''Genet Sel Evol''. 2024 May 2; '''56''' (1):32
Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis. Description: Sysojev, Anton Oberg, et al. Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis. ''Rheumatology (Oxford)''. 2024 May 2; '''63''' (5):1221-1229
History of Diversification and Adaptation from North to South Revealed by Genomic Data: Guanacos from the Desert to Sub-Antarctica. Description: Leon, Fabiola, et al. History of Diversification and Adaptation from North to South Revealed by Genomic Data: Guanacos from the Desert to Sub-Antarctica. ''Genome Biol Evol''. 2024 May 2; '''16''' (5):
Novel putative causal mutations associated with fat traits in Nellore cattle uncovered by eQTLs located in open chromatin regions. Description: Garcia, Ingrid Soares, et al. Novel putative causal mutations associated with fat traits in Nellore cattle uncovered by eQTLs located in open chromatin regions. ''Sci Rep''. 2024 May 2; '''14''' (1):10094
Opportunities for targeted therapies: trametinib as a therapeutic approach to canine oral squamous cell carcinomas. Description: Peralta, Santiago, et al. Opportunities for targeted therapies: trametinib as a therapeutic approach to canine oral squamous cell carcinomas. ''Res Sq''. 2024 May 2;
Population-specific variations in KCNH2 predispose patients to delayed ventricular repolarization upon dihydroartemisinin-piperaquine therapy. Description: Camara, Mahamadou D, et al. Population-specific variations in KCNH2 predispose patients to delayed ventricular repolarization upon dihydroartemisinin-piperaquine therapy. ''Antimicrob Agents Chemother''. 2024 May 2; '''68''' (5):e0139023
SharePro: an accurate and efficient genetic colocalization method accounting for multiple causal signals. Description: Zhang, Wenmin, et al. SharePro: an accurate and efficient genetic colocalization method accounting for multiple causal signals. ''Bioinformatics''. 2024 May 2; '''40''' (5):
A High-Coverage Mesolithic Aurochs Genome and Effective Leveraging of Ancient Cattle Genomes Using Whole Genome Imputation. Description: Erven, Jolijn A M, et al. A High-Coverage Mesolithic Aurochs Genome and Effective Leveraging of Ancient Cattle Genomes Using Whole Genome Imputation. ''Mol Biol Evol''. 2024 May 3; '''41''' (5):
Genetic Causes and Genomic Consequences of Breakdown of Distyly in Linum trigynum. Description: Gutierrez-Valencia, Juanita, et al. Genetic Causes and Genomic Consequences of Breakdown of Distyly in Linum trigynum. ''Mol Biol Evol''. 2024 May 3; '''41''' (5):
The association between single-nucleotide polymorphisms within type 1 interferon pathway genes and human immunodeficiency virus type 1 viral load in antiretroviral-naive participants. Description: Morup, Sara Bohnstedt, et al. The association between single-nucleotide polymorphisms within type 1 interferon pathway genes and human immunodeficiency virus type 1 viral load in antiretroviral-naive participants. ''AIDS Res Ther''. 2024 May 3; '''21''' (1):27
Immune cell signatures and inflammatory mediators: unraveling their genetic impact on chronic kidney disease through Mendelian randomization. Description: Hu, Yongzheng, et al. Immune cell signatures and inflammatory mediators: unraveling their genetic impact on chronic kidney disease through Mendelian randomization. ''Clin Exp Med''. 2024 May 4; '''24''' (1):94
Sex-specific circulating unconventional neutrophils determine immunological outcome of auto-inflammatory Behcet's uveitis. Description: Wang, Qingfeng, et al. Sex-specific circulating unconventional neutrophils determine immunological outcome of auto-inflammatory Behcet's uveitis. ''Cell Discov''. 2024 May 4; '''10''' (1):47
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria. Description: Ojewunmi, Oyesola O, et al. The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria. ''Hum Mol Genet''. 2024 May 4; '''33''' (10):919-929
GWAS of Folate Metabolism With Gene-environment Interaction Analysis Revealed the Possible Role of Lifestyles in the Control of Blood Folate Metabolites in Japanese: The J-MICC Study. Description: Tsukamoto, Mineko, et al. GWAS of Folate Metabolism With Gene-environment Interaction Analysis Revealed the Possible Role of Lifestyles in the Control of Blood Folate Metabolites in Japanese: The J-MICC Study. ''J Epidemiol''. 2024 May 5; '''34''' (5):228-237
Increased susceptibility to Mycobacterium avium complex infection in miniature Schnauzer dogs caused by a codon deletion in CARD9. Description: Mizukami, Keijiro, et al. Increased susceptibility to Mycobacterium avium complex infection in miniature Schnauzer dogs caused by a codon deletion in CARD9. ''Sci Rep''. 2024 May 6; '''14''' (1):10346
Detecting inbreeding depression in structured populations. Description: Lavanchy, Eleonore, et al. Detecting inbreeding depression in structured populations. ''Proc Natl Acad Sci U S A''. 2024 May 7; '''121''' (19):e2315780121
Determinants of mosaic chromosomal alteration fitness. Description: Pershad, Yash, et al. Determinants of mosaic chromosomal alteration fitness. ''Nat Commun''. 2024 May 7; '''15''' (1):3800
Development and verification of a 10K liquid chip for Hainan black goat based on genotyping by pinpoint sequencing of liquid captured targets. Description: Meng, Yong, et al. Development and verification of a 10K liquid chip for Hainan black goat based on genotyping by pinpoint sequencing of liquid captured targets. ''BMC Genom Data''. 2024 May 7; '''25''' (1):44
Genetic polymorphisms associated with adverse pregnancy outcomes in nulliparas. Description: Khan, Raiyan R, et al. Genetic polymorphisms associated with adverse pregnancy outcomes in nulliparas. ''Sci Rep''. 2024 May 7; '''14''' (1):10514
Genetic variation and pesticide exposure influence blood DNA methylation signatures in females with early-stage Parkinson's disease. Description: Schaffner, S L, et al. Genetic variation and pesticide exposure influence blood DNA methylation signatures in females with early-stage Parkinson's disease. ''NPJ Parkinsons Dis''. 2024 May 7; '''10''' (1):98
Characterizing genetic variation on the Z chromosome in Schistosoma japonicum reveals host-parasite co-evolution. Description: Zhou, An, et al. Characterizing genetic variation on the Z chromosome in Schistosoma japonicum reveals host-parasite co-evolution. ''Parasit Vectors''. 2024 May 8; '''17''' (1):207
Complementation testing identifies genes mediating effects at quantitative trait loci underlying fear-related behavior. Description: Chen, Patrick B, et al. Complementation testing identifies genes mediating effects at quantitative trait loci underlying fear-related behavior. ''Cell Genom''. 2024 May 8; '''4''' (5):100545
Distinct positions of genetic and oral histories: Perspectives from India. Description: Biddanda, Arjun, et al. Distinct positions of genetic and oral histories: Perspectives from India. ''HGG Adv''. 2024 May 8; '''5''' (3):100305
Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension. Description: Copeland, Ian, et al. Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension. ''JCI Insight''. 2024 May 8; '''9''' (9):
Exploring the genetic control of sweat gland characteristics in beef cattle for enhanced heat tolerance. Description: Hernandez, Aakilah S, et al. Exploring the genetic control of sweat gland characteristics in beef cattle for enhanced heat tolerance. ''J Anim Sci Biotechnol''. 2024 May 8; '''15''' (1):66
Genome-wide profiling of angiogenic cis-regulatory elements unravels cis-regulatory SNPs for vascular abnormality. Description: Jin, Lihui, et al. Genome-wide profiling of angiogenic cis-regulatory elements unravels cis-regulatory SNPs for vascular abnormality. ''Sci Data''. 2024 May 8; '''11''' (1):467
Transposable elements impact the population divergence of rice blast fungus Magnaporthe oryzae. Description: Lin, Lianyu, et al. Transposable elements impact the population divergence of rice blast fungus Magnaporthe oryzae. ''mBio''. 2024 May 8; '''15''' (5):e0008624
Gut microbial metabolism is linked to variations in circulating non-high density lipoprotein cholesterol. Description: Zhou, Shiyi, et al. Gut microbial metabolism is linked to variations in circulating non-high density lipoprotein cholesterol. ''EBioMedicine''. 2024 May 9; '''104''': 105150
Multiple polygenic risk scores can improve the prediction of systemic lupus erythematosus in Taiwan. Description: Chen, Yu-Chia, et al. Multiple polygenic risk scores can improve the prediction of systemic lupus erythematosus in Taiwan. ''Lupus Sci Med''. 2024 May 9; '''11''' (1):
A time-resolved multi-omics atlas of transcriptional regulation in response to high-altitude hypoxia across whole-body tissues. Description: Yan, Ze, et al. A time-resolved multi-omics atlas of transcriptional regulation in response to high-altitude hypoxia across whole-body tissues. ''Nat Commun''. 2024 May 10; '''15''' (1):3970
Combining Transdiagnostic and Disorder-Level GWAS Enhances Precision of Psychiatric Genetic Risk Profiles in a Multi-Ancestry Sample. Description: Khan, Yousef, et al. Combining Transdiagnostic and Disorder-Level GWAS Enhances Precision of Psychiatric Genetic Risk Profiles in a Multi-Ancestry Sample. ''medRxiv''. 2024 May 10;
Deciphering the causal relationship between plasma and cerebrospinal fluid metabolites and glioblastoma multiforme: a Mendelian Randomization study. Description: Zhou, Zhiwei, et al. Deciphering the causal relationship between plasma and cerebrospinal fluid metabolites and glioblastoma multiforme: a Mendelian Randomization study. ''Aging (Albany NY)''. 2024 May 10; '''16''' (9):8306-8319
Global musical diversity is largely independent of linguistic and genetic histories. Description: Passmore, Sam, et al. Global musical diversity is largely independent of linguistic and genetic histories. ''Nat Commun''. 2024 May 10; '''15''' (1):3964
Sex affects transcriptional associations with schizophrenia across the dorsolateral prefrontal cortex, hippocampus, and caudate nucleus. Description: Benjamin, Kynon J M, et al. Sex affects transcriptional associations with schizophrenia across the dorsolateral prefrontal cortex, hippocampus, and caudate nucleus. ''Nat Commun''. 2024 May 10; '''15''' (1):3980
Population genomics of the invasive Northern Giant Hornet Vespa mandarinia in North America and across its native range. Description: Taylor, Benjamin A, et al. Population genomics of the invasive Northern Giant Hornet Vespa mandarinia in North America and across its native range. ''Sci Rep''. 2024 May 11; '''14''' (1):10803
Serum urate levels and neurodegenerative outcomes: a prospective cohort study and mendelian randomization analysis of the UK Biobank. Description: Zhang, Tingjing, et al. Serum urate levels and neurodegenerative outcomes: a prospective cohort study and mendelian randomization analysis of the UK Biobank. ''Alzheimers Res Ther''. 2024 May 11; '''16''' (1):106
Sweet corn association panel and genome-wide association analysis reveal loci for chilling-tolerant germination. Description: Wu, Zhenxing, et al. Sweet corn association panel and genome-wide association analysis reveal loci for chilling-tolerant germination. ''Sci Rep''. 2024 May 11; '''14''' (1):10791
Deciphering the role of a SINE-VNTR-Alu retrotransposon polymorphism as a biomarker of Parkinson's disease progression. Description: Frohlich, Alexander, et al. Deciphering the role of a SINE-VNTR-Alu retrotransposon polymorphism as a biomarker of Parkinson's disease progression. ''Sci Rep''. 2024 May 13; '''14''' (1):10932
Dissecting the molecular basis of spike traits by integrating gene regulatory networks and genetic variation in wheat. Description: Ai, Guo, et al. Dissecting the molecular basis of spike traits by integrating gene regulatory networks and genetic variation in wheat. ''Plant Commun''. 2024 May 13; '''5''' (5):100879
Evolutionary genomics of socially polymorphic populations of Pogonomyrmex californicus. Description: Errbii, Mohammed, et al. Evolutionary genomics of socially polymorphic populations of Pogonomyrmex californicus. ''BMC Biol''. 2024 May 13; '''22''' (1):109
Genomic insights into the origin and evolution of spelt (Triticum spelta L.) as a valuable gene pool for modern wheat breeding. Description: Wang, Yongfa, et al. Genomic insights into the origin and evolution of spelt (Triticum spelta L.) as a valuable gene pool for modern wheat breeding. ''Plant Commun''. 2024 May 13; '''5''' (5):100883
Genomic regions, candidate genes, and pleiotropic variants associated with physiological and anatomical indicators of heat stress response in lactating sows. Description: de Oliveira, Leticia Fernanda, et al. Genomic regions, candidate genes, and pleiotropic variants associated with physiological and anatomical indicators of heat stress response in lactating sows. ''BMC Genomics''. 2024 May 13; '''25''' (1):467
Most Tibetan weedy barleys originated via recombination between Btr1 and Btr2 in domesticated barley. Description: Gao, Guangqi, et al. Most Tibetan weedy barleys originated via recombination between Btr1 and Btr2 in domesticated barley. ''Plant Commun''. 2024 May 13; '''5''' (5):100828
Genomic analysis uncovers novel candidate genes related to adaptation to tropical climates and milk production traits in native goats. Description: Zhang, Chenxi, et al. Genomic analysis uncovers novel candidate genes related to adaptation to tropical climates and milk production traits in native goats. ''BMC Genomics''. 2024 May 14; '''25''' (1):477
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency. Description: Zhen, Xin, et al. Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency. ''medRxiv''. 2024 May 14;
The landscape of rare genetic variation associated with inflammatory bowel disease and Parkinson's disease comorbidity. Description: Kars, Meltem Ece, et al. The landscape of rare genetic variation associated with inflammatory bowel disease and Parkinson's disease comorbidity. ''Genome Med''. 2024 May 14; '''16''' (1):66
Genetic history of esophageal cancer group in southwestern China revealed by Y-chromosome STRs and genomic evolutionary connection analysis. Description: Jia, Lihua, et al. Genetic history of esophageal cancer group in southwestern China revealed by Y-chromosome STRs and genomic evolutionary connection analysis. ''Heliyon''. 2024 May 15; '''10''' (9):e29867
Genome-wide association study reveals the candidate genes of humerus quality in laying duck. Description: Han, Xu, et al. Genome-wide association study reveals the candidate genes of humerus quality in laying duck. ''Poult Sci''. 2024 May 15; '''103''' (7):103851
Assessing the causal role of immune traits in rheumatoid arthritis by bidirectional Mendelian randomization analysis. Description: Qiu, Mingrui, et al. Assessing the causal role of immune traits in rheumatoid arthritis by bidirectional Mendelian randomization analysis. ''Aging (Albany NY)''. 2024 May 16; '''16''' (10):8687-8696
Associations between immune cell phenotypes and lung cancer subtypes: insights from mendelian randomization analysis. Description: Zheng, Jin-Min, et al. Associations between immune cell phenotypes and lung cancer subtypes: insights from mendelian randomization analysis. ''BMC Pulm Med''. 2024 May 16; '''24''' (1):242
Candidate Genes from an FDA-Approved Algorithm Fail to Predict Opioid Use Disorder Risk in Over 450,000 Veterans. Description: Davis, Christal N, et al. Candidate Genes from an FDA-Approved Algorithm Fail to Predict Opioid Use Disorder Risk in Over 450,000 Veterans. ''medRxiv''. 2024 May 16;
Genomic analysis of severe COVID-19 considering or not asthma comorbidity: GWAS insights from the BQC19 cohort. Description: Amri, Omayma, et al. Genomic analysis of severe COVID-19 considering or not asthma comorbidity: GWAS insights from the BQC19 cohort. ''BMC Genomics''. 2024 May 16; '''25''' (1):482
Identifying drug targets for schizophrenia through gene prioritization. Description: Kraft, Julia, et al. Identifying drug targets for schizophrenia through gene prioritization. ''medRxiv''. 2024 May 16;
Population genomics and epigenomics of Spirodela polyrhiza provide insights into the evolution of facultative asexuality. Description: Wang, Yangzi, et al. Population genomics and epigenomics of Spirodela polyrhiza provide insights into the evolution of facultative asexuality. ''Commun Biol''. 2024 May 16; '''7''' (1):581
Prediction models of persistent taxane-induced peripheral neuropathy among breast cancer survivors using whole-exome sequencing. Description: Engvall, Kristina, et al. Prediction models of persistent taxane-induced peripheral neuropathy among breast cancer survivors using whole-exome sequencing. ''NPJ Precis Oncol''. 2024 May 16; '''8''' (1):102
Asian-European differentiation of schizophrenia-associated genes driven by admixture and natural selection. Description: Chen, Sihan, et al. Asian-European differentiation of schizophrenia-associated genes driven by admixture and natural selection. ''iScience''. 2024 May 17; '''27''' (5):109560
Breaking down causes, consequences, and mediating effects of telomere length variation on human health. Description: Moix, Samuel, et al. Breaking down causes, consequences, and mediating effects of telomere length variation on human health. ''Genome Biol''. 2024 May 17; '''25''' (1):125
AI-enhanced integration of genetic and medical imaging data for risk assessment of Type 2 diabetes. Description: Huang, Yi-Jia, et al. AI-enhanced integration of genetic and medical imaging data for risk assessment of Type 2 diabetes. ''Nat Commun''. 2024 May 18; '''15''' (1):4230
A multi-ancestry genome-wide association study in type 1 diabetes. Description: Michalek, Dominika A, et al. A multi-ancestry genome-wide association study in type 1 diabetes. ''Hum Mol Genet''. 2024 May 18; '''33''' (11):958-968
Combining genome-wide association study and transcriptome analysis to identify molecular markers and genetic basis of population-asynchronous ovarian development in Coilia nasus. Description: Yu, Yue, et al. Combining genome-wide association study and transcriptome analysis to identify molecular markers and genetic basis of population-asynchronous ovarian development in Coilia nasus. ''Zool Res''. 2024 May 18; '''45''' (3):491-505
Variants in the MS4A cluster interact with soluble TREM2 expression on biomarkers of neuropathology. Description: Winfree, Rebecca L, et al. Variants in the MS4A cluster interact with soluble TREM2 expression on biomarkers of neuropathology. ''Mol Neurodegener''. 2024 May 18; '''19''' (1):41
A genome-wide association study identifies a locus associated with knee extension strength in older Japanese individuals. Description: Ito, Shuji, et al. A genome-wide association study identifies a locus associated with knee extension strength in older Japanese individuals. ''Commun Biol''. 2024 May 20; '''7''' (1):513
Causes and consequences of major depressive disorder: An encompassing Mendelian randomization study. Description: Pasman, Joelle A, et al. Causes and consequences of major depressive disorder: An encompassing Mendelian randomization study. ''medRxiv''. 2024 May 21;
Deep learning of left atrial structure and function provides link to atrial fibrillation risk. Description: Pirruccello, James P, et al. Deep learning of left atrial structure and function provides link to atrial fibrillation risk. ''Nat Commun''. 2024 May 21; '''15''' (1):4304
Disentangling the heterogeneity of multiple sclerosis through identification of independent neuropathological dimensions. Description: de Boer, Alyse, et al. Disentangling the heterogeneity of multiple sclerosis through identification of independent neuropathological dimensions. ''Acta Neuropathol''. 2024 May 21; '''147''' (1):90
Genome-first evaluation with exome sequence and clinical data uncovers underdiagnosed genetic disorders in a large healthcare system. Description: Forrest, Iain S, et al. Genome-first evaluation with exome sequence and clinical data uncovers underdiagnosed genetic disorders in a large healthcare system. ''Cell Rep Med''. 2024 May 21; '''5''' (5):101518
Metabolic liability for weight gain in early adulthood. Description: Murthy, Venkatesh L, et al. Metabolic liability for weight gain in early adulthood. ''Cell Rep Med''. 2024 May 21; '''5''' (5):101548
The impact of chronic pain on brain gene expression. Description: Collier, Lily, et al. The impact of chronic pain on brain gene expression. ''medRxiv''. 2024 May 21;
Far-East Asian Toxoplasma isolates share ancestry with North and South/Central American recombinant lineages. Description: Ihara, Fumiaki, et al. Far-East Asian Toxoplasma isolates share ancestry with North and South/Central American recombinant lineages. ''Nat Commun''. 2024 May 22; '''15''' (1):4278
Genome-wide analyses reveals an association between invasive urothelial carcinoma in the Shetland sheepdog and NIPAL1. Description: Parker, Heidi G, et al. Genome-wide analyses reveals an association between invasive urothelial carcinoma in the Shetland sheepdog and NIPAL1. ''NPJ Precis Oncol''. 2024 May 22; '''8''' (1):112
Integrating human endogenous retroviruses into transcriptome-wide association studies highlights novel risk factors for major psychiatric conditions. Description: Duarte, Rodrigo R R, et al. Integrating human endogenous retroviruses into transcriptome-wide association studies highlights novel risk factors for major psychiatric conditions. ''Nat Commun''. 2024 May 22; '''15''' (1):3803
Analysis of admixed Greenlandic siblings shows that the mean genotypic values for metabolic phenotypes differ between Inuit and Europeans. Description: Lin, Long, et al. Analysis of admixed Greenlandic siblings shows that the mean genotypic values for metabolic phenotypes differ between Inuit and Europeans. ''Genome Med''. 2024 May 23; '''16''' (1):71
FastBiCmrMLM: a fast and powerful compressed variance component mixed logistic model for big genomic case-control genome-wide association study. Description: Wang, Jing-Tian, et al. FastBiCmrMLM: a fast and powerful compressed variance component mixed logistic model for big genomic case-control genome-wide association study. ''Brief Bioinform''. 2024 May 23; '''25''' (4):
Genome-wide association study identifies genomic regions associated with key reproductive traits in Korean Hanwoo cows. Description: Haque, Md Azizul, et al. Genome-wide association study identifies genomic regions associated with key reproductive traits in Korean Hanwoo cows. ''BMC Genomics''. 2024 May 23; '''25''' (1):496
Genome-wide association study reveals shared and distinct genetic architecture underlying fatty acid and bioactive oxylipin metabolites in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). Description: Downie, Carolina G, et al. Genome-wide association study reveals shared and distinct genetic architecture underlying fatty acid and bioactive oxylipin metabolites in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). ''medRxiv''. 2024 May 23;
Biobank-wide association scan identifies risk factors for late-onset Alzheimer's disease and endophenotypes. Description: Yan, Donghui, et al. Biobank-wide association scan identifies risk factors for late-onset Alzheimer's disease and endophenotypes. ''Elife''. 2024 May 24; '''12''':
Causal relationship between gut microbiota and intracranial hemorrhage: A two-sample Mendelian randomization study. Description: Jia, Jiameng, et al. Causal relationship between gut microbiota and intracranial hemorrhage: A two-sample Mendelian randomization study. ''Medicine (Baltimore)''. 2024 May 24; '''103''' (21):e38275
Contrasting nidification behaviors facilitate diversification and colonization of the Music frogs under a changing paleoclimate. Description: Lyu, Zhi-Tong, et al. Contrasting nidification behaviors facilitate diversification and colonization of the Music frogs under a changing paleoclimate. ''Commun Biol''. 2024 May 25; '''7''' (1):638
Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors. Description: Olofsson, Isa Amalie, et al. Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors. ''Commun Biol''. 2024 May 27; '''7''' (1):646
Which contributes more to the relict flora distribution pattern in East Asia, geographical processes or climate change? New evidence from the phylogeography of Rehderodendron kwangtungense. Description: Jin, Jiehao, et al. Which contributes more to the relict flora distribution pattern in East Asia, geographical processes or climate change? New evidence from the phylogeography of Rehderodendron kwangtungense. ''BMC Plant Biol''. 2024 May 27; '''24''' (1):459
Whole-genome selection signature differences between Chaohu and Ji'an red ducks. Description: Lin, Ruiyi, et al. Whole-genome selection signature differences between Chaohu and Ji'an red ducks. ''BMC Genomics''. 2024 May 27; '''25''' (1):522
Long-read sequencing for 29 immune cell subsets reveals disease-linked isoforms. Description: Inamo, Jun, et al. Long-read sequencing for 29 immune cell subsets reveals disease-linked isoforms. ''Nat Commun''. 2024 May 28; '''15''' (1):4285
A polygenic score method boosted by non-additive models. Description: Ohta, Rikifumi, et al. A polygenic score method boosted by non-additive models. ''Nat Commun''. 2024 May 29; '''15''' (1):4433
Disentangling heterogeneity in substance use disorder: Insights from genome-wide polygenic scores. Description: Vilar-Ribo, Laura, et al. Disentangling heterogeneity in substance use disorder: Insights from genome-wide polygenic scores. ''Transl Psychiatry''. 2024 May 29; '''14''' (1):221
Genetic variants in C1GALT1 are associated with gastric cancer risk by influencing immune infiltration. Description: Guo, Mengfan, et al. Genetic variants in C1GALT1 are associated with gastric cancer risk by influencing immune infiltration. ''J Biomed Res''. 2024 May 29; '''38''' (4):348-357
Genetic variation of circHIBADH enhances prostate cancer risk through regulating HNRNPA1-related RNA splicing. Description: Cheng, Yifei, et al. Genetic variation of circHIBADH enhances prostate cancer risk through regulating HNRNPA1-related RNA splicing. ''J Biomed Res''. 2024 May 29; '''38''' (4):358-368
Integrative omics analysis elucidates the genetic basis underlying seed weight and oil content in soybean. Description: Yuan, Xiaobo, et al. Integrative omics analysis elucidates the genetic basis underlying seed weight and oil content in soybean. ''Plant Cell''. 2024 May 29; '''36''' (6):2160-2175
Genomic diversity of the locally developed Latvian Darkheaded sheep breed. Description: Gudra, Dita, et al. Genomic diversity of the locally developed Latvian Darkheaded sheep breed. ''Heliyon''. 2024 May 30; '''10''' (10):e31455
Pharmacogenomics of coronary artery response to intravenous gamma globulin in kawasaki disease. Description: Shrestha, Sadeep, et al. Pharmacogenomics of coronary artery response to intravenous gamma globulin in kawasaki disease. ''NPJ Genom Med''. 2024 May 30; '''9''' (1):34
LncRNA gene ANTSR coordinates complementary sex determination in the Argentine ant. Description: Pan, Qiaowei, et al. LncRNA gene ANTSR coordinates complementary sex determination in the Argentine ant. ''Sci Adv''. 2024 May 31; '''10''' (22):eadp1532
Two genome-wide interaction loci modify the association of nonsteroidal anti-inflammatory drugs with colorectal cancer. Description: Drew, David A, et al. Two genome-wide interaction loci modify the association of nonsteroidal anti-inflammatory drugs with colorectal cancer. ''Sci Adv''. 2024 May 31; '''10''' (22):eadk3121
Adaptive and Innate Immunity Are Key Drivers of Age at Onset of Multiple Sclerosis. Description: Misicka, Elina, et al. Adaptive and Innate Immunity Are Key Drivers of Age at Onset of Multiple Sclerosis. ''Neurol Genet''. 2024 Jun; '''10''' (3):e200159
A genome-wide association study of mass spectrometry proteomics using the Seer Proteograph platform. Description: Suhre, Karsten, et al. A genome-wide association study of mass spectrometry proteomics using the Seer Proteograph platform. ''bioRxiv''. 2024 Jun 1;
Analysis of gene expression in the postmortem brain of neurotypical Black Americans reveals contributions of genetic ancestry. Description: Benjamin, Kynon J M, et al. Analysis of gene expression in the postmortem brain of neurotypical Black Americans reveals contributions of genetic ancestry. ''Nat Neurosci''. 2024 Jun; '''27''' (6):1064-1074
Analysis of population structure and genetic diversity of Camellia tachangensis in Guizhou based on SNP markers. Description: Huang, Dejun, et al. Analysis of population structure and genetic diversity of Camellia tachangensis in Guizhou based on SNP markers. ''Mol Biol Rep''. 2024 Jun 1; '''51''' (1):715
Ancient genomes reveal insights into ritual life at Chichen Itza. Description: Barquera, Rodrigo, et al. Ancient genomes reveal insights into ritual life at Chichen Itza. ''Nature''. 2024 Jun; '''630''' (8018):912-919
An eQTL-based approach reveals candidate regulators of LINE-1 RNA levels in lymphoblastoid cells. Description: Bravo, Juan I, et al. An eQTL-based approach reveals candidate regulators of LINE-1 RNA levels in lymphoblastoid cells. ''PLoS Genet''. 2024 Jun; '''20''' (6):e1011311
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease? Description: Senkevich, Konstantin, et al. Are rare heterozygous SYNJ1 variants associated with Parkinson's disease? ''medRxiv''. 2024 Jun 1;
Association between rs1799724 of TNF- alpha gene and early onset preeclampsia in Chinese: A pilot study. Description: Wang, Yujie, et al. Association between rs1799724 of TNF- alpha gene and early onset preeclampsia in Chinese: A pilot study. ''Eur J Obstet Gynecol Reprod Biol X''. 2024 Jun; '''22''': 100303
A Test to Comprehensively Capture the Known Genetic Component of Familial Pulmonary Fibrosis. Description: Villeneuve, Judith, et al. A Test to Comprehensively Capture the Known Genetic Component of Familial Pulmonary Fibrosis. ''Am J Respir Cell Mol Biol''. 2024 Jun; '''70''' (6):437-445
A variant in the 5'UTR of ERBB4 is associated with lifespan in Golden Retrievers. Description: Rebhun, Robert B, et al. A variant in the 5'UTR of ERBB4 is associated with lifespan in Golden Retrievers. ''Geroscience''. 2024 Jun; '''46''' (3):2849-2862
Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry. Description: Jiang, Lan, et al. Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry. ''J Lipid Res''. 2024 Jun; '''65''' (6):100569
Chromosome-level genome assembly and population genomics reveals crucial selection for subgynoecy development in chieh-qua. Description: Wang, Min, et al. Chromosome-level genome assembly and population genomics reveals crucial selection for subgynoecy development in chieh-qua. ''Hortic Res''. 2024 Jun; '''11''' (6):uhae113
Cognitively healthy centenarians are genetically protected against Alzheimer's disease. Description: Tesi, Niccolo', et al. Cognitively healthy centenarians are genetically protected against Alzheimer's disease. ''Alzheimers Dement''. 2024 Jun; '''20''' (6):3864-3875
Combined Genetic Association and Differed Expression Analysis of UBE2L3 Uncovers a Genetic Regulatory Role of (Immuno)proteasome in IgA Nephropathy. Description: Xu, Lin-Lin, et al. Combined Genetic Association and Differed Expression Analysis of UBE2L3 Uncovers a Genetic Regulatory Role of (Immuno)proteasome in IgA Nephropathy. ''Kidney Dis (Basel)''. 2024 Jun; '''10''' (3):167-180
Comparative population genomics reveals convergent and divergent selection in the apricot-peach-plum-mei complex. Description: Yang, Xuanwen, et al. Comparative population genomics reveals convergent and divergent selection in the apricot-peach-plum-mei complex. ''Hortic Res''. 2024 Jun; '''11''' (6):uhae109
De novo assembling a high-quality genome sequence of Amur grape (Vitis amurensis Rupr.) gives insight into Vitis divergence and sex determination. Description: Wang, Pengfei, et al. De novo assembling a high-quality genome sequence of Amur grape (Vitis amurensis Rupr.) gives insight into Vitis divergence and sex determination. ''Hortic Res''. 2024 Jun; '''11''' (6):uhae117
Dynamics of cognitive variability with age and its genetic underpinning in NIHR BioResource Genes and Cognition cohort participants. Description: Rahman, Md Shafiqur, et al. Dynamics of cognitive variability with age and its genetic underpinning in NIHR BioResource Genes and Cognition cohort participants. ''Nat Med''. 2024 Jun; '''30''' (6):1739-1748
Efficient purging of deleterious mutations contributes to the survival of a rare conifer. Description: Wang, Yi, et al. Efficient purging of deleterious mutations contributes to the survival of a rare conifer. ''Hortic Res''. 2024 Jun; '''11''' (6):uhae108
Genetic parameter estimation and molecular foundation of chicken beak shape. Description: Chen, Anqi, et al. Genetic parameter estimation and molecular foundation of chicken beak shape. ''Poult Sci''. 2024 Jun; '''103''' (6):103666
Genome, HLA and polygenic risk score analyses for prevalent and persistent cervical human papillomavirus (HPV) infections. Description: Adebamowo, Sally N, et al. Genome, HLA and polygenic risk score analyses for prevalent and persistent cervical human papillomavirus (HPV) infections. ''Eur J Hum Genet''. 2024 Jun; '''32''' (6):708-716
Genome resources for three modern cotton lines guide future breeding efforts. Description: Sreedasyam, Avinash, et al. Genome resources for three modern cotton lines guide future breeding efforts. ''Nat Plants''. 2024 Jun; '''10''' (6):1039-1051
Genome wide association studies on seven yield-related traits of 183 rice varieties in Bangladesh. Description: Roy, Nilanjan, et al. Genome wide association studies on seven yield-related traits of 183 rice varieties in Bangladesh. ''Plant Direct''. 2024 Jun; '''8''' (6):e593
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Description: Schormair, Barbara, et al. Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. ''Nat Genet''. 2024 Jun; '''56''' (6):1090-1099
Genomic analyses reveal the stepwise domestication and genetic mechanism of curd biogenesis in cauliflower. Description: Chen, Rui, et al. Genomic analyses reveal the stepwise domestication and genetic mechanism of curd biogenesis in cauliflower. ''Nat Genet''. 2024 Jun; '''56''' (6):1235-1244
Genomic and Phenotypic Adaptations of Rattus tanezumi to Cold Limit Its Further Northward Expansion and Range Overlap with R. norvegicus. Description: Zhang, Ming-Yu, et al. Genomic and Phenotypic Adaptations of Rattus tanezumi to Cold Limit Its Further Northward Expansion and Range Overlap with R. norvegicus. ''Mol Biol Evol''. 2024 Jun 1; '''41''' (6):
Haplotype-resolved chromosomal-level genome assembly reveals regulatory variations in mulberry fruit anthocyanin content. Description: Xia, Zhongqiang, et al. Haplotype-resolved chromosomal-level genome assembly reveals regulatory variations in mulberry fruit anthocyanin content. ''Hortic Res''. 2024 Jun; '''11''' (6):uhae120
High-integrity Pueraria montana var. lobata genome and population analysis revealed the genetic diversity of Pueraria genus. Description: Huang, Xuan-Zhao, et al. High-integrity Pueraria montana var. lobata genome and population analysis revealed the genetic diversity of Pueraria genus. ''DNA Res''. 2024 Jun 1; '''31''' (3):
Impact of Immune Cells on Stroke Limited to Specific Subtypes: Evidence from Mendelian Randomization Study. Description: Chen, Chen, et al. Impact of Immune Cells on Stroke Limited to Specific Subtypes: Evidence from Mendelian Randomization Study. ''Neurol Ther''. 2024 Jun; '''13''' (3):599-609
Investigating shared genetic architecture between inflammatory bowel diseases and primary biliary cholangitis. Description: Huang, Wentao, et al. Investigating shared genetic architecture between inflammatory bowel diseases and primary biliary cholangitis. ''JHEP Rep''. 2024 Jun; '''6''' (6):101037
Little evidence of inbreeding depression for birth mass, survival and growth in Antarctic fur seal pups. Description: Paijmans, A J, et al. Little evidence of inbreeding depression for birth mass, survival and growth in Antarctic fur seal pups. ''Sci Rep''. 2024 Jun 1; '''14''' (1):12610
Long-term evolution of Streptococcus mitis and Streptococcus pneumoniae leads to higher genetic diversity within rather than between human populations. Description: Davison, Charlotte, et al. Long-term evolution of Streptococcus mitis and Streptococcus pneumoniae leads to higher genetic diversity within rather than between human populations. ''PLoS Genet''. 2024 Jun; '''20''' (6):e1011317
Polygenic liability for anxiety in association with comorbid anxiety in multiple sclerosis. Description: Kowalec, Kaarina, et al. Polygenic liability for anxiety in association with comorbid anxiety in multiple sclerosis. ''Ann Clin Transl Neurol''. 2024 Jun; '''11''' (6):1393-1404
Risk loci involved in giant cell arteritis susceptibility: a genome-wide association study. Description: Borrego-Yaniz, Gonzalo, et al. Risk loci involved in giant cell arteritis susceptibility: a genome-wide association study. ''Lancet Rheumatol''. 2024 Jun; '''6''' (6):e374-e383
Severe Bottleneck Impacted the Genomic Structure of Egg-Eating Cichlids in Lake Victoria. Description: Imamoto, Minami, et al. Severe Bottleneck Impacted the Genomic Structure of Egg-Eating Cichlids in Lake Victoria. ''Mol Biol Evol''. 2024 Jun 1; '''41''' (6):
Signatures of Adaptation and Purifying Selection in Highland Populations of Dasiphora fruticosa. Description: Yang, Fu-Sheng, et al. Signatures of Adaptation and Purifying Selection in Highland Populations of Dasiphora fruticosa. ''Mol Biol Evol''. 2024 Jun 1; '''41''' (6):
Spinach genomes reveal migration history and candidate genes for important crop traits. Description: Nguyen-Hoang, An, et al. Spinach genomes reveal migration history and candidate genes for important crop traits. ''NAR Genom Bioinform''. 2024 Jun; '''6''' (2):lqae034
Using parent-offspring pairs and trios to estimate indirect genetic effects in education. Description: Trindade Pons, Victoria, et al. Using parent-offspring pairs and trios to estimate indirect genetic effects in education. ''Genet Epidemiol''. 2024 Jun; '''48''' (4):190-199
Whole genome resequencing reveals genomic regions related to red plumage in ducks. Description: Zhang, Xinye, et al. Whole genome resequencing reveals genomic regions related to red plumage in ducks. ''Poult Sci''. 2024 Jun; '''103''' (6):103694
Causal impact of DNA methylation on refracture in elderly individuals with osteoporosis - a prospective cohort study. Description: Wen, Bingtao, et al. Causal impact of DNA methylation on refracture in elderly individuals with osteoporosis - a prospective cohort study. ''BMC Musculoskelet Disord''. 2024 Jun 3; '''25''' (1):432
Computing linkage disequilibrium aware genome embeddings using autoencoders. Description: Tas, Gizem, et al. Computing linkage disequilibrium aware genome embeddings using autoencoders. ''Bioinformatics''. 2024 Jun 3; '''40''' (6):
Factor analysis of lifetime psychopathology and its brain morphometric and genetic correlates in a transdiagnostic sample. Description: Krug, Axel, et al. Factor analysis of lifetime psychopathology and its brain morphometric and genetic correlates in a transdiagnostic sample. ''Transl Psychiatry''. 2024 Jun 3; '''14''' (1):235
Systems genomics of salinity stress response in rice. Description: Gupta, Sonal, et al. Systems genomics of salinity stress response in rice. ''bioRxiv''. 2024 Jun 3;
Transcription factor binding site divergence across maize inbred lines drives transcriptional and phenotypic variation. Description: Galli, Mary, et al. Transcription factor binding site divergence across maize inbred lines drives transcriptional and phenotypic variation. ''bioRxiv''. 2024 Jun 3;
Ancient Sheep Genomes Reveal Four Millennia of North European Short-Tailed Sheep in the Baltic Sea Region. Description: Larsson, Martin N A, et al. Ancient Sheep Genomes Reveal Four Millennia of North European Short-Tailed Sheep in the Baltic Sea Region. ''Genome Biol Evol''. 2024 Jun 4; '''16''' (6):
Optimizing clinico-genomic disease prediction across ancestries: a machine learning strategy with Pareto improvement. Description: Gao, Yan, et al. Optimizing clinico-genomic disease prediction across ancestries: a machine learning strategy with Pareto improvement. ''Genome Med''. 2024 Jun 4; '''16''' (1):76
Risk of diabetes mellitus based on the interactive association between G6PD rs72554664 polymorphism and sex in Taiwan Biobank individuals. Description: Chang, Yen-Lin, et al. Risk of diabetes mellitus based on the interactive association between G6PD rs72554664 polymorphism and sex in Taiwan Biobank individuals. ''Sci Rep''. 2024 Jun 4; '''14''' (1):12802
A high-density linkage map and sex-determination loci in Pacific white shrimp (Litopenaeus vannamei). Description: Garcia, Baltasar F, et al. A high-density linkage map and sex-determination loci in Pacific white shrimp (Litopenaeus vannamei). ''BMC Genomics''. 2024 Jun 5; '''25''' (1):565
A naturally occurring canine model of syndromic congenital microphthalmia. Description: Murgiano, Leonardo, et al. A naturally occurring canine model of syndromic congenital microphthalmia. ''G3 (Bethesda)''. 2024 Jun 5; '''14''' (6):
Genome-wide analysis reveals genomic diversity and signatures of selection in Qinchuan beef cattle. Description: Yu, Hengwei, et al. Genome-wide analysis reveals genomic diversity and signatures of selection in Qinchuan beef cattle. ''BMC Genomics''. 2024 Jun 5; '''25''' (1):558
Novel early-onset Alzheimer-associated genes influence risk through dysregulation of glutamate, immune activation, and intracell signaling pathways. Description: Cruchaga, Carlos, et al. Novel early-onset Alzheimer-associated genes influence risk through dysregulation of glutamate, immune activation, and intracell signaling pathways. ''Res Sq''. 2024 Jun 5;
Robustness in population-structure and demographic-inference results derived from the Aedes aegypti genotyping chip and whole-genome sequencing data. Description: Gomez-Palacio, Andres, et al. Robustness in population-structure and demographic-inference results derived from the Aedes aegypti genotyping chip and whole-genome sequencing data. ''G3 (Bethesda)''. 2024 Jun 5; '''14''' (6):
The Human Genetic Differences in the Outcomes of mRNA Vaccination against COVID-19: A Prospective Cohort Study. Description: Ryu, Ha-Eun, et al. The Human Genetic Differences in the Outcomes of mRNA Vaccination against COVID-19: A Prospective Cohort Study. ''Vaccines (Basel)''. 2024 Jun 5; '''12''' (6):
Genome wide association study and genomic risk prediction of age related macular degeneration in Israel. Description: Grunin, Michelle, et al. Genome wide association study and genomic risk prediction of age related macular degeneration in Israel. ''Sci Rep''. 2024 Jun 6; '''14''' (1):13034
Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents. Description: She, Chun Hing, et al. Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents. ''BMC Genom Data''. 2024 Jun 6; '''25''' (1):51
Genomics of hybrid parallel origin in Aquilegia ecalcarata. Description: Geng, Fang-Dong, et al. Genomics of hybrid parallel origin in Aquilegia ecalcarata. ''BMC Ecol Evol''. 2024 Jun 6; '''24''' (1):75
Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variation. Description: Xu, Zhi Ming, et al. Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variation. ''Am J Hum Genet''. 2024 Jun 6; '''111''' (6):1018-1034
Oral and non-oral lichen planus show genetic heterogeneity and differential risk for autoimmune disease and oral cancer. Description: Reeve, Mary Pat, et al. Oral and non-oral lichen planus show genetic heterogeneity and differential risk for autoimmune disease and oral cancer. ''Am J Hum Genet''. 2024 Jun 6; '''111''' (6):1047-1060
shaPRS: Leveraging shared genetic effects across traits or ancestries improves accuracy of polygenic scores. Description: Kelemen, Martin, et al. shaPRS: Leveraging shared genetic effects across traits or ancestries improves accuracy of polygenic scores. ''Am J Hum Genet''. 2024 Jun 6; '''111''' (6):1006-1017
Unveiling genetic signatures associated with resilience to neonatal diarrhea in lambs through two GWAS approaches. Description: Yaman, Yalcin, et al. Unveiling genetic signatures associated with resilience to neonatal diarrhea in lambs through two GWAS approaches. ''Sci Rep''. 2024 Jun 6; '''14''' (1):13072
A genome-wide association study reveals a polygenic architecture of speech-in-noise deficits in individuals with self-reported normal hearing. Description: Bhatt, Ishan Sunilkumar, et al. A genome-wide association study reveals a polygenic architecture of speech-in-noise deficits in individuals with self-reported normal hearing. ''Sci Rep''. 2024 Jun 7; '''14''' (1):13089
Cancer risks among first-degree relatives of women with a genetic predisposition to breast cancer. Description: Xiao, Qingyang, et al. Cancer risks among first-degree relatives of women with a genetic predisposition to breast cancer. ''J Natl Cancer Inst''. 2024 Jun 7; '''116''' (6):911-919
Family-based GWAS for dental class I malocclusion and clefts. Description: Bezamat, Mariana, et al. Family-based GWAS for dental class I malocclusion and clefts. ''BMC Oral Health''. 2024 Jun 7; '''24''' (1):665
Genome-wide association study of glucocerebrosidase activity modifiers. Description: Somerville, Emma N, et al. Genome-wide association study of glucocerebrosidase activity modifiers. ''Res Sq''. 2024 Jun 7;
Genome-wide determinants of mortality and motor progression in Parkinson's disease. Description: Tan, Manuela M X, et al. Genome-wide determinants of mortality and motor progression in Parkinson's disease. ''NPJ Parkinsons Dis''. 2024 Jun 7; '''10''' (1):113
Mapping and annotating genomic loci to prioritize genes and implicate distinct polygenic adaptations for skin color. Description: Kim, Beomsu, et al. Mapping and annotating genomic loci to prioritize genes and implicate distinct polygenic adaptations for skin color. ''Nat Commun''. 2024 Jun 7; '''15''' (1):4874
Genetic influence on vascular smooth muscle cell apoptosis. Description: McVey, David G, et al. Genetic influence on vascular smooth muscle cell apoptosis. ''Cell Death Dis''. 2024 Jun 8; '''15''' (6):402
Using lifestyle information in polygenic modeling of blood pressure traits: a simple method to reduce bias. Description: Tiezzi, Francesco, et al. Using lifestyle information in polygenic modeling of blood pressure traits: a simple method to reduce bias. ''bioRxiv''. 2024 Jun 8;
Natural variation in protein kinase D modifies alcohol sensitivity in Caenorhabditis elegans. Description: Clites, Benjamin L, et al. Natural variation in protein kinase D modifies alcohol sensitivity in Caenorhabditis elegans. ''bioRxiv''. 2024 Jun 9;
Cytochrome P450 CitCYP97B modulates carotenoid accumulation diversity by hydroxylating beta-cryptoxanthin in Citrus. Description: Zhang, Yingzi, et al. Cytochrome P450 CitCYP97B modulates carotenoid accumulation diversity by hydroxylating beta-cryptoxanthin in Citrus. ''Plant Commun''. 2024 Jun 10; '''5''' (6):100847
Genetic polymorphisms linked to extreme postorthodontic external apical root resorption in Koreans. Description: Liu, Jing, et al. Genetic polymorphisms linked to extreme postorthodontic external apical root resorption in Koreans. ''Prog Orthod''. 2024 Jun 10; '''25''' (1):23
Genome assembly of autotetraploid Actinidia arguta highlights adaptive evolution and enables dissection of important economic traits. Description: Lu, Xue-Mei, et al. Genome assembly of autotetraploid Actinidia arguta highlights adaptive evolution and enables dissection of important economic traits. ''Plant Commun''. 2024 Jun 10; '''5''' (6):100856
Genome-wide enhancer RNA profiling adds molecular links between genetic variation and human cancers. Description: Cai, Yi-Min, et al. Genome-wide enhancer RNA profiling adds molecular links between genetic variation and human cancers. ''Mil Med Res''. 2024 Jun 11; '''11''' (1):36
Genomic and phenomic predictions help capture low-effect alleles promoting seed germination in oilseed rape in addition to QTL analyses. Description: Laurencon, Marianne, et al. Genomic and phenomic predictions help capture low-effect alleles promoting seed germination in oilseed rape in addition to QTL analyses. ''Theor Appl Genet''. 2024 Jun 11; '''137''' (7):156
Genomic insights into the conservation status of the Idle Crayfish Austropotamobius bihariensis Parvulescu, 2019: low genetic diversity in the endemic crayfish species of the Apuseni Mountains. Description: Bonassin, Lena, et al. Genomic insights into the conservation status of the Idle Crayfish Austropotamobius bihariensis Parvulescu, 2019: low genetic diversity in the endemic crayfish species of the Apuseni Mountains. ''BMC Ecol Evol''. 2024 Jun 11; '''24''' (1):78
Germline prediction of immune checkpoint inhibitor discontinuation for immune-related adverse events. Description: Middha, Pooja, et al. Germline prediction of immune checkpoint inhibitor discontinuation for immune-related adverse events. ''medRxiv''. 2024 Jun 11;
Identification of a founder effect involving n.197C>T variant in RMRP gene associated to cartilage-hair hypoplasia syndrome in Brazilian patients. Description: Gomes, Maria Eduarda, et al. Identification of a founder effect involving n.197C>T variant in RMRP gene associated to cartilage-hair hypoplasia syndrome in Brazilian patients. ''Sci Rep''. 2024 Jun 11; '''14''' (1):13436
Protein truncating variants in mitochondrial-related nuclear genes and the risk of chronic liver disease. Description: Yuan, Huangbo, et al. Protein truncating variants in mitochondrial-related nuclear genes and the risk of chronic liver disease. ''BMC Med''. 2024 Jun 11; '''22''' (1):239
Shared genetic effect of kidney function on bipolar and major depressive disorders: a large-scale genome-wide cross-trait analysis. Description: Yu, Simin, et al. Shared genetic effect of kidney function on bipolar and major depressive disorders: a large-scale genome-wide cross-trait analysis. ''Hum Genomics''. 2024 Jun 11; '''18''' (1):60
Analysis-ready VCF at Biobank scale using Zarr. Description: Czech, Eric, et al. Analysis-ready VCF at Biobank scale using Zarr. ''bioRxiv''. 2024 Jun 12;
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk. Description: Jermy, Bradley, et al. A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk. ''Nat Commun''. 2024 Jun 12; '''15''' (1):5007
Epistasis, core-genome disharmony, and adaptation in recombining bacteria. Description: Taylor, Aidan J, et al. Epistasis, core-genome disharmony, and adaptation in recombining bacteria. ''mBio''. 2024 Jun 12; '''15''' (6):e0058124
Genome-wide association study of the common retinal disorder epiretinal membrane: Significant risk loci in each of three American populations. Description: Gelernter, Joel, et al. Genome-wide association study of the common retinal disorder epiretinal membrane: Significant risk loci in each of three American populations. ''Cell Genom''. 2024 Jun 12; '''4''' (6):100582
Identification of biomarkers and potential therapeutic targets for pancreatic cancer by proteomic analysis in two prospective cohorts. Description: Lyu, Jingjing, et al. Identification of biomarkers and potential therapeutic targets for pancreatic cancer by proteomic analysis in two prospective cohorts. ''Cell Genom''. 2024 Jun 12; '''4''' (6):100561
Temporal genomics in Hawaiian crickets reveals compensatory intragenomic coadaptation during adaptive evolution. Description: Zhang, Xiao, et al. Temporal genomics in Hawaiian crickets reveals compensatory intragenomic coadaptation during adaptive evolution. ''Nat Commun''. 2024 Jun 12; '''15''' (1):5001
Genetically predicted 91 circulating inflammatory proteins in relation to risk of urological malignancies: a Mendelian randomization study. Description: Xu, Jianxiong, et al. Genetically predicted 91 circulating inflammatory proteins in relation to risk of urological malignancies: a Mendelian randomization study. ''Aging (Albany NY)''. 2024 Jun 13; '''16''' (12):10366-10379
Genomic analyses of withers height and linear conformation traits in German Warmblood horses using imputed sequence-level genotypes. Description: Reich, Paula, et al. Genomic analyses of withers height and linear conformation traits in German Warmblood horses using imputed sequence-level genotypes. ''Genet Sel Evol''. 2024 Jun 13; '''56''' (1):45
Job-related exhaustion risk variant in UST is associated with dementia and DNA methylation. Description: Sulkava, Sonja, et al. Job-related exhaustion risk variant in UST is associated with dementia and DNA methylation. ''Sci Rep''. 2024 Jun 13; '''14''' (1):13668
Natural variation in BnaA07.MKK9 confers resistance to Sclerotinia stem rot in oilseed rape. Description: Lin, Li, et al. Natural variation in BnaA07.MKK9 confers resistance to Sclerotinia stem rot in oilseed rape. ''Nat Commun''. 2024 Jun 13; '''15''' (1):5059
Assessing the causal relationship between circulating immune cells and abdominal aortic aneurysm by bi-directional Mendelian randomization analysis. Description: Ruan, Weiqiang, et al. Assessing the causal relationship between circulating immune cells and abdominal aortic aneurysm by bi-directional Mendelian randomization analysis. ''Sci Rep''. 2024 Jun 14; '''14''' (1):13733
Does coevolution in refugia drive mimicry in bumble bees? Insights from a South Asian mimicry group. Description: Cui, Jixiang, et al. Does coevolution in refugia drive mimicry in bumble bees? Insights from a South Asian mimicry group. ''Sci Adv''. 2024 Jun 14; '''10''' (24):eadl2286
The Roles of Drift and Selection on Short Stamen Loss in Arabidopsis thaliana along an Elevational Gradient in the Spanish Pyrenees. Description: Buysse, Sophia F, et al. The Roles of Drift and Selection on Short Stamen Loss in Arabidopsis thaliana along an Elevational Gradient in the Spanish Pyrenees. ''bioRxiv''. 2024 Jun 14;
Genome-wide association studies of lifetime and frequency cannabis use in 131,895 individuals. Description: Thorpe, Hayley H A, et al. Genome-wide association studies of lifetime and frequency cannabis use in 131,895 individuals. ''medRxiv''. 2024 Jun 15;
Identification of candidate genes associated with primary feathers of tianfu nonghua ducks based on Genome-wide association studies. Description: Wang, Huazhen, et al. Identification of candidate genes associated with primary feathers of tianfu nonghua ducks based on Genome-wide association studies. ''Poult Sci''. 2024 Jun 15; '''103''' (9):103985
A comprehensive whole genome database of ethnic minority populations. Description: He, Yan, et al. A comprehensive whole genome database of ethnic minority populations. ''Sci Rep''. 2024 Jun 17; '''14''' (1):13954
Causal role of immune cells in prostate cancer: a bidirectional Mendelian-randomization analyses. Description: Zhong, Mingyan, et al. Causal role of immune cells in prostate cancer: a bidirectional Mendelian-randomization analyses. ''Aging (Albany NY)''. 2024 Jun 17; '''16''' (12):10477-10488
Genome-wide association study identifies novel susceptible loci and evaluation of polygenic risk score for chronic obstructive pulmonary disease in a Taiwanese population. Description: Lin, Wei-De, et al. Genome-wide association study identifies novel susceptible loci and evaluation of polygenic risk score for chronic obstructive pulmonary disease in a Taiwanese population. ''BMC Genomics''. 2024 Jun 17; '''25''' (1):607
Geographic origin, ancestry, and death circumstances at the Cornaux/Les Sauges Iron Age bridge, Switzerland. Description: Laffranchi, Zita, et al. Geographic origin, ancestry, and death circumstances at the Cornaux/Les Sauges Iron Age bridge, Switzerland. ''Sci Rep''. 2024 Jun 17; '''14''' (1):12180
Recurrent stroke prediction by applying a stroke polygenic risk score in the Japanese population. Description: Kojima, Naoki, et al. Recurrent stroke prediction by applying a stroke polygenic risk score in the Japanese population. ''medRxiv''. 2024 Jun 17;
Structural variants contribute to phenotypic variation in maize. Description: Catlin, Nathan S, et al. Structural variants contribute to phenotypic variation in maize. ''bioRxiv''. 2024 Jun 17;
Ecological trade-offs drive phenotypic and genetic differentiation of Arabidopsis thaliana in Europe. Description: Bastias, Cristina C, et al. Ecological trade-offs drive phenotypic and genetic differentiation of Arabidopsis thaliana in Europe. ''Nat Commun''. 2024 Jun 18; '''15''' (1):5185
Genetic influences on brain and cognitive health and their interactions with cardiovascular conditions and depression. Description: Zhukovsky, Peter, et al. Genetic influences on brain and cognitive health and their interactions with cardiovascular conditions and depression. ''Nat Commun''. 2024 Jun 18; '''15''' (1):5207
Origin and diversity of the wild cottons (Gossypium hirsutum) of Mound Key, Florida. Description: Ning, Weixuan, et al. Origin and diversity of the wild cottons (Gossypium hirsutum) of Mound Key, Florida. ''Sci Rep''. 2024 Jun 18; '''14''' (1):14046
Strong evidence supports the use of estradiol therapy for the treatment of vaginal inflammation: a two-way Mendelian randomization study. Description: Xu, Xiaosheng, et al. Strong evidence supports the use of estradiol therapy for the treatment of vaginal inflammation: a two-way Mendelian randomization study. ''Eur J Med Res''. 2024 Jun 18; '''29''' (1):339
Interaction between Risk Single-Nucleotide Polymorphisms of Developmental Dyslexia and Parental Education on Reading Ability: Evidence for Differential Susceptibility Theory. Description: Yang, Qing, et al. Interaction between Risk Single-Nucleotide Polymorphisms of Developmental Dyslexia and Parental Education on Reading Ability: Evidence for Differential Susceptibility Theory. ''Behav Sci (Basel)''. 2024 Jun 19; '''14''' (6):
Multi-ancestry Genome-Wide Association Meta-Analysis Identifies Novel Loci in Atopic Dermatitis. Description: Oliva, Meritxell, et al. Multi-ancestry Genome-Wide Association Meta-Analysis Identifies Novel Loci in Atopic Dermatitis. ''medRxiv''. 2024 Jun 19;
The RHCE gene encodes the chicken blood system I. Description: Fulton, Janet E, et al. The RHCE gene encodes the chicken blood system I. ''Genet Sel Evol''. 2024 Jun 19; '''56''' (1):47
Breeding for resilience in finishing pigs can decrease tail biting, lameness and mortality. Description: Gorssen, Wim, et al. Breeding for resilience in finishing pigs can decrease tail biting, lameness and mortality. ''Genet Sel Evol''. 2024 Jun 20; '''56''' (1):48
Effectiveness of colorectal cancer screening integrating non-genetic and genetic risk: a prospective study based on UK Biobank data. Description: Zhang, Yu, et al. Effectiveness of colorectal cancer screening integrating non-genetic and genetic risk: a prospective study based on UK Biobank data. ''Cancer Biol Med''. 2024 Jun 20; '''21''' (8):712-23
Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene. Description: Charng, Wu-Lin, et al. Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene. ''J Med Genet''. 2024 Jun 20; '''61''' (7):699-706
Gliovascular transcriptional perturbations in Alzheimer's disease reveal molecular mechanisms of blood brain barrier dysfunction. Description: Is, Ozkan, et al. Gliovascular transcriptional perturbations in Alzheimer's disease reveal molecular mechanisms of blood brain barrier dysfunction. ''Nat Commun''. 2024 Jun 20; '''15''' (1):4758
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. Description: Magrinelli, Francesca, et al. PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. ''medRxiv''. 2024 Jun 20;
A Mendelian randomization study between metabolic syndrome and its components with prostate cancer. Description: Xia, Long, et al. A Mendelian randomization study between metabolic syndrome and its components with prostate cancer. ''Sci Rep''. 2024 Jun 21; '''14''' (1):14338
The Gene Expression Landscape of Disease Genes. Description: Garcia-Gonzalez, Judit, et al. The Gene Expression Landscape of Disease Genes. ''medRxiv''. 2024 Jun 21;
Uncovering strain- and age-dependent innate immune responses to SARS-CoV-2 infection in air-liquid-interface cultured nasal epithelia. Description: Chang, Jessie J-Y, et al. Uncovering strain- and age-dependent innate immune responses to SARS-CoV-2 infection in air-liquid-interface cultured nasal epithelia. ''iScience''. 2024 Jun 21; '''27''' (6):110009
The association between rs6859 in NECTIN2 gene and Alzheimer's disease is partly mediated by pTau. Description: Rajendrakumar, Aravind Lathika, et al. The association between rs6859 in NECTIN2 gene and Alzheimer's disease is partly mediated by pTau. ''medRxiv''. 2024 Jun 22;
Discovering non-additive heritability using additive GWAS summary statistics. Description: Pattillo Smith, Samuel, et al. Discovering non-additive heritability using additive GWAS summary statistics. ''Elife''. 2024 Jun 24; '''13''':
Genome-wide association study, combined with bulk segregant analysis, identify plant receptors and defense related genes as candidate genes for downy mildew resistance in quinoa. Description: Fondevilla, Sara, et al. Genome-wide association study, combined with bulk segregant analysis, identify plant receptors and defense related genes as candidate genes for downy mildew resistance in quinoa. ''BMC Plant Biol''. 2024 Jun 24; '''24''' (1):594
A trans-oceanic flight of over 4,200 km by painted lady butterflies. Description: Suchan, Tomasz, et al. A trans-oceanic flight of over 4,200 km by painted lady butterflies. ''Nat Commun''. 2024 Jun 25; '''15''' (1):5205
Chromosome-level genome assembly of a cliff plant Taihangia rupestris var. ciliata provides insights into its adaptation and demographic history. Description: Li, Wei-Guo, et al. Chromosome-level genome assembly of a cliff plant Taihangia rupestris var. ciliata provides insights into its adaptation and demographic history. ''BMC Plant Biol''. 2024 Jun 25; '''24''' (1):596
Genome-wide association study identifies host genetic variants influencing oral microbiota diversity and metabolic health. Description: Stankevic, Evelina, et al. Genome-wide association study identifies host genetic variants influencing oral microbiota diversity and metabolic health. ''Sci Rep''. 2024 Jun 26; '''14''' (1):14738
Predictive ability of multi-population genomic prediction methods of phenotypes for reproduction traits in Chinese and Austrian pigs. Description: Wang, Xue, et al. Predictive ability of multi-population genomic prediction methods of phenotypes for reproduction traits in Chinese and Austrian pigs. ''Genet Sel Evol''. 2024 Jun 26; '''56''' (1):49
Runs of homozygosity and selection signature analyses reveal putative genomic regions for artificial selection in layer breeding. Description: Li, Xiaochang, et al. Runs of homozygosity and selection signature analyses reveal putative genomic regions for artificial selection in layer breeding. ''BMC Genomics''. 2024 Jun 26; '''25''' (1):638
Association of ESR1 Germline Variants with TP53 Somatic Variants in Breast Tumors in a Genome-wide Study. Description: Tjader, Nijole P, et al. Association of ESR1 Germline Variants with TP53 Somatic Variants in Breast Tumors in a Genome-wide Study. ''Cancer Res Commun''. 2024 Jun 27; '''4''' (6):1597-1608
Association of PHACTR1 with Coronary Artery Calcium Differs by Sex and Cigarette Smoking. Description: Voorhies, Kirsten, et al. Association of PHACTR1 with Coronary Artery Calcium Differs by Sex and Cigarette Smoking. ''J Cardiovasc Dev Dis''. 2024 Jun 27; '''11''' (7):
Genetic Insights into Azoospermia and Severe Oligozoospermia: Discovering Seven SNPs through GWAS and In Silico Analysis. Description: Chatziparasidou, Alexia, et al. Genetic Insights into Azoospermia and Severe Oligozoospermia: Discovering Seven SNPs through GWAS and In Silico Analysis. ''Curr Issues Mol Biol''. 2024 Jun 27; '''46''' (7):6522-6532
Anthropogenic events and responses to environmental stress are shaping the genomes of Ethiopian indigenous goats. Description: Belay, Shumuye, et al. Anthropogenic events and responses to environmental stress are shaping the genomes of Ethiopian indigenous goats. ''Sci Rep''. 2024 Jun 28; '''14''' (1):14908
Bidirectional causality between idiopathic sudden sensorineural hearing loss and depression: a Mendelian randomization study. Description: Wu, Chuanyu, et al. Bidirectional causality between idiopathic sudden sensorineural hearing loss and depression: a Mendelian randomization study. ''Sci Rep''. 2024 Jun 28; '''14''' (1):14932
Effectiveness and safety of Chaihu-Shugan-San for treating depression based on clinical cases: An updated systematic review and meta-analysis. Description: Zhang, Xiaohang, et al. Effectiveness and safety of Chaihu-Shugan-San for treating depression based on clinical cases: An updated systematic review and meta-analysis. ''Medicine (Baltimore)''. 2024 Jun 28; '''103''' (26):e38668
Family-based genome-wide association analysis of novelty seeking in a Korean schizophrenic population: A pilot study. Description: Kim, Ji Hye, et al. Family-based genome-wide association analysis of novelty seeking in a Korean schizophrenic population: A pilot study. ''Medicine (Baltimore)''. 2024 Jun 28; '''103''' (26):e38694
Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study. Description: Rossi, Niccolo, et al. Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study. ''NPJ Genom Med''. 2024 Jun 28; '''9''' (1):36
Stratified analyses refine association between TLR7 rare variants and severe COVID-19. Description: Boos, Jannik, et al. Stratified analyses refine association between TLR7 rare variants and severe COVID-19. ''HGG Adv''. 2024 Jun 28; '''5''' (4):100323
Continent-wide genomic analysis of the African buffalo (Syncerus caffer). Description: Talenti, Andrea, et al. Continent-wide genomic analysis of the African buffalo (Syncerus caffer). ''Commun Biol''. 2024 Jun 29; '''7''' (1):792
Impaired GK-GKRP interaction rather than direct GK activation worsens lipid profiles and contributes to long-term complications: a Mendelian randomization study. Description: Wang, Ke, et al. Impaired GK-GKRP interaction rather than direct GK activation worsens lipid profiles and contributes to long-term complications: a Mendelian randomization study. ''Cardiovasc Diabetol''. 2024 Jun 29; '''23''' (1):228
Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia. Description: Chen, Lei, et al. Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia. ''Transl Psychiatry''. 2024 Jun 29; '''14''' (1):267
Correlations between growth differentiation factor 15 (GDF-15) serum levels and gene polymorphism with type 2 diabetes mellitus. Description: Liu, Qiumei, et al. Correlations between growth differentiation factor 15 (GDF-15) serum levels and gene polymorphism with type 2 diabetes mellitus. ''Heliyon''. 2024 Jun 30; '''10''' (12):e33044
Spectrum and genotype-phenotype relationship of ALPK3 variants in Chinese patients with hypertrophic cardiomyopathy. Description: Wang, Jing, et al. Spectrum and genotype-phenotype relationship of ALPK3 variants in Chinese patients with hypertrophic cardiomyopathy. ''Heliyon''. 2024 Jun 30; '''10''' (12):e32786
Ancient Plasmodium genomes shed light on the history of human malaria. Description: Michel, Megan, et al. Ancient Plasmodium genomes shed light on the history of human malaria. ''Nature''. 2024 Jul; '''631''' (8019):125-133
An Epigenome-Wide Association Study of DNA Methylation and Proliferative Retinopathy over 28 Years in Type 1 Diabetes. Description: Miller, Rachel G, et al. An Epigenome-Wide Association Study of DNA Methylation and Proliferative Retinopathy over 28 Years in Type 1 Diabetes. ''Ophthalmol Sci''. 2024 Jul-Aug; '''4''' (4):100497
ANO2 Genetic Variants and Anti-VEGF Treatment Response in Neovascular AMD: A Pharmacogenetic Substudy of VIEW 1 and VIEW 2. Description: Guymer, Robyn H, et al. ANO2 Genetic Variants and Anti-VEGF Treatment Response in Neovascular AMD: A Pharmacogenetic Substudy of VIEW 1 and VIEW 2. ''Invest Ophthalmol Vis Sci''. 2024 Jul 1; '''65''' (8):17
Causal relationship and shared genes between air pollutants and amyotrophic lateral sclerosis: A large-scale genetic analysis. Description: Li, Zhihao, et al. Causal relationship and shared genes between air pollutants and amyotrophic lateral sclerosis: A large-scale genetic analysis. ''CNS Neurosci Ther''. 2024 Jul; '''30''' (7):e14812
Causal relationships between immune cell phenotypes and lung adenocarcinoma: A bidirectional two-sample Mendelian randomization study. Description: Li, Bowen, et al. Causal relationships between immune cell phenotypes and lung adenocarcinoma: A bidirectional two-sample Mendelian randomization study. ''Thorac Cancer''. 2024 Jul; '''15''' (21):1673-1680
Clinical and genetic risk factors for progressive fibrosis in metabolic dysfunction-associated steatotic liver disease. Description: Kaplan, David E, et al. Clinical and genetic risk factors for progressive fibrosis in metabolic dysfunction-associated steatotic liver disease. ''Hepatol Commun''. 2024 Jul 1; '''8''' (7):
Deep history of cultural and linguistic evolution among Central African hunter-gatherers. Description: Padilla-Iglesias, Cecilia, et al. Deep history of cultural and linguistic evolution among Central African hunter-gatherers. ''Nat Hum Behav''. 2024 Jul; '''8''' (7):1263-1275
Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Description: Trastulla, Lucia, et al. Distinct genetic liability profiles define clinically relevant patient strata across common diseases. ''Nat Commun''. 2024 Jul 1; '''15''' (1):5534
Distinguishing recrudescence from reinfection in lymphatic filariasis. Description: Choi, Young-Jun, et al. Distinguishing recrudescence from reinfection in lymphatic filariasis. ''EBioMedicine''. 2024 Jul; '''105''': 105188
Effects of inbreeding on reproductive success in endangered North Atlantic right whales. Description: Crossman, Carla A, et al. Effects of inbreeding on reproductive success in endangered North Atlantic right whales. ''R Soc Open Sci''. 2024 Jul; '''11''' (7):240490
Estimation of genetic correlations and genomic prediction accuracy for reproductive and carcass traits in Hanwoo cows. Description: Haque, Md Azizul, et al. Estimation of genetic correlations and genomic prediction accuracy for reproductive and carcass traits in Hanwoo cows. ''J Anim Sci Technol''. 2024 Jul; '''66''' (4):682-701
Evidence for an Association Between a pH-Dependent Potassium Channel, TWIK-1, and the Accuracy of Smooth Pursuit Eye Movements. Description: Bargary, Gary, et al. Evidence for an Association Between a pH-Dependent Potassium Channel, TWIK-1, and the Accuracy of Smooth Pursuit Eye Movements. ''Invest Ophthalmol Vis Sci''. 2024 Jul 1; '''65''' (8):24
Exome sequencing and genome-wide association analyses unveils the genetic predisposition in hydroxychloroquine retinopathy. Description: Chiu, Hsun-I, et al. Exome sequencing and genome-wide association analyses unveils the genetic predisposition in hydroxychloroquine retinopathy. ''Eye (Lond)''. 2024 Jul; '''38''' (10):1926-1932
Exome sequencing identifies novel genetic variants associated with varicose veins. Description: Zhang, Dan-Dan, et al. Exome sequencing identifies novel genetic variants associated with varicose veins. ''PLoS Genet''. 2024 Jul; '''20''' (7):e1011339
Extant and extinct bilby genomes combined with Indigenous knowledge improve conservation of a unique Australian marsupial. Description: Hogg, Carolyn J, et al. Extant and extinct bilby genomes combined with Indigenous knowledge improve conservation of a unique Australian marsupial. ''Nat Ecol Evol''. 2024 Jul; '''8''' (7):1311-1326
Genetic and epigenetic signatures for improved breeding of cultivated blueberry. Description: Wang, Zejia, et al. Genetic and epigenetic signatures for improved breeding of cultivated blueberry. ''Hortic Res''. 2024 Jul; '''11''' (7):uhae138
Genetic and Phenotypic Features of Schizophrenia in the UK Biobank. Description: Legge, Sophie E, et al. Genetic and Phenotypic Features of Schizophrenia in the UK Biobank. ''JAMA Psychiatry''. 2024 Jul 1; '''81''' (7):681-690
Genetic characteristics and selection signatures between Southern Chinese local and commercial chickens. Description: Qi, Lin, et al. Genetic characteristics and selection signatures between Southern Chinese local and commercial chickens. ''Poult Sci''. 2024 Jul; '''103''' (7):103863
Genetic diversity and population structure in five Inner Mongolia cashmere goat populations using whole-genome genotyping. Description: Zhang, Tao, et al. Genetic diversity and population structure in five Inner Mongolia cashmere goat populations using whole-genome genotyping. ''Anim Biosci''. 2024 Jul; '''37''' (7):1168-1176
Genetic-environment associations explain genetic differentiation and variation between western and eastern North Pacific rhinoceros auklet (Cerorhinca monocerata) breeding colonies. Description: Graham, Brendan A, et al. Genetic-environment associations explain genetic differentiation and variation between western and eastern North Pacific rhinoceros auklet (Cerorhinca monocerata) breeding colonies. ''Ecol Evol''. 2024 Jul; '''14''' (7):e11534
Genetic Risk Loci and Familial Associations in Migraine: A Genome-Wide Association Study in the Han Chinese Population of Taiwan. Description: Liu, Yi, et al. Genetic Risk Loci and Familial Associations in Migraine: A Genome-Wide Association Study in the Han Chinese Population of Taiwan. ''J Clin Neurol''. 2024 Jul; '''20''' (4):439-449
Genome assembly and resequencing shed light on evolution, population selection, and sex identification in Vernicia montana. Description: Li, Wenying, et al. Genome assembly and resequencing shed light on evolution, population selection, and sex identification in Vernicia montana. ''Hortic Res''. 2024 Jul; '''11''' (7):uhae141
Genome‑wide association study and polygenic risk scores predict psoriasis and its shared phenotypes in Taiwan. Description: Yang, Jai-Sing, et al. Genome‑wide association study and polygenic risk scores predict psoriasis and its shared phenotypes in Taiwan. ''Mol Med Rep''. 2024 Jul; '''30''' (1):
Genomic evidence reveals three W-autosome fusions in Heliconius butterflies. Description: Rueda-M, Nicol, et al. Genomic evidence reveals three W-autosome fusions in Heliconius butterflies. ''PLoS Genet''. 2024 Jul; '''20''' (7):e1011318
Improving the accuracy of genomic prediction in dairy cattle using the biologically annotated neural networks framework. Description: Wang, Xue, et al. Improving the accuracy of genomic prediction in dairy cattle using the biologically annotated neural networks framework. ''J Anim Sci Biotechnol''. 2024 Jul 1; '''15''' (1):87
Independent Effects of Blood Pressure on Intraocular Pressure and Retinal Ganglion Cell Degeneration: A Mendelian Randomization Study. Description: Rajasundaram, Skanda, et al. Independent Effects of Blood Pressure on Intraocular Pressure and Retinal Ganglion Cell Degeneration: A Mendelian Randomization Study. ''Invest Ophthalmol Vis Sci''. 2024 Jul 1; '''65''' (8):35
Influence of Polygenic Background on the Clinical Presentation of Familial Hypercholesterolemia. Description: Trinder, Mark, et al. Influence of Polygenic Background on the Clinical Presentation of Familial Hypercholesterolemia. ''Arterioscler Thromb Vasc Biol''. 2024 Jul; '''44''' (7):1683-1693
New insights into the evolution and local adaptation of the genus Castanea in east Asia. Description: Nie, Xinghua, et al. New insights into the evolution and local adaptation of the genus Castanea in east Asia. ''Hortic Res''. 2024 Jul; '''11''' (7):uhae147
Plasmodium vivax populations in the western Greater Mekong Subregion evaluated using a genetic barcode. Description: Hu, Yubing, et al. Plasmodium vivax populations in the western Greater Mekong Subregion evaluated using a genetic barcode. ''PLoS Negl Trop Dis''. 2024 Jul; '''18''' (7):e0012299
Polygenic Risk Scores in Predicting Coronary Artery Disease in Symptomatic Patients. A Validation Study. Description: Kujala, Iida, et al. Polygenic Risk Scores in Predicting Coronary Artery Disease in Symptomatic Patients. A Validation Study. ''J Atheroscler Thromb''. 2024 Jul 1; '''31''' (7):1058-1071
Population genomics and distribution modeling revealed the history and suggested a possible future of the endemic Agave aurea (Asparagaceae) complex in the Baja California Peninsula. Description: Klimova, Anastasia, et al. Population genomics and distribution modeling revealed the history and suggested a possible future of the endemic Agave aurea (Asparagaceae) complex in the Baja California Peninsula. ''Ecol Evol''. 2024 Jul; '''14''' (7):e70027
Risk Phenotypes, Comorbidities, Pharmacotherapy, and Electroconvulsive Therapy (ECT) in a Cohort with Difficult-to-Treat Depression in Comparison to an Unmedicated Control Group. Description: Maier, Hannah B, et al. Risk Phenotypes, Comorbidities, Pharmacotherapy, and Electroconvulsive Therapy (ECT) in a Cohort with Difficult-to-Treat Depression in Comparison to an Unmedicated Control Group. ''Pharmacopsychiatry''. 2024 Jul; '''57''' (4):191-203
Sequencing of Kaposi's Sarcoma Herpesvirus (KSHV) genomes from persons of diverse ethnicities and provenances with KSHV-associated diseases demonstrate multiple infections, novel polymorphisms, and low intra-host variance. Description: Marshall, Vickie A, et al. Sequencing of Kaposi's Sarcoma Herpesvirus (KSHV) genomes from persons of diverse ethnicities and provenances with KSHV-associated diseases demonstrate multiple infections, novel polymorphisms, and low intra-host variance. ''PLoS Pathog''. 2024 Jul; '''20''' (7):e1012338
Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Description: Kentistou, Katherine A, et al. Understanding the genetic complexity of puberty timing across the allele frequency spectrum. ''Nat Genet''. 2024 Jul; '''56''' (7):1397-1411
U-shaped association between sleep duration and biological aging: Evidence from the UK Biobank study. Description: Wang, Xuanyang, et al. U-shaped association between sleep duration and biological aging: Evidence from the UK Biobank study. ''Aging Cell''. 2024 Jul; '''23''' (7):e14159
Weighted single-step genome-wide association study to reveal new candidate genes for productive traits of Landrace pig in Korea. Description: Park, Jun, et al. Weighted single-step genome-wide association study to reveal new candidate genes for productive traits of Landrace pig in Korea. ''J Anim Sci Technol''. 2024 Jul; '''66''' (4):702-716
Sirenian genomes illuminate the evolution of fully aquatic species within the mammalian superorder afrotheria. Description: Tian, Ran, et al. Sirenian genomes illuminate the evolution of fully aquatic species within the mammalian superorder afrotheria. ''Nat Commun''. 2024 Jul 2; '''15''' (1):5568
Unveiling the molecular landscape of cognitive aging: insights from polygenic risk scores, DNA methylation, and gene expression. Description: Neto, Sonya, et al. Unveiling the molecular landscape of cognitive aging: insights from polygenic risk scores, DNA methylation, and gene expression. ''Hum Genomics''. 2024 Jul 2; '''18''' (1):75
Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals. Description: Gong, Weikang, et al. Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals. ''Nat Commun''. 2024 Jul 2; '''15''' (1):5540
Adaptive Evolution of Two Distinct Adaptive Haplotypes of Neanderthal Origin at the Immunoglobulin Heavy-chain Locus in East Asian and European Populations. Description: Ma, Xixian, et al. Adaptive Evolution of Two Distinct Adaptive Haplotypes of Neanderthal Origin at the Immunoglobulin Heavy-chain Locus in East Asian and European Populations. ''Mol Biol Evol''. 2024 Jul 3; '''41''' (7):
Ancestral Origins and Admixture History of Kazakhs. Description: Lei, Chang, et al. Ancestral Origins and Admixture History of Kazakhs. ''Mol Biol Evol''. 2024 Jul 3; '''41''' (7):
Ancient and Recent Hybridization in the Oreochromis Cichlid Fishes. Description: Ciezarek, Adam G, et al. Ancient and Recent Hybridization in the Oreochromis Cichlid Fishes. ''Mol Biol Evol''. 2024 Jul 3; '''41''' (7):
Genetic diversity and population structure of wheat landraces in Southern Winter Wheat Region of China. Description: Liu, Ying, et al. Genetic diversity and population structure of wheat landraces in Southern Winter Wheat Region of China. ''BMC Genomics''. 2024 Jul 3; '''25''' (1):664
Genomic Consequences of Isolation and Inbreeding in an Island Dingo Population. Description: Leon-Apodaca, Ana V, et al. Genomic Consequences of Isolation and Inbreeding in an Island Dingo Population. ''Genome Biol Evol''. 2024 Jul 3; '''16''' (7):
Historic dog Furs Unravel the Origin and Artificial Selection of Modern Nordic Lapphund and Elkhound dog Breeds. Description: Wang, Shi-Zhi, et al. Historic dog Furs Unravel the Origin and Artificial Selection of Modern Nordic Lapphund and Elkhound dog Breeds. ''Mol Biol Evol''. 2024 Jul 3; '''41''' (7):
Identification of candidate gene associated with maize northern leaf blight resistance in a multi-parent population. Description: Bi, Yaqi, et al. Identification of candidate gene associated with maize northern leaf blight resistance in a multi-parent population. ''Plant Cell Rep''. 2024 Jul 3; '''43''' (7):189
Imputation of ancient canid genomes reveals inbreeding history over the past 10,000 years. Description: Bougiouri, Katia, et al. Imputation of ancient canid genomes reveals inbreeding history over the past 10,000 years. ''bioRxiv''. 2024 Jul 3;
Multi-omic characterization of allele-specific regulatory variation in hybrid pigs. Description: Quan, Jianping, et al. Multi-omic characterization of allele-specific regulatory variation in hybrid pigs. ''Nat Commun''. 2024 Jul 3; '''15''' (1):5587
Multiple Human Population Movements and Cultural Dispersal Events Shaped the Landscape of Chinese Paternal Heritage. Description: Wang, Mengge, et al. Multiple Human Population Movements and Cultural Dispersal Events Shaped the Landscape of Chinese Paternal Heritage. ''Mol Biol Evol''. 2024 Jul 3; '''41''' (7):
Rapid Adaptation and Interspecific Introgression in the North American Crop Pest Helicoverpa zea. Description: North, Henry L, et al. Rapid Adaptation and Interspecific Introgression in the North American Crop Pest Helicoverpa zea. ''Mol Biol Evol''. 2024 Jul 3; '''41''' (7):
Congenital syndromic Chiari-like malformation (CSCM) in Holstein cattle: towards unravelling of possible genetic causes. Description: Jacinto, Joana Goncalves Pontes, et al. Congenital syndromic Chiari-like malformation (CSCM) in Holstein cattle: towards unravelling of possible genetic causes. ''Acta Vet Scand''. 2024 Jul 4; '''66''' (1):29
Genome wide association study of seedling and adult plant leaf rust resistance in two subsets of barley genetic resources. Description: Amouzoune, Mariam, et al. Genome wide association study of seedling and adult plant leaf rust resistance in two subsets of barley genetic resources. ''Sci Rep''. 2024 Jul 4; '''14''' (1):15428
Abdominal aortic aneurysm and cardiometabolic traits share strong genetic susceptibility to lipid metabolism and inflammation. Description: Zheng, Shufen, et al. Abdominal aortic aneurysm and cardiometabolic traits share strong genetic susceptibility to lipid metabolism and inflammation. ''Nat Commun''. 2024 Jul 5; '''15''' (1):5652
Anatolian genetic ancestry in North Lebanese populations. Description: Platt, Daniel E, et al. Anatolian genetic ancestry in North Lebanese populations. ''Sci Rep''. 2024 Jul 5; '''14''' (1):15518
Genetic and genomic analysis of Belgian Blue's susceptibility for psoroptic mange. Description: Meyermans, Roel, et al. Genetic and genomic analysis of Belgian Blue's susceptibility for psoroptic mange. ''Genet Sel Evol''. 2024 Jul 5; '''56''' (1):52
Genetic diversity of 1,845 rhesus macaques improves genetic variation interpretation and identifies disease models. Description: Wang, Jun, et al. Genetic diversity of 1,845 rhesus macaques improves genetic variation interpretation and identifies disease models. ''Nat Commun''. 2024 Jul 5; '''15''' (1):5658
Polygenic inheritance and its interplay with smoking history in predicting lung cancer diagnosis: a French-Canadian case-control cohort. Description: Boumtje, Veronique, et al. Polygenic inheritance and its interplay with smoking history in predicting lung cancer diagnosis: a French-Canadian case-control cohort. ''EBioMedicine''. 2024 Jul 5; '''106''': 105234
Limbic Network and Papez Circuit Involvement in ALS: Imaging and Clinical Profiles in GGGGCC Hexanucleotide Carriers in C9orf72 and C9orf72-Negative Patients. Description: Christidi, Foteini, et al. Limbic Network and Papez Circuit Involvement in ALS: Imaging and Clinical Profiles in GGGGCC Hexanucleotide Carriers in C9orf72 and C9orf72-Negative Patients. ''Biology (Basel)''. 2024 Jul 6; '''13''' (7):
RECORD, a high-throughput, customizable system that unveils behavioral strategies leveraged by rodents during foraging-like decision-making. Description: Ibanez Alcala, Raquel J, et al. RECORD, a high-throughput, customizable system that unveils behavioral strategies leveraged by rodents during foraging-like decision-making. ''Commun Biol''. 2024 Jul 6; '''7''' (1):822
A comparative analysis reveals the genomic diversity among 8 Muscovy duck populations. Description: Li, Te, et al. A comparative analysis reveals the genomic diversity among 8 Muscovy duck populations. ''G3 (Bethesda)''. 2024 Jul 8; '''14''' (7):
TrG2P: A transfer-learning-based tool integrating multi-trait data for accurate prediction of crop yield. Description: Li, Jinlong, et al. TrG2P: A transfer-learning-based tool integrating multi-trait data for accurate prediction of crop yield. ''Plant Commun''. 2024 Jul 8; '''5''' (7):100975
Natural variation of domestication-related genes contributed to latitudinal expansion and adaptation in soybean. Description: Li, Jing, et al. Natural variation of domestication-related genes contributed to latitudinal expansion and adaptation in soybean. ''BMC Plant Biol''. 2024 Jul 9; '''24''' (1):651
Sex-specific survival gene mutations are discovered as clinical predictors of clear cell renal cell carcinoma. Description: Hwang, Jia, et al. Sex-specific survival gene mutations are discovered as clinical predictors of clear cell renal cell carcinoma. ''Sci Rep''. 2024 Jul 9; '''14''' (1):15800
Tall women with breast cancer have poorer survival than short women. Description: Lehrer, Steven, et al. Tall women with breast cancer have poorer survival than short women. ''medRxiv''. 2024 Jul 9;
eQTLs identify regulatory networks and drivers of variation in the individual response to sepsis. Description: Burnham, Katie L, et al. eQTLs identify regulatory networks and drivers of variation in the individual response to sepsis. ''Cell Genom''. 2024 Jul 10; '''4''' (7):100587
Identification of consensus homozygous regions and their associations with growth and feed efficiency traits in American mink. Description: Davoudi, Pourya, et al. Identification of consensus homozygous regions and their associations with growth and feed efficiency traits in American mink. ''BMC Genom Data''. 2024 Jul 10; '''25''' (1):68
Using high-density SNP data to unravel the origin of the Franches-Montagnes horse breed. Description: Gmel, Annik Imogen, et al. Using high-density SNP data to unravel the origin of the Franches-Montagnes horse breed. ''Genet Sel Evol''. 2024 Jul 10; '''56''' (1):53
Whole exome sequencing analysis identifies genes for alcohol consumption. Description: Kang, Jujiao, et al. Whole exome sequencing analysis identifies genes for alcohol consumption. ''Nat Commun''. 2024 Jul 10; '''15''' (1):5777
Whole-genome analysis reveals distinct adaptation signatures to diverse environments in Chinese domestic pigs. Description: Wang, Zhen, et al. Whole-genome analysis reveals distinct adaptation signatures to diverse environments in Chinese domestic pigs. ''J Anim Sci Biotechnol''. 2024 Jul 10; '''15''' (1):97
Childhood trauma as a mediator between autistic traits and depression: evidence from the ALSPAC birth cohort. Description: Underwood, Jack F G, et al. Childhood trauma as a mediator between autistic traits and depression: evidence from the ALSPAC birth cohort. ''medRxiv''. 2024 Jul 12;
Genetic and multi-omic resources for Alzheimer disease and related dementia from the Knight Alzheimer Disease Research Center. Description: Fernandez, Maria Victoria, et al. Genetic and multi-omic resources for Alzheimer disease and related dementia from the Knight Alzheimer Disease Research Center. ''Sci Data''. 2024 Jul 12; '''11''' (1):768
Calcium deposition in chicken eggshells: role of host genetics and gut microbiota. Description: Jin, Jiaming, et al. Calcium deposition in chicken eggshells: role of host genetics and gut microbiota. ''Poult Sci''. 2024 Jul 14; '''103''' (10):104073
Genetic admixture drives climate adaptation in the bank vole. Description: Hornikova, Michaela, et al. Genetic admixture drives climate adaptation in the bank vole. ''Commun Biol''. 2024 Jul 15; '''7''' (1):863
HiChIP-Based Epigenomic Footprinting Identifies a Promoter Variant of UXS1 That Confers Genetic Susceptibility to Gastroesophageal Cancer. Description: Gnanapragasam, Ansley, et al. HiChIP-Based Epigenomic Footprinting Identifies a Promoter Variant of UXS1 That Confers Genetic Susceptibility to Gastroesophageal Cancer. ''Cancer Res''. 2024 Jul 15; '''84''' (14):2377-2389
Investigating grey matter volumetric trajectories through the lifespan at the individual level. Description: Shi, Runye, et al. Investigating grey matter volumetric trajectories through the lifespan at the individual level. ''Nat Commun''. 2024 Jul 15; '''15''' (1):5954
Meta-analysis of six dairy cattle breeds reveals biologically relevant candidate genes for mastitis resistance. Description: Cai, Zexi, et al. Meta-analysis of six dairy cattle breeds reveals biologically relevant candidate genes for mastitis resistance. ''Genet Sel Evol''. 2024 Jul 15; '''56''' (1):54
Phylogenetic relationships and genetic diversity of the Korean endemic Phedimus latiovalifolius (Crassulaceae) and its close relatives. Description: Cho, Myong-Suk, et al. Phylogenetic relationships and genetic diversity of the Korean endemic Phedimus latiovalifolius (Crassulaceae) and its close relatives. ''Sci Rep''. 2024 Jul 15; '''14''' (1):16255
Effective population size in field pea. Description: Johnson, Josephine Princy, et al. Effective population size in field pea. ''BMC Genomics''. 2024 Jul 16; '''25''' (1):695
Genetic diversity analysis of Inner Mongolia cashmere goats (Erlangshan subtype) based on whole genome re-sequencing. Description: Wang, Ruijun, et al. Genetic diversity analysis of Inner Mongolia cashmere goats (Erlangshan subtype) based on whole genome re-sequencing. ''BMC Genomics''. 2024 Jul 16; '''25''' (1):698
Insights into the genomic homogeneity of Moroccan indigenous sheep breeds though the lens of runs of homozygosity. Description: Kusza, Szilvia, et al. Insights into the genomic homogeneity of Moroccan indigenous sheep breeds though the lens of runs of homozygosity. ''Sci Rep''. 2024 Jul 17; '''14''' (1):16515
A robust cis-Mendelian randomization method with application to drug target discovery. Description: Lin, Zhaotong, et al. A robust cis-Mendelian randomization method with application to drug target discovery. ''Nat Commun''. 2024 Jul 18; '''15''' (1):6072
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder. Description: Mendes, Marla, et al. Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder. ''medRxiv''. 2024 Jul 18;
Identification of Genomic Predictors of Muscle Fiber Size. Description: Guilherme, Joao Paulo L F, et al. Identification of Genomic Predictors of Muscle Fiber Size. ''Cells''. 2024 Jul 18; '''13''' (14):
Investigating gene functions and single-cell expression profiles of de novo variants in orofacial clefts. Description: Itai, Toshiyuki, et al. Investigating gene functions and single-cell expression profiles of de novo variants in orofacial clefts. ''HGG Adv''. 2024 Jul 18; '''5''' (3):100313
Genomic Reference Resource for African Cattle: Genome Sequences and High-Density Array Variants. Description: Tijjani, Abdulfatai, et al. Genomic Reference Resource for African Cattle: Genome Sequences and High-Density Array Variants. ''Sci Data''. 2024 Jul 19; '''11''' (1):801
Hybridization in birds-of-paradise: Widespread ancestral gene flow despite strong sexual selection in a lek-mating system. Description: Blom, Mozes P K, et al. Hybridization in birds-of-paradise: Widespread ancestral gene flow despite strong sexual selection in a lek-mating system. ''iScience''. 2024 Jul 19; '''27''' (7):110300
Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery disease. Description: Lee, Paul C, et al. Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery disease. ''iScience''. 2024 Jul 19; '''27''' (7):110104
Peripheral whole blood microRNA expression in relation to vascular function: a population-based study. Description: Talevi, Valentina, et al. Peripheral whole blood microRNA expression in relation to vascular function: a population-based study. ''J Transl Med''. 2024 Jul 19; '''22''' (1):670
Targeted panel sequencing of pharmacogenes and oncodrivers in colorectal cancer patients reveals genes with prognostic significance. Description: Heczko, Lucie, et al. Targeted panel sequencing of pharmacogenes and oncodrivers in colorectal cancer patients reveals genes with prognostic significance. ''Hum Genomics''. 2024 Jul 19; '''18''' (1):83
Unraveling the metabolomic architecture of autism in a large Danish population-based cohort. Description: Ottosson, Filip, et al. Unraveling the metabolomic architecture of autism in a large Danish population-based cohort. ''BMC Med''. 2024 Jul 19; '''22''' (1):302
Unsupervised clustering identified clinically relevant metabolic syndrome endotypes in UK and Taiwan Biobanks. Description: Lim, Aylwin Ming Wee, et al. Unsupervised clustering identified clinically relevant metabolic syndrome endotypes in UK and Taiwan Biobanks. ''iScience''. 2024 Jul 19; '''27''' (7):109815
MENTOR: Multiplex Embedding of Networks for Team-Based Omics Research. Description: Sullivan, Kyle A, et al. MENTOR: Multiplex Embedding of Networks for Team-Based Omics Research. ''bioRxiv''. 2024 Jul 22;
A genome-guided strategy for climate resilience in American chestnut restoration populations. Description: Sandercock, Alexander M, et al. A genome-guided strategy for climate resilience in American chestnut restoration populations. ''Proc Natl Acad Sci U S A''. 2024 Jul 23; '''121''' (30):e2403505121
Altitude-dependent agro-ecologies impact the microbiome diversity of scavenging indigenous chicken in Ethiopia. Description: Glendinning, Laura, et al. Altitude-dependent agro-ecologies impact the microbiome diversity of scavenging indigenous chicken in Ethiopia. ''Microbiome''. 2024 Jul 23; '''12''' (1):138
Tracing the possible evolutionary trends of Morganella morganii: insights from molecular epidemiology and phylogenetic analysis. Description: Chen, Jiawei, et al. Tracing the possible evolutionary trends of Morganella morganii: insights from molecular epidemiology and phylogenetic analysis. ''mSystems''. 2024 Jul 23; '''9''' (7):e0030624
Using machine learning to combine genetic and environmental data for maize grain yield predictions across multi-environment trials. Description: Fernandes, Igor K, et al. Using machine learning to combine genetic and environmental data for maize grain yield predictions across multi-environment trials. ''Theor Appl Genet''. 2024 Jul 23; '''137''' (8):189
Evaluating genomic inbreeding of two Chinese yak (Bos grunniens) populations. Description: Chen, Shi-Yi, et al. Evaluating genomic inbreeding of two Chinese yak (Bos grunniens) populations. ''BMC Genomics''. 2024 Jul 24; '''25''' (1):712
Detection and evaluation of parameters influencing the identification of heterozygous-enriched regions in Holstein cattle based on SNP chip or whole-genome sequence data. Description: Mulim, Henrique A, et al. Detection and evaluation of parameters influencing the identification of heterozygous-enriched regions in Holstein cattle based on SNP chip or whole-genome sequence data. ''BMC Genomics''. 2024 Jul 26; '''25''' (1):726
Novel loci linked to serum lipid traits are identified in a genome-wide association study of a highly admixed Brazilian population - the 2015 ISA Nutrition. Description: Leite, Jean Michel R S, et al. Novel loci linked to serum lipid traits are identified in a genome-wide association study of a highly admixed Brazilian population - the 2015 ISA Nutrition. ''Lipids Health Dis''. 2024 Jul 26; '''23''' (1):229
Genome-wide SNPs and candidate genes underlying the genetic variations for protein and amino acids in pearl millet (Pennisetum glaucum) germplasm. Description: Singh, Satbeer, et al. Genome-wide SNPs and candidate genes underlying the genetic variations for protein and amino acids in pearl millet (Pennisetum glaucum) germplasm. ''Planta''. 2024 Jul 27; '''260''' (3):63
Multivariate, Multi-omic Analysis in 799,429 Individuals Identifies 134 Loci Associated with Somatoform Traits. Description: Davis, Christal N, et al. Multivariate, Multi-omic Analysis in 799,429 Individuals Identifies 134 Loci Associated with Somatoform Traits. ''medRxiv''. 2024 Jul 29;
Population Performance and Individual Agreement of Coronary Artery Disease Polygenic Risk Scores. Description: Abramowitz, Sarah A, et al. Population Performance and Individual Agreement of Coronary Artery Disease Polygenic Risk Scores. ''medRxiv''. 2024 Jul 29;
The Association between the Abundance of Homozygous Deleterious Variants and the Morbidity of Dog Breeds. Description: Subramanian, Sankar, et al. The Association between the Abundance of Homozygous Deleterious Variants and the Morbidity of Dog Breeds. ''Biology (Basel)''. 2024 Jul 29; '''13''' (8):
The paired immunoglobulin-like type 2 receptor alpha (PILRA) gene polymorphism rs1859788 reduces risk of Alzheimer's Disease in men homozygous for the ApoE epsilon4 allele. Description: Lehrer, Steven, et al. The paired immunoglobulin-like type 2 receptor alpha (PILRA) gene polymorphism rs1859788 reduces risk of Alzheimer's Disease in men homozygous for the ApoE epsilon4 allele. ''Res Sq''. 2024 Jul 29;
A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosis. Description: Pahlevan Kakhki, Majid, et al. A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosis. ''Nat Commun''. 2024 Jul 30; '''15''' (1):6419
Assessing different metrics of pedigree and genomic inbreeding and inbreeding effect on growth, fertility, and feed efficiency traits in a closed-herd Nellore cattle population. Description: Bem, Ricardo D, et al. Assessing different metrics of pedigree and genomic inbreeding and inbreeding effect on growth, fertility, and feed efficiency traits in a closed-herd Nellore cattle population. ''BMC Genomics''. 2024 Jul 30; '''25''' (1):738
Genetic diversity of United States Rambouillet, Katahdin and Dorper sheep. Description: Becker, Gabrielle M, et al. Genetic diversity of United States Rambouillet, Katahdin and Dorper sheep. ''Genet Sel Evol''. 2024 Jul 30; '''56''' (1):56
Genetic predictors of blood pressure traits are associated with preeclampsia. Description: Jasper, Elizabeth A, et al. Genetic predictors of blood pressure traits are associated with preeclampsia. ''Sci Rep''. 2024 Jul 30; '''14''' (1):17613
Genome-wide association studies of body size traits in Tibetan sheep. Description: Liu, Dehui, et al. Genome-wide association studies of body size traits in Tibetan sheep. ''BMC Genomics''. 2024 Jul 30; '''25''' (1):739
Modelling the demographic history of human North African genomes points to a recent soft split divergence between populations. Description: Serradell, Jose M, et al. Modelling the demographic history of human North African genomes points to a recent soft split divergence between populations. ''Genome Biol''. 2024 Jul 30; '''25''' (1):201
The influence of HLA genetic variation on plasma protein expression. Description: Krishna, Chirag, et al. The influence of HLA genetic variation on plasma protein expression. ''Nat Commun''. 2024 Jul 31; '''15''' (1):6469
Whole-genome resequencing identifies candidate genes associated with heat adaptation in chickens. Description: Bai, Hao, et al. Whole-genome resequencing identifies candidate genes associated with heat adaptation in chickens. ''Poult Sci''. 2024 Jul 31; '''103''' (10):104139
Associations of E-proteinoid 3 receptor genetic polymorphisms with salt sensitivity, longitudinal blood pressure changes, and hypertension incidence in Chinese adults. Description: Chang, Ming-Ke, et al. Associations of E-proteinoid 3 receptor genetic polymorphisms with salt sensitivity, longitudinal blood pressure changes, and hypertension incidence in Chinese adults. ''J Clin Hypertens (Greenwich)''. 2024 Aug; '''26''' (8):955-963
Characterisation of runs of homozygosity and inbreeding coefficients in the red-brown Korean native chickens. Description: Macharia, John Kariuki, et al. Characterisation of runs of homozygosity and inbreeding coefficients in the red-brown Korean native chickens. ''Anim Biosci''. 2024 Aug; '''37''' (8):1355-1366
Danzhou chicken: a unique genetic resource revealed by genome-wide resequencing data. Description: Xie, Xinfeng, et al. Danzhou chicken: a unique genetic resource revealed by genome-wide resequencing data. ''Poult Sci''. 2024 Aug; '''103''' (8):103960
Deciphering the Genetic Landscape: Insights Into the Genomic Signatures of Changle Goose. Description: Chen, Hao, et al. Deciphering the Genetic Landscape: Insights Into the Genomic Signatures of Changle Goose. ''Evol Appl''. 2024 Aug; '''17''' (8):e13768
Ecological genomics in the Northern krill uncovers loci for local adaptation across ocean basins. Description: Unneberg, Per, et al. Ecological genomics in the Northern krill uncovers loci for local adaptation across ocean basins. ''Nat Commun''. 2024 Aug 1; '''15''' (1):6297
Enhancing portability of trans-ancestral polygenic risk scores through tissue-specific functional genomic data integration. Description: Crone, Bradley, et al. Enhancing portability of trans-ancestral polygenic risk scores through tissue-specific functional genomic data integration. ''PLoS Genet''. 2024 Aug; '''20''' (8):e1011356
Epigenomic partitioning of a polygenic risk score for asthma reveals distinct genetically driven disease pathways. Description: Stikker, Bernard, et al. Epigenomic partitioning of a polygenic risk score for asthma reveals distinct genetically driven disease pathways. ''Eur Respir J''. 2024 Aug; '''64''' (2):
Estimating overdiagnosis in giant cell arteritis diagnostic pathways using genetic data: genetic association study. Description: Chatzigeorgiou, Charikleia, et al. Estimating overdiagnosis in giant cell arteritis diagnostic pathways using genetic data: genetic association study. ''Rheumatology (Oxford)''. 2024 Aug 1; '''63''' (8):2307-2313
Exploring the Influence of Date Palm Cultivars on Soil Microbiota. Description: Ferreira, Pedro, et al. Exploring the Influence of Date Palm Cultivars on Soil Microbiota. ''Microb Ecol''. 2024 Aug 1; '''87''' (1):103
Extended genome-wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry. Description: Ray, Nicholas R, et al. Extended genome-wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry. ''Alzheimers Dement''. 2024 Aug; '''20''' (8):5247-5261
Gene‒Environment Interaction Between CAST Gene and Eye-Rubbing in the Chinese Keratoconus Cohort Study: A Case-Only Study. Description: Yin, Shanshan, et al. Gene‒Environment Interaction Between CAST Gene and Eye-Rubbing in the Chinese Keratoconus Cohort Study: A Case-Only Study. ''Invest Ophthalmol Vis Sci''. 2024 Aug 1; '''65''' (10):36
Genetic associations with human longevity are enriched for oncogenic genes. Description: Park, Junyoung, et al. Genetic associations with human longevity are enriched for oncogenic genes. ''medRxiv''. 2024 Aug 1;
Genetic variants of m(6)A modification genes are associated with survival of HBV-related hepatocellular carcinoma. Description: Liu, Shuyan, et al. Genetic variants of m(6)A modification genes are associated with survival of HBV-related hepatocellular carcinoma. ''J Cell Mol Med''. 2024 Aug; '''28''' (16):e18517
Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol. Description: Alenbawi, Jamil, et al. Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol. ''Hum Genomics''. 2024 Aug 1; '''18''' (1):85
Genomics of ecological adaptation in Canary Island Descurainia (Brassicaceae) and comparisons with other Brassicaceae. Description: Jackson, Amy C, et al. Genomics of ecological adaptation in Canary Island Descurainia (Brassicaceae) and comparisons with other Brassicaceae. ''Ecol Evol''. 2024 Aug; '''14''' (8):e70144
GWAS Identifies DPP6 as Risk Gene of Cognitive Decline in Parkinson's Disease. Description: Li, Chunyu, et al. GWAS Identifies DPP6 as Risk Gene of Cognitive Decline in Parkinson's Disease. ''J Gerontol A Biol Sci Med Sci''. 2024 Aug 1; '''79''' (8):
Harnessing landrace diversity empowers wheat breeding. Description: Cheng, Shifeng, et al. Harnessing landrace diversity empowers wheat breeding. ''Nature''. 2024 Aug; '''632''' (8026):823-831
Human TMEFF1 is a restriction factor for herpes simplex virus in the brain. Description: Chan, Yi-Hao, et al. Human TMEFF1 is a restriction factor for herpes simplex virus in the brain. ''Nature''. 2024 Aug; '''632''' (8024):390-400
IL17RB genetic variants are associated with acamprosate treatment response in patients with alcohol use disorder: A proteomics-informed genomics study. Description: Ho, Ming-Fen, et al. IL17RB genetic variants are associated with acamprosate treatment response in patients with alcohol use disorder: A proteomics-informed genomics study. ''Brain Behav Immun''. 2024 Aug; '''120''': 304-314
Imatinib treatment and longitudinal growth in pediatric patients with chronic myeloid leukemia: influence of demographic, pharmacological, and genetic factors in the German CML-PAED cohort. Description: Stiehler, Sophie, et al. Imatinib treatment and longitudinal growth in pediatric patients with chronic myeloid leukemia: influence of demographic, pharmacological, and genetic factors in the German CML-PAED cohort. ''Haematologica''. 2024 Aug 1; '''109''' (8):2555-2563
Large carpenter bees show high dispersal in a tropical semi-arid region susceptible to desertification. Description: Brasil, Sandara N R, et al. Large carpenter bees show high dispersal in a tropical semi-arid region susceptible to desertification. ''Ecol Evol''. 2024 Aug; '''14''' (8):e70085
Motor progression trajectories and risk of mild cognitive impairment in Parkinson's disease: A latent class trajectory model from PPMI cohort. Description: Chen, Xi, et al. Motor progression trajectories and risk of mild cognitive impairment in Parkinson's disease: A latent class trajectory model from PPMI cohort. ''CNS Neurosci Ther''. 2024 Aug; '''30''' (8):e14918
Optix and cortex/ivory/mir-193 again: the repeated use of two mimicry hotspot loci. Description: Orteu, Anna, et al. Optix and cortex/ivory/mir-193 again: the repeated use of two mimicry hotspot loci. ''Proc Biol Sci''. 2024 Aug; '''291''' (2027):20240627
Peripheral pathway gene variants in lifelong premature ejaculation: CYP19A1, CYP1A1, and CYP1A2 enzymes polymorphisms in Chinese Han men. Description: Wang, Fei, et al. Peripheral pathway gene variants in lifelong premature ejaculation: CYP19A1, CYP1A1, and CYP1A2 enzymes polymorphisms in Chinese Han men. ''Sex Med''. 2024 Aug; '''12''' (4):qfae056
Plasma Proteomic Signature Predicts Myeloid Neoplasm Risk. Description: Tran, Duc, et al. Plasma Proteomic Signature Predicts Myeloid Neoplasm Risk. ''Clin Cancer Res''. 2024 Aug 1; '''30''' (15):3220-3228
Polygenic risk for schizophrenia and bipolar disorder in relation to cardiovascular biomarkers. Description: Reponen, Elina J, et al. Polygenic risk for schizophrenia and bipolar disorder in relation to cardiovascular biomarkers. ''Eur Arch Psychiatry Clin Neurosci''. 2024 Aug; '''274''' (5):1223-1230
Population structure of Dugong dugon across the Indo-Pacific revealed by historical mitogenomes. Description: Furness, Lydia Hildebrand, et al. Population structure of Dugong dugon across the Indo-Pacific revealed by historical mitogenomes. ''R Soc Open Sci''. 2024 Aug; '''11''' (8):240599
Predictive genetic panel for adult asthma using machine learning methods. Description: Gomes, Luciano Gama da Silva, et al. Predictive genetic panel for adult asthma using machine learning methods. ''J Allergy Clin Immunol Glob''. 2024 Aug; '''3''' (3):100282
RNF213 Variants, Vasospastic Angina, and Risk of Fatal Myocardial Infarction. Description: Hikino, Keiko, et al. RNF213 Variants, Vasospastic Angina, and Risk of Fatal Myocardial Infarction. ''JAMA Cardiol''. 2024 Aug 1; '''9''' (8):723-731
Species divergence and environmental adaptation of Picea asperata complex at the whole genome level. Description: Liu, Yifu, et al. Species divergence and environmental adaptation of Picea asperata complex at the whole genome level. ''Ecol Evol''. 2024 Aug; '''14''' (8):e70126
Statins inhibit paclitaxel-induced PD-L1 expression and increase CD8+ T cytotoxicity for better prognosis in breast cancer. Description: Li, Lei, et al. Statins inhibit paclitaxel-induced PD-L1 expression and increase CD8+ T cytotoxicity for better prognosis in breast cancer. ''Int J Surg''. 2024 Aug 1; '''110''' (8):4716-4726
The jacktree genome and population genomics provides insights for the mechanisms of the germination obstacle and the conservation of endangered ornamental plants. Description: Zhu, Sheng, et al. The jacktree genome and population genomics provides insights for the mechanisms of the germination obstacle and the conservation of endangered ornamental plants. ''Hortic Res''. 2024 Aug; '''11''' (8):uhae166
The relationship between 11 different polygenic longevity scores, parental lifespan, and disease diagnosis in the UK Biobank. Description: Don, Janith, et al. The relationship between 11 different polygenic longevity scores, parental lifespan, and disease diagnosis in the UK Biobank. ''Geroscience''. 2024 Aug; '''46''' (4):3911-3927
Towards cascading genetic risk in Alzheimer's disease. Description: Altmann, Andre, et al. Towards cascading genetic risk in Alzheimer's disease. ''Brain''. 2024 Aug 1; '''147''' (8):2680-2690
Unsupervised representation learning on high-dimensional clinical data improves genomic discovery and prediction. Description: Yun, Taedong, et al. Unsupervised representation learning on high-dimensional clinical data improves genomic discovery and prediction. ''Nat Genet''. 2024 Aug; '''56''' (8):1604-1613
Using viral diversity to identify HIV-1 variants under HLA-dependent selection in a systematic viral genome-wide screen. Description: Neuner-Jehle, Nadia, et al. Using viral diversity to identify HIV-1 variants under HLA-dependent selection in a systematic viral genome-wide screen. ''PLoS Pathog''. 2024 Aug; '''20''' (8):e1012385
Why we thrive beneath a northern sky - genomic signals of selection in apple for adaptation to northern Sweden. Description: Skytte Af Satra, J, et al. Why we thrive beneath a northern sky - genomic signals of selection in apple for adaptation to northern Sweden. ''Heredity (Edinb)''. 2024 Aug; '''133''' (2):67-77
An axis of genetic heterogeneity in autism is indexed by age at diagnosis and is associated with varying developmental and mental health profiles. Description: Zhang, Xinhe, et al. An axis of genetic heterogeneity in autism is indexed by age at diagnosis and is associated with varying developmental and mental health profiles. ''medRxiv''. 2024 Aug 2;
A novel framework with automated horizontal pleiotropy adjustment in mendelian randomization. Description: Lin, Zhaotong. A novel framework with automated horizontal pleiotropy adjustment in mendelian randomization. ''HGG Adv''. 2024 Aug 2; '''5''' (4):100339
European farmhouse brewing yeasts form a distinct genetic group. Description: Preiss, Richard, et al. European farmhouse brewing yeasts form a distinct genetic group. ''Appl Microbiol Biotechnol''. 2024 Aug 2; '''108''' (1):430
Genetic association and machine learning improves discovery and prediction of type 1 diabetes. Description: McGrail, Carolyn, et al. Genetic association and machine learning improves discovery and prediction of type 1 diabetes. ''medRxiv''. 2024 Aug 2;
St. Jude Survivorship Portal: Sharing and Analyzing Large Clinical and Genomic Datasets from Pediatric Cancer Survivors. Description: Matt, Gavriel Y, et al. St. Jude Survivorship Portal: Sharing and Analyzing Large Clinical and Genomic Datasets from Pediatric Cancer Survivors. ''Cancer Discov''. 2024 Aug 2; '''14''' (8):1403-1417
Allelic variability in the Rpp1 locus conferring resistance to Asian soybean rust revealed by genome-wide association. Description: Aoyagi, Luciano Nobuhiro, et al. Allelic variability in the Rpp1 locus conferring resistance to Asian soybean rust revealed by genome-wide association. ''BMC Plant Biol''. 2024 Aug 3; '''24''' (1):743
Comprehensive mapping and modelling of the rice regulome landscape unveils the regulatory architecture underlying complex traits. Description: Zhu, Tao, et al. Comprehensive mapping and modelling of the rice regulome landscape unveils the regulatory architecture underlying complex traits. ''Nat Commun''. 2024 Aug 3; '''15''' (1):6562
Genome-wide association study of therapeutic response to statin drugs in cardiovascular disease. Description: Dabiri, Hamed, et al. Genome-wide association study of therapeutic response to statin drugs in cardiovascular disease. ''Sci Rep''. 2024 Aug 3; '''14''' (1):18005
Functional genetics reveals the contribution of delta opioid receptor to type 2 diabetes and beta-cell function. Description: Meulebrouck, Sarah, et al. Functional genetics reveals the contribution of delta opioid receptor to type 2 diabetes and beta-cell function. ''Nat Commun''. 2024 Aug 5; '''15''' (1):6627
Genetic Signatures of Positive Selection in Human Populations Adapted to High Altitude in Papua New Guinea. Description: Gonzalez-Buenfil, Ram, et al. Genetic Signatures of Positive Selection in Human Populations Adapted to High Altitude in Papua New Guinea. ''Genome Biol Evol''. 2024 Aug 5; '''16''' (8):
Human genetic variation determines 24-hour rhythmic gene expression and disease risk. Description: Guan, Dongyin, et al. Human genetic variation determines 24-hour rhythmic gene expression and disease risk. ''Res Sq''. 2024 Aug 5;
Lack of genetic evidence for NLRP3 inflammasome involvement in Parkinson's disease pathogenesis. Description: Senkevich, Konstantin, et al. Lack of genetic evidence for NLRP3 inflammasome involvement in Parkinson's disease pathogenesis. ''NPJ Parkinsons Dis''. 2024 Aug 5; '''10''' (1):145
All of Us diversity and scale improve polygenic prediction contextually with greatest improvements for under-represented populations. Description: Tsuo, Kristin, et al. All of Us diversity and scale improve polygenic prediction contextually with greatest improvements for under-represented populations. ''bioRxiv''. 2024 Aug 6;
Single cell multiome profiling of pancreatic islets reveals physiological changes in cell type-specific regulation associated with diabetes risk. Description: Mummey, Hannah M, et al. Single cell multiome profiling of pancreatic islets reveals physiological changes in cell type-specific regulation associated with diabetes risk. ''bioRxiv''. 2024 Aug 6;
Exome-wide association study identifies KDELR3 mutations in extreme myopia. Description: Yuan, Jian, et al. Exome-wide association study identifies KDELR3 mutations in extreme myopia. ''Nat Commun''. 2024 Aug 7; '''15''' (1):6703
Genetic determinants and phenotypic consequences of blood T-cell proportions in 207,000 diverse individuals. Description: Poisner, Hannah, et al. Genetic determinants and phenotypic consequences of blood T-cell proportions in 207,000 diverse individuals. ''Nat Commun''. 2024 Aug 7; '''15''' (1):6732
haploMAGIC: accurate phasing and detection of recombination in multiparental populations despite genotyping errors. Description: Montero-Tena, Jose A, et al. haploMAGIC: accurate phasing and detection of recombination in multiparental populations despite genotyping errors. ''G3 (Bethesda)''. 2024 Aug 7; '''14''' (8):
Human genetic structure in Northwest France provides new insights into West European historical demography. Description: Alves, Isabel, et al. Human genetic structure in Northwest France provides new insights into West European historical demography. ''Nat Commun''. 2024 Aug 7; '''15''' (1):6710
Mendelian randomization study on causal association of TEF and circadian rhythm with pulmonary arterial hypertension. Description: Chen, Dandan, et al. Mendelian randomization study on causal association of TEF and circadian rhythm with pulmonary arterial hypertension. ''Respir Res''. 2024 Aug 7; '''25''' (1):301
Whole-genome sequencing analysis of soybean diversity across different countries and selection signature of Korean soybean accession. Description: Cho, Youngbeom, et al. Whole-genome sequencing analysis of soybean diversity across different countries and selection signature of Korean soybean accession. ''G3 (Bethesda)''. 2024 Aug 7; '''14''' (8):
Genomic data reveal a north-south split and introgression history of blood fluke (Schistosoma haematobium) populations from across Africa. Description: Platt, Roy N 2nd, et al. Genomic data reveal a north-south split and introgression history of blood fluke (Schistosoma haematobium) populations from across Africa. ''bioRxiv''. 2024 Aug 8;
Meta-analysis of genome-wide association studies for cancer therapy-related cardiovascular dysfunction and functional mapping highlight an intergenic region close to TP63. Description: Martinez-Campelo, L, et al. Meta-analysis of genome-wide association studies for cancer therapy-related cardiovascular dysfunction and functional mapping highlight an intergenic region close to TP63. ''Sci Rep''. 2024 Aug 8; '''14''' (1):18413
Splicing-specific transcriptome-wide association uncovers genetic mechanisms for schizophrenia. Description: Hervoso, Jonatan L, et al. Splicing-specific transcriptome-wide association uncovers genetic mechanisms for schizophrenia. ''Am J Hum Genet''. 2024 Aug 8; '''111''' (8):1573-1587
Structural and genetic diversity in the secreted mucins MUC5AC and MUC5B. Description: Plender, Elizabeth G, et al. Structural and genetic diversity in the secreted mucins MUC5AC and MUC5B. ''Am J Hum Genet''. 2024 Aug 8; '''111''' (8):1700-1716
15 Years of Longitudinal Genetic, Clinical, Cognitive, Imaging, and Biochemical Measures in DIAN. Description: Daniels, Alisha J, et al. 15 Years of Longitudinal Genetic, Clinical, Cognitive, Imaging, and Biochemical Measures in DIAN. ''medRxiv''. 2024 Aug 9;
Circulating pancreatic enzyme levels are a causal biomarker of type 1 diabetes. Description: Elgamal, Ruth M, et al. Circulating pancreatic enzyme levels are a causal biomarker of type 1 diabetes. ''medRxiv''. 2024 Aug 9;
Variable and interactive effects of Sex, APOE epsilon4 and TREM2 on the deposition of tau in entorhinal and neocortical regions. Description: Giorgio, Joseph, et al. Variable and interactive effects of Sex, APOE epsilon4 and TREM2 on the deposition of tau in entorhinal and neocortical regions. ''Res Sq''. 2024 Aug 9;
Genome-Wide Association Study Meta-Analysis Uncovers Novel Genetic Variants Associated with Olfactory Dysfunction. Description: Imtiaz, Mohammed Aslam, et al. Genome-Wide Association Study Meta-Analysis Uncovers Novel Genetic Variants Associated with Olfactory Dysfunction. ''medRxiv''. 2024 Aug 10;
Genomic variation, environmental adaptation, and feralization in ramie, an ancient fiber crop. Description: Wu, Zeng-Yuan, et al. Genomic variation, environmental adaptation, and feralization in ramie, an ancient fiber crop. ''Plant Commun''. 2024 Aug 12; '''5''' (8):100942
Macular structural integrity estimates are associated with Parkinson's disease genetic risk. Description: Diaz-Torres, Santiago, et al. Macular structural integrity estimates are associated with Parkinson's disease genetic risk. ''Acta Neuropathol Commun''. 2024 Aug 13; '''12''' (1):130
Structural variants linked to Alzheimer's Disease and other common age-related clinical and neuropathologic traits. Description: Vialle, Ricardo A, et al. Structural variants linked to Alzheimer's Disease and other common age-related clinical and neuropathologic traits. ''medRxiv''. 2024 Aug 13;
A metabolome-wide Mendelian randomization study prioritizes causal circulating metabolites for reproductive disorders including primary ovarian insufficiency, polycystic ovary syndrome, and abnormal spermatozoa. Description: Chen, Shuang, et al. A metabolome-wide Mendelian randomization study prioritizes causal circulating metabolites for reproductive disorders including primary ovarian insufficiency, polycystic ovary syndrome, and abnormal spermatozoa. ''J Ovarian Res''. 2024 Aug 14; '''17''' (1):166
Multi-omics insight into the metabolic and cellular characteristics in the pathogenesis of hypothyroidism. Description: Zheng, Shengzhang, et al. Multi-omics insight into the metabolic and cellular characteristics in the pathogenesis of hypothyroidism. ''Commun Biol''. 2024 Aug 14; '''7''' (1):990
Causal relationship between systemic lupus erythematosus and adverse pregnancy outcomes: A two-sample Mendelian randomized study. Description: Zhu, Tao, et al. Causal relationship between systemic lupus erythematosus and adverse pregnancy outcomes: A two-sample Mendelian randomized study. ''Heliyon''. 2024 Aug 15; '''10''' (15):e35401
Selection scan in Native Americans of Mexico identifies FADS2 rs174616: Evidence of gene-diet interactions affecting lipid levels and Delta-6-desaturase activity. Description: Romero-Hidalgo, Sandra, et al. Selection scan in Native Americans of Mexico identifies FADS2 rs174616: Evidence of gene-diet interactions affecting lipid levels and Delta-6-desaturase activity. ''Heliyon''. 2024 Aug 15; '''10''' (15):e35477
Decomposition of phenotypic heterogeneity in autism reveals distinct and coherent genetic programs. Description: Litman, Aviya, et al. Decomposition of phenotypic heterogeneity in autism reveals distinct and coherent genetic programs. ''medRxiv''. 2024 Aug 16;
DNA methylation-estimated phenotypes, telomere length and risk of ischemic stroke: epigenetic age acceleration of screening and a Mendelian randomization study. Description: Maimaiti, Aierpati, et al. DNA methylation-estimated phenotypes, telomere length and risk of ischemic stroke: epigenetic age acceleration of screening and a Mendelian randomization study. ''Aging (Albany NY)''. 2024 Aug 16; '''16''' (16):11970-11993
Genetically predicted metabolites mediate the association between immune cells and metabolic dysfunction-associated steatotic liver disease: a mendelian randomization study. Description: Ye, Dan, et al. Genetically predicted metabolites mediate the association between immune cells and metabolic dysfunction-associated steatotic liver disease: a mendelian randomization study. ''Lipids Health Dis''. 2024 Aug 16; '''23''' (1):249
Genetic architecture of long-distance migration and population genomics of the endangered Japanese eel. Description: Liu, Yan-Fang, et al. Genetic architecture of long-distance migration and population genomics of the endangered Japanese eel. ''iScience''. 2024 Aug 16; '''27''' (8):110563
Genome-wide association reveals a locus in neuregulin 3 associated with gabapentin efficacy in women with chronic pelvic pain. Description: Mackenzie, Scott C, et al. Genome-wide association reveals a locus in neuregulin 3 associated with gabapentin efficacy in women with chronic pelvic pain. ''iScience''. 2024 Aug 16; '''27''' (8):110370
Genome-wide variation study and inter-tissue communication analysis unveil regulatory mechanisms of egg-laying performance in chickens. Description: Wang, Dandan, et al. Genome-wide variation study and inter-tissue communication analysis unveil regulatory mechanisms of egg-laying performance in chickens. ''Nat Commun''. 2024 Aug 16; '''15''' (1):7069
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy. Description: Wang, Hui, et al. Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy. ''Mol Neurodegener''. 2024 Aug 16; '''19''' (1):61
Elucidating the pan-oncologic landscape of S100A9: prognostic and therapeutic corollaries from an integrative bioinformatics and Mendelian randomization analysis. Description: Chen, Yingying, et al. Elucidating the pan-oncologic landscape of S100A9: prognostic and therapeutic corollaries from an integrative bioinformatics and Mendelian randomization analysis. ''Sci Rep''. 2024 Aug 17; '''14''' (1):19071
A roadmap to the molecular human linking multiomics with population traits and diabetes subtypes. Description: Halama, Anna, et al. A roadmap to the molecular human linking multiomics with population traits and diabetes subtypes. ''Nat Commun''. 2024 Aug 19; '''15''' (1):7111
Genetic Variants Associated with Body Mass Index Changes in Korean Adults: The Anseong and Ansan Cohorts of the Korean Genome and Epidemiology Study. Description: Lee, Sang-Im, et al. Genetic Variants Associated with Body Mass Index Changes in Korean Adults: The Anseong and Ansan Cohorts of the Korean Genome and Epidemiology Study. ''Curr Issues Mol Biol''. 2024 Aug 19; '''46''' (8):9074-9081
Deep learning-derived splenic radiomics, genomics, and coronary artery disease. Description: Kamineni, Meghana, et al. Deep learning-derived splenic radiomics, genomics, and coronary artery disease. ''medRxiv''. 2024 Aug 20;
Development and validation of sex-linked molecular markers for rapid and accurate identification of male and female Hippophae tibetana plants. Description: Zeng, Zhefei, et al. Development and validation of sex-linked molecular markers for rapid and accurate identification of male and female Hippophae tibetana plants. ''Sci Rep''. 2024 Aug 20; '''14''' (1):19243
Genomic architecture and population structure of Boreogadus saida from Canadian waters. Description: Bringloe, Trevor T, et al. Genomic architecture and population structure of Boreogadus saida from Canadian waters. ''Sci Rep''. 2024 Aug 20; '''14''' (1):19331
Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance. Description: Thomsen, Hauke, et al. Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance. ''Blood Cancer J''. 2024 Aug 20; '''14''' (1):140
Candidate markers for enhanced host response to PRRS have scarce adverse effects on pigs' growth and production. Description: Laghouaouta, Houda, et al. Candidate markers for enhanced host response to PRRS have scarce adverse effects on pigs' growth and production. ''Porcine Health Manag''. 2024 Aug 21; '''10''' (1):29
Unique genetic and risk-factor profiles in clusters of major depressive disorder-related multimorbidity trajectories. Description: Gezsi, Andras, et al. Unique genetic and risk-factor profiles in clusters of major depressive disorder-related multimorbidity trajectories. ''Nat Commun''. 2024 Aug 21; '''15''' (1):7190
Genome-wide association study of copy number variations in Parkinson's disease. Description: Landoulsi, Zied, et al. Genome-wide association study of copy number variations in Parkinson's disease. ''medRxiv''. 2024 Aug 22;
The CALERIE() Genomic Data Resource. Description: Ryan, C P, et al. The CALERIE() Genomic Data Resource. ''bioRxiv''. 2024 Aug 22;
Epigenetic and genetic risk of Alzheimer disease from autopsied brains in two ethnic groups. Description: Ma, Yiyi, et al. Epigenetic and genetic risk of Alzheimer disease from autopsied brains in two ethnic groups. ''Acta Neuropathol''. 2024 Aug 23; '''148''' (1):27
BDNF Val66Met moderates episodic memory decline and tau biomarker increases in early sporadic Alzheimer's disease. Description: Thomson, Diny, et al. BDNF Val66Met moderates episodic memory decline and tau biomarker increases in early sporadic Alzheimer's disease. ''Arch Clin Neuropsychol''. 2024 Aug 24; '''39''' (6):683-691
Biallelic structural variants in three patients with ERCC8-related Cockayne syndrome and a potential pitfall of copy number variation analysis. Description: Watanabe, Daisuke, et al. Biallelic structural variants in three patients with ERCC8-related Cockayne syndrome and a potential pitfall of copy number variation analysis. ''Sci Rep''. 2024 Aug 26; '''14''' (1):19741
Genetic association of antinuclear antibodies with HLA in JIA patients: a Swedish cohort study. Description: Saleh, Raya, et al. Genetic association of antinuclear antibodies with HLA in JIA patients: a Swedish cohort study. ''Pediatr Rheumatol Online J''. 2024 Aug 26; '''22''' (1):79
Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK Biobank. Description: Hillary, Robert F, et al. Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK Biobank. ''Nat Commun''. 2024 Aug 26; '''15''' (1):7346
Enhancing personalized gene expression prediction from DNA sequences using genomic foundation models. Description: Ramprasad, Pratik, et al. Enhancing personalized gene expression prediction from DNA sequences using genomic foundation models. ''HGG Adv''. 2024 Aug 27; '''5''' (4):100347
Serum proteomic profiling of physical activity reveals CD300LG as a novel exerkine with a potential causal link to glucose homeostasis. Description: Lee-Odegard, Sindre, et al. Serum proteomic profiling of physical activity reveals CD300LG as a novel exerkine with a potential causal link to glucose homeostasis. ''Elife''. 2024 Aug 27; '''13''':
Genetic modifiers and ascertainment drive variable expressivity of complex disorders. Description: Jensen, Matthew, et al. Genetic modifiers and ascertainment drive variable expressivity of complex disorders. ''medRxiv''. 2024 Aug 28;
Integrating Multi-Organ Imaging-Derived Phenotypes and Genomic Information for Predicting the Occurrence of Common Diseases. Description: Liu, Meng, et al. Integrating Multi-Organ Imaging-Derived Phenotypes and Genomic Information for Predicting the Occurrence of Common Diseases. ''Bioengineering (Basel)''. 2024 Aug 28; '''11''' (9):
Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome. Description: Lancaster, Megan C, et al. Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome. ''Nat Commun''. 2024 Aug 29; '''15''' (1):7507
Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism. Description: Sole-Navais, Pol, et al. Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism. ''Nat Commun''. 2024 Aug 30; '''15''' (1):7550
Genome-wide association study based on clustering by obesity-related variables uncovers a genetic architecture of obesity in the Japanese and the UK populations. Description: Takahashi, Ippei, et al. Genome-wide association study based on clustering by obesity-related variables uncovers a genetic architecture of obesity in the Japanese and the UK populations. ''Heliyon''. 2024 Aug 30; '''10''' (16):e36023
A Phenome-Wide Association Study (PheWAS) of Genetic Risk for C-Reactive Protein in Children of European Ancestry: Results From the ABCD Study. Description: Norton, Sara A, et al. A Phenome-Wide Association Study (PheWAS) of Genetic Risk for C-Reactive Protein in Children of European Ancestry: Results From the ABCD Study. ''medRxiv''. 2024 Aug 31;
Genetic association of GJA8 with long-segment Hirschsprung's disease in southern Chinese children. Description: Ma, Zuyi, et al. Genetic association of GJA8 with long-segment Hirschsprung's disease in southern Chinese children. ''Transl Pediatr''. 2024 Aug 31; '''13''' (8):1395-1405
Multipartite network analysis to identify environmental and genetic associations of metabolic syndrome in the Korean population. Description: Shin, Ji-Eun, et al. Multipartite network analysis to identify environmental and genetic associations of metabolic syndrome in the Korean population. ''Sci Rep''. 2024 Aug 31; '''14''' (1):20283
Adaptation of Fusarium Head Blight Pathogens to Changes in Agricultural Practices and Human Migration. Description: Yang, Meixin, et al. Adaptation of Fusarium Head Blight Pathogens to Changes in Agricultural Practices and Human Migration. ''Adv Sci (Weinh)''. 2024 Sep; '''11''' (36):e2401899
Alzheimer's disease genetic pathways impact cerebrospinal fluid biomarkers and imaging endophenotypes in non-demented individuals. Description: Lorenzini, Luigi, et al. Alzheimer's disease genetic pathways impact cerebrospinal fluid biomarkers and imaging endophenotypes in non-demented individuals. ''Alzheimers Dement''. 2024 Sep; '''20''' (9):6146-6160
Ancient Rapanui genomes reveal resilience and pre-European contact with the Americas. Description: Moreno-Mayar, J Victor, et al. Ancient Rapanui genomes reveal resilience and pre-European contact with the Americas. ''Nature''. 2024 Sep; '''633''' (8029):389-397
Association mapping and candidate gene identification for yield traits in European hazelnut (Corylus avellana L.). Description: Baytar, Asena Akkose, et al. Association mapping and candidate gene identification for yield traits in European hazelnut (Corylus avellana L.). ''Plant Direct''. 2024 Sep; '''8''' (8):e625
A Two-Sample Mendelian Randomization Study of Neuroticism and Sleep Bruxism. Description: Strausz, T, et al. A Two-Sample Mendelian Randomization Study of Neuroticism and Sleep Bruxism. ''J Dent Res''. 2024 Sep; '''103''' (10):980-987
Century-long timelines of herbarium genomes predict plant stomatal response to climate change. Description: Lang, Patricia L M, et al. Century-long timelines of herbarium genomes predict plant stomatal response to climate change. ''Nat Ecol Evol''. 2024 Sep; '''8''' (9):1641-1653
Chloroplast and whole-genome sequencing shed light on the evolutionary history and phenotypic diversification of peanuts. Description: Zheng, Zheng, et al. Chloroplast and whole-genome sequencing shed light on the evolutionary history and phenotypic diversification of peanuts. ''Nat Genet''. 2024 Sep; '''56''' (9):1975-1984
Conservation genomics of the wild pumpkin Cucurbita radicans in Central Mexico: The influence of a changing environment on the genetic diversity and differentiation of a rare species. Description: Gasca-Pineda, Jaime, et al. Conservation genomics of the wild pumpkin Cucurbita radicans in Central Mexico: The influence of a changing environment on the genetic diversity and differentiation of a rare species. ''J Plant Res''. 2024 Sep; '''137''' (5):799-813
Ethylene Oxide Hemoglobin Adducts in Cord Blood and Offspring's Size at Birth: The NewGeneris European Cohort Study. Description: Harding, Barbara N, et al. Ethylene Oxide Hemoglobin Adducts in Cord Blood and Offspring's Size at Birth: The NewGeneris European Cohort Study. ''Epidemiology''. 2024 Sep 1; '''35''' (5):710-720
Exploring the influence of a single-nucleotide mutation in EIN4 on tomato fruit firmness diversity through fruit pericarp microstructure. Description: Zhang, Shiwen, et al. Exploring the influence of a single-nucleotide mutation in EIN4 on tomato fruit firmness diversity through fruit pericarp microstructure. ''Plant Biotechnol J''. 2024 Sep; '''22''' (9):2379-2394
From Lawn to Health: Understanding the Prostate Cancer Risk in Light DIY Activities. Description: Yang, Rui, et al. From Lawn to Health: Understanding the Prostate Cancer Risk in Light DIY Activities. ''Am J Mens Health''. 2024 Sep-Oct; '''18''' (5):15579883241287386
Gene pool preservation across time and space In Mongolian-speaking Oirats. Description: Balinova, Natalia, et al. Gene pool preservation across time and space In Mongolian-speaking Oirats. ''Eur J Hum Genet''. 2024 Sep; '''32''' (9):1150-1158
Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences. Description: Burren, Oliver S, et al. Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences. ''Nat Genet''. 2024 Sep; '''56''' (9):1832-1840
Genome-wide association study identified candidate genes for egg production traits in the Longyan Shan-ma duck. Description: Sun, Yanfa, et al. Genome-wide association study identified candidate genes for egg production traits in the Longyan Shan-ma duck. ''Poult Sci''. 2024 Sep; '''103''' (9):104032
Genome-wide meta-analysis identifies ancestry-specific loci for Alzheimer's disease. Description: Ge, Yi-Jun, et al. Genome-wide meta-analysis identifies ancestry-specific loci for Alzheimer's disease. ''Alzheimers Dement''. 2024 Sep; '''20''' (9):6243-6256
HLA-DR3 ~ DQ2 associates with sensory neuropathy in paraneoplastic neurological syndromes with Hu antibodies. Description: Muniz-Castrillo, Sergio, et al. HLA-DR3 ~ DQ2 associates with sensory neuropathy in paraneoplastic neurological syndromes with Hu antibodies. ''J Neurol''. 2024 Sep; '''271''' (9):6336-6342
Multi-Omics Integrative Analyses Identified Two Endotypes of Hip Osteoarthritis. Description: Huang, Jingyi, et al. Multi-Omics Integrative Analyses Identified Two Endotypes of Hip Osteoarthritis. ''Metabolites''. 2024 Sep 1; '''14''' (9):
Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression. Description: Crouse, Jacob J, et al. Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression. ''Mol Psychiatry''. 2024 Sep; '''29''' (9):2765-2773
Prevalence of actionable pharmacogenetic variants and high-risk drug prescriptions: A Swiss hospital-based cohort study. Description: Hodel, Flavia, et al. Prevalence of actionable pharmacogenetic variants and high-risk drug prescriptions: A Swiss hospital-based cohort study. ''Clin Transl Sci''. 2024 Sep; '''17''' (9):e70009
Sex-Specific Susceptibility Loci Associated With Coronary Artery Aneurysms in Patients With Kawasaki Disease. Description: Kim, Jae-Jung, et al. Sex-Specific Susceptibility Loci Associated With Coronary Artery Aneurysms in Patients With Kawasaki Disease. ''Korean Circ J''. 2024 Sep; '''54''' (9):577-586
The Catalan initiative for the Earth BioGenome Project: contributing local data to global biodiversity genomics. Description: Corominas, Montserrat, et al. The Catalan initiative for the Earth BioGenome Project: contributing local data to global biodiversity genomics. ''NAR Genom Bioinform''. 2024 Sep; '''6''' (3):lqae075
The causal relationship between immune cells and atopic dermatitis: A bidirectional Mendelian randomization study. Description: Zhu, Xu, et al. The causal relationship between immune cells and atopic dermatitis: A bidirectional Mendelian randomization study. ''Skin Res Technol''. 2024 Sep; '''30''' (9):e13858
The genetic basis of the kakapo structural color polymorphism suggests balancing selection by an extinct apex predator. Description: Urban, Lara, et al. The genetic basis of the kakapo structural color polymorphism suggests balancing selection by an extinct apex predator. ''PLoS Biol''. 2024 Sep; '''22''' (9):e3002755
Whole-Genome Analyses Reveal the Distinct Taxonomic Status of the Hainan Population of Endangered Rucervus eldii and Its Conservation Implications. Description: Zheng, Chenqing, et al. Whole-Genome Analyses Reveal the Distinct Taxonomic Status of the Hainan Population of Endangered Rucervus eldii and Its Conservation Implications. ''Evol Appl''. 2024 Sep; '''17''' (9):e70010
Whole genome resequencing reveals the adaptability of native chickens to drought, tropical and frigid environments in Xinjiang. Description: Zhang, Lihua, et al. Whole genome resequencing reveals the adaptability of native chickens to drought, tropical and frigid environments in Xinjiang. ''Poult Sci''. 2024 Sep; '''103''' (9):103947
Introgression drives adaptation to the plateau environment in a subterranean rodent. Description: Kang, Yukun, et al. Introgression drives adaptation to the plateau environment in a subterranean rodent. ''BMC Biol''. 2024 Sep 2; '''22''' (1):187
Assessing Mechanisms of Potential Local Adaptation Through a Seascape Genomic Approach in a Marine Gastropod, Littoraria flava. Description: Cortez, Thaina, et al. Assessing Mechanisms of Potential Local Adaptation Through a Seascape Genomic Approach in a Marine Gastropod, Littoraria flava. ''Genome Biol Evol''. 2024 Sep 3; '''16''' (9):
Causal Association Between Atopic Dermatitis and Keratoconus: A Mendelian Randomization Study. Description: Chang, Yuan, et al. Causal Association Between Atopic Dermatitis and Keratoconus: A Mendelian Randomization Study. ''Transl Vis Sci Technol''. 2024 Sep 3; '''13''' (9):13
Chromosome-Scale Genome Assembly and Characterization of Top-Quality Japanese Green Tea Cultivar 'Seimei'. Description: Kawahara, Yoshihiro, et al. Chromosome-Scale Genome Assembly and Characterization of Top-Quality Japanese Green Tea Cultivar 'Seimei'. ''Plant Cell Physiol''. 2024 Sep 3; '''65''' (8):1271-1284
Comparative Population Genomics of Arctic Sled Dogs Reveals a Deep and Complex History. Description: Smith, Tracy A, et al. Comparative Population Genomics of Arctic Sled Dogs Reveals a Deep and Complex History. ''Genome Biol Evol''. 2024 Sep 3; '''16''' (9):
Extensive transmission and variation in a functional receptor for praziquantel resistance in endemic Schistosoma mansoni. Description: Berger, Duncan J, et al. Extensive transmission and variation in a functional receptor for praziquantel resistance in endemic Schistosoma mansoni. ''bioRxiv''. 2024 Sep 3;
Genome-wide discovery of selection signatures in four Anatolian sheep breeds revealed by ddRADseq. Description: Argun Karsli, Bahar, et al. Genome-wide discovery of selection signatures in four Anatolian sheep breeds revealed by ddRADseq. ''Sci Rep''. 2024 Sep 3; '''14''' (1):20518
Mitochondrial Variation in Anopheles gambiae and Anopheles coluzzii: Phylogeographic Legacy and Mitonuclear Associations With Metabolic Resistance to Pathogens and Insecticides. Description: Amaya Romero, Jorge E, et al. Mitochondrial Variation in Anopheles gambiae and Anopheles coluzzii: Phylogeographic Legacy and Mitonuclear Associations With Metabolic Resistance to Pathogens and Insecticides. ''Genome Biol Evol''. 2024 Sep 3; '''16''' (9):
Predictive value of polygenic risk score for prostate cancer incidence and prognosis in the Han Chinese. Description: Hung, Sheng-Chun, et al. Predictive value of polygenic risk score for prostate cancer incidence and prognosis in the Han Chinese. ''Sci Rep''. 2024 Sep 3; '''14''' (1):20453
Transcriptomic response to nitrogen availability reveals signatures of adaptive plasticity during tetraploid wheat domestication. Description: Pieri, Alice, et al. Transcriptomic response to nitrogen availability reveals signatures of adaptive plasticity during tetraploid wheat domestication. ''Plant Cell''. 2024 Sep 3; '''36''' (9):3809-3823
An amplicon panel for high-throughput and low-cost genotyping of Pacific oyster. Description: Sutherland, Ben J G, et al. An amplicon panel for high-throughput and low-cost genotyping of Pacific oyster. ''G3 (Bethesda)''. 2024 Sep 4; '''14''' (9):
Chromosome X-wide association study in case control studies of pathologically confirmed Alzheimer's disease in a European population. Description: Simmonds, Emily, et al. Chromosome X-wide association study in case control studies of pathologically confirmed Alzheimer's disease in a European population. ''Transl Psychiatry''. 2024 Sep 4; '''14''' (1):358
Comparative Genomics Supports Ecologically Induced Selection as a Putative Driver of Banded Penguin Diversification. Description: Leon, Fabiola, et al. Comparative Genomics Supports Ecologically Induced Selection as a Putative Driver of Banded Penguin Diversification. ''Mol Biol Evol''. 2024 Sep 4; '''41''' (9):
Human milk oligosaccharides are associated with maternal genetics and respiratory health of human milk-fed children. Description: Ambalavanan, Amirthagowri, et al. Human milk oligosaccharides are associated with maternal genetics and respiratory health of human milk-fed children. ''Nat Commun''. 2024 Sep 4; '''15''' (1):7735
Inference of Host-Pathogen Interaction Matrices from Genome-Wide Polymorphism Data. Description: Markle, Hanna, et al. Inference of Host-Pathogen Interaction Matrices from Genome-Wide Polymorphism Data. ''Mol Biol Evol''. 2024 Sep 4; '''41''' (9):
Phenome-Wide Association of APOE Alleles in the All of Us Research Program. Description: Khajouei, Ehsan, et al. Phenome-Wide Association of APOE Alleles in the All of Us Research Program. ''medRxiv''. 2024 Sep 4;
The Genetic Architecture of Recombination Rates is Polygenic and Differs Between the Sexes in Wild House Sparrows (Passer domesticus). Description: McAuley, John B, et al. The Genetic Architecture of Recombination Rates is Polygenic and Differs Between the Sexes in Wild House Sparrows (Passer domesticus). ''Mol Biol Evol''. 2024 Sep 4; '''41''' (9):
A genome-wide association study of occupational creativity and its relations with well-being and career success. Description: Li, Wen-Dong, et al. A genome-wide association study of occupational creativity and its relations with well-being and career success. ''Commun Biol''. 2024 Sep 5; '''7''' (1):1092
Sex-specific associations of Notch signaling with chronic HBV infection: a study from Taiwan Biobank. Description: Jen, I-An, et al. Sex-specific associations of Notch signaling with chronic HBV infection: a study from Taiwan Biobank. ''Biol Sex Differ''. 2024 Sep 5; '''15''' (1):69
Cognitive processing speed and accuracy are intrinsically different in genetic architecture and brain phenotypes. Description: Li, Mingyang, et al. Cognitive processing speed and accuracy are intrinsically different in genetic architecture and brain phenotypes. ''Nat Commun''. 2024 Sep 6; '''15''' (1):7786
Genome-wide association studies of Down syndrome associated congenital heart defects. Description: Feldman, Elizabeth R, et al. Genome-wide association studies of Down syndrome associated congenital heart defects. ''medRxiv''. 2024 Sep 6;
Smoking and alcohol by HPV status in head and neck cancer: a Mendelian randomization study. Description: Thakral, Abhinav, et al. Smoking and alcohol by HPV status in head and neck cancer: a Mendelian randomization study. ''Nat Commun''. 2024 Sep 7; '''15''' (1):7835
Single-nucleus multi-omics identifies shared and distinct pathways in Pick's and Alzheimer's disease. Description: Shi, Zechuan, et al. Single-nucleus multi-omics identifies shared and distinct pathways in Pick's and Alzheimer's disease. ''bioRxiv''. 2024 Sep 8;
Cellular indexing of transcriptomes and epitopes (CITE-Seq) in hidradenitis suppurativa identifies dysregulated cell types in peripheral blood and facilitates diagnosis via machine learning. Description: Kumar, Sugandh, et al. Cellular indexing of transcriptomes and epitopes (CITE-Seq) in hidradenitis suppurativa identifies dysregulated cell types in peripheral blood and facilitates diagnosis via machine learning. ''Res Sq''. 2024 Sep 9;
Development and validation of a 66K SNP array for the hard clam (Mercenaria mercenaria). Description: Grouzdev, Denis, et al. Development and validation of a 66K SNP array for the hard clam (Mercenaria mercenaria). ''BMC Genomics''. 2024 Sep 9; '''25''' (1):847
Dual-extraction modeling: A multi-modal deep-learning architecture for phenotypic prediction and functional gene mining of complex traits. Description: Ren, Yanlin, et al. Dual-extraction modeling: A multi-modal deep-learning architecture for phenotypic prediction and functional gene mining of complex traits. ''Plant Commun''. 2024 Sep 9; '''5''' (9):101002
Enhancing genetic association power in endometriosis through unsupervised clustering of clinical subtypes identified from electronic health records. Description: Guare, Lindsay A, et al. Enhancing genetic association power in endometriosis through unsupervised clustering of clinical subtypes identified from electronic health records. ''Res Sq''. 2024 Sep 9;
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes. Description: Farrell, Kurt, et al. Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes. ''Nat Commun''. 2024 Sep 9; '''15''' (1):7880
Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration. Description: Ahmad, Shahzad, et al. Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration. ''Commun Biol''. 2024 Sep 9; '''7''' (1):1103
Host genetics and gut microbiota synergistically regulate feed utilization in egg-type chickens. Description: Zhang, Wenxin, et al. Host genetics and gut microbiota synergistically regulate feed utilization in egg-type chickens. ''J Anim Sci Biotechnol''. 2024 Sep 9; '''15''' (1):123
Long-term longitudinal analysis of 4,187 participants reveals insights into determinants of clonal hematopoiesis. Description: Uddin, Md Mesbah, et al. Long-term longitudinal analysis of 4,187 participants reveals insights into determinants of clonal hematopoiesis. ''Nat Commun''. 2024 Sep 9; '''15''' (1):7858
Streamlined whole-genome genotyping through NGS-enhanced thermal asymmetric interlaced (TAIL)-PCR. Description: Zhao, Sheng, et al. Streamlined whole-genome genotyping through NGS-enhanced thermal asymmetric interlaced (TAIL)-PCR. ''Plant Commun''. 2024 Sep 9; '''5''' (9):100983
Decomposed interaction testing improves detection of genetic modifiers of the relationship of dietary omega-3 fatty acid intake and its plasma biomarkers with hsCRP in the UK Biobank. Description: Westerman, Kenneth E, et al. Decomposed interaction testing improves detection of genetic modifiers of the relationship of dietary omega-3 fatty acid intake and its plasma biomarkers with hsCRP in the UK Biobank. ''medRxiv''. 2024 Sep 10;
Genomic diversity and population structure of Carniolan honey bee in its native habitat. Description: Lukic, Boris, et al. Genomic diversity and population structure of Carniolan honey bee in its native habitat. ''BMC Genomics''. 2024 Sep 10; '''25''' (1):849
A partitioned polygenic risk score reveals distinct contributions to psoriasis clinical phenotypes across a multi-ethnic cohort. Description: Orcales, Faye, et al. A partitioned polygenic risk score reveals distinct contributions to psoriasis clinical phenotypes across a multi-ethnic cohort. ''J Transl Med''. 2024 Sep 11; '''22''' (1):835
Genetic structure, selective characterization and specific molecular identity cards of high-yielding Houdan chickens based on genome-wide SNP. Description: Liu, Cong, et al. Genetic structure, selective characterization and specific molecular identity cards of high-yielding Houdan chickens based on genome-wide SNP. ''Poult Sci''. 2024 Sep 11; '''103''' (12):104325
Multi-ancestry GWAS reveals loci linked to human variation in LINE-1- and Alu-copy numbers. Description: Bravo, Juan I, et al. Multi-ancestry GWAS reveals loci linked to human variation in LINE-1- and Alu-copy numbers. ''bioRxiv''. 2024 Sep 11;
PopMLvis: a tool for analysis and visualization of population structure using genotype data from genome-wide association studies. Description: Elshrif, Mohamed, et al. PopMLvis: a tool for analysis and visualization of population structure using genotype data from genome-wide association studies. ''BMC Bioinformatics''. 2024 Sep 11; '''25''' (1):298
The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes. Description: Amiri Roudbar, Mahmoud, et al. The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes. ''Hum Genomics''. 2024 Sep 11; '''18''' (1):98
Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks. Description: German, Jakob, et al. Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks. ''medRxiv''. 2024 Sep 12;
Causal relationships between dyslexia and the risk of eight dementias. Description: Zhu, Ping, et al. Causal relationships between dyslexia and the risk of eight dementias. ''Transl Psychiatry''. 2024 Sep 12; '''14''' (1):371
Combined Genome-Wide Association Study and Haplotype Analysis Identifies Candidate Genes Affecting Growth Traits of Inner Mongolian Cashmere Goats. Description: Ao, Xiaofang, et al. Combined Genome-Wide Association Study and Haplotype Analysis Identifies Candidate Genes Affecting Growth Traits of Inner Mongolian Cashmere Goats. ''Vet Sci''. 2024 Sep 12; '''11''' (9):
Commonly used genomic arrays may lose information due to imperfect coverage of discovered variants for autism spectrum disorder. Description: Yao, Michael, et al. Commonly used genomic arrays may lose information due to imperfect coverage of discovered variants for autism spectrum disorder. ''J Neurodev Disord''. 2024 Sep 12; '''16''' (1):54
Genetically predicted effects of 10 sleep phenotypes on revision of knee arthroplasty: a mendelian randomization study. Description: Bi, Zhiguo, et al. Genetically predicted effects of 10 sleep phenotypes on revision of knee arthroplasty: a mendelian randomization study. ''J Orthop Surg Res''. 2024 Sep 12; '''19''' (1):563
Genetic regulation of microRNAs in the older adult brain and their contribution to neuropsychiatric conditions. Description: Vattathil, Selina M, et al. Genetic regulation of microRNAs in the older adult brain and their contribution to neuropsychiatric conditions. ''bioRxiv''. 2024 Sep 12;
Genetic variants associated with response to anti-CGRP monoclonal antibody therapy in a chronic migraine Han Chinese population. Description: An, Yu-Chin, et al. Genetic variants associated with response to anti-CGRP monoclonal antibody therapy in a chronic migraine Han Chinese population. ''J Headache Pain''. 2024 Sep 12; '''25''' (1):149
Mitochondrial sequence variants: testing imputation accuracy and their association with dairy cattle milk traits. Description: Dorji, Jigme, et al. Mitochondrial sequence variants: testing imputation accuracy and their association with dairy cattle milk traits. ''Genet Sel Evol''. 2024 Sep 12; '''56''' (1):62
A sex-stratified analysis of the genetic architecture of human brain anatomy. Description: Shafee, Rebecca, et al. A sex-stratified analysis of the genetic architecture of human brain anatomy. ''Nat Commun''. 2024 Sep 13; '''15''' (1):8041
Association of VDR Polymorphisms with Muscle Mass Development in Elite Young Soccer Players: A Pilot Study. Description: Flore, Laura, et al. Association of VDR Polymorphisms with Muscle Mass Development in Elite Young Soccer Players: A Pilot Study. ''Sports (Basel)''. 2024 Sep 13; '''12''' (9):
Genome-wide association studies of thyroid-related hormones, dysfunction, and autoimmunity among 85,421 Chinese pregnancies. Description: Wei, Yuandan, et al. Genome-wide association studies of thyroid-related hormones, dysfunction, and autoimmunity among 85,421 Chinese pregnancies. ''Nat Commun''. 2024 Sep 13; '''15''' (1):8004
NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke. Description: Rodriguez-Flores, Juan Lorenzo, et al. NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke. ''Nat Commun''. 2024 Sep 13; '''15''' (1):8029
Phenotype wide association study links bronchopulmonary dysplasia with eosinophilia in children. Description: Kelchtermans, Jelte, et al. Phenotype wide association study links bronchopulmonary dysplasia with eosinophilia in children. ''Sci Rep''. 2024 Sep 13; '''14''' (1):21391
Genome-wide discovery and integrative genomic characterization of insulin resistance loci using serum triglycerides to HDL-cholesterol ratio as a proxy. Description: DeForest, Natalie, et al. Genome-wide discovery and integrative genomic characterization of insulin resistance loci using serum triglycerides to HDL-cholesterol ratio as a proxy. ''Nat Commun''. 2024 Sep 14; '''15''' (1):8068
Sequence variants influencing the regulation of serum IgG subclass levels. Description: Olafsdottir, Thorunn A, et al. Sequence variants influencing the regulation of serum IgG subclass levels. ''Nat Commun''. 2024 Sep 14; '''15''' (1):8054
A GWAS of ACE Inhibitor-Induced Angioedema in a South African Population. Description: Mugo, Jacquiline W, et al. A GWAS of ACE Inhibitor-Induced Angioedema in a South African Population. ''medRxiv''. 2024 Sep 15;
Haplotype-based pangenomes reveal genetic variations and climate adaptations in moso bamboo populations. Description: Hou, Yinguang, et al. Haplotype-based pangenomes reveal genetic variations and climate adaptations in moso bamboo populations. ''Nat Commun''. 2024 Sep 15; '''15''' (1):8085
Heat stress analysis suggests a genetic basis for tolerance in Macrocystis pyrifera across developmental stages. Description: Harden, Maddelyn, et al. Heat stress analysis suggests a genetic basis for tolerance in Macrocystis pyrifera across developmental stages. ''Commun Biol''. 2024 Sep 15; '''7''' (1):1147
Pervasive findings of directional selection realize the promise of ancient DNA to elucidate human adaptation. Description: Akbari, Ali, et al. Pervasive findings of directional selection realize the promise of ancient DNA to elucidate human adaptation. ''bioRxiv''. 2024 Sep 15;
Atlas of telomeric repeat diversity in Arabidopsis thaliana. Description: Tao, Yueqi, et al. Atlas of telomeric repeat diversity in Arabidopsis thaliana. ''Genome Biol''. 2024 Sep 16; '''25''' (1):244
Genetic-Dependent Brain Signatures of Resilience: Interactions among Childhood Abuse, Genetic Risks and Brain Function. Description: Lu, Han, et al. Genetic-Dependent Brain Signatures of Resilience: Interactions among Childhood Abuse, Genetic Risks and Brain Function. ''bioRxiv''. 2024 Sep 16;
Pedigree reconstruction based on genotype data in chickens. Description: Zhou, Yan, et al. Pedigree reconstruction based on genotype data in chickens. ''Poult Sci''. 2024 Sep 16; '''103''' (12):104327
Analysis of genotyping data reveals the unique genetic diversity represented by the breeds of sheep native to the United Kingdom. Description: Kerr, Eleanor, et al. Analysis of genotyping data reveals the unique genetic diversity represented by the breeds of sheep native to the United Kingdom. ''BMC Genom Data''. 2024 Sep 17; '''25''' (1):82
Chromosome-level genome and population genomics of the intermediate horseshoe bat ( Rhinolophus affinis) reveal the molecular basis of virus tolerance in Rhinolophus and echolocation call frequency variation. Description: Zhao, Le, et al. Chromosome-level genome and population genomics of the intermediate horseshoe bat ( Rhinolophus affinis) reveal the molecular basis of virus tolerance in Rhinolophus and echolocation call frequency variation. ''Zool Res''. 2024 Sep 18; '''45''' (5):1147-1160
Genetic history and biological adaptive landscape of the Tujia people inferred from shared haplotypes and alleles. Description: Chen, Jing, et al. Genetic history and biological adaptive landscape of the Tujia people inferred from shared haplotypes and alleles. ''Hum Genomics''. 2024 Sep 18; '''18''' (1):104
Genomic diversity study of highly crossbred cattle population in a Low and Middle Tropical environment. Description: Guerrero, Luisa Fernanda Naranjo, et al. Genomic diversity study of highly crossbred cattle population in a Low and Middle Tropical environment. ''Trop Anim Health Prod''. 2024 Sep 18; '''56''' (8):258
Identifying genetic variants associated with chromatin looping and genome function. Description: Bhattacharyya, Sourya, et al. Identifying genetic variants associated with chromatin looping and genome function. ''Nat Commun''. 2024 Sep 18; '''15''' (1):8174
Validation of cross-progeny variance genomic prediction using simulations and experimental data in winter elite bread wheat. Description: Oget-Ebrad, Claire, et al. Validation of cross-progeny variance genomic prediction using simulations and experimental data in winter elite bread wheat. ''Theor Appl Genet''. 2024 Sep 18; '''137''' (10):226
Variation in spatial population structure in the Anopheles gambiae species complex. Description: McCann, Robert S, et al. Variation in spatial population structure in the Anopheles gambiae species complex. ''bioRxiv''. 2024 Sep 18;
Whole genome sequence analysis of population structure and insecticide resistance markers in Anopheles melas from the Bijagos Archipelago, Guinea-Bissau. Description: Moss, Sophie, et al. Whole genome sequence analysis of population structure and insecticide resistance markers in Anopheles melas from the Bijagos Archipelago, Guinea-Bissau. ''Parasit Vectors''. 2024 Sep 18; '''17''' (1):396
Atrial fibrillation variant-to-gene prioritization through cross-ancestry eQTL and single-nucleus multiomic analyses. Description: Leblanc, Francis J A, et al. Atrial fibrillation variant-to-gene prioritization through cross-ancestry eQTL and single-nucleus multiomic analyses. ''iScience''. 2024 Sep 20; '''27''' (9):110660
A multi-omics study of brain tissue transcription and DNA methylation revealing the genetic pathogenesis of ADHD. Description: Wang, Jingkai, et al. A multi-omics study of brain tissue transcription and DNA methylation revealing the genetic pathogenesis of ADHD. ''Brief Bioinform''. 2024 Sep 23; '''25''' (6):
Genetic Risk for Alcohol Use Disorder in Relation to Individual Symptom Criteria: Do Polygenic Indices Provide Unique Information for Understanding Severity and Heterogeneity? Description: Kim, Yongguk, et al. Genetic Risk for Alcohol Use Disorder in Relation to Individual Symptom Criteria: Do Polygenic Indices Provide Unique Information for Understanding Severity and Heterogeneity? ''medRxiv''. 2024 Sep 23;
Predicting functional outcome in ischemic stroke patients using genetic, environmental, and clinical factors: a machine learning analysis of population-based prospective cohort study. Description: Chen, Siding, et al. Predicting functional outcome in ischemic stroke patients using genetic, environmental, and clinical factors: a machine learning analysis of population-based prospective cohort study. ''Brief Bioinform''. 2024 Sep 23; '''25''' (6):
Characterization and Expression Analysis of the C-Type Lectin Ladderlectin in Litopenaeus vannamei Post-WSSV Infection. Description: Xue, Qian, et al. Characterization and Expression Analysis of the C-Type Lectin Ladderlectin in Litopenaeus vannamei Post-WSSV Infection. ''Biology (Basel)''. 2024 Sep 24; '''13''' (10):
Proteogenomic analysis integrated with electronic health records data reveals disease-associated variants in Black Americans. Description: Tahir, Usman A, et al. Proteogenomic analysis integrated with electronic health records data reveals disease-associated variants in Black Americans. ''J Clin Invest''. 2024 Sep 24; '''134''' (21):
Identification of genomic regions associated with fatty acid metabolism across blood, liver, backfat and muscle in pigs. Description: Liu, Junhui, et al. Identification of genomic regions associated with fatty acid metabolism across blood, liver, backfat and muscle in pigs. ''Genet Sel Evol''. 2024 Sep 26; '''56''' (1):66
Powerful mapping of cis-genetic effects on gene expression across diverse populations reveals novel disease-critical genes. Description: Akamatsu, Kai, et al. Powerful mapping of cis-genetic effects on gene expression across diverse populations reveals novel disease-critical genes. ''medRxiv''. 2024 Sep 26;
Capitalizing on genebank core collections for rare and novel disease resistance loci to enhance barley resilience. Description: Yuan, Zhihui, et al. Capitalizing on genebank core collections for rare and novel disease resistance loci to enhance barley resilience. ''J Exp Bot''. 2024 Sep 27; '''75''' (18):5940-5954
Causal effects of cardiovascular health on five epigenetic clocks. Description: Sung, Hsien-Liang, et al. Causal effects of cardiovascular health on five epigenetic clocks. ''Clin Epigenetics''. 2024 Sep 27; '''16''' (1):134
Endothelial force sensing signals to parenchymal cells to regulate bile and plasma lipids. Description: Lichtenstein, Laeticia, et al. Endothelial force sensing signals to parenchymal cells to regulate bile and plasma lipids. ''Sci Adv''. 2024 Sep 27; '''10''' (39):eadq3075
Genome-wide association analysis of treatment resistant schizophrenia for variant discovery and polygenic assessment. Description: Lenk, Hasan Cagin, et al. Genome-wide association analysis of treatment resistant schizophrenia for variant discovery and polygenic assessment. ''Hum Genomics''. 2024 Sep 27; '''18''' (1):108
Identifying and characterizing disease subpopulations that most benefit from polygenic risk scores. Description: Isgut, Monica, et al. Identifying and characterizing disease subpopulations that most benefit from polygenic risk scores. ''Sci Rep''. 2024 Sep 27; '''14''' (1):22124
Loss-of-function of RNA-binding protein PRRC2B causes translational defects and congenital cardiovascular malformation. Description: Das, Debojyoti, et al. Loss-of-function of RNA-binding protein PRRC2B causes translational defects and congenital cardiovascular malformation. ''medRxiv''. 2024 Sep 27;
Genetic disease risks of under-represented founder populations in New York City. Description: Isshiki, Mariko, et al. Genetic disease risks of under-represented founder populations in New York City. ''medRxiv''. 2024 Sep 28;
Genetic Predisposition to Prediabetes in the Kazakh Population. Description: Svyatova, Gulnara, et al. Genetic Predisposition to Prediabetes in the Kazakh Population. ''Curr Issues Mol Biol''. 2024 Sep 28; '''46''' (10):10913-10922
Identification of candidate causal variants and target genes at 41 breast cancer risk loci through differential allelic expression analysis. Description: Xavier, Joana M, et al. Identification of candidate causal variants and target genes at 41 breast cancer risk loci through differential allelic expression analysis. ''Sci Rep''. 2024 Sep 28; '''14''' (1):22526
Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK Biobank. Description: Dinneen, Thomas J, et al. Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK Biobank. ''NPJ Genom Med''. 2024 Sep 28; '''9''' (1):43
Association of single nucleotide polymorphisms and gene-environment interactions with major depressive disorder in Chinese. Description: Luan, Di, et al. Association of single nucleotide polymorphisms and gene-environment interactions with major depressive disorder in Chinese. ''Heliyon''. 2024 Sep 30; '''10''' (18):e37504
Genome-wide association studies for pelvic organ prolapse in the Japanese population. Description: Matsunami, Masatoshi, et al. Genome-wide association studies for pelvic organ prolapse in the Japanese population. ''Commun Biol''. 2024 Sep 30; '''7''' (1):1188
Identification of Candidate Genes for Cold Tolerance at Seedling Stage by GWAS in Rice (Oryza sativa L.). Description: Shi, Huimin, et al. Identification of Candidate Genes for Cold Tolerance at Seedling Stage by GWAS in Rice (Oryza sativa L.). ''Biology (Basel)''. 2024 Sep 30; '''13''' (10):
Identification of ubiquitin markers for survival and prognosis of ovarian cancer. Description: Feng, Yiwen, et al. Identification of ubiquitin markers for survival and prognosis of ovarian cancer. ''Heliyon''. 2024 Sep 30; '''10''' (18):e37288
Intestinal flora and inflammatory bowel disease: Causal relationships and predictive models. Description: Bi, Guan-Wei, et al. Intestinal flora and inflammatory bowel disease: Causal relationships and predictive models. ''Heliyon''. 2024 Sep 30; '''10''' (18):e38101
A genome-wide Association study of the Count of Codeine prescriptions. Description: Song, Wenyu, et al. A genome-wide Association study of the Count of Codeine prescriptions. ''Sci Rep''. 2024 Oct 1; '''14''' (1):22780
A high-density linkage map reveals broad- and fine-scale sex differences in recombination in the hihi (stitchbird; Notiomystis cincta). Description: Tan, Hui Zhen, et al. A high-density linkage map reveals broad- and fine-scale sex differences in recombination in the hihi (stitchbird; Notiomystis cincta). ''Heredity (Edinb)''. 2024 Oct; '''133''' (4):262-275
A novel classification framework for genome-wide association study of whole brain MRI images using deep learning. Description: Yu, Shaojun, et al. A novel classification framework for genome-wide association study of whole brain MRI images using deep learning. ''PLoS Comput Biol''. 2024 Oct; '''20''' (10):e1012527
Blood-derived microRNAs are related to cognitive domains in the general population. Description: Melas, Konstantinos, et al. Blood-derived microRNAs are related to cognitive domains in the general population. ''Alzheimers Dement''. 2024 Oct; '''20''' (10):7138-7159
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations. Description: Yahia, Ashraf, et al. Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations. ''Eur J Hum Genet''. 2024 Oct; '''32''' (10):1214-1226
Comprehensive Evaluation of the Genetic Basis of Keratoconus: New Perspectives for Clinical Translation. Description: Cervan-Martin, Miriam, et al. Comprehensive Evaluation of the Genetic Basis of Keratoconus: New Perspectives for Clinical Translation. ''Invest Ophthalmol Vis Sci''. 2024 Oct 1; '''65''' (12):32
Comprehensive genome-wide analysis of genetic loci and candidate genes associated with litter traits in purebred Berkshire pigs of Korea. Description: Park, Jun. Comprehensive genome-wide analysis of genetic loci and candidate genes associated with litter traits in purebred Berkshire pigs of Korea. ''Anim Biosci''. 2024 Oct; '''37''' (10):1702-1711
Continental-scale associations of Arabidopsis thaliana phyllosphere members with host genotype and drought. Description: Karasov, Talia L, et al. Continental-scale associations of Arabidopsis thaliana phyllosphere members with host genotype and drought. ''Nat Microbiol''. 2024 Oct; '''9''' (10):2748-2758
Dissecting the genetic architecture of sunflower disc diameter using genome-wide association study. Description: Delen, Yavuz, et al. Dissecting the genetic architecture of sunflower disc diameter using genome-wide association study. ''Plant Direct''. 2024 Oct; '''8''' (10):e70010
Evaluation of Aedes aegypti control intervention with pyriproxyfen by lcWGS in Manacapuru, Amazonas, Brazil. Description: Leles, Lorena Ferreira de Oliveira, et al. Evaluation of Aedes aegypti control intervention with pyriproxyfen by lcWGS in Manacapuru, Amazonas, Brazil. ''PLoS Negl Trop Dis''. 2024 Oct; '''18''' (10):e0012547
Genetic Analysis of Neurite Outgrowth Inhibitor-Associated Genes in Parkinson's Disease: A Cross-Sectional Cohort Study. Description: Huang, Xiurong, et al. Genetic Analysis of Neurite Outgrowth Inhibitor-Associated Genes in Parkinson's Disease: A Cross-Sectional Cohort Study. ''CNS Neurosci Ther''. 2024 Oct; '''30''' (10):e70070
Genetic architecture of oral glucose-stimulated insulin release provides biological insights into type 2 diabetes aetiology. Description: Madsen, A L, et al. Genetic architecture of oral glucose-stimulated insulin release provides biological insights into type 2 diabetes aetiology. ''Nat Metab''. 2024 Oct; '''6''' (10):1897-1912
Genetic diversity and population structure of superior shea trees (Vitellaria paradoxa subsp. paradoxa) using SNP markers for the establishment of a core collection in Cote d'Ivoire. Description: Attikora, Affi Jean Paul, et al. Genetic diversity and population structure of superior shea trees (Vitellaria paradoxa subsp. paradoxa) using SNP markers for the establishment of a core collection in Cote d'Ivoire. ''BMC Plant Biol''. 2024 Oct 1; '''24''' (1):913
Genetics of suicide ideation. A role for inflammation and neuroplasticity? Description: Turiaco, Fabrizio, et al. Genetics of suicide ideation. A role for inflammation and neuroplasticity? ''Eur Arch Psychiatry Clin Neurosci''. 2024 Oct; '''274''' (7):1527-1541
Genome-wide analysis tracks the emergence of intraspecific polyploids in Phragmites australis. Description: Wang, Cui, et al. Genome-wide analysis tracks the emergence of intraspecific polyploids in Phragmites australis. ''NPJ Biodivers''. 2024 Oct 1; '''3''' (1):29
Genome-Wide and Transcriptome-Wide Association Studies on Northern New England and Ohio Amyotrophic Lateral Sclerosis Cohorts. Description: Li, Siting, et al. Genome-Wide and Transcriptome-Wide Association Studies on Northern New England and Ohio Amyotrophic Lateral Sclerosis Cohorts. ''Neurol Genet''. 2024 Oct; '''10''' (5):e200188
Genome-Wide Association Analysis Identifies LILRB2 Gene for Pathological Myopia. Description: Jiang, Lingxi, et al. Genome-Wide Association Analysis Identifies LILRB2 Gene for Pathological Myopia. ''Adv Sci (Weinh)''. 2024 Oct; '''11''' (40):e2308968
Hepatic WDR23 proteostasis mediates insulin homeostasis by regulating insulin-degrading enzyme capacity. Description: Duangjan, Chatrawee, et al. Hepatic WDR23 proteostasis mediates insulin homeostasis by regulating insulin-degrading enzyme capacity. ''Geroscience''. 2024 Oct; '''46''' (5):4461-4478
Interactions Between Eleven Sleep-Related Characteristics and Diabetic Nephropathy: A Bidirectional Mendelian Randomization Study in European Population. Description: Zheng, Jie, et al. Interactions Between Eleven Sleep-Related Characteristics and Diabetic Nephropathy: A Bidirectional Mendelian Randomization Study in European Population. ''Psychiatry Investig''. 2024 Oct; '''21''' (10):1083-1093
Polygenic Risk Score, Cardiorespiratory Fitness, and Cardiometabolic Risk Factors: WASEDA'S Health Study. Description: Tanisawa, Kumpei, et al. Polygenic Risk Score, Cardiorespiratory Fitness, and Cardiometabolic Risk Factors: WASEDA'S Health Study. ''Med Sci Sports Exerc''. 2024 Oct 1; '''56''' (10):2026-2038
Population-specific putative causal variants shape quantitative traits. Description: Koyama, Satoshi, et al. Population-specific putative causal variants shape quantitative traits. ''Nat Genet''. 2024 Oct; '''56''' (10):2027-2035
Recurrent evolution and selection shape structural diversity at the amylase locus. Description: Bolognini, Davide, et al. Recurrent evolution and selection shape structural diversity at the amylase locus. ''Nature''. 2024 Oct; '''634''' (8034):617-625
Runs of homozygosity analysis for selection signatures in the Yellow Korean native chicken. Description: Kim, Jaewon, et al. Runs of homozygosity analysis for selection signatures in the Yellow Korean native chicken. ''Anim Biosci''. 2024 Oct; '''37''' (10):1683-1691
Single-nucleus transcriptomic profiling of human orbitofrontal cortex reveals convergent effects of aging and psychiatric disease. Description: Frohlich, Anna S, et al. Single-nucleus transcriptomic profiling of human orbitofrontal cortex reveals convergent effects of aging and psychiatric disease. ''Nat Neurosci''. 2024 Oct; '''27''' (10):2021-2032
Synergistic associations of CD33 variants and hypertension with brain and cognitive aging among dementia-free older adults: A population-based study. Description: Zhu, Min, et al. Synergistic associations of CD33 variants and hypertension with brain and cognitive aging among dementia-free older adults: A population-based study. ''Alzheimers Dement''. 2024 Oct; '''20''' (10):7193-7204
The Association Between Periodontal Disease and Cardiovascular Disease: Insights From Imaging, Observational, and Genetic Data. Description: Sanghvi, Mihir M, et al. The Association Between Periodontal Disease and Cardiovascular Disease: Insights From Imaging, Observational, and Genetic Data. ''JACC Adv''. 2024 Oct; '''3''' (10):101241
The genetic landscape of basal ganglia and implications for common brain disorders. Description: Bahrami, Shahram, et al. The genetic landscape of basal ganglia and implications for common brain disorders. ''Nat Commun''. 2024 Oct 1; '''15''' (1):8476
The interplay between polygenic score for tumor necrosis factor-alpha, brain structural connectivity, and processing speed in major depression. Description: Flinkenflugel, Kira, et al. The interplay between polygenic score for tumor necrosis factor-alpha, brain structural connectivity, and processing speed in major depression. ''Mol Psychiatry''. 2024 Oct; '''29''' (10):3151-3159
The role of environmental sensitivity in the mental health of Syrian refugee children: a multi-level analysis. Description: May, Andrew K, et al. The role of environmental sensitivity in the mental health of Syrian refugee children: a multi-level analysis. ''Mol Psychiatry''. 2024 Oct; '''29''' (10):3170-3179
Whole exome sequencing analyses identified novel genes for Alzheimer's disease and related dementia. Description: Zhang, Ya-Ru, et al. Whole exome sequencing analyses identified novel genes for Alzheimer's disease and related dementia. ''Alzheimers Dement''. 2024 Oct; '''20''' (10):7062-7078
Analyses of whole-genome sequences from 185 North American Thoroughbred horses, spanning 5 generations. Description: Bailey, Ernie, et al. Analyses of whole-genome sequences from 185 North American Thoroughbred horses, spanning 5 generations. ''Sci Rep''. 2024 Oct 2; '''14''' (1):22930
Dietary habits and genetic susceptibility: correlations between nutritional intake and genetic risks for schizophrenia and bipolar disorder. Description: Ohi, Kazutaka, et al. Dietary habits and genetic susceptibility: correlations between nutritional intake and genetic risks for schizophrenia and bipolar disorder. ''Transl Psychiatry''. 2024 Oct 2; '''14''' (1):404
Genomic adaptation to small population size and saltwater consumption in the critically endangered Cat Ba langur. Description: Zhang, Liye, et al. Genomic adaptation to small population size and saltwater consumption in the critically endangered Cat Ba langur. ''Nat Commun''. 2024 Oct 2; '''15''' (1):8531
Regionally enriched rare deleterious exonic variants in the UK and Ireland. Description: Halachev, Mihail, et al. Regionally enriched rare deleterious exonic variants in the UK and Ireland. ''Nat Commun''. 2024 Oct 2; '''15''' (1):8454
Changes in sleep patterns in people with a history of depression during the COVID-19 pandemic: a natural experiment. Description: Shin, Mirim, et al. Changes in sleep patterns in people with a history of depression during the COVID-19 pandemic: a natural experiment. ''BMJ Ment Health''. 2024 Oct 3; '''27''' (1):
Connecting dementia risk loci to the CSF proteome identifies pathophysiological leads for dementia. Description: Reus, Lianne M, et al. Connecting dementia risk loci to the CSF proteome identifies pathophysiological leads for dementia. ''Brain''. 2024 Oct 3; '''147''' (10):3522-3533
Genetics of immune response to Epstein-Barr virus: prospects for multiple sclerosis pathogenesis. Description: Huang, Jesse, et al. Genetics of immune response to Epstein-Barr virus: prospects for multiple sclerosis pathogenesis. ''Brain''. 2024 Oct 3; '''147''' (10):3573-3582
Genomic variation of European beech reveals signals of local adaptation despite high levels of phenotypic plasticity. Description: Lazic, Desanka, et al. Genomic variation of European beech reveals signals of local adaptation despite high levels of phenotypic plasticity. ''Nat Commun''. 2024 Oct 3; '''15''' (1):8553
Interactions of the CSF3R polymorphism and early stress on future orientation: evidence for the differential model of stress-related growth. Description: Gan, Yiqun, et al. Interactions of the CSF3R polymorphism and early stress on future orientation: evidence for the differential model of stress-related growth. ''Epidemiol Psychiatr Sci''. 2024 Oct 3; '''33''': e44
Novel risk loci for COVID-19 hospitalization among admixed American populations. Description: Diz-de Almeida, Silvia, et al. Novel risk loci for COVID-19 hospitalization among admixed American populations. ''Elife''. 2024 Oct 3; '''13''':
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height. Description: Hawkes, Gareth, et al. Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height. ''Nat Commun''. 2024 Oct 3; '''15''' (1):8549
Genetic diversity and origin of Kazakh Tobet Dogs. Description: Perfilyeva, Anastassiya, et al. Genetic diversity and origin of Kazakh Tobet Dogs. ''Sci Rep''. 2024 Oct 4; '''14''' (1):23137
Genome-wide association study of cassava brown streak disease resistance in cassava germplasm conserved in South America. Description: Ospina, Jessica A, et al. Genome-wide association study of cassava brown streak disease resistance in cassava germplasm conserved in South America. ''Sci Rep''. 2024 Oct 4; '''14''' (1):23141
Maroon Rice Genomic Diversity Reflects 350 Years of Colonial History. Description: van de Loosdrecht, Marieke S, et al. Maroon Rice Genomic Diversity Reflects 350 Years of Colonial History. ''Mol Biol Evol''. 2024 Oct 4; '''41''' (10):
Multi-ancestry GWAS meta-analyses of lung cancer reveal susceptibility loci and elucidate smoking-independent genetic risk. Description: Gorman, Bryan R, et al. Multi-ancestry GWAS meta-analyses of lung cancer reveal susceptibility loci and elucidate smoking-independent genetic risk. ''Nat Commun''. 2024 Oct 4; '''15''' (1):8629
The goat pan-genome reveals patterns of gene loss during domestication. Description: Liu, Jiaxin, et al. The goat pan-genome reveals patterns of gene loss during domestication. ''J Anim Sci Biotechnol''. 2024 Oct 5; '''15''' (1):132
Genome-wide scan of Flortaucipir PET levels finds JARID2 associated with cerebral tau deposition. Description: Gunasekaran, Tamil Iniyan, et al. Genome-wide scan of Flortaucipir PET levels finds JARID2 associated with cerebral tau deposition. ''medRxiv''. 2024 Oct 7;
QTL discovery for agronomic and quality traits in diploid potato clones using PotatoMASH amplicon sequencing. Description: Vexler, Lea, et al. QTL discovery for agronomic and quality traits in diploid potato clones using PotatoMASH amplicon sequencing. ''G3 (Bethesda)''. 2024 Oct 7; '''14''' (10):
Revealing the evolutionary history and contemporary population structure of Pacific salmon in the Fraser River through genome resequencing. Description: Christensen, Kris A, et al. Revealing the evolutionary history and contemporary population structure of Pacific salmon in the Fraser River through genome resequencing. ''G3 (Bethesda)''. 2024 Oct 7; '''14''' (10):
The association between patterns of exposure to adverse life events and the risk of chronic kidney disease: a prospective cohort study of 140,997 individuals. Description: Li, Chunyang, et al. The association between patterns of exposure to adverse life events and the risk of chronic kidney disease: a prospective cohort study of 140,997 individuals. ''Transl Psychiatry''. 2024 Oct 7; '''14''' (1):424
Cardiovascular risk according to genetic predisposition to gout, lifestyle and metabolic health across prospective European and Korean cohorts. Description: Moon, Ki Won, et al. Cardiovascular risk according to genetic predisposition to gout, lifestyle and metabolic health across prospective European and Korean cohorts. ''RMD Open''. 2024 Oct 8; '''10''' (4):
Giant transposons promote strain heterogeneity in a major fungal pathogen. Description: Gluck-Thaler, Emile, et al. Giant transposons promote strain heterogeneity in a major fungal pathogen. ''bioRxiv''. 2024 Oct 8;
Leveraging large-scale datasets and single cell omics data to develop a polygenic score for cisplatin-induced ototoxicity. Description: Miao, Deanne Nixie R, et al. Leveraging large-scale datasets and single cell omics data to develop a polygenic score for cisplatin-induced ototoxicity. ''Hum Genomics''. 2024 Oct 8; '''18''' (1):112
Optimizing and benchmarking polygenic risk scores with GWAS summary statistics. Description: Zhao, Zijie, et al. Optimizing and benchmarking polygenic risk scores with GWAS summary statistics. ''Genome Biol''. 2024 Oct 8; '''25''' (1):260
Protein-truncating variant in APOL3 increases chronic kidney disease risk in epistasis with APOL1 risk alleles. Description: Zhang, David Y, et al. Protein-truncating variant in APOL3 increases chronic kidney disease risk in epistasis with APOL1 risk alleles. ''JCI Insight''. 2024 Oct 8; '''9''' (19):
The levels of amino acid metabolites in serum induce the pathogenesis of atopic dermatitis by mediating the inflammatory protein S100A12. Description: Zhang, Yaqi, et al. The levels of amino acid metabolites in serum induce the pathogenesis of atopic dermatitis by mediating the inflammatory protein S100A12. ''Sci Rep''. 2024 Oct 8; '''14''' (1):23435
Whole genomes of Amazonian uakari monkeys reveal complex connectivity and fast differentiation driven by high environmental dynamism. Description: Hermosilla-Albala, Nuria, et al. Whole genomes of Amazonian uakari monkeys reveal complex connectivity and fast differentiation driven by high environmental dynamism. ''Commun Biol''. 2024 Oct 8; '''7''' (1):1283
A compendium of genetic variations associated with promoter usage across 49 human tissues. Description: Yuan, Jiapei, et al. A compendium of genetic variations associated with promoter usage across 49 human tissues. ''Nat Commun''. 2024 Oct 9; '''15''' (1):8758
Genome-wide association study of subfoveal choroidal thickness in a longitudinal cohort of older adults. Description: Kim, Hyeong Min, et al. Genome-wide association study of subfoveal choroidal thickness in a longitudinal cohort of older adults. ''Sci Rep''. 2024 Oct 9; '''14''' (1):23545
Polygenic risk and rare variant gene clustering enhance cancer risk stratification for breast and prostate cancers. Description: Kang, Joon Ho, et al. Polygenic risk and rare variant gene clustering enhance cancer risk stratification for breast and prostate cancers. ''Commun Biol''. 2024 Oct 9; '''7''' (1):1289
SFMBT2 regulates plumage color via serum metabolites in Chinese Anyi tile-like gray chickens. Description: Xu, Jiguo, et al. SFMBT2 regulates plumage color via serum metabolites in Chinese Anyi tile-like gray chickens. ''Poult Sci''. 2024 Oct 9; '''103''' (12):104391
Unveiling the Genome-Wide Consequences of Range Expansion and Mating System Transitions in Primula vulgaris. Description: Mora-Carrera, Emiliano, et al. Unveiling the Genome-Wide Consequences of Range Expansion and Mating System Transitions in Primula vulgaris. ''Genome Biol Evol''. 2024 Oct 9; '''16''' (10):
Genome-wide diversity, linkage disequilibrium, and admixture in the main Colombian Creole pig breeds. Description: Ocampo-Gallego, Ricardo Jose, et al. Genome-wide diversity, linkage disequilibrium, and admixture in the main Colombian Creole pig breeds. ''Trop Anim Health Prod''. 2024 Oct 10; '''56''' (8):336
Joint genotype and ancestry analysis identify novel loci associated with atopic dermatitis in African American population. Description: Gautam, Yadu, et al. Joint genotype and ancestry analysis identify novel loci associated with atopic dermatitis in African American population. ''HGG Adv''. 2024 Oct 10; '''5''' (4):100350
Dissecting shared genetic architecture between depression and body mass index. Description: Zhang, Hengyu, et al. Dissecting shared genetic architecture between depression and body mass index. ''BMC Med''. 2024 Oct 11; '''22''' (1):455
Genetics-driven risk predictions leveraging the Mendelian randomization framework. Description: Sens, Daniel, et al. Genetics-driven risk predictions leveraging the Mendelian randomization framework. ''Genome Res''. 2024 Oct 11; '''34''' (9):1276-1285
Genome-wide studies define new genetic mechanisms of IgA vasculitis. Description: Liu, Lili, et al. Genome-wide studies define new genetic mechanisms of IgA vasculitis. ''medRxiv''. 2024 Oct 11;
Matrix sketching framework for linear mixed models in association studies. Description: Burch, Myson, et al. Matrix sketching framework for linear mixed models in association studies. ''Genome Res''. 2024 Oct 11; '''34''' (9):1304-1311
PHACTR1 and APOC1 genetic variants are associated with multi-vessel coronary artery disease. Description: Al Hageh, Cynthia, et al. PHACTR1 and APOC1 genetic variants are associated with multi-vessel coronary artery disease. ''Lipids Health Dis''. 2024 Oct 12; '''23''' (1):332
Signatures of local adaptation and maladaptation to future climate in wild Zizania latifolia. Description: Zou, Yang, et al. Signatures of local adaptation and maladaptation to future climate in wild Zizania latifolia. ''Commun Biol''. 2024 Oct 12; '''7''' (1):1313
Expanding drug targets for 112 chronic diseases using a machine learning-assisted genetic priority score. Description: Chen, Robert, et al. Expanding drug targets for 112 chronic diseases using a machine learning-assisted genetic priority score. ''Nat Commun''. 2024 Oct 15; '''15''' (1):8891
Genetic Underpinnings of Fasting and Oral Glucose-stimulated Based Insulin Sensitivity Indices. Description: Suleman, Sufyan, et al. Genetic Underpinnings of Fasting and Oral Glucose-stimulated Based Insulin Sensitivity Indices. ''J Clin Endocrinol Metab''. 2024 Oct 15; '''109''' (11):2754-2763
A genome-wide association study of adults with community-acquired pneumonia. Description: Suarez-Pajes, Eva, et al. A genome-wide association study of adults with community-acquired pneumonia. ''Respir Res''. 2024 Oct 16; '''25''' (1):374
Investigation of parasite genetic variation and systemic immune responses in patients presenting with different clinical presentations of cutaneous leishmaniasis caused by Leishmania aethiopica. Description: Yizengaw, Endalew, et al. Investigation of parasite genetic variation and systemic immune responses in patients presenting with different clinical presentations of cutaneous leishmaniasis caused by Leishmania aethiopica. ''Infect Dis Poverty''. 2024 Oct 16; '''13''' (1):76
Causal Metabolomic and Lipidomic Analysis of Circulating Plasma Metabolites in Autism: A Comprehensive Mendelian Randomization Study with Independent Cohort Validation. Description: Li, Zhifan, et al. Causal Metabolomic and Lipidomic Analysis of Circulating Plasma Metabolites in Autism: A Comprehensive Mendelian Randomization Study with Independent Cohort Validation. ''Metabolites''. 2024 Oct 17; '''14''' (10):
GWAS-by-subtraction reveals an IOP-independent component of primary open angle glaucoma. Description: Huang, Yu, et al. GWAS-by-subtraction reveals an IOP-independent component of primary open angle glaucoma. ''Nat Commun''. 2024 Oct 17; '''15''' (1):8962
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease. Description: Towns, Clodagh, et al. Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease. ''NPJ Parkinsons Dis''. 2024 Oct 17; '''10''' (1):188
Archaeogenetic analysis revealed East Eurasian paternal origin to the Aba royal family of Hungary. Description: Varga, Gergely I B, et al. Archaeogenetic analysis revealed East Eurasian paternal origin to the Aba royal family of Hungary. ''iScience''. 2024 Oct 18; '''27''' (10):110892
Digital phenotyping from wearables using AI characterizes psychiatric disorders and identifies genetic associations. Description: Liu, Jason J, et al. Digital phenotyping from wearables using AI characterizes psychiatric disorders and identifies genetic associations. ''medRxiv''. 2024 Oct 18;
Hypothesis-based investigation of known AD risk variants reveals the genetic underpinnings of neuropathological lesions observed in Alzheimer's-type dementia. Description: Laureyssen, Celeste, et al. Hypothesis-based investigation of known AD risk variants reveals the genetic underpinnings of neuropathological lesions observed in Alzheimer's-type dementia. ''Acta Neuropathol''. 2024 Oct 18; '''148''' (1):55
Identification and validation of a novel gene ARVCF associated with alcohol dependence among Chinese population. Description: Shi, Xiaoqiang, et al. Identification and validation of a novel gene ARVCF associated with alcohol dependence among Chinese population. ''iScience''. 2024 Oct 18; '''27''' (10):110976
Insights into trait-association of selection signatures and adaptive eQTL in indigenous African cattle. Description: Friedrich, Juliane, et al. Insights into trait-association of selection signatures and adaptive eQTL in indigenous African cattle. ''BMC Genomics''. 2024 Oct 19; '''25''' (1):981
MeHA: A Computational Framework in Revealing the Genetic Basis of Animal Mental Health Traits Under an Intensive Farming System-A Case Study in Pigs. Description: Jiang, Jinyun, et al. MeHA: A Computational Framework in Revealing the Genetic Basis of Animal Mental Health Traits Under an Intensive Farming System-A Case Study in Pigs. ''Biology (Basel)''. 2024 Oct 21; '''13''' (10):
Association between antithrombotic agents use and hepatocellular carcinoma risk: a two-sample mendelian randomization analysis. Description: Yang, Fengyi, et al. Association between antithrombotic agents use and hepatocellular carcinoma risk: a two-sample mendelian randomization analysis. ''J Cancer Res Clin Oncol''. 2024 Oct 22; '''150''' (10):470
Gene-Specific Effects on Brain Volume and Cognition of TMEM106B in Frontotemporal Lobar Degeneration. Description: Vandebergh, Marijne, et al. Gene-Specific Effects on Brain Volume and Cognition of TMEM106B in Frontotemporal Lobar Degeneration. ''Neurology''. 2024 Oct 22; '''103''' (8):e209832
Meta-analysis of genome-wide association studies of stable warfarin dose in patients of African ancestry. Description: Asiimwe, Innocent G, et al. Meta-analysis of genome-wide association studies of stable warfarin dose in patients of African ancestry. ''Blood Adv''. 2024 Oct 22; '''8''' (20):5248-5261
Microevolution of Bartonella grahamii driven by geographic and host factors. Description: Xu, Ailing, et al. Microevolution of Bartonella grahamii driven by geographic and host factors. ''mSystems''. 2024 Oct 22; '''9''' (10):e0108924
A tip of the iceberg: genome survey indicated a complex evolutionary history of Garuga Roxb. species. Description: Zhu, Dongbo, et al. A tip of the iceberg: genome survey indicated a complex evolutionary history of Garuga Roxb. species. ''BMC Genomics''. 2024 Oct 23; '''25''' (1):993
Obstructive sleep apnea and genotype rs6843082 as a risk factor for cerebrovascular accident. Description: Yang, Teng-Chi, et al. Obstructive sleep apnea and genotype rs6843082 as a risk factor for cerebrovascular accident. ''Sci Rep''. 2024 Oct 23; '''14''' (1):25041
Socio-demographic and genetic risk factors for drug adherence and persistence across 5 common medication classes. Description: Cordioli, Mattia, et al. Socio-demographic and genetic risk factors for drug adherence and persistence across 5 common medication classes. ''Nat Commun''. 2024 Oct 23; '''15''' (1):9156
Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysis. Description: Diaz-Torres, Santiago, et al. Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysis. ''Nat Commun''. 2024 Oct 23; '''15''' (1):9116
Genetically predicted gut bacteria, circulating bacteria-associated metabolites and pancreatic ductal adenocarcinoma: a Mendelian randomisation study. Description: Daniel, Neil, et al. Genetically predicted gut bacteria, circulating bacteria-associated metabolites and pancreatic ductal adenocarcinoma: a Mendelian randomisation study. ''Sci Rep''. 2024 Oct 24; '''14''' (1):25144
Two-sample Mendelian Randomization to evaluate the causal relationship between inflammatory arthritis and female-specific cancers. Description: Meisinger, Christa, et al. Two-sample Mendelian Randomization to evaluate the causal relationship between inflammatory arthritis and female-specific cancers. ''J Transl Med''. 2024 Oct 24; '''22''' (1):962
Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development. Description: Ceroni, Fabiola, et al. Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development. ''Nat Commun''. 2024 Oct 26; '''15''' (1):9245
Dynamic changes in hs-CRP and risk of all-cause mortality among middle-aged and elderly adults: findings from a nationwide prospective cohort and mendelian randomization. Description: Wang, Zhonghai, et al. Dynamic changes in hs-CRP and risk of all-cause mortality among middle-aged and elderly adults: findings from a nationwide prospective cohort and mendelian randomization. ''Aging Clin Exp Res''. 2024 Oct 26; '''36''' (1):210
African origin haplotype protective for Alzheimer's disease in APOEepsilon4 carriers: exploring potential mechanisms. Description: Bertholim-Nasciben, Luciana, et al. African origin haplotype protective for Alzheimer's disease in APOEepsilon4 carriers: exploring potential mechanisms. ''bioRxiv''. 2024 Oct 27;
Impact of HHIP gene polymorphisms on phenotypes, serum IL-17 and IL-18 in COPD patients of the Chinese Han population. Description: Zhang, Jiajun, et al. Impact of HHIP gene polymorphisms on phenotypes, serum IL-17 and IL-18 in COPD patients of the Chinese Han population. ''Respir Res''. 2024 Oct 28; '''25''' (1):386
Integrative 3D genomics with multi-omics analysis and functional validation of genetic regulatory mechanisms of abdominal fat deposition in chickens. Description: Shen, Linyong, et al. Integrative 3D genomics with multi-omics analysis and functional validation of genetic regulatory mechanisms of abdominal fat deposition in chickens. ''Nat Commun''. 2024 Oct 28; '''15''' (1):9274
Analyzes of pan-genome and resequencing atlas unveil the genetic basis of jujube domestication. Description: Guo, Mingxin, et al. Analyzes of pan-genome and resequencing atlas unveil the genetic basis of jujube domestication. ''Nat Commun''. 2024 Oct 29; '''15''' (1):9320
Discovery and prioritization of genetic determinants of kidney function in 297,355 individuals from Taiwan and Japan. Description: Chen, Hung-Lin, et al. Discovery and prioritization of genetic determinants of kidney function in 297,355 individuals from Taiwan and Japan. ''Nat Commun''. 2024 Oct 29; '''15''' (1):9317
Exploring mitochondrial blood-based and genetic markers in older adults with mild cognitive impairment and remitted major depressive disorder. Description: Choi, Jaehyoung, et al. Exploring mitochondrial blood-based and genetic markers in older adults with mild cognitive impairment and remitted major depressive disorder. ''Transl Psychiatry''. 2024 Oct 29; '''14''' (1):457
Inversions encounter relaxed genetic constraints and balance birth and death of TPS genes in Curcuma. Description: Liao, Xuezhu, et al. Inversions encounter relaxed genetic constraints and balance birth and death of TPS genes in Curcuma. ''Nat Commun''. 2024 Oct 29; '''15''' (1):9349
PWAS Hub for exploring gene-based associations of common complex diseases. Description: Kelman, Guy, et al. PWAS Hub for exploring gene-based associations of common complex diseases. ''Genome Res''. 2024 Oct 29; '''34''' (10):1674-1686
Accounting for genetic effect heterogeneity in fine-mapping and improving power to detect gene-environment interactions with SharePro. Description: Zhang, Wenmin, et al. Accounting for genetic effect heterogeneity in fine-mapping and improving power to detect gene-environment interactions with SharePro. ''Nat Commun''. 2024 Oct 30; '''15''' (1):9374
Association between cannabis use and brain structure and function: an observational and Mendelian randomisation study. Description: Ishrat, Saba, et al. Association between cannabis use and brain structure and function: an observational and Mendelian randomisation study. ''BMJ Ment Health''. 2024 Oct 30; '''27''' (1):
Amlodipine increases risk of primary open-angle glaucoma. Description: Lehrer, Steven, et al. Amlodipine increases risk of primary open-angle glaucoma. ''Clin Hypertens''. 2024 Nov 1; '''30''' (1):33
Association of rare and common genetic variants in MOCOS with inadequate response to allopurinol. Description: Fanning, Niamh C, et al. Association of rare and common genetic variants in MOCOS with inadequate response to allopurinol. ''Rheumatology (Oxford)''. 2024 Nov 1; '''63''' (11):3025-3032
Genomic insights into the contribution of de novo lipogenesis to intramuscular fat deposition in chicken. Description: Cui, Huanxian, et al. Genomic insights into the contribution of de novo lipogenesis to intramuscular fat deposition in chicken. ''J Adv Res''. 2024 Nov; '''65''': 19-31
High SHBG and Low Bioavailable Testosterone are Strongly Causally Associated with Increased Forearm Fracture Risk in Women: An MR Study Leveraging Novel Female-Specific Data. Description: Quester, Johan, et al. High SHBG and Low Bioavailable Testosterone are Strongly Causally Associated with Increased Forearm Fracture Risk in Women: An MR Study Leveraging Novel Female-Specific Data. ''Calcif Tissue Int''. 2024 Nov; '''115''' (5):648-660
Investigation of genetic polymorphisms in genes encoding growth factors and dental pulp calcification in orthodontic patients. Description: Meyfarth, Sandra Regina Santos, et al. Investigation of genetic polymorphisms in genes encoding growth factors and dental pulp calcification in orthodontic patients. ''J Oral Biol Craniofac Res''. 2024 Nov-Dec; '''14''' (6):712-719
The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two-Sample Mendelian Randomization Study. Description: Li, James L. The Causal Role of Thyroid Hormones in Bipolar Disorders: A Two-Sample Mendelian Randomization Study. ''Endocrinol Diabetes Metab''. 2024 Nov; '''7''' (6):e70009
Upgrading of Grade Group 1 Prostate Cancer at Prostatectomy: Germline Risk Factors in a Prospective Cohort. Description: Liss, Michael A, et al. Upgrading of Grade Group 1 Prostate Cancer at Prostatectomy: Germline Risk Factors in a Prospective Cohort. ''Cancer Epidemiol Biomarkers Prev''. 2024 Nov 1; '''33''' (11):1500-1511
Whole-exome and whole-genome sequencing of 1064 individuals with type 1 diabetes reveals novel genes for diabetic kidney disease. Description: Haukka, Jani K, et al. Whole-exome and whole-genome sequencing of 1064 individuals with type 1 diabetes reveals novel genes for diabetic kidney disease. ''Diabetologia''. 2024 Nov; '''67''' (11):2494-2506
Drosophila Toxicogenomics: genetic variation and sexual dimorphism in susceptibility to 4-Methylimidazole. Description: Collins, Katelynne M, et al. Drosophila Toxicogenomics: genetic variation and sexual dimorphism in susceptibility to 4-Methylimidazole. ''Hum Genomics''. 2024 Nov 4; '''18''' (1):119
*HLA-DQA105 Not Associated With Ustekinumab Loss of Response and Antidrug Antibodies in Ulcerative Colitis and Crohn's Disease Patients.** Description: Colombel, Jean-Frederic, et al. HLA-DQA1*05 Not Associated With Ustekinumab Loss of Response and Antidrug Antibodies in Ulcerative Colitis and Crohn's Disease Patients. ''Inflamm Bowel Dis''. 2024 Nov 4; '''30''' (11):2227-2231
GWAS Meta-analysis of Kidney Function Traits in Japanese Populations. Description: Hishida, Asahi, et al. GWAS Meta-analysis of Kidney Function Traits in Japanese Populations. ''J Epidemiol''. 2024 Nov 5; '''34''' (11):526-534
Relationship between Polygenic Risk Score and the Hypnotics in Bipolar I Disorder. Description: Lee, Hyeon Woo, et al. Relationship between Polygenic Risk Score and the Hypnotics in Bipolar I Disorder. ''Clin Psychopharmacol Neurosci''. 2024 Nov 30; '''22''' (4):585-593
Biology and genetic diversity of Candida krusei isolates from fermented vegetables and clinical samples in China. Description: Zheng, Tianhong, et al. Biology and genetic diversity of Candida krusei isolates from fermented vegetables and clinical samples in China. ''Virulence''. 2024 Dec; '''15''' (1):2411543
Clinical effects of CYP2D6 phenoconversion in patients with psychosis. Description: De Brabander, Emma Y, et al. Clinical effects of CYP2D6 phenoconversion in patients with psychosis. ''J Psychopharmacol''. 2024 Dec; '''38''' (12):1095-1110
Genetic architecture of epigenetic cortical clock age in brain tissue from older individuals: alterations in CD46 and other loci. Description: Grodstein, Francine, et al. Genetic architecture of epigenetic cortical clock age in brain tissue from older individuals: alterations in CD46 and other loci. ''Epigenetics''. 2024 Dec; '''19''' (1):2392050
Genetic association study of TERT gene variants with chronic kidney disease susceptibility in the Chinese population. Description: Su, Yan, et al. Genetic association study of TERT gene variants with chronic kidney disease susceptibility in the Chinese population. ''Ren Fail''. 2024 Dec; '''46''' (1):2300725
Genome-wide characterization of structure variations in the Xiang pig for genetic resistance to African swine fever. Description: Qi, Fenfang, et al. Genome-wide characterization of structure variations in the Xiang pig for genetic resistance to African swine fever. ''Virulence''. 2024 Dec; '''15''' (1):2382762
Genomic analysis of lineage-specific transmission of multidrug resistance tuberculosis in China. Description: Li, Yi-Fan, et al. Genomic analysis of lineage-specific transmission of multidrug resistance tuberculosis in China. ''Emerg Microbes Infect''. 2024 Dec; '''13''' (1):2294858
Identification and functional characterisation of DNA methylation differences between East- and West-originating Finns. Description: Ciantar, Joanna, et al. Identification and functional characterisation of DNA methylation differences between East- and West-originating Finns. ''Epigenetics''. 2024 Dec; '''19''' (1):2397297
PidTools: Algorithm and web tools for crop pedigree identification analysis. Description: Zhang, Yunlong, et al. PidTools: Algorithm and web tools for crop pedigree identification analysis. ''Comput Struct Biotechnol J''. 2024 Dec; '''23''': 2883-2891
Unidentified CYP2D6 genotype does not affect pharmacological treatment for patients with first episode psychosis. Description: De Brabander, Emma Y, et al. Unidentified CYP2D6 genotype does not affect pharmacological treatment for patients with first episode psychosis. ''J Psychopharmacol''. 2024 Dec; '''38''' (12):1111-1121
Genomic insights into mRNA COVID-19 vaccines efficacy: Linking genetic polymorphisms to waning immunity. Description: Hsieh, Min-Jia, et al. Genomic insights into mRNA COVID-19 vaccines efficacy: Linking genetic polymorphisms to waning immunity. ''Hum Vaccin Immunother''. 2024 Dec 31; '''20''' (1):2399382
The relationship between long non-coding gene CASC21 polymorphisms and cervical cancer. Description: Han, Lili, et al. The relationship between long non-coding gene CASC21 polymorphisms and cervical cancer. ''Cancer Biol Ther''. 2024 Dec 31; '''25''' (1):2322207