PubMed Mentions

The links below are to publications on PubMed referring to mach2dat. This list is gathered weekly from PubMed automatically.

Publication/References
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
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
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
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
A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study. Description: Kim, Hyung-cheol, et al. A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study. ''Breast Cancer Res''. 2012 Mar 27; '''14''' (2):R56
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
Assessing the validity of asthma associations for eight candidate genes and age at diagnosis effects. Description: Pino-Yanes, Maria, et al. Assessing the validity of asthma associations for eight candidate genes and age at diagnosis effects. ''PLoS One''. 2013; '''8''' (9):e73157
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
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
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
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 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
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
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
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
Variants of CEP68 gene are associated with acute urticaria/angioedema induced by multiple non-steroidal anti-inflammatory drugs. Description: Cornejo-Garcia, Jose Antonio, et al. Variants of CEP68 gene are associated with acute urticaria/angioedema induced by multiple non-steroidal anti-inflammatory drugs. ''PLoS One''. 2014; '''9''' (3):e90966
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
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
Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis. Description: Acosta-Herrera, Marialbert, et al. Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis. ''Crit Care''. 2015 Jun 16; '''19''': 256
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
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
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
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
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
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma. Description: Shiraishi, Kouya, et al. Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma. ''Nat Commun''. 2016 Aug 9; '''7''': 12451
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
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
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
Trans-ethnic predicted expression genome-wide association analysis identifies a gene for estrogen receptor-negative breast cancer. Description: Gao, Guimin, et al. Trans-ethnic predicted expression genome-wide association analysis identifies a gene for estrogen receptor-negative breast cancer. ''PLoS Genet''. 2017 Sep; '''13''' (9):e1006727
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 variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes. Description: Taira, Makiko, et al. A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes. ''PLoS One''. 2018; '''13''' (12):e0208654
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
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. Description: Kou, Ikuyo, et al. Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. ''Nat Commun''. 2019 Aug 15; '''10''' (1):3685
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
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
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Description: Shah, Sonia, et al. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. ''Nat Commun''. 2020 Jan 9; '''11''' (1):163
Identification of type 2 diabetes loci in 433,540 East Asian individuals. Description: Spracklen, Cassandra N, et al. Identification of type 2 diabetes loci in 433,540 East Asian individuals. ''Nature''. 2020 Jun; '''582''' (7811):240-245
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):
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
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