PubMed Mentions
The links below are to publications on PubMed referring to MaCH-Admix. This list is gathered weekly from PubMed automatically.
Publication/References | |
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 | |
Genetic associations with coronary heart disease: meta-analyses of 12 candidate genetic variants. Description: Ye, Huadan, et al. Genetic associations with coronary heart disease: meta-analyses of 12 candidate genetic variants. ''Gene''. 2013 Nov 15; '''531''' (1):71-7 | |
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 | |
Evaluation of Genome Wide Association Study Associated Type 2 Diabetes Susceptibility Loci in Sub Saharan Africans. Description: Adeyemo, Adebowale A, et al. Evaluation of Genome Wide Association Study Associated Type 2 Diabetes Susceptibility Loci in Sub Saharan Africans. ''Front Genet''. 2015; '''6''': 335 | |
Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci. Description: Buchkovich, Martin L, et al. Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci. ''BMC Med Genomics''. 2015 Jul 26; '''8''': 43 | |
MicroRNAs Classify Different Disease Behavior Phenotypes of Crohn's Disease and May Have Prognostic Utility. Description: Peck, Bailey C E, et al. MicroRNAs Classify Different Disease Behavior Phenotypes of Crohn's Disease and May Have Prognostic Utility. ''Inflamm Bowel Dis''. 2015 Sep; '''21''' (9):2178-87 | |
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 | |
Family-based approaches: design, imputation, analysis, and beyond. Description: Wijsman, Ellen M. Family-based approaches: design, imputation, analysis, and beyond. ''BMC Genet''. 2016 Feb 3; '''17 Suppl 2''': 9 | |
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 | |
Associations of the MCM6-rs3754686 proxy for milk intake in Mediterranean and American populations with cardiovascular biomarkers, disease and mortality: Mendelian randomization. Description: Smith, Caren E, et al. Associations of the MCM6-rs3754686 proxy for milk intake in Mediterranean and American populations with cardiovascular biomarkers, disease and mortality: Mendelian randomization. ''Sci Rep''. 2016 Sep 14; '''6''': 33188 | |
Genome-wide association analysis of secondary imaging phenotypes from the Alzheimer's disease neuroimaging initiative study. Description: Zhu, Wensheng, et al. Genome-wide association analysis of secondary imaging phenotypes from the Alzheimer's disease neuroimaging initiative study. ''Neuroimage''. 2017 Feb 1; '''146''': 983-1002 | |
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 | |
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 | |
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 | |
The moderating role of SES on genetic differences in educational achievement in the Netherlands. Description: de Zeeuw, Eveline L, et al. The moderating role of SES on genetic differences in educational achievement in the Netherlands. ''NPJ Sci Learn''. 2019; '''4''': 13 | |
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 | |
ABTB2 Regulatory Variant as Predictor of Epirubicin-Based Neoadjuvant Chemotherapy in Luminal A Breast Cancer. Description: Gong, Yajie, et al. ABTB2 Regulatory Variant as Predictor of Epirubicin-Based Neoadjuvant Chemotherapy in Luminal A Breast Cancer. ''Front Oncol''. 2020; '''10''': 571517 | |
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 |