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Hepatology (Baltimore, Md.)|April 1, 2024
Variants in autophagy genes MTMR12 and FAM134A are putative modifiers of the hepatic phenotype in α1-antitrypsin deficiencyEdgar N Tafaleng, Jie Li, Yan Wang, et al.Psychophysiology|November 13, 2014
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypesScott I Vrieze, Stephen M Malone, Uma Vaidyanathan, et al.Genetic Epidemiology|August 19, 2010
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndromeAdam E Locke, Kenneth J Dooley, Stuart W Tinker, et al.G3 (Bethesda, Md.)|July 22, 2015
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal DefectsDhanya Ramachandran, Zhen Zeng, Adam E Locke, et al.Nature Genetics|August 30, 2016
Next-generation genotype imputation service and methodsSayantan Das, Lukas Forer, Sebastian Schönherr, et al.Human Molecular Genetics|November 7, 2019
Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distributionYing Wu, K Alaine Broadaway, Chelsea K Raulerson, et al.European Journal of Human Genetics : EJHG|August 25, 2016
Across-cohort QC analyses of GWAS summary statistics from complex traitsGuo-Bo Chen, Sang Hong Lee, Matthew R Robinson, et al.Human Molecular Genetics|September 18, 2015
Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesitySara Hägg, Andrea Ganna, Sander W Van Der Laan, et al.Plos Genetics|October 31, 2017
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM studyJames P Davis, Jeroen R Huyghe, Adam E Locke, et al.Nature Protocols|April 26, 2014
Quality control and conduct of genome-wide association meta-analysesThomas W Winkler, Felix R Day, Damien C Croteau-Chonka, et al.Pageof 8