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Rare and low-frequency coding variants alter human adult height
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms
Ultraconserved elements in the human genome: association and transmission analyses of highly constrained single-nucleotide polymorphisms
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Heritability analysis of nontraditional glycemic biomarkers in the Atherosclerosis Risk in Communities Study
Multiomics integrative analysis identifies allele-specific blood biomarkers associated to Alzheimer's disease etiopathogenesis
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
