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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Rare and low-frequency coding variants alter human adult height
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair