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Exome-wide association study of plasma lipids in >300,000 individuals
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Biological interpretation of genome-wide association studies using predicted gene functions
Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals
Association Analysis of 6,736 U.K. Subjects Provides Replication and ConfirmsTCF7L2as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
Genomic inflation factors under polygenic inheritance
New gene variants alter type 2 diabetes risk predominantly through reduced beta-cell function
Ant colony optimisation to identify genetic variant association with type 2 diabetes