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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
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals
Analysis of protein-coding genetic variation in 60,706 humans
Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Genomic inflation factors under polygenic inheritance