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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Searching for parent-of-origin effects on cardiometabolic traits in imprinted genomic regions
