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12
Exome-wide association study of plasma lipids in >300,000 individuals
Rare and low-frequency coding variants alter human adult height
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
