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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
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
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
Genetic determinants of hair, eye and skin pigmentation in Europeans
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Several common variants modulate heart rate, PR interval and QRS duration