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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
Worldwide population differentiation at disease-associated SNPs
Height-reducing variants and selection for short stature in Sardinia
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
The UK10K project identifies rare variants in health and disease
An interactive genome browser of association results from the UK10K cohorts project
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals
The Emergence of Networks in Human Genome Epidemiology
