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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
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
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
Experimental and Human Evidence for Lipocalin-2 (Neutrophil Gelatinase-Associated Lipocalin [NGAL]) in the Development of Cardiac Hypertrophy and heart failure
Genome-wide analysis identifies 12 loci influencing human reproductive behavior