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American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
American Journal of Human Genetics|February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksGina M Peloso, Paul L Auer, Joshua C Bis, et al.
Scientific Reports|April 29, 2017
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney functionMathias Gorski, Peter J van der Most, Alexander Teumer, et al.
Scientific Reports|May 27, 2017
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney functionMathias Gorski, Peter J van der Most, Alexander Teumer, et al.
The New England Journal of Medicine|March 3, 2016
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease, Nathan O Stitziel, Kathleen E Stirrups, et al.
American Journal of Human Genetics|June 21, 2016
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and InsulinChing-Ti Liu, Sridharan Raghavan, Nisa Maruthur, et al.
Circulation Research|December 1, 2016
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk LociGregory T Jones, Gerard Tromp, Helena Kuivaniemi, et al.
Nature Genetics|September 8, 2015
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseMajid Nikpay, Anuj Goel, Hong-Hee Won, et al.
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