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The New England Journal of Medicine|March 22, 2018
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver DiseaseNoura S Abul-Husn, Xiping Cheng, Alexander H Li, et al.
Science (New York, N.Y.)|December 24, 2016
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR studyFrederick E Dewey, Michael F Murray, John D Overton, et al.
Human Molecular Genetics|April 21, 2017
Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid lociNiha Zubair, Mariaelisa Graff, Jose Luis Ambite, et al.
The New England Journal of Medicine|May 25, 2017
Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular DiseaseFrederick E Dewey, Viktoria Gusarova, Richard L Dunbar, et al.
Journal of the American Heart Association|July 16, 2016
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic AneurysmsFemke N G van 't Hof, Ynte M Ruigrok, Cue Hyunkyu Lee, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature Communications|June 15, 2018
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetesViktoria Gusarova, Colm O'Dushlaine, Tanya M Teslovich, et al.
Nature Genetics|September 13, 2016
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait lociChunyu Liu, Aldi T Kraja, Jennifer A Smith, et al.
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