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Cell|November 19, 2016
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex DiseaseWilliam J Astle, Heather Elding, Tao Jiang, et al.Plos One|November 2, 2018
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic strokeJohn W Cole, Huichun Xu, Kathleen Ryan, et al.Nature Genetics|August 2, 2016
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencingAlejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, et al.The New England Journal of Medicine|November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease, Nathan O Stitziel, Hong-Hee Won, et al.JAMA Cardiology|January 17, 2019
Cardiovascular Risk Factors Associated With Venous ThromboembolismJohn Gregson, Stephen Kaptoge, Thomas Bolton, et al.Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.JAMA|March 27, 2014
Glycated hemoglobin measurement and prediction of cardiovascular disease, Emanuele Di Angelantonio, Pei Gao, et al.Nature Metabolism|October 17, 2020
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individualsLasse Folkersen, Stefan Gustafsson, Qin Wang, et al.Nature Genetics|May 23, 2017
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanismsJoanna M M Howson, Wei Zhao, Daniel R Barnes, et al.International Journal of Population Data Science|March 25, 2025
UK Longitudinal Linkage Collaboration (UK LLC): The National Trusted Research Environment for Longitudinal ResearchAndy Boyd, Katharine M Evans, Emma L Turner, et al.Pageof 31