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Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, 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.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.Circulation. Cardiovascular Genetics|November 23, 2016
Multiethnic Exome-Wide Association Study of Subclinical AtherosclerosisPradeep Natarajan, Joshua C Bis, Lawrence F Bielak, 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.Journal of the American College of Cardiology|February 18, 2017
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery DiseaseThomas R Webb, Jeanette Erdmann, Kathleen E Stirrups, et al.Nature Cardiovascular Research|May 31, 2024
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcificationPaul S de Vries, Matthew P Conomos, Kuldeep Singh, et al.Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.Pageof 18