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Plos One|December 15, 2017
CELSR2 is a candidate susceptibility gene in idiopathic scoliosisElisabet Einarsdottir, Anna Grauers, Jingwen Wang, et al.
European Journal of Cancer (Oxford, England : 1990)|April 18, 2017
Less-favourable prognosis for low-risk endometrial cancer patients with a discordant pre- versus post-operative risk stratificationF A Eggink, C H Mom, K Bouwman, et al.
Human Molecular Genetics|July 29, 2016
Analysis with the exome array identifies multiple new independent variants in lipid lociStavroula Kanoni, Nicholas G D Masca, Kathleen E Stirrups, et al.
European Heart Journal|September 1, 2018
A comprehensive evaluation of the genetic architecture of sudden cardiac arrestForam N Ashar, Rebecca N Mitchell, Christine M Albert, 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.
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 Communications|January 30, 2015
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilityJennifer Wessel, Audrey Y Chu, Sara M Willems, et al.
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