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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.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELEXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Nature Genetics|March 6, 2025
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 casesCarolina Roselli, Ida Surakka, Morten S Olesen, et al.
BMC Cardiovascular Disorders|October 31, 2019
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9Amand F Schmidt, Michael V Holmes, David Preiss, et al.
Nature Genetics|April 19, 2017
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillationIngrid E Christophersen, Michiel Rienstra, Carolina Roselli, et al.
Nature Communications|May 23, 2020
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conductionIoanna Ntalla, Lu-Chen Weng, James H Cartwright, et al.
Nature Genetics|October 31, 2017
Exome-wide association study of plasma lipids in >300,000 individualsDajiang J Liu, Gina M Peloso, Haojie Yu, et al.
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