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Arteriosclerosis, Thrombosis, and Vascular Biology|August 22, 2015
Prediction of Causal Candidate Genes in Coronary Artery Disease LociIngrid Brænne, Mete Civelek, Baiba Vilne, et al.
Circulation. Genomic and Precision Medicine|May 18, 2022
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.
Nature Genetics|October 6, 2021
Polygenic basis and biomedical consequences of telomere length variationVeryan Codd, Qingning Wang, Elias Allara, et al.
Circulation. Genomic and Precision Medicine|October 30, 2020
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome SequencingKeren J Carss, Anna A Baranowska, Javier Armisen, et al.
Cardiovascular Research|June 13, 2020
Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasiaAdrien Georges, Juliette Albuisson, Takiy Berrandou, et al.
The New England Journal of Medicine|April 9, 2015
Genetically determined height and coronary artery diseaseChristopher P Nelson, Stephen E Hamby, Danish Saleheen, et al.
Nature Genetics|July 18, 2017
Association analyses based on false discovery rate implicate new loci for coronary artery diseaseChristopher P Nelson, Anuj Goel, Adam S Butterworth, et al.
American Journal of Human Genetics|February 29, 2020
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere LengthChen Li, Svetlana Stoma, Luca A Lotta, 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.
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