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Cell|March 20, 2025
Asian diversity in human immune cellsKian Hong Kock, Le Min Tan, Kyung Yeon Han, et al.Nature Communications|March 27, 2026
An integrated germline and somatic genomic model for coronary artery diseaseXiong Yang, Min Seo Kim, Xinyu Zhu, et al.Neurology. Genetics|April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.Circulation Research|May 17, 2017
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart DiseaseAkihiro Nomura, Hong-Hee Won, Amit V Khera, 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.Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.Scientific Reports|October 13, 2016
No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-AnalysisChristina Loley, Maris Alver, Themistocles L Assimes, et al.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.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.Pageof 19