Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Analytic Choices Shape Genomic Risk Estimates from Electronic Health Records: Coronary Heart Disease in eMERGE IVJingheng H Chen, Sarah A Knerr, David L Veenstra, et al.
Atherosclerosis|April 1, 2008
ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary interventionSvati H Shah, Elizabeth R Hauser, David Crosslin, et al.
International Journal of Cardiology|August 27, 2019
CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular diseaseJoseph T Glessner, Jin Li, Akshatha Desai, et al.
Annals of Human Genetics|March 29, 2013
Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African AmericansJanina M Jeff, Marylyn D Ritchie, Joshua C Denny, et al.
Frontiers in Genetics|January 8, 2015
Imputation and quality control steps for combining multiple genome-wide datasetsShefali S Verma, Mariza de Andrade, Gerard Tromp, et al.
Medrxiv : the Preprint Server for Health Sciences|May 4, 2026
Determinants of DNA-sequence-based Diagnostic Yield in the CSER ConsortiumYusuph Mavura, David Crosslin, Kathleen Ferar, et al.
American Journal of Human Genetics|March 16, 2007
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery diseaseLiyong Wang, Elizabeth R Hauser, Svati H Shah, et al.
Journal of the American Society of Nephrology : JASN|May 4, 2021
Medical Records-Based Genetic Studies of the Complement SystemAtlas Khan, Ning Shang, Lynn Petukhova, et al.
Pageof 3