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Plos One|November 14, 2013
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizesElijah R Behr, Marylyn D Ritchie, Toshihiro Tanaka, et al.
Circulation|April 29, 2018
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving StatinsWei-Qi Wei, Xiaohui Li, Qiping Feng, et al.
Clinical Pharmacology and Therapeutics|February 21, 2018
Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and ProjectsSimona Volpi, Carol J Bult, Rex L Chisholm, et al.
Communications Biology|October 2, 2018
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLRMaya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
American Journal of Human Genetics|October 11, 2011
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesJoshua C Denny, Dana C Crawford, Marylyn D Ritchie, et al.
Science (New York, N.Y.)|October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene LDLRDaniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
JAMA Oncology|April 21, 2022
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple DiseasesChenjie Zeng, Lisa A Bastarache, Ran Tao, et al.
Circulation|December 16, 2022
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac RepolarizationKevin R Bersell, Tao Yang, Jonathan D Mosley, et al.
The New England Journal of Medicine|November 3, 2016
Fulminant Myocarditis with Combination Immune Checkpoint BlockadeDouglas B Johnson, Justin M Balko, Margaret L Compton, et al.
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