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Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Overcome the Limitation of Phenome-Wide Association Studies (PheWAS): Extension of PheWAS to Efficient and Robust Large-Scale ICD Codes AnalysisYa-Chen Lin, Siwei Zhang, Tess Vessels, et al.
Science Translational Medicine|May 12, 2017
Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variantsJason H Karnes, Lisa Bastarache, Christian M Shaffer, et al.
Pharmacology & Therapeutics|April 17, 2013
The Lambeth Conventions (II): guidelines for the study of animal and human ventricular and supraventricular arrhythmiasMichael J Curtis, Jules C Hancox, András Farkas, et al.
Heart Rhythm|November 13, 2010
Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year oldsJonathan R Skinner, Jackie Crawford, Warren Smith, et al.
Circulation|August 5, 2009
Drug-sensitized zebrafish screen identifies multiple genes, including GINS3, as regulators of myocardial repolarizationDavid J Milan, Albert M Kim, Jeffrey R Winterfield, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2022
Continuous Bayesian variant interpretation accounts for incomplete penetrance among Mendelian cardiac channelopathiesMatthew J O'Neill, Luca Sala, Isabelle Denjoy, et al.
Journal of the American College of Cardiology|October 21, 2017
A Missense Variant in PLEC Increases Risk of Atrial FibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Journal of the American College of Cardiology|June 12, 2012
Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmiaYalda Jamshidi, Ilja M Nolte, Chrysoula Dalageorgou, et al.
Journal of the American Medical Informatics Association : JAMIA|March 31, 2016
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportabilityJacqueline C Kirby, Peter Speltz, Luke V Rasmussen, et al.
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