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Drug Safety|November 30, 2017
Using Human 'Experiments of Nature' to Predict Drug Safety Issues: An Example with PCSK9 InhibitorsRebecca N Jerome, Jill M Pulley, Dan M Roden, et al.
Circulation|August 24, 2005
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndromeLia Crotti, Andrew L Lundquist, Roberto Insolia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2010
Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical recordsLogan Dumitrescu, Marylyn D Ritchie, Kristin Brown-Gentry, et al.
Nature Medicine|March 31, 2009
Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humansHiroshi Watanabe, Nagesh Chopra, Derek Laver, et al.
Journal of Cellular and Molecular Medicine|June 1, 2022
Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessmentScott C Borinstein, David Agamasu, Jonathan S Schildcrout, et al.
Journal of the American Heart Association|June 3, 2022
Genetic Determinants of Body Mass Index and Fasting Glucose Are Mediators of Grade 1 Diastolic DysfunctionNataraja Sarma Vaitinadin, Mingjian Shi, Christian M Shaffer, et al.
Circulation Research|May 14, 2011
Informatic and functional approaches to identifying a regulatory region for the cardiac sodium channelThomas C Atack, Dina Myers Stroud, Hiroshi Watanabe, et al.
Nature Medicine|October 10, 2022
Association of step counts over time with the risk of chronic disease in the All of Us Research ProgramHiral Master, Jeffrey Annis, Shi Huang, et al.
Bioinformatics (Oxford, England)|March 26, 2010
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associationsJoshua C Denny, Marylyn D Ritchie, Melissa A Basford, et al.
Genome Biology|July 2, 2024
Benchmarking computational variant effect predictors by their ability to infer human traitsDaniel R Tabet, Da Kuang, Megan C Lancaster, et al.
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