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Lancet (London, England)|August 10, 2019
Building evidence and measuring clinical outcomes for genomic medicineJosh F Peterson, Dan M Roden, Lori A Orlando, et al.
Journal of Personalized Medicine|July 26, 2018
Physician-Reported Benefits and Barriers to Clinical Implementation of Genomic Medicine: A Multi-Site IGNITE-Network SurveyAniwaa Owusu Obeng, Kezhen Fei, Kenneth D Levy, et al.
Heart Rhythm|November 4, 2010
Modulators of normal electrocardiographic intervals identified in a large electronic medical recordAndrea H Ramirez, Jonathan S Schildcrout, Dana L Blakemore, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|January 8, 2015
Multiplex ligation-dependent probe amplification copy number variant analysis in patients with acquired long QT syndromeVictoria S Williams, Carl J Cresswell, Gerhard Ruspi, et al.
Pharmacogenetics and Genomics|September 16, 2016
Genetic determinants of variability in warfarin response after the dose-titration phaseOtito F Iwuchukwu, Andrea H Ramirez, Yaping Shi, et al.
Circulation|November 3, 2010
Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome scienceJoshua C Denny, Marylyn D Ritchie, Dana C Crawford, et al.
The Journal of Clinical Endocrinology and Metabolism|April 17, 2018
Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine DisordersKathryn M Dahir, Daniel R Tilden, Jeremy L Warner, et al.
American Journal of Human Genetics|April 6, 2010
Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical recordMarylyn D Ritchie, Joshua C Denny, Dana C Crawford, et al.
Journal of the American Medical Informatics Association : JAMIA|January 6, 2021
Comparison of family health history in surveys vs electronic health record data mapped to the observational medical outcomes partnership data model in the All of Us Research ProgramRobert M Cronin, Alese E Halvorson, Cassie Springer, et al.
Circulation. Cardiovascular Genetics|July 18, 2013
Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathyQuinn S Wells, Jason R Becker, Yan R Su, et al.
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