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JAMA Cardiology|January 24, 2019
Association of Thyroid Function Genetic Predictors With Atrial Fibrillation: A Phenome-Wide Association Study and Inverse-Variance Weighted Average Meta-analysisJoe-Elie Salem, M Benjamin Shoemaker, Lisa Bastarache, et al.
Circulation. Cardiovascular Genetics|March 5, 2015
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2Iris C R M Kolder, Michael W T Tanck, Pieter G Postema, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the youngMegan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Scaled multidimensional assays of variant effect identify sequence-function relationships in hypertrophic cardiomyopathyYuta Yamamoto, Kaiser Chua, Alexis Ferrasse, et al.
JAMA Cardiology|May 11, 2022
Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia GenesZachary T Yoneda, Katherine C Anderson, Fei Ye, et al.
Scientific Reports|April 17, 2019
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE networkJacklyn N Hellwege, Sarah Stallings, Eric S Torstenson, et al.
Circulation. Cardiovascular Genetics|April 19, 2017
Investigating the Genetic Architecture of the PR Interval Using Clinical PhenotypesJonathan D Mosley, M Benjamin Shoemaker, Quinn S Wells, et al.
American Journal of Human Genetics|September 5, 2020
Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin AllergyKristi Krebs, Jonas Bovijn, Neil Zheng, et al.
Journal of the American Medical Informatics Association : JAMIA|August 21, 2018
A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environmentsJennifer A Pacheco, Luke V Rasmussen, Richard C Kiefer, et al.
Circulation. Genomic and Precision Medicine|February 3, 2022
Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT SyndromeBelinda Gray, Alban-Elouen Baruteau, Albert A Antolin, et al.
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