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Circulation. Cardiovascular Genetics|November 22, 2011
A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointesStefan Kääb, Dana C Crawford, Moritz F Sinner, et al.
Medrxiv : the Preprint Server for Health Sciences|April 16, 2025
Current Limitations of Electronic Health Record Systems in Supporting Pragmatic Clinical Trials: Insights from the eMERGE ConsortiumKavishwar B Wagholikar, Jennifer Allen Pacheco, Adam S Gordon, et al.
JACC. Clinical Electrophysiology|October 25, 2024
Clinical Characteristics and Outcomes in Patients With Atrial Fibrillation and Pathogenic TTN VariantsZain M Virk, Majd A El-Harasis, Zachary T Yoneda, et al.
Medrxiv : the Preprint Server for Health Sciences|October 31, 2023
Determinants of mosaic chromosomal alteration fitnessYash Pershad, Taralynn Mack, Hannah Poisner, et al.
Learning Health Systems|October 31, 2025
Advancing the science of genomic learning healthcare systemsTeri A Manolio, Renee Rider, Carol J Bult, et al.
Lancet (London, England)|June 13, 2013
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association studyMinoli A Perera, Larisa H Cavallari, Nita A Limdi, et al.
Circulation|December 21, 2018
Probing the Virtual Proteome to Identify Novel Disease BiomarkersJonathan D Mosley, Mark D Benson, J Gustav Smith, et al.
Circulation|October 30, 2016
Genetic Risk Prediction of Atrial FibrillationSteven A Lubitz, Xiaoyan Yin, Henry J Lin, et al.
Science Translational Medicine|June 5, 2015
Global implementation of genomic medicine: We are not aloneTeri A Manolio, Marc Abramowicz, Fahd Al-Mulla, et al.
Circulation. Genomic and Precision Medicine|November 9, 2020
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A FamiliesYanushi D Wijeyeratne, Michael W Tanck, Yuka Mizusawa, et al.
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