Daniel C. Bartos

Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death

Lia Crotti, David J. Tester, Wendy White et al. · JAMA · 2013 · 171 citations · Full text

The cardiomyocyte molecular clock, regulation of <i>Scn5a</i> , and arrhythmia susceptibility

Elizabeth A. Schroder, Mellani Lefta, Xiping Zhang et al. · American Journal of Physiology-Cell Physiology · 2013 · 142 citations · Full text

The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization

Elizabeth A. Schroder, Don E. Burgess, Xiping Zhang et al. · Heart Rhythm · 2015 · 80 citations · Full text

Cardiac Muscle, Cardiomyocyte Molecular Clock, Cellular Physiology +16

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

Daniel C. Bartos, Sabine Duchatelet, Don E. Burgess et al. · Heart Rhythm · 2010 · 72 citations · Full text

Cardiomyopathy, Genetic Disorder, Genetics +6

A <i>KCNQ1</i> Mutation Causes a High Penetrance for Familial Atrial Fibrillation

Daniel C. Bartos, Jeffrey Anderson, Rachel Bastiaenen et al. · Journal of Cardiovascular Electrophysiology · 2012 · 60 citations · Full text