Daniel C. Bartos

Agios Pharmaceuticals (United States) — United States

Medicine · Health Sciences

16h-index1.1kcitations33works0.02yr avg
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Research Topics

Cardiac electrophysiology and arrhythmias(31), Ion channel regulation and function(26), Neuroscience and Neural Engineering(7), Cardiomyopathy and Myosin Studies(4), ECG Monitoring and Analysis(3)

Publications33 total

Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes
International Journal of Molecular Sciences·2022· 19 citedOpen Access
Diastolic Sodium Current in Cardiomyocytes Assessed with Lithium
Biophysical Journal·2020Open Access
High Diastolic Sodium Influx in Heart Failure has Drug-Sensitivities Like Late Sodium Current, but Produces Inward Current at Diastolic Potentials
Biophysical Journal·2017Open Access
Quantitative analysis of the Ca<sup>2+</sup>‐dependent regulation of delayed rectifier K<sup>+</sup> current <i>I</i><sub>Ks</sub> in rabbit ventricular myocytes
The Journal of Physiology·2016· 45 citedOpen Access
Potassium channels in the heart: structure, function and regulation
The Journal of Physiology·2016· 109 citedOpen Access
Abstract 19858: The Promise and Peril of the Molecular Autopsy: Genetic Testing in a Sibling of a Sudden Death in the Young Victim Leads to Misdiagnosis of Long QT Syndrome and ICD Implantation
2016
The Promise and Peril of Precision Medicine
Mayo Clinic Proceedings·2016· 96 citedOpen Access
Ion Channels in the Heart
Comprehensive physiology·2015· 18 cited
Ion Channels in the Heart
Comprehensive physiology·2015· 172 citedOpen Access
The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization
Heart Rhythm·2015· 80 citedOpen Access
Intracellular Calcium Alters IKs Amplitude and Kinetics in Rabbit Myocytes
Biophysical Journal·2015Open Access
Depolarization of Cardiac Membrane Potential Synchronizes Calcium Sparks and Waves in Tissue
Biophysical Journal·2014· 20 citedOpen Access
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation
Heart Rhythm·2013· 25 citedOpen Access
Pharmacological correction of long QT-linked mutations in <i>KCNH2</i> (<i>hERG</i>) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum
American Journal of Physiology-Cell Physiology·2013· 34 citedOpen Access
Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death
JAMA·2013· 171 citedOpen Access
Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residues in the Voltage Sensor
The Journal of Membrane Biology·2013· 21 citedOpen Access
The cardiomyocyte molecular clock, regulation of <i>Scn5a</i> , and arrhythmia susceptibility
American Journal of Physiology-Cell Physiology·2013· 142 citedOpen Access
Cellular Mechanism for the Pharmacological Correction of hERG Mutations Linked to the Long QT Syndrome
Biophysical Journal·2013· 1 citedOpen Access
Malignant Long QT Syndrome KCNQ1 Mutations in the Pore Disrupt the Molecular Basis for Rapid K+ Permeation
Biophysical Journal·2013· 1 citedOpen Access
Mechanistic Basis for Atrial and Ventricular Arrhythmias Caused by KCNQ1 Mutations
UKnowledge (University of Kentucky)·2013Open Access
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Frequent Co-authors

Brian P. Delisle(25), Michael J. Ackerman(12), Don E. Burgess(12), David J. Tester(11), Jennifer L. Smith(8), Craig T. January(8), Donald M. Bers(6), Allison R. Reloj(6), Eleonora Grandi(5), Pascale Guicheney(5), Jonathan N. Johnson(5), Kenneth S. Ginsburg(5), Seiko Ohno(5), Minoru Horie(5), Elizabeth A. Schroder(3), Isabelle Denjoy(3), Véronique Fressart(3), Michael H. Gollob(3), Christie M. McBride(3), Parvathi Nataraj(3)