| Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death E Burashnikov, R Pfeiffer, H Barajas-Martinez, E Delpón, D Hu, M Desai, ... Heart rhythm 7 (12), 1872-1882, 2010 | 535 | 2010 |
| A mutation in the β3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype D Hu, H Barajas-Martinez, E Burashnikov, M Springer, Y Wu, A Varro, ... Circulation: Cardiovascular Genetics 2 (3), 270-278, 2009 | 320 | 2009 |
| Mutations in SCN10A Are Responsible for a Large Fraction of Cases of Brugada Syndrome D Hu, H Barajas-Martínez, R Pfeiffer, F Dezi, J Pfeiffer, T Buch, ... Journal of the American College of Cardiology 64 (1), 66-79, 2014 | 259 | 2014 |
| heart rhythm society (HRS)/Asia pacific heart rhythm society (APHRS)/latin American heart rhythm society (LAHRS) expert consensus statement on the state of genetic testing for … AAM Wilde, C Semsarian, MF Márquez, A Sepehri Shamloo, ... Europace 24 (8), 1307-1367, 2022 | 239 | 2022 |
| Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6) C Templin, JR Ghadri, JS Rougier, A Baumer, V Kaplan, M Albesa, ... European heart journal 32 (9), 1077-1088, 2011 | 239 | 2011 |
| European heart rhythm association (EHRA)/heart rhythm society (HRS)/Asia pacific heart rhythm society (APHRS)/latin American heart rhythm society (LAHRS) expert consensus … AAM Wilde, C Semsarian, MF Márquez, AS Shamloo, MJ Ackerman, ... Europace 24 (8), 1307-1367, 2022 | 204* | 2022 |
| Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8 H Barajas-Martínez, D Hu, T Ferrer, CG Onetti, Y Wu, E Burashnikov, ... Heart Rhythm 9 (4), 548-555, 2012 | 195 | 2012 |
| Maximum Diastolic Potential of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Depends Critically on IKr MX Doss, JM Di Diego, RJ Goodrow, Y Wu, JM Cordeiro, VV Nesterenko, ... PloS one 7 (7), e40288, 2012 | 179 | 2012 |
| Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome I Koncz, Z Gurabi, B Patocskai, BK Panama, T Szél, D Hu, ... Journal of molecular and cellular cardiology 68, 20-28, 2014 | 141 | 2014 |
| ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene D Hu, H Barajas-Martínez, A Terzic, S Park, R Pfeiffer, E Burashnikov, ... International journal of cardiology 171 (3), 431-442, 2014 | 133 | 2014 |
| Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome JM Cordeiro, H Barajas-Martinez, K Hong, E Burashnikov, R Pfeiffer, ... Circulation 114 (19), 2026-2033, 2006 | 131 | 2006 |
| A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1. 5 and Kv4. 3 channel currents D Hu, H Barajas-Martínez, A Medeiros-Domingo, L Crotti, C Veltmann, ... Heart Rhythm 9 (5), 760-769, 2012 | 115 | 2012 |
| Atrial-selective inhibition of sodium-channel current by Wenxin Keli is effective in suppressing atrial fibrillation A Burashnikov, A Petroski, D Hu, H Barajas-Martinez, C Antzelevitch Heart Rhythm 9 (1), 125-131, 2012 | 104 | 2012 |
| Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction D Hu, S Viskin, A Oliva, T Carrier, JM Cordeiro, H Barajas-Martinez, Y Wu, ... Heart Rhythm 4 (8), 1072-1080, 2007 | 86 | 2007 |
| Hypertension as a sequela in patients of SARS-CoV-2 infection G Chen, X Li, Z Gong, H Xia, Y Wang, X Wang, Y Huang, ... PLoS One 16 (4), e0250815, 2021 | 80 | 2021 |
| Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channel HM Barajas-Martínez, D Hu, JM Cordeiro, Y Wu, RJ Kovacs, H Meltser, ... Circulation research 103 (4), 396-404, 2008 | 76 | 2008 |
| Identification of two domains involved in the assembly of transient receptor potential canonical channels PK Lepage, MP Lussier, H Barajas-Martinez, SM Bousquet, AP Blanchard, ... Journal of biological chemistry 281 (41), 30356-30364, 2006 | 73 | 2006 |
| Brugada-like syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay RJ Kanter, R Pfeiffer, D Hu, H Barajas-Martinez, MP Carboni, ... Circulation 125 (1), 14-22, 2012 | 72 | 2012 |
| Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls R Walsh, N Lahrouchi, R Tadros, F Kyndt, C Glinge, PG Postema, ... Genetics in medicine 23 (1), 47-58, 2021 | 65 | 2021 |
| Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect C Veltmann, H Barajas‐Martinez, C Wolpert, M Borggrefe, R Schimpf, ... Journal of the American Heart Association 5 (7), e003379, 2016 | 65 | 2016 |
Charles AntzelevitchDistinguished Professor and Executive Director, Cardiovascular Research, Lankenau Institute forVerified email at mlhs.org
