| CLINICAL PERSPECTIVE C Antzelevitch, GD Pollevick, JM Cordeiro, O Casis, MC Sanguinetti, ... Circulation 115 (4), 442-449, 2007 | 963 | 2007 |
| Sudden death associated with short-QT syndrome linked to mutations in HERG R Brugada, K Hong, R Dumaine, J Cordeiro, F Gaita, M Borggrefe, ... Circulation 109 (1), 30-35, 2004 | 929 | 2004 |
| 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 | 394 | 2010 |
| Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome E Delpón, JM Cordeiro, L Núñez, PEB Thomsen, A Guerchicoff, ... Circulation: Arrhythmia and Electrophysiology 1 (3), 209-218, 2008 | 346 | 2008 |
| De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero K Hong, DR Piper, A Diaz-Valdecantos, J Brugada, A Oliva, ... Cardiovascular research 68 (3), 433-440, 2005 | 302 | 2005 |
| 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 | 266 | 2009 |
| Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations K Hong, J Brugada, A Oliva, A Berruezo-Sanchez, D Potenza, ... Circulation 110 (19), 3023-3027, 2004 | 182 | 2004 |
| 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 | 153 | 2012 |
| Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation LS Ravn, Y Aizawa, GD Pollevick, J Hofman-Bang, JM Cordeiro, U Dixen, ... Heart Rhythm 5 (3), 427-435, 2008 | 144 | 2008 |
| Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome JM Cordeiro, M Marieb, R Pfeiffer, K Calloe, E Burashnikov, ... Journal of molecular and cellular cardiology 46 (5), 695-703, 2009 | 99 | 2009 |
| CLINICAL PERSPECTIVE JM Cordeiro, H Barajas-Martinez, K Hong, E Burashnikov, R Pfeiffer, ... Circulation 114 (19), 2026-2033, 2006 | 97 | 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 | 93 | 2012 |
| 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 | 84 | 2014 |
| Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: Expanding the spectrum of Timothy syndrome J Gillis, E Burashnikov, C Antzelevitch, S Blaser, G Gross, L Turner, ... American Journal of Medical Genetics Part A 158 (1), 182-187, 2012 | 70 | 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 | 69 | 2007 |
| Cryptic 5′ splice site activation in SCN5A associated with Brugada syndrome K Hong, A Guerchicoff, GD Pollevick, A Oliva, R Dumaine, M de Zutter, ... Journal of molecular and cellular cardiology 38 (4), 555-560, 2005 | 69 | 2005 |
| Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome K Vernooy, S Sicouri, R Dumaine, K Hong, A Oliva, E Burashnikov, ... Heart Rhythm 3 (9), 1074-1078, 2006 | 57 | 2006 |
| High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia C Hasdemir, S Payzin, U Kocabas, H Sahin, N Yildirim, A Alp, M Aydin, ... Heart rhythm 12 (7), 1584-1594, 2015 | 54 | 2015 |
| A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death E Nof, JM Cordeiro, GJ Pérez, FS Scornik, K Calloe, B Love, ... Circulation: Cardiovascular Genetics 3 (2), 199-206, 2010 | 51 | 2010 |
| Dual Variation in SCN5A and CACNB2b Underlies the Development of Cardiac Conduction Disease without Brugada Syndrome D Hu, H BARAJAS‐MARTINEZ, VV Nesterenko, R Pfeiffer, A Guerchicoff, ... Pacing and Clinical Electrophysiology 33 (3), 274-285, 2010 | 33 | 2010 |
