Elena Burashnikov
Elena Burashnikov
Verified email at mmrl.edu
Cited by
Cited by
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death
C Antzelevitch, GD Pollevick, JM Cordeiro, O Casis, MC Sanguinetti, ...
Circulation 115 (4), 442-449, 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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Biophysical and Molecular Characterization of a Novel De Novo KCNJ2 Mutation Associated With Andersen-Tawil Syndrome and Catecholaminergic Polymorphic …
H Barajas-Martinez, D Hu, G Ontiveros, G Caceres, M Desai, ...
Circulation: Cardiovascular Genetics 4 (1), 51-57, 2011
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