List of works - Hector Barajas-Martinez

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

scientific article

A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents

scientific article published on 7 December 2011

A temporal window of vulnerability for development of atrial fibrillation with advancing heart failure

article

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

scientific article published on 04 January 2014

Atrial-selective inhibition of sodium-channel current by Wenxin Keli is effective in suppressing atrial fibrillation.

scientific article

Biophysical and molecular characterization of a novel de novo KCNJ2 mutation associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia mimicry

scientific article

Brugada-like syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay.

scientific article

Cellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome.

scientific article published on 25 January 2016

Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome

scientific article

Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.

scientific article

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

scientific article published on 7 September 2020

Identification of a novel de novo mutation associated with PRKAG2 cardiac syndrome and early onset of heart failure

scientific article

Ionic and cellular mechanisms underlying the development of acquired Brugada syndrome in patients treated with antidepressants.

scientific article

LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.

scientific article

Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channel.

scientific article published on 03 July 2008

Maximum diastolic potential of human induced pluripotent stem cell-derived cardiomyocytes depends critically on I(Kr).

scientific article

Mechanisms underlying atrial-selective block of sodium channels by Wenxin Keli: Experimental and theoretical analysis.

scientific article published on 07 January 2016

Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome

scientific article published on 28 December 2013

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

scientific article published on 3 November 2011

Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome

scientific article

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

scientific article

Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

scientific article

Ranolazine effectively suppresses atrial fibrillation in the setting of heart failure.

scientific article

Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes

scientific article published on 01 September 2020

[Genetic and molecular basis for sodium channel-mediated Brugada syndrome].

scientific article

List of works by Hector Barajas-Martinez

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents

A temporal window of vulnerability for development of atrial fibrillation with advancing heart failure

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

Atrial-selective inhibition of sodium-channel current by Wenxin Keli is effective in suppressing atrial fibrillation.

Biophysical and molecular characterization of a novel de novo KCNJ2 mutation associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia mimicry

Brugada-like syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay.

Cellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome.

Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome

Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Identification of a novel de novo mutation associated with PRKAG2 cardiac syndrome and early onset of heart failure

Ionic and cellular mechanisms underlying the development of acquired Brugada syndrome in patients treated with antidepressants.

LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.

Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channel.

Maximum diastolic potential of human induced pluripotent stem cell-derived cardiomyocytes depends critically on I(Kr).

Mechanisms underlying atrial-selective block of sodium channels by Wenxin Keli: Experimental and theoretical analysis.

Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

Ranolazine effectively suppresses atrial fibrillation in the setting of heart failure.

Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes

[Genetic and molecular basis for sodium channel-mediated Brugada syndrome].