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List of works by Hervé Le Marec

0186 : Genotype/phenotype relationship in a large cohort of long QT syndrome patients

0224 : Mental stress unmasked new phenotype of sudden cardiac death related to adrenalin dependent prolongation of the QT interval

14-3-3 is a regulator of the cardiac voltage-gated sodium channel Nav1.5

scientific article

A common antitussive drug, clobutinol, precipitates the long QT syndrome 2

scientific article

A connexin40 mutation associated with a malignant variant of progressive familial heart block type I

scientific article

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human

scientific article

Brugada syndrome: Diagnosis, risk stratification and management

scientific article

Brugada syndrome: report of the second consensus conference.

scientific article

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

scientific article

Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation

scientific article published on 17 July 2013

Cardiac retention of [11C]HED in genotyped long QT patients: a potential amplifier role for severity of the disease

scientific article published on 29 May 2003

Clinical aspects and prognosis of Brugada syndrome in children

scientific article published on 2 April 2007

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

scientific article

Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease

scientific article

Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

scientific article published on 10 June 2016

Effect of baroreflex stimulation using phenylephrine injection on ST segment elevation and ventricular arrhythmia-inducibility in Brugada syndrome patients

scientific article published on 8 January 2009

Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

scholarly article published in Nature Genetics

Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspects

scientific article published on 20 July 2011

Fine-scale human genetic structure in Western France

scientific article published on 3 September 2014

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

scientific article published on 24 August 2015

Genetics of syndromic and non-syndromic mitral valve prolapse

scientific article published on 19 January 2018

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

scientific article published on August 2011

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

scientific article published on August 2011

Identification of large families in early repolarization syndrome

scientific article published in January 2013

Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia

scientific article published on 11 April 2016

MOG1: a new susceptibility gene for Brugada syndrome

scientific article published on 29 March 2011

Mitral valve disease--morphology and mechanisms

scientific article

Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects

scientific article published in May 2003

Novel Brugada SCN5A Mutation Leading to ST Segment Elevation in the Inferior or the Right Precordial Leads ⬇️

scientific article published on February 1, 2003

Outcome after implantation of a cardioverter-defibrillator in patients with Brugada syndrome: a multicenter study

scientific article published on 20 November 2006

Polymorphisms associated with ventricular tachyarrhythmias: rationale, design, and endpoints of the 'diagnostic data influence on disease management and relation of genomics to ventricular tachyarrhythmias in implantable cardioverter/defibrillator p

scientific article

Polymorphisms in the GNAS Gene as Predictors of Ventricular Tachyarrhythmias and Sudden Cardiac Death: Results From the DISCOVERY Trial and Oregon Sudden Unexpected Death Study

scientific article

Response to the Letter by Kattygnarath et al

Risk Stratification and Therapeutic Approach in Brugada Syndrome

scientific article published in September 2012

SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome

scientific article published on 29 September 2009

Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.

scientific article

Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I

article

Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome

article

The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

scientific article

The psychological impact of implantable cardioverter defibrillator implantation on Brugada syndrome patients ⬇️

scientific article published on March 21, 2011

Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation

scientific article

Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

scientific article

Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel

scientific article

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