V. Probst

J. Deharo, Y. Lecarpentier, P. Cosnay, 2010, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Subcutaneous implantable cardioverter defibrillator indication in prevention of sudden cardiac death in difficult clinical situations: A French expert position paper.

C. Leclercq, F. Anselme, S. Boveda, 2020, Archives of cardiovascular diseases.

ThesodiumchannelanditsregulatorysubunitsplayacentralroleinthepathophysiologyofBrugada syndrome (BrS). The identification of rare and common variants that modify the sodium current involved in the devel- opment of BrS favors the predominant role of conduction abnormalities.

R. Redon, V. Probst, F. Kyndt, 2014 .

Brugada Syndrome and Nav1.5

R. Redon, V. Probst, F. Kyndt, 2014 .

Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approach

V. Probst, S. Chatel, F. Kyndt, 2012, Heart.

Mutation Associated With a Malignant Variant ofProgressive Familial Heart

D. Roden, N. Hagiwara, M. Horie, 2012 .

A Connexin40 Mutation Associated With a Malignant Variant of Progressive Familial Heart Block Type I

D. Roden, N. Hagiwara, W. Shimizu, 2012, Circulation. Arrhythmia and electrophysiology.

Common Phenotype in Patients With Mitral Valve Prolapse Who Experienced Sudden Cardiac Death.

C. Leclercq, J. Deharo, D. Hodge, 2018, Circulation.

Benign vs. malignant inferolateral early repolarization: Focus on the T wave.

Ashok J. Shah, J. Ruidavets, J. Kautzner, 2016, Heart rhythm.

Risk Stratification and Therapeutic Approach in Brugada Syndrome.

V. Probst, S. Chatel, H. Marec, 2012, Arrhythmia & electrophysiology review.

Prevalence of diabetes and impact on cardiovascular events and mortality in patients with chronic coronary syndromes, across multiple geographical regions and ethnicities.

T. S. Chee, D. S. Kim, S. H. Lee, 2021, European journal of preventive cardiology.

Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events

S. Priori, E. Behr, A. Mazzanti, 2021, Circulation. Genomic and precision medicine.

TRPM4 non-selective cation channel variants in long QT syndrome

V. Probst, J. Schott, L. Sallé, 2017, BMC Medical Genetics.

Familial Aggregation of Calcific Aortic Valve Stenosis in the Western Part of France

V. Probst, A. Chaventré, J. Schott, 2006, Circulation.

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

R. Redon, C. Dina, N. Makita, 2016, International journal of cardiology.

Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .

Electropharmacological characterization of cardiac repolarization in German shepherd dogs with an inherited syndrome of sudden death: abnormal response to potassium channel blockers.

U. Gerlach, F. Charpentier, V. Probst, 2000, Journal of the American College of Cardiology.

Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form‐associated genes provides new insights for molecular diagnosis and clinical management

R. Redon, C. Dina, F. Sacher, 2022, Human mutation.

Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies

J. Serfaty, J. Trochu, V. Probst, 2020, ESC heart failure.

PQ segment depression in patients with short QT syndrome: a novel marker for diagnosing short QT syndrome?

C. Antzelevitch, M. Borggrefe, J. Blanc, 2014, Heart rhythm.

Dynamic changes in ventricular depolarization during exercise in patients with Brugada syndrome

Alfredo I. Hernández, F. Sacher, V. Probst, 2020, PloS one.

Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre study.

J. Daubert, C. Leclercq, J. Lusson, 2012, European heart journal.

Idiopathic Ventricular Fibrillation

P. Jais, F. Sacher, M. Hocini, 2020, JACC. Clinical electrophysiology.

Prevalence of early repolarization pattern in inferolateral leads in patients with Brugada syndrome.

S. Knecht, F. Sacher, M. Haïssaguerre, 2008, Heart rhythm.

International Triadin Knockout Syndrome Registry: The Clinical Phenotype and Treatment Outcomes of Patients With Triadin Knockout Syndrome

S. Priori, P. Schwartz, C. Napolitano, 2019, Circulation. Genomic and precision medicine.

Cardiac remote monitoring in France.

V. Probst, G. Grimandi, G. Lande, 2014, Archives of cardiovascular diseases.

High Risk of Sustained Ventricular Arrhythmia Recurrence After Acute Myocarditis

É. Marijon, C. Guenancia, V. Probst, 2020, Journal of clinical medicine.

Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients.

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

Process mapping strategies to prevent subcutaneous implantable cardioverter‐defibrillator infections

Timothy R. McClernon, P. Lambiase, B. Knight, 2022, Journal of cardiovascular electrophysiology.

[2018 ESC Guidelines for the diagnosis and management of syncope].

J. Deharo, M. Brignole, P. Elliott, 2018, Kardiologia polska.

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

R. Redon, E. Behr, D. Roden, 2013, Nature Genetics.

Insufficiency of electrocardiogram alone in predicting infrahisian abnormalities in patients with type 1 myotonic dystrophy.

D. Babuty, V. Probst, N. Clementy, 2014, International journal of cardiology.

Implantable cardiac defibrillator leads dysfunction after LVAD implantation

É. Marijon, C. Leclercq, F. Anselme, 2020, Pacing and clinical electrophysiology : PACE.

T-Wave Oversensing in Patients With Brugada Syndrome: True Bipolar Versus Integrated Bipolar Implantable Cardioverter Defibrillator Leads Multicenter Retrospective Study

P. Lambiase, J. Brugada, P. Brugada, 2015, Circulation. Arrhythmia and electrophysiology.

Outcome After Implantation of a Cardioverter-Defibrillator in Patients With Brugada Syndrome: A Multicenter Study–Part 2

M. Field, F. Sacher, M. Hocini, 2006, Circulation.

Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern.

V. Probst, F. Kyndt, J. Schott, 2008, Heart rhythm.

Profile of patients with Brugada syndrome presenting with their first documented arrhythmic event: Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

Zhengrong, E. Behr, C. Napolitano, 2018 .

Continued misuse of orphan drug legislation: a life-threatening risk for mexiletine.

P. Lambiase, S. Priori, E. Behr, 2020, European heart journal.

Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next‐generation sequencing

L. Faivre, C. Thauvin-Robinet, V. Probst, 2017, American journal of medical genetics. Part A.

Ethnic Differences in Patients with Brugada Syndrome and Arrhythmic Events: New Insights from SABRUS.

S. Priori, E. Behr, A. Mazzanti, 2019, Heart rhythm.

Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome.

S. Priori, E. Behr, A. Mazzanti, 2019, Journal of the American College of Cardiology.

Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

S. Priori, E. Behr, C. Napolitano, 2019, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients

S. Priori, E. Behr, C. Napolitano, 2017, Circulation. Arrhythmia and electrophysiology.

Are Women with Severely Symptomatic Brugada Syndrome Different from Men?

M. Field, A. Wilde, M. Borggrefe, 2008, Journal of cardiovascular electrophysiology.

Mental stress test: a rapid, simple, and efficient test to unmask long QT syndrome

R. Redon, F. Charpentier, V. Probst, 2018, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

The QUIDAM study: Hydroquinidine therapy for the management of Brugada syndrome patients at high arrhythmic risk.

F. Sacher, J. Deharo, A. Leenhardt, 2017, Heart rhythm.

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

F. Sacher, M. Haïssaguerre, V. Probst, 2013, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

New Family With Catecholaminergic Polymorphic Ventricular Tachycardia Linked to the Triadin Gene

F. Sacher, C. Rooryck, D. Bozon, 2015, Journal of cardiovascular electrophysiology.

Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block

V. Probst, S. Chatel, J. Schott, 2016, Journal of the American Heart Association.

Progressive Cardiac Conduction Defect is the Prevailing Phenotype in Carriers of a Brugada Syndrome SCN5A Mutation

F. Sacher, D. Escande, V. Probst, 2006, Journal of cardiovascular electrophysiology.

Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28.

J. Trochu, B. Bénichou, J. Gueffet, 2000, Journal of the American College of Cardiology.

Usefulness of fetuin-A and C-reactive protein concentrations for prediction of outcome in acute coronary syndromes (from the French Registry of Acute ST-Elevation Non-ST-Elevation Myocardial Infarction [FAST-MI]).

J. Ferrières, N. Danchin, V. Probst, 2013, The American journal of cardiology.

Predictors of subcutaneous ICD shocks and prognostic impact in patients with structural heart disease.

V. Probst, É. Drumez, J. Labreuche, 2020, The Canadian journal of cardiology.

Prevalence, characteristics, and prognosis role of type 1 ST elevation in the peripheral ECG leads in patients with Brugada syndrome.

F. Sacher, M. Hocini, M. Haïssaguerre, 2013, Heart rhythm.

SCN5A-related cardiac channelopathy

C. Dina, A. Wilde, F. Charpentier, 2012 .

Malignant Purkinje Ectopy induced by Sodium-channel Blocker.

P. Postema, K. Nademanee, M. Haissaguerre, 2022, Heart rhythm.

Generation of human induced pluripotent stem cell lines from two patients affected by catecholamine-induced QT prolongation (CIQTP).

R. Redon, V. Probst, P. Lemarchand, 2021, Stem cell research.

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.

R. Redon, E. Génin, C. Dina, 2018, European heart journal.

Familial Catecholamine-Induced QT Prolongation in Unexplained Sudden Cardiac Death.

R. Redon, F. Charpentier, V. Probst, 2017, Journal of the American College of Cardiology.

2018 ESC Guidelines for the diagnosis and management of syncope

Christophe Leclercq, Raffaello Furlan, Rose Anne Kenny, 2018, European heart journal.

Outcome of Patients with Early Repolarization Pattern and Syncope.

M. Haissaguerre, F. Sacher, J. Deharo, 2022, Heart rhythm.

SCN5A Overlap Syndromes: an open-minded approach.

V. Probst, A. Superti-Furga, Z. Bhuiyan, 2022, Heart rhythm.

Age of First Arrhythmic Event in Brugada Syndrome: Data from the Survey on Arrhythmic Events in Brugada Syndrome (SABRUS) in 678 Patients Age of First Arrhythmic Event in Brugada Syndrome

E. Behr, C. Napolitano, J. Brugada, 2020 .

Correlation of intracardiac electrogram with surface electrocardiogram in Brugada syndrome patients.

F. Sacher, V. Probst, P. Mabo, 2014, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

SCN1Bb, atrial fibrillation, and Brugada syndrome: just another brick in the wall ….

V. Probst, J. Gourraud, H. Le Marec, 2012, Heart rhythm.

Ajmaline challenge: to stop or not to stop...

V. Probst, H. Le Marec, 2009, Heart rhythm.

Monomorphic Ventricular Tachycardia Due to Brugada Syndrome Successfully Treated by Hydroquinidine Therapy in a 3‐Year‐Old Child

V. Probst, J. Schott, P. Boisseau, 2006, Journal of cardiovascular electrophysiology.

S. Matecki, M. Picot, C. Delclaux, 2021 .

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

V. Probst, J. Schott, M. Allouis, 2005, The American journal of cardiology.

Novel SCN5A Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family

D. Escande, S. Demolombe, J. Chevallier, 2001, Circulation.

Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.

R. Redon, N. Hagiwara, M. Horie, 2017, Journal of the American College of Cardiology.

Risk of ventricular arrhythmia in patients with myocardial infarction and non-obstructive coronary arteries and normal ejection fraction

V. Probst, A. Furber, F. Prunier, 2017, World journal of cardiology.

Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy.

R. Redon, A. Rötig, G. Ravenscroft, 2016, American journal of human genetics.

Cardiac Phenotype and Long-Term Follow-Up of Patients With Mutations in NKX2-5 Gene.

V. Probst, F. Kyndt, D. Bonnet, 2016, Journal of the American College of Cardiology.

Safeguarding continuing cardiovascular research excellence and quality publications in France: A working document from the French Society of Cardiology.

M. Gilard, V. Probst, B. Lattuca, 2019, Archives of cardiovascular diseases.

[Familial hypertrophic cardiomyopathy. French study of the duration and outcome of pregnancy].

M. Komajda, M. Desnos, V. Probst, 2002, Archives des maladies du coeur et des vaisseaux.

Long-term prognosis of individuals with right predordial ST-elevation - Brugada syndrome

G. Breithardt, L. Eckardt, M. Borggrefe, 2005 .

745High risk of heart failure in desmoglein-2 mutation carriers in arrhythmogenic right ventricular dysplasia/cardiomyopathy

J. Deharo, P. Cosnay, E. Donal, 2017 .

Brugada syndrome: Keep an eye on the electrocardiogram.

V. Probst, J. Gourraud, 2018, Heart rhythm.

Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype.

J. Trochu, V. Probst, F. Kyndt, 2003, The American journal of cardiology.

Sudden cardiac arrest associated with early repolarization.

Thomas Lavergne, Nicolas Derval, Michel Haïssaguerre, 2008, The New England journal of medicine.

Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis.

Y. Bossé, R. Redon, C. Dina, 2019, Circulation. Genomic and precision medicine.

An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia

J. Skinner, E. Behr, P. Schwartz, 2021, Circulation.

2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families

C. Morillo, E. Kaufman, C. Albert, 2020, Heart rhythm.

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

Olha Koval, Thomas J Hund, Yuejin Wu, 2008, Proceedings of the National Academy of Sciences.

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

R. Redon, K. Strauch, P. Lambiase, 2022, Nature Genetics.

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.

R. Redon, E. Behr, D. Roden, 2015, Cardiovascular research.

Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation.

R. Levine, R. Markwald, R. Norris, 2014, Biochimica et biophysica acta.

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

Dan M Roden, Beverley Balkau, Pierre Lindenbaum, 2013, Nature Genetics.

Circulating PCSK9 levels in acute coronary syndrome: Results from the PC-SCA-9 prospective study.

V. Probst, V. Letocart, C. Le May, 2017, Diabetes & metabolism.

Abnormal Cellular Phenotypes Induced by Three TMPO/LAP2 Variants Identified in Men with Cardiomyopathies

F. Chapon, B. Buendia, C. Rooryck, 2023, Cells.

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

R. Redon, P. Lambiase, P. Ellinor, 2020, Genetics in medicine : official journal of the American College of Medical Genetics.

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

T. Werge, P. Ellinor, S. Priori, 2020, Circulation.

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

J. Towbin, J. Brugada, R. Brugada, 2010, Heart rhythm.

Dose response to nadolol in congenital Long QT Syndrome.

V. Probst, J. Gourraud, B. Guyomarch, 2021, Heart rhythm.

2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families

C. Morillo, E. Kaufman, C. Albert, 2020, Journal of arrhythmia.

Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity.

R. Redon, F. Sacher, V. Probst, 2017, Heart rhythm.

Clinical Yield of Familial Screening After Sudden Death in Young Subjects: The French Experience

R. Redon, F. Sacher, V. Probst, 2017, Circulation. Arrhythmia and electrophysiology.

Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel

V. Probst, S. Chatel, J. Schott, 2013, PloS one.

MOG1: A New Susceptibility Gene for Brugada Syndrome

A. Leenhardt, V. Probst, J. Schott, 2011, Circulation. Cardiovascular genetics.

Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

M Borggrefe, F Gaita, A A M Wilde, 2010, Circulation.

Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies.

H. Tan, F. Sacher, V. Probst, 2009, Heart rhythm.

SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome

A. Wilde, H. Tan, F. Sacher, 2009, Circulation. Cardiovascular genetics.

Clinical Aspects and Prognosis of Brugada Syndrome in Children

A. Wilde, M. Haissaguerre, F. Sacher, 2007, Circulation.

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.

G. Breithardt, W. Haverkamp, L. Eckardt, 2002, Journal of the American College of Cardiology.

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

R. Redon, C. Dina, R. Teusan, 2015, Human molecular genetics.

Inherited progressive cardiac conduction disorders

V. Probst, Vincent Probst, Hugues Abriel, 2015, Current opinion in cardiology.

Parental Electrocardiographic Screening Identifies a High Degree of Inheritance for Congenital and Childhood Nonimmune Isolated Atrioventricular Block

J. Daubert, C. Dina, J. Lusson, 2012, Circulation.

Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org).

S. Priori, D. Roden, J. Brugada, 2009, Heart rhythm.

Heritability of aortic valve stenosis and bicuspid enrichment in families with aortic valve stenosis.

C. Dina, C. Baufreton, V. Probst, 2022, International journal of cardiology.

Genetics of syndromic and non-syndromic mitral valve prolapse

R. Levine, V. Probst, J. Schott, 2018, Heart.

Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy

J. Trochu, I. Young, R. Newbury-Ecob, 2006, Circulation.

Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background

R. Redon, F. Charpentier, V. Probst, 2021, Stem Cell Research.

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

R. Redon, C. Dina, Céline Marionneau, 2016, Journal of the American Heart Association.

A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

R. Redon, F. Charpentier, V. Probst, 2021, Clinical and translational medicine.

Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.

E. Behr, P. Schwartz, A. Wilde, 2016, Heart rhythm.

The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

R. Redon, V. Probst, J. Barc, 2016, Front. Cardiovasc. Med..

Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM 4 Channel

V. Probst, S. Chatel, J. Schott, 2013 .

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease.

D. Escande, S. Demolombe, J. Trochu, 2003, Journal of the American College of Cardiology.

Long-Term Prognosis of Individuals With Right Precordial ST-Segment–Elevation Brugada Syndrome

G. Breithardt, L. Eckardt, M. Borggrefe, 2005, Circulation.

Robustness and relevance of predictive score in sudden cardiac death for patients with Brugada syndrome.

F. Sacher, P. Gourraud, V. Probst, 2020, European heart journal.

OP-EHEA190316_online 3081..3094

R. Redon, C. Dina, Céline Marionneau, 2021 .

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

X. Estivill, M. Caulfield, P. Froguel, 2012, Nature Genetics.

Early Repolarization Disease.

Ashok J. Shah, M. Haissaguerre, P. Jais, 2010, Cardiac electrophysiology clinics.

Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1

R. Porcher, A. Lazarus, F. Chapon, 2016, European heart journal.

Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: results of a systematic screening.

J. Deharo, P. Cosnay, E. Donal, 2014, Heart rhythm.

Defects in Ankyrin-Based Membrane Protein Targeting Pathways Underlie Atrial Fibrillation

X. Wehrens, M. Karck, D. Dobrev, 2011, Circulation.

Fine-scale human genetic structure in Western France

R. Redon, C. Dina, B. Balkau, 2014, European Journal of Human Genetics.

Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes

R. Redon, Toshihiro Tanaka, T. Tsunoda, 2016, Journal of the American Heart Association.

Characteristics of recurrent ventricular fibrillation associated with inferolateral early repolarization role of drug therapy.

H. Heidbuchel, R. Cappato, P. Jais, 2009, Journal of the American College of Cardiology.

A clinical practice guideline for physiotherapists treating patients with chronic obstructive pulmonary disease based on a systematic review of available evidence

M. Decramer, V. Ninane, T. Troosters, 2009, Clinical rehabilitation.

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

F. Sacher, V. Probst, D. Babuty, 2009, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Multifocal Ectopic Purkinje-Related Premature Contractions A New SCN5A -Related Cardiac Channelopathy

C. Dina, A. Wilde, F. Charpentier, 2012 .

Clinical outcome of patients with the Brugada type 1 electrocardiogram without prophylactic implantable cardioverter defibrillator in primary prevention: a cumulative analysis of seven large prospective studies

J. Brugada, L. Calò, V. Probst, 2017, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

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

A. Leenhardt, V. Probst, P. Ray, 2012, Human molecular genetics.

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

P. Ellinor, S. Priori, A. Mazzanti, 2015, Circulation.

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

P. Ellinor, S. Priori, A. Mazzanti, 2015, Circulation.

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

F. Sacher, V. Probst, D. Babuty, 2011, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

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

J. Daubert, D. Escande, V. Probst, 2003, Journal of cardiovascular electrophysiology.

Role of electrophysiological studies in predicting risk of ventricular arrhythmia in early repolarization syndrome.

J. Kautzner, F. Sacher, M. Hocini, 2015, Journal of the American College of Cardiology.

Identification of large families in early repolarization syndrome.

R. Redon, F. Sacher, M. Haïssaguerre, 2013, Journal of the American College of Cardiology.

An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation

M. Haissaguerre, M. Hocini, A. Leenhardt, 2018, Scientific Reports.

Ventricular fibrillation in loop recorder memories in a patient with early repolarization syndrome.

F. Sacher, V. Probst, P. Maury, 2012, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Ventricular Fibrillation with Prominent Early Repolarization Associated with a Rare Variant of KCNJ8/KATP Channel

A. Wilde, E. Schulze-Bahr, Y. Rudy, 2009, Journal of cardiovascular electrophysiology.

Long-term follow-up of patients with short QT syndrome.

Andrea Mazzanti, Paola Dalmasso, Martin Borggrefe, 2011, Journal of the American College of Cardiology.

SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

R. Redon, E. Behr, T. Meitinger, 2020, Circulation. Genomic and precision medicine.

Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

J. Skinner, P. Schwartz, A. Wilde, 2020, Circulation. Arrhythmia and electrophysiology.

Age at Diagnosis of Brugada Syndrome: Influence on Clinical Characteristics and Risk of Arrhythmia.

F. Sacher, V. Probst, N. Clementy, 2019, Heart rhythm.

Number of electrocardiogram leads in the diagnosis of spontaneous Brugada syndrome.

F. Sacher, V. Probst, D. Babuty, 2019, Archives of cardiovascular diseases.

Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest.

J. Skinner, E. Behr, P. Schwartz, 2019, European heart journal.

Clinical presentation and follow-up of women affected by Brugada syndrome.

F. Sacher, V. Probst, D. Babuty, 2019, Heart rhythm.

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups

J. Skinner, E. Behr, P. Schwartz, 2018, European heart journal.

Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants.

E. Behr, M. Sheppard, A. Wilde, 2018, Heart rhythm.

Value of the sodium-channel blocker challenge in Brugada syndrome.

R. Redon, F. Sacher, V. Probst, 2017, International journal of cardiology.

Differential calcium sensitivity in NaV1.5 mixed syndrome mutants

P. Ruben, A. Krahn, V. Probst, 2017, The Journal of physiology.

Brugada syndrome: Diagnosis, risk stratification and management.

V. Probst, J. Barc, J. Gourraud, 2017, Archives of cardiovascular diseases.

Reply to the Editor-Brugada syndrome is not an ECG.

V. Probst, A. Andorin, 2016, Heart rhythm.

Prognostic significance of fever-induced Brugada syndrome.

A. Wilde, S. Viskin, H. Morita, 2016, Heart rhythm.

Monomorphic ventricular tachycardia in patients with Brugada syndrome: A multicenter retrospective study.

P. Lambiase, J. Brugada, P. Brugada, 2016, Heart rhythm.

Increased Tpeak-Tend interval is highly and independently related to arrhythmic events in Brugada syndrome.

F. Sacher, M. Hocini, M. Haïssaguerre, 2015, Heart Rhythm.

Quinidine in Brugada Syndrome: Still a Long Way to Go….

V. Probst, J. Gourraud, 2015, Circulation. Arrhythmia and electrophysiology.

Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

R. Redon, D. Pavin, V. Probst, 2014, Basic Research in Cardiology.

Outcome After Implantation of a Cardioverter-Defibrillator in Patients With Brugada Syndrome: A Multicenter Study

M. O'Neill, F. Sacher, M. Hocini, 2006, Circulation.

Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.

Francesca N. Delling, M. Rienstra, B. Horne, 2022, European heart journal.

18F-Fluorodeoxyglucose Positron Emission Tomography for the Detection of Myocardial Inflammation in Arrhythmogenic Left Ventricular Cardiomyopathy.

J. Serfaty, B. Jamet, V. Probst, 2022, Circulation. Cardiovascular imaging.

Diagnosis and management of subcutaneous implantable cardioverter‐defibrillator infections based on process mapping

Timothy R. McClernon, P. Lambiase, B. Knight, 2020, Pacing and clinical electrophysiology : PACE.

V. Probst, F. Kyndt, J. Schott, 2011, Journal of cardiovascular translational research.

Genetic mechanisms of mitral valve prolapse

R. Levine, A. Hagège, X. Jeunemaître, 2008 .

Prevalence and prognostic role of various conduction disturbances in patients with the Brugada syndrome.

F. Sacher, M. Hocini, M. Haïssaguerre, 2013, The American journal of cardiology.

Response to intravenous ajmaline: a retrospective analysis of 677 ajmaline challenges.

M. Borggrefe, F. Sacher, V. Probst, 2009, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

High risk of heart failure associated with desmoglein‐2 mutations compared to plakophilin‐2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia

J. Deharo, P. Cosnay, E. Donal, 2019, European journal of heart failure.

P. Lambiase, B. Knight, M. Biffi, 2022, Journal of cardiovascular electrophysiology.

Safety, feasibility, and outcome results of cardiac resynchronization with triple-site ventricular stimulation compared to conventional cardiac resynchronization.

C. Leclercq, J. Deharo, F. Anselme, 2016, Heart rhythm.

Heart rate variability and repolarization characteristics in symptomatic and asymptomatic Brugada syndrome

Alfredo I. Hernández, Nathalie Behar, Philippe Mabo, 2016, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Functional Epicardial Conduction Disturbances Due to a SCN5A Variant Associated With Brugada Syndrome

Jesse L. Ashton, F. Sacher, M. Hocini, 2023, JACC. Clinical electrophysiology.

R. Hauer, H. Calkins, E. Behr, 2021, Circulation. Genomic and precision medicine.

Multicenter study of prophylactic ICD implantation in Brugada syndrome

H. Lemarec, F. Sacher, M. Hocini, 2005 .

Abnormal cardiac repolarization and impulse initiation in German shepherd dogs with inherited ventricular arrhythmias and sudden death.

M. Rosen, P. Danilo, F. Charpentier, 1999, Cardiovascular research.

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

Frédéric Sacher, Richard Redon, R. Redon, 2011, Journal of the American College of Cardiology.

Response to the Letter by Kattygnarath et al

A. Leenhardt, V. Probst, J. Schott, 2011 .

Remote implantable cardioverter defibrillator monitoring in a Brugada syndrome population.

M. Wright, F. Sacher, M. Hocini, 2008, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

[Genetic aspects of valvulopathies].

J. Gueffet, V. Probst, A. Chaventré, 2007, Archives des maladies du coeur et des vaisseaux.

P. Lambiase, B. Knight, M. Biffi, 2021, Heart rhythm.

Use of drugs with potential cardiac effect in the setting of SARS-CoV-2 infection

L. Fauchier, C. Leclercq, F. Sacher, 2020, Archives of Cardiovascular Diseases.

Quinidine therapy in children affected by Brugada syndrome: are we far from a safe alternative?

V. Probst, P. Mabo, A. Baruteau, 2009, Cardiology in the Young.

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

Ashutosh Kumar Singh, Jeffrey M. Vinocur, E. Behr, 2023, European heart journal.

A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity

V. Probst, J. Barc, F. Kyndt, 2021, Clinical and translational medicine.

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Andrew D. Johnson, Thomas W. Mühleisen, M. Nalls, 2014, Nature Genetics.

UvA-DARE ( Digital Academic Repository ) Variable Na ( v ) 1 . 5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn 5 a ( + /-) Mouse Model

A. Wilde, Céline Marionneau, D. Escande, 2010 .

Reply to the Editor--PQ-segment depression in short QT syndrome patients: a novel marker for diagnosing short QT syndrome?

C. Antzelevitch, M. Borggrefe, J. Blanc, 2014, Heart rhythm.

Inappropriate therapy after catheter ablation and subcutaneous implantable cardioverter-defibrillator

V. Probst, G. Lande, J. Gourraud, 2020, HeartRhythm case reports.

An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation

M. Haissaguerre, M. Hocini, A. Leenhardt, 2018, Scientific Reports.

From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies

H. Calkins, E. Behr, P. Schwartz, 2023, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Left Ventricular Abnormal Substrate in Brugada Syndrome.

R. Redon, K. Nademanee, M. Haissaguerre, 2023, JACC. Clinical electrophysiology.

Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a +/− Mouse Model

A. Wilde, Céline Marionneau, D. Escande, 2010, PloS one.

The prevalence of left and right bundle branch block morphology ventricular tachycardia amongst patients with arrhythmogenic cardiomyopathy and sustained ventricular tachycardia: insights from the European Survey on Arrhythmogenic Cardiomyopathy.

R. Hauer, L. Fauchier, E. Behr, 2021, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Prevalence of diabetes and impact on cardiovascular events and mortality in patients with chronic coronary syndromes, across multiple geographical regions and ethnicities.

T. S. Chee, D. S. Kim, S. H. Lee, 2022, European journal of preventive cardiology.

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

P. Ellinor, S. Priori, A. Mazzanti, 2016, Circulation.

Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy.

F. Charpentier, Y. Coudière, L. Faivre, 2012, Journal of the American College of Cardiology.

Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies.

H. Tan, F. Sacher, V. Probst, 2009, Heart rhythm.

Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: results of a systematic screening.

J. Deharo, P. Cosnay, E. Donal, 2014, Heart rhythm.

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.

Cardiac Phenotype and Long-Term Follow-Up of Patients With Mutations in NKX2-5 Gene.

V. Probst, F. Kyndt, D. Bonnet, 2016, Journal of the American College of Cardiology.

Parental Electrocardiographic Screening Identifies a High Degree of Inheritance for Congenital and Childhood Nonimmune Isolated Atrioventricular Block

J. Daubert, C. Dina, J. Lusson, 2012, Circulation.

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.

R. Redon, E. Génin, C. Dina, 2019, European heart journal.

A Connexin40 Mutation Associated With a Malignant Variant of Progressive Familial Heart Block Type I

D. Roden, N. Hagiwara, W. Shimizu, 2012, Circulation. Arrhythmia and electrophysiology.

Low rates of inappropriate shocks in contemporary real-world implantable cardioverter defibrillator patients: the CARAT observational study

V. Probst, W. Dichtl, J. de Sousa, 2023, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Early Repolarization Disease.

Ashok J. Shah, M. Haissaguerre, P. Jais, 2010, Cardiac electrophysiology clinics.

The QUIDAM study: Hydroquinidine therapy for the management of Brugada syndrome patients at high arrhythmic risk.

F. Sacher, J. Deharo, A. Leenhardt, 2017, Heart rhythm.

Prevalence and prognostic role of various conduction disturbances in patients with the Brugada syndrome.

F. Sacher, M. Hocini, M. Haïssaguerre, 2013, The American journal of cardiology.

Prevalence of early repolarization pattern in inferolateral leads in patients with Brugada syndrome.

S. Knecht, F. Sacher, M. Haïssaguerre, 2008, Heart rhythm.