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authFullName_s : Julien Barc
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A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

Zeina Al Sayed , Mariam Jouni , Jean‐baptiste Gourraud , Nadjet Belbachir , Julien Barc , et al.
Clinical and Translational Medicine, 2021, 11 (6), ⟨10.1002/ctm2.413⟩
Journal articles hal-03283845v1
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Brugada syndrome: Diagnosis, risk stratification and management

Jean-Baptiste Gourraud , Julien Barc , Aurélie Thollet , Hervé Le Marec , Vincent Probst
Archives of cardiovascular diseases, 2017, Equipe I Equipe IIa, 110 (3), pp.188--195. ⟨10.1016/j.acvd.2016.09.009⟩
Journal articles hal-01832150v1
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Familial Catecholamine-Induced QT Prolongation in Unexplained Sudden Cardiac Death

Francois Huchet , Florence Kyndt , Julien Barc , Aurelie Thollet , Flavien Charpentier , et al.
Journal of the American College of Cardiology, 2017, Equipe I Equipe IIa, 69 (12), pp.1642--1643. ⟨10.1016/j.jacc.2017.01.030⟩
Journal articles hal-01832147v1
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Sodium-channel blocker challenge in the familial screening of Brugada syndrome: safety and predictors of positivity

Dylan Therasse , Frédéric Sacher , Bertrand Petit , Dominique Babuty , Philippe Mabo , et al.
Heart Rhythm, 2017, 14 (10), pp.1442-1448. ⟨10.1016/j.hrthm.2017.06.031⟩
Journal articles hal-01650124v1

Value of the sodium-channel blocker challenge in Brugada syndrome

Dylan Therasse , Frederic Sacher , Dominique Babuty , Philippe Mabo , Jacques Mansourati , et al.
International Journal of Cardiology, 2017, 245, pp.178--180. ⟨10.1016/j.ijcard.2017.05.099⟩
Journal articles hal-01832133v1

FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cells

Amandine Caillaud , Antoine Lévêque , Aurélie Thédrez , Aurore Girardeau , Robin Canac , et al.
STAR Protocols, 2022, 3 (4), pp.101680. ⟨10.1016/j.xpro.2022.101680⟩
Journal articles hal-04060050v1
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Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Iris C. R. M. Kolder , Michael W. T. Tanck , Pieter G. Postema , Julien Barc , Moritz F. Sinner , et al.
Circulation. Cardiovascular Genetics, 2015, 8 (3), pp.447--456. ⟨10.1161/CIRCGENETICS.114.000785⟩
Journal articles hal-01830596v1

The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity

Christiaan C. Veerman , Svitlana Podliesna , Rafik Tadros , Elisabeth M. Lodder , Isabella Mengarelli , et al.
Circulation Research, 2017, Equipe I, 121 (5), pp.537--548. ⟨10.1161/CIRCRESAHA.117.310959⟩
Journal articles hal-01832137v1

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

Pauline Etienne , François Huchet , Nathalie Gaborit , Julien Barc , Aurélie Thollet , et al.
EP-Europace, 2018, Equipe I Equipe IIa, ⟨10.1093/europace/euy078⟩
Journal articles hal-01833912v1
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hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities

Christiaan C. Veerman , Isabella Mengarelli , Kaomei Guan , Michael Stauske , Julien Barc , et al.
Scientific Reports, 2016, Equipe 3, 6 (1), pp.30967. ⟨10.1038/srep30967⟩
Journal articles hal-01831599v1

0211 : Implications of baselines 2010 task force criterias on ventricular arrhythmias in ARVC

Nelly Amara , Jean-Baptiste Gourraud , Arnaud Denis , Philippe Mabo , Aurélie Thollet , et al.
Archives of Cardiovascular Diseases Supplements, Apr 2015, Toulouse, France. pp.169, ⟨10.1016/S1878-6480(15)30103-8⟩
Conference papers hal-01150489v1

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

Elijah R. Behr , Eleonora Savio-Galimberti , Julien Barc , Anders G. Holst , Evmorfia Petropoulou , et al.
Cardiovascular Research, 2015, Equipe 3 Equipe 4, 106 (3), pp.520--529. ⟨10.1093/cvr/cvv042⟩
Journal articles hal-01830983v1
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Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation

Akiko Seki , Taisuke Ishikawa , Xavier Daumy , Hiroyuki Mishima , Julien Barc , et al.
Journal of the American College of Cardiology, 2017, Equipe I, 70 (3), pp.358--370. ⟨10.1016/j.jacc.2017.05.039⟩
Journal articles hal-01832148v1

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

Solena Le Scouarnec , Matilde Karakachoff , Jean-Baptiste Gourraud , Pierre Lindenbaum , Stéphanie Bonnaud , et al.
Human Molecular Genetics, 2015, 24 (10), pp.2757--2763. ⟨10.1093/hmg/ddv036⟩
Journal articles hal-01201946v1
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SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

Yanushi D Wijeyeratne , Michael Tanck , Yuka Mizusawa , Velislav Batchvarov , Julien Barc , et al.
Circulation: Genomic and Precision Medicine, 2020, 13 (6), ⟨10.1161/CIRCGEN.120.002911⟩
Journal articles hal-03099541v1
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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Roddy Walsh , Najim Lahrouchi , Rafik Tadros , Florence Kyndt , Charlotte Glinge , et al.
Genetics in Medicine, 2020, ⟨10.1038/s41436-020-⟩
Journal articles hal-02946962v1
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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Julien Barc , Rafik Tadros , Charlotte Glinge , David Chiang , Mariam Jouni , et al.
Nature Genetics, 2022, 54 (3), pp.232-239. ⟨10.1038/s41588-021-01007-6⟩
Journal articles hal-03589076v1
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The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

Jean-Baptiste Gourraud , Julien Barc , Aurélie Thollet , Solena Le Scouarnec , Hervé Le Marec , et al.
Frontiers in Cardiovascular Medicine, 2016, 3, pp.9. ⟨10.3389/fcvm.2016.00009⟩
Journal articles hal-01831587v1
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SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.

Vincent Probst , Arthur a M Wilde , Julien Barc , Frederic Sacher , Dominique Babuty , et al.
Circulation: Cardiovascular Genetics, 2009, 2 (6), pp.552-7. ⟨10.1161/CIRCGENETICS.109.853374⟩
Journal articles hal-00750425v1
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Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat model

Constance Delwarde , Claire Toquet , Pascal Aumond , Amir Hossein Kayvanjoo , Adrien Foucal , et al.
Cardiovascular Research, 2022, 119 (3), pp.759-771. ⟨10.1093/cvr/cvac136⟩
Journal articles hal-03765601v1

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

Hélène Louis-Dit-Picard , Julien Barc , Daniel Trujillano , Stephanie Miserey-Lenkei , Nabila Bouatia-Naji , et al.
Nature Genetics, 2012, 44 (4), pp.456-460. ⟨10.1038/ng.2218⟩
Journal articles hal-02349651v1
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Clinical Yield of Familial Screening After Sudden Death in Young Subjects

Pauline Quenin , Florence Kyndt , Philippe Mabo , Jacques Mansourati , Dominique Babuty , et al.
Circulation. Arrhythmia and electrophysiology, 2017, 10 (9), Epub ahead of print. ⟨10.1161/CIRCEP.117.005236⟩
Journal articles inserm-01667200v1
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Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy.

Gabriel Laurent , Samuel Saal , Mohamed Yassine Amarouch , Delphine M. Béziau , Roos F. J. Marsman , et al.
Journal of the American College of Cardiology, 2012, 60 (2), pp.144-56. ⟨10.1016/j.jacc.2012.02.052⟩
Journal articles inserm-00719034v1

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

Xavier Daumy , Mohamed-Yassine Amarouch , Pierre Lindenbaum , Stéphanie Bonnaud , Eric Charpentier , et al.
International Journal of Cardiology, 2016, Equipe 3 Equipe 4, 207, pp.349--358. ⟨10.1016/j.ijcard.2016.01.052⟩
Journal articles hal-01831586v1
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Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form associated genes provides new insights for molecular diagnosis and clinical management.

Adeline Goudal , Matilde Karakachoff , Pierre Lindenbaum , Estelle Baron , Stéphanie Bonnaud , et al.
Human Mutation, 2022, 43 (9), pp.1333-1342. ⟨10.1002/humu.24436⟩
Journal articles hal-03722211v1
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Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison

Gildas Loussouarn , Damien Sternberg , Sophie Nicole , Céline Marionneau , Francoise Le Bouffant , et al.
Frontiers in Pharmacology, 2016, 6, pp.314. ⟨10.3389/fphar.2015.00314⟩
Journal articles hal-01270688v1