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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.
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
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 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.
Journal articles
hal-01650124v1
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Value of the sodium-channel blocker challenge in Brugada syndrome
Dylan Therasse
,
Frederic Sacher
,
Dominique Babuty
,
Philippe Mabo
,
Jacques Mansourati
,
et al.
Journal articles
hal-01832133v1
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FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cells
Amandine Caillaud
,
Antoine Lévêque
,
Aurélie Thédrez
,
Aurore Girardeau
,
Robin Canac
,
et al.
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.
Journal articles
hal-01830596v1
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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.
Journal articles
hal-01832137v1
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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.
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.
Journal articles
hal-01831599v1
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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.
Conference papers
hal-01150489v1
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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.
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 articles
hal-01832148v1
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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.
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.
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.
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.
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.
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.
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.
Journal articles
hal-03765601v1
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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.
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.
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 articles
inserm-00719034v1
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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.
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.
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.
Journal articles
hal-01270688v1
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