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Solena Le Scouarnec

Showing results (21-30 of 39) with videos related to

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American Journal of Human Genetics|January 6, 2018
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial AneurysmRomain Bourcier, Solena Le Scouarnec, Stéphanie Bonnaud, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Fine-scale human genetic structure in Western FranceMatilde Karakachoff, Nicolas Duforet-Frebourg, Floriane Simonet, et al.
International Journal of Cardiology|January 29, 2016
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type IXavier Daumy, Mohamed-Yassine Amarouch, Pierre Lindenbaum, et al.
The Journal of Clinical Investigation|May 10, 2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansHiroshi Watanabe, Tamara T Koopmann, Solena Le Scouarnec, et al.
Journal of the American College of Cardiology|August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathyAnnalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Journal of the American Heart Association|June 12, 2016
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada SyndromeVincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, et al.
Human Molecular Genetics|February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
Circulation|March 12, 2021
Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse: Relation to Mitral Regurgitation, Ventricular Remodeling, and ArrhythmiaAnne-Laure Constant Dit Beaufils, Olivier Huttin, Antoine Jobbe-Duval, et al.
Circulation. Genomic and Precision Medicine|March 7, 2020
Genetic Association Analyses Highlight <i>IL6</i>, <i>ALPL</i>, and <i>NAV1</i> As 3 New Susceptibility Genes Underlying Calcific Aortic Valve StenosisSébastien Thériault, Christian Dina, David Messika-Zeitoun, et al.
JACC. Cardiovascular Imaging|May 19, 2023
Machine Learning-Based Phenogrouping in MVP Identifies Profiles Associated With Myocardial Fibrosis and Cardiovascular EventsOlivier Huttin, Nicolas Girerd, Antoine Jobbe-Duval, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|January 6, 2018
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial AneurysmRomain Bourcier, Solena Le Scouarnec, Stéphanie Bonnaud, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Fine-scale human genetic structure in Western FranceMatilde Karakachoff, Nicolas Duforet-Frebourg, Floriane Simonet, et al.
International Journal of Cardiology|January 29, 2016
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type IXavier Daumy, Mohamed-Yassine Amarouch, Pierre Lindenbaum, et al.
The Journal of Clinical Investigation|May 10, 2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansHiroshi Watanabe, Tamara T Koopmann, Solena Le Scouarnec, et al.
Journal of the American College of Cardiology|August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathyAnnalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Journal of the American Heart Association|June 12, 2016
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada SyndromeVincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, et al.
Human Molecular Genetics|February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
Circulation|March 12, 2021
Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse: Relation to Mitral Regurgitation, Ventricular Remodeling, and ArrhythmiaAnne-Laure Constant Dit Beaufils, Olivier Huttin, Antoine Jobbe-Duval, et al.
Circulation. Genomic and Precision Medicine|March 7, 2020
Genetic Association Analyses Highlight <i>IL6</i>, <i>ALPL</i>, and <i>NAV1</i> As 3 New Susceptibility Genes Underlying Calcific Aortic Valve StenosisSébastien Thériault, Christian Dina, David Messika-Zeitoun, et al.
JACC. Cardiovascular Imaging|May 19, 2023
Machine Learning-Based Phenogrouping in MVP Identifies Profiles Associated With Myocardial Fibrosis and Cardiovascular EventsOlivier Huttin, Nicolas Girerd, Antoine Jobbe-Duval, et al.
Pageof 4