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Matilde Karakachoff

Showing results (21-30 of 37) with videos related to

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Heart (British Cardiac Society)|June 22, 2012
Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approachJean Baptiste Gourraud, Florence Kyndt, Swanny Fouchard, et al.
BMJ Open Respiratory Research|March 10, 2022
Evaluation of the Post-COVID-19 Functional Status (PCFS) Scale in a cohort of patients recovering from hypoxemic SARS-CoV-2 pneumoniaNaïla Benkalfate, Emmanuel Eschapasse, Thomas Georges, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2020
Location of intracranial aneurysms is the main factor associated with rupture in the ICAN populationOlivia Rousseau, Matilde Karakachoff, Alban Gaignard, 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.
Human Mutation|July 12, 2022
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical managementAdeline Goudal, Matilde Karakachoff, Pierre Lindenbaum, et al.
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 Heart Journal|July 18, 2025
Arrhythmias in congenitally corrected transposition of the great arteries: an international studyJean-Marc Sellal, Nabil Dib, Matilde Karakachoff, et al.
European Heart Journal|July 5, 2021
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndromeTaisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, 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. 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.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Heart (British Cardiac Society)|June 22, 2012
Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approachJean Baptiste Gourraud, Florence Kyndt, Swanny Fouchard, et al.
BMJ Open Respiratory Research|March 10, 2022
Evaluation of the Post-COVID-19 Functional Status (PCFS) Scale in a cohort of patients recovering from hypoxemic SARS-CoV-2 pneumoniaNaïla Benkalfate, Emmanuel Eschapasse, Thomas Georges, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2020
Location of intracranial aneurysms is the main factor associated with rupture in the ICAN populationOlivia Rousseau, Matilde Karakachoff, Alban Gaignard, 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.
Human Mutation|July 12, 2022
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical managementAdeline Goudal, Matilde Karakachoff, Pierre Lindenbaum, et al.
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 Heart Journal|July 18, 2025
Arrhythmias in congenitally corrected transposition of the great arteries: an international studyJean-Marc Sellal, Nabil Dib, Matilde Karakachoff, et al.
European Heart Journal|July 5, 2021
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndromeTaisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, 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. 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.
Pageof 4