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Solena Le Scouarnec

Showing results (31-40 of 39) with videos related to

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European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
The New England Journal of Medicine|May 9, 2008
Sudden cardiac arrest associated with early repolarizationMichel Haïssaguerre, Nicolas Derval, Frederic Sacher, et al.
Medrxiv : the Preprint Server for Health Sciences|November 1, 2024
Isolated prolapse of the posterior mitral valve leaflet: phenotypic refinement, heritability and genetic etiologyAntoine Rimbert, Damien Duval, Daniel Trujillano, et al.
Nature Communications|April 20, 2024
TAD boundary deletion causes PITX2-related cardiac electrical and structural defectsManon Baudic, Hiroshige Murata, Fernanda M Bosada, et al.
Science Translational Medicine|May 24, 2019
Primary cilia defects causing mitral valve prolapseKatelynn A Toomer, Mengyao Yu, Diana Fulmer, et al.
European Heart Journal|April 10, 2023
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide studyHao Yu Chen, Christian Dina, Aeron M Small, et al.
Circulation|February 6, 2026
Genome and Transcriptome-Wide Analyses Identify Multiple Candidate Genes and a Significant Polygenic Contribution in Bicuspid Aortic ValveSébastien Thériault, Jacob A Holdcraft, Dinara Sharipova, et al.
Nature Genetics|December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease predictionAeron M Small, Ta-Yu Yang, Shinsuke Itoh, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
The New England Journal of Medicine|May 9, 2008
Sudden cardiac arrest associated with early repolarizationMichel Haïssaguerre, Nicolas Derval, Frederic Sacher, et al.
Medrxiv : the Preprint Server for Health Sciences|November 1, 2024
Isolated prolapse of the posterior mitral valve leaflet: phenotypic refinement, heritability and genetic etiologyAntoine Rimbert, Damien Duval, Daniel Trujillano, et al.
Nature Communications|April 20, 2024
TAD boundary deletion causes PITX2-related cardiac electrical and structural defectsManon Baudic, Hiroshige Murata, Fernanda M Bosada, et al.
Science Translational Medicine|May 24, 2019
Primary cilia defects causing mitral valve prolapseKatelynn A Toomer, Mengyao Yu, Diana Fulmer, et al.
European Heart Journal|April 10, 2023
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide studyHao Yu Chen, Christian Dina, Aeron M Small, et al.
Circulation|February 6, 2026
Genome and Transcriptome-Wide Analyses Identify Multiple Candidate Genes and a Significant Polygenic Contribution in Bicuspid Aortic ValveSébastien Thériault, Jacob A Holdcraft, Dinara Sharipova, et al.
Nature Genetics|December 19, 2025
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease predictionAeron M Small, Ta-Yu Yang, Shinsuke Itoh, et al.
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