Get started
Author

Solena Le Scouarnec

Observed names: LE SCOUARNEC, Solena, Le Scouarnec, Selena, Le Scouarnec, Solena, LeScouarnec, Solena, S Le Scouarnec, S. Le Scouarnec, Scouarnec, Solena Le, PhD, Solena Scouarnec
Institutions: Centre National de la Recherche Scientifique, Inserm, Centre Hospitalier Universitaire de Nantes, Institut du Thorax, Université de Nantes, Nantes Université
Observed institutions: University of Iowa, Centre National de la Recherche Scientifique, Université de Bordeaux, Inserm, Université de Bretagne Occidentale, Vanderbilt University, Université Nantes Angers Le Mans, Wellcome Sanger Institute, Centre Hospitalier Universitaire de Bordeaux, Centre Hospitalier Universitaire de Nantes, Centre Hospitalier Universitaire de Tours, Assistance Publique – Hôpitaux de Paris, Centre Hospitalier Régional et Universitaire de Nancy, Centre Hospitalier Universitaire d'Angers, Institut de Myologie, Hôpital Lariboisière, Hôpital Cardiologique du Haut-Lévêque, Pitié-Salpêtrière Hospital, Centre Hospitalier Régional Universitaire de Brest, Clinique Pasteur, Institut du Thorax, Centre Hospitalier Universitaire de Rennes, Université Bordeaux Segalen, Université de Bretagne Occidentale, Université de Nantes, Cranfield University, University of Amsterdam, Vanderbilt University Medical Center, Nantes Université
ORCID: 0000-0003-3444-2125
Observed ORCID: 0000-0003-3444-2125
OpenAlex ID: A5031197087
Sudden Cardiac Arrest Associated with Early Repolarization
2008 · Michel Haïssaguerre, Nicolas Derval, et al. · New England Journal of Medicine · 1,449
PDF
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
2008 · Hiroshi Watanabe, Tamara T. Koopmann, et al. · Journal of Clinical Investigation · 433
SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome
2009 · Vincent Probst, Arthur A.M. Wilde, et al. · Circulation Cardiovascular Genetics · 315
PDF
HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy
2014 · Annalisa Milano, Alexa M.C. Vermeer, et al. · Journal of the American College of Cardiology · 203
PDF
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease
2008 · Solena Le Scouarnec, Naina Bhasin, et al. · Proceedings of the National Academy of Sciences · 170
Defining the Cellular Phenotype of “Ankyrin-B Syndrome” Variants
2007 · Peter J. Mohler, Solena Le Scouarnec, et al. · Circulation · 164
Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse
2021 · Anne-Laure Constant Dit Beaufils, Olivier Huttin, et al. · Circulation · 162
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome
2015 · Solena Le Scouarnec, Matilde Karakachoff, et al. · Human Molecular Genetics · 136
PDF
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
2023 · Hao Yu Chen, Christian Dina, et al. · European Heart Journal · 116
PDF
Primary cilia defects causing mitral valve prolapse
2019 · Katelynn A. Toomer, Mengyao Yu, et al. · Science Translational Medicine · 116
PDF
Characterising chromosome rearrangements: recent technical advances in molecular cytogenetics
2011 · S Le Scouarnec, S M Gribble · Heredity · 99
PDF
Familial Aggregation of Calcific Aortic Valve Stenosis in the Western Part of France
2006 · Vincent Probst, Solena Le Scouarnec, et al. · Circulation · 97
Localized Structural Alterations Underlying a Subset of Unexplained Sudden Cardiac Death
2018 · Michel Haïssaguerre, Mélèze Hocini, et al. · Circulation Arrhythmia and Electrophysiology · 96
Genetic Association Analyses Highlight IL6 , ALPL , and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis
2019 · Sébastien Thériault, Christian Dina, et al. · Circulation Genomic and Precision Medicine · 90
PDF
Identification of Large Families in Early Repolarization Syndrome
2013 · Jean-Baptiste Gourraud, Solena Le Scouarnec, et al. · Journal of the American College of Cardiology · 90
PDF
Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a+/− Mouse Model
2010 · Anne-Laure Leoni, Bruno Gavillet, et al. · PLoS ONE · 85
PDF
Genetics of syndromic and non-syndromic mitral valve prolapse
2018 · Thierry Le Tourneau, Jean Mérot, et al. · Heart · 80
New insights into mitral valve dystrophy: a Filamin-A genotype–phenotype and outcome study
2017 · Thierry Le Tourneau, Solena Le Scouarnec, et al. · European Heart Journal · 79
PDF
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I
2016 · Xavier Daumy, Mohamed-Yassine Amarouch, et al. · International Journal of Cardiology · 63
The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance
2016 · Jean-Baptiste Gourraud, Julien Barc, et al. · Frontiers in Cardiovascular Medicine · 60
PDF
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome
2019 · Nadjet Belbachir, Vincent Portero, et al. · European Heart Journal · 53
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm
2018 · Romain Bourcier, Solena Le Scouarnec, et al. · The American Journal of Human Genetics · 52
PDF
Genetics and pathophysiology of mitral valve prolapse
2023 · Constance Delwarde, Romain Capoulade, et al. · Frontiers in Cardiovascular Medicine · 46
PDF
Fine-scale human genetic structure in Western France
2014 · the D.E.S.I.R. Study Group, Matilde Karakachoff, et al. · European Journal of Human Genetics · 38
Exon organization and novel alternative splicing of the human ANK2 gene: Implications for cardiac function and human cardiac disease
2008 · Shane R. Cunha, Solena Le Scouarnec, et al. · Journal of Molecular and Cellular Cardiology · 37
Works count: 85
Citation count: 4,787
H-index: 27
I10-index: 37
Year
Topic
Type