Solena Le Scouarnec
Solena Le Scouarnec
INSERM UMR 1087 / CNRS UMR 6291, l'institut du thorax, University of Nantes
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Sudden cardiac arrest associated with early repolarization
M Haïssaguerre, N Derval, F Sacher, L Jesel, I Deisenhofer, L de Roy, ...
New England Journal of Medicine 358 (19), 2016-2023, 2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
H Watanabe, TT Koopmann, S Le Scouarnec, T Yang, CR Ingram, ...
The Journal of clinical investigation 118 (6), 2260-2268, 2008
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome
V Probst, AAM Wilde, J Barc, F Sacher, D Babuty, P Mabo, J Mansourati, ...
Circulation: Cardiovascular Genetics 2 (6), 552-557, 2009
PJ Mohler, S Le Scouarnec, I Denjoy, JS Lowe, P Guicheney, L Caron, ...
Circulation 115 (4), 432-441, 2007
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease
S Le Scouarnec, N Bhasin, C Vieyres, TJ Hund, SR Cunha, O Koval, ...
Proceedings of the National Academy of Sciences 105 (40), 15617-15622, 2008
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy
A Milano, AMC Vermeer, EM Lodder, J Barc, AO Verkerk, AV Postma, ...
Journal of the American College of Cardiology 64 (8), 745-756, 2014
Characterising chromosome rearrangements: recent technical advances in molecular cytogenetics
S Le Scouarnec, SM Gribble
Heredity 108 (1), 75-85, 2012
Familial aggregation of calcific aortic valve stenosis in the western part of France
V Probst, S Le Scouarnec, A Legendre, V Jousseaume, P Jaafar, ...
Circulation 113 (6), 856-60, 2006
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome
S Le Scouarnec, M Karakachoff, JB Gourraud, P Lindenbaum, S Bonnaud, ...
Human molecular genetics 24 (10), 2757-2763, 2015
Identification of large families in early repolarization syndrome
JB Gourraud, S Le Scouarnec, F Sacher, S Chatel, N Derval, V Portero, ...
Journal of the American College of Cardiology 61 (2), 164-172, 2013
Variable Nav1. 5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a+/− mouse model
AL Leoni, B Gavillet, JS Rougier, C Marionneau, V Probst, ...
PloS one 5 (2), 2010
The Brugada syndrome: a rare arrhythmia disorder with complex inheritance
JB Gourraud, J Barc, A Thollet, S Le Scouarnec, H Le Marec, JJ Schott, ...
Frontiers in cardiovascular medicine 3, 9, 2016
Exon organization and novel alternative splicing of the human ANK2 gene: implications for cardiac function and human cardiac disease
SR Cunha, S Le Scouarnec, JJ Schott, PJ Mohler
Journal of molecular and cellular cardiology 45 (6), 724-734, 2008
Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIME
P Lindenbaum, S Le Scouarnec, V Portero, R Redon
Bioinformatics 27 (22), 3200-3201, 2011
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I
X Daumy, MY Amarouch, P Lindenbaum, S Bonnaud, E Charpentier, ...
International journal of cardiology 207, 349-358, 2016
Fine-scale human genetic structure in Western France
M Karakachoff, N Duforet-Frebourg, F Simonet, S Le Scouarnec, N Pellen, ...
European Journal of Human Genetics 23 (6), 831-836, 2015
New insights into mitral valve dystrophy: a Filamin-A genotype–phenotype and outcome study
T Le Tourneau, S Le Scouarnec, C Cueff, D Bernstein, JJJ Aalberts, ...
European heart journal 39 (15), 1269-1277, 2018
Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1. 5 sodium channel loss-of-function mutation
T Pambrun, A Mercier, A Chatelier, S Patri, JJ Schott, S Le Scouarnec, ...
Heart Rhythm 11 (8), 1393-1400, 2014
Genetics of syndromic and non-syndromic mitral valve prolapse
T Le Tourneau, J Mérot, A Rimbert, S Le Scouarnec, V Probst, H Le Marec, ...
Heart 104 (12), 978-984, 2018
Dysfunction of the Voltage‐Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome
V Portero, S Le Scouarnec, Z Es‐Salah‐Lamoureux, S Burel, ...
Journal of the American Heart Association 5 (6), e003122, 2016
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