Publications by authors named "Simon Lecointe"

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Isolated prolapse of the posterior mitral valve leaflet: phenotypic refinement, heritability and genetic etiology.
Antoine Rimbert, Damien Duval, Daniel Trujillano, Florence Kyndt, Antoine Jobbe-Duval, Simon Lecointe

medRxiv· October 2024

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Human genetic structure in Northwest France provides new insights into West European historical demography.
Isabel Alves, Joanna Giemza, Michael G B Blum, Carolina Bernhardsson, Stéphanie Chatel, Simon Lecointe

Nat Commun· August 2024

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Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat model.
Constance Delwarde, Claire Toquet, Pascal Aumond, Amir Hossein Kayvanjoo, Adrien Foucal, Simon Lecointe

Cardiovasc Res· May 2023

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Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Julien Barc, Rafik Tadros, Charlotte Glinge, David Y Chiang, Mariam Jouni, Simon Lecointe

Nat Genet· May 2022

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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Julien Barc, Rafik Tadros, Charlotte Glinge, David Y Chiang, Mariam Jouni, Simon Lecointe

Nat Genet· March 2022

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Critical Structural Defects Explain Filamin A Mutations Causing Mitral Valve Dysplasia.
Tatu J K Haataja, Romain Capoulade, Simon Lecointe, Maarit Hellman, Jean Merot

Biophys J· October 2019

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Genetic Association Analyses Highlight , , and As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis.
Sébastien Thériault, Christian Dina, David Messika-Zeitoun, Solena Le Scouarnec, Romain Capoulade, Simon Lecointe

Circ Genom Precis Med· October 2019

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Non-syndromic Mitral Valve Dysplasia Mutation Changes the Force Resilience and Interaction of Human Filamin A.
Tatu J K Haataja, Rafael C Bernardi, Simon Lecointe, Romain Capoulade, Jean Merot

Structure· January 2019

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New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study.
Thierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, Daniel Bernstein, Jan J J Aalberts, Simon Lecointe

Eur Heart J· April 2018

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The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway.
Pauline Labbé, Emilie Faure, Simon Lecointe, Solena Le Scouarnec, Florence Kyndt

Biochim Biophys Acta Mol Cell Res· July 2017

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Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia.
Antoine Rimbert, Matthieu Pichelin, Simon Lecointe, Marie Marrec, Solena Le Scouarnec

Atherosclerosis· July 2016

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Genetic association analyses highlight biological pathways underlying mitral valve prolapse.
Christian Dina, Nabila Bouatia-Naji, Nathan Tucker, Francesca N Delling, Katelynn Toomer, Simon Lecointe

Nat Genet· October 2015

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Fine-scale human genetic structure in Western France.
Matilde Karakachoff, Nicolas Duforet-Frebourg, Floriane Simonet, Solena Le Scouarnec, Nadine Pellen, Simon Lecointe

Eur J Hum Genet· June 2015

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Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.
Delphine M Béziau, Julien Barc, Thomas O'Hara, Laurianne Le Gloan, Mohamed Yassine Amarouch, Simon Lecointe

Basic Res Cardiol· May 2015

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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Connie R Bezzina, Julien Barc, Yuka Mizusawa, Carol Ann Remme, Jean-Baptiste Gourraud, Simon Lecointe

Nat Genet· September 2013

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Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspects.
Aurélie Lardeux, Florence Kyndt, Simon Lecointe, Hervé Le Marec, Jean Merot

J Cardiovasc Transl Res· December 2011

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