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Véronique Fressart
Researcher at Pierre-and-Marie-Curie University
Publications - 4
Citations - 669
Véronique Fressart is an academic researcher from Pierre-and-Marie-Curie University. The author has contributed to research in topics: Sudden cardiac death & Cardiac conduction. The author has an hindex of 4, co-authored 4 publications receiving 573 citations. Previous affiliations of Véronique Fressart include French Institute of Health and Medical Research.
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Journal ArticleDOI
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,Floriane Simonet,Floriane Simonet,Floriane Simonet,Arie O. Verkerk,Peter J. Schwartz,Lia Crotti,Federica Dagradi,Pascale Guicheney,Pascale Guicheney,Véronique Fressart,Véronique Fressart,Antoine Leenhardt,Antoine Leenhardt,Charles Antzelevitch,Susan Bartkowiak,Martin Borggrefe,Rainer Schimpf,Eric Schulze-Bahr,Sven Zumhagen,Elijah R. Behr,Rachel Bastiaenen,Jacob Tfelt-Hansen,Jacob Tfelt-Hansen,Morten S. Olesen,Morten S. Olesen,Stefan Kääb,Britt M. Beckmann,Peter Weeke,Hiroshi Watanabe,Naoto Endo,Tohru Minamino,Minoru Horie,Seiko Ohno,Kanae Hasegawa,Naomasa Makita,Akihiko Nogami,Wataru Shimizu,Takeshi Aiba,Philippe Froguel,Philippe Froguel,Philippe Froguel,Beverley Balkau,Beverley Balkau,Olivier Lantieri,Margherita Torchio,Cornelia Wiese,David Weber,Rianne Wolswinkel,Ruben Coronel,Bas J. Boukens,Stéphane Bézieau,Eric Charpentier,Eric Charpentier,Eric Charpentier,Stéphanie Chatel,Aurore Despres,Françoise Gros,Françoise Gros,Françoise Gros,Florence Kyndt,Simon Lecointe,Pierre Lindenbaum,Vincent Portero,Vincent Portero,Vincent Portero,Jade Violleau,Manfred Gessler,Hanno L. Tan,Dan M. Roden,Vincent M. Christoffels,Hervé Le Marec,Arthur A.M. Wilde,Vincent Probst,Jean-Jacques Schott,Christian Dina,Richard Redon +80 more
TL;DR: The association signals at SCN5A-SCN10A demonstrate that genetic polymorphisms modulating cardiac conduction can also influence susceptibility to cardiac arrhythmia and indicate that common genetic variation can have a strong impact on the predisposition to rare diseases.
Journal ArticleDOI
MOG1: a new susceptibility gene for Brugada syndrome.
Darouna Kattygnarath,Svetlana Maugenre,Nathalie Neyroud,Elise Balse,Carole Ichai,Isabelle Denjoy,Gilles Dilanian,Raphaël P. Martins,Véronique Fressart,Myriam Berthet,Jean-Jacques Schott,Antoine Leenhardt,Vincent Probst,Hervé Le Marec,Bernard Hainque,Alain Coulombe,Stéphane N. Hatem,Pascale Guicheney +17 more
TL;DR: The hypothesis that dominant-negative mutations in MOG1 can impair the trafficking of Nav1.5 to the membrane, leading to INa reduction and clinical manifestation of BrS is supported.
Journal ArticleDOI
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
Alban-Elouen Baruteau,F. Kyndt,Elijah R. Behr,Arja S. Vink,Matthias Lachaud,Anna Joong,Jean-Jacques Schott,Minoru Horie,Isabelle Denjoy,Lia Crotti,Wataru Shimizu,Johan M Bos,Elizabeth A. Stephenson,Leonie C.H. Wong,Dominic Abrams,Andrew M. Davis,Andrew M. Davis,Annika Winbo,Annika Winbo,Anne M. Dubin,Shubhayan Sanatani,Leonardo Liberman,Juan Pablo Kaski,Juan Pablo Kaski,Boris Rudic,Sit Yee Kwok,Claudine Rieubland,Jacob Tfelt-Hansen,George F. Van Hare,Béatrice Guyomarc’h-Delasalle,Nico A. Blom,Yanushi D. Wijeyeratne,Jean-Baptiste Gourraud,Hervé Le Marec,Junichi Ozawa,Véronique Fressart,Jean Marc Lupoglazoff,Federica Dagradi,Carla Spazzolini,Takeshi Aiba,David J. Tester,Laura Zahavich,Virginie Beauséjour-Ladouceur,Mangesh Jadhav,Jonathan R. Skinner,Sonia Franciosi,Andrew D. Krahn,Mena Abdelsayed,Peter C. Ruben,Tak-cheung Yung,Michael J. Ackerman,Arthur A.M. Wilde,Peter J. Schwartz,Vincent Probst +53 more
TL;DR: In this large paediatric cohort of SCN5A mutation-positive subjects, cardiac conduction disorders were the most prevalent phenotype; CEs occurred in about one-third of genotype-positive children, and several independent risk factors were identified, including age ≤1 year at diagnosis, compound mutation, and mutation with both gain- and loss-of-function.
Journal ArticleDOI
Advising a cardiac disease gene positive yet phenotype negative or borderline abnormal athlete: Is sporting disqualification really necessary?
Pascale Richard,Isabelle Denjoy,Véronique Fressart,Mathew G Wilson,François Carré,Philippe Charron +5 more
TL;DR: The aim of this review is to examine the role of genetic testing within the diagnostic algorithm of preparticipation screening of athletes by providing the sports medicine physician with simple cardiac genetic knowledge for the main inherited cardiac conditions known to cause SCD.