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Floriane Simonet
Observed names:
F Simonet,
F. Simonet,
Simonet, F,
Simonet, Floriane
Observed institutions:
Centre National de la Recherche Scientifique,
Inserm,
Centre Hospitalier Universitaire de Nantes,
Hôpital Pontchaillou,
ERN GUARD-Heart,
Institut du Thorax,
Université de Nantes,
Nantes Université
show all 8
ORCID:
0000-0002-6366-7211
Observed ORCID:
0000-0002-6366-7211
OpenAlex ID:
A5042676176
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
2013
·
Connie R Bezzina
, Julien Barc
, et al.
·
Nature Genetics
·
542
Genetic association analyses highlight biological pathways underlying mitral valve prolapse
2015
·
PROMESA investigators
, Christian Dina
, et al.
·
Nature Genetics
·
142
PDF
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
·
138
PDF
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
2022
·
Julien Barc
, Rafik Tadros
, et al.
·
Nature Genetics
·
137
PDF
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
·
89
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
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
Dysfunction of the Voltage‐Gated K + Channel β2 Subunit in a Familial Case of Brugada Syndrome
2016
·
Vincent Portero
, Solena Le Scouarnec
, et al.
·
Journal of the American Heart Association
·
27
PDF
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci
2024
·
Taisuke Ishikawa
, Tatsuo Masuda
, et al.
·
European Heart Journal
·
25
PDF
Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
2013
·
Connie R Bezzina
, Julien Barc
, et al.
·
Nature Genetics
·
20
PDF
Left Ventricular Abnormal Substrate in Brugada Syndrome
2023
·
Ghassen Cheniti
, Michel Haissaguerre
, et al.
·
JACC. Clinical electrophysiology
·
11
Genome and Transcriptome-Wide Analyses Identify Multiple Candidate Genes and a Significant Polygenic Contribution in Bicuspid Aortic Valve
2026
·
Sébastien Thériault
, Jacob A. Holdcraft
, et al.
·
Circulation
·
10
PDF
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background
2021
·
Aurore Girardeau
, Diane Atticus
, et al.
·
Stem Cell Research
·
7
PDF
Genome-Wide Association Study of Accessory Atrioventricular Pathways
2024
·
Hildur M. Aegisdottir
, Laura Andreasen
, et al.
·
JAMA Cardiology
·
5
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
2022
·
Julien Barc
, Rafik Tadros
, et al.
·
Nature Genetics
·
3
PDF
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants
2025
·
Taisuke Ishikawa
, Hiroki Kimoto
, et al.
·
Cardiovascular Research
·
2
Role of common variants and new genes associated with arrhythmogenic cardiomyopathy
2024
·
J Barc
, L Ruffier
, et al.
·
European Heart Journal
·
1
PDF
4 th International Meeting on Laminopathies, Madrid, 9-12 May, 2023
2023
·
Benarroch, Louise
, Bertrand, Anne T.
, et al.
·
Journal of Neuromuscular Diseases
·
1
PDF
Bs-513-02 Genome-wide Association Analyses Identify Novel Brugada Syndrome Risk Loci and Highlight a New Mechanism of Sodium Channel Regulation in Disease Susceptibility
2022
·
Julien Barc
, Rafik Tadros
, et al.
·
Heart Rhythm
·
1
Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome
2020
·
J Barc
, R Trados
, et al.
·
European Heart Journal
·
1
PDF
Gain-of-function Mutation in the Voltage-gated K+ Channel Beta-2 Subunit Is Associated With Brugada Syndrome
2014
·
V. Portero
, S. Le Scouarnec
, et al.
·
Heart Rhythm
·
1
LDLR -3′UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based Studies
2026
·
Antoine Lainé
, Zoé Begué-Racapé
, et al.
·
Arteriosclerosis Thrombosis and Vascular Biology
Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome
2023
·
N Makita
, T Ishikawa
, et al.
·
European Heart Journal
PDF
P.145 Identification of potential genetic modifiers underlying phenotypic variability in a French family with striated muscle laminopathies
2022
·
L. Benarroch
, A. Bertrand
, et al.
·
Neuromuscular Disorders
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Works count:
34
Citation count:
1,306
H-index:
11
I10-index:
13
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