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Estelle Baron
Estelle Baron
inserm
Verified email at univ-nantes.fr
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Cited by
Year
Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy
G Laurent, S Saal, MY Amarouch, DM Béziau, RFJ Marsman, L Faivre, ...
Journal of the American College of Cardiology 60 (2), 144-156, 2012
1772012
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
1492015
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
J Barc, R Tadros, C Glinge, DY Chiang, M Jouni, F Simonet, SJ Jurgens, ...
Nature genetics 54 (3), 232-239, 2022
992022
Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance
J Barc, F Briec, S Schmitt, F Kyndt, M Le Cunff, E Baron, C Vieyres, ...
Journal of the American College of Cardiology 57 (1), 40-47, 2011
882011
Effect of reducing the dose of stavudine on body composition, bone density, and markers of mitochondrial toxicity in HIV-infected subjects: a randomized, controlled study
GA McComsey, VL Re, M O'Riordan, UA Walker, D Lebrecht, E Baron, ...
Clinical infectious diseases 46 (8), 1290-1296, 2008
822008
Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis
S Thériault, C Dina, D Messika-Zeitoun, S Le Scouarnec, R Capoulade, ...
Circulation: Genomic and Precision Medicine 12 (10), e002617, 2019
772019
A connexin40 mutation associated with a malignant variant of progressive familial heart block type I
N Makita, A Seki, N Sumitomo, H Chkourko, S Fukuhara, H Watanabe, ...
Circulation: Arrhythmia and Electrophysiology 5 (1), 163-172, 2012
712012
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
632016
Variants of transient receptor potential melastatin member 4 in childhood atrioventricular block
N Syam, S Chatel, LC Ozhathil, V Sottas, JS Rougier, A Baruteau, ...
Journal of the American Heart Association 5 (5), e001625, 2016
512016
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
332016
Uridine supplementation in HIV lipoatrophy: pilot trial on safety and effect on mitochondrial indices
GA McComsey, M O'riordan, B Setzer, D Lebrecht, E Baron, UA Walker
European journal of clinical nutrition 62 (8), 1031-1037, 2008
312008
Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approach
JB Gourraud, F Kyndt, S Fouchard, E Rendu, P Jaafar, C Gully, K Gacem, ...
Heart 98 (17), 1305-1310, 2012
162012
Genetic population structure across Brittany and the downstream Loire basin provides new insights on the demographic history of Western Europe
I Alves, J Giemza, M Blum, C Bernhardsson, S Chatel, M Karakachoff, ...
bioRxiv, 2022.02. 03.478491, 2022
122022
Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat model
C Delwarde, C Toquet, P Aumond, AH Kayvanjoo, A Foucal, B Le Vely, ...
Cardiovascular Research 119 (3), 759-771, 2023
102023
Effect of NucleomaxX (R) on fat and blood mitochondrial DNA in d4T-treated subjects with clinical lipoatrophy
GA McComsey, M O'Riordan, B Setzer, D Lebrecht, E Baron, UA Walker
ANTIVIRAL THERAPY 10 (8), L49-L50, 2005
82005
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects
M Baudic, H Murata, FM Bosada, US Melo, T Aizawa, P Lindenbaum, ...
Nature communications 15 (1), 3380, 2024
52024
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form‐associated genes provides new insights for molecular diagnosis and clinical management
A Goudal, M Karakachoff, P Lindenbaum, E Baron, S Bonnaud, F Kyndt, ...
Human Mutation 43 (9), 1333-1342, 2022
42022
Local density of states in a one-dimensional photonic crystal with a semiconducting cavity
F Segovia-Chaves, H Vinck-Posada, EP Navarro-Barón
Results in Physics 33, 105129, 2022
42022
Human genetic structure in Northwest France provides new insights into West European historical demography
I Alves, J Giemza, MGB Blum, C Bernhardsson, S Chatel, M Karakachoff, ...
Nature Communications 15 (1), 6710, 2024
22024
Comparative review of USA consumer product safety board data for soccer, ice hockey, and American football from 1990 to 1999
JS Delaney, SE Brien, E Baron
British Journal of Sports Medicine 35 (5), 370-370, 2001
22001
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