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| 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 | 142 | 2015 |
| 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 | 87 | 2011 |
| 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 | 81 | 2008 |
| 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 | 68 | 2012 |
| 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 | 64 | 2022 |
| 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 | 60 | 2016 |
| 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 | 54 | 2019 |
| 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 | 45 | 2016 |
| 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 | 32 | 2016 |
| 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 | 31 | 2008 |
| 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 | 16 | 2012 |
| 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 | 8 | 2005 |
| 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 | 7 | 2023 |
| 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 | 6 | 2022 |
| Genetic association analyses highlight IL6, ALPL, and NAV1 as three new susceptibility genes underlying calcific aortic valve stenosis S Thériault, C Dina, D Messika-Zeitoun, S Le Scouarnec, R Capoulade, ... bioRxiv, 515494, 2019 | 4 | 2019 |
| 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 | 2 | 2022 |
| 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 | 2 | 2022 |
| 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 | 2 | 2001 |
| BS-515-01 NON-CODING DELETION INDUCES 3D CHROMATIN REMODELLING AND PITX2 EXPRESSION DYSREGULATION ASSOCIATED WITH A SYNDROMIC CARDIAC DISORDER M Baudic, H Murata, FM Bosada, US Melo, T Ishikawa, T Aizawa, ... Heart Rhythm 19 (5), S51-S52, 2022 | 1 | 2022 |
