| A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome N Neyroud, F Tesson, I Denjoy, M Leibovici, C Donger, J Barhanin, ... Nature genetics 15 (2), 186-189, 1997 | 1077 | 1997 |
| Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy A Helbling-Leclerc, X Zhang, H Topaloglu, C Cruaud, F Tesson, ... Nature genetics 11 (2), 216-218, 1995 | 747 | 1995 |
| Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation MH Gollob, DL Jones, AD Krahn, L Danis, XQ Gong, Q Shao, X Liu, ... New England Journal of Medicine 354 (25), 2677-2688, 2006 | 668 | 2006 |
| Guidelines for the study of familial dilated cardiomyopathies L Mestroni, B Maisch, WJ McKenna, K Schwartz, P Charron, C Rocco, ... European heart journal 20 (2), 93-102, 1999 | 619 | 1999 |
| Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population P Charron, O Dubourg, M Desnos, R Isnard, A Hagege, A Millaire, ... Circulation 96 (1), 214-219, 1997 | 221 | 1997 |
| Decreased mitochondrial proton leak and reduced expression of uncoupling protein 3 in skeletal muscle of obese diet-resistant women ME Harper, R Dent, S Monemdjou, V Bézaire, L Van Wyck, G Wells, ... Diabetes 51 (8), 2459-2466, 2002 | 156 | 2002 |
| Characterization of a unique genetic variant in the β1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy F Tesson, P Charron, M Peuchmaurd, V Nicaud, F Cambien, L Tiret, ... Journal of molecular and cellular cardiology 31 (5), 1025-1032, 1999 | 154 | 1999 |
| The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation F Tesson, C Dufour, JC Moolman, L Carrier, S Al-Mahdawi, L Chojnowska, ... Journal of molecular and cellular cardiology 29 (2), 831-838, 1997 | 145 | 1997 |
| Genotype–phenotype correlations in familial hypertrophic cardiomyopathy: a comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes P Charron, O Dubourg, M Desnos, R Isnard, A Hagege, G Bonne, ... European heart journal 19 (1), 139-145, 1998 | 142 | 1998 |
| Penetrance of familial hypertrophic cardiomyopathy. P Charron, L Carrier, O Dubourg, F Tesson, M Desnos, P Richard, ... Genetic Counseling (Geneva, Switzerland) 8 (2), 107-114, 1997 | 122 | 1997 |
| In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients N Sylvius, ZT Bilinska, JP Veinot, A Fidzianska, PM Bolongo, S Poon, ... Journal of medical genetics 42 (8), 639-647, 2005 | 115 | 2005 |
| Epidemiology of desmin and cardiac actin gene mutations in a European population of dilated cardiomyopathy F Tesson, N Sylvius, A Pilotto, L Dubosq-Bidot, M Peuchmaurd, ... European heart journal 21 (22), 1872-1876, 2000 | 101 | 2000 |
| Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption P Gupta, ZT Bilinska, N Sylvius, E Boudreau, JP Veinot, S Labib, ... Basic research in cardiology 105, 365-377, 2010 | 100 | 2010 |
| A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16 N Sylvius, F Tesson, C Gayet, P Charron, A Benaiche, L Mangin, ... The American Journal of Human Genetics 68 (1), 241-246, 2001 | 86 | 2001 |
| Lamin A/C and cardiac diseases N Sylvius, F Tesson Current opinion in cardiology 21 (3), 159-165, 2006 | 79 | 2006 |
| Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene P Charron, F Tesson, O Poirier, V Nicaud, M Peuchmaurd, L Tiret, ... European heart journal 20 (21), 1587-1591, 1999 | 78 | 1999 |
| Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children P Charron, O Dubourg, M Desnos, JB Bouhour, R Isnard, A Hagege, ... European heart journal 19 (9), 1377-1382, 1998 | 76 | 1998 |
| Influence of Pro12Ala peroxisome proliferator-activated receptor γ2 polymorphism on glucose response to exercise training in type 2 diabetes KB Adamo, RJ Sigal, K Williams, G Kenny, D Prud’homme, F Tesson Diabetologia 48, 1503-1509, 2005 | 72 | 2005 |
| Peroxisome Proliferator‐activated Receptor γ 2 and Acyl‐CoA Synthetase 5 Polymorphisms Influence Diet Response KB Adamo, R Dent, CD Langefeld, M Cox, K Williams, KM Carrick, ... Obesity 15 (5), 1068-1075, 2007 | 69 | 2007 |
| Lamin A/C mutations in dilated cardiomyopathy F Tesson, M Saj, MM Uvaize, H Nicolas, R Płoski, Z Bilińska Cardiology journal 21 (4), 331-342, 2014 | 68 | 2014 |
