| A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015 | 14604* | 2015 |
| Muscle satellite cells and endothelial cells: close neighbors and privileged partners C Christov, F Chrétien, R Abou-Khalil, G Bassez, G Vallet, FJ Authier, ... Molecular biology of the cell 18 (4), 1397-1409, 2007 | 739 | 2007 |
| Satellite cells attract monocytes and use macrophages as a support to escape apoptosis and enhance muscle growth B Chazaud, C Sonnet, P Lafuste, G Bassez, AC Rimaniol, F Poron, ... The Journal of cell biology 163 (5), 1133-1143, 2003 | 577 | 2003 |
| Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy C Fugier, AF Klein, C Hammer, S Vassilopoulos, Y Ivarsson, A Toussaint, ... Nature medicine 17 (6), 720-725, 2011 | 347 | 2011 |
| Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes K Nguyen, G Bassez, M Krahn, R Bernard, P Laforêt, V Labelle, ... Archives of neurology 64 (8), 1176-1182, 2007 | 294 | 2007 |
| Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2 A Vihola, G Bassez, G Meola, S Zhang, H Haapasalo, A Paetau, ... Neurology 60 (11), 1854-1857, 2003 | 205 | 2003 |
| Unravelling the myotonic dystrophy type 1 clinical spectrum: a systematic registry-based study with implications for disease classification M De Antonio, C Dogan, D Hamroun, M Mati, S Zerrouki, B Eymard, ... Revue neurologique 172 (10), 572-580, 2016 | 181 | 2016 |
| COVID‐19‐related encephalopathy: a case series with brain FDG‐positron‐emission tomography/computed tomography findings C Delorme, O Paccoud, A Kas, A Hesters, S Bombois, P Shambrook, ... European journal of neurology 27 (12), 2651-2657, 2020 | 176 | 2020 |
| Consensus-based care recommendations for adults with myotonic dystrophy type 1 T Ashizawa, C Gagnon, WJ Groh, L Gutmann, NE Johnson, G Meola, ... Neurology: Clinical Practice 8 (6), 507-520, 2018 | 163 | 2018 |
| Confirmation of the type 2 myotonic dystrophy (CCTG) n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins … LL Bachinski, B Udd, G Meola, V Sansone, G Bassez, B Eymard, ... The American Journal of Human Genetics 73 (4), 835-848, 2003 | 161 | 2003 |
| Gender as a modifying factor influencing myotonic dystrophy type 1 phenotype severity and mortality: a nationwide multiple databases cross-sectional observational study C Dogan, M De Antonio, D Hamroun, H Varet, M Fabbro, F Rougier, ... PloS one 11 (2), e0148264, 2016 | 155 | 2016 |
| Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathies K Nguyen, G Bassez, R Bernard, M Krahn, V Labelle, D Figarella‐Branger, ... Human mutation 26 (2), 165-165, 2005 | 142 | 2005 |
| MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1 M Flower, V Lomeikaite, M Ciosi, S Cumming, F Morales, K Lo, ... Brain 142 (7), 1876-1886, 2019 | 140 | 2019 |
| Detection of genomic viral RNA in nerve and muscle of patients with HCV neuropathy FJ Authier, G Bassez, C Payan, L Guillevin, JM Pawlotsky, JD Degos, ... Neurology 60 (5), 808-812, 2003 | 140 | 2003 |
| Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1 G Bassez, A Lazarus, I Desguerre, J Varin, P Laforet, HM Bécane, ... Neurology 63 (10), 1939-1941, 2004 | 138 | 2004 |
| 140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management B Udd, G Meola, R Krahe, C Thornton, LPW Ranum, G Bassez, W Kress, ... Neuromuscular Disorders 16 (6), 403-413, 2006 | 125 | 2006 |
| Analysis of the DYSF mutational spectrum in a large cohort of patients M Krahn, C Béroud, V Labelle, K Nguyen, R Bernard, G Bassez, ... Human mutation 30 (2), E345-E375, 2009 | 124 | 2009 |
| Molecular, physiological, and motor performance defects in DMSXL mice carrying> 1,000 CTG repeats from the human DM1 locus A Huguet, F Medja, A Nicole, A Vignaud, C Guiraud-Dogan, A Ferry, ... PLoS genetics 8 (11), e1003043, 2012 | 123 | 2012 |
| Clinical and histologic findings in autosomal centronuclear myopathy PY Jeannet, G Bassez, B Eymard, P Laforet, JA Urtizberea, A Rouche, ... Neurology 62 (9), 1484-1490, 2004 | 121 | 2004 |
| Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trial K Okkersen, C Jimenez-Moreno, S Wenninger, F Daidj, J Glennon, ... The Lancet Neurology 17 (8), 671-680, 2018 | 106 | 2018 |
Ralf KraheUniversity of Texas MD Anderson Cancer CenterVerified email at mdanderson.org
