| A 10-year study of mortality in a cohort of patients with myotonic dystrophy J Mathieu, P Allard, L Potvin, C Prevost, P Begin Neurology 52 (8), 1658-1658, 1999 | 504 | 1999 |
| ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF JC Engert, P Bérubé, J Mercier, C Doré, P Lepage, B Ge, JP Bouchard, ... Nature genetics 24 (2), 120-125, 2000 | 481 | 2000 |
| Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy J Mathieu, H Boivin, D Meunier, M Gaudreault, P Begin Neurology 56 (3), 336-340, 2001 | 419 | 2001 |
| The K–Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum HC Howard, DB Mount, D Rochefort, N Byun, N Dupré, J Lu, X Fan, ... Nature genetics 32 (3), 384-392, 2002 | 308 | 2002 |
| Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion L Montermini, A Richeter, K Morgan, CM Justice, D Julien, B Castellotti, ... Annals of Neurology: Official Journal of the American Neurological …, 1997 | 302 | 1997 |
| Specific pathological Tau protein variants characterize Pick's disease A Delacourte, Y Robitaille, N Sergeant, L Buée, PR Hof, A Wattez, ... Journal of Neuropathology & Experimental Neurology 55 (2), 159-168, 1996 | 277 | 1996 |
| Measuring participation in children with disabilities using the Assessment of Life Habits L Noreau, C Lepage, L Boissiere, R Picard, P Fougeyrollas, J Mathieu, ... Developmental Medicine & Child Neurology 49 (9), 666-671, 2007 | 207 | 2007 |
| Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans V Bayat, I Thiffault, M Jaiswal, M Tétreault, T Donti, F Sasarman, ... PLoS biology 10 (3), e1001288, 2012 | 200 | 2012 |
| Anesthetic and surgical complications in 219 cases of myotonic dystrophy J Mathieu, P Allard, G Gobeil, M Girard, M De Braekeleer, P Begin Neurology 49 (6), 1646-1650, 1997 | 198 | 1997 |
| Genealogical reconstruction of myotonic dystrophy in the Saguenay‐Lac‐Saint‐Jean area (Quebec, Canada) J Mathieu, M De Braekeleer, C Prevost Neurology 40 (5), 839-839, 1990 | 193 | 1990 |
| Autosomal recessive spastic ataxia of Charlevoix–Saguenay JP Bouchard, A Richter, J Mathieu, D Brunet, TJ Hudson, K Morgan, ... Neuromuscular disorders 8 (7), 474-479, 1998 | 182 | 1998 |
| Relationship between chronic hypercapnia and inspiratory-muscle weakness in myotonic dystrophy P Begin, J Mathieu, J Almirall, A Grassino American journal of respiratory and critical care medicine 156 (1), 133-139, 1997 | 168 | 1997 |
| Myotonic dystrophy: clinical assessment of muscular disability in an isolated population with presumed homogeneous mutation J Mathieu, MD Braekeleer, C Prévost, C Boily Neurology 42 (1), 203-203, 1992 | 161 | 1992 |
| Sleep complaints in patients with myotonic dystrophy L Laberge, P Bégin, J Montplaisir, J Mathieu Journal of sleep research 13 (1), 95-100, 2004 | 155 | 2004 |
| Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy A Duquette, K Roddier, J McNabb‐Baltar, I Gosselin, A St‐Denis, ... Annals of neurology 57 (3), 408-414, 2005 | 141 | 2005 |
| Genes, maternal smoking, and the offspring brain and body during adolescence: design of the Saguenay Youth Study Z Pausova, T Paus, M Abrahamowicz, J Almerigi, N Arbour, M Bernard, ... Human brain mapping 28 (6), 502-518, 2007 | 140 | 2007 |
| Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions ME Arsenault, C Prevost, A Lescault, C Laberge, J Puymirat, J Mathieu Neurology 66 (8), 1248-1250, 2006 | 125 | 2006 |
| A polysomnographic study of daytime sleepiness in myotonic dystrophy type 1 L Laberge, P Bégin, Y Dauvilliers, M Beaudry, M Laforte, S Jean, ... Journal of Neurology, Neurosurgery & Psychiatry 80 (6), 642-646, 2009 | 123 | 2009 |
| Predictors of disrupted social participation in myotonic dystrophy type 1 C Gagnon, J Mathieu, S Jean, L Laberge, M Perron, S Veillette, L Richer, ... Archives of physical medicine and rehabilitation 89 (7), 1246-1255, 2008 | 120 | 2008 |
| Hereditary motor and sensory neuropathy with agenesis of the corpus callosum N Dupré, HC Howard, J Mathieu, G Karpati, M Vanasse, JP Bouchard, ... Annals of neurology 54 (1), 9-18, 2003 | 108 | 2003 |
