TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis E Kabashi, PN Valdmanis, P Dion, D Spiegelman, BJ McConkey, ... Nature genetics 40 (5), 572-574, 2008 | 1850 | 2008 |
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ... Nature genetics 45 (11), 1353-1360, 2013 | 1373 | 2013 |
Siponimod versus placebo in secondary progressive multiple sclerosis (EXPAND): a double-blind, randomised, phase 3 study L Kappos, A Bar-Or, BAC Cree, RJ Fox, G Giovannoni, R Gold, ... The Lancet 391 (10127), 1263-1273, 2018 | 1051 | 2018 |
Neurotrophins promote motor neuron survival and are present in embryonic limb bud CE Henderson, W Camu, C Mettling, A Gouin, K Poulsen, M Karihaloo, ... Nature 363 (6426), 266-270, 1993 | 788 | 1993 |
Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1267-1288, 2018 | 647 | 2018 |
TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1 KK McDonald, A Aulas, L Destroismaisons, S Pickles, E Beleac, W Camu, ... Human molecular genetics 20 (7), 1400-1410, 2011 | 476 | 2011 |
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations S Millecamps, F Salachas, C Cazeneuve, P Gordon, B Bricka, A Camuzat, ... Journal of medical genetics 47 (8), 554-560, 2010 | 364 | 2010 |
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration L Benajiba, I Le Ber, A Camuzat, M Lacoste, C Thomas‐Anterion, ... Annals of neurology 65 (4), 470-473, 2009 | 363 | 2009 |
Effect of natalizumab on disease progression in secondary progressive multiple sclerosis (ASCEND): a phase 3, randomised, double-blind, placebo-controlled trial with an open … R Kapoor, PR Ho, N Campbell, I Chang, A Deykin, F Forrestal, N Lucas, ... The Lancet Neurology 17 (5), 405-415, 2018 | 356 | 2018 |
A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis F Gros-Louis, R Larivière, G Gowing, S Laurent, W Camu, JP Bouchard, ... Journal of Biological Chemistry 279 (44), 45951-45956, 2004 | 274 | 2004 |
A major determinant for binding and aminoacylation of tRNAAla in cytoplasmic alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease P Latour, C Thauvin-Robinet, C Baudelet-Méry, P Soichot, V Cusin, ... The American Journal of Human Genetics 86 (1), 77-82, 2010 | 268 | 2010 |
Neuromyelitis optica in France: a multicenter study of 125 patients N Collongues, R Marignier, H Zephir, C Papeix, F Blanc, C Ritleng, ... Neurology 74 (9), 736-742, 2010 | 264 | 2010 |
Purification of embryonic rat motoneurons by panning on a monoclonal antibody to the low-affinity NGF receptor W Camu, CE Henderson Journal of neuroscience methods 44 (1), 59-70, 1992 | 241 | 1992 |
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis H Daoud, PN Valdmanis, E Kabashi, P Dion, N Dupre, W Camu, ... Journal of medical genetics 46 (2), 112-114, 2009 | 237 | 2009 |
Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes S Millecamps, S Boillée, I Le Ber, D Seilhean, E Teyssou, M Giraudeau, ... Journal of medical genetics 49 (4), 258-263, 2012 | 224 | 2012 |
A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q CK Hand, J Khoris, F Salachas, F Gros-Louis, AAS Lopes, ... The American Journal of Human Genetics 70 (1), 251-256, 2002 | 223 | 2002 |
Recessive Amyotrophic Lateral Sclerosis Families with the D90A SOD1 Mutation Share a Common Founder: Evidence for a Linked Protective Factor A Al-Chalabi, PM Andersen, B Chioza, C Shaw, PC Sham, W Robberecht, ... Human molecular genetics 7 (13), 2045-2050, 1998 | 208 | 1998 |
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study J Gil, B Funalot, A Verschueren, V Danel‐Brunaud, W Camu, ... European journal of neurology 15 (11), 1245-1251, 2008 | 207 | 2008 |
Chitinase 3-like proteins as diagnostic and prognostic biomarkers of multiple sclerosis G Hinsinger, N Galéotti, N Nabholz, S Urbach, V Rigau, C Demattei, ... Multiple Sclerosis Journal 21 (10), 1251-1261, 2015 | 187 | 2015 |
Mutations in FUS cause FALS and SALS in French and French Canadian populations VV Belzil, PN Valdmanis, PA Dion, H Daoud, E Kabashi, A Noreau, ... Neurology 73 (15), 1176-1179, 2009 | 181 | 2009 |