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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 | 1847 | 2008 |
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Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis CH Wu, C Fallini, N Ticozzi, PJ Keagle, PC Sapp, K Piotrowska, P Lowe, ... Nature 488 (7412), 499-503, 2012 | 759 | 2012 |
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 | 648 | 2018 |
Clinical consequences of corticectomies involving the supplementary motor area in man D Laplane, J Talairach, V Meininger, J Bancaud, JM Orgogozo Journal of the neurological sciences 34 (3), 301-314, 1977 | 638 | 1977 |
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ... Nature genetics 48 (9), 1043-1048, 2016 | 629 | 2016 |
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis DA Figlewicz, A Krizus, MG Martinoli, V Meininger, M Dib, GA Rouleau, ... Human molecular genetics 3 (10), 1757-1761, 1994 | 628 | 1994 |
Dyslipidemia is a protective factor in amyotrophic lateral sclerosis L Dupuis, P Corcia, A Fergani, JL Gonzalez De Aguilar, ... Neurology 70 (13), 1004-1009, 2008 | 587 | 2008 |
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis MA Van Es, JH Veldink, CGJ Saris, HM Blauw, PWJ van Vught, A Birve, ... Nature genetics 41 (10), 1083-1087, 2009 | 456 | 2009 |
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 |
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ... Nature genetics 53 (12), 1636-1648, 2021 | 361 | 2021 |
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 | 361 | 2009 |
Intravenous immunoglobulin therapy in multifocal motor neuropathy: a double-blind, placebo-controlled study JM Léger, B Chassande, L Musset, V Meininger, P Bouche, N Baumann Brain 124 (1), 145-153, 2001 | 345 | 2001 |
Glutamate levels in cerebrospinal fluid in amyotrophic lateral sclerosis: a reappraisal using a new HPLC method with coulometric detection in a large cohort of patients O Spreux-Varoquaux, G Bensimon, L Lacomblez, F Salachas, PF Pradat, ... Journal of the neurological sciences 193 (2), 73-78, 2002 | 344 | 2002 |
Sleep disorders and diaphragmatic function in patients with amyotrophic lateral sclerosis I Arnulf, T Similowski, F Salachas, L Garma, S Mehiri, V Attali, ... American journal of respiratory and critical care medicine 161 (3), 849-856, 2000 | 321 | 2000 |
An analysis of extended survival in patients with amyotrophic lateral sclerosis treated with riluzole M Riviere, V Meininger, P Zeisser, T Munsat Archives of neurology 55 (4), 526-528, 1998 | 287 | 1998 |
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study A Shatunov, K Mok, S Newhouse, ME Weale, B Smith, C Vance, ... The Lancet Neurology 9 (10), 986-994, 2010 | 281 | 2010 |
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 |
Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology E Teyssou, T Takeda, V Lebon, S Boillée, B Doukouré, G Bataillon, ... Acta neuropathologica 125, 511-522, 2013 | 273 | 2013 |