Exome sequencing reveals VCP mutations as a cause of familial ALS JO Johnson, J Mandrioli, M Benatar, Y Abramzon, VM Van Deerlin, ... Neuron 68 (5), 857-864, 2010 | 1484 | 2010 |
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 characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 A Chiò, G Borghero, G Restagno, G Mora, C Drepper, BJ Traynor, ... Brain 135 (3), 784-793, 2012 | 241 | 2012 |
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis S Bandres‐Ciga, AJ Noyce, G Hemani, A Nicolas, A Calvo, G Mora, ... Annals of neurology 85 (4), 470-481, 2019 | 176 | 2019 |
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation A Chiò, G Restagno, M Brunetti, I Ossola, A Calvo, G Mora, M Sabatelli, ... Neurobiology of aging 30 (8), 1272-1275, 2009 | 164 | 2009 |
Genetic counselling in ALS: facts, uncertainties and clinical suggestions A Chiò, S Battistini, A Calvo, C Caponnetto, FL Conforti, M Corbo, ... Journal of Neurology, Neurosurgery & Psychiatry 85 (5), 478-485, 2014 | 161 | 2014 |
Factors affecting the diagnostic delay in amyotrophic lateral sclerosis E Cellura, R Spataro, AC Taiello, V La Bella Clinical neurology and neurosurgery 114 (6), 550-554, 2012 | 158 | 2012 |
Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: effect on survival R Spataro, L Ficano, F Piccoli, V La Bella Journal of the neurological sciences 304 (1-2), 44-48, 2011 | 147 | 2011 |
FUS mutations in sporadic amyotrophic lateral sclerosis SL Lai, Y Abramzon, JC Schymick, DA Stephan, T Dunckley, A Dillman, ... Neurobiology of aging 32 (3), 550. e1-550. e4, 2011 | 130 | 2011 |
Complete locked-in and locked-in patients: command following assessment and communication with vibro-tactile P300 and motor imagery brain-computer interface tools C Guger, R Spataro, BZ Allison, A Heilinger, R Ortner, W Cho, V La Bella Frontiers in neuroscience 11, 251, 2017 | 127 | 2017 |
Causes and place of death in Italian patients with amyotrophic lateral sclerosis R Spataro, M Lo Re, T Piccoli, F Piccoli, V La Bella Acta neurologica Scandinavica 122 (3), 217-223, 2010 | 122 | 2010 |
The eye‐tracking computer device for communication in amyotrophic lateral sclerosis R Spataro, M Ciriacono, C Manno, V La Bella Acta Neurologica Scandinavica 130 (1), 40-45, 2014 | 121 | 2014 |
CSF neurofilament proteins as diagnostic and prognostic biomarkers for amyotrophic lateral sclerosis D Rossi, P Volanti, L Brambilla, T Colletti, R Spataro, V La Bella Journal of neurology 265, 510-521, 2018 | 112 | 2018 |
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population M Sabatelli, FL Conforti, M Zollino, G Mora, MR Monsurrò, P Volanti, ... Neurobiology of aging 33 (8), 1848. e15-1848. e20, 2012 | 104 | 2012 |
Sleep–wake disturbances in patients with amyotrophic lateral sclerosis DL Coco, P Mattaliano, R Spataro, A Mattaliano, V La Bella Journal of Neurology, Neurosurgery & Psychiatry 82 (8), 839-842, 2011 | 104 | 2011 |
Tracheostomy mechanical ventilation in patients with amyotrophic lateral sclerosis: clinical features and survival analysis R Spataro, V Bono, S Marchese, V La Bella Journal of the neurological sciences 323 (1-2), 66-70, 2012 | 97 | 2012 |
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis FL Conforti, R Spataro, W Sproviero, R Mazzei, F Cavalcanti, F Condino, ... Neurology 79 (24), 2315-2320, 2012 | 94 | 2012 |
Reaching and grasping a glass of water by locked-in ALS patients through a BCI-controlled humanoid robot R Spataro, A Chella, B Allison, M Giardina, R Sorbello, S Tramonte, ... Frontiers in human neuroscience 11, 68, 2017 | 93 | 2017 |
Consortium, I JO Johnson, J Mandrioli, M Benatar, Y Abramzon, VM Van Deerlin, ... Galassi, G., Scholz, SW, Taylor, JP, Restagno, G., Chio, A., and Traynor, BJ …, 2010 | 69 | 2010 |
Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis JO Johnson, R Chia, DE Miller, R Li, R Kumaran, Y Abramzon, ... JAMA neurology 78 (10), 1236-1248, 2021 | 63 | 2021 |