| 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 | 1464 | 2010 |
| Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ... The Lancet Neurology 11 (4), 323-330, 2012 | 1357 | 2012 |
| Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study A Chiò, A Calvo, C Moglia, L Mazzini, G Mora Journal of Neurology, Neurosurgery & Psychiatry 82 (7), 740-746, 2011 | 637 | 2011 |
| 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 | 627 | 2018 |
| 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 | 614 | 2016 |
| Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ... Nature neuroscience 17 (5), 664-666, 2014 | 542 | 2014 |
| Projected increase in amyotrophic lateral sclerosis from 2015 to 2040 KC Arthur, A Calvo, TR Price, JT Geiger, A Chio, BJ Traynor Nature communications 7 (1), 12408, 2016 | 476 | 2016 |
| Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model HJ Westeneng, TPA Debray, AE Visser, RPA van Eijk, JPK Rooney, ... The Lancet Neurology 17 (5), 423-433, 2018 | 466 | 2018 |
| Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study A Al-Chalabi, A Calvo, A Chio, S Colville, CM Ellis, O Hardiman, ... The Lancet Neurology 13 (11), 1108-1113, 2014 | 428 | 2014 |
| 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 | 335 | 2021 |
| SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis E Rubino, I Rainero, A Chiò, E Rogaeva, D Galimberti, P Fenoglio, ... Neurology 79 (15), 1556-1562, 2012 | 333 | 2012 |
| Epidemiology of ALS in Italy: a 10-year prospective population-based study A Chiò, G Mora, A Calvo, L Mazzini, E Bottacchi, R Mutani Neurology 72 (8), 725-731, 2009 | 325 | 2009 |
| Caregiver burden and patients’ perception of being a burden in ALS A Chio, A Gauthier, A Calvo, P Ghiglione, R Mutani Neurology 64 (10), 1780-1782, 2005 | 318 | 2005 |
| Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy A Montuschi, B Iazzolino, A Calvo, C Moglia, L Lopiano, G Restagno, ... Journal of Neurology, Neurosurgery & Psychiatry 86 (2), 168-173, 2015 | 314 | 2015 |
| A longitudinal study on quality of life and depression in ALS patient–caregiver couples A Gauthier, A Vignola, A Calvo, E Cavallo, C Moglia, L Sellitti, R Mutani, ... Neurology 68 (12), 923-926, 2007 | 314 | 2007 |
| NEK1 variants confer susceptibility to amyotrophic lateral sclerosis KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ... Nature genetics 48 (9), 1037-1042, 2016 | 305 | 2016 |
| A cross sectional study on determinants of quality of life in ALS A Chiò, A Gauthier, A Montuschi, A Calvo, N Di Vito, P Ghiglione, ... Journal of Neurology, Neurosurgery & Psychiatry 75 (11), 1597-1601, 2004 | 262 | 2004 |
| Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ... Nature genetics 53 (3), 294-303, 2021 | 255 | 2021 |
| Neuroimaging in amyotrophic lateral sclerosis: insights into structural and functional changes A Chiò, M Pagani, F Agosta, A Calvo, A Cistaro, M Filippi The Lancet Neurology 13 (12), 1228-1240, 2014 | 244 | 2014 |
| 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 | 237 | 2012 |
Adriano Chio'Professor of Neurology, 'Rita Levi Montalcini' Department of Neuroscience, University of TurinVerified email at unito.it
