| Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study A Chiņ, A Calvo, C Moglia, L Mazzini, G Mora Journal of Neurology, Neurosurgery & Psychiatry 82 (7), 740-746, 2011 | 592 | 2011 |
| 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 | 588 | 2016 |
| 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), 1268-1283. e6, 2018 | 576 | 2018 |
| SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis E Rubino, I Rainero, A Chiņ, E Rogaeva, D Galimberti, P Fenoglio, ... Neurology 79 (15), 1556-1562, 2012 | 327 | 2012 |
| 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 | 307 | 2007 |
| 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 | 299 | 2015 |
| 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 | 275 | 2021 |
| Extensive genetics of ALS: a population-based study in Italy A Chiņ, A Calvo, L Mazzini, R Cantello, G Mora, C Moglia, L Corrado, ... Neurology 79 (19), 1983-1989, 2012 | 193 | 2012 |
| The multistep hypothesis of ALS revisited: the role of genetic mutations A Chiņ, L Mazzini, S D'Alfonso, L Corrado, A Canosa, C Moglia, U Manera, ... Neurology 91 (7), e635-e642, 2018 | 185 | 2018 |
| Functional pattern of brain FDG-PET in amyotrophic lateral sclerosis M Pagani, A Chiņ, MC Valentini, J Öberg, F Nobili, A Calvo, C Moglia, ... Neurology 83 (12), 1067-1074, 2014 | 184 | 2014 |
| Lower serum lipid levels are related to respiratory impairment in patients with ALS A Chio, A Calvo, A Ilardi, E Cavallo, C Moglia, R Mutani, A Palmo, ... Neurology 73 (20), 1681-1685, 2009 | 181 | 2009 |
| Amyotrophic lateral sclerosis outcome measures and the role of albumin and creatinine: a population-based study A Chiņ, A Calvo, G Bovio, A Canosa, D Bertuzzo, F Galmozzi, ... JAMA neurology 71 (9), 1134-1142, 2014 | 180 | 2014 |
| Neurobehavioral symptoms in ALS are negatively related to caregivers’ burden and quality of life A Chiņ, A Vignola, E Mastro, AD Giudici, B Iazzolino, A Calvo, C Moglia, ... European journal of neurology 17 (10), 1298-1303, 2010 | 178 | 2010 |
| Brain hypermetabolism in amyotrophic lateral sclerosis: a FDG PET study in ALS of spinal and bulbar onset A Cistaro, MC Valentini, A Chiņ, F Nobili, A Calvo, C Moglia, A Montuschi, ... European journal of nuclear medicine and molecular imaging 39, 251-259, 2012 | 177 | 2012 |
| Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels F Bartolome, HC Wu, VS Burchell, E Preza, S Wray, CJ Mahoney, NC Fox, ... Neuron 78 (1), 57-64, 2013 | 171 | 2013 |
| 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 | 160 | 2019 |
| Genetic counselling in ALS: facts, uncertainties and clinical suggestions A Chiņ, S Battistini, A Calvo, C Caponnetto, FL Conforti, M Corbo, ... Journal of Neurology, Neurosurgery & Psychiatry 85 (5), 478-485, 2014 | 152 | 2014 |
| Cognitive impairment across ALS clinical stages in a population-based cohort A Chiņ, C Moglia, A Canosa, U Manera, R Vasta, M Brunetti, M Barberis, ... Neurology 93 (10), e984-e994, 2019 | 148 | 2019 |
| Genetic correlation between amyotrophic lateral sclerosis and schizophrenia RL McLaughlin, D Schijven, W Van Rheenen, KR Van Eijk, M O’brien, ... Nature communications 8 (1), 14774, 2017 | 135 | 2017 |
| Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene A Chiņ, G Borghero, M Pugliatti, A Ticca, A Calvo, C Moglia, R Mutani, ... Archives of neurology 68 (5), 594-598, 2011 | 134 | 2011 |
