| Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A S Züchner, IV Mersiyanova, M Muglia, N Bissar-Tadmouri, J Rochelle, ... Nature genetics 36 (5), 449-451, 2004 | 1554 | 2004 |
| Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ... New England Journal of Medicine 361 (17), 1651-1661, 2009 | 1482 | 2009 |
| Collaborative analysis of α-synuclein gene promoter variability and Parkinson disease DM Maraganore, M De Andrade, A Elbaz, MJ Farrer, JP Ioannidis, ... Jama 296 (6), 661-670, 2006 | 528 | 2006 |
| Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 A Bolino, M Muglia, FL Conforti, E LeGuern, MAM Salih, DM Georgiou, ... Nature genetics 25 (1), 17-19, 2000 | 511 | 2000 |
| The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy M De Fusco, A Becchetti, A Patrignani, G Annesi, A Gambardella, ... Nature genetics 26 (3), 275-276, 2000 | 506 | 2000 |
| The challenge of mapping the human connectome based on diffusion tractography KH Maier-Hein, PF Neher, JC Houde, MA Côté, E Garyfallidis, J Zhong, ... Nature communications 8 (1), 1-13, 2017 | 476 | 2017 |
| Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders B Jones, EL Jones, SA Bonney, HN Patel, AR Mensenkamp, ... Nature genetics 34 (1), 29-31, 2003 | 373 | 2003 |
| A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies MA Nalls, R Duran, G Lopez, M Kurzawa-Akanbi, IG McKeith, ... JAMA neurology 70 (6), 727-735, 2013 | 308 | 2013 |
| MR Imaging Index for Differentiation of Progressive Supranuclear Palsy from Parkinson Disease and the Parkinson Variant of Multiple System Atrophy1 A Quattrone, G Nicoletti, D Messina, F Fera, F Condino, P Pugliese, ... Radiology 246 (1), 214-221, 2008 | 307 | 2008 |
| UCHL1 is a Parkinson's disease susceptibility gene DM Maraganore, TG Lesnick, A Elbaz, MC Chartier‐Harlin, T Gasser, ... Annals of neurology 55 (4), 512-521, 2004 | 281 | 2004 |
| Manometry combined with cervical puncture in idiopathic intracranial hypertension JO King, PJ Mitchell, KR Thomson, BM Tress Neurology 58 (1), 26-30, 2002 | 281 | 2002 |
| Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study OA Ross, AI Soto-Ortolaza, MG Heckman, JO Aasly, N Abahuni, G Annesi, ... The Lancet Neurology 10 (10), 898-908, 2011 | 248 | 2011 |
| Apparent diffusion coefficient measurements of the middle cerebellar peduncle differentiate the Parkinson variant of MSA from Parkinson's disease and progressive supranuclear palsy G Nicoletti, R Lodi, F Condino, C Tonon, F Fera, E Malucelli, D Manners, ... Brain 129 (10), 2679-2687, 2006 | 226 | 2006 |
| Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early‐Onset Parkinsonism M Quadri, M Fang, M Picillo, S Olgiati, GJ Breedveld, J Graafland, B Wu, ... Human mutation 34 (9), 1208-1215, 2013 | 224 | 2013 |
| Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial D Pareyson, MM Reilly, A Schenone, GM Fabrizi, T Cavallaro, L Santoro, ... The Lancet Neurology 10 (4), 320-328, 2011 | 220 | 2011 |
| Quetiapine and clozapine in parkinsonian patients with dopaminergic psychosis L Morgante, A Epifanio, E Spina, M Zappia, AE Di Rosa, R Marconi, ... Clinical neuropharmacology 27 (4), 153-156, 2004 | 217 | 2004 |
| Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study M Zappia, G Annesi, G Nicoletti, G Arabia, F Annesi, D Messina, ... Archives of neurology 62 (4), 601-605, 2005 | 207 | 2005 |
| Identification of an Nav1. 1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures M Mantegazza, A Gambardella, R Rusconi, E Schiavon, F Annesi, ... Proceedings of the National Academy of Sciences 102 (50), 18177-18182, 2005 | 196 | 2005 |
| 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 | 187 | 2012 |
| Monoamine oxidase-a genetic variations influence brain activity associated with inhibitory control: new insight into the neural correlates of impulsivity L Passamonti, F Fera, A Magariello, A Cerasa, MC Gioia, M Muglia, ... Biological psychiatry 59 (4), 334-340, 2006 | 187 | 2006 |
Umberto AgugliaFull professor of Neurology, Catanzaro University, ItalyVerified email at unicz.it
