Adriano Chio'

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Andrea CalvoAssociate Professor of Neurology, 'Rita Levi Montalcini' Department of Neuroscience, University ofEmail verificata su unito.it
cristina mogliaUniversity of TorinoEmail verificata su unito.it
Bryan TraynorLaboratory of Neurogenetics, National Institute on AgingEmail verificata su mail.nih.gov
Umberto Manera"Rita Levi Montalcini" Department of NeuroscienceEmail verificata su unito.it
Orla HardimanTrinity College DublinEmail verificata su hardiman.net
Giancarlo LogroscinoFull Professor of Neurology, University of Bari. Director of the Center for NeurodegenerativeEmail verificata su uniba.it
ammar al-chalabiProfessor of Neurology and Complex Disease Genetics, King's College LondonEmail verificata su kcl.ac.uk
Angelina CistaroMD., Prof., CNR Associate ResearcherEmail verificata su irmet.com
andrea faliniprofessore di neuroradiologia, vita-salute universityEmail verificata su hsr.it
Philip Van DammeProfessor of Neuroscience, University of LeuvenEmail verificata su uzleuven.be
"christian lunetta"IRCCS Istituti Clinici Scientifici Maugeri MilanoEmail verificata su icsmaugeri.it
Mamede de CarvalhoFaculdade de Medicina, Instituto de Medicina Molecular, Universidade de Lisboa, Lisbon, PortugalEmail verificata su fm.ul.pt
Federico CasaleTecnico df Ricerca Dip. Neuroscienze Università degli Studi di TorinoEmail verificata su unito.it
mario sabatelliCatholic University of RomeEmail verificata su unicatt.it
Massimo FilippiSan Raffaele Scientific Institute, Vita-Salute San Raffaele UniversityEmail verificata su hsr.it
Flavio NobiliUniversity of GenoaEmail verificata su hsanmartino.it
Maria Giovanna MarrosuProfessor of Neurology, University of CagliariEmail verificata su unica.it
Alan RentonIcahn School of Medicine at Mount SinaiEmail verificata su mssm.edu
Pamela J ShawProfessor of Neurology, University of SheffieldEmail verificata su sheffield.ac.uk
Maurizio A. LeoneIRCCS Casa Sollievo della Sofferenza and Istituto "Mario Negri" IRCCSEmail verificata su iol.it

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Adriano Chio'

Professor of Neurology, 'Rita Levi Montalcini' Department of Neuroscience, University of Turin

Email verificata su unito.it

neurology neuroepidemiology neurogenetics cognition nuclear medicine


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ... Neuron 72 (2), 257-268, 2011	4905	2011
Amyotrophic lateral sclerosis O Hardiman, A Al-Chalabi, A Chio, EM Corr, G Logroscino, W Robberecht, ... Nature reviews Disease primers 3 (1), 1-19, 2017	1997	2017
State of play in amyotrophic lateral sclerosis genetics AE Renton, A Chiò, BJ Traynor Nature neuroscience 17 (1), 17-23, 2014	1835	2014
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	1478	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	1385	2012
Amyotrophic lateral sclerosis MA Van Es, O Hardiman, A Chio, A Al-Chalabi, RJ Pasterkamp, ... The Lancet 390 (10107), 2084-2098, 2017	1289	2017
Prognostic factors in ALS: a critical review A Chio, G Logroscino, O Hardiman, R Swingler, D Mitchell, E Beghi, ... Amyotrophic lateral sclerosis 10 (5-6), 310-323, 2009	1241	2009
EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)–revised report of an EFNS task force EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis: European journal of neurology 19 (3), 360-375, 2012	1154	2012
Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature A Chiò, G Logroscino, BJ Traynor, J Collins, JC Simeone, LA Goldstein, ... Neuroepidemiology 41 (2), 118-130, 2013	1089	2013
Incidence of amyotrophic lateral sclerosis in Europe G Logroscino, BJ Traynor, O Hardiman, A Chiò, D Mitchell, RJ Swingler, ... Journal of Neurology, Neurosurgery & Psychiatry 81 (4), 385-390, 2010	1080	2010
Severely increased risk of amyotrophic lateral sclerosis among Italian professional football players A Chio, G Benzi, M Dossena, R Mutani, G Mora Brain 128 (3), 472-476, 2005	664	2005
Controversies and priorities in amyotrophic lateral sclerosis MR Turner, O Hardiman, M Benatar, BR Brooks, A Chio, M De Carvalho, ... The Lancet Neurology 12 (3), 310-322, 2013	653	2013
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	653	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	647	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	629	2016
Prognosis in amyotrophic lateral sclerosis: a population-based study MA Del Aguila, WT Longstreth, V McGuire, TD Koepsell, G Van Belle Neurology 60 (5), 813-819, 2003	589	2003
Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications R Chia, A Chiò, BJ Traynor The Lancet Neurology 17 (1), 94-102, 2018	588	2018
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	550	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	499	2016
Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS TM Miller, ME Cudkowicz, A Genge, PJ Shaw, G Sobue, RC Bucelli, ... New England Journal of Medicine 387 (12), 1099-1110, 2022	491	2022

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