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G. Charlesworth · SciRah

Researcher profile · Semantic Scholar

G. Charlesworth

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G. Charlesworth — researcher profile on SciRah

h-index: 16
Works: 31
Citations: 1,726

Most-cited papers

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A. Beilina, I. Rudenko, A. Kaganovich, L. Civiero +152 more
2014Proceedings of the National Academy of Sciences of the United States of America356 citations Open access
Semantic Scholar
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
V. Plagnol, M. Nalls, J. Brás, D. Hernandez +96 more
2011PLoS Genetics296 citations Open access
Semantic Scholar
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.
G. Charlesworth, V. Plagnol, Kira M. Holmström, J. Brás +10 more
2012American Journal of Human Genetics253 citations Open access
Semantic Scholar
The genetics of dystonia: new twists in an old tale
G. Charlesworth, K. Bhatia, N. Wood
2013Brain : a journal of neurology114 citations Open access
Semantic Scholar
The Phenotypic Spectrum of DYT24 Due to ANO3 Mutations
M. Stamelou, G. Charlesworth, C. Cordivari, S. Schneider +7 more
2014Movement Disorders104 citations Open access
Semantic Scholar
Mutations in HPCA Cause Autosomal-Recessive Primary Isolated Dystonia
G. Charlesworth, Plamena R. Angelova, Fernando Bartolomé-Robledo, M. Ryten +5 more
2015American Journal of Human Genetics88 citations Open access
Semantic Scholar
Ataxia telangiectasia presenting as dopa-responsive cervical dystonia
G. Charlesworth, M. D. Mohire, S. Schneider, M. Stamelou +2 more
2013Neurology68 citations Open access
Semantic Scholar
Screening for VPS35 mutations in Parkinson's disease
U. Sheerin, G. Charlesworth, J. Brás, R. Guerreiro +6 more
2012Neurobiology of Aging67 citations Open access
Semantic Scholar
SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy
G. Charlesworth, B. Balint, N. Mencacci, L. Carr +2 more
2016Movement Disorders56 citations
Semantic Scholar
C9ORF72 expansions, parkinsonism, and Parkinson disease
J. Cooper-Knock, A. Frolov, J. R. Highley, G. Charlesworth +10 more
2013Neurology56 citations Open access
Semantic Scholar
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1
A. Tucci, G. Charlesworth, U. Sheerin, V. Plagnol +2 more
2012Neuroscience Letters40 citations Open access
Semantic Scholar
Double lesion MRgFUS treatment of essential tremor targeting the thalamus and posterior sub-thalamic area: preliminary study with two year follow-up
A. Jameel, W. Gedroyc, D. Nandi, B. Jones +5 more
2021British Journal of Neurosurgery35 citations Open access
Semantic Scholar
Tremulous cervical dystonia is likely to be familial: Clinical characteristics of a large cohort
I. Rubio-Agusti, I. Pareés, M. Kojovic, M. Stamelou +5 more
2013Parkinsonism & Related Disorders35 citations Open access
Semantic Scholar
Analysis of Parkinson’s Disease Brain–Derived DNA for Alpha-Synuclein Coding Somatic Mutations
C. Proukakis, Maryiam Shoaee, James Morris, T. Brier +7 more
2014Movement Disorders28 citations Open access
Semantic Scholar
Tau acts as an independent genetic risk factor in pathologically proven PD
G. Charlesworth, S. Gandhi, J. Brás, R. Barker +13 more
2012Neurobiology of Aging28 citations Open access
Semantic Scholar
Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation
U. Sheerin, M. Stamelou, G. Charlesworth, T. Shiner +4 more
2012Journal of Neurology18 citations Open access
Semantic Scholar
Primary and secondary dystonic syndromes: an update
G. Charlesworth, K. Bhatia
2013Current Opinion in Neurology15 citations Open access
Semantic Scholar
Acute, localised paroxysmal pain as the initial manifestation of focal seizures: a case report and a brief review of the literature.
G. Charlesworth, I. Soryal, Shelagh M. J. Smith, S. Sisodiya
2009Pain15 citations
Semantic Scholar
The use of the rat isolated vagus nerve for functional measurements of the effect of drugs in vitro.
R. Docherty, G. Charlesworth, K. Farrag, A. Bhattacharjee +1 more
2005Journal of pharmacological and toxicological methods15 citations
Semantic Scholar
Delineating the phenotype of autosomal‐recessive HPCA mutations: Not only isolated dystonia!
B. Balint, G. Charlesworth, R. Erro, N. Wood +1 more
2019Movement Disorders12 citations
Semantic Scholar
Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy
B. Balint, G. Charlesworth, M. Stamelou, L. Carr +3 more
2019European Journal of Neurology12 citations Open access
Semantic Scholar
No pathogenic GNAL mutations in 192 sporadic and familial cases of cervical dystonia
G. Charlesworth, K. Bhatia, Nicholas W. Wood
2013Movement Disorders9 citations Open access
Semantic Scholar
Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
M. Keller, M. Saad, J. Brás, F. Bettella +173 more
20128 citations
Semantic Scholar
Two year data from a preliminary study of double lesion site MRgFUS treatment of Essential Tremor targeting the thalamus and the posterior subthalamic area.
A. Jameel, W. Gedroyc, D. Nandi, B. Jones +5 more
2021medRxiv1 citations Open access
Semantic Scholar
Using next-generation sequencing to understand the aetiology of dystonia and other neurological diseases
G. Charlesworth
20161 citations
Semantic Scholar
Neurodegeneration caused by intronic expansions of C9ORF72 is a clinically heterogeneous but pathologically distinct disease
J. Cooper-Knock, J. R. Highley, Judith A. Hartley, A. Milano +10 more
20131 citations Open access
Semantic Scholar
First stage association analysis of neuropatholically proven PD confirms MAPT as an independent risk factor for PD
G. Charlesworth, S. Gandhi, J. Brás, S. Gentleman +6 more
20121 citations
Semantic Scholar
Étude d’épidémiologie génétique des dystonies familiales en Tunisie
H. Benrhouma, N. Gouider-Khouja, U. Sheerin, G. Charlesworth +2 more
20140 citations
Semantic Scholar
A comprehensive diagnostic test for familial and early onset Parkinson's disease based on next-generation sequencing
N. Mencacci, A. Pittman, U. Sheerin, G. Charlesworth +8 more
20120 citations
Semantic Scholar
Mutations in Nuclear Genes That Affect Mitochondrial Function in Parkinson’s Disease
G. Charlesworth, N. Wood
20120 citations
Semantic Scholar
References Analysis of Parkinson's Disease Brain–derived Dna for Alpha- Synuclein Coding Somatic Mutations
Maryiam Shoaee, James Morris, T. Brier, E. Kara +6 more
0 citations
Semantic Scholar

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