Kevin Talbot
Kevin Talbot
Professor of Neurology, Oxford University
Verified email at ndcn.ox.ac.uk
Title
Cited by
Cited by
Year
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
10052012
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
OV Evgrafov, I Mersiyanova, J Irobi, L Van Den Bosch, I Dierick, CL Leung, ...
Nature genetics 36 (6), 602-606, 2004
6702004
Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS
BJ Turner, K Talbot
Progress in neurobiology 85 (1), 94-134, 2008
5462008
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
5082013
Biomarkers in amyotrophic lateral sclerosis
MR Turner, MC Kiernan, PN Leigh, K Talbot
The Lancet Neurology 8 (1), 94-109, 2009
4522009
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy
J Irobi, K Van Impe, P Seeman, A Jordanova, I Dierick, N Verpoorten, ...
Nature genetics 36 (6), 597-601, 2004
4512004
Selective vulnerability of motor neurons and dissociation of pre-and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy
LM Murray, LH Comley, D Thomson, N Parkinson, K Talbot, ...
Human molecular genetics 17 (7), 949-962, 2008
3702008
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
3022014
Neurofilament light chain: a prognostic biomarker in amyotrophic lateral sclerosis
CH Lu, C Macdonald-Wallis, E Gray, N Pearce, A Petzold, N Norgren, ...
Neurology 84 (22), 2247-2257, 2015
3002015
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
2852014
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy
NR Rodrigues, N Owen, K Talbot, J Ignatius, V Dubowitz, KE Davies
Human Molecular Genetics 4 (4), 631-634, 1995
2791995
Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis
N Filippini, G Douaud, CE Mackay, S Knight, K Talbot, MR Turner
Neurology 75 (18), 1645-1652, 2010
2782010
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
2752018
Long-term effectiveness of dopamine agonists and monoamine oxidase B inhibitors compared with levodopa as initial treatment for Parkinson's disease (PD MED): a large, open …
PD Med Collaborative Group
The Lancet 384 (9949), 1196-1205, 2014
2552014
Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy
D Bäumer, S Lee, G Nicholson, JL Davies, NJ Parkinson, LM Murray, ...
PLoS genetics 5 (12), e1000773, 2009
2522009
Loss of VPS13C function in autosomal-recessive Parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
2432016
Integration of structural and functional magnetic resonance imaging in amyotrophic lateral sclerosis
G Douaud, N Filippini, S Knight, K Talbot, MR Turner
Brain 134 (12), 3470-3479, 2011
2282011
The influence of age and gender on motor and non-motor features of early Parkinson's disease: initial findings from the Oxford Parkinson Disease Center (OPDC) discovery cohort
K Szewczyk-Krolikowski, P Tomlinson, K Nithi, R Wade-Martins, K Talbot, ...
Parkinsonism & related disorders 20 (1), 99-105, 2014
2132014
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
2122017
Genetics of sporadic amyotrophic lateral sclerosis
JC Schymick, K Talbot, BJ Traynor
Human molecular genetics 16 (R2), R233-R242, 2007
2072007
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