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
9742012
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
6582004
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
5322008
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
4902013
Biomarkers in amyotrophic lateral sclerosis
MR Turner, MC Kiernan, PN Leigh, K Talbot
The Lancet Neurology 8 (1), 94-109, 2009
4482009
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
4442004
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
3612008
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
2932014
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
2842015
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
2742014
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
2742010
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
2701995
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
2492018
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 Genet 5 (12), e1000773, 2009
2482009
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
2422014
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
2292011
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
2202016
Genetics of sporadic amyotrophic lateral sclerosis
JC Schymick, K Talbot, BJ Traynor
Human molecular genetics 16 (R2), R233-R242, 2007
2052007
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
1942014
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
1902017
The system can't perform the operation now. Try again later.
Articles 1–20