Kevin Talbot
Kevin Talbot
Professor of Neurology, Oxford University
Verified email at ndcn.ox.ac.uk
TitleCited byYear
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
7132012
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, 2004
5972004
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
4602008
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, 2004
4052004
Biomarkers in amyotrophic lateral sclerosis
MR Turner, MC Kiernan, PN Leigh, K Talbot
The Lancet Neurology 8 (1), 94-109, 2009
3952009
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
3832013
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, 2007
3052007
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
2591995
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
2302010
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
2122009
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
2012014
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
1902011
Genetics of sporadic amyotrophic lateral sclerosis
JC Schymick, K Talbot, BJ Traynor
Human molecular genetics 16 (R2), R233-R242, 2007
1842007
Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?
K Talbot, CP Ponting, AM Theodosiou, NR Rodrigues, R Surtees, ...
Human molecular genetics 6 (3), 497-500, 1997
1821997
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
1722014
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy
HM McLaughlin, R Sakaguchi, C Liu, T Igarashi, D Pehlivan, K Chu, ...
The American Journal of Human Genetics 87 (4), 560-566, 2010
1642010
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
1612014
A two-stage meta-analysis identifies several new loci for Parkinson's disease
International Parkinson's Disease Genomics Consortium, ...
PLoS genetics 7 (6), e1002142, 2011
1582011
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
1572015
Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations
D Bäumer, D Hilton, SML Paine, MR Turner, J Lowe, K Talbot, O Ansorge
Neurology 75 (7), 611-618, 2010
1532010
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