Kevin Talbot

Overview

Best Publications

• Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

  Elisa Majounie;Alan E. Renton;Kin Mok;Elise G. P. Dopper;Elise G. P. Dopper

  1367
  Citations

• Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy

  Oleg V Evgrafov;Irena Mersiyanova;Joy Irobi;Ludo Van Den Bosch

  735
  Citations

• Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

  Aude Nicolas;Kevin P. Kenna;Alan E. Renton;Alan E. Renton;Nicola Ticozzi

  700
  Citations

• Controversies and priorities in amyotrophic lateral sclerosis

  Martin R Turner;Orla Hardiman;Michael Benatar;Benjamin R Brooks

  645
  Citations

• Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS.

  Bradley J Turner;Kevin Talbot;Kevin Talbot

  601
  Citations

• A proposal for new diagnostic criteria for ALS

  Jeremy M. Shefner;Ammar Al-Chalabi;Mark R. Baker;Li-Ying Cui

  525
  Citations

• Biomarkers in amyotrophic lateral sclerosis.

  Martin R Turner;Matthew C Kiernan;P Nigel Leigh;Kevin Talbot

  515
  Citations

• Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model

  Henk Jan Westeneng;Thomas P.A. Debray;Anne E. Visser;Ruben P.A. van Eijk

  506
  Citations

• Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy.

  Joy Irobi;Katrien Van Impe;Pavel Seeman;Albena Jordanova

  498
  Citations

• Neurofilament light chain: A prognostic biomarker in amyotrophic lateral sclerosis.

  Ching-Hua Lu;Corrie Macdonald-Wallis;Elizabeth Gray;Neil Pearce

  491
  Citations

• Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

  Suzanne Lesage;Valérie Drouet;Elisa Majounie;Vincent Deramecourt

  454
  Citations

• Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy

  Lyndsay M. Murray;Laura H. Comley;Derek Thomson;Nick Parkinson

  428
  Citations

• Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

  B N Smith;N Ticozzi;C Fallini;A S Gkazi

  427
  Citations

• Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

  A. Beilina;I. N. Rudenko;A. Kaganovich;L. Civiero

  402
  Citations

• ER Stress and Autophagic Perturbations Lead to Elevated Extracellular α-Synuclein in GBA-N370S Parkinson's iPSC-Derived Dopamine Neurons

  Hugo J.R. Fernandes;Elizabeth M. Hartfield;Helen C. Christian;Evangelia Emmanoulidou

  377
  Citations

• Extracellular vesicles in neurodegenerative disease - pathogenesis to biomarkers

  Alexander G. Thompson;Elizabeth Gray;Sabrina M. Heman-Ackah;Imre Mäger

  354
  Citations

• 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

  Konrad Szewczyk-Krolikowski;Paul Tomlinson;Kannan Nithi;Richard Wade-Martins

  345
  Citations

• Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis

  N Filippini;G Douaud;C E Mackay;S Knight

  330
  Citations

• Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy

  N.R. Rodrigues;N. Owen;K. Talbot;J. Ignatius

  300
  Citations

• Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene

  Aude Nicolas;Kevin P. Kenna;Alan E. Renton;Nicola Ticozzi

  8
  Citations