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| 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 | 746 | 2004 |
| 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 | 625 | 2013 |
| 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 | 609 | 2008 |
| 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 | 576 | 2018 |
| Biomarkers in amyotrophic lateral sclerosis MR Turner, MC Kiernan, PN Leigh, K Talbot The Lancet Neurology 8 (1), 94-109, 2009 | 510 | 2009 |
| Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy J Irobi, KV Impe, P Seeman, A Jordanova, I Dierick, N Verpoorten, ... Nature genetics 36 (6), 597-601, 2004 | 500 | 2004 |
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| 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 | 428 | 2008 |
| Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model HJ Westeneng, TPA Debray, AE Visser, RPA van Eijk, JPK Rooney, ... The Lancet Neurology 17 (5), 423-433, 2018 | 423 | 2018 |
| 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 | 420 | 2014 |
| 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 | 411 | 2014 |
| 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 | 410 | 2016 |
| 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 | 380 | 2014 |
| 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 | 373 | 2017 |
| ER stress and autophagic perturbations lead to elevated extracellular α-synuclein in GBA-N370S Parkinson's iPSC-derived dopamine neurons HJR Fernandes, EM Hartfield, HC Christian, E Emmanoulidou, Y Zheng, ... Stem cell reports 6 (3), 342-356, 2016 | 349 | 2016 |
| A proposal for new diagnostic criteria for ALS JM Shefner, A Al-Chalabi, MR Baker, LY Cui, M de Carvalho, A Eisen, ... Clinical Neurophysiology 131 (8), 2020 | 347 | 2020 |
| Extracellular vesicles in neurodegenerative disease—pathogenesis to biomarkers AG Thompson, E Gray, SM Heman-Ackah, I Mäger, K Talbot, ... Nature Reviews Neurology 12 (6), 346-357, 2016 | 344 | 2016 |
| 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 | 321 | 2010 |
| 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 | 304 | 2014 |
Martin R. TurnerNuffield Department of Clinical Neurosciences, Oxford UniversityVerifierad e-postadress på ndcn.ox.ac.uk
