Johnathan Cooper-Knock
Johnathan Cooper-Knock
Clinical Fellow, University of Sheffield
Verified email at
Cited by
Cited by
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72
J Cooper-Knock, C Hewitt, JR Highley, A Brockington, A Milano, S Man, ...
Brain 135 (3), 751-764, 2012
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
Sequestration of multiple RNA recognition motif-containing proteins by C9orf72 repeat expansions
J Cooper-Knock, MJ Walsh, A Higginbottom, J Robin Highley, ...
Brain 137 (7), 2040-2051, 2014
Gene expression profiling in human neurodegenerative disease
J Cooper-Knock, J Kirby, L Ferraiuolo, PR Heath, M Rattray, PJ Shaw
Nature Reviews Neurology 8 (9), 518-530, 2012
The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype
J Cooper-Knock, PJ Shaw, J Kirby
Acta neuropathologica 127 (3), 333-345, 2014
Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy
J Cooper-Knock, A Higginbottom, MJ Stopford, JR Highley, PG Ince, ...
Acta neuropathologica 130 (1), 63-75, 2015
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions
MD Gallagher, E Suh, M Grossman, L Elman, L McCluskey, ...
Acta neuropathologica 127 (3), 407-418, 2014
C9ORF72 GGGGCC expanded repeats produce splicing dysregulation which correlates with disease severity in amyotrophic lateral sclerosis
J Cooper-Knock, JJ Bury, PR Heath, M Wyles, A Higginbottom, ...
PloS one 10 (5), e0127376, 2015
Loss of nuclear TDP‐43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones
JR Highley, J Kirby, JA Jansweijer, PS Webb, CA Hewamadduma, ...
Neuropathology and applied neurobiology 40 (6), 670-685, 2014
Serum miRNAs miR-206, 143-3p and 374b-5p as potential biomarkers for amyotrophic lateral sclerosis (ALS)
R Waller, EF Goodall, M Milo, J Cooper-Knock, M Da Costa, E Hobson, ...
Neurobiology of aging 55, 123-131, 2017
SRSF1-dependent nuclear export inhibition of C9ORF72 repeat transcripts prevents neurodegeneration and associated motor deficits
GM Hautbergue, LM Castelli, L Ferraiuolo, A Sanchez-Martinez, ...
Nature communications 8 (1), 1-18, 2017
Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72
A Ismail, J Cooper-Knock, JR Highley, A Milano, J Kirby, E Goodall, ...
Journal of Neurology, Neurosurgery & Psychiatry 84 (1), 79-87, 2013
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis
S Bandres‐Ciga, AJ Noyce, G Hemani, A Nicolas, A Calvo, G Mora, ...
Annals of neurology 85 (4), 470-481, 2019
Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation
VL Buchman, J Cooper-Knock, N Connor-Robson, A Higginbottom, ...
Molecular neurodegeneration 8 (1), 1-6, 2013
C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study
J Cooper-Knock, A Frolov, JR Highley, G Charlesworth, J Kirby, A Milano, ...
Neurology 81 (9), 808-811, 2013
The spectrum of C9orf72-mediated neurodegeneration and amyotrophic lateral sclerosis
J Cooper-Knock, J Kirby, R Highley, PJ Shaw
Neurotherapeutics 12 (2), 326-339, 2015
Invited review: decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the art
MJ Walsh, J Cooper‐Knock, JE Dodd, MJ Stopford, SR Mihaylov, J Kirby, ...
Neuropathology and Applied Neurobiology 41 (2), 109-134, 2015
How well do we recognise non-motor symptoms in a British Parkinson’s disease population?
M Hu, J Cooper, R Beamish, E Jones, R Butterworth, L Catterall, ...
Journal of neurology 258 (8), 1513-1517, 2011
C9ORF72 transcription in a frontotemporal dementia case with two expanded alleles
J Cooper-Knock, A Higginbottom, N Connor-Robson, N Bayatti, JJ Bury, ...
Neurology 81 (19), 1719-1721, 2013
Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP‐43‐negative inclusions of C9ORF72‐ALS
JJ Bury, JR Highley, J Cooper‐Knock, EF Goodall, A Higginbottom, ...
Neuropathology 36 (2), 125-134, 2016
The system can't perform the operation now. Try again later.
Articles 1–20