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Not available anywhere: 8
Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations
JS Snowden, J Adams, J Harris, JC Thompson, S Rollinson, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 16 (7-8), 497-505, 2015
Mandates: Alzheimers's UK, UK Medical Research Council
Frontotemporal dementia with amyotrophic lateral sclerosis: A clinical comparison of patients with and without repeat expansions in C9orf72
JS Snowden, J Harris, A Richardson, S Rollinson, JC Thompson, D Neary, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 14 (3), 172-176, 2013
Mandates: UK Medical Research Council, Wellcome Trust
TREM2 analysis and increased risk of Alzheimer's disease
D Finelli, S Rollinson, J Harris, M Jones, A Richardson, A Gerhard, ...
Neurobiology of aging 36 (1), 546. e9-546. e13, 2015
Mandates: UK Medical Research Council, Wellcome Trust
No interaction between tau and TDP‐43 pathologies in either frontotemporal lobar degeneration or motor neurone disease
AC Robinson, JC Thompson, L Weedon, S Rollinson, S Pickering‐Brown, ...
Neuropathology and applied neurobiology 40 (7), 844-854, 2014
Mandates: UK Medical Research Council, Wellcome Trust
Psychosis associated with expansions in the C9orf72 gene: the influence of a 10 base pair gene deletion
JS Snowden, J Harris, J Adams, JC Thompson, AM Richardson, ...
Journal of Neurology, Neurosurgery & Psychiatry 87 (5), 562-563, 2016
Mandates: Alzheimers's UK, UK Medical Research Council, Wellcome Trust
A UBQLN2 variant of unknown significance in frontotemporal lobar degeneration
F Ugwu, S Rollinson, J Harris, A Gerhard, A Richardson, M Jones, ...
Neurobiology of aging 36 (1), 546. e15-546. e16, 2015
Mandates: UK Medical Research Council, Wellcome Trust
CRISPR/Cas9 does not facilitate stable expression of long C9orf72 dipeptides in mice
S Ryan, E Hobbs, S Rollinson, SM Pickering-Brown
Neurobiology of Aging 84, 235. e1-235. e8, 2019
Mandates: Motor Neurone Disease Association, UK, UK Medical Research Council
Left hand dystonia as a recurring feature of a family carrying C9ORF72 mutation
S Luzzi, F Girelli, C Fiori, V Ranaldi, S Baldinelli, V Cameriere, ...
Journal of Neurology, Neurosurgery & Psychiatry 87 (7), 793-795, 2016
Mandates: Wellcome Trust
Available somewhere: 41
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron 72 (2), 257-268, 2011
Mandates: US National Institutes of Health, German Research Foundation
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
Mandates: US National Institutes of Health, German Research Foundation, Motor Neurone …
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), 1267-1288, 2018
Mandates: US National Institutes of Health, US Department of Veterans Affairs, Howard …
Frontotemporal dementia and its subtypes: a genome-wide association study
R Ferrari, DG Hernandez, MA Nalls, JD Rohrer, A Ramasamy, JBJ Kwok, ...
The Lancet Neurology 13 (7), 686-699, 2014
Mandates: US National Institutes of Health, Australian Research Council, National …
Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in …
DMA Mann, S Rollinson, A Robinson, J Bennion Callister, JC Thompson, ...
Acta neuropathologica communications 1, 1-13, 2013
Mandates: UK Medical Research Council, Wellcome Trust
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
Mandates: US National Institutes of Health, UK Medical Research Council, Parkinson's …
Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72
YS Davidson, H Barker, AC Robinson, JC Thompson, J Harris, C Troakes, ...
Acta neuropathologica communications 2, 1-13, 2014
Mandates: UK Medical Research Council, Wellcome Trust
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases
R Ferrari, Y Wang, J Vandrovcova, S Guelfi, A Witeolar, CM Karch, ...
Journal of Neurology, Neurosurgery & Psychiatry 88 (2), 152-164, 2017
Mandates: US National Institutes of Health, Alzheimers's UK, UK Medical Research …
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
C Pottier, X Zhou, RB Perkerson, M Baker, GD Jenkins, DJ Serie, ...
The Lancet Neurology 17 (6), 548-558, 2018
Mandates: US National Institutes of Health, US Department of Veterans Affairs …
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains
W Wei, MJ Keogh, I Wilson, J Coxhead, S Ryan, S Rollinson, H Griffin, ...
Acta neuropathologica communications 5, 1-8, 2017
Mandates: Motor Neurone Disease Association, UK, UK Medical Research Council, National …
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in …
C Pottier, Y Ren, RB Perkerson, M Baker, GD Jenkins, M van Blitterswijk, ...
Acta neuropathologica 137, 879-899, 2019
Mandates: US National Institutes of Health, US Department of Veterans Affairs …
Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9orf72 is linked to TDP‐43 pathology and not …
Y Davidson, AC Robinson, X Liu, D Wu, C Troakes, S Rollinson, ...
Neuropathology and applied neurobiology 42 (3), 242-254, 2016
Mandates: Alzheimers's UK, UK Medical Research Council, Wellcome Trust
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