Stuart Pickering-Brown
Stuart Pickering-Brown
Unknown affiliation
Verified email at manchester.ac.uk
Title
Cited by
Cited by
Year
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
M Hutton, CL Lendon, P Rizzu, M Baker, S Froelich, H Houlden, ...
Nature 393 (6686), 702-705, 1998
35171998
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
32962011
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
M Baker, IR Mackenzie, SM Pickering-Brown, J Gass, R Rademakers, ...
Nature 442 (7105), 916-919, 2006
18012006
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
9082012
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
J Gass, A Cannon, IR Mackenzie, B Boeve, M Baker, J Adamson, R Crook, ...
Human molecular genetics 15 (20), 2988-3001, 2006
5472006
C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins
S Mizielinska, S Grönke, T Niccoli, CE Ridler, EL Clayton, A Devoy, ...
Science 345 (6201), 1192-1194, 2014
4682014
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
JS Snowden, S Rollinson, JC Thompson, JM Harris, CL Stopford, ...
Brain 135 (3), 693-708, 2012
4622012
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
4402019
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699, 2011
4282011
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
H Houlden, M Baker, HR Morris, N MacDonald, S Pickering–Brown, ...
Neurology 56 (12), 1702-1706, 2001
4192001
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
VM Van Deerlin, PMA Sleiman, M Martinez-Lage, A Chen-Plotkin, ...
Nature genetics 42 (3), 234-239, 2010
3992010
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
C Cruchaga, CM Karch, SC Jin, BA Benitez, Y Cai, R Guerreiro, O Harari, ...
Nature 505 (7484), 550-554, 2014
3832014
Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43
YJ Zhang, Y Xu, CA Dickey, E Buratti, F Baralle, R Bailey, ...
Journal of Neuroscience 27 (39), 10530-10534, 2007
3662007
5′ splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10
A Grover, H Houlden, M Baker, J Adamson, J Lewis, G Prihar, ...
Journal of Biological Chemistry 274 (21), 15134-15143, 1999
3151999
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype
IRA Mackenzie, A Baborie, S Pickering-Brown, D Du Plessis, E Jaros, ...
Acta neuropathologica 112 (5), 539-549, 2006
3142006
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies
MA Nalls, R Duran, G Lopez, M Kurzawa-Akanbi, IG McKeith, ...
JAMA neurology 70 (6), 727-735, 2013
3032013
Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43
Y Davidson, T Kelley, IRA Mackenzie, S Pickering-Brown, D Du Plessis, ...
Acta neuropathologica 113 (5), 521-533, 2007
3012007
The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene
IRA Mackenzie, M Baker, S Pickering-Brown, GYR Hsiung, C Lindholm, ...
Brain 129 (11), 3081-3090, 2006
2892006
FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration
H Urwin, KA Josephs, JD Rohrer, IR Mackenzie, M Neumann, A Authier, ...
Acta neuropathologica 120 (1), 33-41, 2010
2492010
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→ T (Arg493X) mutation: an international initiative
R Rademakers, M Baker, J Gass, J Adamson, ED Huey, P Momeni, ...
The Lancet Neurology 6 (10), 857-868, 2007
2212007
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