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Simon Mead
Simon Mead
Deputy Director MRC Prion Unit at UCL; CJD specialist UCLH
Verified email at prion.ucl.ac.uk - Homepage
Title
Cited by
Cited by
Year
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452-1458, 2013
42362013
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
D Harold, R Abraham, P Hollingworth, R Sims, A Gerrish, ML Hamshere, ...
Nature genetics 41 (10), 1088-1093, 2009
32442009
TREM2 variants in Alzheimer's disease
R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ...
New England Journal of Medicine, 2013
29172013
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
P Hollingworth, D Harold, R Sims, A Gerrish, JC Lambert, ...
Nature genetics 43 (5), 429-435, 2011
21182011
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
20802019
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13082018
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
12732012
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
8792017
New insights into the genetic etiology of Alzheimer’s disease and related dementias
C Bellenguez, F Küçükali, IE Jansen, L Kleineidam, S Moreno-Grau, ...
Nature genetics 54 (4), 412-436, 2022
7412022
The heritability and genetics of frontotemporal lobar degeneration
JD Rohrer, R Guerreiro, J Vandrovcova, J Uphill, D Reiman, J Beck, ...
Neurology 73 (18), 1451-1456, 2009
5642009
A stop-codon mutation in the BRI gene associated with familial British dementia
R Vidal, B Frangione, A Rostagno, S Mead, T Révész, G Plant, J Ghiso
Nature 399 (6738), 776-781, 1999
5551999
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
JD Rohrer, JM Nicholas, DM Cash, J Van Swieten, E Dopper, L Jiskoot, ...
The Lancet Neurology 14 (3), 253-262, 2015
5472015
Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy
Z Jaunmuktane, S Mead, M Ellis, JDF Wadsworth, AJ Nicoll, J Kenny, ...
Nature 525 (7568), 247-250, 2015
5422015
Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes
ITS Coyle-Gilchrist, KM Dick, K Patterson, P Vázquez Rodríquez, ...
Neurology 86 (18), 1736-1743, 2016
4982016
Kuru in the 21st century—an acquired human prion disease with very long incubation periods
J Collinge, J Whitfield, E McKintosh, J Beck, S Mead, DJ Thomas, ...
The Lancet 367 (9528), 2068-2074, 2006
4932006
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics
S Mead, MPH Stumpf, J Whitfield, JA Beck, M Poulter, T Campbell, ...
Science 300 (5619), 640-643, 2003
4722003
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
CJ Mahoney, J Beck, JD Rohrer, T Lashley, K Mok, T Shakespeare, ...
Brain 135 (3), 736-750, 2012
4712012
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease
L Jones, PA Holmans, ML Hamshere, D Harold, V Moskvina, D Ivanov, ...
PloS one 5 (11), e13950, 2010
4462010
Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia
JD Rohrer, IOC Woollacott, KM Dick, E Brotherhood, E Gordon, A Fellows, ...
Neurology 87 (13), 1329-1336, 2016
4182016
Common polygenic variation enhances risk prediction for Alzheimer’s disease
V Escott-Price, R Sims, C Bannister, D Harold, M Vronskaya, E Majounie, ...
Brain 138 (12), 3673-3684, 2015
4112015
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