Simon Mead

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	Wszystkie	Od 2020
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232 artykuły

10 artykułów

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Współautorzy

Jonathan RohrerUCL Institute of NeurologyZweryfikowany adres z ucl.ac.uk
Nick C FoxProfessor of Neurology, UCLZweryfikowany adres z ucl.ac.uk
Sebastian BrandnerProfessor of Neuropathology, UCLZweryfikowany adres z ucl.ac.uk
Prof Jonathan M SchottInstitute of Neurology, UCLZweryfikowany adres z ucl.ac.uk
Professor Tamas ReveszEmeritus Professor of Neuropathology, UCL Queen Square Institute of Neurology, Univ Coll LondonZweryfikowany adres z ucl.ac.uk
Tammaryn LashleyInstitute of Neurology, UCL, LondonZweryfikowany adres z ucl.ac.uk
Jonathan DF WadsworthMRC Investigator, MRC Prion Unit at UCLZweryfikowany adres z ucl.ac.uk
Sebastien OurselinProfessor of Healthcare Engineering, King's College LondonZweryfikowany adres z kcl.ac.uk
Rita GuerreiroVan Andel Research InstituteZweryfikowany adres z vai.org
Gerard R. RidgwayOxford Brain Diagnostics LtdZweryfikowany adres z oxfordbraindiagnostics.com
Graham JacksonUCL Institute of Prion DiseasesZweryfikowany adres z prion.ucl.ac.uk
Adrian IsaacsUCL Institute of NeurologyZweryfikowany adres z ucl.ac.uk
Colin MahoneyUniversity of SydneyZweryfikowany adres z sydney.edu.au
Andrew SingletonNational Institute on AgingZweryfikowany adres z mail.nih.gov
Minerva CarrasquilloMayo ClinicZweryfikowany adres z mayo.edu
Jose BrasRegeneron Genetics Center, Regeneron PharmaceuticalsZweryfikowany adres z regeneron.com
Sarah WalkerProfessor of Medical Statistics and Epidemiology, Oxford University and University College LondonZweryfikowany adres z ndm.ox.ac.uk
cath mummeryconsultant neurologistZweryfikowany adres z uclh.nhs.uk
Sarah J TabriziProfessor of Neurology UCLZweryfikowany adres z prion.ucl.ac.uk
Kevin MorganProfessor University of NottinghamZweryfikowany adres z nottingham.ac.uk

Obserwuj

Simon Mead

Deputy Director MRC Prion Unit at UCL; CJD specialist UCLH; NIHR Senior Investigator

Zweryfikowany adres z prion.ucl.ac.uk - Strona główna

Prion Prions Prion disease Prion diseases Genetics


Tytuł Sortuj wg cytatów Sortuj wg roku Sortuj wg tytułu	Cytowane przez Cytowane przez	Rok
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	4746	2013
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	3453	2009
TREM2 variants in Alzheimer's disease R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ... New England Journal of Medicine, 2013	3350	2013
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	2673	2019
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	2322	2011
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	1583	2022
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1557	2018
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	1406	2012
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	1012	2017
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	635	2009
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	601	2015
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	596	2015
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	589	2016
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	584	1999
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	532	2006
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	495	2012
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	489	2003
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	484	2016
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	476	2010
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	470	2015

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