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Tammaryn Lashley
Tammaryn Lashley
Institute of Neurology, UCL, London
E-mail confirmado em ucl.ac.uk
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TREM2 variants in Alzheimer's disease
R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ...
New England Journal of Medicine 368 (2), 117-127, 2013
32542013
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation
JY Li, E Englund, JL Holton, D Soulet, P Hagell, AJ Lees, T Lashley, ...
Nature medicine 14 (5), 501-503, 2008
21362008
Lewy-and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important?
Y Compta, L Parkkinen, SS O'Sullivan, J Vandrovcova, JL Holton, ...
Brain 134 (5), 1493-1505, 2011
6462011
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
6252010
Structure-based classification of tauopathies
Y Shi, W Zhang, Y Yang, AG Murzin, B Falcon, A Kotecha, M van Beers, ...
Nature 598 (7880), 359-363, 2021
5992021
The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease
R Bandopadhyay, AE Kingsbury, MR Cookson, AR Reid, IM Evans, ...
Brain 127 (2), 420-430, 2004
5842004
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
4892012
C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci
S Mizielinska, T Lashley, FE Norona, EL Clayton, CE Ridler, P Fratta, ...
Acta neuropathologica 126, 845-857, 2013
4102013
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
JD Rohrer, T Lashley, JM Schott, JE Warren, S Mead, AM Isaacs, J Beck, ...
Brain 134 (9), 2565-2581, 2011
4082011
Cerebral amyloid angiopathies: a pathologic, biochemical, and genetic view
T Revesz, J Ghiso, T Lashley, G Plant, A Rostagno, B Frangione, ...
Journal of Neuropathology & Experimental Neurology 62 (9), 885-898, 2003
3722003
Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies
T Revesz, JL Holton, T Lashley, G Plant, B Frangione, A Rostagno, ...
Acta neuropathologica 118, 115-130, 2009
3592009
C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis
JD Rohrer, AM Isaacs, S Mizielinska, S Mead, T Lashley, S Wray, K Sidle, ...
The Lancet Neurology 14 (3), 291-301, 2015
2952015
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ...
Nature genetics 53 (3), 294-303, 2021
2772021
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A
AL Brown, OG Wilkins, MJ Keuss, SE Hill, M Zanovello, WC Lee, ...
Nature 603 (7899), 131-137, 2022
2712022
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies
J Bras, R Guerreiro, L Darwent, L Parkkinen, O Ansorge, V Escott-Price, ...
Human molecular genetics 23 (23), 6139-6146, 2014
2672014
Sporadic and familial cerebral amyloid angiopathies
T Revesz, JL Holton, T Lashley, G Plant, A Rostagno, J Ghiso, ...
Brain pathology 12 (3), 343-357, 2002
2652002
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
R Guerreiro, OA Ross, C Kun-Rodrigues, DG Hernandez, T Orme, ...
The Lancet Neurology 17 (1), 64-74, 2018
2622018
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series
NS Ryan, JM Nicholas, PSJ Weston, Y Liang, T Lashley, R Guerreiro, ...
The Lancet Neurology 15 (13), 1326-1335, 2016
2492016
Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule‐binding repeat domains as demonstrated by new specific …
R De Silva, T Lashley, G Gibb, D Hanger, A Hope, A Reid, ...
Neuropathology and applied neurobiology 29 (3), 288-302, 2003
2482003
Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11
H Houlden, J Johnson, C Gardner-Thorpe, T Lashley, D Hernandez, ...
Nature genetics 39 (12), 1434-1436, 2007
2462007
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