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 | 3254 | 2013 |
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 | 2136 | 2008 |
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 | 646 | 2011 |
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 | 625 | 2010 |
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 | 599 | 2021 |
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 | 584 | 2004 |
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 | 489 | 2012 |
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 | 410 | 2013 |
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 | 408 | 2011 |
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 | 372 | 2003 |
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 | 359 | 2009 |
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 | 295 | 2015 |
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 | 277 | 2021 |
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 | 271 | 2022 |
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 | 267 | 2014 |
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 | 265 | 2002 |
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 | 262 | 2018 |
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 | 249 | 2016 |
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 | 248 | 2003 |
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 | 246 | 2007 |