Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis M Neumann, DM Sampathu, LK Kwong, AC Truax, MC Micsenyi, TT Chou, ... Science 314 (5796), 130-133, 2006 | 7313 | 2006 |
Pathological TDP‐43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations IRA Mackenzie, EH Bigio, PG Ince, F Geser, M Neumann, NJ Cairns, ... Annals of Neurology: Official Journal of the American Neurological …, 2007 | 1243 | 2007 |
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update IRA Mackenzie, M Neumann, EH Bigio, NJ Cairns, I Alafuzoff, J Kril, ... Acta neuropathologica 119, 1-4, 2010 | 1211 | 2010 |
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration NJ Cairns, EH Bigio, IRA Mackenzie, M Neumann, VMY Lee, ... Acta neuropathologica 114, 5-22, 2007 | 1211 | 2007 |
TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia IRA Mackenzie, R Rademakers, M Neumann The Lancet Neurology 9 (10), 995-1007, 2010 | 1195 | 2010 |
A harmonized classification system for FTLD-TDP pathology IRA Mackenzie, M Neumann, A Baborie, DM Sampathu, D Du Plessis, ... Acta neuropathologica 122, 111-113, 2011 | 1057 | 2011 |
ALS‐associated fused in sarcoma (FUS) mutations disrupt Transportin‐mediated nuclear import D Dormann, R Rodde, D Edbauer, E Bentmann, I Fischer, A Hruscha, ... The EMBO journal 29 (16), 2841-2857, 2010 | 976 | 2010 |
A new subtype of frontotemporal lobar degeneration with FUS pathology M Neumann, R Rademakers, S Roeber, M Baker, HA Kretzschmar, ... Brain 132 (11), 2922-2931, 2009 | 912 | 2009 |
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis VM Van Deerlin, JB Leverenz, LM Bekris, TD Bird, W Yuan, LB Elman, ... The Lancet Neurology 7 (5), 409-416, 2008 | 889 | 2008 |
Subcellular localization of wild-type and Parkinson's disease-associated mutant α-synuclein in human and transgenic mouse brain PJ Kahle, M Neumann, L Ozmen, V Müller, H Jacobsen, A Schindzielorz, ... Journal of Neuroscience 20 (17), 6365-6373, 2000 | 856 | 2000 |
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 | 631 | 2010 |
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies M Neumann, LK Kwong, EB Lee, E Kremmer, A Flatley, Y Xu, MS Forman, ... Acta neuropathologica 117, 137-149, 2009 | 615 | 2009 |
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions NJ Cairns, M Neumann, EH Bigio, IE Holm, D Troost, KJ Hatanpaa, ... The American journal of pathology 171 (1), 227-240, 2007 | 594 | 2007 |
Frontotemporal lobar degeneration: demographic characteristics of 353 patients JK Johnson, J Diehl, MF Mendez, J Neuhaus, JS Shapira, M Forman, ... Archives of neurology 62 (6), 925-930, 2005 | 589 | 2005 |
Advances in understanding the molecular basis of frontotemporal dementia R Rademakers, M Neumann, IR Mackenzie Nature Reviews Neurology 8 (8), 423-434, 2012 | 515 | 2012 |
Neuropathological background of phenotypical variability in frontotemporal dementia KA Josephs, JR Hodges, JS Snowden, IR Mackenzie, M Neumann, ... Acta neuropathologica 122, 137-153, 2011 | 512 | 2011 |
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations IRA Mackenzie, M Neumann, EH Bigio, NJ Cairns, I Alafuzoff, J Kril, ... Acta neuropathologica 117, 15-18, 2009 | 499 | 2009 |
Misfolded proteinase K–resistant hyperphosphorylated α-synuclein in aged transgenic mice with locomotor deterioration and in human α-synucleinopathies M Neumann, PJ Kahle, BI Giasson, L Ozmen, E Borroni, W Spooren, ... The Journal of clinical investigation 110 (10), 1429-1439, 2002 | 475 | 2002 |
Neurofilament light chain in blood and CSF as marker of disease progression in mouse models and in neurodegenerative diseases M Bacioglu, LF Maia, O Preische, J Schelle, A Apel, SA Kaeser, ... Neuron 91 (1), 56-66, 2016 | 465 | 2016 |
hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations K Mori, S Lammich, IRA Mackenzie, I Forné, S Zilow, H Kretzschmar, ... Acta neuropathologica 125, 413-423, 2013 | 425 | 2013 |