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Rosa Rademakers
Rosa Rademakers
Professor of neuroscience, Mayo Clinic
Verified email at uantwerpen.vib.be
Title
Cited by
Cited by
Year
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
M DeJesus-Hernandez, IR Mackenzie, BF Boeve, AL Boxer, M Baker, ...
Neuron 72 (2), 245-256, 2011
52732011
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
30572013
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
M Baker, IR Mackenzie, SM Pickering-Brown, J Gass, R Rademakers, ...
Nature 442 (7105), 916-919, 2006
22312006
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
M Cruts, I Gijselinck, J Van Der Zee, S Engelborghs, H Wils, D Pirici, ...
Nature 442 (7105), 920-924, 2006
16732006
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
HJ Kim, NC Kim, YD Wang, EA Scarborough, J Moore, Z Diaz, ...
Nature 495 (7442), 467-473, 2013
15232013
Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS
PEA Ash, KF Bieniek, TF Gendron, T Caulfield, WL Lin, ...
Neuron 77 (4), 639-646, 2013
11902013
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
11292010
Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report
PT Nelson, DW Dickson, JQ Trojanowski, CR Jack, PA Boyle, K Arfanakis, ...
Brain 142 (6), 1503-1527, 2019
10322019
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
8582009
TDP‐43 A315T mutation in familial motor neuron disease
MA Gitcho, RH Baloh, S Chakraverty, K Mayo, JB Norton, D Levitch, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
7562008
Progranulin deficiency promotes circuit-specific synaptic pruning by microglia via complement activation
H Lui, J Zhang, SR Makinson, MK Cahill, KW Kelley, HY Huang, Y Shang, ...
Cell 165 (4), 921-935, 2016
6492016
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
J Gass, A Cannon, IR Mackenzie, B Boeve, M Baker, J Adamson, R Crook, ...
Human molecular genetics 15 (20), 2988-3001, 2006
6492006
Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS
TF Gendron, KF Bieniek, YJ Zhang, K Jansen-West, PEA Ash, T Caulfield, ...
Acta neuropathologica 126, 829-844, 2013
6182013
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699-705, 2011
6162011
Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice
YF Xu, TF Gendron, YJ Zhang, WL Lin, S D'Alton, H Sheng, MC Casey, ...
Journal of Neuroscience 30 (32), 10851-10859, 2010
5942010
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
5892010
Longitudinal Modeling of Age-Related Memory Decline and the APOE ε4 Effect
RJ Caselli, AC Dueck, D Osborne, MN Sabbagh, DJ Connor, GL Ahern, ...
New England Journal of Medicine 361 (3), 255-263, 2009
5872009
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5762018
TIA1 mutations in amyotrophic lateral sclerosis and frontotemporal dementia promote phase separation and alter stress granule dynamics
IR Mackenzie, AM Nicholson, M Sarkar, J Messing, MD Purice, C Pottier, ...
Neuron 95 (4), 808-816. e9, 2017
5582017
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
NJ Rutherford, YJ Zhang, M Baker, JM Gass, NCA Finch, YF Xu, ...
PLoS genetics 4 (9), e1000193, 2008
5292008
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