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Marc Cruts
Marc Cruts
Professor of Molecular Genomics
Verified email at molgen.vib-ua.be
Title
Cited by
Cited by
Year
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
16642006
The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS
K Mori, SM Weng, T Arzberger, S May, K Rentzsch, E Kremmer, B Schmid, ...
Science 339 (6125), 1335-1338, 2013
13562013
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β-amyloid precursor protein gene
L Hendriks, CM van Duijn, P Cras, M Cruts, W Hul, F Harskamp, A Warren, ...
Nature genetics 1, 218-221, 1992
11151992
A< i> C9orf72</i> promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene …
I Gijselinck, T Van Langenhove, J van der Zee, K Sleegers, S Philtjens, ...
The Lancet Neurology 11 (1), 54-65, 2012
7632012
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update
K Nuytemans, J Theuns, M Cruts, C Van Broeckhoven
Human mutation 31 (7), 763-780, 2010
6672010
Locus‐specific mutation databases for neurodegenerative brain diseases
M Cruts, J Theuns, C Van Broeckhoven
Human mutation 33 (9), 1340-1344, 2012
5962012
Genetic association of apolipoprotein E with age-related macular degeneration
CCW Klaver, M Kliffen, CM van Duijn, A Hofman, M Cruts, DE Grobbee, ...
The American Journal of Human Genetics 63 (1), 200-206, 1998
5761998
Apolipoprotein E4 allele in a population-based study of early-onset Alzheimer's disease
CM van Duijn, P Knijff, M Cruts, A Wehnert, LM Havekes, C Broeckhoven, ...
Nature genetics 7, 74-78, 1994
5631994
Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins
K Mori, T Arzberger, FA Grässer, I Gijselinck, S May, K Rentzsch, ...
Acta neuropathologica 126 (6), 881-893, 2013
5312013
Estimation of the genetic contribution of presenilin-1 and-2 mutations in a population-based study of presenile Alzheimer disease
M Cruts, CM van Duijn, H Backhovens, M Van den Broeck, A Wehnert, ...
Human Molecular Genetics 7 (1), 43-51, 1998
5171998
Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study
AJC Slooter, M Cruts, S Kalmijn, A Hofman, MMB Breteler, ...
Archives of Neurology 55 (7), 964-968, 1998
4951998
Mean age‐of‐onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
S Kumar‐Singh, J Theuns, B Van Broeck, D Pirici, K Vennekens, ...
Human mutation 27 (7), 686-695, 2006
4642006
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy
K Sleegers, N Brouwers, I Gijselinck, J Theuns, D Goossens, J Wauters, ...
Brain 129 (11), 2977-2983, 2006
4602006
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24. 3
C Van Broeckhoven, H Backhovens, M Cruts, G De Winter, M Bruyland, ...
Nature genetics 2 (4), 335-339, 1992
4581992
The role of tau (MAPT) in frontotemporal dementia and related tauopathies
R Rademakers, M Cruts, C Van Broeckhoven
Human mutation 24 (4), 277-295, 2004
4302004
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 (3), 413-423, 2013
3972013
The genetics and neuropathology of frontotemporal lobar degeneration
A Sieben, T Van Langenhove, S Engelborghs, JJ Martin, P Boon, P Cras, ...
Acta neuropathologica 124 (3), 353-372, 2012
3492012
A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
J van der Zee, I Gijselinck, L Dillen, T Van Langenhove, J Theuns, ...
Human mutation 34 (2), 363-373, 2013
3162013
novoSNP, a novel computational tool for sequence variation discovery
S Weckx, J Del-Favero, R Rademakers, L Claes, M Cruts, P De Jonghe, ...
Genome Research 15 (3), 436-442, 2005
3162005
Presenilin mutations in Alzheimer's disease
M Cruts, C Van Broeckhoven
Human mutation 11 (3), 183-190, 1998
3001998
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