Dinucleotide repeat polymorphism at the D21S145 locus

per Cruts, M., Backhovens, H., Van Broeckhoven, C.
Publicat 1992

Dinucleotide repeat polymorphism at the D1S16 locus

per Cruts, M., Backhovens, H., Van Broeckhoven, C.
Publicat 1992

Apolipoprotein E4 in the temporal variant of frontotemporal dementia

per Rosso, S, van Swieten, J C, Roks, G, van Duijn, C M, Heutink, P, Cruts, M, van Broeckhoven, C
Publicat 2002

A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer disease.

per Tysoe, C, Whittaker, J, Xuereb, J, Cairns, N J, Cruts, M, Van Broeckhoven, C, Wilcock, G, Rubinsztein, D C
Publicat 1998

A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21.

per van Duijn, C. M., Hendriks, L., Farrer, L. A., Backhovens, H., Cruts, M., Wehnert, A., Hofman, A., Van Broeckhoven, C.
Publicat 1994

Genetic association of apolipoprotein E with age-related macular degeneration.

per Klaver, C C, Kliffen, M, van Duijn, C M, Hofman, A, Cruts, M, Grobbee, D E, van Broeckhoven, C, de Jong, P T
Publicat 1998

Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

per Engelborghs, S, Dermaut, B, Goeman, J, Saerens, J, Marien, P, Pickut, B., Van den Broeck, M, Serneels, S, Cruts, M, Van Broeckhoven, C, De Deyn, P P
Publicat 2003

Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

per Engelborghs, S, Dermaut, B, Goeman, J, Saerens, J, Marien, P, Pickut, B., Van den Broeck, M, Serneels, S, Cruts, M, Van Broeckhoven, C, De Deyn, P P
Publicat 2003

The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease.

per Dermaut, B, Cruts, M, Slooter, A J, Van Gestel, S, De Jonghe, C, Vanderstichele, H, Vanmechelen, E, Breteler, M M, Hofman, A, van Duijn, C M, Van Broeckhoven, C
Publicat 1999

Octapeptide repeat insertions in the prion protein gene and early onset dementia

per Croes, E, Theuns, J, Houwing-Duisterma..., J, Dermaut, B, Sleegers, K, Roks, G, Van den Broeck, M, van Harten, B, van Swieten, J C, Cruts, M, Van Broeckhoven, C, van Duijn, C M
Publicat 2004

Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites

per Brouwers, N, Van Cauwenberghe, C, Engelborghs, S, Lambert, J-C, Bettens, K, Le Bastard, N, Pasquier, F, Montoya, A Gil, Peeters, K, Mattheijssens, M, Vandenberghe, R, De Deyn, P P, Cruts, M, Amouyel, P, Sleegers, K, Van Broeckhoven, C
Publicat 2012

The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

per Gijselinck, I, Van Mossevelde, S, van der Zee, J, Sieben, A, Engelborghs, S, De Bleecker, J, Ivanoiu, A, Deryck, O, Edbauer, D, Zhang, M, Heeman, B, Bäumer, V, Van den Broeck, M, Mattheijssens, M, Peeters, K, Rogaeva, E, De Jonghe, P, Cras, P, Martin, J-J, de Deyn, P P, Cruts, M, Van Broeckhoven, C
Publicat a Mol Psychiatry (2016)