Maria Mattheijssens

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Marc Cruts, Ilse Gijselinck, Julie van der Zee et al. · Nature · 2006 · 1.5K citations

Life Sciences, Genetics, Molecular Genetics +11

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee et al. · The Lancet Neurology · 2011 · 628 citations

Life Sciences, Genetics, Molecular Genetics +16

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

Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee et al. · Molecular Psychiatry · 2015 · 247 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Nathalie Brouwers, Caroline Van Cauwenberghe, Sebastiaan Engelborghs et al. · Molecular Psychiatry · 2011 · 232 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genetic contribution of <i>FUS</i> to frontotemporal lobar degeneration

Tim Van Langenhove, Julie van der Zee, Kristel Sleegers et al. · Neurology · 2010 · 220 citations

Life Sciences, Genetics, Molecular Genetics +17