Gijselinck, Ilse
University of Antwerp · Institute Born-Bunge
7 papers on CoChat
Most cited papers
- Verified
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
Cruts, M., Gijselinck, I., van der Zee, J., Engelborghs, S., Wils, H., Pirici, D., Rademakers, R., Vandenberghe, R., Dermaut, B., Martin, J.-J., et al. (2006) · Nature
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 1,512
- Verified
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD
Boeynaems, S., Bogaert, E., Michiels, E., Gijselinck, I., Sieben, A., Jovičić, A., De Baets, G., Scheveneels, W., Steyaert, J., Cuijt, I., et al. (2016) · Scientific Reports
Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative Diseases
Cited by 262
- Verified
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
on behalf of the BELNEU CONSORTIUM, Gijselinck, I., Van Mossevelde, S., van der Zee, J., Sieben, A., Engelborghs, S., De Bleecker, J., Ivanoiu, A., Deryck, O., Edbauer, D., et al. (2016) · Molecular Psychiatry
Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative Diseases
Cited by 242
- Verified
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
Gijselinck, I., Van Mossevelde, S., van der Zee, J., Sieben, A., Philtjens, S., Heeman, B., Engelborghs, S., Vandenbulcke, M., De Baets, G., Bäumer, V., et al. (2015) · Neurology
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 174
- Verified
Clinical features of TBK1 carriers compared with C9orf72,GRN and non-mutation carriers in a Belgian cohort
Van Mossevelde, S., van der Zee, J., Gijselinck, I., Engelborghs, S., Sieben, A., Van Langenhove, T., De Bleecker, J., Baets, J., Vandenbulcke, M., Van Laere, K., et al. (2016) · Brain
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 98
- Verified
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD
van der Zee, J., Rademakers, R., Engelborghs, S., Gijselinck, I., Bogaerts, V., Vandenberghe, R., Santens, P., Caekebeke, J., De Pooter, T., Peeters, K., et al. (2006) · Brain
Alzheimer's disease research and treatmentsAmyotrophic Lateral Sclerosis Research
Cited by 90
- Verified
C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment
Cacace, R., Van Cauwenberghe, C., Bettens, K., Gijselinck, I., van der Zee, J., Engelborghs, S., Vandenbulcke, M., Van Dongen, J., Bäumer, V., Dillen, L., et al. (2013) · Neurobiology of Aging
Alzheimer's disease research and treatmentsAmyotrophic Lateral Sclerosis Research
Cited by 74
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