Ilse Gijselinck
Antwerpen, VLG 2610, Belgium
Last Updated: 09/26/2026
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Found 19 publications
Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.
Journal: Acta neuropathologica
Published: October 05, 2024
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort.
Journal: Neurobiology of aging
Published: April 13, 2017
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.
Journal: JAMA neurology
Published: February 14, 2017
The Genetics of C9orf72 Expansions.
Journal: Cold Spring Harbor perspectives in medicine
Published: January 29, 2017
Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: November 09, 2016
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
Journal: Human mutation
Published: October 10, 2016
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD.
Journal: Scientific reports
Published: August 07, 2015
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
Journal: Brain : a journal of neurology
Published: July 23, 2015
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.
Journal: Neurology
Published: May 19, 2015
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter.
Journal: Molecular psychiatry
Published: May 12, 2015
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.
Journal: Neurology
Published: October 19, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
Journal: Acta neuropathologica
Published: October 17, 2013
Last Updated: 09/26/2026