Veerle Baumer
Antwerpen, VLG, Belgium
Last Updated: 09/26/2026
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Found 8 publications
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.
Journal: JAMA neurology
Published: February 14, 2017
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
Journal: Human mutation
Published: October 10, 2016
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
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.
Journal: JAMA neurology
Published: January 23, 2013
C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment.
Journal: Neurobiology of aging
Published: December 19, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.
Journal: Human mutation
Published: June 29, 2012
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.
Journal: The Lancet. Neurology
Published: December 14, 2011
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Last Updated: 09/26/2026