Karin Peeters
University of Antwerp(BE)
Publications by Year
Research Areas
Parkinson's Disease Mechanisms and Treatments, Amyotrophic Lateral Sclerosis Research, Alzheimer's disease research and treatments, Neurological diseases and metabolism, Genetic Neurodegenerative Diseases
Most-Cited Works
- → Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21(2006)1,517 cited
- → 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(2011)627 cited
- → The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter(2015)246 cited
- → Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites(2011)231 cited
- → Genetic contribution of FUS to frontotemporal lobar degeneration(2010)219 cited
- → A novel presenilin 1 mutation associated with Pick's disease but not β‐amyloid plaques(2004)213 cited
- → Serum biomarker for progranulin‐associated frontotemporal lobar degeneration(2009)204 cited
- → Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia(2013)185 cited
- → Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort(2015)173 cited
- → Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease(2008)167 cited