Julie G. Van Der Zee
Antwerpen, VLG 2610, Belgium
Last Updated: 09/26/2026
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Found 93 publications
Rare ABCA7 mutations in Alzheimer's disease and cerebral amyloid angiopathy pathology.
Journal: Neurobiology of aging
Published: June 17, 2025
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions.
Journal: Nature genetics
Published: February 21, 2025
Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of HTT associated with an early disease onset in C9orf72 carriers.
Journal: Brain communications
Published: October 31, 2024
Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.
Journal: Acta neuropathologica
Published: October 05, 2024
Investigation of the role of miRNA variants in neurodegenerative brain diseases.
Journal: Frontiers in genetics
Published: October 04, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia.
Journal: American journal of human genetics
Published: January 02, 2024
Subclinical epileptiform activity in the Alzheimer continuum: association with disease, cognition and detection method.
Journal: Alzheimer's research & therapy
Published: September 13, 2023
Improved Alzheimer's Disease versus Frontotemporal Lobar Degeneration Differential Diagnosis Combining EEG and Neurochemical Biomarkers: A Pilot Study.
Journal: Journal of Alzheimer's disease : JAD
Published: November 07, 2022
TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early-onset autosomal dominant dementia with amyloid load and parkinsonism.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: July 08, 2022
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum.
Journal: Brain : a journal of neurology
Published: February 15, 2022
Frontotemporal Lobar Degeneration Case with an N-Terminal TUBA4A Mutation Exhibits Reduced TUBA4A Levels in the Brain and TDP-43 Pathology.
Journal: Biomolecules
Published: January 25, 2022
Protein interaction network analysis reveals genetic enrichment of immune system genes in frontotemporal dementia.
Journal: Neurobiology of aging
Published: January 03, 2022
Last Updated: 09/26/2026