Christine Van Broeckhoven

Christine Van Broeckhoven

Antwerpen, VLG 2610, Belgium

Last Updated: 09/26/2026

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Found 211 publications

Rare ABCA7 mutations in Alzheimer's disease and cerebral amyloid angiopathy pathology.

Rare ABCA7 mutations in Alzheimer's disease and cerebral amyloid angiopathy pathology.

Journal: Neurobiology of aging
Published: June 17, 2025

Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.

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.

Investigation of the role of miRNA variants in neurodegenerative brain diseases.

Journal: Frontiers in genetics
Published: October 04, 2024

The SORL1 p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer's disease.

The SORL1 p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer's disease.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: September 03, 2024

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia.

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.

Subclinical epileptiform activity in the Alzheimer continuum: association with disease, cognition and detection method.

Journal: Alzheimer's research & therapy
Published: September 13, 2023

Multivariate GWAS of Alzheimer's disease CSF biomarker profiles implies GRIN2D in synaptic functioning.

Multivariate GWAS of Alzheimer's disease CSF biomarker profiles implies GRIN2D in synaptic functioning.

Journal: Genome medicine
Published: July 24, 2023

Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.

Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.

Journal: Nature communications
Published: February 09, 2023

Improved Alzheimer's Disease versus Frontotemporal Lobar Degeneration Differential Diagnosis Combining EEG and Neurochemical Biomarkers: A Pilot Study.

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

Rare exonic variant affects GRN splicing and contributes to frontotemporal lobar degeneration.

Rare exonic variant affects GRN splicing and contributes to frontotemporal lobar degeneration.

Journal: Neurobiology of aging
Published: September 05, 2022

Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 29, 2022

Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traits.

Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traits.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: April 06, 2022
Showing 1-12 of 211

Last Updated: 09/26/2026