Christine Van Broeckhoven

University of Antwerp — Belgium

Medicine · Health Sciences

141h-index93.4kcitations1.2kworks9.02yr avg
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Research Topics

Alzheimer's disease research and treatments(341), Amyotrophic Lateral Sclerosis Research(170), Neurological diseases and metabolism(141), Parkinson's Disease Mechanisms and Treatments(126), Hereditary Neurological Disorders(118)

Publications1.2k total

Investigation of the role of miRNA variants in neurodegenerative brain diseases
Frontiers in Genetics·2025· 1 citedOpen Access
Rare Abca7 Mutations in Alzheimer's Disease and Cerebral Amyloid Angiopathy Pathology
SSRN Electronic Journal·2025Open Access
Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins
Acta Neuropathologica·2024Open Access
The <i>SORL1</i> p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer’s disease
Proceedings of the National Academy of Sciences·2024· 20 citedOpen Access
Subclinical epileptiform activity in the Alzheimer continuum: association with disease, cognition and detection method
Alzheimer s Research & Therapy·2024· 31 citedOpen Access
Enhanced legumain activity links progranulin deficiency to TDP-43 pathology in frontotemporal lobar degeneration
2024· 5 citedOpen Access
Studying TLR9 loss‐of‐function in iPSC of patients with deleterious mutation
Alzheimer s & Dementia·2023Open Access
Multivariate GWAS of Alzheimer’s disease CSF biomarker profiles implies GRIN2D in synaptic functioning
Genome Medicine·2023· 20 citedOpen Access
The <i>SORL1</i> p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer’s disease
2023· 5 citedOpen Access
Mutated Toll-like receptor 9 increases Alzheimer’s disease risk by compromising innate immunity protection
Molecular Psychiatry·2023· 15 citedOpen Access
Rare exonic variant affects GRN splicing and contributes to frontotemporal lobar degeneration
Neurobiology of Aging·2023· 2 cited
Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
Nature Communications·2023Open Access
Additional file 1 of Multivariate GWAS of Alzheimer’s disease CSF biomarker profiles implies GRIN2D in synaptic functioning
Figshare·2023Open Access
<i>TRIM25</i> mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early‐onset autosomal dominant dementia with amyloid load and parkinsonism
Alzheimer s & Dementia·2022· 9 citedOpen Access
Whole‐exome rare‐variant analysis of Alzheimer's disease and related biomarker traits
Alzheimer s & Dementia·2022· 14 citedOpen Access
Belgian Carriers of Rare <i>ABCA7</i> Mutations Present with Pronounced Cerebral Amyloid Angiopathy and Alzheimer’s Disease
Alzheimer s & Dementia·2022
Microtubule associated protein tau p.R406W patient carriers present with a nonconforming clinical phenotype
Alzheimer s & Dementia·2022
Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?
Genetics in Medicine·2022· 30 citedOpen Access
Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood
Biological Psychiatry·2022· 47 citedOpen Access
Improved Alzheimer’s Disease versus Frontotemporal Lobar Degeneration Differential Diagnosis Combining EEG and Neurochemical Biomarkers: A Pilot Study
Journal of Alzheimer s Disease·2022· 3 citedOpen Access
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Frequent Co-authors

Marc Cruts(18), Kristel Sleegers(12), Sebastiaan Engelborghs(10), John Hardy(8), Cornelia M. van Duijn(8), Karolien Bettens(6), Jessie Theuns(6), Jean‐Charles Lambert(5), Christian Haass(5), Peter De Jonghe(5), Gernot Kleinberger(5), David Mann(4), Martin N. Rossor(4), Alison Goate(4), Dominique Campion(4), Peter Paul De Deyn(4), Benedetta Nacmias(4), Daniela Galimberti(4), Didier Hannequin(4), Ilse Gijselinck(4)