# Christine Van Broeckhoven

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/christine-van-broeckhoven/

## Facts

| Field | Value |
| --- | --- |
| Citations | 94,636 |
| Field | Alzheimer's disease research and treatments |
| h-index | 139 |
| i10-index | 684 |
| Last Known Institution | VIB-UAntwerp Center for Molecular Neurology |
| OpenAlex ID | https://openalex.org/A5039639102 |
| ORCID iD | https://orcid.org/0000-0003-0183-7665 |
| Works | 1,214 |

## Researcher papers

Showing 12 of 17.

- [Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease](https://scholariq.org/papers/genome-wide-association-study-identifies-variants-at-clu-and-picalm-associated/)
- [Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease](https://scholariq.org/papers/genome-wide-association-study-identifies-variants-at-clu-and-cr1-associated-with/)
- [Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease](https://scholariq.org/papers/common-variants-at-abca7-ms4a6a-ms4a4e-epha1-cd33-and-cd2ap-are-associated-with/)
- [De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy](https://scholariq.org/papers/de-novo-mutations-in-the-sodium-channel-gene-scn1a-cause-severe-myoclonic/)
- [VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death](https://scholariq.org/papers/vegf-is-a-modifier-of-amyotrophic-lateral-sclerosis-in-mice-and-humans-and/)
- [TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis](https://scholariq.org/papers/trem2-mutations-implicated-in-neurodegeneration-impair-cell-surface-transport/)
- [APOE and Alzheimer disease: a major gene with semi-dominant inheritance](https://scholariq.org/papers/apoe-and-alzheimer-disease-a-major-gene-with-semi-dominant-inheritance/)
- [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](https://scholariq.org/papers/a-c9orf72-promoter-repeat-expansion-in-a-flanders-belgian-cohort-with-disorders/)
- [Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions](https://scholariq.org/papers/common-variants-at-7p21-are-associated-with-frontotemporal-lobar-degeneration/)
- [Frontotemporal dementia and its subtypes: a genome-wide association study](https://scholariq.org/papers/frontotemporal-dementia-and-its-subtypes-a-genome-wide-association-study/)
- [Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study](https://scholariq.org/papers/phenotype-variability-in-progranulin-mutation-carriers-a-clinical/)
- [Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study](https://scholariq.org/papers/association-of-lrrk2-exonic-variants-with-susceptibility-to-parkinson-s-disease/)

## Researcher topics

- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Researcher university

- [VIB-UAntwerp Center for Molecular Neurology](https://scholariq.org/institutions/vib-uantwerp-center-for-molecular-neurology/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.