# Dominique Campion

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/dominique-campion/

## Facts

| Field | Value |
| --- | --- |
| Citations | 56,239 |
| Field | Alzheimer's disease research and treatments |
| h-index | 87 |
| i10-index | 245 |
| Last Known Institution | Inserm |
| OpenAlex ID | https://openalex.org/A5107927035 |
| ORCID iD | https://orcid.org/0000-0003-1916-7890 |
| Works | 378 |

## Researcher papers

- [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/)
- [Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores](https://scholariq.org/papers/modeling-linkage-disequilibrium-increases-accuracy-of-polygenic-risk-scores/)
- [APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy](https://scholariq.org/papers/app-locus-duplication-causes-autosomal-dominant-early-onset-alzheimer-disease/)
- [Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum](https://scholariq.org/papers/early-onset-autosomal-dominant-alzheimer-disease-prevalence-genetic/)
- [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/)
- [Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus](https://scholariq.org/papers/mirror-extreme-bmi-phenotypes-associated-with-gene-dosage-at-the-chromosome/)
- [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/)
- [<i>TARDBP</i> mutations in motoneuron disease with frontotemporal lobar degeneration](https://scholariq.org/papers/i-tardbp-i-mutations-in-motoneuron-disease-with-frontotemporal-lobar/)
- [Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls](https://scholariq.org/papers/contribution-to-alzheimer-s-disease-risk-of-rare-variants-in-trem2-sorl1-and/)

## Researcher topics

- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Researcher university

- [Inserm](https://scholariq.org/institutions/inserm/)

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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.