# Didier Hannequin

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/didier-hannequin/

## Facts

| Field | Value |
| --- | --- |
| Citations | 40,988 |
| Field | Alzheimer's disease research and treatments |
| h-index | 83 |
| i10-index | 239 |
| Last Known Institution | Assistance Publique – Hôpitaux de Paris |
| OpenAlex ID | https://openalex.org/A5077897163 |
| ORCID iD | https://orcid.org/0000-0003-2662-0999 |
| Works | 403 |

## 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/)
- [Analysis of shared heritability in common disorders of the brain](https://scholariq.org/papers/analysis-of-shared-heritability-in-common-disorders-of-the-brain/)
- [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/)
- [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/)
- [<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/)
- [Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia](https://scholariq.org/papers/identification-of-evolutionarily-conserved-gene-networks-mediating/)

## Researcher topics

- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Dementia and Cognitive Impairment Research](https://scholariq.org/topics/dementia-and-cognitive-impairment-research/)
- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Bioinformatics and Genomic Networks](https://scholariq.org/topics/bioinformatics-and-genomic-networks/)

## Researcher university

- [Assistance Publique – Hôpitaux de Paris](https://scholariq.org/institutions/assistance-publique-hopitaux-de-paris/)

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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.