# Jean‐Charles Lambert

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/jean-charles-lambert/

## Facts

| Field | Value |
| --- | --- |
| Citations | 39,282 |
| Field | Alzheimer's disease research and treatments |
| h-index | 79 |
| i10-index | 231 |
| Last Known Institution | Inserm |
| OpenAlex ID | https://openalex.org/A5004893591 |
| ORCID iD | https://orcid.org/0000-0003-0829-7817 |
| Works | 507 |

## Researcher papers

- [Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease](https://scholariq.org/papers/meta-analysis-of-74-046-individuals-identifies-11-new-susceptibility-loci-for/)
- [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/)
- [Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease](https://scholariq.org/papers/gene-wide-analysis-detects-two-new-susceptibility-genes-for-alzheimer-s-disease/)
- [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/)
- [Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease](https://scholariq.org/papers/excessive-burden-of-lysosomal-storage-disorder-gene-variants-in-parkinson-s/)
- [Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease](https://scholariq.org/papers/unbiased-screen-for-interactors-of-leucine-rich-repeat-kinase-2-supports-a/)
- [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/)
- [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/)
- [Bioinformatics and Genomic Networks](https://scholariq.org/topics/bioinformatics-and-genomic-networks/)
- [Dementia and Cognitive Impairment Research](https://scholariq.org/topics/dementia-and-cognitive-impairment-research/)
- [Neuroinflammation and Neurodegeneration Mechanisms](https://scholariq.org/topics/neuroinflammation-and-neurodegeneration-mechanisms/)

## 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.