# Alexis Brice

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/alexis-brice/

## Facts

| Field | Value |
| --- | --- |
| Citations | 117,212 |
| Field | Parkinson's Disease Mechanisms and Treatments |
| h-index | 156 |
| i10-index | 804 |
| Last Known Institution | Centre National de la Recherche Scientifique |
| OpenAlex ID | https://openalex.org/A5027489586 |
| ORCID iD | https://orcid.org/0000-0002-0941-3990 |
| Works | 1,188 |

## Researcher papers

Showing 12 of 28.

- [Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism](https://scholariq.org/papers/mutations-in-the-i-dj-1-i-gene-associated-with-autosomal-recessive-early-onset/)
- [Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies](https://scholariq.org/papers/identification-of-novel-risk-loci-causal-insights-and-heritable-risk-for/)
- [Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease](https://scholariq.org/papers/multicenter-analysis-of-glucocerebrosidase-mutations-in-parkinson-s-disease/)
- [Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease](https://scholariq.org/papers/large-scale-meta-analysis-of-genome-wide-association-data-identifies-six-new/)
- [Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study](https://scholariq.org/papers/phenotype-genotype-and-worldwide-genetic-penetrance-of-lrrk2-associated/)
- [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/)
- [Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study](https://scholariq.org/papers/frequency-of-the-c9orf72-hexanucleotide-repeat-expansion-in-patients-with/)
- [Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum](https://scholariq.org/papers/early-onset-autosomal-dominant-alzheimer-disease-prevalence-genetic/)
- [Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments](https://scholariq.org/papers/meta-analysis-of-shank-mutations-in-autism-spectrum-disorders-a-gradient-of/)
- [Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis](https://scholariq.org/papers/genome-wide-association-analyses-identify-new-risk-variants-and-the-genetic/)
- [Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology](https://scholariq.org/papers/common-and-rare-variant-association-analyses-in-amyotrophic-lateral-sclerosis/)
- [Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database](https://scholariq.org/papers/comprehensive-research-synopsis-and-systematic-meta-analyses-in-parkinson-s/)

## Researcher topics

- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)

## Researcher university

- [Centre National de la Recherche Scientifique](https://scholariq.org/institutions/centre-national-de-la-recherche-scientifique/)

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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.