# Vincent Meininger

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/vincent-meininger/

## Facts

| Field | Value |
| --- | --- |
| Citations | 22,919 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 80 |
| i10-index | 208 |
| Last Known Institution | Générale de Santé |
| OpenAlex ID | https://openalex.org/A5057953137 |
| ORCID iD | https://orcid.org/0000-0002-6180-7970 |
| Works | 311 |

## Researcher papers

- [TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis](https://scholariq.org/papers/tardbp-mutations-in-individuals-with-sporadic-and-familial-amyotrophic-lateral/)
- [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/)
- [Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-profilin-1-gene-cause-familial-amyotrophic-lateral-sclerosis/)
- [<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/)
- [<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations](https://scholariq.org/papers/i-sod1-i-i-ang-i-i-vapb-i-i-tardbp-i-and-i-fus-i-mutations-in-familial/)
- [Glutamate levels in cerebrospinal fluid in amyotrophic lateral sclerosis: a reappraisal using a new HPLC method with coulometric detection in a large cohort of patients](https://scholariq.org/papers/glutamate-levels-in-cerebrospinal-fluid-in-amyotrophic-lateral-sclerosis-a/)
- [Sleep Disorders and Diaphragmatic Function in Patients with Amyotrophic Lateral Sclerosis](https://scholariq.org/papers/sleep-disorders-and-diaphragmatic-function-in-patients-with-amyotrophic-lateral/)
- [Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology](https://scholariq.org/papers/mutations-in-sqstm1-encoding-p62-in-amyotrophic-lateral-sclerosis-genetics-and/)
- [Reduced expression of the <i>Kinesin-Associated Protein 3</i> ( <i>KIFAP3</i> ) gene increases survival in sporadic amyotrophic lateral sclerosis](https://scholariq.org/papers/reduced-expression-of-the-i-kinesin-associated-protein-3-i-i-kifap3-i-gene/)
- [Causes of death in a post‐mortem series of ALS patients](https://scholariq.org/papers/causes-of-death-in-a-post-mortem-series-of-als-patients/)
- [Impaired glucose tolerance in patients with amyotrophic lateral sclerosis](https://scholariq.org/papers/impaired-glucose-tolerance-in-patients-with-amyotrophic-lateral-sclerosis/)
- [Phenotype difference between ALS patients with expanded repeats in <i>C9ORF72</i> and patients with mutations in other ALS-related genes](https://scholariq.org/papers/phenotype-difference-between-als-patients-with-expanded-repeats-in-i-c9orf72-i/)

## Researcher topics

- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [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/)

## Researcher university

- [Générale de Santé](https://scholariq.org/institutions/generale-de-sante/)

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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.