# Thomas Gasser

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/thomas-gasser-2/

## Facts

| Field | Value |
| --- | --- |
| Citations | 89,923 |
| Field | Parkinson's Disease Mechanisms and Treatments |
| h-index | 137 |
| i10-index | 601 |
| Last Known Institution | German Center for Neurodegenerative Diseases |
| OpenAlex ID | https://openalex.org/A5067744605 |
| ORCID iD | https://orcid.org/0000-0002-1069-1146 |
| Works | 1,389 |

## Researcher papers

Showing 12 of 15.

- [MDS clinical diagnostic criteria for Parkinson's disease](https://scholariq.org/papers/mds-clinical-diagnostic-criteria-for-parkinson-s-disease/)
- [Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology](https://scholariq.org/papers/mutations-in-lrrk2-cause-autosomal-dominant-parkinsonism-with-pleomorphic/)
- [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/)
- [MDS research criteria for prodromal Parkinson's disease](https://scholariq.org/papers/mds-research-criteria-for-prodromal-parkinson-s-disease/)
- [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/)
- [The natural history of multiple system atrophy: a prospective European cohort study](https://scholariq.org/papers/the-natural-history-of-multiple-system-atrophy-a-prospective-european-cohort/)
- [<scp>EFNS</scp>/<scp>MDS</scp>‐<scp>ES</scp> recommendations for the diagnosis of <scp>P</scp>arkinson's disease](https://scholariq.org/papers/scp-efns-scp-scp-mds-scp-scp-es-scp-recommendations-for-the-diagnosis-of-scp-p/)
- [Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture](https://scholariq.org/papers/genome-sequencing-analysis-identifies-new-loci-associated-with-lewy-body/)
- [Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy](https://scholariq.org/papers/loss-of-vps13c-function-in-autosomal-recessive-parkinsonism-causes-mitochondrial/)

## Researcher topics

- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)
- [Nuclear Receptors and Signaling](https://scholariq.org/topics/nuclear-receptors-and-signaling/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Researcher university

- [German Center for Neurodegenerative Diseases](https://scholariq.org/institutions/german-center-for-neurodegenerative-diseases/)

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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.