# Benedikt Schoser

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/benedikt-schoser/

## Facts

| Field | Value |
| --- | --- |
| Citations | 18,427 |
| Field | Lysosomal Storage Disorders Research |
| h-index | 76 |
| i10-index | 252 |
| Last Known Institution | Friedrich Baur Stiftung |
| OpenAlex ID | https://openalex.org/A5039404447 |
| ORCID iD | https://orcid.org/0000-0002-2757-8131 |
| Works | 850 |

## Researcher papers

- [The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene](https://scholariq.org/papers/the-myopathic-form-of-coenzyme-q10-deficiency-is-caused-by-mutations-in-the/)
- [Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial](https://scholariq.org/papers/safety-and-efficacy-of-avalglucosidase-alfa-versus-alglucosidase-alfa-in/)
- [Consensus-based care recommendations for adults with myotonic dystrophy type 1](https://scholariq.org/papers/consensus-based-care-recommendations-for-adults-with-myotonic-dystrophy-type-1/)
- [Polyglucosan body myopathy caused by defective ubiquitin ligase RBCK1](https://scholariq.org/papers/polyglucosan-body-myopathy-caused-by-defective-ubiquitin-ligase-rbck1/)

## Researcher topics

- [Lysosomal Storage Disorders Research](https://scholariq.org/topics/lysosomal-storage-disorders-research/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)
- [Muscle Physiology and Disorders](https://scholariq.org/topics/muscle-physiology-and-disorders/)
- [Cardiomyopathy and Myosin Studies](https://scholariq.org/topics/cardiomyopathy-and-myosin-studies/)

## Researcher university

- [Friedrich Baur Stiftung](https://scholariq.org/institutions/friedrich-baur-stiftung/)

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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.