# Friedrich Baur Stiftung

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/friedrich-baur-stiftung/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 76 |
| Citations | 92,443 |
| City | Altenkunstadt |
| Country | DE |
| Description | Friedrich Baur Stiftung is a research organisation in Altenkunstadt, DE. OpenAlex records 1,466 works and 92,443 citations for it. 205 researchers list it as their most recent affiliation. |
| Homepage | http://www.baur-stiftung.de/index.php/home.html#slide-2 |
| OpenAlex ID | https://openalex.org/I4210133604 |
| Researchers | 205 |
| ROR ID | https://ror.org/032a9fh96 |
| Type | other |
| Works | 1,466 |

## University 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/)

## University top topics

Showing 8 of 25.

- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Muscle Physiology and Disorders](https://scholariq.org/topics/muscle-physiology-and-disorders/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)
- [Lysosomal Storage Disorders Research](https://scholariq.org/topics/lysosomal-storage-disorders-research/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)

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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.