# Rita Horváth

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/rita-horvath/

## Facts

| Field | Value |
| --- | --- |
| Citations | 22,416 |
| Field | Mitochondrial Function and Pathology |
| h-index | 80 |
| i10-index | 319 |
| Last Known Institution | University of Cambridge |
| OpenAlex ID | https://openalex.org/A5036864941 |
| ORCID iD | https://orcid.org/0000-0002-9841-170X |
| Works | 626 |

## Researcher papers

- [Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies](https://scholariq.org/papers/use-of-whole-exome-sequencing-to-determine-the-genetic-basis-of-multiple/)
- [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/)

## Researcher topics

- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [ATP Synthase and ATPases Research](https://scholariq.org/topics/atp-synthase-and-atpases-research/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Researcher university

- [University of Cambridge](https://scholariq.org/institutions/university-of-cambridge/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.