# Holger Prokisch

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/holger-prokisch/

## Facts

| Field | Value |
| --- | --- |
| Citations | 50,445 |
| Field | Mitochondrial Function and Pathology |
| h-index | 102 |
| i10-index | 349 |
| Last Known Institution | Helmholtz Zentrum München |
| OpenAlex ID | https://openalex.org/A5054486997 |
| ORCID iD | https://orcid.org/0000-0003-2379-6286 |
| Works | 654 |

## Researcher papers

- [Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression](https://scholariq.org/papers/large-scale-cis-and-trans-eqtl-analyses-identify-thousands-of-genetic-loci-and/)
- [Systematic identification of trans eQTLs as putative drivers of known disease associations](https://scholariq.org/papers/systematic-identification-of-trans-eqtls-as-putative-drivers-of-known-disease/)
- [Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity](https://scholariq.org/papers/epigenome-wide-association-study-of-body-mass-index-and-the-adverse-outcomes-of/)
- [COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness](https://scholariq.org/papers/coq6-mutations-in-human-patients-produce-nephrotic-syndrome-with-sensorineural/)
- [DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases](https://scholariq.org/papers/dna-methylation-signatures-of-chronic-low-grade-inflammation-are-associated-with/)
- [ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption](https://scholariq.org/papers/adck4-mutations-promote-steroid-resistant-nephrotic-syndrome-through-coq10/)
- [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/)
- [Monogenic variants in dystonia: an exome-wide sequencing study](https://scholariq.org/papers/monogenic-variants-in-dystonia-an-exome-wide-sequencing-study/)
- [Clinical implementation of RNA sequencing for Mendelian disease diagnostics](https://scholariq.org/papers/clinical-implementation-of-rna-sequencing-for-mendelian-disease-diagnostics/)
- [Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function](https://scholariq.org/papers/genetic-variation-influencing-dna-methylation-provides-insights-into-molecular/)
- [Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy](https://scholariq.org/papers/impaired-complex-i-repair-causes-recessive-leber-s-hereditary-optic-neuropathy/)

## 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/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [ATP Synthase and ATPases Research](https://scholariq.org/topics/atp-synthase-and-atpases-research/)

## Researcher university

- [Helmholtz Munich](https://scholariq.org/institutions/helmholtz-munich/)

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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.