# Heymut Omran

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/heymut-omran/

## Facts

| Field | Value |
| --- | --- |
| Citations | 27,066 |
| Field | Genetic and Kidney Cyst Diseases |
| h-index | 89 |
| i10-index | 200 |
| Last Known Institution | Uniwersytecki Szpital Dziecięcy |
| OpenAlex ID | https://openalex.org/A5002534679 |
| ORCID iD | https://orcid.org/0000-0003-0282-6765 |
| Works | 434 |

## Researcher papers

- [When cilia go bad: cilia defects and ciliopathies](https://scholariq.org/papers/when-cilia-go-bad-cilia-defects-and-ciliopathies/)
- [Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure](https://scholariq.org/papers/mutation-of-bsnd-causes-bartter-syndrome-with-sensorineural-deafness-and-kidney/)
- [Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin](https://scholariq.org/papers/nephrocystin-5-a-ciliary-iq-domain-protein-is-mutated-in-senior-loken-syndrome/)
- [Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling](https://scholariq.org/papers/exome-capture-reveals-znf423-and-cep164-mutations-linking-renal-ciliopathies-to/)
- [Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis](https://scholariq.org/papers/mutations-in-a-novel-gene-nphp3-cause-adolescent-nephronophthisis-tapeto-retinal/)
- [Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia](https://scholariq.org/papers/loss-of-nephrocystin-3-function-can-cause-embryonic-lethality-meckel-gruber-like/)
- [DYX1C1 is required for axonemal dynein assembly and ciliary motility](https://scholariq.org/papers/dyx1c1-is-required-for-axonemal-dynein-assembly-and-ciliary-motility/)
- [Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia](https://scholariq.org/papers/zebrafish-ciliopathy-screen-plus-human-mutational-analysis-identifies-c21orf59/)
- [ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6](https://scholariq.org/papers/zmynd10-is-mutated-in-primary-ciliary-dyskinesia-and-interacts-with-lrrc6/)
- [ARMC4 Mutations Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry](https://scholariq.org/papers/armc4-mutations-cause-primary-ciliary-dyskinesia-with-randomization-of-left/)

## Researcher topics

- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)
- [Cystic Fibrosis Research Advances](https://scholariq.org/topics/cystic-fibrosis-research-advances/)
- [Neonatal Respiratory Health Research](https://scholariq.org/topics/neonatal-respiratory-health-research/)
- [Tracheal and airway disorders](https://scholariq.org/topics/tracheal-and-airway-disorders-2/)
- [Protist diversity and phylogeny](https://scholariq.org/topics/protist-diversity-and-phylogeny/)

## Researcher university

- [Uniwersytecki Szpital Dziecięcy](https://scholariq.org/institutions/uniwersytecki-szpital-dzieciecy/)

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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.