# Uniwersytecki Szpital Dziecięcy

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/uniwersytecki-szpital-dzieciecy/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 85.5 |
| Citations | 154,231 |
| City | Krakow |
| Country | PL |
| Description | Uniwersytecki Szpital Dziecięcy is a research organisation in Krakow, PL. OpenAlex records 3,485 works and 154,231 citations for it. 993 researchers list it as their most recent affiliation. |
| Homepage | http://www.szpitalzdrowia.pl/o-szpitalu/english-info/ |
| OpenAlex ID | https://openalex.org/I4210090147 |
| Researchers | 993 |
| ROR ID | https://ror.org/009x1kj44 |
| Type | healthcare |
| Works | 3,485 |

## University 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/)

## University top topics

Showing 8 of 25.

- [Neonatal Respiratory Health Research](https://scholariq.org/topics/neonatal-respiratory-health-research/)
- [Acute Lymphoblastic Leukemia research](https://scholariq.org/topics/acute-lymphoblastic-leukemia-research/)
- [Childhood Cancer Survivors' Quality of Life](https://scholariq.org/topics/childhood-cancer-survivors-quality-of-life/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)
- [Asthma and respiratory diseases](https://scholariq.org/topics/asthma-and-respiratory-diseases/)
- [Congenital Heart Disease Studies](https://scholariq.org/topics/congenital-heart-disease-studies/)
- [Immunodeficiency and Autoimmune Disorders](https://scholariq.org/topics/immunodeficiency-and-autoimmune-disorders/)
- [Hematopoietic Stem Cell Transplantation](https://scholariq.org/topics/hematopoietic-stem-cell-transplantation/)

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