# Thomas Benzing

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/thomas-benzing/

## Facts

| Field | Value |
| --- | --- |
| Citations | 25,866 |
| Field | Renal Diseases and Glomerulopathies |
| h-index | 75 |
| i10-index | 215 |
| Last Known Institution | University of Cologne |
| OpenAlex ID | https://openalex.org/A5050423319 |
| ORCID iD | 0000-0003-0512-1066 |
| Works | 445 |

## Researcher papers

Showing 12 of 26.

- [A Mammalian microRNA Expression Atlas Based on Small RNA Library Sequencing](https://scholariq.org/papers/a-mammalian-microrna-expression-atlas-based-on-small-rna-library-sequencing/)
- [Ciliopathies](https://scholariq.org/papers/ciliopathies/)
- [When cilia go bad: cilia defects and ciliopathies](https://scholariq.org/papers/when-cilia-go-bad-cilia-defects-and-ciliopathies/)
- [Pre-eclampsia: pathogenesis, novel diagnostics and therapies](https://scholariq.org/papers/pre-eclampsia-pathogenesis-novel-diagnostics-and-therapies/)
- [Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways](https://scholariq.org/papers/inversin-the-gene-product-mutated-in-nephronophthisis-type-ii-functions-as-a/)
- [Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination](https://scholariq.org/papers/mutations-in-invs-encoding-inversin-cause-nephronophthisis-type-2-linking-renal/)
- [Nephrin and CD2AP Associate with Phosphoinositide 3-OH Kinase and Stimulate AKT-Dependent Signaling](https://scholariq.org/papers/nephrin-and-cd2ap-associate-with-phosphoinositide-3-oh-kinase-and-stimulate-akt/)
- [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/)
- [Interaction with Podocin Facilitates Nephrin Signaling](https://scholariq.org/papers/interaction-with-podocin-facilitates-nephrin-signaling/)
- [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/)
- [Pilot Study of Extracorporeal Removal of Soluble Fms-Like Tyrosine Kinase 1 in Preeclampsia](https://scholariq.org/papers/pilot-study-of-extracorporeal-removal-of-soluble-fms-like-tyrosine-kinase-1-in/)
- [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/)

## Researcher topics

- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Chronic Kidney Disease and Diabetes](https://scholariq.org/topics/chronic-kidney-disease-and-diabetes/)
- [Biomedical Research and Pathophysiology](https://scholariq.org/topics/biomedical-research-and-pathophysiology/)

## Researcher university

- [University of Cologne](https://scholariq.org/institutions/university-of-cologne/)

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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.