# Andreas Kispert

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/andreas-kispert/

## Facts

| Field | Value |
| --- | --- |
| Citations | 25,527 |
| Field | Congenital heart defects research |
| h-index | 78 |
| i10-index | 177 |
| Last Known Institution | Medizinische Hochschule Hannover |
| OpenAlex ID | https://openalex.org/A5075279504 |
| ORCID iD | https://orcid.org/0000-0002-8154-0257 |
| Works | 245 |

## Researcher papers

- [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/)
- [The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4](https://scholariq.org/papers/the-centrosomal-protein-nephrocystin-6-is-mutated-in-joubert-syndrome-and/)
- [Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible](https://scholariq.org/papers/positional-cloning-uncovers-mutations-in-plce1-responsible-for-a-nephrotic/)
- [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/)
- [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/)
- [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/)
- [Identification of multipotent progenitors in the embryonic mouse kidney by a novel colony-forming assay](https://scholariq.org/papers/identification-of-multipotent-progenitors-in-the-embryonic-mouse-kidney-by-a/)

## Researcher topics

- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Developmental Biology and Gene Regulation](https://scholariq.org/topics/developmental-biology-and-gene-regulation/)
- [Urological Disorders and Treatments](https://scholariq.org/topics/urological-disorders-and-treatments-2/)
- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)

## Researcher university

- [Medizinische Hochschule Hannover](https://scholariq.org/institutions/medizinische-hochschule-hannover/)

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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.