# Jan Halbritter

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/jan-halbritter/

## Facts

| Field | Value |
| --- | --- |
| Citations | 5,860 |
| Field | Genetic and Kidney Cyst Diseases |
| h-index | 39 |
| i10-index | 71 |
| Last Known Institution | Humboldt-Universität zu Berlin |
| OpenAlex ID | https://openalex.org/A5014253128 |
| ORCID iD | 0000-0002-1377-9880 |
| Works | 168 |

## Researcher papers

- [A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome](https://scholariq.org/papers/a-single-gene-cause-in-29-5-of-cases-of-steroid-resistant-nephrotic-syndrome/)
- [Fourteen Monogenic Genes Account for 15% of Nephrolithiasis/Nephrocalcinosis](https://scholariq.org/papers/fourteen-monogenic-genes-account-for-15-of-nephrolithiasis-nephrocalcinosis/)
- [Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy](https://scholariq.org/papers/identification-of-99-novel-mutations-in-a-worldwide-cohort-of-1-056-patients/)
- [Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans](https://scholariq.org/papers/defects-in-the-ift-b-component-ift172-cause-jeune-and-mainzer-saldino-syndromes/)
- [Mutations in <i>RSPH1</i> Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype](https://scholariq.org/papers/mutations-in-i-rsph1-i-cause-primary-ciliary-dyskinesia-with-a-unique-clinical/)
- [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/)
- [ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3](https://scholariq.org/papers/anks6-is-a-central-component-of-a-nephronophthisis-module-linking-nek8-to-invs/)
- [Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis](https://scholariq.org/papers/whole-exome-sequencing-frequently-detects-a-monogenic-cause-in-early-onset/)
- [Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference](https://scholariq.org/papers/genetics-in-chronic-kidney-disease-conclusions-from-a-kidney-disease-improving/)
- [KDIGO 2025 ADPKD guideline: a commentary on diagnosis and management of hepatopancreatic manifestations by the ERA Working Group Genes &amp; Kidney](https://scholariq.org/papers/kdigo-2025-adpkd-guideline-a-commentary-on-diagnosis-and-management-of/)

## Researcher topics

- [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/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Pediatric Urology and Nephrology Studies](https://scholariq.org/topics/pediatric-urology-and-nephrology-studies/)
- [Kidney Stones and Urolithiasis Treatments](https://scholariq.org/topics/kidney-stones-and-urolithiasis-treatments/)

## Researcher university

- [Humboldt-Universität zu Berlin](https://scholariq.org/institutions/humboldt-universitat-zu-berlin/)

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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.