# Detlef Böckenhauer

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/detlef-bockenhauer/

## Facts

| Field | Value |
| --- | --- |
| Citations | 18,626 |
| Field | Ion Transport and Channel Regulation |
| h-index | 72 |
| i10-index | 192 |
| Last Known Institution | Great Ormond Street Hospital |
| OpenAlex ID | https://openalex.org/A5019805529 |
| ORCID iD | 0000-0001-5878-941X |
| Works | 487 |

## Researcher papers

Showing 12 of 21.

- [Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference](https://scholariq.org/papers/nomenclature-for-kidney-function-and-disease-report-of-a-kidney-disease/)
- [Potassium leak channels and the KCNK family of two-p-domain subunits](https://scholariq.org/papers/potassium-leak-channels-and-the-kcnk-family-of-two-p-domain-subunits/)
- [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/)
- [Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities](https://scholariq.org/papers/mutations-in-kelch-like-3-and-cullin-3-cause-hypertension-and-electrolyte/)
- [Whole-genome sequencing of patients with rare diseases in a national health system](https://scholariq.org/papers/whole-genome-sequencing-of-patients-with-rare-diseases-in-a-national-health/)
- [Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and <i>KCNJ10</i> Mutations](https://scholariq.org/papers/epilepsy-ataxia-sensorineural-deafness-tubulopathy-and-i-kcnj10-i-mutations/)
- [Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia](https://scholariq.org/papers/clinical-practice-recommendations-for-the-diagnosis-and-management-of-x-linked/)
- [Risk HLA-DQA1 and PLA <sub>2</sub> R1 Alleles in Idiopathic Membranous Nephropathy](https://scholariq.org/papers/risk-hla-dqa1-and-pla-sub-2-sub-r1-alleles-in-idiopathic-membranous-nephropathy/)
- [Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference](https://scholariq.org/papers/gitelman-syndrome-consensus-and-guidance-from-a-kidney-disease-improving-global/)
- [ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption](https://scholariq.org/papers/adck4-mutations-promote-steroid-resistant-nephrotic-syndrome-through-coq10/)
- [100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.](https://scholariq.org/papers/100-000-genomes-pilot-on-rare-disease-diagnosis-in-health-care-preliminary/)
- [HNF1B Mutations Associate with Hypomagnesemia and Renal Magnesium Wasting](https://scholariq.org/papers/hnf1b-mutations-associate-with-hypomagnesemia-and-renal-magnesium-wasting/)

## Researcher topics

- [Ion Transport and Channel Regulation](https://scholariq.org/topics/ion-transport-and-channel-regulation/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Biomedical Research and Pathophysiology](https://scholariq.org/topics/biomedical-research-and-pathophysiology/)
- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)

## Researcher university

- [Great Ormond Street Hospital](https://scholariq.org/institutions/great-ormond-street-hospital/)

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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.