Detlef Bockenhauer

6PUBLICATIONS
27CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Artificial life and complex adaptive systemsEpigenetics (incl. genome methylation and epigenomics)Gene mappingCellular nervous system
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Publications (6)

|Sep 11, 2025
Fifty Shades of Risk: Population Studies and the Genetic Architecture of Kidney Diseases.

Omid Sadeghi-Alavijeh, Melanie M Y Chan, Horia Stanescu

|Sep 11, 2024
Ascites: Under- and Overfill: Is Amiloride the Answer?

Detlef Bockenhauer, Giulia Florio

|Feb 12, 2022
A Founder Mutation in <i>EHD1</i> Presents with Tubular Proteinuria and Deafness.

Naomi Issler, Sara Afonso, Irith Weissman

|Oct 05, 2021
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA.

Daan Viering, Karl P Schlingmann, Marguerite Hureaux

|Apr 03, 2021
Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness.

Karl P Schlingmann, Aparna Renigunta, Ewout J Hoorn

|Apr 03, 2020
Inherited Tubulopathies of the Kidney: Insights from Genetics.

Mallory L Downie, Sergio C Lopez Garcia, Robert Kleta

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