Richard Warth

University of Regensburg

Germany

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Articles (14)

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2025

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2024

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2023

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2023

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2022

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2021

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2021

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2020

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2020

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2020

Collaborators (9)

Ina Maria Schiessl

Aarhus University

DENMARK

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David Penton

University of Zurich

SWITZERLAND

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Allein Plain

University of Regensburg

GERMANY

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Horia Constantin Stanescu

University College London

UNITED KINGDOM

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Enriko Klootwijk

University College London

UNITED KINGDOM

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Cordula Haas

University of Zurich

SWITZERLAND

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Lydia Tabernero

The University of Manchester

UNITED KINGDOM

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Johannes Loffing

University of Zurich

SWITZERLAND

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Jacqueline Neubauer

University of Zurich

SWITZERLAND

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Richard Warth

Research Interests

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Articles (14)

Somatic mutations in MCOLN3 are associated with aldosterone-producing adenomas.

The ex vivo perfused mouse adrenal gland—a new model to study aldosterone secretion

A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility

Somatic SLC30A1 mutations altering zinc transporter ZnT1 cause aldosterone-producing adenomas and primary aldosteronism.

KidneyGPS: a user-friendly web application to help prioritize kidney function genes and variants based on evidence from genome-wide association studies.

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness

Genetic variants in eleven central and peripheral chemoreceptor genes in sudden infant death syndrome

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness

EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- and Kir5.1-Associated Channelopathies

Distinct Mitochondrial Pathologies Caused by Mutations of the Proximal Tubular Enzymes EHHADH and GATM

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

Collecting system-specific deletion of Kcnj10 predisposes for thiazide- and low-potassium diet-induced hypokalemia

Cellular Pathophysiology of Mutant Voltage-Dependent Ca2+ Channel CACNA1H in Primary Aldosteronism

Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype

Collaborators (9)

Ina Maria Schiessl

David Penton

Allein Plain

Horia Constantin Stanescu

Enriko Klootwijk

Cordula Haas

Lydia Tabernero

Johannes Loffing

Jacqueline Neubauer

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