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Robert Kleta

21PUBLICATIONS

188CO-AUTHORS

Molecular targetsGene expression (incl. microarray and other genome-wide approaches)Electroanalytical chemistryEpigenetics (incl. genome methylation and epigenomics)Gene mapping

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Publications (21)

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|Mar 18, 2026

Familial medullary thyroid carcinoma secondary to an <i>SLC30A9</i> intragenic deletion and translation reinitiation.

Donato Iacovazzo, Federica Begalli, Oniz Suleyman

|Feb 26, 2025

Rare disease gene association discovery in the 100,000 Genomes Project.

Valentina Cipriani, Letizia Vestito, Emma F Magavern

|Apr 04, 2023

The pathophysiology of distal renal tubular acidosis.

Carsten A Wagner, Robert Unwin, Sergio C Lopez-Garcia

|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

Founder mutation in the PMM2 promotor causes hyperinsulinemic hypoglycaemia/polycystic kidney disease (HIPKD).

Sumaya Islam, Mehmet Tekman, Sarah E Flanagan

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Frequent Collaborators

8 joint publications

Detlef Bockenhauer

4 joint publications

Daniel P Gale

3 joint publications

Detlef Bockenhauer

3 joint publications

Richard Warth

2 joint publications

Daan Viering

2 joint publications

Sarah E Flanagan

2 joint publications

Rosa Vargas-Poussou

2 joint publications

Jeroen H F de Baaij

2 joint publications

John A Sayer

2 joint publications

Carsten A Wagner

Frequent Collaborators

8 joint publications

Detlef Bockenhauer

4 joint publications

Daniel P Gale

3 joint publications

Detlef Bockenhauer

3 joint publications

Richard Warth

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