Robert Kleta
21PUBLICATIONS
188CO-AUTHORS
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Publications (21)
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|Mar 18, 2026
Familial medullary thyroid carcinoma secondary to an SLC30A9 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 EHD1 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
