Velibor Tasic
10PUBLICATIONS
81CO-AUTHORS
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Publications (10)
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|Aug 07, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genes.Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena
|Oct 17, 2024
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.Esra Kesdiren, Helge Martens, Frank Brand
|Sep 09, 2023
The Rationale of Complement Blockade of the MCPggaac Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Review.Daniel Turudic, Danka Pokrajac, Velibor Tasic
|Apr 29, 2023
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.Alexandra Barry, Michelle T McNulty, Xiaoyuan Jia
|Mar 16, 2023
Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience.Korbinian M Riedhammer, Jasmina Ćomić, Velibor Tasic
|Nov 27, 2021
Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population.Blanka Stiburkova, Jana Bohatá, Kateřina Pavelcová
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Frequent Collaborators
3 joint publications
Giovanni Montini
3 joint publications
Gian Marco Ghiggeri
3 joint publications
Fangming Lin
3 joint publications
Friedhelm Hildebrandt
3 joint publications
Ali Gharavi
3 joint publications
Simone Sanna-Cherchi
3 joint publications
Maddalena Marasa
3 joint publications
Rik Westland
2 joint publications
Korbinian M Riedhammer
2 joint publications
Helge Martens
