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Velibor Tasic

10PUBLICATIONS

81CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsHaematologyCardiology (incl. cardiovascular diseases)Ecohydrology

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Publications (10)

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|Oct 09, 2025

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena

|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 MCP<sub>ggaac</sub> 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

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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

Frequent Collaborators

3 joint publications

Giovanni Montini

3 joint publications

Gian Marco Ghiggeri

3 joint publications

Fangming Lin

3 joint publications

Friedhelm Hildebrandt

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