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Miguel Verbitsky

7PUBLICATIONS
83CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsCardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)
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Journal

Publications (7)

Sort by Publication Date:
|Jan 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tract.

Lisanne M Vendrig, Juntao Ke, Michael W T Tanck

|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

|Mar 11, 2025
Family History in the Context of CKD.

Francesca Zanoni, Maddalena Marasa, Lucrezia Carlassara

|Nov 30, 2023
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease.

Yask Gupta, David J Friedman, Michelle T McNulty

|Mar 01, 2019
Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Miguel Verbitsky, Rik Westland, Alejandra Perez

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Frequent Collaborators

6 joint publications

Maddalena Marasà

6 joint publications

Simone Sanna-Cherchi

5 joint publications

Friedhelm Hildebrandt

5 joint publications

Ali G Gharavi

4 joint publications

Matthew G Sampson

4 joint publications

Rik Westland

4 joint publications

Gian Marco Ghiggeri

4 joint publications

Giovanni Montini

4 joint publications

Pietro Canetta

4 joint publications

Atlas Khan

Frequent Collaborators

6 joint publications

Maddalena Marasà

6 joint publications

Simone Sanna-Cherchi

5 joint publications

Friedhelm Hildebrandt

5 joint publications

Ali G Gharavi

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