Simone Sanna-Cherchi
15PUBLICATIONS
240CO-AUTHORS
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Publications (15)
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|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
|Sep 30, 2025
Population-scale analysis reveals inherited C1-inhibitor deficiency is a polyphenotypic thrombotic disorder.Alfonso Rodriguez Espada, Amelia K Haj, Sean J Jurgens
|Sep 19, 2025
Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome.Tiffany Tu, Alejandro Ochoa, Amika Sood
|Aug 07, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genes.Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena
|May 02, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletion.Keng Ioi Vong, Sangmoon Lee, Kit Sing Au
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Frequent Collaborators
9 joint publications
Ali Gharavi
7 joint publications
Maddalena Marasà
6 joint publications
Miguel Verbitsky
6 joint publications
GianMarco Ghiggeri
6 joint publications
Friedhelm Hildebrandt
6 joint publications
Krzysztof Kiryluk
5 joint publications
Matthew G Sampson
5 joint publications
Antonio Amoroso
5 joint publications
Rik Westland
5 joint publications
Pietro Canetta
