Simone Sanna-Cherchi

15PUBLICATIONS
240CO-AUTHORS
Infant and child healthCardiology (incl. cardiovascular diseases)Central nervous systemNeurogeneticsGene mapping
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Publications (15)

|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

|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

|Mar 18, 2024
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank.

Justine Ryu, Joel T Rämö, Sean J Jurgens

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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