🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Giovanni Montini

University of Milan

ORCID: 0000-0002-7350-4475

Also affiliated with Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Ospedale Maggiore

Medicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 7 papers. Top paper: “Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease”.

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

medRxiv(2023)10.1101/2023.08.02.23293554
N/A
0.208DataRank · unranked
3 citations

David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang +75 more

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

Nature Communications(2023)10.1038/s41467-023-37985-w
N/A
0DataRank · unranked
50 citations

Michelle T. McNulty, Xiaoyuan Jia, Yask Gupta, Hanna Dêbiec, Yang Luo +65 more

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

Journal of the American Society of Nephrology(2023)10.1681/asn.0000000000000132
N/A
0DataRank · unranked
15 citations

Tze Yin Lim, Juntao Ke, Gina Jin, Miguel Verbitsky, Monica Bodria +77 more

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

Nature Communications(2023)10.1038/s41467-023-43020-9
N/A
0DataRank · unranked
69 citations

David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang +75 more

Exome analysis links kidney malformations to developmental disorders and reveals causal genes

Nature Communications(2025)10.1038/s41467-025-62319-3
N/A
0DataRank · unranked
9 citations

Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil, Andrew Beenken, Miguel Verbitsky +95 more

Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries

Kidney International(2025)10.1016/j.kint.2025.02.026
N/A
0DataRank · unranked
7 citations

Steffen Fieuws, Jonas Hofstetter, David Pitcher, Lotte Vanmeerbeek, Stefanie Haeberle +95 more

Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis

Kidney International(2025)10.1016/j.kint.2025.12.013
N/A
0DataRank · unranked
0 citations

Kristen M. Gibson, Juntao Ke, Zachary T. Sentell, Juliana E Arcila Galvis, Satoshi Koyama +23 more