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

Maria Cristina Aspromonte

University of Padua

ORCID: 0000-0002-4937-6952
Biochemistry, Genetics and Molecular BiologyMaterials Science

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 1%percentile
6.7Author DataRank

Indexed papers

3in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 3 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

The Gene Ontology knowledgebase in 2023

Genetics(2023)10.1093/genetics/iyad031
Top 4%
5.8DataRank
Top 4%2744 citations

James P. Balhoff, Seth Carbon, J. Michael Cherry, Harold Drabkin, Dustin Ebert +90 more

Papers

Driven by 6 papers — median percentile 73. Top paper: “The Gene Ontology knowledgebase in 2023”.

The Gene Ontology knowledgebase in 2023

Genetics(2023)10.1093/genetics/iyad031
Top 4%
5.8DataRank
Top 4%2744 citations

James P. Balhoff, Seth Carbon, J. Michael Cherry, Harold Drabkin, Dustin Ebert +90 more

The Gene Ontology knowledgebase in 2026

Nucleic Acids Research(2025)10.1093/nar/gkaf1292
Top 27%
0.743DataRank
Top 27%95 citations

James P. Balhoff, Seth Carbon, J. Michael Cherry, Dustin Ebert, Marc Feuermann +95 more

CAGI6 ID panel challenge: assessment of phenotype and variant predictions in 415 children with neurodevelopmental disorders (NDDs)

Human Genetics(2025)10.1007/s00439-024-02722-w
Top 70%
0.165DataRank
Top 70%2 citations

Alessio Del Conte, Shaowen Zhu, Wuwei Tan, Yang Shen, Yexian Zhang +24 more

Rare variants in 45 genes account for 25% of cases with NDDs in 415 pediatric patients

Research Square(2023)10.21203/rs.3.rs-3139796/v1
N/A
0DataRank · unranked
2 citations

Alessio Del Conte, Roberta Polli, Demetrio Baldo, Francesco Benedicenti, Elisa Bettella +17 more

CAGI6 ID-Challenge: Assessment of phenotype and variant predictions in 415 children with Neurodevelopmental Disorders (NDDs)

Research Square(2023)10.21203/rs.3.rs-3209168/v1
N/A
0DataRank · unranked
0 citations

Alessio Del Conte, Shaowen Zhu, Wuwei Tan, Yang Shen, Yexian Zhang +24 more

Genetic variants and phenotypic data curated for the CAGI6 intellectual disability panel challenge

Human Genetics(2025)10.1007/s00439-025-02733-1
N/A
0DataRank · unranked
6 citations

Alessio Del Conte, Roberta Polli, Demetrio Baldo, Francesco Benedicenti, Elisa Bettella +18 more