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

Alessandra Murgia

University of Padua

ORCID: 0000-0001-6788-0653

Also affiliated with Città della Speranza Foundation

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 7%percentile
0.165Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

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

Papers

Driven by 5 papers — median percentile 30. Top paper: “CERT1 mutations perturb human development by disrupting sphingolipid homeostasis”.

CERT1 mutations perturb human development by disrupting sphingolipid homeostasis

Journal of Clinical Investigation(2023)10.1172/jci165019
N/A
0.568DataRank · unranked
43 citations

Museer A. Lone, Winston Lee, Laura Capolupo, Sylvia Ho, Adekemi M. Adeyemi +80 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
0.312DataRank · unranked
7 citations

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