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

M. Cristina Digilio

Bambino Gesù Children's Hospital

ORCID: 0000-0002-0205-9634

Also affiliated with Istituti di Ricovero e Cura a Carattere Scientifico

Biochemistry, Genetics and Molecular BiologyMedicine

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 5%percentile
0.461Author 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.

Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62919
Top 41%
0.461DataRank
Top 41%9 citations

Aliska M. Berry, Ian M. Campbell, Xiaonan Zhao, Pengfei Liu, Amanda Gerard +41 more

Papers

Driven by 7 papers — median percentile 59. Top paper: “Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data”.

Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62919
Top 41%
0.461DataRank
Top 41%9 citations

Aliska M. Berry, Ian M. Campbell, Xiaonan Zhao, Pengfei Liu, Amanda Gerard +41 more

Pathway analysis identifies novel non-synonymous variants contributing to extreme vascular outcomes in Williams-Beuren syndrome

medRxiv(2022)10.1101/2022.09.21.22280107
N/A
0DataRank · unranked
0 citations

Charles J. Billington, Niranjan Raja, Zoë C. Wong, Mark Levin, Wolfgang Resch +20 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.30.507111
N/A
0DataRank · unranked
0 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +45 more

Bi-allelic SNAPC4 variants dysregulate global alternative splicing and lead to neuroregression and progressive spastic paraparesis

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.001
N/A
0DataRank · unranked
13 citations

Marie Morimoto, Prashant Sharma, Lyse Ruaud, Newell Belnap, Daniel G. Calame +33 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

npj Genomic Medicine(2023)10.1038/s41525-023-00363-y
N/A
0DataRank · unranked
12 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +47 more

Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams–Beuren Syndrome

Journal of the American Heart Association(2024)10.1161/jaha.123.031377
N/A
0DataRank · unranked
2 citations

Charles J. Billington, Neelam Raja, Zoë C. Wong, Mark Levin, Wolfgang Resch +20 more

Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotyping

medRxiv(2024)10.1101/2024.09.17.24313555
N/A
0DataRank · unranked
0 citations

Carolyn Β. Mervis, Mark Levin, Elisa Biamino, Maria Francesca Bedeschi, M. Cristina Digilio +11 more