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

Luca Brunelli

University of Utah

ORCID: 0000-0002-9542-2243
Biochemistry, Genetics and Molecular BiologyMedicineHealth Professions

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 4%percentile
0.752Author 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.

Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

Genome Medicine(2023)10.1186/s13073-023-01166-7
Top 27%
0.752DataRank
Top 27%29 citations

Edgar J. Hernández, Charlotte A. Hobbs, Sabrina Malone Jenkins, Barry Moore, Edwin F. Juarez +9 more

Papers

Driven by 8 papers — median percentile 73. Top paper: “Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning”.

Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

Genome Medicine(2023)10.1186/s13073-023-01166-7
Top 27%
0.752DataRank
Top 27%29 citations

Edgar J. Hernández, Charlotte A. Hobbs, Sabrina Malone Jenkins, Barry Moore, Edwin F. Juarez +9 more

Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1888
N/A
0DataRank · unranked
8 citations

Najla Al‐Sweel, Andrew Farrell, Rong Mao, Pınar Bayrak‐Toydemir, Christine E. Miller +22 more

Provision and availability of genomic medicine services in Level IV neonatal intensive care units

Genetics in Medicine(2023)10.1016/j.gim.2023.100926
N/A
0DataRank · unranked
18 citations

Katharine Press Callahan, Austin Antoniou, Maya C. del Rosario, Luca Brunelli, Nahed O. ElHassan +8 more

Open-Source Artificial Intelligence System Supports Diagnosis of Mendelian Diseases in Acutely Ill Infants

Children(2023)10.3390/children10060991
N/A
0DataRank · unranked
4 citations

Pablo Botas, Christine E. Miller, Jian Zhao, Sabrina Malone Jenkins, Hunter Best +5 more

A Children’s Rights Framework for Genomic Medicine: Newborn Screening as a Use Case

Medical Research Archives(2024)10.18103/mra.v12i3.5167
N/A
0DataRank · unranked
5 citations

Kee Chan, James Tabery, Warren Binford, Amy Brower, Luca Brunelli

Exploring the Role of Genetic Testing in Decisions to Redirect Care in Critically Ill Infants

American Journal of Hospice and Palliative Medicine®(2024)10.1177/10499091241296544
N/A
0DataRank · unranked
4 citations

Bob Wong, Jamie Seale, Luca Brunelli, Ashley Mowery

Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One)

Frontiers in Genetics(2022)10.3389/fgene.2022.867337
N/A
0DataRank · unranked
21 citations

Kee Chan, Marc S. Williams, Susan A. Berry, Robert J. Currier, Piero Rinaldo +22 more

More Than a Decade of Rapid Genomic Sequencing: Where Are We Now?

Clinical Chemistry(2024)10.1093/clinchem/hvae025
N/A
0DataRank · unranked
0 citations

Luca Brunelli, Michael J. Deem, Emily Farrow, Madhuri Hegde, Zornitza Stark +1 more