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

Erwin Frise

Lawrence Berkeley National Laboratory

ORCID: 0000-0002-9281-4567
Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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: “Fiji: an open-source platform for biological-image analysis”.

Fiji: an open-source platform for biological-image analysis

Nature Methods(2012)10.1038/nmeth.2019
N/A
1.7DataRank · unranked
68810 citations

Ignacio Arganda-Carreras, Erwin Frise, Verena Kaynig, Mark Longair, Tobias Pietzsch +15 more

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

Response to Grosse et al.

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.004
N/A
0DataRank · unranked
1 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Serge Batalov, Wendy Benson +46 more

Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.021
N/A
0DataRank · unranked
11 citations

Meredith S. Wright, Laurie D. Smith, Yupu Liang, William R. Mowrey, Liana Protopsaltis +40 more

Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery

Nature Communications(2025)10.1038/s41467-025-61625-0
N/A
0DataRank · unranked
4 citations

Edgar J. Hernández, Thomas A. Miller, Nathan R. Blue, Raquel M. Zimmerman, Eric R. Griffiths +21 more

MPSE identifies newborns for whole genome sequencing within 48 h of NICU admission

npj Genomic Medicine(2025)10.1038/s41525-025-00506-3
N/A
0DataRank · unranked
0 citations

Edwin F. Juarez, Barry Moore, Edgar J. Hernández, Erwin Frise, Jianrong Li +8 more

Genome x Environment analysis of Sudden Unexpected Infant Death unveils etiologic heterogeneity and strong cannabis and genetic disease risks

medRxiv(2025)10.1101/2025.11.26.25341098
N/A
0DataRank · unranked
0 citations

Gretchen Bandoli, Daniel Helbling, Rebecca J. Baer, Eric Blincow, Bryant Cao +15 more

A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.003
N/A
0DataRank · unranked
171 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Sergey Batalov, Wendy Benson +46 more