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

Erica Sanford Kobayashi

Children’s Institute

ORCID: 0000-0002-3622-8141
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 3%percentile
1.5Author DataRank

Indexed papers

2in 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 2 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.

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

Rapid Whole-Genome Sequencing and Clinical Management in the PICU: A Multicenter Cohort, 2016–2023*

Pediatric Critical Care Medicine(2024)10.1097/pcc.0000000000003522
Top 28%
0.728DataRank
Top 28%23 citations

Jordan Vaught, Lisa Salz, Jennifer Foley, Zaineb Boulil, Heather M. Van Dongen-Trimmer +10 more

The Genomic landscape of short tandem repeats across multiple ancestries

PLoS ONE(2023)10.1371/journal.pone.0279430
N/A
0DataRank · unranked
8 citations

Serge Batalov, Yan Ding, Erica Sanford Kobayashi, Stephen F. Kingsmore, David Dimmock +3 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

Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.020
N/A
0DataRank · unranked
13 citations

Meredith S. Wright, L. Olsen, Brandan Schultz, Liana Protopsaltis, Dan Averbuj +30 more

Approaches to long-read sequencing in a clinical setting to improve diagnostic rate

Scientific Reports(2022)10.1038/s41598-022-20113-x
N/A
0DataRank · unranked
56 citations

Serge Batalov, Aaron M. Wenger, Christine Lambert, Harsharan Dhillon, Richard Hall +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

Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system

Frontiers in Pediatrics(2023)10.3389/fped.2023.1157630
N/A
0DataRank · unranked
11 citations

Elliot A. Perens, Nicole G. Coufal, Erica Sanford Kobayashi, Stephen F. Kingsmore, David Dimmock +1 more