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

Steven E. Scherer

Baylor College of Medicine

ORCID: 0000-0002-3719-3673

Also affiliated with Baylor Genetics

Biochemistry, Genetics and Molecular BiologyPharmacology, Toxicology and PharmaceuticsAgricultural 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 1%percentile
4.6Author 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.

Comparative validation of the D. melanogaster modENCODE transcriptome annotation

Genome Research(2014)10.1101/gr.159384.113
Top 5%
4.6DataRank
Top 5%192 citations

David Sturgill, Jiaxin Qu, Huaiyang Jiang, Soo Park, Nathan Boley +67 more

Papers

Driven by 8 papers — median percentile 95. Top paper: “Comparative validation of the D. melanogaster modENCODE transcriptome annotation”.

Comparative validation of the D. melanogaster modENCODE transcriptome annotation

Genome Research(2014)10.1101/gr.159384.113
Top 5%
4.6DataRank
Top 5%192 citations

David Sturgill, Jiaxin Qu, Huaiyang Jiang, Soo Park, Nathan Boley +67 more

Implementation of preemptive DNA sequence–based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study

Genetics in Medicine(2022)10.1016/j.gim.2022.01.022
N/A
0DataRank · unranked
69 citations

Steven E. Scherer, Suzette J. Bielinski, Donna M. Muzny, Leila A. Jones, John L. Black +95 more

CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis

Journal of Molecular Diagnostics(2022)10.1016/j.jmoldx.2021.12.011
N/A
0DataRank · unranked
47 citations

Erin C. Boone, Steven E. Scherer, Seung‐been Lee, Ibrahim Numanagić, S. Cenk Şahinalp +13 more

Targeted Genotyping in Clinical Pharmacogenomics

Journal of Molecular Diagnostics(2022)10.1016/j.jmoldx.2021.11.008
N/A
0DataRank · unranked
33 citations

Kimberley Harris, Mary Beth Karow, Sandra E. Peterson, Michelle L. Kluge, Katrina E. Kotzer +9 more

Experiences in providing a community educational resource for the All of Us Researcher Workbench

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae226
N/A
0DataRank · unranked
2 citations

Jinyoung Byun, Jun Wang, Stephen Richards, Pamela N. Luna, LaTerrica Williams +11 more

Deep sequencing of candidate genes identified 14 variants associated with smoking abstinence in an ethnically diverse sample

Scientific Reports(2024)10.1038/s41598-024-56750-7
N/A
0DataRank · unranked
0 citations

David W. Wetter, Jian Wang, Robert Yu, George Kypriotakis, Tapsi Kumar +8 more

Toward an integrated resource for pharmacogenomics (PGx): Survey findings from the genomic medicine communities

Genetics in Medicine(2025)10.1016/j.gim.2025.101529
N/A
0DataRank · unranked
4 citations

Li Gong, Kelly E. Caudle, Hetanshi Naik, Philip E. Empey, James M. Hoffman +9 more

The SHR/Akr Y chromosome reveals repeated turnover of the rat pseudoautosomal region

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.28.656580
N/A
0DataRank · unranked
1 citations

Helen Skaletsky, Jennifer F. Hughes, Laura G. Brown, Tatyana Pyntikova, Ting-Jan Cho +15 more