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

Erin M. Ramos

National Institutes of Health

ORCID: 0000-0002-2210-325X

Also affiliated with National Human Genome Research Institute, Office of the Director, Office of Research Infrastructure Programs

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 2%percentile
1.8Author DataRank

Indexed papers

3in 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 3 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.

The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation

Genetics in Medicine(2024)10.1016/j.gim.2024.101228
Top 17%
1.2DataRank
Top 17%59 citations

Danielle R. Azzariti, Larry Babb, Jonathan S. Berg, Leslie G. Biesecker, Zo Bly +28 more

Papers

Driven by 18 papers — median percentile 66. Top paper: “Potential etiologic and functional implications of genome-wide association loci for human diseases and traits”.

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

Proceedings of the National Academy of Sciences(2009)10.1073/pnas.0903103106
N/A
1.2DataRank · unranked
4159 citations

Praveen Sethupathy, Heather A. Junkins, Erin M. Ramos, Jayashri P. Mehta, Francis S. Collins +2 more

The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation

Genetics in Medicine(2024)10.1016/j.gim.2024.101228
Top 17%
1.2DataRank
Top 17%59 citations

Danielle R. Azzariti, Larry Babb, Jonathan S. Berg, Leslie G. Biesecker, Zo Bly +28 more

The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources

medRxiv(2022)10.1101/2022.01.03.21268593
Top 34%
0.575DataRank
Top 34%17 citations

Scott Goehringer, Lawrence Babb, Fowzan S. Alkuraya, Joanna Amberger, Mutaz Amin +41 more

Design and implementation of an action plan for justice, equity, diversity, and inclusion within the Clinical Genome Resource

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.009
N/A
0.165DataRank · unranked
2 citations

Deborah Ritter, Danielle R. Azzariti, Jonathan S. Berg, Joanna E. Bulkley, Mildred K. Cho +12 more

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

UNC Libraries(2020)10.17615/dtq0-px12
Top 100%
0DataRank
Top 100%0 citations

Ozge Ceyhan‐Birsoy, Bryce A. Seifert, Tam P. Sneddon, Natasha T. Strande, Erin M. Ramos +18 more

Phenotype harmonization and cross-study collaboration in GWAS consortia: the GENEVA experience

UNC Libraries(2020)10.17615/e70t-ax35
N/A
0DataRank · unranked
0 citations

Gerardo Heiss, Kristine R. Monroe, Neil E. Caporaso, John A. Heit, Steven J. Kittner +16 more

ClinGen — The Clinical Genome Resource

UNC Libraries(2020)10.17615/js2g-yk58
N/A
0DataRank · unranked
0 citations

Erin M. Ramos, David H. Ledbetter, Carlos D. Bustamante, Stephen T. Sherry, Michael S. Watson +9 more

Using the PhenX Toolkit to Select Standard Measurement Protocols for Your Research Study

Current Protocols(2021)10.1002/cpz1.149
N/A
0DataRank · unranked
30 citations

Stephen Y. Hwang, Jonathan L. Haines, Erin M. Ramos, Catherine A. McCarty, Mary L. Marazita +5 more

Genomic medicine implementation protocols in the PhenX Toolkit: tools for standardized data collection

Genetics in Medicine(2021)10.1038/s41436-021-01183-0
N/A
0DataRank · unranked
4 citations

Kyle B. Brothers, Angela R. Bradbury, Sirisak Chanprasert, Lori A. Orlando, Ali Torkamani +9 more

ClinGen’s Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents

Genetics in Medicine(2022)10.1016/j.gim.2022.02.019
N/A
0DataRank · unranked
13 citations

Charisma L. Jenkins, Joanna E. Bulkley, Marian J. Gilmore, Kristy Lee, Christine M. Pak +17 more

A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources

Journal of the American Medical Informatics Association(2022)10.1093/jamia/ocac057
N/A
0DataRank · unranked
9 citations

Laura Findley, Madison P. Goldrich, Tejinder Rakhra-Burris, Ana Stevens, Pamela A. Williams +34 more

Data compatibility in the addiction sciences: An examination of measure commonality

UNC Libraries(2020)10.17615/zkqc-wn78
N/A
0DataRank · unranked
0 citations

Lisa C. Strader, Andrea M. Hussong, Carol M. Hamilton, Arpana Agrawal, Dana B. Hancock +15 more

Identifying Datasets for Cross-Study Analysis in dbGaP using PhenX

Scientific Data(2022)10.1038/s41597-022-01660-4
N/A
0DataRank · unranked
4 citations

Vesselina Bakalov, Lisa Cox, Michelle Engle, Stephen W. Erickson, Michael Feolo +12 more

The PhenX Toolkit: Measurement Protocols for Assessment of Social Determinants of Health

American Journal of Preventive Medicine(2023)10.1016/j.amepre.2023.03.003
N/A
0DataRank · unranked
33 citations

Cataia Ives, Nancy Lee Jones, Barbara Entwisle, Alicia Fernández, Theresa Cullen +19 more

Toward robust clinical genome interpretation: Developing a consistent terminology to characterize Mendelian disease-gene relationships—allelic requirement, inheritance modes, and disease mechanisms

Genetics in Medicine(2023)10.1016/j.gim.2023.101029
N/A
0DataRank · unranked
17 citations

Marina T. DiStefano, Erin Rooney Riggs, Katherine Josephs, Fowzan S. Alkuraya, Joanna Amberger +21 more

Towards robust clinical genome interpretation: developing a consistent terminology to characterize disease-gene relationships - allelic requirement, inheritance modes and disease mechanisms

medRxiv(2023)10.1101/2023.03.30.23287948
N/A
0DataRank · unranked
7 citations

Marina T. DiStefano, Erin Rooney Riggs, Katherine Josephs, Fowzan S. Alkuraya, Joanna Amberger +21 more

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation

UNC Libraries(2020)10.17615/0tee-nv95
N/A
0DataRank · unranked
1 citations

Christa Lese Martin, Evans, James P., Meredith Weaver, Katrina A.B. Goddard, Margaret Piper +19 more

Improving reporting standards for polygenic scores in risk prediction studies

medRxiv(2020)10.1101/2020.04.23.20077099
N/A
0DataRank · unranked
55 citations

Samuel A. Lambert, Cecelia P. Tamburro, Michael A. Iacocca, Jack W. O’Sullivan, Catherine H. Sillari +28 more