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

Diane T. Smelser

Geisinger Medical Center

ORCID: 0000-0002-3925-8864

Also affiliated with Genomic Health (United States), Geisinger Health System

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 5%percentile
0.355Author 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.

A genome-first approach to characterize DICER1 pathogenic variant prevalence, penetrance and cancer, thyroid, and other phenotypes in 2 population-scale cohorts

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101846
Top 50%
0.355DataRank
Top 50%9 citations

Jeremy S. Haley, Jessica N. Hatton, Uyenlinh L Mirshahi, H. Shanker Rao, Mark Ramos +6 more

Papers

Driven by 6 papers — median percentile 50. Top paper: “Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants”.

Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100242
N/A
0.449DataRank · unranked
19 citations

Natasha T. Strande, Jung Kim, Jeremy S. Haley, Jessica N. Hatton, Megan N. Frone +13 more

A genome-first approach to characterize DICER1 pathogenic variant prevalence, penetrance and cancer, thyroid, and other phenotypes in 2 population-scale cohorts

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101846
Top 50%
0.355DataRank
Top 50%9 citations

Jeremy S. Haley, Jessica N. Hatton, Uyenlinh L Mirshahi, H. Shanker Rao, Mark Ramos +6 more

Genomic ascertainment of CHEK2 -related cancer predisposition

medRxiv(2024)10.1101/2024.08.07.24311613
N/A
0.179DataRank · unranked
1 citations

Jung Kim, Mark Ramos, Jeremy S. Haley, Diane T. Smelser, H. Shanker Rao +6 more

TERT c.3150 G > C (p.K1050N): a founder Ashkenazi Jewish variant associated with telomere biology disorders

npj Genomic Medicine(2025)10.1038/s41525-025-00501-8
N/A
0.104DataRank · unranked
1 citations

Emília M. Pinto, Tianna Zhao, Logan P Zeigler, Jung Kim, Neelam Giri +18 more

Novel polygenic risk score associates with diverticulitis in a multi-institutional, ancestrally diverse cohort

Scientific Reports(2025)10.1038/s41598-025-26455-6
N/A
0DataRank · unranked
1 citations

Thomas E. Ueland, Sarah Abramowitz, John DePaolo, Noah L. Tsao, Jeffrey L. Roberson +8 more

Genome-First Approach to Rare and Common Variant Risk of Thoracic Aortic Aneurysm and Dissection

medRxiv(2025)10.1101/2025.05.18.25327858
N/A
0DataRank · unranked
1 citations

Diane T. Smelser, Dongchuan Guo, Sarah Abramowitz, Gina Biagetti, Renae Judy +12 more