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

Tara Schmidlen

ID Genomics (United States)

ORCID: 0000-0002-9749-112X

Also affiliated with Genomics Medicine (Ireland), Genomics (United Kingdom)

Biochemistry, Genetics and Molecular BiologyPharmacology, Toxicology and PharmaceuticsMedicine

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
0.679Author 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.

Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study

PEC Innovation(2023)10.1016/j.pecinn.2023.100134
Top 29%
0.679DataRank
Top 29%17 citations

Zoe Lindsey‐Mills, Andrew Brangan, Sarah Savage, Tara Schmidlen, Kelly Morgan +6 more

Papers

Driven by 5 papers — median percentile 71. Top paper: “Returning integrated genomic risk and clinical recommendations: The eMERGE study”.

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006
N/A
2.6DataRank · unranked
121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study

PEC Innovation(2023)10.1016/j.pecinn.2023.100134
Top 29%
0.679DataRank
Top 29%17 citations

Zoe Lindsey‐Mills, Andrew Brangan, Sarah Savage, Tara Schmidlen, Kelly Morgan +6 more

Clinical outcomes of a genomic screening program for actionable genetic conditions

Genetics in Medicine(2020)10.1038/s41436-020-0876-4
N/A
0DataRank · unranked
154 citations

H. Lester Kirchner, M. Schwartz, Melissa Kelly, Tara Schmidlen, Laney K. Jones +15 more

Testing a best practices risk result format to communicate genetic risks

Patient Education and Counseling(2020)10.1016/j.pec.2020.10.021
N/A
0DataRank · unranked
27 citations

Debra Roter, Tara Schmidlen, Laura Scheinfeldt, William M. P. Klein, Kyle Davis

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535
N/A
0DataRank · unranked
7 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more