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

Birgit Funke

Icahn School of Medicine at Mount Sinai

ORCID: 0000-0001-6643-3640
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
0.481Author 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.

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.01.014
Top 40%
0.481DataRank
Top 40%8 citations

Alexander Ing, Christian Antolik, Christina Austin‐Tse, Linnea M. Baudhuin, Lucas Bronicki +25 more

Papers

Driven by 9 papers — median percentile 60. Top paper: “Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)”.

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.01.014
Top 40%
0.481DataRank
Top 40%8 citations

Alexander Ing, Christian Antolik, Christina Austin‐Tse, Linnea M. Baudhuin, Lucas Bronicki +25 more

An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy

Human Mutation(2020)10.1002/humu.24061
N/A
0.449DataRank · unranked
19 citations

Naif A. M. Almontashiri, Leslie G. Biesecker, Natalie Berger, Wendy K. Chung, John Garcia +17 more

Elective genomic testing: Practice resource of the National Society of Genetic Counselors

Journal of Genetic Counseling(2023)10.1002/jgc4.1654
N/A
0.442DataRank · unranked
18 citations

David Bick, Louise Bier, Birgit Funke, Matthew Lebo, Katie L. Lewis +6 more

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w
N/A
0.330DataRank · unranked
8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 more

Creation of an Expert Curated Variant List for Clinical Genomic Test Development and Validation: A ClinGen and GeT-RM Collaborative Project

medRxiv(2021)10.1101/2021.06.09.21258594
N/A
0DataRank · unranked
1 citations

Steven M. Harrison, Edward R. Lockhart, Karl V. Voelkerding, Ira M. Lubin, ClinGen Expert Panels +4 more

The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101820
N/A
0DataRank · unranked
2 citations

Vimla S. Aggarwal, A. Bale, Daniel B. Bellissimo, Jessica K. Booker, Yang Cao +30 more

Standardization of Genomic Nomenclature across a Diverse Ecosystem of Stakeholders: Evolution and Challenges

Clinical Chemistry(2025)10.1093/clinchem/hvae195
N/A
0DataRank · unranked
1 citations

Melissa Landrum, Robert R. Freimuth, Birgit Funke, Laura K. Conlin

From Expert Knowledge to Validation Resources

Journal of Molecular Diagnostics(2025)10.1016/j.jmoldx.2025.07.006
N/A
0DataRank · unranked
0 citations

Martine Tremblay, Edward R. Lockhart, Swaroop Aradhya, Pınar Bayrak‐Toydemir, Mark Bowser +12 more

ACMG clinical laboratory standards for next-generation sequencing

UNC Libraries(2020)10.17615/bgw9-dv56
N/A
0DataRank · unranked
0 citations

Heidi L. Rehm, Birgit Funke, Madhuri Hegde, Kerry K. Brown, Elaine Lyon +5 more