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

Rachel A. Ungar

Stanford Medicine

ORCID: 0000-0002-2214-959X

Also affiliated with Stanford University

Biochemistry, Genetics and Molecular Biology

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

0.505Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Transcriptomics and chromatin accessibility in multiple African population samples

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.04.564839

Top 38%

0.505DataRank

Top 38%13 citations

Pagé C. Goddard, Emre Karakoç, Soumya Kundu, Stephanie M. Yan, Daniel Nachun +27 more

Papers

Driven by 12 papers — median percentile 62. Top paper: “Transcriptomics and chromatin accessibility in multiple African population samples”.

Transcriptomics and chromatin accessibility in multiple African population samples

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.04.564839

Top 38%

0.505DataRank

Top 38%13 citations

Pagé C. Goddard, Emre Karakoç, Soumya Kundu, Stephanie M. Yan, Daniel Nachun +27 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

Genome Research(2025)10.1101/gr.279323.124

N/A

0.425DataRank · unranked

11 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101166

N/A

0DataRank · unranked

11 citations

Nicole Legro, Dustin Baldridge, Jimann Shin, Angela Bowman, Berrak Uğur +89 more

Increasing equity in science requires better ethics training: A course by trainees, for trainees

Cell Genomics(2024)10.1016/j.xgen.2024.100554

N/A

0DataRank · unranked

4 citations

Rachel A. Ungar, Alanna L. Pyke, Alvina Adimoelja, Meenakshi Chakraborty, Daniel J. Cotter +11 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

medRxiv(2024)10.1101/2024.03.22.24304565

N/A

0DataRank · unranked

5 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

Impact of genome build on RNA-seq interpretation and diagnostics

medRxiv(2024)10.1101/2024.01.11.24301165

N/A

0DataRank · unranked

0 citations

Pagé C. Goddard, Tanner Jensen, Fabien Degalez, Kevin S. Smith, Christopher Jin +6 more

Transcriptome-wide outlier approach identifies individuals with minor spliceopathies

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.018

N/A

0DataRank · unranked

17 citations

Rodrigo Mendez, Rachel A. Ungar, Devon Bonner, Dena R. Matalon, Gabrielle Lemire +19 more

GREGoR: accelerating genomics for rare diseases

Nature(2025)10.1038/s41586-025-09613-8

N/A

0DataRank · unranked

15 citations

Ben Heavner, Marsha M. Wheeler, Rachel A. Ungar, Jonathan LoTempio, Laurens Wiel +94 more

Transcriptomic signatures of rare variant impacts across sex and the X chromosome

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100463

N/A

0DataRank · unranked

2 citations

Taibo Li, Nikolai G. Vetr, Nicole Ersaro, Alexis Battle, Stephen B. Montgomery +1 more

Transcriptome-wide outlier approach identifies individuals with minor spliceopathies

medRxiv(2025)10.1101/2025.01.02.24318941

N/A

0DataRank · unranked

10 citations

Rodrigo Mendez, Rachel A. Ungar, Devon Bonner, Dena R. Matalon, Gabrielle Lemire +20 more

Functional impact of rare variants and sex across the X-chromosome and autosomes

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.23.634570

N/A

0DataRank · unranked

0 citations

Taibo Li, Nikolai G. Vetr, Nicole M. Ferraro, Alexis Battle, Stephen B. Montgomery +1 more

Impact of genome build on RNA-seq interpretation and diagnostics

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.005

N/A

0DataRank · unranked

13 citations

Pagé C. Goddard, Tanner Jensen, Fabien Degalez, Kevin S. Smith, Christopher Jin +5 more