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

Jonas A. Gustafson

Seattle Children's Hospital

ORCID: 0000-0002-5748-905X

Also affiliated with University of Washington

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 2%percentile
2.1Author 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.

High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

Genome Research(2024)10.1101/gr.279273.124
Top 13%
1.7DataRank
Top 13%78 citations

Sophia B Gibson, Nikhita Damaraju, Miranda Pg Zalusky, Kendra Hoekzema, David Twesigomwe +42 more

Papers

Driven by 15 papers — median percentile 37. Top paper: “High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation”.

High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

Genome Research(2024)10.1101/gr.279273.124
Top 13%
1.7DataRank
Top 13%78 citations

Sophia B Gibson, Nikhita Damaraju, Miranda Pg Zalusky, Kendra Hoekzema, David Twesigomwe +42 more

Pangenome discovery of missing autism variants

medRxiv(2025)10.1101/2025.07.21.25331932
Top 63%
0.216DataRank
Top 63%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +23 more

Using the linear references from the pangenome to discover missing autism variants

Nature Communications(2026)10.1038/s41467-026-68378-4
Top 65%
0.208DataRank
Top 65%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +252 more

AXIN1 mutations in nonsyndromic craniosynostosis

Journal of Neurosurgery Pediatrics(2024)10.3171/2024.5.peds24115
N/A
0.165DataRank · unranked
2 citations

Kshipra Hemal, Jonas A. Gustafson, Le Hao, Irene Valenzuela, Anne Slavotinek +5 more

Damaging variants in FOXI3 cause microtia and craniofacial microsomia

Genetics in Medicine(2022)10.1016/j.gim.2022.09.005
N/A
0DataRank · unranked
21 citations

Andrew T. Timberlake, Justin J. Curran, Michael L. Cunningham, Barbara McDonough, Maria A. Artunduaga +21 more

3-hour genome sequencing and targeted analysis to rapidly assess genetic risk

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101833
N/A
0DataRank · unranked
13 citations

Jonas A. Gustafson, Stephanie C. Bohaczuk, Benjamin J. Mallory, Paxton Reed, Tara Wenger +14 more

CFAP47 is Implicated in X-Linked Polycystic Kidney Disease

Kidney International Reports(2024)10.1016/j.ekir.2024.09.013
N/A
0DataRank · unranked
4 citations

Takuya Fujimaru, Chunyu Liu, Karynne Patterson, Kouhei Yamamoto, Takefumi Suzuki +63 more

Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders

Journal of Medical Genetics(2021)10.1136/jmedgenet-2020-107459
N/A
0DataRank · unranked
10 citations

Maud Wurmser, Simon J. McGowan, Rodrigo Atique, Débora Romeo Bertola, Michael L. Cunningham +11 more

Haploinsufficiency of SF3B2 causes craniofacial microsomia

Nature Communications(2021)10.1038/s41467-021-24852-9
N/A
0DataRank · unranked
89 citations

Casey Griffin, Carrie L. Heike, Anne Hing, Michael L. Cunningham, David Chitayat +24 more

A Diagnostic Blind Spot: Deep intronic SVA_E Insertion identified as the most Common Pathogenic Variant Associated with Canavan Disease

medRxiv(2024)10.1101/2024.12.18.24318806
N/A
0DataRank · unranked
1 citations

Katrina M. Bell, Ramakrishnan Rajagopalan, M. De Silva, Aída Lemes, Cristina Zoco Zabala +24 more

Deep Intronic SVA_E Insertion Identified as the Most Common Pathogenic Variant Associated With Canavan Disease

Neurology Genetics(2025)10.1212/nxg.0000000000200291
N/A
0DataRank · unranked
3 citations

Katrina M. Bell, Ramakrishnan Rajagopalan, M. De Silva, Aída Lemes, Cristina Zoco Zabala +24 more

Complementarity of Long‐Reads and Optical Mapping in Parkinson's Disease for Structural Variants

Annals of Clinical and Translational Neurology(2026)10.1002/acn3.70332
N/A
0DataRank · unranked
0 citations

Theresa Lüth, Susen Schaake, Carolin Gabbert, Marius Möller, Hauke Busch +14 more

Principles and functional consequences of plasmid chromatinization in mammalian cells

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.27.656122
N/A
0DataRank · unranked
1 citations

Thomas W. Tullius, Carina G Biar, Jonas A. Gustafson, Stephanie C. Bohaczuk, Danilo Dubocanin +3 more

Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia Pigmenti

Research Square(2025)10.21203/rs.3.rs-5811417/v1
N/A
0DataRank · unranked
0 citations

Robin D. Clark, Abdallah F. Elias, Casie A. Genetti, Jill A. Madden, Dana Simpson +21 more

Long-read sequencing is required for precision diagnosis of incontinentia pigmenti

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100468
N/A
0DataRank · unranked
0 citations

Robin D. Clark, Abdallah F. Elias, Casie A. Genetti, Jill A. Madden, Dana Simpson +21 more