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

James T. Bennett

Seattle Children's Hospital

ORCID: 0000-0003-2843-5594

Also affiliated with University of Washington, University of Washington Medical Center, Seagen (United States)

MedicineBiochemistry, 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 7%percentile
0.165Author 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.

Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.13.681545
Top 70%
0.165DataRank
Top 70%2 citations

Dominika Maziec, Julia Markowski, Stephanie Georges, Nancy L. Parmalee, Michele Berselli +41 more

Papers

Driven by 14 papers — median percentile 30. Top paper: “Targeted long-read sequencing identifies missing disease-causing variation”.

Targeted long-read sequencing identifies missing disease-causing variation

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.006
N/A
0.825DataRank · unranked
243 citations

Arvis Sulovari, Tianyun Wang, Hailey Loucks, Kendra Hoekzema, Katherine M. Munson +45 more

The Somatic Mosaicism across Human Tissues Network

Nature(2025)10.1038/s41586-025-09096-7
N/A
0.672DataRank · unranked
43 citations

Ji Won Oh, Yujin Angelina Choi, Nam Seop Lim, Boxun Zhao, Adam Voshall +365 more

Targeted long-read sequencing resolves complex structural variants and identifies missing disease-causing variants

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.03.365395
N/A
0.360DataRank · unranked
10 citations

Arvis Sulovari, Tianyun Wang, Hailey Loucks, Kendra Hoekzema, Katherine M. Munson +32 more

Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51786
N/A
0.241DataRank · unranked
4 citations

Ghayda Mirzaa, Elizabeth Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth +28 more

Isolated lateralized overgrowth and the need for tumor screening: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2025)10.1016/j.gim.2025.101480
N/A
0.208DataRank · unranked
3 citations

Aya Abu El Haija, James T. Bennett, Leslie G. Biesecker, Matthew A. Deardorff, Evan R. Hathaway +5 more

Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.13.681545
Top 70%
0.165DataRank
Top 70%2 citations

Dominika Maziec, Julia Markowski, Stephanie Georges, Nancy L. Parmalee, Michele Berselli +41 more

Somatic activating BRAF variants cause isolated lymphatic malformations

medRxiv(2021)10.1101/2021.11.03.21265682
N/A
0DataRank · unranked
1 citations

Dana M. Jensen, Victoria Dmyterko, Giridhar M. Shivaram, Candace T. Myers, Cate Paschal +9 more

Somatic activating BRAF variants cause isolated lymphatic malformations

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100101
N/A
0DataRank · unranked
21 citations

Dana M. Jensen, Victoria Dmyterko, Giridhar M. Shivaram, Candace T. Myers, Cate Paschal +9 more

Primary targeted medical therapy for management of bilateral head and neck lymphatic malformations in infants

International Journal of Pediatric Otorhinolaryngology(2022)10.1016/j.ijporl.2022.111371
N/A
0DataRank · unranked
7 citations

Jonathan N. Perkins, Kaitlyn Zenner, Catherine Bull, Erika Lutsky, Dana M. Jensen +9 more

A dyadic approach to the delineation of diagnostic entities in clinical genomics

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2020.11.013
N/A
0DataRank · unranked
116 citations

Margaret P Adam, Fowzan S. Alkuraya, Anne Amemiya, Michael J. Bamshad, Anita E. Beck +42 more

Clinical RNA sequencing clarifies variants of uncertain significance identified by prior testing

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101886
N/A
0DataRank · unranked
7 citations

Jennifer N. Cech, Cate Paschal, Bri Dingmann, Anna I. Scott, Jenny Thies +24 more

Mapping single-cell diploid chromatin fiber architectures using DAF-seq

Nature Biotechnology(2025)10.1038/s41587-025-02914-3
N/A
0DataRank · unranked
5 citations

Yizi Mao, Benjamin J. Mallory, Mitchell R. Vollger, Stephanie C. Bohaczuk, Christopher B. Oliveira +7 more

CHRNB1‐associated congenital myasthenia syndrome: Expanding the clinical spectrum

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.62011
N/A
0DataRank · unranked
13 citations

Anisha C. Schwarz, Brianna K. Brei, Sarah V. Clowes Candadai, Jenny Thies, Jean K. Mah +5 more

The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children

The Journal of Pediatrics(2020)10.1016/j.jpeds.2020.06.020
N/A
0DataRank · unranked
61 citations

Sarah V. Clowes Candadai, Megan Sikes, Jenny Thies, Heather M. Byers, Jennifer N. Dines +14 more