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

San Jewell

California University of Pennsylvania

ORCID: 0000-0002-6494-8015

Also affiliated with University of Pennsylvania

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 4%percentile
0.756Author 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.

MAJIQlopedia: an encyclopedia of RNA splicing variations in human tissues and cancer

Nucleic Acids Research(2023)10.1093/nar/gkad1043
Top 36%
0.548DataRank
Top 36%20 citations

San Jewell, Kristen W. Lynch, Andrei Thomas‐Tikhonenko, Yoseph Barash, Mathieu Quesnel-Vallières

Papers

Driven by 13 papers — median percentile 50. Top paper: “MAJIQlopedia: an encyclopedia of RNA splicing variations in human tissues and cancer”.

MAJIQlopedia: an encyclopedia of RNA splicing variations in human tissues and cancer

Nucleic Acids Research(2023)10.1093/nar/gkad1043
Top 36%
0.548DataRank
Top 36%20 citations

San Jewell, Kristen W. Lynch, Andrei Thomas‐Tikhonenko, Yoseph Barash, Mathieu Quesnel-Vallières

PolyA_DB v4: systematic polyA site identification and isoform annotation in human and mouse genomes using 3′ end and long-read sequencing data

Nucleic Acids Research(2025)10.1093/nar/gkaf1212
Top 65%
0.208DataRank
Top 65%3 citations

Wei Chun Chen, Luyang Wang, San Jewell, Ayna Mammedova, Seong Woo Han +4 more

Contrasting and Combining Transcriptome Complexity Captured by Short and Long RNA Sequencing Reads

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.21.568046
N/A
0DataRank · unranked
3 citations

San Jewell, Andrei Thomas‐Tikhonenko, Yoseph Barash, Seong Woo Han

Machine learning-optimized targeted detection of alternative splicing

Nucleic Acids Research(2024)10.1093/nar/gkae1260
N/A
0DataRank · unranked
3 citations

Nathaniel Islas, San Jewell, Di Wu, Anupama Jha, Caleb M. Radens +5 more

Contrasting and combining transcriptome complexity captured by short and long RNA sequencing reads

Genome Research(2024)10.1101/gr.278659.123
N/A
0DataRank · unranked
17 citations

San Jewell, Andrei Thomas‐Tikhonenko, Yoseph Barash, Seong Woo Han

Machine learning-optimized targeted detection of alternative splicing

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.20.614162
N/A
0DataRank · unranked
5 citations

Nathaniel Islas, San Jewell, Anupama Jha, Caleb M. Radens, Jeffrey A. Pleiss +4 more

A Deep Dive into Statistical Modeling of RNA Splicing QTLs Reveals New Variants that Explain Neurodegenerative Disease

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.01.610696
N/A
0DataRank · unranked
0 citations

Matthew R. Gazzara, San Jewell, Benjamin D Wales-McGrath, Christopher Devlin Brown, Peter S. Choi +2 more

A deep dive into statistical modeling of RNA splicing QTLs reveals variants that explain neurodegenerative disease

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.10.012
N/A
0DataRank · unranked
1 citations

Matthew R. Gazzara, San Jewell, Benjamin D Wales-McGrath, Kevin Yang, Christopher D. Brown +3 more

G4mer: An RNA language model for transcriptome-wide identification of G-quadruplexes and disease variants from population-scale genetic data

Nature Communications(2025)10.1038/s41467-025-65020-7
N/A
0DataRank · unranked
1 citations

Danielle Gutman, Nathaniel Islas, Bryan B. Guzmán, Alli Jimenez, San Jewell +5 more

Generative modeling for RNA splicing prediction and design

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.20.633986
N/A
0DataRank · unranked
2 citations

Natalie Maus, Anupama Jha, Kevin Yang, Benjamin D Wales-McGrath, San Jewell +5 more

RNA splicing analysis using heterogeneous and large RNA-seq datasets

Nature Communications(2023)10.1038/s41467-023-36585-y
N/A
0DataRank · unranked
120 citations

Joseph K. Aicher, San Jewell, Matthew R. Gazzara, Caleb M. Radens, Anupama Jha +5 more

MAJIQ-CLIN: A novel tool for the identification of Mendelian disease-causing variants from RNA-Seq data

medRxiv(2025)10.1101/2025.01.30.25321185
N/A
0DataRank · unranked
0 citations

Dina Issakova, Barry Slaff, San Jewell, Nicholas F. Lahens, Gregory R. Grant +7 more

A Bayesian model for unsupervised detection of RNA splicing based subtypes in cancers

Nature Communications(2023)10.1038/s41467-022-35369-0
N/A
0DataRank · unranked
9 citations

Mathieu Quesnel-Vallières, San Jewell, Moein Elzubeir, Kristen W. Lynch, Andrei Thomas‐Tikhonenko +2 more