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

Tom Walsh

University of Washington

ORCID: 0000-0002-8875-0310

Also affiliated with University of Washington Medical Center, Mater Misericordiae University Hospital

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 2%percentile
1.8Author 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.

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Clinical Genetics(2020)10.1111/cge.13817
Top 22%
0.929DataRank
Top 22%29 citations

Süleyman Gülsüner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov +45 more

Papers

Driven by 14 papers — median percentile 78. Top paper: “Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia”.

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

Science(2008)10.1126/science.1155174
N/A
1.1DataRank · unranked
1822 citations

Anjene M Addington, Wellcome Trust Case Control Consortium, Anjené M. Addington, Sarah B. Pierce, Alex S. Nord +39 more

Microduplications of 16p11.2 are associated with schizophrenia

Nature Genetics(2009)10.1038/ng.474
N/A
0.990DataRank · unranked
733 citations

Kenneth S. Kendler, Manfred Kayser, Anjene M Addington, Jon McClellan, Milica Pejović-Milovančević +66 more

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Clinical Genetics(2020)10.1111/cge.13817
Top 22%
0.929DataRank
Top 22%29 citations

Süleyman Gülsüner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov +45 more

Inherited predisposition to breast cancer in the Carolina Breast Cancer Study

npj Breast Cancer(2021)10.1038/s41523-020-00214-4
Top 23%
0.869DataRank
Top 23%13 citations

Süleyman Gülsüner, Ming K. Lee, Melissa A. Troester, Andrew F. Olshan, H. Shelton Earp +3 more

Microduplications of 16p11.2 are associated with schizophrenia

UNC Libraries(2020)10.17615/zwts-m549
N/A
0DataRank · unranked
0 citations

Jaya Ganesh, Detelina Grozeva, Vladimir Makarov, Abhishek Bhandari, Ravinesh A. Kumar +27 more

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
0DataRank · unranked
242 citations

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

Germline variants drive myelodysplastic syndrome in young adults

Leukemia(2021)10.1038/s41375-021-01137-0
N/A
0DataRank · unranked
66 citations

Jane E. Churpek, Tom Walsh, Sioḃán Keel, Marja Hakkarainen, Thomas Schroeder +30 more

A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss

Human Molecular Genetics(2023)10.1093/hmg/ddad066
N/A
0DataRank · unranked
1 citations

Ryan J. Carlson, Grace Rabie, Ming K. Lee, Süleyman Gülsüner, Tom Walsh +4 more

Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes

Genome Research(2024)10.1101/gr.279158.124
N/A
0DataRank · unranked
16 citations

Amal Abu Rayyan, Jessica B. Mandell, M. Lee, Greta V Bernier, Barbara M. Norquist +4 more

Resolving the chromatin impact of mosaic variants with targeted Fiber-seq

Genome Research(2024)10.1101/gr.279747.124
N/A
0DataRank · unranked
9 citations

Zachary Amador, Chang Li, Benjamin J. Mallory, Elliott Swanson, Jane Ranchalis +8 more

Genetic regulation of the estrogen receptor and inherited predisposition to breast cancer

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2517736122
N/A
0DataRank · unranked
0 citations

Hannah Kortbawi, Süleyman Gülsüner, Jessica B. Mandell, M. Lee, Tom Walsh +2 more

Genetics of schizophrenia in the South African Xhosa

Science(2020)10.1126/science.aay8833
N/A
0DataRank · unranked
125 citations

Dan J. Stein, Ezra Susser, Goodman Sibeko, Adele Pretorius, Tom Walsh +23 more

Systematic misclassification of missense variants in BRCA1 and BRCA2 “coldspots”

Genetics in Medicine(2020)10.1038/s41436-019-0740-6
N/A
0DataRank · unranked
64 citations

Brian H. Shirts, Thomas P. Slavin, Tom Walsh, Mary‐Claire King, Douglas M. Fowler +2 more

Effects of germline and somatic events in candidate BRCA-like genes on breast-tumor signatures

PLoS ONE(2020)10.1371/journal.pone.0239197
N/A
0DataRank · unranked
30 citations

Brian H. Shirts, Tom Walsh, Süleyman Gülsüner, Mary‐Claire King, Alyssa Parker +3 more