Author

Elizabeth S. Burnside

University of Wisconsin–MadisonORCID 0000-0002-6600-435XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

A. Heather EliasseniD· 1 shared A.V. Patel· 1 shared Ali G. GharaviiD· 1 shared Alicia Yiran ZhouiD· 1 shared Amy TayloriD· 1 shared Amy Trentham‐DietziD· 1 shared Andreas A. Theodorou· 1 shared Andrew HaddadiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Heather EliassenORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineAnnals of OncologyPeer-reviewedApr 25, 2025

Association of Gene Variant Type and Location with Breast Cancer Risk in the General Population

Mwangala P. Akamandisa, Nicholas James Boddicker, Siddhartha Yadav…·Katherine L. Nathanson

This study evaluates breast cancer risks associated with pathogenic variant type and location in BRCA2 and other genes, finding differential risks based on variant position.

11 citationstop 3%

humanGWAS summary statistics

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Genetic & Genomic MedicineCommunications BiologyPeer-reviewedFeb 19, 2024

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Eric Venner, Karynne Patterson, Divya Kalra…·May Okihiro

The paper analyzes pathogenic variant frequencies in the All of Us cohort by ancestry, revealing disparities and potential biases in genomic data.

61 citationstop 1%

humanwhole-genome sequencing

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