Author

Susan P. Etheridge

St. Luke’s Boise Medical CenterORCID 0000-0002-2492-422XUnclaimed 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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Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Organism:human· 1 Research Focus:software / tool· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Martin Tristani‐FirouziiD· 2 shared Alfred L. GeorgeiD· 1 shared Briana L. SawyeriD· 1 shared Dan M. RodeniD· 1 shared Darlene F. Fountain· 1 shared Edgar Javier HernandeziD· 1 shared Elizabeth M. McNallyiD· 1 shared Felix Karthik· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Martin Tristani‐FirouziORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 15, 2024

Identifying barriers to genetic testing in subspecialty cardiac care

Sierra Pond, Genevie Echols, Martin Tristani‐Firouzi…·Briana L. Sawyer

This study identifies barriers to genetic testing in cardiac care by surveying providers, finding insurance issues and specialty differences affect testing uptake.

DOI 10.1101/2024.05.15.24307347

statistical modelbenchmarking

𝕏 PostBluesky

Genetic & Genomic MedicineGenome MedicinePeer-reviewedJan 16, 2024

The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

Megan J. Puckelwartz, Lorenzo L. Pesce, Edgar Javier Hernandez…·Elizabeth M. McNally

This study identifies genetic variants in epilepsy, cardiomyopathy, and arrhythmia genes in a sudden death in the young cohort, finding enrichment of damaging variants and a correlation with younger age at death.

16 citationstop 4%

humanwhole-genome sequencing

𝕏 PostBluesky