Author

Corinne Strawser

Abigail Wexner Research Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Assay:DNA methylation· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Adam P. OstendorfiD· 1 shared Adithe RivaldiiD· 1 shared Allison Daley· 1 shared Allison Thompson· 1 shared Ammar ShaikhouniiD· 1 shared Amy C. GrossiD· 1 shared Ari Zavarella· 1 shared Ashton S. HolubiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperNeuroscience

Adam P. OstendorfORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Somatic variants activating the RAS-MAPK pathway confer susceptibility to hippocampal sclerosis in drug-resistant epilepsy

Lauren Mashburn‐Warren, Ashton S. Holub, Sahibjot Sran, Swetha Ramadesikan, Keaton Suh, Allison Thompson, James J. Anderson, Adithe Rivaldi, Ari Zavarella, Megan Chandler, Allison Daley, Corinne Strawser, Elizabeth A.R. Garfinkle, Jonathan Pindrik, Ammar Shaikhouni, , Tracy A. Bedrosian

The paper identifies somatic RAS-MAPK pathway activating variants in hippocampal sclerosis patients, linking them to seizure-induced injury and suggesting therapeutic targets.

bioRxiv · Apr 9, 2026 · PreprintNeuroscience

SCANBIT facilitates identification of tumor cell populations in scRNAseq data using pseudobulked SNV calls

Matthew V. Cannon, Matthew J. Gust, Amy C. Gross, Maren Cam, James Brandon Reinecke, Leyre Jimenez Garcia, Corinne Strawser, L Ryan, Melissa C. Sammons, Cheng‐Zhong Zhang, Ryan David Roberts

SCANBIT identifies tumor cell populations in scRNA-seq data by using pseudobulked SNV calls, showing that mutational burden affects identification accuracy.

bioRxiv · Jan 28, 2026 · PreprintBioinformatics