Author

Mason Tracewell

Thomas Jefferson UniversityORCID 0000-0003-2749-3848Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Assay:ChIP-seq· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Assay:CRISPR screen· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Samantha M. BarnadaiD· 2 shared Andrew IsopiiD· 1 shared Clément GoubertiD· 1 shared Daniela Tejada-MartíneziD· 1 shared Hailey N. ShankleiD· 1 shared Jonathan KarliniD· 1 shared Julie A. BartaiD· 1 shared Kevin M. KimiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCancer Biology

Samantha M. BarnadaORCID

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2 papers

Recent·Most cited

Cancer BiologybioRxivPreprintFeb 17, 2026

Lung cancer-enriched p53 mutants occupy canonical p53 target genes without activating transcription, revealing a distinct loss-of-function behavior

Mason Tracewell, Hailey N. Shankle, Samantha M. Barnada…·Steven B. McMahon

The paper identifies lung cancer-specific p53 mutants that bind genomic sites but fail to activate transcription, revealing a novel loss-of-function mechanism in lung cancer.

DOI 10.64898/2026.02.14.705936

humanDNA methylation

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GenomicsPLoS GeneticsPeer-reviewedJun 15, 2022

Genomic features underlie the co-option of SVA transposons as cis-regulatory elements in human pluripotent stem cells

Samantha M. Barnada, Andrew Isopi, Daniela Tejada-Martínez…·Marco Trizzino

The paper identifies genomic features that enable SVA transposons to function as cis-regulatory elements in human pluripotent stem cells, showing their impact on gene expression.

30 citations

humanChIP-seq

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