Author

Christine B. Magdongon

Northwestern UniversityORCID 0009-0001-3899-3672Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Cell Biology· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 2 Organism:human· 2 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:experimental assay· 1

Frequent Co-Authors

Amit RahiiD· 2 shared Praveen Kumar Suraneni· 2 shared Adriana G. Landeros· 1 shared Alexander Zaslavsky· 1 shared Arun SreekumariD· 1 shared Basil Baby Mattamana· 1 shared Daniel R. FoltziD· 1 shared Destiny Ariel WallaceiD· 1 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersCancer Biology

Amit RahiORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Molecular BiologyNucleic Acids ResearchPeer-reviewedSep 18, 2026

KSHV-encoded vIRF3 Cooperates with Cellular IRF4 to Drive Super-Enhancer Activity through Complex DNA Elements

Ziyan Liang, Haocong Katherine Ma, Christine B. Magdongon…·Eva Gottwein

This study identifies DNA elements that mediate vIRF3 and IRF4 cooperation in activating super-enhancers, revealing their role in oncogenesis.

DOI 10.1093/nar/gkag942

statistical modelgene regulatory network inference

𝕏 PostBluesky

Cancer BiologyCell Communication and SignalingPeer-reviewedMar 28, 2026

The Hexosamine Biosynthetic Pathway alters the cytoskeleton to modulate cell proliferation and migration in metastatic prostate cancer

Rajina Shakya, Praveen Kumar Suraneni, Amit Rahi…·Dileep Varma

This study investigates how GNPNAT1 knockdown in CRPC cells affects cytoskeletal structure, proliferation, and migration through metabolic and signaling pathways.

3 citationstop 3%

humanmetabolomics

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Cell BiologybioRxivPreprintSep 25, 2023

Nuclear lamin A-associated proteins are required for centromere assembly

Adriana G. Landeros, Destiny Ariel Wallace, Amit Rahi…·Dileep Varma

This study shows that Lamin A-associated proteins are essential for centromere assembly during mitotic exit by interacting with centromere and kinetochore proteins.

2 citations

humanproteomics

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