Author

Robert L. Hollis

Cancer Research UKORCID 0000-0002-1390-3298Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

A. R. S. BlackiD· 1 shared Aikou OkamotoiD· 1 shared Ajitha RajaniD· 1 shared Alan SerrelsiD· 1 shared Alexander E.P. LoftusiD· 1 shared C. Simon HerringtoniD· 1 shared Charlie GourleyiD· 1 shared Clare Bartos· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperImmunology

A. R. S. BlackORCID

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2 papers

Recent·Most cited

ImmunologybioRxivPreprintNov 26, 2025

FAK inhibitor treatment systemically regulates the glioblastoma immune environment via blocking monocyte trafficking

Emily R. Webb, A. R. S. Black, Giovana Carrasco…·Valerie G. Brunton

This study shows that systemic FAK inhibition reduces immunosuppressive macrophages in glioblastoma by blocking monocyte trafficking, enhancing T cell activity and improving survival in a mouse model.

DOI 10.1101/2025.11.26.690731

mousebulk RNA-seq

𝕏 PostBluesky

Cancer BiologyGynecologic OncologyPeer-reviewedMay 27, 2025

Combined genomic and molecular analysis defines prognostic markers of relapse in stage IA-IC1 clear cell ovarian carcinoma

Yasushi Iida, Michael Churchman, Robert L. Hollis…·John P. Thomson

This study identifies ARID1A mutation and low CD3+ TIL levels as prognostic markers for relapse in low-stage clear cell ovarian carcinoma.

2 citations

humanbulk RNA-seq

𝕏 PostBluesky