Author

F. Roncaroli

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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Cancer Biology· 3

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Research Focus:differential expression· 3 Approach:experimental assay· 3 Research Focus:cell-cell communication· 2 Organism:human· 2 Research Focus:spatial domain detection· 2 Assay:bulk RNA-seq· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

J. Minshull· 2 shared A. King· 1 shared A. P. Gilmore· 1 shared A. Pöysti· 1 shared C. Garcia-Diaz· 1 shared D. Brough· 1 shared D. J. Coope· 1 shared D. T. Prescott· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersCancer Biology

J. Minshull

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Hypoxia coordinates the spatial landscape of myeloid cells within glioblastoma to affect outcome

M. J. Haley, L. Bere, J. Minshull, S. Georgaka, N. Garcia-Martin, G. Howell, D. J. Coope, F. Roncaroli, A. King, D. Wedge, S. Allan, O. N. Pathmanaban, D. Brough, K. Couper

The paper maps myeloid cell spatial organisation in glioblastoma and links it to patient survival.

bioRxiv · Jun 30, 2023 · PreprintCancer Biology

Novel Laser Capture Microdissection-Proteomic Analysis Identifies Spatially Distinct Extracellular Matrix Signatures in the Core and Infiltrating Edge of Human Glioblastoma.

R. Pedley, D. T. Prescott, E. Appleton, L. Dingle, J. Minshull, P. I. D'Urso, I. Djoukhadar, A. P. Gilmore, F. Roncaroli, J. Swift

This paper develops an LCM-proteomics protocol to analyze spatial ECM differences in human glioblastoma, identifying distinct matrisome components between tumor epicenter and brain/tumor interface.

bioRxiv · Sep 1, 2022 · PreprintCancer Biology

Glioblastoma cell fate is differentially regulated by the microenvironments of the tumour bulk and infiltrative margin

C. Garcia-Diaz, E. Mereu, M. P. Clements, A. Pöysti, F. Galvez-Cancino, S. P. Castillo, L. Courtot, S. Ruiz, F. Roncaroli, Y. Yuan, S. A. Quezada, H. Heyn, S. Parrinello

This study compares glioblastoma cell fate in tumour bulk and margin, finding distinct neurogenic patterns and immune environments, with margin cells showing developmental-like trajectories and iNPCs linked to interferon signalling.

bioRxiv · Jun 11, 2021 · PreprintCancer Biology