Author

K. Silina

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· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:cell-cell communication· 2 Organism:human· 2 Research Focus:clustering· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1

Frequent Co-Authors

H. Moch· 2 shared M. van den Broek· 2 shared B. Becher· 1 shared B. Sobottka· 1 shared F. Ciompi· 1 shared F. Movahedian Attar· 1 shared F. Pagliarulo· 1 shared H. Castanon· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersPathology

H. Moch

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Multi-resolution deep learning characterizestertiary lymphoid structures in solid tumors

M. van Rijthoven, S. Obahor, F. Pagliarulo, M. van den Broek, P. Schraml, H. Moch, J. van der Laak, F. Ciompi, K. Silina

This paper introduces HookNet-TLS, a deep learning model for automated TLS quantification in cancer pathology slides, achieving human-level performance and prognostic associations.

bioRxiv · Apr 3, 2023Pathology

CD39+PD-1+CD8+ T cells mediate metastatic dormancy in breast cancer

P. Tallon de Lara, H. Castanon, M. Vermeer, N. Nunez, K. Silina, B. Sobottka, J. Urdinez, V. Cecconi, F. Movahedian Attar, S. Hiltbrunner, I. Glarner, H. Moch, S. Tugues, B. Becher, M. van den Broek

This study identifies CD39+PD-1+CD8+ T cells as critical for metastatic dormancy in breast cancer, showing their role in suppressing tumor growth and their potential as a biomarker and immunotherapy target.

bioRxiv · Jun 2, 2020Cancer Biology