Author

M. Fridrikh

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· 2

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

A. Sinha· 2 shared C. A. Powell· 2 shared H. Watanabe· 2 shared J. Zhu· 2 shared M. B. Beasley· 2 shared R. Kong· 2 shared S. Yoo· 2 shared T. Sato· 2 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersCancer Biology

A. Sinha

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2 papers

Recent·Most cited

Classical oncogene family Myc defines unappreciated distinct lineage states of small cell lung cancer

A. S. Patel, S. Yoo, R. Kong, T. Sato, A. Sinha, L. Bao, M. Fridrikh, K. Emoto, G. Nudelman, C. A. Powell, M. B. Beasley, J. Zhu, H. Watanabe

This study identifies distinct lineage states in small cell lung cancer driven by c-Myc and L-Myc, showing their unique roles in molecular subtypes and histology.

bioRxiv · Nov 3, 2020Cancer Biology

Epigenomic profiling discovers trans-lineage SOX2 partnerships driving tumor heterogeneity in lung squamous cell carcinoma

T. Sato, S. Yoo, R. Kong, M. Fridrikh, A. Sinha, P. Chandramani-Shivalingappa, A. Patel, O. Nagano, T. Masuko, M. B. Beasley, C. A. Powell, J. Zhu, H. Watanabe

This study identifies two distinct LUSC subtypes driven by Sox2 partnerships with Brn2 or p63, revealing lineage heterogeneity and potential therapeutic targets.

bioRxiv · Jun 12, 2019Cancer Biology