Author

R. Dahiya

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 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cancer & tumor microenvironment· 2 Research Focus:chromatin & epigenetic regulation· 2 Approach:experimental assay· 2 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

P. Ly· 2 shared A. Guyer· 1 shared A. Mazzagatti· 1 shared A. T. Tebeje· 1 shared C. A. Lovejoy· 1 shared C. L. Walker· 1 shared E. G. Maurais· 1 shared E. S. Kounlavong· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCell Biology

P. Ly

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Author profile →

2 papers

Recent·Most cited

Non-homologous end joining shapes the genomic rearrangement landscape of chromothripsis from mitotic errors

Q. Hu, J. Espejo Valle-Inclan, R. Dahiya, A. Guyer, A. Mazzagatti, E. G. Maurais, J. L. Engel, I. Cortes-Ciriano, P. Ly

This study shows that non-homologous end joining (NHEJ) is the main pathway causing complex genomic rearrangements during chromothripsis from mitotic errors.

bioRxiv · Aug 10, 2023 · PreprintCell Biology

SETD2 safeguards the genome against isochromosome formation

F. Mason, E. S. Kounlavong, A. T. Tebeje, R. Dahiya, T. Guess, L. Vlach, S. R. Norris, C. A. Lovejoy, R. Dere, R. Ohi, P. Ly, C. L. Walker, W. K. Rathmell

This study shows that SETD2 loss leads to chromosome segregation errors and DNA bridging via isochromosome formation, contributing to genomic instability in cancer.

bioRxiv · Oct 25, 2022 · PreprintCancer Biology