Author

Phoebe C. R. Parrish

University of WashingtonORCID 0000-0002-3530-0105Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:experimental assay· 2 Assay:whole-genome sequencing· 2 Assay:CRISPR screen· 1 Research Focus:drug response / drug discovery· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alice H. BergeriD· 2 shared Amira Ellison· 1 shared Amy E. RobertsiD· 1 shared Austin M. GabeliD· 1 shared Barbara R. PoberiD· 1 shared Beth A. KozeliD· 1 shared Beth MartiniD· 1 shared C.A. Morris· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersGenomics

Alice H. BergerORCID

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Author profile →

3 papers

Recent·Most cited

GenomicsbioRxivPreprintJul 27, 2023

A multiplex, prime editing framework for identifying drug resistance variants at scale

Florence M. Chardon, Chase C. Suiter, Riza M. Daza…·Lea M. Starita

This paper introduces prime-SGE, a prime editing framework for assessing drug resistance variants across multiple oncogenes in a single experiment.

17 citations

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintSep 21, 2022

Pathway analysis identifies novel non-synonymous variants contributing to extreme vascular outcomes in Williams-Beuren syndrome

D. Liu, Charles John Billington, N. Raja…·Beth A. Kozel

The paper identifies novel non-synonymous variants associated with extreme vascular outcomes in Williams-Beuren syndrome through whole-genome sequencing and pathway analysis.

DOI 10.1101/2022.09.21.22280107

humanwhole-genome sequencing

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GenomicsCell ReportsPeer-reviewedAug 1, 2021

Discovery of synthetic lethal and tumor suppressive paralog pairs in the human genome

Phoebe C. R. Parrish, James D. Thomas, Austin M. Gabel…·Alice H. Berger

The paper identifies synthetic lethal and tumor suppressive paralog pairs in the human genome using a CRISPR-based approach, revealing new drug targets and essential gene families.

118 citationstop 2%

humanCRISPR screen

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