Author

Meghan T. Harris

Brandeis UniversityORCID 0000-0001-8367-2918Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Molecular Biology· 1 Synthetic Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:CRISPR screen· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Bianca P. LavayeniD· 1 shared Bruce J. McCreedy· 1 shared Daniel R. GettsiD· 1 shared Michael T. MarriD· 1 shared Neha DiwanjiiD· 1 shared Nicholas K. Clark· 1 shared Robert Hofmeister· 1 shared Ruei‐Zeng LiniD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperSynthetic Biology

Bianca P. LavayenORCID

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2 papers

Recent·Most cited

CRISPR-Enabled Autonomous Transposable Element (CREATE) for RNA-based gene editing and delivery

Yuxiao Wang, Ruei‐Zeng Lin, Meghan T. Harris, Bianca P. Lavayen, Neha Diwanji, Bruce J. McCreedy, Robert Hofmeister, Daniel R. Getts

The paper introduces CREATE, an RNA-based gene editing system that delivers large genes without DSBs or DNA templates, achieving specific genomic integration in human cells.

EMBO Reports · Jan 9, 2025Peer-reviewedSynthetic Biology

The Insulin receptor and Insulin like growth factor receptor 5 UTRs support translation initiation independently of eIF4G1

Nicholas K. Clark, Meghan T. Harris, William B. Dahl, Zachary Knotts, Michael T. Marr

The paper shows that the 5' UTRs of Insr and Igf1r transcripts support translation initiation independently of eIF4G1 in both in vitro and cellular settings.

Molecular and Cellular Biology · Sep 19, 2023Peer-reviewedMolecular Biology