Author

Emily M. Hatch

Fred Hutch Cancer CenterORCID 0000-0002-3393-4075Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Emily M. Hatch1 paper

Biology Disciplines

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Cell Biology· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Anna E. MammeliD· 1 shared Anthony Cooke· 1 shared Cole TrapnelliD· 1 shared Dana L. JacksoniD· 1 shared Douglas M. FowleriD· 1 shared Gavin HaiD· 1 shared Heather Z HuangiD· 1 shared Jason J. Stephany· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

Anna E. MammelORCID

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2 papers

Recent·Most cited

RCC1 depletion drives protein transport defects and rupture in micronuclei

Molly G. Zych, Maya Contreras, Manasvita Vashisth, Anna E. Mammel, Gavin Ha, Emily M. Hatch

This study identifies RCC1 depletion as a cause of protein transport defects and micronuclei rupture, linking it to nuclear lamina defects and genome instability.

The Journal of Cell Biology · Jan 9, 2026Peer-reviewedCell Biology

Visual Cell Sorting: A High-throughput, Microscope-based Method to Dissect Cellular Heterogeneity

Nicholas Hasle, Anthony Cooke, Sanjay R Srivatsan, Heather Z Huang, Jason J. Stephany, Zachary Krieger, Dana L. Jackson, Weiliang Tang, Sriram Pendyala, Raymond J. Monnat, Cole Trapnell, Emily M. Hatch, Douglas M. Fowler

This paper introduces a method to physically separate live cells based on visual phenotypes and uses it to study nuclear localization sequences and paclitaxel resistance in human cancers.

bioRxiv · Dec 9, 2019 · PreprintMolecular Biology