Author

DEVORAH STUCKI

University of Utah

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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Cell Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Assay:imaging· 1 Assay:metabolomics· 1 Organism:mouse· 1

Frequent Co-Authors

Marcus G. PezzolesiiD· 2 shared William L. HollandiD· 2 shared Ademuyiwa S. AromolaraniD· 1 shared Adrian M VelardeiD· 1 shared Andrea C. CorbiniD· 1 shared Anshu KumariiD· 1 shared Anthony M. BalynasiD· 1 shared Ashley R. BrattiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersCell Biology

Marcus G. PezzolesiORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Excessive Ca2+-dependent ER-mitochondrial contact stabilization by EFHD1 drives liver injury

David Eberhardt, Emma C. Rekate, Yasmin B Masini, Hannah E. Duron, David M. Mollinedo, Adrian M Velarde, DEVORAH STUCKI, Tara R. Price, Sandra H. J. Lee, Enrique Balderas, Neeraj K Rai, Ashley R. Bratt, Anthony M. Balynas, Chris Stubben, Ryan D. Bia, , Dipayan Chaudhuri

This study identifies EFHD1 as a Ca2+-dependent stabilizer of ER-mitochondrial contacts that drives liver injury in MASH by promoting mitochondrial fragmentation and antiviral stress responses.

bioRxiv · Feb 16, 2026 · PreprintCell Biology

A Draft Pacific Ancestry Pangenome Reference

Connor Littlefield, José M. Lázaro-Guevara, DEVORAH STUCKI, Michael Lansford, Melissa H. Pezzolesi, Emma J. Taylor, Etoni-Ma’asi C. Wolfgramm, Jacob Taloa, Kime Lao, Carlos Dave C. Dumaguit, Perry G. Ridge, Justina P. Tavana, William L. Holland, Kalani L. Raphael, Marcus G. Pezzolesi

The paper develops a Pacific ancestry pangenome reference to improve genetic analysis for an underserved population, showing it reduces variant call errors and captures novel sequence.

bioRxiv · Aug 7, 2024 · PreprintGenomics