Author

Allison M. Culver

University of South Carolina

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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Molecular Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Shannon William DavisiD· 2 shared Anna M. BagnelliD· 1 shared Austin J. Smith· 1 shared Carin M. PapendorpiD· 1 shared Evelyn ChukwurahiD· 1 shared Foster D. RitchieiD· 1 shared Janay M. Clytus· 1 shared Judy Shih-Hwa LiuiD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersMolecular Biology

Shannon William DavisORCID

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2 papers

Recent·Most cited

A frameshift mutation in the murine Prkra gene causes dystonia and exhibits abnormal cerebellar development and reduced eIF2α phosphorylation.

Samuel B. Burnett, Allison M. Culver, Tricia A. Simon, Taylor Rowson, Kenneth Frederick, Kristina J. Palmer, Stephen A. Murray, Shannon William Davis, Rekha C. Patel

This study investigates the effects of a Prkra frameshift mutation in mice, showing reduced eIF2 phosphorylation and cerebellar abnormalities linked to dystonia.

bioRxiv · Jun 4, 2024 · PreprintMolecular Biology

ASH1L REGULATES THE STRUCTURAL DEVELOPMENT OF NEURONAL CIRCUITRY BY MODULATING BDNF/TrkB SIGNALING IN HUMAN NEURONS

Seon Hye Cheon, Allison M. Culver, Anna M. Bagnell, Foster D. Ritchie, Janay M. Clytus, Mikayla M. McCord, Carin M. Papendorp, Evelyn Chukwurah, Austin J. Smith, Mara H. Cowen, Pankaj S. Ghate, Shannon William Davis, Judy Shih-Hwa Liu, Sofia B. Lizarraga

This study shows ASH1L regulates neuronal connectivity by modulating BDNF/TrkB signaling through its interaction with PRC2 in human neurons, linking ASH1L mutations to autism pathogenesis.

bioRxiv · Feb 18, 2020 · PreprintNeuroscience