Author

Cheryl A. Hill

University of MissouriORCID 0000-0002-3179-1437Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Research Focus:differential expression· 3 Assay:DNA methylation· 3 Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:gene regulatory network inference· 2 Assay:bulk RNA-seq· 1 Assay:proteomics· 1

Frequent Co-Authors

Dennis Y. WuiD· 2 shared Harrison W. GabeliD· 2 shared Jenna R. Martin· 2 shared Joseph D. DoughertyiD· 2 shared Susan E. MaloneyiD· 2 shared Thomas PapouiniD· 2 shared Adam W. ClemensiD· 1 shared Alyssa EricksoniD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersNeuroscience

Dennis Y. WuORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

NeuroscienceNeurobiology of DiseasePeer-reviewedMar 3, 2026

ACSS2 mediates prenatal alcohol exposure-related morphological and behavioral phenotypes

Kala M. Dodson, Erica M. Periandri, Anjali Yadav…·Gabor Egervári

This study identifies ACSS2 as a mediator of prenatal alcohol exposure-related phenotypes, showing its role in histone acetylation and developmental changes in the brain.

1 citationtop 5%

mouseproteomics

𝕏 PostBluesky

NeuroscienceCell ReportsPeer-reviewedNov 1, 2023

Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits

Diana C. Beard, Xiyun Zhang, Dennis Y. Wu…·Harrison W. Gabel

This study examines how different DNMT3A mutations cause varied behavioral, epigenetic, and transcriptional issues in neurodevelopmental disorders.

29 citationstop 3%

mouseDNA methylation

𝕏 PostBluesky

NeuroscienceCell ReportsPeer-reviewedNov 1, 2020

DNMT3A haploinsufficiency results in behavioral deficits and global epigenomic dysregulation shared across neurodevelopmental disorders

Diana L. Christian, Dennis Y. Wu, Jenna R. Martin…·Harrison W. Gabel

This study shows that DNMT3A mutations cause behavioral and epigenomic changes in mice, similar to human neurodevelopmental disorders, by disrupting non-CG DNA methylation.

78 citationstop 4%

mouseDNA methylation

𝕏 PostBluesky