Author

Diana C. Beard

Washington University in St. LouisORCID 0000-0002-1799-0771Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Diana C. Beard1 paper · Novartis (Switzerland)

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Harrison W. GabeliD· 2 shared Nicole HamagamiiD· 2 shared Adam W. ClemensiD· 1 shared Alaina UrmaniD· 1 shared Alyssa EricksoniD· 1 shared Audrey McAlindeniD· 1 shared Austin B. LawrenceiD· 1 shared Austin Bell‐HensleyiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersNeuroscience

Harrison W. GabelORCID

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2 papers

Recent·Most cited

Non-CG DNA methylation and MeCP2 stabilize repeated tuning of long genes that distinguish closely related neuron types

J. Russell Moore, Mati T. Nemera, Rinaldo D. D’Souza, Nicole Hamagami, Adam W. Clemens, Diana C. Beard, Alaina Urman, Victoria Rodriguez Mendoza, Harrison W. Gabel

The paper shows that non-CG DNA methylation and MeCP2 regulate long genes to maintain neuron type-specific gene programs at high resolution.

bioRxiv · Jan 30, 2024 · PreprintNeuroscience

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

Diana C. Beard, Xiyun Zhang, Dennis Y. Wu, Jenna R. Martin, Alyssa Erickson, Jane-Valeriane K. Boua, Nicole Hamagami, Raylynn G. Swift, Katherine B. McCullough, Xia Ge, Austin Bell‐Hensley, Hongjun Zheng, Cory W. Palmer, Nicole A. Fuhler, Austin B. Lawrence, , Harrison W. Gabel

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

Cell Reports · Nov 1, 2023Peer-reviewedNeuroscience