Author

Hannah Warren Moore

Greenwood Genetic CenterORCID 0000-0001-6815-2658Unclaimed 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:differential expression· 2 Research Focus:gene regulatory network inference· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Acadia M Thielking· 1 shared Adam J. HarringtoniD· 1 shared Ahlem AssaliiD· 1 shared Aida Bytyci TelegrafiiD· 1 shared Ana PetracoviciiD· 1 shared Benjamin M. SiemseniD· 1 shared Boris KereniD· 1 shared Catherine BridgesiD· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperNeuroscience

Acadia M Thielking

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintOct 30, 2019

MEF2C hypofunction in neuronal and neuroimmune populations cooperate to produce MEF2C haploinsufficiency syndrome-like behaviors in mice

Adam J. Harrington, Catherine Bridges, Kayla Blankenship…·Christopher W. Cowan

This study shows that MEF2C hypofunction in neuronal and neuroimmune populations causes MCHS-like behaviors in mice, highlighting its role in brain development and function.

1 citation

mousebulk RNA-seq

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GeneticsbioRxivPreprintJul 31, 2019

Delineation of the First Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency

David B. Beck, Ana Petracovici, Chongsheng He…·Jill A. Fahrner

This study identifies and characterizes 11 cases of TET3 deficiency, a new Mendelian disorder of DNA demethylation, associated with intellectual disability and developmental delays.

2 citations

humanDNA methylation

𝕏 PostBluesky