Author

Jennifer Crayton

The University of Texas MD Anderson Cancer Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Neuroscience· 1

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Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Research Focus:spatial domain detection· 1 Approach:statistical model· 1

Frequent Co-Authors

C. Marcelo AldaziD· 1 shared Collene R. JeteriD· 1 shared Dhurjhoti SahaiD· 1 shared Jeffrey L. NoebelsiD· 1 shared Kevin G. SancheziD· 1 shared Laura K. FonkeniD· 1 shared Martı́n C. AbbaiD· 1 shared Ryan Seo· 1 shared

Activity by Year

2022-2022 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

C. Marcelo AldazORCID

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1 paper

Recent·Most cited

WWOX P47T loss-of-function mutation induces epilepsy, progressive neuroinflammation, and cerebellar degeneration in mice phenocopying human SCAR12

Tabish Hussain, Kevin G. Sanchez, Jennifer Crayton, Dhurjhoti Saha, Collene R. Jeter, Yue Lu, Martı́n C. Abba, Ryan Seo, Jeffrey L. Noebels, Laura K. Fonken, C. Marcelo Aldaz

This paper describes a mouse model of WWOX P47T mutation that mimics human SCAR12, showing epilepsy, neuroinflammation, and cerebellar degeneration.

bioRxiv · Oct 5, 2022 · PreprintNeuroscience