Author

Shadi Ariyanfar

Virginia TechORCID 0000-0002-3917-7925Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Christopher K. ThompsoniD· 1 shared Deborah J. GoodiD· 1 shared Matthew Adam KocheriD· 1 shared Stuart A. TobetiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

4 top collaborators · 6 mutual co-author links

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1 shared paperNeuroscience

Christopher K. ThompsonORCID

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1 paper

Recent·Most cited

NeurosciencebioRxivPreprintJan 23, 2026

Subcellular partitioning of Nhlh2 mRNA reveals how SNORD116 loss contributes to Prader-Willi Syndrome.

Shadi Ariyanfar, Matthew Adam Kocher, Christopher K. Thompson…·Deborah J. Good

The paper shows that Snord116 regulates Nhlh2 mRNA localization, with loss of Snord116 causing cytoplasmic Nhlh2 mRNA in hypothalamic neurons, impacting Prader-Willi Syndrome.

DOI 10.64898/2026.01.20.700624

mousebulk RNA-seq

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