Author

Christina Michalski

Emory UniversityORCID 0000-0001-9093-5325Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:cell-cell communication· 2 Research Focus:gene regulatory network inference· 2 Research Focus:cell type annotation· 1 Approach:experimental assay· 1

Frequent Co-Authors

Shaojun YuiD· 2 shared Weibo NiuiD· 2 shared Xiangru LiiD· 2 shared Zhaohui Steve QiniD· 2 shared Zhexing WeniD· 2 shared Anna F. LeeiD· 1 shared Anna LehmaniD· 1 shared Anthony Philip CooperiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersNeuroscience

Shaojun YuORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintOct 15, 2026

Synaptic microRNA dysregulation orchestrates aberrant glutamatergic transmission in a human neuronal model of 22q11.2 deletion syndrome

Weibo Niu, Jidong Guo, Ximing Ran…·Zhexing Wen

This study identifies dysregulated synaptic microRNAs in 22q11DS neurons that drive aberrant glutamatergic transmission and synaptic plasticity, linking genetic deletion to psychosis risk.

DOI 10.64898/2026.10.13.758925

humanbulk RNA-seq

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NeurosciencebioRxivPreprintOct 7, 2024

Longitudinal multi-omics reveals pathogenic TSC2 variants disrupt developmental trajectories of human cortical organoids derived from Tuberous Sclerosis Complex

Weibo Niu, Shaojun Yu, Xiangru Li…·Zhexing Wen

This study uses longitudinal multi-omics analysis of cortical organoids to show that TSC2 pathogenic variants disrupt neurodevelopmental trajectories, leading to synaptic and mitochondrial dysfunction.

5 citations

humanscRNA-seq

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Genetic & Genomic MedicineBloodPeer-reviewedJul 5, 2022

Human germline biallelic complete NFAT1 deficiency causes the triad of progressive joint contractures, osteochondromas, and susceptibility to B cell malignancy

Mehul Sharma, Maggie P. Fu, Henry Y. Lu…·Stuart E. Turvey

The paper identifies a human with complete NFAT1 deficiency, revealing its role in joint contractures, osteochondromas, and B cell malignancy through single-cell omic analyses.

19 citations

humanbulk RNA-seq

𝕏 PostBluesky