Author

Hua Xie

Capital Institute of Pediatrics

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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Biology Disciplines

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Genetics· 1 Microbiology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Assay:electrophysiology· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Adam Smith· 1 shared Carson C. ChowiD· 1 shared Chao CheniD· 1 shared Chunyu LiuiD· 1 shared Dian LuiD· 1 shared Dominique R. Dotson· 1 shared Fang LiuiD· 1 shared Fei CheniD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperMicrobiology

Adam Smith

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Author profile →

3 papers

Recent·Most cited

Resolving the Deep Sleep Dual Indeterminacy Problem: Context-Dependent Slow-Wave Activity Modeling Predicts Neurobehavioral Fatigue Where Clinical Sleep Modeling Fails

Shashaank Vattikuti, Hua Xie, Carson C. Chow, Thomas J. Balkin, John Hughes

The paper shows that slow-wave activity (SWA) predicts neurobehavioral fatigue differently during sleep and wakefulness, outperforming clinical sleep metrics in modeling recovery from sleep deprivation.

bioRxiv · Mar 28, 2026 · PreprintPhysiology

Arf GTPases Define BST-2-Independent Pathways for HIV-1 Assembly and Release

Adam Smith, Dominique R. Dotson, Jessica A. Sutton, Hua Xie, Xinhong Dong

This study identifies Arf1 and Arf6 as essential for HIV-1 Gag trafficking, assembly, and release, independent of BST-2 antagonism.

Viruses · Dec 20, 2025Peer-reviewedMicrobiology

Human iPSC-derived neuron of 16p11.2 deletion reveals haplotype-specific expression of MAPK3 and its contribution to variable NDD phenotypes

Fang Liu, Liang Chen, Zhengchang Li, Sen Zhao, Shaofang Shangguan, Haiming Yuan, Ruen Yao, Zailong Qin, Shujie Zhang, Li‐Ping Zou, Zhijie Gao, Qian Chen, Suiwen Wen, Jing Peng, Fei Yin, , Xiaoli Chen

The paper identifies MAPK3 as a driver gene in 16p11.2 deletion-associated neurodevelopmental disorders, showing haplotype-specific expression and cis-regulatory enhancer SNPs contribute to variable phenotypes.

bioRxiv · Jul 10, 2022 · PreprintGenetics