Author

Hua Qiang Xie

Shanghai Jiao Tong UniversityORCID 0009-0007-7586-9279Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:spatial transcriptomics· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Fang CheniD· 1 shared Jiong LiiD· 1 shared Lin XiaoiD· 1 shared Liuning Zhang· 1 shared Long YuiD· 1 shared Richard H. FinnelliD· 1 shared Shuming WangiD· 1 shared Wei Zheng· 1 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Fang ChenORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

NeurosciencebioRxivPreprintNov 22, 2023

Rapid and prolonged response of oligodendrocyte lineage cells in standard acute cuprizone demyelination model revealed by in situ hybridization

Yuehua He, Hua Qiang Xie, Liuning Zhang…·Lin Xiao

The paper uses in situ hybridization to track oligodendrocyte lineage cell dynamics during demyelination and remyelination in a cuprizone model, revealing early mature oligodendrocyte death and prolonged myelin-forming cell activity.

DOI 10.1101/2023.11.22.568377

mousespatial transcriptomics

𝕏 PostBluesky

Genetic & Genomic MedicineiSciencePeer-reviewedApr 12, 2023

Whole-exome Sequencing Study of Hypospadias

Zhongzhong Chen, Yunping Lei, Richard H. Finnell…·Fang Chen

The paper identifies rare damaging variants in outer DNAH genes in 22.5% of severe hypospadias patients, suggesting their role in the condition and potential for genetic counseling.

25 citationstop 2%

humanwhole-exome sequencing

𝕏 PostBluesky