Author

Hoi‐Hung Cheung

Chinese University of Hong KongORCID 0000-0001-7178-9289Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Lingxiao LiuiD· 2 shared Adrian On-Wah LeungiD· 1 shared Alejandro D. IglesiasiD· 1 shared Alexis R. HeidlebaughiD· 1 shared Alina KurolapiD· 1 shared Amanda GerardiD· 1 shared Angad JollyiD· 1 shared Ange‐Line BrueliD· 1 shared

Activity by Year

2023-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersCell Biology

Lingxiao LiuORCID

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3 papers

Recent·Most cited

Cell BiologybioRxivPreprintSep 4, 2025

RNA helicase Ddx21 safeguards fetal HSPC expansion by recruiting Kdm5a to epigenetically sustain ribosomal and hematopoietic gene transcription

Adrian On-Wah Leung, Chang Li, Xianyin Huang…·Hoi‐Hung Cheung

This study identifies Ddx21's role in fetal hematopoiesis by showing it recruits Kdm5a to maintain epigenetic regulation of ribosomal and hematopoietic gene transcription, essential for HSPC expansion.

DOI 10.1101/2025.09.04.674186

mousebulk RNA-seq

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Cell BiologybioRxivPreprintJan 19, 2025

Primate-specific microRNA-1202 regulates dopaminergic neurogenesis by targeting APC2 and modulates WNT/β-catenin signaling pathway in midbrain organoid

Xiaohang Long, Dandan Cao, See-Wing Chan…·Hoi‐Hung Cheung

DOI 10.1101/2025.01.19.633822

humanorganoid / primary culture

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Genetic & Genomic MedicinemedRxivPreprintMar 1, 2023

Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

Daniel G. Calame, Tianyu Guo, Chen Wang…·James R. Lupski

The paper identifies monoallelic DHX9 variants as a cause of neurodevelopmental disorders and Charcot-Marie-Tooth disease, showing genotype-phenotype correlations and cellular dysfunction.

DOI 10.1101/2023.03.01.23286475

humanmouse

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