Author

Ching Moey

The University of QueenslandORCID 0000-0002-5059-7322Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:mouse· 3 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Jens BuntiD· 3 shared Linda J. RichardsiD· 3 shared Elliott H. SherriD· 2 shared Kok Siong CheniD· 2 shared Ruiji Jiang· 2 shared A. James BarkovichiD· 1 shared Alban C. ZiegleriD· 1 shared Alexandra AfenjariD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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3 shared papersNeuroscience

Jens BuntORCID

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3 papers

Recent·Most cited

C12ORF57: a novel principal regulator of synaptic AMPA currents and excitatory neuronal homeostasis

Ruiji Jiang, Malek Chouchane, Kok Siong Chen, Ching Moey, Jens Bunt, Li Jiang, Fowzan Sami Alkuraya, Eman Alobeid, Linda J. Richards, Erik M. Ullian, Elliott H. Sherr

The paper identifies C12ORF57 as a key regulator of synaptic AMPA currents and excitatory neuronal homeostasis, showing its role in synaptic homeostatic downscaling and its disruption in Temtamy syndrome.

bioRxiv · Jan 8, 2025 · PreprintNeuroscience

EMX2 transcriptionally regulates Nfib expression in neural progenitor cells during early cortical development.

Jonathan W. C. Lim, Jens Bunt, Caitlin R. Bridges, Ching Moey, Matisse T. Jacobs, Kok‐Siong Chen, Linda J. Richards

The paper shows EMX2 regulates Nfib expression in neural progenitor cells, both activating and repressing it depending on context, which fine-tunes NFI protein levels during cortical development.

bioRxiv · Dec 26, 2021 · PreprintNeuroscience

Pathogenic DDX3X mutations impair RNA metabolism and neurogenesis during fetal cortical development

Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang, Bethany Johnson-Kerner, Lindsey Suit, Srivats Venkataramanan, Charles J. Sheehan, Fernando C. Alsina, Brieana Fregeau, Kimberly A. Aldinger, Ching Moey, Iryna V. Lobach, Alexandra Afenjar, Dusica Babovic‐Vuksanovic, Stéphane Bezieau, , Elliott H. Sherr

This study identifies DDX3X mutations as causing neurodevelopmental disorders by disrupting RNA metabolism and neurogenesis during fetal cortical development.

Neuron · Mar 4, 2020Peer-reviewedGenetics