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Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development.
Lennox AL, Hoye ML, Jiang R, Johnson-Kerner BL, Suit LA, Venkataramanan S, Sheehan CJ, Alsina FC, Fregeau B, Aldinger KA, Moey C, Lobach I, Afenjar A, Babovic-Vuksanovic D, Bézieau S, Blackburn PR, Bunt J, Burglen L, Campeau PM, Charles P, Chung BHY, Cogné B, Curry C, D'Agostino MD, Di Donato N, Faivre L, Héron D, Innes AM, Isidor B, Keren B, Kimball A, Klee EW, Kuentz P, Küry S, Martin-Coignard D, Mirzaa G, Mignot C, Miyake N, Matsumoto N, Fujita A, Nava C, Nizon M, Rodriguez D, Blok LS, Thauvin-Robinet C, Thevenon J, Vincent M, Ziegler A, Dobyns W, Richards LJ, Barkovich AJ, Floor SN, Silver DL, Sherr EH. Lennox AL, et al. Among authors: moey c. Neuron. 2020 May 6;106(3):404-420.e8. doi: 10.1016/j.neuron.2020.01.042. Epub 2020 Mar 4. Neuron. 2020. PMID: 32135084 Free PMC article.
Aicardi Syndrome Is a Genetically Heterogeneous Disorder.
Ha TT, Burgess R, Newman M, Moey C, Mandelstam SA, Gardner AE, Ivancevic AM, Pham D, Kumar R, Smith N, Patel C, Malone S, Ryan MM, Calvert S, van Eyk CL, Lardelli M, Berkovic SF, Leventer RJ, Richards LJ, Scheffer IE, Gecz J, Corbett MA. Ha TT, et al. Among authors: moey c. Genes (Basel). 2023 Jul 31;14(8):1565. doi: 10.3390/genes14081565. Genes (Basel). 2023. PMID: 37628618 Free PMC article.
Validation of an informant-based cognitive screening tool for Parkinson disease.
Chee KY, Ong KY, Mak CY, Yacob S, Yeo SC, Thrichelam N, Amarnath DD, Thong KS, Moey CH, Ponusamy T, Viswanathan S, Puvanarajah S. Chee KY, et al. Among authors: moey ch. Asia Pac Psychiatry. 2017 Dec;9(4). doi: 10.1111/appy.12278. Epub 2017 Mar 21. Asia Pac Psychiatry. 2017. PMID: 28326670