Parents
Sign in to add mentorKwang Wook Choi | grad student | 2011-2016 | KAIST |
Hugo J. Bellen | post-doc | Baylor College of Medicine |
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Publications
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Tanaka T, Chung HL. (2024) Exploiting fly models to investigate rare human neurological disorders. Neural Regeneration Research. 20: 21-28 |
Liao JZ, Chung HL, Shih C, et al. (2024) Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila. Nature Communications. 15: 3326 |
Chung HL, Ye Q, Park YJ, et al. (2023) Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation. Cell Metabolism |
Ma M, Zhang X, Zheng Y, et al. (2022) The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival. Human Molecular Genetics |
Marcogliese PC, Deal SL, Andrews J, et al. (2022) Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases. Cell Reports. 38: 110517 |
Lu S, Hernan R, Marcogliese PC, et al. (2022) Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures. American Journal of Human Genetics |
Chung HL, Rump P, Lu D, et al. (2022) De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in drosophila. Human Molecular Genetics |
Marcogliese PC, Dutta D, Ray SS, et al. (2022) Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling. Science Advances. 8: eabl5613 |
Manivannan SN, Roovers J, Smal N, et al. (2021) De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies. Brain : a Journal of Neurology |
Manor J, Chung H, Bhagwat PK, et al. (2021) ABCD1 and X-linked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models. Journal of Neuroscience Research |