Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion diseaseJianwen Deng, Daojun Hong, Binbin Zhou et al.|Journal of Medical Genetics|2021Cited by 62
CGG repeat expansion in <i>NOTCH2NLC</i> causes mitochondrial dysfunction and progressive neurodegeneration in <i>Drosophila</i> modelJiaxi Yu, Jianwen Deng, Tongling Liufu et al.|Proceedings of the National Academy of Sciences|2022Cited by 57
The polyG diseases: a new disease entityTongling Liufu, Daojun Hong, Yilei Zheng et al.|Acta Neuropathologica Communications|2022Cited by 38
FUS Mutation Causes Disordered Lipid Metabolism in Skeletal Muscle Associated with ALSBinbin Zhou, Daojun Hong, Xiaobing Li et al.|Molecular Neurobiology|2022Cited by 21
Genetic spectrum in a cohort of patients with distal hereditary motor neuropathyChengsi Wu, Daojun Hong, Haijie Xiang et al.|Annals of Clinical and Translational Neurology|2022Cited by 17