| TDP-43 induces mitochondrial damage and activates the mitochondrial unfolded protein response P Wang, J Deng, J Dong, J Liu, EH Bigio, M Mesulam, T Wang, L Sun, ... PLoS genetics 15 (5), e1007947, 2019 | 205 | 2019 |
| FUS interacts with HSP60 to promote mitochondrial damage J Deng, M Yang, Y Chen, X Chen, J Liu, S Sun, H Cheng, Y Li, EH Bigio, ... PLoS genetics 11 (9), e1005357, 2015 | 190 | 2015 |
| Expression of human FUS protein in Drosophila leads to progressive neurodegeneration Y Chen, M Yang, J Deng, X Chen, Y Ye, L Zhu, J Liu, H Ye, Y Shen, Y Li, ... Protein & cell 2 (6), 477-486, 2011 | 121 | 2011 |
| Expansion of GGC repeat in GIPC1 is associated with oculopharyngodistal myopathy J Deng, J Yu, P Li, X Luan, L Cao, J Zhao, M Yu, W Zhang, H Lv, Z Xie, ... The American Journal of Human Genetics 106 (6), 793-804, 2020 | 118 | 2020 |
| FUS interacts with ATP synthase beta subunit and induces mitochondrial unfolded protein response in cellular and animal models J Deng, P Wang, X Chen, H Cheng, J Liu, K Fushimi, L Zhu, JY Wu Proceedings of the National Academy of Sciences 115 (41), E9678-E9686, 2018 | 114 | 2018 |
| Long-read sequencing identified repeat expansions in the 5′ UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease J Deng, M Gu, Y Miao, S Yao, M Zhu, P Fang, X Yu, P Li, Y Su, J Huang, ... Journal of medical genetics 56 (11), 758-764, 2019 | 113 | 2019 |
| The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3 J Yu, J Deng, X Guo, J Shan, X Luan, L Cao, J Zhao, M Yu, W Zhang, H Lv, ... Brain 144 (6), 1819-1832, 2021 | 100 | 2021 |
| Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: the polyG diseases M Boivin, J Deng, V Pfister, E Grandgirard, M Oulad-Abdelghani, B Morlet, ... Neuron 109 (11), 1825-1835. e5, 2021 | 97 | 2021 |
| An ALS-mutant TDP-43 neurotoxic peptide adopts an anti-parallel β-structure and induces TDP-43 redistribution L Zhu, M Xu, M Yang, Y Yang, Y Li, J Deng, L Ruan, J Liu, S Du, X Liu, ... Human molecular genetics 23 (25), 6863-6877, 2014 | 64 | 2014 |
| Diagnostic value of salivary real‐time quaking‐induced conversion in Parkinson's disease and multiple system atrophy M Luan, Y Sun, J Chen, Y Jiang, F Li, L Wei, W Sun, J Ma, L Song, J Liu, ... Movement Disorders 37 (5), 1059-1063, 2022 | 54 | 2022 |
| Clinical and pathological features in adult-onset NIID patients with cortical enhancement H Liang, B Wang, Q Li, J Deng, L Wang, H Wang, X Li, M Zhu, Y Cai, ... Journal of Neurology 267, 3187-3198, 2020 | 51 | 2020 |
| The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4 J Yu, J Shan, M Yu, L Di, Z Xie, W Zhang, H Lv, L Meng, Y Zheng, Y Zhao, ... The American Journal of Human Genetics 109 (3), 533-541, 2022 | 47 | 2022 |
| PINK1 and Parkin are genetic modifiers for FUS-induced neurodegeneration Y Chen, J Deng, P Wang, M Yang, X Chen, L Zhu, J Liu, B Lu, Y Shen, ... Human molecular genetics 25 (23), 5059-5068, 2016 | 45 | 2016 |
| Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease J Deng, B Zhou, J Yu, X Han, J Fu, X Li, X Xie, M Zhu, Y Zheng, X Guo, ... Journal of medical genetics 59 (5), 462-469, 2022 | 44 | 2022 |
| Cilostazol ameliorates ischemia/reperfusion‐induced tight junction disruption in brain endothelial cells by inhibiting endoplasmic reticulum stress D Nan, H Jin, J Deng, W Yu, R Liu, W Sun, Y Huang The FASEB Journal 33 (9), 10152-10164, 2019 | 31 | 2019 |
| The polyG diseases: a new disease entity T Liufu, Y Zheng, J Yu, Y Yuan, Z Wang, J Deng, D Hong Acta Neuropathologica Communications 10 (1), 79, 2022 | 26 | 2022 |
| Connexin43 promotes angiogenesis through activating the HIF-1α/VEGF signaling pathway under chronic cerebral hypoperfusion W Yu, H Jin, W Sun, D Nan, J Deng, J Jia, Z Yu, Y Huang Journal of Cerebral Blood Flow & Metabolism 41 (10), 2656-2675, 2021 | 25 | 2021 |
| GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy J Yu, X Luan, M Yu, W Zhang, H Lv, L Cao, L Meng, M Zhu, B Zhou, X Wu, ... Annals of Clinical and Translational Neurology 8 (6), 1330-1342, 2021 | 24 | 2021 |
| Novel and recurrent mutations in a cohort of Chinese patients with young-onset amyotrophic lateral sclerosis J Deng, W Wu, Z Xie, Q Gang, M Yu, J Liu, Q Wang, H Lv, W Zhang, ... Frontiers in Neuroscience 13, 1289, 2019 | 24 | 2019 |
| CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia D Tan, C Wei, Z Chen, Y Huang, J Deng, J Li, Y Liu, X Bao, J Xu, Z Hu, ... Movement Disorders 38 (7), 1282-1293, 2023 | 22 | 2023 |
Pidong LiBioMapVerified email at nwafu.edu.cn
