- [41]Hao Deng*, Zhi Song, Jing Li, Qing Huang, Yi Guo, Xiong Deng, Yong Qi, Huarong Yang, Shaojuan Gu.Novel ATPase Cu2+ transporting beta polypeptide mutations in Chinese families with Wilson’s disease[J].Plos One, 2013, 8 (7) : e66526.
- [42]Hao Deng*, Yongxiang Zhao, Wen Zheng, Anding Zhu, Hongbo Xu, Xiong Deng, Zhi Song, Hui Liang.Genetic Analysis of the leucine-rich repeat and lg domain containing nogo receptor-interacting protein 1 gene in essential tremor[J].Journal of Molecular Neuroscience, 2013, 2 (403-407)
- [43]Hao Deng*, Xiaofei Xiu, Anding Zhu, Zhi Song, Wen Zheng, Xiong Deng, Kai Gao.Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease[J].BMC Neurology, 2013, 13: 125.
- [44]Hao Deng*, Sheng Deng, Hongbo Xu, Lamei Yuan, Wei Xiong, Zhi Song, Xiong Deng, Huarong Yang, Yi Guo.Genetic analysis of the S100B gene in Chinese patients with Parkinson disease[J].Neurosci Lett, 2013, 555: 134-136.
- [45]Hao Deng*, Yongxiang Zhao, Lina Gong, Anding Zhu, Shaojuan Gu, Hongbo Xu, Zhi Song, Lamei Yuan.EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease[J].Neurosci Lett, 2013, 543: 69-71.
- [46]Hao Deng*, Lina Gong, Anding Zhu, Yong Qi, Xiong Deng, Kai Gao, Zhi Song, Xiaofei Xiu.Genetic analysis of the FBXO48 gene in Chinese Han patients with Parkinson disease[J].Neurosci Lett, 2013, 541: 224-226.
- [47]Hao Deng*, Xiaohong Zi, Zhi Song, Liu Yu, Shaojuan Gu.Acute myelitis in a patient with Vogt-Koyanagi-Harada disease: case report and review of the literature[J].Journal of Clinical Neurology, 2013, 9 (1) : 61-64.
- [48]Hao Deng*, Yong Qi, Jianguo Zhang, Liping Guan, Wen Zheng, Junhui Yi, Lamei Yuan, Yi Guo.Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencing[J].Indian Journal of Biochemistry & Biophysics, 2013, 50 (4) : 253-258.
- [49]Hao Deng*, Ziqiang Luo, Xiaorong Li, Kai Gao, Wei Xiong, Yongjia Yang, Zuhai Ren, Hongbo Xu, Yi Guo.Genetic analysis of a Chinese Han family with multiple endocrine neoplasia type 2A[J].Indian Journal of Biochemistry & Biophysics, 2012, 50 (1) : 26-31.
- [50]Weidong Le, Zhi Song, Shuhua Chen, Pingyi Xu, Yi Ding, Ming Ming, Hao Deng, Qinghua Tao, Hua Liu.Genetic analysis of NR4A2 gene in a large population of Han Chinese patients with Parkinson's disease[J].European Journal of Neurology, 2013, 20 (3) : 584-587.
- [51]Guiyuan Li, Hao Deng, Xiaorong Li, Wenling Zhang, Xiaorong Li, Fang Wei, Qianjin Liao, Yixin Yang.LPLUNC1 Inhibits Nasopharyngeal Carcinoma Cell Growth via Down-Regulation of the MAP Kinase and Cyclin D1/E2F Pathways[J].PLOS One,, 2013, 8 (5) : e62869.
- [52]Junxiang Tang, Xuejun Fan, Kai Gao, Wen Zheng, Zhi Song, Xiong Deng, Hongbo Xu#, Hao Deng#*.VPS35 mutation in Chinese Han patients with late-onset Parkinson’s disease[J].European Journal of Neurology, 2012, 19 (9) : e96-e97.
- [53]Hao Deng*, Zeshuai Zeng, Xuhong Jiang, Zhi Song, Jin Lei, Hongbo Xu, Wen Zheng, Hui Liang.No evidence of association between the LINGO4 gene and essential tremor[J].Parkinsonism & Related Disorders, 2012, 18 (3) : 303-305.
- [54]Hao Deng*, Zhi Song, Xiangjun Huang, Jianguo Zhang, Linyan Su, Hui Liang, Hongbo Xu, Jin Lei.Gene expression changes in peripheral blood from Chinese Han patients with Tourette syndrome[J].AM J MED GENET B: Neuropsychiatric Genetics, 2012, 159B (8) : 977-980.
- [55]Hao Deng*, Xiangjun Huang, Hui Liang, Hongbo Xu, Linyan Su, Jianguo Zhang, Xiong Deng, Jin Lei.Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome[J].AM J MED GENET B: Neuropsychiatric Genetics, 2012, 159B (1) : 72-76.
- [56]Hao Deng*, Ziqiang Luo, Hongbo Xu, Xiong Deng, Jin Lei, Jianguo Zhang, Linyan Su, Yi Guo.Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome[J].Psychiatric Genetics, 2012, 22 (6) : 300-303.
- [57]Hao Deng*, Zhijian Yang, Hongbo Xu, Weidong Le, Linyan Su, Joseph Jankovic, Xiong Deng, Yi Guo.Mutation screening of the HTR2B gene in patients with Tourette syndrome[J].Neurosci Lett, 2012, 526 (2) : 150-153.
- [58]Hao Deng*, Ziqiang Luo, Hongbo Xu, Linyan Su, Jianguo Zhang, Xiong Deng, Yi Guo.Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD[J].Neurosci Lett, 2012, 517 (1) : 18-20.
- [59]Weidong Le, Pingyi Xu, Ming Ming, Hao Deng, Qinghua Tao, Lai Wei, Hua Liu.Decreased NURR1 and PITX3 gene expression in Chinese patients with Parkinson's disease[J].Eur J Neurol, 2012, 19 (6) : 870-5.
- [60]Jianyu Zhou, Hao Deng, Guoping Yang, Hong Xiang, Lihua Huang, Shuhua Chen, Hong Yuan, Hongwei Lu.Senescent endothelial dysfunction is attributed to the up-regulation of sphingosine-1-phosphate receptor-2 in aged rats[J].Mol Cell Biochem, 2012, 363 (1-2) : 217-224.