Journal Publications

• [1]Hao Deng*, Zhijian Yang, Wei Xiong, Xiong Deng, Zhi Song, Lamei Yuan.Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson’s disease patients[J].Neurosci Lett, 2016, 616: 26-31.
• [2]Zeshuai Zen, Guiyuan Li, Hao Deng, Qianjin Liao, Pan Chen, Jie Yang, Ming Zhou, Wei Xiong, Ke Xu.Integrating ChIP-sequencing and digital gene expression profiling to identify BRD7 downstream genes and construct their regulating network[J].Mol Cell Biochem, 2016, 411 (1-2) : 57-71.
• [3]Hao Deng*, Zhi Song, Yan Yang, Lamei Yuan, Jingjing Xiao, Xiong Deng, Jianguo Zhang, Wen Zheng.Identification of a premature termination mutation in the proline-rich transmembrane protein 2 gene in a Chinese family with febrile seizures[J].Neurobiol, 2016, 53 (2) : 835-41.
• [4]Hao Deng*, Yong Chen*, Bin Ni, Xiong Deng, Wei Xiong, Lamei Yuan, Zhi Song, Ting Tan.Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson’s disease[J].Neurosci Lett, 2016, 612: 189-92.
• [5]Hao Deng*, Yong Chen*, Bin Ni, Xiong Deng, Lamei Yuan, Zhi Song, Ting Tan, Sihan He.Genetic analysis of MC1R variants in Chinese Han patients with sporadic Parkinson’s disease[J].Neurosci Lett, 2016, 611: 101-105.
• [6]Hao Deng*, Zhijian Yang, Hongbo Xu, Xiong Deng, Pengzhi Hu, Yi Guo, Xiangjun Huang, Hong Xia.Identification of a novel MYO15A mutation in a Chinese family with autosomal recessive nonsyndromic hearing loss[J].PLoS One, 2015, 10 (8) : e0136306.
• [7]Lamei Yuan, Ting Tan, Hao Deng#*.Advances in the molecular genetics of non-syndromic polydactyly[J].Expert Rev Mol Med, 2015, 17: e18.
• [8]Joseph Jankovic, Xiaofei Xiu#, Hao Deng#*.Genetic convergence of Parkinson's Disease and lysosomal Storage Disorders[J].Molecular Neurobiology, 2015, 51 (3) : 1554-1568.
• [9]Joseph Jankovic, Yuan Wu#, Hao Deng#*.The EIF4G1 gene and Parkinson Disease[J].Acta Neurol Scand, 2015, 132 (2) : 73-78.
• [10]Joseph Jankovic, Wen Zheng#, Hao Deng#*.Genetics and molecular biology of brain calcification[J].Ageing Res Rev, 2015, 22: 20-38.
• [11]Ting Tan, Hao Deng#*.Advances in the molecular genetics of non-syndromic syndactyly[J].Current Genomics, 2015, 16 (3) : 183-193.
• [12]Sheng Deng, Hong Xia#, Hao Deng#*.Genetic basis of human left-right asymmetry disorders[J].Expert Reviews in Molecular Medicine, 2015, 16: e1.
• [13]Hao Deng*, Yan Yang, Zhijian Yang, Zhi Song, Xiong Deng, Ting Tan, Yi Guo.TCEANC2 rs10788972 and rs12046178 variants in the PARK10 region in Chinese Han patients with sporadic Parkinson's disease[J]. Neurobiology of Aging, 2015, 36 (12) : 3335.e1- e2.
• [14]Yi Guo, Wei Xiong, Weidong Le, Hanxiang Deng, Peter Riederer, Hao Deng#*.Human Genetic Diseases[J].Biomed Res Int, 2014, 2015: 315216.
• [15]Hao Deng*, Yong Chen*, Bin Ni, Zhijian Yang, Zhi Song, Xiong Deng, Lamei Yuan.Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease[J].Neurobiology of Aging, 2015, 36 (10) : 2907.e11-e12.
• [16]Hao Deng*, Wei Xiong, Zhijian Yang, Zhi Song, Lamei Yuan, Xiong Deng, Sheng Deng.Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease[J].Acta Neurologica Belgica, 2015, 115 (3) : 267-271.
• [17]Hao Deng*, Yan Yang, Zhijian Yang, Lamei Yuan, Song Wu, Hongbo Xu, Xiong Deng, Xiangjun Huang.Identification of a novel mutation in the COL2A1 gene in a Chinese family with spondyloepiphyseal dysplasia congenita[J].PLoS One, 2015, 10 (6) : e0127529.
• [18]Hao Deng*, Yulan Shen, Anjie Lu, Pengzhi Hu, An Liu, Hong Xia, Zhijian Yang, Song Wu, Lamei Yuan.Identification of a novel PHEX mutation in a Chinese family with X-linked hypophosphatemic rickets using exome sequencing[J].Biological Chemistry, 2015, 396 (1) : 27-33.
• [19]Hao Deng*, Zhijian Yang, Hongbo Xu, Wei Xiong, Jingjing Xiao, Junhui Yi, Yi Guo, Lamei Yuan.Identification of a novel GJA3 mutation in congenital nuclear cataract[J].Optometry and Vision Science, 2015, 92 (3) : 337-342.
• [20]Hongwei Lu, Alex F. Chen, Hong Yuan, Hao Deng, Hong Xiang, Jie Yang, Shuhua Chen.Role of sphingosine-1-phosphate receptor 1 and sphingosine-1-phosphate receptor 2 in hyperglycemia-induced endothelial cell dysfunction[J].Int J Mol Med, 2015, 35 (4) : 1103-1108.