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HUANG Xiaojun  

  • Graduate Supervisor, Associate Chief Physician
  • Department: Neurology
  • Research Area: Neurology
  • Research Interests: Neurogenetic and Movement Disorders
  • Contact: huangxj@rjlab.cn
Biography Positions Publications Research Projects Patents
  • MD from Shanghai Jiao Tong University School of Medicine, 2013
  • Council Member, Shanghai Association Against Epilepsy
  • Committee Member, Smart Healthcare Technology and Management Subcommittee, Chinese Geriatrics Society
  • Committee Member, EEG & Clinical Neurophysiology Committee, Shanghai Medical Association
  • Secretary, Neuroimmunology, Biochemistry and Genetics Section, Neurology Branch, Shanghai Medical Association
  • Vice Councilor, Hyacinth Huntington’s Disease Care Center
  • Young Committee Member, Chronic Neurological Diseases Committee, Shanghai Association of Chinese Integrative Medicine
  • Secretary, Clinical Genetics Committee, Shanghai Medical Doctor Association
  1. Luo H*, Huang X* (Co-first author), Li Z, Tian W, Fang K, Liu T, Wang S, Tang B, Hu J, Yuan TF, Cao L. An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia. Adv Sci (Weinh). 2024 Mar;11(12):e2306321. doi: 10.1002/advs.202306321.
  2. Huang X*, Fu X, Wu J, Cheng X, Hong X, Li Z, Zheng L, Liu Q, Chen S, Tang B, Zhao Y, Liu X, Li X, Liu X, Zhou Z, Wu L, Fang K, Zhong P, Zhang M, Luan X, Tian W, Tong X, Cao L. Heterozygous KCNJ10 Variants Affecting Kir4.1 Channel Cause Paroxysmal Kinesigenic Dyskinesia. Mov Disord. 2024 Dec;39(12):2199-2210. doi: 10.1002/mds.30025.
  3. Wu J, Cheng X, Ji D, Niu H, Yao S, Lv X, Wang J, Li Z, Zheng H, Cao Y, Zhan F, Zhang M, Tian W, Huang X#(Corresponding Author), Luan X#, Cao L#. The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China. Mov Disord. 2024 May;39(5):798-813. doi: 10.1002/mds.29764.
  4. Li ZY, Tian WT, Huang XJ#(Corresponding Author), Cao L#. The Pathogenesis of Paroxysmal Kinesigenic Dyskinesia: Current Concepts. Mov Disord. 2023 Apr;38(4):537-544. doi: 10.1002/mds.29326.
  5. Tian WT, Zhan FX, Liu ZH, Liu Z, Liu Q, Guo XN, Zhou ZW, Wang SG, Liu XR, Jiang H, Li XH, Zhao GH, Li HY, Tang JG, Bi GH, Zhong P, Yin XM, Liu TT, Ni RL, Zheng HR, Liu XL, Qian XH, Wu JY, Cao YW, Zhang C, Liu SH, Wu YY, Wang QF, Xu T, Hou WZ, Li ZY, Ke HY, Zhu ZY, Zheng L, Wang T, Rong TY, Wu L, Zhang Y, Fang K, Wang ZH, Zhang YK, Zhang M, Zhao YW, Tang BS, Luan XH, Huang XJ#(Corresponding Author), Cao L#. TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study. Mov Disord. 2022 Mar;37(3):545-552. doi: 10.1002/mds.28865.
  6. Cao L*, Huang X* (Co-first author), Wang N, Wu Z, Zhang C, Gu W, Cong S, Ma J, Wei L, Deng Y, Fang Q, Niu Q, Wang J, Wang Z, Yin Y, Tian J, Tian S, Bi H, Jiang H, Liu X, Lü Y, Sun M, Wu J, Xu E, Chen T, Chen T, Chen X, Li W, Li S, Li Q, Song X, Tang Y, Yang P, Yang Y, Zhang M, Zhang X, Zhang Y, Zhang R, Ouyang Y, Yu J, Hu Q, Ke Q, Yao Y, Zhao Z, Zhao X, Zhao G, Liang F, Cheng N, Han J, Peng R, Chen S, Tang B. Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China. Transl Neurodegener. 2021 Feb 16;10(1):7. doi: 10.1186/s40035-021-00231-8.
  7. Huang XJ*, Wang SG, Guo XN, Tian WT, Zhan FX, Zhu ZY, Yin XM, Liu Q, Yin KL, Liu XR, Zhang Y, Liu ZG, Liu XL, Zheng L, Wang T, Wu L, Rong TY, Wang Y, Zhang M, Bi GH, Tang WG, Zhang C, Zhong P, Wang CY, Tang JG, Lu W, Zhang RX, Zhao GH, Li XH, Li H, Chen T, Li HY, Luo XG, Song YY, Tang HD, Luan XH, Zhou HY, Tang BS, Chen SD, Cao L. The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China. Mov Disord. 2020 Aug;35(8):1428-1437. doi: 10.1002/mds.28061.
  8. Tian WT*, Huang XJ* (Co-first author), Mao X, Liu Q, Liu XL, Zeng S, Guo XN, Shen JY, Xu YQ, Tang HD, Yin XM, Zhang M, Tang WG, Liu XR, Tang BS, Chen SD, Cao L. Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients. Mov Disord. 2018 Mar;33(3):459-467. doi: 10.1002/mds.
  9. Huang XJ*, Wang T, Wang JL, Liu XL, Che XQ, Li J, Mao X, Zhang M, Bi GH, Wu L, Zhang Y, Wang JY, Shen JY, Tang BS, Cao L, Chen SD. Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patients. Neurology. 2015 Nov 3;85(18):1546-53. doi: 10.1212/WNL.0000000000002079. 
  10. Cao L*, Huang XJ* (Co-first author), Zheng L, Xiao Q, Wang XJ, Chen SD. Identification of a novel PRRT2 mutation in patients with paroxysmal kinesigenic dyskinesias and c.649dupC as a mutation hot-spot. Parkinsonism Relat Disord. 2012 Jun;18(5):704-6. doi: 10.1016/j.parkreldis.2012.02.006. 
  • 10/01/2024-9/30/2027
    Natural Science Foundation of Shanghai (General Program), ¥200,000, 24ZR1456700
    Mechanisms of Cerebellar-Related Motor Circuits in Paroxysmal Kinesigenic Dyskinesia
    Role: Project leader
  • 12/01/2018-12/31/2018
    Shanghai Municipal Health Commission, ¥20,000, 20164Y0019
    Role of Excitatory Amino Acid Release in the Pathogenesis of Paroxysmal Kinesigenic Dyskinesia
    Role: Project leader
  • 07/01/2017-06/30/2020
    Shanghai Outstanding Young Medical Talents Program (Population and Health System), ¥300,000, 2017YQ079
    Role: Project leader
  • 01/01/2017-12/31/2019
    National Natural Science Foundation of China (General Program), ¥180,000, 81600978
    The Pathogenic Mechanism of PRRT2-Mediated Nav1.2 Channel Dysfunction in Paroxysmal Kinesigenic Dyskinesia
    Role: Project leader
  1. [Li Cao, Yuwen Cao, Wotu Tian, Xiaojun Huang] (2024), “Gene Delivery Vehicle and Gene Therapy Drug for Treating Hereditary Spastic Paraplegia Type 35”, CN202311759513.6

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