Zhao X#, Tang Z, Zhang H, Atianjoh FE, Zhao JY, Liang L, Wang W, Guan X, Kao SC, Tiwari V, Gao YJ, Hoffman PN, Cui H, Li M, Dong X, Tao YX. A long noncoding RNA contributes to neuropathic pain by silencing Kcna2 in primary afferent neurons. Nat Neurosci.2013, 16(8):1024-31（IF：15.251）
Xu J, Zhao J, Zhao X#, LigonsD, Tiwari V, Atianjoh FE, Liang L, Zang W, Njoku D, Raja SN, Yaster M, Tao YX. Morphine tolerance and hyperalgesia mediated through mu opioid receptor-triggered activation of the mammalian target of rapamycin complex 1 pathway in dorsal horn neurons. J Clin Invest. 2014 , 124(2): 592-603. (IF：13.069）
Zhao X#, Sun M, Zhao J, Leyva JA, Zhu H, Yang W, Zeng X, Ao Y, Liu Q, Liu G, Lo WH, Jabs EW, Amzel LM, Shan X, Zhang X. Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.Am J Hum Genet. 2007, 80 (2): 361-71（IF：11.092）
Jiang M, Zhao X#, Han WT, Bian CY, Li XF, Wang G, Ao Y, Li YQ, Yi DX, Zhe Y, Lo HY Wilson, Zhang X, Li JX. A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expression. Hum Genet. 2006, 120 (2): 238-42
Kao SC, Zhao X, Lee CY, Atianjoh FE, Gauda EB, Yaster M, Tao YX. Absence of μ opioid receptor mRNA expression in astrocytes and microglia of rat spinal cord. Neuroreport. 2012, 23(6):378-84.
Cai F, Zhang YD, Zhao X, et al. Screening for AIP gene mutations in a Han Chinese pituitary adenoma cohort followed by LOH analysis. Eur J Endocrinol. 2013, 169: 867–884
Atianjoh FE, Yaster M, Zhao X, Takamiya K, Xia J, Gauda EB, Huganir RL, Tao YX.Spinal cord protein interacting with C kinase 1 is required for the maintenance of complete Freund's djuvant-induced inflammatory pain but not for incision-induced post-operative pain. Pain. 2010, 151(1):226-34.
Xu JT, Zhao X, Yaster M, Tao YX. Expression and distribution of mTOR, p70S6K, 4E-BP1, and their phosphorylated counterparts in rat dorsal root ganglion and spinal cord dorsal horn. Brain Res. 2010; 1336:46-57.
Zhao J, Hua R, Zhao X, Meng Y, Ao Y, Liu Q, Shang D, Sun M, Lo WH, Zhang X. Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia. Br J Dermatol. 2008;158(3): 614-7