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3.Li M, Liu J, Liu D, Duan X, Zhang Q, Wang D, Zheng Q, Bai X, Lu Z. Naringin attenuates cisplatin- and aminoglycoside-induced hair cell injury in the zebrafish lateral line via multiple pathways. J Cell Mol Med. 2021 Jan;25(2):975-989. (共同通訊作者，JCR分區：2)
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6.Bai X, Zhang C, Zhang F, Xiao Y, Jin Y, Wang H, Xu L. Five Novel Mutations in LOXHD1 Gene Were Identified to Gause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families. Biomed Res Int. 2020 Feb 18;2020:1685974. (JCR分區：3)
7.Wang M, Zhou Y, Zhang F, Fan Z, Bai X, Wang H. A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss. BMC Med Genet. 2020 Jul 25;21(1):154. (共同通訊作者，JCR分區：4)
8.Liu F, Cheng X, Dong J, Zhou D, Sun Q, Bai X, Wang D. Imaging modality for measuring the presence and extent of the labral lesions of the shoulder: a systematic review and meta-analysis. BMC Musculoskelet Disord. 2019 Oct 27;20(1):487. (共同通訊作者，JCR分區：3)
9.Zhang M, Han Y, Zhang F, Bai X, Wang H. Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China. Acta Otolaryngol. 2019 Jul;139(7):612-617. (共同通訊作者，JCR分區：4)
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11.Luo J, Bai X, Zhang F, Xiao Y, Gu L, Han Y, Fan Z, Li J, Xu L, Wang H. Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China. Ann Hum Genet. 2017;81(6):258-266. (共同第一作者，JCR分區：4)
12.Bai X, Zhang C, Chen A, Liu W, Li J, Sun Q, Wang H. Protective Effect of Edaravone on Glutamate-Induced Neurotoxicity in Spiral Ganglion Neurons. Neural Plast. 2016;2016:4034218. (JCR分區：3)
13.Zhang C, Wang M, Xiao Y, Zhang F, Zhou Y, Li J, Zheng Q, Bai X, Wang H. A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss. Neural Plast. 2016;2016:1512831. (共同通訊作者，JCR分區：3)
14.Wang M, Zhang F, Xu L, Xiao Y, Li J, Fan Z, Sun Q, Bai X, Wang H. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct. Int J Pediatr Otorhinolaryngol. 2016 Nov;90:170-174. (共同通訊作者，JCR分區：4)
15.Zhang F, Xiao Y, Xu L, Zhang X, Zhang G, Li J, Lv H, Bai X, Wang H. Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay. Biomed Res Int. 2016;2016:1302914. (共同通訊作者，JCR分區：3)
16.Zhang F, Bai X, Xiao Y, Zhang X, Zhang G, Li J, Xu L, Wang H. Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome. Int J Pediatr Otorhinolaryngol. 2016 Jun;85:75-9. (共同第一作者，JCR分區：4)
17.Ma Y, Xiao Y, Zhang F, Han Y, Li J, Xu L, Bai X, Wang H. Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family. Int J Pediatr Otorhinolaryngol. 2016 Apr;83:179-85. (共同通訊作者，JCR分區：4)
18.Xiao Y, Luo J, Zhang F, Li J, Han Y, Zhang D, Wang M, Ma Y, Xu L, Bai X, Wang H. A novel mutation in PAX3 associated with Waardenburg syndrome type I in a Chinese family. Acta Otolaryngol. 2016;136(5):439-45. (共同通訊作者，JCR分區：4)
19.Bai XH, Wang DW, Ji HZ, Zheng L, Lu Y, Tang W, Zhang HY, Xu W, Li JF, Fei ZQ, Wang HB: RbAp48 is Critical for the Proliferation of Hypopharyngeal Carcinoma. ORL J Otorhinolaryngol Relat Spec. 2015;77(5):310-9. (JCR分區：4)
20.Bai X, Lv H, Zhang F, Liu J, Fan Z, Xu L, Han Y, Chai R, Li J, Wang H. Identification of a novel missense mutation in the WFS1 gene as a cause of autosomal dominant nonsyndromic sensorineural hearing loss in all-frequencies. Am J Med Genet A. 2014;164A(12):3052-60. (JCR分區：3)
21.Yan W, Li J, Chai R, Guo W, Xu L, Han Y, Bai X, Wang H. Combining Use of Captopril and Losartan Attenuates the Progress of Streptococcus pneumoniae-Induced Tympanosclerosis through the Suppression of TGF-β1 Expression. PLoS One. 2014;31;9(10):e111620. (共同通訊作者，JCR分區：2)
22.Sheykholeslami K, Thimmappa V, Nava C, Bai X, Yu H, Zheng T, Zhang Z, Li SL, Liu S, Zheng QY. A new mutation of the Atoh1 gene in mice with normal life span allows anaylysis of inner ear and cerebellar phenotype in aging. PLoS One. 2013;8(11):e79791. (共同第一作者，JCR分區：2)
23.Bai XH, Wang DW, Fan ZM, Han YC, Xu L, Zhang GD, Lu SM, Liu WW, Li JF, Wang HB. Helicobacter pylori may cause otitis media with effusion: a pilot study. B-ENT. 2012;8(4):261-4. (JCR分區：4)
24.Wang D, Bai X, Tian Q, Lai Y, Lin EA, Shi Y, Mu X, Feng JQ, Carlson CS, Liu CJ. GEP constitutes a negative feedback loop with MyoD and acts as a novel mediator in controlling skeletal muscle differentiation. Cell Mol Life Sci. 2012;69(11):1855-73. (共同第一作者，JCR分區：2)
25.Guo W, Bai X, Han Y, Xu L, Liu W, Zhang G, Li J, Fan Z, Wang H. Expressions of TGF-β1 and MMP-9 in a guinea pig model of tympanosclerosis: Possible role in the pathogenesis of this disorder. Laryngoscope. 2012;122(9):2037-42. (共同第一作者，JCR分區：2)
26.Bai XH, Wang DW, Luan Y, Yu XP, Liu CJ. Regulation of chondrocyte differentiation by ADAMTS-12 metalloproteinase depends on its enzymatic activity. Cell Mol Life Sci 2009;66(4):667-80. (JCR分區：2)
27.Bai XH, Wang DW, Kong L, Zhang Y, Luan Y, Kobayashi T, Kronenberg HM, Yu XP, Liu CJ. ADAMTS-7, a direct target of PTHrP, adversely regulates endochondral bone growth by associating with and inactivating GEP growth factor. Mol Cell Biol 2009;29(15):4201-19. (JCR分區：2)
