导师姓名： 吴皓 专业代码： 100213
性别： 男 专业名称： 耳鼻咽喉科学
培养单位： 附属第九人民医院 三级学科/
专业领域：
导师类型： 博士生导师 专业学位导师： 兼
联系方式：
邮编： 210000 邮箱地址： wuhao@sh9hospital.org.cn

研究方向 (点击浏览详细信息)
耳科学、耳神经外科学、侧颅底外科学

社会任职
上海医学会耳鼻咽喉头颈外科分会前任主任委员
中华医学会耳鼻咽喉头颈外科分会主任委员
上海市耳鼻咽喉科临床质控中心主任
卫生部新生儿听力筛查专家组组长

科研项目 项目编号项目名称课题来源起止年月批准经费承担职责
shslczdzk00802 上海市临床重点专科建设项目 临床重点专科 2020-01~2024-12 1942.28万元 课题负责人
** 听神经瘤细胞NF2基因状态差异对肿瘤发生发展的作用研究 国家自然科学基金面上项目 2020-01~2023-12 55万元 课题负责人
IMR-NPH202001 用于人工耳蜗抱轴电极微创植入的智能手术机器人及核心组件的研发 上海交通大学医疗机器人项目 2020-01~2022-12 100万元 课题负责人
2018SHZDZX05 灵长类听觉退行性变化机制及治疗研究 基础研究重大 2018-07~2023-06 442.43万元 课题负责人
** 遗传和环境因素对GJB2基因p.V37I突变所致迟发型耳聋表型修饰作用的机制研究 国家自然科学基金重点项目 2018-01~2022-12 299万元 课题负责人
SQ2017YFSF080012 出生缺陷一级预防孕前检测技术设备及应用平台的研发? 科技部重点研发计划 2017-07~2020-12 1918万元 课题负责人
2014BAI04B01 听神经瘤规范化手术治疗策略研究 科技部 2017-05~2017-12 80万元 课题负责人
16CR1005A 先天性耳聋早期双侧人工耳蜗植入的多中心临床研究 申康重大疾病 2016-12~2019-06 200万元 课题负责人
** merlin/p53协同信号的核质穿梭对前庭神经鞘膜瘤生长的影响 国家自然科学基金面上项目 2016-01~2019-12 57万元 课题负责人
** 儿童迟发性耳聋的分子致病机制及基因治疗研究 国自然重点 2014-01~2019-12 290万元 主要责任人
耳鼻重大疾病的早期发现、规范诊治和防控体系研究及推广应用 卫生行业科研专项基金 2012-01~2014-12 2313万元 主要责任人
2012BAI109B02 遗传性耳聋的预防和干预 “国家十二五”科技支撑计划 2012-01~2015-12 50万元 子课题负责人
** 迟发型儿童听力障碍的分子病因及基因型－表型关联研究 国家自然科学基金面上项目 2012-01~2015-12 57万元 课题负责人
2011CB504501 遗传性聋相关新基因识别及其功能的研究 国家973计划 2011-01~2015-08 517万元 子课题负责人
我国耳鼻重大疾病的早期发现、规范诊治和防控 卫生部科研专项经费 2010-07~2013-06 2800万元 课题负责人
C170703 不同生长特性的听神经瘤细胞对听神经瘤生物学行为的影响 国家自然基金，面上项目 2010-01~2012-12 32万元
遗传性耳聋常见基因产前筛查体系的研究 上海市科委，生药项目 ~ 300万元
2008B089 耳科学、耳神经科学及侧颅底外科讲学 上海市科委，白玉兰 ~ 30万元

学术论文 作者论文标题期刊名出版年卷期页码
Huang He*,Chen Hongsai*, Wang Xueling*, Qiu Fangxia, Liu Huihui, Lu Jiawen, Tong Ling, Yang Yuming, Wang Xiansong#,Wu （通讯作者）, Hao#. Degradable and bioadhesive alginate-based composites: An effective hemostatic agent ACS Biomaterials Science & Engineering 2019 5, 10, 5498-5505
Zirong Huo*,Jianqing Chen*,Zhaoyan Wang,Zhihua Zhang#,Hao Wu# （通讯作者） Prognostic Factors of Long-Term Hearing Preservation in Small and Medium-Sized Vestibular Schwannomas After Microsurgery. Otol Neurotol. 2019 40(7):957-964
Chen, Hongsai* ;Huang, He* ;Zhao, Jingjing * ;Wang, Zhigang *;Chang, Mengling ;Xue, Lu ;Zhu, Weidong ;Chai, Yongchuan ;Li, Gen ;Wang, Zhaoyan# ;Wu （通讯作者）, Hao# Age-dependent copy number variations of TP53 tumour suppressor gene associated with altered phosphorylation status of p53 protein in sporadic schwannomas J Neurooncol. 2019 143(3):369-379.
Chen, J-Q*;Tan, H-Y *;Wang, Z-Y* ;Zhu, W-D ;Chai, Y-C ;Jia, H#. ;Wu （通讯作者）, H.# Strategy for facial nerve management during surgical removal of benign jugular foramen tumors: Outcomes and indications Eur Ann Otorhinolaryngol Head Neck Dis 2019 136(3S),S21-S25
Huihui Liu*,Jiawen Lu*,Zhongying Wang,Lei Song,Xueling Wang#,Geng-Lin Li#,Hao Wu# （通讯作者） Functional alteration of ribbon synapses in inner hair cells by noise exposure causing hidden hearing loss Neuroscience Letters 2019 ?707:134268
Chen, Yuming* ;Gu, Jiayi;Liu, Jian ;Tong, Ling;Shi, Fuxin;Wang, Xiaoqin ;Wang, Xueling# ;Yu, Dehong#;Wu （通讯作者）, Hao# Dexamethasone-loaded injectable silk-polyethylene glycol hydrogel alleviates cisplatin-induced ototoxicity International Journal of Nanomedicine 2019 14, 4211–4227
Liu H*, Li G, Lu J, Gao YG, Song L, Li GL#, Wu H#. （通讯作者） Cellular Differences in the Cochlea of CBA and B6 Mice May Underlie Their Difference in Susceptibility to Hearing Loss. Front Cell Neurosci 2019 13, 60
Chen, Jianqing * ;Wu, Yingwei ;Shi, Jun ;Jia, Huan ;Wang, Zhaoyan ;Zhang, Zhihua # ;Wu （通讯作者）, Hao#7 Predictors of round window membrane visibility in pediatric cochlear implant surgery using temporal bone HRCT: A retrospective study. Int J Pediatr Otorhinolaryngol. 2019 121:150-153.
Shuang Yan*, Quan Wang*,Zirong Huo, Tao Yang, Xiaoling Yin,Zhaoyan Wang,Zhihua Zhang#,and Hao Wu# （通讯作者） Gene expression profiles between cystic and solid vestibular schwannoma indicate susceptible molecules and pathways in the cystic formation of vestibular schwannoma. Functional and Integrative Genomics. 2019 19(4):673-684.
Jiawen Lu*, Wenxiao Wang*, Hongchao Liu, Huihui Liu, Hao Wu （通讯作者） Cisplatin induces calcium ion accumulation and hearing loss by causing functional alterations in calcium channels and exocytosis. American Journal of Translational Research 2019 11(11): 6877-6889
Chen, Ying*;Li, Yun;Ren, Yan ;Li, Haifeng;Huang, Meiping ;Jia, Huan;Yang, Tao ;Wang, Zhaoyan ;Huang, Zhiwu#;Wu （通讯作者）, Hao# Identification of a novel CDH23 gene variant associated with non-syndromic progressive hearing loss in a Chinese family: Individualized hearing rehabilitation guided by genetic diagnosis International Journal of Pediatric Otorhinolaryngology 2019 127 (2019) 109649
Peng, Hu * ;Deng, Yue ;Wang, Longhao;Cheng, Yin;Xu, Yaping ;Liao, Jianchun #;Wu （通讯作者）, Hao# Identification of Potential Biomarkers with Diagnostic Value in Pituitary Adenomas Using Prediction Analysis for Microarrays Method J Mol Neurosci 2019 69(3):399-410
Bin Ye*,Quan Wang*,Haixia Hu*,Yilin Shen,Cui Fan,Penghui Chen,Yan Ma,Hao Wu# （通讯作者）,Mingliang Xiang# Restoring autophagic flux attenuates cochlear spiral ganglion neuron degeneration by promoting TFEB nuclear translocation via inhibiting MTOR. Autophagy 2019 15(6): 998–1016.
Wen Kang*,Zhuoer Sun,Xingle Zhao,Xueling Wang#,Yong Tao#,?Hao Wu# （通讯作者） Gene editing based hearing impairment research and therapeutics Neuroscience Letters 2019 709:134326
Jingrong Lu* ,Lingxiang Hu*,Bin Ye,Haixia Hu,Yong Tao,?Yilai Shu ,Hao Chiang,Vikrant Borse ,?Mingliang Xiang,Hao Wu # （通讯作者）,Albert S B Edge,Fuxin Shi # Increased type I and decreased type II hair cells after deletion of Sox2 in the developing mouse utricle Neuroscience 2019 1;422:146-160
You Zhou, Manli Yin, Chenchen Xia, Xueling Wang, Hao Wu# （通讯作者）, Yonghua Ji# Visual deprivation modifies glutamate receptor expression in visual and auditory centers Am J Tra 2019 11(12):7523-7537
Chen, Penghui*; Liu, Haijin*;Lin, Yun;Xu, Jun;Zhu, Weidong ;Wu, Hao#;Yang （通讯作者）, Tao# EYA1 mutations leads to Branchio-Oto syndrome in two Chinese Han deaf families Int J Pediatr Otorhinolaryngol 2019 123:141-145
Tan H(#),Yang J, Wang Z Y, Zhu W D, Chai Y C, Jia H(*), Wu H(*) （通讯作者） Simultaneous supervision by microscope of endoscope-assisted microsurgery via presigmoid retrolabyrinthine approach: A pilot study.Dis. Eur Ann Otorhinolaryngol Head Neck Dis 2018 135(5): S103~S106
Wang Xueling(#), Chen Yuming, Tao Yong, Gao Yunge, Yu Dehong(*), Wu Hao(*) （通讯作者） A666-conjugated nanoparticles target prestin of outer hair cells preventing cisplatin-induced hearing loss International Journal of Nanomedicine 2018 13: 7517~7531
Chen Penghui(#), Chai Yongchuan, Liu Haijin, Li Gen, Wang Longhao, Yang Tao(*),Wu Hao(*) （通讯作者） Postnatal Development of Microglia-Like Cells in Mouse Cochlea Neural Plasticity 2018 2018: **
He L(#), Pang X, Liu H, Chai Y, Wu H(*) （通讯作者）, Yang T(*) Targeted next-generation sequencing and parental genotyping in sporadic Chinese Han deaf patients Clinical Genetics, 2018 93(4): 899~904
Tan Haoyue(#),Jia Huan(#)(*), Li Yun, Zhang Zhihua, Zhu Weidong, Cai Yun, Wang Zhaoyan(*), Wu Hao(*) （通讯作者） Impact of cochlear implantation on the management strategy of patients with neurofibromatosis type 2. European Archives of Oto-Rhino-Laryngology 2018 275(11): 2667~2674
Hongsai Chen#, Lu Xue#, He Huang#, Hantao Wang#, Xiaoman Zhang, Weidong Zhu, Zhigang Wang, Zhaoyan Wang*, Hao Wu* （通讯作者） Synergistic effect of Nutlin-3 combined with MG-132 on schwannoma cells through restoration of merlin and p53 tumour suppressors EBioMedicine 2018 36: 252~265
Xin Lin*,?Gen Li* ,?Yu Zhang* ,?Jingjing Zhao?,?Jiawen Lu? ,?Yunge Gao,?Huihui Liu? ,?Geng-Lin Li ,?Tao Yang ,?Lei Song?# ,?Hao Wu# （通讯作者） Hearing consequences in Gjb2 knock-in mice: Implications for human p.V37I mutation. Aging 2018 11(18):7416-7441
Wang Xueling(#), Wang Longhao, Peng Hu, Yang Tao(*), Wu Hao(*) （通讯作者） A Novel p.G141R Mutation in ILDR1 Leads to Recessive Nonsyndromic Deafness DFNB42 in Two Chinese Han Families Neural Plasticity 2018 2018: **
Hongsai Chen, Lu Xue1, Hantao Wang, Zhaoyan Wang#& Hao Wu# Differential NF2 Gene Status in Sporadic Vestibular Schwannomas and its Prognostic Impact on Tumor Growth Patterns Sci Rep. 2017 7(1):5450
He L, Pang X, Chen P, Wang X, Yang T#, Wu H#. （通讯作者） Carrier re-sequencing reveals rare but benign variants in recessive deafness genes. Sci Rep 2017 7: 11355
Huo?Z#,?Shi?J#,?Shu?Y,?Xiang?M,?Lu?J,?Wu?H* （通讯作者） The?relationship?between?allergic?status?and?adenotonsillar?regrowth:?a?retrospective?research?on?children?after?adenotonsillectomy.? Scientific?Reports 2017 7:46615
Liu H, Luo H, Yang T#, Wu H# （通讯作者）, Chen D#. Association of leukocyte telomere length and the risk of age-related hearing impairment in Chinese Hans. Sci Rep 2017 7: 10106
XIYE LI*, HONGSAI CHEN*, LU XUE, XIUHONG PANG, XIAOMAN ZHANG, ZHENGJIE ZHU, WEIDONG ZHU, ZHAOYAN WANG# and HAO WU# he p53 tumor-suppressor protein plays an essential role in mediating the oncogenic stimulus triggered by loss of expression of another tumor Oncology Letters 2017 14(2):2223-2231
Chen DY, Liu XF, Lin XJ, Zhang D, Chai YC, Yu DH, Sun CL, Wang XL, Zhu WD, Chen Y, Sun LH, Wang XW, Shi FX, Huang ZW, Yang T#, Wu H# （通讯作者） A dominant variant in DMXL2 is linked to nonsyndromic hearing loss. Genetics in Medicine 2017 19(5), 553–558.
Zirong Huo*, Jun Shi,*, Yilai Shu, Mingliang Xiang, Jingrong Lu# Hao Wu#. （通讯作者） The relationship between allergic status and adenotonsillar regrowth: a retrospective research on children after adenotonsillectomy Scientific RepoRts 2017 7: 46615
Haixia Hu,Bin Ye,Le Zhang,Quan Wang ,Zhiwei Liu ,Suying Ji , Qiuju Liu ,Jingrong Lv ,Yan Ma , Ying Xu ,Hao Wu * （通讯作者）,Fude Huang 4* and Mingliang Xiang * Efr3a Insufficiency Attenuates the Degeneration of Spiral Ganglion Neurons after Hair Frontiers in Molecular Neuroscience 2017 3 (10):1-13
Hongsai Chen, Weidong Zhu,Xiye Li ,Lu Xue,Zhaoyan Wang,Hao Wu. （通讯作者） Genetic and epigenetic patterns in patients with the head-and-neck paragangliomas associate with differential clinical characteristics J Cancer Res Clin Oncol 2017 143(6):953-960
Zhu WD, Huang Q, Li XY, Chen HS, Wang ZY, Wu H （通讯作者） Diagnosis and treatment of cavernous hemangioma of the internal auditory canal.J Neurosurg. J Neurosurg 2016 124(3):639-466
Chen Y, Hu L, Wang X, Sun C, Lin X, Li L, Mei L, Huang Z, Yang T#, Wu H#. （通讯作者） Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2 Sci Rep 2016 6: 33279
Gao Z, Kelly MC, Yu DH, Wu H （通讯作者）, Lin X, Chi FL, Chen P Spatial and Age-Dependent Hair Cell Generation in the Postnatal Mammalian Utricle. Mol Neurobiol. 2016 53(3):1601-12
Bin Yi,Shousen Hu,?Chuantao Zuo,Fangyang Jiao,Jingrong Lv,Dongye Chen,Yufei Ma,Jianyong Chen,?Ling Mei,Xueling Wang,Zhiwu Huang* & Hao Wu Effects of long-term salicylate administration on synaptic ultrastructure and metabolic activity in the rat CNS Sci Rep 2016 12;6:24428
Zhu WD, Huang Q, Li XY, Chen HS, Wang ZY, Wu H. （通讯作者） Diagnosis and treatment of cavernous hemangioma of the internal auditory canal. J Neurosurg 2016 2016;124(3):639-466.
???Sun C, Wang X, Chen D, Lin X,?Yu DH ,? Wu H Dexamethasone loaded nanoparticles exert protective effects against Cisplatin-induced hearing loss by systemic administration Neurosci Lett 2016 619:142-8
Sun L, Li X, Shi J, Pang X, Hu Y, Wang X, Wu H#, Yang T# （通讯作者） Molecular etiology and genotype-phenotype correlation of Chinese Han deaf patients with type I and typeII Waardenburg Syndrome Sci Rep 2016 6: 35498
??Yu DH,?Sun C, Zheng Z, Wang X, Chen D, Wu H （通讯作者）, Wang X, Shi F Inner ear delivery of dexamethasone using injectable silk-polyethylene glycol (PEG) hydrogel Int J Pharm 2016 503(1-2):229-37
Shou-Sen Hu, Ling Mei, Jian-Yong Chen, Zhi-Wu Huang*, Hao Wu （通讯作者） Expression of immediate-early genes in the dorsal cochlear nucleus in salicylate-induced tinnitus Eur Arch Otorhinolaryngol? 2016 273(2):325-32.
Pang X, Luo H, Chai Y, Wang X, Sun L, He L, Chen P, Wu H （通讯作者）, Yang T. A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability. PLoS One 2015 10(3):e**
Chen D, Zhu W, Chai Y, Chen Y, Sun L, Yang T#, Wu H （通讯作者） Mutation in PCDH15 may modify the phenotypic expression of the 7511T>C mutation in MT-TS1 in a Chinese Han family with maternally inherited nonsyndromic hearing loss Int J Pediatr Otorhinolaryngol 2015 79(10):1654-1657
Pang X, Wang Z, Chai Y, Chen H, Li L, Sun L, Jia H, Wu H （通讯作者）, Yang T. A Novel Missense Mutation of NOG Interferes With the Dimerization of NOG and Causes Proximal Symphalangism Syndrome in a Chinese Family. Ann Otol Rhinol Laryngol 2015 124(9):745-51
Nie C , Hu H(co-first author), Shen C, Ye B, Wu H＊ （通讯作者）, Xiang M Expression of EFR3A in the Mouse Cochlea during Degeneration of Spiral Ganglion following Hair Cell Loss. PLoS One 2015 Jan 26;10(1):e**
Chen Y,Wang Z,Wang Z,Chen D,Chai Y,Pang X,Sun L,Wang X,Yang T,Wu H （通讯作者） Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss. PLoS One 2015 10(5):e**
ZhaoYan Wang ? HongSai Chen ? Qi Huang ?ZhiHua Zhang ? Jun Yang ? Hao Wu Facial and lower cranial nerve function preservation in lateral Eur Arch Otorhinolaryngol 2015 272:2207–2212
Xiao Man Zhang, MD*, Jun Shi, MD*, Guo Zhen Meng, MD*, Hong Sai Chen （通讯作者）, MD, Li Na Zhang, MD,Zhao Yan Wang, MD, PhD, and Hao Wu, The Effect of Obstructive Sleep Apnea Syndrome on Growth andDevelopment in Nonobese Children: A Parallel Study of Twins J Pediatr 2015 166:646-50).
Jingrong Lu, Weiwen Zhang, Zhentao Wang, Huan Jia, Yan Ma, Hao Wu＊ （通讯作者）, Mingliang Xiang＊ Basal cell adenoma of the parotid gland: clinical and pathological findings in 29 cases. Int J Clin Exp Pathol 2015 8(3):2899-2908
Chai Y, Chen D, Sun L, Li L, Chen Y, Pang X, Zhang L, Wu H （通讯作者）, Yang T. The homozygous p.V37I variant of GJB2 is associated with diverse hearing phenotypes. Clin Genet. 2015 87(4):350-355
Sun C, Wang X, Zheng Z, Chen D, Wang X, Shi F, Yu D, Wu H. （通讯作者） A single dose of dexamethasone encapsulated in polyethylene glycol-coated polylactic acid nanoparticles attenuates cisplatin-induced hearing loss following round window membrane administration. Int J Nanomedicine 2015 10:3567-79
Wang ZT, Chen Y, Chen DY, Chai YC, Pang XH, Sun LH, Wang XW, Yang T, Wu H. （通讯作者） Mutation analysis of seven consanguineous Uyghur families with nonsyndromic deafness. Int J Pediatr Otorhinolaryngol. 2014 78(9):151-3
Chen H, Zhang X, Zhang Z, Yang T, Wang Z, Wu H. （通讯作者） The role of NF2 gene mutations and pathogenesis-related proteins in sporadic vestibular schwannomas in young individuals. Mol Cell Biochem 2014 392(1-2):145-52
Zhang Z, Wang Z, Sun L, Li X, Huang Q, Yang T, Wu H. （通讯作者） Mutation spectrum and differential gene expression in cystic and solid vestibular schwannoma. Genet Med. 2014 16(3):264-70
Wu W, Lü J, Li Y, Kam AC, Fai Tong MC, Huang Z, Wu H. （通讯作者） A new hearing screening system for preschool children Int J Pediatr Otorhinolaryngol. 2014 78(2):1526-
Chai Y, Chen D, Wang X, Wu H, Yang T. （通讯作者） A novel splice site mutation in DFNA5 causes late-onset progressive non-syndromic hearing loss in a Chinese family. Int J Pediatr Otorhinolaryngol. 2014 78(8):12-65
Lü J1, Huang Z, Ma Y, Li Y, Mei L, Yao G, Wang Y, Shen X, Wu H. （通讯作者） Comparison between hearing screening-detected cases and sporadic cases of delayed-onset hearing loss inpreschool-age children Int J Audiol 2014 53(4):123-6
Hu SS, Mei L, Chen JY, Huang ZW, Wu H. （通讯作者） Expression of immediate-early genes in the inferior colliculus and auditory cortex in salicylate-induced tinnitus in rat. Eur J Histochem 2014 58(1):2294
Hu SS, Mei L, Chen JY, Huang ZW, Wu H. （通讯作者） Effects of salicylate on the inflammatory genes expression and synaptic ultrastructure in the cochlear nucleus of rats. Inflammation 2014 37(2):365-73
Zhang L, Hu L, Chai Y, Pang X, Yang T, Wu H. （通讯作者） A Dominant Mutation in the Stereocilia-Expressing GeneTBC1D24 is a Probable Cause for Nonsyndromic Hearing Impairment. Hum Mutat. 2014 35(7):81-8
Chen D, Chai Y, Yang T#, Wu H （通讯作者） Clinical characterization of a novel COCH mutation G87V in a Chinese DFNA9 family Int J Pediatr Otorhinolaryngol. 2013 77（1）: 1711–1715
Zhang Z, Wang Z, Sun L, Li X, Huang Q, Yang T, Wu H （通讯作者） Mutation spectrum and differential gene expression in cystic and solid vestibular schwannoma Genet Med 2013 114（2）:52-60
2.Yang T; Li X; Huang Q; Li L; Chai Y; Sun L; Wang X; Zhu Y; Wang Z; Huang Z; Li Y; Wu H Double heterozygous mutations of MITF and PAX3 result in Waardenburg Syndrome with increased penetrance in pigmentary defects Clin Genet, 2013 83:78-82
Luo H*, Yang T*, Jin X, Pang X, Li J, Chai Y, Li L, Zhang Y, Zhang L, Zhang Z （通讯作者）, Wu W, Zhang Q, Hu X, Sun J, Jiang X, Fan Z, Huang Z, Wu H Association of GRM7 Variants with Different Phenotype Patterns of Age-Related Hearing Impairment in an Elderly Male Han Chinese Population. PLoS One 2013 8(10):77153-77153
Zhang Z, Li Y, Hu L, Wang Z, Huang Q, Wu H （通讯作者） Cochlear implantation in children with cochlear nerve deficiency: a report of nine cases. Int J Pediatr Otorhinolaryngol 2012 1188-1195
Xiaohua Li, Yongchuan Chai, Zheng Tao, Lei Li, Tao Yang, Wu H （通讯作者） Novel mutations in ATP6V0A4 are associated with atypical progressive sensorineural hearing loss in a Chinese patient with distal renal tubular acidosis.2012, 76 (1): 152-154. Int J Pediatr Otorhinolaryngol 2012 152-154
Jingrong Lu, Zhiwu Huang, Tao Yang, Yun Li, Ling Mei, Mingliang Xiang, Yongchuan Chai, Xiaohua Li, Lei Li, Guoyin Yao, Yu Wang, Xiaoming Shen, Hao Wu （通讯作者） Screening for delayed-onset hearing loss in preschool children who previously passed the newborn hearing screening International Journal of Pediatric Otorhinolaryngology 2011 75 (2011): 1045-1049
Jingrong Lu （通讯作者）, Zhiwu Huang, Tao Yang, Yun Li, Ling Mei, Mingliang Xiang, Yongchuan Chai, Xiaohua Li, Lei Li, H. WU, Y. CHEN, Z. Y. WANG,, W. LI, J. Q. LI, L. ZHANG,, Y. J. LU Involvement of P21 (WAF1) in Merlin Deficient Sporadic Vestibular Schwannomas Neuroscience 2010 170 (1):149-155
Jingrong Lu, Zhiwu Huang, Tao Yang, Yun Li, Ling Mei, Mingliang Xiang, Yongchuan Chai, Xiaohua Li, Lei Li, H. Yan Ma （通讯作者）, Tao Yang, Yun Li, Zheng Tao, Zhiwu Huang, Xiaohua Li, Yongchuan Chai, Zhiguo Ouyang, Xiaoming Shen, Hao Wu Genotype – Phenotype Correlation of Two Prevalent GJB2 Mutations in Chinese Newborn Infants Ascertained From the Universal Newborn Hearing Screening Program American Journal of Medical Genetics A, 2010 152 (11): 2912-2915
Wang Z, Lu Y, Tang J, Wang H,Wu H. （通讯作者） The phosphorylation status of merlin in sporadic vestibular Schwannomas. Mol Cell Biochem 2009 201-206
Tao Yang, Jose G. Gurrola II, Hao Wu （共同第一作者）, Sui M. Chiu, Philine Wangemann, Peter M. Synder, Richard J. H. Smith Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome. Am J Hum Genet 2009 84, 651-657
YANG Jun,WU Hao （通讯作者）,ZhangPing,HouDongMing,ChenJie,ZhangShunGuo The pharmacokinetic profiles of dexamethasone and methylprednisolone concentration in perilymph and plasma following systemic and local administration Acta Oto-Laryngologica 2008 128: 496-504
Lü J, Zou J, Wu H （通讯作者）, Cai L. Compensative shuttling of merlin to phosphorylation on serine 518 in vestibular schwannoma. 2008, 118 (1): 169-174. Laryngoscope 2008 169-174
Yang T, Wei X, Chai Y, Li L, Wu H. （通讯作者） Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing. Orphanet J Rare Dis 8(1):85-90.