P. Dai

Xue Gao, Yue-shuai Song, Guo-jian Wang, 2016, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Gene4HL: An Integrated Genetic Database for Hearing Loss

X. Wang, Kuokuo Li, Guihu Zhao, 2021, Frontiers in Genetics.

Multiple synostoses syndrome: Clinical report and retrospective analysis

W. Lu, Yongyi Yuan, Shasha Huang, 2020, American journal of medical genetics. Part A.

Genotype-phenotype variability in Chinese cases of Treacher Collins syndrome

Yongyi Yuan, Shasha Huang, P. Dai, 2019, Acta oto-laryngologica.

Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.

Ping Liu, J Zhang, C. Morton, 2019, American journal of human genetics.

Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

L. Guan, Xue Gao, Guo-jian Wang, 2015, PloS one.

Variant analysis of 92 Chinese Han families with hearing loss

Xu Ma, Shasha Huang, P. Dai, 2022, BMC medical genomics.

The relationship between the GJB3 c.538C>T variant and hearing phenotype in the Chinese population.

Guo-jian Wang, Shasha Huang, D. Kang, 2017, International journal of pediatric otorhinolaryngology.

[Prevention of deafness based on genetic screening and testing].

Yongyi Yuan, P. Dai, 2013, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population

B. Han, L. Wong, E. Schmitt, 2007, Genetics in Medicine.

[Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].

P. Dai, Huijun Yuan, De-liang Huang, 2006, Zhonghua yi xue za zhi.

Clinical characteristics of petrosal cholesteatoma and value of MRI-DWI in the diagnosis

P. Dai, Shi-ming Yang, Dongyi Han, 2019, Acta oto-laryngologica.

Petrous bone cholesteatoma: our experience of 20 years and management of two giant cases affecting rhinopharynx

P. Dai, Shi-ming Yang, Dongyi Han, 2021, European Archives of Oto-Rhino-Laryngology.

Inner Ear Surgery

Shasha Huang, P. Dai, Y. Zou, 2017 .

Congenital Middle Ear Abnormalities With Absence of the Oval Window: Diagnosis, Surgery, and Audiometric Outcomes

Yue-shuai Song, P. Dai, W. Han, 2014, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families

Xue Gao, Shasha Huang, D. Kang, 2018, BMC Medical Genetics.

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

J. Chen, X. Liu, D. Yan, 2011, Journal of Human Genetics.

[Assessment of the curative effective of cochlear implantation in childer with GJB2-associated NSSNHL].

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2014, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

[Mutation of Gap junction protein beta 2 gene and treatment outcome of cochlear implantation in cochlear implantation recipients].

Guo-jian Wang, D. Kang, P. Dai, 2009, Zhonghua yi xue za zhi.

Hearing Loss in Mitochondrial Disorders

Lee-Jun C Wong, Cherng-Lih Perng, L. Wong, 2005, Annals of the New York Academy of Sciences.

Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss.

D. Kang, P. Dai, Huijun Yuan, 2010, Journal of genetics and genomics = Yi chuan xue bao.

Somatic instability of the DNA sequences encoding the polymorphic polyglutamine tract of the AIB1 gene

L. Wong, P. Dai, 2003, Journal of medical genetics.

The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals

Guo-jian Wang, Yongyi Yuan, Shasha Huang, 2015, PloS one.

Sequential Bilateral Cochlear Implantation in a Child with Severe External, Middle, and Inner Ear Malformations: Surgical Considerations and Practical Aspects

Qiuquan Wang, Xue Gao, Guo-jian Wang, 2021, ORL.

Effects of cochlear implant surgical technique on post-operative electrode impedance

X. Xi, Xue Gao, Guo-jian Wang, 2016, Acta oto-laryngologica.

Analysis of revision and reimplantation of cochlear implantations in 45 cases

Lihua Wu, Guo-jian Wang, Yongyi Yuan, 2019, Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery.

Transcriptome analysis of the early stage ifnlr1-mutant zebrafish indicates the immune response to auditory dysfunction.

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2021, Gene expression patterns : GEP.

A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations

Long-xia Wang, D. Cram, Shasha Huang, 2017, Genetics in Medicine.

Preimplantation genetic testing for hereditary hearing loss in Chinese population

S. Blanton, D. Yan, Yuanqing Yao, 2023, Journal of Assisted Reproduction and Genetics.

[Prenatal genetic test and clinical guidance for 213 hereditary deaf families].

Guo-jian Wang, Shasha Huang, D. Kang, 2012, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

[Prenatal diagnosis for hereditary deaf families assisted by genetic testing].

B. Han, Qiuju Wang, Guo-jian Wang, 2007, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation

Guo-jian Wang, Yongyi Yuan, Shasha Huang, 2014, BMC Genetics.

Modified Friedman stage in predicting glossopharyngeal obstruction in obstructive sleep apnea

J. Qin, P. Dai, Dongyi Han, 2017, Acta oto-laryngologica.

Molecular Epidemiology and Functional Assessment of Novel Allelic Variants of SLC26A4 in Non-Syndromic Hearing Loss Patients with Enlarged Vestibular Aqueduct in China

Weiwei Guo, Shiming Yang, Weiwei Guo, 2012, PloS one.

Role of AQP1 in inner ear in motion sickness

P. Dai, S. Xia, Dong‐yi Han, 2011, Physiology & Behavior.

Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.

Guo-jian Wang, Yongyi Yuan, Shasha Huang, 2018, International journal of pediatric otorhinolaryngology.

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.

Ronghua Li, Yaping Qian, D. Kang, 2006, Biochemical and biophysical research communications.

Phenotype and genotype of deaf patients with combined genomic and mitochondrial inheritance models.

Yue-shuai Song, Guo-jian Wang, Yongyi Yuan, 2013, Mitochondrion.

Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genes.

Yue-shuai Song, Guo-jian Wang, Yongyi Yuan, 2013, International Journal of Pediatric Otorhinolaryngology.

Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family

Xue Gao, Shasha Huang, D. Kang, 2020, BioMed Research International.

De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing loss.

Yongyi Yuan, Shasha Huang, D. Kang, 2011, International journal of pediatric otorhinolaryngology.

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability

Xue Gao, Yongyi Yuan, D. Kang, 2019, EBioMedicine.

Study on the relationship between the pathogenic mutations of SLC26A4 and CT phenotypes of inner ear in patient with sensorineural hearing loss

Lihua Wu, P. Dai, Yunliang Liu, 2019, Bioscience reports.

Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2013, Journal of Translational Medicine.

Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation

Xi Lin, Xue Gao, Yongyi Yuan, 2016, BMC Genetics.

Phenotypic Heterogeneity in a DFNA 20 / 26 family segregating a novel ACTG 1 mutation

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2022 .

[Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China].

B. Han, Guo-jian Wang, Yongyi Yuan, 2007, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

[Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].

B. Han, Yongyi Yuan, D. Kang, 2007, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.

P. Dai, Huijun Yuan, Dongyi Han, 2009, Mitochondrion.

Detecting novel mutations and combined Klinefelter syndrome in Usher syndrome cases

Yongyi Yuan, Shasha Huang, P. Dai, 2019, Acta oto-laryngologica.

A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2

Xue Gao, Yongyi Yuan, P. Dai, 2017, BMC Medical Genetics.

A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafness

Yongyi Yuan, P. Dai, A. Huang, 2015, Journal of Translational Medicine.

A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss

Wenxue Tang, Xue Gao, Yue-shuai Song, 2014, PloS one.

Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.

J. Chen, B. Han, Guo-jian Wang, 2008, Mitochondrion.

Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene

Xue Gao, P. Dai, Yi-ming Zhu, 2021, Frontiers in Cell and Developmental Biology.

Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.

D. Kang, P. Dai, M. Guan, 2007, Biochemical and biophysical research communications.

A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss

Yongyi Yuan, P. Dai, Jialing Zeng, 2015, Journal of otology.

[Prevention and interdiction on hereditary deafness].

P. Dai, 2007, Zhonghua yi xue za zhi.

Mutation spectra and founder effect of TMC1 in patients with non‐syndromic deafness in Xiamen area, China

Lihua Wu, Xue Gao, Shasha Huang, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Novel Compound Heterozygous TMC1 Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

L. Guan, Xue Gao, Qing-yan Zhu, 2013, PloS one.

Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

Hui Zhao, Xue Gao, Guo-jian Wang, 2014, PloS one.

Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy

A. Gropman, F. Scaglia, A. Feigenbaum, 2006, Genetics in Medicine.

Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing

L. Guan, Xue Gao, Qing-yan Zhu, 2013, Journal of Translational Medicine.

Two SOX11 variants cause Coffin–Siris syndrome with a new feature of sensorineural hearing loss

Yongyi Yuan, Shasha Huang, P. Dai, 2022, American journal of medical genetics. Part A.

[Study on 2,747 cases of inner ear malformation for its classification in patient with sensorineural hearing loss].

P. Dai, Chengyong Zhou, Baochun Sun, 2015, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

Retrospective study of Langerhans cell histiocytosis in ear, nose and neck.

Guo-jian Wang, Yongyi Yuan, P. Dai, 2019, American journal of otolaryngology.

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness‐associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss

Ronghua Li, Yaping Qian, P. Dai, 2006, American journal of medical genetics. Part A.

Intraoperative CT-guided cochlear implantation in congenital ear deformity

Yue-shuai Song, Guo-jian Wang, Yongyi Yuan, 2012, Acta oto-laryngologica.

Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people

D. Kang, P. Dai, Huijun Yuan, 2015, Acta oto-laryngologica.

Aberrant internal carotid artery causing objective pulsatile tinnitus and conductive hearing loss

Yue-shuai Song, Guo-jian Wang, Yongyi Yuan, 2012, Acta oto-laryngologica.

Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

Hui Zhao, Xue Gao, Guo-jian Wang, 2015, PloS one.

Whole‐Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal‐Recessive Nonsyndromic Hearing Loss DFNB99

Y. Gong, C. Shao, Baichun Jiang, 2015, Human mutation.

Cochlear implantation in a patient with congenital microtia, cochlear hypoplasia, venous anomalies of the temporal bone and laryngomalacia: Challenges and surgical considerations

Yanhui Lu, Xue Gao, P. Dai, 2023, Medicine.

Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome.

L. Bird, M. Muenke, L. Wong, 2001, American journal of medical genetics.

Rapid identification of aminoglycoside-induced deafness gene mutations using multiplex real-time polymerase chain reaction.

Guangxin Xiang, K. Mitchelson, Shasha Huang, 2015, International journal of pediatric otorhinolaryngology.

[Screening for mitochondrial 1555(G) mutation in patients with aminoglycoside antibiotic-induced deafness].

S. Jiang, W. Yang, P. Dai, 1999, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[PTPN11 and the deafness].

P. Dai, H. Xu, Y. Y. Yuan, 2019, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

[Case report and diagnosis of Noonan syndrome with multiple lentigines with deafness as its main clinical feature].

D. Kang, P. Dai, B. Huang, 2019, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.

Wei Li, X. Liu, K. Wrzeszczynski, 2011, American journal of human genetics.

Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2.

Xue Gao, Yongyi Yuan, Shasha Huang, 2020, Stem cell research.

The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.

Yaping Qian, Yongyi Yuan, P. Dai, 2007, Biochemical and biophysical research communications.

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.

Yaping Qian, Yongyi Yuan, P. Dai, 2006, Biochemical and biophysical research communications.

Characterization of SH3GLB1 in the auditory system and its potential role in mitophagy

Yijin Chen, Xue Gao, Guo-jian Wang, 2023, Genes & diseases.

Intraoperative CT-guided cochlear implantation in congenital ear deformity

Yue-shuai Song, Guo-jian Wang, Yongyi Yuan, 2012, Acta oto-laryngologica.