Yongyi Yuan

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.

A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4

Xue Gao, Yongyi Yuan, D. Kang, 2022, Molecular genetics & genomic medicine.

[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.

[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.

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.

Preimplantation genetic testing for hereditary hearing loss in Chinese population

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

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.

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.

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.

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.

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.

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.

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.

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.