Yi Jiang

Evolutionary origin of pathogenic GJB2 alleles in China

Yunchao Liu, Shasha Huang, P. Dai, 2022, Clinical genetics.

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

L. Guan, Xue Gao, Guo-jian Wang, 2018, Journal of Medical Genetics.

Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China

Xiufeng Xu, Lihua Wu, Shasha Huang, 2015, PloS one.

Sheathless acoustic based flow cell sorter for enrichment of rare cells

Xiaodong Wu, Ce Wang, Yuting Ma, 2021, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

Skewed X-chromosome inactivation and next-generation sequencing to identify a novel SMPX variants associated with X-linked hearing loss in a Chinese family.

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2018, International journal of pediatric otorhinolaryngology.

Analysis and Management of Complications in a Cohort of 1,065 Minimally Invasive Cochlear Implantations

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.

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.

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

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

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.

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.

Targeted linked-read sequencing for direct haplotype phasing of parental GJB2/SLC26A4 alleles: A universal and dependable noninvasive prenatal diagnosis method applied to autosomal recessive nonsyndromic hearing loss in at-risk families.

Xue Gao, Yongyi Yuan, Shasha Huang, 2024, The Journal of molecular diagnostics : JMD.