Xue Gao

Ping Liu, Xue Gao, Yi Li, 2019, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome

Yong Feng, Xue Gao, Yongyi Yuan, 2021, BMC Medical Genomics.

Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss

Xue Gao, Yongyi Yuan, Shasha Huang, 2020, Neural plasticity.

Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2022, BMC Medical Genomics.

Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss

Xue Gao, Yongyi Yuan, Shasha Huang, 2022, Frontiers in Genetics.

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.

Molecular diagnose of a large hearing loss population from China by targeted genome sequencing

Yang Wang, Quanfei Huang, Zongfu Cao, 2022, Journal of Human Genetics.

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2018, BioMed research international.

Analysis of genotype–phenotype relationships in 90 Chinese probands with Waardenburg syndrome

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2021, Human Genetics.

Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes

Xue Gao, Yongyi Yuan, P. Dai, 2021, Human Genetics.

Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls

Jianguo Zhang, Hankui Liu, Xue Gao, 2019, European Journal of Human Genetics.

Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six‐generation Chinese family with autosomal dominant hearing loss

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2015, American journal of medical genetics. Part A.

Impact of next-generation sequencing on molecular diagnosis of inherited non-syndromic hearing loss

Xue Gao, P. Dai, 2015 .

Impact of next-generation sequencing on molecular diagnosis of inherited non-syndromic hearing loss

Xue Gao, Pu Dai, Xue Gao, 2014 .

De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome

Weiwei Guo, Ping Chen, Hui Jiang, 2014, Cell Research.

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.

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.

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

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

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.

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.

A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation

Xue Gao, Y. Diao, Meirong Liu, 2018, Medicine.

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.

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 .

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 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.

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.

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.

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.

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.

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.

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.

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

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