M. Han

发表

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.

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.

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.

Gene4HL: An Integrated Genetic Database for Hearing Loss

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

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.

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.

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.

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.

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.

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.

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.

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.

Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

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

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.

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

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

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.

Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2017, Neural plasticity.

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

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

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

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

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.

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

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

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness

Yanyan Zhang, Xun Xu, Hui Jiang, 2014, Genetics in Medicine.

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.