Ming-yu Han

发表

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.

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.

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.

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.

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.

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.

Mastoid and Middle Ear Surgery

Yue-shuai Song, Ming-yu Han, P. Dai, 2017 .

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.

Quantitative assessment of low-level parental mosaicism of SNVs and CNVs in Waardenburg syndrome

Guo-jian Wang, Yongyi Yuan, Shasha Huang, 2022, Human Genetics.

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

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

Gene4HL: An Integrated Genetic Database for Hearing Loss

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