Feifan Zhao

A Novel DFNA36 Mutation in TMC1 Orthologous to the Beethoven (Bth) Mouse Associated with Autosomal Dominant Hearing Loss in a Chinese Family

Yali Zhao, Dayong Wang, Liang Zong et al. · PLoS ONE · 2014 · 71 citations · Full text

Family Members, Genetics, Molecular Genetics +21

Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss

Yali Zhao, Feifan Zhao, Liang Zong et al. · PLoS ONE · 2013 · 65 citations · Full text

Exome Sequencing, Genetics, Pathology +21

Targeted High-Throughput Sequencing Identifies Pathogenic Mutations in KCNQ4 in Two Large Chinese Families with Autosomal Dominant Hearing Loss

Yali Zhao, Yuting Yi, Yun Gao et al. · PLoS ONE · 2014 · 32 citations · Full text

Engineering, Mendelian Disorder, Large Chinese Families +14

Review for metamaterials and metasurfaces based on vanadium dioxide phase change materials

Yao Wu, Weiwei Tao, Feifan Zhao et al. · Optics & Laser Technology · 2024 · 19 citations

Identification of a novel mutation of PJVK in the Chinese non-syndromic hearing loss population with low prevalence of the PJVK mutations

Qiu-Jing Zhang, Lan Lan, Na Li et al. · Acta Oto-Laryngologica · 2015 · 12 citations