Area of research
Sensory Systems · Neurology
Research interest
Research interests include Biology, Hearing loss, Genetic enhancement, Gene, Usher syndrome, and Cell biology.
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis
Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model
Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function
Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome
Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation
Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G
Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss
The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route