Yongchuan Chai

Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing

Tao Yang, Xiaoming Wei, Yongchuan Chai et al. · Orphanet Journal of Rare Diseases · 2013 · 173 citations · Full text

Screening for delayed-onset hearing loss in preschool children who previously passed the newborn hearing screening

Jingrong Lü, Zhiwu Huang, Tao Yang et al. · International Journal of Pediatric Otorhinolaryngology · 2011 · 76 citations

Pediatric Audiology, Delayed-onset Hearing Loss, Early Diagnosis +16

The homozygous p.<scp>V37I</scp> variant of <i><scp>GJB2</scp></i> is associated with diverse hearing phenotypes

Yongchuan Chai, Di Chen, Lianhua Sun et al. · Clinical Genetics · 2014 · 53 citations

Genetics, Genetic Epidemiology, Human Polymorphism +29

The p.V37I Exclusive Genotype Of GJB2: A Genetic Risk-Indicator of Postnatal Permanent Childhood Hearing Impairment

Lei Li, Jingrong Lü, Tao Zheng et al. · PLoS ONE · 2012 · 53 citations · Full text

A Dominant Mutation in the Stereocilia-Expressing Gene<i>TBC1D24</i>is a Probable Cause for Nonsyndromic Hearing Impairment

Luping Zhang, Lingxiang Hu, Yongchuan Chai et al. · Human Mutation · 2014 · 49 citations

Genetics, Molecular Biology, Tbc1d24 Mutations +24