Zhanguo Jin

Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

Xue Zhong Liu, Dongyi Han, Jianzhong Li et al. · The American Journal of Human Genetics · 2009 · 123 citations · Full text

Developmental Biology, Genetic Disorder, Prps1 Gene Cause +5

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

Yi Sun, Jing Chen, Han-Jun Sun et al. · Journal of Human Genetics · 2010 · 36 citations · Full text

Genetic Disorder, Genetics, Audiology +9

Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss

Yi Sun, Jing Cheng, Yanping Lu et al. · Journal of genetics and genomics/Journal of Genetics and Genomics · 2011 · 31 citations

Genetics, Audiology, Auditory Research +5

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

Yu Lu, Xueya Zhou, Zhanguo Jin et al. · Journal of Human Genetics · 2014 · 19 citations · Full text

Genetic Testing, Genetics, Molecular Genetics +18

Preimplantation Genetic Diagnosis for a Chinese Family with Autosomal Recessive Meckel-Gruber Syndrome Type 3 (MKS3)

Yanping Lu, Hongmei Peng, Zhanguo Jin et al. · PLoS ONE · 2013 · 17 citations · Full text

Genetic Testing, Genetics, Pathology +19