Zhijian Yang

Compound heterozygous <i>GJB2</i> mutations associated to a consanguineous Han family with autosomal recessive non-syndromic hearing loss

Hongbo Xu, Xiong Deng, Lamei Yuan et al. · Acta Oto-Laryngologica · 2016 · 57 citations

Life Sciences, Genetics, Molecular Genetics +17

Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease

Lamei Yuan, Xiong Deng, Zhi Song et al. · Neurobiology of Aging · 2015 · 46 citations

Life Sciences, Genetics, Molecular Genetics +13

Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Hong Xia, Xiangjun Huang, Yi Guo et al. · PLoS ONE · 2015 · 33 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Identification of a Novel Mutation in the Titin Gene in a Chinese Family with Limb-Girdle Muscular Dystrophy 2J

Wen Zheng, Han Chen, Xiong Deng et al. · Molecular Neurobiology · 2015 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Identification of a novel <i>PHEX</i> mutation in a Chinese family with X-linked hypophosphatemic rickets using exome sequencing

Lamei Yuan, Song Wu, Hongbo Xu et al. · Biological Chemistry · 2014 · 30 citations

Medicine, Genetics, Molecular Genetics +17