Weining Rong

PRPF4 mutations cause autosomal dominant retinitis pigmentosa

Xue Chen, Yuan Liu, Xunlun Sheng et al. · Human Molecular Genetics · 2014 · 126 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Targeted Sequencing of 179 Genes Associated with Hereditary Retinal Dystrophies and 10 Candidate Genes Identifies Novel and Known Mutations in Patients with Various Retinal Diseases

Xuejuan Chen, Kanxing Zhao, Xunlun Sheng et al. · Investigative Ophthalmology & Visual Science · 2013 · 82 citations

Life Sciences, Genetics, Molecular Genetics +16

CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability

Yuriko Minegishi, Xunlun Sheng, Kazutoshi Yoshitake et al. · Scientific Reports · 2016 · 46 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Association of insulin-like growth factor-1 polymorphisms with high myopia in the Chinese population.

Wenjuan Zhuang, Peizeng Yang, Zili Li et al. · PubMed · 2012 · 37 citations · Full text

Medicine, Endocrinology, Genetics +17

Novel and Recurrent MYO7A Mutations in Usher Syndrome Type 1 and Type 2

Weining Rong, Xue Chen, Kanxing Zhao et al. · PLoS ONE · 2014 · 36 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15