Zixi Sun

Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies

Mingchu Xu, Ya‐Jing Xie, Hana Abouzeid et al. · The American Journal of Human Genetics · 2017 · 77 citations · Full text

Ocular Disease, Developmental Biology, Retina +8

<i>CEP78</i> is mutated in a distinct type of Usher syndrome

Qing Fu, Mingchu Xu, Chen Xue et al. · Journal of Medical Genetics · 2016 · 50 citations · Full text

Mutations in<i>POMGNT1</i>cause non-syndromic retinitis pigmentosa

Mingchu Xu, Takeyuki Yamada, Zixi Sun et al. · Human Molecular Genetics · 2016 · 47 citations · Full text

Prevalence and risk factors for pterygium: a cross-sectional study in Han and Manchu ethnic populations in Hebei, China

Zhouxian Pan, Jiantao Cui, Guangliang Shan et al. · BMJ Open · 2019 · 41 citations · Full text

Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities.

Zixi Sun, Qi Zhou, Huajin Li et al. · PubMed · 2017 · 29 citations · Full text