Jiamin Ouyang

CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection

Jiamin Ouyang, Wenmin Sun, Xueshan Xiao et al. · Human Molecular Genetics · 2019 · 42 citations · Full text

Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3

Xueshan Xiao, Wenmin Sun, Jiamin Ouyang et al. · Human Genetics · 2019 · 31 citations · Full text

Clinical and genetic features of retinoschisis in 120 families with<i>RS1</i>mutations

Sainan Xiao, Wenmin Sun, Xueshan Xiao et al. · British Journal of Ophthalmology · 2021 · 31 citations

Metalloproteinase <i>Adamts16</i> Is Required for Proper Closure of the Optic Fissure

Mingzhe Cao, Jiamin Ouyang, Jingyi Guo et al. · Investigative Ophthalmology & Visual Science · 2018 · 27 citations · Full text

Biallelic mutations in <i>USP45,</i> encoding a deubiquitinating enzyme, are associated with Leber congenital amaurosis

Yi Zhen, Jiamin Ouyang, Wenmin Sun et al. · Journal of Medical Genetics · 2018 · 21 citations