Xueshan Xiao

Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2

Anren Li, Xiaodong Jiao, Francis L. Munier et al. · The American Journal of Human Genetics · 2004 · 280 citations · Full text

Mendelian Disorder, Ophthalmology, Corneal Dystrophy +6

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing

Yan Xu, Liping Guan, Tao Shen et al. · Human Genetics · 2014 · 181 citations

Mendelian Disorder, Known Causative Genes, Exome Sequencing +10

Mitochondrial DNA Haplogroups M7b1′2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G→A Mutation

Yanli Ji, A‐Mei Zhang, Xiaoyun Jia et al. · The American Journal of Human Genetics · 2008 · 131 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +8

Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population

Yi Shi, Jia Qu, Dingding Zhang et al. · The American Journal of Human Genetics · 2011 · 127 citations · Full text

Genetic Variants, Developmental Biology, High Myopia +9

Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis

Lin Li, Xueshan Xiao, Shiqiang Li et al. · PLoS ONE · 2011 · 125 citations · Full text