Fuxin Zhao

Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis

Fei Zhao, Dake Zhang, Qingyi Zhou et al. · EBioMedicine · 2020 · 162 citations · Full text

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

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

Jianxin Lü, Yaping Qian, Zhiyuan Li et al. · Mitochondrion · 2009 · 116 citations

Biology, Mendelian Disorder, Rrna 1555A +9

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation

Pingping Jiang, Xiaofen Jin, Yanyan Peng et al. · Human Molecular Genetics · 2015 · 103 citations · Full text

Exome sequencing reveals CCDC111 mutation associated with high myopia

Fuxin Zhao, Jinyu Wu, Anquan Xue et al. · Human Genetics · 2013 · 88 citations

High Myopia, Genetic Disorder, Medicine +4