Fuxin Zhao
Chinese Academy of Medical Sciences & Peking Union Medical College(CN)Wenzhou Medical University(CN)Chengdu University of Technology(CN)Qinghai University Affiliated Hospital(CN)Affiliated Eye Hospital of Wenzhou Medical College(CN)Jackson Laboratory(US)Shandong University of Science and Technology(CN)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, ATP Synthase and ATPases Research, Metabolism and Genetic Disorders, Ophthalmology and Visual Impairment Studies, Corneal surgery and disorders
Most-Cited Works
- → Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis(2020)165 cited
- → Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population(2011)127 cited
- → Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation(2009)116 cited
- → 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(2015)103 cited
- → Exome sequencing reveals CCDC111 mutation associated with high myopia(2013)89 cited
- → Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation(2009)78 cited