K. Yao

Wei Huang, Shu Zheng, Su-zhan Zhang, 2004, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Evaluation of dry eye after femtosecond laser–assisted cataract surgery

Yibo Yu, K. Yao, Menghan Wu, 2015, Journal of cataract and refractive surgery.

A novel phenotype-genotype correlation with an Arg555Trp mutation of TGFBI gene in Thiel-Behnke corneal dystrophy in a Chinese pedigree

Buyi Zhang, K. Yao, Jinyu Li, 2015, BMC Ophthalmology.

Comparison Study of Anterior Capsule Contraction of Hydrophilic and Hydrophobic Intraocular Lenses Under the Same Size Capsulotomy

Chenqi Luo, K. Yao, Wei Wang, 2022, Translational vision science & technology.

A new heterozygous mutation in the stop codon of CRYAB (p.X176Y) is liable for congenital posterior pole cataract in a Chinese family.

K. Yao, Jinyu Li, Yinhui Yu, 2020, Ophthalmic genetics.

A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family

K. Yao, Jinyu Li, C. Jin, 2010, Molecular vision.

Apoptosis of lens epithelial cells induced by high concentration of glucose is associated with a decrease in caveolin-1 levels

K. Yao, C. Jin, Zhiyong Zhang, 2009, Molecular vision.

A novel splice acceptor site mutation of protein S gene in affected individuals with type I protein S deficiency: allelic exclusion of the mutant gene.

N. Hamasaki, T. Okamura, H. Tsuda, 2001, Thrombosis research.

Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3′ untranslated region

K. Yao, C. Jin, Wei Wang, 2010, Molecular vision.

A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family

Yibo Yu, K. Yao, Jinyu Li, 2014, BMC Medical Genetics.

Ocular manifestations in COVID-19 patients: A systematic review and meta-analysis

Yueyang Zhong, D. Lyu, K. Yao, 2021, Travel Medicine and Infectious Disease.

Targeted Exome Sequencing of Congenital Cataracts Related Genes: Broadening the Mutation Spectrum and Genotype–Phenotype Correlations in 27 Chinese Han Families

Guizhen Sun, X. Gong, K. Yao, 2017, Scientific Reports.

Socio-economic disparity in visual impairment from cataract.

Lixia Lou, Xinyi Chen, K. Yao, 2021, International journal of ophthalmology.

Congenital polymorphic cataract associated with a G to A splice site mutation in the human beta-crystallin gene CRYβA3/A1

Yibo Yu, K. Yao, Jinyu Li, 2012, Molecular vision.

Lanosterol and 25-hydroxycholesterol dissociate crystallin aggregates isolated from cataractous human lens via different mechanisms.

Xiang-jun Chen, Yong-Bin Yan, Li-Dan Hu, 2018, Biochemical and biophysical research communications.

Single Nucleotide Polymorphisms of the Sirtuin 1 (SIRT1) Gene are Associated With age-Related Macular Degeneration in Chinese Han Individuals

Wei Zhang, K. Yao, Yi Zhai, 2015, Medicine.

Yong-Bin Yan, K. Yao, Kai Zhang, 2019, Biochemistry.

A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract

X. Gong, K. Yao, Wei Wang, 2014, PloS one.

Identification and preliminary functional analysis of two novel congenital cataract associated mutations of Cx46 and Cx50

Tingting Xie, K. Yao, Menghan Wu, 2019, Ophthalmic genetics.

Correction: A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract

X. Gong, K. Yao, Wei Wang, 2015, PloS one.

A novel GJA3 mutation associated with congenital nuclear pulverulent and posterior polar cataract in a chinese family

K. Yao, C. Jin, Wei Wang, 2011, Human mutation.

Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family

K. Xia, Renyi Wu, Xiajing Tang, 2009, Molecular vision.

Heterozygous variants c.781G>A and c.1066dup of serine protease 56 cause familial nanophthalmos by impairing serine-type endopeptidase activity

H. Yin, K. Yao, Xiangjun Chen, 2022, The British journal of ophthalmology.

Cataract-causing variant Q70P damages structural stability of βB1-crystallin and increases its tendency to form insoluble aggregates.

Ying Zhang, Yibo Yu, K. Yao, 2023, International journal of biological macromolecules.

The Congenital Cataract-Linked A2V Mutation Impairs Tetramer Formation and Promotes Aggregation of βB2-Crystallin

Jia Xu, Yi-Bo Xi, K. Yao, 2012, PloS one.

Embryonic Surface Ectoderm-specific Mitofusin 2 Conditional Knockout Induces Congenital Cataracts in Mice

Jiangyue Zhao, Yibo Yu, Danhong Wu, 2018, Scientific Reports.

Cataract-Causing S93R Mutant Destabilized Structural Conformation of βB1 Crystallin Linking With Aggregates Formation and Cellular Viability

Wanyue Xu, Li-Dan Hu, Yibo Yu, 2022, Frontiers in Molecular Biosciences.

Multiple cytokine analyses of aqueous humor from the patients with retinitis pigmentosa.

H. Yin, Xinyi Chen, Chenqi Luo, 2019, Cytokine.

Cataract-causing G91del mutant destabilised βA3 heteromers formation linking with structural stability and cellular viability

Wanyue Xu, K. Yao, Xiangjun Chen, 2021, British Journal of Ophthalmology.

The importance of the last strand at the C-terminus in βB2-crystallin stability and assembly.

K. Yao, Xiao-Yao Leng, Sha Wang, 2014, Biochimica et biophysica acta.

Autosomal dominant coralliform cataract related to a missense mutation of the gammaD-crystallin gene.

Wei Huang, Shu Zheng, Su-zhan Zhang, 2004, Chinese Medical Journal.

Heteromeric formation with βA3 protects the low thermal stability of βB1-L116P

Chenqi Luo, K. Yao, Xiangjun Chen, 2022, The British journal of ophthalmology.

The 18th amino acid glycine plays an essential role in maintaining the structural stabilities of γS-crystallin linking with congenital cataract.

Chenqi Luo, K. Yao, Xiangjun Chen, 2023, International journal of biological macromolecules.

A Novel Human Congenital Cataract Mutation in EPHA2 Kinase Domain (p.G668D) Alters Receptor Stability and Function.

K. Yao, Jinyu Li, Yi Zhai, 2019, Investigative ophthalmology & visual science.

Comparative outcomes of femtosecond laser‐assisted cataract surgery and manual phacoemusification: a six‐month follow‐up

Xinyi Chen, K. Yao, Menghan Wu, 2016, Clinical & experimental ophthalmology.

Cataract-linked mutation R188H promotes βB2-crystallin aggregation and fibrillization during acid denaturation.

Yi-Bo Xi, S. Ji, K. Yao, 2014, Biochemical and biophysical research communications.