Xiao-hui Zhang

发表

Patient iPSC-derived retinal organoids: Observable retinal diseases in-a-dish.

Zi-Bing Jin, Xiao-hui Zhang, 2021, Histology and histopathology.

Variant Profiling of a Large Cohort of 138 Chinese Families With Autosomal Dominant Retinitis Pigmentosa

Ting Xiao, Zi-Bing Jin, Xiao-hui Zhang, 2021, Frontiers in Cell and Developmental Biology.

Two novel PRPF31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa

Y. Li, Yang Li, Xiao-hui Zhang, 2013, Molecular vision.

Screening of ABCA4 Gene in a Chinese Cohort With Stargardt Disease or Cone-Rod Dystrophy With a Report on 85 Novel Mutations.

Y. Li, Yang Li, Xiao-hui Zhang, 2016, Investigative ophthalmology & visual science.

UTILIZATION OF FUNDUS AUTOFLUORESCENCE, SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY, AND ENHANCED DEPTH IMAGING IN THE CHARACTERIZATION OF BIETTI CRYSTALLINE DYSTROPHY IN DIFFERENT STAGES

Zhangxing Xu, Xiao-hui Zhang, Xiaoyan Peng, 2015, Retina.

Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4-Related Retinopathy: Deep Intronic Variants and Copy Number Variations

Zi-Bing Jin, Xiao-hui Zhang, Yue Xie, 2022, Investigative ophthalmology & visual science.

Clinical Features and Natural History in a Cohort of Chinese Patients with RPE65-Associated Inherited Retinal Dystrophy

Jianlin Hu, Zi-Bing Jin, Xiao-hui Zhang, 2021, Journal of clinical medicine.

Mutation screening of mitochondrial DNA as well as OPA1 and OPA3 in a Chinese cohort with suspected hereditary optic atrophy.

Y. Li, Yang Li, Xiao-hui Zhang, 2014, Investigative ophthalmology & visual science.

Novel mutations of the RS1 gene in a cohort of Chinese families with X-linked retinoschisis

Y. Li, Yang Li, Xiao-hui Zhang, 2014, Molecular vision.

Comprehensive Molecular Screening in Chinese Usher Syndrome Patients.

Xiao-hui Zhang, Yue Xie, Yang Li, 2018, Investigative ophthalmology & visual science.

Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings

Xiao-hui Zhang, Yue Xie, Xin Zhang, 2022, Investigative ophthalmology & visual science.

Late-onset bilateral lens dislocation and glaucoma associated with a novel mutation in FBN1

Y. Li, Yang Li, Xiao-hui Zhang, 2008, Molecular vision.

Immobilized Fe3O4-Polydopamine-Thermomyces lanuginosus Lipase-Catalyzed Acylation of Flavonoid Glycosides and Their Analogs: An Improved Insight Into Enzymic Substrate Recognition

Qingqing Ji, Zhaoyu Wang, Yanhong Bi, 2021, Frontiers in Bioengineering and Biotechnology.

Genetic and clinical findings in a Chinese cohort with Leber congenital amaurosis and early onset severe retinal dystrophy

Xiao-hui Zhang, Yue Xie, Yang Li, 2019, British Journal of Ophthalmology.

Mutation spectrum of PAX6 and clinical findings in 95 Chinese patients with aniridia

Xiao-hui Zhang, Yue Xie, Yang Li, 2020, Molecular vision.

GPR143 genotypic and ocular phenotypic characterisation in a Chinese cohort with ocular albinism

Xiao-hui Zhang, Yue Xie, Yang Li, 2021, Ophthalmic genetics.

Mitochondrial Mutations in Ethambutol-Induced Optic Neuropathy

Zi-Bing Jin, Xiao-hui Zhang, Quangang Xu, 2021, Frontiers in Cell and Developmental Biology.

Large novel deletions detected in Chinese families with aniridia: correlation between genotype and phenotype

Liang Xu, Yang Li, Xiao-hui Zhang, 2011, Molecular vision.

Generation of an induced pluripotent stem cell line BIOi002-A from a patient with autosomal dominant optic atrophy.

Xiao-hui Zhang, Yue Xie, Yang Li, 2021, Stem cell research.

Clinical findings and RS1 genotype in 90 Chinese families with X-linked retinoschisis

Xiao-hui Zhang, Yue Xie, Yang Li, 2020, Molecular vision.

Screening of BEST1 Gene in a Chinese Cohort With Best Vitelliform Macular Dystrophy or Autosomal Recessive Bestrophinopathy.

Yang Li, Xiao-hui Zhang, Xiaoyan Peng, 2017, Investigative ophthalmology & visual science.

Identification of five novel mutations in the long isoform of the USH2A gene in Chinese families with Usher syndrome type II

Yang Li, Xiao-hui Zhang, B. Dong, 2008, Molecular vision.

Genotype Profile of Global EYS-Associated Inherited Retinal Dystrophy and Clinical Findings in a Large Chinese Cohort

Zi-Bing Jin, Xiao-hui Zhang, Yue Xie, 2021, Frontiers in Cell and Developmental Biology.

GUCY2D mutations in a Chinese cohort with autosomal dominant cone or cone–rod dystrophies

Yang Li, Xiao-hui Zhang, Yue Xie, 2015, Documenta Ophthalmologica.

A novel GUCY2D mutation in a Chinese family with dominant cone dystrophy

Yang Li, Xiao-hui Zhang, B. Dong, 2013, Molecular vision.

Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II

Yang Li, Xiao-hui Zhang, B. Dong, 2011, Molecular vision.

Comprehensive screening of CYP4V2 in a cohort of Chinese patients with Bietti crystalline dystrophy

Xiao-hui Zhang, Xiaoyan Peng, Yue Xie, 2018, Molecular vision.

Sector Retinitis Pigmentosa caused by mutations of the RHO gene

Ting Xiao, Yang Li, Xiao-hui Zhang, 2018, Eye.

Coralliform cataract caused by a novel connexin46 (GJA3) mutation in a Chinese family

Jun Wang, Yang Li, Xiao-hui Zhang, 2012, Molecular vision.

Identification a novel MYOC gene mutation in a Chinese family with juvenile-onset open angle glaucoma

Liang Xu, Yang Li, Xiao-hui Zhang, 2010, Molecular vision.

Identification of two mutations of the RHO gene in two Chinese families with retinitis pigmentosa: Correlation between genotype and phenotype

Yang Li, Xiao-hui Zhang, Zhe Pan, 2012, Molecular vision.

A novel splicing variant of VCAN identified in a Chinese family initially diagnosed with familial exudative vitreoretinopathy

Xiao-hui Zhang, Yue Xie, Jie-Feng Shi, 2022, Molecular genetics & genomic medicine.

Phenotypic diversity observed in a Chinese patient cohort with biallelic variants in Bardet-Biedl syndrome genes

Xiao-hui Zhang, Yue Xie, Yang Li, 2023, Eye.