Chao Qu

发表

Association of genetic variants at MYP10 and MYP15 with high myopia in a Han Chinese population

Lingxi Jiang, Rui Zheng, Xiaoqi Liu, 2019, Ophthalmic genetics.

Near-infrared light protect the photoreceptor from light-induced damage in rats.

Ying Lin, W. Cao, Ying-chuan Fan, 2010, Advances in experimental medicine and biology.

Deep Sc-RNA sequencing decoding the molecular dynamic architecture of the human retina

Lulin Huang, Ling Zhong, Yi Shi, 2022, Science China Life Sciences.

Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese families

B. Gong, Zhenglin Yang, Yi Shi, 2019, Molecular genetics & genomic medicine.

Genetic association of COL1A1 polymorphisms with high myopia in Asian population: a Meta-analysis.

B. Gong, Yi Shi, Zimeng Ye, 2016, International journal of ophthalmology.

Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.

R. Kim, Xianjun Zhu, Lulin Huang, 2016, Genetic testing and molecular biomarkers.

Yanhui Deng, Ling Wan, Lulin Huang, 2021, Genes & diseases.

A Mussel-Inspired Facile Method to Prepare Multilayer-AgNP-Loaded Contact Lens for Early Treatment of Bacterial and Fungal Keratitis.

N. Huang, Xiaoqi Liu, Hui Zhao, 2018, ACS biomaterials science & engineering.

Transforming growth factor β induced mutation-associated phenotype in a Chinese family exhibiting lattice corneal dystrophy.

Xiaoqi Liu, B. Gong, Yi Shi, 2017, Biomedical reports.

Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population

Xiaoqi Liu, B. Gong, Zhenglin Yang, 2018, Ophthalmic genetics.

Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa.

B. Gong, Yi Shi, Fang Lu, 2019, Molecular medicine reports.

Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population

R. Kim, Xianjun Zhu, Lulin Huang, 2016, Scientific Reports.

Genetic association study between INSULIN pathway related genes and high myopia in a Han Chinese population

Xiaoqi Liu, B. Gong, Yi Shi, 2014, Molecular Biology Reports.

Novel Compound Heterozygous CBS Mutations Cause Homocystinuria in a Han Chinese Family

Xiaoqi Liu, B. Gong, Zhenglin Yang, 2015, Scientific Reports.

Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese Families

Peiquan Zhao, Lulin Huang, Zhenglin Yang, 2017, Scientific Reports.

Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis

Dean Y. Li, Xianjun Zhu, C. Mardin, 2019, Genetics in Medicine.

Whole exome sequencing identifies mutations of multiple genes in a Chinese cohort of 95 sporadic probands with presumptive retinitis pigmentosa

Lulin Huang, Zhenglin Yang, Jiyun Yang, 2018, Journal of Bio-X Research.

Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population

R. Kim, Xianjun Zhu, Lulin Huang, 2015, Journal of Human Genetics.

Association between SKIV2L polymorphism rs429608 and age-related macular degeneration: A meta-analysis

Xiaoqi Liu, B. Gong, Yi Shi, 2017, Ophthalmic genetics.

Untargeted metabolomics for uncovering plasma biological markers of wet age-related macular degeneration

Haixin Wang, Yanhui Deng, Lulin Huang, 2021, Aging.

Hard exudate detection based on deep model learned information and multi-feature joint representation for diabetic retinopathy screening

Hui Wang, Zhuoran Wang, Zhenming Peng, 2020, Comput. Methods Programs Biomed..

Local Structure Awareness-Based Retinal Microaneurysm Detection with Multi-Feature Combination

Zhenming Peng, Puying Tang, Chao Qu, 2022, Biomedicines.

Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese Families

Peiquan Zhao, Lulin Huang, Zhenglin Yang, 2017, Scientific Reports.

Identification of a novel homozygous nonsense mutation in the CDHR1 gene in a Chinese family with autosomal recessive retinitis pigmentosa.

B. Gong, Li Gan, Guo Huang, 2020, Clinica chimica acta; international journal of clinical chemistry.

Genetic association study between INSULIN pathway related genes and high myopia in a Han Chinese population

Xiaoqi Liu, B. Gong, Zhenglin Yang, 2014, Molecular Biology Reports.

Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma.

B. Gong, Zhenglin Yang, Yi Shi, 2015, Gene.

Mutation spectrum of CYP1B1 in Chinese patients with primary open-angle glaucoma

Y. Yang, Xiaoqi Liu, B. Gong, 2014, British Journal of Ophthalmology.

Transforming growth factor β induced mutation-associated phenotype in a Chinese family exhibiting lattice corneal dystrophy.

Xiaoqi Liu, B. Gong, Yi Shi, 2017, Biomedical reports.

Dynamic human retinal pigment epithelium (RPE) and choroid architecture based on single-cell transcriptomic landscape analysis

Lulin Huang, B. Gong, Zhenglin Yang, 2022, Genes & diseases.