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Frontiers in Genetics|September 12, 2017
Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese FamilyYu-He Qi, Feng-Juan Gao, Fang-Yuan Hu, et al.
Orphanet Journal of Rare Diseases|December 14, 2019
Expanding the clinical and genetic spectrum of Heimler syndromeFeng-Juan Gao, Fang-Yuan Hu, Ping Xu, et al.
Molecular Vision|September 5, 2017
Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathyXiao-Yan Huang, Hong Zhuang, Ji-Hong Wu, et al.
Investigative Ophthalmology & Visual Science|March 17, 2020
Clinical and Genetic Characteristics of Chinese Patients with Occult Macular DystrophyDan-Dan Wang, Feng-Juan Gao, Jian-Kang Li, et al.
Orphanet Journal of Rare Diseases|May 6, 2021
Frequency and phenotypic characteristics of RPE65 mutations in the Chinese populationFeng-Juan Gao, Dan-Dan Wang, Jian-Kang Li, et al.
The British Journal of Ophthalmology|September 15, 2019
Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathyFeng-Juan Gao, Yu-He Qi, Fang-Yuan Hu, et al.
The British Journal of Ophthalmology|March 20, 2020
Prevalence and genetic-phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal diseaseFeng-Juan Gao, Dan-Dan Wang, Fang Chen, et al.
Frontiers in Genetics|September 24, 2019
ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel VariantsFang-Yuan Hu, Jian-Kang Li, Feng-Juan Gao, et al.
Ophthalmology|May 5, 2019
Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis PigmentosaFeng-Juan Gao, Jian-Kang Li, Han Chen, et al.
Chinese Medical Sciences Journal = Chung-Kuo I Hsueh K'O Hsueh Tsa Chih|June 1, 2023
Chinese Guideline on the Management of Polypoidal Choroidal Vasculopathy (2022)You-Xin Chen, Yu-Qing Zhang, Chang-Zheng Chen, et al.
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