Feng-Juan Gao (Ji-Hong Wu, Jihong Wu)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Venues

NPJ genomic medicine

BMC medical genetics

Orphanet journal of rare diseases

Acta ophthalmologica

This page only lists publications with an associated author ORCID identifier.

Publications

Xubing Liu, Fangyuan Hu, Daowei Zhang, Zhe Li, Jianquan He, Shenghai Zhang, Zhenguo Wang, Yingke Zhao, Jiawen Wu, Chen Liu, Chenchen Li, Xin Li, Feng-Juan Gao
Whole genome sequencing enables new genetic diagnosis for inherited retinal diseases by identifying pathogenic variants. NPJ genomic medicine 9 (1) (2024)
Xubing Liu, Fangyuan Hu, Daowei Zhang, Zhe Li, Jianquan He, Shenghai Zhang, Zhenguo Wang, Yingke Zhao, Jiawen Wu, Chen Liu, Chenchen Li, Xin Li, Feng-Juan Gao
Whole genome sequencing enables new genetic diagnosis for inherited retinal diseases by identifying pathogenic variants. NPJ genomic medicine 9 (1) (2024)
Xubing Liu, Fangyuan Hu, Daowei Zhang, Zhe Li, Jianquan He, Shenghai Zhang, Zhenguo Wang, Yingke Zhao, Jiawen Wu, Chen Liu, Chenchen Li, Xin Li, Feng-Juan Gao
Whole genome sequencing enables new genetic diagnosis for inherited retinal diseases by identifying pathogenic variants. NPJ genomic medicine 9 (1) (2024)
Feng-Juan Gao, Dan-Dan Wang, Fang-Yuan Hu, Ping Xu, Qing Chang, Jian-Kang Li, Wei Liu, Sheng-Hai Zhang, Ge-Zhi Xu, Feng-Juan Gao
Genotypic spectrum and phenotype correlations of EYS-associated disease in a Chinese cohort. Eye (London, England) (2021)
Feng-Juan Gao, Dan-Dan Wang, Jian-Kang Li, Fang-Yuan Hu, Ping Xu, Fang Chen, Yu-He Qi, Wei Liu, Wei Li, Sheng-Hai Zhang, Qing Chang, Ge-Zhi Xu, Feng-Juan Gao
Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population. Orphanet journal of rare diseases 16 (1) (2021)
Feng-Juan Gao, Jian-Hong Dong, Dan-Dan Wang, Fang Chen, Fang-Yuan Hu, Qing Chang, Ping Xu, Wei Liu, Jian-Kang Li, Ying Huang, Feng-Juan Gao, Ge-Zhi Xu
Comprehensive analysis of genetic and clinical characteristics of 30 patients with X-linked juvenile retinoschisis in China. Acta ophthalmologica 99 (4) (2020)
Dan-Dan Wang, Feng-Juan Gao, Fang-Yuan Hu, Sheng-Hai Zhang, Ping Xu, Feng-Juan Gao
Mutation Spectrum of Stickler Syndrome Type I and Genotype-phenotype Analysis in East Asian Population: a systematic review. BMC medical genetics 21 (1) (2020)
Fang-Yuan Hu, Feng-Juan Gao, Jian-Kang Li, Ping Xu, Dan-Dan Wang, Sheng-Hai Zhang, Feng-Juan Gao
Novel variants of ABCA4 in Han Chinese families with Stargardt disease. BMC medical genetics 21 (1) (2020)
Feng-Juan Gao, Guo-Hong Tian, Fang-Yuan Hu, Dan-Dan Wang, Jian-Kang Li, Qing Chang, Fang Chen, Ge-Zhi Xu, Wei Liu, Feng-Juan Gao
Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses. BMC ophthalmology 20 (1) (2020)
Dan-Dan Wang, Feng-Juan Gao, Fang-Yuan Hu, Jian-Kang Li, Sheng-Hai Zhang, Ping Xu, Qing Chang, Rui Jiang, Feng-Juan Gao
Next-generation sequencing-aided precise diagnosis of Stickler syndrome type I. Acta ophthalmologica 98 (4) (2019)
Feng-Juan Gao, Yu-He Qi, Fang-Yuan Hu, Dan-Dan Wang, Ping Xu, Jing-Li Guo, Jian-Kang Li, Yong-Jin Zhang, Wei Li, Fang Chen, Ge-Zhi Xu, Wei Liu, Qing Chang, Ji-Hong Wu
Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy. The British journal of ophthalmology 104 (6) (2019)
Feng-Juan Gao, Fang-Yuan Hu, Ping Xu, Yu-He Qi, Jian-Kang Li, Yong-Jin Zhang, Fang Chen, Qing Chang, Fang Song, Si-Mai Shen, Ge-Zhi Xu, Feng-Juan Gao
Expanding the clinical and genetic spectrum of Heimler syndrome. Orphanet journal of rare diseases 14 (1) (2019)

Feng-Juan Gao.css-eqlu8i{font-size:small;padding-left:4px;} (Ji-Hong Wu, Jihong Wu)

Publication Activity (10 Years)

Top Topics

Top Venues

Feng-Juan Gao (Ji-Hong Wu, Jihong Wu)