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Yang, Jian, Jin, Zi-Bing, Chen, Jie, Huang, Xiu-Feng, Li, Xiao-Man, Liang, Yuan-Bo, Mao, Jian-Yang, Chen, Xin, Zheng, Zhili, Bakshi, Andrew, Zheng, Dong-Dong, Zheng, Mei-Qin, Wray, Naomi R., Visscher, Peter M., Lu, Fan, Qu, Jia
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Published in Proceedings of the National Academy of Sciences - PNAS (18.04.2017)
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Clinical Analysis of Sphenoid Sinus Mucocele With Initial Neurological Symptoms
Chen, Keyang, Cao, Yungang, Wu, Jianbin, Xiang, Haijie, Huang, Xiu‐Feng, Chen, Bobei
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Published in Headache (01.09.2019)
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Periodontal disease increases the host susceptibility to COVID-19 and its severity: a Mendelian randomization study
Wang, Yi, Deng, Hui, Pan, Yihuai, Jin, Lijian, Hu, Rongdang, Lu, Yongyong, Deng, Wenhai, Sun, Weijian, Chen, Chengshui, Shen, Xian, Huang, Xiu-Feng
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Published in Journal of translational medicine (24.12.2021)
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Proteome-wide analysis reveals potential therapeutic targets for Colorectal cancer: a two-sample mendelian randomization study
Cai, Yi-Xin, Wu, Yi-Qing, Liu, Jie, Pan, Huanle, Deng, Wenhai, Sun, Weijian, Xie, Congying, Huang, Xiu-Feng
Published in BMC cancer (04.12.2023)
Published in BMC cancer (04.12.2023)
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Functional characterization of CEP250 variant identified in nonsyndromic retinitis pigmentosa
Huang, Xiu‐Feng, Xiang, Lue, Fang, Xiao‐Long, Liu, Wei‐Qin, Zhuang, You‐Yuan, Chen, Zhen‐Ji, Shen, Ren‐Juan, Cheng, Wan, Han, Ru‐Yi, Zheng, Si‐Si, Chen, Xue‐Jiao, Liu, Xiaoling, Jin, Zi‐Bing
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Published in Human mutation (01.08.2019)
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Advances in the study of Müller glia reprogramming in mammals
Guo, Yi-Ming, Jiang, Xinyi, Min, Jie, Huang, Juan, Huang, Xiu-Feng, Ye, Lu
Published in Frontiers in cellular neuroscience (14.12.2023)
Published in Frontiers in cellular neuroscience (14.12.2023)
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Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing
Huang, Xiu-Feng, Wu, Juan, Lv, Ji-Neng, Zhang, Xiao, Jin, Zi-Bing
Published in Genetics in medicine (01.04.2015)
Published in Genetics in medicine (01.04.2015)
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Single-cell RNA sequencing reveals new subtypes of lens superficial tissue in humans
Zhu, Meng-Chao, Hu, Wei, Lin, Lei, Yang, Qing-Wen, Zhang, Lu, Xu, Jia-Lin, Xu, Yi-Tong, Liu, Jia-Sheng, Zhang, Meng-Di, Tong, Xiao-Yu, Zhu, Kai-Yi, Feng, Ke, Feng, Yi, Su, Jian-Zhong, Huang, Xiu-Feng, Li, Jin
Published in Cell proliferation (01.11.2023)
Published in Cell proliferation (01.11.2023)
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Estrogen is an important mediator of mast cell activation in ovarian endometriomas
Zhu, Tian-Hong, Ding, Shao-Jie, Li, Tian-Tian, Zhu, Li-Bo, Huang, Xiu-Feng, Zhang, Xin-Mei
Published in Reproduction (Cambridge, England) (01.01.2018)
Published in Reproduction (Cambridge, England) (01.01.2018)
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Clinical and Genetic Spectrum of Nine Cases of NLRP3-Associated Autoinflammatory Disease (NLRP3-AID) and Identification of One Novel NLRP3 Mutation by Genetic Variation Analyses
Shangguan, Yaoyao, Ding, Xingru, Ma, Le, Cai, Yi-Xin, Xiang, Shulei, Huang, Xiu-Feng, Shen, Yunyan, Yu, Hai-Guo, Zheng, Wenjie
Published in Journal of Immunology Research (06.03.2024)
Published in Journal of Immunology Research (06.03.2024)
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Mutation spectrum and genotype‐phenotype correlation of inherited retinal dystrophy in Taiwan
Chen, Zhen‐Ji, Lin, Keng‐Hung, Lee, Shi‐Huang, Shen, Ren‐Juan, Feng, Zhuo‐Kun, Wang, Xiao‐Fang, Huang, Xiu‐Feng, Huang, Zhi‐Qin, Jin, Zi‐Bing
Published in Clinical & experimental ophthalmology (01.05.2020)
Published in Clinical & experimental ophthalmology (01.05.2020)
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SLC7A14 linked to autosomal recessive retinitis pigmentosa
Jin, Zi-Bing, Huang, Xiu-Feng, Lv, Ji-Neng, Xiang, Lue, Li, Dong-Qing, Chen, Jiangfei, Huang, Changjiang, Wu, Jinyu, Lu, Fan, Qu, Jia
Published in Nature communications (27.03.2014)
Published in Nature communications (27.03.2014)
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Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families
Huang, Xiu-Feng, Xiang, Ping, Chen, Jie, Xing, Dong-Jun, Huang, Na, Min, Qingjie, Gu, Feng, Tong, Yi, Pang, Chi-Pui, Qu, Jia, Jin, Zi-Bing
Published in PloS one (30.05.2013)
Published in PloS one (30.05.2013)
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Whole‐exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod‐cone dystrophy, cataract, and posterior staphyloma) syndrome
Cai, Xue‐Bi, Wu, Kun‐Chao, Zhang, Xiao, Lv, Ji‐Neng, Jin, Guang‐Hui, Xiang, Lue, Chen, Jie, Huang, Xiu‐Feng, Pan, Deng, Lu, Bin, Lu, Fan, Qu, Jia, Jin, Zi‐Bing
Published in Clinical genetics (01.07.2019)
Published in Clinical genetics (01.07.2019)
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REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival
Veleri, Shobi, Nellissery, Jacob, Mishra, Bibhudatta, Manjunath, Souparnika H, Brooks, Matthew J, Dong, Lijin, Nagashima, Kunio, Qian, Haohua, Gao, Chun, Sergeev, Yuri V, Huang, Xiu-Feng, Qu, Jia, Lu, Fan, Cideciyan, Artur V, Li, Tiansen, Jin, Zi-Bing, Fariss, Robert N, Ratnapriya, Rinki, Jacobson, Samuel G, Swaroop, Anand
Published in Human molecular genetics (15.06.2017)
Published in Human molecular genetics (15.06.2017)
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