Progress in the genetics of uveitis

por Huang, Xiu-Feng, Brown, Matthew A.
Publicado 2022

Novel CHM mutations identified in Chinese families with Choroideremia

por Cai, Xue-Bi, Huang, Xiu-Feng, Tong, Yi, Lu, Qin-Kang, Jin, Zi-Bing
Publicado 2016

Minimal effect of sleep on the risk of age-related macular degeneration: a Mendelian randomization study

por Zhu, Rong-Cheng, Li, Fen-Fen, Wu, Yi-Qing, Yi, Quan-Yong, Huang, Xiu-Feng
Publicado 2023

Whole Exome Sequencing Reveals Genetic Predisposition in a Large Family with Retinitis Pigmentosa

por Wu, Juan, Chen, Lijia, Tam, Oi Sin, Huang, Xiu-Feng, Pang, Chi-Pui, Jin, Zi-Bing
Publicado 2014

Correlation of serum amyloid A levels, clinical manifestations, treatment, and disease activity in patients with acute anterior uveitis

por Dai, Ma-Li, Fan, Shipei, Li, Zhuoran, Yu, Xuewen, Lin, Dan, Huang, Xiu-Feng, Wang, Yuqin
Publicado 2019

Management of heterotopic cesarean scar pregnancy with preservation of intrauterine pregnancy: A case report

por Chen, Zheng-Yun, Zhou, Yong, Qian, Yue, Luo, Jia-Min, Huang, Xiu-Feng, Zhang, Xin-Mei
Publicado 2021

CFI-rs7356506 polymorphisms associated with Vogt-Koyanagi-Harada syndrome

por Dai, Ma-Li, Huang, Xiu-Feng, Wang, Qing-Feng, Cai, Wei-Jun, Jin, Zi-Bing, Wang, Yuqin
Publicado 2016

Blood tests for prediction of deep endometriosis: A case-control study

por Chen, Zheng-Yun, Zhang, Li-Feng, Zhang, Yong-Qing, Zhou, Yong, Li, Xiao-Yong, Huang, Xiu-Feng
Publicado 2021

Causal Relationships Between Glycemic Traits and Myopia

por Li, Fen-Fen, Zhu, Meng-Chao, Shao, Yi-Lei, Lu, Fan, Yi, Quan-Yong, Huang, Xiu-Feng
Publicado 2023

Whole-Exome Sequencing Reveals a Rare Missense Variant in SLC16A9 in a Pedigree with Early-Onset Gout

por Huang, Xiu-Feng, Sun, Li, Zhang, Chunwu, Zhou, Zhenni, Chen, Hui, Zhang, Linhua, Brown, Matthew A., Xia, Xiaoru
Publicado 2020

Proteome-wide analysis reveals potential therapeutic targets for Colorectal cancer: a two-sample mendelian randomization study

por Cai, Yi-Xin, Wu, Yi-Qing, Liu, Jie, Pan, Huanle, Deng, Wenhai, Sun, Weijian, Xie, Congying, Huang, Xiu-Feng
Publicado 2023

‘RetinoGenetics’: a comprehensive mutation database for genes related to inherited retinal degeneration

por Ran, Xia, Cai, Wei-Jun, Huang, Xiu-Feng, Liu, Qi, Lu, Fan, Qu, Jia, Wu, Jinyu, Jin, Zi-Bing
Publicado 2014

‘RetinoGenetics’: a comprehensive mutation database for genes related to inherited retinal degeneration

por Ran, Xia, Cai, Wei-Jun, Huang, Xiu-Feng, Liu, Qi, Lu, Fan, Qu, Jia, Wu, Jinyu, Jin, Zi-Bing
Publicado 2014

Clinical and genetic analyses reveal novel pathogenic ABCA4 mutations in Stargardt disease families

por Lin, Bing, Cai, Xue-Bi, Zheng, Zhi-Li, Huang, Xiu-Feng, Liu, Xiao-Ling, Qu, Jia, Jin, Zi-Bing
Publicado 2016

Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsia

por Li, Fen-Fen, Huang, Xiu-Feng, Chen, Jie, Yu, Xu-Dong, Zheng, Mei-Qin, Lu, Fan, Jin, Zi-Bing, Gan, De-Kang
Publicado 2015

Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations

por Huang, Xiu-Feng, Huang, Zhi-Qin, Lin, Dan, Dai, Ma-Li, Wang, Qing-Feng, Chen, Zhen-Ji, Jin, Zi-Bing, Wang, Yuqin
Publicado 2017

Periodontal disease increases the host susceptibility to COVID-19 and its severity: a Mendelian randomization study

por Wang, Yi, Deng, Hui, Pan, Yihuai, Jin, Lijian, Hu, Rongdang, Lu, Yongyong, Deng, Wenhai, Sun, Weijian, Chen, Chengshui, Shen, Xian, Huang, Xiu-Feng
Publicado 2021

SLC7A14 linked to autosomal recessive retinitis pigmentosa

por Jin, Zi-Bing, Huang, Xiu-Feng, Lv, Ji-Neng, Xiang, Lue, Li, Dong-Qing, Chen, Jiangfei, Huang, Changjiang, Wu, Jinyu, Lu, Fan, Qu, Jia
Publicado 2014

Dysregulated Arginine Metabolism Is Linked to Retinal Degeneration in Cep250 Knockout Mice

por Xiang, Lue, Yang, Qiao-Li, Xie, Bin-Tao, Zeng, Hui-Yi, Ding, Liu-Jun, Rao, Feng-Qin, Yan, Tong, Lu, Fan, Chen, Qi, Huang, Xiu-Feng
Publicado 2023

Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

por 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
Publicado 2013