日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Investigating the Shared Genetic Architecture of 3 Age-Related Ocular Disorders

探究三种年龄相关眼病的共同遗传结构

Bai, Zhan-Pei; Pan, Yi-Suo; Cai, Yi-Xin; Chen, Chong; Tao, Di; Zhao, Xin-Yi; Shen, Yi-Fan; Chen, Feng; Li, Jun-Hua; Qu, Jia; Huang, Xiu-Feng

Genetic and immunologic determinants of BCG disease: from mechanism to prevention

卡介苗病的遗传和免疫学决定因素:从机制到预防

Chen, Feng; Shen, Yifan; Yan, Qianhui; Zheng, Daishan; Chen, Xiaoli; Fang, Longyu; Sun, Mengchen; Zhang, Yuansi; Chu, Maoping; Yang, Enhui; Huang, Xiu-Feng

An integrated multi-omics analysis identifies protein biomarkers and potential drug targets for psoriatic arthritis.

综合多组学分析鉴定出银屑病关节炎的蛋白质生物标志物和潜在药物靶点

Cai Yi-Xin, Zheng Dai-Shan, Chen Xiao-Li, Bai Zhan-Pei, Zhang Jinyi, Deng Wenhai, Huang Xiu-Feng

A machine learning-based model to predict intravenous immunoglobulin resistance in Kawasaki disease

基于机器学习的川崎病静脉注射免疫球蛋白抵抗预测模型

Xia, Yuhan; Huang, Yuezhong; Gong, Min; Liu, Weirong; Meng, Yuanhui; Wu, Huiyang; Zhang, Hui; Zhang, Hao; Weng, Luyi; Chen, Xiao-Li; Qiu, Huixian; Rong, Xing; Wu, Rongzhou; Chu, Maoping; Huang, Xiu-Feng

Clinical features and genetic analysis of nine Chinese children with Dent disease and identification of three novel CLCN5 and OCRL variants

对9名中国Dent病患儿的临床特征和基因分析,并鉴定出3个新的CLCN5和OCRL变异体

Jiang, Xinyi; Lin, Hongzhou; Zhu, Qifan; Chen, Huihui; Huang, Yutong; Huang, Xiu-Feng; Wang, Dexuan

Expanding the COL4A4 variant spectrum: genotype-phenotype correlation in 19 Chinese children using updated Alport kidney disease classification

扩展 COL4A4 变异谱:采用更新的 Alport 肾病分类对 19 名中国儿童进行基因型-表型相关性分析

Huang, Yutong; Lin, Hongzhou; Chen, Huihui; Zhu, Qifan; Jiang, Xinyi; Huang, Xiu-Feng; Wang, Dexuan

Identification of a novel single nucleotide deletion in the NHS causing Nance-Horan syndrome.

鉴定出 NHS 中导致 Nance-Horan 综合征的新型单核苷酸缺失

Huang Teng, Liu Ya-Nan, Ding Dan-Tong, Wang Qiao, Xie Qiu-Ling, Miao Xue-Chuan, Qin Chuan, Huang Xiu-Feng, Li Jin

Identification of mutations associated with congenital cataracts in nineteen Chinese families.

对19个中国家庭中与先天性白内障相关的突变进行鉴定

Sun Hai-Sen, Huang Teng, Liu Zhe-Xuan, Xu Yi-Tong, Wang Ya-Qi, Wang Ming-Cheng, Zhang Shen-Rong, Xu Jia-Lin, Zhu Kai-Yi, Huang Wen-Kai, Huang Xiu-Feng, Li Jin

Editorial: Spondyloarthritis and omics

社论:脊柱关节炎与组学

Huang, Xiu-Feng; Li, Zhixiu

Proteomic analysis reveals potential therapeutic targets for childhood asthma through Mendelian randomization

通过孟德尔随机化进行蛋白质组学分析揭示儿童哮喘的潜在治疗靶点

Wu, Yi-Qing; Cai, Yi-Xin; Chen, Xiao-Li; Chen, Shang-Qin; Huang, Xiu-Feng; Lin, Zhen-Lang