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

Optimized primer and model improve precision of X chromosome telomere length determination in the Han population

优化的引物和模型提高了汉族人群X染色体端粒长度测定的精确度

Zhang, Zhiqi; Sun, Xiangdong; Shi, Jianxiang; Xu, Hongen; Wang, Haoyu; Yang, Zhaohui; Guo, Jiancheng; Yang, Zengguang; Li, Chenxi; Zhu, Jicun; Zhang, Yuexiao; Zheng, Pengyuan; Xue, Xia; Mi, Yang

PAPPA2 c.392G>C Heterozygous Mutation Associates Primary Open-Angle Glaucoma in a Chinese Family.

PAPPA2 c.392G>C 杂合突变与中国家族中的原发性开角型青光眼相关。

Wang Gang, Guo Zilu, Ren Jing, Zhang Ge, Tao Hanlin, Liu Yihan, Zheng Siming, Zhang Xuan, Wang Di, Zhao Rumeng, Cui Huiling, Zhu Shichao, Xu Hongen, Duan Shichao, Li Haijun

CPMOAD: comprehensive preeclampsia multi-omics analysis database

CPMOAD:综合性先兆子痫多组学分析数据库

Fang, Yang; Fan, Mengzhe; Li, Hao; Xu, Hongen; Du, Hongmei; Guo, Yaqing; Gao, Jinshuang; Yuan, Erfeng; Song, Liying; Wang, Yu; Shi, Qianqian; Yu, HaiYang; Yuan, Enwu; Zhao, Xin; Zhang, Linlin

High-accuracy crRNA array assembly strategy for multiplex CRISPR.

用于多重 CRISPR 的高精度 crRNA 阵列组装策略

Zhao Xiangtong, Yang Lixian, Li Peng, Cheng Zijing, Jia Yongshi, Luo Limin, Bi Aihong, Xiong Hanchu, Zhang Haibo, Xu Hongen, Zhang Jinrui, Zhang Yaodong

Genetic diversity and dietary adaptations of the Central Plains Han Chinese population in East Asia

东亚中原汉族人群的遗传多样性和饮食适应性

Qiao, Xiaoyang; Shi, Jianxiang; Xu, Hongen; Liu, Kai; Pu, Youwei; Xue, Xia; Zheng, Wangshan; Guo, Yongbo; Ma, Hao; Wang, Chuan-Chao; Bitsue, Habtom K; Xu, Xiaoyu; Wang, Shanshan; Zhao, Jingru; Guo, Xiangqian; Hou, Xinyue; Wang, Xinwei; Peng, Lei; Qiu, Zan; Su, Bing; Tang, Wenxue; He, Yaoxi; Guo, Jiancheng; Yang, Zhaohui

Rapid cochlear gene therapy in adult deaf mice: Vglut3 rescue via AAV8 achieves day-1 hearing restoration.

成年聋小鼠快速耳蜗基因治疗:通过 AAV8 进行 Vglut3 拯救可在第一天实现听力恢复

Zhang Ting, Zhai Rongqun, Liu Mengli, Xu Hongen, Wang Liang, Tang Wenxue, Chen Bei, Zhao Xingle

SLC26A4 C.317C > A Variant: Functional Analysis and Patient-Derived Induced Pluripotent Stem Line Development.

SLC26A4 C.317C>A 变异:功能分析和患者来源的诱导多能干细胞系开发

Li Yijing, Sun Tao, Hu Sang, Xu Hongen, Zhang Teng, Liu Jinlong, Lu Shuangshuang, Wang Bing, Dan Guo

[Phenotypic and pathogenic variant analysis of an X-linked dominant inherited non-syndromic hearing loss pedigree]

[X连锁显性遗传非综合征性听力损失家系的表型和致病变异分析]

Zhai, Ziyu; Xu, Hongen; Wang, Le; Zhu, Xiaodan; Zhang, Yuan; Li, Ling; Zhang, Xiaosai; Li, Tingxian; Wang, Kaixi; Ye, Fanglei

Early prediction of growth patterns after pediatric kidney transplantation based on height-related single-nucleotide polymorphisms

基于身高相关单核苷酸多态性对儿童肾移植后生长模式进行早期预测

Feng, Yi; Feng, Yonghua; Hu, Mingyao; Xu, Hongen; Wang, Zhigang; Xu, Shicheng; Yan, Yongchuang; Feng, Chenghao; Li, Zhou; Feng, Guiwen; Shang, Wenjun

PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss

PKHD1L1基因参与纤毛外层结构形成,该基因突变会导致常染色体隐性遗传性非综合征型听力损失。

Redfield, Shelby E; De-la-Torre, Pedro; Zamani, Mina; Wang, Hanjun; Khan, Hina; Morris, Tyler; Shariati, Gholamreza; Karimi, Majid; Kenna, Margaret A; Seo, Go Hun; Xu, Hongen; Lu, Wei; Naz, Sadaf; Galehdari, Hamid; Indzhykulian, Artur A; Shearer, A Eliot; Vona, Barbara