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

RNA-Seq of Cultured Peripheral Blood Lymphocytes Improves Identification of Cryptic Splicing Defects in Rare Disease Diagnostics

培养的外周血淋巴细胞的RNA测序提高了罕见病诊断中隐匿性剪接缺陷的识别率

Ren, Jinlin; Dai, Congling; Meng, Fei; Zhang, Pan; Xie, Chunbo; Xiao, Wenjuan; He, Wenbin; Yuan, Shimin; Li, Xiurong; Zhang, Qianjun; Tang, Weiling; Hu, Liang; Chen, Zixu; Lu, Guangxiu; Du, Juan; Zeng, Sicong; Lin, Ge

Novel INSL3 variants cause male infertility with cryptorchidism

新型INSL3变异导致男性隐睾症和不育

Wei, Chunjia; Lu, Wenqing; Li, Yong; Liang, Yaoqiong; Meng, Lanlan; Tan, Chen; Lin, Ge; Tan, Yue-Qiu; Zhang, Qianjun; Tu, Chaofeng; Du, Juan

A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics

非梗阻性无精子症的常见病因:MEI1双等位基因变异及其对不孕症诊断的意义

Tan, Chen; Wang, Tiantian; Tu, Chaofeng; Xie, Chunbo; Chen, Zixu; Yuan, Shimin; Hu, Tongyao; He, Wenbin; Li, Yong; Wang, Yurong; Luo, Chen; Zhang, Qianjun; Nie, Hongchuan; Zhang, Huan; Lu, Guangxiu; Lin, Ge; Tan, Yue-Qiu; Meng, Lanlan; Du, Juan

Integrating AI-generated content tools in higher education: a comparative analysis of interdisciplinary learning outcomes

将人工智能生成内容工具融入高等教育:跨学科学习成果的比较分析

Yan, Zhang; Qianjun, Tang

Genetic rare disease prevention and control: Family-based screening and reproductive interventions in Changsha

遗传罕见病防控:长沙市基于家庭的筛查和生殖干预

Lin, Ge; He, Jun; Wang, Yuankun; Liu, Xiangyan; Du, Juan; Zhang, Qianjun; Zhou, Shihao; Hu, Lanping; He, Jing; Li, Xiurong; Hu, Hao; Hu, Liang; Zhong, Changgao; He, Wen-Bin; Peng, Chan; Xu, Zhen; Zhang, Jingjing; Shu, Yan; Song, Xuan; Zhang, Wenqian; Lu, Guangxiu; Ou, Zhiming; Tan, Yue-Qiu; Liu, Jiyang

Hazard evaluation of goaf based on DBO algorithm coupled with BP neural network

基于DBO算法和BP神经网络的采空区危险性评价

Wang, Wentong; Zhang, Qianjun; Guo, Sha; Li, Zhixing; Li, Zhiguo; Liu, Chuanju

Extended application of PGT-M strategies for small pathogenic CNVs

PGT-M策略在小型致病性CNV中的扩展应用

Hu, Xiao; Wang, Weili; Luo, Keli; Dai, Jing; Zhang, Yi; Wan, Zhenxing; He, Wenbin; Zhang, Shuoping; Yang, Lanlin; Tan, Qin; Li, Wen; Zhang, Qianjun; Gong, Fei; Lu, Guangxiu; Tan, Yue-Qiu; Lin, Ge; Du, Juan

Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagella.

鉴定出与精子鞭毛多种形态异常相关的、导致弱精子畸形的新型纯合ARMC2突变

Zhao Siyi, Liu Qiong, Su Lilan, Meng Lanlan, Tan Chen, Wei Chunjia, Zhang Huan, Luo Tao, Zhang Qianjun, Tan Yue-Qiu, Tu Chaofeng, Chen Houyang, Gao Xingcheng

Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia.

新型 SPEF2 变异体导致男性不育,并可能引起原发性纤毛运动障碍

Lu Wenqing, Li Yong, Meng Lanlan, Tan Chen, Nie Hongchuan, Zhang Qianjun, Song Yuying, Zhang Huan, Tan Yue-Qiu, Tu Chaofeng, Guo Haichun, Wu Longxiang, Du Juan

The mediating effect of family resilience between coping styles and caregiver burden in maintenance hemodialysis patients: a cross-sectional study

家庭韧性在维持性血液透析患者的应对方式与照护者负担之间的中介作用:一项横断面研究

Zhang, Qianjun; Liu, Qiaoling; Zhang, Li; Jin, Yabin; Xiang, Xia; Huang, Xuefang; Mai, Jiezhen; Zhao, Tingfen; Cui, Wen