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

Mutations in CFAP57 disrupt the localization of MYH10 and IFT88, leading to flagellogenesis failure in humans and mice.

CFAP57 的突变会破坏 MYH10 和 IFT88 的定位，导致人类和小鼠的鞭毛发生失败。

期刊:Human Genomics
影响因子:4.3
doi:10.1186/s40246-025-00859-x
Chen Yongjie, Li Lin, Meng Ranran, Li Shanze, Li Yuhua, Jiang Zhaodi, Xu Dan, Lu Zhao, Yin Chenghong, Sha Yanwei, Wang Fengchao
MYH
FAP
MYH10
发表日期：2025
文献求助 收藏

Corrigendum to "Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis" [EBioMedicine 96(2023) 104798]

对“AK9 缺乏通过破坏精子核苷酸稳态导致弱精子症和男性不育”的更正 [EBioMedicine 96(2023) 104798]

期刊:EBioMedicine
影响因子:10.8
doi:10.1016/j.ebiom.2023.104957
Sha, Yanwei; Liu, Wensheng; Li, Shu; Osadchuk, Ludmila V; Chen, Yongjie; Nie, Hua; Gao, Shuai; Xie, Linna; Qin, Weibing; Zhou, Huiliang; Li, Lin
发表日期：2024
文献求助 收藏

Novel bi-allelic DNAH3 variants cause oligoasthenoteratozoospermia

新型双等位基因DNAH3变异导致少弱畸精子症

期刊:Frontiers in Endocrinology
影响因子:4.6
doi:10.3389/fendo.2024.1462509
Li, Shu; Zhang, Zexin; Xie, Linna; Zhao, Yanqiu; Chen, Hongtai; Zhang, Shijia; Cai, Yixiang; Ren, Bingjie; Liu, Wensheng; Tang, Songxi; Sha, Yanwei
发表日期：2024
文献求助 收藏

Biallelic mutations in IQCN, encoding a novel acroplaxome protein, lead to fertilization failure and male infertility with defects in the acrosome and shaping of the spermatid head in humans and mice

IQCN基因的双等位基因突变编码一种新型顶体蛋白，会导致人类和小鼠受精失败和男性不育，并伴有顶体缺陷和精子细胞头部形态异常。

期刊:Life Medicine
影响因子:6
doi:10.1093/lifemedi/lnac050
Sha, Yanwei; Chen, Yongjie; Wang, Xiong; Meng, Ranran; Yang, Xiaoyan; Li, Youzhu; Jin, Pengpeng; Li, Shanze; Chen, Jie; Shao, Tianyu; Xu, Dan; Guo, Yibiao; Jiang, Zhaodi; Li, Yuhua; Yu, Shuntai; Li, Lin; Wang, Fengchao
细胞生物学
发表日期：2023
文献求助 收藏

Homozygous mutation in DNALI1 leads to asthenoteratozoospermia by affecting the inner dynein arms

DNALI1基因的纯合突变会影响内动力蛋白臂，从而导致弱精子畸形症。

期刊:Frontiers in Endocrinology
影响因子:4.6
doi:10.3389/fendo.2022.1058651
Sha, Yanwei; Liu, Wensheng; Nie, Hua; Han, Lu; Ma, Chunjie; Zhang, Xiaoya; Xiao, Ziyi; Qin, Weibing; Jiang, Xiaoming; Wei, Xiaoli
发表日期：2022
文献求助 收藏

Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

DNAH9基因的新变异导致非综合征型重度弱精子症

期刊:Reproductive Biology and Endocrinology
影响因子:4.7
doi:10.1186/s12958-021-00709-0
Tang, Dongdong; Sha, Yanwei; Gao, Yang; Zhang, Jingjing; Cheng, Huiru; Zhang, Junqiang; Ni, Xiaoqing; Wang, Chao; Xu, Chuan; Geng, Hao; He, Xiaojin; Cao, Yunxia
发表日期：2021
文献求助 收藏

Biallelic mutations of CFAP58 are associated with multiple morphological abnormalities of the sperm flagella

CFAP58 的双等位基因突变与精子鞭毛的多种形态异常有关

期刊:Clinical Genetics
影响因子:2.9
doi:10.1111/cge.13898
Yankun Sha, Yanwei Sha, Wensheng Liu, Xingshen Zhu, Mingxiang Weng, Xinzong Zhang, Yifeng Wang, Huiliang Zhou
信号转导
发表日期：2021
文献求助 收藏

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility

双等位基因DNAH8变异导致精子鞭毛多种形态异常和原发性男性不育

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2020.06.004
Liu, Chunyu; Miyata, Haruhiko; Gao, Yang; Sha, Yanwei; Tang, Shuyan; Xu, Zoulan; Whitfield, Marjorie; Patrat, Catherine; Wu, Huan; Dulioust, Emmanuel; Tian, Shixiong; Shimada, Keisuke; Cong, Jiangshan; Noda, Taichi; Li, Hang; Morohoshi, Akane; Cazin, Caroline; Kherraf, Zine-Eddine; Arnoult, Christophe; Jin, Li; He, Xiaojin; Ray, Pierre F; Cao, Yunxia; Touré, Aminata; Zhang, Feng; Ikawa, Masahito
发表日期：2020
文献求助 收藏

Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention

全外显子组测序在卵巢早衰患者中的应用：早期检测和早期干预

期刊:Journal of Ovarian Research
影响因子:4.2
doi:10.1186/s13048-020-00716-6
Liu, Hongli; Wei, Xiaoli; Sha, Yanwei; Liu, Wensheng; Gao, Haijie; Lin, Jin; Li, Youzhu; Tang, Yaling; Wang, Yifeng; Wang, Yanlong; Su, Zhiying
发表日期：2020
文献求助 收藏

Loss-of-function mutation in TSGA10 causes acephalic spermatozoa phenotype in human.

TSGA10 功能丧失突变导致人类出现无头精子表型

期刊:Molecular Genetics & Genomic Medicine
影响因子:1.6
doi:10.1002/mgg3.1284
Ye Yuanyuan, Wei Xiaoli, Sha Yanwei, Li Na, Yan Xiaohong, Cheng Ling, Qiao Duanrui, Zhou Weidong, Wu Rongfeng, Liu Qiaobin, Li Youzhu
其它
Human
发表日期：2020
文献求助 收藏