Ying Shen

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 21

Top Topics

Embryonic Stem Cells

High Fat Diet Induced

Top Venues

Clinical genetics

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Mohan Liu, Lingbo Wang, Yifei Li, Erlei Zhi, Gan Shen, Xiaohui Jiang, Dingming Li, Xinya Zhao, Tiechao Ruan, Chuan Jiang, Xiang Wang, Xueguang Zhang, Yanjiang Zheng, Bangguo Wu, Ningjing Ou, Guicheng Zhao, Siyu Dai, Ruixi Zhou, Li Yang, Yihong Yang, Hanmin Liu, Ying Shen
HSF5 Deficiency Causes Male Infertility Involving Spermatogenic Arrest at Meiotic Prophase I in Humans and Mice. Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Ying-Teng Zhang, Gan Shen, Liang-Chai Zhuo, Xue Yang, Su-Yan Wang, Tie-Chao Ruan, Chuan Jiang, Xiang Wang, Yan Wang, Yi-Hong Yang, Ying Shen
Novel variations in TENT5D lead to teratozoospermia in infertile patients. Andrology 12 (6) (2024)
Tiechao Ruan, Ruixi Zhou, Yihong Yang, Junchen Guo, Chuan Jiang, Xiang Wang, Gan Shen, Siyu Dai, Su-Ren Chen, Ying Shen
Deficiency of IQCH causes male infertility in humans and mice. eLife 12 (2024)
Tiechao Ruan, Ruixi Zhou, Yihong Yang, Junchen Guo, Chuan Jiang, Xiang Wang, Gan Shen, Siyu Dai, Su-Ren Chen, Ying Shen
Deficiency of IQCH causes male infertility in humans and mice. eLife 12 (2024)
Ying-Teng Zhang, Gan Shen, Liang-Chai Zhuo, Xue Yang, Su-Yan Wang, Tie-Chao Ruan, Chuan Jiang, Xiang Wang, Yan Wang, Yi-Hong Yang, Ying Shen
Novel variations in TENT5D lead to teratozoospermia in infertile patients. Andrology (2024)
Tiechao Ruan, Ruixi Zhou, Yihong Yang, Junchen Guo, Chuan Jiang, Xiang Wang, Gan Shen, Siyu Dai, Su-Ren Chen, Ying Shen
Deficiency of IQCH causes male infertility in humans and mice. eLife 12 (2024)
Fan Yang, Huaqin Sun, Yanting Yang, Yanan Wang, Siyu Dai, Ziyuan Lin, Ying Shen, Hongqian Liu
Identification of POLR3B biallelic mutations -associated hypomyelinating leukodystrophy-8 in two siblings. Clinical genetics (2023)
Xiang Wang, Ruixi Zhou, Xiaowei Lu, Siyu Dai, Mohan Liu, Chuan Jiang, Yanting Yang, Ying Shen, Yan Wang, Hanmin Liu
Identification of nonfunctional PABPC1L causing oocyte maturation abnormalities and early embryonic arrest in female primary infertility. Clinical genetics (2023)
Fan Yang, Huaqin Sun, Yanting Yang, Yanan Wang, Siyu Dai, Ziyuan Lin, Ying Shen, Hongqian Liu
Identification of POLR3B biallelic mutations-associated hypomyelinating leukodystrophy-8 in two siblings. Clinical genetics (2023)
Siyu Dai, Yan Liang, Mohan Liu, Yanting Yang, Hongqian Liu, Ying Shen
Novel biallelic mutations in TTC29 cause asthenoteratospermia and male infertility. Molecular genetics & genomic medicine (2022)
Rui Zheng, Yan Wang, Yaqian Li, Juncen Guo, Yuting Wen, Chuan Jiang, Yihong Yang, Ying Shen
FSIP2 plays a role in the acrosome development during spermiogenesis. Journal of medical genetics (2022)
Mohan Liu, Jinhui Li, Yaqian Li, Chuan Jiang, Wenming Xu, Yihong Yang, Ying Shen
The heterozygous mutations of SLC26A8 are not the main actors for male infertility. Human mutation 43 (5) (2022)
Ying Shen, Jing Guo, Xueguang Zhang, Xiang Wang, Shaomi Zhu, Daijuan Chen, Wei Xiong, Guangxiu Lu, Xiaojun Liu, Can Dai, Fei Gong, Yan Wang, Ge Lin, Zhen-Bo Wang, Wen-Ming Xu
Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice. Human reproduction (Oxford, England) 37 (4) (2022)
Xueguang Zhang, Lingbo Wang, Yongyi Ma, Yan Wang, Hongqian Liu, Mohan Liu, Lang Qin, Jinghong Li, Chuan Jiang, Xiaojian Zhang, Xudong Shan, Yuliang Liu, Jinsong Li, Yaqian Li, Rui Zheng, Yongkang Sun, Jianfeng Sun, Xiangyou Leng, Yan Liang, Feng Zhang, XiaoHui Jiang, Yihong Yang, Ying Shen
CEP128 is involved in spermatogenesis in humans and mice. Nature communications 13 (1) (2022)
Chunyu Liu, Ying Shen, Shuyan Tang, Jiaxiong Wang, Yiling Zhou, Shixiong Tian, Huan Wu, Jiangshan Cong, Xiao-Jin He, Li Jin, Yunxia Cao, Yihong Yang, Feng Zhang
Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility. Journal of medical genetics (2022)
Yuting Wen, Xiang Wang, Rui Zheng, Siyu Dai, Jinhui Li, Yihong Yang, Ying Shen
Sequencing of the ZMYND15 gene in a cohort of infertile Chinese men reveals novel mutations in patients with teratozoospermia. Journal of medical genetics (2022)
Sixian Wu, Xiang Wang, Siyu Dai, Guohui Zhang, Jiaojiao Zhou, Ying Shen
A novel missense mutation in GREB1L identified in a three-generation family with renal hypodysplasia/aplasia-3. Orphanet journal of rare diseases 17 (1) (2022)
Xiang Wang, Chuan Jiang, Siyu Dai, Gan Shen, Yihong Yang, Ying Shen
Identification of nonfunctional SPATA20 causing acephalic spermatozoa syndrome in humans. Clinical genetics (2022)
Xueguang Zhang, Rui Zheng, Chen Liang, Haotian Liu, Xiaozhen Zhang, Yongyi Ma, Mohan Liu, Wei Zhang, Yang Yang, Man Liu, Ying-Teng Zhang, Qingjia Ren, Yan Wang, Su-Ren Chen, Yihong Yang, Ying Shen
Loss-of-function mutations in CEP78 cause male infertility in humans and mice. Science advances 8 (40) (2022)
Guohui Zhang, Chuan Jiang, Yushang Yang, Yan Wang, Haimeng Zhou, Siyu Dai, Mohan Liu, Yanting Yang, Li Yang, Qiongyan Shen, Tao Zhang, Xiao-Dong Zhang, Yihong Yang, Ying Shen
Deficiency of cancer/testis antigen gene CT55 causes male infertility in humans and mice. Cell death and differentiation (2022)
Xueguang Zhang, Yihong Yang, Haixia Zhang, Ze Du, Hongqian Liu, Ying Shen
A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous G γ(A γδβ)0 -thalassemia. American journal of hematology 96 (6) (2021)