Qing Sang

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 26

Top Topics

Escherichia Coli

Dna Methylation

Induced Pluripotent Stem Cells

Top Venues

Cellular and molecular life sciences : CMLS

Human reproduction (Oxford, England)

Science (New York, N.Y.)

Journal of assisted reproduction and genetics

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

Publications

Hongbin Zhou, Zhihua Zhang, Ronggui Qu, Hongying Zhu, Yuxi Luo, Qun Li, Jian Mu, Ran Yu, Yang Zeng, Biaobang Chen, Qing Sang, Lei Wang
CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice. Cellular and molecular life sciences : CMLS 81 (1) (2024)
Hongbin Zhou, Zhihua Zhang, Ronggui Qu, Hongying Zhu, Yuxi Luo, Qun Li, Jian Mu, Ran Yu, Yang Zeng, Biaobang Chen, Qing Sang, Lei Wang
CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice. Cellular and molecular life sciences : CMLS 81 (1) (2024)
Tianyu Wu, Yuxi Luo, Meiling Zhang, Biaobang Chen, Xingzhu Du, Hao Gu, Siyuan Xie, Zhiqi Pan, Ran Yu, Ruiqi Hai, Xiangli Niu, Guimin Hao, Li-Ping Jin, Juanzi Shi, Xiao-Xi Sun, Yanping Kuang, Wen Li, Qing Sang, Lei Wang
Mechanisms of minor pole-mediated spindle bipolarization in human oocytes. Science (New York, N.Y.) 385 (6711) (2024)
Hongbin Zhou, Zhihua Zhang, Ronggui Qu, Hongying Zhu, Yuxi Luo, Qun Li, Jian Mu, Ran Yu, Yang Zeng, Biaobang Chen, Qing Sang, Lei Wang
CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice. Cellular and molecular life sciences : CMLS 81 (1) (2024)
Hongbin Zhou, Zhihua Zhang, Ronggui Qu, Hongying Zhu, Yuxi Luo, Qun Li, Jian Mu, Ran Yu, Yang Zeng, Biaobang Chen, Qing Sang, Lei Wang
CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice. Cellular and molecular life sciences : CMLS 81 (1) (2024)
Hongbin Zhou, Zhihua Zhang, Ronggui Qu, Hongying Zhu, Yuxi Luo, Qun Li, Jian Mu, Ran Yu, Yang Zeng, Biaobang Chen, Qing Sang, Lei Wang
CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice. Cellular and molecular life sciences : CMLS 81 (1) (2024)
Tianyu Wu, Yuxi Luo, Meiling Zhang, Biaobang Chen, Xingzhu Du, Hao Gu, Siyuan Xie, Zhiqi Pan, Ran Yu, Ruiqi Hai, Xiangli Niu, Guimin Hao, Li-Ping Jin, Juanzi Shi, Xiao-Xi Sun, Yanping Kuang, Wen Li, Qing Sang, Lei Wang
Mechanisms of minor pole-mediated spindle bipolarization in human oocytes. Science (New York, N.Y.) 385 (6711) (2024)
Qun Li, Lin Zhao, Yang Zeng, Yanping Kuang, Yichun Guan, Biaobang Chen, Shiru Xu, Bin Tang, Ling Wu, Xiaoyan Mao, Xiaoxi Sun, Juanzi Shi, Peng Xu, Feiyang Diao, Songguo Xue, Shihua Bao, Qingxia Meng, Ping Yuan, Wenjun Wang, Ning Ma, Di Song, Bei Xu, Jie Dong, Jian Mu, Zhihua Zhang, Huizhen Fan, Hao Gu, Qiaoli Li, Lin He, Li Jin, Lei Wang, Qing Sang
Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects. Genome biology 24 (1) (2023)
Ruyi Liu, Ronggui Qu, Qun Li, Biaobang Chen, Jian Mu, Yang Zeng, Yuxi Luo, Fangzhou Xu, Lei Wang, Zhihua Zhang, Qing Sang
ARRDC5 deficiency impairs spermatogenesis by affecting SUN5 and NDC1. Development (Cambridge, England) (2023)
Qing Sang, Pierre F Ray, Lei Wang
Understanding the genetics of human infertility. Science (New York, N.Y.) 380 (6641) (2023)
Zhou Zhou, Huizhen Fan, Rong Shi, Yang Zeng, Ruyi Liu, Hao Gu, Qiaoli Li, Qing Sang, Lei Wang, Juanzi Shi, Biaobang Chen
A novel homozygous variant in ZFP36L2 cause female infertility due to oocyte maturation defect. Clinical genetics (2023)
Weijie Wang, Jing Guo, Juanzi Shi, Qun Li, Biaobang Chen, Zhiqi Pan, Ronggui Qu, Jing Fu, Rong Shi, Xia Xue, Jian Mu, Zhihua Zhang, Tianyu Wu, Wenjing Wang, Lin Zhao, Qiaoli Li, Lin He, Xiaoxi Sun, Qing Sang, Ge Lin, Lei Wang
Bi-allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility. EMBO molecular medicine (2023)
Ronggui Qu, Zhihua Zhang, Ling Wu, Qun Li, Jian Mu, Lin Zhao, Zheng Yan, Wenjing Wang, Yang Zeng, Ruyi Liu, Jie Dong, Qiaoli Li, Xiaoxi Sun, Lei Wang, Qing Sang, Biaobang Chen, Yanping Kuang
ADGB variants cause asthenozoospermia and male infertility. Human genetics (2023)
Yang Zeng, Lin Li, Qingchun Li, Jijun Hu, Nana Zhang, Ling Wu, Zheng Yan, Ronggui Qu, Jie Dong, Ruyi Liu, Kwong-Wai Choy, Lei Wang, Qing Sang, Yichun Guan, Biaobang Chen
Genetic screening in patients with ovarian dysfunction. Clinical genetics (2022)
Ruyi Liu, Zheng Yan, Yong Fan, Ronggui Qu, Biaobang Chen, Bin Li, Ling Wu, Haibo Wu, Jian Mu, Lin Zhao, Wenjing Wang, Jie Dong, Yang Zeng, Qiaoli Li, Lei Wang, Qing Sang, Zhihua Zhang, Yanping Kuang
Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertility. Human reproduction (Oxford, England) 37 (7) (2022)
Yang Zeng, Juanzi Shi, Shiru Xu, Rong Shi, Tonghua Wu, Hongyan Li, Xia Xue, Yuanchang Zhu, Biaobang Chen, Qing Sang, Lei Wang
Bi-allelic mutations in MOS cause female infertility characterized by preimplantation embryonic arrest. Human reproduction (Oxford, England) 37 (3) (2022)
Tianyu Wu, Jie Dong, Jing Fu, Yanping Kuang, Biaobang Chen, Hao Gu, Yuxi Luo, Ruihuan Gu, Meiling Zhang, Wen Li, Xi Dong, Xiao-Xi Sun, Qing Sang, Lei Wang
The mechanism of acentrosomal spindle assembly in human oocytes. Science (New York, N.Y.) 378 (6621) (2022)
Zhihua Zhang, Hongbin Zhou, Xujing Deng, Ruixiu Zhang, Ronggui Qu, Jian Mu, Ruyi Liu, Yang Zeng, Biaobang Chen, Lei Wang, Qing Sang, Shi Hua Bao
IQUB deficiency causes male infertility by affecting the activity of p-ERK1/2/RSPH3. Human reproduction (Oxford, England) (2022)
Lin Zhao, Songguo Xue, Zhongyuan Yao, Juanzi Shi, Biaobang Chen, Ling Wu, Lihua Sun, Yao Xu, Zheng Yan, Bin Li, Xiaoyan Mao, Jing Fu, Zhihua Zhang, Jian Mu, Wenjing Wang, Jing Du, Shuai Liu, Jie Dong, Weijie Wang, Qiaoli Li, Lin He, Li Jin, Xiaozhen Liang, Yanping Kuang, Xiaoxi Sun, Lei Wang, Qing Sang
Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development. Protein & cell 11 (12) (2021)
Ruyi Liu, Yifan Zhou, Qiaoli Li, Biaobang Chen, Zhou Zhou, Lan Wang, Lei Wang, Qing Sang, Lei Jin
A novel homozygous missense variant in BTG4 causes zygotic cleavage failure and female infertility. Journal of assisted reproduction and genetics (2021)
Zhou Zhou, Xiaoyan Mao, Biaobang Chen, Jian Mu, Wenjing Wang, Bin Li, Zheng Yan, Jie Dong, Qiaoli Li, Yanping Kuang, Lei Wang, Ling Wu, Qing Sang
A novel splicing variant in DNAH8 causes asthenozoospermia. Journal of assisted reproduction and genetics 38 (6) (2021)
Lei Wang, Qing Sang
MOS is a novel genetic marker for human early embryonic arrest and fragmentation. EMBO molecular medicine 13 (12) (2021)
Jie Dong, Hong Zhang, Xiaoyan Mao, Junhua Zhu, Da Li, Jing Fu, Jijun Hu, Ling Wu, Biaobang Chen, Yiming Sun, Jian Mu, Zhihua Zhang, Xiaoxi Sun, Lin Zhao, Wenjing Wang, Weijie Wang, Zhou Zhou, Yang Zeng, Jing Du, Qiaoli Li, Lin He, Li Jin, Yanping Kuang, Lei Wang, Qing Sang
Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure. Human reproduction (Oxford, England) 36 (8) (2021)
Weijie Wang, Wenjing Wang, Yao Xu, Juanzi Shi, Jing Fu, Biaobang Chen, Jian Mu, Zhihua Zhang, Lin Zhao, Jing Lin, Jing Du, Qiaoli Li, Lin He, Li Jin, Xiao-Xi Sun, Lei Wang, Qing Sang
FBXO43 variants in patients with female infertility characterized by early embryonic arrest. Human reproduction (Oxford, England) 36 (8) (2021)
Zhihua Zhang, Ling Wu, Feiyang Diao, Biaobang Chen, Jing Fu, Xiaoyan Mao, Zheng Yan, Bin Li, Jian Mu, Zhou Zhou, Wenjing Wang, Lin Zhao, Jie Dong, Yang Zeng, Jing Du, Yanping Kuang, Xiaoxi Sun, Lin He, Qing Sang, Lei Wang
Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome. Journal of assisted reproduction and genetics 37 (11) (2020)
Qing Sang, Zhihua Zhang, Juanzi Shi, Xiao-Xi Sun, Bin Li, Zheng Yan, Songguo Xue, Ai Ai, Qifeng Lyu, Wei Li, Jilin Zhang, Ling Wu, Xiaoyan Mao, Biaobang Chen, Jian Mu, Qiaoli Li, Jing Du, Qiang Sun, Li Jin, Lin He, Shujia Zhu, Yanping Kuang, Lei Wang
A pannexin 1 channelopathy causes human oocyte death. Science translational medicine 11 (485) (2020)