Wei Zheng

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 15

Top Topics

Polycystic Ovary Syndrome

Top Venues

Journal of assisted reproduction and genetics

EMBO molecular medicine

Journal of medical genetics

Human reproduction (Oxford, England)

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

Publications

Xian Wan, Huiling Hu, Jiaqi Sun, Fei Meng, Fei Gong, Ge Lin, Hongqing Liao, Wei Zheng
Identification of novel compound heterozygous ZFP36L2 variants implicated in oocyte maturation defects and female infertility. Journal of assisted reproduction and genetics 41 (8) (2024)
Xian Wan, Huiling Hu, Jiaqi Sun, Fei Meng, Fei Gong, Ge Lin, Hongqing Liao, Wei Zheng
Identification of novel compound heterozygous ZFP36L2 variants implicated in oocyte maturation defects and female infertility. Journal of assisted reproduction and genetics 41 (8) (2024)
Xian Wan, Huiling Hu, Jiaqi Sun, Fei Meng, Fei Gong, Ge Lin, Hongqing Liao, Wei Zheng
Identification of novel compound heterozygous ZFP36L2 variants implicated in oocyte maturation defects and female infertility. Journal of assisted reproduction and genetics (2024)
Xian Wan, Huiling Hu, Jiaqi Sun, Fei Meng, Fei Gong, Ge Lin, Hongqing Liao, Wei Zheng
Identification of novel compound heterozygous ZFP36L2 variants implicated in oocyte maturation defects and female infertility. Journal of assisted reproduction and genetics 41 (8) (2024)
Huiling Hu, Xian Wan, Honghui Zhang, Jiaqi Sun, Fei Meng, Shuoping Zhang, Yifan Gu, Fei Gong, Han Zhao, Jing Guo, Wei Zheng
Biallelic variants in α-tubulin isotypes cause female infertility characterised as recurrent preimplantation embryo arrest. Journal of medical genetics (2024)
Xian Wan, Huiling Hu, Jiaqi Sun, Fei Meng, Fei Gong, Ge Lin, Hongqing Liao, Wei Zheng
Identification of novel compound heterozygous ZFP36L2 variants implicated in oocyte maturation defects and female infertility. Journal of assisted reproduction and genetics 41 (8) (2024)
Qi Li, Yize Wang, Wei Zheng, Jing Guo, Shunji Zhang, Fei Gong, Guang-Xiu Lu, Ge Lin, Jing Dai
Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility. Human reproduction (Oxford, England) (2023)
Yin-Li Zhang, Wei Zheng, Peipei Ren, Jiamin Jin, Zhanhong Hu, Qing Liu, Heng-Yu Fan, Fei Gong, Guang-Xiu Lu, Ge Lin, Song-Ying Zhang, Xiaomei Tong
Biallelic variants in MOS cause large polar body in oocyte and human female infertility. Human reproduction (Oxford, England) 37 (8) (2022)
Jing Dai, Qi Li, Qinwei Zhou, Shen Zhang, Junru Chen, Yize Wang, Jing Guo, Yifan Gu, Fei Gong, Yueqiu Tan, Guangxiu Lu, Wei Zheng, Ge Lin
IQCN disruption causes fertilization failure and male infertility due to manchette assembly defect. EMBO molecular medicine 14 (12) (2022)
Jing Dai, Yongzhe Chen, Qi Li, Tianlei Zhang, Qinwei Zhou, Fei Gong, Guangxiu Lu, Wei Zheng, Ge Lin
Pathogenic variant in ACTL7A causes severe teratozoospermia characterized by bubble-shaped acrosomes and male infertility. Molecular human reproduction 28 (8) (2022)
Wei Zheng, Huiling Hu, Shuoping Zhang, Xilin Xu, Yong Gao, Fei Gong, Guangxiu Lu, Ge Lin
The comprehensive variant and phenotypic spectrum of TUBB8 in female infertility. Journal of assisted reproduction and genetics 38 (9) (2021)
Yin-Li Zhang, Wei Zheng, Peipei Ren, Huiling Hu, Xiaomei Tong, Shuo-Ping Zhang, Xiang Li, Haichao Wang, Jun-Chao Jiang, Jiamin Jin, Weijie Yang, Lanrui Cao, Yuanlin He, Yerong Ma, Yingyi Zhang, Yifan Gu, Liang Hu, Keli Luo, Fei Gong, Guang-Xiu Lu, Ge Lin, Heng-Yu Fan, Song-Ying Zhang
Biallelic mutations in MOS cause female infertility characterized by human early embryonic arrest and fragmentation. EMBO molecular medicine 13 (12) (2021)
Wei Zheng, Qian-Qian Sha, Huiling Hu, Fei Meng, Qinwei Zhou, Xueqin Chen, Shuoping Zhang, Yifan Gu, Xian Yan, Lei Zhao, Yurong Zong, Liang Hu, Fei Gong, Guangxiu Lu, Heng-Yu Fan, Jing Guo
Biallelic variants in ZFP36L2 cause female infertility characterised by recurrent preimplantation embryo arrest. Journal of medical genetics (2021)
Wei Zheng, Huiling Hu, Jing Dai, Shuoping Zhang, Yifan Gu, Can Dai, Jing Guo, Xinxin Xu, Yuan Li, Shunji Zhang, Liang Hu, Fei Gong, Guangxiu Lu, Ge Lin
Expanding the genetic and phenotypic spectrum of the subcortical maternal complex genes in recurrent preimplantation embryonic arrest. Clinical genetics 99 (2) (2020)
Jing Dai, Can Dai, Jing Guo, Wei Zheng, Tianlei Zhang, Yuan Li, Changfu Lu, Fei Gong, Guangxiu Lu, Ge Lin
Novel homozygous variations in PLCZ1 lead to poor or failed fertilization characterized by abnormal localization patterns of PLCζ in sperm. Clinical genetics 97 (2) (2019)