Jing Guo (Ge Lin)

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 12

Top Topics

Intellectual Disability

Top Venues

Journal of medical genetics

Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Human reproduction (Oxford, England)

EMBO molecular medicine

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

Publications

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)
Shixiong Tian, Chaofeng Tu, Xiao-Jin He, Lanlan Meng, Jiaxiong Wang, Shuyan Tang, Yang Gao, Chunyu Liu, Huan Wu, Yiling Zhou, Mingrong Lv, Jing Guo, Li Jin, Yunxia Cao, Dongdong Tang, Feng Zhang, Yue-Qiu Tan
Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA. Journal of medical 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)
Jing Guo, Hailian Zhao, Jue Zhang, Xiangjiang Lv, Shen Zhang, Ruibao Su, Wei Zheng, Jing Dai, Fei Meng, Fei Gong, Guangxiu Lu, Yuanchao Xue, Ge Lin
Selective Translation of Maternal mRNA by eIF4E1B Controls Oocyte to Embryo Transition. Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2023)
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)
Tongyao Hu, Lanlan Meng, Chen Tan, Chen Luo, Wen-Bin He, Chaofeng Tu, Huan Zhang, Juan Du, Hongchuan Nie, Guang-Xiu Lu, Jing Guo, Yue-Qiu Tan
Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia. Journal of medical genetics (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)
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)
Hui Li, Liji You, Yufeng Tian, Jing Guo, Xianbao Fang, Chenmin Zhou, Lanying Shi, You-Qiang Su
DPAGT1-Mediated Protein N-Glycosylation Is Indispensable for Oocyte and Follicle Development in Mice. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 7 (14) (2020)
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)
Weili Wang, Chaofeng Tu, Hongchuan Nie, Lanlan Meng, Yong Li, Shimin Yuan, Qianjun Zhang, Juan Du, Junpu Wang, Fei Gong, Liqing Fan, Guang-Xiu Lu, Jing Guo, Yue-Qiu Tan
Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations. Journal of medical genetics 56 (11) (2019)
Jing Guo, Lanying Shi, Xuhong Gong, Mengjie Jiang, Yaoxue Yin, Xiaoyun Zhang, Hong Yin, Hui Li, Chihiro Emori, Koji Sugiura, John J Eppig, You-Qiang Su
Oocyte-dependent activation of MTOR in cumulus cells controls the development and survival of cumulus-oocyte complexes. Journal of cell science 129 (16) (2016)