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Human Reproduction (Oxford, England)|May 26, 2021
Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failureJie Dong, Hong Zhang, Xiaoyan Mao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 27, 2022
Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrestLin Zhao, Qun Li, Yanping Kuang, et al.
The Journal of Clinical Investigation|January 17, 2023
Karyopherin α deficiency contributes to human preimplantation embryo arrestWenjing Wang, Yoichi Miyamoto, Biaobang Chen, et al.
Genome Biology|April 6, 2023
Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defectsQun Li, Lin Zhao, Yang Zeng, et al.
Cell Genomics|September 26, 2025
Genetic landscape of human oocyte/embryo defectsBiaobang Chen, Weijie Wang, Juanzi Shi, et al.
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