Associated Papers
Genetic architecture and phenotypic diversity of oocyte and early embryo competence defects in female infertility.
Zhang C et al.
Nature Medicine, 2026
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
Advances in the genetic etiology of female infertility.
Gu R et al.
Journal of Assisted Reproduction and Genetics, 2024
Variants in NLRP2 and ZFP36L2, non-core components of the human subcortical maternal complex, cause female infertility with embryonic development arrest.
Rui X et al.
Molecular Human Reproduction, 2024
Identification of novel compound heterozygous ZFP36L2 variants implicated in oocyte maturation defects and female infertility.
Wan X et al.
Journal of Assisted Reproduction and Genetics, 2024
A novel homozygous variant in ZFP36L2 cause female infertility due to oocyte maturation defect.
Zhou Z et al.
Clinical Genetics, 2023
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
Biallelic variants in ZFP36L2 cause female infertility characterised by recurrent preimplantation embryo arrest.
Zheng W et al.
Journal of Medical Genetics, 2022
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