Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Genetic architecture and phenotypic diversity of oocyte and early embryo competence defects in female infertility.
Zhang C et al.
Nature Medicine, 2026
Targeting G1-S-checkpoint-compromised cancers with cyclin A/B RxL inhibitors.
Singh S et al.
Nature, 2025
40836083 (PubMed )
Supplement: 41586_2025_9433_MOESM4_ESM.zip › 2024-07-15654B-s4 › Table_S5_052925.xlsx › Tab_6-zscore_CDC20_C_T
Advances in the genetic etiology of female infertility.
Gu R et al.
Journal of Assisted Reproduction and Genetics, 2024
Exonic genetic variants associated with unexpected fertilization failure and zygotic arrest after ICSI: a systematic review.
Torra-Massana M et al.
Zygote (cambridge, England), 2023
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
Novel Mutations in CDC20 Are Associated with Female Infertility Due to Oocyte Maturation Abnormality and Early Embryonic Arrest.
Huang L et al.
Reproductive Sciences (thousand Oaks, Calif.), 2021
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
Identification of Novel Mutations in CDC20: Expanding the Mutational Spectrum for Female Infertility.
Zhao L et al.
Frontiers in Cell and Developmental Biology, 2021
Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development.
Zhao L et al.
Protein & Cell, 2020
R383C mutation of human CDC20 results in idiopathic non-obstructive azoospermia.
Li L et al.
Oncotarget, 2017
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