Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Molecular Guardians of Oocyte Maturation: A Systematic Review on TUBB8, KIF11, and CKAP5 in IVF Outcomes.
Voros C et al.
International Journal of Molecular Sciences, 2025
Identification of novel variants and expansion of the phenotypic spectrum in PATL2, WEE2, and TUBB8 associated with human early embryonic arrest.
Zhao H et al.
Journal of Assisted Reproduction and Genetics, 2025
Novel variants in TUBB8 gene cause multiple phenotypic abnormalities in human oocytes and early embryos.
Hu T et al.
Journal of Ovarian Research, 2023
TUBB8 mutations as a cause of oocyte maturation abnormalities: presentation of oocyte and embryo profiles and novel mutations.
Ebru H et al.
Reproductive Biomedicine Online, 2023
A novel compound heterozygous mutation in TUBB8 causing early embryonic developmental arrest.
Zhang J et al.
Journal of Assisted Reproduction and Genetics, 2023
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility.
Chen B et al.
European Journal of Human Genetics : Ejhg, 2019
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