Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
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
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
Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine.
Zhou Y et al.
Science Advances, 2021
34516913 (PubMed )
Supplement: sciadv.abi6856_tables_s1_to_s8.zip › sciadv.abi6856_Table_S6.xlsx › Sheet1
The comprehensive variant and phenotypic spectrum of TUBB8 in female infertility.
Zheng W et al.
Journal of Assisted Reproduction and Genetics, 2021
Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility.
Okutman O et al.
Genes, 2021
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