Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Novel homozygous variants in ASTL and WEE2 responsible for female infertility characterized by abnormal fertilization.
Xie S et al.
Journal of Assisted Reproduction and Genetics, 2025
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
Gene mutations associated with fertilization failure after in vitro fertilization/intracytoplasmic sperm injection.
Xue Y et al.
Frontiers in Endocrinology, 2022
Clinical exome sequencing identifies novel compound heterozygous mutations of the WEE2 gene in primary infertile women with fertilization failure.
Wang A et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology, 2021
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Novel compound heterozygous mutation in WEE2 is associated with fertilization failure: case report of an infertile woman and literature review.
Tian Y et al.
Bmc Women's Health, 2020
Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure.
Zhou X et al.
Journal of Assisted Reproduction and Genetics, 2019
Novel mutations in WEE2: Expanding the spectrum of mutations responsible for human fertilization failure.
Zhang Z et al.
Clinical Genetics, 2019
Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.
Sang Q et al.
American Journal of Human Genetics, 2018
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