Associated Papers
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
A case report of neonatal incontinentia pigmenti complicated by severe cerebrovascular lesions in one of the male monozygotic twins.
Lin X et al.
Frontiers in Pediatrics, 2024
38832002 (PubMed )
Supplement: Table1.xlsx › filter_variants
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
Investigation of PALB2 Mutation and Correlation With Immunotherapy Biomarker in Chinese Non-Small Cell Lung Cancer Patients.
Zhang J et al.
Frontiers in Oncology, 2021
35087742 (PubMed )
Supplement: Table_1.xlsx › Table3_mut_frequency_v3
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 WEE2 gene variants identified in patients with fertilization failure and female infertility.
Zhao S et al.
Fertility and Sterility, 2019
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