Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
Cryo-EM structure of the human subcortical maternal complex and the associated discovery of infertility-associated variants.
Chi P et al.
Nature Structural & Molecular Biology, 2024
Structural basis of the subcortical maternal complex and its implications in reproductive disorders.
Chi P et al.
Nature Structural & Molecular Biology, 2024
38177687 (PubMed )
Supplement: 41594_2023_1153_MOESM3_ESM.xlsx › Table_S1
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
A novel variant in TLE6 is associated with embryonic developmental arrest (EDA) in familial female infertility.
Akbari M et al.
Scientific Reports, 2022
Gene mutations associated with fertilization failure after in vitro fertilization/intracytoplasmic sperm injection.
Xue Y et al.
Frontiers in Endocrinology, 2022
Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic development.
Liu J et al.
Journal of Assisted Reproduction and Genetics, 2021
Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality.
Zhang M et al.
Frontiers in Genetics, 2021
Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations.
Lin J et al.
Journal of Assisted Reproduction and Genetics, 2020
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