Associated Papers
Novel variants in MEI1 cause female infertility characterized by early embryonic arrest and implantation failure.
Chen B et al.
Journal of Assisted Reproduction and Genetics, 2026
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Novel biallelic MEI1 variants cause female infertility characterized by multiple pronuclei formation and aberrant embryonic development.
Jiao X et al.
Journal of Ovarian Research, 2025
41444636 (PubMed )
Supplement: 13048_2025_1890_MOESM2_ESM.xlsx › Table_S2
Identification of the novel homozygous whole exon deletion in MEI1 underlying azoospermia and embryonic arrest in one consanguineous family.
Liu B et al.
Reproductive Sciences (thousand Oaks, Calif.), 2025
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure.
Dong J et al.
Human Reproduction (oxford, England), 2021
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