Associated Papers
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics.
Tan C et al.
Journal of Assisted Reproduction and Genetics, 2026
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
Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.
Ibrahim R et al.
Reproductive Biology, 2025
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 determinants of testicular sperm extraction outcomes: insights from a large multicentre study of men with non-obstructive azoospermia.
Riera-Escamilla A et al.
Human Reproduction Open, 2025
40896145 (PubMed )
Supplement: hoaf049_supplementary_data.zip › HRO-25-0045-R2-SuppTablesS2-S4_and_S6-S9.xlsx › ST6
Advances in the genetic etiology of female infertility.
Gu R et al.
Journal of Assisted Reproduction and Genetics, 2024
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia.
Zhang Y et al.
Journal of Human Genetics, 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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