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
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
Novel MEI1 mutations cause chromosomal and DNA methylation abnormalities leading to embryonic arrest and implantation failure.
Wu X et al.
Molecular Genetics and Genomics : Mgg, 2024
Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.
Chen S et al.
Human Molecular Genetics, 2020
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