Associated Papers
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 › ST4
Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia.
Zhang Y et al.
Journal of Human Genetics, 2023
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Novel MEI1 compound heterozygous mutation in a sporadic family associated with spermatogenetic failure.
Chen J et al.
Asian Journal of Andrology, 2023
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men.
Krausz C et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2020
Select a paper to view details