Associated Papers
The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study.
Podgrajsek R et al.
Reproductive Biology and Endocrinology : Rb&e, 2025
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
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
Whole exome sequencing analysis of 167 men with primary infertility.
Zhou H et al.
Bmc Medical Genomics, 2024
A novel homozygote nonsense variant of MSH4 leads to primary ovarian insufficiency and non-obstructive azoospermia.
Hashemi Sheikhshabani S et al.
Molecular Biology Reports, 2024
Identification of compound heterozygous variants in MSH4 as a novel genetic cause of diminished ovarian reserve.
Wan Y et al.
Reproductive Biology and Endocrinology : Rb&e, 2023
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia.
Xie C et al.
Human Reproduction Update, 2022
Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia.
Li P et al.
Reproductive Biology and Endocrinology : Rb&e, 2022
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