Associated Papers
The intricate dance of RNA-binding proteins: unveiling the mechanisms behind male infertility.
Gao Y et al.
Human Reproduction Update, 2026
Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility.
Podgrajsek R et al.
The World Journal of Men's Health, 2025
39843174 (PubMed )
Supplement: wjmh-43-908-s001.pdf
Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development.
Kouri C et al.
Ebiomedicine, 2024
38168586 (PubMed )
Supplement: mmc1.pdf
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia.
Huang Y et al.
Bmc Medical Genomics, 2022
Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes.
Ghieh F et al.
Human Reproduction (oxford, England), 2022
Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
Tang D et al.
Reproductive Biology and Endocrinology : Rb&e, 2022
Alterations in synaptonemal complex coding genes and human infertility.
Zhang F et al.
International Journal of Biological Sciences, 2022
The genetic causes of male infertility: a Middle East and North Africa perspective.
Duvuru R et al.
F1000research, 2022
Meiotic chromosome synapsis depends on multivalent SYCE1-SIX6OS1 interactions that are disrupted in cases of human infertility.
Sánchez-Sáez F et al.
Science Advances, 2020
The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.
Pashaei M et al.
Journal of Assisted Reproduction and Genetics, 2020
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