Associated Papers
Molecular characterization of recessively inherited ataxic and neuropathic disorders in consanguineous Pakistani families.
Aslam F et al.
Scientific Reports, 2026
41606223 (PubMed )
Supplement: 41598_2026_37808_MOESM5_ESM.xlsx › Sheet1
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
A partial deletion within the meiosis-specific sporulation domain SPO22 of Tex11 is not associated with infertility in mice.
Ghieh F et al.
Plos One, 2024
Novel mutations of TEX11 are associated with non-obstructive azoospermia.
Song J et al.
Frontiers in Endocrinology, 2023
Genetic defects in human azoospermia.
Ghieh F et al.
Basic and Clinical Andrology, 2019
A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.
Sha Y et al.
Bmc Medical Genetics, 2018
TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.
Yang F et al.
Embo Molecular Medicine, 2015
Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure.
Cannarella R et al.
Asian Journal of Andrology, 0
A new TEX11 mutation causes azoospermia and testicular meiotic arrest.
Yu XC et al.
Asian Journal of Andrology, 0
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