Associated Papers
Tex11 Mutant Mouse Models of Human Azoospermia.
Atkins GR et al.
Biorxiv : the Preprint Server for Biology, 2026
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
Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes.
Rotte N et al.
Embo Molecular Medicine, 2025
40374915 (PubMed )
Supplement: 44321_2025_244_MOESM2_ESM.pdf
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
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Novel mutations of TEX11 are associated with non-obstructive azoospermia.
Song J et al.
Frontiers in Endocrinology, 2023
Targeted next-generation sequencing panel screening of 668 Chinese patients with non-obstructive azoospermia.
An M et al.
Journal of Assisted Reproduction and Genetics, 2021
Select a paper to view details