Associated Papers
Genetic and epigenetic insights into non-obstructive azoospermia: mechanisms, biomarkers, and clinical perspectives.
Wang X 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
Whole exome sequencing analysis of 167 men with primary infertility.
Zhou H et al.
Bmc Medical Genomics, 2024
Loss-of-function variant in TDRD6 cause male infertility with severe oligo-astheno-teratozoospermia in human and mice.
Bi X et al.
Journal of Cellular and Molecular Medicine, 2024
39331689 (PubMed )
Supplement: JCMM-28-e18580-s001.docx
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Genetic control of meiosis surveillance mechanisms in mammals.
Huang Y et al.
Frontiers in Cell and Developmental Biology, 2023
36910159 (PubMed )
Supplement: DataSheet2.PDF
A systematic review on the genetics of male infertility in the era of next-generation sequencing.
Robay A et al.
Arab Journal of Urology, 2018
Mutation in TDRD9 causes non-obstructive azoospermia in infertile men.
Arafat M et al.
Journal of Medical Genetics, 2017
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