Associated Papers
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 identifies rare recessive variants in azoospermia patients from consanguineous Pakistani families.
Uddin I et al.
Molecular Genetics and Genomics : Mgg, 2024
Toward clinical exomes in diagnostics and management of male infertility.
Lillepea K et al.
American Journal of Human Genetics, 2024
ESX1 gene as a potential candidate responsible for male infertility in nonobstructive azoospermia.
Malcher A et al.
Scientific Reports, 2023
Association of ESX1 gene variants with non-obstructive azoospermia in Chinese males.
Ma Q et al.
Scientific Reports, 2021
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