Associated Papers
Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.
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Reproductive Biology, 2025
Genetic insights into the complexity of premature ovarian insufficiency.
Nie L et al.
Reproductive Biology and Endocrinology : Rb&e, 2024
Understanding the Mechanisms of Diminished Ovarian Reserve: Insights from Genetic Variants and Regulatory Factors.
Zhu Q et al.
Reproductive Sciences (thousand Oaks, Calif.), 2024
A novel homozygote nonsense variant of MSH4 leads to primary ovarian insufficiency and non-obstructive azoospermia.
Hashemi Sheikhshabani S et al.
Molecular Biology Reports, 2024
Identification of compound heterozygous variants in MSH4 as a novel genetic cause of diminished ovarian reserve.
Wan Y et al.
Reproductive Biology and Endocrinology : Rb&e, 2023
Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia.
Li P et al.
Reproductive Biology and Endocrinology : Rb&e, 2022
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