Associated Papers
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
The role of RAD51 regulators and variants in primary ovarian insufficiency, endometriosis, and polycystic ovary syndrome.
Witham M et al.
Nar Molecular Medicine, 2024
DNA double-strand break genetic variants in patients with premature ovarian insufficiency.
Ding X et al.
Journal of Ovarian Research, 2023
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia.
Xie C et al.
Human Reproduction Update, 2022
A pathogenic DMC1 frameshift mutation causes nonobstructive azoospermia but not primary ovarian insufficiency in humans.
Cao D et al.
Molecular Human Reproduction, 2021
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
Meiotic Recombination Defects and Premature Ovarian Insufficiency.
Huang C et al.
Frontiers in Cell and Developmental Biology, 2021
DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing.
He WB et al.
Journal of Medical Genetics, 2018
The formation and repair of DNA double-strand breaks in mammalian meiosis.
Qu W et al.
Asian Journal of Andrology, 0
Select a paper to view details