Associated Papers
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
DNA double-strand break genetic variants in patients with premature ovarian insufficiency.
Ding X et al.
Journal of Ovarian Research, 2023
The landscape of genetic variations in non-syndromic primary ovarian insufficiency in the MENA region: a systematic review.
Allouch A et al.
Frontiers in Endocrinology, 2023
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Meiotic Recombination Defects and Premature Ovarian Insufficiency.
Huang C et al.
Frontiers in Cell and Developmental Biology, 2021
Meiotic Cohesin and Variants Associated With Human Reproductive Aging and Disease.
Beverley R et al.
Frontiers in Cell and Developmental Biology, 2021
STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermia.
Jaillard S et al.
Molecular Human Reproduction, 2020
Two rare loss-of-function variants in the STAG3 gene leading to primary ovarian insufficiency.
França MM et al.
European Journal of Medical Genetics, 2019
A STAG3 missense mutation in two sisters with primary ovarian insufficiency.
Colombo R et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2017
Variation analysis of EXO1 gene in Chinese patients with premature ovarian failure.
Su S et al.
Reproductive Biomedicine Online, 2016
STAG3 truncating variant as the cause of primary ovarian insufficiency.
Le Quesne Stabej P et al.
European Journal of Human Genetics : Ejhg, 2016
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing.
Laissue P
Molecular and Cellular Endocrinology, 2015
Mutant cohesin in premature ovarian failure.
Caburet S et al.
The New England Journal of Medicine, 2014
Genetics of primary ovarian insufficiency: new developments and opportunities.
Qin Y et al.
Human Reproduction Update, 0