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
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
Clinical application of whole exome sequencing for recurrent early pregnancy loss.
Liu C et al.
Asian Journal of Surgery, 2024
Pathogenic variants in human DNA damage repair genes mostly arose after the latest human out-of-Africa migration.
He J et al.
Frontiers in Genetics, 2024
Polymorphisms and expression levels of TNP2, SYCP3, and AZFa genes in patients with azoospermia.
Jebur MII et al.
Clinical and Experimental Reproductive Medicine, 2023
Genetic control of meiosis surveillance mechanisms in mammals.
Huang Y et al.
Frontiers in Cell and Developmental Biology, 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
Distinct landscapes of deleterious variants in DNA damage repair system in ethnic human populations.
Qin Z et al.
Life Science Alliance, 2022
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project.
Cong PK et al.
Nature Communications, 2022
A systematic review and standardized clinical validity assessment of genes involved in female reproductive failure.
Volozonoka L et al.
Reproduction (cambridge, England), 2022
Alterations in synaptonemal complex coding genes and human infertility.
Zhang F et al.
International Journal of Biological Sciences, 2022
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Autosomal single-gene disorders involved in human infertility.
Jedidi I et al.
Saudi Journal of Biological Sciences, 2018
Genetic and epigenetic variations associated with idiopathic recurrent pregnancy loss.
Arias-Sosa LA et al.
Journal of Assisted Reproduction and Genetics, 2018
DNA methyltransferase 3A promoter polymorphism is associated with the risk of human spontaneous abortion after assisted reproduction techniques and natural conception.
Liu Y et al.
Journal of Assisted Reproduction and Genetics, 2017
An Association Study of the SLC19A1 Gene Polymorphisms/Haplotypes with Idiopathic Recurrent Pregnancy Loss in an Iranian Population.
Mohtaram S et al.
Genetic Testing and Molecular Biomarkers, 2016
The T657C polymorphism on the SYCP3 gene is associated with recurrent pregnancy loss.
Sazegari A et al.
Journal of Assisted Reproduction and Genetics, 2014
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing.
Mort M et al.
Genome Biology, 2014
Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies.
Roos A et al.
Archives of Gynecology and Obstetrics, 2013
Absence of SYCP3 mutations in women with recurrent miscarriage with at least one trisomic miscarriage.
Hanna CW et al.
Reproductive Biomedicine Online, 2012
SYCP3 mutation may not be associated with recurrent miscarriage caused by aneuploidy.
Mizutani E et al.
Human Reproduction (oxford, England), 2011
Mutations of the SYCP3 gene in women with recurrent pregnancy loss.
Bolor H et al.
American Journal of Human Genetics, 2009