Unraveling the mysteries of early embryonic arrest: genetic factors and molecular mechanisms

J Zhang, J Lv, J Qin, M Zhang, X He, B Ma… - Journal of Assisted …, 2024 - Springer
Early embryonic arrest (EEA) is a critical impediment in assisted reproductive technology
(ART), affecting 40% of infertile patients by halting the development of early embryos from …

Characterization of cryptic complex chromosome rearrangements in balanced chromosomal rearrangement carriers and their PGT-SR clinical outcome assessments

D Cheng, H Ibrahim, K Luo, Y Gu, P Xie, Y Xiao… - Scientific Reports, 2024 - nature.com
Several reports have presented that balanced chromosomal rearrangements (BCRs)
carriers with normal phenotypes may be carriers of complex rearrangements. However, the …

Identification of complex and cryptic chromosomal rearrangements by optical genome mapping

S Shi, P Huang, R Yan, R Li - Molecular Cytogenetics, 2023 - Springer
Background Optical genome mapping (OGM) has developed into a highly promising method
for detecting structural variants (SVs) in human genomes. Complex chromosomal …

Evaluation of genetic risk of apparently balanced chromosomal rearrangement carriers by breakpoint characterization

Y Xiao, D Cheng, K Luo, M Li, Y Tan, G Lin… - Journal of Assisted …, 2024 - Springer
Purpose To report genetic characteristics and associated risk of chromosomal breaks due to
chromosomal rearrangements in large samples. Methods MicroSeq, a technique that …

[HTML][HTML] Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative …

D David, J Fino, R Oliveira, S Dória, CC Morton - Gene, 2023 - Elsevier
Naturally occurring balanced, unbalanced, and complex chromosomal rearrangements
have been reported to cause pathogenic genomic or genetic variants leading to infertility …

Mate-pair genome sequencing reveals structural variants for idiopathic male infertility

Z Dong, J Qian, TSM Law, MHK Chau, Y Cao, S Xue… - Human Genetics, 2023 - Springer
Currently, routine genetic investigation for male infertility includes karyotyping analysis and
PCR for Y chromosomal microdeletions to provide prognostic information such as sperm …

[HTML][HTML] Fertility problems in men carrying a translocation involved in breakpoints on chromosome 17p13: a retrospective, observational study

R Li - Medicine, 2022 - journals.lww.com
Male infertility is a multifactorial reproductive disorder. The effect of genetic factors on male
infertility has been the focus of research. Although a variety of genetic techniques are …

Molecular cytogenomics of human genetic disorders

Z Dong, KW Choy, CC Morton - Human Reproductive and Prenatal …, 2023 - Elsevier
With the advancement of molecular technologies, conventional cytogenetics has been
transited successfully to an era of cytogenomics for the investigation of human genetic …

[PDF][PDF] RESEARCH ADVANCES ON THE ADVERSE EFFECTS OF ANTIBIOTICS ON MALE FERTILITY

R Oniyangi, O Ogunleye, O Ojediran… - 2023 - researchgate.net
With the widespread use of antibiotics, bacterial infection-related morbidity and mortality
have significantly declined, revolutionizing modern medicine. However, concerns have been …

“Progressive motility” in elucidating novel genetic causes of male infertility

F Zhang - Asian Journal of Andrology, 2022 - journals.lww.com
INVITED EDITORIAL intraflagellar transport protein 25 (IFT25) and its interactions with other
IFT particle subunits during flagellogenesis. Genetic defects also affect sperm head. After …