D
Dayuan Shi
Researcher at Zhengzhou University
Publications - 4
Citations - 168
Dayuan Shi is an academic researcher from Zhengzhou University. The author has contributed to research in topics: Histone code & Single-nucleotide polymorphism. The author has an hindex of 3, co-authored 3 publications receiving 79 citations.
Papers
More filters
Journal ArticleDOI
Resetting histone modifications during human parental-to-zygotic transition
Weikun Xia,Jiawei Xu,Guang Yu,Guidong Yao,Kai Xu,Xueshan Ma,Nan Zhang,Bofeng Liu,Tong Li,Zili Lin,Xia Chen,Lijia Li,Qiujun Wang,Dayuan Shi,Senlin Shi,Yile Zhang,Wenyan Song,Haixia Jin,Linli Hu,Zhiqin Bu,Yang Wang,Jie Na,Wei Xie,Yingpu Sun +23 more
TL;DR: By combining chromatin and transcriptome maps, the data unveil a priming phase connecting human parental-to-zygotic epigenetic transition and transcription circuitry and asymmetric H3K27me3 patterning during early lineage specification.
Journal ArticleDOI
Association between the quality of inner cell mass and first trimester miscarriage after single blastocyst transfer.
Dayuan Shi,Jiawei Xu,Meixiang Zhang,Wenbin Niu,Hao Shi,Guidong Yao,Ying Li,Nan Zhang,Yingpu Sun +8 more
TL;DR: Chromosomal aberration of embryo is an important genetic factor for first trimester miscarriage, and the quality of ICM is a potential indicator for euploid miscarriage.
Journal ArticleDOI
Live births following preimplantation genetic testing for dynamic mutation diseases by karyomapping: a report of three cases
Dayuan Shi,Jiawei Xu,Wenbin Niu,Yidong Liu,Hao Shi,Guidong Yao,Senlin Shi,Gang Li,Wenyan Song,Haixia Jin,Yingpu Sun +10 more
TL;DR: Karyomapping is a highly powerful and efficient approach for dynamic mutation detection in preimplantation embryos and the birth of healthy babies that are free of the pathogenic gene for dynamic mutations diseases in patients receiving PGT-M is reported.
Peer ReviewDOI
Genetics Etiologies Associated with Fetal Growth Restriction
Dayuan Shi,Luyao Cai,Luming Sun +2 more
TL;DR: An overview of genetic defects related to FGR is provided to highlight the importance of prenatal genetic counseling and testing for precise diagnosis and management of FGR.