S. Liao

发表

A Novel Variant of the KIF11 Gene, c.2922G>T, Is Associated with Microcephaly by Affecting RNA Splicing

X. Huo, B. Hao, Zhenglong Guo, 2021, Developmental Neuroscience.

Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese families

Hongdan Wang, Dong Wu, S. Liao, 2017, Molecular medicine reports.

METTL3-Mediated N6-Methyladenosine Modification Is Involved in the Dysregulation of NRIP1 Expression in Down Syndrome

Fan Yang, B. Hao, S. Liao, 2021, Frontiers in Cell and Developmental Biology.

Karyotype analysis with amniotic fluid in 12365 pregnant women with indications for genetic amniocentesis and strategies of prenatal diagnosis

S. Liao, H. Xiao, Y. L. Yang, 2016, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Epicardium-Derived Tbx18+ CDCs Transplantation Improve Heart Function in Infarcted Mice

B. Hao, Zhenglong Guo, Mengyuan Geng, 2022, Frontiers in Cardiovascular Medicine.

Case Report: Twin Pregnancy Gives Birth to a Girl with Partial Trisomy 21 Mosaicism after in vitro Fertilization and Embryo Transfer

B. Hao, Zhenglong Guo, Dong Wu, 2022, Frontiers in Genetics.

Experimental endometriosis reduction in rats treated with pioglitazone

Dongyun Zhang, M. He, Hong-yan Liu, 2012 .

Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population

Hong-yan Liu, Hongdan Wang, Xichuan Li, 2018, Scientific Reports.

[Analysis of CYP17A1 gene mutation in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency].

Bing M. Zhang, Shu-xian Cui, S. Liao, 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis

Jingbin Yan, Hongdan Wang, B. Zhu, 2017, Molecular medicine reports.

Maternal natural killer cell immunoglobulin receptor genes and human leukocyte antigen-C ligands influence recurrent spontaneous abortion in the Han Chinese population

Hongdan Wang, S. Liao, Hai Xiao, 2017, Experimental and therapeutic medicine.

Chromatin organizer SATB1 controls the cell identity of CD4+ CD8+ double-positive thymocytes by regulating the activity of super-enhancers

Yongchang Zhu, Y. Kohwi, T. Kohwi-Shigematsu, 2022, Nature Communications.

Chromatin organizer SATB1 controls the cell identity of CD4+ CD8+ double-positive thymocytes by compacting super-enhancers

Yongchang Zhu, Y. Kohwi, T. Kohwi-Shigematsu, 2021 .

The use of cffDNA in fetal sex determination during the first trimester of pregnancy of female DMD carriers.

Dong Wu, S. Liao, Tao Li, 2012, Intractable & rare diseases research.

METTL3-Mediated m6A RNA Methylation of ZBTB4 Interferes With Trophoblast Invasion and Maybe Involved in RSA

Hongdan Wang, S. Liao, Nana Huang, 2022, Frontiers in Cell and Developmental Biology.

A novel c.2326G>A KIT pathogenic variant in piebaldism.

B. Hao, S. Liao, Ke Yang, 2020, American journal of translational research.

Functional Analysis of a Compound Heterozygous Mutation in the VPS13B Gene in a Chinese Pedigree with Cohen Syndrome

Yuanyin Zhao, Y. Ke, S. Liao, 2020, Journal of Molecular Neuroscience.

Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation

Xin Ma, X. Lv, Hong-yan Liu, 2017, Medicine.

[Genetic and prenatal diagnosis for a haemophilia A family with two novel mutations of F8 gene].

B. Zhang, Hong-yan Liu, S. Liao, 2017, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Maternal cell contamination of prenatal samples and the potential effects on prenatal diagnosis results].

Zhao‐Yang Zhang, S. Liao, Tao Li, 2013, Zhonghua fu chan ke za zhi.

Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report.

Hongdan Wang, Tao Wang, Dong Wu, 2017, Molecular medicine reports.

22q11.2 Deletion Syndrome: Copy Number Variation Analysis in Two Patients

Dong Wu, S. Liao, Y. Chu, 2016 .

Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome.

Hong-yan Liu, Hongdan Wang, Xichuan Li, 2017, Clinica chimica acta; international journal of clinical chemistry.

DNA methylation study of fetus genome through a genome-wide analysis

M. He, Hongdan Wang, B. Zhu, 2014, BMC Medical Genomics.

Analysis of etiology, chromosome and prognosis for small left heart system development in 69 fetuses

Yihua He, Lei Huang, Taibing Fan, 2016, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

[Association of polymorphisms of HLA-DRB1 gene with unexplained recurrent spontaneous abortion in ethnic Hans from Henan].

M. He, Dong Wu, S. Liao, 2014, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Phase separation of Epstein-Barr virus EBNA2 protein reorganizes chromatin topology for epigenetic regulation

Yongchang Zhu, B. Hao, Zhaoqiang Li, 2021, Communications Biology.

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

Hongdan Wang, Dong Wu, S. Liao, 2016, Journal of Biomedical Science.

New compound heterozygous mutations of p. Thr101Ilefs 2 and p. Thr306Ale in a child from a Chinese family with 17α-hydroxylase/17, 20-lyase deficiency.

H. Zhang, T. Wang, S. Liao, 2015, Genetics and molecular research : GMR.

Amino acid 118 in the Deafness Causing (DFNA20/26) ACTG1 gene is a Mutational Hot Spot.

X. Liu, D. Yan, R. Mittal, 2018, Gene reports.

Mutations in the RS1 gene in a Chinese family with X-linked juvenile retinoschisis.

Dong Wu, S. Liao, Y. Chu, 2012, Intractable & rare diseases research.