Yiyao Chen

发表

Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening

Xiaoqiang Cai, Congjian Xu, Xiaotian Li, 2022, Cell Discovery.

Classification and Interpretation for 11 FBN1 Variants Responsible for Marfan Syndrome and Pre-implantation Genetic Testing (PGT) for Two Families Successfully Blocked Transmission of the Pathogenic Mutations

D. Lu, Hongjun Fei, Songchang Chen, 2021, Frontiers in Molecular Biosciences.

Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility

D. Lu, Songchang Chen, Zhengwen Jiang, 2021, Journal of Human Genetics.

Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1

Yeqing Qian, Hongjun Fei, Songchang Chen, 2020, Frontiers in Genetics.

Comprehensive preimplantation genetic testing by massively parallel sequencing.

Hui Jiang, Xinming Liang, Xuyang Yin, 2020, Human reproduction.

Prenatal Diagnosis of Chromosomal Mosaicism in Over 18,000 Pregnancies: A Five-Year Single-Tertiary-Center Retrospective Analysis

Xin-Rong Zhao, Yanlin Wang, Shuyuan Li, 2022, Frontiers in Genetics.

Targeted Sequencing and RNA Assay Reveal a Noncanonical JAG1 Splicing Variant Causing Alagille Syndrome

Songchang Chen, Chenming Xu, Junyu Zhang, 2020, Frontiers in Genetics.

Targeted sequencing identifies a novel SH2D1A pathogenic variant in a Chinese family: Carrier screening and prenatal genetic testing

Chenming Xu, Jun-Yu Zhang, Shuyuan Li, 2017, PloS one.

Integrated facial analysis and targeted sequencing identifies a novel KDM6A pathogenic variant resulting in Kabuki syndrome

Hongjun Fei, Songchang Chen, Chenming Xu, 2018, Journal of Bio-X Research.

Case Report: Preimplantation Genetic Testing and Pregnancy Outcomes in Women With Alport Syndrome

Chenming Xu, Zhi-yang Zhou, Zi-Ru Jiang, 2021, Frontiers in Genetics.

Expanding the Scope of Non-invasive Prenatal Testing to Detect Fetal Chromosomal Copy Number Variations

D. Lu, Hongjun Fei, Songchang Chen, 2021, Frontiers in Molecular Biosciences.

Identification of significant biomarkers and pathways associated with gastric carcinogenesis by whole genome-wide expression profiling analysis.

Hongjun Fei, Chenming Xu, Jun-Yu Zhang, 2018, International journal of oncology.

Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility

D. Lu, Li Jin, Songchang Chen, 2021, Journal of human genetics.

Copy number variation sequencing for the products of conception: What is the optimal testing strategy.

Renyi Hua, Lanlan Zhang, Yiyao Chen, 2024, Clinica chimica acta; international journal of clinical chemistry.