Lanlan Zhang

发表

Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders

Wenman Wu, Dazhi Zhang, Songchang Chen, 2022, Human Genomics.

Associations of mitochondrial DNA copy number and deletion rate with early pregnancy loss.

Songchang Chen, Chenming Xu, Li-ya Wang, 2020, Mitochondrion.

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.

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.

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.

A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens

Jianxia Fan, Yeqing Qian, Songchang Chen, 2017, Prenatal diagnosis.

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.

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.