Ying Li

Variant analysis of PEX11B gene from a family with peroxisome biogenesis disorder 14B by whole exome sequencing

Yaqing Guo, Linlin Zhang, Yuan Tian, 2019, Molecular genetics & genomic medicine.

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Yaqing Guo, Erfeng Yuan, Yuan Tian, 2020, Human Genomics.

WNT3 hypomethylation counteracts low activity of the Wnt signaling pathway in the placenta of preeclampsia

Linlin Zhang, Yingying Li, Yangyang Yuan, 2021, Cellular and Molecular Life Sciences.

Detection of WNT2B, WIF1 and β-catenin expression in preeclampsia by placenta tissue microarray.

Linlin Zhang, Yingying Li, Yangyang Yuan, 2018, Clinica chimica acta; international journal of clinical chemistry.

Applying high‐throughput sequencing to identify and evaluate foetal chromosomal deletion and duplication

Linlin Zhang, Yueli Wu, Ling Zhao, 2020, Journal of cellular and molecular medicine.

Genetic examination for fetuses with increased nuchal translucency by exome sequencing

Yingying Li, S. Cui, Y. Zhi, 2022, The journal of obstetrics and gynaecology research.

MicroRNA-302a Functions as a Putative Tumor Suppressor in Colon Cancer by Targeting Akt

Zhiyong Wu, Guo-qing Zhang, Sheng-jie Sun, 2014, PloS one.

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Yaqing Guo, Linlin Zhang, Erfeng Yuan, 2020, Human genomics.

Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication

Yangyang Yuan, Erfeng Yuan, S. Cui, 2023, European Journal of Medical Research.

Altered DNA methylation and transcription of WNT2 and DKK1 genes in placentas associated with early-onset preeclampsia.

Linlin Zhang, Maodong Leng, Yingying Li, 2019, Clinica chimica acta; international journal of clinical chemistry.