Mei-Jiao Suo

Copy number variant analysis for syndromic congenital heart disease in the Chinese population

Feizhen Wu, Weicheng Chen, Guoying Huang, 2022, Human Genomics.

Functional analysis of HECA variants identified in congenital heart disease in the Chinese population

Wei Sheng, Ping Li, Yao Wu, 2022, Journal of clinical laboratory analysis.

PTPN11 Gene Mutations and Its Association with the Risk of Congenital Heart Disease

Guo-ying Huang, Wei Sheng, Zi-qing Xu, 2022, Disease markers.

X‐linked BCOR variants identified in Chinese Han patients with congenital heart disease

Wei Sheng, Ping Li, Guo-Ying Huang, 2022, The journal of gene medicine.

CpG site hypomethylation at ETS1-binding region regulates DLK1 expression in Chinese patients with Tetralogy of Fallot

Weili Yan, Yanyan Qian, Weicheng Chen, 2022, Molecular medicine reports.