Ying Weng

Identification of novel ACAN mutations in two Chinese families and genotype–phenotype correlation in patients with 74 pathogenic ACAN variations

Zhuxi Li, Xiaoping Luo, Yanqin Ying, 2021, Molecular genetics & genomic medicine.

Absence of mutations in human ubiquitin fusion-degradation protein gene in tetralogy of Fallot

Jen-Her Lu, M. Chung, B. Hwang, 2001, Journal of Molecular Medicine.

Deletion at 12q12 increases the risk of developmental delay and intellectual disability

Xiaoping Luo, L. Hou, Ying Weng, 2018, Annals of human genetics.

A High Proportion of Novel ACAN Mutations and Their Prevalence in a Large Cohort of Chinese Short Stature Children

Yiping Shen, J. Chen, Xiaoping Luo, 2021, The Journal of clinical endocrinology and metabolism.