Ying Yang

First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations

D. Wang, Yan Wang, F. Che, 2022, Frontiers in Genetics.

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease

Chong Shen, Lin Yu, Runsheng Chen, 2012, Nature Genetics.

Tri-allelic pattern of short tandem repeats identifies the murderer among identical twins and suggests an embryonic mutational origin.

Yuan-ming Wu, Ying Yang, Li-feng Wang, 2015, Forensic science international. Genetics.

A novel mitochondrial DNA deletion in a patient with Pearson syndrome and neonatal diabetes mellitus provides insight into disease etiology, severity and progression

Yan Wang, Dong Wang, Yuan-ming Wu, 2016, Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis.

WITHDRAWN: A novel mitochondrial DNA deletion in a patient with Pearson syndrome and neonatal diabetes mellitus provides insight into disease etiology, severity and progression.

Yan Wang, Dong Wang, Yuan-ming Wu, 2015, European Journal of Medical Genetics.