Meiyan Zhang

Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy

Nan Li, Li Fang, Qian Liu, 2018, Journal of Medical Genetics.

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach

Jun Zhang, Wei Wang, Hui Jiang, 2016, Genetics in Medicine.

Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case report

Fuyan Lv, Shiguo Liu, Hong Jiang, 2019, BMC Medical Genetics.

A comprehensive assessment of Next‐Generation Sequencing variants validation using a secondary technology

Ye Yin, Hongyun Zhang, Qian Yang, 2019, Molecular genetics & genomic medicine.