Qingwei Wang

Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese families

B. Gong, Zhenglin Yang, Yi Shi, 2019, Molecular genetics & genomic medicine.

Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa.

B. Gong, Yi Shi, Fang Lu, 2019, Molecular medicine reports.

Single nucleotide polymorphisms within NFKBIA are associated with nasopharyngeal carcinoma susceptibility in Chinese Han population.

Shichuan Zhang, W. Ye, S. Deng, 2020, Cytokine.

Detection of serum IgM and IgG for COVID-19 diagnosis

Ping Shuai, Yi Zhang, Dingding Zhang, 2020, Science China Life Sciences.