Wanli Meng

Identification of a novel 10.3 kb deletion causing α0-thalassemia by the third-generation sequencing: pedigree analysis and genetic diagnosis.

Jiaqi Li, Hui Li, Yayun Qin, 2023, Clinical biochemistry.

Case report: Long-read sequencing identified a novel 14.9-kb deletion of the α-globin gene locus in a family with α-thalassemia in China

Aiping Mao, Minhui Ma, Qun Zhu, 2023, Frontiers in Genetics.

Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing.

Aiping Mao, Haihong Shi, Jia-Qi Feng, 2023, Blood cells, molecules & diseases.

Knocking out Analysis of the CpxP gene using Crispr/Cas9 in Escherichia coli MG1655

Xiaoliang He, Xinran Yu, Yuwen Ren, 2020, AMB Express.

Comprehensive Analysis of Fragile X Syndrome: Full Characterization of the FMR1 Locus by Long-Read Sequencing.

D. Liang, Lingqian Wu, Aiping Mao, 2022, Clinical chemistry.