Mao, Aiping

Comprehensive analysis of congenital adrenal hyperplasia using long-read sequencing

Liu, Y., Chen, M., Liu, J., Mao, A., Teng, Y., Yan, H., Zhu, H., Li, Z., Liang, D., & Wu, L. (2022) · Clinical Chemistry

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 80

Long-read sequencing: An effective method for genetic analysis of CYP21A2 variation in congenital adrenal hyperplasia

Li, H., Zhu, X., Yang, Y., Wang, W., Mao, A., Li, J., Bao, S., & Li, J. (2023) · Clinica Chimica Acta

Sexual Differentiation and DisordersGenomics and Rare Diseases

Cited by 23

Improved Genetic Characterization of Congenital Adrenal Hyperplasia by Long-Read Sequencing Compared with Multiplex Ligation-Dependent Probe Amplification Plus Sanger Sequencing

Yuan, D., Cai, R., Mao, A., Tan, J., Zhong, Q., Zeng, D., Tang, N., Wei, X., Huang, J., Zhang, Y., et al. (2024) · The Journal of Molecular Diagnostics

Sexual Differentiation and DisordersGenomics and Rare Diseases

Cited by 13

Targeted long-read sequencing facilitates effective carrier screening for complex monogenic diseases including spinal muscular atrophy, α-/β-thalassemia, 21-hydroxylase deficiency, and fragile-X syndrome

Li, S., Hua, R., Han, X., Xu, Y., Li, M., Gao, L., Ma, R., Meng, W., Mao, A., Wang, J., et al. (2025) · Journal of Translational Medicine

Genomics and Rare DiseasesPrenatal Screening and Diagnostics

Cited by 11