Xi Zhang

Identification of two novel variants of the BCL11B gene in two Chinese pedigrees associated with neurodevelopmental disorders

Ying Yang, F. Che, Liyu Zhang, 2022, Frontiers in Molecular Neuroscience.

Mutations and variants of ONECUT1 in diabetes

Kyle J. Gaulton, Gopika G. Nair, B. Kuster, 2021, Nature Medicine.

A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsy

B. Xiao, H. Long, Hongjun Fang, 2020, Neurological Sciences.

Biallelic TET2 mutations and canonical ASXL1 mutations are frequent and cooccur in Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN): An institutional experience and review of literature

G. Crane, E. Hsi, Yu-Wei Cheng, 2023, EJHaem.

Primary cilia-associated protein IFT172 in ciliopathies

Shilin Luo, Bing Lang, Y. Miao, 2023, Frontiers in Cell and Developmental Biology.