N.‐N. Sun

CHST15 gene germline mutation is associated with the development of familial myeloproliferative neoplasms and higher transformation risk

Yang Zhang, Guoyu Hu, Guangsen Zhang, 2022, Cell Death & Disease.

CEBPA mutation in a case of chronic myeloid leukemia presenting in myeloid blast crisis

Guangsen Zhang, Zhao Cheng, Ji Li, 2017, Leukemia & lymphoma.

Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypes.

Guangsen Zhang, Zhao Cheng, Yong Chen, 2016, Thrombosis research.

A novel Ala275Val mutation in factor X gene influences its structural compatibility and impairs intracellular trafficking and coagulant activity.

Yongheng Chen, Guangsen Zhang, Hongling Peng, 2016, Thrombosis research.

A TET2 rs3733609 C/T genotype is associated with predisposition to the myeloproliferative neoplasms harboring JAK2V617F and confers a proliferative potential on erythroid lineages

Yun-xiao Xu, Hongling Peng, Sufang Liu, 2016, Oncotarget.

A gain‐of‐function mutation in TNFRSF13B is a candidate for predisposition to familial or sporadic immune thrombocytopenia

Z. Cheng, Yongjia Yin, X. Xiao, 2017, Journal of thrombosis and haemostasis : JTH.