Kun Chen

Mediator MED23 Links Pigmentation and DNA Repair through the Transcription Factor MITF.

Xiao Yao, Yichi Xu, Jun Yan, 2017, Cell reports.

Molecular mechanism of a novel Ser362Asn mutation causing inherited FX deficiency in a Chinese family

Linhua Yang, Xiue Liu, X. Qin, 2020, International Journal of Hematology.

Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China

G. Wang, X. Qin, Sicheng Bian, 2023, Global Medical Genetics.