B. Xiang

A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia

T. Cai, Xiang Chen, Haixia Zhang, 2019, BMC Medical Genetics.

Three novel recessive mutations in LAMA2, SYNE1, and TTN are identified in a single case with congenital muscular dystrophy

T. Cai, Xiang Chen, B. Xiang, 2017, Neuromuscular Disorders.

Identification of novel mutations in the HbF repressor gene BCL11A in patients with autism and intelligence disabilities

Jinchen Li, T. Cai, Zhouwen He, 2017, American journal of hematology.

Treadmill Exercise Promotes Neurogenesis in Ischemic Rat Brains via Caveolin-1/VEGF Signaling Pathways

Chan Liu, Fengxia Tu, Qiongyi Pang, 2016, Neurochemical Research.

Targeted deletion of Insm2 in mice result in reduced insulin secretion and glucose intolerance

M. Lan, Zhongsheng Sun, Guanjie Chen, 2018, Journal of Translational Medicine.