Area of research
Cognitive Neuroscience · Radiology, Nuclear Medicine and Imaging
Research interest
Research focused on Dravet syndrome and Single-nucleotide polymorphism, with related work in Basketball, Intravoxel incoherent motion, Hue. Notable publications include 'A Novel Variant of the CHD2 Gene Associated With Developmental Delay and Myoclonic Epilepsy', 'Identification of susceptible genes for complex chronic diseases based on disease risk functional SNPs and interaction networks', and 'Alterations of triple network dynamic connectivity and repetitive behaviors after mini-basketball training program in children with autism spectrum disorder'.
Alterations of triple network dynamic connectivity and repetitive behaviors after mini-basketball training program in children with autism spectrum disorder
Advancing human-use experience for real-world evidence for the registration of traditional Chinese medicine products in China
The impact of a ball sports combination training program on physical fitness and body mass Index in children with autism spectrum disorder
A Novel Variant of the CHD2 Gene Associated With Developmental Delay and Myoclonic Epilepsy
Generation of an iPSC line (SMCPGi001-A) from a patient with Bain type X-linked mental retardation syndrome carrying HNRNPH2 gene mutation
The value of intravoxel incoherent motion imaging in predicting the survival of patients with astrocytoma
Identification of susceptible genes for complex chronic diseases based on disease risk functional SNPs and interaction networks
Distinct activated cortical areas and volumes in Uygur-Chinese bilinguals