Area of research
Oncology · Neurology
Research interest
Research interests include Cerebrovascular and genetic disorders, Cytokine Signaling Pathways and Interactions, Congenital heart defects research, and Chemokine receptors and signaling.
Identification of epigenetic factor KAT2B gene variants for possible roles in congenital heart diseases
Isobaric Tags for Relative and Absolute Quantitation in Proteomic Analysis of Potential Biomarkers in Invasive Cancer, Ductal Carcinoma In Situ, and Mammary Fibroadenoma
Associations of CXCL1 gene 5’UTR variations with ovarian cancer
Comparative analysis of SARS-CoV-2 and its receptor ACE2 with evolutionarily related coronaviruses
RBPJ polymorphisms associated with cerebral infarction diseases in Chinese Han population
Different effection of p.1125Val>Ala and rs11954856 in APC on Wnt signaling pathway
Rs2459976 in<i>ZW10</i>gene associated with congenital heart diseases in Chinese Han population
Characterization of variations in IL23A and IL23R genes: possible roles in multiple sclerosis and other neuroinflammatory demyelinating diseases
Polymorphisms in the CHIT1 gene: Associations with colorectal cancer
Characterization of human bone morphogenetic protein gene variants for possible roles in congenital heart disease
Combined effects of age and polymorphisms in Notch3 in the pathogenesis of cerebral infarction disease
Characterization of soluble N-ethylmaleimide-sensitive factor attachment protein receptor gene STX18 variations for possible roles in congenital heart diseases
Characterization of Transcriptional Repressor Gene MSX1 Variations for Possible Associations with Congenital Heart Diseases
Characterization of SMAD3 Gene Variants for Possible Roles in Ventricular Septal Defects and Other Congenital Heart Diseases
Identification of two novel critical mutations in PCNT gene resulting in microcephalic osteodysplastic primordial dwarfism type II associated with multiple intracranial aneurysms
Inherited neurovascular diseases affecting cerebral blood vessels and smooth muscle
Identification of a novel mutation associated with familial adenomatous polyposis and colorectal cancer
Characterization of Nodal/TGF-Lefty Signaling Pathway Gene Variants for Possible Roles in Congenital Heart Diseases
Identification of a Location at Chromosome 19p in a Big Chinese Family with Charcot-Marie-Tooth Disease
MiR-101 Is Involved in Human Breast Carcinogenesis by Targeting Stathmin1
Identification of a Known Mutation in Notch 3 in Familiar CADASIL in China