Area of research
Rheumatology · Molecular Biology
Research interest
Research focused on Genome-wide association study and Disease, with related work in Plasmodium (life cycle), Plasmodium berghei, Meta-analysis. Notable publications include 'Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome', 'Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups', and 'Meta-analysis Followed by Replication Identifies Loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as Associated with Systemic Lupus Erythematosus in Asians'.
Human antibody targeting <i>Vibrio cholerae</i> O1 O-specific polysaccharide induces an amotile hypovirulent bacterial phenotype: mechanism of protection against cholera
Deep Learning-based Malicious Energy Attack Detection in Sustainable IoT Network
Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups
Excessive deubiquitination of NLRP3-R779C variant contributes to very-early-onset inflammatory bowel disease development
FGFR3 deficiency enhances CXCL12-dependent chemotaxis of macrophages via upregulating CXCR7 and aggravates joint destruction in mice
Disruption of <i>mosGILT</i> in <i>Anopheles gambiae</i> impairs ovarian development and <i>Plasmodium</i> infection
<i>Anopheles gambiae</i> Lacking <i>AgTRIO</i> Inefficiently Transmits <i>Plasmodium berghei</i> to Mice
A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission
Immunization with AgTRIO, a Protein in Anopheles Saliva, Contributes to Protection against Plasmodium Infection in Mice
Identification of ST3AGL4, MFHAS1, CSNK2A2 and CD226 as loci associated with systemic lupus erythematosus (SLE) and evaluation of SLE genetics in drug repositioning
p204 Is Required for Canonical Lipopolysaccharide-induced TLR4 Signaling in Mice
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Meta-analysis Followed by Replication Identifies Loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as Associated with Systemic Lupus Erythematosus in Asians