Area of research
Genetics · Rheumatology
Research interest
Research focused on Genetics and Gene duplication, with related work in MLH1, Missense mutation, Lynch syndrome. Notable publications include 'Assessment of candidate genes and genetic heterogeneity in human non syndromic orofacial clefts specifically non syndromic cleft lip with or without palate', 'Emodin succinyl ester inhibits malignant proliferation and migration of hepatocellular carcinoma by suppressing the interaction of AR and EZH2', and 'Evaluation of a Novel Missense Mutation in ABCB4 Gene Causing Progressive Familial Intrahepatic Cholestasis Type 3'.
Emodin succinyl ester inhibits malignant proliferation and migration of hepatocellular carcinoma by suppressing the interaction of AR and EZH2
Evaluation of a Novel Missense Mutation in<i>ABCB4</i>Gene Causing Progressive Familial Intrahepatic Cholestasis Type 3
SNPs in folate pathway are associated with the risk of nonsyndromic cleft lip with or without cleft palate, a meta-analysis
Functional Characterization of a Missense Variant of <i>MLH1</i> Identified in Lynch Syndrome Pedigree
Combinatorial approach of <i>in silico</i> and <i>in vitro</i> evaluation of <i>MLH1</i> variant associated with Lynch syndrome like metastatic colorectal cancer
Assessment of candidate genes and genetic heterogeneity in human non syndromic orofacial clefts specifically non syndromic cleft lip with or without palate
A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family
WITHDRAWN: A 24-base pair duplication in exon one of HOXD13 gene linked to synpolydactyly type 1 in a Chinese family