Author details

Full Name

Xiangdong Liu

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
33284381	Replication study and meta-analysis indicate a suggestive association of RUNX3 locus with primary biliary cholangitis.	Immunogenetics	2020
20639879	Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis.	Nat Genet	2010
20959405	The IFNG (IFN-gamma) genotype predicts cytogenetic and molecular response to imatinib therapy in chronic myeloid leukemia.	Clin Cancer Res	2010
20578265	Carriage of a tumor necrosis factor polymorphism amplifies the cytotoxic T-lymphocyte antigen 4 attributed risk of primary biliary cirrhosis: evidence for a gene-gene interaction.	Hepatology	2010
19875757	Clinical relevance of vascular endothelial growth factor (VEGFA) and VEGF receptor (VEGFR2) gene polymorphism on the treatment outcome following imatinib therapy.	Ann Oncol	2010
20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Nat Genet	2010
20639880	Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.	Nat Genet	2010
19898481	Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk.	Nat Genet	2009
19141860	Genetic variants in the candidate genes of the apoptosis pathway and susceptibility to chronic myeloid leukemia.	Blood	2009
19584153	Clinical relevance of a pharmacogenetic approach using multiple candidate genes to predict response and resistance to imatinib therapy in chronic myeloid leukemia.	Clin Cancer Res	2009
19333938	CTLA4/ICOS gene variants and haplotypes are associated with rheumatoid arthritis and primary biliary cirrhosis in the Canadian population.	Arthritis Rheum	2009
19276991	Genetic variants in IL-23R and ATG16L1 independently predispose to increased susceptibility to Crohn's disease in a Canadian population.	J Clin Gastroenterol	2009
19458352	Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.	N Engl J Med	2009
19006212	Geroderma osteodysplastica maps to a 4 Mb locus on chromosome 1q24.	Am J Med Genet A	2008
17693570	Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts.	J Med Genet	2008
16671954	The PTPN22 1858T variant is not associated with primary biliary cirrhosis.	Tissue Antigens	2006
16450402	DLG5 variants contribute to Crohn disease risk in a Canadian population.	Hum Mutat	2006
17133579	Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian population.	Arthritis Rheum	2006
15685536	A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease.	Gastroenterology	2005
15986374	Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations.	Arthritis Rheum	2005