Ruizhong Zhang

Evaluation of GWAS-identified SNPs at 6p22 with neuroblastoma susceptibility in a Chinese population.

The Association between GWAS-identified BARD1 Gene SNPs and Neuroblastoma Susceptibility in a Southern Chinese Population.

Identification of Circulating MicroRNAs in Biliary Atresia by Next-Generation Sequencing.

LMO1 gene polymorphisms contribute to decreased neuroblastoma susceptibility in a Southern Chinese population.

Association of potentially functional variants in the XPG gene with neuroblastoma risk in a Chinese population.

Potentially functional polymorphisms in the LIN28B gene contribute to neuroblastoma susceptibility in Chinese children.

Decreased expression of miR-33 in fetal lungs of nitrofen-induced congenital diaphragmatic hernia rat model.

Lack of Associations between Gene Polymorphisms and Neuroblastoma Susceptibility in a Chinese Population.

Silver nanoparticle treatment ameliorates biliary atresia syndrome in rhesus rotavirus inoculated mice.

Common variations within gene and neuroblastoma susceptibility in a Southern Chinese population.

The gene rs1042522 C>G polymorphism and neuroblastoma risk in Chinese children.

gene rs11037575 C>T polymorphism confers neuroblastoma susceptibility in a Southern Chinese population.

Large-scale replication study identified multiple independent SNPs in synergistically associated with Hirschsprung disease in Southern Chinese population.

Genetic Variations of GWAS-Identified Genes and Neuroblastoma Susceptibility: a Replication Study in Southern Chinese Children.

Association of polymorphism in the VEGFA gene 3'-UTR +936T/C with susceptibility to biliary atresia in a Southern Chinese Han population.

rs11655237 C>T confers neuroblastoma susceptibility in Chinese population.

Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population.

Association between Gene Polymorphisms and Neuroblastoma Risk in Chinese Children: A Two-Center Case-Control Study.

Functional Polymorphisms at ERCC1/XPF Genes Confer Neuroblastoma Risk in Chinese Children.

HOTAIR gene polymorphisms contribute to increased neuroblastoma susceptibility in Chinese children.

Associations between lncRNA polymorphisms and neuroblastoma risk in Chinese children.

The intragenic epistatic association of with biliary atresia in Southern Han Chinese population.

Association of VAMP5 and MCC genetic polymorphisms with increased risk of Hirschsprung disease susceptibility in Southern Chinese children.

super-enhancer polymorphism rs2168101 G>T correlates with decreased neuroblastoma risk in Chinese children.

Association of Common Genetic Variants in Pre-microRNAs and Neuroblastoma Susceptibility: A Two-Center Study in Chinese Children.

Association between DSCAM polymorphisms and non-syndromic Hirschsprung disease in Chinese population.

Association of IL18 genetic polymorphisms with increased risk of Biliary atresia susceptibility in Southern Chinese children.

The Role of Neonatal Gr-1 Myeloid Cells in a Murine Model of Rhesus-Rotavirus-Induced Biliary Atresia.

Epistatic Association of CD14 and NOTCH2 Genetic Polymorphisms with Biliary Atresia in a Southern Chinese Population.

Pleiotropic effect of common variants in Hirschsprung disease and neuroblastoma.

rs7973450 A>G increases neuroblastoma risk in Chinese children: a four-center case-control study.

Irrelevance of USF2 rs916145 polymorphism with the risk of biliary atresia susceptibility in Southern Chinese children.

Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia.

PDGFA gene rs9690350 polymorphism increases biliary atresia risk in Chinese children.

Down-regulation of STAT3 enhanced chemokine expression and neutrophil recruitment in biliary atresia.

Modulatory effects of adiponectin on the polarization of tumor-associated macrophages.

Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism.

Role of CD56-expressing immature biliary epithelial cells in biliary atresia.

De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca.

Autoimmune liver disease-related autoantibodies in patients with biliary atresia.

Downregulation of Hes1 expression in experimental biliary atresia and its effects on bile duct structure.

Identification of Genes Associated With Hirschsprung Disease, Based on Whole-Genome Sequence Analysis, and Potential Effects on Enteric Nervous System Development.

Cancer gene mutations in congenital pulmonary airway malformation patients.

CD177 cells produce neutrophil extracellular traps that promote biliary atresia.

Peripheral blood CD177 cells as an early diagnostic marker for biliary atresia: A prospective multicentre study in pediatric patients with cholestasis.