X. Peng

发表

Bioinformatics Analysis and Insights for the Role of COMMD7 in Hepatocellular Carcinoma

X. Yang, N. You, L. Zheng, 2020 .

ABTB2 Regulatory Variant as Predictor of Epirubicin-Based Neoadjuvant Chemotherapy in Luminal A Breast Cancer

Jiang Chang, Bing-he Xu, Yang Yang, 2020, Frontiers in Oncology.

Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer

Jiang Chang, X. Miao, Ying Zhu, 2022, Chinese medical journal.

A genetic variant in PIK3R1 is associated with pancreatic cancer survival in the Chinese population

B. Li, Jiang Chang, X. Miao, 2019, Cancer medicine.

Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese population

Yao Li, Jiang Chang, X. Miao, 2021, Archives of Toxicology.

Systematic Functional Interrogation of Genes in GWAS Loci Identified ATF1 as a Key Driver in Colorectal Cancer Modulated by a Promoter-Enhancer Interaction.

Jiang Chang, X. Miao, Jiaoyuan Li, 2019, American journal of human genetics.

A functional variant rs4442975 modulating FOXA1-binding affinity does not influence the risk or progression of breast cancer in Chinese Han population

Jiang Chang, X. Miao, Jiaoyuan Li, 2016, Oncotarget.

Integrative functional genomics identifies regulatory genetic variant modulating RAB31 expression and altering susceptibility to breast cancer

Jiang Chang, Jiaoyuan Li, Yang Yang, 2018, Molecular carcinogenesis.

Three functional variants were identified to affect RPS24 expression and significantly associated with risk of colorectal cancer

Jiang Chang, X. Miao, Jiaoyuan Li, 2019, Archives of Toxicology.

Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese population

Jiang Chang, X. Miao, Ying Zhu, 2021, Archives of Toxicology.

Genetic variants in m6A modification genes are associated with esophageal squamous-cell carcinoma in the Chinese population.

Jiang Chang, X. Miao, Yang Yang, 2020, Carcinogenesis.

A functional variant in GREM1 confers risk for colorectal cancer by disrupting a hsa-miR-185-3p binding site

Jiang Chang, X. Miao, Jiaoyuan Li, 2017, Oncotarget.

A genetic variant conferred high expression of CAV2 promotes pancreatic cancer progression and associates with poor prognosis.

M. Zhang, Jiang Chang, X. Miao, 2021, European journal of cancer.

A Rare Missense Variant in TCF7L2 Associates with Colorectal Cancer Risk by Interacting with a GWAS-Identified Regulatory Variant in the MYC Enhancer.

Yang Yang, Ying Zhu, Xiaoping Miao, 2018, Cancer research.

Exome-wide analyses identify low-frequency variant in CYP26B1 and additional coding variants associated with esophageal squamous cell carcinoma

Ying Zhu, Wei Chen, Tangchun Wu, 2018, Nature Genetics.

N6-methyladenosine mRNA methylation of PIK3CB regulates AKT signalling to promote PTEN-deficient pancreatic cancer progression

Jiang Chang, X. Miao, Ying Zhu, 2020, Gut.

A functional variant in the boundary of a topological association domain is associated with pancreatic cancer risk

Jiang Chang, X. Miao, Yang Yang, 2019, Molecular carcinogenesis.

Risk SNP-Mediated Enhancer–Promoter Interaction Drives Colorectal Cancer through Both FADS2 and AP002754.2

Jiang Chang, X. Miao, Ying Zhu, 2020, Cancer Research.

Breast cancer risk-associated variants at 6q25.1 influence risk of hepatocellular carcinoma in a Chinese population

Jiang Chang, Jiaoyuan Li, Yang Yang, 2017, Carcinogenesis.

A low‐frequency variant in SMAD7 modulates TGF‐β signaling and confers risk for colorectal cancer in Chinese population

Jiang Chang, X. Miao, Xiaobo Zhou, 2017, Molecular carcinogenesis.

AWESOME: a database of SNPs that affect protein post-translational modifications

Nan Yang, Ying Zhu, Jiang Chang, 2018, Nucleic Acids Res..

A Rare Variant P507L in TPP1 Interrupts TPP1–TIN2 Interaction, Influences Telomere Length, and Confers Colorectal Cancer Risk in Chinese Population

Yang Yang, Ying Zhu, Xiaoping Miao, 2018, Cancer Epidemiology, Biomarkers & Prevention.

ARareVariantP507L inTPP1 InterruptsTPP1–TIN2 Interaction, Influences Telomere Length, and Confers Colorectal Cancer Risk in Chinese Population

Jiang Chang, Jiaoyuan Li, Yang Yang, 2018 .

Integrative analysis identifies genetic variant modulating MICA expression and altering susceptibility to persistent HBV infection

Jiang Chang, Jiaoyuan Li, Yang Yang, 2019, Liver international : official journal of the International Association for the Study of the Liver.

A functional variant in TNXB promoter associates with the risk of esophageal squamous‐cell carcinoma

Jiang Chang, X. Miao, Yang Yang, 2020, Molecular carcinogenesis.

Genetic Predisposition to Colon and Rectal Adenocarcinoma Is Mediated by a Super-enhancer Polymorphism Coactivating CD9 and PLEKHG6

Jiang Chang, X. Miao, Yang Yang, 2020, Cancer Epidemiology, Biomarkers & Prevention.

BRCA1 missense polymorphisms are associated with poor prognosis of pancreatic cancer patients in a Chinese population

Kan Zhai, Jiang Chang, X. Miao, 2017, Oncotarget.

A single nucleotide polymorphism in the 3′-UTR of STAT3 regulates its expression and reduces risk of pancreatic cancer in a Chinese population

Jiang Chang, X. Miao, Jiaoyuan Li, 2016, Oncotarget.

Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations

Chen Wu, D. Lin, Kan Zhai, 2018, Nature Communications.

Evaluation of polymorphisms in microRNA‐binding sites and pancreatic cancer risk in Chinese population

Jiang Chang, X. Miao, Yang Yang, 2019, Journal of cellular and molecular medicine.

ANKLE1 N6‐Methyladenosine‐related variant is associated with colorectal cancer risk by maintaining the genomic stability

Jiang Chang, X. Miao, Yang Yang, 2020, International journal of cancer.

Exome-wide analyses identify low-frequency variant in CYP26B1 and additional coding variants associated with esophageal squamous cell carcinoma

Chen Wu, D. Lin, Kan Zhai, 2018, Nature Genetics.

CancerSplicingQTL: a database for genome-wide identification of splicing QTLs in human cancer

Nan Yang, Ying Zhu, Jiang Chang, 2018, Nucleic Acids Res..

Molecular Carcinogenesis

Jiang Chang, X. Miao, Yang Yang, 2019 .

Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations

Chen Wu, D. Lin, Kan Zhai, 2018, Nature Communications.

Functional characterization of a low-frequency V1937I variant in FASN associated with susceptibility to esophageal squamous cell carcinoma

Jiang Chang, X. Miao, Ying Zhu, 2020, Archives of Toxicology.

Molecular Carcinogenesis

Yang Yang, Ying Zhu, Y. Gong, 2020 .