Jirong Long

发表

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

Jane E. Carpenter, Kyriaki Michailidou, France Labrèche, 2014, Human molecular genetics.

An evaluation of allele frequency estimation accuracy using pooled sequencing data

Yan Guo, Wei Zheng, Jiang Li, 2013, Int. J. Comput. Biol. Drug Des..

dmGWAS: dense module searching for genome-wide association studies in protein-protein interaction networks

Wei Zheng, Peilin Jia, Zhongming Zhao, 2011, Bioinform..

Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians

Wei Lu, Tien Yin Wong, Cheng Hu, 2011, Nature Genetics.

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Michael Jones, Peter Kraft, Arnaud Droit, 2017, Nature Genetics.

Evaluating Genome-Wide Association Study-Identified Breast Cancer Risk Variants in African-American Women

Wei Zheng, Ben Zhang, Douglas F. Easton, 2013, PloS one.

Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer

Ben Zhang, Gong Yang, Keitaro Matsuo, 2012, Nature Genetics.

Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence.

Wei Zheng, Ben Zhang, Jirong Long, 2011, The Lancet. Oncology.

Identification of novel susceptibility loci and genes for prostate cancer risk: A transcriptome-wide association study in over 140,000 European descendants.

Bogdan Pasaniuc, Xingyi Guo, John S Witte, 2019, Cancer research.

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk.

Harvey Risch, Yian A Chen, Mads Thomassen, 2018, Cancer research.

Novel genetic markers of breast cancer survival identified by a genome-wide association study.

Wei Zheng, Ying Zheng, Peter Kraft, 2012, Cancer research.

The use of next generation sequencing technology to study the effect of radiation therapy on mitochondrial DNA mutation.

Yan Guo, Yu Shyr, Fei Ye, 2012, Mutation research.

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Wei Lu, Wei Zheng, Mads Thomassen, 2013, Nature Genetics.

Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci.

Ying Zheng, Min-Ho Shin, Shoichiro Tsugane, 2016, Human molecular genetics.

Gene-environment interactions for breast cancer risk among Chinese women: a report from the Shanghai Breast Cancer Genetics Study.

Wei Lu, Wei Zheng, Ying Zheng, 2013, American journal of epidemiology.

Breast cancer risk variants at 6 q 25 display different phenotype associations and regulate ESR 1 , RMND 1 and CCDC 170

Wei Zheng, Mads Thomassen, Nicholas A. Sinnott-Armstrong, 2016 .

Breast cancer susceptibility associated with rs1219648 (fibroblast growth factor receptor 2) and postmenopausal hormone therapy use in a population-based United States study

Jirong Long, John M. Hampton, Kathleen M. Egan, 2012, Menopause.

Replication study for reported SNP associations with breast cancer survival

Wei Lu, Wei Zheng, Ying Zheng, 2012, Journal of Cancer Research and Clinical Oncology.

The effect of strand bias in Illumina short-read sequencing data

Jiang Li, Yan Guo, Yu Shyr, 2012, BMC Genomics.

Genetic Polymorphisms of Metastasis Suppressor Gene NME1 and Breast Cancer Survival

Wei Zheng, Hui Cai, Jirong Long, 2008, Clinical Cancer Research.

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

Peter Kraft, Mads Thomassen, Daniel J. Park, 2013, Breast Cancer Research.

APOBEC3 deletion polymorphism is associated with breast cancer risk among women of European ancestry.

Wei Zheng, Guoliang Li, Jirong Long, 2013, Carcinogenesis.

A genome-wide association study of breast cancer in women of African ancestry

Clement Adebamowo, Olufunmilayo I. Olopade, Gary K. Chen, 2012, Human Genetics.

Improved Variant Calling Accuracy by Merging Replicates in Whole-Exome Sequencing Studies

Chun Li, Jirong Long, Wei Zheng, 2014, BioMed research international.

A common deletion in the APOBEC3 genes and breast cancer risk.

Wei Lu, Wei Zheng, Ying Zheng, 2013, Journal of the National Cancer Institute.

Genome‐Wide Family‐Based Linkage Analysis of Exome Chip Variants and Cardiometabolic Risk

Carl D Langefeld, Jirong Long, Nicholette D. Palmer, 2014, Genetic epidemiology.

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Patrick Neven, Peter Kraft, Nazneen Rahman, 2015 .

Association analyses of East Asian individuals and trans‐ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

Sanghoon Moon, Cheng Hu, Xu Lin, 2017, Human molecular genetics.

Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4

Bo Dai, Qiang Ding, Henrik Gronberg, 2012, Nature Genetics.

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.

Wei Lu, Päivi Heikkilä, Peter Kraft, 2013, American journal of human genetics.

Genome-wide association studies identify four ER negative–specific breast cancer risk loci

Patrick Neven, Michael Jones, Wei Lu, 2013, Nature Genetics.

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.

Fernando Pires Hartwig, Claude Bouchard, Christian Gieger, 2018, American journal of human genetics.

Relation of FGFR2 genetic polymorphisms to the association between oral contraceptive use and the risk of breast cancer in Chinese women.

Qi Dai, Kai Gu, Jirong Long, 2011, American journal of epidemiology.

Genetic and clinical predictors for breast cancer risk assessment and stratification among Chinese women.

Wei Lu, Ying Zheng, Yu Shyr, 2010, Journal of the National Cancer Institute.

Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family‐Based Linkage and Association in the IRAS Family Study

John Blangero, Carl D Langefeld, Jirong Long, 2017, Annals of human genetics.

Title Identification of a functional genetic variant at 16 q 12 . 1 for breastcancer risk : results from the Asia Breast Cancer Consortium

Wei Lu, Guoliang Li, Kexin Chen, 2010 .

Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk

Yan Guo, Ben Zhang, Min-Ho Shin, 2014, Nature Genetics.

GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.

Harvey Risch, Peter Kraft, Mark McEvoy, 2016, Human molecular genetics.

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

Wei Lu, Nina Ditsch, Julian Peto, 2013, American journal of human genetics.

Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes

Peter Kraft, Jamie Allen, Xingyi Guo, 2018, Human molecular genetics.

Identification of nine new susceptibility loci for endometrial cancer

Peter Kraft, Mark McEvoy, Julian Peto, 2018, Nature Communications.

Identification of a Functional Genetic Variant at 16q12.1 for Breast Cancer Risk: Results from the Asia Breast Cancer Consortium

Wei Lu, Chiun-Sheng Huang, Guoliang Li, 2010, PLoS genetics.

Meat Intake, Heterocyclic Amine Exposure, and Metabolizing Enzyme Polymorphisms in Relation to Colorectal Polyp Risk

Yu Shyr, Reid M. Ness, Jirong Long, 2008, Cancer Epidemiology Biomarkers & Prevention.