Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
出版年份 2017 全文链接
标题
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
作者
关键词
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出版物
NATURE GENETICS
Volume 49, Issue 12, Pages 1767-1778
出版商
Springer Nature
发表日期
2017-10-24
DOI
10.1038/ng.3785
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers
- (2016) Christopher I. Amos et al. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
- The β2-adrenoceptor activates a positive cAMP-calcium feedforward loop to drive breast cancer cell invasion
- (2016) Cindy K. Pon et al. FASEB JOURNAL
- An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression
- (2016) Asaf Wyszynski et al. HUMAN MOLECULAR GENETICS
- Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
- (2016) Alison M Dunning et al. NATURE GENETICS
- F-BOX proteins in cancer cachexia and muscle wasting: Emerging regulators and therapeutic opportunities
- (2016) Ammar Sukari et al. SEMINARS IN CANCER BIOLOGY
- Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
- (2016) Fergus J. Couch et al. Nature Communications
- Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus
- (2016) Kate Lawrenson et al. Nature Communications
- Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1
- (2015) Dylan M. Glubb et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression
- (2015) Hatef Darabi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2
- (2015) N. Orr et al. HUMAN MOLECULAR GENETICS
- Interaction of Heat Shock Protein Cpn10 with the Cyclin E/Cdk2 Substrate Nuclear Protein Ataxia-Telangiectasia (NPAT) Is Involved in Regulating Histone Transcription
- (2015) Li Ling Zheng et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
- (2015) Nasim Mavaddat et al. JNCI-Journal of the National Cancer Institute
- Integrative analysis of 111 reference human epigenomes
- (2015) Anshul Kundaje et al. NATURE
- Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
- (2015) Kyriaki Michailidou et al. NATURE GENETICS
- Partitioning heritability by functional annotation using genome-wide association summary statistics
- (2015) Hilary K Finucane et al. NATURE GENETICS
- LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
- (2015) Brendan K Bulik-Sullivan et al. NATURE GENETICS
- Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
- (2015) Douglas F. Easton et al. NEW ENGLAND JOURNAL OF MEDICINE
- The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
- (2015) et al. SCIENCE
- Cyclin E2 is the predominant E-cyclin associated with NPAT in breast cancer cells
- (2015) Samuel Rogers et al. Cell Division
- Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
- (2015) Nasim Mavaddat et al. JNCI-Journal of the National Cancer Institute
- A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age
- (2014) H. Ahsan et al. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
- A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
- (2014) Suhas S.P. Rao et al. CELL
- Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
- (2014) Roger L. Milne et al. HUMAN MOLECULAR GENETICS
- A promoter-level mammalian expression atlas
- (2014) NATURE
- Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1
- (2014) Qiuyin Cai et al. NATURE GENETICS
- Global view of enhancer-promoter interactome in human cells
- (2014) B. He et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
- (2014) Maya Ghoussaini et al. Nature Communications
- Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers
- (2013) Juliet D. French et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
- (2013) Kerstin B. Meyer et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Super-Enhancers in the Control of Cell Identity and Disease
- (2013) Denes Hnisz et al. CELL
- Integrative eQTL-Based Analyses Reveal the Biology of Breast Cancer Risk Loci
- (2013) Qiyuan Li et al. CELL
- Combinatorial effects of multiple enhancer variants in linkage disequilibrium dictate levels of gene expression to confer susceptibility to common traits
- (2013) O. Corradin et al. GENOME RESEARCH
- Small-Molecule Ligands of Methyl-Lysine Binding Proteins: Optimization of Selectivity for L3MBTL3
- (2013) Lindsey I. James et al. JOURNAL OF MEDICINAL CHEMISTRY
- Genome-wide association studies identify four ER negative–specific breast cancer risk loci
- (2013) Montserrat Garcia-Closas et al. NATURE GENETICS
- Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
- (2013) Stig E Bojesen et al. NATURE GENETICS
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk
- (2013) Kyriaki Michailidou et al. NATURE GENETICS
- Systematic identification of trans eQTLs as putative drivers of known disease associations
- (2013) Harm-Jan Westra et al. NATURE GENETICS
- Systematic discovery and characterization of regulatory motifs in ENCODE TF binding experiments
- (2013) P. Kheradpour et al. NUCLEIC ACIDS RESEARCH
- Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
- (2013) Mia M. Gaudet et al. PLoS Genetics
- Matrix eQTL: ultra fast eQTL analysis via large matrix operations
- (2012) A. A. Shabalin BIOINFORMATICS
- Fast and accurate inference of local ancestry in Latino populations
- (2012) Yael Baran et al. BIOINFORMATICS
- Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
- (2012) N. Mavaddat et al. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
- 19p13.1 Is a Triple-Negative-Specific Breast Cancer Susceptibility Locus
- (2012) K. N. Stevens et al. CANCER RESEARCH
- Evaluation of Association Methods for Analysing Modifiers of Disease Risk in Carriers of High-Risk Mutations
- (2012) Daniel R. Barnes et al. GENETIC EPIDEMIOLOGY
- Annotation of functional variation in personal genomes using RegulomeDB
- (2012) A. P. Boyle et al. GENOME RESEARCH
- A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
- (2012) Afshan Siddiq et al. HUMAN MOLECULAR GENETICS
- Comprehensive molecular portraits of human breast tumours
- (2012) Daniel C. Koboldt et al. NATURE
- Bayesian refinement of association signals for 14 loci in 3 common diseases
- (2012) Julian B Maller et al. NATURE GENETICS
- Genome-wide association analysis identifies three new breast cancer susceptibility loci
- (2012) Maya Ghoussaini et al. NATURE GENETICS
- Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
- (2012) Bryan Howie et al. NATURE GENETICS
- Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
- (2012) Rebecca Hein et al. PLoS One
- Genome-Wide Association Study in East Asians Identifies Novel Susceptibility Loci for Breast Cancer
- (2012) Jirong Long et al. PLoS Genetics
- Genetic modifiers of cancer risk for BRCA1 and BRCA2 mutation carriers
- (2011) R. L. Milne et al. ANNALS OF ONCOLOGY
- RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome
- (2011) Bo Li et al. BMC BIOINFORMATICS
- Gene set analysis of genome-wide association studies: Methodological issues and perspectives
- (2011) Lily Wang et al. GENOMICS
- Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
- (2011) Q. Cai et al. HUMAN MOLECULAR GENETICS
- Beta-Blocker Use Is Associated With Improved Relapse-Free Survival in Patients With Triple-Negative Breast Cancer
- (2011) Amal Melhem-Bertrandt et al. JOURNAL OF CLINICAL ONCOLOGY
- Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study
- (2011) Olivia Fletcher et al. JNCI-Journal of the National Cancer Institute
- A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer
- (2011) Christopher A Haiman et al. NATURE GENETICS
- A linear complexity phasing method for thousands of genomes
- (2011) Olivier Delaneau et al. NATURE METHODS
- A User's Guide to the Encyclopedia of DNA Elements (ENCODE)
- (2011) PLOS BIOLOGY
- GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers
- (2011) Craig H Mermel et al. GENOME BIOLOGY
- METAL: fast and efficient meta-analysis of genomewide association scans
- (2010) C. J. Willer et al. BIOINFORMATICS
- ProbABEL package for genome-wide association analysis of imputed data
- (2010) Yurii S Aulchenko et al. BMC BIOINFORMATICS
- Evaluating the power to discriminate between highly correlated SNPs in genetic association studies
- (2010) Miriam S. Udler et al. GENETIC EPIDEMIOLOGY
- MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
- (2010) Yun Li et al. GENETIC EPIDEMIOLOGY
- A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population
- (2010) Antonis C Antoniou et al. NATURE GENETICS
- Genome-wide association study identifies five new breast cancer susceptibility loci
- (2010) Clare Turnbull et al. NATURE GENETICS
- Analysing biological pathways in genome-wide association studies
- (2010) Kai Wang et al. NATURE REVIEWS GENETICS
- Enrichment Map: A Network-Based Method for Gene-Set Enrichment Visualization and Interpretation
- (2010) Daniele Merico et al. PLoS One
- A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)
- (2009) Gilles Thomas et al. NATURE GENETICS
- Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1
- (2009) Wei Zheng et al. NATURE GENETICS
- Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2
- (2009) Shahana Ahmed et al. NATURE GENETICS
- A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
- (2009) Bryan N. Howie et al. PLoS Genetics
- The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions
- (2008) A C Antoniou et al. BRITISH JOURNAL OF CANCER
- Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer
- (2008) Simon N Stacey et al. NATURE GENETICS
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