About: Polygenes, risk prediction, and targeted prevention of breast cancer

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scientific article published on 01 June 2008

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2008 (uk) artículu científicu espublizáu en xunu de 2008 (ast) scientific article published on 01 June 2008 (en)
publication date	wds:Q81523323-97DD3A59-7974-4853-ABC1-E31F3BFE297D
publication date	2008-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q81523323-36556CC7-0583-4C19-9BE2-7323929C474D
language of work or name	English
cites work	wds:Q81523323-130CAAAB-F7C0-4A9F-90A0-7624E723A989
cites work	Why most published research findings are false
author name string	wds:Q81523323-1F963587-A5FF-4DDD-AF1F-D93C73D420F9
author name string	Bruce A J Ponder
rdfs:label	Polygenes, risk prediction, and targeted prevention of breast cancer (en) Polygenes, risk prediction, and targeted prevention of breast cancer (nl)
skos:prefLabel	Polygenes, risk prediction, and targeted prevention of breast cancer (en) Polygenes, risk prediction, and targeted prevention of breast cancer (nl)
name	Polygenes, risk prediction, and targeted prevention of breast cancer (en) Polygenes, risk prediction, and targeted prevention of breast cancer (nl)
author	wds:Q81523323-2EDD5C71-161F-4B36-A110-31A713B7F623 wds:Q81523323-C78B6DB6-40B6-4B43-8D9C-6F17F23A7E74 wds:Q81523323-EAA3F144-3E82-4258-8A14-3223D4EB72C9
author	Douglas F. Easton Paul D P Pharoah Antonis C Antoniou
title	wds:Q81523323-38B4A853-13BD-401E-A572-CF965CAB8EE3
title	Polygenes, risk prediction, and targeted prevention of breast cancer (en)
page(s)	wds:Q81523323-BC9FBC2C-FD21-47B9-A199-0CA3139B816C
page(s)	2796-2803
instance of	wds:Q81523323-C2394731-557E-40B4-B744-B1ED3EA86A05
instance of	scholarly article
main subject	wds:Q81523323-8F7B0843-12B6-452A-956B-DC49CC559830 wds:Q81523323-D96936F5-2C75-48FB-8110-DA2CF88CF963
main subject	prevention breast cancer
PubMed ID	wds:Q81523323-D8D2E5AC-2027-4195-9D35-5F53E9A244DA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18579814
PubMed ID	18579814
published in	wds:Q81523323-F51EDE1C-C60F-47BD-908A-174873E762DB
published in	The New England Journal of Medicine
issue	wds:Q81523323-1129B707-5CC9-4FAD-82D0-7FB5AE87A064
volume	wds:Q81523323-584F219B-4264-4C29-B10E-EA6CF312C4A5
issue	26
volume	358
DOI	wds:Q81523323-F2B300F4-ED97-40B8-8DA2-A240DF770DEB
DOI	http://dx.doi.org/10.1056/NEJMSA0708739
DOI	10.1056/NEJMSA0708739
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q81523323
is cites work of	Utility of genetic determinants of lipids and cardiovascular events in assessing risk Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer Public health genomics and personalized prevention: lessons from the COGS project Population-based screening in the era of genomics Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals Incorporating genomics into breast and prostate cancer screening: assessing the implications Life insurance: genomic stratification and risk classification Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how? The pursuit of genome-wide association studies: where are we now? Inclusion of gene-gene and gene-environment interactions unlikely to dramatically improve risk prediction for complex diseases The inherited genetics of ovarian and endometrial cancer Prostate cancer risk-associated variants reported from genome-wide association studies: meta-analysis and their contribution to genetic Variation The role of chronic inflammation in obesity-associated cancers Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models Common low-penetrance risk variants associated with breast cancer in Polish women Assessing SNP-SNP interactions among DNA repair, modification and metabolism related pathway genes in breast cancer susceptibility Normal tissue reactions to radiotherapy: towards tailoring treatment dose by genotype A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium Risk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening Potential usefulness of single nucleotide polymorphisms to identify persons at high cancer risk: an evaluation of seven common cancers Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores Prediction of breast cancer risk based on profiling with common genetic variants Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies Clinical implications of genomics for cancer risk genetics Genetic susceptibility to breast cancer Identification of discriminating biomarkers for human disease using integrative network biology Finding the missing heritability of complex diseases Power and predictive accuracy of polygenic risk scores. Genetic prediction of quantitative lipid traits: comparing shrinkage models to gene scores Development of predictive models for airflow obstruction in alpha-1-antitrypsin deficiency. Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study Mutagen sensitivity, tobacco smoking and breast cancer risk: a case-control study Heritability in the genome-wide association era Inclusion of endogenous hormone levels in risk prediction models of postmenopausal breast cancer Genome-wide association studies of cancer A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer Breast cancer risks in women with a family history of breast or ovarian cancer who have tested negative for a BRCA1 or BRCA2 mutation Invited commentary: from genome-wide association studies to gene-environment-wide interaction studies--challenges and opportunities Brain plasticity and genetic factors Beyond odds ratios — communicating disease risk based on genetic profiles Tilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causation Pitfalls of predicting complex traits from SNPs Performance of common genetic variants in breast-cancer risk models Breed-predispositions to cancer in pedigree dogs. Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium Personalized medicine in screening for malignant disease: a review of methods and applications Genome-wide association study (GWAS)-identified disease risk alleles do not compromise human longevity A better coefficient of determination for genetic profile analysis. A multistage association study identifies a breast cancer genetic locus at NCOA7. Dopamine genetic risk score predicts depressive symptoms in healthy adults and adults with depression

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