About: A role for common genomic variants in the assessment of familial breast cancer

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About: A role for common genomic variants in the assessment of familial breast cancer Goto Sponge NotDistinct Permalink

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scientific article published on 29 October 2012

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2012 (uk) scientific article published on 29 October 2012 (en) artículu científicu espublizáu n'ochobre de 2012 (ast)
publication date	wds:Q85312916-5B09137B-D087-4941-81FD-31EDB6BBE91D
publication date	2012-10-29 00:00:00Z (xsd:dateTime)
author name string	wds:Q85312916-2E0BD78B-4A5D-483B-A0F0-613C0D694F04 wds:Q85312916-2E582D08-EE92-4ECE-B9A6-7EB6DB3520AC wds:Q85312916-31C8E6EA-DD95-4742-955D-38D5351397DA wds:Q85312916-3A0B6344-F104-4939-BF3D-4539476E1F35 wds:Q85312916-89F4F0ED-CA07-4007-8D5A-CF910CB3A470 wds:Q85312916-987416B7-0E94-4398-9655-287A12761760 wds:Q85312916-9A199E75-8E6F-4C33-BA62-BE850D95F3DD wds:Q85312916-BEE99564-3A05-41DF-8F46-AD884BEA5520
author name string	Gillian Mitchell Paul A James Jonathan Beesley Alison H Trainer Joanne McKinley Marion Harris Xiao Qing Chen Sarah Sawyer
rdfs:label	A role for common genomic variants in the assessment of familial breast cancer (en) A role for common genomic variants in the assessment of familial breast cancer (nl)
skos:prefLabel	A role for common genomic variants in the assessment of familial breast cancer (en) A role for common genomic variants in the assessment of familial breast cancer (nl)
name	A role for common genomic variants in the assessment of familial breast cancer (en) A role for common genomic variants in the assessment of familial breast cancer (nl)
author	wds:Q85312916-CDB55435-B2D5-4DC9-BFA9-2713D5FAF7B2 wds:Q85312916-E6136E41-BAB8-4118-B166-81968A0F1E49 wds:Q85312916-F9DC85F8-272F-457C-AD4F-F3F71E3D3A8C
author	Georgia Chenevix-Trench David Bowtell Geoffrey J. Lindeman
title	wds:Q85312916-6CC33535-C887-41D5-8081-9B6B8A778E23
title	A role for common genomic variants in the assessment of familial breast cancer (en)
page(s)	wds:Q85312916-4FCF1A9A-B660-4F91-A317-DE0B51CEF860
page(s)	4330-4336
instance of	wds:Q85312916-BCF8974E-8E98-429E-BB05-415718337EBE
instance of	scholarly article
main subject	wds:Q85312916-4A4918AF-6D4C-412F-93DF-1065716D54BF
main subject	breast cancer
PubMed ID	wds:Q85312916-C77AE98E-FEF5-43F5-A2D3-D78AACB9BA3C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23109704
PubMed ID	23109704
published in	wds:Q85312916-ED4A5DAE-E079-4DED-A65B-2A1691C3938C
published in	Journal of Clinical Oncology
issue	wds:Q85312916-BDA32B5E-2777-418A-91A7-78FFB521DE0F
volume	wds:Q85312916-BB6490BC-F5CB-4963-98A6-0C3216EBDB32
issue	35
volume	30
DOI	wds:Q85312916-015A584E-BD1A-46D1-A7EB-4749FDC11EAA
DOI	http://dx.doi.org/10.1200/JCO.2012.41.7469
DOI	10.1200/JCO.2012.41.7469
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q85312916
is cites work of	Prediction of breast cancer risk based on profiling with common genetic variants Clinical implications of genomics for cancer risk genetics Monogenic and polygenic determinants of sarcoma risk: an international genetic study Two decades after BRCA: setting paradigms in personalized cancer care and prevention Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study Behavioral and psychosocial responses to genomic testing for colorectal cancer risk Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab Tumour morphology predicts PALB2 germline mutation status The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia. Discovery and replication of microRNAs for breast cancer risk using genome-wide profiling Common breast cancer risk variants in the post-COGS era: a comprehensive review Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles Long-term prognosis of early-onset breast cancer in a population-based cohort with a known BRCA1/2 mutation status Gene-expression patterns in peripheral blood classify familial breast cancer susceptibility Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context Diagnosis and Management of Hereditary Sarcoma. Breast cancer risk prediction using a clinical risk model and polygenic risk score Genetic variants demonstrating flip-flop phenomenon and breast cancer risk prediction among women of African ancestry. Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks. BRCA1 and BRCA2 5' noncoding region variants identified in breast cancer patients alter promoter activity and protein binding Systematic evaluation of cancer-specific genetic risk score for 11 types of cancer in The Cancer Genome Atlas and Electronic Medical Records and Genomics cohorts Six low-penetrance SNPs for the estimation of breast cancer heritability: A family-based study in Caucasian Italian patients Towards a more precise and individualized assessment of breast cancer risk Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer Genetic risk transmission in a family affected by familial breast cancer Large genomic rearrangements in the familial breast and ovarian cancer gene BRCA1 are associated with an increased frequency of high risk features Genomic Biomarkers for Breast Cancer Risk Population-Wide Genetic Risk Prediction of Complex Diseases: A Pilot Feasibility Study in Macau Population for Precision Public Healthcare Planning. Genetic Testing to Guide Risk-Stratified Screens for Breast Cancer High-risk women's risk perception after receiving personalized polygenic breast cancer risk information. Clinical applications of polygenic breast cancer risk: a critical review and perspectives of an emerging field
is cites work of	wds:Q33916899-3D4B91CE-4CD1-4FA6-A8A4-3A35DDDF39C5 wds:Q37699255-B0072DD5-B5F1-41DA-88A8-17A1FB254AEF wds:Q37583113-1F6F6835-C1CA-4079-A605-8A97AFCEFFA3 wds:Q35832873-127210AD-2366-45A5-8820-1859146D7599 wds:Q52875169-4F8049B3-FEEB-4859-8861-77A0BED64A8D wds:Q92993050-19509EBA-EE84-4B5C-A59C-E95DF51C31AF wds:Q34767345-4E634060-A6AD-487A-9089-F72F15DE84A8 wds:Q32491318-F6E96F70-4936-43B1-86FD-41A2E405C2C6 wds:Q33820594-28EBB197-8CB8-4858-B568-D29C0C128FF9 wds:Q37410693-DF66A406-D702-44F5-AB07-A07863D5612E wds:Q47207156-7CCF9CA6-F0C0-4593-9FD3-9CDB26F1A5BE

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