About: Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

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About: Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk Goto Sponge NotDistinct Permalink

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scientific article (publication date: 2013)

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description	наукова стаття, опублікована у 2013 (uk) artículu científicu espublizáu en 2013 (ast) vědecký článek publikovaný v roce 2013 (cs) 2013 թվականին հրատարակված գիտական հոդված (hy) 2013 թուականին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت عام 2013) (ar) article scientifique (publié 2013) (fr) articolo scientifico (pubblicato il 2013) (it) artigo científico (publicado na 2013) (pt) vedecký článok (publikovaný 2013) (sk) vetenskaplig artikel (publicerad på 2013) (sv) videnskabelig artikel (udgivet 2013) (da) wetenschappelijk artikel (gepubliceerd in 2013) (nl) scientific article (publication date: 2013) (en) im Januar 2013 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q27008356-810A4FF5-1997-4094-95AA-E70045EE9985
publication date	2013-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q27008356-09C7F332-9E16-4219-A240-01BC48983B85
language of work or name	English
cites work	wds:Q27008356-0ACC3C45-DFB7-4991-B5C6-07B201474240 wds:Q27008356-218F08FA-2C8E-40A9-9760-DE909B02AAC5 wds:Q27008356-2855AE86-965F-4841-B4E9-B89C8A8B9268 wds:Q27008356-2B6E80AC-8F14-4318-9590-F0838AA6709F wds:Q27008356-3865100B-2B8F-4135-BA99-1BA78058E2FE wds:Q27008356-3D5E2324-B100-4AC6-A4A7-90286912BD16 wds:Q27008356-3D732379-15DC-44DA-B06E-885DF017F17E wds:Q27008356-47335B27-8B9F-4A6E-83FB-95FDC18B7B85 wds:Q27008356-4D095E98-F014-46AE-8B8A-1F65ED2D693A wds:Q27008356-52919219-0146-4FC9-883E-10FE307BAB19 wds:Q27008356-62B09EC6-6F99-46DC-A344-2DE1C7B489A2 wds:Q27008356-62FFB26A-A72C-4434-864E-70CCEB070940 wds:Q27008356-6A2EB8DB-8C46-418A-B129-47DEA879F204 wds:Q27008356-728225C4-C69B-48DF-9038-FE9A5C787342 wds:Q27008356-764AAE2D-C80A-458A-8356-BD5446D143B4 wds:Q27008356-77F65AD9-FE8F-4C0E-B8BB-67D096DA5CC6 wds:Q27008356-7AB5A051-D221-4EAF-9393-4C36DC6424B1 wds:Q27008356-7D08017B-7FA7-4D4D-B40A-25FC1CB4F3F1 wds:Q27008356-7D1D7022-84DF-49C7-8C7E-A3D94ACD5CB7 wds:Q27008356-7E219397-6839-4082-8A31-6657590B7F58 wds:Q27008356-80AF5E6C-59AB-4BCA-B21F-F3352E9581B5 wds:Q27008356-85318038-A440-4A5D-A449-FD5D50F04F38 wds:Q27008356-868652B9-6010-41BF-8B64-46D7279D716B wds:Q27008356-8A53A0B4-61D7-4FC8-B775-D62FCF8DD4BE wds:Q27008356-8CFF840A-20FE-469B-B7B5-A728FAE32C38 wds:Q27008356-A1C68D35-9AF9-4F74-8F0F-5F7F3E436AD6 wds:Q27008356-A5D40B52-6C21-43DA-B4A7-80753A52F886 wds:Q27008356-A6D439AF-026A-42F3-A579-87FE84C7DFD0 wds:Q27008356-AE1F3B0F-E6DC-4DA3-8F06-E1DD1E58A77C wds:Q27008356-B2E5031E-8CF0-4169-BC65-A3E51BBCCEE7 wds:Q27008356-B87CABD6-9E04-49EA-BFD3-3707D9003E6D wds:Q27008356-C5FBAC77-A5C5-4192-A249-62D0DA181B71 wds:Q27008356-CB5BF339-AAD4-412B-B6CC-C0CF9C316A45 wds:Q27008356-CEB9773A-9D04-4A47-A621-8915D88626DF wds:Q27008356-D02AAEC9-7FFD-42BF-9FD4-8986F93ED9C8 wds:Q27008356-D3781043-F5EF-43FF-B18D-E547C7761FCA wds:Q27008356-DF135470-A002-4179-A20A-93FFCA9BF90D wds:Q27008356-DF5A472F-98DB-4039-B65C-AFE451BFE863 wds:Q27008356-E2AD734B-1BDC-4D52-A63D-6A82EC548C90 wds:Q27008356-E3D547F4-E48D-4864-821D-DAA072C7153F wds:Q27008356-F0130047-969D-49E5-A192-8BF05055D289 wds:Q27008356-F0B57B62-0315-4465-A724-83C3F6A92D64 wds:Q27008356-F33EF7ED-F8C8-470C-8032-E48E749B93C2 wds:Q27008356-F51BE615-EC96-48C9-9114-6685BCE9A006 wds:Q27008356-FEE27CE9-E4BA-4944-A951-CEBCA123460E
cites work	Large-scale genotyping identifies 41 new loci associated with breast cancer risk Variation of breast cancer risk among BRCA1/2 carriers Inactivation of the p53 pathway in retinoblastoma. Genome-wide association studies identify four ER negative-specific breast cancer risk loci The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions Common breast cancer susceptibility loci are associated with triple-negative breast cancer Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer Programs for pedigree analysis: Mendel, Fisher, and dGene Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls A genome-wide association study identifies novel risk loci for type 2 diabetes GenABEL: an R library for genome-wide association analysis Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups A common inversion under selection in Europeans Estimation of the inbreeding coefficient through use of genomic data A genomic background based method for association analysis in related individuals 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 Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers Evaluation of association methods for analysing modifiers of disease risk in carriers of high-risk mutations. A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) Genotype imputation with thousands of genomes Global analysis of the impact of environmental perturbation on cis-regulation of gene expression Targeting Mdm2 and Mdmx in cancer therapy: better living through medicinal chemistry? Global patterns of cis variation in human cells revealed by high-density allelic expression analysis Common variants at 6q22 and 17q21 are associated with intracranial volume Genome-wide association study reveals genetic risk underlying Parkinson's disease Gene expression profiling supports the hypothesis that human ovarian surface epithelia are multipotent and capable of serving as ovarian cancer initiating cells Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

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