Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers - Test2 - elhamkhani - TriplyDB

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

http://www.wikidata.org/entity/Q24655824

about

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers Breast cancer in the personal genomics era Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk Challenging and complex decisions in the management of the BRCA mutation carrier Functional variant of KLOTHO: a breast cancer risk modifier among BRCA1 mutation carriers of Ashkenazi origin Variation in breast cancer risk in BRCA1 and BRCA2 mutation carriers Emergence of FGFR family gene fusions as therapeutic targets in a wide spectrum of solid tumours Screening for replication of genome-wide SNP associations in sporadic ALS Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2: potential modifying effect of BRCA1/BRCA2 mutation carrier status.Single nucleotide polymorphisms associated with risk for contralateral breast cancer in the Women's Environment, Cancer, and Radiation Epidemiology (WECARE) Study Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes Realizing the promise of cancer predisposition genes.Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation.Biological processes, properties and molecular wiring diagrams of candidate low-penetrance breast cancer susceptibility genes.Prevalence of the variant allele rs61764370 T>G in the 3'UTR of KRAS among Dutch BRCA1, BRCA2 and non-BRCA1/BRCA2 breast cancer families.High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series.rs2981582 is associated with FGFR2 expression in normal breast Common genetic variants and modification of penetrance of BRCA2-associated breast cancer Exploring the link between germline and somatic genetic alterations in breast carcinogenesis.Polymorphisms in the TOX3/LOC643714 locus and risk of breast cancer in African-American women.Modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: systematic review and meta-analysis.Eligibility for magnetic resonance imaging screening in the United Kingdom: effect of strict selection criteria and anonymous DNA testing on breast cancer incidence in the MARIBS Study.Fine mapping of the 9q31 Hirschsprung's disease locus.Exploring the link between MORF4L1 and risk of breast cancer.BRCA1 and BRCA2 mutations and treatment strategies for breast cancer.Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers Gene-gene interactions in breast cancer susceptibility.Incorporating tumour pathology information into breast cancer risk prediction algorithms.Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer.Identification of Novel Susceptibility Genes for Breast Cancer - Genome-Wide Association Studies or Evaluation of Candidate Genes?Breast cancer susceptibility: current knowledge and implications for genetic counselling Breast Cancer Risk - Genes, Environment and Clinics.Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.Common low-penetrance risk variants associated with breast cancer in Polish women.Estimating penetrance from multiple case families with predisposing mutations: extension of the 'genotype-restricted likelihood' (GRL) method The risk allele of SNP rs3803662 and the mRNA level of its closest genes TOX3 and LOC643714 predict adverse outcome for breast cancer patients FGFR2 intronic SNPs and breast cancer risk: associations with tumor characteristics and interactions with exogenous exposures and other known breast cancer risk factors.Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers.The inherited genetics of ovarian and endometrial cancer.

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Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

http://www.wikidata.org/entity/Q24655824

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2008 nî lūn-bûn

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2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2008 թվականի ապրիլին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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Common breast cancer-predispos ...... A1 and BRCA2 mutation carriers

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J.AJHG.2008.02.008

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American Journal of Human Genetics

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Agnès Chompret

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Andrew K Godwin

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Ans M W van den Ouweland

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Beatrix Versmold

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Bella Kaufman

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Carol Chu

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Christian Sutter

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Claude Houdayer

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Corinne Capoulade

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Csilla I Szabo

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P2860

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

Genome-wide association study identifies novel breast cancer susceptibility loci

Variation of breast cancer risk among BRCA1/2 carriers.

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics.

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes.

Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations.

Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish population

An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA)

RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.

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10.1016/J.AJHG.2008.02.008

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4

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82

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Dominique Stoppa-Lyonnet

Georgia Chenevix-Trench

Rita Schmutzler

Heli Nevanlinna

Paolo Peterlongo

Katherine L Nathanson

Marion Gauthier-Villars

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2008-04-01T00:00:00Z

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