| scholarly article | Q13442814 |
| P50 | author | Fergus J. Couch | Q63018779 |
| Celine M. Vachon | Q74173260 | ||
| P2093 | author name string | Jenna Lilyquist | |
| Kathryn J Ruddy | |||
| P2860 | cites work | DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers | Q21144874 |
| PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene | Q24615080 | ||
| Genome-wide association studies identify four ER negative-specific breast cancer risk loci | Q24622610 | ||
| Genome-wide association study identifies novel breast cancer susceptibility loci | Q24645441 | ||
| Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers | Q24655824 | ||
| Gene-environment interaction and risk of breast cancer | Q26772236 | ||
| Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk | Q27008356 | ||
| A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1 | Q28115843 | ||
| Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations | Q28215462 | ||
| A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer | Q28303909 | ||
| Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer | Q28924377 | ||
| Large-scale genotyping identifies 41 new loci associated with breast cancer risk | Q29416989 | ||
| Genetic modifiers of CHEK2*1100delC-associated breast cancer risk | Q37739048 | ||
| Long Noncoding RNAs CUPID1 and CUPID2 Mediate Breast Cancer Risk at 11q13 by Modulating the Response to DNA Damage. | Q38640565 | ||
| Health Disparities and Triple-Negative Breast Cancer in African American Women: A Review | Q38868959 | ||
| Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study | Q39006292 | ||
| Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium | Q40282176 | ||
| Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer | Q40346126 | ||
| Genetic variations in the Hippo signaling pathway and breast cancer risk in African American women in the AMBER Consortium | Q40638709 | ||
| Genetic susceptibility to breast cancer | Q41130542 | ||
| Rates for breast cancer characteristics by estrogen and progesterone receptor status in the major racial/ethnic groups | Q44121727 | ||
| Association of a common variant of the CASP8 gene with reduced risk of breast cancer | Q45188733 | ||
| Association analysis identifies 65 new breast cancer risk loci. | Q45979098 | ||
| Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer | Q46103372 | ||
| Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium | Q47190168 | ||
| The associations of sequence variants in DNA-repair and cell-cycle genes with cancer risk: genotype-phenotype correlations. | Q47800993 | ||
| High constant incidence in twins and other relatives of women with breast cancer. | Q53403578 | ||
| A common coding variant in CASP8 is associated with breast cancer risk | Q57250674 | ||
| Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer | Q57251792 | ||
| Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk | Q36858843 | ||
| Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer | Q36859142 | ||
| An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriers | Q36882665 | ||
| Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer | Q36897003 | ||
| Gene-based analysis of the fibroblast growth factor receptor signaling pathway in relation to breast cancer in African American women: the AMBER consortium | Q36961082 | ||
| CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls | Q37048943 | ||
| A genome-wide association study of breast cancer in women of African ancestry | Q37109758 | ||
| Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs). | Q37236216 | ||
| Admixture Mapping of African-American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes | Q37271961 | ||
| Beyond GWASs: illuminating the dark road from association to function | Q37298148 | ||
| Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation | Q37342144 | ||
| Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. | Q37356243 | ||
| Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1. | Q37367871 | ||
| Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. | Q37369631 | ||
| Genetic variations in vitamin D-related pathways and breast cancer risk in African American women in the AMBER consortium | Q37381735 | ||
| The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers | Q37401496 | ||
| Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers | Q37434133 | ||
| Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). | Q37481884 | ||
| Genetic variation in the insulin, insulin-like growth factor, growth hormone, and leptin pathways in relation to breast cancer in African-American women: the AMBER consortium | Q37482022 | ||
| A collaborative study of the etiology of breast cancer subtypes in African American women: the AMBER consortium | Q37623331 | ||
| Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer | Q29417100 | ||
| Identification of the breast cancer susceptibility gene BRCA2 | Q29616290 | ||
| Breast Cancer Screening in the Precision Medicine Era: Risk-Based Screening in a Population-Based Trial. | Q30238753 | ||
| Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics | Q33330850 | ||
| Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk. | Q33565679 | ||
| Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers | Q33614244 | ||
| A functionally significant SNP in TP53 and breast cancer risk in African-American women | Q33731355 | ||
| Fine scale mapping of the breast cancer 16q12 locus | Q33878276 | ||
| CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies | Q33910280 | ||
| Gene-environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study | Q33935171 | ||
| Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers | Q33947829 | ||
| Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1. | Q34023796 | ||
| Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions | Q34038964 | ||
| Population structure in admixed populations: effect of admixture dynamics on the pattern of linkage disequilibrium. | Q34043712 | ||
| A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). | Q34085748 | ||
| Genome-wide association study identifies five new breast cancer susceptibility loci | Q34114293 | ||
| A comprehensive examination of breast cancer risk loci in African American women | Q34211808 | ||
| Evaluating genome-wide association study-identified breast cancer risk variants in African-American women | Q34339783 | ||
| Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium | Q34379032 | ||
| ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles | Q34546389 | ||
| A genome-wide scan for breast cancer risk haplotypes among African American women | Q34611972 | ||
| 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) | Q34623703 | ||
| Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer | Q34631785 | ||
| Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers | Q34801008 | ||
| Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2. | Q34806825 | ||
| Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk | Q35061252 | ||
| Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation | Q35064451 | ||
| 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 | Q35089479 | ||
| Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk | Q35102646 | ||
| Genetic predisposition to in situ and invasive lobular carcinoma of the breast | Q35151684 | ||
| Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans | Q35389444 | ||
| Replication of breast cancer GWAS susceptibility loci in the Women's Health Initiative African American SHARe Study | Q35456134 | ||
| Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers | Q35523236 | ||
| Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. | Q35524465 | ||
| Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium | Q35565707 | ||
| Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) | Q35737888 | ||
| Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures | Q35752042 | ||
| A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer | Q35755874 | ||
| 19p13.1 is a triple-negative-specific breast cancer susceptibility locus | Q35871567 | ||
| Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry | Q35883587 | ||
| 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. | Q35889575 | ||
| Common breast cancer susceptibility loci are associated with triple-negative breast cancer | Q35891162 | ||
| Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. | Q35940158 | ||
| Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer | Q35996692 | ||
| Mammographic breast density and breast cancer: evidence of a shared genetic basis | Q36043843 | ||
| Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression | Q36066735 | ||
| An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression | Q36073563 | ||
| Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus | Q36124728 | ||
| The contributions of breast density and common genetic variation to breast cancer risk | Q36137764 | ||
| A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers | Q36152991 | ||
| Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers | Q36352389 | ||
| Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers | Q36393232 | ||
| A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. | Q36435849 | ||
| RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies | Q36512097 | ||
| Genetic susceptibility loci for subtypes of breast cancer in an African American population | Q36514074 | ||
| Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
| Fine-mapping of the 6q25 locus identifies a novel SNP associated with breast cancer risk in African-American women | Q36587625 | ||
| Breast Cancer Risk Prediction Using Clinical Models and 77 Independent Risk-Associated SNPs for Women Aged Under 50 Years: Australian Breast Cancer Family Registry | Q36619329 | ||
| Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk | Q36720814 | ||
| Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors | Q36720821 | ||
| Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers | Q36742577 | ||
| Family history, age, and risk of breast cancer. Prospective data from the Nurses' Health Study | Q36743855 | ||
| Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers | Q36839777 | ||
| Genome-wide association analysis identifies three new breast cancer susceptibility loci | Q36842233 | ||
| Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls | Q36856357 | ||
| P921 | main subject | genetic variation | Q349856 |
| P577 | publication date | 2018-01-30 | |
| P1433 | published in | Cancer Epidemiology, Biomarkers & Prevention | Q326334 |
| P1476 | title | Common Genetic Variation and Breast Cancer Risk - Past, present, and future |
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