| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1012888138 |
| P356 | DOI | 10.1007/S10549-016-4053-Z |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1007/s10549-016-4053-z |
| P932 | PMC publication ID | 5226879 |
| P698 | PubMed publication ID | 27848153 |
| P50 | author | Jack A. Taylor | Q42767532 |
| Katie O'Brien | Q57900263 | ||
| Dmitri Zaykin | Q61987553 | ||
| Clarice Weinberg | Q89866315 | ||
| Dale Sandler | Q37376725 | ||
| P2093 | author name string | Min Shi | |
| P2860 | cites work | A flexible and accurate genotype imputation method for the next generation of genome-wide association studies | Q21129496 |
| An integrated map of genetic variation from 1,092 human genomes | Q22122153 | ||
| Breast cancers among very young premenopausal women (United States). | Q44442730 | ||
| Association of genetic variants at TOX3, 2q35 and 8q24 with the risk of familial and early-onset breast cancer in a South-American population. | Q46762978 | ||
| Pooled analysis of prospective cohort studies on height, weight, and breast cancer risk | Q47229226 | ||
| Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population. | Q51311827 | ||
| FGFR2 intronic polymorphisms interact with reproductive risk factors of breast cancer: results of a case control study in Japan. | Q51627790 | ||
| Estimating age-specific breast cancer risks: a descriptive tool to identify age interactions. | Q51770859 | ||
| Genetic variants in FGFR2 and MAP3K1 are associated with the risk of familial and early-onset breast cancer in a South-American population. | Q54466712 | ||
| DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome | Q61946715 | ||
| A pilot genome-wide association study of early-onset breast cancer | Q81234958 | ||
| TOX3 is a neuronal survival factor that induces transcription depending on the presence of CITED1 or phosphorylated CREB in the transcriptionally active complex | Q24318759 | ||
| 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 | ||
| Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk | Q27008356 | ||
| A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer | Q28303909 | ||
| Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approach | Q28394471 | ||
| Breast cancer subtypes and previously established genetic risk factors: a bayesian approach | Q28397311 | ||
| Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium | Q28474694 | ||
| Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer | Q28924377 | ||
| A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study | Q28943278 | ||
| A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese | Q28943445 | ||
| Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility | Q28943457 | ||
| A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study | Q28943473 | ||
| Large-scale genotyping identifies 41 new loci associated with breast cancer risk | Q29416989 | ||
| A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. | Q29417036 | ||
| Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer | Q29417100 | ||
| Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease | Q30665466 | ||
| A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting | Q32074789 | ||
| Common genetic variants and modification of penetrance of BRCA2-associated breast cancer | Q33742096 | ||
| Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation | Q33811527 | ||
| Evaluation of polygenic risk scores for predicting breast and prostate cancer risk | Q33873837 | ||
| Modification of breast cancer risk according to age and menopausal status: a combined analysis of five population-based case-control studies | Q33957073 | ||
| Correlation of breast cancer susceptibility loci with patient characteristics, metastasis-free survival, and mRNA expression of the nearest genes | Q33958257 | ||
| Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1. | Q34023796 | ||
| 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 | ||
| Polymorphisms in second intron of the FGFR2 gene are associated with the risk of early-onset breast cancer in Chinese Han women | Q34177903 | ||
| A linear complexity phasing method for thousands of genomes | Q34237936 | ||
| Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. | Q34375940 | ||
| Allowing for missing parents in genetic studies of case-parent triads | Q34389420 | ||
| 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 | Q34472668 | ||
| A genome-wide scan for breast cancer risk haplotypes among African American women | Q34611972 | ||
| A genome-wide association scan on estrogen receptor-negative breast cancer | Q34613513 | ||
| Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer | Q34631785 | ||
| Genome-wide association study of breast cancer in the Japanese population | Q35021642 | ||
| 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 | ||
| Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium | Q35119701 | ||
| Replication of five GWAS-identified loci and breast cancer risk among Hispanic and non-Hispanic white women living in the Southwestern United States | Q35154043 | ||
| Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium | Q35166701 | ||
| Replication of breast cancer GWAS susceptibility loci in the Women's Health Initiative African American SHARe Study | Q35456134 | ||
| Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium | Q35565707 | ||
| A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer | Q35755874 | ||
| Common breast cancer susceptibility loci are associated with triple-negative breast cancer | Q35891162 | ||
| Challenges and opportunities in the targeting of fibroblast growth factor receptors in breast cancer | Q36245320 | ||
| Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression | Q36354441 | ||
| A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. | Q36435849 | ||
| Family-based designs in the age of large-scale gene-association studies | Q36451033 | ||
| Role of birthweight in the etiology of breast cancer | Q36528661 | ||
| Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
| 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 | ||
| Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. | Q36670312 | ||
| Case-sibling studies that acknowledge unstudied parents and permit the inclusion of unmatched individuals | Q36693431 | ||
| A genome-wide association study of breast cancer in women of African ancestry | Q37109758 | ||
| The influence of genetic variation in 30 selected genes on the clinical characteristics of early onset breast cancer | Q37131378 | ||
| BRCA1 and BRCA2: different roles in a common pathway of genome protection | Q37149848 | ||
| Evaluation of potential regulatory function of breast cancer risk locus at 6q25.1. | Q37220500 | ||
| Comparison of genetic variation of breast cancer susceptibility genes in Chinese and German populations. | Q37235167 | ||
| Curses--winner's and otherwise--in genetic epidemiology | Q37243708 | ||
| Hormone-dependent effects of FGFR2 and MAP3K1 in breast cancer susceptibility in a population-based sample of post-menopausal African-American and European-American women | Q37292711 | ||
| Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. | Q37369631 | ||
| Evaluation of 11 breast cancer susceptibility loci in African-American women | Q37382245 | ||
| Common genetic variants associated with breast cancer in Korean women and differential susceptibility according to intrinsic subtype | Q38476052 | ||
| Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study | Q39006292 | ||
| Analyzing 395,793 samples shows significant association between rs999737 polymorphism and breast cancer | Q39210546 | ||
| Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study | Q39605778 | ||
| A family-based, genome-wide association study of young-onset breast cancer: inherited variants and maternally mediated effects. | Q40906978 | ||
| Young age at diagnosis correlates with worse prognosis and defines a subset of breast cancers with shared patterns of gene expression | Q42661638 | ||
| A combined analysis of genome-wide association studies in breast cancer | Q42676622 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genome-wide association study | Q1098876 |
| P304 | page(s) | 333-344 | |
| P577 | publication date | 2016-11-15 | |
| P1433 | published in | Breast Cancer Research and Treatment | Q326085 |
| P1476 | title | Previous GWAS hits in relation to young-onset breast cancer | |
| P478 | volume | 161 |
| Q64912700 | Evaluation of significant genome-wide association studies risk - SNPs in young breast cancer patients. |
| Q44643445 | Fibroblast Growth Factor Receptor 2 Signaling in Breast Cancer |
| Q89866318 | Interactions between a Polygenic Risk Score and Non-genetic Risk Factors in Young-Onset Breast Cancer |
| Q95265125 | Machine Learning Supports Long Noncoding RNAs as Expression Markers for Endometrial Carcinoma |
| Q52653738 | Significant association between ERCC2 and MTHR polymorphisms and breast cancer susceptibility in Moroccan population: genotype and haplotype analysis in a case-control study. |
| Q90264934 | Significant association of TOX3/LOC643714 locus-rs3803662 and breast cancer risk in a cohort of Iranian population |
Search more.