Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium.
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Selection in reported epidemiological risks: an empirical assessmentGenome-wide association study identifies novel breast cancer susceptibility lociAssembly of inflammation-related genes for pathway-focused genetic analysisEpidemiology and pathophysiology of alcohol and breast cancer: Update 2012The Pro allele of the p53 codon 72 polymorphism is associated with decreased intratumoral expression of BAX and p21, and increased breast cancer riskA genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart StudyImpact of XRCC2 Arg188His polymorphism on cancer susceptibility: a meta-analysis.Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in Cancer.Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases.Constrained Maximum Likelihood Estimation for Model Calibration Using Summary-level Information from External Big Data Sources.Genetic variants in hormone-related genes and risk of breast cancer.Association between common variation in 120 candidate genes and breast cancer risk.Association between the BRCA2 N372H variant and male breast cancer risk: a population-based case-control study in Tuscany, Central Italy.TGFB1 and TGFBR1 polymorphisms and breast cancer risk in the Nurses' Health Study.Mutation analysis of the MDM4 gene in German breast cancer patientsA field synopsis on low-penetrance variants in DNA repair genes and cancer susceptibility.An analysis of growth, differentiation and apoptosis genes with risk of renal cancer.A method of predicting changes in human gene splicing induced by genetic variants in context of cis-acting elementsSubtyping of breast cancer by immunohistochemistry to investigate a relationship between subtype and short and long term survival: a collaborative analysis of data for 10,159 cases from 12 studiesCombined effects of single nucleotide polymorphisms TP53 R72P and MDM2 SNP309, and p53 expression on survival of breast cancer patients.Can genes for mammographic density inform cancer aetiology?Association between the BRCA2 rs144848 polymorphism and cancer susceptibility: a meta-analysis.Influence of XRCC1 Genetic Polymorphisms on Ionizing Radiation-Induced DNA Damage and Repair.Understanding susceptibility to breast cancer metastasis: the genetic approach.Germline variation in TP53 regulatory network genes associates with breast cancer survival and treatment outcome.Breast Cancer Risk - Genes, Environment and Clinics.Interaction among apoptosis-associated sequence variants and joint effects on aggressive prostate cancer.Relevance of LIG4 gene polymorphisms with cancer susceptibility: evidence from a meta-analysisCommon non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association ConsortiumAssociation of BRCA2 N372H polymorphism with cancer susceptibility: a comprehensive review and meta-analysis.Associations of progesterone receptor polymorphisms with age at menarche and menstrual cycle lengthAssessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study.Associating GWAS Information with the Notch Signaling Pathway Using Transcription Profiling.Five polymorphisms and breast cancer risk: results from the Breast Cancer Association ConsortiumIn search of breast cancer culprits: suspecting the suspected and the unsuspectedRefined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia.An integrative genomics approach to biomarker discovery in breast cancerRAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer familiesAssociations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association ConsortiumAn original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
P2860
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P2860
Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Commonly studied single-nucleo ...... Cancer Association Consortium.
@en
type
label
Commonly studied single-nucleo ...... Cancer Association Consortium.
@en
prefLabel
Commonly studied single-nucleo ...... Cancer Association Consortium.
@en
P2860
P356
P1476
Commonly studied single-nucleo ...... Cancer Association Consortium.
@en
P2093
Breast Cancer Association Consortium
P2860
P304
P356
10.1093/JNCI/DJJ374
P407
P577
2006-10-01T00:00:00Z