Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium
about
Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approachBreast cancer subtypes and previously established genetic risk factors: a bayesian approachA polymorphism rs12325489C>T in the lincRNA-ENST00000515084 exon was found to modulate breast cancer risk via GWAS-based association analysesGenome-wide association study in east Asians identifies novel susceptibility loci for breast cancerA genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer StudyGenetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinomaA 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.Functional annotation of putative regulatory elements at cancer susceptibility LociSignificant overlap between human genome-wide association-study nominated breast cancer risk alleles and rat mammary cancer susceptibility loci.Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutationBreast cancer risk assessment using genetic variants and risk factors in a Singapore Chinese population.Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1.Evaluation of breast cancer susceptibility loci in Chinese women.Evaluating genome-wide association study-identified breast cancer risk variants in African-American womenGenome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25.A novel multiplex tetra-primer ARMS-PCR for the simultaneous genotyping of six single nucleotide polymorphisms associated with female cancers.Associations of two common genetic variants with breast cancer risk in a chinese population: a stratified interaction analysisGenetic variants at 12p11 and 12q24 are associated with breast cancer risk in a Chinese population.Evaluation of nanofluidics technology for high-throughput SNP genotyping in a clinical settingGenome-wide association study of breast cancer in the Japanese population.Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans.Replication of breast cancer GWAS susceptibility loci in the Women's Health Initiative African American SHARe Study.Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium.Combined effect of low-penetrant SNPs on breast cancer risk.Novel genetic markers of breast cancer survival identified by a genome-wide association study.Proper Use of Allele-Specific Expression Improves Statistical Power for cis-eQTL Mapping with RNA-Seq DataAdmixture mapping identifies a locus on 6q25 associated with breast cancer risk in US LatinasAssociation of three SNPs in TOX3 and breast cancer risk: Evidence from 97275 cases and 128686 controls.Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.Genetic and Epigenetic Regulation of TOX3 Expression in Breast CancerGenome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians.Interaction between common breast cancer susceptibility variants, genetic ancestry, and nongenetic risk factors in Hispanic women.A sequence-based method to predict the impact of regulatory variants using random forest.Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expressionGenetic susceptibility loci for subtypes of breast cancer in an African American population.TOX3 protein expression is correlated with pathological characteristics in breast cancer.Gene-environment interactions for breast cancer risk among Chinese women: a report from the Shanghai Breast Cancer Genetics Study.A common deletion in the APOBEC3 genes and breast cancer risk.Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls.New breast cancer risk variant discovered at 10q25 in East Asian women.
P2860
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P2860
Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Identification of a functional ...... Asia Breast Cancer Consortium
@ast
Identification of a functional ...... Asia Breast Cancer Consortium
@en
Identification of a functional ...... Asia Breast Cancer Consortium
@nl
type
label
Identification of a functional ...... Asia Breast Cancer Consortium
@ast
Identification of a functional ...... Asia Breast Cancer Consortium
@en
Identification of a functional ...... Asia Breast Cancer Consortium
@nl
prefLabel
Identification of a functional ...... Asia Breast Cancer Consortium
@ast
Identification of a functional ...... Asia Breast Cancer Consortium
@en
Identification of a functional ...... Asia Breast Cancer Consortium
@nl
P2093
P2860
P50
P3181
P1433
P1476
Identification of a functional ...... Asia Breast Cancer Consortium
@en
P2093
Guoliang Li
Hiroji Iwata
Hong Zheng
Hongbing Shen
Jiajun Shi
Jiarong Cheng
Jirong Long
P2860
P304
P3181
P356
10.1371/JOURNAL.PGEN.1001002
P407
P50
P577
2010-06-24T00:00:00Z