Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium

scientific article

Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1371/JOURNAL.PGEN.1001002
P3181OpenCitations bibliographic resource ID2696948
P932PMC publication ID2891809
P698PubMed publication ID20585626
P5875ResearchGate publication ID44807320

P50authorLoic Le MarchandQ28360612
Keitaro MatsuoQ30506416
Hiroji IwataQ90659986
Wanqing WenQ99208333
Kazuo TajimaQ113693872
Furu WangQ114328054
Sum Yin ChanQ114328057
Yoshio KasugaQ114328058
Martha J. ShrubsoleQ37371925
Sandra Deming-HalversonQ42438267
Chiun-Sheng HuangQ42677843
Motoki IwasakiQ43288528
Ui-Soon KhooQ57306450
Shoichiro TsuganeQ57476727
Jiajun ShiQ58825553
Qiuyin CaiQ59194517
Chun LiQ64183498
Wei ZhengQ67482021
Xiao-Ou ShuQ67482510
Ming-Feng HouQ72856113
Christopher A. HaimanQ73606228
Brian E. HendersonQ73660621
Jirong LongQ73800661
Yu-Tang GaoQ73862394
Chen-Yang ShenQ73926370
Hongbing ShenQ87650948
Yong-Bing XiangQ87875811
Zhibin HuQ88410186
P2093author name stringHong Zheng
Kexin Chen
Wei Lu
Ying Zheng
Bo Huang
Wenjing Wang
Lina Zhang
Guoliang Li
Kai Gu
Mark C Kelley
Kelvin Y K Chan
Shimian Qu
Jiarong Cheng
P2860cites workGenome-wide association study identifies novel breast cancer susceptibility lociQ24645441
Principal components analysis corrects for stratification in genome-wide association studiesQ27860975
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancerQ28303909
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).Q34085748
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancerQ34631785
A multiethnic cohort in Hawaii and Los Angeles: baseline characteristicsQ35786223
Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.Q36670312
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.Q37356243
Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.Q37369631
Functional polymorphisms in the BRCA1 promoter influence transcription and are associated with decreased risk for breast cancer in Chinese women.Q37436858
Association of menstrual and reproductive factors with breast cancer risk: results from the Shanghai Breast Cancer StudyQ39540042
Gene-environment Interactions and Polymorphism Studies of Cancer Risk in the Hospital-based Epidemiologic Research Program at Aichi Cancer Center II (HERPACC-II)Q44181217
Serum organochlorines and breast cancer risk in Japanese women: a case-control studyQ46230466
Genetic variants in fibroblast growth factor receptor 2 (FGFR2) contribute to susceptibility of breast cancer in Chinese womenQ46323110
Association of genetic polymorphisms of ER-alpha and the estradiol-synthesizing enzyme genes CYP17 and CYP19 with breast cancer risk in Chinese womenQ46384021
A tandem repeat of human telomerase reverse transcriptase (hTERT) and risk of breast cancer development and metastasis in Chinese women.Q53322181
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancerQ57251792
Genetic variants of BLM interact with RAD51 to increase breast cancer susceptibilityQ64387482
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectbreast cancerQ128581
P304page(s)e1001002
P577publication date2010-06-24
P1433published inPLOS GeneticsQ1893441
P1476titleIdentification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium
P478volume6

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cites work (P2860)
Q60961227A Comprehensive cis-eQTL Analysis Revealed Target Genes in Breast Cancer Susceptibility Loci Identified in Genome-wide Association Studies
Q36769624A common deletion in the APOBEC3 genes and breast cancer risk
Q37296991A common variant in the SIAH2 locus is associated with estrogen receptor-positive breast cancer in the Chinese Han population
Q40906978A family-based, genome-wide association study of young-onset breast cancer: inherited variants and maternally mediated effects.
Q48345502A functional BRCA1 coding sequence genetic variant contributes to prognosis of triple-negative breast cancer, especially after radiotherapy
Q37697205A functional variant rs4442975 modulating FOXA1-binding affinity does not influence the risk or progression of breast cancer in Chinese Han population
Q57918178A genetic risk predictor for breast cancer using a combination of low-penetrance polymorphisms in a Japanese population
Q28943473A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
Q29417036A 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.
Q34685625A novel multiplex tetra-primer ARMS-PCR for the simultaneous genotyping of six single nucleotide polymorphisms associated with female cancers
Q38958555A polygenic risk score for breast cancer risk in a Taiwanese population.
Q28539203A polymorphism rs12325489C>T in the lincRNA-ENST00000515084 exon was found to modulate breast cancer risk via GWAS-based association analyses
Q36329488A sequence-based method to predict the impact of regulatory variants using random forest
Q35856257Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas
Q35937737Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population
Q92135575Association of rs4784227-CASC16 (LOC643714 locus) and rs4782447-ACSF3 polymorphisms and their association with breast cancer risk among Iranian population
Q35913571Association of three SNPs in TOX3 and breast cancer risk: Evidence from 97275 cases and 128686 controls
Q34757714Associations of two common genetic variants with breast cancer risk in a chinese population: a stratified interaction analysis
Q33892384Breast cancer risk assessment using genetic variants and risk factors in a Singapore Chinese population
Q36354441Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression
Q28397311Breast cancer subtypes and previously established genetic risk factors: a bayesian approach
Q42695563Chromatin accessibility prediction via a hybrid deep convolutional neural network
Q35682030Combined effect of low-penetrant SNPs on breast cancer risk.
Q36856357Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls
Q37235167Comparison of genetic variation of breast cancer susceptibility genes in Chinese and German populations.
Q40238343Evaluating genetic variants associated with breast cancer risk in high and moderate-penetrance genes in Asians
Q34339783Evaluating genome-wide association study-identified breast cancer risk variants in African-American women
Q34116018Evaluation of breast cancer susceptibility loci in Chinese women
Q34801132Evaluation of nanofluidics technology for high-throughput SNP genotyping in a clinical setting
Q37220500Evaluation of potential regulatory function of breast cancer risk locus at 6q25.1.
Q64912700Evaluation of significant genome-wide association studies risk - SNPs in young breast cancer patients.
Q55040393Evaluation of three polygenic risk score models for the prediction of breast cancer risk in Singapore Chinese.
Q35389444Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans
Q30367526Functional annotation of putative regulatory elements at cancer susceptibility Loci
Q40420307GERV: a statistical method for generative evaluation of regulatory variants for transcription factor binding.
Q36661778Gene-environment interactions for breast cancer risk among Chinese women: a report from the Shanghai Breast Cancer Genetics Study
Q64251583Genetic Epidemiology of Breast Cancer in Latin America
Q37065332Genetic ancestry modifies the association between genetic risk variants and breast cancer risk among Hispanic and non-Hispanic white women
Q36180327Genetic and Epigenetic Regulation of TOX3 Expression in Breast Cancer
Q42371580Genetic and environmental factors and serum hormones, and risk of estrogen receptor-positive breast cancer in pre- and postmenopausal Japanese women
Q50057756Genetic determinants of sporadic breast cancer in Sri Lankan women.
Q36514074Genetic susceptibility loci for subtypes of breast cancer in an African American population
Q33811527Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation
Q34776778Genetic variants at 12p11 and 12q24 are associated with breast cancer risk in a Chinese population
Q28943516Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma
Q41355586Genetic variants in long noncoding RNA H19 contribute to the risk of breast cancer in a southeast China Han population
Q36227599Genome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians.
Q34023796Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1.
Q35565707Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
Q39647103Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci
Q28924377Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer
Q34375940Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25.
Q35021642Genome-wide association study of breast cancer in the Japanese population
Q37509093Genomic Disparities in Breast Cancer Among Latinas.
Q61448654Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas
Q40591033Identification of novel susceptibility markers for the risk of overall breast cancer as well as subtypes defined by hormone receptor status in the Chinese population
Q91404921Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population
Q36249029Interaction between common breast cancer susceptibility variants, genetic ancestry, and nongenetic risk factors in Hispanic women
Q37037670New breast cancer risk variant discovered at 10q25 in East Asian women
Q35803492Novel genetic markers of breast cancer survival identified by a genome-wide association study
Q37487782Prediction of breast cancer risk based on common genetic variants in women of East Asian ancestry
Q40474074Previous GWAS hits in relation to young-onset breast cancer.
Q35841465Proper Use of Allele-Specific Expression Improves Statistical Power for cis-eQTL Mapping with RNA-Seq Data
Q35456134Replication of breast cancer GWAS susceptibility loci in the Women's Health Initiative African American SHARe Study
Q28394471Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approach
Q37645149Risk-association of five SNPs in TOX3/LOC643714 with breast cancer in southern China.
Q33745676Significant overlap between human genome-wide association-study nominated breast cancer risk alleles and rat mammary cancer susceptibility loci
Q36640318TOX3 protein expression is correlated with pathological characteristics in breast cancer
Q37200793The Role of Constitutional Copy Number Variants in Breast Cancer
Q37644934The breast cancer susceptibility-related polymorphisms at the TOX3/LOC643714 locus associated with lung cancer risk in a Han Chinese population

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