Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.
about
Isolated populations and complex disease gene identificationGenome-wide association studies and the clinic: a focus on breast cancerThe landscape of long noncoding RNAs in the human transcriptomeGenome-wide association studies: how predictable is a person’s cancer risk?Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disordersPrevalence in the United States of selected candidate gene variants. Third National Health and Nutrition Examination Survey, 1991- 1994Breast cancer in the personal genomics eraComprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortiumAssociation analyses identify six new psoriasis susceptibility loci in the Chinese populationScreening and association testing of common coding variation in steroid hormone receptor co-activator and co-repressor genes in relation to breast cancer risk: the Multiethnic CohortCommon genetic variation in candidate genes and susceptibility to subtypes of breast cancerCandidate gene-environment interactions in breast cancerThe gene desert mammary carcinoma susceptibility locus Mcs1a regulates Nr2f1 modifying mammary epithelial cell differentiation and proliferationThe genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevanceCancer evolution and individual susceptibilityUsing lifetime risk estimates in personal genomic profiles: estimation of uncertaintyReplication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approachBreast cancer subtypes and previously established genetic risk factors: a bayesian approachIdentification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer ConsortiumRealizing the promise of population biobanks: a new model for translationRare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening studyDataSHIELD: resolving a conflict in contemporary bioscience--performing a pooled analysis of individual-level data without sharing the dataSize matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiologyGenome-wide association study in east Asians identifies novel susceptibility loci for breast cancerPotential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibilityA genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer StudyLarge-scale genotyping identifies 41 new loci associated with breast cancer risk.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.Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.A HapMap harvest of insights into the genetics of common diseaseSequence variants at the TERT-CLPTM1L locus associate with many cancer typesDetecting signals in pharmacogenomic genome-wide association studiesSingle nucleotide polymorphisms associated with risk for contralateral breast cancer in the Women's Environment, Cancer, and Radiation Epidemiology (WECARE) StudyDirect-to-Consumer Genetic and Genomic Testing: Preparing Nurse Practitioners for Genomic Healthcare.Genetic polymorphism of the OPG gene associated with breast cancer.Breast cancer prediction using genome wide single nucleotide polymorphism data.Association between 5p12 genomic markers and breast cancer susceptibility: evidence from 19 case-control studies.Power to detect risk alleles using genome-wide tag SNP panelsCopy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics.
P2860
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P2860
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.
description
2007 nî lūn-bûn
@nan
2007 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Common variants on chromosomes ...... ceptor-positive breast cancer.
@ast
Common variants on chromosomes ...... ceptor-positive breast cancer.
@en
Common variants on chromosomes ...... ceptor-positive breast cancer.
@nl
type
label
Common variants on chromosomes ...... ceptor-positive breast cancer.
@ast
Common variants on chromosomes ...... ceptor-positive breast cancer.
@en
Common variants on chromosomes ...... ceptor-positive breast cancer.
@nl
altLabel
Common variants on chromosomes ...... eceptor–positive breast cancer
@en
prefLabel
Common variants on chromosomes ...... ceptor-positive breast cancer.
@ast
Common variants on chromosomes ...... ceptor-positive breast cancer.
@en
Common variants on chromosomes ...... ceptor-positive breast cancer.
@nl
P2093
P2860
P50
P356
P1433
P1476
Common variants on chromosomes ...... ceptor-positive breast cancer.
@en
P2093
Agnar Helgason
Alejandro Tres
Andrei Manolescu
Barbro Werelius
Dorine W Swinkels
Eduardo Polo
Esther Millastre
Gardar Myrdal
Gisli Masson
Helgi Sigurdsson
P2860
P2888
P304
P356
10.1038/NG2064
P407
P50
P577
2007-05-27T00:00:00Z