A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
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Genome-wide and candidate gene association study of cigarette smoking behaviorsSilencing of keratinocyte growth factor receptor restores 5-fluorouracil and tamoxifen efficacy on responsive cancer cellsGenome-wide association studies and the clinic: a focus on breast cancerGenome-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- 1994Genome-wide association study of glioma and meta-analysisImputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33A subset-based approach improves power and interpretation for the combined analysis of genetic association studies of heterogeneous traitsEthnic background and genetic variation in the evaluation of cancer risk: a systematic reviewFine mapping versus replication in whole-genome association studiesGRM7 variants confer susceptibility to age-related hearing impairmentRisk of breast and prostate cancer is not associated with increased homozygosity in outbred populationsGenome-wide association study identifies a locus at 7p15.2 associated with endometriosisBreast 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 consortiumA large-scale candidate gene association study of age at menarche and age at natural menopauseGenome-wide association studies identify four ER negative-specific breast cancer risk lociGenome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancerGenome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locusGenome-wide association studies identify loci associated with age at menarche and age at natural menopauseGenetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in CaucasiansCommon variations in BARD1 influence susceptibility to high-risk neuroblastomaVariation of breast cancer risk among BRCA1/2 carriers.Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variantsCandidate gene polymorphisms for ischemic stroke.Screening 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 CohortTargeting RTK Signaling Pathways in CancerCandidate gene-environment interactions in breast cancerGenome-wide association study of selenium concentrationsThe gene desert mammary carcinoma susceptibility locus Mcs1a regulates Nr2f1 modifying mammary epithelial cell differentiation and proliferationAntitumor effects and molecular mechanisms of ponatinib on endometrial cancer cells harboring activating FGFR2 mutationsThe genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevanceInhibition of the fibroblast growth factor receptor (FGFR) pathway: the current landscape and barriers to clinical applicationPaternal age effect mutations and selfish spermatogonial selection: causes and consequences for human diseaseTelomerase reverse transcriptase locus polymorphisms and cancer risk: a field synopsis and meta-analysisIdentification of ten loci associated with height highlights new biological pathways in human growthMultiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.Genetic polymorphisms in the 9p21 region associated with risk of multiple cancersInherited variation in immune genes and pathways and glioblastoma risk
P2860
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P2860
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
description
2007 nî lūn-bûn
@nan
2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2007年の論文
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2007年学术文章
@wuu
2007年学术文章
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2007年学术文章
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2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
name
A genome-wide association stud ...... c postmenopausal breast cancer
@ast
A genome-wide association stud ...... c postmenopausal breast cancer
@en
A genome-wide association stud ...... c postmenopausal breast cancer
@nl
type
label
A genome-wide association stud ...... c postmenopausal breast cancer
@ast
A genome-wide association stud ...... c postmenopausal breast cancer
@en
A genome-wide association stud ...... c postmenopausal breast cancer
@nl
prefLabel
A genome-wide association stud ...... c postmenopausal breast cancer
@ast
A genome-wide association stud ...... c postmenopausal breast cancer
@en
A genome-wide association stud ...... c postmenopausal breast cancer
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
A genome-wide association stud ...... c postmenopausal breast cancer
@en
P2093
Christine D Berg
Daniela S Gerhard
Eugenia E Calle
Gilles Thomas
Joseph F Fraumeni
Michael J Thun
Regina G Ziegler
Robert N Hoover
Robert Welch
P2860
P2888
P3181
P356
10.1038/NG2075
P407
P50
P577
2007-07-01T00:00:00Z