A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).
about
The landscape of long noncoding RNAs in the human transcriptomeJoint associations between genetic variants and reproductive factors in glioma risk among womenComprehensive 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 genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinomaComprehensive genomic studies: emerging regulatory, strategic, and quality assurance challenges for biorepositoriesBase excision repair and cancerThe gene desert mammary carcinoma susceptibility locus Mcs1a regulates Nr2f1 modifying mammary epithelial cell differentiation and proliferationA Cross-Cancer Genetic Association Analysis of the DNA Repair and DNA Damage Signaling Pathways for Lung, Ovary, Prostate, Breast, and Colorectal Cancer.Cancer evolution and individual susceptibilityReplication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approachCross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal CancerBreast 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 ConsortiumGenome sequence of the date palm Phoenix dactylifera LGenome-wide association study in east Asians identifies novel susceptibility loci for breast cancerGenome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucomaPotential 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.Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.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.Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modelingSingle nucleotide polymorphisms associated with risk for contralateral breast cancer in the Women's Environment, Cancer, and Radiation Epidemiology (WECARE) StudyBreast cancer prediction using genome wide single nucleotide polymorphism data.High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic ArraysAssociation between 5p12 genomic markers and breast cancer susceptibility: evidence from 19 case-control studies.Hereditary breast cancer: ever more pieces to the polygenic puzzle.Genome-wide mechanisms of nuclear receptor action.Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.Leveraging genetic variability across populations for the identification of causal variants.Germline mutation in the RAD51B gene confers predisposition to breast cancer.Design of association studies with pooled or un-pooled next-generation sequencing data.Integrated analysis of germline and somatic variants in ovarian cancer.Beyond genome-wide association studies: genetic heterogeneity and individual predisposition to cancer.Using principal components of genetic variation for robust and powerful detection of gene-gene interactions in case-control and case-only studies.Significant overlap between human genome-wide association-study nominated breast cancer risk alleles and rat mammary cancer susceptibility loci.Exploring the link between germline and somatic genetic alterations in breast carcinogenesis.
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P2860
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
A multistage genome-wide assoc ...... 1p11.2 and 14q24.1 (RAD51L1).
@ast
A multistage genome-wide assoc ...... 1p11.2 and 14q24.1 (RAD51L1).
@en
A multistage genome-wide assoc ...... alleles at 1p11.2 and 14q24.1
@nl
type
label
A multistage genome-wide assoc ...... 1p11.2 and 14q24.1 (RAD51L1).
@ast
A multistage genome-wide assoc ...... 1p11.2 and 14q24.1 (RAD51L1).
@en
A multistage genome-wide assoc ...... alleles at 1p11.2 and 14q24.1
@nl
prefLabel
A multistage genome-wide assoc ...... 1p11.2 and 14q24.1 (RAD51L1).
@ast
A multistage genome-wide assoc ...... 1p11.2 and 14q24.1 (RAD51L1).
@en
A multistage genome-wide assoc ...... alleles at 1p11.2 and 14q24.1
@nl
P2093
P2860
P50
P356
P1433
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A multistage genome-wide assoc ...... 1p11.2 and 14q24.1 (RAD51L1).
@en
P2093
Alice Sigurdson
Beata Peplonska
Bruce H Alexander
Christine D Berg
Daniela S Gerhard
Eugenia E Calle
Gilles Thomas
Jesus Gonzalez-Bosquet
Joseph F Fraumeni
P2860
P2888
P304
P356
10.1038/NG.353
P407
P50
P577
2009-03-29T00:00:00Z
P5875
P6179
1000555917