Genome-wide association study identifies three new melanoma susceptibility loci.
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Comparison of family history and SNPs for predicting risk of complex diseaseImputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33Pancreatic Cancer GeneticsEpidemiology and Inherited Predisposition for Sporadic Pancreatic AdenocarcinomaMeta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian womenCross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic AssociationsTERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publicationsCommon genetic variants in the 9p21 region and their associations with multiple tumoursA genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemiaGenome-wide association study identifies multiple risk loci for chronic lymphocytic leukemiaGenetic variants at 9p21.3 are associated with risk of esophageal squamous cell carcinoma in a Chinese populationIdentification of a melanoma susceptibility locus and somatic mutation in TET2.Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.A variant in FTO shows association with melanoma risk not due to BMIRealizing the promise of cancer predisposition genes.Development and validation of a melanoma risk score based on pooled data from 16 case-control studies.Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients.An adaptive threshold determination method of feature screening for genomic selection.Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanomaVariants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma.Calculation of exact p-values when SNPs are tested using multiple genetic modelsHaplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.Melanoma genetics.Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppressionNext generation sequencing techniques in neurological diseases: redefining clinical and molecular associations.Cyclin D1 G870A polymorphism contributes to colorectal cancer susceptibility: evidence from a systematic review of 22 case-control studiesA novel test of informative missingness using inconsistent linkage disequilibrium signals between case-parent triads and incomplete data.Genetics of familial melanoma: 20 years after CDKN2A.MicroRNA related polymorphisms and breast cancer risk.Replication and predictive value of SNPs associated with melanoma and pigmentation traits in a Southern European case-control studyGenetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish populationVariants at the 9p21 locus and melanoma riskJoint effect of multiple common SNPs predicts melanoma susceptibilityFine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regionsAddressing population-specific multiple testing burdens in genetic association studies.Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer riskInvolvement of ANXA5 and ILKAP in susceptibility to malignant melanoma.Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study.Prediction of the damage-associated non-synonymous single nucleotide polymorphisms in the human MC1R gene
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P2860
Genome-wide association study identifies three new melanoma susceptibility loci.
description
2011 nî lūn-bûn
@nan
2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Genome-wide association study identifies three new melanoma susceptibility loci.
@ast
Genome-wide association study identifies three new melanoma susceptibility loci.
@en
Genome-wide association study identifies three new melanoma susceptibility loci.
@en-gb
type
label
Genome-wide association study identifies three new melanoma susceptibility loci.
@ast
Genome-wide association study identifies three new melanoma susceptibility loci.
@en
Genome-wide association study identifies three new melanoma susceptibility loci.
@en-gb
prefLabel
Genome-wide association study identifies three new melanoma susceptibility loci.
@ast
Genome-wide association study identifies three new melanoma susceptibility loci.
@en
Genome-wide association study identifies three new melanoma susceptibility loci.
@en-gb
P2093
P2860
P50
P356
P1433
P1476
Genome-wide association study identifies three new melanoma susceptibility loci.
@en
P2093
Alisa M Goldstein
Anne E Cust
Bart Janssen
Christian Ingvar
David E Elder
Donato Calista
Eitan Friedman
Elizabeth M Gillanders
Esther Azizi
P2860
P2888
P304
P356
10.1038/NG.959
P407
P50
P5008
P577
2011-10-09T00:00:00Z
P5875
P6179
1033916692