Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.
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Genetic Variations Involved in Vitamin E StatusImputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohortGenome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulinComparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data setA reference panel of 64,976 haplotypes for genotype imputation.1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.The influence of ACE ID and ACTN3 R577X polymorphisms on lower-extremity function in older women in response to high-speed power trainingWhole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes.Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypesGenetics of proteasome diseases.Genetic Variations Associated with Vitamin A Status and Vitamin A Bioavailability.Genetic susceptibility to type 2 diabetes and obesity: from genome-wide association studies to rare variants and beyond.Genome-wide association studies of cancer in diverse populations.Host-related factors explaining interindividual variability of carotenoid bioavailability and tissue concentrations in humansVitamin E and Alzheimer's Disease-Is It Time for Personalized Medicine?Estimating genome-wide significance for whole-genome sequencing studiesGenome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence.Comparing genetic variants detected in the 1000 genomes project with SNPs determined by the International HapMap Consortium.Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.Evaluation and application of summary statistic imputation to discover new height-associated loci.Molecular pathology of cutaneous melanomaGenome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
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P2860
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.
description
2013 nî lūn-bûn
@nan
2013 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Imputation of variants from th ...... ed by HapMap based imputation.
@ast
Imputation of variants from th ...... ed by HapMap based imputation.
@en
Imputation of variants from th ...... ed by HapMap based imputation.
@nl
type
label
Imputation of variants from th ...... ed by HapMap based imputation.
@ast
Imputation of variants from th ...... ed by HapMap based imputation.
@en
Imputation of variants from th ...... ed by HapMap based imputation.
@nl
prefLabel
Imputation of variants from th ...... ed by HapMap based imputation.
@ast
Imputation of variants from th ...... ed by HapMap based imputation.
@en
Imputation of variants from th ...... ed by HapMap based imputation.
@nl
P2093
P2860
P50
P1433
P1476
Imputation of variants from th ...... ed by HapMap based imputation.
@en
P2093
Andrew R Wood
David Melzer
Dena G Hernandez
Hou-Feng Zheng
J Brent Richards
J Raphael Gibbs
John R B Perry
Michael A Nalls
Tim D Spector
Toshiko Tanaka
P2860
P304
P356
10.1371/JOURNAL.PONE.0064343
P407
P577
2013-05-16T00:00:00Z