A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
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WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture riskGenome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffeeGenome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13)Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association studyDNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriersCommon variants in left/right asymmetry genes and pathways are associated with relative hand skillCommon genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessChapter 11: Genome-wide association studiesGene-wide characterization of common quantitative trait loci for ABCB1 mRNA expression in normal liver tissues in the Chinese populationQuantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome associationThe genetic architecture of adaptations to high altitude in EthiopiaEpigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing populationChimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatelliteTREM2 Variants in Alzheimer's DiseaseMeta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's diseaseGenome-wide association study of Tourette's syndromeA genome-wide association study of anorexia nervosa.TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosisSequence variants in SLC16A11 are a common risk factor for type 2 diabetes in MexicoIFITM3 restricts the morbidity and mortality associated with influenzaCohort Profile: TwinsUK and healthy ageing twin studyPCSK6 is associated with handedness in individuals with dyslexiaComprehensive evaluation of imputation performance in African AmericansIdentification of multiple genetic susceptibility loci in Takayasu arteritisDense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosisGenotype imputation with thousands of genomesIdentification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypesGenome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial MorphologyThe fine-scale genetic structure of the British populationMaking sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genomeProgress and promise in understanding the genetic basis of common diseasesApplication of computational methods in genetic study of inflammatory bowel diseaseInsights into the genetic architecture of diabetic nephropathyThe genetics of major depressionDisease mechanisms in rheumatology--tools and pathways: defining functional genetic variants in autoimmune diseasesExome sequencing and complex disease: practical aspects of rare variant association studiesPyPedia: using the wiki paradigm as crowd sourcing environment for bioinformatics protocolsDNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient.Epigenomic elements analyses for promoters identify ESRRG as a new susceptibility gene for obesity-related traitsAssociation of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals
P2860
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P2860
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունիսին 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 flexible and accurate genoty ...... enome-wide association studies
@ast
A flexible and accurate genoty ...... enome-wide association studies
@en
A flexible and accurate genoty ...... enome-wide association studies
@en-gb
A flexible and accurate genoty ...... enome-wide association studies
@nl
type
label
A flexible and accurate genoty ...... enome-wide association studies
@ast
A flexible and accurate genoty ...... enome-wide association studies
@en
A flexible and accurate genoty ...... enome-wide association studies
@en-gb
A flexible and accurate genoty ...... enome-wide association studies
@nl
altLabel
A Flexible and Accurate Genoty ...... enome-Wide Association Studies
@en
prefLabel
A flexible and accurate genoty ...... enome-wide association studies
@ast
A flexible and accurate genoty ...... enome-wide association studies
@en
A flexible and accurate genoty ...... enome-wide association studies
@en-gb
A flexible and accurate genoty ...... enome-wide association studies
@nl
P2860
P3181
P1433
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A flexible and accurate genoty ...... enome-wide association studies
@en
P2093
Bryan N Howie
P2860
P304
P3181
P356
10.1371/JOURNAL.PGEN.1000529
P407
P577
2009-06-01T00:00:00Z