Use of unphased multilocus genotype data in indirect association studies.
about
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetranceTP53-binding protein variants and breast cancer risk: a case-control studyPolymorphism discovery and association analyses of the interferon genes in type 1 diabetesGenetic association mapping via evolution-based clustering of haplotypesAllowing for missing data at highly polymorphic genes when testing for maternal, offspring and maternal-fetal genotype incompatibility effects.Understanding the accuracy of statistical haplotype inference with sequence data of known phase.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.Fine mapping--19th century style.Fine-scale mapping in case-control samples using locus scoring and haplotype-sharing methods.Discovery, linkage disequilibrium and association analyses of polymorphisms of the immune complement inhibitor, decay-accelerating factor gene (DAF/CD55) in type 1 diabetesHow well do HapMap SNPs capture the untyped SNPs?Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.Applicability of DNA pools on 500 K SNP microarrays for cost-effective initial screens in genomewide association studiesA systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure.Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variationComprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritisSingle-marker and two-marker association tests for unphased case-control genotype data, with a power comparisonRegion-based analysis in genome-wide association study of Framingham Heart Study blood lipid phenotypesPCA-based bootstrap confidence interval tests for gene-disease association involving multiple SNPsA data-adaptive sum test for disease association with multiple common or rare variants.Statistical challenges for genome-wide association studies of suicidality using family data.The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.Estrogen receptor genotype and risk of cognitive impairment in elders: findings from the Health ABC study.Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia.Common SNPs in FTO gene are associated with obesity related anthropometric traits in an island population from the eastern Adriatic coast of Croatia.USING LINEAR PREDICTORS TO IMPUTE ALLELE FREQUENCIES FROM SUMMARY OR POOLED GENOTYPE DATA.An omnibus test for family-based association studies with multiple SNPs and multiple phenotypesGWAS to Sequencing: Divergence in Study Design and AnalysisModifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping resultsNo evidence of association or interaction between the IL4RA, IL4, and IL13 genes in type 1 diabetesA high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.Localization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag single-nucleotide polymorphisms.Family-based association test using normal approximation to gene dropping null distribution.Imputation without doing imputation: a new method for the detection of non-genotyped causal variants.Power of association tests in the presence of multiple causal variants.Cumulative risk on the oxytocin receptor gene (OXTR) underpins empathic communication difficulties at the first stages of romantic love.Joint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power.Regression-based association analysis with clustered haplotypes through use of genotypes.High-resolution association mapping of quantitative trait loci: a population-based approach.
P2860
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P2860
Use of unphased multilocus genotype data in indirect association studies.
description
2004 nî lūn-bûn
@nan
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Use of unphased multilocus genotype data in indirect association studies.
@ast
Use of unphased multilocus genotype data in indirect association studies.
@en
type
label
Use of unphased multilocus genotype data in indirect association studies.
@ast
Use of unphased multilocus genotype data in indirect association studies.
@en
prefLabel
Use of unphased multilocus genotype data in indirect association studies.
@ast
Use of unphased multilocus genotype data in indirect association studies.
@en
P2093
P356
P1433
P1476
Use of unphased multilocus genotype data in indirect association studies.
@en
P2093
David Clayton
Jason Cooper
Juliet Chapman
P304
P356
10.1002/GEPI.20032
P577
2004-12-01T00:00:00Z