Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms.
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Analysis of KLF transcription factor family gene variants in type 2 diabetesPower and sample size calculations in the presence of phenotype errors for case/control genetic association studiesEstimating haplotype frequencies in pooled DNA samples when there is genotyping errorSize matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiologyFamily-based genome-wide association scan of attention-deficit/hyperactivity disorder"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.Impact of genotyping errors on the type I error rate and the power of haplotype-based association methods.LRTae: improving statistical power for genetic association with case/control data when phenotype and/or genotype misclassification errors are presentEvaluating the concordance between sequencing, imputation and microarray genotype calls in the GAW18 data.Optimal genotype determination in highly multiplexed SNP data.The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.Detection of genotyping errors by Hardy-Weinberg equilibrium testing.Characteristics of replicated single-nucleotide polymorphism genotypes from COGA: Affymetrix and Center for Inherited Disease Research.A detailed Hapmap of the Sitosterolemia locus spanning 69 kb; differences between Caucasians and African-AmericansChronic renal insufficiency among Asian Indians with type 2 diabetes: I. Role of RAAS gene polymorphisms.Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes.The merits of testing Hardy-Weinberg equilibrium in the analysis of unmatched case-control data: a cautionary note.Association of TGFbeta1, TNFalpha, CCR2 and CCR5 gene polymorphisms in type-2 diabetes and renal insufficiency among Asian IndiansIncorporation of genetic model parameters for cost-effective designs of genetic association studies using DNA pooling.Linkage disequilibrium-based quality control for large-scale genetic studiesEstimating the single nucleotide polymorphism genotype misclassification from routine double measurements in a large epidemiologic sample.Computing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio testDeviations from hardy-weinberg equilibrium in parental and unaffected sibling genotype dataMissing call bias in high-throughput genotyping.Common variants of inflammatory cytokine genes are associated with risk of nephropathy in type 2 diabetes among Asian Indians.Testing Hardy-Weinberg equilibrium and homogeneity of Hardy-Weinberg disequilibrium using complex survey data.Incorporating duplicate genotype data into linear trend tests of genetic association: methods and cost-effectivenessOn quality control measures in genome-wide association studies: a test to assess the genotyping quality of individual probands in family-based association studies and an application to the HapMap data.Assessing the utility of whole-genome amplified serum DNA for array-based high throughput genotyping.Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary studyAssociation analysis of ADPRT1, AKR1B1, RAGE, GFPT2 and PAI-1 gene polymorphisms with chronic renal insufficiency among Asian Indians with type-2 diabetes.In vitro vs in silico detected SNPs for the development of a genotyping array: what can we learn from a non-model species?Genome-wide association scan of attention deficit hyperactivity disorderOptimal two-stage design for case-control association analysis incorporating genotyping errors.Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failureDetection of Mendelian consistent genotyping errors in pedigrees.ALG: automated genotype calling of Luminex assaysParaoxonase 1 (PON1) polymorphisms, haplotypes and activity in predicting cad risk in North-West Indian Punjabis.Approximate and exact tests of Hardy-Weinberg equilibrium using uncertain genotypes.Pharmacogenetic evaluation of ABCB1, Cyp2C9, Cyp2C19 and methylene tetrahydrofolate reductase polymorphisms in teratogenicity of anti-epileptic drugs in women with epilepsy
P2860
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P2860
Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Power and sample size calculat ...... ngle nucleotide polymorphisms.
@en
Power and sample size calculat ...... ngle nucleotide polymorphisms.
@nl
type
label
Power and sample size calculat ...... ngle nucleotide polymorphisms.
@en
Power and sample size calculat ...... ngle nucleotide polymorphisms.
@nl
prefLabel
Power and sample size calculat ...... ngle nucleotide polymorphisms.
@en
Power and sample size calculat ...... ngle nucleotide polymorphisms.
@nl
P2093
P356
P1433
P1476
Power and sample size calculat ...... ngle nucleotide polymorphisms.
@en
P2093
Derek Gordon
Michael Nothnagel
Stephen J Finch
P356
10.1159/000066696
P577
2002-01-01T00:00:00Z