| Repeated measurement sampling in genetic association analysis with genotyping errors |
|
|
|
|
|
|
|
|
|
| Sex‐specific QTL effects on variation in paraoxonase 1 (PON1) activity in Mexican Americans |
|
|
|
|
|
|
|
|
|
| Simple methods for assessing haplotype‐environment interactions in case‐only and case‐control studies |
|
|
|
|
|
|
|
|
|
| Explorative two‐locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures‐related photosensitivity loci |
|
|
|
|
|
|
|
|
|
| Informative‐Transmission Disequilibrium Test (i‐TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring |
|
|
|
|
|
|
|
|
|
| Interpretation of simultaneous linkage and family‐based association tests in genome screens |
|
|
|
|
|
|
|
|
|
| MCMC‐based linkage analysis for complex traits on general pedigrees: multipoint analysis with a two‐locus model and a polygenic component |
|
|
|
|
|
|
|
|
|
| Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage |
|
|
|
|
|
|
|
|
|
| Family‐based association analysis with ordered categorical phenotypes, covariates and interactions |
|
|
|
|
|
|
|
|
|
| Genetic influences on mannan‐binding lectin (MBL) and mannan‐binding lectin associated serine protease‐2 (MASP‐2) activity |
|
|
|
|
|
|
|
|
|
| Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent‐of‐origin (<i>POO</i>) effects in the presence of missing parental genotypes when unaffected si |
|
|
|
|
|
|
|
|
|
| Family‐based association tests for ordinal traits adjusting for covariates |
|
|
|
|
|
|
|
|
|
| The elusive goal of pedigree weights |
|
|
|
|
|
|
|
|
|
| A new multimarker test for family‐based association studies |
|
|
|
|
|
|
|
|
|
| The admixture maximum likelihood test: a novel experiment‐wise test of association between disease and multiple SNPs |
|
|
|
|
|
|
|
|
|
| Quantifying the amount of missing information in genetic association studies |
|
|
|
|
|
|
|
|
|
| Testing Untyped Alleles (TUNA)—applications to genome‐wide association studies |
|
|
|
|
|
|
|
|
|
| Imputation methods to improve inference in SNP association studies |
|
|
|
|
|
|
|
|
|
| Simultaneous estimation of gene‐gene and gene‐environment interactions for numerous loci using double penalized log–likelihood |
|
|
|
|
|
|
|
|
|
| Gene‐dropping vs. empirical variance estimation for allele‐sharing linkage statistics |
|
|
|
|
|
|
|
|
|
| Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment |
|
|
|
|
|
|
|
|
|
| A comparison of methods for intermediate fine mapping |
|
|
|
|
|
|
|
|
|
| Perils and pitfalls of permutation tests for distinguishing the effects of neighbouring polymorphisms |
|
|
|
|
|
|
|
|
|
| An efficient family‐based association test using multiple markers |
|
|
|
|
|
|
|
|
|
| Familial aggregation of ischemic stroke in young women: the Stroke Prevention in Young Women Study |
|
|
|
|
|
|
|
|
|
| Semiparametric variance‐component models for linkage and association analyses of censored trait data |
|
|
|
|
|
|
|
|
|
| A scan statistic for identifying chromosomal patterns of SNP association |
|
|
|
|
|
|
|
|
|
| Quantifying bias due to allele misclassification in case‐control studies of haplotypes |
|
|
|
|
|
|
|
|
|
| Comparison of SNP tagging methods using empirical data: association study of 713 SNPs on chromosome 12q14.3–12q24.21 for asthma and total serum IgE in an African Caribbean population |
|
|
|
|
|
|
✓ |
✓ |
African Caribbean |
| A sliding‐window weighted linkage disequilibrium test |
|
|
|
|
|
|
|
|
|
| The effect of reduction in cross‐validation intervals on the performance of multifactor dimensionality reduction |
|
|
|
|
|
|
|
|
|
| Molecular evolution of 5′ flanking regions of 87 candidate genes for atherosclerotic cardiovascular disease |
|
|
|
|
|
✓ |
✓ |
✓ |
European‐Americans; African‐Americans |
| Contrasting multi‐site genotypic distributions among discordant quantitative phenotypes: the <i>APOA1/C3/A4/A5</i> gene cluster and cardiovascular disease risk factors |
|
|
|
|
|
✓ |
|
|
European‐American |
| Stratified false discovery control for large‐scale hypothesis testing with application to genome‐wide association studies |
|
|
|
|
|
|
|
|
|
| Simple estimates of haplotype relative risks in case‐control data |
|
|
|
|
|
|
|
|
|
| Resampling‐based multiple hypothesis testing procedures for genetic case‐control association studies |
|
|
|
|
|
|
|
|
|
| Sex differences in genetic and environmental determinants of pulse pressure |
|
|
|
|
|
|
|
|
|
| Using sex‐averaged genetic maps in multipoint linkage analysis when identity‐by‐descent status is incompletely known |
|
|
|
|
|
|
|
|
|
| Distribution and magnitude of type I error of model‐based multipoint lod scores: implications for multipoint mod scores |
|
|
|
|
|
|
|
|
|
| Estimating the power of variance component linkage analysis in large pedigrees |
|
|
|
|
|
|
✓ |
✓ |
Sardinians |
| A comparison of several methods for haplotype frequency estimation and haplotype reconstruction for tightly linked markers from general pedigrees |
|
|
|
|
|
|
|
|
|
| Power‐based, phase‐informed selection of single nucleotide polymorphisms for disease association screens |
|
|
|
|
|
|
|
|
|
| Nonparametric linkage analysis using person‐specific covariates |
|
|
|
|
|
|
|
|
|
| Omnibus permutation tests of the association of an ensemble of genetic markers with disease in case‐control studies |
|
|
|
|
|
|
|
|
|
| Variance component models for X‐linked QTLs |
|
|
|
|
|
|
|
|
|
| Linkage analysis with gene‐environment interaction: model illustration and performance of ordered subset analysis |
|
|
|
|
|
|
|
|
|
| Optimal two‐stage genotyping designs for genome‐wide association scans |
|
|
|
|
|
|
|
|
|
| Improving the power of association tests for quantitative traits in family studies |
|
|
|
|
|
|
|
|
|
| The v‐MFG test: investigating maternal, offspring and maternal‐fetal genetic incompatibility effects on disease and viability |
|
|
|
|
|
|
|
|
|
| An evaluation of the replicate pool method: quick estimation of genome‐wide linkage peak <i>p</i>‐values |
|
|
|
|
|
|
|
|
|
| Testing for genetic heterogeneity in the genome search meta‐analysis method |
|
|
|
|
|
|
|
|
|
| Power comparison of generalizations of the mean test for affected sib pairs in case of incompletely informative markers |
|
|
|
|
|
|
|
|
|
| A Bayesian toolkit for genetic association studies |
|
|
|
|
|
|
|
|
|
| Haplotype analysis in the presence of informatively missing genotype data |
|
|
|
|
|
|
|
|
|
| Centralizing the non‐central chi‐square: a new method to correct for population stratification in genetic case‐control association studies |
|
|
|
|
|
|
|
|
|
| Improved association analyses of disease subtypes in case‐parent triads |
|
|
|
|
|
|
|
|
|
| Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring |
|
|
|
|
|
|
|
|
|
| Estimation and testing of genotype and haplotype effects in case‐control studies: comparison of weighted regression and multiple imputation procedures |
|
|
|
|
|
|
|
|
|
| Haplotype association analysis for late onset diseases using nuclear family data |
|
|
|
|
|
|
|
|
|
| Using endophenotypes for pathway clusters to map complex disease genes |
|
|
|
|
|
|
|
|
|