| Mining gold dust under the genome wide significance level: a two‐stage approach to analysis of GWAS |
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| Inferring genetic causal effects on survival data with associated endo‐phenotypes |
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| Predicting multiallelic genes using unphased and flanking single nucleotide polymorphisms |
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| Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring |
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| Bayesian analysis of rare variants in genetic association studies |
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| Direct assessment of multiple testing correction in case-control association studies with related individuals |
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| Ancestry informative marker panels for African Americans based on subsets of commercially available SNP arrays |
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| Postassociation cleaning using linkage disequilibrium information |
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| Meta-analysis of gene-environment interaction: joint estimation of SNP and SNP × environment regression coefficients |
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| The Maximum-Likelihood-Binomial method revisited: a robust approach for model-free linkage analysis of quantitative traits in large sibships |
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| Analysis of untyped SNPs: maximum likelihood and imputation methods |
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| Abstracts from the nineteenth annual meeting of the International Genetic Epidemiology Society |
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| Distribution of model‐based multipoint heterogeneity lod scores |
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| Meta‐analysis of sex‐specific genome‐wide association studies |
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| Using biological knowledge to discover higher order interactions in genetic association studies |
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| SNP Selection in genome‐wide and candidate gene studies via penalized logistic regression |
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| Evaluating haplotype effects in case‐control studies via penalized‐likelihood approaches: prospective or retrospective analysis? |
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| A simple and fast two‐locus quality control test to detect false positives due to batch effects in genome‐wide association studies |
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| Association statistics under the PPL framework |
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| MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes |
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| A generic coalescent‐based framework for the selection of a reference panel for imputation |
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Hispanic population; admixed populations |
| Evaluating the power to discriminate between highly correlated SNPs in genetic association studies |
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shared ancestry; populations with different LD patterns |
| Bayesian mixture models for the incorporation of prior knowledge to inform genetic association studies |
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| Using cases to strengthen inference on the association between single nucleotide polymorphisms and a secondary phenotype in genome‐wide association studies |
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| An “almost exhaustive” search‐based sequential permutation method for detecting epistasis in disease association studies |
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| Analyze multivariate phenotypes in genetic association studies by combining univariate association tests |
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| Joint testing of genotype and ancestry association in admixed families |
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| Genotype‐based association mapping of complex diseases: gene‐environment interactions with multiple genetic markers and measurement error in environmental exposures |
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| Letter to the Editor |
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| Bayesian variable selection for survival regression in genetics |
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| <i>P</i>‐value based analysis for shared controls design in genome‐wide association studies |
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| Powerful multi‐marker association tests: unifying genomic distance‐based regression and logistic regression |
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| Adjusting for covariates in logistic regression models |
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| Meta‐analysis of genetic association studies and adjustment for multiple testing of correlated SNPs and traits |
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| CAPL: a novel association test using case‐control and family data and accounting for population stratification |
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| A review of statistical methods for testing genetic anticipation: looking for an answer in Lynch syndrome |
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| A multipoint method for meta‐analysis of genetic association studies |
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| Identifying candidate causal variants via trans‐population fine‐mapping |
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| Impact of repeated measures and sample selection on genome‐wide association studies of fasting glucose |
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| Estimation of <i>P</i>‐value of MAX test with double triangle diagram for 2 × 3 SNP case‐control tables |
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| A Bayesian approach to genetic association studies with family‐based designs |
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| Risk prediction using genome‐wide association studies |
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| Pathway‐based analysis for genome‐wide association studies using supervised principal components |
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| Testing for non‐random mating: evidence for ancestry‐related assortative mating in the Framingham heart study |
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North‐South European cline; European descent |
| African and non‐African admixture components in African Americans and an African Caribbean population |
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African vs. European ancestry; European admixture; European |
| Imputation aware meta‐analysis of genome‐wide association studies |
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| On the genome‐wide analysis of copy number variants in family‐based designs: methods for combining family‐based and population‐based information for testing dichotomous or quantitative traits, or comp |
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| Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome |
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| Quality control and quality assurance in genotypic data for genome‐wide association studies |
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| Genome‐wide association studies using haplotype clustering with a new haplotype similarity |
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| A variance components factor model for genetic association studies: A Bayesian analysis |
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| Pooled versus individual genotyping in a breast cancer genome‐wide association study |
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| Resequencing of pooled DNA for detecting disease associations with rare variants |
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| Comparison of association mapping methods in a complex pedigreed population |
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| Risk categorization for complex disorders according to genotype relative risk and precision in parameter estimates |
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| The longitudinal nonparametric test as a new tool to explore gene‐gene and gene‐time effects in cohorts |
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| A statistical method for scanning the genome for regions with rare disease alleles |
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| Ordered subset analysis for case‐control studies |
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| Effect of including environmental data in investigations of gene‐disease associations in the presence of qualitative interactions |
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| Identifying genetic interactions in genome‐wide data using Bayesian networks |
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| Detection of SNP‐SNP interactions in trios of parents with schizophrenic children |
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Ashkenazi Jewish descent |
| Equivalence of three score tests for association mapping of quantitative trait loci under selective genotyping |
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| Design of association studies with pooled or un‐pooled next‐generation sequencing data |
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| Using evidence for population stratification bias in combined individual‐ and family‐level genetic association analyses of quantitative traits |
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| Modeling maternal‐offspring gene‐gene interactions: the extended‐MFG test |
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| Estimating gene penetrance from family data |
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| Entropy‐supported marker selection and Mantel statistics for haplotype sharing analysis |
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| Score‐based adjustment for confounding by population stratification in genetic association studies |
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| Joint linkage and segregation analysis under multiallelic trait inheritance: simplifying interpretations for complex traits |
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| The gene, environment association studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions |
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| Screen and clean: a tool for identifying interactions in genome‐wide association studies |
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| Optimizing the power of genome‐wide association studies by using publicly available reference samples to expand the control group |
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