| Regionally Smoothed Meta-Analysis Methods for GWAS Datasets |
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| A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information |
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| Adaptive Set-Based Methods for Association Testing |
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| Issue Information |
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| Contents |
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| A Framework for Interpreting Type I Error Rates from a Product‐Term Model of Interaction Applied to Quantitative Traits |
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| Modeling X Chromosome Data Using Random Forests: Conquering Sex Bias |
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| USAT: A Unified Score‐Based Association Test for Multiple Phenotype‐Genotype Analysis |
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| Meta‐Analysis of Rare Variant Association Tests in Multiethnic Populations |
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European; African, Japanese American, Latina, African Americans, multiethnic, ethnicities |
| Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort |
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European subjects; non-Hispanic white |
| Small Sample Kernel Association Tests for Human Genetic and Microbiome Association Studies |
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| Causal Genetic Inference Using Haplotypes as Instrumental Variables |
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| Three Approaches to Modeling Gene‐Environment Interactions in Longitudinal Family Data: Gene‐Smoking Interactions in Blood Pressure |
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| Many Phenotypes Without Many False Discoveries: Error Controlling Strategies for Multitrait Association Studies |
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| Multiple SNP Set Analysis for Genome‐Wide Association Studies Through Bayesian Latent Variable Selection |
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| Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array |
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German; German population; German cases; German controls |
| Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study |
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| Genetic Variants Influencing Joint Damage in Mexican Americans and European Americans With Rheumatoid Arthritis |
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European Americans; Mexican Americans |
| Semiparametric Allelic Tests for Mapping Multiple Phenotypes: Binomial Regression and Mahalanobis Distance |
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| An Adaptive Association Test for Multiple Phenotypes with GWAS Summary Statistics |
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| Issue Information |
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| Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X Chromosome |
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| A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits |
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| Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event |
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| Epithelial‐Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk |
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women of European ancestry; Asians |
| SEQMINER: An R‐Package to Facilitate the Functional Interpretation of Sequence‐Based Associations |
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| The 2015 Annual Meeting of the International Genetic Epidemiology Society |
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| Prognostic and Predictive Values and Statistical Interactions in the Era of Targeted Treatment |
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| SNP Set Association Testing for Survival Outcomes in the Presence of Intrafamilial Correlation |
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| Issue Information |
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| Sequence Kernel Association Analysis of Rare Variant Set Based on the Marginal Regression Model for Binary Traits |
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| A Novel Statistic for Global Association Testing Based on Penalized Regression |
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| Approximate score‐based testing with application to multivariate trait association analysis |
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| Computing a Synthetic Chronic Psychosocial Stress Measurement in Multiple Datasets and its Application in the Replication of G × E Interactions of the <i>EBF1</i> Gene |
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| Contemporary Considerations for Constructing a Genetic Risk Score: An Empirical Approach |
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| A Fast Multiple‐Kernel Method With Applications to Detect Gene‐Environment Interaction |
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| Genome‐Wide Analysis of Gene‐Gene and Gene‐Environment Interactions Using Closed‐Form Wald Tests |
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| Powerful Set‐Based Gene‐Environment Interaction Testing Framework for Complex Diseases |
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| Issue Information |
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| iGWAS: Integrative Genome‐Wide Association Studies of Genetic and Genomic Data for Disease Susceptibility Using Mediation Analysis |
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| SPS: A Simulation Tool for Calculating Power of Set‐Based Genetic Association Tests |
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| Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction |
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European Americans |
| Biology‐Driven Gene‐Gene Interaction Analysis of Age‐Related Cataract in the eMERGE Network |
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European Americans |
| Robust and Powerful Affected Sibpair Test for Rare Variant Association |
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| Influence of Smoking Status and Intensity on Discovery of Blood Pressure Loci Through Gene‐Smoking Interactions |
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| Issue Information |
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| Kernel Approach for Modeling Interaction Effects in Genetic Association Studies of Complex Quantitative Traits |
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| Fast eQTL Analysis for Twin Studies |
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| Testing for Polygenic Effects in Genome‐Wide Association Studies |
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| Genetic Analyses Benefit From Using Less Heterogeneous Phenotypes: An Illustration With the Hospital Anxiety and Depression Scale (HADS) |
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| Robust Inference of Population Structure for Ancestry Prediction and Correction of Stratification in the Presence of Relatedness |
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| Pleiotropy Analysis of Quantitative Traits at Gene Level by Multivariate Functional Linear Models |
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eight European cohorts |
| Issue Information |
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| A Powerful Approach to Test an Optimally Weighted Combination of Rare Variants in Admixed Populations |
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| Permutation Testing in the Presence of Polygenic Variation |
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| Methods for Association Analysis and Meta‐Analysis of Rare Variants in Families |
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| Novel Bayes Factors That Capture Expert Uncertainty in Prior Density Specification in Genetic Association Studies |
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| Deciphering Genome Environment Wide Interactions Using Exposed Subjects Only |
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| LEAP: Biomarker Inference Through Learning and Evaluating Association Patterns |
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| Gene‐Gene Interaction Among <i>WNT</i> Genes for Oral Cleft in Trios |
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European trios; Asian trios |
| Testing the Effect of Rare Compound‐Heterozygous and Recessive Mutations in Case–Parent Sequencing Studies |
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| Meta‐analysis of Genome‐Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology |
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17,248 individuals of European ancestry; 6,841 individuals of Asian ancestry |
| A Retrospective Likelihood Approach for Efficient Integration of Multiple Omics Factors in Case‐Control Association Studies |
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| Interaction Association Analysis of Imputed SNPs in Case‐Control and Follow‐Up Studies |
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| Informed Genome‐Wide Association Analysis With Family History As a Secondary Phenotype Identifies Novel Loci of Lung Cancer |
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| A Genome‐Wide Association Study of Early Spontaneous Preterm Delivery |
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| Issue Information |
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| Population Genetics Identifies Challenges in Analyzing Rare Variants |
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