| Properties of global‐ and local‐ancestry adjustments in genetic association tests in admixed populations |
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global ancestry, local ancestry, admixed populations, ancestral populations, ancestry-adjusted, ance |
| Kernel machine methods for integrative analysis of genome‐wide methylation and genotyping studies |
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| On the substructure controls in rare variant analysis: Principal components or variance components? |
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| Integrating genome‐wide association study summaries and element‐gene interaction datasets identified multiple associations between elements and complex diseases |
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| A deeper look at two concepts of measuring gene–gene interactions: logistic regression and interaction information revisited |
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| Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations |
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| Two‐phase designs for joint quantitative‐trait‐dependent and genotype‐dependent sampling in post‐GWAS regional sequencing |
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| A robust and powerful two‐step testing procedure for local ancestry adjusted allelic association analysis in admixed populations |
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African American ("African American participants"; "African Americans") |
| Methods for meta‐analysis of multiple traits using GWAS summary statistics |
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| Multifactorial disease risk calculator: Risk prediction for multifactorial disease pedigrees |
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| Gene‐based genetic association test with adaptive optimal weights |
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| Predictive accuracy of combined genetic and environmental risk scores |
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| Using imputed genotype data in the joint score tests for genetic association and gene–environment interactions in case‐control studies |
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| A unified partial likelihood approach for X‐chromosome association on time‐to‐event outcomes |
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| Estimating the number of potential family members eligible for <i>BRCA1</i> and <i>BRCA2</i> mutation testing in a “Traceback” approach |
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| Issue Information |
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| Family‐based tests for associating haplotypes with general phenotype data |
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| Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes |
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| An integrative approach to assess X‐chromosome inactivation using allele‐specific expression with applications to epithelial ovarian cancer |
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| Multiethnic polygenic risk scores improve risk prediction in diverse populations |
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European samples; European ancestry; European; Latino; Native American; South Asian; African |
| On meta‐ and mega‐analyses for gene–environment interactions |
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| An ancestry‐based approach for detecting interactions |
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the fraction of European/African ancestry in African Americans; African American and Latino admixed individuals |
| Integrative sparse principal component analysis of gene expression data |
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| Testing for the indirect effect under the null for genome‐wide mediation analyses |
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| Rare‐variant association tests in longitudinal studies, with an application to the Multi‐Ethnic Study of Atherosclerosis (MESA) |
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Multi‐Ethnic |
| On the testing of Hardy‐Weinberg proportions and equality of allele frequencies in males and females at biallelic genetic markers |
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| Impact of sample collection participation on the validity of estimated measures of association in the National Birth Defects Prevention Study when assessing gene‐environment interactions |
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| Corrigendum |
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| Estimation of a significance threshold for epigenome‐wide association studies |
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| Issue Information |
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| Phenotype validation in electronic health records based genetic association studies |
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| Mendelian randomization with fine‐mapped genetic data: Choosing from large numbers of correlated instrumental variables |
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| Evolutionarily derived networks to inform disease pathways |
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| Analysis of cancer gene expression data with an assisted robust marker identification approach |
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| The more you test, the more you find: The smallest <i>P</i>‐values become increasingly enriched with real findings as more tests are conducted |
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| Iterative hard thresholding for model selection in genome‐wide association studies |
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| A multivariate distance‐based analytic framework for microbial interdependence association test in longitudinal study |
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| Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels |
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| A functional U‐statistic method for association analysis of sequencing data |
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| The 2017 Annual Meeting of the International Genetic Epidemiology Society |
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| Issue Information |
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| An efficient study design to test parent‐of‐origin effects in family trios |
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| Adaptive testing for association between two random vectors in moderate to high dimensions |
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| A comparison of methods for inferring causal relationships between genotype and phenotype using additional biological measurements |
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| Joint genotype‐ and ancestry‐based genome‐wide association studies in admixed populations |
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| Improving power for rare‐variant tests by integrating external controls |
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| Accommodating missingness in environmental measurements in gene‐environment interaction analysis |
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| Integrative eQTL analysis of tumor and host omics data in individuals with bladder cancer |
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| A genetic stochastic process model for genome‐wide joint analysis of biomarker dynamics and disease susceptibility with longitudinal data |
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| Detecting genetic association through shortest paths in a bidirected graph |
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| Issue Information |
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| Integrative gene set enrichment analysis utilizing isoform‐specific expression |
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| Region‐based association tests for sequencing data on survival traits |
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| PhredEM: a phred-score-informed genotype-calling approach for next-generation sequencing studies |
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| Polygenic scores via penalized regression on summary statistics |
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| Inferring gene regulatory relationships with a high-dimensional robust approach |
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| Conditional analysis of multiple quantitative traits based on marginal GWAS summary statistics |
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| Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels |
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| Issue Information |
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| Inclusion of biological knowledge in a Bayesian shrinkage model for joint estimation of SNP effects |
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| A novel association test for multiple secondary phenotypes from a case-control GWAS |
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| BinomiRare: A robust test of the association of a rare variant with a disease for pooled analysis and meta-analysis, with application to the HCHS/SOL |
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| A genome‐wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study |
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Mexican‐origin Americans / Mexican Americans |
| A combination test for detection of gene-environment interaction in cohort studies |
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| Semiparametric methods for estimation of a nonlinear exposure‐outcome relationship using instrumental variables with application to Mendelian randomization |
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| On the association analysis of genome‐sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows |
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| Are rare variants really independent? |
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| Issue Information |
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| gsSKAT: Rapid gene set analysis and multiple testing correction for rare‐variant association studies using weighted linear kernels |
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| Genetic risk models: Influence of model size on risk estimates and precision |
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| Gene‐based segregation method for identifying rare variants in family‐based sequencing studies |
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| Adaptive testing for multiple traits in a proportional odds model with applications to detect SNP-brain network associations |
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| Detecting association of rare and common variants based on cross-validation prediction error |
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| Bayesian latent variable models for hierarchical clustered count outcomes with repeated measures in microbiome studies |
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| A powerful statistical framework for generalization testing in GWAS, with application to the HCHS/SOL |
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| Issue Information |
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