| Improved two‐step testing of genome‐wide gene–environment interactions |
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| Efficient identification of trait‐associated loss‐of‐function variants in the UK Biobank cohort by exome‐sequencing based genotype imputation |
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UKB homogeneous European participants |
| Methods for large‐scale single mediator hypothesis testing: Possible choices and comparisons |
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| Adaptive Bayesian variable clustering via structural learning of breast cancer data |
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| Issue Information |
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| Multivariate analysis of a missense variant in <i>CREBRF</i> reveals associations with measures of adiposity in people of Polynesian ancestries |
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| Sparse prediction informed by genetic annotations using the logit normal prior for Bayesian regression tree ensembles |
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| Statistical methods for <i>cis</i>‐Mendelian randomization with two‐sample summary‐level data |
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| An empirical Bayes approach to improving population‐specific genetic association estimation by leveraging cross‐population data |
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non‐European ancestry; European ancestry population; trans‐ancestry GWAS |
| Mediation analysis of multiple mediators with incomplete omics data |
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| Issue Information |
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| Abstracts |
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| An exploration of linkage fine‐mapping on sequences from case‐control studies |
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| Statistical learning for sparser fine‐mapped polygenic models: The prediction of LDL‐cholesterol |
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| Investigating the prediction of CpG methylation levels from SNP genotype data to help elucidate relationships between methylation, gene expression and complex traits |
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| Genetic heterogeneity: Challenges, impacts, and methods through an associative lens |
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| Issue Information |
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| Including diverse and admixed populations in genetic epidemiology research |
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| Deconvolution analysis of cell‐type expression from bulk tissues by integrating with single‐cell expression reference |
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| Sparse group variable selection for gene–environment interactions in the longitudinal study |
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| Control for population stratification in genetic association studies based on GWAS summary statistics |
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| Statistical power of transcriptome‐wide association studies |
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| A Bayesian hierarchical model for improving measurement of 5mC and 5hmC levels: Toward revealing associations between phenotypes and methylation states |
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| Novel HLA associations with outcomes of <i>Mycobacterium tuberculosis</i> exposure and sarcoidosis in individuals of African ancestry using nearest‐neighbor feature selection |
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individuals of African ancestry |
| Post hoc power is not informative |
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| Clarifying the causes of consistent and inconsistent findings in genetics |
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| Analysis of parent‐of‐origin effects for secondary phenotypes using case–control mother–child pair data |
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| Disentangling the effects of traits with shared clustered genetic predictors using multivariable Mendelian randomization |
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| Adjusting for collider bias in genetic association studies using instrumental variable methods |
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| Statistical methods for Mendelian models with multiple genes and cancers |
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| Issue Information |
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| Selection bias when inferring the effect direction in Mendelian randomization |
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| Gene‐environment interaction in type 2 diabetes in Korean cohorts: Interaction of a type 2 diabetes polygenic risk score with triglyceride and cholesterol on fasting glucose levels |
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Korean cohorts; multiethnic data |
| Benchmarking statistical methods for analyzing parent–child dyads in genetic association studies |
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multiethnic mother–child pairs |
| Gene‐level association analysis of ordinal traits with functional ordinal logistic regressions |
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| Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank |
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| RAVAQ: An integrative pipeline from quality control to region‐based rare variant association analysis |
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| Secondary analyses for genome‐wide association studies using expression quantitative trait loci |
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| A two‐sample robust Bayesian Mendelian Randomization method accounting for linkage disequilibrium and idiosyncratic pleiotropy with applications to the COVID‐19 outcomes |
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| Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes |
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| Issue Information |
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| The influence of unmeasured confounding on the MR Steiger approach |
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| Interaction between genetics and smoking in determining risk of coronary artery diseases |
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participants of European ancestry |
| Integrating external controls in case–control studies improves power for rare‐variant tests |
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| Collider bias from selecting disease samples distorts causal inferences |
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| Issue Information |
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| Genome‐wide association studies of 27 accelerometry‐derived physical activity measurements identified novel loci and genetic mechanisms |
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| Genome‐wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores |
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