Works matching IS 07410395 AND DT 2025 AND VI 49 AND IP 1
Results: 30
Genetically Predicted Gene Expression Effects on Changes in Red Blood Cell and Plasma Polyunsaturated Fatty Acids.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22613
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A Novel Statistical Method for Unmasking Sex‐Specific Genomics Signatures in Complex Traits.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22612
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Transferability of Single‐ and Cross‐Tissue Transcriptome Imputation Models Across Ancestry Groups.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22611
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Identifying Disease Associated Multi‐Omics Network With Mixed Graphical Models Based on Markov Random Field Model.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22605
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Using Family History Data to Improve the Power of Association Studies: Application to Cancer in UK Biobank.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22609
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Integrative Multi‐Omics Approach for Improving Causal Gene Identification.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22601
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Refinement of a Published Gene‐Physical Activity Interaction Impacting HDL‐Cholesterol: Role of Sex and Lipoprotein Subfractions.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22607
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Multivariable MR Can Mitigate Bias in Two‐Sample MR Using Covariable‐Adjusted Summary Associations.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22606
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General Kernel Machine Methods for Multi‐Omics Integration and Genome‐Wide Association Testing With Related Individuals.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22610
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A Novel One‐Sample Mendelian Randomization Approach for Count‐Type Outcomes That Is Robust to Correlated and Uncorrelated Pleiotropic Effects.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22602
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Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow‐Up Studies.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22608
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Estimating Causal Effects on a Disease Progression Trait Using Bivariate Mendelian Randomisation.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22600
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Fine‐Mapping the Results From Genome‐Wide Association Studies of Primary Biliary Cholangitis Using SuSiE and h2‐D2.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22592
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A Mixed‐Effect Kernel Machine Regression Model for Integrative Analysis of Alpha Diversity in Microbiome Studies.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22596
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Enhancing Gene Expression Predictions Using Deep Learning and Functional Annotations.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22595
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GWASBrewer: An R Package for Simulating Realistic GWAS Summary Statistics.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22594
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Powerful Rare‐Variant Association Analysis of Secondary Phenotypes.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22589
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Correction to the 2024 Annual Meeting of the International Genetic Epidemiology Society.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22599
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- Article
Ethical, Legal, and Social Implications of Gene‐Environment Interaction Research.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22591
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Comparing Ancestry Standardization Approaches for a Transancestry Colorectal Cancer Polygenic Risk Score.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22590
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PSAP‐Genomic‐Regions: A Method Leveraging Population Data to Prioritize Coding and Non‐Coding Variants in Whole Genome Sequencing for Rare Disease Diagnosis.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22593
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Polygenic hazard score models for the prediction of Alzheimer's free survival using the lasso for Cox's proportional hazards model.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22581
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Predicting Lung Cancer in Korean Never‐Smokers With Polygenic Risk Scores.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22586
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Use of genetic correlations to examine selection bias.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22584
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Exploring pleiotropy in Mendelian randomisation analyses: What are genetic variants associated with 'cigarette smoking initiation' really capturing?
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22583
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Genetic Associations of Persistent Opioid Use After Surgery Point to OPRM1 but Not Other Opioid‐Related Loci as the Main Driver of Opioid Use Disorder.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22588
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Exploring and Accounting for Genetically Driven Effect Heterogeneity in Mendelian Randomization.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22587
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Issue Information.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22569
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- Article
Gene−Air Pollution Interaction and Diversity of Genetic Sampling: The Southern California Children's Health Study.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.70000
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Using clustering of genetic variants in Mendelian randomization to interrogate the causal pathways underlying multimorbidity from a common risk factor.
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- Genetic Epidemiology, 2025, v. 49, n. 1, p. 1, doi. 10.1002/gepi.22582
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