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Genetic Epidemiology is a peer-reviewed medical journal for research on the genetic epidemiology of human traits in families and populations. It is published by John Wiley & Sons on behalf of the International Genetic Epidemiology Society. According to the Journal Citation Reports, the journal has a 2020 impact factor of 2.135. Source: Wikipedia (en)
Editions published in Genetic Epidemiology 200
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Polygenic Epidemiology
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Determining Which Phenotypes Underlie a Pleiotropic Signal
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JAM: A Scalable Bayesian Framework for Joint Analysis of Marginal SNP Effects
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Review of the Gene-Environment Interaction Literature in Cancer: What Do We Know?
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Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project
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Toward the integration of Omics data in epidemiological studies: still a "long and winding road".
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A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits
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Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models
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Genetic data simulators and their applications: an overview
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A Fast Multiple-Kernel Method With Applications to Detect Gene-Environment Interaction
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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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Three Approaches to Modeling Gene-Environment Interactions in Longitudinal Family Data: Gene-Smoking Interactions in Blood Pressure.
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Modeling X Chromosome Data Using Random Forests: Conquering Sex Bias
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A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information
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The association between global DNA methylation and telomere length in a longitudinal study of boilermakers
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Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees
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Challenges of linkage analysis in the era of whole-genome sequencing
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A variational Bayes discrete mixture test for rare variant association
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Using item response theory to model multiple phenotypes and their joint heritability in family data.
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A generalized genetic random field method for the genetic association analysis of sequencing data
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An empirical comparison of meta-analysis and mega-analysis of individual participant data for identifying gene-environment interactions
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Harmonization of study and reference data by PhaseLift: saving time when imputing study data
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Methods for collapsing multiple rare variants in whole-genome sequence data
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Value of Mendelian laws of segregation in families: data quality control, imputation, and beyond
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Testing genetic association with rare and common variants in family data
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Genetic prediction in the Genetic Analysis Workshop 18 sequencing data
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Longitudinal data analysis for genetic studies in the whole-genome sequencing era.
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Longitudinal data analysis in genome-wide association studies
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Applications of machine learning and data mining methods to detect associations of rare and common variants with complex traits
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A custom correlation coefficient (CCC) approach for fast identification of multi-SNP association patterns in genome-wide SNPs data
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Adjusting family relatedness in data-driven burden test of rare variants
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Comparing computational methods for identification of allele-specific expression based on next generation sequencing data.
Subject - wd:Q5532864