Genetic Epidemiology

Papers
(The TQCC of Genetic Epidemiology is 2. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-06-01 to 2026-06-01.)
ArticleCitations
A gene‐based association test of interactions for maternal–fetal genotypes identifies genes associated with nonsyndromic congenital heart defects349
A Brief History behind the journal Genetic Epidemiology and the International Genetic Epidemiology Society133
Statistics to prioritize rare variants in family‐based sequencing studies with disease subtypes69
Deconvolution analysis of cell‐type expression from bulk tissues by integrating with single‐cell expression reference48
Are trait‐associated genes clustered together in a gene network?45
Statistical power of transcriptome‐wide association studies24
A Novel One‐Sample Mendelian Randomization Approach for Count‐Type Outcomes That Is Robust to Correlated and Uncorrelated Pleiotropic Effects20
Bias and mean squared error in Mendelian randomization with invalid instrumental variables16
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MELODY: Mediation Analysis in Logistic Regression for High‐Dimensional Mediators and a Binary Outcome15
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Integrative Harmonization of Phenotypic and Genomic Data Improves Bone Mineral Density Prediction in Multi‐Study Osteoporosis Research11
Multivariable MR Can Mitigate Bias in Two‐Sample MR Using Covariable‐Adjusted Summary Associations10
Gene‐level association analysis of bivariate ordinal traits with functional regressions10
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Causation and familial confounding as explanations for the associations of polygenic risk scores with breast cancer: Evidence from innovative ICE FALCON and ICE CRISTAL analyses9
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Uncovering Ethnicity‐Specific Recessive Loci for Alzheimer's Disease in 89 Dominican Families Using Family‐Based WGS Analysis7
A Robust Association Test Leveraging Unknown Genetic Interactions: Application to Cystic Fibrosis Lung Disease7
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Sensitivity analyses gain relevance by fixing parameters observable during the empirical analyses6
Multivariate analysis of a missense variant in CREBRF reveals associations with measures of adiposity in people of Polynesian ancestries6
Effect of case and control definitions on genome‐wide association study (GWAS) findings6
Control for population stratification in genetic association studies based on GWAS summary statistics5
Investigating the prediction of CpG methylation levels from SNP genotype data to help elucidate relationships between methylation, gene expression and complex traits5
Structured testing of genetic association with mixed clinical outcomes5
A Mixed‐Effect Kernel Machine Regression Model for Integrative Analysis of Alpha Diversity in Microbiome Studies5
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Novel HLA associations with outcomes of Mycobacterium tuberculosis exposure and sarcoidosis in individuals of African ancestry using nearest‐neighbor feature selection4
Correction to “Multivariable MR Can Mitigate Bias in Two‐Sample MR Using Covariable‐Adjusted Summary Associations”4
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Ethical, Legal, and Social Implications of Gene‐Environment Interaction Research4
Methods for large‐scale single mediator hypothesis testing: Possible choices and comparisons4
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Dimension Reduction Using Local Principal Components for Regression‐Based Multi‐SNP Analysis in 1000 Genomes and the Canadian Longitudinal Study on Aging (CLSA)3
Phenotypic variance partitioning by transcriptomic gene expression levels and environmental variables for anthropometric traits using GTEx data3
Statistical learning for sparser fine‐mapped polygenic models: The prediction of LDL‐cholesterol3
Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow‐Up Studies3
Meta‐analysis of breast cancer risk for individuals with PALB2 pathogenic variants3
Parent‐of‐Origin Effects in Childhood Asthma at Seven Years of Age3
Genome‐Wide Association Analyses in Family Triads and Dyads Following Assisted Reproductive Technology3
simmrd: An open‐source tool to perform simulations in Mendelian randomization3
Evaluating a Mendelian Risk Prediction Model That Aggregates Across Genes and Cancers2
Data‐adaptive and pathway‐based tests for association studies between somatic mutations and germline variations in human cancers2
Sparse group variable selection for gene–environment interactions in the longitudinal study2
Use of genetic correlations to examine selection bias2
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Improved two‐step testing of genome‐wide gene–environment interactions2
Shared and Distinct Genetic Factors Underlying Bile Acid Regulation and Intrahepatic Cholestasis of Pregnancy2
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Limitation of permutation‐based differential correlation analysis2
Genetic heterogeneity: Challenges, impacts, and methods through an associative lens2
Using parent‐offspring pairs and trios to estimate indirect genetic effects in education2
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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 Disorder2
Comparison of regmed and BayesNetty for exploring causal models with many variables2
Sex‐Specific Association Between Polymorphisms in Estrogen Receptor Alpha Gene (ESR1) and Depression: A Genome‐Wide Association Study of All of Us and UK Biobank Data2
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Bias correction for inverse variance weighting Mendelian randomization2
Correction to “Abstracts”2
General Kernel Machine Methods for Multi‐Omics Integration and Genome‐Wide Association Testing With Related Individuals2
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Using Family History Data to Improve the Power of Association Studies: Application to Cancer in UK Biobank2
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