| Transcriptome-wide association studies accounting for colocalization using Egger regression |
15 |
| Estimation of a significance threshold for epigenome-wide association studies |
13 |
| The eMERGE genotype set of 717 subjects imputed to similar to 40 million variants genome wide and association with the herpes zoster medical record phenotype |
13 |
| Generalizing polygenic risk scores from Europeans to Hispanics/Latinos |
11 |
| Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes |
9 |
| Bias in Mendelian randomization due to assortative mating |
9 |
| Methods for meta-analysis of multiple traits using GWAS summary statistics |
8 |
| Predictive accuracy of combined genetic and environmental risk scores |
8 |
| Integrated analysis of genomics, longitudinal metabolomics, and Alzheimer's risk factors among 111 cohort participants |
7 |
| Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohorts |
6 |
| Integrating eQTL data with GWAS summary statistics in pathway-based analysis with application to schizophrenia |
6 |
| Ancestry-specific association mapping in admixed populations |
6 |
| A fully adjusted two-stage procedure for rank-normalization in genetic association studies |
6 |
| A multiple mediator analysis approach to quantify the effects of the ADH1B and ALDH2 genes on hepatocellular carcinoma risk |
6 |
| Interaction of a genetic risk score with physical activity, physical inactivity, and body mass index in relation to venous thromboembolism risk |
5 |
| Properties of global- and local-ancestry adjustments in genetic association tests in admixed populations |
5 |
| Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes |
5 |
| A large-scale exome array analysis of venous thromboembolism |
4 |
| The accuracy of LD Score regression as an estimator of confounding and genetic correlations in genome-wide association studies |
4 |
| Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP data |
4 |
| Implementing MR-PRESSO and GCTA-GSMR for pleiotropy assessment in Mendelian randomization studies from a practitioner's perspective |
4 |
| Imputed gene associations identify replicable trans-acting genes enriched in transcription pathways and complex traits |
4 |
| A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals |
4 |
| A review of kernel methods for genetic association studies |
4 |
| A hierarchical clustering method for dimension reduction in joint analysis of multiple phenotypes |
3 |
| POLARIS: Polygenic LD-adjusted risk score approach for set-based analysis of GWAS data |
3 |
| A flexible and parallelizable approach to genome-wide polygenic risk scores |
3 |
| A small-sample kernel association test for correlated data with application to microbiome association studies |
3 |
| FastSKAT: Sequence kernel association tests for very large sets of markers |
3 |
| Spinning convincing stories for both true and false association signals |
3 |
| Kernel machine methods for integrative analysis of genome-wide methylation and genotyping studies |
3 |
| Generalized Hotelling's test for paired compositional data with application to human microbiome studies |
2 |
| Integrating genome-wide association study summaries and element-gene interaction datasets identified multiple associations between elements and complex diseases |
2 |
| A simple and accurate method to determine genomewide significance for association tests in sequencing studies |
2 |
| Constrained instruments and their application to Mendelian randomization with pleiotropy |
2 |
| Extended methods for gene-environment-wide interaction scans in studies of admixed individuals with varying degrees of relationships |
2 |
| System for Quality-Assured Data Analysis: Flexible, reproducible scientific workflows |
2 |
| Summary statistic analyses can mistake confounding bias for heritability |
2 |
| A robust and powerful two-step testing procedure for local ancestry adjusted allelic association analysis in admixed populations |
2 |
| On the testing of Hardy-Weinberg proportions and equality of allele frequencies in males and females at biallelic genetic markers |
2 |
| An ancestry-based approach for detecting interactions |
2 |
| A unified partial likelihood approach for X-chromosome association on time-to-event outcomes |
2 |
| Generalized multifactor dimensionality reduction approaches to identification of genetic interactions underlying ordinal traits |
2 |
| ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available |
2 |
| Bayesian variable selection using partially observed categorical prior information in fine-mapping association studies |
2 |
| Robust meta-analysis of biobank-based genome-wide association studies with unbalanced binary phenotypes |
2 |
| A network approach to prioritizing susceptibility genes for genome-wide association studies |
2 |
| Bayesian meta-analysis across genome-wide association studies of diverse phenotypes |
2 |
| Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI |
2 |
| The evidential statistical paradigm in genetics |
2 |
