Zhu et al., 2023
ViewHTML| Publication | Publication Date | Title | 
|---|---|---|
| Zhu et al. | Amplification is the primary mode of gene-by-sex interaction in complex human traits | |
| Uffelmann et al. | Genome-wide association studies | |
| Weiner et al. | Polygenic architecture of rare coding variation across 394,783 exomes | |
| Hysi et al. | Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability | |
| Goldgar et al. | Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2 | |
| Hutchinson et al. | Fine-mapping genetic associations | |
| US20200327956A1 (en) | Methods of selection, reporting and analysis of genetic markers using broad-based genetic profiling applications | |
| Pirinen et al. | Assessing allele-specific expression across multiple tissues from RNA-seq read data | |
| Liang et al. | The lengths of admixture tracts | |
| de la Fuente | From ‘differential expression’to ‘differential networking’–identification of dysfunctional regulatory networks in diseases | |
| MacArthur et al. | Guidelines for investigating causality of sequence variants in human disease | |
| Vinkhuyzen et al. | Estimation and partition of heritability in human populations using whole-genome analysis methods | |
| Nuzhdin et al. | Genotype–phenotype mapping in a post-GWAS world | |
| Wu et al. | Joint analysis of GWAS and multi-omics QTL summary statistics reveals a large fraction of GWAS signals shared with molecular phenotypes | |
| Qi et al. | From genetic associations to genes: methods, applications, and challenges | |
| Little et al. | Strengthening the reporting of genetic association studies (STREGA)—an extension of the strengthening the reporting of observational studies in epidemiology (STROBE) statement | |
| Maguluri et al. | Big Data Solutions For Mapping Genetic Markers Associated With Lifestyle Diseases | |
| Slatkin | Disequilibrium mapping of a quantitative-trait locus in an expanding population | |
| Shin et al. | GxEsum: a novel approach to estimate the phenotypic variance explained by genome-wide GxE interaction based on GWAS summary statistics for biobank-scale data | |
| Liu et al. | Conditional transcriptome-wide association study for fine-mapping candidate causal genes | |
| Kerner et al. | A genome-wide case-only test for the detection of digenic inheritance in human exomes | |
| López-Bigas et al. | Highly consistent patterns for inherited human diseases at the molecular level | |
| Weissenkampen et al. | Methods for the analysis and interpretation for rare variants associated with complex traits | |
| David | A current guide to candidate gene association studies | |
| Yurko et al. | A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk |