9 papers found
Significant impact of miRNA–target gene networks on genetics of human complex traits
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
The UK10K project identifies rare variants in health and disease
MultiMeta: an R package for meta-analyzing multi-phenotype genome-wide association studies: Table 1.
FORGE: A tool to discover cell specific enrichments of GWAS associated SNPs in regulatory regions
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