Transcriptome-wide association studies (TWAS) integrate genome-wide association studies (GWAS) and gene expression datasets to identify gene–trait associations. In this …
Abstract Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated …
Previous genome-wide association studies (GWASs) of stroke—the second leading cause of death worldwide—were conducted predominantly in populations of European ancestry …
Missing heritability in genome-wide association studies defines a major problem in genetic analyses of complex biological traits,. The solution to this problem is to identify all causal …
The development of transcriptome-wide association studies (TWAS) has enabled researchers to better identify and interpret causal genes in many diseases. However, there …
Bipolar disorder is a heritable mental illness with complex etiology. We performed a genome- wide association study of 41,917 bipolar disorder cases and 371,549 controls of European …
Biobanks facilitate genome-wide association studies (GWASs), which have mapped genomic loci across a range of human diseases and traits. However, most biobanks are …
Most genetic variants identified from genome-wide association studies (GWAS) in humans are noncoding, indicating their role in gene regulation. Previous studies have shown …
Primary open-angle glaucoma (POAG), is a heritable common cause of blindness world- wide. To identify risk loci, we conduct a large multi-ethnic meta-analysis of genome-wide …