Many common human diseases are complex and are expected to be highly heterogeneous,
with multiple causative loci and multiple rare and common variants at some of the causative …

Genome-wide association studies (GWAS) have become a preferred method to identify new
genetic susceptibility loci. This technique aims to understanding the molecular etiology of …

Recent studies in population of European ancestry have shown that 30%∼ 50% of
heritability for human complex traits such as height and body mass index, and common …

Background Recent genome-wide association (GWA) studies have provided compelling
evidence of association between genetic variants and common complex diseases. These …

Genome-wide association studies (GWAS) on diverse ancestry groups are lacking, resulting
in deficits of genetic discoveries and polygenic scores. We conducted GWAS for 76 …

Despite the recent explosive rise in number of genetic markers for complex disease traits
identified in genome-wide association studies, there is still a large gap between the known …

Genome‐wide association studies (GWAS) have identified many single nucleotide
polymorphisms (SNP s) associated with complex traits. However, the genetic heritability of …

To facilitate broad and convenient integrative visualization of and access to GWAS data, we
have created the GWAS Central resource (http://www. gwascentral. org). This database …

The establishment of high-throughput single-nucleotide polymorphism (SNP)-typing
technologies has enabled astonishing progress to be made in genome-wide association …

Polygenic scores (PGS) have been widely used to predict disease risk using variants
identified from genome-wide association studies (GWAS). To date, most GWAS have been …