<p>We identified 12 common diseases with five or more independent cross-ethnic risk alleles from Varimed. Similar with <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002621#pgen-1002621-g003" target="_blank">Figure 3</a>, we plotted the average increased RAFs in the East Asia regions in the HGDP for each of 12 diseases, against the null distributions of frequency-matched control genomic alleles and risk alleles for other diseases. We ordered these 12 diseases by the increased RAF for a direct comparison. T2D was the only disease showing significantly lower RAFs in the East Asian populations. Two-side p values were calculated by comparing dotted vertical lines against the null distributions of frequency-matched c...
<div><p>Genome-wide association studies (GWAS) have detected many disease associations. However, the...
Background: Searching for associations between genetic variants and complex diseases has been a very...
Asian populations are under-represented in human genomics research. Here, we characterize clinically...
<p>Eleven independent cross-ethnic T2D risk alleles were combined as an ensemble to calculate the av...
<p>The frequencies of six cross-ethnic T2D risk alleles were shown as dark blue wedges across the 53...
Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele frequenc...
<p>Risk-allele frequencies (RAF) were shown as heights of bars across the 11 HapMap populations at 1...
Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele frequenc...
<div><p>Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele ...
<p>Similar with <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002621#p...
<p><i>X</i> axis: log(OR) for the replication stage of the discovery European GWAS. <i>Y</i> axis: l...
<p>Illustration of haplotype forms identified by haploPS that span the longest genetic distance arou...
The successes of genome-wide association (GWA) studies have mainly come from studies performed in po...
<p>A high T2D Genetic Risk Score (GRS) had been previously shown to significantly associate with inc...
<p>The density plots were drawn for the histograms of log(PGR) values across 11 HapMap3 population g...
<div><p>Genome-wide association studies (GWAS) have detected many disease associations. However, the...
Background: Searching for associations between genetic variants and complex diseases has been a very...
Asian populations are under-represented in human genomics research. Here, we characterize clinically...
<p>Eleven independent cross-ethnic T2D risk alleles were combined as an ensemble to calculate the av...
<p>The frequencies of six cross-ethnic T2D risk alleles were shown as dark blue wedges across the 53...
Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele frequenc...
<p>Risk-allele frequencies (RAF) were shown as heights of bars across the 11 HapMap populations at 1...
Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele frequenc...
<div><p>Many disease-susceptible SNPs exhibit significant disparity in ancestral and derived allele ...
<p>Similar with <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002621#p...
<p><i>X</i> axis: log(OR) for the replication stage of the discovery European GWAS. <i>Y</i> axis: l...
<p>Illustration of haplotype forms identified by haploPS that span the longest genetic distance arou...
The successes of genome-wide association (GWA) studies have mainly come from studies performed in po...
<p>A high T2D Genetic Risk Score (GRS) had been previously shown to significantly associate with inc...
<p>The density plots were drawn for the histograms of log(PGR) values across 11 HapMap3 population g...
<div><p>Genome-wide association studies (GWAS) have detected many disease associations. However, the...
Background: Searching for associations between genetic variants and complex diseases has been a very...
Asian populations are under-represented in human genomics research. Here, we characterize clinically...