<p>A) Odds ratios and confidence intervals for the different comparisons are shown. The frequency distribution of the minor rs2302685 allele was analysed in different cohorts and combined samples: odds ratios and 95% confidence interval for the allele frequency are shown for patients with specific disease subtypes of ileal CD (classified as either L1 (solely ileal) or L3 (ileal and colonic involvement)) compared to healthy control individuals. The early onset as well as the penetrating behaviour subgroup displays an significantly increased Minor allele frequencies (MAF). B) An especially high risk for early onset ileal CD is found for homozygous minor C - allele carriers. This becomes apparent in the high odds ratios for such individuals in...
BACKGROUND & AIMS: Recent studies reported a role for more than 70 genes or loci in the susceptibili...
<p>Frequencies of carriers of at least one short (S-allele) for the intron 2 microsatellite repeat p...
In most complex diseases, much of the heritability remains unaccounted for by common variants. It ha...
<p>The different distribution of genotypes is demonstrated for each group and subgroup: controls, ul...
<p>For each variable, the number of patients included is given. P<sub>CC</sub><i>P</i>-value for tes...
The percent of subjects recruited at each of the three IBD centers with complete genotype and clinic...
Although genome-wide association studies (GWAS) have separately identified many genetic susceptibili...
<p>P value for genotype frequencies was obtained testing for differences between homo- and heterozyg...
variants still represent the most important predictors for CD susceptibility and phenotype, we eval...
<p>The average relative frequency of each taxa is shown for ileal CD, colitis and control subjects f...
<p>Chi-square test used for <i>P</i>-values. Odds ratio and confidence interval estimated using 2×2 ...
<p>Chi-square test used for <i>P</i>-values. Odds ratio and confidence interval estimated using 2×2 ...
CARD15 on chromosome 16 is the only IBD susceptibility gene identified among several mapped loci. It...
<p>The genotypes for which the risk was calculated are marked in bold. The Bonferroni adjusted p-val...
Crohn’s disease (CD) is a pathologic condition with different clinical expressions that may reflect ...
BACKGROUND & AIMS: Recent studies reported a role for more than 70 genes or loci in the susceptibili...
<p>Frequencies of carriers of at least one short (S-allele) for the intron 2 microsatellite repeat p...
In most complex diseases, much of the heritability remains unaccounted for by common variants. It ha...
<p>The different distribution of genotypes is demonstrated for each group and subgroup: controls, ul...
<p>For each variable, the number of patients included is given. P<sub>CC</sub><i>P</i>-value for tes...
The percent of subjects recruited at each of the three IBD centers with complete genotype and clinic...
Although genome-wide association studies (GWAS) have separately identified many genetic susceptibili...
<p>P value for genotype frequencies was obtained testing for differences between homo- and heterozyg...
variants still represent the most important predictors for CD susceptibility and phenotype, we eval...
<p>The average relative frequency of each taxa is shown for ileal CD, colitis and control subjects f...
<p>Chi-square test used for <i>P</i>-values. Odds ratio and confidence interval estimated using 2×2 ...
<p>Chi-square test used for <i>P</i>-values. Odds ratio and confidence interval estimated using 2×2 ...
CARD15 on chromosome 16 is the only IBD susceptibility gene identified among several mapped loci. It...
<p>The genotypes for which the risk was calculated are marked in bold. The Bonferroni adjusted p-val...
Crohn’s disease (CD) is a pathologic condition with different clinical expressions that may reflect ...
BACKGROUND & AIMS: Recent studies reported a role for more than 70 genes or loci in the susceptibili...
<p>Frequencies of carriers of at least one short (S-allele) for the intron 2 microsatellite repeat p...
In most complex diseases, much of the heritability remains unaccounted for by common variants. It ha...