It has been reported that celiac disease (CD) is strongly associated with the HLA-DQ2 alleles DQA1*0501 and DQB1*0201. However, this association only accounts for a portion of the genetic component of CD. Several non-HLA loci and candidate genes that potentially contribute to CD susceptibility have been reported, but have not been confirmed. The aim of this study was to identify loci that contribute to disease susceptibility in a CD population from Finland. We performed a genomewide linkage scan and identified two regions of significant linkage to CD (6p and 2q23-32) and one region of suggestive linkage (10p). We also performed targeted typing and analyses that replicated the associations of the HLA and CTLA4 loci
We tested 310,605 SNPs for association in 778 individuals with celiac disease and 1,422 controls. Ou...
Celiac disease (CD) is a model for common complex disorders with a high degree of heritability. The ...
Item does not contain fulltextUsing variants from the 1000 Genomes Project pilot European CEU datase...
Celiac disease (CD), or gluten-sensitive enteropathy, is a common multifactorial disorder resulting ...
Celiac disease (CD), or gluten-sensitive enteropathy, is a common multifactorial disorder resulting ...
Celiac disease (CD) is a gluten-induced enteropathy, which results from the interplay between enviro...
Abstract Background Celiac disease has a strong genetic association with HLA. However, this associat...
Celiac disease (CD) is a complex genetic disorder with multiple contributing genes. Linkage studies ...
Celiac disease (CD), a malabsorption disorder of the small intestine, results from ingestion of glut...
Celiac disease is a common autoimmune disease caused by sensitivity to the dietary protein gluten. F...
Celiac disease is a common autoimmune disease caused by sensitivity to the dietary protein gluten. F...
SummaryCeliac disease (CD), a malabsorption disorder of the small intestine, results from ingestion ...
Celiac Disease (CD) or Gluten Sensitive Enteropathy (GSE) is a life-long disorder. It is characteriz...
OBJECTIVES: There are significant geographical differences in the prevalence and incidence of celiac...
We tested 310,605 SNPs for association in 778 individuals with celiac disease and 1,422 controls. Ou...
We tested 310,605 SNPs for association in 778 individuals with celiac disease and 1,422 controls. Ou...
Celiac disease (CD) is a model for common complex disorders with a high degree of heritability. The ...
Item does not contain fulltextUsing variants from the 1000 Genomes Project pilot European CEU datase...
Celiac disease (CD), or gluten-sensitive enteropathy, is a common multifactorial disorder resulting ...
Celiac disease (CD), or gluten-sensitive enteropathy, is a common multifactorial disorder resulting ...
Celiac disease (CD) is a gluten-induced enteropathy, which results from the interplay between enviro...
Abstract Background Celiac disease has a strong genetic association with HLA. However, this associat...
Celiac disease (CD) is a complex genetic disorder with multiple contributing genes. Linkage studies ...
Celiac disease (CD), a malabsorption disorder of the small intestine, results from ingestion of glut...
Celiac disease is a common autoimmune disease caused by sensitivity to the dietary protein gluten. F...
Celiac disease is a common autoimmune disease caused by sensitivity to the dietary protein gluten. F...
SummaryCeliac disease (CD), a malabsorption disorder of the small intestine, results from ingestion ...
Celiac Disease (CD) or Gluten Sensitive Enteropathy (GSE) is a life-long disorder. It is characteriz...
OBJECTIVES: There are significant geographical differences in the prevalence and incidence of celiac...
We tested 310,605 SNPs for association in 778 individuals with celiac disease and 1,422 controls. Ou...
We tested 310,605 SNPs for association in 778 individuals with celiac disease and 1,422 controls. Ou...
Celiac disease (CD) is a model for common complex disorders with a high degree of heritability. The ...
Item does not contain fulltextUsing variants from the 1000 Genomes Project pilot European CEU datase...