Crohn disease (CD), an inflammatory bowel disease, is a multifactorial trait with the highest frequency in Ashkenazi Jewish (AJ) individuals of Central European origin. Recently, three common predisposing CARD15 mutations (R702W, G908R, and 1007fs) and a polymorphism (P268S) were identified. To determine whether CARD15 mutations account for the higher prevalence of CD in AJ individuals, the haplotypes and allele frequencies of the common mutations and variants were assessed in 219 members of 50 AJ and 53 members of 10 Sephardi/Oriental Jewish (SOJ) multiplex families with CD, in 36 AJ patients with sporadic CD, and in 246 AJ and 82 SOJ controls. A higher frequency of CARD15 mutations was found in AJ patients from multiplex families with CD ...
Objective Genetic heterogeneity and incomplete phenotype penetrance complicate genetic analysis of C...
BACKGROUND: Crohn's disease (CD) has been associated with CARD15/NOD2 mutations in Caucasians. The R...
BACKGROUND: Crohn's disease (CD) has been associated with CARD15/NOD2 mutations in Caucasians. The R...
Crohn disease (CD), an inflammatory bowel disease, is a multifactorial trait with the highest freque...
Crohn disease (CD) exhibits a 2–4-fold increased frequency in Jews as compared with other ethnic/rac...
Background & AimsCrohn’s disease (CD) is a highly heritable disease that is particularly common in t...
Crohn's disease (CD) is a complex disorder resulting from the interaction of intestinal microbiota w...
As part of a broader collaborative network of exome sequencing studies, we developed a jointly calle...
Background & Aims: Crohn’s disease (CD) is a highly heritable disease that is particularly commo...
As part of a broader collaborative network of exome sequencing studies, we developed a jointly calle...
The caspase recruitment domain gene (CARD15) was recently identified as the underlying gene associat...
As part of a broader collaborative network of exome sequencing studies, we developed a jointly calle...
Current debate focuses on the relevance of linkage disequilibrium (LD), ethnicity and underlying hap...
Objectives: Crohn disease is a chronic inflammatory bowel disorder that is caused by environmental a...
Objective Genetic heterogeneity and incomplete phenotype penetrance complicate genetic analysis of C...
BACKGROUND: Crohn's disease (CD) has been associated with CARD15/NOD2 mutations in Caucasians. The R...
BACKGROUND: Crohn's disease (CD) has been associated with CARD15/NOD2 mutations in Caucasians. The R...
Crohn disease (CD), an inflammatory bowel disease, is a multifactorial trait with the highest freque...
Crohn disease (CD) exhibits a 2–4-fold increased frequency in Jews as compared with other ethnic/rac...
Background & AimsCrohn’s disease (CD) is a highly heritable disease that is particularly common in t...
Crohn's disease (CD) is a complex disorder resulting from the interaction of intestinal microbiota w...
As part of a broader collaborative network of exome sequencing studies, we developed a jointly calle...
Background & Aims: Crohn’s disease (CD) is a highly heritable disease that is particularly commo...
As part of a broader collaborative network of exome sequencing studies, we developed a jointly calle...
The caspase recruitment domain gene (CARD15) was recently identified as the underlying gene associat...
As part of a broader collaborative network of exome sequencing studies, we developed a jointly calle...
Current debate focuses on the relevance of linkage disequilibrium (LD), ethnicity and underlying hap...
Objectives: Crohn disease is a chronic inflammatory bowel disorder that is caused by environmental a...
Objective Genetic heterogeneity and incomplete phenotype penetrance complicate genetic analysis of C...
BACKGROUND: Crohn's disease (CD) has been associated with CARD15/NOD2 mutations in Caucasians. The R...
BACKGROUND: Crohn's disease (CD) has been associated with CARD15/NOD2 mutations in Caucasians. The R...