Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
- 19 October 2004
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 49 (12), 664-668
- https://doi.org/10.1007/s10038-004-0204-x
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populationsEuropean Journal of Human Genetics, 2003
- Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's diseaseJournal of Human Genetics, 2002
- CARD15/NOD2 Mutational Analysis and Genotype-Phenotype Correlation in 612 Patients with Inflammatory Bowel DiseaseAmerican Journal of Human Genetics, 2002
- A high-throughput SNP typing system for genome-wide association studiesJournal of Human Genetics, 2001
- Association between a Single-Nucleotide Polymorphism in the Promoter of the Human Interleukin-3 Gene and Rheumatoid Arthritis in Japanese Patients, and Maximum-Likelihood Estimation of Combinatorial Effect That Two Genetic Loci Have on Susceptibility to the DiseaseAmerican Journal of Human Genetics, 2001
- Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's diseaseJournal of Human Genetics, 2001
- Two stage genome–wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12Nature Genetics, 1996
- Mapping of a susceptibility locus for Crohn's disease on chromosome 16Nature, 1996
- Classification of Inflammatory Bowel DiseaseScandinavian Journal of Gastroenterology, 1989
- Counting methods (EM algorithm) in human pedigree analysis: Linkage and segregation analysisAnnals of Human Genetics, 1977