Related references
Note: Only part of the references are listed.Association of TNFSF15 with Crohn's disease in Koreans
Suk-Kyun Yang et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2008)
Association Between Genetic Variants in the IL-23R Gene and Early-Onset Crohn's Disease: Results From a Case-Control and Family-Based Study Among Canadian Children
Devendra K. Amre et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2008)
The ATG16L1 Gene Variants rs2241879 and rs2241880 (T300A) Are Strongly Associated With Susceptibility to Crohn's Disease in the German Population
Jurgen Glas et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2008)
ATG16L1 T300A Shows Strong Associations With Disease Subgroups in a Large Australian IBD Population: Further Support for Significant Disease Heterogeneity
Elizabeth V. Fowler et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2008)
Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's Disease Risk in a Population-Based Case-Control Study: Evidence of Gene-Gene Interactions
Toshihiko Okazaki et al.
INFLAMMATORY BOWEL DISEASES (2008)
IL23R haplotypes provide a large population attributable risk for Crohn's disease
Kent D. Taylor et al.
INFLAMMATORY BOWEL DISEASES (2008)
Autophagy gene ATG16L1 influences susceptibility and disease location but not childhood-onset in Crohn's disease in northern Europe
J. Van Limbergen et al.
INFLAMMATORY BOWEL DISEASES (2008)
Epidemiology of inflammatory bowel disease in the Songpa-Kangdong district, Seoul, Korea, 1986-2005: A KASID study
Suk-Kyun Yang et al.
INFLAMMATORY BOWEL DISEASES (2008)
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Jeffrey C. Barrett et al.
NATURE GENETICS (2008)
New links to the pathogenesis of Crohn disease provided by genome-wide association scans
Christopher G. Mathew
NATURE REVIEWS GENETICS (2008)
IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand Caucasians with inflammatory bowel disease
Rebecca L. Roberts et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2007)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton et al.
NATURE (2007)
IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease
Mark Tremelling et al.
GASTROENTEROLOGY (2007)
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
Jochen Hampe et al.
NATURE GENETICS (2007)
Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients
Keiko Yamazaki et al.
JOURNAL OF HUMAN GENETICS (2007)
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
Richard H. Duerr et al.
SCIENCE (2006)
Association study of TNFSF15 polymorphisms in Japanese patients with inflammatory bowel disease
Y. Kakuta et al.
GUT (2006)
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease
K Yamazaki et al.
HUMAN MOLECULAR GENETICS (2005)
Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
K Yamazaki et al.
JOURNAL OF HUMAN GENETICS (2004)
Genetic variation in DLG5 is associated with inflammatory bowel disease
M Stoll et al.
NATURE GENETICS (2004)
Functional variants of OCTN cation transporter genes are associated with Crohn disease
VD Peltekova et al.
NATURE GENETICS (2004)
NOD2/CARD15 gene polymorphisms and Crohn's disease in the Chinese population
RWL Leong et al.
ALIMENTARY PHARMACOLOGY & THERAPEUTICS (2003)
Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations
PJP Croucher et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2003)
Inflammatory bowel disease
DK Podolsky
NEW ENGLAND JOURNAL OF MEDICINE (2002)
Lack of common NOD2 variants in Japanese patients with Crohn's disease
N Inoue et al.
GASTROENTEROLOGY (2002)
Epidemiology of inflammatory bowel disease in Asia
SK Yang et al.
INFLAMMATORY BOWEL DISEASES (2001)
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
J Hampe et al.
LANCET (2001)
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
JP Hugot et al.
NATURE (2001)
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
Y Ogura et al.
NATURE (2001)
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci
JD Rioux et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)