Susceptibility loci reported in genome‐wide association studies are associated with Crohn’s disease in Canadian children
Devendra Amre(Centre Hospitalier Universitaire Sainte-Justine), Émile Lévy(Université de Montréal), Houda Fegury(Centre Hospitalier Universitaire Sainte-Justine), Ernest G. Seidman(Université de Montréal), Philippe Lambrette(Centre Hospitalier Universitaire Sainte-Justine), Colette Deslandres(Centre Hospitalier Universitaire Sainte-Justine), Alfreda Krupoves(Université de Montréal), Kenneth Morgan(University of London), Guy Grimard(Université de Montréal), David M. Israel(University of British Columbia), Jinsong Dong(Chinese Academy of Agricultural Sciences), David Mack(Children's Hospital of Eastern Ontario), Irina Costea(Université de Montréal)
Cited by 36
Related Papers
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
|Nature Genetics|1999|1.7k
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
|Nature Genetics|2010|680
SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis
|The American Journal of Human Genetics|2006|493
Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy
|Journal of Allergy and Clinical Immunology|2011|479