Pages that link to "Q24649802"

The following pages link to A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 (Q24649802):

Displaying 50 items.

• celiac disease (Q11088) ‎ (← links)
• HLA-DQA1 (Q18026947) ‎ (← links)
• A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci (Q21145042) ‎ (← links)
• Spectrum of gluten-related disorders: consensus on new nomenclature and classification (Q21245301) ‎ (← links)
• Accurate and robust genomic prediction of celiac disease using statistical learning (Q21563352) ‎ (← links)
• Recent Insights Into the Genetics of Inflammatory Bowel Disease (Q22250935) ‎ (← links)
• Celiac disease: prevalence, diagnosis, pathogenesis and treatment (Q22305490) ‎ (← links)
• Celiac disease and non-celiac gluten sensitivity (Q22306535) ‎ (← links)
• Lacritin and other new proteins of the lacrimal functional unit (Q24320688) ‎ (← links)
• The Oslo definitions for coeliac disease and related terms (Q24601971) ‎ (← links)
• Multiple common variants for celiac disease influencing immune gene expression (Q24608614) ‎ (← links)
• Common variants conferring risk of schizophrenia (Q24614376) ‎ (← links)
• The biological functions of T helper 17 cell effector cytokines in inflammation (Q24614431) ‎ (← links)
• Shared and distinct genetic variants in type 1 diabetes and celiac disease (Q24623113) ‎ (← links)
• Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection (Q24632121) ‎ (← links)
• A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis (Q24634112) ‎ (← links)
• Testing for antireticulin antibodies in patients with celiac disease is obsolete: a review of recommendations for serologic screening and the literature (Q24634400) ‎ (← links)
• Human dectin-1 deficiency and mucocutaneous fungal infections (Q24645008) ‎ (← links)
• Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions (Q24645332) ‎ (← links)
• Newly identified genetic risk variants for celiac disease related to the immune response (Q24654340) ‎ (← links)
• Intestinal Microbiota and Celiac Disease: Cause, Consequence or Co-Evolution? (Q26796606) ‎ (← links)
• Risk factors for celiac disease (Q26798375) ‎ (← links)
• Genomic risk prediction of complex human disease and its clinical application (Q26799562) ‎ (← links)
• Therapeutic approaches for celiac disease (Q26825413) ‎ (← links)
• The neuroimmunology of schizophrenia (Q26859392) ‎ (← links)
• Immune development and intestinal microbiota in celiac disease (Q27026098) ‎ (← links)
• Structural and Functional Studies of trans -Encoded HLA-DQ2.3 (DQA1*03:01/DQB1*02:01) Protein Molecule (Q27677454) ‎ (← links)
• Coeliac disease: a unique model for investigating broken tolerance in autoimmunity (Q28073430) ‎ (← links)
• Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling (Q28236179) ‎ (← links)
• Recent advances in the genetics of autoimmune disease (Q28238782) ‎ (← links)
• Coeliac disease (Q28242747) ‎ (← links)
• Coeliac disease and autoimmune disease-genetic overlap and screening (Q28266589) ‎ (← links)
• Gluten sensitivity: from gut to brain (Q28273729) ‎ (← links)
• Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci (Q28281906) ‎ (← links)
• Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease (Q28286971) ‎ (← links)
• Evaluation of European coeliac disease risk variants in a north Indian population (Q28395308) ‎ (← links)
• Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus (Q28924360) ‎ (← links)
• Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci (Q28943258) ‎ (← links)
• A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease (Q28943307) ‎ (← links)
• A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease (Q28943417) ‎ (← links)
• ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study (Q28943532) ‎ (← links)
• Wnt signaling and Dupuytren's disease (Q29417139) ‎ (← links)
• Integrating common and rare genetic variation in diverse human populations (Q29547220) ‎ (← links)
• A HapMap harvest of insights into the genetics of common disease (Q29614875) ‎ (← links)
• Identification of Non-HLA Genes Associated with Celiac Disease and Country-Specific Differences in a Large, International Pediatric Cohort (Q30277090) ‎ (← links)
• Contrasting the Genetic Background of Type 1 Diabetes and Celiac Disease Autoimmunity (Q30278631) ‎ (← links)
• Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes (Q30300266) ‎ (← links)
• Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease (Q30426720) ‎ (← links)
• Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data (Q30832807) ‎ (← links)
• Variants in neuropeptide Y receptor 1 and 5 are associated with nutrient-specific food intake and are under recent selection in Europeans. (Q30873841) ‎ (← links)