SNP information rs9271366

Research and publications:

  18462017   Mapping the genetic architecture of gene expression in human liver.

  19010793   Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.

  19143821   Association of MHC SNP genotype with susceptibility to type 1 diabetes: a modified survival approach.

  19838195   A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus

  20045101   Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.

  20169177   Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus.

  20405052   The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

  20441431   Recent advances in the genetics of systemic lupus erythematosus.

  20546594   An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.

  21049023   A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis.

  21247752   Revealing the genetic basis of multiple sclerosis: are we there yet?

  21408207   Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.

  21654846   SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients.

  21695597   MHC region and risk of systemic lupus erythematosus in African American women.

  21699788   Haplotype HLA-Cw*1202-B*5201-DRB1*1502 increases the risk of ulcerative colitis, but reduces the risk of Crohn's disease.

  21829388   Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA.

  21873553   Genetic analysis of adult-onset autoimmune diabetes.

  22077970   Abundant pleiotropy in human complex diseases and traits.

  22233601   Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at MSH5, HLA-DPB1 and HLA-G.

  22253788   Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations.

  22761632   Role of MHC-linked susceptibility genes in the pathogenesis of human and murine lupus.

  23326239   A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).

  23511034   Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians.

  24727690   Single nucleotide polymorphism (SNP)-strings: an alternative method for assessing genetic associations.

  26278503   Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans.

  26606652   Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.

  27156530   Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility.

  27250029   Genetic polymorphisms in TNIP1 increase the risk of gastric carcinoma.

  27540591   Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies.

  27552900   Combining HLA-DRB1-DQB1 and Mycobacterium Avium Subspecies Paratubercolosis (MAP) antibodies in Sardinian multiple sclerosis patients: associated or independent risk factors?

  27651918   I too, am America: a review of research on systemic lupus erythematosus in African-Americans.

  27812365   Shared Genetic Etiology of Autoimmune Diseases in Patients from a Biorepository Linked to De-identified Electronic Health Records.

  31032751   Genetic Alleles Associated with SLE Susceptibility and Clinical Manifestations in Hispanic Patients from the Dominican Republic.

  31052430   Genetic Studies of Inflammatory Bowel Disease-Focusing on Asian Patients.

  31297130   C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients.