Published in Hum Immunol on August 12, 2008
Molecular genetics of atherosclerosis. Hum Genet (2009) 0.95
Magnetic resonance imaging of bone marrow cell-mediated interleukin-10 gene therapy of atherosclerosis. PLoS One (2011) 0.79
CD14(bright)CD16+ intermediate monocytes are induced by interleukin-10 and positively correlate with disease activity in rheumatoid arthritis. Arthritis Res Ther (2017) 0.76
IL-10 gene polymorphisms and their association with immune traits in four rabbit populations. J Vet Med Sci (2013) 0.75
Multiple common variants for celiac disease influencing immune gene expression. Nat Genet (2010) 6.90
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat Genet (2011) 6.36
Association of the major histocompatibility complex with response to infliximab therapy in rheumatoid arthritis patients. Arthritis Rheum (2004) 2.45
MDR1 gene: susceptibility in Spanish Crohn's disease and ulcerative colitis patients. Inflamm Bowel Dis (2006) 1.54
TNFRSF1A polymorphisms rs1800693 and rs4149584 in patients with multiple sclerosis. Neurology (2013) 1.47
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. Nat Genet (2010) 1.32
Combined therapy with idebenone and deferiprone in patients with Friedreich's ataxia. Cerebellum (2011) 1.21
The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases. Ann Rheum Dis (2009) 1.17
Coenzyme Q(10)-responsive ataxia: 2-year-treatment follow-up. Mov Disord (2010) 1.08
IFIH1-GCA-KCNH7 locus: influence on multiple sclerosis risk. Eur J Hum Genet (2008) 1.08
Sex and body mass index specific regulation of blood pressure by CYP19A1 gene variants. Hypertension (2007) 1.06
MHC susceptibility genes to IgA deficiency are located in different regions on different HLA haplotypes. J Immunol (2002) 1.06
Role of the MHC2TA gene in autoimmune diseases. Ann Rheum Dis (2006) 1.06
CD40: novel association with Crohn's disease and replication in multiple sclerosis susceptibility. PLoS One (2010) 1.01
Role of the PXR gene locus in inflammatory bowel diseases. Inflamm Bowel Dis (2007) 1.00
A polymorphism in PTPN2 gene is associated with an earlier onset of type 1 diabetes. Immunogenetics (2011) 0.98
Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients. Eur J Hum Genet (2009) 0.96
Association of the organic cation transporter OCTN genes with Crohn's disease in the Spanish population. Eur J Hum Genet (2006) 0.96
Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis. Inflamm Bowel Dis (2011) 0.96
Interleukin-10 polymorphisms in Spanish patients with IBD. Inflamm Bowel Dis (2005) 0.95
High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency. PLoS Genet (2012) 0.94
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. Brain (2013) 0.94
Influence of the inducible nitric oxide synthase gene (NOS2A) on inflammatory bowel disease susceptibility. Immunogenetics (2007) 0.93
IL23R and IL12B polymorphisms in Spanish IBD patients: no evidence of interaction. Inflamm Bowel Dis (2008) 0.93
High prevalence of viable Mycobacterium avium subspecies paratuberculosis in Crohn's disease. World J Gastroenterol (2010) 0.93
Gender-specific association of the PTPN22 C1858T polymorphism with achalasia. Hum Immunol (2007) 0.92
Novel association of the interleukin 2-interleukin 21 region with inflammatory bowel disease. Am J Gastroenterol (2009) 0.92
Large-scale gene expression in bone marrow mesenchymal stem cells: a putative role for COL10A1 in osteoarthritis. Ann Rheum Dis (2010) 0.90
IBD1 and IBD3 determine location of Crohn's disease in the Spanish population. Inflamm Bowel Dis (2004) 0.90
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1. PLoS One (2012) 0.90
Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain. J Neuroimmunol (2010) 0.90
Immunological mechanisms that associate with oligoclonal IgM band synthesis in multiple sclerosis. Clin Immunol (2010) 0.89
Environment-gene interaction in multiple sclerosis: human herpesvirus 6 and MHC2TA. Hum Immunol (2007) 0.89
Role of ATG16L1 Thr300Ala polymorphism in inflammatory bowel disease: a Study in the Spanish population and a meta-analysis. Inflamm Bowel Dis (2009) 0.89
Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genes. Mult Scler (2011) 0.89
Evidence for the association of the SLC22A4 and SLC22A5 genes with type 1 diabetes: a case control study. BMC Med Genet (2006) 0.88
Role of the human endogenous retrovirus HERV-K18 in autoimmune disease susceptibility: study in the Spanish population and meta-analysis. PLoS One (2013) 0.88
Macrophage migration inhibitory factor gene: influence on rheumatoid arthritis susceptibility. Hum Immunol (2007) 0.87
Suggested association of NOS2A polymorphism in idiopathic achalasia: no evidence in a large case-control study. Am J Gastroenterol (2009) 0.86
Role of SLC22A4, SLC22A5, and RUNX1 genes in rheumatoid arthritis. J Rheumatol (2006) 0.86
TRAIL/TRAIL receptor system and susceptibility to multiple sclerosis. PLoS One (2011) 0.86
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. J Med Genet (2012) 0.86
6q23 polymorphisms in rheumatoid arthritis Spanish patients. Rheumatology (Oxford) (2009) 0.86
Interleukin-10 polymorphisms in Spanish multiple sclerosis patients. J Neuroimmunol (2002) 0.86
IFN-beta pharmacogenomics in multiple sclerosis. Pharmacogenomics (2010) 0.85
Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis. J Med Genet (2012) 0.85
FcRL3 and multiple sclerosis pathogenesis: role in autoimmunity? J Neuroimmunol (2007) 0.84
Association of MYO9B haplotype with type 1 diabetes. Hum Immunol (2008) 0.84
Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population. BMC Med Genet (2007) 0.84
Severity of ulcerative colitis is associated with a polymorphism at diamine oxidase gene but not at histamine N-methyltransferase gene. World J Gastroenterol (2006) 0.83
Ca2+/calmodulin-dependent modulation of cell cycle elements pRb and p27kip1 involved in the enhanced proliferation of lymphoblasts from patients with Alzheimer dementia. Neurobiol Dis (2003) 0.83
Association of IL10 promoter polymorphisms with idiopathic achalasia. Hum Immunol (2011) 0.83
Analysis of the influence of two CD24 genetic variants in Crohn's disease and ulcerative colitis. Hum Immunol (2011) 0.83
Polymorphisms in the IL2, IL2RA and IL2RB genes in multiple sclerosis risk. Eur J Hum Genet (2010) 0.83
Polymorphisms in the selenoprotein S gene: lack of association with autoimmune inflammatory diseases. BMC Genomics (2008) 0.83
Influence of IL6R rs8192284 polymorphism status in disease activity in rheumatoid arthritis. J Rheumatol (2010) 0.82
C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition. Hum Immunol (2005) 0.82
CD209 in inflammatory bowel disease: a case-control study in the Spanish population. BMC Med Genet (2007) 0.82
Study of polymorphisms in 4q27, 10p15, and 22q13 regions in autoantibodies stratified type 1 diabetes patients. Autoimmunity (2011) 0.82
Polymorphisms in the transforming growth factor-beta gene (TGF-beta) and the risk of advanced alcoholic liver disease. Liver Int (2005) 0.82
Fine mapping and functional analysis of the multiple sclerosis risk gene CD6. PLoS One (2013) 0.81
Functional polymorphism of the NFKB1 gene promoter is not relevant in predisposition to celiac disease. Scand J Gastroenterol (2006) 0.81
Herpesvirus active replication in multiple sclerosis: a genetic control? J Neurol Sci (2011) 0.81
HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV. Retrovirology (2014) 0.81
Analysis of the REL polymorphism rs13031237 in autoimmune diseases. Ann Rheum Dis (2010) 0.81
Study of chromosomal region 5p13.1 in Crohn's disease, ulcerative colitis, and rheumatoid arthritis. Hum Immunol (2010) 0.81
NO role of NOS2A susceptibility polymorphisms in rheumatoid arthritis. Nitric Oxide (2009) 0.80