PubRank

Elena Urcelay

Author PubWeight™ 83.36‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Multiple common variants for celiac disease influencing immune gene expression. Nat Genet 2010 6.90
2 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat Genet 2011 6.36
3 TNFRSF1A polymorphisms rs1800693 and rs4149584 in patients with multiple sclerosis. Neurology 2013 1.47
4 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. Nat Genet 2010 1.32
5 The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases. Ann Rheum Dis 2009 1.17
6 IFIH1-GCA-KCNH7 locus: influence on multiple sclerosis risk. Eur J Hum Genet 2008 1.08
7 MHC susceptibility genes to IgA deficiency are located in different regions on different HLA haplotypes. J Immunol 2002 1.06
8 Role of the MHC2TA gene in autoimmune diseases. Ann Rheum Dis 2006 1.06
9 CD40: novel association with Crohn's disease and replication in multiple sclerosis susceptibility. PLoS One 2010 1.01
10 Role of the PXR gene locus in inflammatory bowel diseases. Inflamm Bowel Dis 2007 1.00
11 A polymorphism in PTPN2 gene is associated with an earlier onset of type 1 diabetes. Immunogenetics 2011 0.98
12 Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients. Eur J Hum Genet 2009 0.96
13 Association of the organic cation transporter OCTN genes with Crohn's disease in the Spanish population. Eur J Hum Genet 2006 0.96
14 Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis. Inflamm Bowel Dis 2011 0.96
15 Interleukin-10 polymorphisms in Spanish patients with IBD. Inflamm Bowel Dis 2005 0.95
16 High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency. PLoS Genet 2012 0.94
17 MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. Brain 2013 0.94
18 Influence of the inducible nitric oxide synthase gene (NOS2A) on inflammatory bowel disease susceptibility. Immunogenetics 2007 0.93
19 IL23R and IL12B polymorphisms in Spanish IBD patients: no evidence of interaction. Inflamm Bowel Dis 2008 0.93
20 High prevalence of viable Mycobacterium avium subspecies paratuberculosis in Crohn's disease. World J Gastroenterol 2010 0.93
21 Gender-specific association of the PTPN22 C1858T polymorphism with achalasia. Hum Immunol 2007 0.92
22 Novel association of the interleukin 2-interleukin 21 region with inflammatory bowel disease. Am J Gastroenterol 2009 0.92
23 Large-scale gene expression in bone marrow mesenchymal stem cells: a putative role for COL10A1 in osteoarthritis. Ann Rheum Dis 2010 0.90
24 IBD1 and IBD3 determine location of Crohn's disease in the Spanish population. Inflamm Bowel Dis 2004 0.90
25 Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1. PLoS One 2012 0.90
26 Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain. J Neuroimmunol 2010 0.90
27 Environment-gene interaction in multiple sclerosis: human herpesvirus 6 and MHC2TA. Hum Immunol 2007 0.89
28 Immunological mechanisms that associate with oligoclonal IgM band synthesis in multiple sclerosis. Clin Immunol 2010 0.89
29 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
30 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
31 Evidence for the association of the SLC22A4 and SLC22A5 genes with type 1 diabetes: a case control study. BMC Med Genet 2006 0.88
32 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
33 Macrophage migration inhibitory factor gene: influence on rheumatoid arthritis susceptibility. Hum Immunol 2007 0.87
34 Suggested association of NOS2A polymorphism in idiopathic achalasia: no evidence in a large case-control study. Am J Gastroenterol 2009 0.86
35 Role of SLC22A4, SLC22A5, and RUNX1 genes in rheumatoid arthritis. J Rheumatol 2006 0.86
36 6q23 polymorphisms in rheumatoid arthritis Spanish patients. Rheumatology (Oxford) 2009 0.86
37 TRAIL/TRAIL receptor system and susceptibility to multiple sclerosis. PLoS One 2011 0.86
38 Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. J Med Genet 2012 0.86
39 IFN-beta pharmacogenomics in multiple sclerosis. Pharmacogenomics 2010 0.85
40 Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis. J Med Genet 2012 0.85
41 FcRL3 and multiple sclerosis pathogenesis: role in autoimmunity? J Neuroimmunol 2007 0.84
42 Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population. BMC Med Genet 2007 0.84
43 Role of IL-10 promoter polymorphisms in the development of severe aorto-iliac occlusive disease. Hum Immunol 2008 0.84
44 Association of IL10 promoter polymorphisms with idiopathic achalasia. Hum Immunol 2011 0.83
45 Polymorphisms in the IL2, IL2RA and IL2RB genes in multiple sclerosis risk. Eur J Hum Genet 2010 0.83
46 Polymorphisms in the selenoprotein S gene: lack of association with autoimmune inflammatory diseases. BMC Genomics 2008 0.83
47 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
48 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
49 Analysis of the influence of two CD24 genetic variants in Crohn's disease and ulcerative colitis. Hum Immunol 2011 0.83
50 Study of polymorphisms in 4q27, 10p15, and 22q13 regions in autoantibodies stratified type 1 diabetes patients. Autoimmunity 2011 0.82
51 CD209 in inflammatory bowel disease: a case-control study in the Spanish population. BMC Med Genet 2007 0.82
52 C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition. Hum Immunol 2005 0.82
53 Influence of IL6R rs8192284 polymorphism status in disease activity in rheumatoid arthritis. J Rheumatol 2010 0.82
54 Fine mapping and functional analysis of the multiple sclerosis risk gene CD6. PLoS One 2013 0.81
55 Functional polymorphism of the NFKB1 gene promoter is not relevant in predisposition to celiac disease. Scand J Gastroenterol 2006 0.81
56 Analysis of the REL polymorphism rs13031237 in autoimmune diseases. Ann Rheum Dis 2010 0.81
57 Study of chromosomal region 5p13.1 in Crohn's disease, ulcerative colitis, and rheumatoid arthritis. Hum Immunol 2010 0.81
58 HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV. Retrovirology 2014 0.81
59 Herpesvirus active replication in multiple sclerosis: a genetic control? J Neurol Sci 2011 0.81
60 IL4 in the 5q31 context: association studies of type 1 diabetes and rheumatoid arthritis in the Spanish population. Immunogenetics 2007 0.80
61 NO role of NOS2A susceptibility polymorphisms in rheumatoid arthritis. Nitric Oxide 2009 0.80
62 DRB1*03:01 haplotypes: differential contribution to multiple sclerosis risk and specific association with the presence of intrathecal IgM bands. PLoS One 2012 0.80
63 Interleukin-10 haplotypes in Celiac Disease in the Spanish population. BMC Med Genet 2006 0.79
64 Evidence of epistasis between TNFRSF14 and TNFRSF6B polymorphisms in patients with rheumatoid arthritis. Arthritis Rheum 2010 0.79
65 The IL6-174G/C polymorphism is associated with celiac disease susceptibility in girls. Hum Immunol 2009 0.79
66 Lack of association of NKX2-3, IRGM, and ATG16L1 inflammatory bowel disease susceptibility variants with celiac disease. Hum Immunol 2009 0.79
67 MSH5 is not a genetic predisposing factor for immunoglobulin A deficiency but marks the HLA-DRB1*0102 subgroup carrying susceptibility. Hum Immunol 2010 0.79
68 Th1 cytokine polymorphisms in spanish patients with type 1 diabetes. Hum Immunol 2005 0.78
69 FcRL3 gene promoter variant is associated with peripheral arthritis in Crohn's disease. Inflamm Bowel Dis 2009 0.78
70 Plasma soluble IL-6 receptor concentration in rheumatoid arthritis: associations with the rs8192284 IL6R polymorphism and with disease activity. Rheumatol Int 2010 0.78
71 Combined influence of genetic and environmental factors in age of rheumatoid arthritis onset. Rheumatol Int 2011 0.78
72 Genetic markers linked to rheumatoid arthritis are also strongly associated with articular manifestations in ulcerative colitis patients. Hum Immunol 2006 0.78
73 Interleukin-6 gene variation in Spanish patients with immunoglobulin-A deficiency. Hum Immunol 2008 0.77
74 Interleukin-10 polymorphisms in Spanish IgA deficiency patients: a case-control and family study. BMC Med Genet 2006 0.77
75 MDR1 polymorphisms and response to azathioprine therapy in patients with Crohn's disease. Inflamm Bowel Dis 2007 0.77
76 Localization of Type 1 Diabetes susceptibility in the ancestral haplotype 18.2 by high density SNP mapping. Genomics 2009 0.77
77 Polymorphisms in interleukin-10 gene according to mutations of NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn's disease. World J Gastroenterol 2006 0.76
78 A recombined haplotype in the major histocompatibility region contains a cluster of genes conferring high susceptibility to ulcerative colitis in the Spanish population. Inflamm Bowel Dis 2005 0.76
79 CD46 in a Spanish cohort of multiple sclerosis patients: genetics, mRNA expression and response to interferon-beta treatment. Mult Scler 2010 0.76
80 Alternative splicing and proteolytic rupture contribute to the generation of soluble IL-6 receptors (sIL-6R) in rheumatoid arthritis. Cytokine 2013 0.76
81 Strong protective effect of DR3 against ulcerative colitis in the Spanish population. Am J Gastroenterol 2007 0.76
82 Candidate gene study of TRAIL and TRAIL receptors: association with response to interferon beta therapy in multiple sclerosis patients. PLoS One 2013 0.75
83 A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population. BMC Med Genet 2006 0.75
84 Early B-cell Factor gene association with multiple sclerosis in the Spanish population. BMC Neurol 2005 0.75
85 Lack of association between the functional c-kit rs6554199 polymorphism and achalasia in a Spanish population. Hum Immunol 2012 0.75
86 Shared epitope and anti-cyclic citrullinated peptide antibodies: relationship with age at onset and duration of disease in rheumatoid arthritis. J Rheumatol 2009 0.75
87 Lack of evidence of a role of XBP1 and PRDM1 polymorphisms in Spanish patients with immunoglobulin A deficiency. Hum Immunol 2009 0.75
88 ICAM1 R241 is not associated with celiac disease in the Spanish population. Hum Immunol 2008 0.75
89 [Influence of mutations of proteinase-activated receptors F2R/PAR1 and F2RL1/PAR2 on inflammatory bowel disease]. Med Clin (Barc) 2008 0.75