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A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis

artículo científico publicado en 2010

A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis ⬇️

artículo científico publicado en 2016

A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish/Norwegian celiac disease families

scientific article published on 06 June 2007

A gene in the telomeric HLA complex distinct from HLA-A is involved in predisposition to juvenile idiopathic arthritis

artículo científico publicado en 2002

A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis

artículo científico publicado en 2009

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort

artículo científico publicado en 2010

Abundant genetic overlap between blood lipids and immune-mediated diseases indicates shared molecular genetic mechanisms

artículo científico publicado en 2015

Accurate Adapter Information Is Crucial for Reproducibility and Reusability in Small RNA Seq Studies

scientific article published on 28 October 2019

Allele imputation for the killer cell immunoglobulin-like receptor KIR3DL1/S1

artículo científico publicado en 2022

An Association Study of Interleukin 18 Receptor Genes (IL18R1 and IL18RAP) in Lumbar Disc Degeneration

artículo científico publicado en 2012

An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis

artículo científico publicado en 2012

An extension to: Systematic assessment of commercially available low-input miRNA library preparation kits

scientific article published on 21 May 2020

Analysis of MAdCAM-1 and ICAM-1 polymorphisms in 365 Scandinavian patients with primary sclerosing cholangitis

artículo científico publicado en 2006

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

artículo científico publicado en 2013

Antineutrophil antibodies define clinical and genetic subgroups in primary sclerosing cholangitis

artículo científico publicado en 2016

Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease

artículo científico publicado en 2007

Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort

artículo científico publicado en 2006

Association analysis of the interleukin 17A gene in Caucasian rheumatoid arthritis patients from Norway and New Zealand

artículo científico publicado en 2009

Association of CD247 polymorphisms with rheumatoid arthritis: a replication study and a meta-analysis

artículo científico publicado en 2013

Association to the Glypican-5 gene in multiple sclerosis

article

Associations between APOE genotypes and disease susceptibility, joint damage and lipid levels in patients with rheumatoid arthritis

artículo científico publicado en 2013

Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal study

artículo científico publicado en 2007

CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigm

artículo científico publicado en 2004

CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases

Catechol-O-methyltransferase (COMT) gene polymorphisms are associated with baseline disability but not long-term treatment outcome in patients with chronic low back pain

artículo científico publicado en 2015

Celiac disease genetics: current concepts and practical applications

artículo científico publicado en 2005

Cholangiocarcinoma in primary sclerosing cholangitis is associated with NKG2D polymorphisms

scientific article published on 01 January 2008

Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles

scientific article published on 04 July 2003

Correction: Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms

artículo científico publicado en 2015

Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy.

artículo científico publicado en 2011

Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy.

artículo científico publicado en 2011

Correlation between gene expression and MRI STIR signals in patients with chronic low back pain and Modic changes indicates immune involvement

artículo científico publicado en 2022

Discussion on the role of hemochromatosis susceptibility gene mutation in protecting against iron deficiency in celiac disease ⬇️

artículo científico publicado el 1 de mayo de 2003

Distinct ACPA fine specificities, formed under the influence of HLA shared epitope alleles, have no effect on radiographic joint damage in rheumatoid arthritis

artículo científico publicado en 2011

ERAP2 is associated with ankylosing spondylitis in HLA-B27-positive and HLA-B27-negative patients

artículo científico publicado en 2015

Effects of coffee consumption, smoking, and hormones on risk for primary sclerosing cholangitis

artículo científico publicado en 2013

Efficacy of antibiotic treatment in patients with chronic low back pain and Modic changes (the AIM study): double blind, randomised, placebo controlled, multicentre trial

artículo científico publicado en 2019

Electrostatic modifications of the human leukocyte antigen-DR P9 peptide-binding pocket and susceptibility to primary sclerosing cholangitis

artículo científico publicado en 2011

Environmental exposures and the risk of multiple sclerosis investigated in a Norwegian case-control study

artículo científico publicado en 2014

Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritis

artículo científico publicado en 2014

Erratum: Corrigendum: Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus

scholarly article published in Nature Genetics

Evidence for PTPN22 R620W Polymorphism As the Sole Common Risk Variant for Rheumatoid Arthritis in the 1p13.2 Region

article

FCRL3 –169C/C Genotype Is Associated with Anti-citrullinated Protein Antibody-positive Rheumatoid Arthritis and with Radiographic Progression ⬇️

artículo científico publicado el 1 de septiembre de 2011

FOXP3 polymorphisms in type 1 diabetes and coeliac disease.

artículo científico publicado en 2006

Fetal and Maternal Genetic Variants Influencing Neonatal Vitamin D Status

artículo científico publicado en 2017

GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways

scientific article published on 31 October 2019

Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study

artículo científico publicado en 2012

Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors

artículo científico publicado en 2016

Genetic polymorphisms associated with inflammatory bowel disease do not confer risk for primary sclerosing cholangitis

artículo científico publicado en 2006

Genetic risk scores and number of autoantibodies in patients with rheumatoid arthritis

artículo científico publicado en 2013

Genetic risk variants for autoimmune diseases that influence gene expression in thymus.

artículo científico publicado en 2016

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

artículo científico publicado en 2015

Genome-wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A, and Identification of ZBTB10 and Three Distinct HLA Associations

artículo científico publicado en 2015

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

artículo científico publicado en 2017

Genome-wide ancestry patterns in Rapanui suggest pre-European admixture with Native Americans

artículo científico publicado en 2014

Genome-wide association analysis in primary sclerosing cholangitis

artículo científico publicado en 2009

Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus

artículo científico publicado en 2010

HLA -A, -C, -B, -DRB1, -DQB1 and -DPB1 allele and haplotype frequencies in 4514 healthy Norwegians

artículo científico publicado en 2018

HLA and sleep parameter associations in post-H1N1 narcolepsy type 1 patients and first-degree relatives

artículo científico publicado en 2020

HLA associated genetic predisposition to autoimmune diseases: Genes involved and possible mechanisms

artículo científico publicado en 2005

HLA-C alleles confer risk for anti-citrullinated peptide antibody-positive rheumatoid arthritis independent of HLA-DRB1 alleles

artículo científico publicado en 2013

HLA-DRB3*01:01 exhibits a dose-dependent impact on HPA-1a antibody levels in HPA-1a-immunized women

High nocturnal sleep fragmentation is associated with low T lymphocyte P2Y11 protein levels in narcolepsy type 1

artículo científico publicado en 2021

Human Leukocyte Antigen alleles associated with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)

artículo científico publicado en 2020

Identification of a Natural Killer Cell Receptor Allele That Prolongs Survival of Cytomegalovirus-Positive Glioblastoma Patients.

artículo científico publicado en 2016

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

artículo científico publicado en 2013

Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy

artículo científico publicado en 2011

Importance of human leukocyte antigen (HLA) class I and II alleles on the risk of multiple sclerosis

artículo científico publicado en 2012

Increased coagulation activity and genetic polymorphisms in the F5, F10 and EPCR genes are associated with breast cancer: a case-control study

artículo científico publicado en 2014

Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis

artículo científico publicado en 2012

Intravenous Cyclophosphamide in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. An Open-Label Phase II Study

artículo científico publicado en 2020

Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis

artículo científico publicado en 2009

LYP inhibits T-cell activation when dissociated from CSK.

artículo científico publicado en 2012

Lack of Association among Peptidyl Arginine Deiminase Type 4 Autoantibodies, PADI4 Polymorphisms, and Clinical Characteristics in Rheumatoid Arthritis

scientific article published on 01 June 2018

Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis

artículo científico publicado en 2007

Lack of association with the CD28/CTLA4/ICOS gene region among Norwegian multiple sclerosis patients

article

Late onset myasthenia gravis is associated with HLA DRB1*15:01 in the Norwegian population

artículo científico publicado en 2012

Long-term muscular outcome and predisposing and prognostic factors in juvenile dermatomyositis: A case-control study

artículo científico publicado en 2010

Low frequency and rare coding variation contributes to multiple sclerosis risk

Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1.

artículo científico publicado en 2015

Maternal Microchimerism in Cord Blood and Risk of Celiac Disease in Childhood

artículo científico publicado en 2020

Maternal and Newborn Vitamin D-Binding Protein, Vitamin D Levels, Vitamin D Receptor Genotype, and Childhood Type 1 Diabetes

scientific article published on 28 January 2019

Maternal and neonatal vitamin D status, genotype and childhood celiac disease.

artículo científico publicado en 2017

Maternal microchimerism in cord blood and risk of childhood-onset type 1 diabetes

artículo científico publicado en 2019

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

artículo científico publicado en 2015

Methotrexate Treatment of Newly Diagnosed RA Patients Is Associated With DNA Methylation Differences at Genes Relevant for Disease Pathogenesis and Pharmacological Action

artículo científico publicado en 2021

MicroRNA Expression Differences in Blood-Derived CD19+ B Cells of Methotrexate Treated Rheumatoid Arthritis Patients

artículo científico publicado en 2021

Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing

artículo científico publicado en 2020

Multiple loci in the HLA complex are associated with Addison's disease

artículo científico publicado en 2011

Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis

artículo científico publicado en 2010

New gene map for multiple sclerosis

artículo científico publicado en 2011

No evidence of type 1 diabetes susceptibility genes in the region centromeric of the HLA complex

artículo científico publicado en 2003

Novel genetic association of theVTCN1region with rheumatoid arthritis

artículo científico publicado en 2012

Oligoclonal band phenotypes in MS differ in their HLA class II association, while specific KIR ligands at HLA class I show association to MS in general

scholarly article by Marte W. Gustavsen et al published September 2014 in Journal of Neuroimmunology

Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles

artículo científico publicado en 2013

Particular genetic variants of ligands for natural killer cell receptors may contribute to the HLA associated risk of primary sclerosing cholangitis

artículo científico publicado en 2007

Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis

artículo científico publicado en 2007

Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease

artículo científico publicado en 2004

Polymorphisms in the steroid and xenobiotic receptor gene influence survival in primary sclerosing cholangitis

scientific article published on 01 September 2006

Polymorphisms of the BDNF gene show neither association with multiple sclerosis susceptibility nor clinical course ⬇️

artículo científico publicado el 15 de febrero de 2012

Prenatal iron exposure and childhood type 1 diabetes.

artículo científico publicado en 2018

Primary sclerosing cholangitis in genetically diverse populations listed for liver transplantation: unique clinical and human leukocyte antigen associations

artículo científico publicado en 2010

Protection against anti-citrullinated protein antibody-positive rheumatoid arthritis is predominantly associated with HLA-DRB1*1301: a meta-analysis of HLA-DRB1 associations with anti-citrullinated protein antibody-positive and anti-citrullinated pr

artículo científico publicado en 2010

Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population

artículo científico publicado en 2014

Replication of association of the interleukin 23 receptor rs1343151 variant with rheumatoid arthritis in Caucasian sample sets

scholarly article

Rheumatoid Arthritis Patients, Both Newly Diagnosed and Methotrexate Treated, Show More DNA Methylation Differences in CD4+ Memory Than in CD4+ Naïve T Cells

artículo científico publicado en 2020

Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08

scientific journal article

Small duct primary sclerosing cholangitis without inflammatory bowel disease is genetically different from large duct disease

artículo científico publicado en 2014

Systematic assessment of commercially available low-input miRNA library preparation kits

artículo científico publicado en 2019

The HLA profiles of mixed connective tissue disease differ distinctly from the profiles of clinically related connective tissue diseases

artículo científico publicado en 2014

The Influence of the Autoimmunity-Associated Ancestral HLA Haplotype AH8.1 on the Human Gut Microbiota: A Cross-Sectional Study

artículo científico publicado en 2015

The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples

scientific article published on 01 February 2011

The SH2D2A gene and susceptibility to multiple sclerosis

artículo científico publicado en 2008

The autoimmune-predisposing variant of lymphoid tyrosine phosphatase favors T helper 1 responses.

artículo científico publicado en 2013

The effect of infliximab in patients with chronic low back pain and Modic changes (the BackToBasic study): study protocol of a randomized, double blind, placebo-controlled, multicenter trial

scientific article published on 21 October 2020

Transcriptome profiling of human thymic CD4+ and CD8+ T cells compared to primary peripheral T cells

scientific article published on 11 May 2020

Transcriptomes of antigen presenting cells in human thymus

scientific article published on 01 July 2019

Treatment outcome of chronic low back pain and radiographic lumbar disc degeneration are associated with inflammatory and matrix degrading gene variants: a prospective genetic association study

artículo científico publicado en 2013

Two HLA class I genes independently associated with multiple sclerosis

artículo científico publicado en 2010

VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis

artículo científico publicado en 2014

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

artículo científico publicado en 2016

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