| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1014266187 |
| P356 | DOI | 10.1038/JHG.2015.99 |
| P698 | PubMed publication ID | 26290150 |
| P2093 | author name string | Xin Wu | |
| Huji Xu | |||
| Haiyan Chen | |||
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease | Q22251069 | ||
| Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease | Q22251082 | ||
| A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease | Q22251291 | ||
| TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis | Q24293476 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| Transgenic mice expressing human tumour necrosis factor: a predictive genetic model of arthritis | Q24564656 | ||
| Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo | Q24629443 | ||
| Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects | Q24631241 | ||
| Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes | Q24632382 | ||
| Identification of multiple genetic susceptibility loci in Takayasu arteritis | Q24632711 | ||
| Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis | Q24633290 | ||
| Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants | Q24646663 | ||
| Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways | Q24653432 | ||
| Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis | Q24656576 | ||
| Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region | Q24657139 | ||
| A haplotype map of the human genome | Q24679827 | ||
| Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease | Q27860821 | ||
| Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis | Q28183279 | ||
| New allele frequency database: http://www.allelefrequencies.net | Q28204761 | ||
| A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes | Q28248848 | ||
| A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis | Q28267921 | ||
| Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients | Q28304174 | ||
| The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritis | Q28306666 | ||
| Genetically distinct subsets within ANCA-associated vasculitis | Q28943363 | ||
| Disturbed Th17/Treg balance in patients with rheumatoid arthritis | Q84644585 | ||
| Targeting tumor necrosis factor alpha in psoriasis and psoriatic arthritis | Q94705801 | ||
| Identification of IL-18 and Th17 cells in salivary glands of patients with Sjögren's syndrome, and amplification of IL-17-mediated secretion of inflammatory cytokines from salivary gland cells by IL-18. | Q39953212 | ||
| Assessing the role of HLA-linked and unlinked determinants of disease | Q40593830 | ||
| Interleukin 17 induces cartilage collagen breakdown: novel synergistic effects in combination with proinflammatory cytokines | Q41866942 | ||
| A common genetic background for inflammatory bowel disease and ankylosing spondylitis: a genealogic study in Iceland | Q42627585 | ||
| Joint erosion in rheumatoid arthritis: interactions between tumour necrosis factor alpha, interleukin 1, and receptor activator of nuclear factor kappaB ligand (RANKL) regulate osteoclasts | Q43049903 | ||
| Association of single nucleotide polymorphisms in the IL-12 (IL-12A and B) and IL-12 receptor (IL-12Rbeta1 and beta2) genes and gene-gene interactions with atopic dermatitis in Koreans | Q43538727 | ||
| Behçet disease and the HLA system | Q43853415 | ||
| Ethnic differences in allele frequency of autoimmune-disease-associated SNPs. | Q44144728 | ||
| TNF skews monocyte differentiation from macrophages to dendritic cells | Q44205364 | ||
| Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland | Q46088274 | ||
| Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis. | Q46147942 | ||
| High Association of an HL-A Antigen, W27, with Ankylosing Spondylitis | Q48012715 | ||
| Association of the TSHR gene with Graves' disease: the first disease specific locus. | Q50758182 | ||
| Blockade of Dickkopf (DKK)-1 induces fusion of sacroiliac joints. | Q51756072 | ||
| Up-regulation of macrophage inflammatory protein-3 alpha/CCL20 and CC chemokine receptor 6 in psoriasis. | Q52026606 | ||
| The overexpression of heparin-binding epidermal growth factor is responsible for Th17-induced airway remodeling in an experimental asthma model. | Q54425160 | ||
| Human Lymphocyte Antigen Association in Ankylosing Spondylitis | Q54441822 | ||
| Cytokines and Behcet's disease | Q57217995 | ||
| Common genes in autoimmune diseases: a link between immune-mediated diseases | Q57307059 | ||
| Association ofERAP1, but notIL23R, with ankylosing spondylitis in a Han Chinese population | Q57667591 | ||
| Revisiting genome wide association studies (GWAS) in coeliac disease: replication study in Spanish population and expression analysis of candidate genes | Q63314034 | ||
| HL-A antigens in psoriasis with special reference to the clinical type, age of onset, exacerbations after respiratory infections and occurrence of arthritis | Q67364463 | ||
| A population-based study of multiple sclerosis in twins | Q69671085 | ||
| Prevention of Th2-like cell responses by coadministration of IL-12 and IL-18 is associated with inhibition of antigen-induced airway hyperresponsiveness, eosinophilia, and serum IgE levels | Q77484106 | ||
| Familial clustering of rheumatoid arthritis with other autoimmune diseases | Q77694552 | ||
| Dickkopf-1 is a master regulator of joint remodeling | Q79610564 | ||
| Multiple lessons for multiple sclerosis | Q79690005 | ||
| Guilt beyond a reasonable doubt | Q80540702 | ||
| Cutting edge: a variant of the IL-23R gene associated with inflammatory bowel disease induces loss of microRNA regulation and enhanced protein production | Q83289684 | ||
| Shared familial aggregation of susceptibility to autoimmune diseases | Q84483470 | ||
| Genetics of rheumatoid arthritis contributes to biology and drug discovery | Q29417000 | ||
| Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. | Q29417005 | ||
| Interleukin-12 and the regulation of innate resistance and adaptive immunity | Q29614602 | ||
| Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility | Q29614872 | ||
| A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1 | Q29614873 | ||
| Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci | Q30417517 | ||
| High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis | Q30419111 | ||
| Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. | Q30419116 | ||
| Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease | Q30426720 | ||
| Pervasive sharing of genetic effects in autoimmune disease | Q30431030 | ||
| Co-occurrence and comorbidities in patients with immune-mediated inflammatory disorders: an exploration using US healthcare claims data, 2001-2002. | Q31041292 | ||
| Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions | Q33474863 | ||
| Autoimmune disease classification by inverse association with SNP alleles | Q33521311 | ||
| The genetic basis for the association of the 8.1 ancestral haplotype (A1, B8, DR3) with multiple immunopathological diseases | Q33630699 | ||
| Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene | Q33645905 | ||
| Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology | Q33797864 | ||
| The IL23R R381Q gene variant protects against immune-mediated diseases by impairing IL-23-induced Th17 effector response in humans | Q33833964 | ||
| Prioritizing candidate disease genes by network-based boosting of genome-wide association data. | Q33887815 | ||
| Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. | Q33942125 | ||
| A gene-environment interaction between smoking and shared epitope genes in HLA-DR provides a high risk of seropositive rheumatoid arthritis | Q33982255 | ||
| Helminth-host immunological interactions: prevention and control of immune-mediated diseases | Q34030215 | ||
| Langerhans cell migration | Q34049853 | ||
| Ankylosing spondylitis and HL-A 27. | Q34051631 | ||
| Construction and initial characterization of a mouse-human chimeric anti-TNF antibody | Q34060890 | ||
| Tumor necrosis factor: biology and therapeutic inhibitors | Q34065153 | ||
| IL-17 is increased in asthmatic airways and induces human bronchial fibroblasts to produce cytokines | Q34090258 | ||
| Immune-mediated disease genetics: the shared basis of pathogenesis | Q34303522 | ||
| Location of tumour necrosis factor alpha by immunohistochemistry in chronic inflammatory bowel disease | Q34377789 | ||
| Treatment of rheumatoid arthritis with tumour necrosis factor inhibitors | Q34588629 | ||
| The common genetic hypothesis of autoimmune/inflammatory disease | Q34607762 | ||
| Th17 and natural Treg cell population dynamics in systemic lupus erythematosus | Q34978528 | ||
| Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk | Q35125868 | ||
| Genetic interrelationship between insulin-dependent diabetes mellitus, the autoimmune thyroid diseases, and rheumatoid arthritis | Q35200726 | ||
| New Perspectives and Emerging Therapies for Immune-mediated Inflammatory Disorders | Q35541936 | ||
| The intricate role of complement component C4 in human systemic lupus erythematosus | Q35627095 | ||
| Obesity in autoimmune diseases: not a passive bystander | Q38237025 | ||
| Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes | Q38518470 | ||
| Salivary gland tissue expression of interleukin-23 and interleukin-17 in Sjögren's syndrome: findings in humans and mice | Q39912433 | ||
| Expression of IL-17, IL-23 and their receptors in minor salivary glands of patients with primary Sjögren's syndrome | Q35676007 | ||
| Blockade of the EGF receptor induces a deranged chemokine expression in keratinocytes leading to enhanced skin inflammation | Q35791607 | ||
| Gene map of the extended human MHC. | Q35968433 | ||
| Serum interleukin-17 & nitric oxide levels in patients with primary Sjögren's syndrome. | Q36064302 | ||
| Tumour necrosis factor inhibitors. | Q36227991 | ||
| Interleukin 12 inhibits antigen-induced airway hyperresponsiveness, inflammation, and Th2 cytokine expression in mice | Q36365451 | ||
| Immune-mediated inflammatory diseases (IMIDs) and biologic therapy: a medical revolution | Q36778450 | ||
| Concordance rates of insulin dependent diabetes mellitus: a population based study of young Danish twins | Q36905127 | ||
| A polymorphism in the coding region of Il12b promotes IL-12p70 and IL-23 heterodimer formation | Q36905411 | ||
| Immune-mediated diseases: where do we stand? | Q36916194 | ||
| IL-17/Th17 targeting: on the road to prevent chronic destructive arthritis? | Q37015036 | ||
| The epidermal growth factor receptor system in skin repair and inflammation | Q37020092 | ||
| Anti-tumor necrosis factor ameliorates joint disease in murine collagen-induced arthritis | Q37253521 | ||
| Epidemiology of autoimmune diseases in Denmark | Q37278627 | ||
| Th17 cytokines interleukin (IL)-17 and IL-22 modulate distinct inflammatory and keratinocyte-response pathways. | Q37298535 | ||
| Systemic and local interleukin-17 and linked cytokines associated with Sjögren's syndrome immunopathogenesis | Q37316528 | ||
| Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis | Q37441841 | ||
| Interleukin-17 and its target genes: mechanisms of interleukin-17 function in disease | Q37735334 | ||
| The role of dendritic cells in the pathogenesis of systemic lupus erythematosus | Q37737799 | ||
| Epidemiology of immune-mediated inflammatory diseases: incidence, prevalence, natural history, and comorbidities. | Q37740847 | ||
| IL-17 receptor signaling and T helper 17-mediated autoimmune demyelinating disease | Q37865163 | ||
| The potential role of interleukin-17 in severe asthma | Q37902959 | ||
| Biology and signal transduction pathways of the Lymphotoxin-αβ/LTβR system | Q37966050 | ||
| Role of IL-17 in psoriasis and psoriatic arthritis | Q37987880 | ||
| Genetic variations in interleukin-12 related genes in immune-mediated diseases | Q38028141 | ||
| Human genetics offers an emerging picture of common pathways and mechanisms in autoimmunity | Q38049938 | ||
| Th17 cells in type 1 diabetes | Q38068028 | ||
| Geographical variability and environmental risk factors in inflammatory bowel disease | Q38075524 | ||
| Mapping of immune-mediated disease genes. | Q38120034 | ||
| Genetic insights into common pathways and complex relationships among immune-mediated diseases | Q38126785 | ||
| Inflammatory pathways in spondyloarthritis | Q38130805 | ||
| Genetics of autoimmunity: an update. | Q38173983 | ||
| Th17 and regulatory T cell balance in autoimmune and inflammatory diseases | Q38177967 | ||
| Extraintestinal manifestations and complications in inflammatory bowel disease: from shared genetics to shared biological pathways | Q38205103 | ||
| The role of tumour necrosis factor in the pathogenesis of immune-mediated diseases | Q38207758 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 675-681 | |
| P577 | publication date | 2015-08-20 | |
| P1433 | published in | Journal of Human Genetics | Q6295302 |
| P1476 | title | The genomic landscape of human immune-mediated diseases | |
| P478 | volume | 60 |
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