| scholarly article | Q13442814 |
| P50 | author | Richard Flavell | Q2149481 |
| Lauren A Zenewicz | Q51354756 | ||
| P2093 | author name string | Judy H Cho | |
| Clara Abraham | |||
| P2860 | cites work | Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project | Q21061203 |
| Genetic diagnosis by whole exome capture and massively parallel DNA sequencing | Q22066282 | ||
| Finding the missing heritability of complex diseases | Q22122198 | ||
| Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease | Q22251069 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| Targeted capture and massively parallel sequencing of 12 human exomes | Q24615381 | ||
| Genome-scale DNA methylation maps of pluripotent and differentiated cells | Q24621431 | ||
| A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus | Q24629130 | ||
| Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes | Q24632382 | ||
| Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants | Q24646663 | ||
| Innate immunity and intestinal microbiota in the development of Type 1 diabetes | Q24647312 | ||
| A core gut microbiome in obese and lean twins | Q24649648 | ||
| A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 | Q24649802 | ||
| Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes | Q24651119 | ||
| Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways | Q24653432 | ||
| Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci | Q24656799 | ||
| TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study | Q24657292 | ||
| Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci | Q24658255 | ||
| A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus | Q28236839 | ||
| Recent advances in the genetics of autoimmune disease | Q28238782 | ||
| Of mice and not men: differences between mouse and human immunology | Q28246229 | ||
| A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes | Q28248848 | ||
| Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus | Q28261767 | ||
| Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX | Q28265206 | ||
| A genome-wide association study identifies IL23R as an inflammatory bowel disease gene | Q28270603 | ||
| Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant | Q28280659 | ||
| Genetics of gene expression and its effect on disease | Q29614591 | ||
| A genome-wide association study of global gene expression | Q29614592 | ||
| Risk alleles for multiple sclerosis identified by a genomewide study | Q29614890 | ||
| Genetic mapping in human disease | Q29614943 | ||
| NOD2 stimulation induces autophagy in dendritic cells influencing bacterial handling and antigen presentation | Q29615617 | ||
| Nod1 and Nod2 direct autophagy by recruiting ATG16L1 to the plasma membrane at the site of bacterial entry | Q29615618 | ||
| Inflammatory bowel disease | Q29616286 | ||
| Interleukin-22, a T(H)17 cytokine, mediates IL-23-induced dermal inflammation and acanthosis | Q29620506 | ||
| Prediction and interaction in complex disease genetics: experience in type 1 diabetes | Q33479555 | ||
| Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. | Q33942125 | ||
| DNA methylation profiles in monozygotic and dizygotic twins. | Q34924376 | ||
| Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk | Q35125868 | ||
| IL-22 ameliorates intestinal inflammation in a mouse model of ulcerative colitis | Q36303708 | ||
| Systemic lupus erythematosus: all roads lead to type I interferons | Q36608558 | ||
| IL-15 trans-presentation promotes human NK cell development and differentiation in vivo | Q37061837 | ||
| Two independent alleles at 6q23 associated with risk of rheumatoid arthritis | Q37120830 | ||
| Rheumatoid arthritis association at 6q23. | Q37172071 | ||
| REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis | Q37248628 | ||
| A modular analysis framework for blood genomics studies: application to systemic lupus erythematosus | Q37308037 | ||
| Instability of the transcription factor Foxp3 leads to the generation of pathogenic memory T cells in vivo | Q37312884 | ||
| IL-22 and inflammation: leukin' through a glass onion | Q37328260 | ||
| Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource | Q37358904 | ||
| Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases | Q37413517 | ||
| Aire | Q37419376 | ||
| Molecular networks as sensors and drivers of common human diseases | Q37594580 | ||
| Innate and adaptive interleukin-22 protects mice from inflammatory bowel disease | Q39902875 | ||
| Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis | Q41846939 | ||
| Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases | Q43089300 | ||
| Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility | Q44808056 | ||
| Genetic variation in PTPN22 corresponds to altered function of T and B lymphocytes | Q44932416 | ||
| Systemic lupus erythematosus. | Q53495545 | ||
| Autoimmune disease in first-degree relatives of patients with multiple sclerosis. A UK survey | Q73822014 | ||
| Familial clustering of rheumatoid arthritis with other autoimmune diseases | Q77694552 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 791-797 | |
| P577 | publication date | 2010-03-01 | |
| P1433 | published in | Cell | Q655814 |
| P1476 | title | Unraveling the genetics of autoimmunity | |
| P478 | volume | 140 |
| Q42741761 | A TPL2 (MAP3K8) disease-risk polymorphism increases TPL2 expression thereby leading to increased pattern recognition receptor-initiated caspase-1 and caspase-8 activation, signalling and cytokine secretion |
| Q48004039 | A functional genomics predictive network model identifies regulators of inflammatory bowel disease |
| Q34130800 | A functional variant in ERAP1 predisposes to multiple sclerosis |
| Q36006358 | Acute myeloid leukemia developing in patients with autoimmune diseases |
| Q38396248 | Animal models of Multiple Sclerosis. |
| Q38601283 | Anti-cardiac troponin antibodies in clinical human disease: a systematic review |
| Q46899903 | Association of autoimmune diseases with oral lichen planus: a cross-sectional, clinical study |
| Q33676951 | Autoimmunity and the gut |
| Q34537272 | Autoimmunity and tumor immunology: two facets of a probabilistic immune system |
| Q26996644 | B cells take the front seat: dysregulated B cell signals orchestrate loss of tolerance and autoantibody production |
| Q33935390 | Balancing selection is common in the extended MHC region but most alleles with opposite risk profile for autoimmune diseases are neutrally evolving |
| Q47323461 | Bioconjugate Strategies for the Induction of Antigen-Specific Tolerance in Autoimmune Diseases. |
| Q57612857 | Brief Report: Candidate gene study in systemic sclerosis identifies a rare and functional variant of the TNFAIP3 locus as a risk factor for polyautoimmunity |
| Q35882582 | CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model |
| Q35178495 | CD4+FOXP3+ T regulatory cells in human autoimmunity: more than a numbers game |
| Q35885484 | COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis |
| Q36835759 | Characterization of pathogenic human monoclonal autoantibodies against GM-CSF. |
| Q34595104 | Clinical and pathological implications of concurrent autoimmune thyroid disorders and papillary thyroid cancer |
| Q34440616 | Clues to immune tolerance: the monogenic autoimmune syndromes |
| Q33837769 | Coherent somatic mutation in autoimmune disease |
| Q47112329 | Convergent downstream candidate mechanisms of independent intergenic polymorphisms between co-classified diseases implicate epistasis among noncoding elements |
| Q45959876 | Cutting-edge issues in organ-specific autoimmunity. |
| Q53541598 | Decreased UBASH3A mRNA Expression Levels in Peripheral Blood Mononuclear Cells from Patients with Systemic Lupus Erythematosus. |
| Q46091266 | Dog leukocyte antigen class II-associated genetic risk testing for immune disorders of dogs: simplified approaches using Pug dog necrotizing meningoencephalitis as a model |
| Q37149410 | Effective Arrestin-Specific Immunotherapy of Experimental Autoimmune Uveitis with RTL: A Prospect for Treatment of Human Uveitis |
| Q34310285 | Effector CD4+ T cell expression signatures and immune-mediated disease associated genes |
| Q34216556 | Enhancing the understanding of asthma |
| Q36755979 | Environment and primary biliary cirrhosis: electrophilic drugs and the induction of AMA. |
| Q58805285 | Evidence for sexual conflict over major histocompatibility complex diversity in a wild songbird |
| Q30009882 | Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene. |
| Q40144087 | Exploring the interplay between autoimmunity and cancer to find the target therapeutic hotspots. |
| Q40435291 | Ficolin Gene Polymorphisms in Systemic Lupus Erythematosus and Rheumatoid Arthritis |
| Q36057301 | Follicular Helper T Cells in Autoimmunity. |
| Q37714788 | Gene-gene interaction of BLK, TNFSF4, TRAF1, TNFAIP3, and REL in systemic lupus erythematosus |
| Q34659651 | Genetic association of rs1520333 G/A polymorphism in the IL7 gene with multiple sclerosis susceptibility in Isfahan population |
| Q54372307 | Genetic polymorphisms in CTLA4 and SLC4A2 are differentially associated with the pathogenesis of primary biliary cirrhosis in Japanese patients. |
| Q34384366 | Human regulatory T cells in autoimmune diseases |
| Q53214604 | IL-4, IL-10 and high sensitivity-CRP as potential serum biomarkers of persistent/recurrent disease in papillary thyroid carcinoma with/without Hashimoto's thyroiditis. |
| Q42258001 | IRF5 risk polymorphisms contribute to interindividual variance in pattern recognition receptor-mediated cytokine secretion in human monocyte-derived cells |
| Q90001905 | Immunogenicity of a rheumatoid arthritis protective sequence when acquired through microchimerism |
| Q34567654 | Impact of inflammatory bowel disease and high-dose steroid exposure on pupillary responses to negative information in pediatric depression |
| Q26864276 | Innate and adaptive immunity in inflammatory bowel disease |
| Q38689233 | Integrative Genetic and Epigenetic Analysis Uncovers Regulatory Mechanisms of Autoimmune Disease |
| Q83082263 | Mechanisms and pathophysiology of autoimmune disease |
| Q35899439 | Mechanisms of human autoimmunity |
| Q37119854 | Modeling the heterogeneity of multiple sclerosis in animals |
| Q37973770 | Monogenic autoimmunity |
| Q36479570 | Monozygotic twins with CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy |
| Q37627889 | NFIL3-deficient mice develop microbiota-dependent, IL-12/23-driven spontaneous colitis |
| Q48001628 | Nature, nurture, and microbes: The development of multiple sclerosis |
| Q37282406 | New insight on the Xq28 association with systemic sclerosis |
| Q35057902 | New mechanism of oral immunity to mucosal candidiasis in hyper-IgE syndrome |
| Q34428954 | Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation |
| Q27001015 | Possible implication of bacterial infection in acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation |
| Q50602849 | Psoriasis concurrent with inflammatory bowel disease. |
| Q51593866 | Quantitative disease resistance: to better understand parasite-mediated selection on major histocompatibility complex. |
| Q64039246 | Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS |
| Q42367245 | Recent advances in understanding autoimmune thyroid disease: the tallest tree in the forest of polyautoimmunity. |
| Q38020963 | Regulatory T cells in the central nervous system |
| Q99234081 | Sex matters: impact on pathogenesis, presentation and treatment of inflammatory bowel disease |
| Q42640015 | Shared genetic factors may not explain the raised risk of comorbid inflammatory diseases in multiple sclerosis |
| Q21135491 | Shared molecular and functional frameworks among five complex human disorders: a comparative study on interactomes linked to susceptibility genes |
| Q41553112 | The Genetic Architecture of Type 1 Diabetes |
| Q34097022 | The IL18RAP region disease polymorphism decreases IL-18RAP/IL-18R1/IL-1R1 expression and signaling through innate receptor-initiated pathways |
| Q39806420 | The deubiquitinase A20 mediates feedback inhibition of interleukin-17 receptor signaling |
| Q59353940 | The potential role for infections in the pathogenesis of autoimmune Addison's disease |
| Q58693536 | The role of polymorphic ERAP1 in autoinflammatory disease |
| Q35193892 | Therapeutic cancer vaccines and translating vaccinomics science to the global health clinic: emerging applications toward proof of concept |
| Q34580271 | Three multiplex snapshot assays for SNP genotyping in candidate innate immune genes. |
| Q35309080 | Towards systemic sclerosis and away from primary biliary cirrhosis: the case of PTPN22. |
| Q34675319 | Worldwide population distribution of the common LCE3C-LCE3B deletion associated with psoriasis and other autoimmune disorders |
Search more.