| scholarly article | Q13442814 |
| P356 | DOI | 10.1101/CSHPERSPECT.A007260 |
| P8608 | Fatcat ID | release_42lvcp3a4nh35oyebd3y5fwg2u |
| P932 | PMC publication ID | 3282406 |
| P698 | PubMed publication ID | 22383754 |
| P50 | author | Adrian Liston | Q37384388 |
| An Goris | Q38326110 | ||
| P2860 | cites work | Extreme Evolutionary Disparities Seen in Positive Selection across Seven Complex Diseases | Q21136175 |
| Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 | ||
| MULTIFACTORIAL GENETICSUNDERSTANDING QUANTITATIVE GENETIC VARIATION | Q22121996 | ||
| Finding the missing heritability of complex diseases | Q22122198 | ||
| Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortium | Q22122334 | ||
| Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus. | Q52196099 | ||
| Highly variable expression of tissue-restricted self-antigens in human thymus: implications for self-tolerance and autoimmunity. | Q53569120 | ||
| Generalized resistance to thymic deletion in the NOD mouse; a polygenic trait characterized by defective induction of Bim. | Q53877408 | ||
| Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome | Q55670225 | ||
| Beyond odds ratios — communicating disease risk based on genetic profiles | Q58047301 | ||
| Incidence of CSF abnormalities in siblings of multiple sclerosis patients and unrelated controls | Q58321078 | ||
| Deregulated T cell activation and autoimmunity in mice lacking interleukin-2 receptor beta | Q72287439 | ||
| Variation is the spice of life | Q73594237 | ||
| Spontaneous autoimmune thyroiditis in NOD.H-2h4 mice | Q77380426 | ||
| Human DQ8 can substitute for murine I-Ag7 in the selection of diabetogenic T cells restricted to I-Ag7 | Q77801073 | ||
| Polygenic susceptibility to breast cancer and implications for prevention | Q78029012 | ||
| Homeostasis of peripheral CD4+ T cells: IL-2R alpha and IL-2 shape a population of regulatory cells that controls CD4+ T cell numbers | Q78404451 | ||
| Haplotype 4 of the multiple sclerosis-associated interleukin-7 receptor alpha gene influences the frequency of recent thymic emigrants | Q82498114 | ||
| Genetic risk prediction--are we there yet? | Q83658297 | ||
| A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease | Q22251291 | ||
| The allelic structure of common disease | Q22337147 | ||
| An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains | Q24313206 | ||
| Functionally defective germline variants of sialic acid acetylesterase in autoimmunity | Q24322817 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci | Q24618592 | ||
| Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls | Q24628710 | ||
| Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes | Q24632382 | ||
| Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis | Q24635370 | ||
| Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes | Q24651119 | ||
| Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes | Q24652324 | ||
| Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis | Q24656576 | ||
| Control of regulatory T cell development by the transcription factor Foxp3 | Q27860489 | ||
| The International HapMap Project | Q27860695 | ||
| Foxp3 programs the development and function of CD4+CD25+ regulatory T cells | Q27860714 | ||
| Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease | Q27860821 | ||
| Positional cloning of the APECED gene | Q28116470 | ||
| Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease | Q28201947 | ||
| Aire regulates negative selection of organ-specific T cells | Q28213185 | ||
| 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 | ||
| A genome-wide association study identifies IL23R as an inflammatory bowel disease gene | Q28270603 | ||
| HLA , CTLA-4 and PTPN22 : the shared genetic master-key to autoimmunity? | Q28277382 | ||
| Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant | Q28280659 | ||
| Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci | Q28281906 | ||
| Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus | Q28289699 | ||
| Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease | Q28300680 | ||
| Emerging patterns of risk factor make-up enable subclassification of rheumatoid arthritis | Q28304210 | ||
| Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction | Q28308221 | ||
| Interleukin-2 receptor α chain regulates the size and content of the peripheral lymphoid compartment | Q28587823 | ||
| Ulcerative colitis-like disease in mice with a disrupted interleukin-2 gene | Q28593669 | ||
| Risk alleles for multiple sclerosis in multiplex families. | Q34985640 | ||
| IL-21 drives secondary autoimmunity in patients with multiple sclerosis, following therapeutic lymphocyte depletion with alemtuzumab (Campath-1H) | Q34988311 | ||
| Integration of genetic risk factors into a clinical algorithm for multiple sclerosis susceptibility: a weighted genetic risk score | Q34997074 | ||
| Specific interaction between genotype, smoking and autoimmunity to citrullinated alpha-enolase in the etiology of rheumatoid arthritis | Q35011877 | ||
| Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort | Q35022304 | ||
| Estimation of effect size distribution from genome-wide association studies and implications for future discoveries | Q36191121 | ||
| Spontaneous autoimmunity prevented by thymic expression of a single self-antigen | Q36228141 | ||
| Gene dosage--limiting role of Aire in thymic expression, clonal deletion, and organ-specific autoimmunity. | Q36399327 | ||
| Aggregation of multiple sclerosis genetic risk variants in multiple and single case families | Q36438926 | ||
| The complex genetics of multiple sclerosis: pitfalls and prospects | Q37090601 | ||
| Unravelling the association of partial T-cell immunodeficiency and immune dysregulation | Q37190443 | ||
| Detecting shared pathogenesis from the shared genetics of immune-related diseases | Q37353862 | ||
| Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource | Q37358904 | ||
| Recent insights in the epidemiology of autoimmune diseases: improved prevalence estimates and understanding of clustering of diseases | Q37438934 | ||
| Genome-wide association studies on IgE regulation: are genetics of IgE also genetics of atopic disease? | Q37782212 | ||
| Genome-wide association studies: results from the first few years and potential implications for clinical medicine | Q37827862 | ||
| The MHC, disease and selection | Q37832010 | ||
| Promise and pitfalls of the Immunochip | Q37846258 | ||
| The genes influencing the susceptibility to IDDM in humans | Q40575824 | ||
| Genetic analysis of autoimmune disease | Q40980040 | ||
| Imaging brain damage in first-degree relatives of sporadic and familial multiple sclerosis | Q48638410 | ||
| Natural selection on genes that underlie human disease susceptibility | Q28757653 | ||
| Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 | Q28943305 | ||
| A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. | Q29417009 | ||
| Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease | Q29417151 | ||
| A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis | Q29417158 | ||
| The future of genetic studies of complex human diseases | Q29547215 | ||
| Common SNPs explain a large proportion of the heritability for human height | Q29547221 | ||
| Risk alleles for multiple sclerosis identified by a genomewide study | Q29614890 | ||
| An essential role for Scurfin in CD4+CD25+ T regulatory cells | Q29618395 | ||
| X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy | Q29619109 | ||
| The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 | Q29619324 | ||
| CTLA-4 control over Foxp3+ regulatory T cell function | Q29619413 | ||
| Regulatory T cells prevent catastrophic autoimmunity throughout the lifespan of mice | Q29622850 | ||
| Derivation of diabetes-resistant congenic lines from the nonobese diabetic mouse | Q30305858 | ||
| Structure of an autoimmune T cell receptor complexed with class II peptide-MHC: insights into MHC bias and antigen specificity | Q31142850 | ||
| Defining the role of the MHC in autoimmunity: a review and pooled analysis | Q33330857 | ||
| Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus | Q33375065 | ||
| Prediction and interaction in complex disease genetics: experience in type 1 diabetes | Q33479555 | ||
| What role for genetics in the prediction of multiple sclerosis? | Q33695782 | ||
| The role of genetic factors in autoimmune disease: implications for environmental research | Q33741165 | ||
| Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come | Q33772946 | ||
| Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations? | Q33799136 | ||
| Prediction and pathogenesis in type 1 diabetes. | Q33818896 | ||
| Nonobese diabetic congenic strain analysis of autoimmune diabetes reveals genetic complexity of the Idd18 locus and identifies Vav3 as a candidate gene. | Q33918365 | ||
| The prevalence of 30 ICD-10 autoimmune diseases in Denmark | Q33941529 | ||
| Structure of a human autoimmune TCR bound to a myelin basic protein self-peptide and a multiple sclerosis-associated MHC class II molecule | Q33947114 | ||
| A high-density screen for linkage in multiple sclerosis | Q34021149 | ||
| Genetic association between juvenile rheumatoid arthritis and polymorphism in the SH2D2A gene | Q34319025 | ||
| Meta-analysis of genome-wide linkage studies across autoimmune diseases | Q34325606 | ||
| Inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreporting | Q34386225 | ||
| Normal regulatory alpha/beta T cells effectively eliminate abnormally activated T cells lacking the interleukin 2 receptor beta in vivo | Q34506140 | ||
| A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region | Q34525819 | ||
| Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis | Q34657157 | ||
| TGF-beta and IL-6 drive the production of IL-17 and IL-10 by T cells and restrain T(H)-17 cell-mediated pathology | Q34712326 | ||
| Immunopathology of interleukin (IL) 2-deficient mice: thymus dependence and suppression by thymus-dependent cells with an intact IL-2 gene | Q34719199 | ||
| Genome-based prediction of common diseases: advances and prospects | Q34851798 | ||
| Validating, augmenting and refining genome-wide association signals | Q34976245 | ||
| The epigenetics of autoimmunity | Q34979322 | ||
| P433 | issue | 3 | |
| P921 | main subject | autoimmune disease | Q8084905 |
| P577 | publication date | 2012-03-01 | |
| P1433 | published in | Cold Spring Harbor Perspectives in Biology | Q3927509 |
| P1476 | title | The immunogenetic architecture of autoimmune disease | |
| P478 | volume | 4 |
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| Q55035559 | An Increased Frequency in HLA Class I Alleles and Haplotypes Suggests Genetic Susceptibility to Influenza A (H1N1) 2009 Pandemic: A Case-Control Study. |
| Q38467857 | An integrative pipeline for multi-modal discovery of disease relationships |
| Q47846903 | Anti-inflammatory roles of p38α MAPK in macrophages are context dependent and require IL-10. |
| Q38422793 | Autoimmune/inflammatory syndrome induced by adjuvant (ASIA) evolution after silicone implants. Who is at risk? |
| Q47323461 | Bioconjugate Strategies for the Induction of Antigen-Specific Tolerance in Autoimmune Diseases. |
| Q36389114 | Cellular stress and innate inflammation in organ-specific autoimmunity: lessons learned from vitiligo |
| Q36366934 | Familial Aggregation and Segregation Analysis in Families Presenting Autoimmunity, Polyautoimmunity, and Multiple Autoimmune Syndrome |
| Q52345322 | Familial multiple sclerosis and association with other autoimmune diseases. |
| Q36057301 | Follicular Helper T Cells in Autoimmunity. |
| Q37607787 | High prevalence of autoimmune disease in the rare inflammatory bone disorder sternocostoclavicular hyperostosis: survey of a Dutch cohort. |
| Q38392912 | Immune biomarkers: the promises and pitfalls of personalized medicine. |
| Q36193674 | Impact of V-ets Erythroblastosis Virus E26 Oncogene Homolog 1 Gene Polymorphisms Upon Susceptibility to Autoimmune Diseases: A Meta-Analysis |
| Q35767935 | Integrated Analyses of Gene Expression Profiles Digs out Common Markers for Rheumatic Diseases. |
| Q45855746 | Liver cystic echinococcosis and human host immune and autoimmune follow-up: A review |
| Q35899439 | Mechanisms of human autoimmunity |
| Q35241027 | Meta-analysis of microRNA-146a rs2910164 G>C polymorphism association with autoimmune diseases susceptibility, an update based on 24 studies |
| Q40760203 | Natural resistance to experimental feline infectious peritonitis virus infection is decreased rather than increased by positive genetic selection |
| Q39061447 | Network-based analysis of differentially expressed genes in cerebrospinal fluid (CSF) and blood reveals new candidate genes for multiple sclerosis. |
| Q33421946 | Poly-autoimmunity in patients with myasthenia gravis: A single-center experience. |
| Q36382352 | Progress in multiple sclerosis genetics |
| Q47101422 | SIAE Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies |
| Q37533248 | Sex-biased chromatin and regulatory cross-talk between sex chromosomes, autosomes, and mitochondria. |
| Q37351905 | Shared Genetic Etiology of Autoimmune Diseases in Patients from a Biorepository Linked to De-identified Electronic Health Records |
| Q40507763 | The effect of genetic bottlenecks and inbreeding on the incidence of two major autoimmune diseases in standard poodles, sebaceous adenitis and Addison's disease |
| Q89650535 | The microbiome in autoimmune rheumatic disease |
| Q37693206 | Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription |
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