Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus.

scientific article published on 26 July 2002

Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1086/342290
P932PMC publication ID379191
P698PubMed publication ID12145745
P5875ResearchGate publication ID11236347

P50authorPeter K. GregersenQ7175067
Carl D. LangefeldQ102208371
Henry A. ErlichQ110157647
Patrick M GaffneyQ64978394
P2093author name stringKathy L Moser
Timothy W Behrens
Stephen S Rich
Emily C Baechler
Robert R Graham
James T Elder
Philip E Stuart
Rajan P Nair
Teodorica L Bugawan
Linda E Green
Damini Jawaheer
Ward A Ortmann
Richard A King
Peter R Rodine
Karl J Espe
Katherine B Shark
Kristine E Rohlf
Scott A Selby
P2860cites workConditional ETDT analysis of the human leukocyte antigen region in type 1 diabetesQ73607038
Conditional linkage disequilibrium analysis of a complex disease superlocus, IDDM1 in the HLA region, reveals the presence of independent modifying gene effects influencing the type 1 diabetes risk encoded by the major HLA-DQB1, -DRB1 disease lociQ73707657
Genetic susceptibility to systemic lupus erythematosusQ74578130
The genetics of lupusQ77329110
Recent advances in the genetics of systemic lupus erythematosusQ77629430
The genetics of human systemic lupus erythematosusQ77892094
Methods for the study of histocompatibility genesQ79518294
Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortiumQ22122334
A sibship test for linkage in the presence of association: the sib transmission/disequilibrium testQ24538716
PedCheck: a program for identification of genotype incompatibilities in linkage analysisQ24539016
Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)Q24671756
Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosusQ24799685
Intensely punctate meiotic recombination in the class II region of the major histocompatibility complexQ28190352
A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair familiesQ28776415
The future of genetic studies of complex human diseasesQ29547215
Genomics of the major histocompatibility complex: haplotypes, duplication, retroviruses and diseaseQ33630704
Association analysis using refined microsatellite markers localizes a susceptibility locus for psoriasis vulgaris within a 111 kb segment telomeric to the HLA-C geneQ33878843
A test for linkage and association in general pedigrees: the pedigree disequilibrium testQ34141820
Genome screening in human systemic lupus erythematosus: results from a second Minnesota cohort and combined analyses of 187 sib-pair familiesQ34145111
Genetics and molecular genetics of the MHC.Q34188439
Delineating the genetic basis of systemic lupus erythematosusQ34376876
Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C.Q34390693
Allele-sharing models: LOD scores and accurate linkage testsQ35249919
Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritisQ35834701
The role of somatic mutation in the pathogenic anti-DNA responseQ36135271
Autoantigens targeted in systemic lupus erythematosus are clustered in two populations of surface structures on apoptotic keratinocytesQ36363024
Systemic exposure to irradiated apoptotic cells induces autoantibody productionQ36401434
HLA-DR, DQ and DP typing using PCR amplification and immobilized probesQ38336692
Genetic analysis of autoimmune diseaseQ40980040
The critical region for Behçet disease in the human major histocompatibility complex is reduced to a 46-kb segment centromeric of HLA-B, by association analysis using refined microsatellite mappingQ42014366
Induction of dendritic cell differentiation by IFN-alpha in systemic lupus erythematosus.Q53718320
Polygenic control of susceptibility to murine systemic lupus erythematosusQ57903408
Dissection of the HLA association with multiple sclerosis in the founder isolated population of SardiniaQ63285869
TNF-308A and HLA-DR3 alleles contribute independently to susceptibility to systemic lupus erythematosusQ73374738
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectsystemic lupus erythematosusQ1485
visualizationQ451553
P304page(s)543-553
P577publication date2002-07-26
P1433published inAmerican Journal of Human GeneticsQ4744249
P1476titleVisualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus
P478volume71

Reverse relations

cites work (P2860)
Q30278514A Central Role for HLA-DR3 in Anti-Smith Antibody Responses and Glomerulonephritis in a Transgenic Mouse Model of Spontaneous Lupus
Q36854313A compass that points to lupus: genetic studies on type I interferon pathway.
Q37161006A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
Q108910610A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response
Q40424563A role for HLA-DRB1*1101 and DRB1*0801 in cognitive ability and its decline with age.
Q34144851A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles
Q34955602An extensive screen of the HLA region reveals an independent association of HLA class I and class II with susceptibility for systemic lupus erythematosus
Q33942125Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.
Q42604970Association of HLA-DRB1*15 and HLADQB1*06 with SLE in Saudis
Q36058691Association of HLA-G 3' Untranslated Region Polymorphisms with Systemic Lupus Erythematosus in a Japanese Population: A Case-Control Association Study.
Q33455772Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.
Q30418064Autoimmunity, end organ damage, and the origin of autoantibodies and autoreactive T cells in systemic lupus erythematosus.
Q38425837Biomarkers in lupus nephritis
Q34513460Bromodomain coactivators in cancer, obesity, type 2 diabetes, and inflammation
Q87418244Certain HLA alleles are associated with stress-triggered Graves' disease and influence its course
Q38534421Clinical Role of Human Leukocyte Antigen in Health and Disease.
Q40153873Clinical, serologic, and immunogenetic characterization (HLA-DRB1) of late-onset lupus erythematosus in a Colombian population
Q44303693Cumulative association of eight susceptibility genes with systemic lupus erythematosus in a Japanese female population.
Q35882070Current advances in the human lupus genetics
Q36392330Current status of lupus genetics
Q33330857Defining the role of the MHC in autoimmunity: a review and pooled analysis
Q30433491Differential responses to Smith D autoantigen by mice with HLA-DR and HLA-DQ transgenes: dominant responses by HLA-DR3 transgenic mice with diversification of autoantibodies to small nuclear ribonucleoprotein, double-stranded DNA, and nuclear antige
Q35834701Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis
Q54649175Extended haplotype analysis reveals an association of TNF polymorphisms with susceptibility to systemic lupus erythematosus beyond HLA-DR3.
Q57329898Familial aggregation and linkage analysis of autoantibody traits in pedigrees multiplex for systemic lupus erythematosus
Q35788507Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A
Q37030621General aspects of the genetics of SLE.
Q34363380Genes and Sjögren's syndrome
Q81541374Genes and autoimmune diseases - a complex inheritance
Q57461894Genetic association of IRF5 with SLE in Mexicans: higher frequency of the risk haplotype and its homozygozity than Europeans
Q51123536Genetic control of the spontaneous activation of CD4+ Th cells in systemic lupus erythematosus-prone (NZB x NZW) F1 mice.
Q35600184Genetic epidemiology of type 1 diabetes
Q35102487Genetic susceptibility to systemic lupus erythematosus in the genomic era
Q36593309Genetics of SLE in mice
Q36670483Genetics of autoimmune diseases--disorders of immune homeostasis
Q38907309HLA Class II with Lupus Nephritis in Moroccan Patients
Q91393861HLA and kidney disease: from associations to mechanisms
Q36392275HLA class II DR and DQ genotypes and haplotypes associated with rheumatic fever among a clinically homogeneous patient population of Latvian children
Q36379492HLA class II disease associations in southern Africa
Q45171706HLA class II, MICA and PRL gene polymorphisms: the common contribution to the systemic lupus erythematosus development in Czech population.
Q30424263HLA-DR3 restricted T cell epitope mimicry in induction of autoimmune response to lupus-associated antigen SmD
Q40607323HLA-DRB1 the notorious gene in the mosaic of autoimmunity
Q21092448High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions
Q35570872Horizons in Sjögren's syndrome genetics
Q35073646Identical twins:one with anti-glomerular basement membrane glomerulonephritis,the other with systemic lupus erythematosus.
Q35877841Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study
Q30837981Identification of two independent risk factors for lupus within the MHC in United Kingdom families
Q33909567Linkage at 12q24 with systemic lupus erythematosus (SLE) is established and confirmed in Hispanic and European American families
Q44039154Localization of Type 1 Diabetes susceptibility in the ancestral haplotype 18.2 by high density SNP mapping.
Q33487803MHC class II polymorphism is associated with a canine SLE-related disease complex
Q35637001MHC class II, tumour necrosis factor alpha, and lymphotoxin alpha gene haplotype associations with serological subsets of systemic lupus erythematosus
Q53665656MHC microsatellite diversity and linkage disequilibrium among common HLA-A, HLA-B, DRB1 haplotypes: implications for unrelated donor hematopoietic transplantation and disease association studies.
Q35549151MHC region and risk of systemic lupus erythematosus in African American women
Q61283020Maternal HLA class II compatibility in men with systemic lupus erythematosus
Q82287091Meta-analysis of TNF-alpha promoter -308 A/G polymorphism and SLE susceptibility
Q40288584Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus
Q57330853Microsatellite typing for DRB1 alleles: application to the analysis of HLA associations with rheumatoid arthritis
Q48283822No excess of autoimmune diseases in multiple sclerosis families from the Netherlands.
Q86113674One novel susceptibility locus associate with systemic lupus erythematosus in Chinese Han population
Q30425180Pathogenesis of systemic lupus erythematosus revisited 2011: end organ resistance to damage, autoantibody initiation and diversification, and HLA-DR.
Q36486336Pediatric systemic lupus erythematosus: management issues in primary practice
Q46532671Peptides from antibodies to DNA elicit cytokine release from peripheral blood mononuclear cells of patients with systemic lupus erythematosus: relation of cytokine pattern to disease duration
Q61658983Prevalence and evolutionary origins of autoimmune susceptibility alleles in natural mouse populations
Q33964547Recent advances in the genetics of systemic lupus erythematosus
Q34330648Regulation of major histocompatibility complex class II gene expression, genetic variation and disease
Q28943379Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08
Q36065912Role of MHC-linked susceptibility genes in the pathogenesis of human and murine lupus
Q28278154Role of an intronic polymorphism in the PDCD1 gene with the risk of sporadic systemic lupus erythematosus and the occurrence of antiphospholipid antibodies
Q35986928Role of cytokines in systemic lupus erythematosus: recent progress from GWAS and sequencing
Q46950949SNP haplotypes and allele frequencies show evidence for disruptive and balancing selection in the human leukocyte receptor complex
Q34756777Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus
Q37852786Shared genetics in coeliac disease and other immune-mediated diseases
Q80093540Specific combinations of HLA-DR2 and DR3 class II haplotypes contribute graded risk for disease susceptibility and autoantibodies in human SLE
Q34032957Spontaneous lupus-like syndrome in HLA-DQ2 transgenic mice with a mixed genetic background.
Q81318245Systemic lupus erythematosus susceptibility loci defined by genome scan meta-analysis
Q37930475Systemic lupus erythematosus, the brain, and anti-NR2 antibodies
Q35156161Systemic lupus erythematosus: from genes to organ damage
Q36673286Systemic lupus erythematosus: multiple immunological phenotypes in a complex genetic disease.
Q36687918Systems biology in systemic lupus erythematosus: integrating genes, biology and immune function
Q35124114Teasing apart the complex genetics of human autoimmunity: lessons from rheumatoid arthritis
Q28080256The Importance of Patient-Specific Factors for Hepatic Drug Response and Toxicity
Q35553401The genetics of primary Sjögren’s syndrome
Q28391462The role of HLA-DR-DQ haplotypes in variable antibody responses to anthrax vaccine adsorbed
Q35896644Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at MSH5, HLA-DPB1 and HLA-G
Q36365695Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans
Q36614958Unraveling the genetics of systemic lupus erythematosus
Q34082914Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for systemic lupus erythematosus within the MHC.

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