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A High Prevalence of Anti-EBNA1 Heteroantibodies in Systemic Lupus Erythematosus (SLE) Supports Anti-EBNA1 as an Origin for SLE Autoantibodies.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.830993
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- Article
Peptide Mimics of a Major Lupus Epitope of SmB/B′.
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- Annals of the New York Academy of Sciences, 2003, v. 987, n. 1, p. 215, doi. 10.1111/j.1749-6632.2003.tb06051.x
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- Article
Genetic susceptibility to SLE: new insights from fine mapping and genome-wide association studies.
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- 2009
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- Publication type:
- research
Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 6, p. 1656
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- Publication type:
- Article
Evaluation of imputation-based association in and around the integrin-α-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE).
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 6, p. 1171, doi. 10.1093/hmg/ddp007
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- Publication type:
- Article
Genetic variation in the CRP promoter: association with systemic lupus erythematosus.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1147, doi. 10.1093/hmg/ddn004
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- Publication type:
- Article
The US Department of Veterans Affairs Science and Health Initiative to Combat Infectious and Emerging Life-Threatening Diseases (VA SHIELD): A Biorepository Addressing National Health Threats.
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- Open Forum Infectious Diseases, 2022, v. 9, n. 12, p. 1, doi. 10.1093/ofid/ofac641
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- Article
Characterization of an Autoantigen Associated With Chronic Ulcerative Stomatitis: The CUSP Autoantigen is a Member of the p53 Family[sup 1].
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- Journal of Investigative Dermatology, 1999, v. 113, n. 2, p. 0, doi. 10.1046/j.1523-1747.1999.00651.x
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- Publication type:
- Article
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome.
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- Nature Genetics, 2013, v. 45, n. 11, p. 1284, doi. 10.1038/ng.2792
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- Publication type:
- Article
Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus.
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- Nature Genetics, 2011, v. 43, n. 3, p. 253, doi. 10.1038/ng.766
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- Publication type:
- Article
A nonsynonymous functional variant in integrin-α<sub>M</sub> (encoded by ITGAM) is associated with systemic lupus erythematosus.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 152, doi. 10.1038/ng.71
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- Publication type:
- Article
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.
- Published in:
- Nature Genetics, 2005, v. 37, n. 5, p. 478, doi. 10.1038/ng1540
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- Publication type:
- Article
Preferential Binding to Elk-1 by SLE-Associated <i>IL10</i> Risk Allele Upregulates <i>IL10</i> Expression.
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- PLoS Genetics, 2013, v. 9, n. 10, p. 1, doi. 10.1371/journal.pgen.1003870
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- Publication type:
- Article
Trans-Ancestral Studies Fine Map the SLE-Susceptibility Locus <i>TNFSF4</i>.
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- PLoS Genetics, 2013, v. 9, n. 7, p. 1, doi. 10.1371/journal.pgen.1003554
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- Publication type:
- Article
MicroRNA-3148 Modulates Allelic Expression of Toll-Like Receptor 7 Variant Associated with Systemic Lupus Erythematosus.
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- PLoS Genetics, 2013, v. 9, n. 2, p. 1, doi. 10.1371/journal.pgen.1003336
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- Publication type:
- Article
A Comprehensive Analysis of Shared Loci between Systemic Lupus Erythematosus (SLE) and Sixteen Autoimmune Diseases Reveals Limited Genetic Overlap.
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- PLoS Genetics, 2011, v. 7, n. 12, p. 1, doi. 10.1371/journal.pgen.1002406
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- Publication type:
- Article
Association of Genetic Variants in Complement Factor H and Factor H-Related Genes with Systemic Lupus Erythematosus Susceptibility.
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- PLoS Genetics, 2011, v. 7, n. 5, p. 1, doi. 10.1371/journal.pgen.1002079
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- Publication type:
- Article
Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome‐Wide Association Study and Inverse Variance–Weighted Meta‐Analysis.
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- Arthritis & Rheumatology, 2020, v. 72, n. 9, p. 1483, doi. 10.1002/art.41291
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- Publication type:
- Article
Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease.
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- Arthritis & Rheumatology, 2016, v. 68, n. 5, p. 1272, doi. 10.1002/art.39545
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- Publication type:
- Article
X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome.
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- Arthritis & Rheumatology, 2016, v. 68, n. 5, p. 1290, doi. 10.1002/art.39560
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- Publication type:
- Article
Whole-Exome Sequencing Reveals Overlap Between Macrophage Activation Syndrome in Systemic Juvenile Idiopathic Arthritis and Familial Hemophagocytic Lymphohistiocytosis.
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- Arthritis & Rheumatology, 2014, v. 66, n. 12, p. 3486, doi. 10.1002/art.38793
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- Publication type:
- Article
PTPN22 Association in Systemic Lupus Erythematosus (SLE) with Respect to Individual Ancestry and Clinical Sub-Phenotypes.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0069404
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- Publication type:
- Article
Genome-Wide Association Study of African and European Americans Implicates Multiple Shared and Ethnic Specific Loci in Sarcoidosis Susceptibility.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043907
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- Article
Osteopontin and Systemic Lupus Erythematosus Association: A Probable Gene-Gender Interaction.
- Published in:
- PLoS ONE, 2008, v. 3, n. 3, p. 1, doi. 10.1371/journal.pone.0001757
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- Publication type:
- Article
Common Variants within MECP2 Confer Risk of Systemic Lupus Erythematosus.
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- PLoS ONE, 2008, v. 3, n. 3, p. 1, doi. 10.1371/journal.pone.0001727
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- Publication type:
- Article
IRF5 gene polymorphisms in melanoma.
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- Journal of Translational Medicine, 2012, v. 10, n. 1, p. 170, doi. 10.1186/1479-5876-10-170
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- Publication type:
- Article
Desmoplakin and periplakin genetically and functionally contribute to eosinophilic esophagitis.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26939-9
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- Publication type:
- Article
The Role of Genetic Variation Near Interferon-Kappa in Systemic Lupus Erythematosus.
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- Journal of Biomedicine & Biotechnology, 2010, p. 1, doi. 10.1155/2010/706825
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- Publication type:
- Article
Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma.
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- Toxicological Sciences, 2015, v. 146, n. 1, p. 192, doi. 10.1093/toxsci/kfv084
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- Article
Unraveling the genetics of systemic lupus erythematosus.
- Published in:
- Springer Seminars in Immunopathology, 2006, v. 28, n. 2, p. 119, doi. 10.1007/s00281-006-0040-5
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- Publication type:
- Article
Identification of a Sjögren's syndrome susceptibility locus at OAS1 that influences isoform switching, protein expression, and responsiveness to type I interferons.
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- PLoS Genetics, 2017, v. 13, n. 6, p. 1, doi. 10.1371/journal.pgen.1006820
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- Publication type:
- Article
Validation of low‐coverage whole‐genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth.
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- Human Mutation, 2021, v. 42, n. 12, p. 1602, doi. 10.1002/humu.24279
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- Article
Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African Americans.
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- Human Molecular Genetics, 2018, v. 27, n. 21, p. 3813, doi. 10.1093/hmg/ddy280
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- Article
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 24, p. 4836, doi. 10.1093/hmg/ddx362
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- Article
Shared and distinct interactions of type 1 and type 2 Epstein-Barr Nuclear Antigen 2 with the human genome.
- Published in:
- BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-10183-8
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- Publication type:
- Article