Autoimmune disease: why and where it occurs

Fas Ligand-Induced Apoptosis as a Mechanism of Immune Privilege

Griffith, T. S., Brunner, T., Fletcher, S. M., Green, D. R., & Ferguson, T. A. (1995) · Science · doi:10.1126/science.270.5239.1189 · Cited by 1,990

Epidemiology and estimated population burden of selected autoimmune diseases in the United States

Jacobson, D. L., Gange, S. J., Rose, N. R., & Graham, N. M. H. (1997) · Clinical Immunology and Immunopathology · doi:10.1006/clin.1997.4412 · Cited by 1,667

Molecular mimicry in T cell-mediated autoimmunity: Viral peptides activate human T cell clones specific for myelin basic protein

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Positional cloning of the APECED gene

Nagamine, K., Peterson, P., Scott, H. S., Kudoh, J., Minoshima, S., Heino, M., Krohn, K. J. E., Lalioti, M. D., Mullis, P. E., Antonarakis, S. E., et al. (1997) · Nature Genetics · doi:10.1038/ng1297-393 · Cited by 1,439

Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies

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Visualization of peptide-specific T cell immunity and peripheral tolerance induction in vivo.

Kearney, E. R., Pape, K., Loh, D., & Jenkins, M. (1994) · Immunity · doi:10.1016/1074-7613(94)90084-1 · Cited by 1,126

bcl-2 transgene inhibits T cell death and perturbs thymic self-censorship

Strasser, A., Harris, A. W., & Cory, S. (1991) · Cell · doi:10.1016/0092-8674(91)90362-3 · Cited by 1,054

Multiple Sclerosis: A Coordinated Immunological Attack against Myelin in the Central Nervous System

Steinman, L. (1996) · Cell · doi:10.1016/s0092-8674(00)81107-1 · Cited by 892

Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus

Vafiadis, P., Bennett, S. T., Todd, J. A., Nadeau, J., Grabs, R., Goodyer, C. G., Wickramasinghe, S., Colle, E., & Polychronakos, C. (1997) · Nature Genetics · doi:10.1038/ng0397-289 · Cited by 809

Spontaneous Autoimmune Disease in FcγRIIB-Deficient Mice Results from Strain-Specific Epistasis

Bolland, S. M., & Ravetch, J. V. (2000) · Immunity · doi:10.1016/s1074-7613(00)00027-3 · Cited by 757

A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis

Begovich, A. B., Carlton, V. E. H., Honigberg, L. A., Schrodi, S. J., Chokkalingam, A. P., Alexander, H. C., Ardlie, K., Huang, Q., Smith, A. M., Spoerke, J. M., et al. (2004) · The American Journal of Human Genetics · doi:10.1086/422827 · Cited by 1,501

IL-6 in inflammation, autoimmunity and cancer

Hirano, T. (2021) · International Immunology · doi:10.1093/intimm/dxaa078 · Cited by 1,453

A Large-Scale Genetic Association Study Confirms IL12B and Leads to the Identification of IL23R as Psoriasis-Risk Genes

Cargill, M., Schrodi, S. J., Chang, M., Garcia, V. E., Brandon, R., Callis, K. P., Matsunami, N., Ardlie, K. G., Civello, D., Catanese, J. J., et al. (2007) · The American Journal of Human Genetics · doi:10.1086/511051 · Cited by 1,086

Altered thymic T-cell selection due to a mutation of the ZAP-70 gene causes autoimmune arthritis in mice

Sakaguchi, N., Takahashi, T., Hata, H., Nomura, T., Tagami, T., Yamazaki, S., Sakihama, T., Matsutani, T., Negishi, I., Nakatsuru, S., et al. (2003) · Nature · doi:10.1038/nature02119 · Cited by 881

A Proposed Classification of the Immunological Diseases

McGonagle, D., & McDermott, M. (2006) · PLoS Medicine · doi:10.1371/journal.pmed.0030297 · Cited by 841

Immunologic Aspects of Chronic Obstructive Pulmonary Disease

Cosío, M. G., Saetta, M. P., & Agustí, A. G. N. (2009) · New England Journal of Medicine · doi:10.1056/nejmra0804752 · Cited by 823

Cytokines and autoimmunity

O’Shea, J. J., Ma, A. I., & Lipsky, P. E. (2002) · Nature reviews. Immunology · doi:10.1038/nri702 · Cited by 677

NALP1 in Vitiligo-Associated Multiple Autoimmune Disease

Jin, Y., Mailloux, C. M., Gowan, K., Riccardi, S. L., LaBerge, G. S., Bennett, D. C., Fain, P. R., & Spritz, R. A. (2007) · New England Journal of Medicine · doi:10.1056/nejmoa061592 · Cited by 635

Synovial fibroblasts: key players in rheumatoid arthritis

Huber, L. C., Distler, O., Tarner, I. H., Gay, R. E., Gay, S., & Pap, T. (2006) · Lara D. Veeken · doi:10.1093/rheumatology/kel065 · Cited by 608

Interleukin-17 promotes autoimmunity by triggering a positive-feedback loop via interleukin-6 induction

Ogura, H., Murakami, M., Okuyama, Y., Tsuruoka, M., Kitabayashi, C., Kanamoto, M., Nishihara, M., Iwakura, Y., & Hirano, T. (2008) · Immunity · doi:10.1016/j.immuni.2008.07.018 · Cited by 564

The interplay between cytokines, inflammation, and antioxidants: mechanistic insights and therapeutic potentials of various antioxidants and anti-cytokine compounds

Bhol, N. K., Bhanjadeo, M. M., Singh, A. K., Dash, U. C., Ojha, R. R., Majhi, S., Duttaroy, A. K., & Jena, A. B. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117177 · Cited by 570

Carbohydrate mimicry between human ganglioside GM1 and Campylobacter jejuni lipooligosaccharide causes Guillain–Barré syndrome

Yuki, N., Susuki, K., Koga, M., Nishimoto, Y., Odaka, M., Hirata, K., Taguchi, K., Miyatake, T., Furukawa, K., Kobata, T., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402391101 · Cited by 497

Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

Wise, C. A. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.8.961 · Cited by 443

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities

Kochi, Y., Yamada, R., Suzuki, A., Harley, J. B., Shirasawa, S., Sawada, T., Bae, S., Tokuhiro, S., Chang, X., Sekine, A., et al. (2005) · Nature Genetics · doi:10.1038/ng1540 · Cited by 394

Polyglandular Autoimmune Syndromes: Immunogenetics and Long-Term Follow-Up

Dittmar, M., & Kahaly, G. J. (2003) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2002-021845 · Cited by 367

Evolution in Health and Disease

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The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis

Lee, Y. H., Rho, Y. H., Choi, S. J., Ji, J. D., Song, G. G., Nath, S. K., & Harley, J. B. (2006) · Rheumatology · doi:10.1093/rheumatology/kel170 · Cited by 318

Emerging role of air pollution in autoimmune diseases

Zhao, C., Xu, Z., Wu, G., Mao, Y., Liu, L., Qian-Wu, Dan, Y., Tao, S., Zhang, Q., Sam, N. B., et al. (2019) · Autoimmunity Reviews · doi:10.1016/j.autrev.2018.12.010 · Cited by 321

Autoimmunity through Cytokine-Induced Dendritic Cell Activation

Banchereau, J., Pascual, V., & Palucka, A. K. (2004) · Immunity · doi:10.1016/s1074-7613(04)00108-6 · Cited by 295

Rheumatoid arthritis: Recent advances on its etiology, role of cytokines and pharmacotherapy

Alam, J., Jantan, I., & Bukhari, S. N. A. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.05.055 · Cited by 286

IFN-α Induces Early Lethal Lupus in Preautoimmune (New Zealand Black × New Zealand White)F1 but Not in BALB/c Mice

Mathian, A., Weinberg, A. G., Gallegos, M., Banchereau, J., & Koutouzov, S. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.5.2499 · Cited by 270

Autoantibodies in Patients with Chronic Obstructive Pulmonary Disease

Feghali‐Bostwick, C. A., Gadgil, A. S., Otterbein, L. E., Pilewski, J. M., Stoner, M. W., Csizmadia, E., Zhang, Y., Sciurba, F. C., & Duncan, S. R. (2007) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200701-014oc · Cited by 268

A defect in central tolerance in NOD mice

Kishimoto, H., & Sprent, J. (2001) · Nature Immunology · doi:10.1038/ni726 · Cited by 268

Fibrosis: ultimate and proximate causes

Thannickal, V. J., Zhou, Y., Gaggar, A., & Duncan, S. R. (2014) · Journal of Clinical Investigation · doi:10.1172/jci74368 · Cited by 249

PTPN22 Genetic Variation: Evidence for Multiple Variants Associated with Rheumatoid Arthritis

Carlton, V. E. H., Hu, X., Chokkalingam, A. P., Schrodi, S. J., Brandon, R. C., Alexander, H. C., Chang, M., Catanese, J. J., Leong, D. U., Ardlie, K., et al. (2005) · The American Journal of Human Genetics · doi:10.1086/468189 · Cited by 240

Fc Receptor-Like Molecules

Davis, R. S. (2007) · Annual Review of Immunology · doi:10.1146/annurev.immunol.25.022106.141541 · Cited by 225

NLRP1 haplotypes associated with vitiligo and autoimmunity increase interleukin-1β processing via the NLRP1 inflammasome

Levandowski, C. B., Mailloux, C. M., Ferrara, T. M., Gowan, K., Ben, S., Jin, Y., McFann, K. K., Holland, P. J., Fain, P. R., Dinarello, C. A., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1222808110 · Cited by 213

Curcumin: A natural modulator of immune cells in systemic lupus erythematosus

Momtazi‐Borojeni, A. A., Haftcheshmeh, S. M., Esmaeili, S., Johnston, T. P., Abdollahi, E., & Sahebkar, A. (2017) · Autoimmunity Reviews · doi:10.1016/j.autrev.2017.11.016 · Cited by 212

A Defect in Tryptophan Catabolism Impairs Tolerance in Nonobese Diabetic Mice

Grohmann, U., Fallarino, F., Bianchi, R., Orabona, C., Vacca, C., Fioretti, M. C., & Puccetti, P. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20030633 · Cited by 212

The Master Switch: The Role of Mast Cells in Autoimmunity and Tolerance

Sayed, B. A., Christy, A. L., Quirion, M. R., & Brown, M. A. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090320 · Cited by 214

Characterizing the Dysfunctional NK Cell: Assessing the Clinical Relevance of Exhaustion, Anergy, and Senescence

Judge, S. J., Murphy, W. J., & Canter, R. J. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00049 · Cited by 216

Cutting Edge: Molecular Portrait of Human Autoimmune Disease

Maas, K. H., Chan, S. K., Parker, J. S., Slater, A. M., Moore, J. H., Olsen, N. J., & Aune, T. M. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.1.5 · Cited by 202

HLA in coeliac disease: Unravelling the complex genetics of a complex disorder

Louka, A. S., & Sollid, L. M. (2003) · Tissue Antigens · doi:10.1034/j.1399-0039.2003.00017.x · Cited by 192

Patients with idiopathic pulmonary fibrosis with antibodies to heat shock protein 70 have poor prognoses

Kahloon, R. A., Xue, J., Bhargava, A., Csizmadia, E., Otterbein, L., Kass, D. J., Bon, J., Soejima, M., Levesque, M. C., Lindell, K. O., et al. (2013) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201203-0506oc · Cited by 190

The Pathogenesis of Biliary Atresia: Evidence for a Virus-Induced Autoimmune Disease

Mack, C. L. (2007) · Seminars in Liver Disease · doi:10.1055/s-2007-985068 · Cited by 183

Autoimmunity in human primary immunodeficiency diseases

Arkwright, P. D., Abinun, M., & Cant, A. J. (2002) · Blood · doi:10.1182/blood.v99.8.2694 · Cited by 180

Autoimmune arthritis associated with mutated interleukin (IL)-6 receptor gp130 is driven by STAT3/IL-7-dependent homeostatic proliferation of CD4+ T cells

Sawa, S.-I., Kamimura, D., Jin, G.-H., Morikawa, H., Kamon, H., Nishihara, M., Ishihara, K., Murakami, M., & Hirano, T. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20052187 · Cited by 176

NF-κB and STAT1 control CXCL1 and CXCL2 gene transcription

Burke, S. J., Lu, D., Sparer, T. E., Masi, T. J., Goff, M. R., Karlstad, M. D., & Collier, J. J. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00347.2013 · Cited by 180

Interleukin 6 in autoimmune and inflammatory diseases: a personal memoir

HIRANO, T. (2010) · Proceedings of the Japan Academy, Series B · doi:10.2183/pjab.86.717 · Cited by 172

A Comprehensive Analysis of Shared Loci between Systemic Lupus Erythematosus (SLE) and Sixteen Autoimmune Diseases Reveals Limited Genetic Overlap

Ramos, P. S., Criswell, L. A., Moser, K. L., Comeau, M. E., Williams, A. H., Pajewski, N. M., Chung, S. A., Graham, R., Zidovetzki, R., Kelly, J. A., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002406 · Cited by 172

Modeling Inflammation in Zebrafish for the Development of Anti-inflammatory Drugs

Xie, Y., Meijer, A. H., & Schaaf, M. J. M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.620984 · Cited by 164

Expression of IP-10/CXCL10 and MIG/CXCL9 in the Thyroid and Increased Levels of IP-10/CXCL10 in the Serum of Patients with Recent-Onset Graves' Disease

Romagnani, P., Rotondi, M., Lazzeri, E., Lasagni, L., Francalanci, M., Buonamano, A., Milani, S., Vitti, P., Chiovato, L., Tonacchera, M., et al. (2002) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64171-5 · Cited by 159

Immunogenetic Risk and Protective Factors for the Idiopathic Inflammatory Myopathies

OʼHanlon, T. P., Carrick, D. M., Targoff, I. N., Arnett, F. C., Reveille, J. D., Carrington, M. N., Gao, X., Oddis, C. V., Morel, P. A., Malley, J. D., et al. (2006) · Medicine · doi:10.1097/01.md.0000217525.82287.eb · Cited by 161

The common variants/multiple disease hypothesis of common complex genetic disorders

Becker, K. G. (2003) · Medical Hypotheses · doi:10.1016/s0306-9877(03)00332-3 · Cited by 157

Cellular and Humoral Autoreactivity in Idiopathic Pulmonary Fibrosis

Feghali‐Bostwick, C. A., Tsai, C. G., Valentine, V. G., Kantrow, S. P., Stoner, M. W., Pilewski, J. M., Gadgil, A. S., George, M. P., Gibson, K. F., Choi, A. M. K., et al. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.4.2592 · Cited by 158

Macrophage: Key player in the pathogenesis of autoimmune diseases

Yang, S. C., Zhao, M., & Jia, S. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1080310 · Cited by 165

Inflammatory Bowel Disease: Autoimmune or Immune‐mediated Pathogenesis?

Wen, Z., & Fiocchi, C. (2004) · Journal of Immunology Research · doi:10.1080/17402520400004201 · Cited by 158

Viruses as adjuvants for autoimmunity: evidence from Coxsackievirus‐induced myocarditis

Fairweather, D., Frisancho‐Kiss, S., & Rose, N. R. (2005) · Reviews in Medical Virology · doi:10.1002/rmv.445 · Cited by 155

Role of Cytokines in the Pathogenesis and Suppression of Thyroid Autoimmunity

Ganesh, B. B., Bhattacharya, P., Gopisetty, A., & Prabhakar, B. S. (2011) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2011.0049 · Cited by 157

T-cell signalling and autoimmunity: molecular mechanisms of disease

Ohashi, P. S. (2002) · Nature reviews. Immunology · doi:10.1038/nri822 · Cited by 148

There is no evidence of an inverse relationship between TH2-mediated atopy and TH1-mediated autoimmune disorders: Lack of support for the hygiene hypothesis

Sheikh, A., Smeeth, L. L., & Hubbard, R. (2003) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2003.8 · Cited by 148

Ganglioside mimicry and peripheral nerve disease

Yuki, N. (2007) · Muscle & Nerve · doi:10.1002/mus.20762 · Cited by 142

Molecular underpinning of B‐cell anergy

Yarkoni, Y., Getahun, A., & Cambier, J. C. (2010) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00936.x · Cited by 131

Is Eradication Therapy Useful as the First Line of Treatment in Helicobacter pylori-Positive Idiopathic Thrombocytopenic Purpura? Analysis of 207 Eradicated Chronic ITP Cases in Japan

Fujimura, K., Kuwana, M., Kurata, Y., Imamura, M., Harada, H., Sakamaki, H., Teramura, M., Koda, K., Nomura, S., Sugihara, S., et al. (2005) · International Journal of Hematology · doi:10.1532/ijh97.04146 · Cited by 130

Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3-p32.2

Alkhateeb, A. M. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.6.661 · Cited by 130

Loss of Tolerance and Autoimmunity Affecting Multiple Organs in STAT5A/5B -Deficient Mice

Snow, J. W., Abraham, N., Ma, M. C., HERNDIER, B. G., Pastuszak, A. W., & Goldsmith, M. A. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.10.5042 · Cited by 128

Regulatory T Cell Plasticity and Stability and Autoimmune Diseases

Qiu, R., Zhou, L., Ma, Y., Zhou, L., Liang, T., Shi, L., Long, J., & Yuan, D. (2018) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-018-8721-0 · Cited by 132

Neurocognitive effects of stress: a metaparadigm perspective

Kim, E. J., & Kim, J. J. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-01986-4 · Cited by 154

Constitutive OX40/OX40 Ligand Interaction Induces Autoimmune-Like Diseases

Murata, K., Nose, M., Ndhlovu, L. C., Sato, T., Sugamura, K., & Ishii, N. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.8.4628 · Cited by 125

Circulating proteasomes are markers of cell damage and immunologic activity in autoimmune diseases.

Egerer, K., Kuckelkorn, U., Rudolph, P. E., Rückert, J. C., Dörner, T., Burmester, G. R., Kloetzel, P. M., & Feist, E. (2002) · PubMed · Cited by 123

Epitope specificity and significance in systemic autoimmune diseases

Mähler, M., & Fritzler, M. J. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05127.x · Cited by 121

Genetics of rheumatoid arthritis: Underlying evidence of ethnic differences

Kochi, Y., Suzuki, A., Yamada, R., & Yamamoto, K. (2009) · Journal of Autoimmunity · doi:10.1016/j.jaut.2009.02.020 · Cited by 121

Autoimmunity gene expression portrait: specific signature that intersects or differentiates between multiple sclerosis and systemic lupus erythematosus

Mandel, M., Gurevich, M., Pauzner, R., Kaminski, N., & Achiron, A. (2004) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2004.02587.x · Cited by 117

Micronutrients in autoimmune diseases: possible therapeutic benefits of zinc and vitamin D

Weßels, I., & Rink, L. (2019) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2019.108240 · Cited by 123

Type 1 Diabetes and Autoimmune Thyroid Disease—The Genetic Link

Frommer, L., & Kahaly, G. J. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.618213 · Cited by 119

Bacterial Infections Promote T Cell Recognition of Self-Glycolipids

Libero, G. D., Moran, A. P., Gober, H.-J., Rossy, E., Shamshiev, A. T., Chelnokova, O., Mazorra, Z., Vendetti, S., Sacchi, A., Prendergast, M. M., et al. (2005) · Immunity · doi:10.1016/j.immuni.2005.04.013 · Cited by 115

The R620W Polymorphism of the Protein Tyrosine Phosphatase PTPN22 Is Not Associated with Multiple Sclerosis

Begovich, A. B., Caillier, S. J., Alexander, H. C., Penko, J. M., Hauser, S. L., Barcellos, L. F., & Oksenberg, J. R. (2004) · The American Journal of Human Genetics · doi:10.1086/427244 · Cited by 114

Molecular mimicry of mitochondrial and nuclear autoantigens in primary biliary cirrhosis

Shimoda, S., Nakamura, M., Ishibashi, H., Kawano, A., Kamihira, T., Sakamoto, N., Matsushita, S., Tanaka, A., Worman, H. J., Gershwin, M. E., et al. (2003) · Gastroenterology · doi:10.1016/s0016-5085(03)00387-1 · Cited by 113

Viral fusogenic membrane glycoproteins kill solid tumor cells by nonapoptotic mechanisms that promote cross presentation of tumor antigens by dendritic cells.

Bateman, A. R., Harrington, K. J., Kottke, T., Ahmed, A. U., Melcher, A. A., Gough, M. J., Linardakis, E., Riddle, D. S., Dietz, A. B., Lohse, C. M., et al. (2002) · PubMed · Cited by 109

Clonal tracking of autoaggressive T cells in polymyositis by combining laser microdissection, single-cell PCR, and CDR3-spectratype analysis

Hofbauer, M., Wiesener, S. C., Babbe, H., Roers, A., Wekerle, H., Dornmair, K., Hohlfeld, R., & Goebels, N. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0236183100 · Cited by 110

Guillain-Barré syndrome and anti-ganglioside antibodies: A clinician-scientist’s journey

YUKI, N. (2012) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.88.299 · Cited by 109

PTPN22: Its role in SLE and autoimmunity

Chung, S. A., & Criswell, L. A. (2007) · Autoimmunity · doi:10.1080/08916930701510848 · Cited by 112

The autoimmune origin of atherosclerosis

Blasi, C. (2008) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2008.05.025 · Cited by 109

Addressing Parents’ Concerns: Do Vaccines Cause Allergic or Autoimmune Diseases?

Offit, P. A., & Hackett, C. J. (2003) · PEDIATRICS · doi:10.1542/peds.111.3.653 · Cited by 107

Macroprolactinemia: Diagnostic, Clinical, and Pathogenic Significance

Shimatsu, A., & Hattori, N. (2012) · Clinical and Developmental Immunology · doi:10.1155/2012/167132 · Cited by 108

MHC class II super-enhancer increases surface expression of HLA-DR and HLA-DQ and affects cytokine production in autoimmune vitiligo

Cavalli, G., Hayashi, M., Jin, Y., Yorgov, D., Santorico, S. A., Holcomb, C. L., Rastrou, M. V., Erlich, H., Tengesdal, I. W., Dagna, L., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1523482113 · Cited by 105

Apoptosis in response to microbial infection induces autoreactive TH17 cells

Campisi, L., Barbet, G., Ding, Y., Esplugues, E., Flavell, R. A., & Blander, J. M. (2016) · Nature Immunology · doi:10.1038/ni.3512 · Cited by 105

Genome‐wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility

Julià, A., Ballina, J., Cañete, J. D., Balsa, A., Tornero‐Molina, J., Naranjo, A., Alperi‐López, M., Erra, A., Pascual‐Salcedo, D., Barceló, P., et al. (2008) · Arthritis & Rheumatism · doi:10.1002/art.23623 · Cited by 104

The Devil in the Details: The Emerging Role of Anticitrulline Autoimmunity in Rheumatoid Arthritis

van Gaalen, F. A., Ioan‐Facsinay, A., Huizinga, T. W. J., & Toes, R. E. M. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.9.5575 · Cited by 104

The Use of Human Mesenchymal Stem Cells as Therapeutic Agents for the in vivo Treatment of Immune-Related Diseases: A Systematic Review

Leyendecker, A., Pinheiro, C. C. G., Amano, M. T., & Bueno, D. F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02056 · Cited by 106

Immunogenetic Risk and Protective Factors for the Idiopathic Inflammatory Myopathies

OʼHanlon, T. P., Carrick, D. M., Arnett, F. C., Reveille, J. D., Carrington, M. N., Gao, X., Oddis, C. V., Morel, P. A., Malley, J. D., Malley, K. G., et al. (2005) · Medicine · doi:10.1097/01.md.0000189818.63141.8c · Cited by 102

Development of Autoimmunity in IL-14α-Transgenic Mice

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FCRL3, an Autoimmune Susceptibility Gene, Has Inhibitory Potential on B-Cell Receptor-Mediated Signaling

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