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PLoS Genetics, ISSN 1553-7390, 08/2011, Volume 7, Issue 8, pp. e1002216 - e1002216
Journal Article
PLoS Genetics, ISSN 1553-7390, 02/2013, Volume 9, Issue 2, pp. e1003222 - e1003222
Journal Article
Diabetologia, ISSN 0012-186X, 7/2013, Volume 56, Issue 7, pp. 1615 - 1622
Islet autoantibody-positive children progress to type 1 diabetes at variable rates. In our study, we asked whether characteristic autoantibody and/or gene... 
Progression | Islet autoantibody | Medicine & Public Health | Human Physiology | Type 1 diabetes | Metabolic Diseases | Internal Medicine | Susceptibility genes | T-CELL FUNCTION | DIAGNOSIS | IA-2 AUTOANTIBODIES | APPEARANCE | RISK | ANTIBODY STANDARDIZATION PROGRAM | PREDICTION | INSULIN | AUTOIMMUNITY | ENDOCRINOLOGY & METABOLISM | GENOME-WIDE ASSOCIATION | Zinc Transporter 8 | Humans | Insulin - immunology | Child, Preschool | Infant | Male | Lectins, C-Type - genetics | Interferon-Induced Helicase, IFIH1 | Interleukin-18 Receptor beta Subunit - genetics | Interleukin-2 Receptor alpha Subunit - genetics | Female | Diabetes Mellitus, Type 1 - immunology | Child | Microfilament Proteins - genetics | Infant, Newborn | Monosaccharide Transport Proteins - genetics | Genetic Predisposition to Disease - genetics | Receptor-Like Protein Tyrosine Phosphatases, Class 8 - immunology | Protein Tyrosine Phosphatase, Non-Receptor Type 22 - genetics | Diabetes Mellitus, Type 1 - pathology | CTLA-4 Antigen - genetics | Genotype | Protein Tyrosine Phosphatase, Non-Receptor Type 2 - genetics | Receptor, ErbB-3 - genetics | Proteins - genetics | DEAD-box RNA Helicases - genetics | Autoantibodies - immunology | HLA-DQ Antigens - genetics | Interleukin-10 - genetics | Adolescent | Polymorphism, Single Nucleotide - genetics | Cation Transport Proteins - immunology | Autoimmunity | Development and progression | Autoantibodies | Children | Genes | Index Medicus
Journal Article
PLoS Genetics, ISSN 1553-7390, 03/2011, Volume 7, Issue 3, pp. e1001323 - e1001323
Journal Article
Blood, ISSN 0006-4971, 09/2007, Volume 110, Issue 5, pp. 1516 - 1518
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 08/2016, Volume 99, Issue 2, pp. 366 - 374
Journal Article
American Journal of Transplantation, ISSN 1600-6135, 03/2013, Volume 13, Issue 3, pp. 663 - 675
Atypical hemolytic and uremic syndrome (aHUS) is a severe disease strongly associated with genetic abnormalities in the complement alternative pathway. In... 
Acute rejection | endothelial cell damage | mutations and polymorphisms in complement alternative pathway | thrombotic microangiopathy | atypical hemolytic and uremic syndrome | renal transplantation | SURGERY | FACTOR-B | HUS | FACTOR-I | FACTOR-H-AUTOANTIBODIES | TRANSPLANTATION | KIDNEY-TRANSPLANTATION | MUTATIONS | CD46 | PREDISPOSE | MEMBRANE COFACTOR PROTEIN | Recurrence | Genetic Testing | Prognosis | Humans | Middle Aged | Male | Young Adult | Hemolytic-Uremic Syndrome - genetics | Complement Factor B - genetics | Adult | Complement System Proteins - genetics | Female | Hemolytic-Uremic Syndrome - therapy | Retrospective Studies | Complement C3 - genetics | Biomarkers - metabolism | Risk Factors | Biomarkers - analysis | Kidney Transplantation | Mutation - genetics | Fibrinogen - genetics | Graft Survival - genetics | Adolescent | Membrane Cofactor Protein - genetics | Aged | Complement Factor H - genetics | Graft Rejection - genetics | Atypical Hemolytic Uremic Syndrome | Medical research | Kidneys | Genes | Organ transplant recipients | Medicine, Experimental | Genetic research | Transplantation | Clinical trials | Mutation | Transplants & implants | Drug therapy | Index Medicus | Biological Markers | Complement C3 | Life Sciences | Immunology | Fibrinogen | Hemolytic-Uremic Syndrome | Antigens, CD46 | Graft Survival | Complement Factor H | Complement System Proteins | Complement Factor B | Graft Rejection
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2013, Volume 8, Issue 4, pp. e61045 - e61045
Introduction: Rheumatoid arthritis (RA) is a systemic, chronic inflammatory disease influenced by both genetic and environmental factors, leading to joint... 
MODIFYING ANTIRHEUMATIC DRUGS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | EARLY RHEUMATOID-ARTHRITIS | CYCLIC CITRULLINATED PEPTIDE | FUNCTIONAL HAPLOTYPE | PROGNOSTIC-FACTORS | JAPANESE POPULATION | JOINT DAMAGE | MULTIDISCIPLINARY SCIENCES | SHARED EPITOPE | DISEASE-ACTIVITY | Genetic Predisposition to Disease - genetics | Hydrolases - genetics | HLA-DRB1 Chains - genetics | Humans | Middle Aged | Genetic Loci - genetics | Male | Peptides, Cyclic - immunology | Disease Progression | Arthritis, Rheumatoid - pathology | Arthritis, Rheumatoid - diagnostic imaging | Arthritis, Rheumatoid - genetics | Arthrography | Antibodies - immunology | Female | Polymorphism, Single Nucleotide | Protein-Arginine Deiminases | Cohort Studies | Autoimmunity | Rheumatoid factor | Histocompatibility antigens | HLA histocompatibility antigens | Development and progression | Arthritis | Disease susceptibility | Risk factors | Genetic polymorphisms | Antigenic determinants | Haplotypes | Multiple regression analysis | Destruction | Genes | Medical records | Genomes | Gender | Arginine deiminase | Arginine | Protein-arginine deiminase | Drb1 protein | Population | Genetic factors | Age | Deoxyribonucleic acid--DNA | Autoantibodies | Rheumatology | Environmental factors | Regression analysis | Citrulline | Risk analysis | Patients | Loci | CCR6 protein | Meta-analysis | CD83 antigen | Rheumatoid arthritis | Alleles | Histocompatibility antigen HLA | Genetic testing | PTPN2 protein | Smoking | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2015, Volume 47, Issue 4, pp. 381 - 386
Journal Article