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Principal components analysis corrects for stratification in genome-wide association studies

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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A comprehensive review of genetic association studies

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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

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A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

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A genome-wide search for human type 1 diabetes susceptibility genes

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Genetically Dependent ERBB3 Expression Modulates Antigen Presenting Cell Function and Type 1 Diabetes Risk

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Update in Endocrine Autoimmunity

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Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations

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The ubiquitin ligase adaptor Ndfip1 regulates T cell-mediated gastrointestinal inflammation and inflammatory bowel disease susceptibility

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Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals

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Mitochondrial network regulation and its potential interference with inflammatory signals in pancreatic beta cells

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Restoring Regulatory T Cells in Type 1 Diabetes

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Insulin Transactivator MafA Regulates Intrathymic Expression of Insulin and Affects Susceptibility to Type 1 Diabetes

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Mapping the prescriptiome to fractures in men—a national analysis of prescription history and fracture risk

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Physical Activity Benefits the Skeleton of Children Genetically Predisposed to Lower Bone Density in Adulthood

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Integrative analyses of TEDDY Omics data reveal lipid metabolism abnormalities, increased intracellular ROS and heightened inflammation prior to autoimmunity for type 1 diabetes

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Quantitative Differences in the Urinary Proteome of Siblings Discordant for Type 1 Diabetes Include Lysosomal Enzymes

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The type I diabetes association of the IL2RA locus

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Detecting Local Haplotype Sharing and Haplotype Association

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Prediction of gene expression with cis-SNPs using mixed models and regularization methods

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Genetic Risk Scores Implicated in Adult Bone Fragility Associate With Pediatric Bone Density

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Disease-specific biases in alternative splicing and tissue-specific dysregulation revealed by multitissue profiling of lymphocyte gene expression in type 1 diabetesPreprint

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Genome‐wide association studies (GWAS): impact on elucidating the aetiology of diabetes

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Molecular Mechanisms of Eosinophilic Esophagitis

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Human CLEC16A regulates autophagy through modulating mTOR activity

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Effect of experimental diabetes on craniofacial growth in rats

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Change you can B(cell)eive in: recent progress confirms a critical role for B cells in type 1 diabetes

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Altered Immune Regulation in Type 1 Diabetes

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Clec16a is Critical for Autolysosome Function and Purkinje Cell Survival

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Identifying shared genetic loci and common risk genes of rheumatoid arthritis associated with three autoimmune diseases based on large-scale cross-trait genome-wide association studies

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Genetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritis

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The search for the genetic contribution to autoimmune thyroid disease: the never ending story?

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Type 1 diabetes as an autoimmune disease: the evidence

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Genome-wide association studies in type 1 diabetes

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A neurologist’s guide to genome-wide association studies

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Genetic Association between the Interleukin-2 Receptor-α Gene and Mode of Onset of Type 1 Diabetes in the Japanese Population

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PTPN22 Gene Polymorphism (C1858T) Is Associated with Susceptibility to Type 1 Diabetes: A Meta‐Analysis of 19,495 Cases and 25,341 Controls

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PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

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Single-nucleotide polymorphisms in the IL2RA gene are associated with age at diagnosis in late-onset Finnish type 1 diabetes subjects

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Endocrine autoimmune disease: genetics become complex

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CLEC16A—An Emerging Master Regulator of Autoimmunity and Neurodegeneration

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More CLEC16A gene variants associated with multiple sclerosis

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SNP-specific extraction of haplotype-resolved targeted genomic regions

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Functional SOCS1 polymorphisms are associated with variation in obesity in whites

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Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes

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Understanding the genetic and epigenetic basis of common variable immunodeficiency disorder through omics approaches

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Making Insulin and Staying Out of Autoimmune Trouble: The Beta-Cell Conundrum

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Progress in Understanding Type 1 Diabetes Through Its Genetic Overlap with Other Autoimmune Diseases

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Genetic polymorphisms in susceptibility to Type 1 Diabetes

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Balancing selection is common in the extended MHC region but most alleles with opposite risk profile for autoimmune diseases are neutrally evolving

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Trying to understand the genetics of atopic dermatitis

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ThePCDH1gene and asthma in early childhood

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Evaluating cost efficiency of SNP chips in genome‐wide association studies

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Intron 4 a/b polymorphism of the endothelial nitric oxide synthase gene is associated with both type 1 and type 2 diabetes in a genetically homogeneous population

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The role of non-HLA single nucleotide polymorphisms in multiple sclerosis susceptibility

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Pre-diagnostic genotyping identifies T1D subjects with impaired Treg IL-2 signaling and an elevated proportion of FOXP3+IL-17+ cells

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The β-Cell Genomic Landscape in T1D: Implications for Disease Pathogenesis

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Genetic overlap between type 1 diabetes and other autoimmune diseases

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Protective role of the HLA–A*02 allele in Portuguese patients with multiple sclerosis

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Genetics of Type 1 Diabetes and Autoimmune Thyroid Disease

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BMD‐Associated Variation at the Osterix Locus Is Correlated With Childhood Obesity in Females

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A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci among Red Blood Cell Transfusion Recipients with Sickle Cell Disease

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Accurate measurement of gene copy number for human alpha-defensin DEFA1A3

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Genomics in cardiac metabolism

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Integrative genomics analysis of various omics data and networks identify risk genes and variants vulnerable to childhood-onset asthma

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Genetic determinants of diabetes are similarly associated with other immune-mediated diseases

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Evidence for two independent associations with type 1 diabetes at the 12q13 locus

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Popper revisited: GWAS here, last year

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Principal Component Analysis Characterizes Shared Pathogenetics from Genome-Wide Association Studies

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Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia

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Phenome-Wide Association Study to Explore Relationships between Immune System Related Genetic Loci and Complex Traits and Diseases

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Genome-wide association studies in type 1 diabetes, inflammatory bowel disease and other immune-mediated disorders

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Mass spectrometry is only one piece of the puzzle in clinical proteomics

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Predicting Type 1 Diabetes Candidate Genes using Human Protein-Protein Interaction Networks

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The Osteopontin Gene +1239A/C Single Nucleotide Polymorphism is Associated with Type 1 Diabetes Mellitus in the Italian Population

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Polymorphisms in the Inflammatory Genes CIITA, CLEC16A and IFNG Influence BMD, Bone Loss and Fracture in Elderly Women

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Involvement of CLEC16A in Activation of Astrocytes After LPS Treated

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Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes

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Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population: Table 1

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CLEC16A regulates splenocyte and NK cell function in part through MEK signaling

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Modeling dynamic changes in type 1 diabetes progression: Quantifying $\beta$-cell variation after the appearance of islet-specific autoimmune responses

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Fine Mapping and Functional Studies of Risk Variants for Type 1 Diabetes at Chromosome 16p13.13

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Intron polymorphism in the KIAA0350 gene is reproducibly associated with susceptibility to type 1 diabetes (T1D) in the Han Chinese population

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Use of Induced Pluripotent Stem Cells to Build Isogenic Systems and Investigate Type 1 Diabetes

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Joint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power

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Identifying causal variants at loci with multiple signals of association

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GOP-1 promotes apoptotic cell degradation by activating the small GTPase Rab2 in C. elegans

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Functional evaluation of the role of C-type lectin domain family 16A at the chromosome 16p13 locus

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The missing heritability in type 1 diabetes

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The Rise and Fall of the Common Disease–Common Variant (CD–CV) Hypothesis: How the Sickle Cell Disease Paradigm Led Us All Astray (Or Did It?)

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Intron polymorphism in the KIAA0350 gene is reproducibly associated with susceptibility to type 1 diabetes (T1D) in the Han Chinese population

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Genome-wide association studies in type 1 diabetes

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A Human Type 1 Diabetes Susceptibility Locus Maps to Chromosome 21q22.3

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