Risk Alleles for Multiple Sclerosis Identified by a Genomewide Study

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A haplotype map of the human genome

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A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene

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A genome-wide association study identifies novel risk loci for type 2 diabetes

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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

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Revised diagnostic criteria for neuromyelitis optica

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Multiple sclerosis

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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

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Multiple sclerosis

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Multiple Sclerosis: An Immune or Neurodegenerative Disorder?

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Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

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PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations

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Human genetic variation and its contribution to complex traits

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Autoimmune T cell responses in the central nervous system

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SNP Genotyping Using the Sequenom MassARRAY iPLEX Platform

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How to Interpret a Genome-wide Association Study

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The genetics and immunopathogenesis of inflammatory bowel disease

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A copy number variation map of the human genome

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A HapMap harvest of insights into the genetics of common disease

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Multiple Sclerosis: Mechanisms and Immunotherapy

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Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

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Dysregulated Epstein-Barr virus infection in the multiple sclerosis brain

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An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

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Revisiting IL-2: Biology and therapeutic prospects

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New IBD genetics: common pathways with other diseases

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Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

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Environmental factors and multiple sclerosis

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Mechanisms of neurodegeneration and axonal dysfunction in multiple sclerosis

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Vitamin D and multiple sclerosis

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Opposing regulation of the locus encoding IL-17 through direct, reciprocal actions of STAT3 and STAT5

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Deconstructing the Peptide-MHC Specificity of T Cell Recognition

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Detecting shared pathogenesis from the shared genetics of immune-related diseases

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Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

The Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene) (2009) · Nature Genetics · doi:10.1038/ng.396 · Cited by 550

Multiple sclerosis: risk factors, prodromes, and potential causal pathways

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Glial influence on the blood brain barrier

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Sex and gender issues in multiple sclerosis

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Expression of the Multiple Sclerosis-Associated MHC Class II Allele HLA-DRB1*1501 Is Regulated by Vitamin D

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The epidemiology of multiple sclerosis

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Genetics of type 1A diabetes

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Multiple sclerosis

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Antiviral immune responses: triggers of or triggered by autoimmunity?

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Epidemiology of multiple sclerosis

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Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis

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Epstein–Barr virus and multiple sclerosis

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Identification of Therapeutic Targets for Quiescent, Chemotherapy-Resistant Human Leukemia Stem Cells

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Long non-coding RNAs in nervous system function and disease

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Recent Insights Into the Genetics of Inflammatory Bowel Disease

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Class II HLA interactions modulate genetic risk for multiple sclerosis

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Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo

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Oncogenic IL7R gain-of-function mutations in childhood T-cell acute lymphoblastic leukemia

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Multiple sclerosis genetics

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Pathway and network-based analysis of genome-wide association studies in multiple sclerosis

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Frontotemporal dementia and its subtypes: a genome-wide association study

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Rheumatoid arthritis association at 6q23

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Cytokine and cytokine receptor gene polymorphisms and their functionality

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Analysis of CD161 expression on human CD8 + T cells defines a distinct functional subset with tissue-homing properties

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Genomics and the Multifactorial Nature of Human Autoimmune Disease

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Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci

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The genetics of multiple sclerosis: SNPs to pathways to pathogenesis

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An update on immunopathogenesis, diagnosis, and treatment of multiple sclerosis

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The challenge of multiple sclerosis: How do we cure a chronic heterogeneous disease?

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Potassium Channel KIR4.1 as an Immune Target in Multiple Sclerosis

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Recent Advances in the Genetics of Autoimmune Disease

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Multiple sclerosis—a quiet revolution

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Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record

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Myelin Regeneration: A Recapitulation of Development?

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Autoimmune diseases: insights from genome-wide association studies

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Fine-Mapping the Genetic Association of the Major Histocompatibility Complex in Multiple Sclerosis: HLA and Non-HLA Effects

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Daclizumab in active relapsing multiple sclerosis (CHOICE study): a phase 2, randomised, double-blind, placebo-controlled, add-on trial with interferon beta

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Incidence of multiple sclerosis in multiple racial and ethnic groups

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Functional inflammatory profiles distinguish myelin-reactive T cells from patients with multiple sclerosis

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CD4+FOXP3+ T Regulatory Cells in Human Autoimmunity: More Than a Numbers Game

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Epigenetic principles and mechanisms underlying nervous system functions in health and disease

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The genetics of multiple sclerosis: an up‐to‐date review

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Epigenome-wide differences in pathology-free regions of multiple sclerosis–affected brains

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Unravelling the human genome–phenome relationship using phenome-wide association studies

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Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource

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Tissue-Specific Genetic Control of Splicing: Implications for the Study of Complex Traits

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Analysis of 17 autoimmune disease-associated variants in type 1 diabetes identifies 6q23/TNFAIP3 as a susceptibility locus

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NKT Cell-Dependent Amelioration of a Mouse Model of Multiple Sclerosis by Altering Gut Flora

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Interleukin‐2 in the development and control of inflammatory disease

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Natural Naive CD4+CD25+CD127low Regulatory T Cell (Treg) Development and Function Are Disturbed in Multiple Sclerosis Patients: Recovery of Memory Treg Homeostasis during Disease Progression

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Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer Disease

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Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

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A shift from adaptive to innate immunity: a potential mechanism of disease progression in multiple sclerosis

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The cytokine milieu in the interplay of pathogenic Th1/Th17 cells and regulatory T cells in autoimmune disease

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The IL-2 – IL-2 receptor pathway in health and disease: The role of the soluble IL-2 receptor

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The Generation R Study Biobank: a resource for epidemiological studies in children and their parents

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Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene

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IL2RA Genetic Heterogeneity in Multiple Sclerosis and Type 1 Diabetes Susceptibility and Soluble Interleukin-2 Receptor Production

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Is multiple sclerosis a mitochondrial disease?

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