Chris Cotsapas
educated at: University of New South Wales, Imperial College London
occupation: researcher
Articles 51
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Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
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Shared associations identify causal relationships between gene expression and immune cell phenotypes
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Genome-wide association studies of multiple sclerosis.
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Analysis of shared heritability in common disorders of the brain
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Erratum: Genome-wide association studies of multiple sclerosis
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Low frequency and rare coding variation contributes to multiple sclerosis risk
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Integrative Genetic and Epigenetic Analysis Uncovers Regulatory Mechanisms of Autoimmune Disease
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Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation
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Novel determinants of mammalian primary microRNA processing revealed by systematic evaluation of hairpin-containing transcripts and human genetic variation
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Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types.
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Microbiota control immune regulation in humanized mice.
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The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility
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Network Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of Mutation
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Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity.
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Survey of variation in human transcription factors reveals prevalent DNA binding changes
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Progress and challenges for treating Type 1 diabetes
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Analysis of shared heritability in common disorders of the brain
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NR1H3 p.Arg415Gln is not associated to multiple sclerosis risk
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Large-scale trans-eQTLs affect hundreds of transcripts and mediate patterns of transcriptional co-regulation
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Integrative genetic and epigenetic analysis uncovers regulatory mechanisms of autoimmune disease
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Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.
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Genetic variants associated with autoimmunity drive NFκB signaling and responses to inflammatory stimuli
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Genetic analysis for a shared biological basis between migraine and coronary artery disease
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Class II HLA interactions modulate genetic risk for multiple sclerosis
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Changes in T-cell subsets identify responders to FcR-nonbinding anti-CD3 mAb (teplizumab) in patients with type 1 diabetes
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Network analysis of genome-wide selective constraint reveals a gene network active in early fetal brain intolerant of mutation
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MHC associations with clinical and autoantibody manifestations in European SLE.
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Pleiotropy in complex traits: challenges and strategies
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Weight loss after gastric bypass is associated with a variant at 15q26.1.
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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
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Protein array-based profiling of CSF identifies RBPJ as an autoantigen in multiple sclerosis
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Immune-mediated disease genetics: the shared basis of pathogenesis
Human - wd:Q42293286