about
Genome-wide detection and characterization of positive selection in human populationsPleiotropy in complex traits: challenges and strategiesGenetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell linesNetwork Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of MutationGenetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosusCommon body mass index-associated variants confer risk of extreme obesity.Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.Pervasive sharing of genetic effects in autoimmune disease.Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology.MHC associations with clinical and autoantibody manifestations in European SLE.Fine mapping in 94 inbred mouse strains using a high-density haplotype resource.Immune-mediated disease genetics: the shared basis of pathogenesis.Heritability of the weight loss response to gastric bypass surgery.Genetic variants associated with autoimmunity drive NFκB signaling and responses to inflammatory stimuliUnraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in EuropeansGenetic dissection of gene regulation in multiple mouse tissues.Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity.Genetic analysis for a shared biological basis between migraine and coronary artery disease.Survey of variation in human transcription factors reveals prevalent DNA binding changes.Weight loss after gastric bypass is associated with a variant at 15q26.1.Class II HLA interactions modulate genetic risk for multiple sclerosis.Changes in T-cell subsets identify responders to FcR-nonbinding anti-CD3 mAb (teplizumab) in patients with type 1 diabetesProgress and challenges for treating Type 1 diabetes.Two independent alleles at 6q23 associated with risk of rheumatoid arthritisIntra- and inter-individual genetic differences in gene expressionIdentifying genetic components of drug response in mice.Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.Protein array-based profiling of CSF identifies RBPJ as an autoantigen in multiple sclerosis.Human genetics offers an emerging picture of common pathways and mechanisms in autoimmunity.Integrative Genetic and Epigenetic Analysis Uncovers Regulatory Mechanisms of Autoimmune Disease.Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation.Novel determinants of mammalian primary microRNA processing revealed by systematic evaluation of hairpin-containing transcripts and human genetic variation.Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types.Microbiota control immune regulation in humanized mice.Gene expression profiles in zebrafish (Danio rerio) liver cells exposed to a mixture of pharmaceuticals at environmentally relevant concentrations.Genome-wide association studies of multiple sclerosis.Analysis of shared heritability in common disorders of the brainThe Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibilityHierarchical Bayes variable selection and microarray experimentsNormalization procedures and detection of linkage signal in genetical-genomics experiments
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Chris Cotsapas
@ast
Chris Cotsapas
@en
Chris Cotsapas
@es
Chris Cotsapas
@nl
Chris Cotsapas
@sl
type
label
Chris Cotsapas
@ast
Chris Cotsapas
@en
Chris Cotsapas
@es
Chris Cotsapas
@nl
Chris Cotsapas
@sl
prefLabel
Chris Cotsapas
@ast
Chris Cotsapas
@en
Chris Cotsapas
@es
Chris Cotsapas
@nl
Chris Cotsapas
@sl
P106
P31
P496
0000-0002-7772-5910