List of works - Chris Cotsapas

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

scientific article published on 29 September 2013

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Analysis of shared heritability in common disorders of the brain

Changes in T-cell subsets identify responders to FcR-nonbinding anti-CD3 mAb (teplizumab) in patients with type 1 diabetes

scientific article published on 31 October 2015

Class II HLA interactions modulate genetic risk for multiple sclerosis

scientific article published on 07 September 2015

Common body mass index-associated variants confer risk of extreme obesity

scientific article

Common body mass index-associated variants confer risk of extreme obesity

Erratum: Genome-wide association studies of multiple sclerosis

scholarly article published in Clinical & translational immunology

Fine mapping in 94 inbred mouse strains using a high-density haplotype resource

scientific article

Gene expression profiles in zebrafish (Danio rerio) liver cells exposed to a mixture of pharmaceuticals at environmentally relevant concentrations.

scientific article published on 30 August 2007

Genetic Variation and the Control of Transcription

scientific article published on 01 January 2003

Genetic analysis for a shared biological basis between migraine and coronary artery disease

scientific article published on June 2015

Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines

scientific article

Genetic dissection of gene regulation in multiple mouse tissues.

scientific article published on 12 June 2006

Genetic variants associated with autoimmunity drive NFκB signaling and responses to inflammatory stimuli

scientific article

Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus

scientific journal article

Genome-wide association studies of multiple sclerosis.

scientific article

Genome-wide detection and characterization of positive selection in human populations

scientific article

Heritability of the weight loss response to gastric bypass surgery

scientific article

Hierarchical Bayes variable selection and microarray experiments

Human genetics offers an emerging picture of common pathways and mechanisms in autoimmunity

scientific article published on 05 October 2012

Identifying genetic components of drug response in mice

scientific article published on September 2008

Immune-mediated disease genetics: the shared basis of pathogenesis

scientific article

Integrative Genetic and Epigenetic Analysis Uncovers Regulatory Mechanisms of Autoimmune Disease

scientific article

Integrative genetic and epigenetic analysis uncovers regulatory mechanisms of autoimmune disease

Intra- and inter-individual genetic differences in gene expression

scientific article published on 08 May 2009

Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation

scientific article published on March 2017

Large-scale trans-eQTLs affect hundreds of transcripts and mediate patterns of transcriptional co-regulation

Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types.

scientific article published on 20 February 2017

Low frequency and rare coding variation contributes to multiple sclerosis risk

MHC associations with clinical and autoantibody manifestations in European SLE.

scientific article

Microbiota control immune regulation in humanized mice

scientific article published on 2 November 2017

NR1H3 p.Arg415Gln is not associated to multiple sclerosis risk

Network Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of Mutation

scientific article

Network analysis of genome-wide selective constraint reveals a gene network active in early fetal brain intolerant of mutation

article

Normalization procedures and detection of linkage signal in genetical-genomics experiments

scientific article published on 01 August 2006

Novel determinants of mammalian primary microRNA processing revealed by systematic evaluation of hairpin-containing transcripts and human genetic variation

scientific article published on 13 January 2017

Pervasive sharing of genetic effects in autoimmune disease

scientific article

Pleiotropy in complex traits: challenges and strategies

scientific article

Progress and challenges for treating Type 1 diabetes

scientific article published on 17 May 2016

Protein array-based profiling of CSF identifies RBPJ as an autoantigen in multiple sclerosis

scientific article published on 06 August 2013

Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology

scientific article

Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity.

scientific article published on 16 February 2016

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

scientific article

Shared associations identify causal relationships between gene expression and immune cell phenotypes

scientific article published on 04 March 2021

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.

scientific article published in May 2015

Survey of variation in human transcription factors reveals prevalent DNA binding changes

scientific article

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

scholarly article published 13 July 2017

Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

scientific article

Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans

scientific article

Weight loss after gastric bypass is associated with a variant at 15q26.1.

scientific article published on May 2013

List of works by Chris Cotsapas

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

Analysis of shared heritability in common disorders of the brain

Analysis of shared heritability in common disorders of the brain

Changes in T-cell subsets identify responders to FcR-nonbinding anti-CD3 mAb (teplizumab) in patients with type 1 diabetes

Class II HLA interactions modulate genetic risk for multiple sclerosis

Common body mass index-associated variants confer risk of extreme obesity

Common body mass index-associated variants confer risk of extreme obesity

Erratum: Genome-wide association studies of multiple sclerosis

Fine mapping in 94 inbred mouse strains using a high-density haplotype resource

Gene expression profiles in zebrafish (Danio rerio) liver cells exposed to a mixture of pharmaceuticals at environmentally relevant concentrations.

Genetic Variation and the Control of Transcription

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines

Genetic dissection of gene regulation in multiple mouse tissues.

Genetic variants associated with autoimmunity drive NFκB signaling and responses to inflammatory stimuli

Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus

Genome-wide association studies of multiple sclerosis.

Genome-wide detection and characterization of positive selection in human populations

Heritability of the weight loss response to gastric bypass surgery

Hierarchical Bayes variable selection and microarray experiments

Human genetics offers an emerging picture of common pathways and mechanisms in autoimmunity

Identifying genetic components of drug response in mice

Immune-mediated disease genetics: the shared basis of pathogenesis

Integrative Genetic and Epigenetic Analysis Uncovers Regulatory Mechanisms of Autoimmune Disease

Integrative genetic and epigenetic analysis uncovers regulatory mechanisms of autoimmune disease

Intra- and inter-individual genetic differences in gene expression

Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation

Large-scale trans-eQTLs affect hundreds of transcripts and mediate patterns of transcriptional co-regulation

Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types.

Low frequency and rare coding variation contributes to multiple sclerosis risk

MHC associations with clinical and autoantibody manifestations in European SLE.

Microbiota control immune regulation in humanized mice

NR1H3 p.Arg415Gln is not associated to multiple sclerosis risk

Network Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of Mutation

Network analysis of genome-wide selective constraint reveals a gene network active in early fetal brain intolerant of mutation

Normalization procedures and detection of linkage signal in genetical-genomics experiments

Novel determinants of mammalian primary microRNA processing revealed by systematic evaluation of hairpin-containing transcripts and human genetic variation

Pervasive sharing of genetic effects in autoimmune disease

Pleiotropy in complex traits: challenges and strategies

Progress and challenges for treating Type 1 diabetes

Protein array-based profiling of CSF identifies RBPJ as an autoantigen in multiple sclerosis

Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology

Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity.

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

Shared associations identify causal relationships between gene expression and immune cell phenotypes

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.

Survey of variation in human transcription factors reveals prevalent DNA binding changes

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans

Weight loss after gastric bypass is associated with a variant at 15q26.1.