Lista de obras - Oliver Burren - Dominio Público Uruguay

A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region

artículo científico publicado en 2006

A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples

artículo científico publicado en 2014

A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations

artículo científico publicado en 2014

A rareIL2RAhaplotype identifies SNP rs61839660 as causal for autoimmunity

A type I interferon transcriptional signature precedes autoimmunity in children genetically at risk for type 1 diabetes.

artículo científico publicado en 2014

Approaches and advances in the genetic causes of autoimmune disease and their implications

artículo científico publicado en 2018

CHiCP: a web-based tool for the integrative and interactive visualization of promoter capture Hi-C datasets.

artículo científico publicado en 2016

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

artículo científico publicado en 2009

Chromosome contacts in activated T cells identify autoimmune disease candidate genes

artículo científico publicado en 2017

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

artículo científico publicado en 2014

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

artículo científico publicado en 2004

Discovery, linkage disequilibrium and association analyses of polymorphisms of the immune complement inhibitor, decay-accelerating factor gene (DAF/CD55) in type 1 diabetes

artículo científico publicado en 2006

Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping

artículo científico publicado en 2015

Epigenetic analysis of regulatory T cells using multiplex bisulfite sequencing.

artículo científico publicado en 2015

Erratum: Corrigendum: Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls

artículo científico publicado en 2015

Evidence that Cd101 is an autoimmune diabetes gene in nonobese diabetic mice

scientific journal article

Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers

artículo científico publicado en 2015

Gene-gene interactions in the NOD mouse model of type 1 diabetes.

scientific article published on January 2008

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

artículo científico publicado en 2010

Inherited variation in vitamin D genes is associated with predisposition to autoimmune disease type 1 diabetes

artículo científico publicado en 2011

Integration of disease association and eQTL data using a Bayesian colocalisation approach highlights six candidate causal genes in immune-mediated diseases

artículo científico publicado en 2015

Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters

artículo científico publicado en 2016

Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene

artículo científico publicado en 2011

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

artículo científico publicado en 2013

No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes

artículo científico publicado en 2005

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

artículo científico publicado en 2007

Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.

artículo científico publicado en 2007

Seven newly identified loci for autoimmune thyroid disease

artículo científico publicado en 2012

Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls

artículo científico publicado en 2015

T1DBase, a community web-based resource for type 1 diabetes research

artículo científico publicado en 2005

T1DBase: integration and presentation of complex data for type 1 diabetes research

artículo científico publicado en 2006

T1DBase: update 2011, organization and presentation of large-scale data sets for type 1 diabetes research

artículo científico publicado en 2010

Testing the possible negative association of type 1 diabetes and atopic disease by analysis of the interleukin 4 receptor gene.

artículo científico publicado en 2003

The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants

VSEAMS: a pipeline for variant set enrichment analysis using summary GWAS data identifies IKZF3, BATF and ESRRA as key transcription factors in type 1 diabetes ⬇️

artículo científico publicado en 2014

Widespread seasonal gene expression reveals annual differences in human immunity and physiology

artículo científico publicado en 2015

Lista de obras de Oliver Burren

A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region

A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples

A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations

A rareIL2RAhaplotype identifies SNP rs61839660 as causal for autoimmunity

A type I interferon transcriptional signature precedes autoimmunity in children genetically at risk for type 1 diabetes.

Approaches and advances in the genetic causes of autoimmune disease and their implications

CHiCP: a web-based tool for the integrative and interactive visualization of promoter capture Hi-C datasets.

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

Chromosome contacts in activated T cells identify autoimmune disease candidate genes

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

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

Discovery, linkage disequilibrium and association analyses of polymorphisms of the immune complement inhibitor, decay-accelerating factor gene (DAF/CD55) in type 1 diabetes

Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping

Epigenetic analysis of regulatory T cells using multiplex bisulfite sequencing.

Erratum: Corrigendum: Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls

Evidence that Cd101 is an autoimmune diabetes gene in nonobese diabetic mice

Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers

Gene-gene interactions in the NOD mouse model of type 1 diabetes.

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Inherited variation in vitamin D genes is associated with predisposition to autoimmune disease type 1 diabetes

Integration of disease association and eQTL data using a Bayesian colocalisation approach highlights six candidate causal genes in immune-mediated diseases

Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters

Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes

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

Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.

Seven newly identified loci for autoimmune thyroid disease

Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls

T1DBase, a community web-based resource for type 1 diabetes research

T1DBase: integration and presentation of complex data for type 1 diabetes research

T1DBase: update 2011, organization and presentation of large-scale data sets for type 1 diabetes research

Testing the possible negative association of type 1 diabetes and atopic disease by analysis of the interleukin 4 receptor gene.

The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants

VSEAMS: a pipeline for variant set enrichment analysis using summary GWAS data identifies IKZF3, BATF and ESRRA as key transcription factors in type 1 diabetes ⬇️

Widespread seasonal gene expression reveals annual differences in human immunity and physiology