Lista de obras -

A novel autoantibody to a 155-kd protein is associated with dermatomyositis

artículo científico publicado en 2006

Brief Report: Association of Myositis Autoantibodies, Clinical Features, and Environmental Exposures at Illness Onset With Disease Course in Juvenile Myositis

artículo científico publicado en 2015

Changes in the pattern of DNA methylation associate with twin discordance in systemic lupus erythematosus

artículo científico publicado en 2009

Clinical, serologic, and immunogenetic features of familial idiopathic inflammatory myopathy

artículo científico publicado en 1998

Cytokine gene polymorphisms as risk and severity factors for juvenile dermatomyositis

artículo científico publicado en 2008

Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups

artículo científico publicado en 2015

Differences in idiopathic inflammatory myopathy phenotypes and genotypes between Mesoamerican Mestizos and North American Caucasians: ethnogeographic influences in the genetics and clinical expression of myositis

artículo científico publicado en 2002

Expression of interferon-regulated genes in juvenile dermatomyositis versus Mendelian autoinflammatory interferonopathies

scientific article published on 06 April 2020

Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups

scientific article published on 28 May 2019

Gene Expression Profiles from Disease Discordant Twins Suggest Shared Antiviral Pathways and Viral Exposures among Multiple Systemic Autoimmune Diseases

artículo científico publicado en 2015

Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis

artículo científico publicado en 2015

Gene expression profiles from discordant monozygotic twins suggest that molecular pathways are shared among multiple systemic autoimmune diseases

artículo científico publicado en 2011

Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders

artículo científico publicado en 2013

HLA polymorphisms in African Americans with idiopathic inflammatory myopathy: allelic profiles distinguish patients with different clinical phenotypes and myositis autoantibodies

artículo científico publicado en 2006

Immunogenetic risk and protective factors for juvenile dermatomyositis in Caucasians.

artículo científico publicado en 2006

Immunoglobulin gene polymorphisms are susceptibility factors in clinical and autoantibody subgroups of the idiopathic inflammatory myopathies.

artículo científico publicado en 2008

Plasma proteomic profiles from disease-discordant monozygotic twins suggest that molecular pathways are shared in multiple systemic autoimmune diseases.

artículo científico publicado en 2011

Post-zygotic and inter-individual structural genetic variation in a presumptive enhancer element of the locus between the IL10Rβ and IFNAR1 genes

artículo científico publicado en 2013

Twins discordant for myositis and systemic lupus erythematosus show markedly enriched autoantibodies in the affected twin supporting environmental influences in pathogenesis.

artículo científico publicado en 2014

Lista de obras de

A novel autoantibody to a 155-kd protein is associated with dermatomyositis

Brief Report: Association of Myositis Autoantibodies, Clinical Features, and Environmental Exposures at Illness Onset With Disease Course in Juvenile Myositis

Changes in the pattern of DNA methylation associate with twin discordance in systemic lupus erythematosus

Clinical, serologic, and immunogenetic features of familial idiopathic inflammatory myopathy

Cytokine gene polymorphisms as risk and severity factors for juvenile dermatomyositis

Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups

Differences in idiopathic inflammatory myopathy phenotypes and genotypes between Mesoamerican Mestizos and North American Caucasians: ethnogeographic influences in the genetics and clinical expression of myositis

Expression of interferon-regulated genes in juvenile dermatomyositis versus Mendelian autoinflammatory interferonopathies

Focused HLA analysis in Caucasians with myositis identifies significant associations with autoantibody subgroups

Gene Expression Profiles from Disease Discordant Twins Suggest Shared Antiviral Pathways and Viral Exposures among Multiple Systemic Autoimmune Diseases

Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis

Gene expression profiles from discordant monozygotic twins suggest that molecular pathways are shared among multiple systemic autoimmune diseases

Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders

HLA polymorphisms in African Americans with idiopathic inflammatory myopathy: allelic profiles distinguish patients with different clinical phenotypes and myositis autoantibodies

Immunogenetic risk and protective factors for juvenile dermatomyositis in Caucasians.

Immunoglobulin gene polymorphisms are susceptibility factors in clinical and autoantibody subgroups of the idiopathic inflammatory myopathies.

Plasma proteomic profiles from disease-discordant monozygotic twins suggest that molecular pathways are shared in multiple systemic autoimmune diseases.

Post-zygotic and inter-individual structural genetic variation in a presumptive enhancer element of the locus between the IL10Rβ and IFNAR1 genes

Twins discordant for myositis and systemic lupus erythematosus show markedly enriched autoantibodies in the affected twin supporting environmental influences in pathogenesis.