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Using the tools of proteomics to understand the pathogenesis of idiopathic inflammatory myopathies

Current opinion in rheumatology, 2019-11, Vol.31 (6), p.617-622

2019

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Broadening our understanding of the genetics of Juvenile Idiopathic Arthritis (JIA): Interrogation of three dimensional chromatin structures and genetic regulatory elements within JIA-associated risk loci

PloS one, 2020-07, Vol.15 (7), p.e0235857-e0235857

2020

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Whole blood transcriptome biomarkers of unruptured intracranial aneurysm

PloS one, 2020-11, Vol.15 (11), p.e0241838-e0241838

2020

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Analysis of chromatin data supports a role for CD14+ monocytes/macrophages in mediating genetic risk for juvenile idiopathic arthritis

Frontiers in immunology, 2022-09, Vol.13, p.913555

2022

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A systematic strategy for identifying causal single nucleotide polymorphisms and their target genes on Juvenile arthritis risk haplotypes

BMC medical genomics, 2024-07, Vol.17 (1), p.185-14, Article 185

2024

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Circulating neutrophil transcriptome may reveal intracranial aneurysm signature

PloS one, 2018-01, Vol.13 (1), p.e0191407-e0191407

2018

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Using Chromatin Architecture to Understand the Genetics and Transcriptomics of Juvenile Idiopathic Arthritis

Frontiers in immunology, 2018-12, Vol.9, p.2964-2964

2018

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CD4+ T cells from children with active juvenile idiopathic arthritis show altered chromatin features associated with transcriptional abnormalities

Scientific reports, 2021-02, Vol.11 (1), p.4011-4011, Article 4011

2021

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Biomarkers from circulating neutrophil transcriptomes have potential to detect unruptured intracranial aneurysms

Journal of translational medicine, 2018-12, Vol.16 (1), p.373-373, Article 373

2018

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Genetic insights into juvenile idiopathic arthritis derived from deep whole genome sequencing

Scientific reports, 2017-06, Vol.7 (1), p.2657-10, Article 2657

2017

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Genomic characterization of remission in juvenile idiopathic arthritis

Arthritis research & therapy, 2013-08, Vol.15 (4), p.R100-R100, Article R100

2013

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Broadening our understanding of genetic risk for scleroderma/systemic sclerosis by querying the chromatin architecture surrounding the risk haplotypes

BMC medical genomics, 2021-04, Vol.14 (1), p.114-12, Article 114

2021

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Classification models using circulating neutrophil transcripts can detect unruptured intracranial aneurysm

Journal of translational medicine, 2020-10, Vol.18 (1), p.392-392, Article 392

2020

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The feasibility of developing biomarkers from peripheral blood mononuclear cell RNAseq data in children with juvenile idiopathic arthritis using machine learning approaches

Arthritis research & therapy, 2019-11, Vol.21 (1), p.230-10, Article 230

2019

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Mapping of Variable DNA Methylation Across Multiple Cell Types Defines a Dynamic Regulatory Landscape of the Human Genome

G3 : genes - genomes - genetics, 2016-04, Vol.6 (4), p.973-986

2016

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Epigenetic landscapes of intracranial aneurysm risk haplotypes implicate enhancer function of endothelial cells and fibroblasts in dysregulated gene expression

BMC medical genomics, 2021-06, Vol.14 (1), p.162-14, Article 162

2021

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Whole blood expression profiling from the TREAT trial: insights for the pathogenesis of polyarticular juvenile idiopathic arthritis

Arthritis research & therapy, 2016-07, Vol.18 (1), p.157-157, Article 157

2016

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Epigenetic landscapes suggest that genetic risk for intracranial aneurysm operates on the endothelium

BMC medical genomics, 2019-10, Vol.12 (1), p.149-149, Article 149

2019

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Plasma exosomes from children with juvenile dermatomyositis are taken up by human aortic endothelial cells and are associated with altered gene expression in those cells

Pediatric rheumatology online journal, 2019-07, Vol.17 (1), p.41-41, Article 41

2019

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Identification of Circulating Gene Expression Signatures of Intracranial Aneurysm in Peripheral Blood Mononuclear Cells

Diagnostics (Basel), 2021-06, Vol.11 (6), p.1092

2021

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Systemic lupus erythematosus in American Indian/Alaska natives: Incorporating our new understanding of the biology of trauma

Seminars in arthritis and rheumatism, 2023-12, Vol.63, p.152245-152245, Article 152245

2023

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Health inequities in the rheumatic diseases of childhood

Current opinion in rheumatology, 2022-09

2022

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“Racism as a public health issue” APS racism series: at the intersection of equity, science, and social justice

Pediatric research, 2020-11, Vol.88 (5), p.696-698

2020

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Facing the Truth and Moving Forward: The Complicity of Pediatricians with Racism in the United States

Academic pediatrics, 2024-09, Vol.24 (7), p.S204-S207

2024

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Reduced Nicotinamide Adenine Dinucleotide Phosphate Oxidase-Independent Resistance to Aspergillus fumigatus in Alveolar Macrophages

The Journal of immunology (1950), 2008-05, Vol.180 (10), p.6854-6867

2008

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Using the tools of proteomics to understand the pathogenesis of idiopathic inflammatory myopathies

Broadening our understanding of the genetics of Juvenile Idiopathic Arthritis (JIA): Interrogation of three dimensional chromatin structures and genetic regulatory elements within JIA-associated risk loci

Whole blood transcriptome biomarkers of unruptured intracranial aneurysm

Analysis of chromatin data supports a role for CD14+ monocytes/macrophages in mediating genetic risk for juvenile idiopathic arthritis

A systematic strategy for identifying causal single nucleotide polymorphisms and their target genes on Juvenile arthritis risk haplotypes

Circulating neutrophil transcriptome may reveal intracranial aneurysm signature

Using Chromatin Architecture to Understand the Genetics and Transcriptomics of Juvenile Idiopathic Arthritis

CD4+ T cells from children with active juvenile idiopathic arthritis show altered chromatin features associated with transcriptional abnormalities

Biomarkers from circulating neutrophil transcriptomes have potential to detect unruptured intracranial aneurysms

Genetic insights into juvenile idiopathic arthritis derived from deep whole genome sequencing

Genomic characterization of remission in juvenile idiopathic arthritis

Broadening our understanding of genetic risk for scleroderma/systemic sclerosis by querying the chromatin architecture surrounding the risk haplotypes

Classification models using circulating neutrophil transcripts can detect unruptured intracranial aneurysm

The feasibility of developing biomarkers from peripheral blood mononuclear cell RNAseq data in children with juvenile idiopathic arthritis using machine learning approaches

Mapping of Variable DNA Methylation Across Multiple Cell Types Defines a Dynamic Regulatory Landscape of the Human Genome

Epigenetic landscapes of intracranial aneurysm risk haplotypes implicate enhancer function of endothelial cells and fibroblasts in dysregulated gene expression

Whole blood expression profiling from the TREAT trial: insights for the pathogenesis of polyarticular juvenile idiopathic arthritis

Epigenetic landscapes suggest that genetic risk for intracranial aneurysm operates on the endothelium

Plasma exosomes from children with juvenile dermatomyositis are taken up by human aortic endothelial cells and are associated with altered gene expression in those cells

Identification of Circulating Gene Expression Signatures of Intracranial Aneurysm in Peripheral Blood Mononuclear Cells

Systemic lupus erythematosus in American Indian/Alaska natives: Incorporating our new understanding of the biology of trauma

Health inequities in the rheumatic diseases of childhood

“Racism as a public health issue” APS racism series: at the intersection of equity, science, and social justice

Facing the Truth and Moving Forward: The Complicity of Pediatricians with Racism in the United States

Reduced Nicotinamide Adenine Dinucleotide Phosphate Oxidase-Independent Resistance to Aspergillus fumigatus in Alveolar Macrophages

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