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Author Details

Matthew T Weirauch
University of Cincinnati College of Medicine
2003
166
50
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37645953High-throughput identification of functional regulatory SNPs in systemic lupus erythematosus.bioRxiv2024
37645953High-throughput identification of functional regulatory SNPs in systemic lupus erythematosus.bioRxiv2024
35918104Vitamin D receptor and STAT6 interactome governs oesophageal epithelial barrier responses to IL-13 signalling.Gut2023
35918104Vitamin D receptor and STAT6 interactome governs oesophageal epithelial barrier responses to IL-13 signalling.Gut2023
37745430After the Infection: A Survey of Pathogens and Non-communicable Human Disease.medRxiv2023
37662191Lineage tracing of newly accrued nuclei in skeletal myofibers uncovers distinct transcripts and interplay between nuclear populations.bioRxiv2023
37995687Nuclear RNA catabolism controls endogenous retroviruses, gene expression asymmetry, and dedifferentiation.Mol Cell2023
37794597Effector memory T cells induce innate inflammation by triggering DNA damage and a non-canonical STING pathway in dendritic cells.Cell Rep2023
37031202Single cell transcriptomic analysis of HPV16-infected epithelium identifies a keratinocyte subpopulation implicated in cancer.Nat Commun2023
36585519Gene-environment interactions and their impact on human health.Genes Immun2023
36824978Macrophage epigenetic memories of early life injury drive neonatal nociceptive priming.bioRxiv2023
37337107Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.Nat Genet2023
36949074A DNA tumor virus globally reprograms host 3D genome architecture to achieve immortal growth.Nat Commun2023
37455310A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth.BMC Med2023
37114997Prediction of cooperative homeodomain DNA binding sites from high-throughput-SELEX data.Nucleic Acids Res2023
37531635VExD: a curated resource for human gene expression alterations following viral infection.G3 (Bethesda)2023
36719906maxATAC: Genome-scale transcription-factor binding prediction from ATAC-seq with deep neural networks.PLoS Comput Biol2023
37662191Lineage tracing of newly accrued nuclei in skeletal myofibers uncovers distinct transcripts and interplay between nuclear populations.bioRxiv2023
37794597Effector memory T cells induce innate inflammation by triggering DNA damage and a non-canonical STING pathway in dendritic cells.Cell Rep2023
37745430After the Infection: A Survey of Pathogens and Non-communicable Human Disease.medRxiv2023
37995687Nuclear RNA catabolism controls endogenous retroviruses, gene expression asymmetry, and dedifferentiation.Mol Cell2023
37531635VExD: a curated resource for human gene expression alterations following viral infection.G3 (Bethesda)2023
37455310A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth.BMC Med2023
36949074A DNA tumor virus globally reprograms host 3D genome architecture to achieve immortal growth.Nat Commun2023
37114997Prediction of cooperative homeodomain DNA binding sites from high-throughput-SELEX data.Nucleic Acids Res2023
37337107Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.Nat Genet2023
37031202Single cell transcriptomic analysis of HPV16-infected epithelium identifies a keratinocyte subpopulation implicated in cancer.Nat Commun2023
36719906maxATAC: Genome-scale transcription-factor binding prediction from ATAC-seq with deep neural networks.PLoS Comput Biol2023
36585519Gene-environment interactions and their impact on human health.Genes Immun2023
36824978Macrophage epigenetic memories of early life injury drive neonatal nociceptive priming.bioRxiv2023
34111451TSLP disease-associated genetic variants combined with airway TSLP expression influence asthma risk.J Allergy Clin Immunol2022
35595084Multiancestral polygenic risk score for pediatric asthma.J Allergy Clin Immunol2022
35388006Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery.Nat Commun2022
35576187Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis.PLoS Genet2022
36000549β-catenin cancer-enhancing genomic regions axis is involved in the development of fibrolamellar hepatocellular carcinoma.Hepatol Commun2022
35863348"Stripe" transcription factors provide accessibility to co-binding partners in mammalian genomes.Mol Cell2022
36253972Frontotemporal degeneration genetic risk loci and transcription regulation as a possible mechanistic link to disease risk.Medicine (Baltimore)2022
34111451TSLP disease-associated genetic variants combined with airway TSLP expression influence asthma risk.J Allergy Clin Immunol2022
35252945CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.Cell Genom2022
35263148Blocking UBE2N abrogates oncogenic immune signaling in acute myeloid leukemia.Sci Transl Med2022
35576187Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis.PLoS Genet2022
35595084Multiancestral polygenic risk score for pediatric asthma.J Allergy Clin Immunol2022
35388006Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery.Nat Commun2022
36000549β-catenin cancer-enhancing genomic regions axis is involved in the development of fibrolamellar hepatocellular carcinoma.Hepatol Commun2022
35863348"Stripe" transcription factors provide accessibility to co-binding partners in mammalian genomes.Mol Cell2022
36253972Frontotemporal degeneration genetic risk loci and transcription regulation as a possible mechanistic link to disease risk.Medicine (Baltimore)2022
35252945CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.Cell Genom2022
35263148Blocking UBE2N abrogates oncogenic immune signaling in acute myeloid leukemia.Sci Transl Med2022
33382170Second-hand smoke and NFE2L2 genotype interaction increases paediatric asthma risk and severity.Clin Exp Allergy2021
34294116Genomics and transcriptomics yields a system-level view of the biology of the pathogen Naegleria fowleri.BMC Biol2021
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Collaborators

Cincinnati Children's Hospital Medical Center
Co-authored papers 34
University of Toronto
Co-authored papers 21
US Department of Veterans Affairs Medical Center
Co-authored papers 13
Co-authored papers 11
University of Toronto
Co-authored papers 11
Cincinnati Children's Hospital Medical Center
Co-authored papers 10
Cincinnati Children's Hospital Medical Center
Co-authored papers 7
University of Lausanne
Co-authored papers 6
Wayne State University
Co-authored papers 6
University of Illinois at Champaign-Urbana
Co-authored papers 6
Center for Epigenetics and Metabolism, University of California irvine
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 5
Cincinnati Children's Hospital
Co-authored papers 5
University of Geneva Medical School
Co-authored papers 5
University of California at Santa Cruz
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 5
University of Rochester
Co-authored papers 5
Co-authored papers 4
USDA-ARS
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
USDA Agricultural Research Service
Co-authored papers 4
Sloan Kettering Institute
Co-authored papers 4
Co-authored papers 4
University of Toronto
Co-authored papers 4
Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation
Co-authored papers 4
Co-authored papers 4
Icahn School of Medicine at Mount Sinai
Co-authored papers 4
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Baylor College of Medicine
Co-authored papers 4