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Author Details
Full Name
Matthew T Weirauch
Affiliation
University of Cincinnati College of Medicine
ORCID
Career Start Year
2003
Papers
166
H Index
50
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37645953
High-throughput identification of functional regulatory SNPs in systemic lupus erythematosus.
bioRxiv
2024
37645953
High-throughput identification of functional regulatory SNPs in systemic lupus erythematosus.
bioRxiv
2024
35918104
Vitamin D receptor and STAT6 interactome governs oesophageal epithelial barrier responses to IL-13 signalling.
Gut
2023
35918104
Vitamin D receptor and STAT6 interactome governs oesophageal epithelial barrier responses to IL-13 signalling.
Gut
2023
37745430
After the Infection: A Survey of Pathogens and Non-communicable Human Disease.
medRxiv
2023
37662191
Lineage tracing of newly accrued nuclei in skeletal myofibers uncovers distinct transcripts and interplay between nuclear populations.
bioRxiv
2023
37995687
Nuclear RNA catabolism controls endogenous retroviruses, gene expression asymmetry, and dedifferentiation.
Mol Cell
2023
37794597
Effector memory TÂ cells induce innate inflammation by triggering DNA damage and a non-canonical STING pathway in dendritic cells.
Cell Rep
2023
37031202
Single cell transcriptomic analysis of HPV16-infected epithelium identifies a keratinocyte subpopulation implicated in cancer.
Nat Commun
2023
36585519
Gene-environment interactions and their impact on human health.
Genes Immun
2023
36824978
Macrophage epigenetic memories of early life injury drive neonatal nociceptive priming.
bioRxiv
2023
37337107
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.
Nat Genet
2023
36949074
A DNA tumor virus globally reprograms host 3D genome architecture to achieve immortal growth.
Nat Commun
2023
37455310
A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth.
BMC Med
2023
37114997
Prediction of cooperative homeodomain DNA binding sites from high-throughput-SELEX data.
Nucleic Acids Res
2023
37531635
VExD: a curated resource for human gene expression alterations following viral infection.
G3 (Bethesda)
2023
36719906
maxATAC: Genome-scale transcription-factor binding prediction from ATAC-seq with deep neural networks.
PLoS Comput Biol
2023
37662191
Lineage tracing of newly accrued nuclei in skeletal myofibers uncovers distinct transcripts and interplay between nuclear populations.
bioRxiv
2023
37794597
Effector memory TÂ cells induce innate inflammation by triggering DNA damage and a non-canonical STING pathway in dendritic cells.
Cell Rep
2023
37745430
After the Infection: A Survey of Pathogens and Non-communicable Human Disease.
medRxiv
2023
37995687
Nuclear RNA catabolism controls endogenous retroviruses, gene expression asymmetry, and dedifferentiation.
Mol Cell
2023
37531635
VExD: a curated resource for human gene expression alterations following viral infection.
G3 (Bethesda)
2023
37455310
A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth.
BMC Med
2023
36949074
A DNA tumor virus globally reprograms host 3D genome architecture to achieve immortal growth.
Nat Commun
2023
37114997
Prediction of cooperative homeodomain DNA binding sites from high-throughput-SELEX data.
Nucleic Acids Res
2023
37337107
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.
Nat Genet
2023
37031202
Single cell transcriptomic analysis of HPV16-infected epithelium identifies a keratinocyte subpopulation implicated in cancer.
Nat Commun
2023
36719906
maxATAC: Genome-scale transcription-factor binding prediction from ATAC-seq with deep neural networks.
PLoS Comput Biol
2023
36585519
Gene-environment interactions and their impact on human health.
Genes Immun
2023
36824978
Macrophage epigenetic memories of early life injury drive neonatal nociceptive priming.
bioRxiv
2023
34111451
TSLP disease-associated genetic variants combined with airway TSLP expression influence asthma risk.
J Allergy Clin Immunol
2022
35595084
Multiancestral polygenic risk score for pediatric asthma.
J Allergy Clin Immunol
2022
35388006
Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery.
Nat Commun
2022
35576187
Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis.
PLoS Genet
2022
36000549
β-catenin cancer-enhancing genomic regions axis is involved in the development of fibrolamellar hepatocellular carcinoma.
Hepatol Commun
2022
35863348
"Stripe" transcription factors provide accessibility to co-binding partners in mammalian genomes.
Mol Cell
2022
36253972
Frontotemporal degeneration genetic risk loci and transcription regulation as a possible mechanistic link to disease risk.
Medicine (Baltimore)
2022
34111451
TSLP disease-associated genetic variants combined with airway TSLP expression influence asthma risk.
J Allergy Clin Immunol
2022
35252945
CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.
Cell Genom
2022
35263148
Blocking UBE2N abrogates oncogenic immune signaling in acute myeloid leukemia.
Sci Transl Med
2022
35576187
Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis.
PLoS Genet
2022
35595084
Multiancestral polygenic risk score for pediatric asthma.
J Allergy Clin Immunol
2022
35388006
Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery.
Nat Commun
2022
36000549
β-catenin cancer-enhancing genomic regions axis is involved in the development of fibrolamellar hepatocellular carcinoma.
Hepatol Commun
2022
35863348
"Stripe" transcription factors provide accessibility to co-binding partners in mammalian genomes.
Mol Cell
2022
36253972
Frontotemporal degeneration genetic risk loci and transcription regulation as a possible mechanistic link to disease risk.
Medicine (Baltimore)
2022
35252945
CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.
Cell Genom
2022
35263148
Blocking UBE2N abrogates oncogenic immune signaling in acute myeloid leukemia.
Sci Transl Med
2022
33382170
Second-hand smoke and NFE2L2 genotype interaction increases paediatric asthma risk and severity.
Clin Exp Allergy
2021
34294116
Genomics and transcriptomics yields a system-level view of the biology of the pathogen Naegleria fowleri.
BMC Biol
2021
1 - 50 of 332
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Co-authored papers
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Wayne State University
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Co-authored papers
5
Bahram Namjou
Cincinnati Children's Hospital
Co-authored papers
5
Evgeny M Zdobnov
University of Geneva Medical School
Co-authored papers
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Joshua M Stuart
University of California at Santa Cruz
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Donna M Muzny
Baylor College of Medicine
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Kim C Worley
Baylor College of Medicine
Co-authored papers
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John H Werren
University of Rochester
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Ross C Hardison
Co-authored papers
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USDA-ARS
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Stephen Richards
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