Matthew D. Thompson Data-verified
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Assistant Professor
faculty
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Biography and Research Information
OverviewAI-generated summary
Matthew D. Thompson, Assistant Professor at the University of Arkansas for Medical Sciences, investigates trends in cancer treatment and patient survival outcomes. His work includes analyses of real-world data to understand prescription patterns for systemic anticancer therapies in advanced non-small cell lung cancer. Thompson has also published research on the role and regulation of helicases at the replication fork, structural features of Dda helicase, and the application of multi-omics data integration for understanding triple-negative breast cancer.
His research has extended to pharmacokinetic modeling for dose selection of immune-activating products in oncology and assessing the use of bone-targeting agents in patients with bone metastasis. Thompson collaborates with researchers at the University of Arkansas for Medical Sciences, including Maroof Zafar, Emory G. Malone, Lindsey Hazeslip, and Duah Alkam, with whom he has co-authored multiple publications. He has an h-index of 16, with 77 total publications and 868 total citations.
Metrics
- h-index: 16
- Publications: 77
- Citations: 874
Selected Publications
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Untargeted CUT&Tag reads are enriched at accessible chromatin and restrict identification of potential G4-forming sequences in G4-targeted CUT&Tag experiments (2025)
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Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB (2025)
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Untargeted CUT&Tag and BG4 CUT&Tag are both enriched at G-quadruplexes and accessible chromatin (2024)
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Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB (2024)
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Role and Regulation of Pif1 Family Helicases at the Replication Fork (2022)
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Monitoring helicase-catalyzed unwinding of multiple duplexes simultaneously (2022)
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A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp> (2021)
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Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer (2021)
Collaboration Network
Top Collaborators
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- Role and Regulation of Pif1 Family Helicases at the Replication Fork
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Untargeted CUT&Tag reads are enriched at accessible chromatin and restrict identification of potential G4-forming sequences in G4-targeted CUT&Tag experiments
- Untargeted CUT&Tag and BG4 CUT&Tag are both enriched at G-quadruplexes and accessible chromatin
Showing 5 of 9 shared publications
- Supplementary Data from Urinary Metabolite Risk Biomarkers of Lung Cancer: A Prospective Cohort Study
- Supplementary Figure 7 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 5 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Data from Urinary Metabolite Risk Biomarkers of Lung Cancer: A Prospective Cohort Study
- Supplementary Figure 7 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 5 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Cancer Pharmacology
- Cancer Pharmacology
- Cancer Pharmacology
- Cancer Pharmacology
- Cancer Pharmacology
- Treatment patterns and survival outcomes for patients with non-small cell lung cancer in the UK in the preimmunology era: a REAL-Oncology database analysis from the I-O Optimise initiative
- Trends in the prescription of systemic anticancer therapy and mortality among patients with advanced non-small cell lung cancer: a real-world retrospective observational cohort study from the I-O optimise initiative
- Assessment of bone-targeting agents use in patients with bone metastasis from breast, lung or prostate cancer using structured and unstructured electronic health records from a regional UK-based hospital
- Algorithms to identify radiotherapy intent in unresected non-metastatic non-small-cell lung cancer: an I-O Optimise analysis
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Supplementary Figure 7 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 5 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 7 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 5 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 7 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 5 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Treatment patterns and survival outcomes for patients with non-small cell lung cancer in the UK in the preimmunology era: a REAL-Oncology database analysis from the I-O Optimise initiative
- Trends in the prescription of systemic anticancer therapy and mortality among patients with advanced non-small cell lung cancer: a real-world retrospective observational cohort study from the I-O optimise initiative
- Assessment of bone-targeting agents use in patients with bone metastasis from breast, lung or prostate cancer using structured and unstructured electronic health records from a regional UK-based hospital
- Treatment patterns and survival outcomes for patients with non-small cell lung cancer in the UK in the preimmunology era: a REAL-Oncology database analysis from the I-O Optimise initiative
- Trends in the prescription of systemic anticancer therapy and mortality among patients with advanced non-small cell lung cancer: a real-world retrospective observational cohort study from the I-O optimise initiative
- Algorithms to identify radiotherapy intent in unresected non-metastatic non-small-cell lung cancer: an I-O Optimise analysis
- Treatment patterns and survival outcomes for patients with non-small cell lung cancer in the UK in the preimmunology era: a REAL-Oncology database analysis from the I-O Optimise initiative
- Trends in the prescription of systemic anticancer therapy and mortality among patients with advanced non-small cell lung cancer: a real-world retrospective observational cohort study from the I-O optimise initiative
- Algorithms to identify radiotherapy intent in unresected non-metastatic non-small-cell lung cancer: an I-O Optimise analysis
- Role and Regulation of Pif1 Family Helicases at the Replication Fork
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Monitoring helicase-catalyzed unwinding of multiple duplexes simultaneously
- Supplementary Figure 5 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 5 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
- Supplementary Figure 1 from Unique and Novel Urinary Metabolomic Features in Malignant versus Benign Adrenal Neoplasms
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