Stephen G. Jones
Assistant Professor
Also affiliated: Centers for Disease Control and Prevention (2015); United States Fish and Wildlife Service (2005); Vanderbilt University (2015); Sherwood Forest Hospitals NHS Foundation Trust (2015–2024); Schaffner (Switzerland) (2015); Queen's Medical Centre (2002); BlueCross BlueShield of South Carolina Foundation (2009–2016); Manor Hospital (2009); Mass General Brigham (2019)
Peds Pediatrics, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Stephen G. Jones, an Assistant Professor at the University of Arkansas for Medical Sciences, focuses his research on public health and epidemiological studies. His work has investigated the spatial implications of data analysis methods in healthcare research, including the influence of spatial resolution on disease cluster detection. Jones has also examined demographic factors affecting emergency department utilization within Medicaid populations and explored the clinical utility of advanced microbiology testing tools. He has published 43 papers, accumulating 475 citations and an h-index of 11. His collaborations include several shared publications with researchers at the University of Arkansas for Medical Sciences, such as Stacie M. Jones, Fatimah Al‐Doori, Matthew Bell, and John Alberty.
Metrics
- h-index: 11
- Publications: 43
- Citations: 475
Positions
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Assistant Professor publications 2025University of Arkansas for Medical Sciences Peds Pediatrics, College of Medicine Institutional directory
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University of Arkansas for Medical Sciences publications 2025Pediatrics ORCID
Selected Publications
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Incidental Detection of Acute Leukemia During Genetic Evaluation of Neurodevelopmental Disorder in a Pediatric Clinic: A Case Report (2026)
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Trofinetide-Induced Enterocolitis Syndrome in a Child with Rett Syndrome (2025)
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Potential neonatal toxicity of new psychoactive substances (2023)
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Prediction of milk plasma ratio for amphoteric substances (2022)
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Identifying cytochrome P450s involved in oxidative metabolism of synthetic cannabinoid N‐(adamantan‐1‐yl)‐1‐(5‐fluoropentyl)‐1H‐indole‐3‐carboxamide (STS‐135) (2020)
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Comparaisons continentales des caractéristiques des patients dans PALISADE, étude de phase 3 d’AR101 dans l’allergie à l’arachide (2019)
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Enzymatic analysis of glucuronidation of synthetic cannabinoid 1-naphthyl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate (FDU-PB-22) (2019)
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Sublingual Immunotherapy for Peanut Allergy: A Randomized, Double-Blind, Placebo-Controlled Multicenter Trial (CoFAR) (2012)
Collaboration Network
Top Collaborators
- Potential neonatal toxicity of new psychoactive substances
- Identifying cytochrome P450s involved in oxidative metabolism of synthetic cannabinoid N‐(adamantan‐1‐yl)‐1‐(5‐fluoropentyl)‐1H‐indole‐3‐carboxamide (STS‐135)
- Enzymatic analysis of glucuronidation of synthetic cannabinoid 1-naphthyl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate (FDU-PB-22)
- Prediction of milk plasma ratio for amphoteric substances
- Identifying cytochrome P450s involved in oxidative metabolism of synthetic cannabinoid N‐(adamantan‐1‐yl)‐1‐(5‐fluoropentyl)‐1H‐indole‐3‐carboxamide (STS‐135)
- Enzymatic analysis of glucuronidation of synthetic cannabinoid 1-naphthyl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate (FDU-PB-22)
- Identifying cytochrome P450s involved in oxidative metabolism of synthetic cannabinoid N‐(adamantan‐1‐yl)‐1‐(5‐fluoropentyl)‐1H‐indole‐3‐carboxamide (STS‐135)
- Enzymatic analysis of glucuronidation of synthetic cannabinoid 1-naphthyl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate (FDU-PB-22)
- Identifying cytochrome P450s involved in oxidative metabolism of synthetic cannabinoid N‐(adamantan‐1‐yl)‐1‐(5‐fluoropentyl)‐1H‐indole‐3‐carboxamide (STS‐135)
- Enzymatic analysis of glucuronidation of synthetic cannabinoid 1-naphthyl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate (FDU-PB-22)
- Identifying cytochrome P450s involved in oxidative metabolism of synthetic cannabinoid N‐(adamantan‐1‐yl)‐1‐(5‐fluoropentyl)‐1H‐indole‐3‐carboxamide (STS‐135)
- Enzymatic analysis of glucuronidation of synthetic cannabinoid 1-naphthyl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate (FDU-PB-22)
- Identifying cytochrome P450s involved in oxidative metabolism of synthetic cannabinoid N‐(adamantan‐1‐yl)‐1‐(5‐fluoropentyl)‐1H‐indole‐3‐carboxamide (STS‐135)
- Enzymatic analysis of glucuronidation of synthetic cannabinoid 1-naphthyl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate (FDU-PB-22)
- Sublingual Immunotherapy for Peanut Allergy: A Randomized, Double-Blind, Placebo-Controlled Multicenter Trial (CoFAR)
- Comparaisons continentales des caractéristiques des patients dans PALISADE, étude de phase 3 d’AR101 dans l’allergie à l’arachide
- Potential neonatal toxicity of new psychoactive substances
- Prediction of milk plasma ratio for amphoteric substances
- Release of Soluble Protein from Peanut and Its Adsorption by Activated Charcoal In Vitro and In Vivo
- Release of Soluble Protein from Peanut and Its Adsorption by Activated Charcoal In Vitro and In Vivo
- Release of Soluble Protein from Peanut and Its Adsorption by Activated Charcoal In Vitro and In Vivo
- Release of Soluble Protein from Peanut and Its Adsorption by Activated Charcoal In Vitro and In Vivo
- Release of Soluble Protein from Peanut and Its Adsorption by Activated Charcoal In Vitro and In Vivo
- Enzymatic analysis of glucuronidation of synthetic cannabinoid 1-naphthyl 1-(4-fluorobenzyl)-1H-indole-3-carboxylate (FDU-PB-22)
- Comparaisons continentales des caractéristiques des patients dans PALISADE, étude de phase 3 d’AR101 dans l’allergie à l’arachide
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