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Presence Current · Arkansas
Last published 2026
Sources OpenAlex · ORCID
Refreshed 2026-10-05

Shannon Rose

High Impact

Associate Professor

Also affiliated: Rutgers, The State University of New Jersey (1990–1991); Arkansas Children's Hospital (2009–2025); University of Minnesota (1990–1991); Scripps Health (1990–1991); Harvard University (1990–1994); University of Tennessee Health Science Center (2025); The University of Melbourne (1956); University of California, San Francisco (1990–1991); University of Arkansas Medical Center (2023); Council of Science Editors (1991); University of California, San Diego (1990–1991); Shannon Applied Biotechnology Centre (2024); Hospices Civils de Lyon (2008); Hôpital Edouard Herriot (2008); Arkansas Children's Nutrition Center (2018–2022); Scripps Clinic (1990–1991); Arkansas Department of Agriculture (2019); National Health and Medical Research Council (1956); Weizmann Institute of Science (1990–1994); University of California, Berkeley (1990–1991)

34 h-index 91 pubs 5,143 cited

  • Humans
  • Child
  • Autism Spectrum Disorder
  • Male
  • Mitochondria
  • Female
  • Oxidative Stress
  • Case-Control Studies
  • Autistic Disorder
  • Child, Preschool
  • Cell Line
  • Insulin Resistance
  • Glutathione
  • Biomarkers
  • Reactive Oxygen Species

Biography and Research Information

OverviewAI-generated summary

Shannon Rose's research focuses on understanding the biological mechanisms underlying Autism Spectrum Disorder (ASD), with a particular emphasis on mitochondrial dysfunction, oxidative stress, and metabolic imbalances. Rose has investigated these areas through studies involving human subjects, including children, and utilizing cell lines derived from individuals with ASD.

Publications detail findings related to oxidative damage and inflammation in the autism brain, as well as metabolic imbalances associated with methylation dysregulation and oxidative damage in children with ASD. Further work has explored the clinical and molecular characteristics of mitochondrial dysfunction in ASD and the potential of butyrate to enhance mitochondrial function during oxidative stress in cell lines from boys with autism. Rose's research also includes studies on cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism, and the impact of oxidative stress on mitochondrial function in a subset of autism lymphoblastoid cell lines. Additionally, Rose has investigated the therapeutic potential of folinic acid in improving verbal communication in children with autism.

Rose's scholarly contributions are reflected in an h-index of 34 and over 5,000 citations across 91 publications. Rose collaborates with several researchers at the University of Arkansas for Medical Sciences, including Leanna Delhey, Elisabet Børsheim, Craig Porter, and Pritmohinder S. Gill.

Metrics

  • h-index: 34
  • Publications: 91
  • Citations: 5,143

Positions

  • Associate Professor 2024–present
    University of Tennessee Health Science Center College of Nursing, Department of Health Promotion and Disease Prevention ORCID
  • Associate Professor publications 2008–2025
    University of Arkansas for Medical Sciences ORCID
  • Assistant Professor 2017–2024
    University of Arkansas for Medical Sciences Pediatrics ORCID
  • Postdoctoral Fellow 2012–2017
    University of Arkansas for Medical Sciences Pediatrics ORCID

Selected Publications

  • Mitochondrial respiratory function in human platelets: Influence of sample preparation, assay buffer, and instrumental platform (2025)
    Physiological Reports DOI OpenAlex
  • Correlating maternal and cord-blood inflammatory markers and BDNF with human fetal brain activity recorded by magnetoencephalography: An exploratory study (2024)
    Brain Behavior & Immunity - Health 4 citations DOI OpenAlex
  • Platelets, inflammation, and purinergic receptors in chronic kidney disease (2024)
    Kidney International 15 citations DOI OpenAlex
  • Regulatory T cells and bioenergetics of peripheral blood mononuclear cells linked to pediatric obesity (2024)
    Immunometabolism 3 citations DOI OpenAlex
  • Correlation of fetal heart rate dynamics to inflammatory markers and brain-derived neurotrophic factor during pregnancy (2024)
    Journal of Perinatal Medicine 2 citations DOI OpenAlex
  • Nitrosative Stress in Autism: Supportive Evidence and Implications for Mitochondrial Dysfunction (2024)
    Advanced Science 13 citations DOI OpenAlex
  • Circulating microRNA levels differ in the early stages of insulin resistance in prepubertal children with obesity (2022)
    Life Sciences 14 citations DOI OpenAlex
  • Air Pollution and Maximum Temperature Are Associated with Neurodevelopmental Regressive Events in Autism Spectrum Disorder (2022)
    Journal of Personalized Medicine 8 citations DOI OpenAlex
  • Metabolomic Signatures of Autism Spectrum Disorder (2022)
    Journal of Personalized Medicine 53 citations DOI OpenAlex
  • Blood RNA Sequencing Indicates Upregulated BATF2 and LY6E and Downregulated ISG15 and MT2A Expression in Children with Autism Spectrum Disorder (2022)
    International Journal of Molecular Sciences 6 citations DOI OpenAlex
  • Integrated microRNA–mRNA Expression Profiling Identifies Novel Targets and Networks Associated with Autism (2022)
    Journal of Personalized Medicine 14 citations DOI OpenAlex
  • Effect of excess weight and insulin resistance on DNA methylation in prepubertal children (2022)
    Scientific Reports 10 citations DOI OpenAlex
  • A Personalized Approach to Evaluating and Treating Autism Spectrum Disorder (2022)
    Journal of Personalized Medicine 17 citations DOI OpenAlex
  • Blood RNA Sequencing Confirms Upregulated BATF2 and FCGR1A Expression in Children with Autism Spectrum Disorder (2021)
    Research Square DOI OpenAlex
  • MicroRNA Expression Profiles in Autism Spectrum Disorder: Role for miR-181 in Immunomodulation (2021)
    Journal of Personalized Medicine 21 citations DOI OpenAlex

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Collaboration Network

138 Collaborators 46 Institutions 7 Countries

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