Kimberly Stephens
Assistant Professor
Also affiliated: Franciscan University of Steubenville (2021); University of Maryland, Baltimore (2017); American Nurses Association (2020); Arkansas Children's Hospital (2021–2026); Capital One (United States) (2018); Innovations for Poverty Action (2007); Cleveland Clinic (2016); University of North Carolina Health Care (2025); University of Nevada, Reno (2006–2007); Howard Hughes Medical Institute (2018); Johns Hopkins University (2014–2023); University of Idaho (1999); Aerospace Testing Alliance (United States) (2021); Duquesne University (2016–2021); BRAC (2016); University of California, San Francisco (2010–2013); GlaxoSmithKline (United Kingdom) (2010); University of Washington (2003); Western Connecticut State University (2017); University of Arkansas Medical Center (2021–2024); Johns Hopkins Medicine (2014–2023); Allegheny General Hospital (2023); Society of Health and Physical Educators (2021); University of Alabama at Birmingham (2025); Yale University (2013–2017); Stephens College (2011–2016); Shadyside Hospital (2022); Department of Physiological Sciences (2017); Kinetic Art & Technology (United States) (2014); Zero to Three (2018); Renown Regional Medical Center (2006–2008); Swanson Center (2016); Committee on Publication Ethics (2018); University of Washington Applied Physics Laboratory (2003); Printed Electronics (United Kingdom) (2018); Arkansas Children's Nutrition Center (2021–2026); Arkansas Children’s Foundation (2021); Institute of Cell Biology and Neurobiology (2012); Community Hospital (2018); Cleveland Clinic Akron General (2016); RJ Lee Group (United States) (2017); University at Buffalo, State University of New York (2007); Washington State University (1993–1996); Waynesburg University (2014–2023); University of California, Davis (2000–2012); Friedrich Miescher Institute (1993); Michigan State University (1981); Walter Reed Army Institute of Research (2022)
Faculty Researcher
Peds Pediatrics, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Kimberly Stephens, an Assistant Professor at the University of Arkansas for Medical Sciences, leads a research group focusing on areas including epigenetics, neuroscience, and child health. Her work has been recognized with a designation as a high-impact researcher, evidenced by an h-index of 24 and over 1,800 citations across 167 publications. Stephens' research interests span molecular mechanisms, such as the de novo methylation of histone H3K23 by EHMT1/GLP and EHMT2/G9a, and the role of transcription factors like CCAAT enhancer binding protein gamma (C/EBP-γ).
Her publications also address the heritability of neuropsychiatric traits through human brain region-specific variably methylated regions and the global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain. Stephens has also investigated the impact of early life factors on child health, including the gut microbiome and implementing trauma-informed strategies for mothers of infants with neonatal abstinence syndrome. Further research explores quality improvement tools and the management of remote employees using leadership models.
Metrics
- h-index: 24
- Publications: 169
- Citations: 1,829
Selected Publications
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Degraded myelin is associated with cold hypersensitivity in paclitaxel-induced peripheral neuropathy (2026)
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Loss of FAM60A disrupts Sin3/HDAC control of the Hippo signaling and promotes oncogenic YAP1 activation (2026)
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Impact of Early Life Stress on the Composition of Gut Microbiome (2026)
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DNMT3B Controls Enhancer-Linked Chromatin and Cell Cycle Networks in Acute Myeloid Leukemia (2026)
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A Novel Model of Paclitaxel-Induced Peripheral Neuropathy Produces aClinically Relevant Phenotype in Mice (2026)
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Abstract 2281 Epigenetic Drivers and Subtype-Specific Roles of DNMT3B in Acute Myeloid Leukemia (2025)
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Stress During Lactation: A Hidden Link to Offspring Bone Health (2025)
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Impact of Maternal Care Behaviors on Mechanical Sensitivity of Adult Offspring (2025)
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ID: 342895 Assessment of Psychosocial Factors and Success of Neuromodulation Trials for Treatment of Persistent Pain (2024)
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Effect of Early Life Stress on Skeletal Health (2024)
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Spinal cord stimulation attenuates paclitaxel-induced gait impairment and mechanical hypersensitivity via peripheral neuroprotective mechanisms in tumor-bearing rats (2024)
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Behavioral Effects of Repeated Paclitaxel Cycles on Paclitaxel-Induced Peripheral Neuropathy Resolution (2024)
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The Persistence Of Rodent Mechanical Hypersensitivity Following Chronic Constriction Injury From Chronic Early-Life Stress (2024)
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Impact of psychosocial factors on the success of neuromodulation treatment for patients with persistent pain (2024)
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The Role of Early Life Gut Mycobiome on Child Health (2024)
Collaboration Network
Top Collaborators
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- De novo methylation of histone H3K23 by the methyltransferases EHMT1/GLP and EHMT2/G9a
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
Showing 5 of 24 shared publications
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Additional file 10 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 15 shared publications
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Additional file 10 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 15 shared publications
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Additional file 10 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 15 shared publications
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Additional file 10 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 15 shared publications
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Additional file 10 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 15 shared publications
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Additional file 10 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 15 shared publications
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Additional file 10 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 15 shared publications
- Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Human brain region-specific variably methylated regions (VMRs) are enriched for heritability of distinct neuropsychiatric traits
- Additional file 10 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 15 shared publications
- Global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- Spinal Cord Stimulation Increases Chemoefficacy and Prevents Paclitaxel-Induced Pain via CX3CL1
- Spinal cord stimulation attenuates paclitaxel-induced gait impairment and mechanical hypersensitivity via peripheral neuroprotective mechanisms in tumor-bearing rats
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- 63438 Differential chromatin accessibility at dorsal root ganglia enhancers is associated with nerve injury
Showing 5 of 10 shared publications
- Global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- 63438 Differential chromatin accessibility at dorsal root ganglia enhancers is associated with nerve injury
- Dynamics of Global Gene Expression and Chromatin Accessibility of the Peripheral Nervous System in Animal Models of Persistent Pain
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
Showing 5 of 8 shared publications
- CCAAT enhancer binding protein gamma (C/EBP-γ): An understudied transcription factor
- Global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- Dynamics of Global Gene Expression and Chromatin Accessibility of the Peripheral Nervous System in Animal Models of Persistent Pain
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
Showing 5 of 8 shared publications
- Additional file 9 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 8 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 11 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 5 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 13 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
Showing 5 of 8 shared publications
- Global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- 63438 Differential chromatin accessibility at dorsal root ganglia enhancers is associated with nerve injury
- Dynamics of Global Gene Expression and Chromatin Accessibility of the Peripheral Nervous System in Animal Models of Persistent Pain
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
Showing 5 of 7 shared publications
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- 63438 Differential chromatin accessibility at dorsal root ganglia enhancers is associated with nerve injury
- Dynamics of Global Gene Expression and Chromatin Accessibility of the Peripheral Nervous System in Animal Models of Persistent Pain
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
- Transcription Factor Affinity at Dorsal Root Ganglia Enhancers after Nerve Injury
Showing 5 of 7 shared publications
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