Kimberly Stephens
Assistant Professor
Also affiliated: University of Nevada, Reno (2007–2008); Howard Hughes Medical Institute (2018); Johns Hopkins University (2016–2023); University of Idaho (1999); University of California, San Francisco (2010–2017); Florida International University (2017); Western Connecticut Health Network (2017); Johns Hopkins Medicine (2016–2022); Renown Health (2008); Yale University (2017); Renown Regional Medical Center (2007–2008); Apex Innovations (United States) (2007); Arkansas Children’s Foundation (2021); Arkansas Children's Research Institute (2021–2026); University at Buffalo, State University of New York (2007); University of California, Davis (2000–2012); Walter Reed Army Institute of Research (2022)
Peds Pediatrics, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Kimberly Stephens leads a research group at the University of Arkansas for Medical Sciences, focusing on investigations into sex differences in gene regulation following nerve injury, as evidenced by her 2019 publication on this topic. Her work also extends to exploring associations between cytokine gene variations and persistent breast pain in women post-breast cancer surgery, a subject of her 2013 publication. Stephens has contributed to studies on the success of enteral nutrition and its relation to ICU-acquired infections, and the implementation of human trafficking education in emergency departments.
Her research interests also encompass the alteration of pulmonary neuroendocrine cells during airway injury repair and the implementation of practice standards for electrocardiographic monitoring. Stephens holds a substantial publication record, with 169 total publications and 1,840 citations, contributing to an h-index of 25. She is recognized as a highly cited researcher. Key collaborators include Sean D. Taverna, Bryan E. White, Samrat Roy Choudhury, and Johnathan Goree, all from the University of Arkansas for Medical Sciences, with whom she shares multiple publications.
Metrics
- h-index: 19
- Publications: 93
- Citations: 1,019
Positions
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Assistant Professor 2025–presentUniversity of Arkansas for Medical Sciences Peds Pediatrics, College of Medicine Institutional directory
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Postdoctoral fellow 2013–2019Johns Hopkins School of Medicine Pharmacology & Molecular Sciences ORCID
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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Myelin Degradation as a Driver of Persistent, Exclusive Cold Hypersensitivity in a Model of Chemotherapy-Induced Peripheral Neuropathy (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 a Clinically Relevant Phenotype in Mice (2026)
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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
- Identification of Regulatory Elements in Primary Sensory Neurons Involved in Trauma-Induced Neuropathic Pain
Showing 5 of 28 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 19 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 19 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 19 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 19 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 19 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 19 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 19 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 19 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
- Identification of Regulatory Elements in Primary Sensory Neurons Involved in Trauma-Induced Neuropathic Pain
- Dynamics of global gene expression and chromatin accessibility of the peripheral nervous system in animal models of persistent pain
Showing 5 of 10 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 10 shared publications
- The Role of Early Life Gut Mycobiome on Child Health
- A Novel Model of Paclitaxel-Induced Peripheral Neuropathy Produces a Clinically Relevant Phenotype in Mice
- Stress During Lactation: A Hidden Link to Offspring Bone Health
- The Persistence Of Rodent Mechanical Hypersensitivity Following Chronic Constriction Injury From Chronic Early-Life Stress
- Behavioral Effects of Repeated Paclitaxel Cycles on Paclitaxel-Induced Peripheral Neuropathy Resolution
Showing 5 of 9 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 17 of Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits
- Additional file 14 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
- Identification of Regulatory Elements in Primary Sensory Neurons Involved in Trauma-Induced Neuropathic 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
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
- Identification of Regulatory Elements in Primary Sensory Neurons Involved in Trauma-Induced Neuropathic 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
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