Erin Willis
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Also affiliated: University of North Carolina at Chapel Hill (2024); Arkansas Children's Hospital (2018–2022); Eastern New Mexico University (2016); University of Pittsburgh (2010); Lee University (2022); University of Colorado Boulder (2015–2026); University of Arkansas Medical Center (2017); University of Colorado System (2018–2026); University of Missouri–Kansas City (2022); University of Memphis (2012–2015)
Formerly Arkansas Affiliated with UAMS through 2022; recent publications list University of Colorado Boulder.
Research Areas
Biomedical Subjects
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Biography and Research Information
OverviewAI-generated summary
Erin Willis researches health communication, focusing on how individuals share and consume health information, particularly through social media platforms. Their work investigates the role of "patient influencers" in pharmaceutical marketing and the communication of health literacy concerning prescription medications. Willis has also explored the use of natural language processing to extract consumer insights from social media data for public health crisis management. Additionally, their research has examined vaccine hesitancy among young adults and the broader implications of medical advice disseminated by social media influencers. Willis's scholarship also touches upon the utility of behavioral biometrics for user authentication and demographic characteristic detection.
With a career marked by 87 publications and 1,257 citations, Willis holds an h-index of 18. Key collaborators include Murat Gökden, Vikki Stefans, Aravindhan Veerapandiyan, and Akilandeswari Aravindhan, all from the University of Arkansas for Medical Sciences.
Metrics
- h-index: 18
- Publications: 87
- Citations: 1,303
Selected Publications
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First-Line Rituximab in Pediatric-Onset Multiple Sclerosis: Clinical and MRI Outcomes in a Retrospective Cohort (2026)
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Reversible Pulmonary Arterial Hypertension Due to Fenfluramine in a Young Child: A Case Report (2026)
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Responsive Neurostimulation for Treatment of SCN1A-Associated Developmental and Epileptic Encephalopathies (2026)
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Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in <i>FKRP</i> Gene (2022)
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Underutilization of epilepsy surgery: Part I: A scoping review of barriers (2021)
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Charcot–Marie–Tooth Disease Type 4J and Multiple Sclerosis (2019)
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Immunotherapy in Autoimmune and Neuroinflammation-Related Epilepsies (2018)
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Clinicopathologic Findings of CARS2 Mutation (2018)
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KIAA2022-related disorders can cause Jeavons (eyelid myoclonia with absence) syndrome (2018)
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A Not Uncommon Cause of Stroke Mimicker in Children (2017)
Collaboration Network
Top Collaborators
- Underutilization of epilepsy surgery: Part I: A scoping review of barriers
- KIAA2022-related disorders can cause Jeavons (eyelid myoclonia with absence) syndrome
- Clinicopathologic Findings of CARS2 Mutation
- Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene
- Intractable epileptic spasms in a patient with Pontocerebellar hypoplasia: Severe phenotype of type 2 or another subtype?
Showing 5 of 13 shared publications
- Clinicopathologic Findings of CARS2 Mutation
- Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in <i>FKRP</i> Gene
- Charcot–Marie–Tooth Disease Type 4J and Multiple Sclerosis
- Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in <i>FKRP</i> Gene
- Reversible Pulmonary Arterial Hypertension Due to Fenfluramine in a Young Child: A Case Report
- First-Line Rituximab in Pediatric-Onset Multiple Sclerosis: Clinical and MRI Outcomes in a Retrospective Cohort
- Absence status after starting clobazam in a patient with syndrome of continuous spike and wave during slow sleep (CSWS)
- Myoclonic epilepsy evolved into West syndrome: a patient with a novel de novo KCNQ2 mutation
- Myoclonic epilepsy evolved into West syndrome: a patient with a novel de novo KCNQ2 mutation
- A Not Uncommon Cause of Stroke Mimicker in Children
- Immunotherapy in Autoimmune and Neuroinflammation-Related Epilepsies
- Charcot–Marie–Tooth Disease Type 4J and Multiple Sclerosis
- Underutilization of epilepsy surgery: Part I: A scoping review of barriers
- Underutilization of epilepsy surgery: Part I: A scoping review of barriers
- Underutilization of epilepsy surgery: Part I: A scoping review of barriers
- Underutilization of epilepsy surgery: Part I: A scoping review of barriers
- Underutilization of epilepsy surgery: Part I: A scoping review of barriers
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