Publications
239
Citations
12,836
Est. group size
~4
Recurring co-author estimate
Active years
46
Publishing since 1981
Karen McCoy's research focuses on cystic fibrosis (CF), a genetic disease that causes thick mucus buildup affecting the lungs, digestive system, and other organs. Her work spans clinical trials of new CF drugs (including CFTR modulators and inhaled therapies), studies of lung disease progression in children, and research on co-occurring conditions such as autism spectrum disorder in CF patients. Much of her work involves multicenter clinical studies evaluating drug safety, effectiveness, and impact on lung function, bacterial infections, and immune responses.
Publication output has remained fairly steady over the past decade, averaging just under 7 papers per year in the last 5 years, with a notable peak in 2023.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- A Precious Child's Legacy: Insights Into Advanced Lung and Liver Disease in Children With Cystic Fibrosis
Pediatric Pulmonology · 2026
- Highly Effective Modulator Therapies Restore Neutrophil Dysfunction in People with Cystic Fibrosis
American Journal of Respiratory Cell and Molecular Biology · 2026
- 101 Interim summary of SPL84-002, a Phase 2 study in pwCF carrying the 3849 +10 Kb C- >T mutation evaluating the safety, tolerability, pharmacokinetics, and preliminary efficacy of SPL84
Journal of Cystic Fibrosis · 2025
- Clinical management of pediatric patients with cystic fibrosis and autism spectrum disorder
Pediatric Pulmonology · 2023
- Impact of elexacaftor–tezacaftor–ivacaftor on bacterial colonization and inflammatory responses in cystic fibrosis
Pediatric Pulmonology · 2022
- Cystic Fibrosis and Autism Spectrum Disorder: Unique challenges of this dual diagnosis
2022
- Aquagenic wrinkling in children under two years of age: Could this be a potential clinical referral tool for cystic fibrosis among non-screened populations?
Journal of Cystic Fibrosis · 2021
- IMPACT OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR MODULATOR ELEXACAFTOR-TEZACAFTOR-IVACAFTOR ON LUNG FUNCTION, BMI, BACTERIAL COLONIZATION, AND ADAPTIVE IMMUNE RESPONSES IN PATIENTS WITH CYSTIC FIBROSIS
CHEST Journal · 2021
- 544: Safety and tolerability of single and repeat doses of MRT5005, an inhaled CFTR mRNA replacement therapy, in adult CF patients
Journal of Cystic Fibrosis · 2021
- 575: Improved clinical outcome in an N1303K-CFTR patient treated with elexacaftor/tezacaftor/ivacaftor based on in vitro experimental evidence
Journal of Cystic Fibrosis · 2021
- Cystic Fibrosis Macrophage Function and Clinical Outcomes After Elexacaftor/Tezacaftor/Ivacaftor Initiation
2021
- Mucus plugging, air trapping, and bronchiectasis are important outcome measures in assessing progressive childhood cystic fibrosis lung disease
Pediatric Pulmonology · 2020
- Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation
UNC Libraries · 2020
- Pragmatic evaluation of a midstream urine collection technique for infants in the emergency department
Canadian Journal of Emergency Medicine · 2020
- Practitioner Due Diligence: Real-World Lumacaftor/Ivacaftor Use
The Journal of Pediatric Pharmacology and Therapeutics · 2020
- Journal of Cystic Fibrosis×12
- Pediatric Pulmonology×10
- CHEST Journal×8
- The Lancet Respiratory Medicine×5
- UNC Libraries×5
- James F. Chmiel
Medicine · Indiana University
- Estelle Cormet‐Boyaka
Medicine · The Ohio State University
- Michelle S. Howenstine
Medicine · Indiana University
- Charles Clem
Medicine · Indiana University
- Mariah Eisner
Medicine · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile