Publications
181
Citations
3,973
Est. group size
~1
Recurring co-author estimate
Active years
50
Publishing since 1976
Don B. Sanders conducts clinical research on cystic fibrosis, a genetic condition that affects the lungs and other organs. The work focuses on how to measure and treat lung decline, including studies of pulmonary flare-ups (exacerbations), antibiotic use, lung function testing at home, the airway microbiome (the community of microbes in the lungs), and newer gene-targeted drug therapies.
Publication activity has been steady over the past decade, averaging around 11 papers per year in the last five years.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- An observational study of the lung microbiome and lung function in young children with cystic fibrosis across two countries with differing antibiotic practices
Microbial Pathogenesis · 2025
- WS07.06Early change in forced vital capacity as a determinant of outcome in pulmonary exacerbations of cystic fibrosis
Journal of Cystic Fibrosis · 2025
- 649 Quality of clinically performed home spirometry in children with cystic fibrosis
Journal of Cystic Fibrosis · 2025
- 650 Defining the clinical use of home spirometry in children with cystic fibrosis
Journal of Cystic Fibrosis · 2025
- Correlates of FEV₁ deficit in pulmonary exacerbations of cystic fibrosis and associated clinical outcomes
Journal of Cystic Fibrosis · 2025
- Evaluating the association of antibiotic spectrum and treatment responses of cystic fibrosis pulmonary exacerbations
Journal of Cystic Fibrosis · 2025
- Effects of Therapeutic Antibiotic Exposure on the Oropharyngeal and Fecal Microbiota in Infants With Cystic Fibrosis
Pediatric Pulmonology · 2025
- Systematic comparison of methods for offline breath sampling
Analytical and Bioanalytical Chemistry · 2025
- Longitudinal Monitoring of Volatile Organic Compounds in Exhaled Breath Samples Collected from Children Diagnosed With Cystic Fibrosis
American Journal of Respiratory and Critical Care Medicine · 2025
- Standards for the care of people with cystic fibrosis (CF); recognising and addressing CF health issues
Journal of Cystic Fibrosis · 2024
- Impact of the expanded label for elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with no F508del variant in the USA
European Respiratory Journal · 2024
- Characteristics of individuals with cystic fibrosis in the United States ineligible for ivacaftor and elexacaftor/tezacaftor/ivacaftor
Journal of Cystic Fibrosis · 2024
- Treatment of small as well as large declines in lung function enhances recovery to baseline in people with CF
Pediatric Pulmonology · 2024
- Symptom Phenotyping in Adults With Cystic Fibrosis During a Large Randomized Clinical Trial
2024
- Impact of Treating Small and Large Declines in Lung Function in Cystic Fibrosis
2024
- Journal of Cystic Fibrosis×47
- Pediatric Pulmonology×11
- Annals of the American Thoracic Society×6
- American Journal of Respiratory and Critical Care Medicine×5
- PMC×5
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 11, 2026.
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