Numerical modeling of the effects of nasal mucosal thickness and dehydration on air conditioning for a 5-year-old with cystic fibrosis. Respiratory Physiology and Neurobiology. 2026; 346:104652.
Poster: 682A longitudinal retrospective analysis of environmental exposure effects on Th2 inflammatory markers and pulmonary function in people with cystic fibrosis. Journal of Cystic Fibrosis. 2026; 25:374.
Poster: 679Characterizing spatial variability in CF lung function: A US Midwest cohort study. Journal of Cystic Fibrosis. 2026; 25:372.
Poster: 677PRISM-CF: A prototype dashboard to contextualize polygenic risk scores with environmental and clinical factors in cystic fibrosis. Journal of Cystic Fibrosis. 2026; 25:370-371.
Poster: 187Effects of diesel exhaust particles in an aged mouse model of cystic fibrosis disease. Journal of Cystic Fibrosis. 2026; 25:92-93.
Poster: 83The NET effect on NF-κB–activation in CF epithelia and the impact of ETI. Journal of Cystic Fibrosis. 2026; 25:42.
Poster: 191Comparing MRI scoring approaches to characterize early sinonasal disease in pediatric cystic fibrosis. Journal of Cystic Fibrosis. 2026; 25:96.
Sinusitis and Olfaction Improve in Young Children with Cystic Fibrosis Treated with ETI. Annals of the American Thoracic Society. 2026.
Lung mucus burden and treatment response assessed by MRI in the post-modulator era. Journal of Cystic Fibrosis. 2026; 25(4):711-717.
Structural and Functional Pulmonary MRI to Predict Pulmonary Exacerbations in Cystic Fibrosis. Chest. 2026; 169(4):919-931.
Xenon-129 magnetic resonance imaging detects ongoing ventilation improvements in people with cystic fibrosis receiving highly effective modulator therapy. Annals of the American Thoracic Society. 2026; 23(2):303-307.
Longitudinal Monitoring of Lumacaftor/Ivacaftor Response in Young Children with Cystic Fibrosis Lung Disease Using 129Xe MRI. Academic Radiology. 2025; 32(10):6238-6249.
TGF-β induces excessive pulmonary IL-6 secretion in cystic fibrosis via PI3K. American Journal of Physiology - Lung Cellular and Molecular Physiology. 2025; 329(4):L470-L479.
Optimizing Xenon 129 Ventilation MRI in Cystic Fibrosis with Spiral Imaging and Flip-Angle Correction. Radiology: Cardiothoracic Imaging. 2025; 7(5):e240574.
88 Neutrophil extracellular traps increase human bronchial epithelial iron release and promote Pseudomonas aeruginosa growth. Journal of Cystic Fibrosis. 2025; 24:s45-s46.
732 A genetic algorithm-derived single index model for integrating environmental risk into longitudinal lung function prediction in cystic fibrosis. Journal of Cystic Fibrosis. 2025; 24:s437b-ss438.
710 Near-road air pollution inhibits long-term modulator effectiveness. Journal of Cystic Fibrosis. 2025; 24:s425-s426.
743 Effects of environmental and social epidemiological factors on cytokine response in people with cystic fibrosis. Journal of Cystic Fibrosis. 2025; 24:s447-s448.
Hypercubes to identify geomarkers of rapid cystic fibrosis lung disease progression. BMC Medical Informatics and Decision Making. 2025; 25(1):304.
The impact of highly effective modulator therapy on sinusitis and dysosmia in young children with cystic fibrosis: a prospective study protocol. ERJ Open Research. 2025; 11(1).
Robust identification of environmental exposures and community characteristics predictive of rapid lung disease progression. Science of the Total Environment. 2024; 950:175348.
Quantifying abnormal alveolar microstructure in cystic fibrosis lung disease via hyperpolarized 129Xe diffusion MRI. Journal of Cystic Fibrosis. 2024; 23(5):926-935.
327 Comparison of human nasal and fisher rat thyroid cell-based theratyping results. Journal of Cystic Fibrosis. 2024; 23:s173-s174.
198 Neutrophil extracellular traps increase Pseudomonal density in human bronchial epithelia. Journal of Cystic Fibrosis. 2024; 23:s110.
Heterogeneity in Neutrophil Extracellular Traps from Healthy Human Subjects. International Journal of Molecular Sciences. 2023; 25(1).
98 Neutrophil extracellular traps disrupt bronchial epithelial junctional integrity and promote infection. Journal of Cystic Fibrosis. 2023; 22:s51.
168 Impact of TGF-β exposure on IL-6 secretion in cystic fibrosis airway epithelia. Journal of Cystic Fibrosis. 2023; 22:s89.
CFTR dysfunction in smooth muscle drives TGFβ dependent airway hyperreactivity. Respiratory Research. 2023; 24(1):198.
380 Neutrophil extracellular traps disrupt bronchial epithelial barrier function: Alpha-1 antitrypsin to the rescue. Journal of Cystic Fibrosis. 2022; 21:s223.
27 Effect of SARS-CoV-2 on long-term physical and mental health symptoms in people with cystic fibrosis and their caregivers. Journal of Cystic Fibrosis. 2022; 21:s16-s17.
Alpha-1 antitrypsin limits neutrophil extracellular trap disruption of airway epithelial barrier function. Frontiers in Immunology. 2022; 13:1023553.