WS13.4 Refining the CFTR genotype–function–phenotype relationship using registry and primary cell data. Journal of Cystic Fibrosis. 2026; 25:s26.
EPS2.03 Allele-specific editing in primary human nasal epithelial cells with compound heterozygous genotypes. Journal of Cystic Fibrosis. 2026; 25:s39.
ECFS statement on theratyping and theranostics in the context of rare and ultrarare CFTR variants in people with CF. Journal of Cystic Fibrosis. 2026.
Who will win the race for the first CFTR gene replacement therapy? Molecular Therapy. 2026; 34(4):1874-1876.
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.
710 Near-road air pollution inhibits long-term modulator effectiveness. Journal of Cystic Fibrosis. 2025; 24:s425-s426.
88 Neutrophil extracellular traps increase human bronchial epithelial iron release and promote Pseudomonas aeruginosa growth. Journal of Cystic Fibrosis. 2025; 24:s45-s46.
659 Lung function decline persists among healthy children with CF taking elexacaftor/tezacaftor/ivacaftor. Journal of Cystic Fibrosis. 2025; 24:s394.
314 Impact of routine pulmonary medications on modulator-rescued CFTR in cystic fibrosis cells. Journal of Cystic Fibrosis. 2025; 24:s175.
Use of Bronchoscopic Cryotherapy for Recanalization and Cryoextraction in Pediatric Population: A Five-Year Single Center Experience. American Journal of Respiratory and Critical Care Medicine. 2025; 211(Supplement_1):a7710-a7710.
Aligning Expectations With Outcomes: A Prospective Study of Pediatric Bronchoscopy in the ICU Setting. American Journal of Respiratory and Critical Care Medicine. 2025; 211(Supplement_1):a2303-a2303.
Spike and Slab Regression for Nonstationary Gaussian Linear Mixed Effects Modeling of Rapid Disease Progression. Environmetrics. 2025; 36(1).
Evaluation of elexacaftor-tezacaftor-ivacaftor treatment in individuals with cystic fibrosis and CFTRN1303K in the USA: a prospective, multicentre, open-label, single-arm trial. The Lancet Respiratory Medicine. 2024; 12(12):947-957.
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.
A personalized medicine approach to optimize care for a pediatric cystic fibrosis patient with atypical clinical symptoms. Pediatric Pulmonology. 2024; 59(1):229-232.
Upper Airway Disease in Cystic Fibrosis. In: Hodson and Geddes' Cystic Fibrosis. Taylor & Francis; 2023:325-330.
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.
Gradual increase in sweat chloride concentration is associated with a higher risk of CRMS/CFSPID to CF reclassification. Pediatric Pulmonology. 2023; 58(4):1074-1084.
Phenotypic Alteration of an Established Human Airway Cell Line by Media Selection. International Journal of Molecular Sciences. 2023; 24(2).
Novel Applications of Biomarkers and Personalized Medicine in Cystic Fibrosis. Clinics in Chest Medicine. 2022; 43(4):617-630.
683 Characteristics of cystic fibrosis transmembrane conductance regulator modulator response in nasal cell models derived from patients with rare cystic fibrosis transmembrane conductance regulator variants. Journal of Cystic Fibrosis. 2022; 21:s373.
606 Focused clinical trials of modulator response for rare cystic fibrosis genotypes. Journal of Cystic Fibrosis. 2022; 21:s336.
380 Neutrophil extracellular traps disrupt bronchial epithelial barrier function: Alpha-1 antitrypsin to the rescue. Journal of Cystic Fibrosis. 2022; 21:s223.
When CFSPID becomes CF. Journal of Cystic Fibrosis. 2022; 21(1):e23-e27.
CRISPRi links COVID-19 GWAS loci to LZTFL1 and RAVER1. EBioMedicine. 2022; 75:103806.
Alpha-1 antitrypsin limits neutrophil extracellular trap disruption of airway epithelial barrier function. Frontiers in Immunology. 2022; 13:1023553.