Gerry McElvaney

Royal College of Surgeons in Ireland — Ireland

Medicine · Health Sciences

1h-index1citations24works0.02yr avg
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Research Topics

Cystic Fibrosis Research Advances(8), Protease and Inhibitor Mechanisms(5), Pediatric health and respiratory diseases(3), Asthma and respiratory diseases(2), Neonatal Respiratory Health Research(2)

Publications24 total

32 Assessment of the changes to the respiratory tract microbiome of CF patients 4 years on ETI
Journal of Cystic Fibrosis·2025
175 Do CT images accurately identify inflammatory ‘hotspots’ in the CF lung?
Journal of Cystic Fibrosis·2025
Late Breaking Abstract - Real-world evidence for severe Alpha-1 Antitrypsin Deficiency: Life-years gained for augmentation therapy versus standard care
2025
Late Breaking Abstract - Targeting senescence to reduce inflammation in alpha-1 antitrypsin deficiency (AATD)
2025
Senescence is Elevated in Airway and Liver Cells in Alpha-1 Antitrypsin Deficiency and is Tractable to Targeted Therapy
American Journal of Respiratory and Critical Care Medicine·2025
The ZZ Family Study: A Preliminary Proband Analysis
American Journal of Respiratory and Critical Care Medicine·2025
Interlobar Differences in Airway Cell Counts, Cell Differentials and Protease Levels in People With Cystic Fibrosis on Highly Effective Modulator Therapy
American Journal of Respiratory and Critical Care Medicine·2025
An update from the Irish national alpha-1 antitrypsin deficiency targeted detection programme
Epidemiology·2023
Cellular stress and senescence in alpha-1 antitrypsin deficiency: therapeutic opportunities
2023
Research priorities in alpha-1 antitrypsin deficiency (AATD) for healthcare professionals
2020
322 longitudinal analysis of the lower airway microbiota in pwcf during periods of clinical stability
Research Portal (Queen's University Belfast)·2019
356 association between multi-drug resistant pseusdomonas aeruginosa and viable bacterial community profiles in sputum
Research Portal (Queen's University Belfast)·2019
414 Baseline microbial community composition in clinically stable CF patients compared to those experiencing episodes of pulmonary exacerbation.
Research Portal (Queen's University Belfast)·2018
415 comparison of microbial community composition in cf patients with and without cf-related diabetes
Research Portal (Queen's University Belfast)·2018
MZ carrier state in alpha-1 antitrypsin deficiency: Summary of the 16th Gordon L. Snider critical issues workshop, Bethesda, Maryland, November 13, 2017
Translational Science of Rare Diseases·2018Open Access
P073 Use of qPCR to analyse changes in total bacterial and Pseudomonas aeruginosa load in cystic fibrosis patients when clinically stable and during exacerbations
Journal of Cystic Fibrosis·2018Open Access
Supplemental Oxygen Enhances the Effects of Interval Training On Exercise Capacity in Cystic Fibrosis
Medicine & Science in Sports & Exercise·2017
Regulation of interleukin-8 by miR-17 during chronic inflammation in cystic fibrosis
2015· 1 cited
MiR-31 regulates IRF-1 function in cystic fibrosis epithelial cells
2014
WS21.6 Comparison of the CF airway microbiome obtained by bronchoscopy vs. sputum
Journal of Cystic Fibrosis·2014Open Access
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Frequent Co-authors

J.S. Elborn(7), Michael M. Tunney(6), Gillian Lavelle(6), Richard C. Boucher(6), Marianne S. Muhlebach(6), Cedric Gunaratnam(6), Tomás P. Carroll(6), Joseph Hatch(5), G.G. Einarsson(5), Laura J. Sherrard(5), D.F. Gilpin(5), Mark P. Murphy(5), E. Johnston(4), Bryan Zorn(4), Catherine M. Greene(3), Matthew C. Wolfgang(3), Ronen Reuveny(3), Niall M. Moyna(3), Katherine O’Neill(3), L. McIlreavey(3)