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• Conference paper
  Huang Y, Ma S-F, Oldham JM, Adegunsoye A, Zhu D, Murray S, Kim JS, Bonham C, Strickland E, Linderholm AL, Lee CT, Paul T, Mannem H, Maher TM, Molyneaux PL, Strek ME, Martinez FJ, Noth Iet al., 2024,

  Machine Learning of Plasma Proteomics Classifies Diagnosis of Interstitial Lung Disease

  , International Conference of the American-Thoracic-Society (ATS), Publisher: AMER THORACIC SOC, Pages: 444-454, ISSN: 1073-449X
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• Journal article
  Calamita E, Liu WH, Ogger PP, Griffin L, Michalaki C, Murphy F, Worrell J, McCarthy C, Agro A, Hertz M, Maher TM, Lloyd CM, Molyneaux P, Kumar V, Byrne AJet al., 2024,

  Type 1 Invariant Natural Killer T Cells Drive Lung Fibrosis

  , AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, Vol: 210, Pages: 521-523, ISSN: 1073-449X
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• Journal article
  Thillai M, Oldham JM, Ruggiero A, Kanavati F, McLellan T, Saini G, Johnson SR, Ble F-X, Azim A, Ostridge K, Platt A, Belvisi M, Maher TM, Molyneaux PLet al., 2024,

  Deep Learning-based Segmentation of Computed Tomography Scans Predicts Disease Progression and Mortality in Idiopathic Pulmonary Fibrosis

  , AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, Vol: 210, Pages: 465-472, ISSN: 1073-449X
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• Journal article
  Mall MA, Burgel P-R, Castellani C, Davies JC, Salathe M, Taylor-Cousar JLet al., 2024,

  Cystic fibrosis.

  , Nat Rev Dis Primers, Vol: 10

  Cystic fibrosis is a rare genetic disease caused by mutations in CFTR, the gene encoding cystic fibrosis transmembrane conductance regulator (CFTR). The discovery of CFTR in 1989 has enabled the unravelling of disease mechanisms and, more recently, the development of CFTR-directed therapeutics that target the underlying molecular defect. The CFTR protein functions as an ion channel that is crucial for correct ion and fluid transport across epithelial cells lining the airways and other organs. Consequently, CFTR dysfunction causes a complex multi-organ disease but, to date, most of the morbidity and mortality in people with cystic fibrosis is due to muco-obstructive lung disease. Cystic fibrosis care has long been limited to treating symptoms using nutritional support, airway clearance techniques and antibiotics to suppress airway infection. The widespread implementation of newborn screening for cystic fibrosis and the introduction of a highly effective triple combination CFTR modulator therapy that has unprecedented clinical benefits in up to 90% of genetically eligible people with cystic fibrosis has fundamentally changed the therapeutic landscape and improved prognosis. However, people with cystic fibrosis who are not eligible based on their CFTR genotype or who live in countries where they do not have access to this breakthrough therapy remain with a high unmet medical need.

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• Journal article
  Howlett P, Gan J, Lesosky M, Feary Jet al., 2024,

  Relationship between cumulative silica exposure and silicosis: a systematic review and dose-response meta-analysis

  , THORAX, ISSN: 0040-6376
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• Journal article
  Feary J, Devaraj A, Burton M, Chua F, Coker RK, Datta A, Hewitt R, Kokosi M, Kouranos V, Reynolds CJ, Ross CL, Smith V, Ward K, Wickremasinghe M, Szram Jet al., 2024,

  Artificial stone silicosis: a UK case series

  , THORAX, ISSN: 0040-6376
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• Journal article
  Koreshkov M, Antreich SJ, Bismarck A, Fritz I, Reimhult E, Takatsuna Y, Zirbs Ret al., 2024,

  Sustainable food packaging using modified SiO₂ nanofillers in biodegradable polymers

  , MATERIALS CHEMISTRY FRONTIERS, Vol: 8, Pages: 2754-2763
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• Journal article
  Meldrum OW, Donaldson GC, Narayana JK, Ivan FX, Jaggi TK, Mac Aogain M, Finney LJ, Allinson JP, Wedzicha JA, Chotirmall SHet al., 2024,

  Accelerated Lung Function Decline and Mucus-Microbe Evolution in Chronic Obstructive Pulmonary Disease

  , AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, Vol: 210, Pages: 298-310, ISSN: 1073-449X
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• Journal article
  Blank M, Wilson RC, Wan Y, Peters J, Davies F, Tyszczuk L, Pichon B, Riezk A, Demirjian A, Brown CS, Gilchrist M, Holmes A, Rawson TMet al., 2024,

  Exploring real-world vancomycin target attainment in neonatal intensive care in the context of Staphylococcal infections: a retrospective observational cohort study

  , Journal of Infection, Vol: 89, ISSN: 0163-4453
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• Journal article
  Jaillais Y, Bayer E, Bergmann DC, Botella MA, Boutte Y, Bozkurt TO, Caillaud M-C, Germain V, Grossmann G, Heilmann I, Hemsley PA, Kirchhelle C, Martiniere A, Miao Y, Mongrand S, Mueller S, Noack LC, Oda Y, Ott T, Pan X, Pleskot R, Potocky M, Robert S, Rodriguez CS, Simon-Plas F, Russinova E, Van Damme D, Van Norman JM, Weijers D, Yalovsky S, Yang Z, Zelazny E, Gronnier Jet al., 2024,

  Guidelines for naming and studying plasma membrane domains in plants

  , NATURE PLANTS, Vol: 10, Pages: 1172-1183, ISSN: 2055-026X
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