| Year |
Citation |
Score |
| 2023 |
McNally P, Linnane B, Williamson M, Elnazir B, Short C, Saunders C, Kirwan L, David R, Kemner-Van de Corput MPC, Tiddens HAWM, Davies JC, Cox DW. The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6-11 with cystic fibrosis in a real-world setting. Respiratory Research. 24: 199. PMID 37568199 DOI: 10.1186/s12931-023-02497-0 |
0.304 |
|
| 2021 |
McNally P, Butler D, Karpievitch YV, Linnane B, Ranganathan S, Stick SM, Hall GL, Schultz A. Ivacaftor and Airway Inflammation in Preschool Children with Cystic Fibrosis. American Journal of Respiratory and Critical Care Medicine. PMID 34077699 DOI: 10.1164/rccm.202012-4332LE |
0.343 |
|
| 2021 |
Linnane B, Walsh AM, Walsh CJ, Crispie F, O'Sullivan O, Cotter PD, McDermott M, Renwick J, McNally P. The Lung Microbiome in Young Children with Cystic Fibrosis: A Prospective Cohort Study. Microorganisms. 9. PMID 33652802 DOI: 10.3390/microorganisms9030492 |
0.37 |
|
| 2020 |
Hutchinson I, McNally P. Appearance of Pancreatic Sufficiency and Discontinuation of Pancreatic Enzyme Replacement Therapy (PERT) in Children with Cystic Fibrosis on Ivacaftor. Annals of the American Thoracic Society. PMID 32931706 DOI: 10.1513/Annalsats.202006-614Rl |
0.324 |
|
| 2020 |
O Loughlin DW, Coughlan S, De Gascun CF, McNally P, Cox DW. The role of rhinovirus infections in young children with cystic fibrosis. Journal of Clinical Virology : the Official Publication of the Pan American Society For Clinical Virology. 129: 104478. PMID 32521465 DOI: 10.1016/J.Jcv.2020.104478 |
0.399 |
|
| 2020 |
Rowland M, McGee A, Broderick A, Drumm B, Connolly L, Daly LE, Drummond J, Fitzpatrick E, Linnane B, McCormick PA, McNally P, Rainford L, Bourke B. Repeatability of transient elastography in children. Pediatric Research. PMID 32357363 DOI: 10.1038/S41390-020-0916-4 |
0.325 |
|
| 2020 |
Useckaite Z, Ward MP, Trappe A, Reilly R, Lennon J, Davage H, Matallanas D, Cassidy H, Dillon ET, Brennan K, Doyle SL, Carter S, Donnelly S, Linnane B, McKone EF, ... McNally P, et al. Increased extracellular vesicles mediate inflammatory signalling in cystic fibrosis. Thorax. PMID 32265339 DOI: 10.1136/Thoraxjnl-2019-214027 |
0.422 |
|
| 2020 |
De Santi C, Fernández Fernández E, Gaul R, Vencken S, Glasgow A, Oglesby IK, Hurley K, Hawkins F, Mitash N, Mu F, Raoof R, Henshall DC, Cutrona MB, Simpson JC, Harvey BJ, ... ... McNally P, et al. Precise Targeting of miRNA Sites Restores CFTR Activity in CF Bronchial Epithelial Cells. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 32059764 DOI: 10.1016/J.Ymthe.2020.02.001 |
0.386 |
|
| 2020 |
Mooney C, McKiernan PJ, Raoof R, Henshall DC, Linnane B, McNally P, Glasgow AMA, Greene CM. Plasma microRNA levels in male and female children with cystic fibrosis. Scientific Reports. 10: 1141. PMID 31980676 DOI: 10.1038/S41598-020-57964-1 |
0.3 |
|
| 2020 |
Butler D, Montegue T, O’Sullivan N, Cox D, McNally P. P160 Study to Evaluate the Additional Gains of Upper and Lower Lobe Sampling in children with Cystic Fibrosis (SEAGULLS): safety and microbiological yield Journal of Cystic Fibrosis. 19. DOI: 10.1016/S1569-1993(20)30495-1 |
0.361 |
|
| 2020 |
Trappe A, Useckaite Z, Ward M, Davage H, Lennon J, Carter S, McKone E, Donnelly S, McNally P, Coppinger J. ePS3.02 Increased extracellular vesicles mediate inflammatory signalling in cystic fibrosis Journal of Cystic Fibrosis. 19. DOI: 10.1016/S1569-1993(20)30302-7 |
0.333 |
|
| 2019 |
Hulme KM, Linnane B, McNally PG. Lower Airway Infection in Preschool Children with Cystic Fibrosis - An International Comparison. American Journal of Respiratory and Critical Care Medicine. PMID 31769996 DOI: 10.1164/rccm.201910-2064LE |
0.302 |
|
| 2019 |
H'ng E, Jackson A, Lennon J, McNally P. P096 Pseudomonas aeruginosa prevalence rates over 12 years in Irish children with cystic fibrosis Journal of Cystic Fibrosis. 18. DOI: 10.1016/S1569-1993(19)30390-X |
0.39 |
|
| 2019 |
Hulme K, Lennon J, McLoughlin R, Linnane B, McNally P. P074 The prevalence of pathogenic organisms in the airways of Irish preschool children with cystic fibrosis Journal of Cystic Fibrosis. 18. DOI: 10.1016/S1569-1993(19)30368-6 |
0.403 |
|
| 2018 |
Linnane B, McNally P. Six-lobe bronchoalveolar lavage in children with cystic fibrosis. The Lancet. Respiratory Medicine. PMID 30037714 DOI: 10.1016/S2213-2600(18)30295-9 |
0.418 |
|
| 2018 |
Muhlebach MS, Hatch JE, Einarsson GG, McGrath SJ, Gilipin DF, Lavelle G, Mirkovic B, Murray MA, McNally P, Gotman N, Davis Thomas S, Wolfgang MC, Gilligan PH, McElvaney NG, Elborn JS, et al. Anaerobic bacteria cultured from CF airways correlate to milder disease-a multisite study. The European Respiratory Journal. PMID 29946004 DOI: 10.1183/13993003.00242-2018 |
0.355 |
|
| 2018 |
Glasgow A, Vencken S, Santi CD, Raoof R, Henshall D, Linnane B, Mcnally P, Greene C. The TLR4 regulator miR-21 is downregulated in the paediatric cystic fibrosis airway European Respiratory Journal. DOI: 10.1183/13993003.Congress-2018.Pa3420 |
0.303 |
|
| 2018 |
Linnane B, Cotter P, O'Sullivan O, Crisbie F, Walsh A, Renwick J, Mcnally P. Prospective case-control study describing the lower airway microbiome in pre-school children with cystic fibrosis European Respiratory Journal. 52. DOI: 10.1183/13993003.Congress-2018.Oa509 |
0.435 |
|
| 2017 |
Ringholz FC, Higgins G, Hatton A, Sassi A, Moukachar A, Fustero-Torre C, Hollenhorst M, Sermet-Gaudelus I, Harvey BJ, McNally P, Urbach V. Resolvin D1 regulates epithelial ion transport and inflammation in cystic fibrosis airways. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29233471 DOI: 10.1016/j.jcf.2017.11.017 |
0.3 |
|
| 2017 |
Ringholz FC, Higgins G, Hatton A, Sassi A, Moukachar A, Fustero-Torre C, Hollenhorst M, Sermet-Gaudelus I, Harvey BJ, McNally P, Urbach V. Resolvin D1 regulates epithelial ion transport and inflammation in cystic fibrosis airways. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29233471 DOI: 10.1016/j.jcf.2017.11.017 |
0.3 |
|
| 2017 |
Ringholz FC, Higgins G, Hatton A, Sassi A, Moukachar A, Fustero-Torre C, Hollenhorst M, Sermet-Gaudelus I, Harvey BJ, McNally P, Urbach V. Resolvin D1 regulates epithelial ion transport and inflammation in cystic fibrosis airways. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29233471 DOI: 10.1016/j.jcf.2017.11.017 |
0.3 |
|
| 2017 |
Ringholz FC, Higgins G, Hatton A, Sassi A, Moukachar A, Fustero-Torre C, Hollenhorst M, Sermet-Gaudelus I, Harvey BJ, McNally P, Urbach V. Resolvin D1 regulates epithelial ion transport and inflammation in cystic fibrosis airways. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29233471 DOI: 10.1016/J.Jcf.2017.11.017 |
0.403 |
|
| 2017 |
McNally P, O'Rourke J, Fantino E, Chacko A, Pabary R, Turnbull A, Grant T, O'Sullivan N, Wainwright C, Linnane B, Davies JC, Sly PD. Pooling of bronchoalveolar lavage in children with cystic fibrosis does not adversely affect the microbiological yield or sensitivity in detecting pulmonary inflammation. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29157921 DOI: 10.1016/J.Jcf.2017.10.016 |
0.418 |
|
| 2017 |
Treston B, Mullane D, Onwuneme C, Nazir BE, Greally PC, McNally P. EPS4.8 Atopy in children with cystic fibrosis is associated with lower body mass index and worse pulmonary function Journal of Cystic Fibrosis. 16. DOI: 10.1016/S1569-1993(17)30309-0 |
0.383 |
|
| 2016 |
Higgins G, Fustero Torre C, Tyrrell J, McNally P, Harvey BJ, Urbach V. Lipoxin A4 prevents tight junction disruption and delays the colonisation of cystic fibrosis bronchial epithelial cells by Pseudomonas aeruginosa. American Journal of Physiology. Lung Cellular and Molecular Physiology. ajplung.00368.2015. PMID 27084849 DOI: 10.1152/Ajplung.00368.2015 |
0.417 |
|
| 2016 |
Camper N, Glasgow AM, Osbourn M, Quinn DJ, Small DM, McLean DT, Lundy FT, Elborn JS, McNally P, Ingram RJ, Weldon S, Taggart CC. A secretory leukocyte protease inhibitor variant with improved activity against lung infection. Mucosal Immunology. 9: 669-76. PMID 26376365 DOI: 10.1038/Mi.2015.90 |
0.393 |
|
| 2016 |
McKiernan P, Mooney C, Henshall D, Linnane B, McNally P, Greene C. Serum microRNA levels in paediatric females versus males with cystic fibrosis European Respiratory Journal. 48. DOI: 10.1183/13993003.Congress-2016.Pa898 |
0.324 |
|
| 2016 |
Fitzgerald C, George S, Linnane B, Chroinin MN, Mullane D, Herzig M, Greally P, Elnazir B, Healy F, McNally P, Javadpour S, Cox DR, Fitzpatrick P. 185 Irish Comparative Outcome Study (ICOS): a comparison of early childhood growth trajectories in children clinically diagnosed with cystic fibrosis with those diagnosed through newborn bloodspot screening Journal of Cystic Fibrosis. 15. DOI: 10.1016/S1569-1993(16)30423-4 |
0.346 |
|
| 2015 |
Mirković B, Murray MA, Lavelle GM, Molloy K, Azim AA, Gunaratnam C, Healy F, Slattery D, McNally P, Hatch J, Wolfgang M, Tunney MM, Muhlebach MS, Devery R, Greene CM, et al. Short-chain Fatty Acids Cause an IL-8 Response in Cystic Fibrosis Airways via Increased GPR41. American Journal of Respiratory and Critical Care Medicine. PMID 26266556 DOI: 10.1164/Rccm.201505-0943Oc |
0.315 |
|
| 2015 |
McGovern E, McNally P, O'Sullivan M, Phelan E, Sumner K, Best DH, McMahon CJ. Infantile pulmonary capillary haemangiomatosis: a lethal form of pulmonary hypertension. Cardiology in the Young. 1-6. PMID 26175015 DOI: 10.1017/S1047951115001006 |
0.365 |
|
| 2015 |
Oglesby IK, Vencken SF, Agrawal R, Gaughan K, Molloy K, Higgins G, McNally P, McElvaney NG, Mall MA, Greene CM. miR-17 overexpression in cystic fibrosis airway epithelial cells decreases interleukin-8 production. The European Respiratory Journal. 46: 1350-60. PMID 26160865 DOI: 10.1183/09031936.00163414 |
0.397 |
|
| 2015 |
Higgins G, Ringholz F, Buchanan P, McNally P, Urbach V. Physiological impact of abnormal lipoxin A₄ production on cystic fibrosis airway epithelium and therapeutic potential. Biomed Research International. 2015: 781087. PMID 25866809 DOI: 10.1155/2015/781087 |
0.451 |
|
| 2015 |
Glasgow AM, Small DM, Scott A, McLean DT, Camper N, Hamid U, Hegarty S, Parekh D, O'Kane C, Lundy FT, McNally P, Elborn JS, McAuley DF, Weldon S, Taggart CC. A role for whey acidic protein four-disulfide-core 12 (WFDC12) in the regulation of the inflammatory response in the lung. Thorax. 70: 426-32. PMID 25770093 DOI: 10.1136/Thoraxjnl-2014-206488 |
0.341 |
|
| 2015 |
Linnane B, Vaish S, Clarke D, O'Sullivan N, McNally P. The findings of a clinical surveillance bronchoalveolar lavage programme in pre-school patients with cystic fibrosis. Pediatric Pulmonology. 50: 327-32. PMID 25408378 DOI: 10.1002/Ppul.23118 |
0.396 |
|
| 2015 |
Small DM, Zani ML, Quinn DJ, Dallet-Choisy S, Glasgow AM, O'Kane C, McAuley DF, McNally P, Weldon S, Moreau T, Taggart CC. A functional variant of elafin with improved anti-inflammatory activity for pulmonary inflammation. Molecular Therapy : the Journal of the American Society of Gene Therapy. 23: 24-31. PMID 25189740 DOI: 10.1038/Mt.2014.162 |
0.353 |
|
| 2014 |
Renwick J, McNally P, John B, DeSantis T, Linnane B, Murphy P. The microbial community of the cystic fibrosis airway is disrupted in early life. Plos One. 9: e109798. PMID 25526264 DOI: 10.1371/Journal.Pone.0109798 |
0.448 |
|
| 2014 |
Al-Alawi M, Buchanan P, Verriere V, Higgins G, McCabe O, Costello RW, McNally P, Urbach V, Harvey BJ. Physiological levels of lipoxin A4 inhibit ENaC and restore airway surface liquid height in cystic fibrosis bronchial epithelium. Physiological Reports. 2. PMID 25107986 DOI: 10.14814/Phy2.12093 |
0.365 |
|
| 2014 |
Weldon S, McNally P, McAuley DF, Oglesby IK, Wohlford-Lenane CL, Bartlett JA, Scott CJ, McElvaney NG, Greene CM, McCray PB, Taggart CC. miR-31 dysregulation in cystic fibrosis airways contributes to increased pulmonary cathepsin S production. American Journal of Respiratory and Critical Care Medicine. 190: 165-74. PMID 24940638 DOI: 10.1164/Rccm.201311-1986Oc |
0.41 |
|
| 2014 |
Ringholz FC, Buchanan PJ, Clarke DT, Millar RG, McDermott M, Linnane B, Harvey BJ, McNally P, Urbach V. Reduced 15-lipoxygenase 2 and lipoxin A4/leukotriene B4 ratio in children with cystic fibrosis. The European Respiratory Journal. 44: 394-404. PMID 24696116 DOI: 10.1183/09031936.00106013 |
0.455 |
|
| 2014 |
Higgins G, Buchanan P, Perriere M, Al-Alawi M, Costello RW, Verriere V, McNally P, Harvey BJ, Urbach V. Activation of P2RY11 and ATP release by lipoxin A4 restores the airway surface liquid layer and epithelial repair in cystic fibrosis. American Journal of Respiratory Cell and Molecular Biology. 51: 178-90. PMID 24588705 DOI: 10.1165/Rcmb.2012-0424Oc |
0.388 |
|
| 2014 |
O'Donovan C, Greally P, Canny G, McNally P, Hussey J. Active video games as an exercise tool for children with cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 13: 341-6. PMID 24189057 DOI: 10.1016/J.Jcf.2013.10.008 |
0.329 |
|
| 2014 |
Ringholz F, Devins M, McNally P. Managing end stage lung disease in children. Paediatric Respiratory Reviews. 15: 75-80; quiz 80-1. PMID 23948571 DOI: 10.1016/J.Prrv.2013.07.002 |
0.308 |
|
| 2013 |
Buchanan PJ, McNally P, Harvey BJ, Urbach V. Lipoxin Aâ‚„-mediated KATP potassium channel activation results in cystic fibrosis airway epithelial repair. American Journal of Physiology. Lung Cellular and Molecular Physiology. 305: L193-201. PMID 23686859 DOI: 10.1152/Ajplung.00058.2013 |
0.388 |
|
| 2013 |
Walsh A, Canny G, McMahon CJ, Redmond JM, McNally P. Hemoptysis from bronchial varices associated with pulmonary vein stenosis: role of surgical repair. Pediatric Pulmonology. 48: 838-40. PMID 22997173 DOI: 10.1002/Ppul.22659 |
0.334 |
|
| 2013 |
Small D, Zani M, Quinn D, Weldon S, McAuley D, McNally P, Moreau T, Taggart C. S99 A Functional Variant of Elafin with Improved Anti-Inflammatory Activity Thorax. 68. DOI: 10.1136/Thoraxjnl-2013-204457.106 |
0.341 |
|
| 2013 |
Glasgow A, Weldon S, Scott A, McLean D, Camper N, Lundy F, McNally P, Elborn JS, Taggart C. 163 A role for the WFDC protein, WAP2, in the regulation of inflammatory response in the lung Journal of Cystic Fibrosis. 12. DOI: 10.1016/S1569-1993(13)60305-7 |
0.311 |
|
| 2012 |
Verrière V, Higgins G, Al-Alawi M, Costello RW, McNally P, Chiron R, Harvey BJ, Urbach V. Lipoxin A4 stimulates calcium-activated chloride currents and increases airway surface liquid height in normal and cystic fibrosis airway epithelia. Plos One. 7: e37746. PMID 22662206 DOI: 10.1371/Journal.Pone.0037746 |
0.4 |
|
| 2012 |
Ringholz F, McNally P, Urbach V. 608 Reduced Lipoxin A4/Leukotriene B4Ratio in Early Cf Bal - Impaired Airway Epithelial Lipoxin A4Synthesis Capacity Archives of Disease in Childhood. 97. DOI: 10.1136/Archdischild-2012-302724.0608 |
0.455 |
|
| 2012 |
Renwick J, McNally P, Linnane B, Greally P, Elnazir B, Lynch S, Murphy PG. WS20.5 The airway microbiome in children with cystic fibrosis Journal of Cystic Fibrosis. 11. DOI: 10.1016/S1569-1993(12)60145-3 |
0.435 |
|
| 2012 |
Higgins G, Verriere V, Harvey BJ, McNally P, Urbach V. WS15.2 Airway surface liquid layer height in cystic fibrosis bronchial epithelial cells is increased by lipoxin A4 via an apical ATP release activating a P2Y receptor pathway Journal of Cystic Fibrosis. 11. DOI: 10.1016/S1569-1993(12)60104-0 |
0.339 |
|
| 2012 |
Weldon S, McNally P, McAuley D, Scott C, Mall M, Randell S, Wohlford-Lenane C, Bartlett J, McCray P, Taggart C. WS9.5 CF epithelial cells are a source of pulmonary cathepsin S via increased IRF-1 Journal of Cystic Fibrosis. 11: S20. DOI: 10.1016/S1569-1993(12)60064-2 |
0.367 |
|
| 2011 |
Linnane B, McNally P. Bronchoalveolar lavage-directed therapy in children with cystic fibrosis and Pseudomonas aeruginosa infection. Jama. 306: 1761; author reply 1. PMID 22028348 DOI: 10.1001/Jama.2011.1518 |
0.37 |
|
| 2011 |
McNally P, Coughlan C, Bergsson G, Doyle M, Taggart C, Adorini L, Uskokovic MR, El-Nazir B, Murphy P, Greally P, Greene CM, McElvaney NG. Vitamin D receptor agonists inhibit pro-inflammatory cytokine production from the respiratory epithelium in cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 10: 428-34. PMID 21784717 DOI: 10.1016/J.Jcf.2011.06.013 |
0.331 |
|
| 2011 |
Vega-Carrascal I, Reeves EP, Niki T, Arikawa T, McNally P, O'Neill SJ, Hirashima M, McElvaney NG. Dysregulation of TIM-3-galectin-9 pathway in the cystic fibrosis airways. Journal of Immunology (Baltimore, Md. : 1950). 186: 2897-909. PMID 21263071 DOI: 10.4049/Jimmunol.1003187 |
0.434 |
|
| 2011 |
McNally P, Ervine E, Shields MD, Dimitrov BD, El Nazir B, Taggart CC, Greene CM, McElvaney NG, Greally P. High concentrations of pepsin in bronchoalveolar lavage fluid from children with cystic fibrosis are associated with high interleukin-8 concentrations. Thorax. 66: 140-3. PMID 21160087 DOI: 10.1136/Thx.2009.130914 |
0.41 |
|
| 2009 |
Weldon S, McNally P, McElvaney NG, Elborn JS, McAuley DF, Wartelle J, Belaaouaj A, Levine RL, Taggart CC. Decreased levels of secretory leucoprotease inhibitor in the Pseudomonas-infected cystic fibrosis lung are due to neutrophil elastase degradation. Journal of Immunology (Baltimore, Md. : 1950). 183: 8148-56. PMID 20007580 DOI: 10.4049/Jimmunol.0901716 |
0.414 |
|
| 2009 |
Bergsson G, Reeves EP, McNally P, Chotirmall SH, Greene CM, Greally P, Murphy P, O'Neill SJ, McElvaney NG. LL-37 complexation with glycosaminoglycans in cystic fibrosis lungs inhibits antimicrobial activity, which can be restored by hypertonic saline. Journal of Immunology (Baltimore, Md. : 1950). 183: 543-51. PMID 19542465 DOI: 10.4049/Jimmunol.0803959 |
0.421 |
|
| 2008 |
Guyot N, Butler MW, McNally P, Weldon S, Greene CM, Levine RL, O'Neill SJ, Taggart CC, McElvaney NG. Elafin, an elastase-specific inhibitor, is cleaved by its cognate enzyme neutrophil elastase in sputum from individuals with cystic fibrosis. The Journal of Biological Chemistry. 283: 32377-85. PMID 18799464 DOI: 10.1074/Jbc.M803707200 |
0.429 |
|
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