Follow
Prof. Edward F. McKone
Prof. Edward F. McKone
University College Dublin
Verified email at svhg.ie
Title
Cited by
Cited by
Year
A CFTR potentiator in patients with cystic fibrosis and the G551D mutation
BW Ramsey, J Davies, NG McElvaney, E Tullis, SC Bell, P Dřevínek, ...
New England Journal of Medicine 365 (18), 1663-1672, 2011
23952011
Elexacaftor–tezacaftor–ivacaftor for cystic fibrosis with a single Phe508del allele
PG Middleton, MA Mall, P Dřevínek, LC Lands, EF McKone, D Polineni, ...
New England Journal of Medicine 381 (19), 1809-1819, 2019
15232019
Lumacaftor–ivacaftor in patients with cystic fibrosis homozygous for Phe508del CFTR
CE Wainwright, JS Elborn, BW Ramsey, G Marigowda, X Huang, M Cipolli, ...
New England Journal of Medicine 373 (3), 220-231, 2015
15032015
Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind …
HGM Heijerman, EF McKone, DG Downey, E Van Braeckel, SM Rowe, ...
The Lancet 394 (10212), 1940-1948, 2019
9942019
The future of cystic fibrosis care: a global perspective
SC Bell, MA Mall, H Gutierrez, M Macek, S Madge, JC Davies, PR Burgel, ...
The Lancet Respiratory Medicine 8 (1), 65-124, 2020
7752020
Tezacaftor–ivacaftor in patients with cystic fibrosis homozygous for Phe508del
JL Taylor-Cousar, A Munck, EF McKone, CK Van Der Ent, A Moeller, ...
New england journal of medicine 377 (21), 2013-2023, 2017
7732017
VX-445–tezacaftor–ivacaftor in patients with cystic fibrosis and one or two Phe508del alleles
D Keating, G Marigowda, L Burr, C Daines, MA Mall, EF McKone, ...
New england journal of medicine 379 (17), 1612-1620, 2018
6242018
Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study
EF McKone, SS Emerson, KL Edwards, ML Aitken
The Lancet 361 (9370), 1671-1676, 2003
4942003
Restoring cystic fibrosis transmembrane conductance regulator function reduces airway bacteria and inflammation in people with cystic fibrosis and chronic lung infections
KB Hisert, SL Heltshe, C Pope, P Jorth, X Wu, RM Edwards, M Radey, ...
American journal of respiratory and critical care medicine 195 (12), 1617-1628, 2017
3522017
VX-659–tezacaftor–ivacaftor in patients with cystic fibrosis and one or two Phe508del alleles
JC Davies, SM Moskowitz, C Brown, A Horsley, MA Mall, EF McKone, ...
New england journal of medicine 379 (17), 1599-1611, 2018
3402018
Assessment of safety and efficacy of long-term treatment with combination lumacaftor and ivacaftor therapy in patients with cystic fibrosis homozygous for the F508del-CFTR …
MW Konstan, EF McKone, RB Moss, G Marigowda, S Tian, D Waltz, ...
The lancet Respiratory medicine 5 (2), 107-118, 2017
3112017
CFTR genotype as a predictor of prognosis in cystic fibrosis
EF McKone, CH Goss, ML Aitken
Chest 130 (5), 1441-1447, 2006
2952006
Sustained benefit from ivacaftor demonstrated by combining clinical trial and cystic fibrosis patient registry data
GS Sawicki, EF McKone, DJ Pasta, SJ Millar, JS Wagener, CA Johnson, ...
American journal of respiratory and critical care medicine 192 (7), 836-842, 2015
2472015
Long-term safety and efficacy of ivacaftor in patients with cystic fibrosis who have the Gly551Asp-CFTR mutation: a phase 3, open-label extension study (PERSIST)
EF McKone, D Borowitz, P Drevinek, M Griese, MW Konstan, ...
The lancet Respiratory medicine 2 (11), 902-910, 2014
2362014
Lung transplant referral for individuals with cystic fibrosis: Cystic Fibrosis Foundation consensus guidelines
KJ Ramos, PJ Smith, EF McKone, JM Pilewski, A Lucy, SE Hempstead, ...
Journal of Cystic Fibrosis 18 (3), 321-333, 2019
1902019
Delayed neutrophil apoptosis enhances NET formation in cystic fibrosis
RD Gray, G Hardisty, KH Regan, M Smith, CT Robb, R Duffin, A Mackellar, ...
Thorax 73 (2), 134-144, 2018
1882018
Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes
PJ Barry, MA Mall, A Álvarez, C Colombo, KM de Winter-De Groot, I Fajac, ...
New England Journal of Medicine 385 (9), 815-825, 2021
1802021
A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele
ET Zemanick, JL Taylor-Cousar, J Davies, RL Gibson, MA Mall, ...
American journal of respiratory and critical care medicine 203 (12), 1522-1532, 2021
1792021
Ambient air pollution, lung function, and airway responsiveness in asthmatic children
D Ierodiakonou, A Zanobetti, BA Coull, S Melly, DS Postma, HM Boezen, ...
Journal of allergy and clinical immunology 137 (2), 390-399, 2016
1622016
A multinational report to characterise SARS-CoV-2 infection in people with cystic fibrosis
R Cosgriff, S Ahern, SC Bell, K Brownlee, PR Burgel, C Byrnes, H Corvol, ...
Journal of cystic fibrosis 19 (3), 355-358, 2020
1472020
The system can't perform the operation now. Try again later.
Articles 1–20