Garry R Cutting


1988 …2019
If you made any changes in Pure, your changes will be visible here soon.

Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 2 Similar Profiles
Cystic Fibrosis Medicine & Life Sciences
Cystic Fibrosis Transmembrane Conductance Regulator Medicine & Life Sciences
Mutation Medicine & Life Sciences
Regulator Genes Medicine & Life Sciences
Lung Diseases Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Genes Medicine & Life Sciences
Chloride Channels Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1988 2019

Acquired cystic fibrosis transmembrane conductance regulator dysfunction and radiographic bronchiectasis in current and former smokers: A cross-sectional study

Teerapuncharoen, K., Michael Wells, J., Vamsee Raju, S., Raraigh, K. S., Aksit, M. A., Cutting, G. R., Rasmussen, L., Hrudaya Nath, P., Bhatt, S. P., Solomon, G. M., Dransfield, M. T. & Rowe, S. M., Jan 1 2019, In : Annals of the American Thoracic Society. 16, 1, p. 150-153 4 p.

Research output: Contribution to journalLetter

Cystic Fibrosis Transmembrane Conductance Regulator
Cross-Sectional Studies

49 - Genetics and Pathophysiology of Cystic Fibrosis

Cutting, G. R., Engelhardt, J. & Zeitlin, P. L., Mar 8 2018, Kendig's Disorders of the Respiratory Tract in Children. Elsevier Inc., p. 757-768.e6

Research output: Chapter in Book/Report/Conference proceedingChapter

Cystic Fibrosis
Mucociliary Clearance
Precision Medicine
Chronic Obstructive Pulmonary Disease

AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations

Darrah, R. J., Jacono, F. J., Joshi, N., Mitchell, A. L., Sattar, A., Campanaro, C. K., Litman, P., Frey, J., Nethery, D. E., Barbato, E. S., Hodges, C. A., Corvol, H., Cutting, G. R., Knowles, M. R., Strug, L. J. & Drumm, M. L., Jan 1 2018, (Accepted/In press) In : Journal of Cystic Fibrosis.

Research output: Contribution to journalArticle

Cystic Fibrosis
Genome-Wide Association Study
Lung Diseases

Airway mucosal host defense is key to genomic regulation of cystic fibrosis lung disease severity

Polineni, D., Dang, H., Gallins, P. J., Jones, L. C., Pace, R. G., Stonebraker, J. R., Commander, L. A., Krenicky, J. E., Zhou, Y. H., Corvol, H., Cutting, G. R., Drumm, M. L., Strug, L. J., Boyle, M. P., Durie, P. R., Chmiel, J. F., Zou, F., Wright, F. A., O’Neal, W. K. & Knowles, M. R., Jan 1 2018, In : American Journal of Respiratory and Critical Care Medicine. 197, 1, p. 79-93 15 p.

Research output: Contribution to journalArticle

Cystic Fibrosis
Lung Diseases
Genome-Wide Association Study
Gene Expression
Cystic Fibrosis Transmembrane Conductance Regulator

Capitalizing on the heterogeneous effects of CFTR nonsense and frameshift variants to inform therapeutic strategy for cystic fibrosis

Sharma, N., Evans, T. A., Pellicore, M. J., Davis, E., Aksit, M. A., McCague, A. F., Joynt, A. T., Lu, Z., Han, S. T., Anzmann, A. F., Lam, A. T. N., Thaxton, A., West, N. E., Merlo, C., Gottschalk, L. B., Raraigh, K. S., Sosnay, P. R., Cotton, C. U. & Cutting, G. R., Nov 1 2018, In : PLoS genetics. 14, 11, e1007723.

Research output: Contribution to journalArticle

cystic fibrosis
Cystic Fibrosis
Nonsense Codon