Garry R. Cutting

University of North Carolina at Chapel Hill — United States

Medicine · Health Sciences

84h-index25.5kcitations374works8.82yr avg
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Research Topics

Cystic Fibrosis Research Advances(216), Neonatal Respiratory Health Research(107), Tracheal and airway disorders(59), Genomics and Rare Diseases(49), Congenital Ear and Nasal Anomalies(23)

Publications372 total

Base editing and nanoparticle transfection of airway cell types essential for treatment of cystic fibrosis
2025
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients.
UNC Libraries·2025Open Access
MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric
UNC Libraries·2025Open Access
Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis
UNC Libraries·2025Open Access
Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients
UNC Libraries·2025Open Access
288 Evidence against synonymous polymorphism neutrality with rare CFTR variants that display altered modulator responsiveness and clinical phenotype
Journal of Cystic Fibrosis·2025
Diseases Common in Persons With Cystic Fibrosis Among <i>CFTR</i> Heterozygotes
JAMA Internal Medicine·2025· 1 cited
MagicalRsq: Machine-learning-based genotype imputation quality calibration
UNC Libraries·2025Open Access
Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria
Genetics in Medicine·2025· 30 citedOpen Access
<i>CHP2</i> Modifies Chronic <i>Pseudomonas aeruginosa</i> Airway Infection Risk in Cystic Fibrosis
Annals of the American Thoracic Society·2025Open Access
Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1B
JCI Insight·2024· 2 citedOpen Access
Author Correction: Standardizing variant naming in literature with VariantValidator to increase diagnostic rates
Nature Genetics·2024Open Access
Standardizing variant naming in literature with VariantValidator to increase diagnostic rates
Nature Genetics·2024· 10 citedOpen Access
Genetic modifiers of body mass index in individuals with cystic fibrosis
The American Journal of Human Genetics·2024· 1 citedOpen Access
343 Identification of candidate sites for superexon insertion in CFTR intron 1
Journal of Cystic Fibrosis·2024
Deep resequencing of CFTR in 762 F508del homozygotes reveals clusters of non-coding variants associated with cystic fibrosis disease traits
UNC Libraries·2024Open Access
Ligand-free biodegradable poly(beta-amino ester) nanoparticles for targeted systemic delivery of mRNA to the lungs
Biomaterials·2024· 21 citedOpen Access
Investigation of CFTR Function in Human Nasal Epithelial Cells Informs Personalized Medicine
American Journal of Respiratory Cell and Molecular Biology·2024· 6 citedOpen Access
Establishment of a conditionally reprogrammed primary eccrine sweat gland culture for evaluation of tissue-specific CFTR function
Journal of Cystic Fibrosis·2024· 3 citedOpen Access
The clinical utility of sequencing the entirety of CFTR
Journal of Cystic Fibrosis·2024· 3 cited
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Frequent Co-authors

William B. Guggino(9), Scott M. Blackman(7), Peter R. Durie(6), Julian Zielenski(6), Michael R. Knowles(6), Beryl J. Rosenstein(5), Johanna M. Rommens(5), Milan Maçek(5), Steven M. Harrison(5), John E. Mickle(5), Kathleen Naughton(5), Rachel Karchin(4), Mary Corey(4), Marc S. Greenblatt(4), Sean V. Tavtigian(4), Leslie G. Biesecker(4), Rhonda G. Pace(4), Jaclyn R. Stonebraker(4), Joseph M. Collaco(4), Lei Sun(4)