Garry R. Cutting

Affiliations: 
Johns Hopkins University, Baltimore, MD 
Area:
Molecular Biology, Genetics, Cell Biology
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"Garry Cutting"
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Publications

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Bihler H, Sivachenko A, Millen L, et al. (2024) In vitro modulator responsiveness of 655 CFTR variants found in people with cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
Kleinfelder K, Lotti V, Eramo A, et al. (2023) analysis and theratyping of an ultra-rare CFTR genotype (W57G/A234D) in primary human rectal and nasal epithelial cells. Iscience. 26: 108180
Mention K, Cavusoglu-Doran K, Joynt AT, et al. (2023) Use of adenine base editing and homology-independent targeted integration strategies to correct the cystic fibrosis causing variant, W1282X. Human Molecular Genetics
Joynt AT, Kavanagh EW, Newby GA, et al. (2023) Protospacer modification improves base editing of a canonical splice site variant and recovery of CFTR function in human airway epithelial cells. Molecular Therapy. Nucleic Acids. 33: 335-350
Joynt AT, Cutting GR, Sharma N. (2022) Genetics of Cystic Fibrosis: Clinical Implications. Clinics in Chest Medicine. 43: 591-602
Aksit MA, Ling H, Pace RG, et al. (2022) Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis. American Journal of Human Genetics. 109: 1894-1908
Raraigh KS, Paul KC, Goralski JL, et al. (2022) CFTR bearing variant p.Phe312del exhibits function inconsistent with phenotype and negligible response to ivacaftor. Jci Insight. 7
Sun Q, Liu W, Rosen JD, et al. (2022) Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients. Hgg Advances. 3: 100090
Saferali A, Qiao D, Kim W, et al. (2022) variants are associated with chronic bronchitis in smokers. The European Respiratory Journal
Collaco JM, Raraigh KS, Betz J, et al. (2021) Accurate assignment of disease liability to genetic variants using only population data. Genetics in Medicine : Official Journal of the American College of Medical Genetics
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