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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: Apr 25, 2024
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Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID.
Deanna M Green et al. Pediatrics 2024
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Genetic testing for diffuse lung diseases in children.
Aaron Hamvas et al. Pediatr Pulmonol 2023
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Perceptions of airway gene therapy for cystic fibrosis.
Donnelley Martin et al. Expert opinion on biological therapy 2022
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Gene therapy for cystic fibrosis: Challenges and prospects.
Sui Hongshu et al. Frontiers in pharmacology 2022 131015926
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Effect of Physical Activity Program on the Quality of Life of Children with Cystic Fibrosis at School Age: A Randomized Clinical Trail.
Hakim Ashrafalsadat et al. Tanaffos 2022 21(1) 63-69
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Screening for idiopathic pulmonary fibrosis using comorbidity signatures in electronic health records.
Onishchenko Dmytro et al. Nature medicine 2022
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The Effectiveness of Nintedanib in Patients with Idiopathic Pulmonary Fibrosis, Familial Pulmonary Fibrosis and Progressive Fibrosing Interstitial Lung Diseases: A Real-World Study.
Cameli Paolo et al. Biomedicines 2022 10(8)
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Genetic testing in interstitial lung disease: An international survey.
Terwiel Michelle et al. Respirology (Carlton, Vic.) 2022
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Perceptions of Genetic Testing: A Mixed-methods Study of Patients with Pulmonary Fibrosis and their First-degree Relatives.
Grant-Orser Amanda et al. Annals of the American Thoracic Society 2022
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State-of-the-art review of lung imaging in cystic fibrosis with recommendations for pulmonologists and radiologists from the "iMAging managEment of cySTic fibROsis" (MAESTRO) consortium.
Ciet Pierluigi et al. European respiratory review : an official journal of the European Respiratory Society 2022 31(163)
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X-Linked Agammaglobulinemia: Infection Frequency and Infection-Related Mortality in the USIDNET Registry.
O'Toole Dana et al. Journal of clinical immunology 2022
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Elexacaftor/Tezacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for the F508del Mutation and Advanced Lung Disease: A 48-Week Observational Study.
Carnovale Vincenzo et al. Journal of clinical medicine 2022 11(4)
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Seasonal variation of lung function in cystic fibrosis: longitudinal modeling to compare a Midwest US cohort to international populations.
Gecili Emrah et al. The Science of the total environment 2022 776
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Toward a Conversational Agent to Support the Self-Management of Adults and Young Adults With Sickle Cell Disease: Usability and Usefulness Study.
Issom David-Zacharie et al. Frontiers in digital health 2021 3600333
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Effectiveness and safety of elexacaftor/tezacaftor/ivacaftor in patients with cystic fibrosis and advanced lung disease with the Phe508del/minimal function genotype.
Carnovale Vincenzo et al. Respiratory medicine 2021 189106646
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Staphylococcus aureus and Cystic Fibrosis-A Close Relationship. What Can We Learn from Sequencing Studies?
Rumpf Christine et al. Pathogens (Basel, Switzerland) 2021 10(9)
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Ethical dilemma: ELX/TEZ/IVA or Lung Transplantation in Cystic Fibrosis and End Stage Lung Disease?
Breuer Oded et al. Chest 2021
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Quantification of Phenotypic Variability of Lung Disease in Children with Cystic Fibrosis.
Stahl Mirjam et al. Genes 2021 12(6)
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Use of a Genomic Classifier in Patients with Interstitial Lung Disease: A Systematic Review.
Kheir Fayez et al. Annals of the American Thoracic Society 2021
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Gene Therapy: A Possible Alternative to CFTR Modulators?
Mercier J et al. Frontiers in pharmacology 2021 12648203
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Risk factors for illness severity among pregnant women with confirmed SARS-CoV-2 infection - Surveillance for Emerging Threats to Mothers and Babies Network, 20 state, local, and territorial health departments, March 29, 2020 -January 8, 2021
RR Galang et al, MEDRXIV, March 1, 2021
Family History of Pulmonary Fibrosis Predicts Worse Survival in Patients with Interstitial Lung Disease.
Cutting Claire et al. Chest 2021 Jan
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Current and novel therapeutic strategies for the management of cystic fibrosis.
Gbian Douweh Leyla et al. Expert opinion on drug delivery 2021 Jan
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TPMT and HLA-DQA1-HLA-DRB genetic profiling to guide the use of azathioprine in the treatment of interstitial lung disease: First experience.
Taha Nada et al. Pulmonary pharmacology & therapeutics 2021 Jan 66101988
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Host genetic effects in pneumonia.
Chen Hung-Hsin et al. American journal of human genetics 2020 Dec
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Early disease surveillance in young children with cystic fibrosis: A qualitative analysis of parent experiences.
Douglas Tonia A et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2020 Oct
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Protocol for Project Fizzyo, an analytic longitudinal observational cohort study of physiotherapy for children and young people with cystic fibrosis, with interrupted time-series design.
Raywood Emma et al. BMJ open 2020 Oct 10(10) e039587
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Newborn screening alone insufficient to improve pulmonary outcomes for cystic fibrosis.
Barreda Christina B et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2020 Jun
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Comparative diagnostic efficacy of serum Krebs von den Lungen-6 and surfactant D for connective tissue disease-associated interstitial lung diseases: A meta-analysis.
Zhong Danli et al. Medicine 2020 Apr 99(16) e19695
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Alpha-1 Antitrypsin Deficiency and Pregnancy.
Gaeckle Nate T et al. COPD 2020 Apr 1-7
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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