Cystic fibrosis ▲ Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)

Last Posted: Dec-16-2016 7AM

 Cystic Fibrosis expanded expanded

Associations between genetics, medical status, physical exercise and psychological well-being in adults with cystic fibrosis.
Backström-Eriksson Lena et al. BMJ open respiratory research 2016 3(1) e000141

Differences in Outcomes between Early and Late Diagnosis of Cystic Fibrosis in the Newborn Screening Era.
Coffey Michael J et al. The Journal of pediatrics 2016 Nov

Babies with CF Not Diagnosed in Newborn Screenings Do More Poorly, Study Finds
J Fernandez, CF Foundation, November 18, 2016

More information on this topic

Last Updated: Dec 14, 2016

• Associations between genetics, medical status, physical exercise and psychological well-being in adults with cystic fibrosis.
  Backström-Eriksson Lena et al. BMJ open respiratory research 2016 3(1) e000141
• Babies with CF Not Diagnosed in Newborn Screenings Do More Poorly, Study Finds
  J Fernandez, CF Foundation, November 18, 2016
• Differences in Outcomes between Early and Late Diagnosis of Cystic Fibrosis in the Newborn Screening Era.
  Coffey Michael J et al. The Journal of pediatrics 2016 Nov
• Cystic fibrosis: to screen or not to screen? Involving a Citizens' jury in decisions on screening carrier.
  Mosconi Paola et al. Health expectations : an international journal of public participation in health care and health policy 2015 Dec 18(6) 1956-67
• Identification of Burkholderia and Uncommon Glucose Non-fermenting Gram-Negative Bacilli Isolated from Patients with Cystic Fibrosis using Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS).
  Plongla Rongpong, Panagea Theofano, Pincus David H, Jones Melissa C, Gilligan Peter H.Journal of clinical microbiology 2016 Oct
• CFTR pharmacology.
  Zegarra-Moran Olga et al. Cellular and molecular life sciences : CMLS 2016 Oct
• Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives.
  Schmidt Béla Z et al. Clinical pharmacology : advances and applications 2016 127-140
• Cystic fibrosis: a clinical view.
  Castellani Carlo et al. Cellular and molecular life sciences : CMLS 2016 Oct
• Genetic medicines for CF: Hype versus reality.
  Alton Eric W F W et al. Pediatric pulmonology 2016 Oct (S44) S5-S17
• New App for Cystic Fibrosis Patients Helps to Manage Symptoms
  Global Genes, 2016
• Parent Experience With False-Positive Newborn Screening Results for Cystic Fibrosis.
  Hayeems Robin Z et al. Pediatrics 2016 Aug
• Non-invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis.
  Hill Melissa et al. Prenatal diagnosis 2015 Oct 35(10) 950-8
• Showing Value in Newborn Screening: Challenges in Quantifying the Effectiveness and Cost-Effectiveness of Early Detection of Phenylketonuria and Cystic Fibrosis
  Disease: NA; Type: Data; State: Multiple States
• Toward quality improvement in cystic fibrosis newborn screening: Progress and continuing challenges.
  Farrell Philip M et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2016 May
• The Cystic Fibrosis Foundation Patient Registry: Design and Methods of a National Observational Disease Registry.
  Knapp Emily A et al. Annals of the American Thoracic Society 2016 Apr

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• Pathogen (4)

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• Guidelines (5)
• Tier Table (1)
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• Huamn (15)
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Relevant Resources

• Genetics and Genomics Competencies Center (G2C2)
• NIH Genetic Testing Registry
• NIH MedGen Database
• Online Mendelian Inheritance in Man (OMIM)
• PharmGKB