Evidence map›Paper›PMID 17202292›Full record

ReviewProceedings of the American Thoracic Society2007

Strategies for identifying modifier genes in cystic fibrosis.

Michael P Boyle

Abstract readReview
In one paragraph

Review in Proceedings of the American Thoracic Society, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Role of theInternational journal of molecular sciences · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Saturation of the human phenome.Current genomics · 2010
    Article
  13. Myeloperoxidase-dependent oxidative metabolism of nitric oxide in the cystic fibrosis airway.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2010
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Atypical cystic fibrosis and CFTR-related diseases.Clinical reviews in allergy & immunology · 2008
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Michael P BoyleDepartment of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA. mboyle@jhmi.edu

Funding

Genetic Modifiers of Cystic Fibrosis: Sibling StudyR01HL068927 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CUTTING, GARRY R · 2001 to 2011
$8.9M
Genetic Modifiers of Cystic FibrosisK23HL071847 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BOYLE, MICHAEL P · 2003 to 2007
$657k
NHLBI NIH HHS K23-HL071847NHLBI NIH HHS R01-HL68927PHS HHS R025CR02
6 · The paper itself

Abstract

Even in patients with cystic fibrosis (CF) with identical CFTR genotypes, there is a wide range in the severity of lung disease, with some individuals facing death or lung transplantation early in life and others demonstrating mild lung disease well into adulthood. Although numerous environmental factors have been identified that influence CF pulmonary phenotype, there is now growing evidence that polymorphic variants in genes besides CFTR play an important role in determining severity of CF lung disease. This article reviews the most recent findings regarding genetic modifiers in CF and also discusses in detail the strategies currently being used to identify novel modifiers of CF pulmonary phenotype. These include single- and multicenter studies, twin and sib studies, microarray approaches, and whole genome association studies.

Indexed as

Polymorphism, GeneticCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorGenotypeHumansMutationOligonucleotide Array Sequence AnalysisPhenotypeCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID17202292
PMCPMC2647615

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.