Evidence map›Paper›PMID 9708232›Full record

ReviewThorax1998

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

D J Davidson, D J Porteous

Abstract readReview
In one paragraph

Review in Thorax, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Multidisciplinary approach to patients with manifestations and pulmonary complications of cystic fibrosis.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
  8. 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

2 authors.

D J DavidsonMRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
D J Porteous

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genes, RecessiveAnimalsBacterial InfectionsCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDisease Models, AnimalGene DeletionHumansMiceMutationCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID9708232
PMCPMC1745224

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.