Evidence map›Paper›PMID 28601843›Full record

ArticleGut2018

Emmanuelle Masson, Jian-Min Chen, David N Cooper, Claude Férec

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Gut, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 3 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

5 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Role of the CommonGenes · 2020
    Pooled it
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Emmanuelle MassonInstitut National de la Santé et de la Recherche Médicale (INSERM), U1078 Brest, France.
Jian-Min ChenInstitut National de la Santé et de la Recherche Médicale (INSERM), U1078 Brest, France.ORCID 0000-0002-2424-3969
David N CooperFaculté de Médecine et des Sciences de la Santé, Université de Bretagne Occidentale (UBO), Brest, France.
Claude FérecInstitut National de la Santé et de la Recherche Médicale (INSERM), U1078 Brest, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DNA Copy Number VariationsPolymorphism, GeneticGenetic Predisposition to DiseaseMutationPancreatitisTrypsinTrypsinchronic pancreatitiscopy number variantduplicationpromoter variantPRSS1gene

Identifiers

PMID28601843

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.