Evidence map›Paper›PMID 34828289›Full record

ArticleGenes2021

Chronic Pancreatitis: The True Pathogenic Culprit within the

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

Open access · goldAbstract read
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Phenotypic and Genetic Diversity in Diabetes Across Populations.The Journal of clinical endocrinology and metabolism · 2025
    Review
  5. Review
  6. Review
  7. Article
  8. Article
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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

6 authors at 2 institutions in 3 countries.

Na PuInserm, Univ Brest, EFS, UMR 1078, GGB, F-29200 Brest, France.
Emmanuelle MassonInserm, Univ Brest, EFS, UMR 1078, GGB, F-29200 Brest, France.
David N CooperInstitute of Medical Genetics, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK.ORCID 0000-0002-8943-8484
Emmanuelle GéninInserm, Univ Brest, EFS, UMR 1078, GGB, F-29200 Brest, France.ORCID 0000-0003-4117-2813
Claude FérecInserm, Univ Brest, EFS, UMR 1078, GGB, F-29200 Brest, France.
Jian-Min ChenInserm, Univ Brest, EFS, UMR 1078, GGB, F-29200 Brest, France.ORCID 0000-0002-2424-3969
Inserm · FRCardiff University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A diverse range of loss-of-function variants in the

Indexed as

Mutation, MissenseBinding SitesGene FrequencyGenetic Predisposition to DiseaseHumansLinkage DisequilibriumLoss of Function MutationPancreatitis, ChronicPromoter Regions, GeneticTrypsin Inhibitor, Kazal PancreaticSPINK1 protein, humanTrypsin Inhibitor, Kazal Pancreaticchronic pancreatitisenhancerlinkage disequilibriumregulatory variantSPINK1 gene

Identifiers

PMID34828289
PMCPMC8619230
OpenAlexW3210059080

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.