Evidence map›Paper›PMID 25602001›Full record

ArticleCMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne2015

Old meets new: identifying founder mutations in genetic disease.

Jane A Evans

Open access · goldAbstract readComment
In one paragraph

Article in CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Autosomal recessiveFrontiers in immunology · 2023
    Article
  5. TheCancers · 2021
    Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Jane A EvansBiochemistry and Medical Genetics, University of Manitoba, Winnipeg, Man. jevans@ms.umanitoba.ca.
University of Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Founder EffectCarbohydrate Metabolism, Inborn ErrorsFemaleGlycogen Debranching Enzyme SystemGlycogen Storage Disease Type IIIHumansInuitMaleMutationSucrase-Isomaltase ComplexGlycogen Debranching Enzyme SystemSucrase-Isomaltase Complex

Identifiers

PMID25602001
PMCPMC4312142
OpenAlexW1979984878

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.