Evidence map›Paper›PMID 28361094›Full record

ArticleMolecular genetics & genomic medicine2017

Genetic contributions to stuttering: the current evidence.

Carlos Frigerio-Domingues, Dennis Drayna

Abstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. The Significance of a Higher Prevalence of ADHD and ADHD Symptoms in Children Who Stutter.Journal of speech, language, and hearing research : JSLHR · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Factors Associated With Symptoms of Anxiety and Depression in Children Who Stutter.Language, speech, and hearing services in schools · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Stuttering as a spectrum disorder: A hypothesis.Current research in neurobiology · 2023
    Review
  19. Article
  20. Article
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.

Carlos Frigerio-DominguesNational Institute on Deafness and Other Communication Disorders Porter Neuroscience Research Center National Institutes of Health.
Dennis DraynaNational Institute on Deafness and Other Communication Disorders Porter Neuroscience Research Center National Institutes of Health.ORCID 0000-0002-1730-4532

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence for genetic factors in persistent developmental stuttering has accumulated over the past four decades, and the genes that underlie this disorder are starting to be identified. The genes identified to date, all point to deficits in intracellular trafficking in this disorder.

Identifiers

PMID28361094
PMCPMC5370225

What OpenQuestion holds

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Registered trials

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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.