Evidence map›Paper›PMID 28224991›Full record

ArticleEuropean journal of human genetics : EJHG2017

Prevalence of congenital amusia.

Isabelle Peretz, Dominique T Vuvan

Open access · bronzeAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 133 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Beyond the notes: Clarifying the role of expressivity in conveying musical emotion.Quarterly journal of experimental psychology (2006) · 2026
    Article
  4. Article
  5. Article
  6. Effects of vocal-motor interference on vocal pitch imitation.Attention, perception & psychophysics · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Web-based psychoacoustics of binaural hearing: Two validation experiments.The Journal of the Acoustical Society of America · 2023
    Article
  16. Article
  17. Article
  18. FORUM: Remote testing for psychological and physiological acoustics.The Journal of the Acoustical Society of America · 2022
    Article
  19. Congenital amusia-pathology of musical disorder.Journal of applied genetics · 2022
    Review
  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 at 1 institution in 1 country.

Isabelle PeretzBRAMS Laboratory and Department of Psychology, University of Montreal, Montreal, QC, Canada.
Dominique T VuvanBRAMS Laboratory and Department of Psychology, University of Montreal, Montreal, QC, Canada.
Université de Montréal · CA

Funding

CIHR
6 · The paper itself

Abstract

Congenital amusia (commonly known as tone deafness) is a lifelong musical disorder that affects 4% of the population according to a single estimate based on a single test from 1980. Here we present the first large-based measure of prevalence with a sample of 20 000 participants, which does not rely on self-referral. On the basis of three objective tests and a questionnaire, we show that (a) the prevalence of congenital amusia is only 1.5%, with slightly more females than males, unlike other developmental disorders where males often predominate; (b) self-disclosure is a reliable index of congenital amusia, which suggests that congenital amusia is hereditary, with 46% first-degree relatives similarly affected; (c) the deficit is not attenuated by musical training and (d) it emerges in relative isolation from other cognitive disorder, except for spatial orientation problems. Hence, we suggest that congenital amusia is likely to result from genetic variations that affect musical abilities specifically.

Indexed as

Genetic VariationAdolescentAdultAgedAuditory Perceptual DisordersFemaleHumansMaleMiddle AgedPrevalenceSex Factors

Identifiers

PMID28224991
PMCPMC5437896
OpenAlexW2511357225

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.