Evidence map›Paper›PMID 30815537›Full record

ArticleWellcome open research2018

Language phenotypes in children with sex chromosome trisomies.

Dorothy V M Bishop, Annie Brookman-Byrne, Nikki Gratton, Elaine Gray, Georgina Holt, Louise Morgan, Sarah Morris, Eleanor Paine, Holly Thornton, Paul A Thompson

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Wellcome open research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. A cross-sectional study of early language abilities in children with sex chromosome trisomy (XXY, XXX, XYY) aged 1-6 years.Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence · 2022
    Article
  9. Observational
  10. Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis.American journal of medical genetics. Part C, Seminars in medical genetics · 2020
    Article
  11. Review
  12. Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child.American journal of medical genetics. Part C, Seminars in medical genetics · 2020
    Article
  13. Article
  14. 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

10 authors at 1 institution in 1 country.

Dorothy V M BishopDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.ORCID https://orcid.org/0000-0002-2448-4033
Annie Brookman-ByrneDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.ORCID https://orcid.org/0000-0001-7953-8062
Nikki GrattonDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.
Elaine GrayDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.
Georgina HoltDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.ORCID https://orcid.org/0000-0003-4233-8731
Louise MorganDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.
Sarah MorrisDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.ORCID https://orcid.org/0000-0002-5659-9492
Eleanor PaineDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.
Holly ThorntonDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.
Paul A ThompsonDepartment of Experimental Psychology, University of Oxford, Oxford, Oxon, OX2 6GG, UK.ORCID https://orcid.org/0000-0001-9940-6913
University of Oxford · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ascertainment biasKlinefelter syndromeparent reportpsychometric testingTrisomy XvariabilityXYY syndrome

Identifiers

PMID30815537
PMCPMC6376256
OpenAlexW2899993386

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.