Evidence map›Paper›PMID 15477871›Full record

ArticleMolecular psychiatry2005

No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia.

N A Cope, G Hill, M van den Bree, D Harold, V Moskvina, E K Green, M J Owen, J Williams, M C O'Donovan

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
7.7field-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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2013
    Pooled it
  2. Article
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  13. Review
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  17. Review
  18. Genetics of developmental dyslexia.European child & adolescent psychiatry · 2010
    Review
  19. Article
  20. The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2008
    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

9 authors at 1 institution in 1 country.

N A Cope
G Hill
M van den Bree
D Harold
V Moskvina
E K Green
M J Owen
J Williams
M C O'Donovan
University of Wales · GB

Funding

Medical Research Council G9810900
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosomes, Human, Pair 15Genetic MarkersAdolescentChildDyslexiaGenetic Predisposition to DiseaseHumansGenetic Markers

Identifiers

PMID15477871
OpenAlexW2009605026

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.