Evidence map›Paper›PMID 23028439›Full record

ArticlePloS one2012

Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population.

Yuping Zhang, Jun Li, Twila Tardif, Margit Burmeister, Sandra M Villafuerte, Catherine McBride-Chang, Hong Li, Bingjie Shi, Weilan Liang, Zhixiang Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

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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

11 authors at 6 institutions in 2 countries.

Yuping ZhangState Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China.
Jun Li
Twila Tardif
Margit Burmeister
Sandra M Villafuerte
Catherine McBride-Chang
Hong Li
Bingjie Shi
Weilan Liang
Zhixiang Zhang
Hua Shu
Beijing Normal University · CNUniversity of Michigan–Ann Arbor · USChinese University of Hong Kong · CNMichigan United · USPeking University · CNPeking University First Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several independent studies have supported the association of DYX1C1 with dyslexia, but its role in general reading development remains unclear. Here, we investigated the contribution of this gene to reading, with a focus on orthographic skills, in a sample of 284 unrelated Chinese children aged 5 to 11 years who were participating in the Chinese Longitudinal Study of Reading Development. We tested this association using a quantitative approach for Chinese character reading, Chinese character dictation, orthographic judgment, and visual skills. Significant or marginally significant associations were observed at the marker rs11629841 with children's orthographic judgments at ages 7 and 8 years (all P values<0.020). Significant associations with Chinese character dictation (all P values<0.013) were also observed for this single-nucleotide polymorphism (SNP) at ages 9, 10, and 11 years. Further analyses revealed that the association with orthographic skills was specific to the processing of specific components of characters (P values<0.046). No association was found at either SNP of rs3743205 or rs57809907. Our findings suggest that DYX1C1 influences reading development in the general Chinese population and supports a universal effect of this gene.

Indexed as

Genetic Predisposition to DiseaseAsian PeopleChildChild, PreschoolChinaCytoskeletal ProteinsDyslexiaFemaleGenotypeHumansJudgmentMaleNerve Tissue ProteinsNuclear ProteinsPhenotypePolymorphism, Single NucleotideCytoskeletal ProteinsDNAAF4 protein, humanNerve Tissue ProteinsNuclear Proteins

Identifiers

PMID23028439
PMCPMC3441603
OpenAlexW2116324693

What OpenQuestion holds

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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.