Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population (Q28603932)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27100778%20AND%20SRC:MED&resulttype=core&format=json

2 April 2020

title

Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population (English)

1 reference

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2 April 2020

4

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2 April 2020

author name string

Yuping Zhang

1

1 reference

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2 April 2020

Jun Li

2

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2 April 2020

Shuang Song

3

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2 April 2020

Margit Burmeister

5

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2 April 2020

Sandra M Villafuerte

6

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2 April 2020

Mengmeng Su

7

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2 April 2020

Catherine McBride

8

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2 April 2020

Hua Shu

9

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2 April 2020

language of work or name

English

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publication date

21 April 2016

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2 April 2020

1 reference

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2 April 2020

volume

11

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2 April 2020

issue

4

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2 April 2020

page(s)

e0153603

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Creative Commons Attribution 4.0 International

2 April 2020

copyright license

start time

21 April 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

17 March 2017

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Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

17 March 2017

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DCDC2 is associated with reading disability and modulates neuronal development in the brain

17 March 2017

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Modeling the Etiology of Individual Differences in Early Reading Development: Evidence for Strong Genetic Influences

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The genetic and environmental etiologies of individual differences in early reading growth in Australia, the United States, and Scandinavia

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The Genetic and Environmental Foundation of the Simple View of Reading in Chinese

29 September 2017

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29 September 2017

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Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.

29 September 2017

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29 September 2017

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29 September 2017

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Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat

29 September 2017

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29 September 2017

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3 June 2018

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21 January 2018

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Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

21 January 2018

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The role of gene DCDC2 in German dyslexics.

21 January 2018

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21 January 2018

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Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.

21 January 2018

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Orthographic depth and its impact on universal predictors of reading: a cross-language investigation.

21 January 2018

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Developmental trajectories of reading development and impairment from ages 3 to 8 years in Chinese children.

21 January 2018

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Phonological awareness in young Chinese children.

21 January 2018

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Statistical power analyses using G*Power 3.1: tests for correlation and regression analyses.

21 January 2018

1 reference

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Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.

21 January 2018

1 reference

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21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/27100778

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0153603

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27100778%20AND%20SRC:MED&resulttype=core&format=json

2 April 2020

ADS bibcode

2016PLoSO..1153603Z

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27100778%20AND%20SRC:MED&resulttype=core&format=json

2 April 2020

2 references