(Q48700980)

14 February 2018

title

No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy. (English)

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14 February 2018

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6

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author name string

Giulia Bellini

1

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14 February 2018

Carmela Bravaccio

2

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14 February 2018

Filippo Calamoneri

3

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14 February 2018

Maria Donatella Cocuzza

4

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14 February 2018

Pasquale Fiorillo

5

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14 February 2018

Domenico Mazzone

7

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14 February 2018

Emanuele Miraglia del Giudice

8

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14 February 2018

Geoffredo Scuccimarra

9

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14 February 2018

Roberto Militerni

10

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14 February 2018

Antonio Pascotto

11

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14 February 2018

publication date

1 January 2005

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14 February 2018

Journal of Molecular Neuroscience

published in

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14 February 2018

volume

27

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14 February 2018

issue

3

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14 February 2018

page(s)

311-314

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14 February 2018

https://scigraph.springernature.com/pub.10.1385/jmn:27:3:311

exact match

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cites work

A new gene (DYX3) for dyslexia is located on chromosome 2

1 reference

12 December 2020

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

1 reference

12 December 2020

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

1 reference

12 December 2020

Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.

1 reference

12 December 2020

A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5.

1 reference

12 December 2020

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

1 reference

12 December 2020

A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.

1 reference

12 December 2020

A dominant gene for developmental dyslexia on chromosome 3

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12 December 2020

Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p.

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12 December 2020

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.

1 reference

12 December 2020

The first candidate gene for dyslexia: Turning the page of a new chapter of research

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12 December 2020

Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability.

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12 December 2020

Cross-national comparisons of developmental dyslexia in Italy and the United States

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12 December 2020

Developmental dyslexia

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12 December 2020

X-chromosome as a marker for population history: linkage disequilibrium and haplotype study in Eurasian populations

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12 December 2020

Annotation: Genetics of reading and spelling disorder

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12 December 2020

Dyslexia: cultural diversity and biological unity

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12 December 2020

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

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12 December 2020

The genetics of dyslexia

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12 December 2020

Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families

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12 December 2020

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

1 reference

12 December 2020

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

1 reference

12 December 2020

Identifiers

DOI

10.1385/JMN:27:3:311

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14 February 2018

Dimensions Publication ID

1022843220

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14 February 2018