Strong motion deficits in dyslexia associated with DCDC2 gene alteration (Q36956227)

17 August 2017

Strong motion deficits in dyslexia associated with DCDC2 gene alteration (English)

1 reference

17 August 2017

0 references

Maria Concetta Morrone

Maria Concetta Morrone

5

0 references

Sara Mascheretti

Sara Mascheretti

3

0 references

Cecilia Marino

Cecilia Marino

2

0 references

Guido M. Cicchini

Guido Marco Cicchini

1

0 references

author name string

Daniela Perani

4

1 reference

PMCID

4888943

17 August 2017

language of work or name

English

0 references

publication date

1 May 2015

1 reference

17 August 2017

Journal of Neuroscience

1 reference

17 August 2017

35

1 reference

17 August 2017

21

1 reference

17 August 2017

8059-8064

1 reference

Speed discrimination predicts word but not pseudo-word reading rate in adults and children.

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Molecular genetics of dyslexia: an overview

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

The dyslexia-associated gene DCDC2 is required for spike-timing precision in mouse neocortex

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Abnormal visual motion processing is not a cause of dyslexia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

DCDC2 genetic variants and susceptibility to developmental dyslexia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

A dyslexia-associated variant in DCDC2 changes gene expression

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Contrast responsivity in MT+ correlates with phonological awareness and reading measures in children

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Genetics of dyslexia: the evolving landscape

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

The Italian preadolescent mental health project (PrISMA): rationale and methods.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

The tale is in the tail: an alternative hypothesis for psychophysical performance variability in dyslexia.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Evidence for a magnocellular defect in developmental dyslexia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Specific reading disability: differences in contrast sensitivity as a function of spatial frequency.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Developmental dyslexia: four consecutive patients with cortical anomalies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Cytoarchitectonic abnormalities in developmental dyslexia: A case study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Contrast sensitivity and coherent motion detection measured at photopic luminance levels in dyslexics and controls.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Auditory cytoarchitectonic abnormalities in a case of familial developmental dyslexia.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Dyslexia: a deficit in visuo-spatial attention, not in phonological processing.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

The role of gene DCDC2 in German dyslexics.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Inversion of perceived direction of motion caused by spatial undersampling in two children with periventricular leukomalacia.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Directional motion contrast sensitivity in developmental dyslexia.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Two visual motion processing deficits in developmental dyslexia associated with different reading skills deficits.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Contrast sensitivity in subgroups of developmental dyslexia.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Disabled readers suffer from visual and auditory impairments but not from a specific magnocellular deficit.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

To see but not to read; the magnocellular theory of dyslexia.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

QUEST: a Bayesian adaptive psychometric method.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4888943

Psychophysical evidence for a magnocellular pathway deficit in dyslexia

4 September 2018

1 reference

12 December 2020

Spatio-temporal contrast sensitivity, coherent motion, and visible persistence in developmental dyslexia

1 reference

12 December 2020

Visual deficits in pre-readers at familial risk for dyslexia

1 reference

12 December 2020

Selective depression of motion sensitivity during saccades

1 reference

12 December 2020

10.1523/JNEUROSCI.5077-14.2015

Identifiers

DOI

1 reference

17 August 2017

1 reference

17 August 2017

1 reference

PMCID

4888943