(Q30529633)

English

Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

0 references

reading disability

1 reference

based on heuristic

inferred from title

Cheryl M Lacadie

6

object named as

Cheryl Lacadie

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

author name string

Natalie Cope

1

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

John D Eicher

2

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Haiying Meng

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Christopher J Gibson

4

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Karl Hager

5

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Robert K Fulbright

7

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

R Todd Constable

8

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Grier P Page

9

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Jeffrey R Gruen

10

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

language of work or name

0 references

publication date

27 June 2012

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

63

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

148-156

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Imaging genetics of FOXP2 in dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

DCDC2 genetic variants and susceptibility to developmental dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

DCDC2, KIAA0319 and CMIP are associated with reading-related traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

A dyslexia-associated variant in DCDC2 changes gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

An fMRI study of multimodal semantic and phonological processing in reading disabled adolescents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Functional abnormalities in the dyslexic brain: a quantitative meta-analysis of neuroimaging studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals-A Preliminary Voxel Based Morphometry Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Relations among speech, language, and reading disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

More accurate Talairach coordinates for neuroimaging using non-linear registration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Effects of stimulus difficulty and repetition on printed word identification: an fMRI comparison of nonimpaired and reading-disabled adolescent cohorts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

False positives in imaging genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Functional and morphometric brain dissociation between dyslexia and reading ability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Brain abnormalities underlying altered activation in dyslexia: a voxel based morphometry study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Dyslexia (specific reading disability).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Geometric strategies for neuroanatomic analysis from MRI.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Neurobiological studies of reading and reading disability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Dyslexia: cultural diversity and biological unity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Explicit and implicit processing of words and pseudowords by adult developmental dyslexics: A search for Wernicke's Wortschatz?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Functional connectivity of the angular gyrus in normal reading and dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Enhancement of MR images using registration for signal averaging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Functional disruption in the organization of the brain for reading in dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Is developmental dyslexia a disconnection syndrome? Evidence from PET scanning

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Evidence for a genetic aetiology in reading disability of twins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

Failure to activate the left temporoparietal cortex in dyslexia. An oxygen 15 positron emission tomographic study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

20 June 2018

The role of gene DCDC2 in German dyslexics.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Left lateralized white matter microstructure accounts for individual differences in reading ability and disability.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Children's reading performance is correlated with white matter structure measured by diffusion tensor imaging.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Imaging brain connectivity in children with diverse reading ability.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Gray matter alteration in dyslexia: converging evidence from volumetric and voxel-by-voxel MRI analyses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Disruption of posterior brain systems for reading in children with developmental dyslexia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Preliminary evidence of widespread morphological variations of the brain in dyslexia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Morphological alteration of temporal lobe gray matter in dyslexia: an MRI study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Microstructure of temporo-parietal white matter as a basis for reading ability: evidence from diffusion tensor magnetic resonance imaging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

A positron emission tomographic study of impaired word recognition and phonological processing in dyslexic men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3518451

26 November 2018

Persistence of dyslexia: the Connecticut Longitudinal Study at adolescence

1 reference

https://pubmed.ncbi.nlm.nih.gov/22750057

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional reductions of gray matter volume in familial dyslexia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22750057

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.NEUROIMAGE.2012.06.037

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

DBLP publication ID

journals/neuroimage/CopeEMGHLFCPG12

1 reference

DBLP Dataset 2021-01-02

28 January 2021

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

ResearchGate publication ID

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