DCDC2 is associated with reading disability and modulates neuronal development in the brain (Q24294360)

5 July 2017

title

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

1 reference

Doublecortin domain containing 2

5 July 2017

0 references

0 references

1 reference

GOA release 2020-03-11

neuron migration

1 reference

GOA release 2020-03-11

1 reference

9

Joel Gelernter

0 references

Sally Shaywitz

13

object named as

Sally E Shaywitz

1 reference

5 July 2017

14

Bennett A Shaywitz

1 reference

5 July 2017

Haiying Meng

1

1 reference

5 July 2017

Shelley D Smith

2

1 reference

5 July 2017

Karl Hager

3

1 reference

5 July 2017

Matthew Held

4

1 reference

5 July 2017

Jonathan Liu

5

1 reference

5 July 2017

Richard K Olson

6

1 reference

5 July 2017

Bruce F Pennington

7

1 reference

5 July 2017

John C DeFries

8

1 reference

5 July 2017

Thomas O'Reilly-Pol

10

1 reference

5 July 2017

Stefan Somlo

11

1 reference

5 July 2017

Pawel Skudlarski

12

1 reference

5 July 2017

Karen Marchione

15

1 reference

5 July 2017

Yu Wang

16

1 reference

5 July 2017

Murugan Paramasivam

17

1 reference

5 July 2017

Joseph J LoTurco

18

1 reference

5 July 2017

Grier P Page

19

1 reference

5 July 2017

Jeffrey R Gruen

20

1 reference

5 July 2017

language of work or name

English

0 references

publication date

8 November 2005

1 reference

5 July 2017

number of pages

6

1 reference

Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

1 reference

5 July 2017

volume

102

1 reference

5 July 2017

issue

47

1 reference

5 July 2017

page(s)

17053-17058

1 reference

describes a project that uses

5 July 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC1278934/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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=1278934

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

A transcription map of the 6p22.3 reading disability locus identifying candidate genes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Functional connectivity of the angular gyrus in normal reading and dyslexia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Haploview: analysis and visualization of LD and haplotype maps

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

The neural code for written words: a proposal

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Neurotrophins and netrins require calcineurin/NFAT signaling to stimulate outgrowth of embryonic axons

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Lissencephaly and other malformations of cortical development: 1995 update

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

RNAi reveals doublecortin is required for radial migration in rat neocortex

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Dyslexia (specific reading disability).

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Evidence for linkage and association with reading disability on 6p21.3-22.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Rapid amplification of plasmid and phage DNA using Phi 29 DNA polymerase and multiply-primed rolling circle amplification

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Male sexual dysfunction in mice bearing targeted mutant alleles of the PEA3 ets gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Developmental dyslexia: four consecutive patients with cortical anomalies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Evidence for a genetic aetiology in reading disability of twins.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Specific deficits in component reading and language skills: genetic and environmental influences.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

The genetics of specific reading disability

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

Pedigree tests of transmission disequilibrium

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1278934

GOLD--graphical overview of linkage disequilibrium

29 November 2018

1 reference

12 December 2020

Peaks of linkage are localized by a BAC/PAC contig of the 6p reading disability locus

1 reference

12 December 2020

Dyslexia (Specific Reading Disability)

1 reference

12 December 2020

Specific reading disability: identification of an inherited form through linkage analysis

1 reference

12 December 2020

Auxological and biochemical evaluation of pubertal suppression with the GnRH agonist leuprolide acetate in early and precocious puberty

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0508591102

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1073/PNAS.0508591102

1 reference

OpenCitations bibliographic resource ID

5 July 2017

0 references

707382

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

5 July 2017

1 reference