(Q36160444)

12 August 2017

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

1 reference

12 August 2017

0 references

Elena L. Grigorenko

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14506298

13 March 2024

language of work or name

English

0 references

publication date

23 September 2003

1 reference

12 August 2017

3

1 reference

full work available at URL

inferred from page(s)

https://europepmc.org/articles/pmc208730?pdf=render

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14506298

https://europepmc.org/articles/PMC208730

13 March 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14506298

https://europepmc.org/articles/PMC208730?pdf=render

13 March 2024

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14506298

https://doi.org/10.1073/pnas.2134926100

13 March 2024

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14506298

https://pnas.org/doi/pdf/10.1073/pnas.2134926100

13 March 2024

1 reference

Crossref

DOI

10.1073/PNAS.2134926100

https://api.crossref.org/works/10.1073/PNAS.2134926100

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

13 March 2024

published in

1 reference

12 August 2017

100

1 reference

12 August 2017

20

1 reference

12 August 2017

11190-11192

1 reference

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

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Catechol O -methyltransferase val 158 -met genotype and individual variation in the brain response to amphetamine

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Pre-frontal executive committee for perception, working memory, attention, long-term memory, motor control, and thinking: a tutorial review

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Atypical brain activation of reading processes in children with developmental dyslexia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Developmental dyslexia: genetic dissection of a complex cognitive trait

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Dyslexia: nature and nurture

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

A major susceptibility locus for specific language impairment is located on 13q21.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

FOXP2 is not a major susceptibility gene for autism or specific language impairment

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

A genomewide scan identifies two novel loci involved in specific language impairment

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

A forkhead-domain gene is mutated in a severe speech and language disorder

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Dyslexia: cultural diversity and biological unity

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Two translocations of chromosome 15q associated with dyslexia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Evidence for linkage of spelling disability to chromosome 15

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

The prefrontal landscape: implications of functional architecture for understanding human mentation and the central executive

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Pharmacological modulation of behavioral and neuronal correlates of repetition priming.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Definition and treatment of dyslexia: a report by the Committee on Dyslexia of the Health Council of The Netherlands.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Evidence for the independent familial transmission of attention deficit hyperactivity disorder and learning disabilities: results from a family genetic study.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=208730

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides

23 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.2134926100

Comorbidity of reading disability and attention-deficit/hyperactivity disorder: differences by gender and subtype

21 January 2018

1 reference

12 December 2020

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q

1 reference

12 December 2020

Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder

1 reference

12 December 2020

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

1 reference

12 December 2020

Attention deficit hyperactivity disorder, reading disability, and personality disorders in a prison population

1 reference

12 December 2020

Arithmetic disabilities with and without reading difficulties: A comparison of arithmetic errors

series ordinal

25

1 reference

Crossref

DOI

10.1073/PNAS.2134926100

https://api.crossref.org/works/10.1073/PNAS.2134926100

13 March 2024

Identifiers

DOI

10.1073/PNAS.2134926100

1 reference

12 August 2017

0 references

1 reference

PMC publication ID

208730

12 August 2017

1 reference

PMC publication ID

208730