A new gene (DYX3) for dyslexia is located on chromosome 2 (Q24681637)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

31 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

31 October 2019

0 references

Fagerheim T

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

31 October 2019

Raeymaekers P

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

31 October 2019

Tønnessen FE

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

31 October 2019

Pedersen M

4

1 reference

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31 October 2019

Tranebjaerg L

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

31 October 2019

Lubs HA

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

31 October 2019

language of work or name

English

0 references

publication date

1 September 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

31 October 2019

published in

1 reference

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31 October 2019

volume

36

1 reference

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31 October 2019

issue

9

1 reference

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31 October 2019

page(s)

664-669

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

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

31 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Evidence for linkage of spelling disability to chromosome 15

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Calcineurin A alpha (PPP3CA), calcineurin A beta (PPP3CB) and calcineurin B (PPP3R1) are located on human chromosomes 4, 10q21-->q22 and 2p16-->p15 respectively

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

A comprehensive genetic map of the human genome based on 5,264 microsatellites

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Strategies for multilocus linkage analysis in humans

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Quantitative trait locus for reading disability on chromosome 6

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Parametric and nonparametric linkage analysis: a unified multipoint approach

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Neurobiological Basis of Speech: A Case for the Preeminence of Temporal Processing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Linkage strategies for genetically complex traits. I. Multilocus models

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Evidence for major gene transmission of developmental dyslexia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Using genetics to dissect cognition

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

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=1734428

Impaired visual word processing in dyslexia revealed with magnetoencephalography

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734428

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

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10507721

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cosegregation of balanced translocation (1;2) with retarded speech development and dyslexia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10507721

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Contrast sensitivity in dyslexia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10507721

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721 AND SRC:MED&resulttype=core&format=json

31 October 2019

PubMed publication ID

10507721

1 reference