Allelic variants of DYX1C1 are not associated with dyslexia in India (Q33735905)

29 July 2017

title

Allelic variants of DYX1C1 are not associated with dyslexia in India (English)

1 reference

29 July 2017

0 references

1 reference

Pushpa Saviour

1

1 reference

29 July 2017

Satish Kumar

2

1 reference

29 July 2017

U Kiran

3

1 reference

29 July 2017

Rajasekhara Reddy Ravuri

4

1 reference

29 July 2017

V R Rao

5

1 reference

29 July 2017

Nallur Basappa Ramachandra

6

1 reference

29 July 2017

language of work or name

1 reference

1 September 2008

1 reference

Indian Journal of Human Genetics

29 July 2017

published in

1 reference

29 July 2017

volume

14

1 reference

29 July 2017

issue

3

1 reference

29 July 2017

page(s)

99-102

1 reference

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

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

A dominant gene for developmental dyslexia on chromosome 3

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

Evidence for linkage of spelling disability to chromosome 15

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

Quantitative trait locus for reading disability on chromosome 6

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2840802

30 October 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/20300304

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20300304

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A children's behaviour questionnaire for completion by teachers: preliminary findings

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20300304

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.4103/0971-6866.45002

1 reference

29 July 2017

1 reference

29 July 2017

1 reference