(Q52058164)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15702132%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia (English)

1 reference

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8 January 2020

0 references

2

1 reference

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8 January 2020

Massimo Molteni

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15702132%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Cecilia Marino

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15702132%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Maria Nobile

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15702132%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

author name string

Maria Luisa Lorusso

3

1 reference

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8 January 2020

Laura Vanzin

4

1 reference

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8 January 2020

Nello Salandi

5

1 reference

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8 January 2020

Alessandra Citterio

7

1 reference

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8 January 2020

Silvana Beri

8

1 reference

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8 January 2020

Valentina Crespi

9

1 reference

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8 January 2020

Marco Battaglia

10

1 reference

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8 January 2020

publication date

1 April 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15702132%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

8 January 2020

published in

1 reference

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8 January 2020

volume

13

1 reference

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8 January 2020

issue

4

1 reference

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8 January 2020

page(s)

491-499

1 reference

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201356

8 January 2020

exact match

0 references

cites work

Developmental dyslexia: genetic dissection of a complex cognitive trait

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Visual motion sensitivity and reading.

21 January 2018

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The neurological basis of developmental dyslexia: an overview and working hypothesis

21 January 2018

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

21 January 2018

1 reference

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Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

A dominant gene for developmental dyslexia on chromosome 3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

Quantitative trait locus for reading disability on chromosome 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

Evidence for linkage of spelling disability to chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

Two translocations of chromosome 15q associated with dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

The family based association test method: strategies for studying general genotype--phenotype associations.

21 January 2018

1 reference

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

21 January 2018

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Genetics of learning disabilities

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

Transmission/disequilibrium tests for extended marker haplotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

Transmission/disequilibrium tests using multiple tightly linked markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

7 January 2021

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201356

7 January 2021