(Q28288962)

1

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A Citterio

2

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A Facoetti

4

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G Menozzi

5

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L Vanzin

6

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M L Lorusso

7

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M Nobile

8

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M Molteni

Genes, Brain and Behavior

9

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language of work or name

English

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publication date

October 2007

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published in

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volume

6

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issue

7

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page(s)

640-6

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cites work

Quantitative trait locus for reading disability on chromosome 6

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

A dominant gene for developmental dyslexia on chromosome 3

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

Dyslexia: cultural diversity and biological unity

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

Evidence for linkage of spelling disability to chromosome 15

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1601-183X.2006.00291.X

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

21 April 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Developmental dyslexia: genetic dissection of a complex cognitive trait

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Power and design considerations for a general class of family-based association tests: quantitative traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

PBAT: tools for family-based association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

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/10.1111%2FJ.1601-183X.2006.00291.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Genetic influences on language impairment and phonological short-term memory.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Two translocations of chromosome 15q associated with dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Generalist genes and learning disabilities

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Biological abnormality of impaired reading is constrained by culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Linkage of speech sound disorder to reading disability loci.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Twin study of the etiology of comorbidity between reading disability and attention-deficit/hyperactivity disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X

Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2006.00291.X