Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. (Q30498012)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165691%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

title

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects (English)

1 reference

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18 January 2020

0 references

5

1 reference

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18 January 2020

Dianne F Newbury

1

1 reference

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18 January 2020

Silvia Paracchini

2

1 reference

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18 January 2020

John Stein

8

1 reference

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18 January 2020

Anthony Monaco

10

1 reference

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18 January 2020

author name string

T S Scerri

3

1 reference

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18 January 2020

L Winchester

4

1 reference

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18 January 2020

Alex J Richardson

6

1 reference

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18 January 2020

J Walter

7

1 reference

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18 January 2020

J B Talcott

9

1 reference

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18 January 2020

language of work or name

English

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publication date

17 December 2010

1 reference

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18 January 2020

1 reference

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18 January 2020

volume

41

1 reference

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18 January 2020

issue

1

1 reference

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18 January 2020

page(s)

90-104

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https://scigraph.springernature.com/pub.10.1007/s10519-010-9424-3

18 January 2020

exact match

0 references

cites work

Recent advances in the genetics of language impairment

1 reference

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Genetics of developmental dyslexia

20 June 2018

1 reference

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Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

20 June 2018

1 reference

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Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment

20 June 2018

1 reference

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Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation

20 June 2018

1 reference

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CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

20 June 2018

1 reference

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CMIP and ATP2C2 modulate phonological short-term memory in language impairment

20 June 2018

1 reference

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

20 June 2018

1 reference

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A common variant associated with dyslexia reduces expression of the KIAA0319 gene

20 June 2018

1 reference

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Gene associated with seizures, autism, and hepatomegaly in an Amish girl

20 June 2018

1 reference

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Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient

20 June 2018

1 reference

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A functional genetic link between distinct developmental language disorders

20 June 2018

1 reference

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Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

20 June 2018

1 reference

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Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

20 June 2018

1 reference

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A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea

20 June 2018

1 reference

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Relations among speech, language, and reading disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

PLINK: a tool set for whole-genome association and population-based linkage analyses

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Severe receptive language disorder in childhood--familial aspects and long-term outcomes: results from a Scottish study.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Association of short-term memory with a variant within DYX1C1 in developmental dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

No gene is an island: the flip-flop phenomenon

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Heritable risk factors associated with language impairments

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

The genetics of developmental dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

20 June 2018

1 reference

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Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Are specific language impairment and dyslexia distinct disorders?

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

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PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Developmental dyslexia and specific language impairment: same or different?

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Family-based association study of DYX1C1 variants in autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

A dominant gene for developmental dyslexia on chromosome 3

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

On the "specifics" of specific reading disability and specific language impairment

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

A general test of association for quantitative traits in nuclear families

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Varieties of developmental dyslexia.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Whole genome amplification from a single cell: implications for genetic analysis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Genetic analyses of roundabout (ROBO) axon guidance receptors in autism.

20 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

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/10.1007%2FS10519-010-9424-3

Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

Further evidence for DYX1C1 as a susceptibility factor for dyslexia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

Children at family risk of dyslexia: a follow-up in early adolescence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-010-9424-3

Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

The Cambridge Language and Speech Project (CLASP). I . Detection of language difficulties at 36 to 39 months.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3029677

The Children's Test of Nonword Repetition: a test of phonological working memory

26 November 2018

1 reference

12 December 2020

Is preschool language impairment a risk factor for dyslexia in adolescence?

1 reference

12 December 2020

The extent to which psychometric tests differentiate subgroups of children with SLI

1 reference

12 December 2020

Characteristics of children attending language units in England: a national study of 7-year-olds

1 reference

12 December 2020

10.1007/S10519-010-9424-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165691%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

18 January 2020

1052399530

0 references

Fatcat ID

release_67z2djhlpne7dmoeuwcji6qnr4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/67z2djhlpne7dmoeuwcji6qnr4

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21165691%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference