(Q38271952)

English

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample (English)

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

0 references

Ellen M. Wijsman

7

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Virginia W. Berninger

6

object named as

Virginia W Berninger

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

author name string

Beate Peter

1

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Wendy H Raskind

2

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Mark Matsushita

3

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Mark Lisowski

4

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Tiffany Vu

5

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Zoran Brkanac

8

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

9 November 2010

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Journal of Neurodevelopmental Disorders

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

3

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

1

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

39-49

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Functional magnetic resonance imaging sequential-finger movement activation differentiating good and poor writers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

A multidisciplinary approach to understanding developmental dyslexia within working-memory architecture: genotypes, phenotypes, brain, and instruction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

A functional genetic link between distinct developmental language disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

A review of family-based tests for linkage disequilibrium between a quantitative trait and a genetic marker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Relations among speech, language, and reading disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Writing problems in developmental dyslexia: under-recognized and under-treated

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Cognitive and behavioral dysfunction in children with hypothalamic hamartoma and epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Neuropsychology and genetics of speech, language, and literacy disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

The genetic bases of speech sound disorders: evidence from spoken and written language

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Parental phenotypes in family-based association analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

A longitudinal investigation of reading outcomes in children with language impairments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

FOXP2: novel exons, splice variants, and CAG repeat length stability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

FOXP2 is not a major susceptibility gene for autism or specific language impairment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Prevalence of specific language impairment in kindergarten children.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

6 September 2017

Multiple transcription start sites for FOXP2 with varying cellular specificities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

14 September 2017

Lifespan trajectory of myelin integrity and maximum motor speed

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

27 September 2017

Toward an understanding of developmental language and reading disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

23 June 2018

Relationship of finger function to beginning writing: application to diagnosis of writing disabilities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

23 June 2018

Reliability and validity of a computerized neurocognitive test battery, CNS Vital Signs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

31 August 2018

Exploring dyslexics' phonological deficit I: lexical vs sub-lexical and input vs output processes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

31 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

31 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

31 August 2018

Sensory processing, reading, IQ, and attention.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

31 August 2018

The science of reading and dyslexia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

31 August 2018

Familial aggregation of dyslexia phenotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

31 August 2018

Associated movements as a measure of developmental age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3163991

31 August 2018

Pedigree tests of transmission disequilibrium

1 reference

https://api.crossref.org/works/10.1007%2FS11689-010-9065-0

21 January 2018

Psycholinguistic markers for specific language impairment (SLI)

1 reference

https://pubmed.ncbi.nlm.nih.gov/21484596

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Circumventing multiple testing: a multilocus Monte Carlo approach to testing for association

1 reference

https://pubmed.ncbi.nlm.nih.gov/21484596

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association of reading disability, behavioral disorders, and language impairment among second-grade children

1 reference

https://pubmed.ncbi.nlm.nih.gov/21484596

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of speed in repetitive and successive finger-movements in normal children

1 reference

https://pubmed.ncbi.nlm.nih.gov/21484596

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11689-010-9065-0

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38271952&oldid=2201506909"