(Q34858439)

4 August 2017

title

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16 (English)

1 reference

4 August 2017

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2

Annette Estes

1 reference

4 August 2017

Ellen M Wijsman

10

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Nancy J Minshew

7

object named as

Nancy J Minshew

1 reference

4 August 2017

8

Geraldine Dawson

1 reference

4 August 2017

Nicola H Chapman

1

1 reference

4 August 2017

Jeff Munson

3

1 reference

4 August 2017

Raphael Bernier

4

1 reference

4 August 2017

Sara J Webb

5

1 reference

4 August 2017

Joseph H Rothstein

6

1 reference

4 August 2017

Gerard D Schellenberg

9

1 reference

4 August 2017

publication date

21 October 2010

1 reference

4 August 2017

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4 August 2017

volume

129

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4 August 2017

issue

1

1 reference

4 August 2017

page(s)

59-70

1 reference

https://scigraph.springernature.com/pub.10.1007/s00439-010-0899-z

4 August 2017

exact match

0 references

cites work

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A genome-wide linkage and association scan reveals novel loci for autism

8 July 2018

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8 July 2018

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A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

8 July 2018

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Genome-wide linkage in Utah autism pedigrees

8 July 2018

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

8 July 2018

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Common genetic variants on 5p14.1 associate with autism spectrum disorders

8 July 2018

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8 July 2018

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Examining executive functioning in children with autism spectrum disorder, attention deficit hyperactivity disorder and typical development

8 July 2018

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Evidence for latent classes of IQ in young children with autism spectrum disorder

8 July 2018

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Genome-wide linkage analyses of quantitative and categorical autism subphenotypes

8 July 2018

1 reference

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Further defining the language impairment of autism: is there a specific language impairment subtype?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

The genetics of autistic disorders and its clinical relevance: a review of the literature

8 July 2018

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An Investigation of Language Impairment in Autism: Implications for Genetic Subgroups

8 July 2018

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Segregation analysis of a complex quantitative trait: approaches for identifying influential data points

8 July 2018

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A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.

8 July 2018

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Replication of autism linkage: fine-mapping peak at 17q21.

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods

8 July 2018

1 reference

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A combined linkage-physical map of the human genome

8 July 2018

1 reference

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Evidence for sex-specific risk alleles in autism spectrum disorder

8 July 2018

1 reference

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A genomewide screen of 345 families for autism-susceptibility loci

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Identifying neurocognitive phenotypes in autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

A genomewide screen for autism susceptibility loci

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Improved inference of relationship for pairs of individuals

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Expression of T-cadherin (CDH13, H-Cadherin) in human brain and its characteristics as a negative growth regulator of epidermal growth factor in neuroblastoma cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

An autosomal genomic screen for autism. Collaborative linkage study of autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Present and future possibilities for defining a phenotype for specific language impairment

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

A genomic screen of autism: evidence for a multilocus etiology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

MCMC segregation and linkage analysis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Wechsler IQ profiles in diagnosis of high-functioning autism.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Genetics of autism: characteristics of affected and unaffected children from 37 multiplex families.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

A case-control family history study of autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Autism as a strongly genetic disorder: evidence from a British twin study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Genetic and clinical correlations of Xp21 muscular dystrophy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Infantile autism: a genetic study of 21 twin pairs

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Ability profiles in children with autism: influence of age and IQ.

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-010-0899-Z

Association between extreme autistic traits and intellectual disability: insights from a general population twin study.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

A quantitative trait locus analysis of social responsiveness in multiplex autism families

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Evidence for multiple loci from a genome scan of autism kindreds.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Characteristics of the broader phenotype in autism: a study of siblings using the children's communication checklist-2.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Linkage analyses of IQ in the collaborative study on the genetics of alcoholism (COGA) sample.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

A girl with pervasive developmental disorder and complex chromosome rearrangement involving 8p and 10p.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

The application of short forms of the Wechsler Intelligence scales in adults and children with high functioning autism.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Genomic screen and follow-up analysis for autistic disorder.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Symptom domains in autism and related conditions: evidence for familiality

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Familial factors influence level of functioning in pervasive developmental disorder.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

Asperger's syndrome and autism: neurocognitive aspects.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082447

The Swedish WAIS-R factor structure and cognitive profiles for adults with dyslexia

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20963441

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00439-010-0899-Z

1 reference

Dimensions Publication ID

4 August 2017

1013080517

0 references

Fatcat ID

release_xv5ysb4qpvgorlqvo5ccndz32q

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/xv5ysb4qpvgorlqvo5ccndz32q

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

3082447

1 reference

4 August 2017

1 reference