(Q24305575)

GOA release 2020-03-11

vocalization behavior

1 reference

GOA release 2020-03-11

author

Michael Wigler

8

0 references

Daniel Geschwind

13

0 references

Jonathan Sebat

Jonathan Sebat

7

0 references

Christa Lese Martin

9

Christa L Martin

0 references

Rita M. Cantor

12

Rita M Cantor

0 references

David H. Ledbetter

10

David H Ledbetter

0 references

Stanley F Nelson

11

Stanley F Nelson

0 references

author name string

Maricela Alarcón

1

0 references

Brett S Abrahams

2

0 references

Jennifer L Stone

3

0 references

Jacqueline A Duvall

4

0 references

Julia V Perederiy

5

0 references

Jamee M Bomar

American Journal of Human Genetics

6

0 references

language of work or name

English

0 references

publication date

January 2008

0 references

published in

0 references

volume

82

0 references

issue

1

0 references

page(s)

150-9

0 references

describes a project that uses

limma

1 reference

Europe PubMed Central

22 June 2022

https://europepmc.org/article/PMC/2253955

inferred from PubMed Central ID database lookup

cites work

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

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Strong association of de novo copy number mutations with autism

19 March 2017

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19 March 2017

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19 March 2017

1 reference

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19 March 2017

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19 March 2017

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19 March 2017

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

19 March 2017

1 reference

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Linear models and empirical bayes methods for assessing differential expression in microarray experiments

19 March 2017

1 reference

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19 March 2017

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19 March 2017

1 reference

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

19 March 2017

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Epidemiology of autistic disorder and other pervasive developmental disorders

19 March 2017

1 reference

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FOXP2 and the neuroanatomy of speech and language

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Large-scale copy number polymorphism in the human genome

19 March 2017

1 reference

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

19 March 2017

1 reference

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Genetic studies of autistic disorder and chromosome 7

19 March 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Whole-genome patterns of common DNA variation in three human populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Genome-wide analyses of human perisylvian cerebral cortical patterning.

7 April 2017

1 reference

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Development of structure and function in the infant brain: implications for cognition, language and social behaviour.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Why the frontal cortex in autism might be talking only to itself: local over-connectivity but long-distance disconnection

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

High-throughput SNP genotyping on universal bead arrays

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Toward a developmental neurobiology of autism.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Autism as a paradigmatic complex genetic disorder

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Evidence for sex-specific risk alleles in autism spectrum disorder

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Human chromosome 7 circa 2004: a model for structural and functional studies of the human genome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Decoding randomly ordered DNA arrays

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Annotation: the neural basis of social impairments in autism: the role of the dorsal medial-frontal cortex and anterior cingulate system

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

On the nature and evolution of the neural bases of human language

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Defining the broader phenotype of autism: genetic, brain, and behavioral perspectives.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

A Drosophila neurexin is required for septate junction and blood-nerve barrier formation and function

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Joint attention and language in autism and developmental language delay

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

A longitudinal study of joint attention and language development in autistic children

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Analytic computation of the expectation of the linkage disequilibrium coefficient r2.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Two-stage designs for gene-disease association studies with sample size constraints

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Genetic and environmental influence on language impairment in 4-year-old same-sex and opposite-sex twins.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

CHOISS for selection of single nucleotide polymorphism markers on interval regularity.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Incorporating language phenotypes strengthens evidence of linkage to autism

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Cognitive Deficits in Parents from Multiple‐incidence Autism Families

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253955

Techview: molecular biology. Bead-based fiber-optic arrays

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18179893

12 December 2020

inferred from PubMed ID database lookup

BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18179893

12 December 2020

inferred from PubMed ID database lookup

Linkage disequilibrium in finite populations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18179893

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1016/J.AJHG.2007.09.005

1 reference

1 reference

1 reference

PubMed publication ID

18179893

1 reference