(Q24643479)

9

0 references

Tanya M Teslovich

4

object named as

Tanya M Teslovich

0 references

author name string

Dan E Arking

1

0 references

David J Cutler

2

0 references

Camille W Brune

3

0 references

Kristen West

5

0 references

Morna Ikeda

6

0 references

Alexis Rea

7

0 references

Moltu Guy

8

0 references

Aravinda Chakravarti

American Journal of Human Genetics

11

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language of work or name

English

0 references

publication date

January 2008

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published in

0 references

volume

82

0 references

issue

1

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page(s)

160-4

0 references

cites work

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=2253968

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

Genetics of austim: complex aetiology for a heterogeneous disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

Common fragile sites, extremely large genes, neural development and cancer

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

Pervasive developmental disorders in preschool children: confirmation of high prevalence

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

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=2253968

Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

Analysis of family resemblance. I. Introduction

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

Combining information from multiple sources in the diagnosis of 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=2253968

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253968

10.1016/J.AJHG.2007.09.015

28 November 2018

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ch4so5uyfndjrbeob34v2ufp6a

30 July 2022

release_ch4so5uyfndjrbeob34v2ufp6a

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ch4so5uyfndjrbeob34v2ufp6a

30 July 2022

OpenCitations bibliographic resource ID

1954818

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://api.fatcat.wiki/v0/release/ch4so5uyfndjrbeob34v2ufp6a

30 July 2022

https://api.fatcat.wiki/v0/release/ch4so5uyfndjrbeob34v2ufp6a

1 reference

30 July 2022