(Q46952080)

26 December 2017

title

Sex-specific association of a common variant of the XG gene with autism spectrum disorders (English)

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26 December 2017

main subject

autism spectrum disorder

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autism

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author name string

Shun-Chiao Chang

1

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26 December 2017

David L Pauls

2

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26 December 2017

Christoph Lange

3

1 reference

26 December 2017

Roksana Sasanfar

4

1 reference

26 December 2017

Susan L Santangelo

5

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26 December 2017

publication date

1 October 2013

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26 December 2017

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

published in

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26 December 2017

volume

162B

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26 December 2017

issue

7

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26 December 2017

page(s)

742-750

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26 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

A genome-wide scan for common alleles affecting risk for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Individual common variants exert weak effects on the risk for autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Intestinal lymphocyte populations in children with regressive autism: evidence for extensive mucosal immunopathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

The immune response in autism: a new frontier for autism research

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Decreased transforming growth factor beta1 in autism: a potential link between immune dysregulation and impairment in clinical behavioral outcomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Association of the alpha4 integrin subunit gene (ITGA4) with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Concordance by sex in sibling pairs with schizophrenia is paternally inherited. Evidence for a pseudoautosomal locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

CD99 is essential for leukocyte diapedesis in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

PBDX is the XG blood group gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

The human pseudoautosomal regions: a review for genetic epidemiologists

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

A new sex-specific genetic map of the human pseudoautosomal regions (PAR1 and PAR2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Genetics of austim: complex aetiology for a heterogeneous disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Exploring the cognitive phenotype of autism: weak "central coherence" in parents and siblings of children with autism: I. Experimental tests

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Executive function in parents of children with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Disruption of neurexin 1 associated with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Brief report: immune factors in autism: a critical review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

The pursuit of genome-wide association studies: where are we now?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Effects of familial risk factors and place of birth on the risk of autism: a nationwide register-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

CD99 activates T cells via a costimulatory function that promotes raft association of TCR complex and tyrosine phosphorylation of TCR zeta

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

CD99 signals caspase-independent T cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Lymphocyte function in autism and Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Sex differences in developmental reading disability: new findings from 4 epidemiological studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Evidence for sex-specific risk alleles in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

High density SNP association study of a major autism linkage region on chromosome 17.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Immune abnormalities in patients with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Database resources of the National Center for Biotechnology Information

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

Neurexin 1alpha structural variants associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32165

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.32165

1 reference

26 December 2017

1 reference

26 December 2017