(Q44565309)

4 December 2017

title

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder (English)

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autism spectrum disorderکیرم دعنت

4 December 2017

main subject

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autism

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single-nucleotide polymorphism

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4 December 2017

Hreinn Stefansson

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Fritz Poustka

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4 December 2017

Kari Stefansson

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4 December 2017

Christine M Freitag

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4 December 2017

David Collier

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4 December 2017

Sabine M Klauck

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4 December 2017

Ragnheidur Fossdal

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4 December 2017

Pierandrea Muglia

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4 December 2017

Roel A Ophoff

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4 December 2017

Evald Saemundsen

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4 December 2017

Stefan Hreidarsson

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4 December 2017

Evangelos Vassos

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4 December 2017

Sarah Curran

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4 December 2017

Patrick Bolton

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4 December 2017

Kinga Rozsnyai

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4 December 2017

Andreas Chiocchetti

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4 December 2017

Eftichia Duketis

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4 December 2017

Sabine Schlitt

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4 December 2017

Irene Lee

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4 December 2017

ITAN

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4 December 2017

Martin Poot

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4 December 2017

Wouter Staal

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4 December 2017

Maretha V de Jonge

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4 December 2017

David Skuse

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4 December 2017

Will Mandy

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4 December 2017

Páll Magnusson

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4 December 2017

publication date

8 June 2011

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

4 December 2017

published in

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4 December 2017

volume

156B

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4 December 2017

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4 December 2017

page(s)

633-639

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Advances in autism genetics: on the threshold of a new neurobiology

4 December 2017

cites work

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https://api.crossref.org/works/10.1002%2FAJMG.B.31201

Case report: autistic disorder in Kabuki syndrome

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

21 January 2018

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

21 January 2018

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Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

21 January 2018

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Hotspots of large rare deletions in the human genome

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Replicating genotype-phenotype associations

21 January 2018

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

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21 January 2018

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Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees

21 January 2018

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21 January 2018

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21 January 2018

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Novel de novo SHANK3 mutation in autistic patients

21 January 2018

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The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm

21 January 2018

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

21 January 2018

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Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

21 January 2018

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

21 January 2018

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

21 January 2018

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The C20orf133 gene is disrupted in a patient with Kabuki syndrome

21 January 2018

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GWAMA: software for genome-wide association meta-analysis

21 January 2018

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Finding the missing heritability of complex diseases

21 January 2018

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Structural variation of chromosomes in autism spectrum disorder

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.31201

The discriminative ability and diagnostic utility of the ADOS-G, ADI-R, and GARS for children in a clinical setting

21 January 2018

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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

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How many genetic variants remain to be discovered?

21 January 2018

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Genetic risk sum score comprised of common polygenic variation is associated with body mass index

21 January 2018

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Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

21 January 2018

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Advancing paternal age and autism

21 January 2018

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The future of genetic studies of complex human diseases

21 January 2018

1 reference

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A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples

21 January 2018

1 reference

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Strong association of de novo copy number mutations with autism

21 January 2018

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Rethinking the nature of genetic vulnerability to autistic spectrum disorders

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.31201

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.31201

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

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The role of genetic variation in the causation of mental illness: an evolution-informed framework

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31201

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.31201

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.31201

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31201

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.31201

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4 December 2017

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