(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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single-nucleotide polymorphism

4 December 2017

main subject

autism spectrum disorder

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autism

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17

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4 December 2017

Hreinn Stefansson

25

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Fritz Poustka

7

object named as

Fritz Poustka

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26

Kari Stefansson

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9

Christine M Freitag

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27

David Collier

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5

Sabine M Klauck

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21

Ragnheidur Fossdal

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11

Pierandrea Muglia

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16

Roel A Ophoff

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24

Evald Saemundsen

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23

Stefan Hreidarsson

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4 December 2017

20

Evangelos Vassos

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4 December 2017

Sarah Curran

1

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4 December 2017

Patrick Bolton

2

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4 December 2017

Kinga Rozsnyai

3

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4 December 2017

Andreas Chiocchetti

4

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4 December 2017

Eftichia Duketis

6

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4 December 2017

Sabine Schlitt

8

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4 December 2017

Irene Lee

10

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4 December 2017

ITAN

12

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4 December 2017

Martin Poot

13

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4 December 2017

Wouter Staal

14

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4 December 2017

Maretha V de Jonge

15

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4 December 2017

David Skuse

18

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Will Mandy

19

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Páll Magnusson

22

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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

issue

6

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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

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

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

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Novel de novo SHANK3 mutation in autistic patients

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

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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

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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

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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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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

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

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

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Rethinking the nature of genetic vulnerability to autistic spectrum disorders

21 January 2018

1 reference

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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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

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

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

1 reference

4 December 2017

1 reference