(Q37177974)

18 August 2017

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population (English)

1 reference

18 August 2017

0 references

autism spectrum disorder

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0 references

17

1 reference

18 August 2017

13

Thomas Werge

1 reference

18 August 2017

Stephan J Sanders

9

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Verneri Anttila

Verneri Anttila

3

0 references

Jakob Grove

Jakob Grove

6

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Beate St Pourcain

Beate St Pourcain

2

0 references

Preben Bo Mortensen

Preben Bo Mortensen

19

0 references

George Davey Smith

George Davey Smith

22

0 references

Kaitlin E Samocha

Kaitlin E Samocha

8

0 references

Joanna Martin

Joanna Martin

11

0 references

Angelica Ronald

Angelica Ronald

21

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Mads Vilhelm Hollegaard

12

Mads V Hollegaard

1 reference

18 August 2017

23

Mark J Daly

1 reference

18 August 2017

10

Stephan Ripke

1 reference

18 August 2017

16

Benjamin M Neale

1 reference

18 August 2017

Elise B Robinson

1

1 reference

18 August 2017

Jack A Kosmicki

4

1 reference

18 August 2017

Brendan Bulik-Sullivan

5

1 reference

18 August 2017

Julian Maller

7

1 reference

18 August 2017

David M Hougaard

14

1 reference

18 August 2017

iPSYCH-SSI-Broad Autism Group

15

1 reference

18 August 2017

David Skuse

18

1 reference

18 August 2017

Anders D Børglum

20

1 reference

18 August 2017

language of work or name

English

0 references

publication date

21 March 2016

1 reference

18 August 2017

1 reference

18 August 2017

48

1 reference

18 August 2017

5

1 reference

18 August 2017

552-555

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.3529

18 August 2017

0 references

cites work

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

An atlas of genetic correlations across human diseases and traits

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Copy number variations and cognitive phenotypes in unselected populations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Excess of rare, inherited truncating mutations in autism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

The contribution of de novo coding mutations to autism spectrum disorder

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Synaptic, transcriptional and chromatin genes disrupted in autism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Autism spectrum disorder severity reflects the average contribution of de novo and familial influences

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

A framework for the interpretation of de novo mutation in human disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Biological insights from 108 schizophrenia-associated genetic loci

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Most genetic risk for autism resides with common variation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

CNVs conferring risk of autism or schizophrenia affect cognition in controls

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Cohort profile: the 'children of the 90s'—the index offspring of the Avon Longitudinal Study of Parents and Children

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Cohort Profile: the Avon Longitudinal Study of Parents and Children: ALSPAC mothers cohort

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%)

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Stability of autistic traits in the general population: further evidence for a continuum of impairment

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

GCTA: a tool for genome-wide complex trait analysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

The Simons Simplex Collection: a resource for identification of autism genetic risk factors

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Sibling recurrence and the genetic epidemiology of autism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

A method and server for predicting damaging missense mutations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Common disorders are quantitative traits

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Genetic heterogeneity between the three components of the autism spectrum: a twin study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Autism spectrum disorders and autistic like traits: similar etiology in the extreme end and the normal variation

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Measuring autistic traits: heritability, reliability and validity of the Social and Communication Disorders Checklist.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

3 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.3529

Common disorders are quantitative traits

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4986048

4 December 2018

Identifiers

DOI

10.1038/NG.3529

1 reference

18 August 2017

1 reference

18 August 2017

1 reference