(Q34063817)

30 July 2017

title

Most genetic risk for autism resides with common variation (English)

1 reference

30 July 2017

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19

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30 July 2017

Trent Gaugler

1

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Stephan J. Sanders

Stephan J Sanders

3

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Kathryn Roeder

Kathryn Roeder

18

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Sven Sandin

Sven Sandin

12

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Lambertus Klei

2

Lambertus Klei

1 reference

30 July 2017

16

Christina M Hultman

1 reference

30 July 2017

9

Yudi Pawitan

1 reference

30 July 2017

13

Pamela Sklar

1 reference

30 July 2017

11

Stephan Ripke

1 reference

30 July 2017

15

Abraham Reichenberg

1 reference

30 July 2017

10

Jennifer Reichert

1 reference

30 July 2017

17

Bernie Devlin

1 reference

30 July 2017

4

Corneliu A Bodea

1 reference

30 July 2017

7

Milind Mahajan

1 reference

30 July 2017

Arthur P Goldberg

5

1 reference

30 July 2017

Ann B Lee

6

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30 July 2017

Dina Manaa

8

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30 July 2017

Oscar Svantesson

14

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30 July 2017

language of work or name

English

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publication date

20 July 2014

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full work available at URL

30 July 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137411

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published in

Nature Genetics

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30 July 2017

volume

46

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30 July 2017

issue

8

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30 July 2017

page(s)

881-885

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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

CNVs conferring risk of autism or schizophrenia affect cognition in controls

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Evaluating empirical bounds on complex disease genetic architecture

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Common genetic variants, acting additively, are a major source of risk for autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

De Novo Gene Disruptions in Children on the Autistic Spectrum

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Patterns and rates of exonic de novo mutations in autism spectrum disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Genetic architecture in autism spectrum disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

The mystery of missing heritability: Genetic interactions create phantom heritability

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

The conundrums of understanding genetic risks for autism spectrum disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Synthetic associations created by rare variants do not explain most GWAS results

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

GCTA: a tool for genome-wide complex trait analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Synthetic associations in the context of genome-wide association scan signals

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Rare variants create synthetic genome-wide associations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

Strong association of de novo copy number mutations with autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

5 July 2018

The heritability of IQ

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4137411

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

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.3039

Linking the SWI/SNF complex to prostate cancer.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.3039

inferred from DOI database lookup

7 January 2021

based on heuristic

The familial risk of autism

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.3039

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.3039

1 reference

Dimensions Publication ID

30 July 2017

0 references

1 reference

30 July 2017

1 reference