(Q34408880)

2 August 2017

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

1 reference

2 August 2017

autism spectrum disorder

0 references

0 references

Elise B Robinson

1

0 references

Kaitlin E Samocha

object named as

Kaitlin E Samocha

series ordinal

2

0 references

Mark Joseph Daly

series ordinal

7

object named as

Mark J Daly

1 reference

2 August 2017

5

Benjamin M Neale

1 reference

2 August 2017

6

Roy H Perlis

1 reference

2 August 2017

Jack A Kosmicki

3

1 reference

PubMed ID

25288738

2 August 2017

Lauren McGrath

series ordinal

4

1 reference

PubMed ID

25288738

2 August 2017

language of work or name

English

0 references

publication date

6 October 2014

1 reference

Proceedings of the National Academy of Sciences of the United States of America

2 August 2017

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

2 August 2017

111

1 reference

2 August 2017

42

1 reference

2 August 2017

15161-15165

1 reference

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

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Most genetic risk for autism resides with common variation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

De novo mutations in schizophrenia implicate synaptic networks

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

The role of de novo mutations in the genetics of autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Examining and interpreting the female protective effect against autistic behavior

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Optimal outcome in individuals with a history of autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Trajectories of autism severity in children using standardized ADOS scores

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Mood disorders in mothers of children on the autism spectrum are associated with higher functioning autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Autism genetics: searching for specificity and convergence

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Genetic architectures of psychiatric disorders: the emerging picture and its implications

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Family history of schizophrenia and bipolar disorder as risk factors for autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

De Novo Gene Disruptions in Children on the Autistic Spectrum

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Genetic contributions to stability and change in intelligence from childhood to old age.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Genome-wide association studies establish that human intelligence is highly heritable and polygenic

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Sibling recurrence and the genetic epidemiology of autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Defining the broader, medium and narrow autism phenotype among parents using the Autism Spectrum Quotient (AQ).

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Is autism really a coherent syndrome in boys, or girls?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Epidemiology of autistic disorder and other pervasive developmental disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Prevalence of depression by race/ethnicity: findings from the National Health and Nutrition Examination Survey III

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Familial mental retardation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210299

Rare inherited variation in autism: beginning to see the forest and a few trees

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1409204111

Diagnostic exome sequencing in persons with severe intellectual disability

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1409204111

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1409204111

21 January 2018

Identifiers

DOI

10.1073/PNAS.1409204111

1 reference

2 August 2017

0 references

1 reference

2 August 2017

1 reference

PubMed ID

25288738