(Q43117326)

14 November 2017

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

1 reference

14 November 2017

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Jason L Stein

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Daniel H Geschwind

1 reference

14 November 2017

Neelroop N Parikshak

1 reference

PMC publication ID

3691080

14 November 2017

language of work or name

English

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publication date

1 January 2013

1 reference

14 November 2017

1 reference

14 November 2017

1 reference

14 November 2017

1 reference

14 November 2017

209-211

1 reference

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

Autism genetics: searching for specificity and convergence

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

De Novo Gene Disruptions in Children on the Autistic Spectrum

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

Genetic architecture in autism spectrum disorder

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

A systematic survey of loss-of-function variants in human protein-coding genes

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3691080

10.1016/J.NEURON.2013.01.010

25 May 2018

Identifiers

DOI

1 reference

14 November 2017

1 reference

PMC publication ID

3691080

14 November 2017

PubMed publication ID

23352155

1 reference

PMC publication ID

3691080