(Q37834918)

English

Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: a systematic review and meta-analysis

scientific article published on May 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

24 August 2017

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1 reference

Europe PubMed Central

Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: a systematic review and meta-analysis (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 August 2017

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systematic review

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based on heuristic

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author name string

Kyle M Walsh

1

1 reference

Europe PubMed Central

PubMed publication ID

24 August 2017

Michael B Bracken

2

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Europe PubMed Central

PubMed publication ID

24 August 2017

language of work or name

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publication date

1 May 2011

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Europe PubMed Central

PubMed publication ID

24 August 2017

Genetics in Medicine

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Europe PubMed Central

PubMed publication ID

24 August 2017

13

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Europe PubMed Central

PubMed publication ID

24 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

24 August 2017

377-384

1 reference

Europe PubMed Central

PubMed publication ID

24 August 2017

The genetics of autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Autism: the quest for the genes

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Advancing paternal age and autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Functional impact of global rare copy number variation in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

The genetics of autistic disorders and its clinical relevance: a review of the literature

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Identification and characterization of the tuberous sclerosis gene on chromosome 16

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Advances in autism genetics: on the threshold of a new neurobiology

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Association between microdeletion and microduplication at 16p11.2 and autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Microduplications of 16p11.2 are associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Copy-number variations associated with neuropsychiatric conditions

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Structural variation of chromosomes in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Recurrent 16p11.2 microdeletions in autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Further characterization of the new microdeletion syndrome of 16p11.2-p12.2.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Large, rare chromosomal deletions associated with severe early-onset obesity

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Measuring inconsistency in meta-analyses

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Clinical genetic testing for patients with autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

The role of rare structural variants in the genetics of autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Once and Again—Issues Surrounding Replication in Genetic Association Studies

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182076C0C

21 January 2018

Identifiers

10.1097/GIM.0B013E3182076C0C

1 reference

Europe PubMed Central

PubMed publication ID

24 August 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 August 2017

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