(Q22251090)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

review article

1 reference

title

Copy-number variations associated with neuropsychiatric conditions (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1

Edwin H Jr Cook

Edwin H Jr

Cook

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

2

Stephen W Scherer

Stephen W

Scherer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

language of work or name

English

0 references

publication date

1 October 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

volume

455

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

issue

7215

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

page(s)

919-923

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

Detection of large-scale variation in the human genome

24 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Frequency of new copy number variation in humans

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Genomic rearrangements and sporadic disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Genome architecture, rearrangements and genomic disorders

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Contemplating effects of genomic structural variation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Genetics and genomics of behavioral and psychiatric disorders

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Psychiatric genetics: progress amid controversy

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Autism as a paradigmatic complex genetic disorder

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Structural variation of chromosomes in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Recurrent 16p11.2 microdeletions in autism

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Identifying autism loci and genes by tracing recent shared ancestry

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Strong association of de novo copy number mutations with sporadic schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Large recurrent microdeletions associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Diagnostic genome profiling in mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Ethical implications of array comparative genomic hybridization in complex phenotypes: points to consider in research

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Relative impact of nucleotide and copy number variation on gene expression phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

A unified genetic theory for sporadic and inherited autism

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Autism: highly heritable but not inherited

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Challenges and standards in integrating surveys of structural variation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Deletions of NF1 gene and exons detected by multiplex ligation-dependent probe amplification

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

NF1 microduplication first clinical report: association with mild mental retardation, early onset of baldness and dental enamel hypoplasia?

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Increase inGSK3β gene copy number variation in bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Alpha-synuclein locus duplication as a cause of familial Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

An individual with Gilles de la Tourette syndrome and Smith-Magenis microdeletion syndrome: is chromosome 17p11.2 a candidate region for Tourette syndrome putative susceptibility genes?

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Familial deletion within NLGN4 associated with autism and Tourette syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

An interview with... Cliff Tabin

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07458

7 January 2021

Identifiers

DOI

10.1038/NATURE07458

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18923514%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

24 December 2019

1002940116

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017