Rare chromosomal deletions and duplications increase risk of schizophrenia (Q22337245)

Célia Maria de Oliveira Barreto Coimbra Carvalho

0 references

Christopher P. Morley

Christopher P. Morley

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Douglas M. Ruderfer

Douglas M. Ruderfer

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Benjamin S Pickard

Benjamin Pickard

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Andrew McQuillin

Andrew McQuillin

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Derek W. Morris

Derek W Morris

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Stuart Macgregor

Stuart MacGregor

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Draga Toncheva

Draga Toncheva

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Aiden Corvin

Aiden Corvin

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George Kirov

George Kirov

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A Macedo

macedo, a

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David Curtis

David Curtis

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Peter Holmans

Peter Holmans

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James Walters

James Walters

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Michael Gill

Michael Gill

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Michael C O'Donovan

Michael C O'Donovan

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Peter M. Visscher

Visscher PM

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Paul Lichtenstein

Structural variation of chromosomes in autism spectrum disorder

paul lichtenstein

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language of work or name

English

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publication date

11 September 2008

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published in

Nature

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volume

455

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issue

7210

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page(s)

237-41

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cites work

1 reference

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Strong association of de novo copy number mutations with autism

19 March 2017

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Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

19 March 2017

1 reference

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

19 March 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

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Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

19 March 2017

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

19 March 2017

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Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

19 March 2017

1 reference

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Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

19 March 2017

1 reference

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

19 March 2017

1 reference

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Integrated detection and population-genetic analysis of SNPs and copy number variation

19 March 2017

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Genome architecture, rearrangements and genomic disorders

7 April 2017

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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

7 April 2017

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

27 September 2017

1 reference

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Chromosome 22 deletion syndrome and schizophrenia

27 September 2017

1 reference

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Identification of DNA copy-number aberrations by array-comparative genomic hybridization in patients with schizophrenia

27 September 2017

1 reference

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Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

27 September 2017

1 reference

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

27 September 2017

1 reference

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Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms

27 September 2017

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Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome.

30 May 2018

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CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

29 November 2018

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DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.

29 November 2018

1 reference

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Linkage of schizophrenia with chromosome 1q loci in Taiwanese families.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912847

Evidence for linkage disequilibrium between the alpha 7-nicotinic receptor gene (CHRNA7) locus and schizophrenia in Azorean families

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912847

Schizophrenia, the heteromodal association neocortex and development: potential for a neurogenetic approach.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912847

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18668038

12 December 2020

inferred from PubMed ID database lookup

Association study of CHRFAM7A copy number and 2bp deletion polymorphisms with schizophrenia and bipolar affective disorder

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18668038

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNATURE07239

7 January 2021

inferred from DOI database lookup

Large recurrent microdeletions associated with schizophrenia

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNATURE07239

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NATURE07239

1 reference

Dimensions Publication ID

1040865418

0 references

1 reference

1 reference

PubMed publication ID

18668038

1 reference