Linked Life Data

20439386

Source:http://linkedlifedata.com/resource/pubmed/id/20439386

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2010-8-9
pubmed:abstractText
Structural variations of DNA, such as copy number variations (CNVs), are recognized to contribute both to normal genomic variability and to risk for human diseases. For example, schizophrenia has an established connection with 22q11.2 deletions. Recent genome-wide studies have provided initial evidence that CNVs at other loci may also be associated with schizophrenia. In this article, the authors provide a brief overview of CNVs, review recent findings related to schizophrenia, outline implications for clinical practice and diagnostic subtyping, and make recommendations for future reports on CNVs to improve interpretation of results.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1535-7228
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
167
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
899-914
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.
pubmed:affiliation
Clinical Genetics Research Program, Centre for Addiction and Mental Health, 33 Russell St., Toronto, Ontario, Canada. anne.bassett@utoronto.ca
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural