Linked Life Data

17164797

Source:http://linkedlifedata.com/resource/pubmed/id/17164797

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2007-2-22
pubmed:abstractText
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, genome-wide association studies are now becoming a reality. In this paper, we discuss the utility of these approaches to detect genetic risk variants involved in complex disease susceptibility and, in the best case scenario where a signal is detected, how helpful it will be to the understanding of the pathological process.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1018-4813
pubmed:author
pubmed:issnType
Print
pubmed:volume
15
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
260-3
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?
pubmed:affiliation
1INSERM U535, University Paris Sud, Villejuif F-94817, France. bourgain@vjf.inserm.fr
pubmed:publicationType
Journal Article