Identification of Common Genetic Variants Predisposing to Neurobehavioral Disease by way of Genome-Wide SNP Association Studies
Correspondence: (Login to view email address)
- The Translational Genomics Research Institute
- Document Type:
- Presentation
- Date:
- Received 13 December 2008 01:07 UTC; Posted 15 December 2008
- Subjects:
- Genetics & Genomics
- Abstract:
Dr. David Craig began by explaining expression and linkage studies. He then focused on genome-wide association studies (GWAS), giving examples from Diabetes Type 2 and Alzheimer’s research. Dr. Craig concluded with the recognition that GWAS cannot at the present adequately account for environmental influences on disease.
To watch Dr. Craig’s presentation, please see the Panel 3 Google Video posting.
- Collection:
- Stanford University: CIRGE Symposium May 9, 2008
- Presented at:
- CIRGE Symposium: Capturing Complexity, 09 May 2008
Discussion
- Votes:
-
0 votes
- Comments:
-
0 comments
- (Login to share with a colleague)
Additional information
- License:
- This document is licensed to the public under the Creative Commons Attribution 3.0 License
- How to cite this document:
-
Craig, David. Identification of Common Genetic Variants Predisposing to Neurobehavioral Disease by way of Genome-Wide SNP Association Studies. Available from Nature Precedings <http://dx.doi.org/10.1038/npre.2008.2652.1> (2008)
- Version info:
-
Other versions of this document in Nature Precedings
None.
Other versions of this document elsewhere on the web
None known.
