Interpretation of Association Signals and Identification of Causal Variants from Genome-wide Association Studies
Open Access
- 14 May 2010
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 86 (5), 730-742
- https://doi.org/10.1016/j.ajhg.2010.04.003
Abstract
No abstract availableKeywords
This publication has 59 references indexed in Scilit:
- Finding the missing heritability of complex diseasesNature, 2009
- Common vs. rare allele hypotheses for complex diseasesCurrent Opinion in Genetics & Development, 2009
- Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancersHuman Genetics, 2008
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence DataAmerican Journal of Human Genetics, 2008
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsNature, 2007
- Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDLNature Genetics, 2007
- The Genetic Basis of Complex TraitsPublished by Springer Science and Business Media LLC ,2007
- A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCNature Genetics, 2006
- Detecting recent positive selection in the human genome from haplotype structureNature, 2002
- Population genetics—making sense out of sequenceNature Genetics, 1999