Leveraging Genetic Variability across Populations for the Identification of Causal Variants
- 8 January 2010
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 86 (1), 23-33
- https://doi.org/10.1016/j.ajhg.2009.11.016
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)Nature Genetics, 2009
- Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1Nature Genetics, 2009
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetesNature Genetics, 2008
- Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33Proceedings of the National Academy of Sciences of the United States of America, 2008
- So Many Correlated Tests, So Little Time! Rapid Adjustment of P Values for Multiple Correlated TestsAmerican Journal of Human Genetics, 2007
- A second generation human haplotype map of over 3.1 million SNPsNature, 2007
- Genome-wide association study identifies novel breast cancer susceptibility lociNature, 2007
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectNature, 2007
- Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studiesNature Genetics, 2006
- A haplotype map of the human genomeNature, 2005