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1.
Figure 2.

Figure 2. From: Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases.

A vision for collaboration among disease- and gene-specific investigators, systematic reviewers, and online publishers. HuGENet, Human Genome Epidemiology Network; HVP, Human Variome Project; P3G, Public Population Project in Genomics.

Muin J. Khoury, et al. Am J Epidemiol. 2009 August 1;170(3):269-279.
2.
Figure 1.

Figure 1. From: Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases.

A) Levels of statistical significance for associations of genetic loci with P values of 10−5 or lower identified through genome-wide association studies (GWAS) and entered in the National Human Genome Research Institute catalog of GWAS as of October 14, 2008 (38, 39); data are limited to those loci that have binary outcome phenotypes (n = 223). For details on selection of loci in the catalog, see Hindorff et al. (38) and Manolio et al. (39). B) Odds ratios (per allele) for the 223 associations. C) Odds ratios for the 142 of the 233 associations that had P values less than 10−7. Not shown are the 5, 13, and 7 outliers that had values outside of the depicted range in the 3 panels, respectively.

Muin J. Khoury, et al. Am J Epidemiol. 2009 August 1;170(3):269-279.

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