1 |
Butte, A., Califano, A., Friend, S., Ideker, T., and Schadt, E. (2011). Integrative Network-based Association Studies: Leveraging cell regulatory models in the post-GWAS era. Nature Precedings doi:10.1038/npre.2011.5732.1
DOI
|
2 |
GIANT Consortium. (2010). Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467, 832-838.
DOI
ScienceOn
|
3 |
The International HapMap Consortium. (2003). The International HapMap Project. Nature 426, 789-796.
DOI
ScienceOn
|
4 |
Thorisson, G.A., and Stein, L.D. (2003). The SNP Consortium website: past, present and future. Nucl. Acids Res. 31, 124-127.
DOI
|
5 |
Wang, K., Li, M., and Hakonarson, H. (2010). Analysing biological pathways in Genome-wide association studies. Nat. Rev. Genet. 11, 843-854.
DOI
ScienceOn
|
6 |
Wang, W.Y., Barratt, B.J., Clayton, D.G., and Todd, J.A. (2005). Genome-wide association studies: theoretical and practical concerns. Nat. Rev. Genet. 6, 109-118.
DOI
|
7 |
Yang, J., Benyamin, B., McEvoy, B.P., Gordon, S., Henders, A.K., Nyholt, D.R., Madden, P.A., Heath, A.C., Martin, N.G., Montgomery, G.W., Goddard, M.E., and Visscher, P.M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42, 565-569.
DOI
|
8 |
Hudson, T. (2011). Genomics and Clinical Relevance. Science 331, 547.
|
9 |
Hindorff, L.A., Sethupathy, P., Junkins, H.A., Ramos, E.M., Mehta, J.P., Collins, F.S., and Manolio, T.A. (2009). Potential etiologic and functional implications of genome- wide association loci for human diseases and traits. Proc. Natl. Acad Sci. USA 106, 9362-9367.
DOI
|
10 |
Huang, D.W., Sherman, B.T., and Lempicki, R.A. (2009). Systematic and integrative analysis of large gene lists using DAVID Bioinformatics Resources. Nat. Protoc. 4, 44-57.
|
11 |
Lander, E.S. (2011). Initial impact of the sequencing of the human genome. Nature 470, 187-197.
DOI
|
12 |
Manolio, T.A., Collins, F.S., Cox, N.J., Goldstein, D.B., Hindorff, L.A., Hunter, D.J., McCarthy, M.I., Ramos, E.M., Cardon, L.R., Chakravarti, A., Cho, J.H., Guttmacher, A.E., Kong, A., Kruglyak, L., Mardis, E., Rotimi, C.N., Slatkin, M., Valle, D., Whittemore, A.S., Boehnke, M., Clark, A.G., Eichler, E.E., Gibson, G., Haines, J.L., Mackay, T.F., McCarroll, S.A., and Visscher, P.M. (2009). Finding the missing heritability of complex diseases. Nature 461, 747-753.
DOI
|
13 |
Mardis, E.R. (2011). A decade's perspective on DNA sequencing technology. Nature 470, 198-203.
DOI
|
14 |
Nature Editorial. (2010). The human genome at ten. Nature 464, 649-650.
DOI
|
15 |
Monteiro, A.N.A., Coetzee, G.A., Freedman, M.L., Biasi, M.D., Casey, G., Duggan, D., Risch, A., Plass, C., Liu, P., James, M., Vikis, H.G., Tichelaar, J.W., You, M., Gayther, S.A., and Mills, I.G. (2010). Principles for the post-GWAS functional characterisation of risk loci. Nature Precedings. doi:10.1038/npre.2010. 5162.
DOI
|
16 |
Nam, D., Kim, J., Kim, S.Y., and Kim, S. (2010). GSA-SNP: a general approach for gene set analysis of polymorphisms. Nucl. Acids Res. 38, 749-754.
DOI
ScienceOn
|
17 |
Nam, D., Kim, S.Y., Gene-set approach for expression pattern analysis. (2008). Brief Bioinform. 9, 189-197.
DOI
|