Subramanian A, Tamayo P, Mootha VK, et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci U S A. 2005;102(43):15545-50. doi:10.1073/pnas.0506580102
Nusbaum C, Zody MC, Borowsky ML, et al. DNA sequence and analysis of human chromosome 18. Nature. 2005;437(7058):551-5. doi:10.1038/nature03983
Petryshen TL, Middleton FA, Tahl AR, et al. Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia. Mol Psychiatry. 2005;10(12):1074-88, 1057. doi:10.1038/sj.mp.4001739
Tengs T, Lee JC, Paez G, et al. A transforming MET mutation discovered in non-small cell lung cancer using microarray-based resequencing. Cancer Lett. 2006;239(2):227-33. doi:10.1016/j.canlet.2005.08.007
Trinh TT, Rioux JD. The promise and perils of interpreting genetic associations in Crohn’s disease. Gut. 2005;54(10):1354-7. doi:10.1136/gut.2005.070920
Giallourakis C, Henson C, Reich M, Xie X, Mootha VK. Disease gene discovery through integrative genomics. Annu Rev Genomics Hum Genet. 2005;6:381-406. doi:10.1146/annurev.genom.6.080604.162234
Freedman ML, Penney KL, Stram DO, et al. A haplotype-based case-control study of BRCA1 and sporadic breast cancer risk. Cancer Res. 2005;65(16):7516-22. doi:10.1158/0008-5472.CAN-05-0132
Gillette MA, Mani DR, Carr SA. Place of pattern in proteomic biomarker discovery. J Proteome Res. 2005;4(4):1143-54. doi:10.1021/pr0500962
Chandra S, Muir C, Silva M, Carr S. Imaging biomarkers in drug development: an overview of opportunities and open issues. J Proteome Res. 2005;4(4):1134-7. doi:10.1021/pr0500915
Sawcer S, Ban M, Maranian M, et al. A high-density screen for linkage in multiple sclerosis. Am J Hum Genet. 2005;77(3):454-67. doi:10.1086/444547