Pugh TJ, Morozova O, Attiyeh EF, et al. The genetic landscape of high-risk neuroblastoma. Nat Genet. 2013;45(3):279-84. doi:10.1038/ng.2529
Cibulskis K, Lawrence MS, Carter SL, et al. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol. 2013;31(3):213-9. doi:10.1038/nbt.2514
Grossman SR, Andersen KG, Shlyakhter I, et al. Identifying recent adaptations in large-scale genomic data. Cell. 2013;152(4):703-13. doi:10.1016/j.cell.2013.01.035
Genovese G, Handsaker RE, Li H, et al. Using population admixture to help complete maps of the human genome. Nat Genet. 2013;45(4):406-14, 414e1. doi:10.1038/ng.2565
Genovese G, Friedman DJ, Pollak MR. APOL1 variants and kidney disease in people of recent African ancestry. Nat Rev Nephrol. 2013;9(4):240-4. doi:10.1038/nrneph.2013.34
Kiezun A, Pulit SL, Francioli LC, et al. Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency. PLoS Genet. 2013;9(2):e1003301. doi:10.1371/journal.pgen.1003301
Moorjani P, Patterson N, Loh PR, et al. Reconstructing Roma history from genome-wide data. PLoS One. 2013;8(3):e58633. doi:10.1371/journal.pone.0058633
Dulak AM, Stojanov P, Peng S, et al. Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity. Nat Genet. 2013;45(5):478-86. doi:10.1038/ng.2591
Garraway LA, Lander ES. Lessons from the cancer genome. Cell. 2013;153(1):17-37. doi:10.1016/j.cell.2013.03.002
Van Allen EM, Wagle N, Levy MA. Clinical analysis and interpretation of cancer genome data. J Clin Oncol. 2013;31(15):1825-33. doi:10.1200/JCO.2013.48.7215