Stieglitz E, Taylor-Weiner AN, Chang TY, et al. The genomic landscape of juvenile myelomonocytic leukemia. Nat Genet. 2015;47(11):1326-1333. doi:10.1038/ng.3400
Sham PC, Purcell SM. Statistical power and significance testing in large-scale genetic studies. Nat Rev Genet. 2014;15(5):335-46. doi:10.1038/nrg3706
Fraser HB, Xie X. Common polymorphic transcript variation in human disease. Genome Res. 2009;19(4):567-75. doi:10.1101/gr.083477.108
Henn MR, Boutwell CL, Charlebois P, et al. Whole genome deep sequencing of HIV-1 reveals the impact of early minor variants upon immune recognition during acute infection. PLoS Pathog. 2012;8(3):e1002529. doi:10.1371/journal.ppat.1002529
Turchin MC, Chiang CWK, Palmer CD, et al. Evidence of widespread selection on standing variation in Europe at height-associated SNPs. Nat Genet. 2012;44(9):1015-9. doi:10.1038/ng.2368
Li Q, Seo JH, Stranger B, et al. Integrative eQTL-based analyses reveal the biology of breast cancer risk loci. Cell. 2013;152(3):633-41. doi:10.1016/j.cell.2012.12.034
McLaren PJ, Coulonges C, Ripke S, et al. Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls. PLoS Pathog. 2013;9(7):e1003515. doi:10.1371/journal.ppat.1003515
Okada Y, Wu D, Trynka G, et al. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature. 2014;506(7488):376-81. doi:10.1038/nature12873
Agler C, Nielsen DM, Urkasemsin G, et al. Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24. PLoS Genet. 2014;10(2):e1003991. doi:10.1371/journal.pgen.1003991
Saxena R, Bjonnes A, Prescott J, et al. Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort. Circ Cardiovasc Genet. 2014;7(3):287-95. doi:10.1161/CIRCGENETICS.113.000412