Yeo TW, De Jager PL, Gregory SG, et al. A second major histocompatibility complex susceptibility locus for multiple sclerosis. Ann Neurol. 2007;61(3):228-36. doi:10.1002/ana.21063
Newton-Cheh C, Hirschhorn JN. Genetic association studies of complex traits: design and analysis issues. Mutat Res. 2005;573(1-2):54-69. doi:10.1016/j.mrfmmm.2005.01.006
Daniels R, Ndiaye D, Wall M, et al. Rapid, field-deployable method for genotyping and discovery of single-nucleotide polymorphisms associated with drug resistance in Plasmodium falciparum. Antimicrob Agents Chemother. 2012;56(6):2976-86. doi:10.1128/AAC.05737-11
Cuomo CA, Desjardins CA, Bakowski MA, et al. Microsporidian genome analysis reveals evolutionary strategies for obligate intracellular growth. Genome Res. 2012;22(12):2478-88. doi:10.1101/gr.142802.112
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
Han B, Kang EY, Raychaudhuri S, de Bakker PIW, Eskin E. Fast pairwise IBD association testing in genome-wide association studies. Bioinformatics. 2014;30(2):206-13. doi:10.1093/bioinformatics/btt609
Hamrefors V, Hedblad B, Hindy G, et al. Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21. PLoS One. 2014;9(1):e85893. doi:10.1371/journal.pone.0085893
Duncan LE, Holmans PA, Lee PH, et al. Pathway analyses implicate glial cells in schizophrenia. PLoS One. 2014;9(2):e89441. doi:10.1371/journal.pone.0089441
Garraway LA. A Notch for noncoding RNA in melanoma. N Engl J Med. 2014;370(20):1950-1. doi:10.1056/NEJMcibr1402173
Speed D, O’Brien TJ, Palotie A, et al. Describing the genetic architecture of epilepsy through heritability analysis. Brain. 2014;137(Pt 10):2680-9. doi:10.1093/brain/awu206