Hayeck TJ, Zaitlen NA, Loh PR, et al. Mixed model with correction for case-control ascertainment increases association power. Am J Hum Genet. 2015;96(5):720-30. doi:10.1016/j.ajhg.2015.03.004
Sadd BM, Barribeau SM, Bloch G, et al. The genomes of two key bumblebee species with primitive eusocial organization. Genome Biol. 2015;16:76. doi:10.1186/s13059-015-0623-3
Peyrot WJ, Lee SH, Milaneschi Y, et al. The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects. Mol Psychiatry. 2015;20(6):735-43. doi:10.1038/mp.2015.50
Gesierich B, Opherk C, Rosand J, et al. APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL. J Cereb Blood Flow Metab. 2016;36(1):199-203. doi:10.1038/jcbfm.2015.85
Westra HJ, Arends D, Esko T, et al. Cell Specific eQTL Analysis without Sorting Cells. PLoS Genet. 2015;11(5):e1005223. doi:10.1371/journal.pgen.1005223
Melé M, Ferreira PG, Reverter F, et al. Human genomics. The human transcriptome across tissues and individuals. Science. 2015;348(6235):660-5. doi:10.1126/science.aaa0355
Surakka I, Horikoshi M, Mägi R, et al. The impact of low-frequency and rare variants on lipid levels. Nat Genet. 2015;47(6):589-97. doi:10.1038/ng.3300
Mukamal KJ, Jensen MK, Pers TH, Pai JK, Kraft P, Rimm EB. Multilocus heterozygosity and coronary heart disease: nested case-control studies in men and women. PLoS One. 2015;10(5):e0124847. doi:10.1371/journal.pone.0124847
Franke L, Bannoudi H el, Jansen DTSL, et al. Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes. Eur J Hum Genet. 2016;24(2):263-70. doi:10.1038/ejhg.2015.95
Chen CY, Han J, Hunter DJ, Kraft P, Price AL. Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction. Genet Epidemiol. 2015;39(6):427-38. doi:10.1002/gepi.21906