Raj T, Shulman JM, Keenan BT, et al. Alzheimer disease susceptibility loci: evidence for a protein network under natural selection. Am J Hum Genet. 2012;90(4):720-6. doi:10.1016/j.ajhg.2012.02.022
Raychaudhuri S, Rich SS. Autoimmunity: insights from human genomics. Curr Opin Immunol. 2012;24(5):513-5. doi:10.1016/j.coi.2012.09.006
Price AL, Zaitlen NA, Reich D, Patterson N. Response to Sul and Eskin. Nat Rev Genet. 2013;14(4):300. doi:10.1038/nrg2813-c2
Agarwala V, Flannick J, Sunyaev S, GoT2D Consortium, Altshuler D. Evaluating empirical bounds on complex disease genetic architecture. Nat Genet. 2013;45(12):1418-27. doi:10.1038/ng.2804
Malik R, Bevan S, Nalls MA, et al. Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies. Stroke. 2014;45(2):394-402. doi:10.1161/STROKEAHA.113.002938
Tragante V, Barnes MR, Ganesh SK, et al. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. Am J Hum Genet. 2014;94(3):349-60. doi:10.1016/j.ajhg.2013.12.016
Deelen P, Menelaou A, van Leeuwen EM, et al. Improved imputation quality of low-frequency and rare variants in European samples using the ’Genome of The Netherlands’. Eur J Hum Genet. 2014;22(11):1321-6. doi:10.1038/ejhg.2014.19
Mäkinen VP, Civelek M, Meng Q, et al. Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease. PLoS Genet. 2014;10(7):e1004502. doi:10.1371/journal.pgen.1004502
Levinson DF, Mostafavi S, Milaneschi Y, et al. Genetic studies of major depressive disorder: why are there no genome-wide association study findings and what can we do about it?. Biol Psychiatry. 2014;76(7):510-2. doi:10.1016/j.biopsych.2014.07.029
Smith G, Luk K, Schulz CA, et al. Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis. JAMA. 2014;312(17):1764-71. doi:10.1001/jama.2014.13959