Siegert S, Seo J, Kwon EJ, et al. The schizophrenia risk gene product miR-137 alters presynaptic plasticity. Nat Neurosci. 2015;18(7):1008-16. doi:10.1038/nn.4023
Hägg S, Fall T, Ploner A, et al. Adiposity as a cause of cardiovascular disease: a Mendelian randomization study. Int J Epidemiol. 2015;44(2):578-86. doi:10.1093/ije/dyv094
Ng E, Lind M, Lindgren C, et al. Genome-wide association study of toxic metals and trace elements reveals novel associations. Hum Mol Genet. 2015;24(16):4739-45. doi:10.1093/hmg/ddv190
Sul JH, Raj T, de Jong S, et al. Accurate and fast multiple-testing correction in eQTL studies. Am J Hum Genet. 2015;96(6):857-68. doi:10.1016/j.ajhg.2015.04.012
Pendergraft WF, Nachman PH. Recent pathogenetic advances in ANCA-associated vasculitis. Presse Med. 2015;44(6 Pt 2):e223-9. doi:10.1016/j.lpm.2015.04.007
Draisma HHM, Pool R, Kobl M, et al. Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Nat Commun. 2015;6:7208. doi:10.1038/ncomms8208
Housley WJ, Fernandez SD, Vera K, et al. Genetic variants associated with autoimmunity drive NFκB signaling and responses to inflammatory stimuli. Sci Transl Med. 2015;7(291):291ra93. doi:10.1126/scitranslmed.aaa9223
Jansen H, Loley C, Lieb W, et al. Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk. Atherosclerosis. 2015;241(2):419-26. doi:10.1016/j.atherosclerosis.2015.05.033
Hohman TJ, Cooke-Bailey JN, Reitz C, et al. Global and local ancestry in African-Americans: Implications for Alzheimer’s disease risk. Alzheimers Dement. 2016;12(3):233-43. doi:10.1016/j.jalz.2015.02.012
Usher CL, Handsaker RE, Esko T, et al. Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. Nat Genet. 2015;47(8):921-5. doi:10.1038/ng.3340