Weng LC, Tang W, Rich SS, et al. A genetic association study of D-dimer levels with 50K SNPs from a candidate gene chip in four ethnic groups. Thromb Res. 2014;134(2):462-7. doi:10.1016/j.thromres.2014.05.018
Okada Y, Han B, Tsoi LC, et al. Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes. Am J Hum Genet. 2014;95(2):162-72. doi:10.1016/j.ajhg.2014.07.002
van der Valk RJP, Kreiner-Møller E, Kooijman MN, et al. A novel common variant in DCST2 is associated with length in early life and height in adulthood. Hum Mol Genet. 2015;24(4):1155-68. doi:10.1093/hmg/ddu510
Gottlieb DJ, Hek K, Chen TH, et al. Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Mol Psychiatry. 2015;20(10):1232-9. doi:10.1038/mp.2014.133
Tiihonen J, Rautiainen MR, Ollila HM, et al. Genetic background of extreme violent behavior. Mol Psychiatry. 2015;20(6):786-92. doi:10.1038/mp.2014.130
Benyamin B, Esko T, Ried JS, et al. Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nat Commun. 2014;5:4926. doi:10.1038/ncomms5926
Yu L, Chibnik LB, Srivastava GP, et al. Association of Brain DNA methylation in SORL1, ABCA7, HLA-DRB5, SLC24A4, and BIN1 with pathological diagnosis of Alzheimer disease. JAMA Neurol. 2015;72(1):15-24. doi:10.1001/jamaneurol.2014.3049
Ruderfer DM, Lim ET, Genovese G, et al. No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia. Eur J Hum Genet. 2015;23(4):555-7. doi:10.1038/ejhg.2014.228
Ramanan VK, Nho K, Shen L, et al. FASTKD2 is associated with memory and hippocampal structure in older adults. Mol Psychiatry. 2015;20(10):1197-204. doi:10.1038/mp.2014.142
Golan D, Lander ES, Rosset S. Measuring missing heritability: inferring the contribution of common variants. Proc Natl Acad Sci U S A. 2014;111(49):E5272-81. doi:10.1073/pnas.1419064111