Chen CW, Koche RP, Sinha AU, et al. DOT1L inhibits SIRT1-mediated epigenetic silencing to maintain leukemic gene expression in MLL-rearranged leukemia. Nat Med. 2015;21(4):335-43. doi:10.1038/nm.3832
Canhao H, Rodrigues AM, Santos MJ, et al. TRAF1/C5 but not PTPRC variants are potential predictors of rheumatoid arthritis response to anti-tumor necrosis factor therapy. Biomed Res Int. 2015;2015:490295. doi:10.1155/2015/490295
Beaudoin M, Gupta RM, Won HH, et al. Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries. Arterioscler Thromb Vasc Biol. 2015;35(6):1472-9. doi:10.1161/ATVBAHA.115.305534
Palta P, Kaplinski L, Nagirnaja L, et al. Haplotype phasing and inheritance of copy number variants in nuclear families. PLoS One. 2015;10(4):e0122713. doi:10.1371/journal.pone.0122713
Zhang CZ, Adalsteinsson VA, Francis J, et al. Calibrating genomic and allelic coverage bias in single-cell sequencing. Nat Commun. 2015;6:6822. doi:10.1038/ncomms7822
Lai KMV, Gong G, Atanasio A, et al. Diverse Phenotypes and Specific Transcription Patterns in Twenty Mouse Lines with Ablated LincRNAs. PLoS One. 2015;10(4):e0125522. doi:10.1371/journal.pone.0125522
Moutsianas L, Agarwala V, Fuchsberger C, et al. The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease. PLoS Genet. 2015;11(4):e1005165. doi:10.1371/journal.pgen.1005165
Viatte S, Plant D, Han B, et al. Association of HLA-DRB1 haplotypes with rheumatoid arthritis severity, mortality, and treatment response. JAMA. 2015;313(16):1645-56. doi:10.1001/jama.2015.3435
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
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