Charlton J, Downing TL, Smith ZD, et al. Author Correction: Global delay in nascent strand DNA methylation. Nat Struct Mol Biol. 2018;25(4):355. doi:10.1038/s41594-018-0055-3
Publications
Alrohaif H, Topf A, Evangelista T, Lek M, McArthur D, Lochmüller H. Whole-exome sequencing identifies mutations in in a mild form of Carey-Fineman-Ziter syndrome. Neurol Genet. 2018;4(2):e226. doi:10.1212/NXG.0000000000000226
Clatworthy AE, Romano KP, Hung DT. Whole-organism phenotypic screening for anti-infectives promoting host health. Nat Chem Biol. 2018;14(4):331-341. doi:10.1038/s41589-018-0018-3
Hindy G, Engström G, Larsson SC, et al. Role of Blood Lipids in the Development of Ischemic Stroke and its Subtypes: A Mendelian Randomization Study. Stroke. 2018;49(4):820-827. doi:10.1161/STROKEAHA.117.019653
Charlton J, Downing TL, Smith ZD, et al. Global delay in nascent strand DNA methylation. Nat Struct Mol Biol. 2018;25(4):327-332. doi:10.1038/s41594-018-0046-4
Malik R, Chauhan G, Traylor M, et al. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2018;50(4):524-537. doi:10.1038/s41588-018-0058-3
Chen Z, Lichtor PA, Berliner AP, Chen JC, Liu DR. Evolution of sequence-defined highly functionalized nucleic acid polymers. Nat Chem. 2018;10(4):420-427. doi:10.1038/s41557-018-0008-9
Dunn EC, Sofer T, Wang MJ, et al. Genome-wide association study of depressive symptoms in the Hispanic Community Health Study/Study of Latinos. J Psychiatr Res. 2018;99:167-176. doi:10.1016/j.jpsychires.2017.12.010
Landry LG, Rehm HL. Association of Racial/Ethnic Categories With the Ability of Genetic Tests to Detect a Cause of Cardiomyopathy. JAMA Cardiol. 2018;3(4):341-345. doi:10.1001/jamacardio.2017.5333
Gilles ME, Hao L, Huang L, et al. Personalized RNA Medicine for Pancreatic Cancer. Clin Cancer Res. 2018;24(7):1734-1747. doi:10.1158/1078-0432.CCR-17-2733