Emdin CA, Khera AV, Natarajan P, et al. Genetic Association of Waist-to-Hip Ratio With Cardiometabolic Traits, Type 2 Diabetes, and Coronary Heart Disease. JAMA. 2017;317(6):626-634. doi:10.1001/jama.2016.21042
Publications
Grossman SR, Zhang X, Wang L, et al. Systematic dissection of genomic features determining transcription factor binding and enhancer function. Proc Natl Acad Sci U S A. 2017;114(7):E1291-E1300. doi:10.1073/pnas.1621150114
Yu L, Lutz MW, Wilson RS, et al. TOMM40’523 variant and cognitive decline in older persons with APOE ε3/3 genotype. Neurology. 2017;88(7):661-668. doi:10.1212/WNL.0000000000003614
Kar SP, Adler E, Tyrer J, et al. Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci. Br J Cancer. 2017;116(4):524-535. doi:10.1038/bjc.2016.426
Bargiela D, Bianchi MT, Westover B, et al. Selection of first-line therapy in multiple sclerosis using risk-benefit decision analysis. Neurology. 2017;88(7):677-684. doi:10.1212/WNL.0000000000003612
Fishbein L, Leshchiner I, Walter V, et al. Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma. Cancer Cell. 2017;31(2):181-193. doi:10.1016/j.ccell.2017.01.001
Levin BJ, Huang YY, Peck SC, et al. A prominent glycyl radical enzyme in human gut microbiomes metabolizes trans-4-hydroxy-l-proline. Science. 2017;355(6325). doi:10.1126/science.aai8386
Cuomo CA, Bakkeren G, Khalil HB, et al. Comparative Analysis Highlights Variable Genome Content of Wheat Rusts and Divergence of the Mating Loci. G3 (Bethesda). 2017;7(2):361-376. doi:10.1534/g3.116.032797
Marouli E, Graff M, Medina-Gomez C, et al. Rare and low-frequency coding variants alter human adult height. Nature. 2017;542(7640):186-190. doi:10.1038/nature21039
Kreiner E, Waage J, Standl M, et al. Shared genetic variants suggest common pathways in allergy and autoimmune diseases. J Allergy Clin Immunol. 2017. doi:10.1016/j.jaci.2016.10.055