Manning A, Highland HM, Gasser J, et al. A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. 2017;66(7):2019-2032. doi:10.2337/db16-1329
Publications
Shpigler HY, Saul MC, Murdoch EE, et al. Behavioral, transcriptomic and epigenetic responses to social challenge in honey bees. Genes Brain Behav. 2017;16(6):579-591. doi:10.1111/gbb.12379
Patrick E, Rajagopal S, Wong HKA, et al. Dissecting the role of non-coding RNAs in the accumulation of amyloid and tau neuropathologies in Alzheimer’s disease. Mol Neurodegener. 2017;12(1):51. doi:10.1186/s13024-017-0191-y
Houweling PJ, Berman YD, Turner N, et al. Exploring the relationship between α-actinin-3 deficiency and obesity in mice and humans. Int J Obes (Lond). 2017;41(7):1154-1157. doi:10.1038/ijo.2017.72
Zhou F, Liu Y, Rohde C, et al. AML1-ETO requires enhanced C/D box snoRNA/RNP formation to induce self-renewal and leukaemia. Nat Cell Biol. 2017;19(7):844-855. doi:10.1038/ncb3563
Rothhammer V, Borucki DM, Sanchez MIG, et al. Dynamic regulation of serum aryl hydrocarbon receptor agonists in MS. Neurol Neuroimmunol Neuroinflamm. 2017;4(4):e359. doi:10.1212/NXI.0000000000000359
Khalili H, de Silva PS, Ananthakrishnan AN, et al. Dietary Iron and Heme Iron Consumption, Genetic Susceptibility, and Risk of Crohn’s Disease and Ulcerative Colitis. Inflamm Bowel Dis. 2017;23(7):1088-1095. doi:10.1097/MIB.0000000000001161
Hung J, Lopes SCP, Nery OA, et al. Applying Faster R-CNN for Object Detection on Malaria Images. Conference on Computer Vision and Pattern Recognition Workshops. IEEE Computer Society Conference on Computer Vision and Pattern Recognition. Workshops. 2017;2017:808-813. doi:10.1109/cvprw.2017.112
Lohmann K, Redin C, Tönnies H, et al. Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia. JAMA Neurol. 2017;74(7):806-812. doi:10.1001/jamaneurol.2017.0666
Aung T, Ozaki M, Lee MC, et al. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nat Genet. 2017;49(7):993-1004. doi:10.1038/ng.3875