Merino J, Leong A, Posner DC, et al. Genetically Driven Hyperglycemia Increases Risk of Coronary Artery Disease Separately From Type 2 Diabetes. Diabetes Care. 2017;40(5):687-693. doi:10.2337/dc16-2625
Publications
Walesky C, Goessling W. WNTing no RASt for hepatocellular carcinoma. Hepatology. 2017;65(5):1435-1437. doi:10.1002/hep.29157
Holmberg FE, Seidelin JB, Yin X, et al. Culturing human intestinal stem cells for regenerative applications in the treatment of inflammatory bowel disease. EMBO Mol Med. 2017;9(5):558-570. doi:10.15252/emmm.201607260
Florez JC. Pharmacogenetics in type 2 diabetes: precision medicine or discovery tool? Diabetologia. 2017;60(5):800-807. doi:10.1007/s00125-017-4227-1
Carlston CM, O’Donnell-Luria AH, Underhill HR, et al. Pathogenic ASXL1 somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz Syndrome. Hum Mutat. 2017;38(5):517-523. doi:10.1002/humu.23203
Deming Y, Li Z, Kapoor M, et al. Genome-wide association study identifies four novel loci associated with Alzheimer’s endophenotypes and disease modifiers. Acta Neuropathol. 2017;133(5):839-856. doi:10.1007/s00401-017-1685-y
Abbott J, Ye T, Qin L, et al. CMOS nanoelectrode array for all-electrical intracellular electrophysiological imaging. Nat Nanotechnol. 2017;12(5):460-466. doi:10.1038/nnano.2017.3
Dukik K, Muñoz JF, Jiang Y, et al. Novel taxa of thermally dimorphic systemic pathogens in the Ajellomycetaceae (Onygenales). Mycoses. 2017;60(5):296-309. doi:10.1111/myc.12601
Wamsley B, Fishell G. Genetic and activity-dependent mechanisms underlying interneuron diversity. Nat Rev Neurosci. 2017;18(5):299-309. doi:10.1038/nrn.2017.30
Wang W, Li C, Chen Q, et al. Striatopallidal dysfunction underlies repetitive behavior in Shank3-deficient model of autism. J Clin Invest. 2017;127(5):1978-1990. doi:10.1172/JCI87997