Cassa CA, Weghorn D, Balick DJ, et al. Estimating the selective effects of heterozygous protein-truncating variants from human exome data. Nat Genet. 2017;49(5):806-810. doi:10.1038/ng.3831
Publications
Wang X, Yang K, Xie Q, et al. Purine synthesis promotes maintenance of brain tumor initiating cells in glioma. Nat Neurosci. 2017;20(5):661-673. doi:10.1038/nn.4537
Lassen KG, Xavier RJ. Genetic control of autophagy underlies pathogenesis of inflammatory bowel disease. Mucosal Immunol. 2017;10(3):589-597. doi:10.1038/mi.2017.18
Hill A, Loh PR, Bharadwaj RB, et al. Stepwise Distributed Open Innovation Contests for Software Development: Acceleration of Genome-Wide Association Analysis. Gigascience. 2017;6(5):1-10. doi:10.1093/gigascience/gix009
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
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