Shukla SA, Howitt BE, Wu CJ, Konstantinopoulos PA. Predicted neoantigen load in non-hypermutated endometrial cancers: Correlation with outcome and tumor-specific genomic alterations. Gynecol Oncol Rep. 2017;19:42-45. doi:10.1016/j.gore.2016.12.009
Publications
de Lange KM, Moutsianas L, Lee JC, et al. Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. Nat Genet. 2017;49(2):256-261. doi:10.1038/ng.3760
Shaw ND, Brand H, Kupchinsky ZA, et al. SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nat Genet. 2017;49(2):238-248. doi:10.1038/ng.3743
Luo Y, de Lange KM, Jostins L, et al. Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7. Nat Genet. 2017;49(2):186-192. doi:10.1038/ng.3761
Gong Y, Schumacher SE, Wu WH, Tang F, Beroukhim R, Chan TA. Pan-Cancer Analysis Links PARK2 to BCL-XL-Dependent Control of Apoptosis. Neoplasia. 2017;19(2):75-83. doi:10.1016/j.neo.2016.12.006
Davidson SM, Jonas O, Keibler MA, et al. Direct evidence for cancer-cell-autonomous extracellular protein catabolism in pancreatic tumors. Nat Med. 2017;23(2):235-241. doi:10.1038/nm.4256
Lyons SM, Fay MM, Akiyama Y, Anderson PJ, Ivanov P. RNA biology of angiogenin: Current state and perspectives. RNA Biol. 2017;14(2):171-178. doi:10.1080/15476286.2016.1272746
Krienen FM, Sherwood CC. Gradients of Connectivity in the Cerebral Cortex. Trends Cogn Sci. 2017;21(2):61-63. doi:10.1016/j.tics.2016.12.002
Maussion G, Cruceanu C, Rosenfeld JA, et al. Implication of LRRC4C and DPP6 in neurodevelopmental disorders. Am J Med Genet A. 2017;173(2):395-406. doi:10.1002/ajmg.a.38021
Pasaniuc B, Price AL. Dissecting the genetics of complex traits using summary association statistics. Nat Rev Genet. 2017;18(2):117-127. doi:10.1038/nrg.2016.142