Muñoz JF, Farrer RA, Desjardins CA, et al. Genome Diversity, Recombination, and Virulence across the Major Lineages of Paracoccidioides. mSphere. 2016;1(5). doi:10.1128/mSphere.00213-16
Publications
Li G, Cunin P, Wu D, et al. The Rheumatoid Arthritis Risk Variant CCR6DNP Regulates CCR6 via PARP-1. PLoS Genet. 2016;12(9):e1006292. doi:10.1371/journal.pgen.1006292
Walesky C, Goessling W. Nature and nurture: Environmental toxins and biliary atresia. Hepatology. 2016;64(3):717-9. doi:10.1002/hep.28701
High FA, Bhayani P, Wilson JM, Bult CJ, Donahoe PK, Longoni M. De novo frameshift mutation in COUP-TFII (NR2F2) in human congenital diaphragmatic hernia. Am J Med Genet A. 2016;170(9):2457-61. doi:10.1002/ajmg.a.37830
Flannick J, Florez JC. Type 2 diabetes: genetic data sharing to advance complex disease research. Nat Rev Genet. 2016;17(9):535-49. doi:10.1038/nrg.2016.56
Wright JB, Sanjana NE. CRISPR Screens to Discover Functional Noncoding Elements. Trends Genet. 2016;32(9):526-9. doi:10.1016/j.tig.2016.06.004
Scott EM, Halees A, Itan Y, et al. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Nat Genet. 2016;48(9):1071-6. doi:10.1038/ng.3592
Kar SP, Beesley J, Olama AAA, et al. Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types. Cancer Discov. 2016;6(9):1052-67. doi:10.1158/2159-8290.CD-15-1227
Provine NM, Larocca RA, Aid M, et al. Immediate Dysfunction of Vaccine-Elicited CD8+ T Cells Primed in the Absence of CD4+ T Cells. J Immunol. 2016;197(5):1809-22. doi:10.4049/jimmunol.1600591
Ku T, Swaney J, Park JY, et al. Multiplexed and scalable super-resolution imaging of three-dimensional protein localization in size-adjustable tissues. Nat Biotechnol. 2016;34(9):973-81. doi:10.1038/nbt.3641