Thomas JC, Godfrey PA, Feldgarden M, Robinson A. Draft genome sequences of Staphylococcus aureus sequence type 34 (ST34) and ST42 hybrids. J Bacteriol. 2012;194(10):2740-1. doi:10.1128/JB.00248-12
Marbach D, Lamparter D, Quon G, Kellis M, Kutalik Z, Bergmann S. Tissue-specific regulatory circuits reveal variable modular perturbations across complex diseases. Nat Methods. 2016;13(4):366-70. doi:10.1038/nmeth.3799
Sudmant PH, Rausch T, Gardner EJ, et al. An integrated map of structural variation in 2,504 human genomes. Nature. 2015;526(7571):75-81. doi:10.1038/nature15394
Rioux JD, Daly MJ, Silverberg MS, et al. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat Genet. 2001;29(2):223-8. doi:10.1038/ng1001-223
Patterson N, Petersen DC, van der Ross RE, et al. Genetic structure of a unique admixed population: implications for medical research. Hum Mol Genet. 2010;19(3):411-9. doi:10.1093/hmg/ddp505
Patterson N, Price AL, Reich D. Population structure and eigenanalysis. PLoS Genet. 2006;2(12):e190. doi:10.1371/journal.pgen.0020190
Singer JB, Hill AE, Burrage LC, et al. Genetic dissection of complex traits with chromosome substitution strains of mice. Science. 2004;304(5669):445-8. doi:10.1126/science.1093139
Mather KJ, Christophi CA, Jablonski KA, et al. Common variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/2), adiponectin concentrations, and diabetes incidence in the Diabetes Prevention Program. Diabet Med. 2012;29(12):1579-88. doi:10.1111/j.1464-5491.2012.03662.x
Chmielecki J, Crago AM, Rosenberg M, et al. Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors. Nat Genet. 2013;45(2):131-2. doi:10.1038/ng.2522
Liu DJ, Peloso GM, Zhan X, et al. Meta-analysis of gene-level tests for rare variant association. Nat Genet. 2014;46(2):200-4. doi:10.1038/ng.2852