Malik AN, Vierbuchen T, Hemberg M, et al. Genome-wide identification and characterization of functional neuronal activity-dependent enhancers. Nat Neurosci. 2014;17(10):1330-9. doi:10.1038/nn.3808
Zaitlen N, Pasaniuc B, Sankararaman S, et al. Leveraging population admixture to characterize the heritability of complex traits. Nat Genet. 2014;46(12):1356-62. doi:10.1038/ng.3139
Adib-Samii P, Devan W, Traylor M, et al. Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke. Stroke. 2015;46(2):348-53. doi:10.1161/STROKEAHA.114.006849
Ge T, Nichols TE, Lee PH, et al. Massively expedited genome-wide heritability analysis (MEGHA). Proc Natl Acad Sci U S A. 2015;112(8):2479-84. doi:10.1073/pnas.1415603112
Beaudoin M, Gupta RM, Won HH, et al. Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries. Arterioscler Thromb Vasc Biol. 2015;35(6):1472-9. doi:10.1161/ATVBAHA.115.305534
Swaminathan B, Thorleifsson G, Jöud M, et al. Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. Nat Commun. 2015;6:7213. doi:10.1038/ncomms8213
Hayes G, Urbanek M, Ehrmann DA, et al. Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Nat Commun. 2015;6:7502. doi:10.1038/ncomms8502
Finucane HK, Bulik-Sullivan B, Gusev A, et al. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nat Genet. 2015;47(11):1228-35. doi:10.1038/ng.3404
Vieira NM, Elvers I, Alexander MS, et al. Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype. Cell. 2015;163(5):1204-13. doi:10.1016/j.cell.2015.10.049
Kilpeläinen TO, Carli JFM, Skowronski AA, et al. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. Nat Commun. 2016;7:10494. doi:10.1038/ncomms10494