Turchin MC, Chiang CWK, Palmer CD, et al. Evidence of widespread selection on standing variation in Europe at height-associated SNPs. Nat Genet. 2012;44(9):1015-9. doi:10.1038/ng.2368
Patterson N, Moorjani P, Luo Y, et al. Ancient admixture in human history. Genetics. 2012;192(3):1065-93. doi:10.1534/genetics.112.145037
Florez JC, Jablonski KA, McAteer JB, et al. Effects of genetic variants previously associated with fasting glucose and insulin in the Diabetes Prevention Program. PLoS One. 2012;7(9):e44424. doi:10.1371/journal.pone.0044424
Sankararaman S, Patterson N, Li H, Pääbo S, Reich D. The date of interbreeding between Neandertals and modern humans. PLoS Genet. 2012;8(10):e1002947. doi:10.1371/journal.pgen.1002947
Zaitlen N, Lindström S, Pasaniuc B, et al. Informed conditioning on clinical covariates increases power in case-control association studies. PLoS Genet. 2012;8(11):e1003032. doi:10.1371/journal.pgen.1003032
Smith G, Avery CL, Evans DS, et al. Impact of ancestry and common genetic variants on QT interval in African Americans. Circ Cardiovasc Genet. 2012;5(6):647-55. doi:10.1161/CIRCGENETICS.112.962787
Koren A, Polak P, Nemesh J, et al. Differential relationship of DNA replication timing to different forms of human mutation and variation. Am J Hum Genet. 2012;91(6):1033-40. doi:10.1016/j.ajhg.2012.10.018
Trynka G, Sandor C, Han B, et al. Chromatin marks identify critical cell types for fine mapping complex trait variants. Nat Genet. 2013;45(2):124-30. doi:10.1038/ng.2504
Diogo D, Kurreeman F, Stahl EA, et al. Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis. Am J Hum Genet. 2013;92(1):15-27. doi:10.1016/j.ajhg.2012.11.012
Ruderfer DM, Chambert K, Moran J, et al. Mosaic copy number variation in schizophrenia. Eur J Hum Genet. 2013;21(9):1007-11. doi:10.1038/ejhg.2012.287