Xue Y, Mezzavilla M, Haber M, et al. Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations. Nat Commun. 2017;8:15927. doi:10.1038/ncomms15927
Hajdinjak M, Fu Q, Hübner A, et al. Reconstructing the genetic history of late Neanderthals. Nature. 2018;555(7698):652-656. doi:10.1038/nature26151
Nakatsuka N, Moorjani P, Rai N, et al. The promise of discovering population-specific disease-associated genes in South Asia. Nat Genet. 2017;49(9):1403-1407. doi:10.1038/ng.3917
Prasad B, Saxena R, Goel N, Patel SR. Genetic Ancestry for Sleep Research: Leveraging Health Inequalities to Identify Causal Genetic Variants. Chest. 2018;153(6):1478-1496. doi:10.1016/j.chest.2018.03.024
Harney E, May H, Shalem D, et al. Ancient DNA from Chalcolithic Israel reveals the role of population mixture in cultural transformation. Nat Commun. 2018;9(1):3336. doi:10.1038/s41467-018-05649-9
Skoglund P, Mallick S, Patterson N, Reich D. No evidence for unknown archaic ancestry in South Asia. Nat Genet. 2018;50(5):632-633. doi:10.1038/s41588-018-0097-9
Lazaridis I. The evolutionary history of human populations in Europe. Curr Opin Genet Dev. 2018;53:21-27. doi:10.1016/j.gde.2018.06.007
Chao MJ, Kim KH, Shin JW, et al. Population-specific genetic modification of Huntington’s disease in Venezuela. PLoS Genet. 2018;14(5):e1007274. doi:10.1371/journal.pgen.1007274
Gazal S, Loh PR, Finucane HK, et al. Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations. Nat Genet. 2018;50(11):1600-1607. doi:10.1038/s41588-018-0231-8
Rivas MA, Avila BE, Koskela J, et al. Insights into the genetic epidemiology of Crohn’s and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 2018;14(5):e1007329. doi:10.1371/journal.pgen.1007329