Kurki MI, Gaál EI, Kettunen J, et al. High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms. PLoS Genet. 2014;10(1):e1004134. doi:10.1371/journal.pgen.1004134
Lipson M, Loh PR, Patterson N, et al. Reconstructing Austronesian population history in Island Southeast Asia. Nat Commun. 2014;5:4689. doi:10.1038/ncomms5689
Yan S, Yuan S, Xu Z, et al. Likelihood-based complex trait association testing for arbitrary depth sequencing data. Bioinformatics. 2015;31(18):2955-62. doi:10.1093/bioinformatics/btv307
Yu B, Pulit SL, Hwang SJ, et al. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk. Circ Cardiovasc Genet. 2016;9(1):64-70. doi:10.1161/CIRCGENETICS.115.001215
Myers S, Fefferman C, Patterson N. Can one learn history from the allelic spectrum?. Theor Popul Biol. 2008;73(3):342-8. doi:10.1016/j.tpb.2008.01.001
Boettger LM, Handsaker RE, Zody MC, McCarroll SA. Structural haplotypes and recent evolution of the human 17q21.31 region. Nat Genet. 2012;44(8):881-5. doi:10.1038/ng.2334
Lange LA, Hu Y, Zhang H, et al. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am J Hum Genet. 2014;94(2):233-45. doi:10.1016/j.ajhg.2014.01.010
Carneiro M, Rubin CJ, di Palma F, et al. Rabbit genome analysis reveals a polygenic basis for phenotypic change during domestication. Science. 2014;345(6200):1074-9. doi:10.1126/science.1253714
Roosing S, Hofree M, Kim S, et al. Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome. Elife. 2015;4:e06602. doi:10.7554/eLife.06602
Richards AL, Leonenko G, Walters JT, et al. Exome arrays capture polygenic rare variant contributions to schizophrenia. Hum Mol Genet. 2016;25(5):1001-7. doi:10.1093/hmg/ddv620