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.

Goto A, Chen BH, Chan K-HK, et al. Genetic variants in sex hormone pathways and the risk of type 2 diabetes among African American, Hispanic American, and European American postmenopausal women in the US. J Diabetes. 2018;10(6):524-533. doi:10.1111/1753-0407.12648.

Manning A, Highland HM, Gasser J, et al. A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. 2017;66(7):2019-2032. doi:10.2337/db16-1329.

Huang AY, Yu D, Davis LK, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 2017;94(6):1101-1111.e7. doi:10.1016/j.neuron.2017.06.010.

Vetter C, Dashti HS, Lane JM, et al. Night Shift Work, Genetic Risk, and Type 2 Diabetes in the UK Biobank. Diabetes Care. 2018;41(4):762-769. doi:10.2337/dc17-1933.

Bigdeli TB, Ripke S, Peterson RE, et al. Genetic effects influencing risk for major depressive disorder in China and Europe. Transl Psychiatry. 2017;7(3):e1074. doi:10.1038/tp.2016.292.

Flannick J, Fuchsberger C, Mahajan A, et al. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci Data. 2017;4:170179. doi:10.1038/sdata.2017.179.

Stein MB, McCarthy MJ, Chen C-Y, et al. Genome-wide analysis of insomnia disorder. Mol Psychiatry. 2018;23(11):2238-2250. doi:10.1038/s41380-018-0033-5.

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.

Tukiainen T, Pirinen M, Sarin A-P, et al. Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation. PLoS Genet. 2014;10(2):e1004127. doi:10.1371/journal.pgen.1004127.