Groen-Blokhuis MM, Middeldorp CM, Kan KJ, et al. Attention-deficit/hyperactivity disorder polygenic risk scores predict attention problems in a population-based sample of children. J Am Acad Child Adolesc Psychiatry. 2014;53(10):1123-9.e6. doi:10.1016/j.jaac.2014.06.014
Foroud T, Lai D, Koller D, et al. Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7. Stroke. 2014;45(11):3194-9. doi:10.1161/STROKEAHA.114.006096
van der Valk RJP, Kreiner-Møller E, Kooijman MN, et al. A novel common variant in DCST2 is associated with length in early life and height in adulthood. Hum Mol Genet. 2015;24(4):1155-68. doi:10.1093/hmg/ddu510
Wood AR, Esko T, Yang J, et al. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet. 2014;46(11):1173-86. doi:10.1038/ng.3097
Coffee and Caffeine Genetics Consortium, Cornelis MC, Byrne EM, et al. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Mol Psychiatry. 2015;20(5):647-56. doi:10.1038/mp.2014.107
Pers TH, Timshel P, Hirschhorn JN. SNPsnap: a Web-based tool for identification and annotation of matched SNPs. Bioinformatics. 2015;31(3):418-20. doi:10.1093/bioinformatics/btu655
Weisenfeld NI, Yin S, Sharpe T, et al. Comprehensive variation discovery in single human genomes. Nat Genet. 2014;46(12):1350-5. doi:10.1038/ng.3121
Obaldia N, Baro NK, Calzada JE, et al. Clonal outbreak of Plasmodium falciparum infection in eastern Panama. J Infect Dis. 2015;211(7):1087-96. doi:10.1093/infdis/jiu575
Smith G, Luk K, Schulz CA, et al. Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis. JAMA. 2014;312(17):1764-71. doi:10.1001/jama.2014.13959
Gottlieb DJ, Hek K, Chen TH, et al. Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Mol Psychiatry. 2015;20(10):1232-9. doi:10.1038/mp.2014.133