Longoni M, High FA, Russell MK, et al. Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics. Proc Natl Acad Sci U S A. 2014;111(34):12450-5. doi:10.1073/pnas.1412509111
Körberg IB, Sundström E, Meadows JRS, et al. A simple repeat polymorphism in the MITF-M promoter is a key regulator of white spotting in dogs. PLoS One. 2014;9(8):e104363. doi:10.1371/journal.pone.0104363
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
Tada H, Won HH, Melander O, Yang J, Peloso GM, Kathiresan S. Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease. Circ Cardiovasc Genet. 2014;7(5):583-7. doi:10.1161/CIRCGENETICS.113.000420
Ye CJ, Feng T, Kwon HK, et al. Intersection of population variation and autoimmunity genetics in human T cell activation. Science. 2014;345(6202):1254665. doi:10.1126/science.1254665
Gire SK, Goba A, Andersen KG, et al. Genomic surveillance elucidates Ebola virus origin and transmission during the 2014 outbreak. Science. 2014;345(6202):1369-72. doi:10.1126/science.1259657
1000 Genomes Project Consortium, Abecasis GR, Auton A, et al. An integrated map of genetic variation from 1,092 human genomes. Nature. 2012;491(7422):56-65. doi:10.1038/nature11632
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
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