Karczewski KJ, Snyder MP. Integrative omics for health and disease. Nat Rev Genet. 2018;19(5):299-310. doi:10.1038/nrg.2018.4
Zhu Z, Anttila V, Smoller JW, Lee PH. Statistical power and utility of meta-analysis methods for cross-phenotype genome-wide association studies. PLoS One. 2018;13(3):e0193256. doi:10.1371/journal.pone.0193256
Landry LG, Rehm HL. Association of Racial/Ethnic Categories With the Ability of Genetic Tests to Detect a Cause of Cardiomyopathy. JAMA Cardiol. 2018;3(4):341-345. doi:10.1001/jamacardio.2017.5333
Pardiñas AF, Holmans P, Pocklington AJ, et al. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat Genet. 2018;50(3):381-389. doi:10.1038/s41588-018-0059-2
Whitton H, Singh LN, Patrick MA, et al. Changes at the nuclear lamina alter binding of pioneer factor Foxa2 in aged liver. Aging Cell. 2018;17(3):e12742. doi:10.1111/acel.12742
Anttila V, Wessman M, Kallela M, Palotie A. Genetics of migraine. Handb Clin Neurol. 2018;148:493-503. doi:10.1016/B978-0-444-64076-5.00031-4
Archer TC, Sengupta S, Pomeroy SL. Brain cancer genomics and epigenomics. Handb Clin Neurol. 2018;148:785-797. doi:10.1016/B978-0-444-64076-5.00050-8
Olalde I, Brace S, Allentoft ME, et al. The Beaker phenomenon and the genomic transformation of northwest Europe. Nature. 2018;555(7695):190-196. doi:10.1038/nature25738
Mathieson I, Alpaslan-Roodenberg S, Posth C, et al. The genomic history of southeastern Europe. Nature. 2018;555(7695):197-203. doi:10.1038/nature25778
Aneichyk T, Hendriks WT, Yadav R, et al. Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly. Cell. 2018;172(5):897-909.e21. doi:10.1016/j.cell.2018.02.011