Sklar P, Smoller JW, Fan J, et al. Whole-genome association study of bipolar disorder. Mol Psychiatry. 2008;13(6):558-69. doi:10.1038/sj.mp.4002151
Onuchic V, Lurie E, Carrero I, et al. Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory loci. Science. 2018;361(6409). doi:10.1126/science.aar3146
Shungin D, Deng WQ, Varga TV, et al. Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions. PLoS Genet. 2017;13(6):e1006812. doi:10.1371/journal.pgen.1006812
Polimanti R, Amstadter AB, Stein MB, et al. A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder. Genome Med. 2017;9(1):99. doi:10.1186/s13073-017-0491-4
Van der Auwera S, Peyrot WJ, Milaneschi Y, et al. Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD. Am J Med Genet B Neuropsychiatr Genet. 2018;177(1):40-49. doi:10.1002/ajmg.b.32593
Huang H, Duggal P, Thio CL, et al. Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection. Sci Rep. 2017;7(1):15843. doi:10.1038/s41598-017-16011-2
Singh T, Walters JTR, Johnstone M, et al. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nat Genet. 2017;49(8):1167-1173. doi:10.1038/ng.3903
Nakatsuka N, Moorjani P, Rai N, et al. The promise of discovering population-specific disease-associated genes in South Asia. Nat Genet. 2017;49(9):1403-1407. doi:10.1038/ng.3917
Robinson MR, English G, Moser G, et al. Genotype-covariate interaction effects and the heritability of adult body mass index. Nat Genet. 2017;49(8):1174-1181. doi:10.1038/ng.3912
Nelson CP, Goel A, Butterworth AS, et al. Association analyses based on false discovery rate implicate new loci for coronary artery disease. Nat Genet. 2017;49(9):1385-1391. doi:10.1038/ng.3913