Flannick J, Mercader JM, Fuchsberger C, et al. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Nature. 2019;570(7759):71-76. doi:10.1038/s41586-019-1231-2.

Kalim S, Wald R, Yan AT, et al. Extended Duration Nocturnal Hemodialysis and Changes in Plasma Metabolite Profiles. Clin J Am Soc Nephrol. 2018;13(3):436-444. doi:10.2215/CJN.08790817.

Roselli C, Chaffin MD, Weng L-C, et al. Multi-ethnic genome-wide association study for atrial fibrillation. Nat Genet. 2018;50(9):1225-1233. doi:10.1038/s41588-018-0133-9.

Winsvold BS, Palta P, Eising E, et al. Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study. Cephalalgia. 2018;38(2):312-322. doi:10.1177/0333102417690111.

Liang J, Le TH, Edwards DRV, et al. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. PLoS Genet. 2017;13(5):e1006728. doi:10.1371/journal.pgen.1006728.

Witt SH, Streit F, Jungkunz M, et al. Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Transl Psychiatry. 2017;7(6):e1155. doi:10.1038/tp.2017.115.

Waage J, Standl M, Curtin JA, et al. Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat Genet. 2018;50(8):1072-1080. doi:10.1038/s41588-018-0157-1.

Eriksson D, Dalin F, Eriksson GN, et al. Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1. J Clin Endocrinol Metab. 2018;103(1):179-186. doi:10.1210/jc.2017-01957.

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.

Foo JC, Streit F, Treutlein J, et al. Shared genetic etiology between alcohol dependence and major depressive disorder. Psychiatr Genet. 2018;28(4):66-70. doi:10.1097/YPG.0000000000000201.