Kosmicki JA, Samocha KE, Howrigan DP, et al. Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples. Nat Genet. 2017;49(4):504-510. doi:10.1038/ng.3789
Duncan L, Yilmaz Z, Gaspar H, et al. Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa. Am J Psychiatry. 2017;174(9):850-858. doi:10.1176/appi.ajp.2017.16121402
Winsvold BS, Bettella F, Witoelar A, et al. Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants. PLoS One. 2017;12(9):e0185663. doi:10.1371/journal.pone.0185663
Zepeda-Mendoza CJ, Ibn-Salem J, Kammin T, et al. Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements. Am J Hum Genet. 2017;101(2):206-217. doi:10.1016/j.ajhg.2017.06.011
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
DeBoever C, Tanigawa Y, Lindholm ME, et al. Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study. Nat Commun. 2018;9(1):1612. doi:10.1038/s41467-018-03910-9
Mukherjee S, Saxena R, Palmer LJ. The genetics of obstructive sleep apnoea. Respirology. 2018;23(1):18-27. doi:10.1111/resp.13212
Zhao Z, Bi W, Zhou W, VandeHaar P, Fritsche LG, Lee S. UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test. Am J Hum Genet. 2020;106(1):3-12. doi:10.1016/j.ajhg.2019.11.012
Chen CY, Lee PH, Castro VM, et al. Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records. Transl Psychiatry. 2018;8(1):86. doi:10.1038/s41398-018-0133-7
Bick AG, Weinstock JS, Nandakumar SK, et al. Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. 2020;586(7831):763-768. doi:10.1038/s41586-020-2819-2