Liu DJ, Peloso GM, Zhan X, et al. Meta-analysis of gene-level tests for rare variant association. Nat Genet. 2014;46(2):200-4. doi:10.1038/ng.2852.

Tada H, Won H-H, 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.

Benyamin B, Esko T, Ried JS, et al. Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nat Commun. 2014;5:4926. doi:10.1038/ncomms5926.

Jain M, Ngoy S, Sheth SA, et al. A systematic survey of lipids across mouse tissues. Am J Physiol Endocrinol Metab. 2014;306(8):E854-68. doi:10.1152/ajpendo.00371.2013.

Mukamal KJ, Jensen MK, Pers TH, Pai JK, Kraft P, Rimm EB. Multilocus heterozygosity and coronary heart disease: nested case-control studies in men and women. PLoS One. 2015;10(5):e0124847. doi:10.1371/journal.pone.0124847.

Lettre G, Hirschhorn JN. Small island, big genetic discoveries. Nat Genet. 2015;47(11):1224-5. doi:10.1038/ng.3426.

Salihovic S, Ganna A, Fall T, et al. The metabolic fingerprint of p,p’-DDE and HCB exposure in humans. Environ Int. 2016;88:60-6. doi:10.1016/j.envint.2015.12.015.

Clapham KR, Chu AY, Wessel J, et al. A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans. BMC Endocr Disord. 2016;16:7. doi:10.1186/s12902-016-0088-8.

Zuris JA, Thompson DB, Shu Y, et al. Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo. Nat Biotechnol. 2015;33(1):73-80. doi:10.1038/nbt.3081.

Teslovich TM, Musunuru K, Smith AV, et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 2010;466(7307):707-13. doi:10.1038/nature09270.