Munz, M., Willenborg, C., Richter, G., Jockel-Schneider, Y., Graetz, C., Staufenbiel, I., … Schaefer, A. (2018). A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddy015 (Original work published 2018)

Marouli, E., Graff, M., Medina-Gomez, C., Lo, K., Wood, A., Kjaer, T., … Lettre, G. (2017). Rare and low-frequency coding variants alter human adult height. Nature, 542(7640), 186-190. https://doi.org/10.1038/nature21039 (Original work published 2017)