Ritchie Lab - A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes.

Park, J., Levin, M. G., Haggerty, C. M., Hartzel, D. N., Judy, R., Kember, R. L., Reza, N., Ritchie, M. D., Owens, A. T., Damrauer, S. M., & Rader, D. J. (2020). A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes. Genetics in Medicine : Official Journal of the American College of Medical Genetics., 22(1), 102–111. https://doi.org/10.1038/s41436-019-0625-8