Ritchie Lab - Exome-by-phenome-wide rare variant gene burden association with electronic health record phenotypes.

Park, J., Katz, N., Zhang, X., Lucas, A. M., Verma, A., Judy, R. L., Kember, R. L., Chen, J., Damrauer, S. M., Ritchie, M. D., & Rader, D. J. (2019). Exome-by-phenome-wide rare variant gene burden association with electronic health record phenotypes. Biorxiv. https://doi.org/10.1101/798330