Phenotype-genotype association grid: a convenient method for summarizing multiple association analyses

by Levy, Daniel, DePalma, Steven R, Benjamin, Emelia J, O'Donnell, Christopher J, Parise, Helen, Hirschhorn, Joel N, Vasan, Ramachandran S, Izumo, Seigo, Larson, Martin G
Published 2006

NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity

by Abou Hassan, Ossama K., Fahed, Akl C., Batrawi, Manal, Arabi, Mariam, Refaat, Marwan M., DePalma, Steven R., Seidman, J. G., Seidman, Christine E., Bitar, Fadi F., Nemer, Georges M.
Published 2015

Genome-Wide Assessment for Genetic Variants Associated with Ventricular Dysfunction after Primary Coronary Artery Bypass Graft Surgery

by Fox, Amanda A., Pretorius, Mias, Liu, Kuang-Yu, Collard, Charles D., Perry, Tjorvi E., Shernan, Stanton K., De Jager, Philip L., Hafler, David A., Herman, Daniel S., DePalma, Steven R., Roden, Dan M., Muehlschlegel, Jochen D., Donahue, Brian S., Darbar, Dawood, Seidman, J. G., Body, Simon C., Seidman, Christine E.
Published 2011

Loss of RNA expression and allele-specific expression associated with congenital heart disease

by McKean, David M., Homsy, Jason, Wakimoto, Hiroko, Patel, Neil, Gorham, Joshua, DePalma, Steven R., Ware, James S., Zaidi, Samir, Ma, Wenji, Patel, Nihir, Lifton, Richard P., Chung, Wendy K., Kim, Richard, Shen, Yufeng, Brueckner, Martina, Goldmuntz, Elizabeth, Sharp, Andrew J., Seidman, Christine E., Gelb, Bruce D., Seidman, J. G.
Published 2016