Hays, T., Hernan, R., Disco, M., Griffin, E. L., Goldshtrom, N., Vargas, D., Krishnamurthy, G., Bomback, M., Rehman, A. U., Wilson, A. T., Guha, S., Phadke, S., Okur, V., Robinson, D., Felice, V., Abhyankar, A., Jobanputra, V., & Chung, W. K. (2023). Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease. Circulation: Genomic and Precision Medicine, 16(5), 415–420. https://doi.org/10.1161/circgen.122.004050

Jang, M. Y., Patel, P. N., Pereira, A. C., Willcox, J. A. L., Haghighi, A., Tai, A. C., Ito, K., Morton, S. U., Gorham, J. M., McKean, D. M., DePalma, S. R., Bernstein, D., Brueckner, M., Chung, W. K., Giardini, A., Goldmuntz, E., Kaltman, J. R., Kim, R., Newburger, J. W., … Seidman, J. G. (2023). Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease. Circulation: Genomic and Precision Medicine, 16(3), 224–231. https://doi.org/10.1161/circgen.122.003924

Lewis, M. J., Hsieh, A., Qiao, L., Tan, R., Kazzi, B., Channing, A., Griffin, E. L., Jobanputra, V., Su, J., Shahryar, C., Kochilas, L., Gaynor, J. W., Lee, T., Goldmuntz, E., Russell, M., Mital, S., Tristani, M., Brueckner, M., Newburger, J., … Chung, W. K. (2023). Association of Predicted Damaging De Novo Variants on Ventricular Function in Individuals With Congenital Heart Disease. Circulation: Genomic and Precision Medicine, 16(2). https://doi.org/10.1161/circgen.122.003900

Griffin, E. L., Nees, S. N., Morton, S. U., Wynn, J., Patel, N., Jobanputra, V., Robinson, S., Kochav, S. M., Tao, A., Andrews, C., Cross, N., Geva, J., Lanzilotta, K., Ritter, A., Taillie, E., Thompson, A., Meyer, C., Akers, R., King, E. C., … Chung, W. K. (2023). Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation: Genomic and Precision Medicine, 16(2). https://doi.org/10.1161/circgen.122.003791

Dikilitas, O., Sherafati, A., Saadatagah, S., Satterfield, B. A., Kochan, D. C., Anderson, K. C., Chung, W. K., Hebbring, S. J., Salvati, Z. M., Sharp, R. R., Sturm, A. C., Gibbs, R. A., Rowley, R., Venner, E., Linder, J. E., Jones, L. K., Perez, E. F., Peterson, J. F., Jarvik, G. P., … Kullo, I. J. (2023). Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results. Circulation: Genomic and Precision Medicine, 16(2). https://doi.org/10.1161/circgen.122.003816

Khera, A. V., Wang, M., Chaffin, M., Emdin, C. A., Samani, N. J., Schunkert, H., Watkins, H., McPherson, R., Erdmann, J., Elosua, R., Boerwinkle, E., Ardissino, D., Butterworth, A. S., Di Angelantonio, E., Naheed, A., Danesh, J., Chowdhury, R., Krumholz, H. M., Sheu, W. H.-H., … Kathiresan, S. (2022). Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease. Circulation: Genomic and Precision Medicine, 15(6). https://doi.org/10.1161/circgen.121.003598

Shimada, Y. J., Raita, Y., Liang, L. W., Maurer, M. S., Hasegawa, K., Fifer, M. A., & Reilly, M. P. (2022). Prediction of Major Adverse Cardiovascular Events in Patients With Hypertrophic Cardiomyopathy Using Proteomics Profiling. Circulation: Genomic and Precision Medicine, 15(6). https://doi.org/10.1161/circgen.121.003546

Tortigue, M., Nield, L. E., Karakachoff, M., McLeod, C. J., Belli, E., Babu-Narayan, S. V., Prigent, S., Boet, A., Conway, M., Elder, R. W., Ladouceur, M., Khairy, P., Kowalik, E., Kalfa, D. M., Barron, D. J., Mussa, S., Hiippala, A., Temple, J., Abadir, S., … Baruteau, A.-E. (2022). Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International Study. Circulation: Genomic and Precision Medicine, 15(3). https://doi.org/10.1161/circgen.121.003464

Morton, S. U., Pereira, A. C., Quiat, D., Richter, F., Kitaygorodsky, A., Hagen, J., Bernstein, D., Brueckner, M., Goldmuntz, E., Kim, R. W., Lifton, R. P., Porter, G. A., Tristani-Firouzi, M., Chung, W. K., Roberts, A., Gelb, B. D., Shen, Y., Newburger, J. W., Seidman, J. G., & Seidman, C. E. (2022). Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity. Circulation: Genomic and Precision Medicine, 15(2). https://doi.org/10.1161/circgen.121.003500