recent publications

• academic article

  • Shen, G. Q., Li, L., Girelli, D., Seidelmann, S. B., Rao, S., Fan, C., Park, J. E., Xi, Q., Li, J., Hu, Y., Olivieri, O., Marchant, K., et al. An lrp8 variant is associated with familial and premature coronary artery disease and myocardial infarction American Journal of Human Genetics  2007 81:780-791  DOI:10.1086/521581  PMID:17847002  PMCID:PMC2227927
  • Luke, M. M., Kane, J. P., Liu, D. M., Rowland, C. M., Shiffman, D., Cassano, J., Catanese, J. J., Pullinger, C. R., Leong, D. U., Arellano, A. R., Tong, C. H., Movsesyan, I., et al. A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease Arteriosclerosis, Thrombosis, and Vascular Biology  2007 27:2030-2036  DOI:10.1161/atvbaha.107.141291  PMID:17569884
  • Shiffman, D., Ellis, S. G., Rowland, C. M., Malloy, M. J., Luke, M. M., Iakoubova, O. A., Pullinger, C. R., Cassano, J., Aouizerat, B. E., Fenwick, R. G., Reitz, R. E., Catanese, J. J., et al. Identification of four gene variants associated with myocardial infarction American Journal of Human Genetics  2005 77:596-605  DOI:10.1086/491674  PMID:16175505  PMCID:PMC1275608
  • Bhagavatula, M. R. K., Fan, C., Shen, G. Q., Cassano, J., Plow, E. F., Topol, E. J., Wang, Q. Transcription factor mef2a mutations in patients with coronary artery disease Human Molecular Genetics  2004 13:3181-3188  DOI:10.1093/hmg/ddh329  PMID:15496429  PMCID:PMC1579761