Allele-specific enhancers mediate associations between LCAT and ABCA1 polymorphisms and HDL metabolism

por Howard, Alicia D., Wang, Xiaochun, Prasad, Megana, Sahu, Avinash Das, Aniba, Radhouane, Miller, Michael, Hannenhalli, Sridhar, Chang, Yen-Pei Christy
Publicado 2019

Rare coding variants in RCN3 are associated with blood pressure

por He, Karen Y., Kelly, Tanika N., Wang, Heming, Liang, Jingjing, Zhu, Luke, Cade, Brian E., Assimes, Themistocles L., Becker, Lewis C., Beitelshees, Amber L., Bielak, Lawrence F., Bress, Adam P., Brody, Jennifer A., Chang, Yen-Pei Christy, Chang, Yi-Cheng, de Vries, Paul S., Duggirala, Ravindranath, Fox, Ervin R., Franceschini, Nora, Furniss, Anna L., Gao, Yan, Guo, Xiuqing, Haessler, Jeffrey, Hung, Yi-Jen, Hwang, Shih-Jen, Irvin, Marguerite Ryan, Kalyani, Rita R., Liu, Ching-Ti, Liu, Chunyu, Martin, Lisa Warsinger, Montasser, May E., Muntner, Paul M., Mwasongwe, Stanford, Naseri, Take, Palmas, Walter, Reupena, Muagututi’a Sefuiva, Rice, Kenneth M., Sheu, Wayne H.-H., Shimbo, Daichi, Smith, Jennifer A., Snively, Beverly M., Yanek, Lisa R., Zhao, Wei, Blangero, John, Boerwinkle, Eric, Chen, Yii-Der Ida, Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Fornage, Myriam, He, Jiang, Hou, Lifang, Kaplan, Robert C., Kardia, Sharon L. R., Kenny, Eimear E., Kooperberg, Charles, Lloyd-Jones, Donald, Loos, Ruth J. F., Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., North, Kari E., Peyser, Patricia A., Psaty, Bruce M., Raffield, Laura M., Rao, D. C., Redline, Susan, Reiner, Alex P., Rich, Stephen S., Rotter, Jerome I., Taylor, Kent D., Tracy, Russell, Vasan, Ramachandran S., Morrison, Alanna C., Levy, Daniel, Chakravarti, Aravinda, Arnett, Donna K., Zhu, Xiaofeng
Publicado 2022