| Autor: |
Boerwinkle, Eric, Vojinovic, Dina, Becker, Diane M., Van Setten, Jessica, Heckbert, Susan R., Bowden, Donald W., Oudkerk, Matthijs, Heiss, Gerardo, Yao, Jie, Deary, Ian J., Goodarzi, Mark O., Bis, Joshua C., Rotter, Jerome I., Fuster, Valentin, Išgum, Ivana, Guo, Xiuqing, Taylor, Kent D., Lyytikäinen, Leo-Pekka, Li-Gao, Ruifang, Rivadeneira, Fernando, Kavousi, Maryam, Sartori, Samantha, Dörr, Marcus, Smith, Albert V., Psaty, Bruce M., Kathiresan, Sekar, Völzke, Henry, Kral, Brian G., O'Donnell, Christopher J., Baber, Usman, Newman, Anne B., Rader, Daniel J., Peyser, Patricia A., Mehran, Roxana, Nguyen, Khanh-Dung, Tada, Hayato, Trompet, Stella, De Mutsert, Renée, Feitosa, Mary F., De Jong, Pim A., Natarajan, Pradeep, Mitchell, Braxton D., Yanek, Lisa R., Massaro, Joe, Vaidya, Dhananjay, Peloso, Gina M., Turner, Stephen T., Franco, Oscar H., Bielak, Lawrence F., Borecki, Ingrid B., Harris, Tamara B., Hoffmann, Udo, Raitakari, Olli T., Marioni, Riccardo E., Jukema, J. Wouter, Gudnason, Vilmundur, Mook-Kanamori, Dennis O., Teumer, Alexander, Cupples, L. Adrienne, Kardia, Sharon L.R., Amin, Najaf, Post, Wendy, Hwang, Shih-Jen, Chen, Yii-Der Ida, Pankow, James S., Mathias, Rasika, Rosendaal, Frits, Stitziel, Nathan O., North, Kari E., Wassel, Christina L., Wardlaw, Joanna M., Lehtimäki, Terho, Van Duijn, Cornelia M., Jhun, Min A, Yerges-Armstrong, Laura M., Isaacs, Aaron, Reilly, Dermot F., De Koning, Harry, Franceschini, Nora, Van Der Lugt, Aad, Becker, Lewis C., Felix, Stephan B., Raffield, Laura M., Dehghan, Abbas, Wojczynski, Mary K., Weiss, Stefan, Wilson, James G., Kähönen, Mika, Launer, Lenore J., Mosley, Thomas H., Demirkan, Ayse, O'Connell, Jeffrey R., De Vos, Bob D., Schminke, Ulf, Province, Michael A., Völker, Uwe, Carr, J. Jeffrey, Uitterlinden, Andre G., Cox, Amanda J., Hofman, Albert |
| Jazyk: |
angličtina |
| Rok vydání: |
2016 |
| Předmět: |
|
| DOI: |
10.17615/tpdv-s479 |
| Popis: |
The burden of subclinical atherosclerosis in asymptomatic individuals is heritable and associated with elevated risk of developing clinical coronary heart disease (CHD). We sought to identify genetic variants in protein-coding regions associated with subclinical atherosclerosis and the risk of subsequent CHD. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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