Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
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author: Vilmundur Gudnason, Albert Hofman, Bruce M. Psaty, André Uitterlinden, Eric Boerwinkle, Thomas Meitinger, Charles Kooperberg, Myriam Fornage, Caroline Hayward, Cornelia M. van Duijn, Albert V. Smith, Kristian Hveem, Igor Rudan, Omri Gottesman, Gail P. Jarvik, Ellen M Schmidt, Emily H Turner, Adam E Locke, Goo Jun, Christian Fuchsberger, Lisa W. Martin, Cristen J. Willer, Pål Sætrom, Douglas M. Ruderfer, Themistocles L Assimes, Michael Y. Tsai, He Zhang, Jerome I Rotter, Mark McCarthy, Michael Boehnke, Ruth J. Loos, Erwin Böttinger, Sekar Kathiresan, Leif Groop, Aaron R. Folsom, David Altshuler, Stacey Gabriel, Cecilia Lindgren, David S Siscovick, Joshua C Bis, Ingrid B Borecki, Adolfo Correa, Kari E North, Nora Franceschini, Mary Feitosa, Thomas Lumley, James G. Wilson, Ulrike Peters, L. Adrienne Cupples, Alisa Manning, Christopher J O'Donnell, Deborah A Nickerson, Christie M. Ballantyne, Johanna Jakobsdottir, Deborah N Farlow, Michael E Griswold, Leslie A. Lange, Wendy S. Post, Paul L Auer, Gonçalo Abecasis, Russell P Tracy, Gina M Peloso, Herman A Taylor, Oddgeir L Holmen, Mark J Rieder, Hyun Min Kang, Jacy Crosby, Alexander P Reiner, Kyle J Gaulton, Eli A. Stahl, Jennifer E Huffman, Stephen S Rich, Jason Flannick, David R Crosslin, Rebecca D. Jackson, Chris Bizon, Yingchang Lu, Ethan Mather Lange, Pamela J Schreiner, Daniel Levy, Aaron Isaacs
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