Abstract 9613: Randomized Evaluation of Anacetrapib Lipid-Modifying Therapy in Patients With HeteroZygous Familial HypercholesterolEmia (REALIZE Study) by Kastelein, John J, Besseling, Joost, Shah, Sukrut, Bergeron, Jean, Langslet, Gisle, Hovingh, G Kees, Al-Saady, Naab, Koeijvoets, Michiel, Hunter, John, Johnson-Levonas, Amy O, Fable, Jennifer, Sapre, Aditi, Mitchel, Yale

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The Genetics of High-Density Lipoprotein Metabolism: Clinical Relevance for Therapeutic Approaches: HIGH-DENSITY LIPOPROTEIN AS A THERAPEUTIC TARGET: THE NEXT FRONTIER IN CORONARY... by STRANG, Aart C, KEES HOVINGH, G, STROES, Erik S. G, KASTELEIN, John J. P

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THE TRP719ARG VARIANT OF KIF6 AND CARDIOVASCULAR OUTCOMES IN STATIN-TREATED, CORONARY STABLE PATIENTS OF THE TNT AND IDEAL PROSPECTIVE STUDIES by Arsenault, Benoit, Boekholdt, S. Matthijs, Hovingh, G. Kees, Hyde, Craig L, DeMicco, David A, Chatterjee, Aurobindo L, Barter, Philip, Deedwania, Prakash, Waters, David D, LaRosa, John C, Pedersen, Terje R, Kastelein, John JP

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HOMOZYGOUS AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN THE NETHERLANDS: PREVALENCE, GENOTYPE-PHENOTYPE RELATIONSHIP AND CLINICAL OUTCOME by Sjouke, Barbara, Kusters, Dorothe, Kindt, Iris, Besseling, Joost, Defesche, Joep, Sijbrands, Eric, van Lennep, Jeanine Roeters, Stalenhoef, Anton, Wiegman, Albert, de Graaf, Jacqueline, Fouchier, Sigrid, Kastelein, John, Hovingh, G Kees

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eNOS Activation by HDL Is Impaired in Genetic CETP Deficiency: e95925 by Gomaraschi, Monica, Ossoli, Alice, Pozzi, Silvia, Nilsson, Peter, Cefalu, Angelo B, Averna, Maurizio, Kuivenhoven, Jan Albert, Hovingh, G Kees, Veglia, Fabrizio, Franceschini, Guido

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Complete and Partial LCAT Deficiency are Differentially Associated with Atherosclerosis by Oldoni, Federico, Baldassarre, Damiano, Castelnuovo, Samuela, Ossoli, Alice, Amato, Mauro, van Capelleveen, Julian, Hovingh, G Kees, De Groot, Eric, Bochem, Andrea, Simonelli, Sara, Barbieri, Simone, Veglia, Fabrizio, Franceschini, Guido, Kuivenhoven, Jan Albert, Holleboom, Adriaan G, Calabresi, Laura

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Abstract 16849: Alirocumab Dosing in a Real World Setting: Data From an Open-label Treatment Extension to the ODYSSEY Program for Patients With Heterozygous Familial Hypercholester... by Hovingh, G Kees, Guyton, John R, Langslet, Gisle, Dufour, Robert, Baccara-Dinet, Marie T, Din-Bell, Chantal, Manvelian, Garen, Farnier, Michel A

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Carriers of lecithin cholesterol acyltransferase gene mutations have accelerated atherogenesis as assessed by carotid 3.0-T magnetic resonance imaging [corrected] by Duivenvoorden, Raphaël, Holleboom, Adriaan G, van den Bogaard, Bas, Nederveen, Aart J, de Groot, Eric, Hutten, Barbara A, Schimmel, Alinda W, Hovingh, G Kees, Kastelein, John J P, Kuivenhoven, Jan Albert, Stroes, Erik S G

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Measurement of arterial wall thickness as a surrogate marker for atherosclerosis: Atherosclerosis: evolving vascular biology and clinical implications by DE GROOT, Eric, KEES HOVINGH, G, WIEGMAN, Albert, DURIEZ, Patrick, SMIT, Andries J, FRUCHART, Jean-Charles, KASTELEIN, John J. P

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Characteristics of Patients in the 10th and 90th Percentile of LDL-C Reductions with Alirocumab: ODYSSEY Pooled Analyses by Rosenson, Robert S., Roth, Eli M., Ray, Kausik K., Hovingh, G Kees, Bays, Harold E., Laufs, Ulrich, Rader, Daniel J., Baccara-Dinet, Marie T., Thompson, Desmond, Louie, Michael J., Leiter, Lawrence A.

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A novel ApoA-I mutation (L178P) leads to endothelial dysfunction, increased arterial wall thickness, and premature coronary artery disease. Commentary by HOVINGH, G. Kees, BROWNLIE, Alison, HAYDEN, Michael R, KUIVENHOVEN, Jan Albert, KASTELEIN, John J. P, BALLANTYNE, Christie M, NAMBI, Vijay, BISOENDIAL, Radjesh J, DUBE, Marie Pierre, LEVELS, Johannes H. M, PETERSEN, Wilma, DULLAART, Robin P. F, STROES, Erik S. G, ZWINDERMAN, Aeilko H, DE GROOT, Eric

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Recognition and Treatment of Homozygous Familial Hypercholesterolemia by Primary Care Physicians: a Survey from the National Lipid Association by Hemphill, Linda, Goldberg, Anne, Hovingh, Kees, Cohen, Jerome, Karalis, Dean G.

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Effect of statin therapy on muscle symptoms: an individual participant data meta-analysis of large-scale, randomised, double-blind trials by Reith, Christina, Baigent, Colin, Blackwell, Lisa, Spata, Enti, Davies, Kelly, Wilson, Kate, Armitage, Jane, Preiss, David, Simes, John, Collins, Rory, Barnes, Elizabeth, Fulcher, Jordan, Herrington, William G, Kirby, Adrienne, Mihaylova, Borislava, O'Connell, Rachel, Amarenco, Pierre, Barter, Philip, Betteridge (deceased), D John, Blazing, Michael, Bosch, Jackie, Braunwald, Eugene, Clearfield, Michael, Cobbe, Stuart, Colhoun, Helen M, Dahlöf, Björn, de Lemos, James, Downs, John R, Durrington, Paul N, Fellström, Bengt, Franzosi, Maria Grazia, Fuller (deceased), John, Furberg, Curt, Glynn, Robert, Gordon, David, Gotto Jr, Antonio, Gupta, Ajay, Hawkins, C Morton, Hitman, Graham A, Holdaas (deceased), Hallvard, Jardine, Alan, Jukema, J Wouter, Kean, Sharon, Kjekshus, John, Knatterud (deceased), Genell, Knopp (deceased), Robert H, Koren, Michael, Krane, Vera, Latini, Roberto, Lonn, Eva, Lucci, Donata, Macfarlane, Peter, MacMahon, Stephen, Maggioni, Aldo, Marchioli, Roberto, Marschner, Ian, Moyé, Lemuel, Murphy, Sabina, Neil, Andrew, Nicolis, Enrico B, Packard, Chris, Parish, Sarah, Peto, Richard, Pfeffer, Marc, Pressel, Sara, Rahman, Mahboob, Ridker, Paul M, Robertson, Michele, Sacks, Frank, Schmieder, Roland, Serruys, Patrick W, Sever, Peter, Shaw (deceased), John, Shepherd (deceased), James, Simpson, Lara, Sleight (deceased), Peter, Tavazzi, Luigi, Tognoni, Gianni, Wanner, Christoph, Wedel, Hans, Weis, Stephen, Welch, K Michael, White, Harvey, Wilhelmsen, Lars, Young, Robin, Yusuf, Salim, Zannad, Faiez, Arashi, Hiroyuki, Clarke, Robert, Flather, Marcus, Goldbourt, Uri, Goto, Shinya, Hopewell, Jemma, Kearney, Patricia, Kitas, George, Newman, Connie, Schwartz, Greg, Smeeth, Liam, Tobert, Jonathan, Yamaguchi, Junichi

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Correction to: Recognition and Treatment of Homozygous Familial Hypercholesterolemia by Primary Care Physicians: a Survey from the National Lipid Association by Hemphill, Linda, Goldberg, Anne, Hovingh, Kees, Cohen, Jerome, Karalis, Dean G

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Association of exome sequences with plasma C-reactive protein levels in >9000 participants by Schick, Ursula M, Auer, Paul L, Bis, Joshua C, Lin, Honghuang, Wei, Peng, Pankratz, Nathan, Lange, Leslie A, Brody, Jennifer, Stitziel, Nathan O, Kim, Daniel S, Carlson, Christopher S, Fornage, Myriam, Haessler, Jeffery, Hsu, Li, Jackson, Rebecca D, Kooperberg, Charles, Leal, Suzanne M, Psaty, Bruce M, Boerwinkle, Eric, Tracy, Russell, Ardissino, Diego, Shah, Svati, Willer, Cristen, Loos, Ruth, Melander, Olle, Mcpherson, Ruth, Hovingh, Kees, Reilly, Muredach, Watkins, Hugh, Girelli, Domenico, Fontanillas, Pierre, Chasman, Daniel I, Gabriel, Stacey B, Gibbs, Richard, Nickerson, Deborah A, Kathiresan, Sekar, Peters, Ulrike, Dupuis, Josée, Wilson, James G, Rich, Stephen S, Morrison, Alanna C, Benjamin, Emelia J, Gross, Myron D, Reiner, Alex P

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Lipoprotein profiles in human heterozygote carriers of a functional mutation P297S in scavenger receptor class B1 by Ljunggren, Stefan A., Levels, Johannes H.M., Hovingh, Kees, Holleboom, Adriaan G., Vergeer, Menno, Argyri, Letta, Gkolfinopoulou, Christina, Chroni, Angeliki, Sierts, Jeroen A., Kastelein, John J., Kuivenhoven, Jan Albert, Lindahl, Mats, Karlsson, Helen

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Association of exome sequences with plasma C-reactive protein levels in >9000 participants by Schick, Ursula M, Auer, Paul L, Bis, Joshua C, Lin, Honghuang, Wei, Peng, Pankratz, Nathan, Lange, Leslie A, Brody, Jennifer, Stitziel, Nathan O, Kim, Daniel S, Carlson, Christopher S, Fornage, Myriam, Haessler, Jeffery, Hsu, Li, Jackson, Rebecca D, Kooperberg, Charles, Leal, Suzanne M, Psaty, Bruce M, Boerwinkle, Eric, Tracy, Russell, Ardissino, Diego, Shah, Svati, Willer, Cristen, Loos, Ruth, Melander, Olle, Mcpherson, Ruth, Hovingh, Kees, Reilly, Muredach, Watkins, Hugh, Girelli, Domenico, Fontanillas, Pierre, Chasman, Daniel I, Gabriel, Stacey B, Gibbs, Richard, Nickerson, Deborah A, Kathiresan, Sekar, Peters, Ulrike, Dupuis, Josée, Wilson, James G, Rich, Stephen S, Morrison, Alanna C, Benjamin, Emelia J, Gross, Myron D, Reiner, Alex P

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ApoA-I mutations, L202P and K131del, in HDL from heterozygotes with low HDL-C by Ljunggren, Stefan, Levels, Johannes H. M., Turkina, Maria V., Sundberg, Sofie, Bochem, Andrea E., Hovingh, Kees, Holleboom, Adriaan G., Lindahl, Mats, Kuivenhoven, Jan Albert, Karlsson, Helen

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