From endothelial dysfunction to atherosclerosis von Sitia, S, Tomasoni, L, Atzeni, F, Ambrosio, G, Cordiano, C, Catapano, A, Tramontana, S, Perticone, F, Naccarato, P, Camici, P, Picano, E, Cortigiani, L, Bevilacqua, M, Milazzo, L, Cusi, D, Barlassina, C, Sarzi-Puttini, P, Turiel, M

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Simulation and Analysis of Thermal Insulators Applied to Post-Disaster Temporary Shelters in Tropical Countries von da Costa, Bruno B. F., Silva, Caio F. P., Maciel, Ana Carolina F., Cusi, Herson D. P., Maquera, Gladys, Haddad, Assed N.

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R990G polymorphism of calcium-sensing receptor does produce a gain-of-function and predispose to primary hypercalciuria von Vezzoli, G., Terranegra, A., Arcidiacono, T., Biasion, R., Coviello, D., Syren, M.L., Paloschi, V., Giannini, S., Mignogna, G., Rubinacci, A., Ferraretto, A., Cusi, D., Bianchi, G., Soldati, L.

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Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis von Invernizzi, P, Ransom, M, Raychaudhuri, S, Kosoy, R, Lleo, A, Shigeta, R, Franke, A, Bossa, F, Amos, C I, Gregersen, P K, Siminovitch, K A, Cusi, D, de Bakker, P I W, Podda, M, Gershwin, M E, Seldin, M F

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Dietary style and acid load in an Italian population of calcium kidney stone formers von Vezzoli, G, Dogliotti, E, Terranegra, A, Arcidiacono, T, Macrina, L, Tavecchia, M, Pivari, F, Mingione, A, Brasacchio, C, Nouvenne, A, Meschi, T, Cusi, D, Spotti, D, Montanari, E, Soldati, L

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Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: Association with the functional IRAK1 196Phe/532Ser haplotype von Dieudé, P., Bouaziz, M., Guedj, M., Riemekasten, G., Airò, P., Müller, M., Cusi, D., Matucci‐Cerinic, M., Melchers, I., Koenig, W., Salvi, E., Wichmann, H. E., Cuomo, G., Hachulla, E., Diot, E., Hunzelmann, N., Caramaschi, P., Mouthon, L., Riccieri, V., Distler, J., Tarner, I., Avouac, J., Meyer, O., Kahan, A., Chiocchia, G., Boileau, C., Allanore, Y.

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6C.02: EXOME SEQUENCING IN SEVEN FAMILIES AND GENE-BASED ASSOCIATION STUDIES SUPPORT GENETIC HETEROGENEITY AND SUGGEST POSSIBLE CANDIDATES FOR FIBROMUSCULAR DYSPLASIA von Kiando, S, Plouin, P.F, Barlassina, M.C, Cusi, D, Galan, P, Lathrop, M, Jeunemaitre, X, Bouatia-Naji, N

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[OP.7C.04] GENETIC ASSOCIATION STUDY IDENTIFIES COMMON VARIATION IN PHACTR1 TO ASSOCIATE WITH FIBROMUSCULAR DYSPLASIA von Kiando, S, Tucker, N, Castro-vega, L, Cusi, D, Galan, P, J.-P, Empana, Olin, J, Gornik, H, Plouin, P.-F, Kullo, I, Milan, D, Ganesh, S, Boutouyrie, P, Kovacic, J, Jeunemaitre, X, Bouatia-naji, N

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THU0519 Xanthine Oxidase Gene Variants and Their Association with Blood Pressure and Incident Hypertension: A Population Study von Scheepers, L.E., Wei, F., Stolarz-Skrzypek, K., Malyutina, S., Tikhonoff, V., Thijs, L., Salvi, E., Barlassina, C., Filipovský, J., Casiglia, E., Nikitin, Y.P., Kawecka-Jaszcz, K., Manunta, P., Cusi, D., Boonen, A., Staessen, J.A., Arts, I.C.

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The -665 CT polymorphism in the eNOS gene predicts cardiovascular mortality and morbidity in white Europeans von Olivi, L, Gu, Y.-M, Salvi, E, Liu, Y.-P, Thijs, L, Velayutham, D, Jin, Y, Jacobs, L, D'Avila, F, Petit, T, Barcella, M, Lanzani, C, Kuznetsova, T, Manunta, P, Barlassina, C, Cusi, D, Staessen, J.A

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The −665 C>T polymorphism in the eNOS gene predicts cardiovascular mortality and morbidity in white Europeans von Olivi, L, Gu, Y-M, Salvi, E, Liu, Y-P, Thijs, L, Velayutham, D, Jin, Y, Jacobs, L, D'Avila, F, Petit, T, Barcella, M, Lanzani, C, Kuznetsova, T, Manunta, P, Barlassina, C, Cusi, D, Staessen, J A

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Evidence for malaria selection of a CR1 haplotype in Sardinia von Kosoy, R, Ransom, M, Chen, H, Marconi, M, Macciardi, F, Glorioso, N, Gregersen, P K, Cusi, D, Seldin, M F

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Polymorphisms of CaSR gene decreasing CaSR expression predispose to calcium nephrolithiasis von Vezzoli, G, Aloia, A, Terranegra, A, Dogliotti, E, Arcidiacono, T, Rainone, F, Mingione, A, Spotti, D, Cusi, D, Hendy, G.N, Soldati, L

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Vitamin D receptor activation and prevention of arterial ageing von Cozzolino, M, Stucchi, A, Rizzo, M.A, Soldati, L, Cusi, D, Ciceri, P, Brenna, I, Elli, F, Gallieni, M

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Reprint of: Vitamin D receptor activation and prevention of arterial ageing von Cozzolino, M, Stucchi, A, Rizzo, M.A, Soldati, L, Cusi, D, Ciceri, P, Brenna, I, Elli, F, Gallieni, M

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Genome-wide association study of obsessive-compulsive disorder von Stewart, S E, Yu, D, Scharf, J M, Neale, B M, Fagerness, J A, Arnold, P D, Evans, P D, Gamazon, E R, McGrath, L, Haddad, S, Crane, J, Hezel, D, Illman, C, Mayerfeld, C, Konkashbaev, A, Liu, C, Pluzhnikov, A, Tikhomirov, A, Rauch, S L, Maier, W, Ruhrmann, S, Grabe, H-J, Lennertz, L, Wagner, M, Bellodi, L, Cavallini, M C, Richter, M A, Cook, E H, Kennedy, J L, Rosenberg, D, Stein, D J, Hemmings, S M J, Azzam, A, Chavira, D A, Fournier, E, Garrido, H, Sheppard, B, Umaña, P, Murphy, D L, Wendland, J R, Veenstra-VanderWeele, J, Denys, D, Blom, R, Deforce, D, Van Nieuwerburgh, F, Walitza, S, Egberts, K, Renner, T, Miguel, E C, Cappi, C, Hounie, A G, Conceição do Rosário, M, Sampaio, A S, Vallada, H, Lanzagorta, N, Camarena, B, Delorme, R, Leboyer, M, Pato, C N, Pato, M T, Voyiaziakis, E, Heutink, P, Cath, D C, Posthuma, D, Smit, J H, Samuels, J, Bienvenu, O J, Cullen, B, Fyer, A J, Grados, M A, Greenberg, B D, McCracken, J T, Riddle, M A, Wang, Y, Coric, V, Leckman, J F, Pittenger, C, Eapen, V, Black, D W, Ophoff, R A, Strengman, E, Cusi, D, Turiel, M, Frau, F, Macciardi, F, Gibbs, J R, Cookson, M R, Singleton, A, Hardy, J, Crenshaw, A T, Parkin, M A, Mirel, D B, Conti, D V, Purcell, S, Nestadt, G, Hanna, G L, Jenike, M A, Knowles, J A, Cox, N, Pauls, D L

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Genetic Drivers of Kidney Defects in the DiGeorge Syndrome von Lopez-Rivera, Esther, Liu, Yangfan P, Verbitsky, Miguel, Anderson, Blair R, Capone, Valentina P, Otto, Edgar A, Yan, Zhonghai, Mitrotti, Adele, Martino, Jeremiah, Steers, Nicholas J, Fasel, David A, Vukojevic, Katarina, Deng, Rong, Racedo, Silvia E, Liu, Qingxue, Werth, Max, Westland, Rik, Vivante, Asaf, Makar, Gabriel S, Bodria, Monica, Sampson, Matthew G, Gillies, Christopher E, Vega-Warner, Virginia, Maiorana, Mariarosa, Petrey, Donald S, Honig, Barry, Lozanovski, Vladimir J, Salomon, Rémi, Heidet, Laurence, Carpentier, Wassila, Gaillard, Dominique, Carrea, Alba, Gesualdo, Loreto, Cusi, Daniele, Izzi, Claudia, Scolari, Francesco, van Wijk, Joanna A.E, Arapovic, Adela, Saraga-Babic, Mirna, Saraga, Marijan, Kunac, Nenad, Samii, Ali, McDonald-McGinn, Donna M, Crowley, Terrence B, Zackai, Elaine H, Drozdz, Dorota, Miklaszewska, Monika, Tkaczyk, Marcin, Sikora, Przemyslaw, Szczepanska, Maria, Mizerska-Wasiak, Malgorzata, Krzemien, Grazyna, Szmigielska, Agnieszka, Zaniew, Marcin, Darlow, John M, Puri, Prem, Barton, David, Casolari, Emilio, Furth, Susan L, Warady, Bradley A, Gucev, Zoran, Hakonarson, Hakon, Flogelova, Hana, Tasic, Velibor, Latos-Bielenska, Anna, Materna-Kiryluk, Anna, Allegri, Landino, Wong, Craig S, Drummond, Iain A, D’Agati, Vivette, Imamoto, Akira, Barasch, Jonathan M, Hildebrandt, Friedhelm, Kiryluk, Krzysztof, Lifton, Richard P, Morrow, Bernice E, Jeanpierre, Cecile, Papaioannou, Virginia E, Ghiggeri, Gian Marco, Gharavi, Ali G, Katsanis, Nicholas, Sanna-Cherchi, Simone

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1400 DISCOVERY OF A DIRECT ASSOCIATION BETWEEN PRIMARY BILIARY CIRRHOSIS AND LOW BONE MASS: IDENTIFICATION OF TNFSF11/RANKL AS A RISK LOCUS FOR PATIENTS WITH PBC von Hirschfield, G.M, Juran, B.D, Invernizzi, P, Atkinson, E.J, Li, Y, Xie, G, Kosoy, R, Ransom, M, Sun, Y, Bianchi, I, Schlicht, E.M, Lleo, A, Coltescu, C, Bernuzzi, F, Lammert, C, Shigetta, R, Chan, L.L, Balschun, T, Marconi, M, Cusi, D, Mason, A.L, Myers, R.P, Milkiewicz, P, Odin, J.A, Luketic, V.A, Bacon, B, Bodenheimer, H, Liakina, V, Vincent, C, Levy, C, Franke, A, Gregerson, P.K, Annese, V, Gershwin, M.E, de Andrade, M, Amos, C.I, Lazaridis, K.N, Seldin, M.F, Siminovitch, K.A

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Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits von Winkler, Thomas W., Graff, Misa, Young, Kristin, Deng, Xuan, Heard-Costa, Nancy L., Eicher, John D., Wu, Joseph, Alfred, Tamuno, Cadby, Gemma, Direk, Nese, Eriksson, Joel, Fischer, Krista, Gorski, Mathias, Komulainen, Pirjo, Lim, Unhee, Lyytikäinen, Leo-Pekka, Smith, Albert Vernon, Smith, Jennifer A., Teumer, Alexander, Verweij, Niek, Vitart, Veronique, Wu, Ying, Yengo, Loic, Hua Zhao, Jing, Blangero, John, Buyske, Steve, Campbell, Harry, Collins, Francis S., de Craen, Anton J. M., de Geus, Eco J. C., Eiriksdottir, Gudny, Faul, Jessica D., Ford, Ian, Grallert, Harald, Hallmans, Göran, Hamsten, Anders, Hartman, Catharina A., Hassinen, Maija, Hernandez, Dena, Hocking, Lynne J., Homuth, Georg, Jan Hottenga, Jouke, Huang, Jie, Hung, Joseph, Jarvelin, Marjo-Riitta, Juonala, Markus, Karlsson, Magnus, Kolcic, Ivana, Kolovou, Genovefa, Kuusisto, Johanna, Lakka, Timo A., Leander, Karin, Lee, Nanette R., Lind, Lars, Lobbens, Stephane, Luben, Robert, Lubke, Gitta, Lupoli, Sara, Marques-Vidal, Pedro, Menni, Cristina, Peyser, Patricia A., Pisinger, Charlotta, Ridker, Paul M., Bien, Stephanie A., Rudan, Igor, Sennblad, Bengt, Stott, David J., Thorand, Barbara, Uitterlinden, Andre G., Wild, Sarah, Willemsen, Gonneke, Wolffenbuttel, Bruce H. R., Zillikens, M Carola, Baldassarre, Damiano, Böger, Carsten A., Boomsma, Dorret I., Bouchard, Claude, Chen, Yii-DerIda, Chines, Peter S., Froguel, Philippe, Haiman, Christopher A., Johnson, Andrew D., Kardia, Sharon L. R., Lehtimäki, Terho, März, Winfried, Morris, Andrew P., Palmer, Lyle J., Peters, Annette, Polasek, Ozren, Psaty, Bruce M., Smith, Blair H., Sørensen, Thorkild I. A., Frayling, Timothy M., Barroso, Inês, Hirschhorn, Joel N., Hunter, David J., van Duijn, Cornelia M., Mohlke, Karen L., Marchini, Jonathan, Liu, Ching-Ti

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Two Point Mutations within the Adducin Genes are Involved in Blood Pressure Variation von Bianchi, Giuseppe, Tripodi, Grazia, Casari, Giorgio, Salardi, Sergio, Barber, Barry R., Garcia, Rodolfo, Leoni, Patricia, Torielli, Lucia, Cusi, Daniele, Ferrandi, Mara, Pinna, Lorenzo A., Baralle, Francisco E., Ferrari, Patrizia

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