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    Meta‐analysis of individual‐patient data from EVAR‐1, DREAM, OVER and ACE trials comparing outcomes of endovascular or open repair for abdominal aortic aneurysm over 5 years by Sweeting, M. J., Sculpher, M. J., Poole‐Wilson, the late P.A., Johnston, L., Bradbury, A. W., Higman, D. J., Wyatt, M. G., Taylor, P. R., Wilkinson, A. R., Lavelle, J. M., McPherson, S., Kessell, D. O., Gould, D. A., Collins, M. A., Braithwaite, B., Platts, A., Matson, M., Morris, G., Aukett, M., Gough, M., Kivela, M., Murray, S., Spencer, S., Bak, A. A. A., Buth, J., Grobbee, D. E., van Sambeek, M. R. H. M., de Mol, B. A. J. M., Reekers, J., van Sambeek, M. R. H. M., Verhoeven, E. L. G., van der Ham, A. C., ten Haken, G. B., van der Vliet, A. J., Wisselink, W., Smeets, H. J., Cushing, C., Katz, D. A., Matts, J. P., Kasirajan, K., Paap, C., Veeraswamy, R., Lilly, M. P., Ellis, K., Dosluoglu, H. H., Eschberger, K., Meadows, W., Ruf, M., Pinault, G., Chand, P., Yales, C., Lee, N., Cerveira, J. J., Zickler, R. W., O'Sullivan, M. T., Bush, R. L., Guinn, G., Nachreiner, R., Kimbrough, J., Ashe, L., Bishop, V., Cayne, N., Rockman, C., Johanning, J., Bahmani, D. D., Golden, M. A., Mitchell, M. E., Tzeng, E., Forbes, B. A., Yan, K., Glickerman, D. G., Shames, M., Leon, L. R., Mills, J. L., Psalms, S. B., Sidawy, A., Wong, J., DeVirgillio, C., Rigberg, D. A., Watelet, J., Hemery, F., Ady, N., Blin, V., Becquemin, J.‐P., Allaire, E., Chevalier, P., Baque, J., Veyret, C., Watelet, J., Clavier, E., C, Dupreix, Langanay, T., Koussa, M., Pillet, J.‐C., Lescalie, F., Krause, D., Cardon, J.‐M., Braesco, J., Tailboux, L., Varty, K.

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    New insights into the genetic etiology of Alzheimer's disease and related dementias by Amin, Najaf, Naj, Adam C, Grenier-Boley, Benjamin, Boland, Anne, van der Lee, Sven J, Yang, Qiong, de Rojas, Itziar, Yaqub, Amber, Chapuis, Julien, Alarcón-Martín, Emilio, Tsolaki, Anthoula, Antúnez, Carmen, Bailly, Henri, Barral, Sandra, Pastor, Ana Belén, Below, Jennifer E, Benussi, Luisa, Binetti, Giuliano, Boada, Mercè, Bråthen, Geir, Bresner, Catherine, Brodaty, Henry, Brusco, Luis Ignacio, Burholt, Vanessa, Cuccaro, Michael L, Clark, Christopher, Custodero, Carlo, Dalmasso, Maria Carolina, Daniele, Antonio, Debette, Stéphanie, Dichgans, Martin, Escott-Price, Valentina, Ferreira, Catarina B, Fladby, Tormod, Fließbach, Klaus, García-Alberca, Jose Maria, Garcia-Madrona, Sebastian, Garcia-Ribas, Guillermo, Giegling, Ina, Grande, Giulia, Gudnason, Vilmundur, Haapasalo, Annakaisa, Hampel, Harald, Hanon, Olivier, Hardy, John, Harwood, Janet, Hoffmann, Per, Hulsman, Marc, Kilander, Lena, Kornhuber, Johannes, Lage, Carmen, Love, Seth, Löwemark, Malin, Marquié, Marta, Mead, Simon, Medina, Miguel, Mir, Pablo, Mol, Merel, Ngandu, Tiia, Ortega, Gemma, Paolo, Caffarra, Pasquier, Florence, Pastor, Pau, Polak, Thomas, Priller, Josef, Thomassen, Jesper Qvist, Rainero, Innocenzo, Rajabli, Farid, Reinders, Marcel J T, Reitz, Christiane, Rongve, Arvid, Rosende-Roca, Maitée, Rujescu, Dan, Sakka, Paraskevi, Sánchez-Arjona, María Bernal, Sánchez-Valle, Raquel, Scamosci, Michela, Scheltens, Philip, Scherbaum, Norbert, Snijders, Gijsje J L, Spalletta, Gianfranco, Tartan, Juan Pablo, Tárraga, Lluís, Tesí, Niccolo, Traykov, Latchezar, Ulstein, Ingun, van Rooij, Jeroen, van Swieten, John, Vandenberghe, Rik, Wagner, Michael, Wiltfang, Jens, Yannakoulia, Mary, Zulaica, Miren, Sachdev, Perminder, Ikram, M Arfan, de Mendonça, Alexandre, Hort, Jakub, Ingelsson, Martin, Sims, Rebecca, Ruiz, Agustín

    Published in Nature genetics
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    X-chromosome-wide association study for Alzheimer's disease by Le Borgne, Julie, Gomez, Lissette, Heikkinen, Sami, Amin, Najaf, Ahmad, Shahzad, Choi, Seung Hoan, Bis, Joshua, Grenier-Boley, Benjamin, Rodriguez, Omar Garcia, Kleineidam, Luca, Young, Juan, Tripathi, Kumar Parijat, Wang, Lily, Varma, Achintya, Campos-Martin, Rafael, van der Lee, Sven, Damotte, Vincent, de Rojas, Itziar, Palmal, Sagnik, Lipton, Richard, Reiman, Eric, McKee, Ann, De Jager, Philip, Bush, William, Small, Scott, Levey, Allan, Saykin, Andrew, Foroud, Tatiana, Albert, Marilyn, Hyman, Bradley, Petersen, Ronald, Younkin, Steven, Sano, Mary, Wisniewski, Thomas, Vassar, Robert, Schneider, Julie, Henderson, Victor, Roberson, Erik, DeCarli, Charles, LaFerla, Frank, Brewer, James, Swerdlow, Russell, Van Eldik, Linda, Hamilton-Nelson, Kara, Paulson, Henry, Naj, Adam, Lopez, Oscar, Chui, Helena, Crane, Paul, Grabowski, Thomas, Kukull, Walter, Asthana, Sanjay, Craft, Suzanne, Strittmatter, Stephen, Cruchaga, Carlos, Leverenz, James, Goate, Alison, Kamboh, M Ilyas, George-Hyslop, Peter St, Valladares, Otto, Kuzma, Amanda, Cantwell, Laura, Riemenschneider, Matthias, Morris, John, Slifer, Susan, Dalmasso, Carolina, Castillo, Atahualpa, Küçükali, Fahri, Peters, Oliver, Schneider, Anja, Dichgans, Martin, Rujescu, Dan, Scherbaum, Norbert, Deckert, Jürgen, Riedel-Heller, Steffi, Hausner, Lucrezia, Molina-Porcel, Laura, Düzel, Emrah, Grimmer, Timo, Wiltfang, Jens, Heilmann-Heimbach, Stefanie, Moebus, Susanne, Tegos, Thomas, Scarmeas, Nikolaos, Dols-Icardo, Oriol, Moreno, Fermin, Pérez-Tur, Jordi, Bullido, María J, Pastor, Pau, Sánchez-Valle, Raquel, Álvarez, Victoria, Boada, Mercè, García-González, Pablo, Puerta, Raquel, Mir, Pablo, Real, Luis M, Piñol-Ripoll, Gerard, García-Alberca, Jose María, Royo, Jose Luís, Rodriguez-Rodriguez, Eloy

    Published in Molecular psychiatry
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    Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders by Gillentine, Madelyn A, Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N, De Vries, Bert B A, Vissers, Lisenka E L M, Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A, Bhat, Gifty, Cobian, Katherine, Bird, Lynne M, Friedman, Jennifer, Wright, Meredith S, Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K, White, Kerry M, Elpeleg, Orly, Berger, Itai, Espineli, Edward J, Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjærsgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L Manace, Mckee, Shane, Mirzaa, Ghayda M, Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E H, van Gassen, Koen L I, Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K, Nowakowski, Tomasz, Bernier, Raphael A, Eichler, Evan E

    Published in Genome medicine
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