Treffer 1 - 20 von 23 für Suche 'GUILLEN, Myriam', Suchdauer: 1,44s Treffer weiter einschränken
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    Novel genetic loci associated with hippocampal volume von Chauhan, Ganesh, Hofer, Edith, Desrivières, Sylvane, Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Arfanakis, Konstantinos, Aribisala, Benjamin S., Athanasiu, Lavinia, Axelsson, Tomas, Chakravarty, M. Mallar, Cuellar-Partida, Gabriel, Doan, Nhat Trung, Giddaluru, Sudheer, Goldman, Aaron L., Gottesman, Rebecca F., Griswold, Michael E., Holmes, Avram J., Jia, Tianye, Karbalai, Nazanin, Kasperaviciute, Dalia, Liewald, David C. M., Luciano, Michelle, Marquand, Andre F., Matarin, Mar, Muñoz Maniega, Susana, Loohuis, Loes M. Olde, Oosterlaan, Jaap, Rommelse, Nanda, Ropele, Stefan, Shin, Jean, Sprooten, Emma, Trabzuni, Daniah, Trompet, Stella, Vaidya, Dhananjay, Van der Grond, Jeroen, Westlye, Lars T., Windham, Beverly G., Woldehawariat, Girma, Yanek, Lisa R., Almasy, Laura, Andreassen, Ole A., van Bokhoven, Hans, Boomsma, Dorret I., Brunner, Han G., De Craen, Anton J. M., Deary, Ian J., Debette, Stéphanie, DeCarli, Charles, Drevets, Wayne C., Fedko, Iryna O., Fernández, Guillén, Fisher, Simon E., Fleischman, Debra A., Ford, Ian, Francks, Clyde, Fukunaga, Masaki, Gudnason, Vilmundur, Hashimoto, Ryota, Heslenfeld, Dirk J., Ho, Beng-Choon, Hoekstra, Pieter J., Hofman, Albert, Homuth, Georg, Hottenga, Jouke-Jan, Jönsson, Erik G., Jukema, J. Wouter, McDonald, Colm, McIntosh, Andrew M., Mecocci, Patrizia, Melle, Ingrid, Montgomery, Grant W., Morris, Derek W., Mosley, Thomas H., Mühleisen, Thomas W., Nauck, Matthias, Ohi, Kazutaka, Olvera, Rene L., Penninx, Brenda W. J. H., Romanczuk-Seiferth, Nina, Saykin, Andrew J., Schmidt, Helena, Schofield, Peter R., Sigursson, Sigurdur, Smith, Colin, Soininen, Hilkka, Toga, Arthur W., Traynor, Bryan J., Hernández, Maria C. Valdés, van ’t Ent, Dennis, Van Tol, Marie-Jose, Völzke, Henry, Wassink, Thomas H., Westman, Eric, White, Tonya, Wong, Tien Y., Zielke, Ronald H., Launer, Lenore J., Medland, Sarah E., Ikram, M. Arfan

    Veröffentlicht in Nature communications

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    Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults von Hofer, Edith, Roshchupkin, Gennady V., Adams, Hieab H. H., Knol, Maria J., Lin, Honghuang, Li, Shuo, Zare, Habil, Ahmad, Shahzad, Armstrong, Nicola J., Satizabal, Claudia L., Bernard, Manon, Bis, Joshua C., Gillespie, Nathan A., Luciano, Michelle, Mishra, Aniket, Scholz, Markus, Teumer, Alexander, Xia, Rui, Jian, Xueqiu, Mosley, Thomas H., Saba, Yasaman, Pirpamer, Lukas, Seiler, Stephan, Becker, James T., Carmichael, Owen, Rotter, Jerome I., Psaty, Bruce M., Lopez, Oscar L., Amin, Najaf, van der Lee, Sven J., Yang, Qiong, Himali, Jayandra J., Maillard, Pauline, Beiser, Alexa S., DeCarli, Charles, Karama, Sherif, Lewis, Lindsay, Harris, Mat, Bastin, Mark E., Deary, Ian J., Veronica Witte, A., Beyer, Frauke, Loeffler, Markus, Mather, Karen A., Schofield, Peter R., Thalamuthu, Anbupalam, Kwok, John B., Wright, Margaret J., Ames, David, Trollor, Julian, Jiang, Jiyang, Brodaty, Henry, Wen, Wei, Vernooij, Meike W., Hofman, Albert, Uitterlinden, André G., Niessen, Wiro J., Wittfeld, Katharina, Bülow, Robin, Völker, Uwe, Pausova, Zdenka, Bruce Pike, G., Maingault, Sophie, Crivello, Fabrice, Tzourio, Christophe, Amouyel, Philippe, Mazoyer, Bernard, Neale, Michael C., Franz, Carol E., Lyons, Michael J., Panizzon, Matthew S., Andreassen, Ole A., Dale, Anders M., Logue, Mark, Grasby, Katrina L., Jahanshad, Neda, Painter, Jodie N., Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P., Lind, Penelope A., Pizzagalli, Fabrizio, Stein, Jason L., Thompson, Paul M., Medland, Sarah E., Sachdev, Perminder S., Kremen, William S., Wardlaw, Joanna M., Villringer, Arno, van Duijn, Cornelia M., Grabe, Hans J., Longstreth, William T., Fornage, Myriam, Paus, Tomas, Debette, Stephanie, Ikram, M. Arfan, Schmidt, Helena, Schmidt, Reinhold, Seshadri, Sudha

    Veröffentlicht in Nature communications

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    Widening of the genetic and clinical spectrum of Lamb–Shaffersyndrome, a neurodevelopmental disorder due to SOX5haploinsufficiency von Ash, Zawerton, Mignot Cyril, Sigafoos Ashley, Blackburn, Patrick R, Haseeb Abdul, McWalter Kirsty, Ichikawa Shoji, Nava, Caroline, Keren, Boris, Perrine, Charles, Marey Isabelle, Tabet Anne-Claude, Levy, Jonathan, Perrin, Laurence, Hartmann, Andreas, Lesca Gaetan, Schluth-Bolard Caroline, Monin, Pauline, Dupuis-Girod, Sophie, Guillen Sacoto Maria J, Schnur, Rhonda E, Zhu Zehua, Poisson, Alice, Salima, El Chehadeh, Alembik Yves, Ange-Line, Bruel, Lehalle Daphné, Nambot Sophie, Moutton Sébastien, Odent Sylvie, Jaillard Sylvie, Dubourg Christèle, Hilhorst-Hofstee Yvonne, Barbaro-Dieber Tina, Ortega, Lucia, Bhoj, Elizabeth J, Masser-Frye, Diane, Bird, Lynne M, Lindstrom, Kristin, Ramsey, Keri M, Narayanan Vinodh, Fassi, Emily, Willing, Marcia, Cole, Trevor, Salter, Claire G, Akilapa Rhoda, Vandersteen, Anthony, Canham, Natalie, Rump, Patrick, Gerkes, Erica H, Klein Wassink-Ruiter Jolien S, Bijlsma Emilia, Hoffer, Mariëtte J, Vargas, Marcelo, Wojcik Antonina, Cherik Florian, Francannet Christine, Rosenfeld, Jill A, Machol Keren, Scott, Daryl A, Bacino, Carlos A, Wang, Xia, Clark, Gary D, Bertoli, Marta, Zwolinski, Simon, Thomas, Rhys H, Akay Ela, Chang, Richard C, Bressi Rebekah, Sanchez Russo Rossana, Srour Myriam, Russell, Laura, Goyette, Anne-Marie E, Dupuis Lucie, Mendoza-Londono, Roberto, Karimov, Catherine, Maries, Joseph, Nizon Mathilde, Cogné Benjamin, Kuechler Alma, Piton Amélie, Klee, Eric W, Lefebvre Véronique, Clark, Karl J, Depienne Christel

    Veröffentlicht in Genetics in medicine

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    Quality improvement collaborative for improving patient care delivery in Argentine public health sector intensive care units von Loudet, Cecilia Inés, Jorro Barón, Facundo, Reina, Rosa, Arias López, María del Pilar, Alegría, Silvia Liliana, Barrios, Cecilia del Valle, Buffa, Rodolfo, Cabana, María Laura, Cunto, Eleonora Roxana, Fernández Nievas, Simón, García, Mariel Ayelén, Gibbons, Luz, Izzo, Gabriela, Llanos, María Natalia, Meregalli, Claudia, Joaquín Mira, José, Ratto, María Elena, Rivet, Mariano Luis, Roberti, Javier, Silvestri, Ana María, Tévez, Analía, Uranga, Leonardo Joaquín, Zakalik, Graciela, Rodríguez, Viviana, García-Elorrio, Ezequiel, Paggi, Laura, Becerra, Jacqueline Vilca, Rodríguez, Ivanna, Gelmetti, José, Paglia, Agustina, Villacorta, Magali, Luna, Fernando, Vanini, Christian, Sirino, Alicia, Balasini, Carina, Bastías Saez, Elizabeth Johanna, Fumale, Mariela Viviana, Castillo, Leticia Fernanda, Valle Rodríguez, Alejandra del, Vitale, Andrea Elizabeth, Vernetti, Yanina Luz, Chambi, Eliseo Velásquez, Flores, Aracelly Pérez, Hurtado, Itala Talamas, Verduguez, Marta, Bortoli, Verónica, Carmona, Maximiliano, Caponi, Matías, Chocobar, Melisa, Badilla, Flavia, Videla, Gisela, Conil, Cecilia, Chediack, Viviana, Resguardo, Analía Ileana, Susana González, Silvia, Muñoz, Elizabeth Rodríguez, Gregori, Rosana, Almeida, José Antonio, Domínguez, Cecilia Verónica, Tejerina, Olga Zulema, Tejerina, Susana, Tintilay, Cintya, Lamas, Malena, Gutiérrez, Dalma, Báez, Patricia, Aguiar, Valeria, Galán, Josefa, Gauna, María Eugenia, Kutscherauer, Daniela Olmos, Marcolini, Andrea, Fernández, Fernando David, Castellano, Luis Fernando, Catalini, Silvia Edith, Aramayo, Gladys Myriam, Calejman, Luciano Inowlocki, Torrico, María Luz, González, Liliana, Villavicencio, Vilma, Ortega, Javier Julián, Taborda, Pablo Nicolás, Moreno, Martín Américo, Moyano, Silvina Maricel, Vacas, Sebastian, Valle Fernández, Claudia del, Sánchez, Gabriela, Mamani, Clemente, Guillén, Sabrina, Maciel, Karina, Fernández, Silvia Laura, Plotnikow, Gustavo, Pereyra, Cecilia Florencia, Anzorena, Inés Suárez, Lescano, Marianela, Guglielmino, Marina

    Veröffentlicht in BMJ open quality

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    Genetic variants for head size share genes and pathways with cancer von Knol, Maria J., Mishra, Aniket, van der Auwera, Sandra, Duperron, Marie-Gabrielle, Pawlak, Mikolaj A., Shin, Jean, Li, Gloria H.Y., Amod, Alyssa R., Tsuchida, Ami, Aygün, Nil, Beyer, Frauke, Bis, Joshua C., Bos, Daniel, Caspers, Svenja, Catheline, Gwenaëlle, Enlund-Cerullo, Maria, Helmer, Catherine, Jack, Clifford R., Jahanshad, Neda, Li, Shuo, Longstreth, W.T., Arfanakis, Konstantinos, Aribisala, Benjamin S., Bastin, Mark E., Cheng, Ching-Yu, Gottesman, Rebecca F., Liewald, David C.M., Lopez, Lorna M., Lopez, Oscar, Niessen, Wiro J., Sacco, Ralph L., Völzke, Henry, Yanek, Lisa, Yang, Jingyun, Bernard, Manon, Boomsma, Dorret I., Brickman, Adam M., Brodaty, Henry, Buitelaar, Jan K., Carr, Vaughan J., Chakravarty, M. Mallar, Ching, Christopher R.K., Corvin, Aiden, Curran, Joanne E., den Braber, Anouk, Erk, Susanne, Fedko, Iryna O., Fernández, Guillén, Fisher, Simon E., Ge, Tian, Goldman, Aaron L., Green, Robert C., Greven, Corina U., Hashimoto, Ryota, Henskens, Frans, Ho, Beng-Choon, Holmes, Avram J., Jablensky, Assen, Jia, Tianye, Kwok, John B., Lawrie, Stephen M., McDonald, Colm, McMahon, Katie L., McWhirter, Olvera, Rene L., Pandolfo, Massimo, Pantelis, Christos, Pappa, Irene, Reppermund, Simone, Rose, Emma Jane, Schall, Ulrich, Schumann, Gunter, Shen, Li, Soininen, Hilkka, Sprooten, Emma, Turner, Jessica A., Van Haren, Neeltje E.M., van 't Ent, Dennis, Wen, Wei, Wright, Margaret J., Wu, Jingqin, Medland, Sarah E., Miyamoto, Susumu, Moebus, Susanne, Muetzel, Ryan, Nagata, Manabu, Palmer, Nicholette D., Quidé, Yann, Roshchupkin, Gennady V., Schreiner, Pamela J., Shapland, Chin Yang, Sidney, Stephen, Uhlmann, Anne, Wittfeld, Katharina, Yang, Qiong, Brunner, Han G., Le Grand, Quentin, Bowden, Donald W., Cheung, Ching-Lung, Thompson, Paul M.

    Veröffentlicht in CELL REPORTS MEDICINE

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