Treffer 1 - 20 von 72 für Suche 'Weber, M Nick', Suchdauer: 1,47s Treffer weiter einschränken
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    Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores von de Rojas, Itziar, Tesi, Niccolo, Zettergren, Anna, Montrreal, Laura, Antonell, Anna, Bis, Joshua C., González-Perez, Antonio, Calero, Miguel, Blesa, Rafael, Sotolongo-Grau, Oscar, Benaque, Alba, Benussi, Alberto, de Mendonça, Alexandre, Arias Pastor, Alfonso, Espinosa, Ana, Sanabria, Ángela, DeStefano, Anita L., Schneider, Anja, Haapasalo, Annakaisa, Tybjærg-Hansen, Anne, Hartmann, Annette M., Spottke, Annika, Corbatón-Anchuelo, Arturo, Arosio, Beatrice, Nacmias, Benedetta, Kunkle, Brian W., Charbonnier, Camille, Martínez Rodríguez, Carmen, Reynolds, Chandra A., Fenoglio, Chiara, Van Broeckhoven, Christine, Clark, Christopher, Buiza-Rueda, Dolores, Alcolea, Daniel, Grünblatt, Edna, Dardiotis, Efthimios, Conti, Elisa, Boerwinkle, Eric, Ferri, Evelyn, Pasquier, Florence, Mangialasche, Francesca, Hadjigeorgiou, Georgios, Spalletta, Gianfranco, Soininen, Hilkka, Rainero, Innocenzo, Hort, Jakub, Kornhuber, Johannes, Pineda, Juan A., Fortea, Juan, Popp, Julius, Buerger, Katharina, Molina-Porcel, Laura, Wang, Li-San, Farotti, Lucia, Tsolaki, Magda, Rosende-Roca, Maitée, Hulsman, Marc, Spallazzi, Marco, Bernal Sánchez-Arjona, María, Dalmasso, Maria Carolina, Fernández-Fuertes, Marta, Herrmann, Martin J., Vyhnalek, Martin, Yannakoulia, Mary, Schmid, Matthias, Armstrong, Nicola J., Skrobot, Olivia Anna, Quenez, Olivier, Bossù, Paola, Caffarra, Paolo, Dionigi Rossi, Paolo, Sakka, Paraskevi, Riederer, Peter, Kalaria, Rajesh N., Mayeux, Richard, Vandenberghe, Rik, Sorbi, Sandro, Hägg, Sara, Engelborghs, Sebastiaan, Helisalmi, Seppo, Kern, Silke, Boschi, Silvia, Fostinelli, Silvia, Gil, Silvia, Ciccone, Simona, Djurovic, Srdjan, Riedel-Heller, Steffi, Kuulasmaa, Teemu, del Ser, Teodoro, Ngandu, Tiia, García-Alberca, Jose María, Lleó, Alberto, Real, Luis M., Mir, Pablo, Scheltens, Philip, Holstege, Henne, Amouyel, Philippe, Blennow, Kaj, Andreassen, Ole A., Posthuma, Danielle

    Veröffentlicht in NATURE COMMUNICATIONS

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    Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals von Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.


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