Treffer 1 - 8 von 8 für Suche 'Hardy, Nazli W.', Suchdauer: 2,74s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5

    Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von van Rheenen, Wouter, van der Spek, Rick a A, Bakker, Mark K, van Vugt, Joke J F A, Hop, Paul J, Zwamborn, Ramona a J, de Klein, Niek, Westra, Harm-Jan, Bakker, Olivier B, Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs H P, van Eijk, Kristel R, Kooyman, Maarten, Byrne, Ross P, Doherty, Mark, Heverin, Mark, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley N, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Shaw, Pamela J, Hardy, John, Orrell, Richard W, Sendtner, Michael, Meyer, Thomas, Başak, Nazli, van der Kooi, Anneke J, Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Lauria, Giuseppe, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, d'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Canosa, Antonio, Grassano, Maurizio, Beghi, Ettore, Pupillo, Elisabetta, Logroscino, Giancarlo, Nefussy, Beatrice, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Zabari, Michal, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'H, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stéphanie, Meininger, Vincent, Salachas, François, Mora Pardina, Jesus S, Assialioui, Abdelilah, Rojas-García, Ricardo, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Payan, Christine a M, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan, Braun, Alice, Kraft, Julia

    Veröffentlicht in Nature genetics

    Volltext
    Artikel
  6. 6
  7. 7

    Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von van Rheenen, Wouter, Shatunov, Aleksey, Dekker, Annelot M, McLaughlin, Russell L, Diekstra, Frank P, Pulit, Sara L, van der Spek, Rick A.A, Võsa, Urmo, de Jong, Simone, Robinson, Matthew R, Yang, Jian, Fogh, Isabella, van Doormaal, Perry Tc, Tazelaar, Gijs H.P, Koppers, Max, Blokhuis, Anna M, Sproviero, William, Jones, Ashley R, Kenna, Kevin P, van Eijk, Kristel R, Harschnitz, Oliver, Schellevis, Raymond D, Brands, William J, Medic, Jelena, Menelaou, Androniki, Vajda, Alice, Ticozzi, Nicola, Lin, Kuang, Rogelj, Boris, Vrabec, Katarina, Ravnik-Glavač, Metka, Koritnik, Blaž, Zidar, Janez, Leonardis, Lea, Grošelj, Leja Dolenc, Millecamps, Stéphanie, Salachas, François, Meininger, Vincent, de Carvalho, Mamede, Pinto, Susana, Mora, Jesus S, Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen E, Shaw, Pamela J, Hardy, John, Orrell, Richard W, Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Topp, Simon, Petri, Susanne, Abdulla, Susanne, Drepper, Carsten, Sendtner, Michael, Meyer, Thomas, Ophoff, Roel A, Staats, Kim A, Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, Van Deerlin, Vivianna M, Trojanowski, John Q, Elman, Lauren, McCluskey, Leo, Basak, A. Nazli, Tunca, Ceren, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R, Maurel, Cindy, Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A.M, Saker-Delye, Safaa, Dürr, Alexandra, Wood, Nicholas W, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-François, Uitterlinden, Andre G, Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charles, Blauw, Hylke M, van der Kooi, Anneke J

    Veröffentlicht in Nature Genetics

    Volltext
    Artikel
  8. 8

    Using global team science to identify genetic parkinson's disease worldwide von Vollstedt, Eva‐Juliane, Klein, Christine, Ahmad‐Annuar, Azlina, Al‐Mubarak, Bashayer, Annesi, Grazia, Barber, Thomas R., Bardien, Soraya, Başak, A. Nazlı, Bhatia, Kailash, Binkofski, Ferdinand, Bozi, Maria, Brice, Alexis, Brighina, Laura, Brockmann, Kathrin, Brücke, Thomas, Chen‐Plotkin, Alice, Ju Chung, Sun, Clark, Lorraine, Corvol, Jean‐Christophe, Cosentino, Carlos, Cras, Patrick, Crosiers, David, De Michele, Giuseppe, De Rosa, Anna, Erer, Sevda, Ertan, Sibel, Farrer, Matthew, Fiala, Ondrej, Foroud, Tatiana, Friedman, Andrzej, Frigerio, Roberta, Garraux, Gaetan, Gomez‐Esteban, Juan Carlos, Hardy, John, Hassan, Anhar, Hedera, Peter, Hentati, Faycal, Inca‐Martinez, Miguel, Infante, Jon, Jankovic, Joseph, Jesús, Silvia, Kasten, Meike, Kataoka, Hiroshi, Kim, Yun Joong, Koziorowski, Dariusz, Krüger, Rejko, Krygowska‐Wajs, Anna, Kulisevsky, Jaime, Lai, Dongbing, Lang, Anthony, LeDoux, Mark, Lesage, Suzanne, Lim, Shen‐Yang, Lin, Chin‐Hsien, Lopera, Francisco, Lopez, Grisel, Lu, Chin‐Song, Lynch, Tim, Maraganore, Demetrius, Marder, Karen, Mazzetti, Pilar, Mirelman, Anat, Morris, Huw, Naito, Anna, Ozelius, Laurie J., Padmanabhan, Shalini, Paisán‐Ruiz, Coro, Petkovic, Sonja, Petrucci, Simona, Pimentel, Márcia, Pirker, Walter, Pulkes, Teeratorn, Puschmann, Andreas, Quattrone, Aldo, Sammler, Esther, Sazci, Ali, Schrag, Anette, Sharma, Manu, Sidransky, Ellen, Petersen, Maria Skaalum, Sue, Carolyn M., Swan, Matthew, Swanberg, Maria, Taba, Pille, Tan, Manuela, Tan, Ai Huey, Tan, Eng‐King, Tayebi, Nahid, Thaler, Avner, Thomas, Astrid, Toda, Tatsushi, Torres, Luis, Valente, Enza Maria, Van Broeckhoven, Christine, Wood, Nicholas W., Wszolek, Zbigniew K., Wu, Ruey‐Meei, Yoshino, Hiroyo, Zhang, Baorong, Zimprich, Alexander

    Veröffentlicht in Annals of neurology

    Volltext
    Artikel