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    Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von Bakker, Mark K., van Vugt, Joke J. F. A., Hop, Paul J., Westra, Harm-Jan, Deelen, Patrick, Hannon, Eilis, Dolzhenko, Egor, 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, Smith, Bradley N., Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Sendtner, Michael, Meyer, Thomas, Başak, Nazli, van der Kooi, Anneke J., Ratti, Antonia, Fogh, Isabella, Lauria, Giuseppe, Corti, Stefania, Sorarù, Gianni, Filosto, Massimiliano, Chiò, Adriano, Calvo, Andrea, Brunetti, Maura, Nefussy, Beatrice, Osmanovic, Alma, Lerner, Yossef, Gotkine, Marc, Bell, Shaughn, Vourc’h, Patrick, Corcia, Philippe, Salachas, François, Mora Pardina, Jesus S., Rojas-García, Ricardo, Ross, Jay P., Weishaupt, Jochen H., Brenner, David, Bensimon, Gilbert, Payan, Christine A. M., Saker-Delye, Safa, Wood, Nicholas W., Rademakers, Rosa, Lieb, Wolfgang, Olsen, Catherine M., Uitterlinden, Andre G., Hofman, Albert, Rietschel, Marcella, Traynor, Bryan J., Mitne Neto, Miguel, Cauchi, Ruben J., Gaur, Nayana, Ilse, Benjamin, Stubendorff, Beatrice, Witte, Otto W., Steinbach, Robert, Graff, Caroline, Ataulina, Anastasia, Rogelj, Boris, Koritnik, Blaž, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Stević, Zorica, Drory, Vivian, Povedano, Monica, Blair, Ian P., Kiernan, Matthew C., Furlong, Sarah, Mathers, Susan, Nicholson, Garth A., Pamphlett, Roger, Rowe, Dominic B., Williams, Kelly L., Mather, Karen A., Sachdev, Perminder S., Wallace, Leanne, Pinto, Susana, Rouleau, Guy A., Breen, Gerome, Brown, Robert H., Andersen, Peter M., McRae, Allan F., Davey Smith, George, Gaunt, Tom R., Eberle, Michael A., Wray, Naomi R., Van Damme, Philip, Veldink, Jan H.

    Veröffentlicht in Nature genetics

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    Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biolo... von Bakker, Mark K., van Vugt, Joke J. F. A., Hop, Paul J., Westra, Harm-Jan, Deelen, Patrick, Hannon, Eilis, Dolzhenko, Egor, 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, Smith, Bradley N., Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Sendtner, Michael, Meyer, Thomas, Başak, Nazli, van der Kooi, Anneke J., Ratti, Antonia, Fogh, Isabella, Lauria, Giuseppe, Corti, Stefania, Sorarù, Gianni, Filosto, Massimiliano, Chiò, Adriano, Calvo, Andrea, Brunetti, Maura, Nefussy, Beatrice, Osmanovic, Alma, Lerner, Yossef, Gotkine, Marc, Bell, Shaughn, Vourc’h, Patrick, Corcia, Philippe, Salachas, François, Mora Pardina, Jesus S., Rojas-García, Ricardo, Ross, Jay P., Weishaupt, Jochen H., Brenner, David, Bensimon, Gilbert, Payan, Christine A. M., Saker-Delye, Safa, Wood, Nicholas W., Rademakers, Rosa, Lieb, Wolfgang, Olsen, Catherine M., Uitterlinden, Andre G., Hofman, Albert, Rietschel, Marcella, Traynor, Bryan J., Mitne Neto, Miguel, Cauchi, Ruben J., Gaur, Nayana, Ilse, Benjamin, Stubendorff, Beatrice, Witte, Otto W., Steinbach, Robert, Graff, Caroline, Ataulina, Anastasia, Rogelj, Boris, Koritnik, Blaž, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Stević, Zorica, Drory, Vivian, Povedano, Monica, Blair, Ian P., Kiernan, Matthew C., Furlong, Sarah, Mathers, Susan, Nicholson, Garth A., Pamphlett, Roger, Rowe, Dominic B., Williams, Kelly L., Mather, Karen A., Sachdev, Perminder S., Wallace, Leanne, Pinto, Susana, Rouleau, Guy A., Breen, Gerome, Brown, Robert H., Andersen, Peter M., McRae, Allan F., Davey Smith, George, Gaunt, Tom R., Eberle, Michael A., Wray, Naomi R., Van Damme, Philip, Veldink, Jan H.

    Veröffentlicht in Nature genetics

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    Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von Rheenen, Wouter van, Spek, Rick A. A. van der, Vugt, Joke J. F. A. van, Klein, Niek de, Bakker, Olivier B, Siciliano, Gabriele, Breen, Gerome, Weber, Markus, Silani, Vincenzo, Amouyel, Philippe, Curtis, Charles J, Mill, Jonathan, Filosto, Massimiliano, Hardiman, Orla, Runz, Heiko, Chandran, Siddharthan, Damme, Philip van, Gagliardi, Stella, Cichon, Sven, Hardy, John, Calvo, Andrea, Kooyman, Maarten, Ratti, Antonia, Garton, Fleur C, Fogh, Isabella, Brunetti, Maura, Mazzini, Letizia, Logroscino, Giancarlo, Nefussy, Beatrice, Rinaldi, Fabrizio, Weishaupt, Jochen H, Baloh, Robert H, Vito, Nicoletta di, Zoccolella, Stefano, Heverin, Mark, Glass, Jonathan D, Rota, Eugenia, Ilse, Benjamin, Payan, Christine A. M, Saker-Delye, Safa, Aguggia, Marco, Perrone, Patrizia, Mundi, Ciro, Passarella, Bruno, Delodovici, Maria Luisa, Furlong, Sarah, Manera, Umberto, Bombaci, Alessandro, Meineri, Piero, Mauro, Alessandro, Leone, Maurizio, Mathers, Susan, Gellera, Cinzia, Andersen, Peter M, D’alfonso, Sandra, Bertolotto, Antonio, Slalom Consortium, Dotta, Michele, Pignatta, Pietro, Groen, Ewout J. N, Cotelli, Maria Sofia, Mattei, Marco de, Sapio, Alessia di, Corcia, Philippe, Mccombe, Pamela A, Parals Consortium, Peverelli, Silvia, Cereda, Cristina, Bo, Roberto del, Hofman, Albert, Van Eijk, Kristel R, Tittmann, Lukas, Cauchi, Ruben J, Lomen-Hoerth, Catherine, Brylev, Lev, Grosskreutz, Julian, Roediger, Annekathrin, Pamphlett, Roger, Fominykh, Vera, Lieb, Wolfgang, Millecamps, Stéphanie, Ataulina, Anastasia, Zidar, Janez, Rowe, Dominic B, Peotta, Laura, Glavač, Damjan, Rietschel, Marcella, Meininger, Vincent, Smith, Bradley N, Cugnasco, Paolo, Papurello, Diego Maria, Sorarù, Gianni, Mather, Karen A, Wallace, Leanne, Carvalho, Mamede de, Pinto, Susana, Marco, Giovanni de, Al Khleifat, Ahmad, Eberle, Michael A, Braun, Alice


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