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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 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

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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 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, Basak, Nazli, van der Kooi, Anneke J, Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Lauria, Giuseppe, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, D'Alfonso, Sandra, Soraru, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chio, 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, Stephanie, Meininger, Vincent, Salachas, Francois, Mora Pardina, Jesus S, Assialioui, Abdelilah, Rojas-Garcia, 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

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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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    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 van der, Bakker, Mark, Berg, Leonard van den, Veldink, Jan, Vugt, Joke van, Hop, Paul, Zwamborn, Ramona, Klein, Niek de, Westra, Harm-Jan, Bakker, Olivier, Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot, Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs, Eijk, Kristel van, Kooyman, Maarten, Byrne, Ross, Doherty, Mark, Heverin, Mark, Khleifat, Ahmad Al, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen, Shaw, Pamela, Hardy, John, Orrell, Richard, Sendtner, Michael, Meyer, Thomas, Basak, Nazli, Kooi, Anneke van der, Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Pinter, Guiseppe Lauria, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, D'Alfonso, Sandra, Soraru, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chio, 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, Bell, Shaugn, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stephanie, Meininger, Vincent, Salachas, Francois, Pardina, Jesus Mora, Assialioui, Abdelilah, Rojas-García, Ricardo, Dion, Patrick, Ross, Jay, Ludolph, Albert, Weishaupt, Jochen, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Payan, Christine, Saker-Delye, Safa, Wood, Nicholas, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan

    Veröffentlicht in Research Square

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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 Hop, Paul J, Bakker, Olivier B, Baird, Denis, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Kooyman, Maarten, Byrne, Ross P, Heverin, Mark, Al Khleifat, Ahmad, Ticozzi, Nicola, Cooper-Knock, Johnathan, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Orrell, Richard W, van der Kooi, Anneke J, Fogh, Isabella, Gellera, Cinzia, Corti, Stefania, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Grassano, Maurizio, Pupillo, Elisabetta, Logroscino, Giancarlo, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Meininger, Vincent, Salachas, François, Assialioui, Abdelilah, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Kraft, Julia, Hofman, Albert, Cichon, Sven, Nöthen, Markus M, Traynor, Bryan J, Singleton, Andrew B, Wiedau-Pazos, Martina, Van Deerlin, Vivianna, Roediger, Annekathrin, Stubendorff, Beatrice, Graff, Caroline, Brylev, Lev, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Drory, Vivian, Povedano, Monica, Furlong, Sarah, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Rowe, Dominic B, Williams, Kelly, Henders, Anjali K, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Glass, Jonathan D, Brown, Robert H, Landers, John E, Andersen, Peter Munch, Groen, Ewout J. N, Fan, Dongsheng, McRae, Allan F, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Franke, Lude, van den Berg, Leonard H, Veldink, Jan, Universitat Autònoma de Barcelona

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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 Hop, Paul J, Bakker, Olivier B, Baird, Denis, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Kooyman, Maarten, Byrne, Ross P, Heverin, Mark, Al Khleifat, Ahmad, Ticozzi, Nicola, Cooper-Knock, Johnathan, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Orrell, Richard W, van der Kooi, Anneke J, Fogh, Isabella, Gellera, Cinzia, Corti, Stefania, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Grassano, Maurizio, Pupillo, Elisabetta, Logroscino, Giancarlo, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Meininger, Vincent, Salachas, François, Assialioui, Abdelilah, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Kraft, Julia, Hofman, Albert, Cichon, Sven, Nöthen, Markus M, Traynor, Bryan J, Singleton, Andrew B, Wiedau-Pazos, Martina, Roediger, Annekathrin, Gaur, Nayana, Stubendorff, Beatrice, Graff, Caroline, Brylev, Lev, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Drory, Vivian, Povedano, Monica, Furlong, Sarah, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Rowe, Dominic B, Henders, Anjali K, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Glass, Jonathan D, Brown, Robert H, Landers, John E, Andersen, Peter Munch, Groen, Ewout J. N, Fan, Dongsheng, McRae, Allan F, Gaunt, Tom, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Franke, Lude, van den Berg, Leonard H, Veldink, Jan H, Universitat Autònoma de Barcelona

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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 biol... von Hop, Paul J, Bakker, Olivier B, Baird, Denis, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Kooyman, Maarten, Byrne, Ross P, Heverin, Mark, Al Khleifat, Ahmad, Ticozzi, Nicola, Cooper-Knock, Johnathan, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Orrell, Richard W, van der Kooi, Anneke J, Fogh, Isabella, Gellera, Cinzia, Corti, Stefania, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Grassano, Maurizio, Pupillo, Elisabetta, Logroscino, Giancarlo, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Meininger, Vincent, Salachas, François, Assialioui, Abdelilah, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Kraft, Julia, Hofman, Albert, Cichon, Sven, Nöthen, Markus M, Traynor, Bryan J, Singleton, Andrew B, Wiedau-Pazos, Martina, Van Deerlin, Vivianna, Roediger, Annekathrin, Stubendorff, Beatrice, Graff, Caroline, Brylev, Lev, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Drory, Vivian, Povedano, Monica, Furlong, Sarah, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Rowe, Dominic B, Williams, Kelly, Henders, Anjali K, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Glass, Jonathan D, Brown, Robert H, Landers, John E, Andersen, Peter Munch, Groen, Ewout J. N, Fan, Dongsheng, McRae, Allan F, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Franke, Lude, van den Berg, Leonard H, Veldink, Jan, Universitat Autònoma de Barcelona

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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 biol... von Hop, Paul J, Bakker, Olivier B, Baird, Denis, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Kooyman, Maarten, Byrne, Ross P, Heverin, Mark, Al Khleifat, Ahmad, Ticozzi, Nicola, Cooper-Knock, Johnathan, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Orrell, Richard W, van der Kooi, Anneke J, Fogh, Isabella, Gellera, Cinzia, Corti, Stefania, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Grassano, Maurizio, Pupillo, Elisabetta, Logroscino, Giancarlo, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Meininger, Vincent, Salachas, François, Assialioui, Abdelilah, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Kraft, Julia, Hofman, Albert, Cichon, Sven, Nöthen, Markus M, Traynor, Bryan J, Singleton, Andrew B, Wiedau-Pazos, Martina, Roediger, Annekathrin, Gaur, Nayana, Stubendorff, Beatrice, Graff, Caroline, Brylev, Lev, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Drory, Vivian, Povedano, Monica, Furlong, Sarah, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Rowe, Dominic B, Henders, Anjali K, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Glass, Jonathan D, Brown, Robert H, Landers, John E, Andersen, Peter Munch, Groen, Ewout J. N, Fan, Dongsheng, McRae, Allan F, Gaunt, Tom, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Franke, Lude, van den Berg, Leonard H, Veldink, Jan H, Universitat Autònoma de Barcelona

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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, van der Spek, Rick A.A, Bakker, Mark, Vugt, Joke J.F.A. van, Hop, Paul, Zwamborn, Ramona A.J, Klein, Niek de, Westra, Harm-Jan, Bakker, Olivier, Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot, Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs H.P, van Eijk, Kristel, Kooyman, Maarten, Byrne, Ross, Doherty, Mark, Heverin, Mark, Khleifat, Ahmad Al, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen, Shaw, Pamela, Hardy, John, Orrell, Richard, Sendtner, Michael, Meyer, Thomas, Başak, Nazli, van der Kooi, Anneke, Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Lauria Pinter, 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, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stéphanie, Meininger, Vincent, Salachas, François, Pardina, Jesus Mora, Assialioui, Abdelilah, Rojas-García, Ricardo, Dion, Patrick, Ross, Jay, Ludolph, Albert, Weishaupt, Jochen, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Dürr, Alexandra, Payan, Christine A.M, Saker-Delye, Safa, Wood, Nicholas, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan, Braun, Alice, Kraft, Julia

    Veröffentlicht in medRxiv
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