Treffer 1 - 18 von 18 für Suche 'BRAUN, Johnathan J', Suchdauer: 0,92s Treffer weiter einschränken
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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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  15. 15

    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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  17. 17

    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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    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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