Treffer 1 - 20 von 42 für Suche 'Byrne, Lukas', Suchdauer: 1,70s 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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    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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    Transforming Obesity Prevention for CHILDren (TOPCHILD) Collaboration: protocol for a systematic review with individual participant data meta-analysis of behavioural interventions... von Hunter, Kylie E, Johnson, Brittany J, Askie, Lisa, Golley, Rebecca K, Baur, Louise A, Taylor, Rachael W, Wolfenden, Luke, Wood, Charles T, Mihrshahi, Seema, Hayes, Alison J, Rissel, Chris, Robledo, Kristy P, O'Connor, Denise A, Espinoza, David, Staub, Lukas P, Barba, Angie, Libesman, Sol, Smith, Wendy A, Sue-See, Michelle, Hesketh, Kylie D, Bryant, Maria, Paul, Ian M, Wen, Li Ming, Larsen, Junilla K, O'Reilly, Sharleen L, Wasser, Heather M, Savage, Jennifer S, Ong, Ken K, Salvy, Sarah-Jeanne, Gross, Rachel S, Rasmussen, Finn E, Linares, Ana Maria, Øverby, Nina Cecilie, González Acero, Carolina, Lakshman, Rajalakshmi, Thompson, Amanda L, Maffeis, Claudio, Oken, Emily, Pérez-Expósito, Ana B, Banna, Jinan C, Røed, Margrethe, Anzman-Frasca, Stephanie, Taylor, Barry J, Seidler, Anna Lene, Johnson, Brittany, Barba, Angie, Aberoumand, Mason, Libesman, Sol, Williams, Jonathan, Baur, Louise, Chadwick, Paul, Espinoza, David, Marschner, Ian, O’Connor, Denise, Rissel, Chris, Robledo, Kristy, Sanders, Lee, Staub, Lukas, Taki, Sarah, Taylor, Rachael, Wolfenden, Luke, Wood, Charles, Anzman-Frasca, Stephanie, Bryant, Maria, Byrne, Rebecca, Campbell, Karen, Rivera, Maribel Campos, Corpeleijn, Eva, Daniels, Lynne, Haye, Kayla dela, Fiks, Alexander, Ghaderi, Ata, Acero, Carolina González, Goran, Michael, Hesketh, Kylie, Jacobvitz, Deborah, Joshipura, Kaumudi, Karssen, Levie, Lakshman, Rajalakshmi, Larsen, Junilla K, Linares, Ana Maria, Maffeis, Claudio, Messito, Mary Jo, Oken, Emily, Øverby, Nina, Palacios, Cristina, Paul, Ian M, Raat, Hein, Rasmussen, Finn, Røed, Margrethe, Salvy, Sarah-Jeanne, Stough, Cathleen Odar, Taylor, Barry, Thompson, Amanda, Thomson, Jessica, Verbestel, Vera, Vitolo, Márcia Regina, Wasser, Heather, Wen, Li Ming, Widen, Elizabeth

    Veröffentlicht in BMJ open

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