Treffer 1 - 20 von 114 für Suche 'GELLER ANDRE', Suchdauer: 1,73s Treffer weiter einschränken
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    Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies von Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J., Bast, Thomas, Baum, Larry, Becker, Albert J., Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Buono, Russell J., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cavalleri, Gianpiero L., Cherny, Stacey S., Chinthapalli, Krishna, Coffey, Alison J., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J., Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A., Freytag, Saskia, Gaus, Verena, Geller, Eric B., Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gui, Hongsheng, Guo, Youling, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L., Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Krause, Roland, Krenn, Martin, Kunz, Wolfram S., Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Malovini, Alberto, Marson, Anthony G., Mayer, Thomas, McCormack, Mark, Mills, James L., Mirza, Nasir, Moerzinger, Martina, Møller, Rikke S., Molloy, Anne M., Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M., Nürnberg, Peter, O’Brien, Terence J., Oliver, Karen L.

    Veröffentlicht in Nature communications

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    GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture von Stevelink, Remi, Campbell, Ciarán, Chen, Siwei, Abou-Khalil, Bassel, Adesoji, Oluyomi M., Afawi, Zaid, Amadori, Elisabetta, Anderson, Alison, Anderson, Joseph, Andrade, Danielle M., Annesi, Grazia, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bast, Thomas, Baum, Larry, Baumgartner, Tobias, Baykan, Betül, Bebek, Nerses, Becker, Albert J., Becker, Felicitas, Bennett, Caitlin A., Berghuis, Bianca, Berkovic, Samuel F., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blatt, Ilan, Bobbili, Dheeraj R., Borggraefe, Ingo, Bosselmann, Christian, Braatz, Vera, Bradfield, Jonathan P., Brockmann, Knut, Brody, Lawrence C., Buono, Russell J., Busch, Robyn M., Caglayan, Hande, Campbell, Ellen, Canafoglia, Laura, Canavati, Christina, Cascino, Gregory D., Castellotti, Barbara, Catarino, Claudia B., Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherny, Stacey S., Cheung, Ching-Lung, Chinthapalli, Krishna, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Clark, Peggy O., Cole, Andrew J., Compston, Alastair, Coppola, Antonietta, Cosico, Mahgenn, Cossette, Patrick, Craig, John J., Cusick, Caroline, Daly, Mark J., Davis, Lea K., de Haan, Gerrit-Jan, Delanty, Norman, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Di Vito, Lidia, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Elger, Christian E., Ellis, Colin A., Eriksson, Johan G., Faucon, Annika, Feng, Yen-Chen A., Ferguson, Lisa, Ferraro, Thomas N., Ferri, Lorenzo, Feucht, Martha, Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, Franke, Andre, French, Jacqueline A., Freri, Elena, Gagliardi, Monica, Gambardella, Antonio, Geller, Eric B., Giangregorio, Tania, Gjerstad, Leif

    Veröffentlicht in Nature genetics

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    Ultra-rare genetic variation in common epilepsies: a case-control sequencing study von Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

    Veröffentlicht in Lancet neurology

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    Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study von Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

    Veröffentlicht in Epilepsia (Copenhagen)

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    Common variants at 12q15 and 12q24 are associated with infant head circumference von Taal, H Rob, St Pourcain, Beate, Thiering, Elisabeth, Das, Shikta, Mook-Kanamori, Dennis O, Warrington, Nicole M, Kaakinen, Marika, Kreiner-Møller, Eskil, Bradfield, Jonathan P, Freathy, Rachel M, Geller, Frank, Guxens, Mònica, Cousminer, Diana L, Kerkhof, Marjan, Timpson, Nicholas J, Ikram, M Arfan, Beilin, Lawrence J, Bønnelykke, Klaus, Buxton, Jessica L, Charoen, Pimphen, Chawes, Bo Lund Krogsgaard, Eriksson, Johan, Evans, David M, Hofman, Albert, Kemp, John P, Kim, Cecilia E, Klopp, Norman, Lahti, Jari, Lye, Stephen J, McMahon, George, Mentch, Frank D, Müller-Nurasyid, Martina, O'Reilly, Paul F, Prokopenko, Inga, Rivadeneira, Fernando, Steegers, Eric A P, Sunyer, Jordi, Tiesler, Carla, Yaghootkar, Hanieh, Breteler, Monique M B, Debette, Stéphanie, Fornage, Myriam, Gudnason, Vilmundur, Launer, Lenore J, van der Lugt, Aad, Mosley, Thomas H, Seshadri, Sudha, Smith, Albert V, Vernooij, Meike W, Blakemore, Alexandra I F, Chiavacci, Rosetta M, Feenstra, Bjarke, Fernandez-Banet, Julio, Grant, Struan F A, Hartikainen, Anna-Liisa, van der Heijden, Albert J, Iñiguez, Carmen, Lathrop, Mark, McArdle, Wendy L, Mølgaard, Anne, Newnham, John P, Palmer, Lyle J, Palotie, Aarno, Pouta, Annneli, Ring, Susan M, Sovio, Ulla, Standl, Marie, Uitterlinden, Andre G, Wichmann, H-Erich, Vissing, Nadja Hawwa, DeCarli, Charles, van Duijn, Cornelia M, McCarthy, Mark I, Koppelman, Gerard H, Estivill, Xavier, Hattersley, Andrew T, Melbye, Mads, Bisgaard, Hans, Pennell, Craig E, Widen, Elisabeth, Hakonarson, Hakon, Smith, George Davey, Heinrich, Joachim, Jarvelin, Marjo-Riitta, Jaddoe, Vincent W V

    Veröffentlicht in Nature genetics

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    Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations von Smith, Alexander W., Carpay, Johannes A., Devinsky, Orrin, Braun, Kees P. J., Smit, Dirk J. A., Avbersek, Andreja, Becker, Albert J., Berkovic, Samuel F., Boysen, Katja E., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Chinthapalli, Krishna, Coffey, Alison J., Coppola, Antonietta, Cossette, Patrick, De Jonghe, Peter, Dlugos, Dennis J., Feucht, Martha, Freytag, Saskia, Geller, Eric B., Guo, Youling, Hakonarson, Hakon, Haut, Sheryl, Heinzen, Erin L., Hengsbach, Christian, Johnson, Michael R., Kälviäinen, Reetta, Kirsch, Heidi E., Lau, Yu‐Lung, Lehesjoki, Anna‐Elina, Lerche, Holger, Lieb, Wolfgang, Malovini, Alberto, McCormack, Mark, Molloy, Anne M., Rau, Sarah, Schachter, Steven C., Vari, Maria S., Weber, Yvonne G., Weisenberg, Judith, Wolff, Markus, Yang, Wanling, Zara, Federico, Howrigan, Daniel P., Cerrato, Felecia, Gabriel, Stacey B., Daly, Mark J., Neale, Benjamin M., Lowenstein, Daniel H., Cossette, Patrick, Cotsapas, Chris, Petrovski, Slavé, Sisodiya, Sanjay M., Freyer, Catharine, McKenna, Kevin, Bennett, Caitlin A., Burgess, Rosemary, O'Brien, Terence J., Stamberger, Hannah, Krestel, Heinz, Gallati, Sabina, Papacostas, Savvas S., Tanteles, George A., Klein, Karl Martin, Rademacher, Michael, Afawi, Zaid, Korczyn, Amos D., Kanaan, Moien, Lemke, Johannes R., Wolking, Stefan, Schulze‐Bonhage, Andreas, Schubert‐Bast, Susanne, Korinthenberg, Rudolf, Dennig, Dieter, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Rees, Mark I., Schneider, Natascha, Sills, Graeme J., Shukralla, Arif, McCormack, Mark, Canafoglia, Laura, Franceschetti, Silvana, Iacomino, Michele, Stella Vari, Maria, Salpietro, Vincenzo, Labate, Angelo, Manna, Lorella, Parrini, Elena, Inoue, Yushi, Topaloglu, Pınar, Yücesan, Emrah, Poduri, Annapurna, Buono, Russell J., Sperling, Michael R., Lo, Warren, Hegde, Manu, Helbig, Katherine L.

    Veröffentlicht in Epilepsia (Copenhagen)

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