Search Results - Weber, Michele L.

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    GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture by Campbell, Ciarán, Chen, Siwei, Andrade, Danielle M, Annesi, Grazia, Auce, Pauls, Bebek, Nerses, Berkovic, Samuel F, Beydoun, Ahmad, Blatt, Ilan, Borggraefe, Ingo, Bradfield, Jonathan P, Brody, Lawrence C, Canafoglia, Laura, Castellotti, Barbara, Cerrato, Felecia, Cherny, Stacey S, Cheung, Ching-Lung, Cole, Andrew J, Cossette, Patrick, Daly, Mark J, Dlugos, Dennis J, Doherty, Colin P, Ellis, Colin A, Feucht, Martha, Franceschetti, Silvana, French, Jacqueline A, Gambardella, Antonio, Granata, Tiziana, Guerrini, Renzo, Haas, Kevin F, Howrigan, Daniel P, Jamnadas-Khoda, Jennifer, Jehi, Lara, Kanai, Masahiro, Kantanen, Anne-Mari, Kara, Bülent, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kegele, Josua, King, Chontelle, Klein, Karl M, Korczyn, Amos D, Koupparis, Andreas, Krey, Ilona, Kurki, Mitja I, Lauxmann, Stephen, Leech, Stephanie L, Lehesjoki, Anna-Elina, Lesca, Gaetan, Leu, Costin, Lewin, Naomi, Lopes-Cendes, Iscia, Magnusson, Sigurdur, Marson, Anthony G, May, Patrick, McGraw, Christopher M, Mei, Davide, Montomoli, Martino, Mostacci, Barbara, Muccioli, Lorenzo, Müller-Schlüter, Karen, Neubauer, Bernd, Nothnagel, Michael, Pendziwiat, Manuela, Pondrelli, Federica, Powell, Rob H. W, Privitera, Michael, Ragona, Francesca, Regan, Brigid M, Sadleir, Lynette G, Sander, Josemir W, Scala, Marcello, Sham, Pak, Sheidley, Beth R, Shih, Jerry J, Smith, Michael C, Sonsma, Anja C. M, Sperling, Michael R, Stephani, Ulrich, Stewart, William C, Stipa, Carlotta, Striano, Pasquale, Tan, K. Meng, Thomas, G. Neil, Timonen, Oskari, Todaro, Marian, Topaloğlu, Pınar, Tumiene, Birute, Utkus, Algirdas, van Baalen, Andreas, Visscher, Frank, Weber, Yvonne G, Weisenberg, Judith, Widdess-Walsh, Peter, Wolff, Markus, Wolking, Stefan, Yapıcı, Zuhal, Zagaglia, Sara, Zara, Federico, Zhou, Wei

    Published in Nature genetics
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    Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals by Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.

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