Search Results - Schlüter, Hannah M

Refine Results
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9

    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.

    Get full text
    Article
  10. 10
  11. 11
  12. 12
  13. 13
  14. 14
  15. 15
  16. 16

    Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals by Povysil, Gundula, Allen, Andrew S., Howrigan, Daniel P., Tashman, Katherine, Cerrato, Felecia, Cusick, Caroline, Heyne, Henrike, Churchhouse, Claire, Watts, Nick, Lal, Dennis, Gupta, Namrata, Cavalleri, Gianpiero L., Hakonarson, Hakon, Marson, Anthony G., Petrovski, Slavé, Sisodiya, Sanjay M., Depondt, Chantal, Scheffer, Ingrid E., Krause, Roland, Regan, Brigid M., Leu, Costin, Leech, Stephanie L., Todaro, Marian, Stamberger, Hannah, Kousiappa, Ioanna, Tanteles, George A., Christou, Yiolanda, Laššuthová, Petra, Knake, Susanne, Kunz, Wolfram S., Zsurka, Gábor, Surges, Rainer, Rademacher, Annika, von Spiczak, Sarah, Kanaan, Moien, Canavati, Christina, Lemke, Johannes R., Krey, Ilona, Weber, Yvonne G., Wolking, Stefan, Kegele, Josua, Borggräfe, Ingo, Mayer, Thomas, Brockmann, Knut, Madeleyn, Rene, Saarela, Anni, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Derambure, Philippe, Hirsch, Edouard, Chassoux, Francine, Chung, Seo-Kyung, Schneider, Natascha, Balestrini, Simona, Zagaglia, Sara, Johnson, Michael R., Auce, Pauls, Barišić, Nina, Canafoglia, Laura, Franceschetti, Silvana, Castellotti, Barbara, Granata, Tiziana, Ragona, Francesca, Iacomino, Michele, Riva, Antonella, Vari, Maria Stella, Salpietro, Vincenzo, Mancardi, Maria Margherita, Nobili, Lino, Bisulli, Francesca, Pippucci, Tommaso, Licchetta, Laura, Tinuper, Paolo, Gambardella, Antonio, Labate, Angelo, Annesi, Grazia, Manna, Lorella, Parrini, Elena, Bianchini, Claudia, Montomoli, Martino, Hirose, Shinichi, Yamakawa, Kazuhiro, Beydoun, Ahmad, Sadleir, Lynette G., Topaloglu, Pınar, Baykan, Betül, Özkara, YeşÇiğdem, Ho, Chen-Jui, Chou, I-Jun, Shain, Catherine, Goldman, Alicia, Busch, Robyn M., Jehi, Lara, Ferguson, Lisa, Clark, Peggy O., Privitera, Michael, Schachter, Steven, Cosico, Mahgenn, Lowenstein, Daniel H., Goldstein, David B.

    Get full text
    Article
  17. 17
  18. 18

    Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes by Chen, Siwei, Abou-Khalil, Bassel W., Afawi, Zaid, Ali, Quratulain Zulfiqar, Amadori, Elisabetta, Anderson, Alison, Anderson, Joe, Andrade, Danielle M., Annesi, Grazia, Arslan, Mutluay, Auce, Pauls, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Banks, Eric, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bass, Nick, Baum, Larry W., Baumgartner, Tobias H., Baykan, Betül, Bebek, Nerses, Becker, Felicitas, Bennett, Caitlin A., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blackwood, Douglas, Blatt, Ilan, Borggräfe, Ingo, Bosselmann, Christian, Braatz, Vera, Brand, Harrison, Brockmann, Knut, Buono, Russell J., Busch, Robyn M., Caglayan, S. Hande, Canafoglia, Laura, Canavati, Christina, Castellotti, Barbara, Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherian, Christina, Cherny, Stacey S., Cheung, Ching-Lung, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Ciullo, Valentina, Clark, Peggy O., Cole, Andrew J., Cosico, Mahgenn, Cossette, Patrick, Cotsapas, Chris, Cusick, Caroline, Daly, Mark J., Davis, Lea K., Jonghe, Peter De, Delanty, Norman, Dennig, Dieter, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Vito, Lidia Di, Dickerson, Faith, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Ellis, Colin A., Epstein, Leon, Evans, Meghan, Faucon, Annika, Feng, Yen-Chen Anne, Ferguson, Lisa, Ferraro, Thomas N., Silva, Izabela Ferreira Da, Ferri, Lorenzo, Feucht, Martha, Fields, Madeline C., Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, French, Jacqueline A., Freri, Elena, Fu, Jack M., Gabriel, Stacey, Gagliardi, Monica, Gambardella, Antonio, Gauthier, Laura, Giangregorio, Tania, Gili, Tommaso, Glauser, Tracy A., Goldberg, Ethan, Goldman, Alica, Goldstein, David B.

    Published in Nature neuroscience
    Get full text
    Article
  19. 19
  20. 20

    Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations by 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.

    Published in Epilepsia (Copenhagen)
    Get full text
    Article