Browse by People

Collapse authors list.
Allen, Andrew S, Berkovic, Samuel F, Bridgers, Joshua, Cossette, Patrick, Dlugos, Dennis, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Heinzen, Erin L, Jiang, Yu et al (show 104 more authors) , Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G ORCID: 0000-0002-6861-8806, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slave, Poduri, Annapurna, Ren, Zhong, Scheffer, Ingrid E, Sherr, Elliott, Wang, Quanli, Balling, Rudi, Barisic, Nina, Baulac, Stephanie, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Depienne, Christel, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Jaehn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Leguern, Eric, Lehesjoki, Anna-Elina, Lemke, Johannes R, Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Moller, Rikke S, Muhle, Hiltrud, Pal, Deb, Palotie, Aarno, Rosenow, Felix, Selmer, Kaja, Serratosa, Jose M, Sisodiya, Sanjay, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weber, Yvonne, Weckhuysen, Sarah, Zara, Federico, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F, Berkovic, Samuel F, Bluvstein, Judith, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P, Fiol, Miguel E, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Glauser, Tracy, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Kossoff, Eric H, Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H, McGuire, Shannon M, Motika, Paul V, Novotny, Edward J, Ottman, Ruth, Paolicchi, Juliann M, Parent, Jack, Park, Kristen, Poduri, Annapurna, Scheffer, Ingrid E, Shellhaas, Renee A, Sherr, Elliott, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen PG, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter and Winawer, Melodie R (2017) Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (7). pp. 894-899.

Collapse authors list.
Montanucci, Ludovica, Lewis-Smith, David, Collins, Ryan L, Niestroj, Lisa-Marie, Parthasarathy, Shridhar, Xian, Julie, Ganesan, Shiva, Macnee, Marie, Bruenger, Tobias, Thomas, Rhys H et al (show 313 more authors) , Talkowski, Michael, Helbig, Ingo, Leu, Costin, Lal, Dennis, Motelow, Joshua E, Povysil, Gundula, Dhindsa, Ryan S, Stanley, Kate E, Allen, Andrew S, Goldstein, David B, Feng, Yen-Chen Anne, Howrigan, Daniel P, Abbott, Liam E, Tashman, Katherine, Cerrato, Felecia, Cusick, Caroline, Singh, Tarjinder, Heyne, Henrike, Byrnes, Andrea E, Churchhouse, Claire, Watts, Nick, Solomonson, Matthew, Lal, Dennis, Gupta, Namrata, Neale, Benjamin M, Berkovic, Samuel F, Lerche, Holger, Goldstein, David B, Lowenstein, Daniel H, Berkovic, Samuel F, Lerche, Holger, Goldstein, David B, Lowenstein, Daniel H, Cavalleri, Gianpiero L, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Dixon-Salazar, Tracy, Guerrini, Renzo, Hakonarson, Hakon, Heinzen, Erin L, Dhindsa, Ryan S, Stanley, Kate E, Helbig, Ingo, Kwan, Patrick, Marson, Anthony G, Petrovski, Slave, Kamalakaran, Sitharthan, Sisodiya, Sanjay M, Stewart, Randy, Weckhuysen, Sarah, Depondt, Chantal, Dlugos, Dennis J, Scheffer, Ingrid E, Striano, Pasquale, Freyer, Catharine, Krause, Roland, May, Patrick, McKenna, Kevin, Regan, Brigid M, Bennett, Caitlin A, Leech, Stephanie L, Leu, Costin, Lewis-Smith, David, Berkovic, Samuel F, Scheffer, Ingrid E, Regan, Brigid M, Bennett, Caitlin A, Leech, Stephanie L, O'Brien, Terence J, Petrovski, Slave, Todaro, Marian, Kwan, Patrick, Weckhuysen, Sarah, De Jonghe, Peter, Stamberger, Hannah, Depondti, Chantal, Andrade, Danielle M, Ali, Quratulain Zulfiqar, Sadoway, Tara R, Krestel, Heinz, Schaller, Andre, Papacostas, Savvas S, Kousiappa, Ioanna, Tanteles, George A, Yiolanda, Christou, Sterbova, Katalin, Vlckova, Marketa, Sedlackova, Lucie, Lassuthova, Petra, Klein, Karl Martin, Rosenow, Felix, Reif, Philipp S, Knake, Susanne, Neubauer, Bernd A, Zimprich, Friedrich, Feucht, Martha, Reinthaler, Eva, Kunz, Wolfram S, Zsurka, Gabor, Surges, Rainer, Baumgartner, Tobias H, von Wrede, Randi, Helbig, Ingo, Klein, Karl Martin, Pendziwiat, Manuela, Muhle, Hiltrud, Rademacher, Annika, van Baalen, Andreas, von Spiczak, Sarah, Stephani, Ulrich, Afawi, Zaid, Korczyn, Amos D, Kanaan, Moien, Canavati, Christina, Kurlemann, Gerhard, Mueller-Schlueter, Karen, Kluger, Gerhard, Haeusler, Martin, Blatt, Ilan, Lemke, Johannes R, Krey, Ilona, Lerche, Holger, Weber, Yvonne G, Wolking, Stefan, Becker, Felicitas, Lauxmann, Stephan, Bosselmann, Christian, Kegele, Josua, Hengsbach, Christian, Rau, Sarah, Steinhoff, Bernhard J, Schulze-Bonhage, Andreas, Borggrafe, Ingo, Schankin, Christoph J, Schubert-Bast, Susanne, Schreiber, Herbert, Mayer, Thomas, Korinthenberg, Rudolf, Brockmann, Knut, Wolff, Markus, Kurlemann, Gerhard, Dennig, Dieter, Madeleyn, Rene, Kegele, Josua, Kalviainen, Reetta, Saarela, Anni, Timonen, Oskari, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Rheims, Sylvain, Lesca, Gaetan, Ryvlin, Philippe, Maillard, Louis, Valton, Luc, Derambure, Philippe, Bartolomei, Fabrice, Hirsch, Edouard, Michel, Veronique, Chassoux, Francine, Rees, Mark I, Chung, Seo-Kyung, Pickrell, William O, Powell, Robert HW, Baker, Mark D, Fonferko-Shadrach, Beata, Lawthom, Charlotte, Anderson, Joe, Sisodiya, Sanjay M, Schneider, Natascha, Balestrini, Simona, Zagaglia, Sara, Braatz, Vera, Marson, Anthony G ORCID: 0000-0002-6861-8806, Johnson, Michael R, Auce, Pauls, Sills, Graeme J, Kwan, Patrick, Baum, Larry W, Sham, Pakc, Cherny, Stacey S, Lui, Colin HT, Cavalleri, Gianpiero L, Delanty, Norman, Doherty, Colin P, Shukralla, Arif, El-Naggar, Hany, Widdess-Walsh, Peter, Barisic, Nina, Canafoglia, Laura, Franceschetti, Silvana, Castellotti, Barbara, Granata, Tiziana, Ragona, Francesca, Striano, Pasquale, Zara, Federico, Iacomino, Michele, Riva, Antonella, Madia, Francesca, Vari, Maria Stella, Salpietro, Vincenzo, Scala, Marcello, Mancardi, Maria Margherita, Lino, Nobili, Amadori, Elisa, Giacomini, Thea, Bisulli, Francesca, Pippucci, Tommaso, Licchetta, Laura, Minardi, Raffaella, Tinuper, Paolo, Muccioli, Lorenzo, Mostacci, Barbara, Gambardella, Antonio, Labate, Angelo, Annesi, Grazia, Manna, Lorella, Gagliardi, Monica, Guerrini, Renzo, Parrini, Elena, Mei, Davide, Vetro, Annalisa, Bianchini, Claudia, Montomoli, Martino, Doccini, Viola, Barba, Carmen, Hirose, Shinichi, Ishii, Atsushi, Suzuki, Toshimitsu, Inoue, Yushi, Yamakawa, Kazuhiro, Beydoun, Ahmad, Nasreddine, Wassim, Khoueiry-Zgheib, Nathalie, Tumiene, Birute, Utkus, Algirdas, Sadleir, Lynette G, King, Chontelle, Caglayan, S Hande, Arslan, Mutluay, Yapici, Zuhal, Topaloglu, Pinar, Kara, Bulent, Yis, Uluc, Turkdogan, Dilsad, Gundogdu-Eken, Asli, Bebek, Nerses, Ugur-Iseri, Sibel, Baykan, Betul, Salman, Baris, Haryanyan, Garen, Yucesan, Emrah, Kesim, Yesim, Ozkara, Cigdem, Tsai, Meng-Han, Ho, Chen-Jui, Lin, Chih-Hsiang, Lin, Kuang-Lin, Chou, I-Jun, Poduri, Annapurna, Shiedley, Beth R, Shain, Catherine, Noebels, Jeffrey L, Goldman, Alicia, Busch, Robyn M, Jehi, Lara, Najm, Imad M, Lal, Dennis, Ferguson, Lisa, Khoury, Jean, Glauser, Tracy A, Clark, Peggy O, Buono, Russell J, Ferraro, Thomas N, Sperling, Michael R, Dlugos, Dennis J, Lo, Warren, Privitera, Michael, French, Jacqueline A, Cossette, Patrick, Schachter, Steven, Hakonarson, Hakon, Lowenstein, Daniel H, Kuzniecky, Ruben I, Dlugos, Dennis J, Devinsky, Orrin, Lowenstein, Daniel H, Kuzniecky, Ruben I, French, Jacqueline A, Hegde, Manu, Greenberg, David A, Helbig, Ingo, Ellis, Colin A, Goldberg, Ethan, Helbig, Katherine L, Lewis-Smith, David, Cosico, Mahgenn, Vaidiswaran, Priya, Fitch, Eryn, Newton, Charles RJC, Kariuki, SymonM, Wagner, Ryan G, Owusu-Agyei, Seth, Cole, Andrew J, McGraw, ChristopherM, Siena, S Anthony, Davis, Lea, Hucks, Donald, Faucon, Annika, Wu, David, Abou-Khalil, Bassel W, Haas, Kevin and Taneja, Randip S (2023) Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals. NATURE COMMUNICATIONS, 14 (1). 4392-.

Collapse authors list.
May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline et al (show 88 more authors) , Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Guerrero-Lopez, Rosa, Baulac, Stephanie, Marini, Carla, Thiele, Holger, Altmueller, Janine, Jabbari, Kamel, Ruppert, Ann-Kathrin, Jurkowski, Wiktor, Lal, Dennis, Rusconi, Raffaella, Cestele, Sandrine, Terragni, Benedetta, Coombs, Ian D, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Everett, Kate, Moller, Rikke S, Hjalgrim, Helle, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, De Jonghe, Peter, Sisodiya, Sanjay M, Nabbout, Rima, Franceschetti, Silvana, Coppola, Antonietta, Vari, Maria S, Trenite, Dorothee Kasteleijn-Nolst, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, Francois, Carmant, Lionel, Lortie, Anne, Desbiens, Richard, Clement, Jean-Francois, Cieuta-Walti, Cecile, Sills, Graeme J ORCID: 0000-0002-3389-8713, Auce, Pauls, Francis, Ben ORCID: 0000-0002-2130-5976, Johnson, Michael R, Marson, Anthony G ORCID: 0000-0002-6861-8806, Berghuis, Bianca, Sander, Josemir W, Avbersek, Andreja, McCormack, Mark, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Krenn, Martin, Zimprich, Fritz, Peter, Sarah, Nikanorova, Marina, Kraaij, Robert, van Rooij, Jeroen, Balling, Rudi, Ikram, M Arfan, Uitterlinden, Andre G, Avanzini, Giuliano, Schorge, Stephanie, Petrou, Steven, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby PC, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nuernberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland and Lerche, Holger (2018) Rare coding variants in genes encoding GABA_A receptors in genetic generalised epilepsies: an exome-based case-control study. LANCET NEUROLOGY, 17 (8). pp. 699-708.

Collapse authors list.
Wolking, Stefan, Moreau, Claudia, Nies, Anne T, Schaeffeler, Elke, McCormack, Mark, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Krenn, Martin, Moller, Rikke S et al (show 21 more authors) , Nikanorova, Marina, Weber, Yvonne G, Weckhuysen, Sarah, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Johnson, Michael R, Koeleman, Bobby PC, Kunz, Wolfram S, Marson, Anthony G ORCID: 0000-0002-6861-8806, Sander, Josemir W, Sills, Graeme J, Striano, Pasquale, Zara, Federico, Zimprich, Fritz, Schwab, Matthias, Krause, Roland, Sisodiya, Sanjay M, Cossette, Patrick, Girard, Simon L and Lerche, Holger (2020) Testing association of rare genetic variants with resistance to three common antiseizure medications. EPILEPSIA, 61 (4). pp. 657-666.