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Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

by May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline, Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Baulac, Stéphanie, Marini, Carla, Thiele, Holger, Jabbari, Kamel, Ruppert, Ann-Kathrin, Lal, Dennis, Cestèle, Sandrine, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, Sisodiya, Sanjay M, Nabbout, Rima, Coppola, Antonietta, Vari, Maria S, Kasteleijn-Nolst Trenité, Dorothée, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, François, Carmant, Lionel, Desbiens, Richard, Cieuta-Walti, Cécile, Sills, Graeme J, Auce, Pauls, Johnson, Michael R, Marson, Anthony G, Berghuis, Bianca, Avbersek, Andreja, McCormack, Mark, Delanty, Norman, Depondt, Chantal, Zimprich, Fritz, Peter, Sarah, van Rooij, Jeroen, Ikram, M Arfan, Avanzini, Giuliano, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby P C, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nürnberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland, Lerche, Holger, May, Patrick, Girard, Simon, Bobbili, Dheeraj R, Schubert, Julian, Arfan Ikram, M, Maljevic, Snezana, Cossette, Patrick, Lerche, Holger, Ferlazzo, Edoardo, La Neve, Angela, Vignoli, Aglaia, Crichiutti, Giovanni, Gambardella, Antonio, Belcastro, Vincenzo, Bianchi, Amedeo, Yalçın, Destina, Dizdarer, Gulsen, Arslan, Kezban, Yapıcı, Zuhal, Kuşcu, Demet, Leu, Costin, Heggeli, Kristin, Willis, Joseph, Jorgensen, Andrea, Srivastava, Prashant, Rau, Sarah
Published in Lancet neurology (01.08.2018)

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Rare coding variants in genes encoding GABA A receptors in genetic generalised epilepsies: an exome-based case-control study

by May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline, Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Guerrero-López, Rosa, Baulac, Stéphanie, Marini, Carla, Thiele, Holger, Altmüller, Janine, Jabbari, Kamel, Ruppert, Ann-Kathrin, Jurkowski, Wiktor, Lal, Dennis, Rusconi, Raffaella, Cestèle, Sandrine, Terragni, Benedetta, Coombs, Ian D, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Everett, Kate, Møller, Rikke S, Hjalgrim, Helle, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, Jonghe, Peter De, Sisodiya, Sanjay M, Nabbout, Rima, Franceschetti, Silvana, Coppola, Antonietta, Vari, Maria S, Kasteleijn-Nolst Trenité, Dorothée, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, François, Carmant, Lionel, Lortie, Anne, Desbiens, Richard, Clément, Jean-François, Cieuta-Walti, Cécile, Sills, Graeme J, Auce, Pauls, Francis, Ben, Johnson, Michael R, Marson, Anthony G, 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, André G, Avanzini, Giuliano, Schorge, Stephanie, Petrou, Steven, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby P C, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nürnberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland, Lerche, Holger
Published in Lancet neurology (01.08.2018)

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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) (01.07.2021)

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