Number of items: 6.
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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.
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Mitchell, James W ORCID: 0000-0002-6465-0382, Noble, Adam ORCID: 0000-0002-8070-4352, Baker, Gus, Batchelor, Rachel, Brigo, Francesco, Christensen, Jakob, French, Jacqueline, Gil-Nagel, Antonio, Guekht, Alla, Jette, Nathalie et al (show 12 more authors) , Kälviäinen, Reetta, Leach, John Paul, Maguire, Melissa, O'Brien, Terence, Rosenow, Felix, Ryvlin, Philippe, Tittensor, Phil, Tripathi, Manjari, Trinka, Eugen, Wiebe, Samuel, Williamson, Paula R ORCID: 0000-0001-9802-6636 and Marson, Tony
(2022)
Protocol for the development of an international Core Outcome Set for treatment trials in adults with epilepsy: the EPilepsy outcome Set for Effectiveness Trials Project (EPSET).
Trials, 23 (1).
p. 943.
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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.
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Mirza, Nasir, Stevelink, Remi, Taweel, Basel ORCID: 0000-0002-6157-2438, Koeleman, Bobby PC, Marson, Anthony G, Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J et al (show 151 more authors) , Bast, Thomas, Baum, Larry, Becker, Albert J, Berghuis, Felicitas Becker 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 GF, 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, Trenite, Dorothee Kasteleijn-Nolst, Kirsch, Heidi E, Knowlton, Robert C, Koeleman, Bobby PC, Krause, Roland, Krenn, Martin, Kunz, Wolfram S, Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D, Lopes-Cendes, Iscia, Lowenstein, Daniel H, Malovini, Alberto, Marson, Anthony G ORCID: 0000-0002-6861-8806, Mayer, Thomas, McCormack, Mark, Mills, James L, Mirza, Nasir ORCID: 0000-0002-3538-0117, 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, Palotie, Aarno, Pangilinan, Faith, Peter, Sarah, Petrovski, Slavé, Poduri, Annapurna, Privitera, Michael, Radtke, Rodney, Rau, Sarah, Reif, Philipp S, Reinthaler, Eva M, Rosenow, Felix, Sander, Josemir W, Sander, Thomas, Scattergood, Theresa, Schachter, Steven C, Schankin, Christoph J, Scheffer, Ingrid E, Schmitz, Bettina, Schoch, Susanne, Sham, Pak C, Shih, Jerry J, Sills, Graeme J, Sisodiya, Sanjay M, Slattery, Lisa, Smith, Alexander, Smith, David F, Smith, Michael C, Smith, Philip E, Sonsma, Anja CM, Speed, Doug, Sperling, Michael R, Steinhoff, Bernhard J, Stephani, Ulrich, Stevelink, Remi, Strauch, Konstantin, Striano, Pasquale, Stroink, Hans, Surges, Rainer, Tan, K Meng, Thio, Liu Lin, Thomas, G Neil, Todaro, Marian, Tozzi, Rossana, Vari, Maria S, Vining, Eileen PG, Visscher, Frank, Spiczak, Sarah von, Walley, Nicole M, Weber, Yvonne G, Wei, Zhi, Weisenberg, Judith, Whelan, Christopher D, Widdess-Walsh, Peter, Wolff, Markus, Wolking, Stefan, Yang, Wanling, Zara, Federico and Zimprich, Fritz
(2021)
Using common genetic variants to find drugs for common epilepsies.
Brain Communications, 3 (4).
fcab287-.
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Hatton, Sean N, Huynh, Khoa H, Bonilha, Leonardo, Abela, Eugenio, Alhusaini, Saud, Altmann, Andre, Alvim, Marina KM, Balachandra, Akshara R, Bartolini, Emanuele, Bender, Benjamin et al (show 66 more authors) , Bernasconi, Neda, Bernasconi, Andrea, Bernhardt, Boris, Bargallo, Nuria, Caldairou, Benoit, Caligiuri, Maria E, Carr, Sarah JA, Cavalleri, Gianpiero L, Cendes, Fernando, Concha, Luis, Davoodi-bojd, Esmaeil, Desmond, Patricia M, Devinsky, Orrin, Doherty, Colin P, Domin, Martin, Duncan, John S, Focke, Niels K, Foley, Sonya F, Gambardella, Antonio, Gleichgerrcht, Ezequiel, Guerrini, Renzo, Hamandi, Khalid, Ishikawa, Akaria, Keller, Simon S ORCID: 0000-0001-5247-9795, Kochunov, Peter V, Kotikalapudi, Raviteja, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, Kwan, Patrick, Labate, Angelo, Langner, Soenke, Lenge, Matteo, Liu, Min, Lui, Elaine, Martin, Pascal, Mascalchi, Mario, Moreira, Jose CV, Morita-Sherman, Marcia E, O'Brien, Terence J, Pardoe, Heath R, Pariente, Jose C, Ribeiro, Leticia F, Richardson, Mark P, Rocha, Cristiane S, Rodriguez-Cruces, Raul, Rosenow, Felix, Severino, Mariasavina, Sinclair, Benjamin, Soltanian-Zadeh, Hamid, Striano, Pasquale, Taylor, Peter N, Thomas, Rhys H, Tortora, Domenico, Velakoulis, Dennis, Vezzani, Annamaria, Vivash, Lucy, von Podewils, Felix, Vos, Sjoerd B, Weber, Bernd, Winston, Gavin P, Yasuda, Clarissa L, Zhu, Alyssa H, Thompson, Paul M, Whelan, Christopher D, Jahanshad, Neda, Sisodiya, Sanjay M and McDonald, Carrie R
(2020)
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study.
Brain, 143 (8).
pp. 2454-2473.
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Hatton, Sean N ORCID: 0000-0002-9149-8726, Huynh, Khoa H, Bonilha, Leonardo, Abela, Eugenio ORCID: 0000-0002-9356-1450, Alhusaini, Saud, Altmann, Andre ORCID: 0000-0002-9265-2393, Alvim, Marina KM, Balachandra, Akshara R, Bartolini, Emanuele, Bender, Benjamin et al (show 66 more authors) , Bernasconi, Neda, Bernasconi, Andrea, Bernhardt, Boris, Bargallo, Núria, Caldairou, Benoit, Caligiuri, Maria E, Carr, Sarah JA, Cavalleri, Gianpiero L, Cendes, Fernando ORCID: 0000-0001-9336-9568, Concha, Luis, Davoodi-Bojd, Esmaeil, Desmond, Patricia M, Devinsky, Orrin ORCID: 0000-0003-0044-4632, Doherty, Colin P, Domin, Martin, Duncan, John S, Focke, Niels K, Foley, Sonya F, Gambardella, Antonio, Gleichgerrcht, Ezequiel, Guerrini, Renzo ORCID: 0000-0002-7272-7079, Hamandi, Khalid, Ishikawa, Akari, Keller, Simon S, Kochunov, Peter V, Kotikalapudi, Raviteja, Kreilkamp, Barbara AK, Kwan, Patrick, Labate, Angelo, Langner, Soenke, Lenge, Matteo, Liu, Min, Lui, Elaine, Martin, Pascal, Mascalchi, Mario, Moreira, José CV, Morita-Sherman, Marcia E, O'Brien, Terence J, Pardoe, Heath R ORCID: 0000-0002-0123-2167, Pariente, José C, Ribeiro, Letícia F, Richardson, Mark P ORCID: 0000-0001-8925-3140, Rocha, Cristiane S, Rodríguez-Cruces, Raúl, Rosenow, Felix, Severino, Mariasavina, Sinclair, Benjamin, Soltanian-Zadeh, Hamid, Striano, Pasquale, Taylor, Peter N, Thomas, Rhys H ORCID: 0000-0003-2062-8623, Tortora, Domenico ORCID: 0000-0002-5621-4046, Velakoulis, Dennis, Vezzani, Annamaria, Vivash, Lucy ORCID: 0000-0002-1182-0907, von Podewils, Felix, Vos, Sjoerd B, Weber, Bernd, Winston, Gavin P, Yasuda, Clarissa L, Zhu, Alyssa H, Thompson, Paul M, Whelan, Christopher D, Jahanshad, Neda, Sisodiya, Sanjay M and McDonald, Carrie R
(2020)
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study.
Brain : a journal of neurology, 143 (8).
2454 - 2473.
This list was generated on Sun Sep 10 23:16:34 2023 BST.