Number of items: 3.
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Larivière, Sara, Rodríguez-Cruces, Raúl, Royer, Jessica, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis, Keller, Simon S ORCID: 0000-0001-5247-9795, Cendes, Fernando, Yasuda, Clarissa, Bonilha, Leonardo et al (show 52 more authors) , Gleichgerrcht, Ezequiel, Focke, Niels K, Domin, Martin, von Podewills, Felix, Langner, Soenke, Rummel, Christian, Wiest, Roland, Martin, Pascal, Kotikalapudi, Raviteja, O’Brien, Terence J, Sinclair, Benjamin, Vivash, Lucy, Desmond, Patricia M, Alhusaini, Saud, Doherty, Colin P, Cavalleri, Gianpiero L, Delanty, Norman, Kälviäinen, Reetta, Jackson, Graeme D, Kowalczyk, Magdalena, Mascalchi, Mario, Semmelroch, Mira, Thomas, Rhys H, Soltanian-Zadeh, Hamid, Davoodi-Bojd, Esmaeil, Zhang, Junsong, Lenge, Matteo, Guerrini, Renzo, Bartolini, Emanuele, Hamandi, Khalid, Foley, Sonya, Weber, Bernd, Depondt, Chantal, Absil, Julie, Carr, Sarah JA, Abela, Eugenio, Richardson, Mark P, Devinsky, Orrin, Severino, Mariasavina, Striano, Pasquale, Tortora, Domenico, Hatton, Sean N, Vos, Sjoerd B, Duncan, John S, Whelan, Christopher D, Thompson, Paul M, Sisodiya, Sanjay M, Bernasconi, Andrea, Labate, Angelo, McDonald, Carrie R, Bernasconi, Neda and Bernhardt, Boris C
(2020)
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study.
Science Advances, 6 (47).
eabc6457-eabc6457.
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Larivière, Sara, Royer, Jessica, Rodríguez-Cruces, Raúl, Paquola, Casey, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis, Keller, Simon S ORCID: 0000-0001-5247-9795, Cendes, Fernando, Yasuda, Clarissa L et al (show 64 more authors) , Bonilha, Leonardo, Gleichgerrcht, Ezequiel, Focke, Niels K, Domin, Martin, von Podewills, Felix, Langner, Soenke, Rummel, Christian, Wiest, Roland, Martin, Pascal, Kotikalapudi, Raviteja, O’Brien, Terence J, Sinclair, Benjamin, Vivash, Lucy, Desmond, Patricia M, Lui, Elaine, Vaudano, Anna Elisabetta, Meletti, Stefano, Tondelli, Manuela, Alhusaini, Saud, Doherty, Colin P, Cavalleri, Gianpiero L, Delanty, Norman, Kälviäinen, Reetta, Jackson, Graeme D, Kowalczyk, Magdalena, Mascalchi, Mario, Semmelroch, Mira, Thomas, Rhys H, Soltanian-Zadeh, Hamid, Davoodi-Bojd, Esmaeil, Zhang, Junsong, Winston, Gavin P, Griffin, Aoife, Singh, Aditi, Tiwari, Vijay K, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, Lenge, Matteo, Guerrini, Renzo, Hamandi, Khalid, Foley, Sonya, Rüber, Theodor, Weber, Bernd, Depondt, Chantal, Absil, Julie, Carr, Sarah JA, Abela, Eugenio, Richardson, Mark P, Devinsky, Orrin, Severino, Mariasavina, Striano, Pasquale, Tortora, Domenico, Kaestner, Erik, Hatton, Sean N, Vos, Sjoerd B, Caciagli, Lorenzo, Duncan, John S, Whelan, Christopher D, Thompson, Paul M, Sisodiya, Sanjay M, Bernasconi, Andrea, Labate, Angelo, McDonald, Carrie R, Bernasconi, Neda and Bernhardt, Boris C
(2022)
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression.
Nature Communications, 13 (1).
4320-.
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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-.
This list was generated on Sun Jan 14 14:45:59 2024 GMT.