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McCormack, M, Gui, Hongsheng, Ingason, Andrés, Speed, Doug, Wright, Galen EB, Zhang, Eunice J, Secolin, Rodrigo, Yasuda, Clarissa, Kwok, Maxwell, Wolking, Stefan et al (show 2 more authors) , Becker, Felicitas and Rau, Sarah (2017) Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology, 90 (4).

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Larivière, Sara, Rodríguez-Cruces, Raúl, Royer, Jessica, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis, Keller, Simon, Cendes, Fernando, Yasuda, Clarissa, Bonilha, Leonardo et al (show 52 more authors) , Gleichgerrcht, Ezequiel, Focke, Niels, Domin, Martin, Podewills, Felix von, Langner, Soenke, Rummel, Christian, Wiest, Roland, Martin, Pascal, Kotikalapudi, Raviteja, O’Brien, Terence, Sinclair, Benjamin, Vivash, Lucy, Desmond, Patricia, Alhusaini, Saud, Doherty, Colin, Cavalleri, Gianpiero, Delanty, Norman, Kälviäinen, Reetta, Jackson, Graeme, Kowalczyk, Magdalena, Mascalchi, Mario, Semmelroch, Mira, Thomas, Rhys, 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, Abela, Eugenio, Richardson, Mark, Devinsky, Orrin, Severino, Mariasavina, Striano, Pasquale, Tortora, Domenico, Hatton, Sean, Vos, Sjoerd, Duncan, John, Whelan, Christopher, Thompson, Paul, Sisodiya, Sanjay, Bernasconi, Andrea, Labate, Angelo, McDonald, Carrie, Bernasconi, Neda and Bernhardt, Boris (2020) Network-based atrophy modelling in the common epilepsies: a worldwide ENIGMA study.

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Hatton, Sean ORCID: 0000-0002-9149-8726, Huynh, Khoa, Bonilha, Leonardo, Abela, Eugenio, Alhusaini, Saud, Altmann, Andre ORCID: 0000-0002-9265-2393, Alvim, Marina KM, Balachandra, Akshara, Bartolini, Emanuele, Bender, Benjamin et al (show 64 more authors) , Bernasconi, Neda, Bernasconi, Andrea, Bernhardt, Boris, Bargallo, Núria, Caldairou, Benoit, Caligiuri, Maria Eugenia, Carr, Sarah JA, Cavalleri, Gianpiero, Cendes, Fernando, Concha, Luis, Davoodi-bojd, Esmaeil, Desmond, Patricia, Devinsky, Orrin, Doherty, Colin, Domin, Martin, Duncan, John, Focke, Niels, Foley, Sonya, Gambardella, Antonio, Gleichgerrcht, Ezequiel, Guerrini, Renzo, Hamandi, Khalid, Ishikawa, Akaria, Keller, Simon, Kochunov, Peter, 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, José CV, Morita-Sherman, Marcia, O’Brien, Terence, Pardoe, Heath, Pariente, José, Ribeiro, Letícia, Richardson, Mark, Rocha, Cristiane, Rodríguez-Cruces, Raúl, Rosenow, Felix, Severino, Mariasavina, Sinclair, Benjamin, Soltanian-Zadeh, Hamid, Striano, Pasquale, Taylor, Peter, Thomas, Rhys, Tortora, Domenico, Velakoulis, Dennis, Vezzani, Annamaria ORCID: 0000-0003-0573-6175, Vivash, Lucy ORCID: 0000-0002-1182-0907, von Podewils, Felix, Vos, Sjoerd, Weber, Bernd, Winston, Gavin, Yasuda, Clarissa, Thompson, Paul, Jahanshad, Neda, Sisodiya, Sanjay and McDonald, Carrie (2019) White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA Epilepsy study.

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Altmann, Andre ORCID: 0000-0002-9265-2393, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa ORCID: 0000-0002-9578-018X, Tolomeo, Daniele, Reynolds, Regina, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo et al (show 88 more authors) , Botía, Juan, Absil, Julie, Alhusaini, Saud, Alvim, Marina, Auvinen, Pia, Bargallo, Nuria, Bartolini, Emanuele, Bender, Benjamin, Bergo, Felipe, Bernardes, Tauana, Bernasconi, Andrea, Bernasconi, Neda, Bernhardt, Boris, Blackmon, Karen, Braga, Barbara, Caligiuri, Maria Eugenia, Calvo, Anna, Carlson, Chad, Carr, Sarah, Cavalleri, Gianpiero, Cendes, Fernando, Chen, Jian, Chen, Shuai, Cherubini, Andrea, Concha, Luis, David, Philippe, Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Doherty, Colin, Domin, Martin, Focke, Niels, Foley, Sonya, Franca, Wendy, Gambardella, Antonio, Guerrini, Renzo, Hamandi, Khalid, Hibar, Derrek, Isaev, Dmitry, Jackson, Graeme, Jahanshad, Neda, Kalviainen, Reetta, Keller, Simon, Kochunov, Peter, Kotikalapudi, Raviteja, Kowalczyk, Magdalena, Kuzniecky, Ruben, Kwan, Patrick, Labate, Angelo, Langner, Soenke, Lenge, Matteo, Liu, Min, Martin, Pascal, Mascalchi, Mario, Meletti, Stefano, Morita, Marcia, O’Brien, Terence, Pariente, Jose, Richardson, Mark, Rodriguez-Cruces, Raul, Rummel, Christian, Saavalainen, Taavi, Semmelroch, Mira, Severino, Mariasavina, Striano, Pasquale, Thesen, Thomas, Thomas, Rhys, Tondelli, Manuela, Tortora, Domenico, Vaudano, Anna Elisabetta, Vivash, Lucy, von Podewils, Felix, Wagner, Jan, Weber, Bernd, Wiest, Roland, Yasuda, Clarissa, Zhang, Guohao, Zhang, Junsong, Leu, Costin ORCID: 0000-0003-0598-3301, Avbersek, Andreja, Thorn, Maria, Whelan, Christopher, Thompson, Paul, McDonald, Carrie, Vezzani, Annamaria ORCID: 0000-0003-0573-6175, Sisodiya, Sanjay, ENIGMA-Epilepsy Working Group, and EpiPGX Consortium, (2018) A systems-level analysis highlights microglial activation as a modifying factor in common forms of human epilepsy.