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Wolking, Stefan, Moreau, Claudia, McCormack, Mark, Krause, Roland, Krenn, Martin, Berkovic, Samuel, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Johnson, Michael R et al (show 14 more authors) , Koeleman, Bobby PC, Kunz, Wolfram S, Lerche, Holger, Marson, Anthony G ORCID: 0000-0002-6861-8806, O'Brien, Terence J, Petrovski, Slave, Sander, Josemir W, Sills, Graeme J, Striano, Pasquale, Zara, Federico, Zimprich, Fritz, Sisodiya, Sanjay M, Girard, Simon L and Cossette, Patrick (2021) Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy. ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 8 (7). pp. 1376-1387.

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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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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.

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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-.