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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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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.