Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy by Reinthaler, Eva M., Lal, Dennis, Jurkowski, Wiktor, Feucht, Martha, Steinböck, Hannelore, Gruber‐Sedlmayr, Ursula, Ronen, Gabriel M., Geldner, Julia, Haberlandt, Edda, Neophytou, Birgit, Hahn, Andreas, Altmüller, Janine, Thiele, Holger, Toliat, Mohammad R., Lerche, Holger, Nürnberg, Peter, Sander, Thomas, Neubauer, Bernd A., Zimprich, Fritz

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Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes by Reinthaler, Eva M., Dejanovic, Borislav, Lal, Dennis, Semtner, Marcus, Merkler, Yvonne, Reinhold, Annika, Pittrich, Dorothea A., Hotzy, Christoph, Feucht, Martha, Steinböck, Hannelore, Gruber-Sedlmayr, Ursula, Ronen, Gabriel M., Neophytou, Birgit, Geldner, Julia, Haberlandt, Edda, Muhle, Hiltrud, Ikram, M. Arfan, van Duijn, Cornelia M., Uitterlinden, Andre G., Hofman, Albert, Altmüller, Janine, Kawalia, Amit, Toliat, Mohammad R., Nürnberg, Peter, Lerche, Holger, Nothnagel, Michael, Thiele, Holger, Sander, Thomas, Meier, Jochen C., Schwarz, Günter, Neubauer, Bernd A., Zimprich, Fritz

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Rare variants in [gamma]-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes by Reinthaler, Eva M, Dejanovic, Borislav, Lal, Dennis, Semtner, Marcus, Merkler, Yvonne, Reinhold, Annika, Pittrich, Dorothea A, Hotzy, Christoph, Feucht, Martha, Steinbock, Hannelore, Gruber-Sedlmayr, Ursula, Ronen, Gabriel M, Neophytou, Birgit, Geldner, Julia, Haberlandt, Edda, Muhle, Hiltrud, Ikram, M Arfan, van Duijn, Cornelia M, Uitterlinden, Andre G, Hofman, Albert, Altmuller, Janine, Kawalia, Amit, Toliat, Mohammad R, Nurnberg, Peter, Lerche, Holger, Nothnagel, Michael, Thiele, Holger, Sander, Thomas, Meier, Jochen C, Schwarz, Gunter, Neubauer, Bernd A, Zimprich, Fritz

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Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy by Bobbili, Dheeraj R, Lal, Dennis, May, Patrick, Reinthaler, Eva M, Jabbari, Kamel, Thiele, Holger, Nothnagel, Michael, Jurkowski, Wiktor, Feucht, Martha, Nürnberg, Peter, Lerche, Holger, Zimprich, Fritz, Krause, Roland, Neubauer, Bernd A, Feucht, Martha, Steinböck, Hannelore, Neophytou, Birgit, Geldner, Julia, Gruber-Sedlmayr, Ursula, Haberlandt, Edda, Ronen, Gabriel M, Altmüller, Janine, Lal, Dennis, Sander, Thomas, Krause, Roland, May, Patrick, Balling, Rudi, Neubauer, Bernd A

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Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes by Lal, Dennis, Reinthaler, Eva M, Dejanovic, Borislav, May, Patrick, Thiele, Holger, Lehesjoki, Anna-Elina, Schwarz, Günter, Riesch, Erik, Ikram, M Arfan, van Duijn, Cornelia M, Uitterlinden, Andre G, Hofman, Albert, Steinböck, Hannelore, Gruber-Sedlmayr, Ursula, Neophytou, Birgit, Zara, Federico, Hahn, Andreas, Gormley, Padhraig, Becker, Felicitas, Weber, Yvonne G, Cilio, Maria Roberta, Kunz, Wolfram S, Krause, Roland, Zimprich, Fritz, Lemke, Johannes R, Nürnberg, Peter, Sander, Thomas, Lerche, Holger, Neubauer, Bernd A

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