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	1.	RBFOX1 and RBFOX3 mutations in rolandic epilepsy. [electronic resource] by Lal, Dennis Reinthaler, Eva M Altmüller, Janine Toliat, Mohammad R Thiele, Holger Nürnberg, Peter Lerche, Holger Hahn, Andreas Møller, Rikke S Muhle, Hiltrud Sander, Thomas Zimprich, Fritz Neubauer, Bernd A Producer: 20140607 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy. [electronic resource] 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 Producer: 20140929 In: Epilepsia vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	DEPDC5 mutations in genetic focal epilepsies of childhood. [electronic resource] by Lal, Dennis Reinthaler, Eva M Schubert, Julian Muhle, Hiltrud Riesch, Erik Kluger, Gerhard Jabbari, Kamel Kawalia, Amit Bäumel, Christine Holthausen, Hans Hahn, Andreas Feucht, Martha Neophytou, Birgit Haberlandt, Edda Becker, Felicitas Altmüller, Janine Thiele, Holger Lemke, Johannes R Lerche, Holger Nürnberg, Peter Sander, Thomas Weber, Yvonne Zimprich, Fritz Neubauer, Bernd A Producer: 20140811 In: Annals of neurology vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. [electronic resource] 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 Reinthaler, Eva M Zimprich, Fritz Feucht, Martha Steinböck, Hannelore Neophytou, Birgit Geldner, Julia Gruber-Sedlmayr, Ursula Haberlandt, Edda Ronen, Gabriel M Altmüller, Janine Lal, Dennis Nürnberg, Peter Sander, Thomas Thiele, Holger Krause, Roland May, Patrick Balling, Rudi Lerche, Holger Neubauer, Bernd A Producer: 20181211 In: European journal of human genetics : EJHG vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Rare gene deletions in genetic generalized and Rolandic epilepsies. [electronic resource] by Jabbari, Kamel Bobbili, Dheeraj R Lal, Dennis Reinthaler, Eva M Schubert, Julian Wolking, Stefan Sinha, Vishal Motameny, Susanne Thiele, Holger Kawalia, Amit Altmüller, Janine Toliat, Mohammad Reza Kraaij, Robert van Rooij, Jeroen Uitterlinden, André G Ikram, M Arfan Zara, Federico Lehesjoki, Anna-Elina Krause, Roland Zimprich, Fritz Sander, Thomas Neubauer, Bernd A May, Patrick Lerche, Holger Nürnberg, Peter Producer: 20190208 In: PloS one vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	TPP2 mutation associated with sterile brain inflammation mimicking MS. [electronic resource] by Reinthaler, Eva M Graf, Elisabeth Zrzavy, Tobias Wieland, Thomas Hotzy, Christoph Kopecky, Chantal Pferschy, Sandra Schmied, Christiane Leutmezer, Fritz Keilani, Mohammad Lill, Christina M Hoffjan, Sabine Epplen, Jörg T Zettl, Uwe K Hecker, Michael Deutschländer, Angela Meuth, Sven G Ahram, Mamoun Mustafa, Baha El-Khateeb, Mohammed Vilariño-Güell, Carles Sadovnick, A Dessa Zimprich, Fritz Tomkinson, Birgitta Strom, Tim Kristoferitsch, Wolfgang Lassmann, Hans Zimprich, Alexander Publication details: Neurology. Genetics Dec 2018 In: Neurology. Genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes. [electronic resource] 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 Producer: 20160801 In: PloS one vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes. [electronic resource] 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 Producer: 20150803 In: Annals of neurology vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease. [electronic resource] by Vilariño-Güell, Carles Zimprich, Alexander Martinelli-Boneschi, Filippo Herculano, Bruno Wang, Zhe Matesanz, Fuencisla Urcelay, Elena Vandenbroeck, Koen Leyva, Laura Gris, Denis Massaad, Charbel Quandt, Jacqueline A Traboulsee, Anthony L Encarnacion, Mary Bernales, Cecily Q Follett, Jordan Yee, Irene M Criscuoli, Maria G Deutschländer, Angela Reinthaler, Eva M Zrzavy, Tobias Mascia, Elisabetta Zauli, Andrea Esposito, Federica Alcina, Antonio Izquierdo, Guillermo Espino-Paisán, Laura Mena, Jorge Antigüedad, Alfredo Urbaneja-Romero, Patricia Ortega-Pinazo, Jesús Song, Weihong Sadovnick, A Dessa Producer: 20191106 In: PLoS genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. [electronic resource] by Reinthaler, Eva M Lal, Dennis Lebon, Sebastien Hildebrand, Michael S Dahl, Hans-Henrik M Regan, Brigid M Feucht, Martha Steinböck, Hannelore Neophytou, Birgit Ronen, Gabriel M Roche, Laurian Gruber-Sedlmayr, Ursula Geldner, Julia Haberlandt, Edda Hoffmann, Per Herms, Stefan Gieger, Christian Waldenberger, Melanie Franke, Andre Wittig, Michael Schoch, Susanne Becker, Albert J Hahn, Andreas Männik, Katrin Toliat, Mohammad R Winterer, Georg Lerche, Holger Nürnberg, Peter Mefford, Heather Scheffer, Ingrid E Berkovic, Samuel F Beckmann, Jacques S Sander, Thomas Jacquemont, Sebastien Reymond, Alexandre Zimprich, Fritz Neubauer, Bernd A Producer: 20150723 In: Human molecular genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies. [electronic resource] by Lal, Dennis Ruppert, Ann-Kathrin Trucks, Holger Schulz, Herbert de Kovel, Carolien G Kasteleijn-Nolst Trenité, Dorothée Sonsma, Anja C M Koeleman, Bobby P Lindhout, Dick Weber, Yvonne G Lerche, Holger Kapser, Claudia Schankin, Christoph J Kunz, Wolfram S Surges, Rainer Elger, Christian E Gaus, Verena Schmitz, Bettina Helbig, Ingo Muhle, Hiltrud Stephani, Ulrich Klein, Karl M Rosenow, Felix Neubauer, Bernd A Reinthaler, Eva M Zimprich, Fritz Feucht, Martha Møller, Rikke S Hjalgrim, Helle De Jonghe, Peter Suls, Arvid Lieb, Wolfgang Franke, Andre Strauch, Konstantin Gieger, Christian Schurmann, Claudia Schminke, Ulf Nürnberg, Peter Sander, Thomas Producer: 20160427 In: PLoS genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. [electronic resource] by Lemke, Johannes R Lal, Dennis Reinthaler, Eva M Steiner, Isabelle Nothnagel, Michael Alber, Michael Geider, Kirsten Laube, Bodo Schwake, Michael Finsterwalder, Katrin Franke, Andre Schilhabel, Markus Jähn, Johanna A Muhle, Hiltrud Boor, Rainer Van Paesschen, Wim Caraballo, Roberto Fejerman, Natalio Weckhuysen, Sarah De Jonghe, Peter Larsen, Jan Møller, Rikke S Hjalgrim, Helle Addis, Laura Tang, Shan Hughes, Elaine Pal, Deb K Veri, Kadi Vaher, Ulvi Talvik, Tiina Dimova, Petia Guerrero López, Rosa Serratosa, José M Linnankivi, Tarja Lehesjoki, Anna-Elina Ruf, Susanne Wolff, Markus Buerki, Sarah Wohlrab, Gabriele Kroell, Judith Datta, Alexandre N Fiedler, Barbara Kurlemann, Gerhard Kluger, Gerhard Hahn, Andreas Haberlandt, D Edda Kutzer, Christina Sperner, Jürgen Becker, Felicitas Weber, Yvonne G Feucht, Martha Steinböck, Hannelore Neophythou, Birgit Ronen, Gabriel M Gruber-Sedlmayr, Ursula Geldner, Julia Harvey, Robert J Hoffmann, Per Herms, Stefan Altmüller, Janine Toliat, Mohammad R Thiele, Holger Nürnberg, Peter Wilhelm, Christian Stephani, Ulrich Helbig, Ingo Lerche, Holger Zimprich, Fritz Neubauer, Bernd A Biskup, Saskia von Spiczak, Sarah Producer: 20131126 In: Nature genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. [electronic resource] by Kasperaviciute, Dalia Catarino, Claudia B Matarin, Mar Leu, Costin Novy, Jan Tostevin, Anna Leal, Bárbara Hessel, Ellen V S Hallmann, Kerstin Hildebrand, Michael S Dahl, Hans-Henrik M Ryten, Mina Trabzuni, Daniah Ramasamy, Adaikalavan Alhusaini, Saud Doherty, Colin P Dorn, Thomas Hansen, Jörg Krämer, Günter Steinhoff, Bernhard J Zumsteg, Dominik Duncan, Susan Kälviäinen, Reetta K Eriksson, Kai J Kantanen, Anne-Mari Pandolfo, Massimo Gruber-Sedlmayr, Ursula Schlachter, Kurt Reinthaler, Eva M Stogmann, Elisabeth Zimprich, Fritz Théâtre, Emilie Smith, Colin O'Brien, Terence J Meng Tan, K Petrovski, Slave Robbiano, Angela Paravidino, Roberta Zara, Federico Striano, Pasquale Sperling, Michael R Buono, Russell J Hakonarson, Hakon Chaves, João Costa, Paulo P Silva, Berta M da Silva, António M de Graan, Pierre N E Koeleman, Bobby P C Becker, Albert Schoch, Susanne von Lehe, Marec Reif, Philipp S Rosenow, Felix Becker, Felicitas Weber, Yvonne Lerche, Holger Rössler, Karl Buchfelder, Michael Hamer, Hajo M Kobow, Katja Coras, Roland Blumcke, Ingmar Scheffer, Ingrid E Berkovic, Samuel F Weale, Michael E Delanty, Norman Depondt, Chantal Cavalleri, Gianpiero L Kunz, Wolfram S Sisodiya, Sanjay M Producer: 20131125 In: Brain : a journal of neurology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)