Auflistung Universitätsbibliographie nach Autor "Weber, Yvonne G."

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Auflistung Universitätsbibliographie nach Autor "Weber, Yvonne G."

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  • Diagnostic implications of genetic copy number variation in epilepsy plus
    Coppola, Antonietta; Cellini, Elena; Stamberger, Hannah; Saarentaus, Elmo; Cetica, Valentina; Lal, Dennis; Djemie, Tania; Bartnik-Glaska, Magdalena; Ceulemans, Berten; Cross, J. Helen; Deconinck, Tine; De Masi, Salvatore; Dorn, Thomas; Guerrini, Renzo; Hoffman-Zacharska, Dorotha; Kooy, Frank; Lagae, Lieven; Lench, Nicholas; Lemke, Johannes R.; Lucenteforte, Ersilia; Madia, Francesca; Mefford, Heather C.; Morrogh, Deborah; Nuernberg, Peter; Palotie, Aarno; Schoonjans, An-Sofie; Striano, Pasquale; Szczepanik, Elzbieta; Tostevin, Anna; Vermeesch, Joris R.; Van Esch, Hilde; Van Paesschen, Wim; Waters, Jonathan J.; Weckhuysen, Sarah; Zara, Federico; Jonghe, Peter De; Sisodiya, Sanjay M.; Marini, Carla; Lehesjioki, Anna-Elina; Craiu, Dana; Talvik, Tiina; Caglayan, Hande; Serratosa, Jose; Sterbova, Katalin; Moller, Rikke S.; Hjalgrim, Helle; Lerche, Holger; Weber, Yvonne; Helbig, Ingo; von Spiczak, Sarah; Barba, Carmen; Bogaerts, Anneleen; Boni, Antonella; Galizia, Elisabeth Caruana; Chiari, Sara; Clementella, Claudia; Di Gacomo, Gianpiero; Ferrari, Annarita; Guarducci, Silvia; Giglio, Sabrina; Holmgren, Philip; Leu, Costin; Mari, Francesco; Melani, Federico; Novara, Francesca; Pantaleo, Marilena; Peeters, Elke; Pisano, Tiziana; Rosati, Anna; Sander, Josemir; Schoeler, Natasha; Stankiewicz, Pawel; Striano, Salvatore; Suls, Arvid; Traverso, Monica; Vandeweyer, Geert; Van Dijck, Anke; Zuffardi, Orsetta (2019)
  • Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
    Becker, Felicitas; Schubert, Julian; Weckhuysen, Sarah; Suls, Arvid; Grueninger, Steffen; Korn-Merker, Elisabeth; Hofmann-Peters, Anne; Sperner, Juergen; Cross, Helen; Hallmann, Kerstin; Elger, Christian E.; Kunz, Wolfram S.; Madeleyen, Rene; Lerche, Holger; Weber, Yvonne G. (2015)
  • Drosophila melanogaster as a versatile model organism to study genetic epilepsies: An overview
    Fischer, Florian P. P.; Karge, Robin A. A.; Weber, Yvonne G. G.; Koch, Henner; Wolking, Stefan; Voigt, Aaron (2023)
  • Epilepsie - Wichtige Therapieempfehlungen für Praxis und Klinik
    Klamer, S.; Weber, Y. G.; Lerche, H. (2012)
  • Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
    Kasperaviciute, Dalia; Catarino, Claudia B.; Matarin, Mar; Leu, Costin; Novy, Jan; Tostevin, Anna; Leal, Barbara; 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, Joerg; Kraemer, Guenter; Steinhoff, Bernhard J.; Zumsteg, Dominik; Duncan, Susan; Kaelviaeinen, Reetta K.; Eriksson, Kai J.; Kantanen, Anne-Mari; Pandolfo, Massimo; Gruber-Sedlmayr, Ursula; Schlachter, Kurt; Reinthaler, Eva M.; Stogmann, Elisabeth; Zimprich, Fritz; Theatre, Emilie; Smith, Colin; O'Brien, Terence J.; Tan, K. Meng; Petrovski, Slave; Robbiano, Angela; Paravidino, Roberta; Zara, Federico; Striano, Pasquale; Sperling, Michael R.; Buono, Russell J.; Hakonarson, Hakon; Chaves, Joao; Costa, Paulo P.; Silva, Berta M.; da Silva, Antonio 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; Roessler, 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. (2013)
  • Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes
    Lal, Dennis; Reinthaler, Eva M.; Dejanovici, Borislav; May, Patrick; Thiele, Holger; Lehesjoki, Anna-Elina; Schwarz, Gunter; Riesch, Erik; Ikram, M. Arfan; van Duijn, Cornelia M.; Uitterlinden, Andre G.; Hofman, Albert; Steinboeck, 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.; Nuernberg, Peter; Sander, Thomas; Lerche, Holger; Neubauer, Bernd A. (2016)
  • Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy
    Moller, Rikke S.; Weber, Yvonne G.; Klitten, Laura L.; Trucks, Holger; Muhle, Hiltrud; Kunz, Wolfram S.; Mefford, Heather C.; Franke, Andre; Kautza, Monika; Wolf, Peter; Dennig, Dieter; Schreiber, Stefan; Rueckert, Ina-Maria; Wichmann, H.-Erich; Ernst, Jan P.; Schurmann, Claudia; Grabe, Hans J.; Tommerup, Niels; Stephani, Ulrich; Lerche, Holger; Hjalgrim, Helle; Helbig, Ingo; Sander, Thomas (2013)
  • Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy
    Lal, Dennis; Pernhorst, Katharina; Klein, Karl Martin; Reif, Philipp; Tozzi, Rossana; Toliat, Mohammad R.; Winterer, Georg; Neubauer, Bernd; Nuernberg, Peter; Rosenow, Felix; Becker, Felicitas; Lerche, Holger; Kunz, Wolfram S.; Kurki, Mitja I.; Hoffmann, Per; Becker, Albert J.; Perucca, Emilio; Zara, Federico; Sander, Thomas; Weber, Yvonne G. (2015)
  • FIRES and NORSE are distinct entities
    Körtevélyessy, Péter; Lerche, Holger; Weber, Yvonne (2012)
  • Focal epilepsy in Glucose transporter type 1 (Glut1) defects: case reports and a review of literature
    Wolking, Stefan; Becker, Felicitas; Bast, Thomas; Wiemer-Kruel, Adelheid; Mayer, Thomas; Lerche, Holger; Weber, Yvonne G. (2014)
  • Galanin pathogenic mutations in temporal lobe epilepsy
    Guipponi, Michel; Chentouf, Amina; Webling, Kristin E. B.; Freimann, Krista; Crespel, Arielle; Nobile, Carlo; Lemke, Johannes R.; Hansen, Jorg; Dorn, Thomas; Lesca, Gaetan; Ryvlin, Philippe; Hirsch, Edouard; Rudolf, Gabrielle; Rosenberg, Dominique Sarah; Weber, Yvonne; Becker, Felicitas; Helbig, Ingo; Muhle, Hiltrud; Salzmann, Annick; Chaouch, Malika; Oubaiche, Mohand Laid; Ziglio, Serena; Gehrig, Corinne; Santoni, Federico; Pizzato, Massimo; Langel, Ulo; Antonarakis, Stylianos E. (2015)
  • Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
    Lal, Dennis; May, Patrick; Perez-Palma, Eduardo; Samocha, Kaitlin E.; Kosmicki, Jack A.; Robinson, Elise B.; Moller, Rikke S.; Krause, Roland; Nuernberg, Peter; Weckhuysen, Sarah; De Jonghe, Peter; Guerrini, Renzo; Niestroj, Lisa M.; Du, Juliana; Marini, Carla; Ware, James S.; Kurki, Mitja; Gormley, Padhraig; Tang, Sha; Wu, Sitao; Biskup, Saskia; Poduri, Annapurna; Neubauer, Bernd A.; Koeleman, Bobby P. C.; Helbig, Katherine L.; Weber, Yvonne G.; Helbig, Ingo; Majithia, Amit R.; Palotie, Aarno; Daly, Mark J. (2020)
  • Genetic Biomarkers in Epilepsy
    Weber, Yvonne G.; Nies, Anne T.; Schwab, Matthias; Lerche, Holger (2014)
  • Genetic generalized epilepsies in adults - challenging assumptions and dogmas
    Vorderwuelbecke, Bernd J.; Wandschneider, Britta; Weber, Yvonne; Holtkamp, Martin (2022)
  • Genetic testing before epilepsy surgery-An exploratory survey and case collection from German epilepsy centers
    Bosselmann, Christian Malte; San Antonio-Arce, Victoria; Schulze-Bonhage, Andreas; Fauser, Susanne; Zacher, Pia; Mayer, Thomas; Aparicio, Javier; Albers, Kristina; Cloppenborg, Thomas; Kunz, Wolfram; Surges, Rainer; Syrbe, Steffen; Weber, Yvonne; Wolking, Stefan (2022)
  • Genetik der epileptischen Enzephalopathien
    Wolking, S.; Weber, Y. G. (2015)
  • Genetik der idiopathischen Epilepsien
    Weber, Y. G.; Lerche, H. (2013)
  • Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
    Steffens, Michael; Leu, Costin; Ruppert, Ann-Kathrin; Zara, Federico; Striano, Pasquale; Robbiano, Angela; Capovilla, Giuseppe; Tinuper, Paolo; Gambardella, Antonio; Bianchi, Amedeo; La Neve, Angela; Crichiutti, Giovanni; de Kovel, Carolien G. F.; Trenite, Dorothee Kasteleijn-Nolst; de Haan, Gerrit-Jan; Lindhout, Dick; Gaus, Verena; Schmitz, Bettina; Janz, Dieter; Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger; Steinhoff, Bernhard J.; Kleefuss-Lie, Ailing A.; Kunz, Wolfram S.; Surges, Rainer; Elger, Christian E.; Muhle, Hiltrud; von Spiczak, Sarah; Ostertag, Philipp; Helbig, Ingo; Stephani, Ulrich; Moller, Rikke S.; Hjalgrim, Helle; Dibbens, Leanne M.; Bellows, Susannah; Oliver, Karen; Mullen, Saul; Scheffer, Ingrid E.; Berkovic, Samuel F.; Everett, Kate V.; Gardiner, Mark R.; Marini, Carla; Guerrini, Renzo; Lehesjoki, Anna-Elina; Siren, Auli; Guipponi, Michel; Malafosse, Alain; Thomas, Pierre; Nabbout, Rima; Baulac, Stephanie; Leguern, Eric; Guerrero, Rosa; Serratosa, Jose M.; Reif, Philipp S.; Rosenow, Felix; Moerzinger, Martina; Feucht, Martha; Zimprich, Fritz; Kapser, Claudia; Schankin, Christoph J.; Suls, Arvid; Smets, Katrin; De Jonghe, Peter; Jordanova, Albena; Caglayan, Hande; Yapici, Zuhal; Yalcin, Destina A.; Baykan, Betul; Bebek, Nerses; Ozbek, Ugur; Gieger, Christian; Wichmann, Heinz-Erich; Balschun, Tobias; Ellinghaus, David; Franke, Andre; Meesters, Christian; Becker, Tim; Wienker, Thomas F.; Hempelmann, Anne; Schulz, Herbert; Rueschendorf, Franz; Leber, Markus; Pauck, Steffen M.; Trucks, Holger; Toliat, Mohammad R.; Nuernberg, Peter; Avanzini, Giuliano; Koeleman, Bobby P. C.; Sander, Thomas (2012)
  • Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
    Leu, Costin; de Kovel, Carolien G. F.; Zara, Federico; Striano, Pasquale; Pezzella, Marianna; Robbiano, Angela; Bianchi, Amedeo; Bisulli, Francesca; Coppola, Antonietta; Giallonardo, Anna Teresa; Beccaria, Francesca; Trenite, Dorothee Kasteleijn-Nolst; Lindhout, Dick; Gaus, Verena; Schmitz, Bettina; Janz, Dieter; Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger; Kleefuss-Lie, Ailing A.; Hallman, Kerstin; Kunz, Wolfram S.; Elger, Christian E.; Muhle, Hiltrud; Stephani, Ulrich; Moller, Rikke S.; Hjalgrim, Helle; Mullen, Saul; Scheffer, Ingrid E.; Berkovic, Samuel F.; Everett, Kate V.; Gardiner, Mark R.; Marini, Carla; Guerrini, Renzo; Lehesjoki, Anna-Elina; Siren, Auli; Nabbout, Rima; Baulac, Stephanie; Leguern, Eric; Serratosa, Jose M.; Rosenow, Felix; Feucht, Martha; Unterberger, Iris; Covanis, Athanasios; Suls, Arvid; Weckhuysen, Sarah; Kaneva, Radka; Caglayan, Hande; Turkdogan, Dilsad; Baykan, Betul; Bebek, Nerses; Ozbek, Ugur; Hempelmann, Anne; Schulz, Herbert; Rueschendorf, Franz; Trucks, Holger; Nuernberg, Peter; Avanzini, Giuliano; Koeleman, Bobby P. C.; Sander, Thomas (2012)
  • Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
    Abou-Khalil, Bassel; Auce, Pauls; Avbersek, Andreja; Bahlo, Melanie; Balding, David J.; Bast, Thomas; Baum, Larry; Becker, Albert J.; Becker, Felicitas; Berghuis, 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 G. F.; 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, Andres; Jamnadas-Khoda, Jennifer; Johnson, Michael R.; Kalviainen, Reetta; Kantanen, Anne-Mari; Kasperaviciute, Dalia; Trenite, Dorothee Kasteleijn-Nolst; Kirsch, Heidi E.; Knowlton, Robert C.; Koeleman, Bobby P. C.; Krause, Roland; Krenn, Martin; Kunz, Wolfram S.; Kuzniecky, Ruben; Kwan, Patrick; Lal, Dennis; Lau, Yu-Lung; Lehesjoki, Anna-Elina; Lerche, Holger; Leu, Costin; Lieb, Wolfgang; Lindhout, Dick; Lo, Warren D.; Lopes-Cendes, Iscia; Lowenstein, Daniel H.; Malovini, Alberto; Marson, Anthony G.; Mayer, Thomas; McCormack, Mark; Mills, James L.; Mirza, Nasir; Moerzinger, Martina; Moller, Rikke S.; Molloy, Anne M.; Muhle, Hiltrud; Newton, Mark; Ng, Ping-Wing; Noethen, Markus M.; Nuernberg, Peter; O'Brien, Terence J.; Oliver, Karen L.; Palotie, Aarno (2018)