Auflistung Universitätsbibliographie nach Autor "Weber, Yvonne G."

DSpace Repositorium (Manakin basiert)

Auflistung Universitätsbibliographie nach Autor "Weber, Yvonne G."

Sortiert nach: Sortierung: Ergebnisse:

  • Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data
    Allen, Andrew S.; Berkovic, Samuel F.; Bridgers, Joshua; Cossette, Patrick; Dlugos, Dennis; Epstein, Michael P.; Glauser, Tracy; Goldstein, David B.; Heinzen, Erin L.; Jiang, Yu; Johnson, Michael R.; Kuzniecky, Ruben; Lowenstein, Daniel H.; Marson, Anthony G.; Mefford, Heather C.; O'Brien, Terence J.; Ottman, Ruth; Petrou, Steven; Petrovski, Slave; Poduri, Annapurna; Ren, Zhong; Scheffer, Ingrid E.; Sherr, Elliott; Wang, Quanli; Balling, Rudi; Barisic, Nina; Baulac, Stephanie; Caglayan, Hande; Craiu, Dana; De Jonghe, Peter; Depienne, Christel; Guerrini, Renzo; Helbig, Ingo; Hjalgrim, Helle; Hoffman-Zacharska, Dorota; Jaehn, Johanna; Klein, Karl Martin; Koeleman, Bobby; Komarek, Vladimir; Krause, Roland; Leguern, Eric; Lehesjoki, Anna-Elina; Lemke, Johannes R.; Lerche, Holger; Linnankivi, Tarja; Marini, Carla; May, Patrick; Moller, Rikke S.; Muhle, Hiltrud; Pal, Deb; Palotie, Aarno; Rosenow, Felix; Selmer, Kaja; Serratosa, Jose M.; Sisodiya, Sanjay; Stephani, Ulrich; Sterbova, Katalin; Striano, Pasquale; Suls, Arvid; Talvik, Tiina; von Spiczak, Sarah; Weber, Yvonne; Weckhuysen, Sarah; Zara, Federico; Abou-Khalil, Bassel; Alldredge, Brian K.; Amrom, Dina; Andermann, Eva; Andermann, Frederick; Bautista, Jocelyn F.; Berkovic, Samuel F.; Bluvstein, Judith; Cascino, Gregory D.; Consalvo, Damian; Crumrine, Patricia; Devinsky, Orrin; Dlugos, Dennis; Epstein, Michael P.; Fiol, Miguel E.; Fountain, Nathan B.; French, Jacqueline; Friedman, Daniel; Glauser, Tracy; Haas, Kevin; Haut, Sheryl R.; Hayward, Jean; Joshi, Sucheta; Kanner, Andres; Kirsch, Heidi E.; Kossoff, Eric H.; Kuperman, Rachel; Kuzniecky, Ruben; Lowenstein, Daniel H.; McGuire, Shannon M.; Motika, Paul V.; Novotny, Edward J.; Ottman, Ruth; Paolicchi, Juliann M.; Parent, Jack; Park, Kristen; Poduri, Annapurna (2017)
  • Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia
    Yap, Zheng Yie; Efthymiou, Stephanie; Seiffert, Simone; Parra, Karen Vargas; Lee, Sukyeong; Nasca, Alessia; Maroofian, Reza; Schrauwen, Isabelle; Pendziwiat, Manuela; Jung, Sunhee; Bhoj, Elizabeth; Striano, Pasquale; Mankad, Kshitij; Vona, Barbara; Cuddapah, Sanmati; Wagner, Anja; Alvi, Javeria Raza; Davoudi-Dehaghani, Elham; Fallah, Mohammad-Sadegh; Gannavarapu, Srinitya; Lamperti, Costanza; Legati, Andrea; Murtaza, Bibi Nazia; Nadeem, Muhammad Shahid; Rehman, Mujaddad Ur; Saeidi, Kolsoum; Salpietro, Vincenzo; von Spiczak, Sarah; Sandoval, Abigail; Zeinali, Sirous; Zeviani, Massimo; Reich, Adi; Jang, Cholsoon; Helbig, Ingo; Barakat, Tahsin Stefan; Ghezzi, Daniele; Leal, Suzanne M.; Weber, Yvonne; Houlden, Henry; Yoon, Wan Hee (2021)
  • Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies
    Lal, Dennis; Ruppert, Ann-Kathrin; Trucks, Holger; Schulz, Herbert; de Kovel, Carolien G.; Trenite, Dorothee Kasteleijn-Nolst; 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; Moller, Rikke S.; Hjalgrim, Helle; De Jonghe, Peter; Suls, Arvid; Lieb, Wolfgang; Franke, Andre; Strauch, Konstantin; Gieger, Christian; Schurmann, Claudia; Schminke, Ulf; Nuernberg, Peter; Sander, Thomas (2015)
  • Characteristics and healthcare situation of adult patients with tuberous sclerosis complex in German epilepsy centers
    Hamer, Hajo M.; Pfaefflin, Margarete; Baier, Hartmut; Boesebeck, Frank; Franz, Melanie; Holtkamp, Martin; Kurlemann, Gerhard; May, TheodorW.; Mayer, Thomas; Metzner, Mirjam; Steinhoff, Bernhard J.; Stodieck, Stefan; Straub, Hans-Beatus; Weber, Yvonne G.; Brandt, Christian (2018)
  • Current practice in diagnostic genetic testing of the epilepsies
    Krey, Ilona; Platzer, Konrad; Esterhuizen, Alina; Berkovic, Samuel F.; Helbig, Ingo; Hildebrand, Michael S.; Lerche, Holger; Lowenstein, Daniel; Moller, Rikke S.; Poduri, Annapurna; Sadleir, Lynette; Sisodiya, Sanjay M.; Weckhuysen, Sarah; Wilmshurst, Jo M.; Weber, Yvonne; Lemke, Johannes R. (2022)
  • Delirium Screening in Aphasic Patients With the Intensive Care Delirium Screening Checklist (ICDSC) : A Prospective Cohort Study
    Bosselmann, Christian; Zurloh, Jan; Stefanou, Maria-Ioanna; Stadler, Vera; Weber, Yvonne; Lerche, Holger; Poli, Sven; Ziemann, Ulf; Mengel, Annerose (2019)
  • DEPDC5 Mutations in Genetic Focal Epilepsies of Childhood
    Lal, Dennis; Reinthaler, Eva M.; Schubert, Julian; Muhle, Hiltrud; Riesch, Erik; Kluger, Gerhard; Jabbari, Kamel; Kawalia, Amit; Baeumel, Christine; Holthausen, Hans; Hahn, Andreas; Feucht, Martha; Neophytou, Birgit; Haberlandt, Edda; Becker, Felicitas; Altmueller, Janine; Thiele, Holger; Lemke, Johannes R.; Lerche, Holger; Nuernberg, Peter; Sander, Thomas; Weber, Yvonne; Zimprich, Fritz; Neubauer, Bernd A. (2014)
  • Development of a rapid functional assay that predicts GLUT1 disease severity
    Zaman, Sasha M.; Mullen, Saul A.; Petrovski, Slave; Maljevic, Snezana; Gazina, Elena, V; Phillips, A. Marie; Jones, Gabriel Davis; Hildebrand, Michael S.; Damiano, John; Auvin, Stephane; Lerche, Holger; Weber, Yvonne G.; Berkovic, Samuel F.; Scheffer, Ingrid E.; Reid, Christopher A.; Petrou, Steven (2018)
  • 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)
  • 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)
  • 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)
  • 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 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 identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
    Montanucci, Ludovica; Lewis-Smith, David; Collins, Ryan L.; Niestroj, Lisa-Marie; Parthasarathy, Shridhar; Xian, Julie; Ganesan, Shiva; Macnee, Marie; Bruenger, Tobias; Thomas, Rhys H.; Talkowski, Michael; Helbig, Ingo; Leu, Costin; Lal, Dennis; Motelow, Joshua E.; Povysil, Gundula; Dhindsa, Ryan S.; Stanley, Kate E.; Allen, Andrew S.; Goldstein, David B.; Feng, Yen-Chen Anne; Howrigan, Daniel P.; Abbott, Liam E.; Tashman, Katherine; Cerrato, Felecia; Cusick, Caroline; Singh, Tarjinder; Heyne, Henrike; Byrnes, Andrea E.; Churchhouse, Claire; Watts, Nick; Solomonson, Matthew; Lal, Dennis; Gupta, Namrata; Neale, Benjamin M.; Berkovic, Samuel F.; Lerche, Holger; Goldstein, David B.; Lowenstein, Daniel H.; Berkovic, Samuel F.; Lerche, Holger; Goldstein, David B.; Lowenstein, Daniel H.; Cavalleri, Gianpiero L.; Cossette, Patrick; Cotsapas, Chris; De Jonghe, Peter; Dixon-Salazar, Tracy; Guerrini, Renzo; Hakonarson, Hakon; Heinzen, Erin L.; Dhindsa, Ryan S.; Stanley, Kate E.; Helbig, Ingo; Kwan, Patrick; Marson, Anthony G.; Petrovski, Slave; Kamalakaran, Sitharthan; Sisodiya, Sanjay M.; Stewart, Randy; Weckhuysen, Sarah; Depondt, Chantal; Dlugos, Dennis J.; Scheffer, Ingrid E.; Striano, Pasquale; Freyer, Catharine; Krause, Roland; May, Patrick; McKenna, Kevin; Regan, Brigid M.; Bennett, Caitlin A.; Leech, Stephanie L.; Leu, Costin; Lewis-Smith, David; Berkovic, Samuel F.; Scheffer, Ingrid E.; Regan, Brigid M.; Bennett, Caitlin A.; Leech, Stephanie L.; O'Brien, Terence J.; Petrovski, Slave; Todaro, Marian; Kwan, Patrick; Weckhuysen, Sarah; De Jonghe, Peter; Stamberger, Hannah; Depondti, Chantal; Andrade, Danielle M.; Ali, Quratulain Zulfiqar; Sadoway, Tara R.; Krestel, Heinz; Schaller, Andre; Papacostas, Savvas S.; Kousiappa, Ioanna; Tanteles, George A.; Yiolanda, Christou; Sterbova, Katalin; Vlckova, Marketa; Sedlackova, Lucie; Lassuthova, Petra; Klein, Karl Martin (2023)