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  2. Zdanowicz, Katarzyna [Author]; Gebauer, Daniel [Author]; Speck, Kerstin [Author]; Steinbock, Oliver [Author]; Beckmann, Birgit [Author]; Marx, Steffen [Author]; Koschemann, Marc [Author]

    Distributed fiber optic sensors for measuring strains of concrete, steel, and textile reinforcement : Possible fields of application

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    Mass.: Wiley, Malden, [2024]

    Published in: Structural concrete ; 23,6 (2022), Seite 3367-3382

  4. 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

    Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy

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    Wiley, 2014

    Published in: Epilepsia, 55 (2014) 8

  5. 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; [...]

    Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy

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    Springer Science and Business Media LLC, 2018

    Published in: European Journal of Human Genetics, 26 (2018) 2, Seite 258-264

  6. Lal, Dennis; Reinthaler, Eva M.; Dejanovic, Borislav; May, Patrick; Thiele, Holger; Lehesjoki, Anna-Elina; Schwarz, Günter; Riesch, Erik; Ikram, M. Arfan; Duijn, Cornelia M. van; 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; [...]

    Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes

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    Public Library of Science (PLoS), 2016

    Published in: PLOS ONE, 11 (2016) 3, Seite e0150426

  7. 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; [...]

    Rare variants in γ‐aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes

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    Wiley, 2015

    Published in: Annals of Neurology, 77 (2015) 6, Seite 972-986

  8. 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; [...]

    Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

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    Springer Science and Business Media LLC, 2013

    Published in: Nature Genetics, 45 (2013) 9, Seite 1067-1072

  9. 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; [...]

    16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

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    Oxford University Press (OUP), 2014

    Published in: Human Molecular Genetics, 23 (2014) 22, Seite 6069-6080