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  2. Kubisch, Peter [Musical director]; Drehmann, Stephan [Editor] ; Mittelsächsische Theater und Philharmonie

    Berliner Luft : Musik einer Metropole : ein Programm mit dem Opernchor des Mittelsächsischen Theaters

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    [Freiberg]: Mittelsächsisches Theater, 06.02.2019

    Published in: Mittelsächsische Theater und Philharmonie: Mittelsächsisches Theater ; 2019-02-08

    Saxon Bibliography (Sächsische Bibliografie)
  3. Schöllhorn, Johannes [Other]; Parra, Hèctor [Other]; Nunes, Emmanuel [Other]; Dufourt, Hugues [Other]; Gander, Bernhard [Other]; Sharp, Elliott [Other]; Froleyks, Stephan [Other]; Royé, Gijsbrecht [Other]; Ott, Daniel [Other]; Aperghis, Georges [Other]; Kaul, Matthias [Other]; Kubisch, Christina [Other]; Davis, Gareth [Performer]; Hodges, Nicolas [Performer]; Rundel, Peter [Performer] ; Trío Arbós, JACK Quartet Musikgruppe, Arditti String Quartet, Ensemble R, Kulturforum Witten, Wittener Tage für Neue Kammermusik 41. 2009 Witten

    Wittener Tage für neue Kammermusik 2009 : CD Dokumentation live (2 Compact-Discs in Box)

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    Witten: Kulturforum, P 2009

  6. Kubisch, Stephan (gnd 139007318) [Author] ; Timmermann, Dirk AkademischeR BetreuerIn [Contributor]; Schwiegelshohn, Uwe AkademischeR BetreuerIn [Contributor]; Tavangarian, Djamshid AkademischeR BetreuerIn [Contributor]; Universität Rostock Fakultät für Informatik und Elektrotechnik (gnd: 10085032-7) Grad-verleihende Institution [Contributor]

    Architekturen für Ethernet-basierte Teilnehmerzugangsnetzwerke und deren Umsetzung in Hardware

    Thesis
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    Universität Rostock Rostock, 2009 2009

  7. Volk, Alexander E.; Lang-Roth, Ruth; Yigit, Goekhan; Borck, Guntram; Nuernberg, Gudrun; Rosenkranz, Stephan; Nuernberg, Peter; Kubisch, Christian; Beutner, Dirk

    A Novel MYO6 Splice Site Mutation Causes Autosomal Dominant Sensorineural Hearing Loss Type DFNA22 with a Favourable Outcome after Cochlear Implantation

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    S. Karger AG, 2013

    Published in: Audiology and Neurotology

  8. Lessel, Davor; Muhammad, Tariq; Casar Tena, Teresa; Moepps, Barbara; Burkhalter, Martin D.; Hitz, Marc-Phillip; Toka, Okan; Rentzsch, Axel; Schubert, Stephan; Schalinski, Adelheid; Bauer, Ulrike M. M.; Kubisch, Christian; Ware, Stephanie M.; Philipp, Melanie

    The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5

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    Springer Science and Business Media LLC, 2016

    Published in: Scientific Reports

  9. Rapp Christina, K.; Postma, AlexV.; Knoflach, Katrin; Volk, AlexanderE.; Lemke, JohannesR.; Ackermann, Maximilian; Regamey, Nicolas; Latzin, Philipp; Celant, Lucas; Jansen, SamaraM.; Bogaard, HarmJ.; Ilgun, Aho; Alders, Mariëlle; van Spaendonck-Zwarts, KarinY.; Jonigk, Danny; Klein, Christoph; Gräf, Stephan; Kubisch, Christian; Houweling, ArjanC.; Griese, Matthias

    Biallelic variants in the calpain regulatory subunit, CAPNS1, cause pulmonary arterial hypertension

    Conference Proceedings
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    Georg Thieme Verlag, 2023

    Published in: Klinische Pädiatrie

  10. Müller, Kathrin; Brenner, David; Weydt, Patrick; Meyer, Thomas; Grehl, Torsten; Petri, Susanne; Grosskreutz, Julian; Schuster, Joachim; Volk, Alexander E; Borck, Guntram; Kubisch, Christian; Klopstock, Thomas; Zeller, Daniel; Jablonka, Sibylle; Sendtner, Michael; Klebe, Stephan; Knehr, Antje; Günther, Kornelia; Weis, Joachim; Claeys, Kristl G; Schrank, Berthold; Sperfeld, Anne-Dorte; Hübers, Annemarie; Otto, Markus; [...]

    Comprehensive analysis of the mutation spectrum in 301 German ALS families

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    BMJ, 2018

    Published in: Journal of Neurology, Neurosurgery & Psychiatry

  11. Borck, Guntram; Rehman, Atteeq Ur; Lee, Kwanghyuk; Pogoda, Hans-Martin; Kakar, Naseebullah; von Ameln, Simon; Grillet, Nicolas; Hildebrand, Michael S.; Ahmed, Zubair M.; Nürnberg, Gudrun; Ansar, Muhammad; Basit, Sulman; Javed, Qamar; Morell, Robert J.; Nasreen, Nabilah; Shearer, A. Eliot; Ahmad, Adeel; Kahrizi, Kimia; Shaikh, Rehan S.; Ali, Rana A.; Khan, Shaheen N.; Goebel, Ingrid; Meyer, Nicole C.; Kimberling, William J.; [...]

    Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

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    Elsevier BV, 2011

    Published in: The American Journal of Human Genetics

  12. Brenner, David; Rosenbohm, Angela; Yilmaz, Rüstem; Müller, Kathrin; Grehl, Torsten; Petri, Susanne; Meyer, Thomas; Grosskreutz, Julian; Weydt, Patrick; Ruf, Wolfgang; Neuwirth, Christoph; Weber, Markus; Pinto, Susana; Claeys, Kristl G; Schrank, Berthold; Jordan, Berit; Knehr, Antje; Günther, Kornelia; Hübers, Annemarie; Zeller, Daniel; Kubisch, Christian; Jablonka, Sibylle; Sendtner, Michael; Klopstock, Thomas; [...]

    Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations

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    Oxford University Press (OUP), 2019

    Published in: Brain

  13. Brenner, David; Yilmaz, Rüstem; Müller, Kathrin; Grehl, Torsten; Petri, Susanne; Meyer, Thomas; Grosskreutz, Julian; Weydt, Patrick; Ruf, Wolfgang; Neuwirth, Christoph; Weber, Markus; Pinto, Susana; Claeys, Kristl G; Schrank, Berthold; Jordan, Berit; Knehr, Antje; Günther, Kornelia; Hübers, Annemarie; Zeller, Daniel; Kubisch, Christian; Jablonka, Sibylle; Sendtner, Michael; Klopstock, Thomas; de Carvalho, Mamede; [...]

    Hot-spot KIF5A mutations cause familial ALS

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    Oxford University Press (OUP), 2018

    Published in: Brain

  14. Bryois, Julien; Skene, Nathan G.; Hansen, Thomas Folkmann; Kogelman, Lisette J. A.; Watson, Hunna J.; Liu, Zijing; Adan, Roger; Alfredsson, Lars; Ando, Tetsuya; Andreassen, Ole; Baker, Jessica; Bergen, Andrew; Berrettini, Wade; Birgegård, Andreas; Boden, Joseph; Boehm, Ilka; Boni, Claudette; Boraska Perica, Vesna; Brandt, Harry; Breen, Gerome; Bryois, Julien; Buehren, Katharina; Bulik, Cynthia; Burghardt, Roland; [...]

    Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

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    Springer Science and Business Media LLC, 2020

    Published in: Nature Genetics

  15. Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K.; Walters, Raymond K.; Bras, Jose; Duncan, Laramie; Escott-Price, Valentina; Falcone, Guido J.; Gormley, Padhraig; Malik, Rainer; Patsopoulos, Nikolaos A.; Ripke, Stephan; Wei, Zhi; Yu, Dongmei; Lee, Phil H.; Turley, Patrick; Grenier-Boley, Benjamin; Chouraki, Vincent; Kamatani, Yoichiro; Berr, Claudine; Letenneur, Luc; Hannequin, Didier; Amouyel, Philippe; Boland, Anne; [...]

    Analysis of shared heritability in common disorders of the brain

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    American Association for the Advancement of Science (AAAS), 2018

    Published in: Science