Publications - Daniel Bader

  • 2015

  • Tobias B Haack, Christian Staufner, Marlies G Köpke, Beate K Straub, Stefan Kölker, Christian Thiel, Peter Freisinger, Ivo Baric, Patrick J McKiernan, Nicola Dikow, Inga Harting, Flemming Beisse, Peter Burgard, Urania Kotzaeridou, Joachim Kühr, Urban Himbert, Robert W Taylor, Felix Distelmaier, Jerry Vockley, Lina Ghaloul-Gonzalez, Johannes Zschocke, Laura S Kremer, Elisabeth Graf, Thomas Schwarzmayr, Daniel M Bader, Julien Gagneur, Thomas Wieland, Caterina Terrile, Tim M Strom, Thomas Meitinger, Georg F Hoffmann, Holger Prokisch Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy The American Journal of Human Genetics (2015)

  • J Arloth, DM Bader, S Röh, A Altmann Re-Annotator: Annotation Pipeline for Microarrays bioRxiv (2015)

  • Daniel M Bader, Stefan Wilkening, Gen Lin, Manu M Tekkedil, Kim Dietrich, Lars M Steinmetz, Julien Gagneur Negative feedback buffers effects of regulatory variants Molecular Systems Biology (2015)

     

  • 2013

  • Carina Quast, Serena Cuboni, Daniel Bader, André Altmann, Peter Weber, Janine Arloth, Simone Röh, Tanja Brückl, Marcus Ising, Anna Kopczak, Angelika Erhardt, Felix Hausch, Susanne Lucae, Elisabeth B. Binder Functional Coding Variants in SLC6A15, a Possible Risk Gene for Major Depression. Plos One (2013)

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  • 2012

  • Quast, Carina and Altmann, Andre and Weber, Peter and Arloth, Janine and Bader, Daniel and Heck, Angela and Pfister, Hildegard and Muller-Myhsok, Bertram and Erhardt, Angelika and Binder, Elisabeth B, Rare variants in TMEM132D in a case--control sample for panic disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics (2012)

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  • Altmann, Andre and Weber, Peter and Bader, Daniel and Preuss, Michael and Binder, Elisabeth B and Muller-Myhsok, Bertram. A beginners guide to SNP calling from high-throughput DNA-sequencing data. Human Genetics (2012)

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