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Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers.

  • Peter Horak
  • , Christoph Heining
  • , Simon Kreutzfeldt
  • , Barbara Hutter
  • , Andreas Mock
  • , Jennifer Hüllein
  • , Martina Fröhlich
  • , Sebastian Uhrig
  • , Arne Jahn
  • , Andreas Rump
  • , Laura Gieldon
  • , Lino Möhrmann
  • , Dorothea Hanf
  • , Veronica Teleanu
  • , Christoph E Heilig
  • , Daniel B Lipka
  • , Michael Allgäuer
  • , Leo Ruhnke
  • , Andreas Laßmann
  • , Volker Endris
  • Olaf Neumann, Roland Penzel, Katja Beck, Daniela Richter, Ulrike Winter, Stephan Wolf, Katrin Pfütze, Christina Geörg, Bettina Meißburger, Ivo Buchhalter, Marinela Augustin (Co-author), Walter E Aulitzky, Peter Hohenberger, Matthias Kroiss, Peter Schirmacher, Richard F Schlenk, Ulrich Keilholz, Frederick Klauschen, Gunnar Folprecht, Sebastian Bauer, Jens Thomas Siveke, Christian H Brandts, Thomas Kindler, Melanie Boerries, Anna L Illert, Nikolas von Bubnoff, Philipp J Jost, Karsten Spiekermann, Michael Bitzer, Klaus Schulze-Osthoff, Christof von Kalle, Barbara Klink, Benedikt Brors, Albrecht Stenzinger, Evelin Schröck, Daniel Hübschmann, Wilko Weichert, Hanno Glimm, Stefan Fröhling

Research output: Contribution to journalOriginal Articlepeer-review

210 Citations (Web of Science)
Original languageEnglish
Pages (from-to)2780-2795
JournalCANCER DISCOVERY
Volume11
Issue number11
DOIs
Publication statusPublished - 2021

Keywords

  • VEMURAFENIB
  • ONCOLOGY
  • REPAIR
  • MEDICINE
  • BURDEN
  • TUMORS

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