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Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers

  • A Jahn
  • , A Rump
  • , TJ Widmann
  • , C Heining
  • , P Horak
  • , B Hutter
  • , N Paramasivam
  • , S Uhrig
  • , L Gieldon
  • , S Drukewitz
  • , A Kubler
  • , M Bermudez
  • , K Hackmann
  • , J Porrmann
  • , J Wagner
  • , M Arlt
  • , M Franke
  • , J Fischer
  • , Z Kowalzyk
  • , D William
  • V Weth, S Oster, M Frohlich, J Hullein, CV Gonzalez, S Kreutzfeldt, A Mock, CE Heilig, DB Lipka, L Mohrmann, D Hanf, M Oles, V Teleanu, M Allgauer, L Ruhnke, O Kutz, A Knurr, A Lassmann, V Endris, O Neumann, R Penzel, K Beck, D Richter, U Winter, S Wolf, K Pfutze, C Georg, B Meissburger, I Buchhalter, Marinela Augustin (Co-author), WE Aulitzky, P Hohenberger, M Kroiss, P Schirmacher, RF Schlenk, U Keilholz, F Klauschen, G Folprecht, S Bauer, JT Siveke, CH Brandts, T Kindler, M Boerries, AL Illert, N von Bubnoff, PJ Jost, KH Metzeler, M Bitzer, K Schulze-Osthoff, C von Kalle, B Brors, A Stenzinger, W Weichert, D Hubschmann, S Frohling, H Glimm, E Schrock, B Klink

Research output: Contribution to journalOriginal Articlepeer-review

49 Citations (Web of Science)
Original languageEnglish
Pages (from-to)1186-1199
JournalANNALS OF ONCOLOGY
Volume33
Issue number11
DOIs
Publication statusPublished - 2022

Keywords

  • GERMLINE VARIANTS
  • SEQUENCE VARIANTS
  • MEDICAL GENETICS
  • AMERICAN-COLLEGE
  • OVARIAN-CANCER
  • BREAST-CANCER
  • GENOMICS
  • RISK
  • GENES
  • CLASSIFICATION

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