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Borchert, Florian, Mock, Andreas, Tomczak, Aurelie, Huegel, Jonas, Alkarkoukly, Samer 
ORCID: 0000-0003-1891-1366, Knurr, Alexander, Volckmar, Anna-Lena ORCID: 0000-0002-1036-5391, Stenzinger, Albrecht, Schirmacher, Peter, Debus, Juergen, Jaeger, Dirk, Longerich, Thomas, Froehling, Stefan, Eils, Roland ORCID: 0000-0002-0034-4036, Bougatf, Nina, Sax, Ulrich and Schapranow, Matthieu-P
(2021).
Knowledge bases and software support for variant interpretation in precision oncology.
Brief. Bioinform., 22 (6).
OXFORD:
OXFORD UNIV PRESS.
ISSN 1477-4054
Fassunke, Jana, Ihle, Michaela Angelika, Lenze, Dido, Lehmann, Annika, Hummel, Michael, Vollbrecht, Claudia, Penzel, Roland, Volckmar, Anna-Lena, Stenzinger, Albrecht, Endris, Volker, Jung, Andreas, Lehmann, Ulrich, Zeugner, Silke, Baretton, Gustavo, Kreipe, Hans, Schirmacher, Peter, Kirchner, Thomas, Dietel, Manfred, Buettner, Reinhard and Merkelbach-Bruse, Sabine (2017). EGFR T790M mutation testing of non-small cell lung cancer tissue and blood samples artificially spiked with circulating cell-free tumor DNA: results of a round robin trial. Virchows Arch., 471 (4). S. 509 - 521. NEW YORK: SPRINGER. ISSN 1432-2307
Hinney, Anke ORCID: 0000-0001-5659-0706, Scherag, Andre ORCID: 0000-0002-9406-4704, Jarick, Ivonne, Albayrak, Oezguer, Puetter, Carolin, Pechlivanis, Sonali, Dauvermann, Maria R., Beck, Sebastian, Weber, Heike ORCID: 0000-0002-9421-1292, Scherag, Susann, Nguyen, Trang T., Volckmar, Anna-Lena, Knoll, Nadja, Faraone, Stephen V., Neale, Benjamin M., Franke, Barbara ORCID: 0000-0003-4375-6572, Cichon, Sven ORCID: 0000-0002-9475-086X, Hoffmann, Per ORCID: 0000-0002-6573-983X, Noethen, Markus M., Schreiber, Stefan, Joeckel, Karl-Heinz, Wichmann, H. -Erich, Freitag, Christine, Lempp, Thomas, Meyer, Jobst, Gilsbach, Susanne, Herpertz-Dahlmann, Beate, Sinzig, Judith ORCID: 0000-0002-3693-3318, Lehmkuhl, Gerd, Renner, Tobias J., Warnke, Andreas, Romanos, Marcel ORCID: 0000-0001-7628-8299, Lesch, Klaus-Peter ORCID: 0000-0001-8348-153X, Reif, Andreas, Schimmelmann, Benno G. and Hebebrand, Johannes
(2011).
Genome-Wide Association Study in German Patients With Attention Deficit/Hyperactivity Disorder.
Am. J. Med. Genet. B, 156B (8).
S. 888 - 898.
MALDEN:
WILEY-BLACKWELL.
ISSN 1552-4841