Ultra-fast deep-learned CNS tumour classification during surgery von Vermeulen, C., Pagès-Gallego, M., Kester, L., Kranendonk, M. E. G., Wesseling, P., Verburg, N., de Witt Hamer, P., Kooi, E. J., Dankmeijer, L., van der Lugt, J., van Baarsen, K., Hoving, E. W., Tops, B. B. J., de Ridder, J.

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Processing of primary microRNAs by the microprocessor complex von Denli, A.M, Tops, B.B.J, Plasterk, R.H.A, Ketting, R.F, Hannon, G.J

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Adrenal Nodularity and Somatic Mutations in Primary Aldosteronism: One Node Is the Culprit? von Dekkers, T, ter Meer, M, Lenders, J. W. M, Hermus, A. R. M, Schultze Kool, L, Langenhuijsen, J. F, Nishimoto, K, Ogishima, T, Mukai, K, Azizan, E. A. B, Tops, B, Deinum, J, Küsters, B

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NTRK rearrangements in a subset of NF1-related malignant peripheral nerve sheath tumors as novel actionable target von Hiemcke-Jiwa, L. S., Meister, M. T., Martin, E., Dierselhuis, M. P., Haveman, L. M., Meijers, R. W. J., Tops, B. B. J., Wesseling, P., van Diest, P. J., van Gorp, J. M., Hehir-Kwa, J. Y., van Belzen, I. A. E. M., Bonenkamp, J. J., van Noesel, M. M., Flucke, U., Kester, L. A.

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PATZ1 fusions define a novel molecularly distinct neuroepithelial tumor entity with a broad histological spectrum von Alhalabi, Karam T., Stichel, Damian, Sievers, Philipp, Peterziel, Heike, Sommerkamp, Alexander C., Sturm, Dominik, Wittmann, Andrea, Sill, Martin, Jäger, Natalie, Beck, Pengbo, Pajtler, Kristian W., Snuderl, Matija, Jour, George, Delorenzo, Michael, Martin, Allison M., Levy, Adam, Dalvi, Nagma, Hansford, Jordan R., Gottardo, Nicholas G., Uro-Coste, Emmanuelle, Maurage, Claude-Alain, Godfraind, Catherine, Vandenbos, Fanny, Pietsch, Torsten, Kramm, Christof, Filippidou, Maria, Kattamis, Antonis, Jones, Chris, Øra, Ingrid, Mikkelsen, Torben Stamm, Zapotocky, Michal, Sumerauer, David, Scheie, David, McCabe, Martin, Wesseling, Pieter, Tops, Bastiaan B. J., Kranendonk, Mariëtte E. G., Karajannis, Matthias A., Bouvier, Nancy, Papaemmanuil, Elli, Dohmen, Hildegard, Acker, Till, von Hoff, Katja, Schmid, Simone, Miele, Evelina, Filipski, Katharina, Kitanovski, Lidija, Krskova, Lenka, Gojo, Johannes, Haberler, Christine, Alvaro, Frank, Ecker, Jonas, Selt, Florian, Milde, Till, Witt, Olaf, Oehme, Ina, Kool, Marcel, von Deimling, Andreas, Korshunov, Andrey, Pfister, Stefan M., Sahm, Felix, Jones, David T. W.

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Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases von Ten Broek, Roel W., Eijkelenboom, Astrid, Vleuten, Carine J. M., Kamping, Eveline J., Kets, Marleen, Verhoeven, Bas H., Grünberg, Katrien, Schultze Kool, Leo J., Tops, Bastiaan B. J., Ligtenberg, Marjolijn J. L., Flucke, Uta

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Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification von Keck, Michaela-Kristina, Sill, Martin, Wittmann, Andrea, Joshi, Piyush, Stichel, Damian, Beck, Pengbo, Okonechnikow, Konstantin, Sievers, Philipp, Wefers, Annika K., Roncaroli, Federico, Avula, Shivaram, McCabe, Martin G., Hayden, James T., Wesseling, Pieter, Øra, Ingrid, Nistér, Monica, Kranendonk, Mariëtte E. G., Tops, Bastiaan B. J., Zapotocky, Michal, Zamecnik, Josef, Vasiljevic, Alexandre, Fenouil, Tanguy, Meyronet, David, von Hoff, Katja, Schüller, Ulrich, Loiseau, Hugues, Figarella-Branger, Dominique, Kramm, Christof M., Sturm, Dominik, Scheie, David, Rauramaa, Tuomas, Pesola, Jouni, Gojo, Johannes, Haberler, Christine, Brandner, Sebastian, Jacques, Tom, Sexton Oates, Alexandra, Saffery, Richard, Koscielniak, Ewa, Baker, Suzanne J., Yip, Stephen, Snuderl, Matija, Ud Din, Nasir, Samuel, David, Schramm, Kathrin, Blattner-Johnson, Mirjam, Selt, Florian, Ecker, Jonas, Milde, Till, von Deimling, Andreas, Korshunov, Andrey, Perry, Arie, Pfister, Stefan M., Sahm, Felix, Solomon, David A., Jones, David T. W.

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Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas von Weren, Robbert D.A., Mensenkamp, Arjen R., Simons, Michiel, Eijkelenboom, Astrid, Sie, Aisha S., Ouchene, Hicham, Asseldonk, Monique, Gomez‐Garcia, Encarna B., Blok, Marinus J., Hullu, Joanne A., Nelen, Marcel R., Hoischen, Alexander, Bulten, Johan, Tops, Bastiaan B.J., Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L.

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Pleuropulmonary blastoma (PPB) and other DICER1-associated high-grade malignancies are morphologically, genetically and epigenetically related – A comparative study of 4 PPBs and 6... von Hiemcke-Jiwa, L.S., van Belle, S., Eijkelenboom, A., Merks, J.H.M., van Noesel, M.M., Kaal, S.E.J., Pijnenborg, J.M.A., Bulten, J., Tops, B.B.J., van de Ven, C.P., van Gorp, J.M., de Krijger, R.R., Cheesman, E., Kelsey, A.M., Kester, L.A., Flucke, U.

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EWSR1-ATF1 chimeric transcript in a myoepithelial tumor of soft tissue: a case report von Flucke, Uta, MD, Mentzel, Thomas, MD, Verdijk, Marian A., MSc, Slootweg, Pieter J., MD, DMD, PhD, Creytens, David H., MD, Suurmeijer, Albert J.H., MD, PhD, Tops, Bastiaan B.J., PhD

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NR4A3 rearrangement reliably distinguishes between the clinicopathologically overlapping entities myoepithelial carcinoma of soft tissue and cellular extraskeletal myxoid chondrosa... von Flucke, Uta, Tops, Bastiaan B. J., Verdijk, Marian A. J., van Cleef, Patricia J. H., van Zwam, Peter H., Slootweg, Pieter J., Bovée, Judith V. M. G., Riedl, Robert G., Creytens, David H., Suurmeijer, Albert J. H., Mentzel, Thomas

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Infantile fibrosarcoma with an EGFR kinase domain duplication: Underlining a close relationship with congenital mesoblastic nephroma and highlighting a similar morphological spectr... von van Spronsen, R., Kester, L.A., Knops, R.R.G., van de Sande, M.A.J., van Leenders, G.J.L.H., de Laat, P.C.J., Stortelder, E., Korpershoek, E., van Noesel, M.M., Meister, M.T., Koerkamp, M.J.A. Groot, de Graaf, N., Giovannoni, I., Tops, B.B.J., de Krijger, R.R., ter Horst, S.A.J., Flucke, U., Alaggio, R., Hiemcke-Jiwa, L.S.

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GOPC:ROS1 and other ROS1 fusions represent a rare but recurrent drug target in a variety of glioma types von Sievers, Philipp, Stichel, Damian, Sill, Martin, Schrimpf, Daniel, Sturm, Dominik, Selt, Florian, Ecker, Jonas, Kazdal, Daniel, Miele, Evelina, Kranendonk, Mariëtte E. G., Tops, Bastiaan B. J., Kohlhof-Meinecke, Patricia, Beschorner, Rudi, Kramm, Christof M., Hasselblatt, Martin, Reifenberger, Guido, Capper, David, Wesseling, Pieter, Stenzinger, Albrecht, Milde, Till, Korshunov, Andrey, Witt, Olaf, Pfister, Stefan M., Wick, Wolfgang, von Deimling, Andreas, Jones, David T. W., Sahm, Felix

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Development of a semi-conductor sequencing-based panel for genotyping of colon and lung cancer by the Onconetwork consortium von Tops, Bastiaan B J, Normanno, Nicola, Kurth, Henriette, Amato, Eliana, Mafficini, Andrea, Rieber, Nora, Le Corre, Delphine, Rachiglio, Anna Maria, Reiman, Anne, Sheils, Orla, Noppen, Christoph, Lacroix, Ludovic, Cree, Ian A, Scarpa, Aldo, Ligtenberg, Marjolijn J L, Laurent-Puig, Pierre

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Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material von Steeghs, Elisabeth M. P., Kroeze, Leonie I., Tops, Bastiaan B. J., van Kempen, Leon C., ter Elst, Arja, Kastner-van Raaij, Annemiek W. M., Hendriks-Cornelissen, Sandra J. B., Hermsen, Mandy J. W., Jansen, Erik A. M., Nederlof, Petra M., Schuuring, Ed, Ligtenberg, Marjolijn J. L., Eijkelenboom, Astrid

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Systematic discovery of gene fusions in pediatric cancer by integrating RNA-seq and WGS von van Belzen, Ianthe A E M, Cai, Casey, van Tuil, Marc, Badloe, Shashi, Strengman, Eric, Janse, Alex, Verwiel, Eugène T P, van der Leest, Douwe F M, Kester, Lennart, Molenaar, Jan J, Meijerink, Jules, Drost, Jarno, Peng, Weng Chuan, Kerstens, Hindrik H D, Tops, Bastiaan B J, Holstege, Frank C P, Kemmeren, Patrick, Hehir-Kwa, Jayne Y

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Correction to: Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification von Keck, Michaela-Kristina, Sill, Martin, Wittmann, Andrea, Joshi, Piyush, Stichel, Damian, Beck, Pengbo, Okonechnikow, Konstantin, Sievers, Philipp, Wefers, Annika K., Roncaroli, Federico, Avula, Shivaram, McCabe, Martin G., Hayden, James T., Wesseling, Pieter, Øra, Ingrid, Nistér, Monica, Kranendonk, Mariëtte E. G., Tops, Bastiaan B. J., Zapotocky, Michal, Zamecnik, Josef, Vasiljevic, Alexandre, Fenouil, Tanguy, Meyronet, David, von Hoff, Katja, Schüller, Ulrich, Loiseau, Hugues, Figarella-Branger, Dominique, Kramm, Christof M., Sturm, Dominik, Scheie, David, Rauramaa, Tuomas, Pesola, Jouni, Gojo, Johannes, Haberler, Christine, Brandner, Sebastian, Jacques, Tom, Sexton Oates, Alexandra, Saffery, Richard, Koscielniak, Ewa, Baker, Suzanne J., Yip, Stephen, Snuderl, Matija, Ud Din, Nasir, Samuel, David, Schramm, Kathrin, Blattner-Johnson, Mirjam, Selt, Florian, Ecker, Jonas, Milde, Till, von Deimling, Andreas, Korshunov, Andrey, Perry, Arie, Pfister, Stefan M., Sahm, Felix, Solomon, David A., Jones, David T. W.

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HER2, chromosome 17 polysomy and DNA ploidy status in breast cancer; a translational study von Halilovic, Altuna, Verweij, Dagmar I., Simons, Annet, Stevens-Kroef, Marian J. P. L., Vermeulen, Susan, Elsink, Janet, Tops, Bastiaan B. J., Otte-Höller, Irene, van der Laak, Jeroen A. W. M., van de Water, Carlijn, Boelens, Oliver B. A., Schlooz-Vries, Margrethe S., Dijkstra, Jeroen R., Nagtegaal, Iris D., Tol, Jolien, van Cleef, Patricia H. J., Span, Paul N., Bult, Peter

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EWSR1-The Most Common Rearranged Gene in Soft Tissue Lesions, Which Also Occurs in Different Bone Lesions: An Updated Review von Flucke, Uta, van Noesel, Max M., Siozopoulou, Vasiliki, Creytens, David, Tops, Bastiaan B. J., van Gorp, Joost M., Hiemcke-Jiwa, Laura S.

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Identification of a novel MET mutation in high-grade glioma resulting in an auto-active intracellular protein von Navis, Anna C., van Lith, Sanne A. M., van Duijnhoven, Sander M. J., de Pooter, Maaike, Yetkin-Arik, Bahar, Wesseling, Pieter, Hendriks, Wiljan J. A. J., Venselaar, Hanka, Timmer, Marco, van Cleef, Patricia, van Bergen en Henegouwen, Paul, Best, Myron G., Wurdinger, Thomas D., Tops, Bastiaan B. J., Leenders, William P. J.

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