A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma von Salaverria, Itziar, Martin-Guerrero, Idoia, Wagener, Rabea, Kreuz, Markus, Kohler, Christian W., Richter, Julia, Pienkowska-Grela, Barbara, Adam, Patrick, Burkhardt, Birgit, Claviez, Alexander, Damm-Welk, Christine, Drexler, Hans G., Hummel, Michael, Jaffe, Elaine S., Küppers, Ralf, Lefebvre, Christine, Lisfeld, Jasmin, Löffler, Markus, Macleod, Roderick A.F., Nagel, Inga, Oschlies, Ilske, Rosolowski, Maciej, Russell, Robert B., Rymkiewicz, Grzegorz, Schindler, Detlev, Schlesner, Matthias, Scholtysik, René, Schwaenen, Carsten, Spang, Rainer, Szczepanowski, Monika, Trümper, Lorenz, Vater, Inga, Wessendorf, Swen, Klapper, Wolfram, Siebert, Reiner

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The acrocentric part of der(Y)t(Y;acro)(q12;p1?2) contains D15Z1 sequences in the majority of cases von Fuchs, Sigrid, Lisfeld, Jasmin, Kankel, Stefanie, Person, Luisa, Liehr, Thomas

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ALK-positive anaplastic large cell lymphoma limited to the skin: clinical, histopathological and molecular analysis of 6 pediatric cases. A report from the ALCL99 study von Oschlies, Ilske, Lisfeld, Jasmin, Lamant, Laurence, Nakazawa, Atsuko, d'Amore, Emanuele S G, Hansson, Ulrika, Hebeda, Konnie, Simonitsch-Klupp, Ingrid, Maldyk, Jadwiga, Müllauer, Leonhard, Tinguely, Marianne, Stücker, Markus, Ledeley, Marie-Cecile, Siebert, Reiner, Reiter, Alfred, Brugières, Laurence, Klapper, Wolfram, Woessmann, Wilhelm

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Therapy in Primary Mediastinal B-Cell Lymphoma von Woessmann, Wilhelm, Lisfeld, Jasmin, Burkhardt, Birgit, Cashen, Amanda F, Christian, Beth A, Bartlett, Nancy L, Wilson, Wyndham H, Grant, Cliona, Dunleavy, Kieron

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Recurrent loss of heterozygosity in 1p36 associated with TNFRSF14 mutations in IRF4 translocation negative pediatric follicular lymphomas von Martin-Guerrero, Idoia, Salaverria, Itziar, Burkhardt, Birgit, Szczepanowski, Monika, Baudis, Michael, Bens, Susanne, de Leval, Laurence, Garcia-Orad, Africa, Horn, Heike, Lisfeld, Jasmin, Pellissery, Shoji, Klapper, Wolfram, Oschlies, Ilske, Siebert, Reiner

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A combination of long- and short-read genomics reveals frequent p-arm breakpoints within chromosome 21 complex genomic rearrangements von Schuy, Jakob, Sæther, Kristine Bilgrav, Lisfeld, Jasmin, Ek, Marlene, Grochowski, Christopher M., Lun, Ming Yin, Hastie, Alex, Rudolph, Susanne, Fuchs, Sigrid, Neveling, Kornelia, Hempel, Maja, Hoischen, Alexander, Pettersson, Maria, Carvalho, Claudia M.B., Eisfeldt, Jesper, Lindstrand, Anna

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The landscape of genomic alterations across childhood cancers von Gröbner, Susanne N., Worst, Barbara C., Weischenfeldt, Joachim, Buchhalter, Ivo, Kleinheinz, Kortine, Rudneva, Vasilisa A., Johann, Pascal D., Balasubramanian, Gnana Prakash, Segura-Wang, Maia, Brabetz, Sebastian, Bender, Sebastian, Hutter, Barbara, Sturm, Dominik, Pfaff, Elke, Hübschmann, Daniel, Zipprich, Gideon, Heinold, Michael, Eils, Jürgen, Lawerenz, Christian, Erkek, Serap, Lambo, Sander, Waszak, Sebastian, Blattmann, Claudia, Borkhardt, Arndt, Kuhlen, Michaela, Eggert, Angelika, Fulda, Simone, Gessler, Manfred, Wegert, Jenny, Kappler, Roland, Baumhoer, Daniel, Burdach, Stefan, Kirschner-Schwabe, Renate, Kontny, Udo, Kulozik, Andreas E., Lohmann, Dietmar, Hettmer, Simone, Eckert, Cornelia, Bielack, Stefan, Nathrath, Michaela, Niemeyer, Charlotte, Richter, Günther H., Schulte, Johannes, Siebert, Reiner, Westermann, Frank, Molenaar, Jan J., Vassal, Gilles, Witt, Hendrik, Burkhardt, Birgit, Kratz, Christian P., Witt, Olaf, van Tilburg, Cornelis M., Kramm, Christof M., Fleischhack, Gudrun, Dirksen, Uta, Rutkowski, Stefan, Frühwald, Michael, von Hoff, Katja, Wolf, Stephan, Klingebiel, Thomas, Koscielniak, Ewa, Landgraf, Pablo, Koster, Jan, Resnick, Adam C., Zhang, Jinghui, Liu, Yanling, Zhou, Xin, Waanders, Angela J., Zwijnenburg, Danny A., Raman, Pichai, Brors, Benedikt, Weber, Ursula D., Northcott, Paul A., Pajtler, Kristian W., Kool, Marcel, Piro, Rosario M., Korbel, Jan O., Schlesner, Matthias, Eils, Roland, Jones, David T. W., Lichter, Peter, Chavez, Lukas, Zapatka, Marc, Pfister, Stefan M.

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Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma von López, Cristina, Kleinheinz, Kortine, Aukema, Sietse M., Rohde, Marius, Bernhart, Stephan H., Hübschmann, Daniel, Wagener, Rabea, Toprak, Umut H., Raimondi, Francesco, Kreuz, Markus, Waszak, Sebastian M., Huang, Zhiqin, Sieverling, Lina, Paramasivam, Nagarajan, Seufert, Julian, Sungalee, Stephanie, Russell, Robert B., Bausinger, Julia, Kretzmer, Helene, Ammerpohl, Ole, Bergmann, Anke K., Binder, Hans, Borkhardt, Arndt, Brors, Benedikt, Claviez, Alexander, Doose, Gero, Feuerbach, Lars, Haake, Andrea, Hansmann, Martin-Leo, Hoell, Jessica, Hummel, Michael, Korbel, Jan O., Lawerenz, Chris, Lenze, Dido, Radlwimmer, Bernhard, Richter, Julia, Rosenstiel, Philip, Rosenwald, Andreas, Schilhabel, Markus B., Stein, Harald, Stilgenbauer, Stephan, Stadler, Peter F., Szczepanowski, Monika, Weniger, Marc A., Zapatka, Marc, Eils, Roland, Lichter, Peter, Loeffler, Markus, Möller, Peter, Trümper, Lorenz, Klapper, Wolfram, Hoffmann, Steve, Küppers, Ralf, Burkhardt, Birgit, Schlesner, Matthias, Siebert, Reiner

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Autosomal dominantly inherited myopathy likely caused by the TNNT1 variant p.(Asp65Ala) von Holling, Tess, Lisfeld, Jasmin, Johannsen, Jessika, Matschke, Jakob, Song, Feizhi, Altmeppen, Hermann Clemens, Kutsche, Kerstin

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A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a von Harms, Frederike L., Weiss, Deike, Lisfeld, Jasmin, Alawi, Malik, Kutsche, Kerstin

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The genomic and transcriptional landscape of primary central nervous system lymphoma von Radke, Josefine, Ishaque, Naveed, Koll, Randi, Gu, Zuguang, Schumann, Elisa, Sieverling, Lina, Uhrig, Sebastian, Hübschmann, Daniel, Toprak, Umut H., López, Cristina, Hostench, Xavier Pastor, Borgoni, Simone, Juraeva, Dilafruz, Pritsch, Fabienne, Paramasivam, Nagarajan, Balasubramanian, Gnana Prakash, Schlesner, Matthias, Sahay, Shashwat, Weniger, Marc, Pehl, Debora, Radbruch, Helena, Osterloh, Anja, Korfel, Agnieszka, Misch, Martin, Onken, Julia, Faust, Katharina, Vajkoczy, Peter, Moskopp, Dag, Wang, Yawen, Jödicke, Andreas, Trümper, Lorenz, Anagnostopoulos, Ioannis, Lenze, Dido, Küppers, Ralf, Hummel, Michael, Schmitt, Clemens A., Wiestler, Otmar D., Wolf, Stephan, Unterberg, Andreas, Eils, Roland, Herold-Mende, Christel, Brors, Benedikt, Siebert, Reiner, Wiemann, Stefan, Heppner, Frank L.

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Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing von RICHTER, Julia, SCHLESNER, Matthias, LENZE, Dido, SZCZEPANOWSKI, Monika, PAULSEN, Maren, LIPINSKI, Simone, RUSSELL, Robert B, ADAM-KLAGES, Sabine, APIC, Gordana, CLAVIEZ, Alexander, HASENCLEVER, Dirk, HOVESTADT, Volker, HOFFMANN, Steve, HORNIG, Nadine, KORBEL, Jan O, KUBE, Dieter, LANGENBERGER, David, LAWERENZ, Chris, LISFELD, Jasmin, MEYER, Katharina, PICELLI, Simone, PISCHIMAROV, Jordan, RADLWIMMER, Bernhard, KREUZ, Markus, RAUSCH, Tobias, ROHDE, Marius, SCHILHABEL, Markus, SCHOLTYSIK, René, SPANG, Rainer, TRAUTMANN, Heiko, ZENZ, Thorsten, BORKHARDT, Arndt, DREXLER, Hans G, MÖLLER, Peter, LEICH, Ellen, MACLEOD, Roderick A. F, POTT, Christiane, SCHREIBER, Stefan, TRÜMPER, Lorenz, LOEFFLER, Markus, STADLER, Peter F, LICHTER, Peter, EILS, Roland, KÜPPERS, Ralf, HUMMEL, Michael, BURKHARDT, Birgit, KLAPPER, Wolfram, ROSENSTIEL, Philip, ROSENWALD, Andreas, BRORS, Benedikt, SIEBERT, Reiner, ROSOLOWSKI, Maciej, AMMERPOHL, Ole, WAGENER, Rabea, BERNHART, Stephan H

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INPP4A-related genetic and phenotypic spectrum and functional relevance of subcellular targeting of INPP4A isoforms von Hecher, Laura, Harms, Frederike L., Lisfeld, Jasmin, Alawi, Malik, Denecke, Jonas, Kutsche, Kerstin

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Non‐anaplastic peripheral T‐cell lymphoma in children and adolescents – a retrospective analysis of the NHL‐BFM study group von Kontny, Udo, Oschlies, Ilske, Woessmann, Willi, Burkhardt, Birgit, Lisfeld, Jasmin, Salzburg, Janina, Janda, Ales, Attarbaschi, Andishe, Niggli, Felix, Zimmermann, Martin, Reiter, Alfred, Klapper, Wolfram

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MYC/MIZ1-dependent gene repression inversely coordinates the circadian clock with cell cycle and proliferation von Shostak, Anton, Ruppert, Bianca, Ha, Nati, Bruns, Philipp, Toprak, Umut H., Eils, Roland, Schlesner, Matthias, Diernfellner, Axel, Brunner, Michael

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MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells von Doose, Gero, Haake, Andrea, Bernhart, Stephan H., López, Cristina, Duggimpudi, Sujitha, Wojciech, Franziska, Bergmann, Anke K., Borkhardt, Arndt, Burkhardt, Birgit, Claviez, Alexander, Dimitrova, Lora, Haas, Siegfried, Hoell, Jessica I., Hummel, Michael, Karsch, Dennis, Klapper, Wolfram, Kleo, Karsten, Kretzmer, Helene, Kreuz, Markus, Küppers, Ralf, Lawerenz, Chris, Lenze, Dido, Loeffler, Markus, Mantovani-Löffler, Luisa, Möller, Peter, Ott, German, Richter, Julia, Rohde, Marius, Rosenstiel, Philip, Rosenwald, Andreas, Schilhabel, Markus, Schneider, Markus, Scholz, Ingrid, Stilgenbauer, Stephan, Stunnenberg, Hendrik G., Szczepanowski, Monika, Trümper, Lorenz, Weniger, Marc A., Hoffmann, Steve, Siebert, Reiner, Iaccarino, Ingram

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Whole-Exome Sequencing in Critically Ill Neonates and Infants: Diagnostic Yield and Predictability of Monogenic Diagnosis von Scholz, Tasja, Blohm, Martin Ernst, Kortüm, Fanny, Bierhals, Tatjana, Lessel, Davor, van der Ven, Amelie T., Lisfeld, Jasmin, Herget, Theresia, Kloth, Katja, Singer, Dominique, Perez, Anna, Obi, Nadia, Johannsen, Jessika, Denecke, Jonas, Santer, René, Kubisch, Christian, Deindl, Philipp, Hempel, Maja

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Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort von Ven, Amelie T., Johannsen, Jessika, Kortüm, Fanny, Wagner, Matias, Tsiakas, Konstantinos, Bierhals, Tatjana, Lessel, Davor, Herget, Theresia, Kloth, Katja, Lisfeld, Jasmin, Scholz, Tasja, Obi, Nadia, Wortmann, Saskia, Prokisch, Holger, Kubisch, Christian, Denecke, Jonas, Santer, René, Hempel, Maja

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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant von Aerden, Mio, Denommé-Pichon, Anne-Sophie, Bonneau, Dominique, Bruel, Ange-Line, Delanne, Julian, Gérard, Bénédicte, Mazel, Benoît, Philippe, Christophe, Pinson, Lucile, Prouteau, Clément, Putoux, Audrey, Tran Mau-Them, Frédéric, Viora-Dupont, Éléonore, Vitobello, Antonio, Ziegler, Alban, Piton, Amélie, Isidor, Bertrand, Francannet, Christine, Maillard, Pierre-Yves, Julia, Sophie, Philippe, Anais, Schaefer, Elise, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette, Legius, Eric, Theunis, Miel, Keren, Boris, Buratti, Julien, Charles, Perrine, Courtin, Thomas, Misra-Isrie, Mala, van Haelst, Mieke, Waisfisz, Quinten, Wieczorek, Dagmar, Schmetz, Ariane, Herget, Theresia, Kortüm, Fanny, Lisfeld, Jasmin, Debray, François-Guillaume, Bramswig, Nuria C, Atallah, Isis, Fodstad, Heidi, Jouret, Guillaume, Almoguera, Berta, Tahsin-Swafiri, Saoud, Santos-Simarro, Fernando, Palomares-Bralo, Maria, López-González, Vanesa, Kibaek, Maria, Tørring, Pernille M, Renieri, Alessandra, Bruno, Lucia Pia, Õunap, Katrin, Wojcik, Monica, Hsieh, Tzung-Chien, Krawitz, Peter, Van Esch, Hilde

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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant von Aerden, Mio, Denomme-Pichon, Anne-Sophie, Bonneau, Dominique, Bruel, Ange-Line, Delanne, Julian, Gerard, Benedicte, Mazel, Benoit, Philippe, Christophe, Pinson, Lucile, Prouteau, Clement, Putoux, Audrey, Tran Mau-Them, Frederic, Viora-Dupont, Eleonore, Vitobello, Antonio, Ziegler, Alban, Piton, Amelie, Isidor, Bertrand, Francannet, Christine, Maillard, Pierre-Yves, Julia, Sophie, Philippe, Anais, Schaefer, Elise, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette, Legius, Eric, Theunis, Miel, Keren, Boris, Buratti, Julien, Charles, Perrine, Courtin, Thomas, Misra-Isrie, Mala, van Haelst, Mieke, Waisfisz, Quinten, Wieczorek, Dagmar, Schmetz, Ariane, Herget, Theresia, Kortuem, Fanny, Lisfeld, Jasmin, Debray, Francois-Guillaume, Bramswig, Nuria C, Atallah, Isis, Fodstad, Heidi, Jouret, Guillaume, Almoguera, Berta, Tahsin-Swafiri, Saoud, Santos-Simarro, Fernando, Palomares-Bralo, Maria, Lopez-Gonzalez, Vanesa, Kibaek, Maria, Torring, Pernille M, Renieri, Alessandra, Bruno, Lucia Pia, Ounap, Katrin, Wojcik, Monica, Hsieh, Tzung-Chien, Krawitz, Peter, Van Esch, Hilde

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