13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking von Yang, Minjun, Safavi, Setareh, Woodward, Eleanor L., Duployez, Nicolas, Olsson-Arvidsson, Linda, Ungerbäck, Jonas, Sigvardsson, Mikael, Zaliova, Marketa, Zuna, Jan, Fioretos, Thoas, Johansson, Bertil, Nord, Karolin H., Paulsson, Kajsa

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A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma von Walther, Charles, Tayebwa, Johnbosco, Lilljebjörn, Henrik, Magnusson, Linda, Nilsson, Jenny, von Steyern, Fredrik Vult, Øra, Ingrid, Domanski, Henryk A, Fioretos, Thoas, Nord, Karolin H, Fletcher, Christopher DM, Mertens, Fredrik

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Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary f... von Mohajeri, Arezoo, Tayebwa, Johnbosco, Collin, Anna, Nilsson, Jenny, Magnusson, Linda, von Steyern, Fredrik Vult, Brosjö, Otte, Domanski, Henryk A., Larsson, Olle, Sciot, Raf, Debiec-Rychter, Maria, Hornick, Jason L., Mandahl, Nils, Nord, Karolin H., Mertens, Fredrik

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GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma von Nord, Karolin H, Lilljebjörn, Henrik, Vezzi, Francesco, Nilsson, Jenny, Magnusson, Linda, Tayebwa, Johnbosco, de Jong, Danielle, Bovée, Judith V M G, Hogendoorn, Pancras C W, Szuhai, Karoly

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Methylation and copy number profiling: emerging tools to differentiate osteoblastoma from malignant mimics? von Ameline, Baptiste, Nathrath, Michaela, Nord, Karolin H., de Flon, Felix Haglund, Bovée, Judith V.M.G., Krieg, Andreas H., Höller, Sylvia, Hench, Jürgen, Baumhoer, Daniel

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Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the Wnt/beta-catenin signaling pathway von Nord, Karolin H, Nilsson, Jenny, Arbajian, Elsa, Vult von Steyern, Fredrik, Brosjö, Otte, Cleton-Jansen, Anne-Marie, Szuhai, Karoly, Hogendoorn, Pancras C W

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Genetic profiling of a chondroblastoma‐like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a... von Saba, Karim H., Cornmark, Louise, Rissler, Marianne, Fioretos, Thoas, Åström, Kristina, Haglund, Felix, Rosenberg, Andrew E., Brosjö, Otte, Nord, Karolin H.

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Retained Heterodisomy Is Associated with High Gene Expression in Hyperhaploid Inflammatory Leiomyosarcoma von Nord, Karolin H, Paulsson, Kajsa, Veerla, Srinivas, Wejde, Johan, Brosjö, Otte, Mandahl, Nils, Mertens, Fredrik

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Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors von Gebre-Medhin, Samuel, Nord, Karolin H, Möller, Emely, Mandahl, Nils, Magnusson, Linda, Nilsson, Jenny, Jo, Vickie Y, Vult von Steyern, Fredrik, Brosjö, Otte, Larsson, Olle, Domanski, Henryk A, Sciot, Raf, Debiec-Rychter, Maria, Fletcher, Christopher D.M, Mertens, Fredrik

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Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma von Nord, Karolin H., Magnusson, Linda, Isaksson, Margareth, Nilsson, Jenny, Lilljebjörn, Henrik, Domanski, Henryk A., Kindblom, Lars-Gunnar, Mandahl, Nils, Mertens, Fredrik, Rowley, Janet D.

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NTRK fusions in osteosarcoma are rare and non‐functional events von Ameline, Baptiste, Saba, Karim H, Kovac, Michal, Magnusson, Linda, Witt, Olaf, Bielack, Stefan, Nathrath, Michaela, Nord, Karolin H, Baumhoer, Daniel

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CDK4 is co-amplified with either TP53 promoter gene fusions or MDM2 through distinct mechanisms in osteosarcoma von Saba, Karim H., Difilippo, Valeria, Styring, Emelie, Nilsson, Jenny, Magnusson, Linda, van den Bos, Hilda, Wardenaar, René, Spierings, Diana C. J., Foijer, Floris, Nathrath, Michaela, Haglund de Flon, Felix, Baumhoer, Daniel, Nord, Karolin H.

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Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia von Safavi, S, Forestier, E, Golovleva, I, Barbany, G, Nord, K H, Moorman, A V, Harrison, C J, Johansson, B, Paulsson, K

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Inactivation of RB1, CDKN2A, and TP53 have distinct effects on genomic stability at side‐by‐side comparison in karyotypically normal cells von Andersson, Natalie, Saba, Karim H., Magnusson, Linda, Nilsson, Jenny, Karlsson, Jenny, Nord, Karolin H., Gisselsson, David

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Clonal evolution through loss of chromosomes and subsequent polyploidization in chondrosarcoma von Olsson, Linda, Paulsson, Kajsa, Bovée, Judith V M G, Nord, Karolin H

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FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma von Macchia, Gemma, Trombetta, Domenico, Möller, Emely, Mertens, Fredrik, Storlazzi, Clelia T, Debiec-Rychter, Maria, Sciot, Raf, Nord, Karolin H

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Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas von Macchia, Gemma, Nord, Karolin H., Zoli, Monica, Purgato, Stefania, D'Addabbo, Pietro, Whelan, Christopher W., Carbone, Lucia, Perini, Giovanni, Mertens, Fredrik, Rocchi, Mariano, Storlazzi, Clelia Tiziana

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Loss of NF2 defines a genetic subgroup of non‐FOS‐rearranged osteoblastoma von Saba, Karim H, Cornmark, Louise, Hofvander, Jakob, Magnusson, Linda, Nilsson, Jenny, Bos, Hilda, Spierings, Diana CJ, Foijer, Floris, Staaf, Johan, Brosjö, Otte, Sumathi, Vaiyapuri P, Lam, Suk Wai, Szuhai, Karoly, Bovée, Judith VMG, Kovac, Michal, Baumhoer, Daniel, Styring, Emelie, Nord, Karolin H

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Alkali‐like myosin light chain‐1 (myl1) is an early marker for differentiating fast muscle cells in zebrafish von Burguière, A. C., Nord, H., von Hofsten, J.

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Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma von Arbajian, Elsa, Puls, Florian, Magnusson, Linda, Thway, Khin, Fisher, Cyril, Sumathi, Vaiyapuri P, Tayebwa, Johnbosco, Nord, Karolin H, Kindblom, Lars-Gunnar, Mertens, Fredrik

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