FIP1L1-PDGFRα D842V, a novel panresistant mutant, emerging after treatment of FIP1L1-PDGFRα T674I eosinophilic leukemia with single agent sorafenib von Lierman, E, Michaux, L, Beullens, E, Pierre, P, Marynen, P, Cools, J, Vandenberghe, P

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A Tyrosine Kinase Created by Fusion of the PDGFRA and FIP1L1 Genes as a Therapeutic Target of Imatinib in Idiopathic Hypereosinophilic Syndrome von Cools, Jan, DeAngelo, Daniel J, Gotlib, Jason, Stover, Elizabeth H, Legare, Robert D, Cortes, Jorges, Kutok, Jeffrey, Clark, Jennifer, Galinsky, Ilene, Griffin, James D, Cross, Nicholas C.P, Tefferi, Ayalew, Malone, James, Alam, Rafeul, Schrier, Stanley L, Schmid, Janet, Rose, Michal, Vandenberghe, Peter, Verhoef, Gregor, Boogaerts, Marc, Wlodarska, Iwona, Kantarjian, Hagop, Marynen, Peter, Coutre, Steven E, Stone, Richard, Gilliland, D. Gary

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Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of publ... von Menten, B, Maas, N, Thienpont, B, Buysse, K, Vandesompele, J, Melotte, C, de Ravel, T, Van Vooren, S, Balikova, I, Backx, L, Janssens, S, De Paepe, A, De Moor, B, Moreau, Y, Marynen, P, Fryns, J-P, Mortier, G, Devriendt, K, Speleman, F, Vermeesch, J R

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FOXP1, a gene highly expressed in a subset of diffuse large B-cell lymphoma, is recurrently targeted by genomic aberrations von WLODARSKA, I, VEYT, E, DE WOLF-PEETERS, C, DE PAEPE, P, VANDENBERGHE, P, NOOIJEN, P, THEATE, I, MICHAUX, L, SAGAERT, X, MARYNEN, P, HAGEMEIJER, A

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Role of cardiac myocyte tissue factor in heart hemostasis von PAWLINSKI, R., TENCATI, M., HOLSCHER, T., PEDERSEN, B., VOET, T., TILLEY, R. E., MARYNEN, P., MACKMAN, N.

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Clinical and molecular features of FIP1L1-PDFGRA (+) chronic eosinophilic leukemias von VANDENBERGHE, P, WLODARSKA, I, MAEREVOET, M, VERHOEF, G, COOLS, J, GILLILAND, D. G, HAGEMEIJER, A, MARYNEN, P, MICHAUX, L, ZACHEE, P, BOOGAERTS, M, VANSTRAELEN, D, HERREGODS, M-C, VAN HOOF, A, SELLESLAG, D, ROUFOSSE, F

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Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map von Van Buggenhout, G, Melotte, C, Dutta, B, Froyen, G, Van Hummelen, P, Marynen, P, Matthijs, G, de Ravel, T, Devriendt, K, Fryns, J P, Vermeesch, J R

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Allele-specific copy number analysis of tumors von Van Loo, Peter, Nordgard, Silje H., Lingjærde, Ole Christian, Russnes, Hege G., Rye, Inga H., Sun, Wei, Weigman, Victor J., Marynen, Peter, Zetterberg, Anders, Naume, Bjørn, Perou, Charles M., Børresen-Dale, Anne-Lise, Kristensen, Vessela N.

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A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias von SPELEMAN, F, CAUWELIER, B, BOOGAERTS, M, DE MOERLOOSE, B, BENOIT, Y, SELLESLAG, D, BILLIET, J, ROBERT, A, HUGUET, F, VANDENBERGHE, P, DE PAEPE, A, MARYNEN, P, DASTUGUE, N, HAGEMEIJER, A, COOLS, J, VERHASSELT, B, POPPE, B, VAN ROY, N, VANDESOMPELE, J, GRAUX, C, UYTTEBROECK, A

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Novel PORCN mutations in focal dermal hypoplasia von Froyen, G, Govaerts, K, Van Esch, H, Verbeeck, J, Tuomi, M-L, Heikkilä, H, Torniainen, S, Devriendt, K, Fryns, J-P, Marynen, P, Järvelä, I, Ala-Mello, S

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Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL von Pospisilova, H, Baens, M, Michaux, L, Stul, M, Van Hummelen, P, Van Loo, P, Vermeesch, J, Jarosova, M, Zemanova, Z, Michalova, K, Van den Berghe, I, Alexander, H D, Hagemeijer, A, Vandenberghe, P, Cools, J, De Wolf-Peeters, C, Marynen, P, Wlodarska, I

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Gene prioritization through genomic data fusion von Aerts, Stein, Lambrechts, Diether, Maity, Sunit, Van Loo, Peter, Coessens, Bert, De Smet, Frederik, Tranchevent, Leon-Charles, De Moor, Bart, Marynen, Peter, Hassan, Bassem, Carmeliet, Peter, Moreau, Yves

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Translocations t(11;18)(q21;q21) and t(14;18)(q32;q21) are the main chromosomal abnormalities involving MLT/MALT1 in MALT lymphomas von PENAS, E. M, HINZ, K, DIERLAMM, J, RÖSER, K, COPIE-BERGMAN, C, WLODARSKA, I, MARYNEN, P, HAGEMEIJER, A, GAULARD, P, LÖNING, T, HOSSIELD, D. K

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Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males von Van Esch, Hilde, Bauters, Marijke, Ignatius, Jaakko, Jansen, Mieke, Raynaud, Martine, Hollanders, Karen, Lugtenberg, Dorien, Bienvenu, Thierry, Jensen, Lars Riff, Gécz, Jozef, Moraine, Claude, Marynen, Peter, Fryns, Jean-Pierre, Froyen, Guy

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A new NDE1 PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome von La Starza, R, Rosati, R, Roti, G, Gorello, P, Bardi, A, Crescenzi, B, Pierini, V, Calabrese, O, Baens, M, Folens, C, Cools, J, Marynen, P, Martelli, M F, Mecucci, C, Cuneo, A

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Efficacy of the Kinase Inhibitor SU11248 against Gastrointestinal Stromal Tumor Mutants Refractory to Imatinib Mesylate von PRENEN, Hans, COOLS, Jan, MENTENS, Nicole, FOLENS, Cedric, SCIOT, Raf, SCHÖFFSKI, Patrick, VAN OOSTEROM, Allan, MARYNEN, Peter, DEBIEC-RYCHTER, Maria

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X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms von Frints, SGM, Froyen, G, Marynen, P, Fryns, J-P

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Detection of t(11;18)(q21;q21) by interphase fluorescence in situ hybridization using API2 and MLT specific probes von DIERLAMM, Judith, BAENS, Mathijs, HAGEMEIJER, Anne, HOSSFELD, Dieter Kurt, DE WOLF-PEETERS, Christiane, MARYNEN, Peter, STEFANOVA-OUZOUNOVA, Margarita, HINZ, Kristina, WLODARSKA, Iwona, MAES, Brigitte, STEYLS, Anja, DRIESSEN, Ann, VERHOEF, Gregor, GAULARD, Philippe

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Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants von Debiec-Rychter, Maria, Cools, Jan, Dumez, Herlinde, Sciot, Raf, Stul, Michel, Mentens, Nicole, Vranckx, Hilde, Wasag, Bartosz, Prenen, Hans, Roesel, Johannes, Hagemeijer, Anne, Van Oosterom, Allan, Marynen, Peter

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Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis von Levine, Ross L., Wadleigh, Martha, Cools, Jan, Ebert, Benjamin L., Wernig, Gerlinde, Huntly, Brian J.P., Boggon, Titus J., Wlodarska, Iwona, Clark, Jennifer J., Moore, Sandra, Adelsperger, Jennifer, Koo, Sumin, Lee, Jeffrey C., Gabriel, Stacey, Mercher, Thomas, D’Andrea, Alan, Fröhling, Stefan, Döhner, Konstanze, Marynen, Peter, Vandenberghe, Peter, Mesa, Ruben A., Tefferi, Ayalew, Griffin, James D., Eck, Michael J., Sellers, William R., Meyerson, Matthew, Golub, Todd R., Lee, Stephanie J., Gilliland, D. Gary

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