Recurrent Chromosome Abnormalities Define Nonoverlapping Unique Subgroups of Tumors in Patients With Chronic Lymphocytic Leukemia and Known Karyotypic Abnormalities von Jimenez-Zepeda, Victor H, Chng, Wee Joo, Schop, Roelandt F.J, Braggio, Esteban, Leis, Jose F, Kay, Neil, Fonseca, Rafael

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Identification of Copy Number Abnormalities and Inactivating Mutations in Two Negative Regulators of Nuclear Factor-κB Signaling Pathways in Waldenström's Macroglobulinemia von BRAGGIO, Esteban, KEATS, Jonathan J, AZAB, Feda, GREIPP, Philip, GERTZ, Morie, HAYMAN, Suzanne, RAJKUMAR, S. Vincent, CARPTEN, John, CHEST, Marta, BARRETT, Michael, STEWART, A. Keith, DOGAN, Ahmet, LELEU, Xavier, LEIF BERGSAGEL, P, GHOBRIAL, Irene M, FONSECA, Rafael, VAN WIER, Scott, JIMENEZ-ZEPEDA, Victor H, VALDEZ, Riccardo, SCHOP, Roelandt F. J, PRICE-TROSKA, Tammy, HENDERSON, Kimberly, SACCO, Antonio

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Search for a natural killer: a case report von Louter, Leonora, Schop, Roelandt F. J., van der Meer, Adriaan J.

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First-Line Treatment of Waldenström’s Macroglobulinaemia: Considerations Based on the Dutch National Guideline von Amaador, Karima, Kersten, Marie José, Visser, Hein P. J., Nieuwenhuizen, Laurens, Schop, Roelandt F. J., Chamuleau, Martine E. D., Velders, Gerjo A., Minnema, Monique C., Vos, Josephine Mathilde Iris

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Waldenström macroglobulinemia neoplastic cells lack immunoglobulin heavy chain locus translocations but have frequent 6q deletions von Schop, Roelandt F.J., Kuehl, W. Michael, Van Wier, Scott A., Ahmann, Gregory J., Price-Troska, Tammy, Bailey, Richard J., Jalal, Syed M., Qi, Ying, Kyle, Robert A., Greipp, Philip R., Fonseca, Rafael

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Extensive genetic alterations of the HLA region, including homozygous deletions of HLA class II genes in B-cell lymphomas arising in immune-privileged sites von Riemersma, Sietske A., Jordanova, Ekaterina S., Schop, Roelandt F.J., Philippo, Katja, Looijenga, Leendert H.J., Schuuring, Ed, Kluin, Philip M.

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Deletions of 17p13.1 and 13q14 are uncommon in Waldenström macroglobulinemia clonal cells and mostly seen at the time of disease progression von Schop, Roelandt F.J, Jalal, Syed M, Van Wier, Scott A, Ahmann, Gregory J, Bailey, Richard J, Kyle, Robert A, Greipp, Philip R, Rajkumar, S.Vincent, Gertz, Morie A, Lust, John A, Lacy, Martha Q, Dispenzieri, Angela, Witzig, Thomas E, Fonseca, Rafael

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Genetics and cytogenetics of Waldenstrom's macroglobulinemia von Schop, Roelandt F.J., Fonseca, Rafael

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High-Resolution Genomic Analysis in Waldenström's Macroglobulinemia Identifies Disease-Specific and Common Abnormalities with Marginal Zone Lymphomas von Braggio, Esteban, Keats, Jonathan J., Leleu, Xavier, Van Wier, Scott, Jimenez-Zepeda, Victor Hugo, Schop, Roelandt F.J., Chesi, Marta, Barrett, Michael, Stewart, Alexander Keith, Dogan, Ahmet, Bergsagel, Peter Leif, Ghobrial, Irene M., Fonseca, Rafael

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Identification of Copy Number Abnormalities and Inactivating Mutations in Two Negative Regulators of Nuclear Factor-κB Signaling Pathways in Waldenström's Macroglobulinemia von Braggio, Esteban, Keats, Jonathan J., Leleu, Xavier, Van Wier, Scott, Jimenez-Zepeda, Victor H., Valdez, Riccardo, Schop, Roelandt F.J., Price-Troska, Tammy, Henderson, Kimberly, Sacco, Antonio, Azab, Feda, Greipp, Philip, Gertz, Morie, Hayman, Suzanne, Rajkumar, S. Vincent, Carpten, John, Chesi, Marta, Barrett, Michael, Stewart, A. Keith, Dogan, Ahmet, Bergsagel, P. Leif, Ghobrial, Irene M., Fonseca, Rafael

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High Density Oligonucleotide Array CGH Analysis of CLL Reveals Areas of Recurrent Genomic Gain or Loss von Schop, Roelandt F.J., Mancini, Catherine, Chng, Wee-Joo, Tschumper, Renee C., Jelinek, Diane F., Kay, Neil E., Bergsagel, Peter Leif, Carpten, John D., Fonseca, Rafael

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One Half of Patients with Waldenström Macroglobulinemia Have Large Deletions of Chromosome 6q von Van Wier, Scott, Chng, Wee-Joo, Ahmann, Greg, Rempel, Rachel, Al Masri, Azzah, Gertz, Morie, Dispenzieri, Angela, Greipp, Philip, Schop, Roelandt F.J., Fonseca, Rafael

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One Half of Patients with Waldenström Macroglobulinemia Have Large Deletions of Chromosome 6q von Van Wier, Scott, Chng, Wee-Joo, Ahmann, Greg, Rempel, Rachel, Al Masri, Azzah, Gertz, Morie, Dispenzieri, Angela, Greipp, Philip, Schop, Roelandt F.J., Fonseca, Rafael

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6q Deletion in Waldenström Macroglobulinemia Is the Most Common Cytogenetic Abnormality and Is Associated with Aggressive Disease with a Trend towards Worse Survival von Schop, Roelandt F.J., Ocio, Enrique M., Gonzalez, Belen, Gutierrez, Norma C., Moro, Maria Jesus, Aguilera, Carmen, Hernández, Jose, García-Sanz, Ramon, Xu, Ruifang, Hernandez-Rivas, Jesus M., Greipp, Philip R., Dispenzieri, Angela, Jalal, Syed M., Lacy, Martha Q., Gonzalez-Paz, Natalia, Gertz, Morie A., San Miguel, Jesús F., Fonseca, Rafael

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6q Deletion in Waldenström Macroglobulinemia Is the Most Common Cytogenetic Abnormality and Is Associated with Aggressive Disease with a Trend towards Worse Survival von Schop, Roelandt F.J., Ocio, Enrique M., Gonzalez, Belen, Gutierrez, Norma C., Moro, Maria Jesus, Aguilera, Carmen, Hernández, Jose, García-Sanz, Ramon, Xu, Ruifang, Hernandez-Rivas, Jesus M., Greipp, Philip R., Dispenzieri, Angela, Jalal, Syed M., Lacy, Martha Q., Gonzalez-Paz, Natalia, Gertz, Morie A., San Miguel, Jesús F., Fonseca, Rafael

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6q deletion discriminates Waldenström macroglobulinemia from IgM monoclonal gammopathy of undetermined significance von Schop, Roelandt F.J., Van Wier, Scott A., Xu, Ruifang, Ghobrial, Irene, Ahmann, Gregory J., Greipp, Philip R., Kyle, Robert A., Dispenzieri, Angela, Lacy, Martha Q., Rajkumar, S. Vincent, Gertz, Morie A., Fonseca, Rafael

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