Works by van Wezel, Tom

Results: 80
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    Multicenter Comparison of Molecular Tumor Boards in The Netherlands: Definition, Composition, Methods, and Targeted Therapy Recommendations.

    Published in:
    Oncologist, 2021, v. 26, n. 8, p. e1347, doi. 10.1002/onco.13580
    By:
    • Koopman, Bart;
    • Groen, Harry J.M.;
    • Ligtenberg, Marjolijn J.L.;
    • Grünberg, Katrien;
    • Monkhorst, Kim;
    • de Langen, Adrianus J.;
    • Boelens, Mirjam C.;
    • Paats, Marthe S.;
    • von der Thüsen, Jan H.;
    • Dinjens, Winand N.M.;
    • Solleveld, Nienke;
    • van Wezel, Tom;
    • Gelderblom, Hans;
    • Hendriks, Lizza E.;
    • Speel, Ernst‐Jan M.;
    • Theunissen, Tom E.;
    • Kroeze, Leonie I.;
    • Mehra, Niven;
    • Piet, Berber;
    • van der Wekken, Anthonie J.
    Publication type:
    Article
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    Germline variant affecting p53β isoforms predisposes to familial cancer.

    Published in:
    Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52551-8
    By:
    • Schubert, Stephanie A.;
    • Ruano, Dina;
    • Joruiz, Sebastien M.;
    • Stroosma, Jordy;
    • Glavak, Nikolina;
    • Montali, Anna;
    • Pinto, Lia M.;
    • Rodríguez-Girondo, Mar;
    • Barge-Schaapveld, Daniela Q. C. M.;
    • Nielsen, Maartje;
    • van Nesselrooij, Bernadette P. M.;
    • Mensenkamp, Arjen R.;
    • van Leerdam, Monique E.;
    • Sharp, Thomas H.;
    • Morreau, Hans;
    • Bourdon, Jean-Christophe;
    • de Miranda, Noel F. C. C.;
    • van Wezel, Tom
    Publication type:
    Article
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    Robust detection of translocations in lymphoma FFPE samples using targeted locus capture-based sequencing.

    Published in:
    Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23695-8
    By:
    • Allahyar, Amin;
    • Pieterse, Mark;
    • Swennenhuis, Joost;
    • Los-de Vries, G. Tjitske;
    • Yilmaz, Mehmet;
    • Leguit, Roos;
    • Meijers, Ruud W. J.;
    • van der Geize, Robert;
    • Vermaat, Joost;
    • Cleven, Arjen;
    • van Wezel, Tom;
    • Diepstra, Arjan;
    • van Kempen, Léon C.;
    • Hijmering, Nathalie J.;
    • Stathi, Phylicia;
    • Sharma, Milan;
    • Melquiond, Adrien S. J.;
    • de Vree, Paula J. P.;
    • Verstegen, Marjon J. A. M.;
    • Krijger, Peter H. L.
    Publication type:
    Article
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    Neurofibromas in LZTR1 schwannomatosis.

    Published in:
    Clinical Genetics, 2022, v. 101, n. 5/6, p. 571, doi. 10.1111/cge.14121
    By:
    • Groen, Justus L.;
    • Moghadasi, Setareh;
    • Spruijt, Liesbeth;
    • Korpershoek, Esther;
    • Ierland, Yvette van;
    • Tom van Wezel, J.;
    • Duinen, Sjoerd van;
    • Malessy, Martijn J. A.;
    • Lesnik Oberstein, Saskia A. J.
    Publication type:
    Article
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    Molecular analysis using SalvGlandDx improves risk of malignancy estimation and diagnosis of salivary gland cytopathology: An exploratory multicenter study.

    Published in:
    Cancer Cytopathology, 2024, v. 132, n. 7, p. 435, doi. 10.1002/cncy.22814
    By:
    • Freiberger, Sandra N.;
    • Ikenberg, Kristian;
    • van Egmond, Demi;
    • Claerhout, Sofie;
    • van Wezel, Tom;
    • Bempt, Isabelle Vanden;
    • van Rossem, Jeroen N.;
    • Mueller, Simon A.;
    • Clement, Paul M;
    • Poorten, Vincent Vander;
    • Cohen, Danielle;
    • Hauben, Esther;
    • Rupp, Niels J.
    Publication type:
    Article
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    Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 12, p. 1256, doi. 10.1038/ng.1004
    By:
    • Pansuriya, Twinkal C;
    • van Eijk, Ronald;
    • d'Adamo, Pio;
    • van Ruler, Maayke A J H;
    • Kuijjer, Marieke L;
    • Oosting, Jan;
    • Cleton-Jansen, Anne-Marie;
    • van Oosterwijk, Jolieke G;
    • Verbeke, Sofie L J;
    • Meijer, Daniëlle;
    • van Wezel, Tom;
    • Nord, Karolin H;
    • Sangiorgi, Luca;
    • Toker, Berkin;
    • Liegl-Atzwanger, Bernadette;
    • San-Julian, Mikel;
    • Sciot, Raf;
    • Limaye, Nisha;
    • Kindblom, Lars-Gunnar;
    • Daugaard, Soeren
    Publication type:
    Article
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    Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers.

    Published in:
    Nature Genetics, 2002, v. 31, n. 3, p. 295, doi. 10.1038/ng903
    By:
    • Ruivenkamp, Claudia A.L.;
    • van Wezel, Tom;
    • Zanon, Carlo;
    • Stassen, Alphons P.M.;
    • Vlcek, Cestmir;
    • Csikós, Tamás;
    • Klous, Anita M.;
    • Tripodis, Nikos;
    • Perrakis, Anastassis;
    • Boerrigter, Lucie;
    • Groot, Peter C.;
    • Lindeman, Jan;
    • Mooi, Wolter J.;
    • Meijjer, Gerrit A.;
    • Scholten, Gert;
    • Dauwerse, Hans;
    • Paces, Vaclav;
    • van Zandwijk, Nico;
    • van Ommen, Gert Jan B.
    Publication type:
    Article
    12

    Real-world routine diagnostic molecular analysis for TP53 mutational status is recommended over p53 immunohistochemistry in B-cell lymphomas.

    Published in:
    Virchows Archiv: European Journal of Pathology, 2024, v. 485, n. 4, p. 643, doi. 10.1007/s00428-023-03676-6
    By:
    • de Haan, Lorraine M.;
    • de Groen, Ruben A. L.;
    • de Groot, Fleur A.;
    • Noordenbos, Troy;
    • van Wezel, Tom;
    • van Eijk, Ronald;
    • Ruano, Dina;
    • Diepstra, Arjan;
    • Koens, Lianne;
    • Nicolae-Cristea, Alina;
    • Hartog, Wietske C. E. den;
    • Terpstra, Valeska;
    • Ahsmann, Els;
    • Dekker, Tim J. A.;
    • Sijs-Szabo, Aniko;
    • Veelken, Hendrik;
    • Cleven, Arjen H. G.;
    • Jansen, Patty M.;
    • Vermaat, Joost S. P.
    Publication type:
    Article
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    Cell-of-origin classification using the Hans and Lymph2Cx algorithms in primary cutaneous large B-cell lymphomas.

    Published in:
    Virchows Archiv: European Journal of Pathology, 2022, v. 480, n. 3, p. 667, doi. 10.1007/s00428-021-03265-5
    By:
    • Schrader, Anne M. R.;
    • de Groen, Ruben A. L.;
    • Willemze, Rein;
    • Jansen, Patty M.;
    • Quint, Koen D.;
    • van Wezel, Tom;
    • van Eijk, Ronald;
    • Ruano, Dina;
    • Tensen, Cornelis P.;
    • Hauben, Esther;
    • Woei-A-Jin, F. J. S. H.;
    • Busschots, Anne M.;
    • van den Berg, Anke;
    • Diepstra, Arjan;
    • Vermeer, Maarten H.;
    • Vermaat, Joost S. P.
    Publication type:
    Article
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    Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients.

    Published in:
    PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0157381
    By:
    • Jansen, Anne M. L.;
    • Geilenkirchen, Marije A.;
    • van Wezel, Tom;
    • Jagmohan-Changur, Shantie C.;
    • Ruano, Dina;
    • van der Klift, Heleen M.;
    • van den Akker, Brendy E. W. M.;
    • Laros, Jeroen F. J.;
    • van Galen, Michiel;
    • Wagner, Anja;
    • Letteboer, Tom G. W.;
    • Gómez-García, Encarna B.;
    • Tops, Carli M. J.;
    • Vasen, Hans F.;
    • Devilee, Peter;
    • Hes, Frederik J.;
    • Morreau, Hans;
    • Wijnen, Juul T.
    Publication type:
    Article
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    Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.

    Published in:
    2015
    By:
    • Yu, Willie;
    • McPherson, John R;
    • Stevenson, Mark;
    • van Eijk, Ronald;
    • Heng, Hong Lee;
    • Newey, Paul;
    • Gan, Anna;
    • Ruano, Dina;
    • Huang, Dachuan;
    • Poon, Song Ling;
    • Ong, Choon Kiat;
    • van Wezel, Tom;
    • Cavaco, Branca;
    • Rozen, Steven G;
    • Tan, Patrick;
    • Teh, Bin T;
    • Thakker, Rajesh V;
    • Morreau, Hans
    Publication type:
    journal article
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    Loss of bone morphogenetic protein signaling in fibroblasts results in CXCL12-driven serrated polyp development.

    Published in:
    Journal of Gastroenterology, 2023, v. 58, n. 1, p. 25, doi. 10.1007/s00535-022-01928-x
    By:
    • Ouahoud, Sarah;
    • Westendorp, Barbara Florien;
    • Voorneveld, Philip Willen;
    • Abudukelimu, Subinuer;
    • Koelink, Pim Johan;
    • Pascual Garcia, Elena;
    • Buuren, Jessica Flora Isabella;
    • Harryvan, Tom Jacob;
    • Lenos, Kristiaan Jan;
    • van Wezel, Tom;
    • Offerhaus, Johan Arnold;
    • Fariña-Sarasqueta, Arantza;
    • Crobach, Stijn;
    • Slingerland, Marije;
    • Hardwick, James Christopher Henry;
    • Hawinkels, Lukas Jacobus Antonius Christiaan
    Publication type:
    Article
    28

    Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.

    Published in:
    International Journal of Cancer, 2013, v. 132, n. 7, p. 1556, doi. 10.1002/ijc.27843
    By:
    • Talseth‐Palmer, Bente A.;
    • Wijnen, Juul T.;
    • Brenne, Ingvild S.;
    • Jagmohan‐Changur, Shantie;
    • Barker, Daniel;
    • Ashton, Katie A.;
    • Tops, Carli M.;
    • Evans, Tiffany‐Jane;
    • McPhillips, Mary;
    • Groombridge, Claire;
    • Suchy, Janina;
    • Kurzawski, Grzegorz;
    • Spigelman, Allan;
    • Møller, Pål;
    • Morreau, Hans M.;
    • Van Wezel, Tom;
    • Lubinski, Jan;
    • Vasen, Hans F.A.;
    • Scott, Rodney J.
    Publication type:
    Article
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    Correspondence: SEMA4A variation and risk of colorectal cancer.

    Published in:
    Nature Communications, 2016, v. 7, n. 3, p. 10611, doi. 10.1038/ncomms10611
    By:
    • Kinnersley, Ben;
    • Chubb, Daniel;
    • Dobbins, Sara E.;
    • Frampton, Matthew;
    • Buch, Stephan;
    • Timofeeva, Maria N.;
    • Castellví-Bel, Sergi;
    • Farrington, Susan M.;
    • Forsti, Asta;
    • Hampe, Jochen;
    • Hemminki, Kari;
    • Hofstra, Robert M. W.;
    • Northwood, Emma;
    • Palles, Claire;
    • Pinheiro, Manuela;
    • Ruiz-Ponte, Clara;
    • Schafmayer, Clemens;
    • Teixeira, Manuel R.;
    • Westers, Helga;
    • van Wezel, Tom
    Publication type:
    Article
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    Multicenter In-House Evaluation of an Amplicon-Based Next−Generation Sequencing Panel for Comprehensive Molecular Profiling: Multicenter Evaluation of the OCA Plus Panel: E. Jantus-Lewintre et al.

    Published in:
    Molecular Diagnosis & Therapy, 2025, v. 29, n. 2, p. 249, doi. 10.1007/s40291-024-00766-2
    By:
    • Jantus-Lewintre, Eloisa;
    • Rappa, Alessandra;
    • Ruano, Dina;
    • van Egmond, Demi;
    • Gallach, Sandra;
    • Gozuyasli, Dilce;
    • Durães, Cecília;
    • Costa, José Luis;
    • Camps, Carlos;
    • Lacroix, Ludovic;
    • Kashofer, Karl;
    • van Wezel, Tom;
    • Barberis, Massimo
    Publication type:
    Article
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    Evaluation of BRCA1/2 testing rates in epithelial ovarian cancer patients: lessons learned from real-world clinical data.

    Published in:
    Familial Cancer, 2025, v. 24, n. 2, p. 1, doi. 10.1007/s10689-025-00467-7
    By:
    • Lanjouw, Lieke;
    • Kramer, Claire J. H.;
    • Elst, Arja ter;
    • de Bock, Geertruida H.;
    • Gaarenstroom, Katja N.;
    • Yigit, Refika;
    • Berger, Lieke P. V.;
    • van Asperen, Christi J.;
    • Commandeur-Jan, Sabrina Z.;
    • van der Hall, Dimas M. X.;
    • Jalving, Mathilde;
    • Kagie, Marjolein J.;
    • van der Stoep, Nienke;
    • van Wezel, Tom;
    • Mourits, Marian J. E.;
    • Bosse, Tjalling;
    • Bart, Joost
    Publication type:
    Article
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    Targeted next generation sequencing screening of Lynch syndrome in Tunisian population.

    Published in:
    Familial Cancer, 2019, v. 18, n. 3, p. 343, doi. 10.1007/s10689-019-00130-y
    By:
    • Ben Sghaier, Rihab;
    • Jansen, Anne Maria Lucia;
    • Bdioui, Ahlem;
    • Van Wezel, Tom;
    • ksiaa, Mehdi;
    • Elgolli, Lamia;
    • Ben Fatma, Leila;
    • Ben Ahmed, Slim;
    • Azzouz, Mohamed Msaddak;
    • Hellara, Olfa;
    • Elghali, Amine;
    • Darbel, Fathi;
    • Skandrani, Karim;
    • Mokkni, Moncef;
    • Gdissa, Ameni;
    • Ltaief, Rached;
    • Saad, Ali;
    • Hmila, Fahmi;
    • Gribaa, Moez;
    • Morreau, Hans
    Publication type:
    Article
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    SNP association study in PMS2-associated Lynch syndrome.

    Published in:
    Familial Cancer, 2018, v. 17, n. 4, p. 507, doi. 10.1007/s10689-017-0061-3
    By:
    • ten Broeke, Sanne W.;
    • Elsayed, Fadwa A.;
    • Pagan, Lisa;
    • Olderode-Berends, Maran J. W.;
    • Garcia, Encarna Gomez;
    • Gille, Hans J. P.;
    • van Hest, Liselot P.;
    • Letteboer, Tom G. W.;
    • van der Kolk, Lizet E.;
    • Mensenkamp, Arjen R.;
    • van Os, Theo A.;
    • Spruijt, Liesbeth;
    • Redeker, Bert J. W.;
    • Suerink, Manon;
    • Vos, Yvonne J.;
    • Wagner, Anja;
    • Wijnen, Juul T.;
    • Steyerberg, E. W.;
    • Tops, Carli M. J.;
    • van Wezel, Tom
    Publication type:
    Article
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    Genetic Stability of Driver Alterations in Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type and Their Relapses: A Rationale for the Use of Molecular-Based Methods for More Effective Disease Monitoring.

    Published in:
    Cancers, 2022, v. 14, n. 20, p. 5152, doi. 10.3390/cancers14205152
    By:
    • Schrader, Anne M. R.;
    • de Groen, Ruben A. L.;
    • Willemze, Rein;
    • Jansen, Patty M.;
    • Quint, Koen D.;
    • Cleven, Arjen H. G.;
    • van Wezel, Tom;
    • van Eijk, Ronald;
    • Ruano, Dina;
    • Veelken, J. H.;
    • Tensen, Cornelis P.;
    • Neelis, Karen J.;
    • Daniels, Laurien A.;
    • Hauben, Esther;
    • Woei-A-Jin, F. J. S. H.;
    • Busschots, A. M.;
    • Vermeer, Maarten H.;
    • Vermaat, Joost S. P.
    Publication type:
    Article
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