Works by Ligtenberg, Marjolijn J. L.

Results: 58
    1

    Comprehensive clinicopathological and genomic profiling of gallbladder cancer reveals actionable targets in half of patients.

    Published in:
    NPJ Precision Oncology, 2022, v. 6, n. 1, p. 1, doi. 10.1038/s41698-022-00327-y
    By:
    • de Bitter, Tessa J. J.;
    • de Reuver, Philip R.;
    • de Savornin Lohman, Elise A. J.;
    • Kroeze, Leonie I.;
    • Vink-Börger, Marianne E.;
    • van Vliet, Shannon;
    • Simmer, Femke;
    • von Rhein, Daniel;
    • Jansen, Erik A. M.;
    • Verheij, Joanne;
    • van Herpen, Carla M. L.;
    • Nagtegaal, Iris D.;
    • Ligtenberg, Marjolijn J. L.;
    • van der Post, Rachel S.
    Publication type:
    Article
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    Identification of Fusion Genes and Targets for Genetically Matched Therapies in a Large Cohort of Salivary Gland Cancer Patients.

    Published in:
    Cancers, 2022, v. 14, n. 17, p. 4156, doi. 10.3390/cancers14174156
    By:
    • Lassche, Gerben;
    • van Helvert, Sjoerd;
    • Eijkelenboom, Astrid;
    • Tjan, Martijn J. H.;
    • Jansen, Erik A. M.;
    • van Cleef, Patricia H. J.;
    • Verhaegh, Gerald W.;
    • Kamping, Eveline J.;
    • Grünberg, Katrien;
    • van Engen-van Grunsven, Adriana C. H.;
    • Ligtenberg, Marjolijn J. L.;
    • van Herpen, Carla M. L.
    Publication type:
    Article
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    Comprehensive Assessment of Incidence, Risk Factors, and Mechanisms of Impaired Medical and Psychosocial Health Outcomes among Adolescents and Young Adults with Cancer: Protocol of the Prospective Observational COMPRAYA Cohort Study.

    Published in:
    Cancers, 2021, v. 13, n. 10, p. 2348, doi. 10.3390/cancers13102348
    By:
    • Husson, Olga;
    • Ligtenberg, Marjolijn J. L.;
    • van de Poll-Franse, Lonneke V.;
    • Prins, Judith B.;
    • van den Bent, Martin J.;
    • van Eenbergen, Mies C.;
    • Fles, Renske;
    • Manten-Horst, Eveliene;
    • Gietema, Jourik A.;
    • van der Graaf, Winette T. A.;
    • Soffietti, Riccardo
    Publication type:
    Article
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    External Quality Assessment for KRAS Testing Is Needed: Setup of a European Program and Report of the First Joined Regional Quality Assessment Rounds.

    Published in:
    Oncologist, 2011, v. 16, n. 4, p. 467, doi. 10.1634/theoncologist.2010-0429
    By:
    • BELLON, ELLEN;
    • LIGTENBERG, MARJOLIJN J. L.;
    • TEJPAR, SABINE;
    • COX, KAREN;
    • DE HERTOGH, GERT;
    • DE STRICKER, KARIN;
    • EDSJÖ, ANDERS;
    • GORGOULIS, VASSILIS;
    • HÖFLER, GERALD;
    • JUNG, ANDREAS;
    • KOTSINAS, ATHANASSIOS;
    • LAURENT-PUIG, PIERRE;
    • LÓPEZ-RÍOS, FERNANDO;
    • HANSEN, TINE PLATO;
    • ROULEAU, ETIENNE;
    • VANDENBERGHE, PETER;
    • VAN KRIEKEN, JOHAN J. M.;
    • DEQUEKER, ELISABETH
    Publication type:
    Article
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    Micro-costing diagnostics in oncology: from single-gene testing to whole- genome sequencing.

    Published in:
    2021
    By:
    • Pasmans, Clémence T. B.;
    • Tops, Bastiaan B. J.;
    • Steeghs, Elisabeth M. P.;
    • Coupé, Veerle M. H.;
    • Grünberg, Katrien;
    • de Jong, Eiko K;
    • Schuuring, Ed M. D.;
    • Willems, Stefan M.;
    • Ligtenberg, Marjolijn J. l.;
    • Retèl, Valesca P.;
    • van Snellenberg, Hans;
    • de Bruijn, Ewart;
    • Cuppen, Edwin;
    • Frederix, Geert W. J.;
    • Pasmans, Clémence Tb;
    • Tops, Bastiaan Bj;
    • Steeghs, Elisabeth Mp;
    • Coupé, Veerle Mh;
    • Schuuring, Ed Md;
    • Ligtenberg, Marjolijn Jl
    Publication type:
    journal article
    19

    Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 112, doi. 10.1038/ng.283
    By:
    • Ligtenberg, Marjolijn J. L.;
    • Kuiper, Roland P.;
    • Tsun Leung Chan;
    • Goossens, Monique;
    • Hebeda, Konnie M.;
    • Voorendt, Marsha;
    • Lee, Tracy Y. H.;
    • Bodmer, Danielle;
    • Hoenselaar, Eveline;
    • Hendriks-Cornelissen, Sandra J. B.;
    • Wai Yin Tsui;
    • Chi Kwan Kong;
    • Brunner, Han G.;
    • van Kessel, Ad Geurts;
    • Siu Tsan Yuen;
    • van Krieken, J Han J. M.;
    • Leung, Suet Yi;
    • Hoogerbrugge, Nicoline
    Publication type:
    Article
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    Impact of DNA damage repair defects and aggressive variant features on response to carboplatin‐based chemotherapy in metastatic castration‐resistant prostate cancer.

    Published in:
    International Journal of Cancer, 2021, v. 148, n. 2, p. 385, doi. 10.1002/ijc.33306
    By:
    • Slootbeek, Peter H. J.;
    • Duizer, Marleen L.;
    • Doelen, Maarten J.;
    • Kloots, Iris S. H.;
    • Kuppen, Malou C. P.;
    • Westgeest, Hans M.;
    • Uyl‐de Groot, Carin A.;
    • Pamidimarri Naga, Samhita;
    • Ligtenberg, Marjolijn J. L.;
    • Oort, Inge M.;
    • Gerritsen, Winald R.;
    • Schalken, Jack A.;
    • Kroeze, Leonie I.;
    • Bloemendal, Haiko J.;
    • Mehra, Niven
    Publication type:
    Article
    22

    Evaluation of yield and experiences of age‐related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch syndrome.

    Published in:
    International Journal of Cancer, 2020, v. 147, n. 8, p. 2150, doi. 10.1002/ijc.33117
    By:
    • Vos, Janet R.;
    • Fakkert, Ingrid E.;
    • Spruijt, Liesbeth;
    • Willems, Riki W.;
    • Langenveld, Sera;
    • Mensenkamp, Arjen R.;
    • Leter, Edward M.;
    • Nagtegaal, Iris D.;
    • Ligtenberg, Marjolijn J. L.;
    • Hoogerbrugge, Nicoline
    Publication type:
    Article
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    An evaluation of the challenges to developing tumor BRCA1 and BRCA2 testing methodologies for clinical practice.

    Published in:
    Human Mutation, 2018, v. 39, n. 3, p. 394, doi. 10.1002/humu.23375
    By:
    • Ellison, Gillian;
    • Ahdesmäki, Miika;
    • Luke, Sally;
    • Waring, Paul M.;
    • Wallace, Andrew;
    • Wright, Ronnie;
    • Röthlisberger, Benno;
    • Ludin, Katja;
    • Merkelbach‐Bruse, Sabine;
    • Heydt, Carina;
    • Ligtenberg, Marjolijn J. L.;
    • Mensenkamp, Arjen R.;
    • de Castro, David Gonzalez;
    • Jones, Thomas;
    • Vivancos, Ana;
    • Kondrashova, Olga;
    • Pauwels, Patrick;
    • Weyn, Christine;
    • Hahnen, Eric;
    • Hauke, Jan
    Publication type:
    Article
    27

    Two intronic mutations in the adrenoleukodystrophy gene.

    Published in:
    Human Mutation, 1995, v. 6, n. 3, p. 272, doi. 10.1002/humu.1380060316
    By:
    • Kemp, Stephan;
    • Ligtenberg, Marjolijn J. L.;
    • van Geel, Björn M.;
    • Barth, Peter G.;
    • Sarde, Claude-Olivier;
    • van Oost, Bernard A.;
    • Bolhuis, Pieter A.
    Publication type:
    Article
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    Noonan syndrome, the SOS1 gene and embryonal rhabdomyosarcoma.

    Published in:
    Genes, Chromosomes & Cancer, 2010, v. 49, n. 7, p. 635, doi. 10.1002/gcc.20773
    By:
    • Jongmans, Marjolijn C. J.;
    • Hoogerbrugge, Peter M.;
    • Hilkens, Linda;
    • Flucke, Uta;
    • van der Burgt, Ineke;
    • Noordam, Kees;
    • Ruiterkamp-Versteeg, Martina;
    • Yntema, Helger G.;
    • Nillesen, Willy M.;
    • Ligtenberg, Marjolijn J. L.;
    • van Kessel, Ad Geurts;
    • Kuiper, Roland P.;
    • Hoogerbrugge, Nicoline
    Publication type:
    Article
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    Implementation of Novel Molecular Biomarkers for Non-small Cell Lung Cancer in the Netherlands: How to Deal With Increasing Complexity.

    Published in:
    Frontiers in Oncology, 2020, v. 9, p. 1, doi. 10.3389/fonc.2019.01521
    By:
    • van den Broek, Daan;
    • Hiltermann, T. Jeroen N.;
    • Biesma, Bonne;
    • Dinjens, Winand N. M.;
    • 't Hart, Nils A.;
    • Hinrichs, John W. J.;
    • Leers, Mathie P. G.;
    • Monkhorst, Kim;
    • van Oosterhout, Matthijs;
    • Scharnhorst, Volkher;
    • Schuuring, Ed;
    • Speel, Ernst-Jan M.;
    • van den Heuvel, Michel M.;
    • van Schaik, Ron H. N.;
    • von der Thüsen, Jan;
    • Willems, Stefan M.;
    • de Visser, Leonie;
    • Ligtenberg, Marjolijn J. L.
    Publication type:
    Article
    42

    Implementation of Novel Molecular Biomarkers for Non-small Cell Lung Cancer in the Netherlands: How to Deal With Increasing Complexity.

    Published in:
    Frontiers in Oncology, 2020, v. 10, p. 1, doi. 10.3389/fonc.2019.01521
    By:
    • van den Broek, Daan;
    • Hiltermann, T. Jeroen N.;
    • Biesma, Bonne;
    • Dinjens, Winand N. M.;
    • 't Hart, Nils A.;
    • Hinrichs, John W. J.;
    • Leers, Mathie P. G.;
    • Monkhorst, Kim;
    • van Oosterhout, Matthijs;
    • Scharnhorst, Volkher;
    • Schuuring, Ed;
    • Speel, Ernst-Jan M.;
    • van den Heuvel, Michel M.;
    • van Schaik, Ron H. N.;
    • von der Thüsen, Jan;
    • Willems, Stefan M.;
    • de Visser, Leonie;
    • Ligtenberg, Marjolijn J. L.
    Publication type:
    Article
    43

    Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation.

    Published in:
    European Journal of Human Genetics, 2011, v. 19, n. 8, p. 870, doi. 10.1038/ejhg.2011.37
    By:
    • Jongmans, Marjolijn C. J.;
    • van der Burgt, Ineke;
    • Hoogerbrugge, Peter M.;
    • Noordam, Kees;
    • Yntema, Helger G.;
    • Nillesen, Willy M.;
    • Kuiper, Roland P.;
    • Ligtenberg, Marjolijn J. L.;
    • van Kessel, Ad Geurts;
    • van Krieken, J. Han J. M.;
    • Kiemeney, Lambertus A. L. M.;
    • Hoogerbrugge, Nicoline
    Publication type:
    Article
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    Genome sequencing as a generic diagnostic strategy for rare disease.

    Published in:
    Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01301-y
    By:
    • Schobers, Gaby;
    • Derks, Ronny;
    • den Ouden, Amber;
    • Swinkels, Hilde;
    • van Reeuwijk, Jeroen;
    • Bosgoed, Ermanno;
    • Lugtenberg, Dorien;
    • Sun, Su Ming;
    • Corominas Galbany, Jordi;
    • Weiss, Marjan;
    • Blok, Marinus J.;
    • Olde Keizer, Richelle A. C. M.;
    • Hofste, Tom;
    • Hellebrekers, Debby;
    • de Leeuw, Nicole;
    • Stegmann, Alexander;
    • Kamsteeg, Erik-Jan;
    • Paulussen, Aimee D. C.;
    • Ligtenberg, Marjolijn J. L.;
    • Bradley, Xiangqun Zheng
    Publication type:
    Article
    47

    Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility.

    Published in:
    PLoS Genetics, 2016, v. 12, n. 2, p. 1, doi. 10.1371/journal.pgen.1005880
    By:
    • de Voer, Richarda M.;
    • Hahn, Marc-Manuel;
    • Weren, Robbert D. A.;
    • Mensenkamp, Arjen R.;
    • Gilissen, Christian;
    • van Zelst-Stams, Wendy A.;
    • Spruijt, Liesbeth;
    • Kets, C. Marleen;
    • Zhang, Junxiao;
    • Venselaar, Hanka;
    • Vreede, Lilian;
    • Schubert, Nil;
    • Tychon, Marloes;
    • Derks, Ronny;
    • Schackert, Hans K.;
    • Geurts van Kessel, Ad;
    • Hoogerbrugge, Nicoline;
    • Ligtenberg, Marjolijn J. L.;
    • Kuiper, Roland P.
    Publication type:
    Article
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    A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.

    Published in:
    Nature Genetics, 2015, v. 47, n. 6, p. 668, doi. 10.1038/ng.3287
    By:
    • Weren, Robbert D A;
    • Kets, C Marleen;
    • de Voer, Richarda M;
    • Verwiel, Eugène T P;
    • Spruijt, Liesbeth;
    • van Zelst-Stams, Wendy A G;
    • Jongmans, Marjolijn C;
    • Gilissen, Christian;
    • Hehir-Kwa, Jayne Y;
    • Hoischen, Alexander;
    • Kamping, Eveline J;
    • Geurts van Kessel, Ad;
    • Kuiper, Roland P;
    • Hoogerbrugge, Nicoline;
    • Ligtenberg, Marjolijn J L;
    • Shendure, Jay;
    • Boyle, Evan A;
    • Nagtegaal, Iris D;
    • Tops, Bastiaan B J;
    • van Krieken, J Han J M
    Publication type:
    Article
    50

    Development of a semi-conductor sequencing-based panel for genotyping of colon and lung cancer by the Onconetwork consortium.

    Published in:
    BMC Cancer, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12885-015-1015-5
    By:
    • Tops, Bastiaan B. J.;
    • Normanno, Nicola;
    • Kurth, Henriette;
    • Amato, Eliana;
    • Mafficini, Andrea;
    • Rieber, Nora;
    • Le Corre, Delphine;
    • Rachiglio, Anna Maria;
    • Reiman, Anne;
    • Sheils, Orla;
    • Noppen, Christoph;
    • Lacroix, Ludovic;
    • Cree, Ian A.;
    • Scarpa, Aldo;
    • Ligtenberg, Marjolijn J. L.;
    • Laurent-Puig, Pierre
    Publication type:
    Article