1. 2019
  2. Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non-CDKN2A/CDK4 melanoma families

    Dutch Working Group for Clinical Oncogenetics, Potjer, T. P., Bollen, S., Grimbergen, A. J. E. M., van Doorn, R., Gruis, N. A., van Asperen, C. J., Hes, F. J. & van der Stoep, N., 15 May 2019, In : International Journal of Cancer. 144, 10, p. 2453-2464 12 p.

    Research output: Contribution to journalArticleResearchpeer-review

  3. Targetable Gene Fusions Identified in Radioactive Iodine-Refractory Advanced Thyroid Carcinoma

    van der Tuin, K., Ventayol, M., Corver, W., Khalifa, M., Ruano, D., Corssmit, E. P., Hes, F. J., Links, T. P., Smit, J., Plantinga, T. S., Kapiteijn, E., Van Wezel, T. & Morreau, H., 1 Apr 2019, In : European Journal of Endocrinology. 180, 4, p. 235-241 7 p.

    Research output: Contribution to journalArticleResearchpeer-review

  4. Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

    Grolleman, J. E., de Voer, R. M., Elsayed, F. A., Nielsen, M., Weren, R. D. A., Palles, C., Ligtenberg, M. J. L., Vos, J. R., Ten Broeke, S. W., de Miranda, N. F. C. C., Kuiper, R. A., Kamping, E. J., Jansen, E. A. M., Vink-Börger, M. E., Popp, I., Lang, A., Spier, I., Hüneburg, R., James, P. A., Li, N. & 33 othersStaninova, M., Lindsay, H., Cockburn, D., Spasic-Boskovic, O., Clendenning, M., Sweet, K., Capellá, G., Sjursen, W., Høberg-Vetti, H., Jongmans, M. C., Neveling, K., Geurts van Kessel, A., Morreau, H., Hes, F. J., Sijmons, R. H., Schackert, H. K., Ruiz-Ponte, C., Dymerska, D., Lubinski, J., Rivera, B., Foulkes, W. D., Tomlinson, I. P., Valle, L., Buchanan, D. D., Kenwrick, S., Adlard, J., Dimovski, A. J., Campbell, I. G., Aretz, S., Schindler, D., van Wezel, T., Hoogerbrugge, N. & Kuiper, R. P., 11 Feb 2019, In : Cancer Cell. 35, 2, p. 256-266.e5 11 p.

    Research output: Contribution to journalArticleResearchpeer-review

  5. Mathematical Models for Tumor Growth and the Reduction of Overtreatment

    Heesterman, B. L., Bokhorst, J-M., de Pont, L. M. H., Verbist, B. M., Bayley, J-P., van der Mey, A. G. L., Corssmit, E. P. M., Hes, F. J., van Benthem, P. P. G. & Jansen, J. C., Feb 2019, In : Journal of neurological surgery. Part B, Skull base. 80, 1, p. 72-78 7 p.

    Research output: Contribution to journalArticleResearchpeer-review

  6. Increased Mortality in SDHB but Not in SDHD Pathogenic Variant Carriers

    Rijken, J. A., van Hulsteijn, L. T., Dekkers, O. M., Niemeijer, N. D., Leemans, C. R., Eijkelenkamp, K., van der Horst-Schrivers, A. N. A., Kerstens, M. N., van Berkel, A., Timmers, H. J. L. M., Kunst, H. P. M., Bisschop, P. H. L. T., Dreijerink, K. M. A., van Dooren, M. F., Hes, F. J., Jansen, J. C., Corssmit, E. P. M. & Hensen, E. F., 17 Jan 2019, In : Cancers. 11, 1, 11 p., e103.

    Research output: Contribution to journalArticleResearchpeer-review

  7. 2018
  8. Cancer Risks for PMS2-Associated Lynch Syndrome

    Ten Broeke, S. W., van der Klift, H. M., Tops, C. M. J., Aretz, S., Bernstein, I., Buchanan, D. D., de la Chapelle, A., Capella, G., Clendenning, M., Engel, C., Gallinger, S., Gomez Garcia, E., Figueiredo, J. C., Haile, R., Hampel, H. L., Hopper, J. L., Hoogerbrugge, N., von Knebel Doeberitz, M., Le Marchand, L., Letteboer, T. G. W. & 28 othersJenkins, M. A., Lindblom, A., Lindor, N. M., Mensenkamp, A. R., Møller, P., Newcomb, P. A., van Os, T. A. M., Pearlman, R., Pineda, M., Rahner, N., Redeker, E. J. W., Olderode-Berends, M. J. W., Rosty, C., Schackert, H. K., Scott, R., Senter, L., Spruijt, L., Steinke-Lange, V., Suerink, M., Thibodeau, S., Vos, Y. J., Wagner, A., Winship, I., Hes, F. J., Vasen, H. F. A., Wijnen, J. T., Nielsen, M. & Win, A. K., 10 Oct 2018, In : Journal of Clinical Oncology. 36, 29, p. 2961-2968 8 p.

    Research output: Contribution to journalArticleResearchpeer-review

  9. CM-Score: a validated scoring system to predict CDKN2A germline mutations in melanoma families from Northern Europe

    Dutch Working Group for Clinical Oncogenetics, Oct 2018, In : Journal of Medical Genetics. 55, 10, p. 661-668 8 p.

    Research output: Contribution to journalArticleResearchpeer-review

  10. Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility

    Weren, R. D. A., van der Post, R. S., Vogelaar, I. P., van Krieken, J. H., Spruijt, L., Lubinski, J., Jakubowska, A., Teodorczyk, U., Aalfs, C. M., van Hest, L. P., Oliveira, C., Kamping, E. J., Schackert, H. K., Ranzani, G. N., Gómez García, E. B., Hes, F. J., Holinski-Feder, E., Genuardi, M., Ausems, M. G. E. M., Sijmons, R. H. & 6 othersWagner, A., van der Kolk, L. E., Cats, A., Bjørnevoll, I., Hoogerbrugge, N. & Ligtenberg, M. J. L., Oct 2018, In : Journal of Medical Genetics. 55, 10, p. 669-674 6 p.

    Research output: Contribution to journalArticleResearchpeer-review

  11. Clinical and Molecular Characteristics May Alter Treatment Strategies of Thyroid Malignancies in DICER1 Syndrome

    van der Tuin, K., de Kock, L., Kamping, E. J., Hannema, S. E., Pouwels, M-J. M., Niedziela, M., van Wezel, T., Hes, F. J., Jongmans, M. C., Foulkes, W. D. & Morreau, H., 26 Sep 2018, In : Journal of Clinical Endocrinology and Metabolism. 104, 2, p. 277-284 8 p.

    Research output: Contribution to journalArticleResearchpeer-review

  12. Clinical progression and metachronous paragangliomas in a large cohort of SDHD germline variant carriers

    Heesterman, B. L., de Pont, L. M. H., van der Mey, A. G., Bayley, J-P., Corssmit, E. P., Hes, F. J., Verbist, B. M., van Benthem, P. P. G. & Jansen, J. C., Sep 2018, In : European Journal of Human Genetics. 26, 9, p. 1339-1347 9 p.

    Research output: Contribution to journalArticleResearchpeer-review

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