Works by Vasen, Hans F.A.


Results: 13
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    Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of lynch syndrome patients.

    Published in:
    Human Mutation, 2010, v. 31, n. 5, p. 578, doi. 10.1002/humu.21229
    By:
    • van der Klift, Heleen M.;
    • Tops, Carli M.J.;
    • Bik, Elsa C.;
    • Boogaard, Merel W.;
    • Borgstein, Anne-Marijke;
    • Hansson, Kerstin B.M.;
    • Ausems, Margreet G.E.M.;
    • Garcia, Encarna Gomez;
    • Green, Andrew;
    • Hes, Frederik J.;
    • Izatt, Louise;
    • van Hest, Liselotte P.;
    • Alonso, Angel M.;
    • Vriends, Annette H.J.T.;
    • Wagner, Anja;
    • van Zelst-Stams, Wendy A.G.;
    • Vasen, Hans F.A.;
    • Morreau, Hans;
    • Devilee, Peter;
    • Wijnen, Juul T.
    Publication type:
    Article
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    Revised Bethesda Guidelines for Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) and Microsatellite Instability.

    Published in:
    JNCI: Journal of the National Cancer Institute, 2004, v. 96, n. 4, p. 261, doi. 10.1093/jnci/djh034
    By:
    • Umar, Asad;
    • Boland, C. Richard;
    • Terdiman, Jonathan P.;
    • Syngal, Sapna;
    • de la Chapelle, Albert;
    • Rüschoff, Josef;
    • Fishel, Richard;
    • Lindor, Noralane M.;
    • Burgart, Lawrence J.;
    • Hamelin, Richard;
    • Hamilton, Stanley R.;
    • Hiatt, Robert A.;
    • Jass, Jeremy;
    • Lindblom, Annika;
    • Lynch, Henry T.;
    • Peltomaki, Païvi;
    • Ramsey, Scott D.;
    • Rodriguez-Bigas, Miguel A.;
    • Vasen, Hans F.A.
    Publication type:
    Article
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    Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: A prospective analysis.

    Published in:
    International Journal of Cancer, 2015, v. 136, n. 3, p. 668, doi. 10.1002/ijc.29032
    By:
    • Heemskerk‐Gerritsen, Bernadette A.M.;
    • Rookus, Matti A.;
    • Aalfs, Cora M.;
    • Ausems, Margreet G.E.M.;
    • Collée, Johanna M.;
    • Jansen, Liesbeth;
    • Kets, C. Marleen;
    • Keymeulen, Kristien B.M.I.;
    • Koppert, Linetta B.;
    • Meijers‐Heijboer, Hanne E.J.;
    • Mooij, Thea M.;
    • Tollenaar, Rob A.E.M.;
    • Vasen, Hans F.A.;
    • HEBON;
    • Hooning, Maartje J.;
    • Seynaeve, Caroline
    Publication type:
    Article
    10

    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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