Familial Cancer, 1389-9600

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  1. 2019

  2. Risk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predisposition

    Lars J. Lindberg, Wia Wegen-Haitsma, Steen Ladelund, Lars Smith-Hansen, Christina Therkildsen, Inge Bernstein & Mef Nilbert, 2019, In : Familial Cancer. 18, 2, p. 183-191

    Research output: Contribution to journal › Article

  3. 2018

  4. Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries

    Anne Brédart, Jean Luc Kop, Antonis C. Antoniou, Alex P. Cunningham, Antoine de Pauw, Marc Tischkowitz, Hans Ehrencrona, Sylvie Dolbeault, Léonore Robieux, Kerstin Rhiem, Douglas F. Easton, Peter Devilee, Dominique Stoppa-Lyonnet & Rita Schmutlzer, 2018, In : Familial Cancer. 17, 1, p. 31-41

    Research output: Contribution to journal › Article

  5. 2017

  7. Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing

    Anna Rohlin, Eva Rambech, Anders Kvist, Therese Törngren, Frida Eiengård, Ulf Lundstam, Theofanis Zagoras, Samuel Gebre-Medhin, Åke Borg, Jan Björk, Mef Nilbert & Margareta Nordling, 2017 Apr, In : Familial Cancer. 16, 2, p. 195-203

    Research output: Contribution to journal › Article

  8. 2016

  9. No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families.

    Henriette Roed Nielsen, Janne Petersen, Lotte Krogh, Mef Nilbert & Anne-Bine Skytte, 2016 Oct, In : Familial Cancer. 15, 4, p. 523–528

    Research output: Contribution to journal › Article

  10. BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.

    Henriette Roed Nielsen, Mef Nilbert, Janne Petersen, Steen Ladelund, Mads Thomassen, Inge Søkilde Pedersen, Thomas V O Hansen, Anne-Bine Skytte, Åke Borg & Christina Therkildsen, 2016, In : Familial Cancer. 15, 4, p. 507-512

    Research output: Contribution to journal › Article

  11. 2014

  12. Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome.

    Jenny-Maria Jönsson, Katarina Bartuma, Mev Dominguez, Katja Harbst, Zohreh Ketabi, Susanne Malander, Mats Jönsson, Ana Carneiro, Anna Måsbäck, Göran B Jönsson & Mef Nilbert, 2014, In : Familial Cancer. 13, 4, p. 537-545 9 p.

    Research output: Contribution to journal › Article

  13. 2012

  14. Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation

    Christina Therkildsen, Anna Isinger-Ekstrand, Steen Ladelund, Anja Nissen, Eva Rambech, Inge Bernstein & Mef Nilbert, 2012, In : Familial Cancer. 11, 4, p. 579-585

    Research output: Contribution to journal › Article

  16. 2011

  17. Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals

    Mev Dominguez, Felipe Carneiro da Silva, Erika Maria Monteiro dos Santos, Bianca Garcia Lisboa, Ligia Petrolini de Oliveira, Fabio de Oliveira Ferreira, Israel Gomy, Wilson Toshihiko Nakagawa, Samuel Aguiar Junior, Mariana Redal, Carlos Vaccaro, Adriana Della Valle, Carlos Sarroca, Dirce Maria Carraro & Benedito Mauro Rossi, 2011, In : Familial Cancer. 10, 4, p. 641-647

    Research output: Contribution to journal › Article

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