Familial Cancer, 1389-9600

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  1. 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 journalArticle

  2. 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 journalArticle

  3. The added value of PMS2 immunostaining in the diagnosis of hereditary nonpolyposis colorectal cancer.

    Britta Halvarsson, Annika Lindblom, Eva Rambech, Kristina Lagerstedt & Mef Nilbert, 2006, In : Familial Cancer. 5, 4, p. 353-358

    Research output: Contribution to journalArticle

  4. The added value of PMS2 staining for the diagnosis of hereditary nonpolyposis colorectal cancer

    Britta Halvarsson, Mef Nilbert, E. Rambech & A. Lindblom, 2006, In : Familial Cancer. 5, p. 353

    Research output: Contribution to journalArticle

  5. Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

    Anna Isinger Ekstrand, Christina Therkildsen, Inge Bernstein & Mef Nilbert, 2011, In : Familial Cancer. 10, p. 239-243

    Research output: Contribution to journalArticle

  6. 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 journalArticle

  7. 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 journalArticle

  8. 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 journalArticle

  9. 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 journalArticle

  10. Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum

    Mef Nilbert, Christina Therkildsen, Anja Nissen, Måns Åkerman & Inge Bernstein, 2009, In : Familial Cancer. 8, 3, p. 209-213

    Research output: Contribution to journalArticle

  11. Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study

    Helle Vendel Petersen, Mary Jane Esplen, Steen Ladelund, Inge Bernstein, Lone Sunde, Christina Carlsson & Mef Nilbert, 2011, In : Familial Cancer. 10, 4, p. 633-639

    Research output: Contribution to journalArticle

  12. 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 journalArticle

  13. 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 journalArticle