Familial Cancer, 1389-9600

Tidskrift

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  1. Artikel i vetenskaplig tidskrift
  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, I : Familial Cancer. 18, 2, s. 183-191

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. 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, I : Familial Cancer. 17, 1, s. 31-41

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. 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, I : Familial Cancer. 16, 2, s. 195-203

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. 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 okt, I : Familial Cancer. 15, 4, s. 523–528

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. 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, I : Familial Cancer. 15, 4, s. 507-512

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. 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, I : Familial Cancer. 13, 4, s. 537-545 9 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. 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, I : Familial Cancer. 11, 4, s. 579-585

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients.

    Susanne Magnusson, Thomas Wiebe, Ulf Kristoffersson, Helena Jernström & Håkan Olsson, 2012, I : Familial Cancer. 11, s. 145-155

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer

    Maria Henningson, Maria Hietala, Therese Törngren, Håkan Olsson & Helena Jernström, 2011, I : Familial Cancer. 10, 2, s. 173-185

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. 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, I : Familial Cancer. 10, 4, s. 641-647

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. 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, I : Familial Cancer. 10, 4, s. 633-639

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. Can a phenotype for recessive inheritance in breast cancer be defined?

    Carolina Ellberg, Göran B Jönsson & Håkan Olsson, 2010, I : Familial Cancer. 9, 4, s. 525-530

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer.

    Anna Isinger Ekstrand, Mats Jönsson, Annika Lindblom, Åke Borg & Mef Nilbert, 2010, I : Familial Cancer. 9, s. 125-129

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  17. Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.

    Susanne Magnusson, Åke Borg, Ulf Kristoffersson, Mef Nilbert, Thomas Wiebe & Håkan Olsson, 2008, I : Familial Cancer. 7, s. 331-337

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. Absence of the common IGF1 19 CA-repeat allele is more common among BRCA1 mutation carriers than among non-carriers from BRCA1 families.

    Maria Henningson, Erika Bågeman, Therese Törngren, Åke Borg, Håkan Olsson & Helena Jernström, 2007, I : Familial Cancer. 6, 4, s. 445-452

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  19. 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, I : Familial Cancer. 5, 4, s. 353-358

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift