Familial Cancer, 1389-9600
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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. 183-191Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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. 31-41Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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. 195-203Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer
Martin P. Nilsson, Christof Winter, Ulf Kristoffersson, Martin Rehn, Christer Larsson, Lao H. Saal & Niklas Loman, 2017 apr, I: Familial Cancer. 16, 2, s. 187-193Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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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. 523–528Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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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. 507-512Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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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. 579-585Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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. 145-155Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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. 173-185Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift