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  1. Article

    Open Access

    Matched analysis of circulating selenium with the breast cancer selenotranscriptome: a multicentre prospective study

    Low serum selenium and altered tumour RNA expression of certain selenoproteins are associated with a poor breast cancer prognosis. Selenoprotein expression stringently depends on selenium availability, hence c...

    Kamil Demircan, Ylva Bengtsson, Thilo Samson Chillon in Journal of Translational Medicine (2023)

  2. Article

    Open Access

    Author Correction: Validation of the BOADICEA model for predicting the likelihood of carrying pathogenic variants in eight breast and ovarian cancer susceptibility genes

    Nanna Bæk Møller, Desirée Sofie Boonen, Elisabeth Simone Feldner in Scientific Reports (2023)

  3. Article

    Open Access

    Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer

    Genetic screening for pathogenic variants (PVs) in cancer predisposition genes can affect treatment strategies, risk prediction and preventive measures for patients and families. For decades, hereditary breast...

    Anna Öfverholm, Therese Törngren, Anna Rosén, Brita Arver, Zakaria Einbeigi in BMC Cancer (2023)

  4. Article

    Open Access

    Obesity-associated changes in molecular biology of primary breast cancer

    Obesity is associated with an increased risk of develo** breast cancer (BC) and worse prognosis in BC patients, yet its impact on BC biology remains understudied in humans. This study investigates how the bi...

    Ha-Linh Nguyen, Tatjana Geukens, Marion Maetens, Samuel Aparicio in Nature Communications (2023)

  5. Article

    Open Access

    Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

    The distribution of ovarian tumour characteristics differs between germline BRCA1 and BRCA2 pathogenic variant carriers and non-carriers. In this study, we assessed the utility of ovarian tumour characteristics a...

    Denise G. O’Mahony, Susan J. Ramus, Melissa C. Southey in British Journal of Cancer (2023)

  6. Article

    Open Access

    Validation of the BOADICEA model for predicting the likelihood of carrying pathogenic variants in eight breast and ovarian cancer susceptibility genes

    BOADICEA is a comprehensive risk prediction model for breast and/or ovarian cancer (BC/OC) and for carrying pathogenic variants (PVs) in cancer susceptibility genes. In addition to BRCA1 and BRCA2, BOADICEA versi...

    Nanna Bæk Møller, Desirée Sofie Boonen, Elisabeth Simone Feldner in Scientific Reports (2023)

  7. Article

    Open Access

    Molecular characteristics of breast tumors in patients screened for germline predisposition from a population-based observational study

    Pathogenic germline variants (PGVs) in certain genes are linked to higher lifetime risk of develo** breast cancer and can influence preventive surgery decisions and therapy choices. Public health programs of...

    Deborah F. Nacer, Johan Vallon-Christersson, Nicklas Nordborg in Genome Medicine (2023)

  8. Article

    Open Access

    RNA sequencing-based single sample predictors of molecular subtype and risk of recurrence for clinical assessment of early-stage breast cancer

    Multigene assays for molecular subtypes and biomarkers can aid management of early invasive breast cancer. Using RNA-sequencing we aimed to develop single-sample predictor (SSP) models for clinical markers, su...

    Johan Staaf, Jari Häkkinen, Cecilia Hegardt, Lao H. Saal in npj Breast Cancer (2022)

  9. Article

    Open Access

    Spatial deconvolution of HER2-positive breast cancer delineates tumor-associated cell type interactions

    In the past decades, transcriptomic studies have revolutionized cancer treatment and diagnosis. However, tumor sequencing strategies typically result in loss of spatial information, critical to understand cell...

    Alma Andersson, Ludvig Larsson, Linnea Stenbeck, Fredrik Salmén in Nature Communications (2021)

  10. Article

    Open Access

    A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients

    The risk of breast cancer associated with CHEK2:c.1100delC is 2–threefold but higher in carriers with a family history of breast cancer than without, suggesting that other genetic loci in combination with CHEK2:c...

    Camilla Wendt, Taru A. Muranen, Lotta Mielikäinen in Scientific Reports (2021)

  11. Article

    Open Access

    Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

    A Correction to this paper has been published: https://doi.org/10.1038/s41467-021-23162-4

    Juliette Coignard, Michael Lush, Jonathan Beesley, Tracy A. O’Mara in Nature Communications (2021)

  12. Article

    Open Access

    Correction to: Molecular analyses of triple-negative breast cancer in the young and elderly

    An amendment to this paper has been published and can be accessed via the original article.

    Mattias Aine, Ceren Boyaci, Johan Hartman, Jari Häkkinen in Breast Cancer Research (2021)

  13. Article

    Open Access

    Distinct mechanisms of resistance to fulvestrant treatment dictate level of ER independence and selective response to CDK inhibitors in metastatic breast cancer

    Resistance to endocrine treatment in metastatic breast cancer is a major clinical challenge. Clinical tools to predict both drug resistance and possible treatment combination approaches to overcome it are lack...

    Kamila Kaminska, Nina Akrap, Johan Staaf, Carla L. Alves in Breast Cancer Research (2021)

  14. Article

    Open Access

    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

    Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial factors. About 50 common variants have been shown to modify BC risk for mutation carriers. All but three, were identifi...

    Juliette Coignard, Michael Lush, Jonathan Beesley, Tracy A. O’Mara in Nature Communications (2021)

  15. Article

    Open Access

    Molecular analyses of triple-negative breast cancer in the young and elderly

    Breast cancer in young adults has been implicated with a worse outcome. Analyses of genomic traits associated with age have been heterogenous, likely because of an incomplete accounting for underlying molecula...

    Mattias Aine, Ceren Boyaci, Johan Hartman, Jari Häkkinen in Breast Cancer Research (2021)

  16. Article

    Open Access

    The spatial RNA integrity number assay for in situ evaluation of transcriptome quality

    The RNA integrity number (RIN) is a frequently used quality metric to assess the completeness of rRNA, as a proxy for the corresponding mRNA in a tissue. Current methods operate at bulk resolution and provide ...

    Linda Kvastad, Konstantin Carlberg, Ludvig Larsson in Communications Biology (2021)

  17. Article

    Open Access

    Breast cancer survival in Nordic BRCA2 mutation carriers—unconventional association with oestrogen receptor status

    The natural history of breast cancer among BRCA2 carriers has not been clearly established. In a previous study from Iceland, positive ER status was a negative prognostic factor. We sought to identify factors tha...

    Elinborg J. Olafsdottir, Ake Borg, Maj-Britt Jensen in British Journal of Cancer (2020)

  18. No Access

    Article

    Integrating spatial gene expression and breast tumour morphology via deep learning

    Spatial transcriptomics allows for the measurement of RNA abundance at a high spatial resolution, making it possible to systematically link the morphology of cellular neighbourhoods and spatially localized gen...

    Bryan He, Ludvig Bergenstråhle, Linnea Stenbeck in Nature Biomedical Engineering (2020)

  19. Article

    Open Access

    Comprehensive molecular comparison of BRCA1 hypermethylated and BRCA1 mutated triple negative breast cancers

    Homologous recombination deficiency (HRD) is a defining characteristic in BRCA-deficient breast tumors caused by genetic or epigenetic alterations in key pathway genes. We investigated the frequency of BRCA1 prom...

    Dominik Glodzik, Ana Bosch, Johan Hartman, Mattias Aine in Nature Communications (2020)

  20. Article

    Open Access

    Prognostic implications of the expression levels of different immunoglobulin heavy chain-encoding RNAs in early breast cancer

    The extent and composition of the immune response in a breast cancer is one important prognostic factor for the disease. The aim of the current work was to refine the analysis of the humoral component of an im...

    Christer Larsson, Anna Ehinger, Sofia Winslow, Karin Leandersson in npj Breast Cancer (2020)

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