Skip to main content

and
  1. Article

    Open Access

    Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

    Previous studies have demonstrated that common breast cancer susceptibility alleles are differentially associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. It is currently unknown how thes...

    Anna Marie Mulligan, Fergus J Couch, Daniel Barrowdale in Breast Cancer Research (2011)

  2. Article

    Open Access

    The Angelina Jolie effect: how high celebrity profile can have a major impact on provision of cancer related services

    It is frequent for news items to lead to a short lived temporary increase in interest in a particular health related service, however it is rare for this to have a long lasting effect. In 2013, in the UK in pa...

    D Gareth R Evans, Julian Barwell, Diana M Eccles, Amanda Collins in Breast Cancer Research (2014)

  3. Article

    Open Access

    Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

    More than 70 common alleles are known to be involved in breast cancer (BC) susceptibility, and several exhibit significant heterogeneity in their associations with different BC subtypes. Although there are dif...

    Karoline B Kuchenbaecker, Susan L Neuhausen, Mark Robson in Breast Cancer Research (2014)

  4. Article

    Open Access

    An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

    Individuals carrying pathogenic mutations in the BRCA1 and BRCA2 genes have a high lifetime risk of breast cancer. BRCA1 and BRCA2 are involved in DNA double-strand break repair, DNA alterations that can be cause...

    Sophie Blein, Claire Bardel, Vincent Danjean, Lesley McGuffog in Breast Cancer Research (2015)

  5. Article

    Open Access

    Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

    Prostate-specific antigen (PSA) and PSA-velocity (PSAV) have been used to identify men at risk of prostate cancer (PrCa). The IMPACT study is evaluating PSA screening in men with a known genetic predisposition...

    Christos Mikropoulos, Christina G Hutten Selkirk, Sibel Saya in British Journal of Cancer (2018)

  6. Article

    Open Access

    Erratum: Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

    Correction to: British Journal of Cancer (2018) 118, 266–276; doi:10.1038/bjc.2017.429; published online 04 January 2018 The authors would like to acknowledge the following information for this manuscript: Chr...

    Christos Mikropoulos, Christina G Hutten Selkirk, Sibel Saya in British Journal of Cancer (2018)

  7. Article

    Open Access

    Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

    Height and body mass index (BMI) are associated with higher ovarian cancer risk in the general population, but whether such associations exist among BRCA1/2 mutation carriers is unknown.

    Frank Qian, Matti A. Rookus, Goska Leslie, Harvey A. Risch in British Journal of Cancer (2019)

  8. Article

    Open Access

    The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

    Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic variants in DNA repair genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 are associated with breast cancer risk. FANCM, whic...

    Gisella Figlioli, Massimo Bogliolo, Irene Catucci, Laura Caleca in npj Breast Cancer (2019)

  9. Article

    Open Access

    Evaluation of tumour surveillance protocols and outcomes in von Hippel-Lindau disease in a national health service

    Von Hippel-Lindau (VHL) disease is an inherited tumour predisposition syndrome and a paradigm for the importance of early diagnosis and surveillance. However, there is limited information on the “real world” m...

    Eamonn R. Maher, Julian Adlard, Julian Barwell in British Journal of Cancer (2022)