Brca1 Mutation Risk

BRCA1 Mutation Risk is a genetic risk assessment construct that quantifies the increased susceptibility to breast and ovarian cancers conferred by pathogenic variants in the BRCA1 tumor suppressor gene, distinguishing it from other hereditary cancer risks by its specific association with BRCA1 gene dysfunction.

759

Publications

70.6K

Citations

6.4K

Authors

1.7K

Institutions

Publications per year

2017–2026

135

Authors

6.4K

  1. SA
    Steven A. Narod

    University of Toronto, Canada

    76 publications · 9.5K citations

    44

    h-index

  2. JL
    Jan Lubiński

    Pomeranian Medical University, Poland

    80 publications · 6.8K citations

    43

    h-index

  3. SL
    Susan L. Neuhausen

    City of Hope, United States

    53 publications · 7.3K citations

    39

    h-index

  4. DF
    Douglas F. Easton

    University of Cambridge, United Kingdom

    53 publications · 8K citations

    38

    h-index

  5. DG
    D. Gareth Evans

    University of Manchester, United Kingdom

    50 publications · 6.6K citations

    33

    h-index

1–5 of 6.4K

Venues

  1. Breast Cancer Research and Treatment

    64 publications · 3K citations

    36

    h-index

  2. Journal of Clinical Oncology

    35 publications · 7.3K citations

    31

    h-index

  3. PubMed

    Repository · 34 publications · 4.8K citations

    23

    h-index

  4. JNCI Journal of the National Cancer Institute

    25 publications · 7.6K citations

    23

    h-index

  5. British Journal of Cancer

    BJC · 26 publications · 2.4K citations

    22

    h-index

1–5