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November 25, 2013Journal of Medical Genetics

Ovarian cancer familial relative risks by tumour subtypes and by known ovarian cancer genetic susceptibility variants

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Abstract

These estimates could be useful in the counselling of relatives of patients with ovarian cancer.

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Cite This Study

Jervis et al. (2013) studied this question.

synapsesocial.com/papers/69de5f89bf539e227055874e https://doi.org/10.1136/jmedgenet-2013-102015

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Breast and Ovarian Cancer in Relatives of Cancer Patients, with and without BRCA MutationsOriginal Research · 2006 · 40 citations
2Tagging Single Nucleotide Polymorphisms in the BRIP1 Gene and Susceptibility to Breast and Ovarian CancerGWAS · 2007 · 60 citations
3RAD51C Germline Mutations in Breast and Ovarian Cancer Cases from High-Risk FamiliesOriginal Research · 2011 · 72 citations
4Ovarian cancer among 8005 women from a breast cancer family history clinic: no increased risk of invasive ovarian cancer in families testing negative for <i>BRCA1</i> and <i>BRCA2</i>Cohort Study · 2013 · 24 citations
5Cancer mortality in relatives of women with ovarian cancer: The OPCS studyCohort Study · 1996 · 125 citations