Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Journal of medical genetics - 1 Feb 2014

Jervis Sarah, Song Honglin, Lee Andrew, Dicks Ed, Tyrer Jonathan, Harrington Patricia, Easton Douglas F, Jacobs Ian J, Pharoah Paul P D, Antoniou Antonis C

Abstract excerpt

BACKGROUND: Family history is one of the most important risk factors for epithelial ovarian cancer (EOC). Little is known, however, on how EOC familial relative risks (FRRs) vary by factors such as tumour subtype or the combined effects of common EOC susceptibility alleles. In addition, no data currently exist on the FRRs associated with EOC after exclusion of BRCA1 or BRCA2 mutation carriers. METHODS: EOC FRRs...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Genes, BRCA1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, BRCA2

Share to Neoplasms, Cystic, Mucinous, and Serous

Share to Ovarian Neoplasms

Share to Polymorphism, Single Nucleotide

Share to Young Adult

Source

Identifiers

PMID: 24277755
DOI: 10.1136/jmedgenet-2013-102015

Genes

BRCA1
BRCA2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Ovarian cancer familial relative risks by tumour subtypes and by known ovarian cancer genetic susceptibility variants.PMID 24277755Read ↗

Familial risk of epithelial ovarian cancer after accounting for gynaecological surgery: a population-based study.Semantic proximity Read ↗

Epithelial ovarian cancer risk: A review of the current genetic landscapeSemantic proximity Read ↗

Familial risks of ovarian cancer by age at diagnosis, proband type and histologySemantic proximity Read ↗

Genetic epidemiology of ovarian cancer and prospects for polygenic risk prediction.Semantic proximity Read ↗

Ovarian and breast cancer risks to women in families with two or more cases of ovarian cancer.Semantic proximity Read ↗

Long-term risk of cancer among the first-degree relatives of epithelial ovarian cancer patients: A cohort study with 48 years of follow up.Semantic proximity Read ↗

Familial relative risks for breast cancer by pathological subtype: a population-based cohort study.Semantic proximity Read ↗

A risk prediction algorithm for ovarian cancer incorporating BRCA1, BRCA2, common alleles and other familial effects.Semantic proximity Read ↗

Family history of breast cancer as a risk factor for ovarian cancer in a prospective study.Semantic proximity Read ↗

Ovarian cancer risk factors in relation to family history.Semantic proximity Read ↗

Breast and ovarian cancer in relatives of cancer patients, with and without BRCA mutations.Semantic proximity Read ↗

Role of common genetic variants in ovarian cancer susceptibility and outcome: progress to date from the Ovarian Cancer Association Consortium (OCAC).Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.