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

Changing patterns of referral into a family history clinic and detection of ovarian cancer: a retrospective 10-year review.

Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology - 1 Oct 2022

Smallwood K G, Crockett S, Huang V, Cullimore V, Davies J, Satti G, Phillips A

Abstract excerpt

This study examines whether a change in the criteria for genetic testing for ovarian cancer risk changed the nature of referrals into our Familial Cancer service. This is a retrospective review of 273 women who underwent risk reducing surgery (RRS). The primary outcome was to establish whether there was an increase in women having RRS with a confirmed genetic mutation. Secondary outcomes included the incidence of...

Read the complete abstract on PubMed

Topics

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

Share to Genes, BRCA1
Share to Genes, BRCA2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genetic Testing

Share to Mutation

Share to Ovarian Neoplasms

Share to Referral and Consultation

Source

Identifiers

PMID: 35980980
DOI: 10.1080/01443615.2022.2111253

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Changing patterns of referral into a family history clinic and detection of ovarian cancer: a retrospective 10-year review.PMID 35980980Read ↗

Genetic risk assessment for women with epithelial ovarian cancer: referral patterns and outcomes in a university gynecologic oncology clinic.Semantic proximity Read ↗

Changing patterns of referrals and outcomes of genetic participation in gynaecological-oncology multidisciplinary care.Semantic proximity Read ↗

Outcome of preventive surgery and screening for breast and ovarian cancer in BRCA mutation carriers.Semantic proximity Read ↗

Cancer family history triage: a key step in the decision to offer screening and genetic testing.Semantic proximity Read ↗

Evaluation of questionnaire on cancer family history in identifying patients at increased genetic risk in general practice.Semantic proximity Read ↗

Prophylactic oophorectomy rates in relation to a guideline update on referral to genetic counseling.Semantic proximity Read ↗

Improving referral for genetic risk assessment in ovarian cancer using an electronic medical record system.Semantic proximity Read ↗

Referral of Ovarian Cancer Patients for Genetic Counselling by Oncologists: Need for Improvement.Semantic proximity Read ↗

Prevalence of family history of breast and ovarian cancer in a single primary care practice using a self-administered questionnaire.Semantic proximity Read ↗

Characteristics associated with genetic counseling referral and BRCA1/2 testing among women in a large integrated health system.Semantic proximity Read ↗

In the wake of Angelina - managing a family history of breast cancer.Semantic proximity Read ↗

Changes in specialists' perspectives on cancer genetic testing, prophylactic surgery and insurance discrimination: then and now.Semantic proximity Read ↗

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