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

Missed opportunities: Genetic counseling and testing among an ethnically diverse cohort of women with endometrial cancer.

Gynecologic oncology - 1 Oct 2018

Lee Jessica, Gubernick Lindsay R, Brodsky Allison L, Fehniger Julia E, Levine Douglas A, Gerber Deanna, Asgari Shabnam A, Cantor Anna, Martineau Jessica T, Ginsburg Ophira M, Smith Julia A, Pothuri Bhavana

Abstract excerpt

OBJECTIVES: Lynch syndrome (LS) accounts for the majority of inherited endometrial cancers (EC), and the identification of probands presents a unique opportunity to treat and prevent multiple cancers. The diagnosis of EC can provide the indication for women with specific risk factors to undergo genetic testing (GT). We sought to evaluate genetic counseling referrals (GCR) and subsequent GT rates in an ethnically...

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers, Tumor
Share to Colorectal Neoplasms, Hereditary Nonpolyposis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mismatch Repair

Share to Early Detection of Cancer

Share to Endometrial Neoplasms

Share to Genetic Counseling

Share to Predictive Value of Tests

Share to Referral and Consultation

Source

Identifiers

PMID: 30077346
DOI: 10.1016/j.ygyno.2018.07.023

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

Missed opportunities: Genetic counseling and testing among an ethnically diverse cohort of women with endometrial cancer.PMID 30077346Read ↗

Missing a chance to prevent: disparities in completion of genetic evaluation in high-risk patients with endometrial cancer.Semantic proximity Read ↗

Lost opportunities for mismatch repair (MMR) screening among minority women with endometrial cancer.Semantic proximity Read ↗

Clinicopathologic characteristics and outcomes of endometrial Cancer patients with mismatch repair deficiency in the era of universal Lynch syndrome screening.Semantic proximity Read ↗

Clinicopathologic features of endometrial cancer with mismatch repair deficiencySemantic proximity Read ↗

Pathogenic germline variants in patients with endometrial cancer of diverse ancestrySemantic proximity Read ↗

Updates in gynecologic care for individuals with lynch syndromeSemantic proximity Read ↗

Current and future role of genetic screening in gynecologic malignancies.Semantic proximity Read ↗

Genetic Susceptibility to Endometrial Cancer: Risk Factors and Clinical ManagementSemantic proximity Read ↗

Comparison of screening strategies for Lynch syndrome in patients with newly diagnosed endometrial cancer: a prospective cohort study in ChinaSemantic proximity Read ↗

An Analysis of Clinical, Surgical, Pathological and Molecular Characteristics of Endometrial Cancer According to Mismatch Repair Status. A Multidisciplinary Approach.Semantic proximity Read ↗

How Should We Test for Lynch Syndrome? A Review of Current Guidelines and Future StrategiesSemantic proximity Read ↗

Mismatch Repair Universal Screening of Endometrial Cancers (MUSE) in a Canadian CohortSemantic proximity Read ↗

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