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

Inherited Cancer Susceptibility Gene Sequence Variations Among Patients With Appendix Cancer

11 Nov 2022

Abstract excerpt

Importance: Germline sequence variations in APC, BMPR1A, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, PMS2, PTEN, SMAD4, STK11, and TP53 genes are associated with susceptibility to gastrointestinal cancers. As a rare cancer, the evaluation of appendiceal cancer (AC) predisposition has been limited. Objective: To assess the prevalence and spectrum of inherited cancer susceptibility gene sequence variations in...

Read the complete abstract on PubMed

Topics

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

Share to Gastric Cancer Management and Outcomes
Share to Ovarian cancer diagnosis and treatment

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 36368039
DOI: 10.1001/jamaoncol.2022.5425

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inherited Cancer Susceptibility Gene Sequence Variations Among Patients With Appendix CancerPMID 36368039Read ↗

Investigation of Hereditary Cancer Predisposition Genes of Patients with Colorectal Cancer: Single-centre Experience.Semantic proximity Read ↗

The Impact of Germline Alterations in Appendiceal Adenocarcinoma.Semantic proximity Read ↗

Analysis of germline genetic variants that cause hereditary colorectal cancer in bahiaSemantic proximity Read ↗

The guidelines for clinical practice for carriers of germline mutations in the Lynch syndrome predisposition genes MLH1, MSH2, MSH6, PMS2 and large deletions of EPCAM (4.2024).Semantic proximity Read ↗

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.Semantic proximity Read ↗

Genetic/Familial High-Risk Assessment: Colorectal, Endometrial, and Gastric, Version 3.2024, NCCN Clinical Practice Guidelines In Oncology.Semantic proximity Read ↗

Genetic Landscape of Lynch Syndrome in a High-Risk Serbian Cohort: Predominance of MLH1 Variants and Implications for Risk-Based Testing.Semantic proximity Read ↗

Prevalence of Pathogenic Germline Variants in Patients With Gastric Cancer Ascertained Through Multigene Panel TestingSemantic proximity Read ↗

Genetic testing for inherited colorectal cancer and polyposis, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).Semantic proximity Read ↗

Germline susceptibility variants impact clinical outcome and therapeutic strategies for stage III colorectal cancerSemantic proximity Read ↗

Targeted sequencing of 36 known or putative colorectal cancer susceptibility genesSemantic proximity Read ↗

Germline Genetic Features of Young Individuals With Colorectal Cancer.Semantic proximity Read ↗

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