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

Genetic Variants in Patients With a Family History of Pancreatic Cancer: Impact of Multigene Panel Testing.

Pancreas - 1 Apr 2021

Zhu Huili, Welinsky Sara, Soper Emily R, Brown Karen L, Abul-Husn Noura S, Lucas Aimee L

Abstract excerpt

OBJECTIVES: Up to 15% of pancreatic cancer is hereditary. We aim to study the prevalence of pathogenic germline variants (PGVs) in patients referred for genetic counseling with a family history (FH) of pancreatic cancer. METHODS: We performed a retrospective single institution cohort study of individuals who underwent cancer genetic counseling with a FH of pancreatic cancer. RESULTS: We identified 314 patients....

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Aged, 80 and over
Share to Biomarkers, Tumor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Genetic Testing

Share to Germ-Line Mutation

Share to Pancreatic Neoplasms

Share to Risk Factors

Source

Identifiers

PMID: 33939675
DOI: 10.1097/MPA.0000000000001804

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic Variants in Patients With a Family History of Pancreatic Cancer: Impact of Multigene Panel Testing.PMID 33939675Read ↗

The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.Semantic proximity Read ↗

Multigene Hereditary Cancer Panels Reveal High-Risk Pancreatic Cancer Susceptibility GenesSemantic proximity Read ↗

Discovering Hereditary Risk Through Surveillance: A Prospective Genetic Analysis of Individuals With Familial Pancreatic Cancer.Semantic proximity Read ↗

Impact of changing guidelines on genetic testing and surveillance recommendations in a contemporary cohort of breast cancer survivors with family history of pancreatic cancer.Semantic proximity Read ↗

Clinical Impact of Pathogenic Germline Variants in Pancreatic Cancer: Results From a Multicenter, Prospective, Universal Genetic Testing Study.Semantic proximity Read ↗

Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients.Semantic proximity Read ↗

Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer.Semantic proximity Read ↗

Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer.Semantic proximity Read ↗

Prospective study of germline genetic testing in incident cases of pancreatic adenocarcinoma.Semantic proximity Read ↗

Familial Pancreatic Cancer: A Critical Review.Semantic proximity Read ↗

Germline Testing for Individuals with Pancreatic Adenocarcinoma and Novel Genetic Risk Factors.Semantic proximity Read ↗

Universal Panel Testing of Pancreatic Cancer Cases for Cancer PredispositionSemantic proximity Read ↗

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