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

Acceptability of, and Information Needs Regarding, Next-Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study.

Journal of genetic counseling - 1 Apr 2016

Meiser Bettina, Storey Ben, Quinn Veronica, Rahman Belinda, Andrews Lesley

Abstract excerpt

Next generation sequencing (NGS) for patients at risk of hereditary cancer syndromes can also identify non-cancer related mutations, as well as variants of unknown significance. This study aimed to determine what benefits and shortcomings patients perceive in relation to NGS, as well as their interest and information preferences in regards to such testing. Eligible patients had previously received inconclusive...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Counseling
Share to High-Throughput Nucleotide Sequencing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Informed Consent

Share to Neoplastic Syndromes, Hereditary

Share to Patient Acceptance of Health Care

Share to Patient Satisfaction

Share to Qualitative Research

Share to Risk Assessment

Source

Identifiers

PMID: 26259529
DOI: 10.1007/s10897-015-9861-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Acceptability of, and Information Needs Regarding, Next-Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study.PMID 26259529Read ↗

Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview studySemantic proximity Read ↗

Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines.Semantic proximity Read ↗

Experiences with obtaining informed consent for genomic sequencingSemantic proximity Read ↗

“Is It Worth Knowing?” Focus Group Participants’ Perceived Utility of Genomic Preconception Carrier ScreeningSemantic proximity Read ↗

Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patientsSemantic proximity Read ↗

Evaluation of laboratory perspectives on hereditary cancer panels.Semantic proximity Read ↗

"Would you test your children without their consent?" and other sticky dilemmas in the field of cancer genetic testing.Semantic proximity Read ↗

Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care.Semantic proximity Read ↗

Informed consent for exome sequencing research in families with genetic disease: The emerging issue of incidental findingsSemantic proximity Read ↗

Genomic Sequencing in Pediatric Oncology: Perspectives of Parents and Adolescents on Ethical IssuesSemantic proximity Read ↗

Old Challenges or New Issues? Genetic Health Professionals' Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing.Semantic proximity Read ↗

The Experiences and Needs of Individuals with a Variant of Uncertain Significance on Genetic Tests for Hereditary Cancer Syndromes:A Grounded Theory Study.Semantic proximity Read ↗

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