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

Next generation sequencing in psychiatric research: what study participants need to know about research findings.

The international journal of neuropsychopharmacology - 1 Oct 2013

Mathieu Ghislaine, Groisman Iris Jaitovich, Godard Beatrice

Abstract excerpt

The use of next generation sequencing (NGS) technologies in psychiatric genetics research and its potential to generate individual research results will likely have far reaching implications for predictive and diagnostic practices. The extent of this impact may not be easily understood by psychiatric research participants during the consent process. The traditional consent process for studies involving human...

Read the complete abstract on PubMed

Topics

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

Share to Biomedical Research
Share to Comprehension

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomics

Share to High-Throughput Nucleotide Sequencing

Share to Incidental Findings

Share to Informed Consent

Share to Mental Disorders

Share to Predictive Value of Tests

Source

Identifiers

PMID: 23725748
DOI: 10.1017/S1461145713000527

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

Next generation sequencing in psychiatric research: what study participants need to know about research findings.PMID 23725748Read ↗

Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next‐Generation Sequencing and Informed Consent in DiagnosticsSemantic proximity Read ↗

Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics researchSemantic proximity Read ↗

Ethical issues in medical-sequencing research: implications of genotype-phenotype studies for individuals and populations.Semantic proximity Read ↗

The Challenge of Informed Consent and Return of Results in Translational Genomics: Empirical Analysis and RecommendationsSemantic proximity Read ↗

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

Improved ethical guidance for the return of results from psychiatric genomics research.Semantic proximity Read ↗

Return of Results in Psychiatric Genetics Research: Perceptions of Best Practices in a Global Sample of Psychiatric Genetics ResearchersSemantic proximity Read ↗

Next-Generation Sequencing and the Return of Results.Semantic proximity Read ↗

A Closer Look at the Recommended Criteria for Disclosing Genetic Results: Perspectives of Medical Genetic Specialists, Genomic Researchers, and Institutional Review Board ChairsSemantic proximity Read ↗

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

Revealing the results of whole-genome sequencing and whole-exome sequencing in research and clinical investigations: some ethical issues: Table 1Semantic proximity Read ↗

Managing the ethical challenges of next-generation sequencing in genomic medicineSemantic proximity Read ↗

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