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

Response to open peer commentaries on "Genomic inheritances: disclosing individual research results from whole-exome sequencing to deceased participants' relatives".

The American journal of bioethics : AJOB - 1 Jan 2012

Hull Sara Chandros, Chan Ben, Biesecker Leslie G, Berkman Benjamin E

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to Genetic Testing
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Truth Disclosure

Source

Open in PubMed Open full text

Identifiers

PMID: 23215942
DOI: 10.1080/15265161.2012.739836
PMCID: PMC4142508

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Response to open peer commentaries on "Genomic inheritances: disclosing individual research results from whole-exome sequencing to deceased participants' relatives".PMID 23215942Read ↗

Genomic inheritances: disclosing individual research results from whole-exome sequencing to deceased participants' relatives.Semantic proximity Read ↗

Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility.Semantic 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 ↗

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

Patients' views on incidental findings from clinical exome sequencingSemantic proximity Read ↗

Recommendations for returning genomic incidental findings? We need to talk!Semantic proximity Read ↗

Return of Results in Genomic Research Using Large-Scale or Whole Genome Sequencing: Toward a New NormalSemantic proximity Read ↗

Incidental Findings with Genomic Testing: Implications for Genetic Counseling PracticeSemantic proximity Read ↗

Research participants in NGS studies want to know about incidental findings.Semantic proximity Read ↗

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

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

Genetics. Genomic research and human subject privacy.Semantic proximity Read ↗

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