Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG)

scientific article published on 22 December 2018

Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG) is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/S41436-018-0391-Z
P698PubMed publication ID30578420

P50authorDavid T. MillerQ91603806
P2093author name stringJoshua L Deignan
Reed E Pyeritz
Jodi D Hoffman
James O'Leary
Robert G Best
Ingrid Holm
David Flannery
ACMG Social Ethical Legal Issues Committee
Karen L David
Leslie Manace Brenman
Lynn Bush
P2860cites workPerformance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research ConsortiumQ28601251
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular PathologyQ34465792
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and GenomicsQ34544874
Managing the ethical challenges of next-generation sequencing in genomic medicineQ38239811
HIPAA's Individual Right of Access to Genomic Data: Reconciling Safety and Civil RightsQ47198411
Duty to re-contact.Q53492995
Points to consider in the clinical application of genomic sequencingQ84730858
The coming explosion in genetic testing--is there a duty to recontact?Q85087734
P433issue4
P921main subjectgenomicsQ222046
medical geneticsQ1071953
P304page(s)769-771
P577publication date2018-12-22
P1433published inGenetics in MedicineQ15765508
P1476titlePatient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG)
P478volume21

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cites work (P2860)
Q92738841A duty to recontact in genetics: context matters
Q90438987A pediatric perspective on genomics and prevention in the twenty-first century
Q94671482CFTR variant testing: a technical standard of the American College of Medical Genetics and Genomics (ACMG)
Q99402854Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis
Q90103411Preemptively Precise: Returning and Updating Pharmacogenetic Test Results to Realize the Benefits of Preemptive Testing
Q91731430Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes
Q93012834Response to Knoppers et al

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