Literature DB >> 9762534

Multiplex genetic testing. The Council on Ethical and Judicial Affairs, American Medical Association.

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Abstract

As panels of multiple genetic tests become increasingly available, clinicians face new challenges in helping patients understand the nature of these tests. Diagnostic tests for conditions that inevitably lead to disease, "susceptibility" tests that reveal heightened risk of disease, and tests for carrier status raise different concerns about informed consent and pose different needs for counseling. Clinicians must understand the implications of different kinds of tests, and of different arrays of tests in multiple panels, if multiplex tests are to be used wisely in clinical practice.

Entities:  

Keywords:  American Medical Association; Genetics and Reproduction

Mesh:

Year:  1998        PMID: 9762534

Source DB:  PubMed          Journal:  Hastings Cent Rep        ISSN: 0093-0334            Impact factor:   2.683


  5 in total

1.  The ethics and impact on behaviour of knowledge about one's own genome. Interview by Judy Jones.

Authors:  M Levitt
Journal:  BMJ       Date:  1999-11-13

2.  Parents' attitudes toward pediatric genetic testing for common disease risk.

Authors:  Kenneth P Tercyak; Sharon Hensley Alford; Karen M Emmons; Isaac M Lipkus; Benjamin S Wilfond; Colleen M McBride
Journal:  Pediatrics       Date:  2011-04-18       Impact factor: 7.124

3.  Informed Choice in Direct-to-Consumer Genetic Testing for Alzheimer and Other Diseases: Lessons from Two Cases.

Authors:  Donna A Messner
Journal:  New Genet Soc       Date:  2011

4.  On averages and peaks: how do people integrate attitudes about multiple diseases to reach a decision about multiplex genetic testing?

Authors:  Shoshana Shiloh; Christopher H Wade; J Scott Roberts; Sharon Hensley Alford; Barbara B Biesecker
Journal:  Med Decis Making       Date:  2012-11-05       Impact factor: 2.583

5.  Cancer risk assessment using genetic panel testing: considerations for clinical application.

Authors:  Susan Hiraki; Erica S Rinella; Freya Schnabel; Ruth Oratz; Harry Ostrer
Journal:  J Genet Couns       Date:  2014-03-07       Impact factor: 2.537

  5 in total

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