Leila Jamal, Jill O. Robinson, Kurt D. Christensen, Jennifer Blumenthal-Barby, Melody J. Slashinski, Denise Lautenbach Perry, Jason L. Vassy, Julia Wycliff, Robert C. Green & Amy L. McGuire
Ajob Empirical Bioethics 8 (2):82-88 (2017)
AbstractThis article has no associated abstract. (fix it)
Added to PP
Historical graph of downloads
References found in this work
No references found.
Citations of this work
Trust and the Ethical Challenges in the Use of Whole Genome Sequencing for Tuberculosis Surveillance: A Qualitative Study of Stakeholder Perspectives.Carly Jackson, Jennifer L. Gardy, Hedieh C. Shadiloo & Diego S. Silva - 2019 - BMC Medical Ethics 20 (1):43.
Understanding Variations in Secondary Findings Reporting Practices Across U.S. Genome Sequencing Laboratories.Sara L. Ackerman & Barbara A. Koenig - 2018 - Ajob Empirical Bioethics 9 (1):48-57.
Similar books and articles
On the Justifiability of ACMG Recommendations for Reporting of Incidental Findings in Clinical Exome and Genome Sequencing.Thomas May - 2015 - Journal of Law, Medicine and Ethics 43 (1):134-142.
Ethical and Legal Implications of Whole Genome and Whole Exome Sequencing in African Populations.Galen Wright, Pieter Koornhof, Adebowale Adeyemo & Nicki Tiffin - 2013 - BMC Medical Ethics 14 (1):21.
The $1000 Genome: Ethical and Legal Issues in Whole Genome Sequencing of Individuals. [REVIEW]John A. Robertson - 2003 - American Journal of Bioethics 3 (3):35-42.
The Elusive Ideal of Inclusiveness: Lessons From a Worldwide Survey of Neurologists on the Ethical Issues Raised by Whole-Genome Sequencing.Thierry Hurlimann, Iris Jaitovich Groisman & Béatrice Godard - 2017 - BMC Medical Ethics 18 (1):28.
Whole-Genome Sequencing and Disability in the NICU: Exploring Practical and Ethical Challenges.Michael J. Deem - 2016 - Pediatrics 137 (s1):S47-S55.
Understanding Culture and Culture Management in the English NHS: A Comparison of Professional and Patient Perspectives.Frederick H. Konteh, Russell Mannion & Huw T. O. Davies - 2011 - Journal of Evaluation in Clinical Practice 17 (1):111-117.
Social Networkers' Attitudes Toward Direct-to-Consumer Personal Genome Testing.Amy McGuire, Christina Diaz, Tao Wang & Susan Hilsenbeck - 2009 - American Journal of Bioethics 9 (6-7):3-10.
Whole Genome Sequencing of Children’s DNA for Research: Points to Consider.Kristien Hens - 2011 - Journal of Clinical Research and Bioethics 2 (7).
The Role of Whole Genome and Whole Exome Sequencing in Preventive Genomic Sequencing Programs.Gabrielle Bertier, Ma'N. H. Zawati & Yann Joly - 2015 - American Journal of Bioethics 15 (7):22-24.
The Role of Patients in Clinical Ethics Support: A Snapshot of Practices and Attitudes in the United Kingdom.Ainsley J. Newson - 2009 - Clinical Ethics 4 (3):139-145.
Privacy Issues in Clinical Genomic Medicine, or Marcus Welby, M.D., Meets the $1000 Genome. [REVIEW]Sheri Alpert - 2008 - Cambridge Quarterly of Healthcare Ethics 17 (4):373-384.
Ethical Challenges in Integrating Patient-Care with Clinical Research in a Resource-Limited Setting: Perspectives From Papua New Guinea. [REVIEW]Moses Laman, William Pomat, Peter Siba & Inoni Betuela - 2013 - BMC Medical Ethics 14 (1):29.
Parents Perspectives on Whole Genome Sequencing for Their Children: Qualified Enthusiasm?J. A. Anderson, M. S. Meyn, C. Shuman, R. Zlotnik Shaul, L. E. Mantella, M. J. Szego, S. Bowdin, N. Monfared & R. Z. Hayeems - 2017 - Journal of Medical Ethics 43 (8):535-539.
Consent to Clinical Research--Adequately Voluntary or Substantially Influenced?S. Hewlett - 1996 - Journal of Medical Ethics 22 (4):232-237.
A Philosophical Analysis of Informed Consent for Whole Genome Sequencing in Biobank Research by Use of Beauchamp and Childress’ Four Principles of Biomedical Ethics.Ebbesen M. & Sundby A. - 2015 - Journal of Clinical Research and Bioethics 6 (6).