Publications by authors named "Ellen W Clayton"

27Publications

Health and kinship matter: Learning about direct-to-consumer genetic testing user experiences via online discussions.

PLoS One 2020 8;15(9):e0238644. Epub 2020 Sep 8.

Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0238644PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478842PMC
September 2020

From Ventilators to Vaccines: Reframing the Ethics of Resource Allocation.

Am J Bioeth 2020 07;20(7):W15-W16

Center for Biomedical Ethics and Society, Vanderbilt University Medical Center.

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http://dx.doi.org/10.1080/15265161.2020.1782530DOI Listing
July 2020

Balancing Expediency and Scientific Rigor in Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Development.

J Infect Dis 2020 06;222(2):180-182

Division of Pediatric Infectious Diseases, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

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http://dx.doi.org/10.1093/infdis/jiaa234DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239154PMC
June 2020

Patient perspectives on variant reclassification after cancer susceptibility testing.

Mol Genet Genomic Med 2020 Jul 24;8(7):e1275. Epub 2020 Apr 24.

Vanderbilt University School of Medicine, Nashville, TN, USA.

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http://dx.doi.org/10.1002/mgg3.1275DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336756PMC
July 2020

What Results Should Be Returned from Opportunistic Screening in Translational Research?

J Pers Med 2020 Mar 1;10(1). Epub 2020 Mar 1.

Center for Biomedical Ethics and Society, Vanderbilt University Medical Center, Nashville, TN 37235, USA.

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http://dx.doi.org/10.3390/jpm10010013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151595PMC
March 2020

Patients' willingness to reconsider cancer genetic testing after initially declining: Mention it again.

J Genet Couns 2020 02 25;29(1):18-24. Epub 2019 Sep 25.

Vanderbilt University School of Medicine, Nashville, TN, USA.

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http://dx.doi.org/10.1002/jgc4.1174DOI Listing
February 2020

A systematic literature review of individuals' perspectives on privacy and genetic information in the United States.

PLoS One 2018 31;13(10):e0204417. Epub 2018 Oct 31.

Center for Genetic Privacy & Identity in Community Settings, Vanderbilt University Medical Center, Nashville, TN, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0204417PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209148PMC
March 2019

Physicians' perspectives on receiving unsolicited genomic results.

Genet Med 2019 02 5;21(2):311-318. Epub 2018 Jul 5.

Vanderbilt University Medical Center, Nashville, Tennessee, USA.

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http://dx.doi.org/10.1038/s41436-018-0047-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294706PMC
February 2019

Response to Patryn and Zagaja.

Genet Med 2016 07 14;18(7):751. Epub 2016 Apr 14.

Division of Genetics and Genomics and The Manton Center for Orphan Diseases Research, Boston Children's Hospital, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1038/gim.2016.27DOI Listing
July 2016

Ethical, legal, and social implications of incorporating genomic information into electronic health records.

Genet Med 2013 Oct 12;15(10):810-6. Epub 2013 Sep 12.

Department of Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan, USA.

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http://dx.doi.org/10.1038/gim.2013.117DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926430PMC
October 2013

The role of distress in uptake and response to predisposition genetic testing: the BMPR2 experience.

Genet Test Mol Biomarkers 2012 Mar 15;16(3):203-9. Epub 2011 Nov 15.

Department of Human Services and Rehabilitation, Western Washington University, Bellingham, Washington 98225, USA.

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http://dx.doi.org/10.1089/gtmb.2011.0059DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306587PMC
March 2012

Two large-scale surveys on community attitudes toward an opt-out biobank.

Am J Med Genet A 2011 Dec 7;155A(12):2982-90. Epub 2011 Nov 7.

Center for Biomedical Ethics and Society, Vanderbilt University Medical Center, Nashville, Tennessee 37203, USA.

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http://dx.doi.org/10.1002/ajmg.a.34304DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3222722PMC
December 2011

Attitudes and beliefs of sports medicine providers to sickle cell trait screening of student athletes.

Clin J Sport Med 2011 Nov;21(6):480-5

Department of Medicine, University of Chicago, Chicago, Illinois 60637, USA.

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http://dx.doi.org/10.1097/JSM.0b013e31822e8634DOI Listing
November 2011

What patients and their relatives think about testing for BMPR2.

J Genet Couns 2008 Oct 13;17(5):452-8. Epub 2008 Sep 13.

Department of Human and Organizational Development, Vanderbilt University, Nashville, TN, USA.

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http://dx.doi.org/10.1007/s10897-008-9172-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3730255PMC
October 2008

Religion, conscience, and controversial clinical practices.

N Engl J Med 2007 May;356(18):1889-92; author reply 1889-92

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May 2007

Natural settings trials--improving the introduction of clinical genetic tests.

J Law Med Ethics 2004 ;32(1):106-10

Center for Genetics and Health Policy, Department of Pediatrics, Vanderbilt University School of Medicine, USA.

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http://dx.doi.org/10.1111/j.1748-720x.2004.tb00454.xDOI Listing
June 2004

Pharmacogenomics and children: meeting the ethical challenges.

Am J Pharmacogenomics 2003 ;3(6):399-404

Department of Pediatrics, Center for Genetics and Health Policy, Vanderbilt University, Nashville, Tennessee 37232-0165, USA.

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http://dx.doi.org/10.2165/00129785-200303060-00007DOI Listing
February 2004