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Ellen Wright Clayton

Biographic Data

ID6083109
NAMEEllen Wright Clayton
GIVEN NAMESEllen Wright
FAMILY NAMEClayton
SIGNATURECLAYTON E W
AFFILIATIONSVanderbilt University
ORCID0000-0002-0308-4110
VERIFIEDYes
TOTAL WORKS8
TOTAL CITATIONS1
WORKS AS AUTHOR8
WORKS AS EDITOR0
FIRST PUBLICATION YEAR1995
LATEST PUBLICATION YEAR2021
H-INDEX1
  • Ethical issues in genetics and infectious diseases research

    Open Access•Alexis Walker, Vence L Bonham et al.•ARTICLE•Ethics Medicine and Public Health•2021

  • Commercial Interests, the Technological Imperative, and Advocates

    Open Access•Stacey Pereira, Ellen Wright Clayton•ARTICLE•The Hastings Center Report•2018

    While the NSIGHT program was driven by a desire to define and gather data about both the benefits and harms of introducing genomic sequencing into the care of newborns, it remains to be seen how much influence these data will have in shaping the use of this technology in newborns. Ultimately, three additional forces—commercial interests, the technological imperative, and advocates—may play a significant role in shaping the use of sequencing in ne…

  • Protecting Life While Preserving Liberty

    Open Access•Lindsey C McKernan, Ellen Wright Clayton et al.•ARTICLE•Frontiers in Psychiatry•2018

    In the United States, suicide increased by 24% in the past 20 years, and suicide risk identification at point-of-care remains a cornerstone of the effort to curb this epidemic (1). As risk identification is difficult because of symptom under-reporting, timing, or lack of screening, healthcare systems rely increasingly on risk scoring and now artificial intelligence (AI) to assess risk. AI remains the science of solving problems and accomplishing …

  • Clinical and Ethical Considerations in Managing Carrier Detection

    Lainie Friedman Ross, Ellen Wright Clayton•ARTICLE•American Journal of Public Health•2009•Cited by: 1•References: 6

    letter

  • So What Are We Going to Do about Research Using Clinical Information and Samples

    Ellen Wright Clayton•ARTICLE•IRB Ethics and Human Research•2004

  • The International HapMap Project

    Open Access•Richard A Gibbs, John W Belmont et al.•ARTICLE•Nature•2003

    The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. An international consortium is developing a map of these patterns across the genome by determining the genotypes of one million or more sequence variants, their frequencies and the degree of association between them, in DNA samples from populations with a…

  • Case Study

    Ellen Wright Clayton, Eric Kodish•ARTICLE•The Hastings Center Report•1999

    Baby Aaron was brought to the children's hospital emergency department at three months of age. His parents, members of the Amish community, told the ER doctor that the baby seemed to be having trouble breathing and was not growing well. After examining the baby, the physician was suspicious of congestive heart failure. An echocardiogram demonstrated significant congenital heart disease. A pediatric cardiologist was consulted. She informed the par…

  • The Dispersion of Genetic Technologies and the Law

    Ellen Wright Clayton•ARTICLE•The Hastings Center Report•1995

    http://dx.doi.org/10.2307/3562124

  • Clinical and Ethical Considerations in Managing Carrier Detection

    Lainie Friedman Ross, Ellen Wright Clayton•ARTICLE•American Journal of Public Health•2009•Cited by: 1•References: 6

    letter

  • The Dispersion of Genetic Technologies and the Law

    Ellen Wright Clayton•ARTICLE•The Hastings Center Report•1995

    http://dx.doi.org/10.2307/3562124

  • Case Study

    Ellen Wright Clayton, Eric Kodish•ARTICLE•The Hastings Center Report•1999

    Baby Aaron was brought to the children's hospital emergency department at three months of age. His parents, members of the Amish community, told the ER doctor that the baby seemed to be having trouble breathing and was not growing well. After examining the baby, the physician was suspicious of congestive heart failure. An echocardiogram demonstrated significant congenital heart disease. A pediatric cardiologist was consulted. She informed the par…

  • The International HapMap Project

    Open Access•Richard A Gibbs, John W Belmont et al.•ARTICLE•Nature•2003

    The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. An international consortium is developing a map of these patterns across the genome by determining the genotypes of one million or more sequence variants, their frequencies and the degree of association between them, in DNA samples from populations with a…

  • So What Are We Going to Do about Research Using Clinical Information and Samples

    Ellen Wright Clayton•ARTICLE•IRB Ethics and Human Research•2004

  • Clinical and Ethical Considerations in Managing Carrier Detection

    Lainie Friedman Ross, Ellen Wright Clayton•ARTICLE•American Journal of Public Health•2009•Cited by: 1•References: 6

    letter

  • Commercial Interests, the Technological Imperative, and Advocates

    Open Access•Stacey Pereira, Ellen Wright Clayton•ARTICLE•The Hastings Center Report•2018

    While the NSIGHT program was driven by a desire to define and gather data about both the benefits and harms of introducing genomic sequencing into the care of newborns, it remains to be seen how much influence these data will have in shaping the use of this technology in newborns. Ultimately, three additional forces—commercial interests, the technological imperative, and advocates—may play a significant role in shaping the use of sequencing in ne…

  • Protecting Life While Preserving Liberty

    Open Access•Lindsey C McKernan, Ellen Wright Clayton et al.•ARTICLE•Frontiers in Psychiatry•2018

    In the United States, suicide increased by 24% in the past 20 years, and suicide risk identification at point-of-care remains a cornerstone of the effort to curb this epidemic (1). As risk identification is difficult because of symptom under-reporting, timing, or lack of screening, healthcare systems rely increasingly on risk scoring and now artificial intelligence (AI) to assess risk. AI remains the science of solving problems and accomplishing …

  • Ethical issues in genetics and infectious diseases research

    Open Access•Alexis Walker, Vence L Bonham et al.•ARTICLE•Ethics Medicine and Public Health•2021

Medicine (4 works) · Biology (3 works) · Computer Science (3 works) · Genomics and Rare Diseases (3 works) · Political science (3 works) · Psychology (3 works) · Engineering (2 works) · Engineering ethics (2 works) · Genetics (2 works) · Genome (2 works)

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