Gail E Henderson

Summary

Affiliation: University of North Carolina
Country: USA

Publications

  1. pmc Clinical trials and medical care: defining the therapeutic misconception
    Gail E Henderson
    University of North Carolina at ChapelHill, Chapel Hill, North Carolina, United Statesof America
    PLoS Med 4:e324. 2007
  2. doi request reprint Is informed consent broken?
    Gail E Henderson
    Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, 333 South Columbia Street, Rm 347 MacNider, Chapel Hill, NC 2799 7240, USA
    Am J Med Sci 342:267-72. 2011
  3. ncbi request reprint Therapeutic misconception in early phase gene transfer trials
    Gail E Henderson
    School of Medicine, University of NC at Chapel Hill, CB 7240, Chapel Hill, NC 27599 7240, USA
    Soc Sci Med 62:239-53. 2006
  4. ncbi request reprint Uncertain benefit: investigators' views and communications in early phase gene transfer trials
    Gail E Henderson
    Department of Social Medicine, University of North Carolina School of Medicine, Chapel Hill, NC 27599 7240, USA
    Mol Ther 10:225-31. 2004
  5. doi request reprint Great expectations: views of genetic research participants regarding current and future genetic studies
    Gail Henderson
    Department of Social Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599 7240, USA
    Genet Med 10:193-200. 2008
  6. ncbi request reprint Consent forms and the therapeutic misconception: the example of gene transfer research
    Nancy M P King
    University of North Carolina at Chapel Hill, USA
    IRB 27:1-8. 2005
  7. ncbi request reprint Confidentiality: more than a linkage file and a locked drawer
    Michele M Easter
    Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, USA
    IRB 26:13-7. 2004
  8. ncbi request reprint The many meanings of care in clinical research
    Michele M Easter
    Department of Social Medicine, University of North Carolina at Chapel Hill, NC 27499 7240, USA
    Sociol Health Illn 28:695-712. 2006
  9. ncbi request reprint What research ethics should learn from genomics and society research: lessons from the ELSI Congress of 2011
    Gail E Henderson
    Department of Social Medicine, School of Medicine, Center for Genomics and Society, University of North Carolina Chapel Hill, Chapel Hill, NC, USA
    J Law Med Ethics 40:1008-24. 2012
  10. ncbi request reprint Vulnerability to influence: a two-way street
    Gail E Henderson
    University of North Carolina School of Medicine, USA
    Am J Bioeth 4:50-2; discussion W32. 2004

Detail Information

Publications20

  1. pmc Clinical trials and medical care: defining the therapeutic misconception
    Gail E Henderson
    University of North Carolina at ChapelHill, Chapel Hill, North Carolina, United Statesof America
    PLoS Med 4:e324. 2007
  2. doi request reprint Is informed consent broken?
    Gail E Henderson
    Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, 333 South Columbia Street, Rm 347 MacNider, Chapel Hill, NC 2799 7240, USA
    Am J Med Sci 342:267-72. 2011
    ..Because more research is conducted under these new conditions, the very nature of the researcher-subject relationship is shifting and will require new governance mechanisms to promote the original goals of informed consent...
  3. ncbi request reprint Therapeutic misconception in early phase gene transfer trials
    Gail E Henderson
    School of Medicine, University of NC at Chapel Hill, CB 7240, Chapel Hill, NC 27599 7240, USA
    Soc Sci Med 62:239-53. 2006
    ..We hope that this work will deepen the discussion of how to define and measure TM, and refine the specification of factors that are related to subjects' TM...
  4. ncbi request reprint Uncertain benefit: investigators' views and communications in early phase gene transfer trials
    Gail E Henderson
    Department of Social Medicine, University of North Carolina School of Medicine, Chapel Hill, NC 27599 7240, USA
    Mol Ther 10:225-31. 2004
    ..This dilemma cannot be effectively addressed by individual investigators alone, but must be acknowledged and openly discussed by the scientific community at large...
  5. doi request reprint Great expectations: views of genetic research participants regarding current and future genetic studies
    Gail Henderson
    Department of Social Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599 7240, USA
    Genet Med 10:193-200. 2008
    ..We explored attitudes toward genetic research participation among people in a case-control genetic epidemiology study of colon cancer, the North Carolina Colorectal Cancer Study (NCCCS)...
  6. ncbi request reprint Consent forms and the therapeutic misconception: the example of gene transfer research
    Nancy M P King
    University of North Carolina at Chapel Hill, USA
    IRB 27:1-8. 2005
  7. ncbi request reprint Confidentiality: more than a linkage file and a locked drawer
    Michele M Easter
    Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, USA
    IRB 26:13-7. 2004
  8. ncbi request reprint The many meanings of care in clinical research
    Michele M Easter
    Department of Social Medicine, University of North Carolina at Chapel Hill, NC 27499 7240, USA
    Sociol Health Illn 28:695-712. 2006
    ....
  9. ncbi request reprint What research ethics should learn from genomics and society research: lessons from the ELSI Congress of 2011
    Gail E Henderson
    Department of Social Medicine, School of Medicine, Center for Genomics and Society, University of North Carolina Chapel Hill, Chapel Hill, NC, USA
    J Law Med Ethics 40:1008-24. 2012
    ....
  10. ncbi request reprint Vulnerability to influence: a two-way street
    Gail E Henderson
    University of North Carolina School of Medicine, USA
    Am J Bioeth 4:50-2; discussion W32. 2004
  11. pmc Parents' online portrayals of pediatric treatment and research options
    Rebecca Schaffer
    University of North Carolina at Chapel Hill, USA
    J Empir Res Hum Res Ethics 4:73-87. 2009
    ..Our discussion of these findings clarifies the potential for parent-authored websites to inform and influence families considering research and treatment options for their seriously ill children...
  12. ncbi request reprint The invisible hand in clinical research: the study coordinator's critical role in human subjects protection
    Arlene M Davis
    University of North Carolina School of Medicine, USA
    J Law Med Ethics 30:411-9. 2002
  13. pmc Studying genetic research participants: lessons from the "Learning About Research in North Carolina" study
    Giselle Corbie-Smith
    Department of Social Medicine, Cecil G Sheps Center for Health Services Research, University of North Carolina, 725 Martin Luther King Jr Boulevard, Chapel Hill, NC 27599, USA
    Cancer Epidemiol Biomarkers Prev 17:2019-24. 2008
    ..In this article, we give an overview of the LeARN study, summarizing the methods we used, challenges we encountered, and lessons learned about recruiting participants who have previously participated in genetic research...
  14. pmc Conceptualizing race in research
    Giselle Corbie-Smith
    Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, 27599, USA
    J Natl Med Assoc 100:1235-43. 2008
    ..Given this continued controversy, we examined how investigators interpret the concept of "race" and whether their views of race are reflected in their published work...
  15. pmc Relationships and communication in minority participation in research: multidimensional and multidirectional
    Giselle Corbie-Smith
    Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, North Carolina 27599 7240, USA
    J Natl Med Assoc 99:489-98. 2007
    ..These relationships can both facilitate the recruitment process as well as aid in the interpretation of research findings...
  16. pmc Public willingness to participate in and public opinions about genetic variation research: a review of the literature
    Rene Sterling
    School of Public Health, University of North Carolina, Chapel Hill, NC 27599 7240, USA
    Am J Public Health 96:1971-8. 2006
    ..We review empirical studies of public willingness to participate in and opinions about genetic research with particular attention to differences in consent and opinion by racial/ethnic group membership...
  17. doi request reprint Stewardship practices of U.S. biobanks
    Gail E Henderson
    Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
    Sci Transl Med 5:215cm7. 2013
    ..Biobanks now need guidance to fully articulate stewardship practices that ensure respect for contributors while facilitating research. ..
  18. pmc Biobanks in the United States: how to identify an undefined and rapidly evolving population
    Gregory J Boyer
    1 Department of Health Policy and Management, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
    Biopreserv Biobank 10:511-7. 2012
    ..Furthermore, our approach demonstrates that with the appropriate tools it is possible to develop a systematic and comprehensive database to investigate undefined populations...
  19. pmc The role of race and trust in tissue/blood donation for genetic research
    Jada Bussey-Jones
    School of Medicine, Emory University, Atlanta, Georgia 30331, USA
    Genet Med 12:116-21. 2010
    ....
  20. ncbi request reprint Assessing benefits in clinical research: why diversity in benefit assessment can be risky
    Larry R Churchill
    Vanderbilt University, USA
    IRB 25:1-8. 2003