These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

255 related articles for article (PubMed ID: 18316466)

  • 1. Duty to disclose what? Querying the putative obligation to return research results to participants.
    Miller FA; Christensen R; Giacomini M; Robert JS
    J Med Ethics; 2008 Mar; 34(3):210-3. PubMed ID: 18316466
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Informing study participants of research results: an ethical imperative.
    Fernandez CV; Kodish E; Weijer C
    IRB; 2003; 25(3):12-9. PubMed ID: 14569989
    [No Abstract]   [Full Text] [Related]  

  • 3. The search for clarity in communicating research results to study participants.
    Shalowitz DI; Miller FG
    J Med Ethics; 2008 Sep; 34(9):e17. PubMed ID: 18757617
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The emergence of an ethical duty to disclose genetic research results: international perspectives.
    Knoppers BM; Joly Y; Simard J; Durocher F
    Eur J Hum Genet; 2006 Nov; 14(11):1170-8. PubMed ID: 16868560
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Misusing informed consent: a critique of limitations on research subjects' access to genetic research results.
    Banks TM
    Sask Law Rev; 2000; 63(2):539-80. PubMed ID: 12666671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A legal duty to disclose individual research findings to research subjects?
    Gordon MP
    Food Drug Law J; 2009; 64(1):225-60. PubMed ID: 19998747
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The return of individual research findings in paediatric genetic research.
    Hens K; Nys H; Cassiman JJ; Dierickx K
    J Med Ethics; 2011 Mar; 37(3):179-83. PubMed ID: 21059631
    [TBL] [Abstract][Full Text] [Related]  

  • 8. When do genetic researchers have a duty to recontact study participants?
    Wade CH; Kalfoglou AL
    Am J Bioeth; 2006; 6(6):26-7; author reply W10-2. PubMed ID: 17085400
    [No Abstract]   [Full Text] [Related]  

  • 9. Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy.
    Bredenoord AL; Onland-Moret NC; Van Delden JJ
    Hum Mutat; 2011 Aug; 32(8):861-7. PubMed ID: 21538687
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Information disclosure in population-based research involving genetics: a framework for the practice of ethics in epidemiology.
    Kristman VL; Kreiger N
    Ann Epidemiol; 2008 Apr; 18(4):335-41. PubMed ID: 18083547
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Obligations in offering to disclose genetic research results.
    Fernandez CV; Weijer C
    Am J Bioeth; 2006; 6(6):44-6; author reply W10-2. PubMed ID: 17085409
    [No Abstract]   [Full Text] [Related]  

  • 12. Is it ethical to deny genetic research participants individualised results?
    Affleck P
    J Med Ethics; 2009 Apr; 35(4):209-13. PubMed ID: 19332574
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Letting the gene out of the bottle: a comment on returning individual research results to participants.
    Ossorio PN
    Am J Bioeth; 2006; 6(6):24-5; author reply W10-2. PubMed ID: 17085399
    [No Abstract]   [Full Text] [Related]  

  • 14. Thresholds and boundaries in the disclosure of individual genetic research results.
    Dressler LG; Juengst ET
    Am J Bioeth; 2006; 6(6):18-20; author reply W10-2. PubMed ID: 17085396
    [No Abstract]   [Full Text] [Related]  

  • 15. Taking our obligations to research participants seriously: disclosing individual results of genetic research.
    Manolio TA
    Am J Bioeth; 2006; 6(6):32-4; author reply W10-2. PubMed ID: 17085403
    [No Abstract]   [Full Text] [Related]  

  • 16. Ethical conduct of radiology research with human participants.
    Burger I; Kass N
    J Am Coll Radiol; 2006 Dec; 3(12):932-9. PubMed ID: 17412204
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A duty to participate in research: does social context matter?
    de Melo-Martin I
    Am J Bioeth; 2008 Oct; 8(10):28-36. PubMed ID: 19003704
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The kindness of strangers: the donative contract between subjects and researchers and the non-obligation to return individual results of genetic research.
    Meyer MN
    Am J Bioeth; 2008 Nov; 8(11):44-6. PubMed ID: 19061109
    [No Abstract]   [Full Text] [Related]  

  • 19. Considering the nature of individual research results.
    Beskow LM
    Am J Bioeth; 2006; 6(6):38-40; author reply W10-2. PubMed ID: 17085406
    [No Abstract]   [Full Text] [Related]  

  • 20. Genetic testing and human subjects in research.
    Laidlaw SA; Raffel LJ; Daar JF
    Whittier Law Rev; 2002; 24(2):429-72. PubMed ID: 15085855
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.