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 *

474 related articles for article (PubMed ID: 26678513)

  • 1. Balancing Benefits and Risks of Immortal Data: Participants' Views of Open Consent in the Personal Genome Project.
    Zarate OA; Brody JG; Brown P; Ramirez-Andreotta MD; Perovich L; Matz J
    Hastings Cent Rep; 2016; 46(1):36-45. PubMed ID: 26678513
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Consent to 'personal' genomics and privacy. Direct-to-consumer genetic tests and population genome research challenge traditional notions of privacy and consent.
    Knoppers BM
    EMBO Rep; 2010 Jun; 11(6):416-9. PubMed ID: 20448662
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Open Questions.
    Kaebnick GE
    Hastings Cent Rep; 2016; 46(1):2. PubMed ID: 26786031
    [No Abstract]   [Full Text] [Related]  

  • 4. Ethical and legal implications of whole genome and whole exome sequencing in African populations.
    Wright GE; Koornhof PG; Adeyemo AA; Tiffin N
    BMC Med Ethics; 2013 May; 14():21. PubMed ID: 23714101
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Human Genome Project and public perception: truth and consequences.
    Pelias MZ; Markward NJ
    Emory Law J; 2000; 49(3):837-58. PubMed ID: 12645564
    [No Abstract]   [Full Text] [Related]  

  • 6. Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.
    Oliver JM; Slashinski MJ; Wang T; Kelly PA; Hilsenbeck SG; McGuire AL
    Public Health Genomics; 2012; 15(2):106-14. PubMed ID: 22213783
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genomic research and data-mining technology: implications for personal privacy and informed consent.
    Tavani HT
    Ethics Inf Technol; 2004; 6(1):15-28. PubMed ID: 16969958
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Promise and Perils of Open Medical Data.
    Hoffman S
    Hastings Cent Rep; 2016; 46(1):6-7. PubMed ID: 26786035
    [No Abstract]   [Full Text] [Related]  

  • 9. Genomic anonymity: have we already lost it?
    Greenbaum D; Du J; Gerstein M
    Am J Bioeth; 2008 Oct; 8(10):71-4. PubMed ID: 19003717
    [No Abstract]   [Full Text] [Related]  

  • 10. American Society of Clinical Oncology policy statement: oversight of clinical research.
    American Society of Clinical Oncology
    J Clin Oncol; 2003 Jun; 21(12):2377-86. PubMed ID: 12721281
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Community participation and representation in genetic studies: testing the application of fundamental ethical principles.
    Brito A
    St Thomas Law Rev; 2001; 13(4):935-43. PubMed ID: 12661583
    [No Abstract]   [Full Text] [Related]  

  • 12. Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
    Sanderson SC; Linderman MD; Suckiel SA; Diaz GA; Zinberg RE; Ferryman K; Wasserstein M; Kasarskis A; Schadt EE
    Eur J Hum Genet; 2016 Jan; 24(1):14-20. PubMed ID: 26036856
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.
    Henderson GE; Wolf SM; Kuczynski KJ; Joffe S; Sharp RR; Parsons DW; Knoppers BM; Yu JH; Appelbaum PS
    J Law Med Ethics; 2014; 42(3):344-55. PubMed ID: 25264092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. "A Question of Trust" and "a Leap of Faith"-Study Participants' Perspectives on Consent, Privacy, and Trust in Smart Home Research: Qualitative Study.
    Kennedy MR; Huxtable R; Birchley G; Ives J; Craddock I
    JMIR Mhealth Uhealth; 2021 Nov; 9(11):e25227. PubMed ID: 34842551
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PGTandMe: social networking-based genetic testing and the evolving research model.
    Koch VG
    Health Matrix Clevel; 2012; 22(1):33-74. PubMed ID: 22616542
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Ethical issues of personal genome: a legal perspective--ethical and legal ramifications of personal genome research].
    Maruyama E
    Nihon Rinsho; 2009 Jun; 67(6):1209-13. PubMed ID: 19507516
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ethical aspects of participation in the database of genotypes and phenotypes of the National Center for Biotechnology Information: the Cancer and Leukemia Group B Experience.
    Peppercorn J; Shapira I; Deshields T; Kroetz D; Friedman P; Spears P; Collyar DE; Shulman LN; Dressler L; Bertagnolli MM
    Cancer; 2012 Oct; 118(20):5060-8. PubMed ID: 22415847
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Legal, ethical, and social issues in human genome research.
    Greely HT
    Annu Rev Anthropol; 1998; 27():473-502. PubMed ID: 15977340
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The project data sphere initiative: accelerating cancer research by sharing data.
    Green AK; Reeder-Hayes KE; Corty RW; Basch E; Milowsky MI; Dusetzina SB; Bennett AV; Wood WA
    Oncologist; 2015 May; 20(5):464-e20. PubMed ID: 25876994
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Consent Issues in Genetic Research: Views of Research Participants.
    Goodman D; Johnson CO; Wenzel L; Bowen D; Condit C; Edwards KL
    Public Health Genomics; 2016; 19(4):220-8. PubMed ID: 27376949
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.