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 *

131 related articles for article (PubMed ID: 30525978)

  • 1. Patients' perspectives on opt-out consent for observational research: systematic review and focus group.
    Cardillo L; Cahill F; Wylie H; Williams A; Zylstra J; Davies A; Fullwood L; Van Hemelrijck M
    Br J Nurs; 2018 Dec; 27(22):1321-1329. PubMed ID: 30525978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. "Let's get the best quality research we can": public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study.
    Hill EM; Turner EL; Martin RM; Donovan JL
    BMC Med Res Methodol; 2013 Jun; 13():72. PubMed ID: 23734773
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Randomised Controlled Trial of Consent Procedures for the Use of Residual Tissues for Medical Research: Preferences of and Implications for Patients, Research and Clinical Practice.
    Rebers S; Vermeulen E; Brandenburg AP; Stoof TJ; Zupan-Kajcovski B; Bos WJ; Jonker MJ; Bax CJ; van Driel WJ; Verwaal VJ; van den Brekel MW; Grutters JC; Tupker RA; Plusjé L; de Bree R; Schagen van Leeuwen JH; Vermeulen EG; de Leeuw RA; Brohet RM; Aaronson NK; Van Leeuwen FE; Schmidt MK
    PLoS One; 2016; 11(3):e0152509. PubMed ID: 27028128
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Acceptability of opt-out consent in a hospital patient population.
    Boulos D; Morand E; Foo M; Trivedi JD; Lai R; Huntersmith R; Zhang K; Stark CB; Le S
    Intern Med J; 2018 Jan; 48(1):84-87. PubMed ID: 29314513
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Patients' experiences and preferences for opt-in models and health professional involvement in biobanking consent: A cross-sectional survey of Australian cancer outpatients.
    Fradgley EA; Chong SE; Cox ME; Gedye C; Paul CL
    Asia Pac J Clin Oncol; 2019 Feb; 15(1):31-37. PubMed ID: 29573159
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recall and Retention of Consent Procedure Contents and Decisions: Results of a Randomized Controlled Trial.
    Rebers S; Vermeulen E; Brandenburg AP; Aaronson NK; Schmidt MK
    Public Health Genomics; 2018; 21(1-2):27-36. PubMed ID: 30199881
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Willingness to participate in pragmatic dialysis trials: the importance of physician decisional autonomy and consent approach.
    Courtright KR; Halpern SD; Joffe S; Ellenberg SS; Karlawish J; Madden V; Gabler NB; Szymanski S; Yadav KN; Dember LM
    Trials; 2017 Oct; 18(1):474. PubMed ID: 29020994
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Why persons choose to opt out of an exception from informed consent cardiac arrest trial.
    Nelson MJ; Deiorio NM; Schmidt TA; Zive DM; Griffiths D; Newgard CD
    Resuscitation; 2013 Jun; 84(6):825-30. PubMed ID: 23402968
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Patient Perspectives About Decisions to Share Medical Data and Biospecimens for Research.
    Kim J; Kim H; Bell E; Bath T; Paul P; Pham A; Jiang X; Zheng K; Ohno-Machado L
    JAMA Netw Open; 2019 Aug; 2(8):e199550. PubMed ID: 31433479
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Research participants' perceptions and views on consent for biobank research: a review of empirical data and ethical analysis.
    D'Abramo F; Schildmann J; Vollmann J
    BMC Med Ethics; 2015 Sep; 16():60. PubMed ID: 26354520
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 'What if I'm not dead?' - Myth-busting and organ donation.
    Miller J; Currie S; O'Carroll RE
    Br J Health Psychol; 2019 Feb; 24(1):141-158. PubMed ID: 30345605
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Patients' experiences on donation of their residual biological samples and the impact of these experiences on the type of consent given for the future research use of the tissue: a systematic review.
    Chan TW; Mackey S; Hegney DG
    Int J Evid Based Healthc; 2012 Mar; 10(1):9-26. PubMed ID: 22405414
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Opt-out plus, the patients' choice: preferences of cancer patients concerning information and consent regimen for future research with biological samples archived in the context of treatment.
    Vermeulen E; Schmidt MK; Aaronson NK; Kuenen M; van der Valk P; Sietses C; van den Tol P; van Leeuwen FE
    J Clin Pathol; 2009 Mar; 62(3):275-8. PubMed ID: 19017681
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A comparison of institutional review board professionals' and patients' views on consent for research on medical practices.
    Kraft SA; Cho MK; Constantine M; Lee SS; Kelley M; Korngiebel D; James C; Kuwana E; Meyer A; Porter K; Diekema D; Capron AM; Alicic R; Wilfond BS; Magnus D
    Clin Trials; 2016 Oct; 13(5):555-65. PubMed ID: 27257125
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage.
    Berry JG; Ryan P; Gold MS; Braunack-Mayer AJ; Duszynski KM;
    J Med Ethics; 2012 Oct; 38(10):619-25. PubMed ID: 22518045
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recruiting patients to medical research: double blind randomised trial of "opt-in" versus "opt-out" strategies.
    Junghans C; Feder G; Hemingway H; Timmis A; Jones M
    BMJ; 2005 Oct; 331(7522):940. PubMed ID: 16157604
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Participant recruitment in sensitive surveys: a comparative trial of 'opt in' versus 'opt out' approaches.
    Hunt KJ; Shlomo N; Addington-Hall J
    BMC Med Res Methodol; 2013 Jan; 13():3. PubMed ID: 23311340
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Use of electronic patient records for research: views of patients and staff in general practice.
    Stevenson F; Lloyd N; Harrington L; Wallace P
    Fam Pract; 2013 Apr; 30(2):227-32. PubMed ID: 23132893
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dissenting from care.data: an analysis of opt-out forms.
    Vezyridis P; Timmons S
    J Med Ethics; 2016 Dec; 42(12):792-796. PubMed ID: 27884968
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Research recruitment and consent methods in a pandemic: a qualitative study of COVID-19 patients' perspectives.
    Small SS; Lau E; McFarlane K; Archambault PM; Longstaff H; Hohl CM
    BMC Med Res Methodol; 2023 May; 23(1):113. PubMed ID: 37170077
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.