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 *

338 related articles for article (PubMed ID: 25359560)

  • 1. Testing an online, dynamic consent portal for large population biobank research.
    Thiel DB; Platt J; Platt T; King SB; Fisher N; Shelton R; Kardia SL
    Public Health Genomics; 2015; 18(1):26-39. PubMed ID: 25359560
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
    Sanderson SC; Brothers KB; Mercaldo ND; Clayton EW; Antommaria AHM; Aufox SA; Brilliant MH; Campos D; Carrell DS; Connolly J; Conway P; Fullerton SM; Garrison NA; Horowitz CR; Jarvik GP; Kaufman D; Kitchner TE; Li R; Ludman EJ; McCarty CA; McCormick JB; McManus VD; Myers MF; Scrol A; Williams JL; Shrubsole MJ; Schildcrout JS; Smith ME; Holm IA
    Am J Hum Genet; 2017 Mar; 100(3):414-427. PubMed ID: 28190457
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.
    Antommaria AHM; Brothers KB; Myers JA; Feygin YB; Aufox SA; Brilliant MH; Conway P; Fullerton SM; Garrison NA; Horowitz CR; Jarvik GP; Li R; Ludman EJ; McCarty CA; McCormick JB; Mercaldo ND; Myers MF; Sanderson SC; Shrubsole MJ; Schildcrout JS; Williams JL; Smith ME; Clayton EW; Holm IA
    AJOB Empir Bioeth; 2018; 9(3):128-142. PubMed ID: 30240342
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biobank research and the right to privacy.
    Ursin LO
    Theor Med Bioeth; 2008; 29(4):267-85. PubMed ID: 18855123
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 'Cool! and creepy': engaging with college student stakeholders in Michigan's biobank.
    Platt T; Platt J; Thiel DB; Fisher N; Kardia SL
    J Community Genet; 2014 Oct; 5(4):349-62. PubMed ID: 24916145
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Confidentiality, informed consent and children's participation in the Saudi biobank governance: a comparative study.
    Alahmad GH; Dierickx K
    East Mediterr Health J; 2014 Dec; 20(11):681-9. PubMed ID: 25601806
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Biobank research, informed consent and society. Towards a new alliance?
    D'Abramo F
    J Epidemiol Community Health; 2015 Nov; 69(11):1125-8. PubMed ID: 25669218
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Communicating Identifiability Risks to Biobank Donors.
    Kasperbauer TJ; Gjerris M; Waldemar G; Sandøe P
    Camb Q Healthc Ethics; 2018 Jan; 27(1):123-136. PubMed ID: 29214966
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Confidentiality, informed consent, and children's participation in research involving stored tissue samples: interviews with medical professionals from the Middle East.
    Alahmad G; Al Jumah M; Dierickx K
    Narrat Inq Bioeth; 2015; 5(1):53-66. PubMed ID: 25981282
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A proposed approach to informed consent for biobanks in China.
    Liu M; Hu Q
    Bioethics; 2014 May; 28(4):181-6. PubMed ID: 22762502
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Attitudes toward medical and genetic confidentiality in the Saudi research biobank: An exploratory survey.
    Alahmad G; Hifnawy T; Abbasi B; Dierickx K
    Int J Med Inform; 2016 Mar; 87():84-90. PubMed ID: 26806715
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Biobanking research on oncological residual material: a framework between the rights of the individual and the interest of society.
    Caenazzo L; Tozzo P; Pegoraro R
    BMC Med Ethics; 2013 Apr; 14():17. PubMed ID: 23547565
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Experience with establishment and operation of a biobank].
    Stege A; Hummel M
    Pathologe; 2008 Nov; 29 Suppl 2():214-7. PubMed ID: 18712392
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biobanking in the subcontinent: exploring concerns.
    Jafarey AM; Shekhani SS; Shirazi B
    Indian J Med Ethics; 2017; 2(4):248-254. PubMed ID: 28803222
    [TBL] [Abstract][Full Text] [Related]  

  • 15. IRB review and public health biobanking: a case study of the Michigan BioTrust for Health.
    Mongoven A; McGee H
    IRB; 2012; 34(3):11-6. PubMed ID: 22830178
    [No Abstract]   [Full Text] [Related]  

  • 16. Fair Shares and Sharing Fairly: A Survey of Public Views on Open Science, Informed Consent and Participatory Research in Biobanking.
    Joly Y; Dalpé G; So D; Birko S
    PLoS One; 2015; 10(7):e0129893. PubMed ID: 26154134
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The moral concerns of biobank donors: the effect of non-welfare interests on willingness to donate.
    De Vries RG; Tomlinson T; Kim HM; Krenz CD; Ryan KA; Lehpamer N; Kim SY
    Life Sci Soc Policy; 2016; 12():3. PubMed ID: 26968989
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Storage policies and use of the Danish Newborn Screening Biobank.
    Nørgaard-Pedersen B; Hougaard DM
    J Inherit Metab Dis; 2007 Aug; 30(4):530-6. PubMed ID: 17632694
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Public opinion about the importance of privacy in biobank research.
    Kaufman DJ; Murphy-Bollinger J; Scott J; Hudson KL
    Am J Hum Genet; 2009 Nov; 85(5):643-54. PubMed ID: 19878915
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reconsidering the value of consent in biobank research.
    Allen J; McNamara B
    Bioethics; 2011 Mar; 25(3):155-66. PubMed ID: 19659851
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.