Literature DB >> 17145906

Genetic testing without consent: the implications of the new Human Tissue Act 2004.

A Lucassen1, J Kaye.   

Abstract

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Year:  2006        PMID： 17145906      PMCID： PMC2563345          DOI： 10.1136/jme.2005.013631

Source DB:  PubMed          Journal:  J Med Ethics        ISSN： 0306-6800            Impact factor:   2.903


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  4 in total

1.  GP reprimanded for testing patients for HIV without consent.

Authors:  C Dyer
Journal:  BMJ       Date:  2000-01-15

2.  Protecting and promoting privacy in an uncertain world: further defences of ignorance and the right not to know.

Authors:  G T Laurie
Journal:  Eur J Health Law       Date:  2000-06

3.  Confidentiality and serious harm in genetics - preserving the confidentiality of one patient and preventing harm to relatives.

Authors:  Anneke Lucassen; Michael Parker
Journal:  Eur J Hum Genet       Date:  2004-02       Impact factor: 4.246

Review 4.  Genetic information: a joint account?

Authors:  Michael Parker; Anneke M Lucassen
Journal:  BMJ       Date:  2004-07-17
  4 in total
  3 in total

Review 1.  From Beyond the Grave: Use of Medical Information from the Deceased to Guide Care of Living Relatives.

Authors:  Shereen Tadros; Helena Carley; Anneke Lucassen
Journal:  Curr Genet Med Rep       Date:  2020-11-24

2.  Using biomarkers in acute medicine to prevent hearing loss: should this require specific consent?

Authors:  Peta Coulson-Smith; Anneke Lucassen
Journal:  J Med Ethics       Date:  2020-07-13       Impact factor: 2.903

3.  'A Procedure Without a Problem', or the face transplant that didn't happen. The Royal Free, the Royal College of Surgeons and the challenge of surgical firsts.

Authors:  Fay Bound Alberti; Victoria Hoyle
Journal:  Med Humanit       Date:  2021-10-12
  3 in total

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