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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Elizabeth Chapman

Arthur Rank Hospice

Brookfields Hospital


United Kingdom


Name/email consistency: medium



  • Arthur Rank Hospice, Brookfields Hospital, Cambridge, United Kingdom. 2008
  • The Centre for Family Research, University of Cambridge, UK. 2002 - 2007
  • Adult Cystic Fibrosis Centre, Papworth NHS Trust, Papworth Everard, Cambridge CB3 8RE United Kingdom. 2005
  • Arthur Rank Hospice, Cambridge, UK. 2005


  1. Clinical evaluation of theMood and Symptom Questionnaire (MSQ) in a day therapy unit in a palliative support centre in the United Kingdom. Chapman, E., Whale, J., Landy, A., Hughes, D., Saunders, M. Palliat. Support. Care (2008) [Pubmed]
  2. Psychosocial issues for patients with ventricular assist devices: a qualitative pilot study. Chapman, E., Parameshwar, J., Jenkins, D., Large, S., Tsui, S. Am. J. Crit. Care (2007) [Pubmed]
  3. End of life care for adult cystic fibrosis patients: facilitating a good enough death. Chapman, E., Landy, A., Lyon, A., Haworth, C., Bilton, D. J. Cyst. Fibros. (2005) [Pubmed]
  4. Challenging the representations of cancer pain: experiences of a multidisciplinary pain management group in a palliative care unit. Chapman, E., Hughes, D., Landy, A., Whale, J., Saunders, M. Palliative. &. Supportive. Care (2005) [Pubmed]
  5. Patients' knowledge of cystic fibrosis: genetic determinism and implications for treatment. Chapman, E., Bilton, D. J. Genet. Couns (2004) [Pubmed]
  6. Patient impact of negative representations of HIV. Chapman, E. AIDS. Patient. Care. STDS (2002) [Pubmed]
  7. Ethical dilemmas in testing for late onset conditions: reactions to testing and perceived impact on other family members. Chapman, E. J. Genet. Couns (2002) [Pubmed]
  8. Difficult decisions: social and ethical implications of changing medical technology. Chapman, E. Community. Genet (2002) [Pubmed]
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