Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Brown, Lindsey
Parker, Michael
and
Dixon-Woods1, Mary
2008.
Whose Interest? British Newspaper Reporting of use of Medical Records for Research.
Journal of Health Services Research & Policy,
Vol. 13,
Issue. 3,
p.
140.
Hansson, M G
2009.
Ethics and biobanks.
British Journal of Cancer,
Vol. 100,
Issue. 1,
p.
8.
Dixon-Woods, Mary
and
Tarrant, Carolyn
2009.
Why do people cooperate with medical research? Findings from three studies.
Social Science & Medicine,
Vol. 68,
Issue. 12,
p.
2215.
JACKSON, C.
DIXON-WOODS, M.
TOBIN, M.
YOUNG, B.
HENEY, D.
and
PRITCHARD-JONES, K.
2009.
Seeking consent to tissue banking: a survey of health professionals in childhood cancer.
European Journal of Cancer Care,
Vol. 18,
Issue. 4,
p.
391.
Morris, Norma
and
Schneider, Margaret
2010.
Volunteer Research Subjects’ Experience of Participation in Research on a Novel Diagnostic Technology for Breast Cancer.
Qualitative Health Research,
Vol. 20,
Issue. 1,
p.
81.
Hoeyer, Klaus
2010.
After Novelty: The Mundane Practices of Ensuring a Safe and Stable Supply of Bone.
Science as Culture,
Vol. 19,
Issue. 2,
p.
123.
Hansson, Mats G
2010.
Taking the Patient‘s Side: The Ethics of Pharmacogenetics.
Personalized Medicine,
Vol. 7,
Issue. 1,
p.
75.
Tutton, Richard
2010.
Encyclopedia of Life Sciences.
Johnsson, Linus
Helgesson, Gert
Rafnar, Thorunn
Halldorsdottir, Ingibjorg
Chia, Kee-Seng
Eriksson, Stefan
and
Hansson, Mats G
2010.
Hypothetical and factual willingness to participate in biobank research.
European Journal of Human Genetics,
Vol. 18,
Issue. 11,
p.
1261.
Morrell, Bronwen
Lipworth, Wendy
Axler, Renata
Kerridge, Ian
and
Little, Miles
2011.
Cancer as Rubbish: Donation of Tumor Tissue for Research.
Qualitative Health Research,
Vol. 21,
Issue. 1,
p.
75.
Wilson, Duncan
2011.
Tissue Culture in Science and Society.
p.
117.
Vermeulen, Eric
Schmidt, Marjanka K
Cornel, Martina C
Knoppers, Bartha Maria
van Leeuwen, Flora E
and
Aaronson, Neil K
2011.
Connective tissue: Cancer patients’ attitudes towards medical research using excised (tumour) tissue.
BioSocieties,
Vol. 6,
Issue. 4,
p.
466.
Lipworth, Wendy
Forsyth, Rowena
and
Kerridge, Ian
2011.
Tissue donation to biobanks: a review of sociological studies.
Sociology of Health & Illness,
Vol. 33,
Issue. 5,
p.
792.
Gaffney, Eoin F.
Madden, Deirdre
and
Thomas, Geraldine A.
2012.
Molecular Profiling.
Vol. 823,
Issue. ,
p.
59.
Soto, Carmen
Tarrant, Carolyn
Pritchard-Jones, Kathy
and
Dixon-Woods, Mary
2012.
Consent to tissue banking for research: qualitative study and recommendations.
Archives of Disease in Childhood,
Vol. 97,
Issue. 7,
p.
632.
Nicol, Dianne
and
Critchley, Christine
2012.
Benefit sharing and biobanking in Australia.
Public Understanding of Science,
Vol. 21,
Issue. 5,
p.
534.
Hansson, Mats G.
Simonsson, Bengt
Feltelius, Nils
Forsberg, Joanna Stjernschantz
and
Hasford, Joerg
2012.
Medical registries represent vital patient interests and should not be dismantled by stricter regulation.
Cancer Epidemiology,
Vol. 36,
Issue. 6,
p.
575.
Hoeyer, Klaus L.
2013.
Commercialization of Tissue-Based Research: Time to Move Beyond the Gift/Market Dichotomy.
Biopreservation and Biobanking,
Vol. 11,
Issue. 6,
p.
397.
Masterton, Malin
Renberg, Tobias
Hansson, Mats G
and
Sporrong, Sofia Kälvemark
2014.
Ethical review boards are poor advocates for patient perspectives.
Research Ethics,
Vol. 10,
Issue. 3,
p.
169.
Salvaterra, Elena
Locatelli, Federica
Strazzer, Sandra
Borgatti, Renato
D''angelo, Grazia
and
Lenzi, Leonardo
2014.
Paediatric Biobanks: Opinions, Feelings and Attitudes of Parents towards the Specimen Donation of Their Sick Children to a Hypothetical Biobank.
Pathobiology,
Vol. 81,
Issue. 5-6,
p.
304.