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Health, Risk & Society Volume 14, 2012 - Issue 7-8
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Original articles

Evidence-based familial risk explanations in cancer genetic counselling

Negotiating and communicating health risk

Gøril Thomassen Department of Language and Communication Studies, Norwegian University of Science and Technology, Trondheim, NorwayCorrespondence[email protected]
&
Srikant Sarangi Health Communication Research Centre, School of English, Communication and Philosophy, Cardiff University, Cardiff, UK
Pages 607-626 | Received 05 Jan 2012, Accepted 04 Jul 2012, Published online: 02 Oct 2012

Citations (11)

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Read on this site (2)

Tone Aasen & John-Arne Skolbekken. (2014) Preparing for and communicating uncertainty in cancer genetic counselling sessions in Norway: an interpretative phenomenological analysis. Health, Risk & Society 16:4, pages 370-389.
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Olga Zayts & Srikant Sarangi. (2013) Modes of risk explanation in telephone consultations between nurses and parents for a genetic condition. Health, Risk & Society 15:2, pages 194-215.
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Articles from other publishers (9)

Olga Zayts‐Spence, Jasmine L. F. Fung & Brian H. Y. Chung. (2021) ‘Do language and culture really matter?’: A trans‐disciplinary investigation of cultural diversity in genetic counseling in Hong Kong . Journal of Genetic Counseling 30:1, pages 75-84.
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Gøril Thomassen Hammerstad, Srikant Sarangi & Inga Bjørnevoll. (2020) Diagnostic uncertainties, ethical tensions, and accounts of role responsibilities in genetic counseling communication. Journal of Genetic Counseling 29:6, pages 1159-1172.
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Kimberly A. Kaphingst, Emily Peterson, Jingsong Zhao, Anna Gaysynsky, Ashley Elrick, Soo Jung Hong, Melinda Krakow, Manusheela Pokharel, Chelsea L. Ratcliff, William M. P. Klein, Muin J. Khoury & Wen-Ying Sylvia Chou. (2018) Cancer communication research in the era of genomics and precision medicine: a scoping review. Genetics in Medicine 21:8, pages 1691-1698.
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Jason L. Vassy, J. Kelly Davis, Christine Kirby, Ian J. Richardson, Robert C. Green, Amy L. McGuire & Peter A. Ubel. (2018) How Primary Care Providers Talk to Patients about Genome Sequencing Results: Risk, Rationale, and Recommendation. Journal of General Internal Medicine 33:6, pages 877-885.
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Anne Kerr, Emily Ross, Gwen Jacques & Sarah Cunningham-Burley. (2018) The sociology of cancer: a decade of research. Sociology of Health & Illness 40:3, pages 552-576.
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Tanya Stivers & Stefan Timmermans. (2017) The Actionability of Exome sequencing testing results. Sociology of Health & Illness 39:8, pages 1542-1556.
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Jean Paul, Sylvia Metcalfe, Lesley Stirling, Brenda Wilson & Jan Hodgson. (2015) Analyzing communication in genetic consultations—A systematic review. Patient Education and Counseling 98:1, pages 15-33.
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Olga Zayts & Stephanie Schnurr. (2014) More than ‘information provider’ and ‘counselor’: Constructing and negotiating roles and identities of nurses in genetic counseling sessions. Journal of Sociolinguistics 18:3, pages 345-369.
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Srikant Sarangi. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences.

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