Citations (31)
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Dinah A. Tetteh. (2019) Visibility of the ovaries and breasts: an analysis of Angelina Jolie’s medical announcements. Feminist Media Studies 19:5, pages 651-666.
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Sophie Rees. (2018) No one scans you and says ‘you’re alright now’: the experience of embodied risk for young women living with a history of breast cancer. Health, Risk & Society 20:7-8, pages 312-324.
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Emily Ross, Tineke Broer, Anne Kerr & Sarah Cunningham-Burley. (2018) Identity, community and care in online accounts of hereditary colorectal cancer syndrome. New Genetics and Society 37:2, pages 117-136.
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Maggie Mort, Celia Mary Roberts, Mette Kragh Furbo, Joann Wilkinson & Adrian Mackenzie. (2016) Biosensing: how citizens’ views illuminate emerging health and social risks. Health, Risk & Society 17:7-8, pages 605-623.
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Alexandra Farren Gibson, Christina Lee & Shona Crabb. (2015) ‘Take ownership of your condition’: Australian women’s health and risk talk in relation to their experiences of breast cancer. Health, Risk & Society 17:2, pages 132-148.
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Lisa R. Rubin, Allison Werner-Lin, Michal Sagi, Ina Cholst, Rikki Stern, Debra Lilienthal & Karen Hurley. (2014) ‘The BRCA Clock is Ticking!’: Negotiating medical concerns and reproductive goals in preimplantation genetic diagnosis. Human Fertility 17:3, pages 159-164.
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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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Deborah Lupton. (2013) Risk and emotion: towards an alternative theoretical perspective. Health, Risk & Society 15:8, pages 634-647.
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Annmarie Ruston. (2009) Isolation: A threat and means of spatial control. Living with risk in a deprived neighbourhood. Health, Risk & Society 11:3, pages 257-268.
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Holly Etchegary, Louise Lemyre, Brenda Wilson & Dan Krewski. (2009) Is genetic makeup a perceived health risk: analysis of a national survey of Canadians. Journal of Risk Research 12:2, pages 223-237.
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Nick Pidgeon, Peter Simmons, Sophie Sarre, Karen Henwood & Noel Smith. (2008) The ethics of socio-cultural risk research. Health, Risk & Society 10:4, pages 321-329.
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GillianA. Bendelow. (2006) Pain, suffering and risk. Health, Risk & Society 8:1, pages 59-70.
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Articles from other publishers (19)
Alison Hicks. (2023) Risky (information) business: an informational risk research agenda. Journal of Documentation 79:5, pages 1147-1163.
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M. A. Rubel, A. Werner-Lin, F. K. Barg & B. A. Bernhardt. (2017) Expert Knowledge Influences Decision-Making for Couples Receiving Positive Prenatal Chromosomal Microarray Testing Results. Culture, Medicine, and Psychiatry 41:3, pages 382-406.
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Lea Hagoel. 2017. Alleviating World Suffering. Alleviating World Suffering
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Jörgen Sparf. (2016) Disability and Vulnerability: Interpretations of Risk in Everyday Life. Journal of Contingencies and Crisis Management 24:4, pages 244-252.
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Nina Hallowell, Shirlene Badger, Sue Richardson, Carlos Caldas, Richard H. Hardwick, Rebecca C. Fitzgerald & Julia Lawton. (2016) An investigation of the factors effecting high-risk individuals’ decision-making about prophylactic total gastrectomy and surveillance for hereditary diffuse gastric cancer (HDGC). Familial Cancer 15:4, pages 665-676.
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Ganzamungu Zihindula & Pranitha Maharaj. (2015) Risk of Sexual Violence: Perspectives and Experiences of Women in a Hospital in the Democratic Republic of Congo. Journal of Community Health 40:4, pages 736-743.
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Isabelle Pellegrini, Niki Prodromou, Isabelle Coupier, Laetitia Huiart, Jessica Moretta, Catherine Noguès & Claire Julian-Reynier. (2014) Avoir un enfant et accéder au DPN/DPI pour des femmes porteuses d’une mutation BRCA ? Malades et indemnes appréhendent la question différemment. Bulletin du Cancer 101:11, pages 1001-1008.
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Claire Balmer, Frances Griffiths & Janet Dunn. (2014) A qualitative systematic review exploring lay understanding of cancer by adults without a cancer diagnosis. Journal of Advanced Nursing 70:8, pages 1688-1701.
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Felicity K. Boardman. (2014) Knowledge is power? The role of experiential knowledge in genetically ‘risky’ reproductive decisions. Sociology of Health & Illness 36:1, pages 137-150.
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Iain Wilkinson. (2013) The problem of suffering as a driving force of rationalization and social change. The British Journal of Sociology 64:1, pages 123-141.
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Sahra Gibbon, Eirini Kampriani & Andrea zur Nieden. (2010) BRCA patients in Cuba, Greece and Germany: Comparative perspectives on public health, the state and the partial reproduction of ‘neoliberal’ subjects. BioSocieties 5:4, pages 440-466.
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Catherine M. Will, David Armstrong & Theresa M. Marteau. (2010) Genetic unexceptionalism: Clinician accounts of genetic testing for familial hypercholesterolaemia. Social Science & Medicine 71:5, pages 910-917.
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Wendy L. Lipworth, Heather M. Davey, Stacy M. Carter, Claire Hooker & Wendy Hu. (2010) Beliefs and beyond: what can we learn from qualitative studies of lay people’s understandings of cancer risk?. Health Expectations 13:2, pages 113-124.
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Daniel H. Lende & Alicia Lachiondo. (2008) Embodiment and Breast Cancer Among African American Women. Qualitative Health Research 19:2, pages 216-228.
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Holly EtchegaryBeth PotterHeather HowleyMario CappelliDoug CoyleIan GrahamMark WalkerBrenda Wilson. (2008) The Influence of Experiential Knowledge on Prenatal Screening and Testing Decisions. Genetic Testing 12:1, pages 115-124.
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Holly Etchegary & Colin Perrier. (2007) Information Processing in the Context of Genetic Risk: Implications for Genetic‐Risk Communication. Journal of Genetic Counseling 16:4, pages 419-432.
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Paula M. Saukko, Suzanne H. Richards, Maggie H. Shepherd & John L. Campbell. (2006) Are genetic tests exceptional? Lessons from a qualitative study on thrombophilia. Social Science & Medicine 63:7, pages 1947-1959.
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