Citations (16)
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Catarina Seidi, Marta Patrão, Sara Guerra, Carla Roma Oliveira, Álvaro Mendes & Liliana Sousa. (2023) The Experience of Receiving and Transmitting a Genetic Disease. Journal of Constructivist Psychology 36:2, pages 232-247.
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Mark Gaspar, Troy Grennan, Irving Salit & Daniel Grace. (2018) Confronting comorbidity risks within HIV biographies: gay men’s integration of HPV-associated anal cancer risk into their narratives of living with HIV. Health, Risk & Society 20:5-6, pages 276-296.
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Bob Heyman, Andy Alaszewski & Patrick Brown. (2013) Probabilistic thinking and health risks: An editorial. Health, Risk & Society 15:1, pages 1-11.
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Bob Heyman. (2010) Screening for health risks: A second editorial. Health, Risk & Society 12:2, pages 81-84.
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Bob Heyman. (2010) Screening for health risks: A social science perspective. Health, Risk & Society 12:1, pages 1-6.
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Bob Heyman. (2010) Book review. Health, Risk & Society 12:1, pages 77-79.
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Articles from other publishers (10)
Neil Fahy, Charlotte Rice, Nayana Lahiri, Roopal Desai & Joshua Stott. (2023) Genetic risk for Huntington Disease and reproductive decision‐making: A systematic review. Clinical Genetics 104:2, pages 147-162.
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Jasmin Eppel‐Meichlinger, Andrea Kobleder & Hanna Mayer. (2022) Developing a theoretical definition of self‐organization: A principle‐based concept analysis in the context of uncertainty in chronic illness. Nursing Forum 57:5, pages 954-962.
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Yael Hochman & Gabriela Spector‐Mersel. (2020) Three strategies for doing narrative resistance: Navigating between master narratives. British Journal of Social Psychology 59:4, pages 1043-1061.
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Michael Halpin. (2018) Science and Suffering: Genetics and the Lived Experience of Illness. Social Problems 65:3, pages 360-376.
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Allison Werner-Lin, Frances K. Barg, Katherine S. Kellom, Kallyn J. Stumm, Lisa Pilchman, Ashley N. Tomlinson & Barbara A. Bernhardt. (2016) Couple’s Narratives of Communion and Isolation Following Abnormal Prenatal Microarray Testing Results. Qualitative Health Research 26:14, pages 1975-1987.
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Petra Lilja Andersson, Åsa Petersén, Caroline Graff & Anna-Karin Edberg. (2016) Ethical aspects of a predictive test for Huntington’s Disease. Nursing Ethics 23:5, pages 565-575.
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Kevin Dew, Anne Scott & Allison KirkmanKevin Dew, Anne Scott & Allison Kirkman. 2016. Social, Political and Cultural Dimensions of Health. Social, Political and Cultural Dimensions of Health
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Karen Forrest Keenan, Sheila A. Simpson, Zosia Miedzybrodzka, David A. Alexander & June Semper. (2013) How Do Partners Find out About the Risk of Huntington’s Disease in Couple Relationships?. Journal of Genetic Counseling 22:3, pages 336-344.
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Hervé Corvellec. (2011) The narrative structure of risk accounts. Risk Management 13:3, pages 101-121.
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Kelly Amanda Raspberry & Debra Skinner. (2011) Negotiating desires and options: How mothers who carry the fragile X gene experience reproductive decisions. Social Science & Medicine 72:6, pages 992-998.
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