1. Almqvist, E., Robins Wahlin, T.-B., Haegermark, A., Lundin, A., Winblad, B., & Anvret, M. (1994). Problems within the sibship experienced during predictive testing for Huntington’s disease. Abstract from 4th European meeting on psychosocial aspects of genetics, Heidelberg University, 12th–14th of September, 1994.
2. Almqvist, E. W., Bloch, M., Brinkman, R., Craufurd, D., Hayden, M. R., & on behalf on an international Huntington disease collaborative group. (1999). A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease. American Journal of Human Genetics, 64, 1293–1304.
3. Almqvist, E. W., Brinkman, R., Wiggins, S., & Hayden, M. R. (2003). Psychological consequences and predictors of adverse events in the first 5 years after predictive testing for Huntington’s disease. Clinical Genetics, 64, 300–309.
4. Codori, A.-M., & Brandt, J. (1994). Psychological costs and benefits of predictive testing for Huntington’s disease. American Journal of Medical Genetics, 54, 174–184.
5. Creswell, J. W., & Poth, C. N. (2017). Qualitative inquiry and research design: choosing among five approaches (4th ed.). Los Angeles: Sage Publications.