Publikationen

Zeitschriftenartikel

Dowrick, A., Evered, J. A., Navarro Dias de Souza, A., Thier, A., Inês Gandolfo Conceição, M.,
Holmberg, C. & Mahtani-Chugani, V. (2023). Sharing uncertainty: Comparing patient narratives of
help-seeking in the first year of the Covid-19 pandemic across the UK, USA, Brazil, Germany and
Spain. SSM - Qualitative Research in Health, 4(1), 100306. 

Dowrick, A., Grob, R., Sawada., A., Thier, A., Holmberg, C. & Sakuma Sato, R.(2023). Navigating responsible bio-political citizenship: Cross-country comparison of stigma in Covid-19 illness narratives in Germany, Japan, the UK and the USA. SSM - Qualitative Research in Health, 4(1), 100291. 

Holmberg, C., Nettleton, S., Sakuma Sato, R., Mahtani-Chugani, V., Driessen, A., Ormel, l., Wynn, M.,
Verhej, N., Alma, M. & Thier, A. (2023). Doing isolation – Caring Citizens. A cross-country comparative
analysis of patient experiences with isolation practices during the early phase of the Covid-19
pandemic. SSM - Qualitative Research in Health, 4(60), 100364.

Schultze, M., Breuning, M., Heyde, M. von der, Kaiser, M., Müller-Nordhorn, J. & Holmberg, C. (2022).
Presenting scientifically-derived illness experiences online - Evaluation of the use of the DIPEx
Germany website. Patient education and counseling, 105(7), 2328–2337.

Kaiser M., Adami S., Lucius-Hoene G., Muller-Nordhorn J., Goerling U, Breuning M., Holmberg C. (2021). Learning-by-doing: the importance of experiential knowledge sharing for meeting the information needs of people with colorectal cancer in Germany-a qualitative study. BMJ Open, 11(2):e038460.

Blödt S., Müller-Nordhorn J., Seifert G., Holmberg C. (2021). Trust, medical expertise and humaneness: A qualitative study on people with cancer' satisfaction with medical care. Health Expect., 24(2):317-26.

Schultze M., Müller‐Nordhorn J., Holmberg C. (2020). Discussing the effects of prostate cancer beyond biographical disruption and new normalcy: the experiences of men with prostate cancer in Germany. Sociology of health & illness, 42(6), p.1359-78

Holmberg C., Adami S. (2020). Leben mit dem Stoma. Der Onkologe. 2020; 26(12):1162.

Breuning M., Schäfer-Fauth L., Lucius-Hoene G., Holmberg C. (2020). Connecting one’s own illness story to the illness experiences of others on a website - An evaluation study using the think aloud method. Patient Education and Counseling, 103(1), p. 199-207.

Blödt S., Kaiser M., Adam Y., Adami S., Schultze M., Müller-Nordhorn J., Holmberg C. (2018). Understanding the role of health information in patients’ experiences: secondary analysis of qualitative narrative interviews with people diagnosed with cancer in Germany. BMJ open, 8(3):e019576-e.

Adami S., Breuning M., Bengel J., Bischoff A., Peng-Keller S. (2018). Chronische Schmerzpatientinnen und -patienten sprechen über ihre Spiritualität. Spiritual Care, 7(3), p. 243-53.

Giesler J. M., Keller B., Repke T., Leonhart R., Weis J., Muckelbauer R.,..., Holmberg C. (2017). Effect of a Website That Presents Patients' Experiences on Self-Efficacy and Patient Competence of Colorectal Cancer Patients: Web-Based Randomized Controlled Trial. Journal of medical Internet research, 19(10):e334-e.

Engler J., Güthlin C., Dahlhaus A., Kojima E., Müller‐Nordhorn J., Weißbach L., Holmberg C. (2017). Physician cooperation in outpatient cancer care. An amplified secondary analysis of qualitative interview data. European journal of cancer care, 26(6):e12675-n/a.

Breuning M., Lucius-Hoene G., Burbaum C., Himmel W., Bengel J. (2017). Subjektive Krankheitserfahrungen und Patientenorientierung: Das Website-Projekt DIPEx Germany. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 60(4):453-61.

Engler J., Adami S., Adam Y., Keller B., Repke T., Fügemann H,..., Holmberg C. (2016). Using others' experiences. Cancer patients' expectations and navigation of a website providing narratives on prostate, breast and colorectal cancer. Patient Educ Couns, 99(8), p. 1325-32.

Breuning M., Hettmer S., Strahm B., Bengel J., Niemeyer C. (2016). Krebskranke Kinder und ihre Familien: Verständnis für das Erleben. Deutsches Ärzteblatt,113(51), p. 2362-3.

Lucius-Hoene G., Groth S., Becker A.-K., Dvorak F., Breuning M., Himmel W. (2013). Wie erleben Patienten die Veröffentlichung ihrer Krankheitserfahrungen im Internet? Die Rehabilitation, 52(3), p. 196-201.

Lucius-Hoene G., Thiele U., Breuning M., Haug S. (2012). Doctors' voices in patients' narratives: coping with emotions in storytelling. Chronic illness; 8(3), p.163-75.

Bücher & Buchbeiträge

Silberzahn-Jandt, G., Thier, A., Holmberg, C. (2023). „wer hilft mir, wenn jetzt was ist?“. In: Ohlbrecht, H., Seltrecht, A. (eds) Pflege: Systemrelevant – und nun?. Gesundheit und Gesellschaft. Springer VS, Wiesbaden. 

Holmberg C:, Breuning M. (2021). Personal Experience of Illness. In: Scrimshaw SC, Lane SD, Rubinstein RA, Fisher J, editors. Sage Handbook of Social Studies in Health and Medicine, p. 143-161.

Holmberg C. Krankheitsnarrative in der Versorgungsforschung. In: Netzwerk Qualitative Gesundheitsforschung, editor. Perspektiven qualitativer Gesundheitsforschung 2020; p. 99-115.

Lucius-Hoene G., Holmberg C., Meyer T., editors (2018). Illness Narratives in Practice: Potentials and Challenges of Using Narratives in Health-related Contexts. Oxford: Oxford University Press.

Lucius-Hoene G., Breuning M., Helfferich C. (2018). Illness narratives in practice: Which questions do we have to face when collecting and using them? In: Lucius-Hoene G., Holmberg C., Meyer T., editors. Illness Narratives in Practice: Potentials and Challenges of Using Narratives in Health-related Contexts. Oxford: Oxford University Press.

Palant A., Himmel W. (2018). How to use illness narratives in medical education: First teaching experiences with the German DIPEx website project. In: Lucius-Hoene G., Holmberg C., Meyer T., editors. Illness Narratives in Practice: Potentials and Challenges of Using Narratives in Health-related Contexts. Oxford: Oxford University Press; p. 152-63.

Lucius-Hoene G., Breuning M., Palant A. (2015). Patientenerfahrungen als Ressource: Die Website krankheitserfahrungen. de. In: Amelung V. E., Eble S., Hildebrandt H., Kieps F., Längel R., Ozegowski S., et al., editors. Patientenorientierung Schlüssel für mehr Qualität (Schriftenreihe des Bundesverbandes Managed Care). Berlin: MWV Medizinisch Wissenschaftliche Verlagsgesellschaft; p. 248-53.

Posterbeiträge

Thier, A. K., Schultze, M., Spura, A., Buhs, B. & Holmberg, C. (2023). Versorgungserfahrungen von
Menschen mit Post-Covid während der Pandemie (2020-2022). In Das Gesundheitswesen,
Gesundheitskompetenz in Krisenzeiten. Georg Thieme Verlag.