Jennifer Viberg Johansson

Ethics of Health Data Infrastructures: Toward Continuous Governance and Public Trust

Inoue, Yusuke; Viberg Johansson, Jennifer

Ingår i Journal of Medical Internet Research, 2026

• DOI för Ethics of Health Data Infrastructures: Toward Continuous Governance and Public Trust
• Ladda ner fulltext (pdf) av Ethics of Health Data Infrastructures: Toward Continuous Governance and Public Trust

Patient Preferences in Neuromuscular Diseases: Insights for Future Drug Development

Jimenez-Moreno, Aura Cecilia; Blain, Alasdair; Pinto, Cathy Anne; Soekhai, Vikas et al.

Ingår i JIMD Reports, 2026

• DOI för Patient Preferences in Neuromuscular Diseases: Insights for Future Drug Development
• Ladda ner fulltext (pdf) av Patient Preferences in Neuromuscular Diseases: Insights for Future Drug Development

Införande av rehabiliteringskoordinator inom psykiatrisk specialistsjukvård: En registerbaserad uppföljning

Andersén, Åsa; Berglund, Erik; Anderzén, Ingrid; Viberg Johansson, Jennifer

2026

• Ladda ner fulltext (pdf) av Införande av rehabiliteringskoordinator inom psykiatrisk specialistsjukvård: En registerbaserad uppföljning

Motor fatigue and fatigability in early multiple sclerosis patients: an analysis of clinical, radiological and psychological underpinnings

Betti, Matteo; Masciulli, C.; Addazio, I.; Ballerini, C. et al.

Ingår i Neurological Sciences, 2026

• DOI för Motor fatigue and fatigability in early multiple sclerosis patients: an analysis of clinical, radiological and psychological underpinnings
• Ladda ner fulltext (pdf) av Motor fatigue and fatigability in early multiple sclerosis patients: an analysis of clinical, radiological and psychological underpinnings

Colorectal cancer risk: stereotypical assumptions and competing values - a qualitative study with the general public

Sundell, Erica; Hedström, Mariann; Nihlén Fahlquist, Jessica; Viberg Johansson, Jennifer et al.

Ingår i BMC Public Health, 2026

• DOI för Colorectal cancer risk: stereotypical assumptions and competing values - a qualitative study with the general public
• Ladda ner fulltext (pdf) av Colorectal cancer risk: stereotypical assumptions and competing values - a qualitative study with the general public

Ethics of Health Data Infrastructures: Toward Continuous Governance and Public Trust

Inoue, Yusuke; Viberg Johansson, Jennifer

Ingår i Journal of Medical Internet Research, 2026

• DOI för Ethics of Health Data Infrastructures: Toward Continuous Governance and Public Trust
• Ladda ner fulltext (pdf) av Ethics of Health Data Infrastructures: Toward Continuous Governance and Public Trust

Patient Preferences in Neuromuscular Diseases: Insights for Future Drug Development

Jimenez-Moreno, Aura Cecilia; Blain, Alasdair; Pinto, Cathy Anne; Soekhai, Vikas et al.

Ingår i JIMD Reports, 2026

• DOI för Patient Preferences in Neuromuscular Diseases: Insights for Future Drug Development
• Ladda ner fulltext (pdf) av Patient Preferences in Neuromuscular Diseases: Insights for Future Drug Development

Motor fatigue and fatigability in early multiple sclerosis patients: an analysis of clinical, radiological and psychological underpinnings

Betti, Matteo; Masciulli, C.; Addazio, I.; Ballerini, C. et al.

Ingår i Neurological Sciences, 2026

• DOI för Motor fatigue and fatigability in early multiple sclerosis patients: an analysis of clinical, radiological and psychological underpinnings
• Ladda ner fulltext (pdf) av Motor fatigue and fatigability in early multiple sclerosis patients: an analysis of clinical, radiological and psychological underpinnings

Colorectal cancer risk: stereotypical assumptions and competing values - a qualitative study with the general public

Sundell, Erica; Hedström, Mariann; Nihlén Fahlquist, Jessica; Viberg Johansson, Jennifer et al.

Ingår i BMC Public Health, 2026

• DOI för Colorectal cancer risk: stereotypical assumptions and competing values - a qualitative study with the general public
• Ladda ner fulltext (pdf) av Colorectal cancer risk: stereotypical assumptions and competing values - a qualitative study with the general public

Perceptions of lifestyle-related risk communication in patients with breast and colorectal cancer: a qualitative interview study in Sweden

Grauman, Åsa; Sundell, Erica; Viberg Johansson, Jennifer; Cavalli-Bjorkman, Nina et al.

Ingår i Archives of Public Health, 2024

• DOI för Perceptions of lifestyle-related risk communication in patients with breast and colorectal cancer: a qualitative interview study in Sweden
• Ladda ner fulltext (pdf) av Perceptions of lifestyle-related risk communication in patients with breast and colorectal cancer: a qualitative interview study in Sweden

Comparing and modeling the use of online recommender systems

Engström, Emma; Vartanova, Irina; Viberg Johansson, Jennifer; Persson, Minna et al.

Ingår i Computers in Human Behavior Reports, 2024

• DOI för Comparing and modeling the use of online recommender systems
• Ladda ner fulltext (pdf) av Comparing and modeling the use of online recommender systems

'Humans think outside the pixels': Radiologists' perceptions of using artificial intelligence for breast cancer detection in mammography screening in a clinical setting

Viberg Johansson, Jennifer; Engström, Emma

Ingår i Health Informatics Journal, 2024

• DOI för 'Humans think outside the pixels': Radiologists' perceptions of using artificial intelligence for breast cancer detection in mammography screening in a clinical setting
• Ladda ner fulltext (pdf) av 'Humans think outside the pixels': Radiologists' perceptions of using artificial intelligence for breast cancer detection in mammography screening in a clinical setting

Women's perceptions and attitudes towards the use of AI in mammography in Sweden: a qualitative interview study

Viberg Johansson, Jennifer; Dembrower, Karin; Strand, Fredrik; Grauman, Åsa

Ingår i BMJ Open, 2024

• DOI för Women's perceptions and attitudes towards the use of AI in mammography in Sweden: a qualitative interview study
• Ladda ner fulltext (pdf) av Women's perceptions and attitudes towards the use of AI in mammography in Sweden: a qualitative interview study

Patients accept therapy using embryonic stem cells for Parkinson's disease: a discrete choice experiment

Schölin Bywall, Karin; Drevin, Jennifer; Groothuis-Oudshoorn, Catharina; Veldwijk, Jorien et al.

Ingår i BMC Medical Ethics, 2023

• DOI för Patients accept therapy using embryonic stem cells for Parkinson's disease: a discrete choice experiment
• Ladda ner fulltext (pdf) av Patients accept therapy using embryonic stem cells for Parkinson's disease: a discrete choice experiment

Public Preferences for Digital Health Data Sharing: Discrete Choice Experiment Study in 12 European Countries.

Biasiotto, Roberta; Viberg Johansson, Jennifer; Alemu, Melaku Birhanu; Romano, Virginia et al.

Ingår i Journal of Medical Internet Research, 2023

• DOI för Public Preferences for Digital Health Data Sharing: Discrete Choice Experiment Study in 12 European Countries.

Experiences of individuals with rheumatoid arthritis interacting with health care and the use of a digital self-care application: a qualitative interview study

Viberg Johansson, Jennifer; Blyckert, Hanna; Schölin Bywall, Karin

Ingår i BMJ Open, 2023

• DOI för Experiences of individuals with rheumatoid arthritis interacting with health care and the use of a digital self-care application: a qualitative interview study
• Ladda ner fulltext (pdf) av Experiences of individuals with rheumatoid arthritis interacting with health care and the use of a digital self-care application: a qualitative interview study

Physical function and severe side effects matter most to patients with RA (< 5 years): a discrete choice experiment assessing preferences for personalized RA treatment

Schölin Bywall, Karin; Esbensen, Bente Appel; Heidenvall, Marie; Erlandsson, Inger et al.

Ingår i BMC Rheumatology, 2023

• DOI för Physical function and severe side effects matter most to patients with RA (< 5 years): a discrete choice experiment assessing preferences for personalized RA treatment
• Ladda ner fulltext (pdf) av Physical function and severe side effects matter most to patients with RA (< 5 years): a discrete choice experiment assessing preferences for personalized RA treatment

Comparing Outcomes of a Discrete Choice Experiment and Case 2 Best-Worst Scaling: An Application to Neuromuscular Disease Treatment

Soekhai, Vikas; Donkers, Bas; Viberg Johansson, Jennifer; Jimenez-Moreno, Cecilia et al.

Ingår i Patient, s. 239-253, 2023

• DOI för Comparing Outcomes of a Discrete Choice Experiment and Case 2 Best-Worst Scaling: An Application to Neuromuscular Disease Treatment
• Ladda ner fulltext (pdf) av Comparing Outcomes of a Discrete Choice Experiment and Case 2 Best-Worst Scaling: An Application to Neuromuscular Disease Treatment

Public perceptions of myocardial infarction: Do illness perceptions predict preferences for health check results

Grauman, Åsa; Viberg, Jennifer; Falahee, Marie; Veldwijk, Jorien

Ingår i Preventive Medicine Reports, s. 101683-101683, 2022

• DOI för Public perceptions of myocardial infarction: Do illness perceptions predict preferences for health check results
• Ladda ner fulltext (pdf) av Public perceptions of myocardial infarction: Do illness perceptions predict preferences for health check results

Functional capacity vs side effects: treatment attributes to consider when individualising treatment for patients with rheumatoid arthritis

Schölin Bywall, Karin; Esbensen, Bente Appel; Lason, Marta; Heidenvall, Marie et al.

Ingår i Clinical Rheumatology, s. 695-704, 2022

• DOI för Functional capacity vs side effects: treatment attributes to consider when individualising treatment for patients with rheumatoid arthritis
• Ladda ner fulltext (pdf) av Functional capacity vs side effects: treatment attributes to consider when individualising treatment for patients with rheumatoid arthritis

Making space for patients’ preferences in precision medicine: a qualitative study exploring perspectives of patients with rheumatoid arthritis

Schölin Bywall, Karin; Viberg, Jennifer; Erlandsson, Inger; Heidenvall, Marie et al.

Ingår i BMJ Open, 2022

• DOI för Making space for patients’ preferences in precision medicine: a qualitative study exploring perspectives of patients with rheumatoid arthritis
• Ladda ner fulltext (pdf) av Making space for patients’ preferences in precision medicine: a qualitative study exploring perspectives of patients with rheumatoid arthritis

What ethical approaches are used by scientists when sharing health data?: An interview study

Viberg, Jennifer; Bentzen, Heidi Beate; Mascalzoni, Deborah

Ingår i BMC Medical Ethics, 2022

• DOI för What ethical approaches are used by scientists when sharing health data?: An interview study
• Ladda ner fulltext (pdf) av What ethical approaches are used by scientists when sharing health data?: An interview study

Patients' views on using human embryonic stem cells to treat Parkinson's disease: an interview study

Drevin, Jennifer; Nyholm, Dag; Widner, Håkan; Van Vliet, Trinette et al.

Ingår i BMC Medical Ethics, 2022

• DOI för Patients' views on using human embryonic stem cells to treat Parkinson's disease: an interview study
• Ladda ner fulltext (pdf) av Patients' views on using human embryonic stem cells to treat Parkinson's disease: an interview study

Preference Variation: Where Does Health Risk Attitude Come Into the Equation?

Huls, Samare P. I.; Veldwijk, Jorien; Swait, Joffre D.; Viberg Johansson, Jennifer et al.

Ingår i Value in Health, s. 2044-2052, 2022

• DOI för Preference Variation: Where Does Health Risk Attitude Come Into the Equation?
• Ladda ner fulltext (pdf) av Preference Variation: Where Does Health Risk Attitude Come Into the Equation?

Governing health data across changing contexts: A focus group study of citizen’s views in England, Iceland, and Sweden

Shah, N.; Viberg Johansson, Jennifer; Haraldsdóttir, E.; Bentzen, H.B. et al.

Ingår i International Journal of Medical Informatics, 2021

• DOI för Governing health data across changing contexts: A focus group study of citizen’s views in England, Iceland, and Sweden

Preferences of the Public for Sharing Health Data: Discrete Choice Experiment

Viberg Johansson, Jennifer; Bentzen, Heidi Beate; Shah, Nisha; Haraldsdóttir, Eik et al.

Ingår i JMIR Medical Informatics, 2021

• DOI för Preferences of the Public for Sharing Health Data: Discrete Choice Experiment
• Ladda ner fulltext (pdf) av Preferences of the Public for Sharing Health Data: Discrete Choice Experiment

Governance mechanisms for sharing of health data: An approach towards selecting attributes for complex discrete choice experiment studies

Viberg, Jennifer; Shah, Nisha; Haraldsdóttir, Eik; Bentzen, Heidi Beate et al.

Ingår i Technology in society, s. 101625-101625, 2021

• DOI för Governance mechanisms for sharing of health data: An approach towards selecting attributes for complex discrete choice experiment studies

A study protocol for quantifying patient preferences in neuromuscular disorders: a case study of the IMI PREFER Project [version 1; peer review: 1 approved]

Jimenez-Moreno, Aura Cecilia; Pinto, Cathy Anne; Levitan, Bennett; Whichello, Chiara et al.

Ingår i Wellcome Open Research, 2020

• DOI för A study protocol for quantifying patient preferences in neuromuscular disorders: a case study of the IMI PREFER Project [version 1; peer review: 1 approved]
• Ladda ner fulltext (pdf) av A study protocol for quantifying patient preferences in neuromuscular disorders: a case study of the IMI PREFER Project [version 1; peer review: 1 approved]

Mimicking Real-Life Decision Making in Health: Allowing Respondents Time to Think in a Discrete Choice Experiment

Veldwijk, Jorien; Viberg Johansson, Jennifer; Donkers, Bas; de Bekker-Grob, Esther W.

Ingår i Value in Health, s. 945-952, 2020

• DOI för Mimicking Real-Life Decision Making in Health: Allowing Respondents Time to Think in a Discrete Choice Experiment

Research participants' preferences for receiving genetic risk information: a discrete choice experiment

Viberg, Jennifer; Langenskiöld, Sophie; Segerdahl, Pär; Hansson, Mats G. et al.

Ingår i Genetics in Medicine, s. 2381-2389, 2019

• DOI för Research participants' preferences for receiving genetic risk information: a discrete choice experiment

Making sense of genetic risk: A qualitative focus-group study of healthy participants in genomic research

Viberg, Jennifer; Segerdahl, Pär; Hösterey Ugander, Ulrika; Hansson, Mats G. et al.

Ingår i Patient Education and Counseling, s. 422-427, 2018

• DOI för Making sense of genetic risk: A qualitative focus-group study of healthy participants in genomic research

Mimicking Real Life Decision-Making In Health: Allowing Respondents Time-To-Think In A Discrete Choice Experiment

Veldwijk, J.; Viberg Johansson, Jennifer; Donkers, B.; de Bekker-Grob, E.

Ingår i Value in Health, 2017

Freedom of Choice about Incidental Findings can frustrate participants’ true preferences

Viberg, Jennifer; Segerdahl, Pär; Langenskiöld, Sophie; Hansson, Mats G

Ingår i Bioethics, s. 203-209, 2016

• DOI för Freedom of Choice about Incidental Findings can frustrate participants’ true preferences

Incidental findings: the time is not yet ripe for a policy for biobanks

Viberg, Jennifer; Hansson, Mats G.; Langenskiöld, Sophie; Segerdahl, Pär

Ingår i European Journal of Human Genetics, s. 437-441, 2014

• DOI för Incidental findings: the time is not yet ripe for a policy for biobanks

INDIVIDUAL GENETIC RESEARCH RESULTS: Uncertainties, Conceptions, and Preferences

Viberg Johansson, Jennifer

2018

• Ladda ner fulltext (pdf) av INDIVIDUAL GENETIC RESEARCH RESULTS: Uncertainties, Conceptions, and Preferences

Incidental Findings: The Time Is not yet Ripe for a Policy for Biobanks

Viberg, Jennifer; Hansson, Mats G.; Langenskiöld, Sophie; Segerdahl, Pär

Ingår i Ethics, Law and Governance of Biobanking, Springer, 2015

Införande av rehabiliteringskoordinator inom psykiatrisk specialistsjukvård: En registerbaserad uppföljning

Andersén, Åsa; Berglund, Erik; Anderzén, Ingrid; Viberg Johansson, Jennifer

2026

• Ladda ner fulltext (pdf) av Införande av rehabiliteringskoordinator inom psykiatrisk specialistsjukvård: En registerbaserad uppföljning