Mats G. Hansson

Preferences, attitudes and views regarding genetic newborn screening (gNBS) for rare diseases: a systematic review of the literature and synthesis from 2009 to 2022

Martin, Sylvia; Kyosovska-Peshtenska, Gergana; Audi, Jennifer; Zarakowska, Kaja et al.

Ingår i Orphanet Journal of Rare Diseases, 2026

• DOI för Preferences, attitudes and views regarding genetic newborn screening (gNBS) for rare diseases: a systematic review of the literature and synthesis from 2009 to 2022
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“Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project

Martin, Sylvia; Piperkova, Aneta; Zschüntzsch, Jana; Sky, Edith Gross et al.

Ingår i AI and Ethics, s. 4843-4853, 2025

• DOI för “Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project
• Ladda ner fulltext (pdf) av “Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project

Determination of prednisolone concentration in human breast milk and plasma of breastfed infants: study protocol of a Swedish multicentre low-intervention clinical trial

Svedenkrans, Jenny; Hellgren, Karin; Backlund, Karin; Perrin, Nina et al.

Ingår i BMJ Open, 2025

• DOI för Determination of prednisolone concentration in human breast milk and plasma of breastfed infants: study protocol of a Swedish multicentre low-intervention clinical trial

Setting up mother–infant pair lactation studies with biobanking for research according to regulatory requirements

Hansson, Mats G.; Björkgren, Ida; Svedenkrans, Jenny; Backman, Helena et al.

Ingår i British Journal of Clinical Pharmacology, 2025

• DOI för Setting up mother–infant pair lactation studies with biobanking for research according to regulatory requirements

“Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project

Martin, Sylvia; Piperkova, Aneta; Zschüntzsch, Jana; Sky, Edith Gross et al.

Ingår i AI and Ethics, s. 4843-4853, 2025

• DOI för “Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project

“Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project

Martin, Sylvia; Piperkova, Aneta; Zschüntzsch, Jana; Sky, Edith Gross et al.

Ingår i AI and Ethics, s. 4843-4853, 2025

• DOI för “Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project
• Ladda ner fulltext (pdf) av “Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project

Determination of prednisolone concentration in human breast milk and plasma of breastfed infants: study protocol of a Swedish multicentre low-intervention clinical trial

Svedenkrans, Jenny; Hellgren, Karin; Backlund, Karin; Perrin, Nina et al.

Ingår i BMJ Open, 2025

• DOI för Determination of prednisolone concentration in human breast milk and plasma of breastfed infants: study protocol of a Swedish multicentre low-intervention clinical trial

Setting up mother–infant pair lactation studies with biobanking for research according to regulatory requirements

Hansson, Mats G.; Björkgren, Ida; Svedenkrans, Jenny; Backman, Helena et al.

Ingår i British Journal of Clinical Pharmacology, 2025

• DOI för Setting up mother–infant pair lactation studies with biobanking for research according to regulatory requirements

“Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project

Martin, Sylvia; Piperkova, Aneta; Zschüntzsch, Jana; Sky, Edith Gross et al.

Ingår i AI and Ethics, s. 4843-4853, 2025

• DOI för “Code of ethical practice” for sharing and access to personal data for AI-/ ML-based technologies in rare diseases genetic NBS research project: a collaborative construction in a European IMI project

Determination of prednisolone concentration in human breast milk and plasma of breastfed infants: study protocol of a Swedish multicentre low-intervention clinical trial

Svedenkrans, Jenny; Hellgren, Karin; Backlund, Karin; Perrin, Nina et al.

Ingår i BMJ Open, 2025

• DOI för Determination of prednisolone concentration in human breast milk and plasma of breastfed infants: study protocol of a Swedish multicentre low-intervention clinical trial
• Ladda ner fulltext (pdf) av Determination of prednisolone concentration in human breast milk and plasma of breastfed infants: study protocol of a Swedish multicentre low-intervention clinical trial

Patient preferences in genetic newborn screening for rare diseases: study protocol

MARTIN, Sylvia; Angolini, Emanuele; Audi, Jennifer; Bertini, Enrico et al.

Ingår i BMJ Open, 2024

• DOI för Patient preferences in genetic newborn screening for rare diseases: study protocol

Legal obstacles jeopardise research in personalised medicine – experiences from a Nordic collaboration within rheumatology

Glintborg, Bente; Hansson, Mats G.; Hammer, Hilde Berner; Klareskog, Lars et al.

Ingår i Scandinavian Journal of Public Health, s. 1019-1025, 2024

• DOI för Legal obstacles jeopardise research in personalised medicine – experiences from a Nordic collaboration within rheumatology

Legal obstacles jeopardise research in personalised medicine - experiences from a Nordic collaboration within rheumatology

Glintborg, Bente; Hansson, Mats G.; Hammer, Hilde Berner; Klareskog, Lars et al.

Ingår i Scandinavian Journal of Public Health, s. 1019-1025, 2024

• DOI för Legal obstacles jeopardise research in personalised medicine - experiences from a Nordic collaboration within rheumatology

Patient preferences in genetic newborn screening for rare diseases: study protocol

Martin, Sylvia; Angolini, Emanuele; Audi, Jennifer; Bertini, Enrico et al.

Ingår i BMJ Open, 2024

• DOI för Patient preferences in genetic newborn screening for rare diseases: study protocol
• Ladda ner fulltext (pdf) av Patient preferences in genetic newborn screening for rare diseases: study protocol

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

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

Bywall, Karin Schölin; 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

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

Bywall, Karin Schölin; 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

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

A proposal for an international Code of Conduct for data sharing in genomics

Matar, Amal; Hansson, Mats; Slokenberga, Santa; Panagiotopoulos, Adam et al.

Ingår i Developing World Bioethics, s. 344-357, 2023

• DOI för A proposal for an international Code of Conduct for data sharing in genomics
• Ladda ner fulltext (pdf) av A proposal for an international Code of Conduct for data sharing in genomics

Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe

Garnier, Nicolas; Berghout, Joanne; Zygmunt, Aldona; Singh, Deependra et al.

Ingår i PLOS ONE, 2023

• DOI för Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe
• Ladda ner fulltext (pdf) av Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe

The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

Laurie, Steven; Piscia, Davide; Matalonga, Leslie; Corvo, Alberto et al.

Ingår i Human Mutation, s. 717-733, 2022

• DOI för The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases
• Ladda ner fulltext (pdf) av The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

Laurie, Steven; Piscia, Davide; Matalonga, Leslie; Corvo, Alberto et al.

Ingår i Human Mutation, 2022

• DOI för The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

Attitudes and values among the Swedish general public to using human embryonic stem cells for medical treatment

Grauman, Åsa; Hansson, Mats G.; Nyholm, Dag; Jiltsova, Elena et al.

Ingår i BMC Medical Ethics, 2022

• DOI för Attitudes and values among the Swedish general public to using human embryonic stem cells for medical treatment
• Ladda ner fulltext (pdf) av Attitudes and values among the Swedish general public to using human embryonic stem cells for medical treatment

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

Would you consider donating your left-over embryos to treat Parkinson’s disease? Interviews with individuals that underwent IVF in Sweden

Schölin Bywall, Karin; Holte, Jan; Brodin, Thomas; Hansson, Mats G. et al.

Ingår i BMC Medical Ethics, 2022

• DOI för Would you consider donating your left-over embryos to treat Parkinson’s disease? Interviews with individuals that underwent IVF in Sweden
• Ladda ner fulltext (pdf) av Would you consider donating your left-over embryos to treat Parkinson’s disease? Interviews with individuals that underwent IVF in Sweden

Does being exposed to an educational tool influence patient preferences?: The influence of an educational tool on patient preferences assessed by a discrete choice experiment

Schölin Bywall, Karin; Veldwijk, Jorien; Hansson, Mats G.; Baecklund, Eva et al.

Ingår i Patient Education and Counseling, s. 2577-2585, 2021

• DOI för Does being exposed to an educational tool influence patient preferences?: The influence of an educational tool on patient preferences assessed by a discrete choice experiment

Does being exposed to an educational tool influence patient preferences? The influence of an educational tool on patient preferences assessed by a discrete choice experiment.

Bywall, Karin Schölin; Veldwijk, Jorien; Hansson, Mats G.; Baecklund, Eva et al.

Ingår i Patient Education and Counseling, s. 2577-2585, 2021

• DOI för Does being exposed to an educational tool influence patient preferences? The influence of an educational tool on patient preferences assessed by a discrete choice experiment.

Communicating test results from a general health checkup: the public’s preferences from a discrete choice experiment survey

Grauman, Åsa; Hansson, Mats G.; James, Stefan; Hauber, Brett et al.

Ingår i Patient Related Outcome Measures, s. 649-660, 2021

• DOI för Communicating test results from a general health checkup: the public’s preferences from a discrete choice experiment survey
• Ladda ner fulltext (pdf) av Communicating test results from a general health checkup: the public’s preferences from a discrete choice experiment survey

Good general health and lack of family history influence the underestimation of cardiovascular risk: A cross sectional study

Grauman, Åsa; Veldwijk, Jorien; James, Stefan; Hansson, Mats G. et al.

Ingår i European Journal of Cardiovascular Nursing, s. 676-683, 2021

• DOI för Good general health and lack of family history influence the underestimation of cardiovascular risk: A cross sectional study
• Ladda ner fulltext (pdf) av Good general health and lack of family history influence the underestimation of cardiovascular risk: A cross sectional study

Patient preferences on rheumatoid arthritis second-line treatment: a discrete choice experiment of Swedish patients

Schölin Bywall, Karin; Kihlbom, Ulrik; Hansson, Mats; Falahee, Marie et al.

Ingår i Arthritis Research & Therapy, 2020

• DOI för Patient preferences on rheumatoid arthritis second-line treatment: a discrete choice experiment of Swedish patients
• Ladda ner fulltext (pdf) av Patient preferences on rheumatoid arthritis second-line treatment: a discrete choice experiment of Swedish patients

Swepis har lett till överilade ändringar i förlossningsrutiner: [SWEPIS has led to rash changes in routines within Swedish obstetric care]

Drevin, Jennifer; Hansson, Mats

Ingår i Läkartidningen, 2020

Pretend Play as an Intervention for Children With Cancer: A Feasibility Study

Frygner-Holm, Sara; Russ, Sandra; Quitmann, Julia; Ring, Lena et al.

Ingår i Journal of Pediatric Oncology Nursing, s. 65-75, 2020

• DOI för Pretend Play as an Intervention for Children With Cancer: A Feasibility Study

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

Values and value conflicts in implementation and use of preconception expanded carrier screening: an expert interview study

Matar, Amal; Hansson, Mats G.; Höglund, Anna T

Ingår i BMC Medical Ethics, 2019

• DOI för Values and value conflicts in implementation and use of preconception expanded carrier screening: an expert interview study
• Ladda ner fulltext (pdf) av Values and value conflicts in implementation and use of preconception expanded carrier screening: an expert interview study

The Position of Neuromuscular Patients in Shared Decision Making. Report from the 235th ENMC Workshop: Milan, Italy, January 19-20, 2018

Lochmueller, Hanns; Ambrosini, Anna; van Engelen, Baziel; Hansson, Mats G. et al.

Ingår i JOURNAL OF NEUROMUSCULAR DISEASES, s. 161-172, 2019

• DOI för The Position of Neuromuscular Patients in Shared Decision Making. Report from the 235th ENMC Workshop: Milan, Italy, January 19-20, 2018

Exploring research participants' perceptions of cardiovascular risk information-Room for improvement and empowerment

Grauman, Åsa; Hansson, Mats G.; James, Stefan K; Veldwijk, Jorien et al.

Ingår i Patient Education and Counseling, s. 1528-1534, 2019

• DOI för Exploring research participants' perceptions of cardiovascular risk information-Room for improvement and empowerment
• Ladda ner fulltext (pdf) av Exploring research participants' perceptions of cardiovascular risk information-Room for improvement and empowerment

Short-term mental distress in research participants after receiving cardiovascular risk information

Grauman, Åsa; Hansson, Mats G.; Puranen, Arvid; James, Stefan et al.

Ingår i PLOS ONE, 2019

• DOI för Short-term mental distress in research participants after receiving cardiovascular risk information
• Ladda ner fulltext (pdf) av Short-term mental distress in research participants after receiving cardiovascular risk information

Patient Perspectives on the Value of Patient Preference Information in Regulatory Decision Making: A Qualitative Study in Swedish Patients with Rheumatoid Arthritis

Schölin Bywall, Karin; Veldwijk, Jorien; Hansson, Mats G.; Kihlbom, Ulrik

Ingår i Patient, s. 297-305, 2019

• DOI för Patient Perspectives on the Value of Patient Preference Information in Regulatory Decision Making: A Qualitative Study in Swedish Patients with Rheumatoid Arthritis
• Ladda ner fulltext (pdf) av Patient Perspectives on the Value of Patient Preference Information in Regulatory Decision Making: A Qualitative Study in Swedish Patients with Rheumatoid Arthritis

"A perfect society": Swedish policymakers' ethical and social views on preconception expanded carrier screening

Matar, Amal; Hansson, Mats G.; Höglund, Anna T.

Ingår i Journal of Community Genetics, s. 267-280, 2019

• DOI för "A perfect society": Swedish policymakers' ethical and social views on preconception expanded carrier screening
• Ladda ner fulltext (pdf) av "A perfect society": Swedish policymakers' ethical and social views on preconception expanded carrier screening

Genetics and risk - an exploration of conceptual approaches to genetic risk

Hansson, Mats G.; Bouder, Frederic; Howard, Heidi Carmen

Ingår i Journal of Risk Research, s. 101-108, 2018

• DOI för Genetics and risk - an exploration of conceptual approaches to genetic risk

Perceptions of first-degree relatives of patients with rheumatoid arthritis about lifestyle modifications and pharmacological interventions to reduce the risk of rheumatoid arthritis development: a qualitative interview study

Simons, Gwenda; Stack, Rebecca J.; Stoffer-Marx, Michaela; Englbrecht, Matthias et al.

Ingår i BMC Rheumatology, 2018

• DOI för Perceptions of first-degree relatives of patients with rheumatoid arthritis about lifestyle modifications and pharmacological interventions to reduce the risk of rheumatoid arthritis development: a qualitative interview study
• Ladda ner fulltext (pdf) av Perceptions of first-degree relatives of patients with rheumatoid arthritis about lifestyle modifications and pharmacological interventions to reduce the risk of rheumatoid arthritis development: a qualitative interview study

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

Perceptions of predictive testing for those at risk of developing a chronic inflammatory disease: a meta-synthesis of qualitative studies

Bayliss, Kerin; Raza, Karim; Simons, Gwenda; Falahee, Marie et al.

Ingår i Journal of Risk Research, s. 167-189, 2018

• DOI för Perceptions of predictive testing for those at risk of developing a chronic inflammatory disease: a meta-synthesis of qualitative studies

Giving Patients’ Preferences a Voice in Medical Treatment Life Cycle: The PREFER Public–Private Project

de Bekker-Grob, Esther; Berlin, Conny; Levitan, Bennet; Raza, Karim et al.

Ingår i Patient, s. 263-266, 2017

• DOI för Giving Patients’ Preferences a Voice in Medical Treatment Life Cycle: The PREFER Public–Private Project

Patients' Perceptions of Their Relatives' Risk of Developing Rheumatoid Arthritis and of the Potential for Risk Communication, Prediction, and Modulation

Falahee, Marie; Simons, Gwenda; Buckley, Christopher D.; Hansson, M G et al.

Ingår i Arthritis care & research, s. 1558-1565, 2017

• DOI för Patients' Perceptions of Their Relatives' Risk of Developing Rheumatoid Arthritis and of the Potential for Risk Communication, Prediction, and Modulation

Genetics and risk – an exploration of conceptual approaches to genetic risk

Hansson, Mats G.; Bouder, Frederic; Howard, Heidi C.

Ingår i Journal of Risk Research, s. 101-108, 2017

• DOI för Genetics and risk – an exploration of conceptual approaches to genetic risk

Giving Patients’ Preferences a Voice in Medical Treatment Life Cycle: The PREFER Public–Private Project

de Bekker-Grob, Esther W.; Berlin, Conny; Levitan, Bennett; Raza, Karim et al.

Ingår i Patient, s. 263-266, 2017

• DOI för Giving Patients’ Preferences a Voice in Medical Treatment Life Cycle: The PREFER Public–Private Project

Rheumatoid Arthritis Patients’ Perspectives On The Value Of Patient Preferences In Regulatory Decision-Making During Drug Development: A Qualitative Study

Schölin Bywall, Karin; Veldwijk, Jorien; Hansson, Mats G.; Kihlbom, Ulrik

Ingår i Value in Health, 2017

• DOI för Rheumatoid Arthritis Patients’ Perspectives On The Value Of Patient Preferences In Regulatory Decision-Making During Drug Development: A Qualitative Study

The risk of re-identification versus the need to identify individuals in rare disease research

Hansson, Mats G.; Lochmuller, Hanns; Riess, Olaf; Schaefer, Franz et al.

Ingår i European Journal of Human Genetics, s. 1553-1558, 2016

• DOI för The risk of re-identification versus the need to identify individuals in rare disease research
• Ladda ner fulltext (pdf) av The risk of re-identification versus the need to identify individuals in rare disease research

Anxiety delivered direct-to-consumer: are we asking the right questions about the impacts of DTC genetic testing?

Oliveri, S.; Howard, Heidi Carmen; Renzi, C.; Hansson, Mats G. et al.

Ingår i Journal of Medical Genetics, s. 798-799, 2016

• DOI för Anxiety delivered direct-to-consumer: are we asking the right questions about the impacts of DTC genetic testing?

Anxiety delivered direct-to-consumer: are we asking the right questions about the impacts of DTC genetic testing?

Oliveri, Serena; Howard, Heidi C.; Renzi, Chiara; Hansson, Mats G. et al.

Ingår i Journal of Medical Genetics, s. 798-799, 2016

• DOI för Anxiety delivered direct-to-consumer: are we asking the right questions about the impacts of DTC genetic testing?

Perceptions of risk and predictive testing held by the first-degree relatives of patients with rheumatoid arthritis in England, Austria and Germany: a qualitative study

Stack, Rebecca J.; Stoffer, Michaela; Englbrecht, Mathias; Mosor, Erika et al.

Ingår i BMJ Open, 2016

• DOI för Perceptions of risk and predictive testing held by the first-degree relatives of patients with rheumatoid arthritis in England, Austria and Germany: a qualitative study
• Ladda ner fulltext (pdf) av Perceptions of risk and predictive testing held by the first-degree relatives of patients with rheumatoid arthritis in England, Austria and Germany: a qualitative study

The risk of re-identification versus the need to identify individuals in rare disease research

Hansson, Mats G.; Lochmüller, Hanns; Riess, Olaf; Schaefer, Franz et al.

Ingår i European Journal of Human Genetics, s. 1553-1558, 2016

• DOI för The risk of re-identification versus the need to identify individuals in rare disease research

Let the Individuals Directly Concerned Decide: A Solution to Tragic Choices in Genetic Risk Information

Oliveri, Serena; Pravettoni, Gabriella; Fioretti, Chiara; Hansson, Mats G.

Ingår i Public Health Genomics, s. 307-313, 2016

• DOI för Let the Individuals Directly Concerned Decide: A Solution to Tragic Choices in Genetic Risk Information

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

Ethics rounds: An appreciated form of ethics support

Silén, Marit; Ramklint, Mia; Hansson, Mats G; Haglund, Kristina

Ingår i Nursing Ethics, s. 203-213, 2016

• DOI för Ethics rounds: An appreciated form of ethics support

Let the Individuals Directly Concerned Decide: A Solution to Tragic Choices in Genetic Risk Information

Oliveri, Serena; Pravettoni, Gabriella; Fioretti, Chiara; Hansson, Mats G.

Ingår i Public Health Genomics, s. 307-313, 2016

• DOI för Let the Individuals Directly Concerned Decide: A Solution to Tragic Choices in Genetic Risk Information

Perceptions Of Testing To Predict Future Development Of Rheumatoid Arthritis Among The First-Degree Relatives Of People With Rheumatoid Arthritis: A Qualitative Exploration

Stack, Rebecca J.; Falahee, Marie; Stoffer, Michaela; Stamm, Tanja et al.

Ingår i Rheumatology, s. 110-110, 2015

Broad Consent for Research With Biological Samples: Workshop Conclusions

Grady, Christine; Eckstein, Lisa; Berkman, Ben; Brock, Dan et al.

Ingår i American Journal of Bioethics, s. 34-42, 2015

• DOI för Broad Consent for Research With Biological Samples: Workshop Conclusions

Hope for a cure and altruism are the main motives behind participation in phase 3 clinical cancer trials

Godskesen, Tove; Hansson, Mats G.; Nygren, Peter; Nordin, Karin et al.

Ingår i European Journal of Cancer Care, s. 133-141, 2015

• DOI för Hope for a cure and altruism are the main motives behind participation in phase 3 clinical cancer trials

The Swedish CArdioPulmonary BioImage Study: objectives and design

Bergström, G; Berglund, G; Blomberg, A; Brandberg, J et al.

Ingår i Journal of Internal Medicine, s. 645-659, 2015

• DOI för The Swedish CArdioPulmonary BioImage Study: objectives and design
• Ladda ner fulltext (pdf) av The Swedish CArdioPulmonary BioImage Study: objectives and design

Ethics rounds do not improve the handling of ethical issues by psychiatric staff

Silén, Marit; Haglund, Kristina; Hansson, Mats G.; Ramklint, Mia

Ingår i Nordic Journal of Psychiatry, s. 1700-1707, 2015

• DOI för Ethics rounds do not improve the handling of ethical issues by psychiatric staff

Ethical, Legal and Societal Implications of Biobanking at European Level: A Common Service of the European Biobank and Biomolecular Research Infrastructure

Cambon-Thomsen, Anne; Bovenberg, Jasper; Lavitrano, Marialuisa; Hansson, Mats G. et al.

Ingår i Tissue Antigens, s. 372-372, 2015

International Charter of principles for sharing bio-specimens and data

Mascalzoni, Deborah; Dove, Edward S; Rubinstein, Yaffa; Dawkins, Hugh J S et al.

Ingår i European Journal of Human Genetics, s. 721-728, 2015

• DOI för International Charter of principles for sharing bio-specimens and data
• Ladda ner fulltext (pdf) av International Charter of principles for sharing bio-specimens and data

Öppenheten förstör chansen till patent

Arvidsson, Per I.; Domeij, Bengt; Hansson, Mats G.; Landegren, Ulf et al.

Ingår i Svenska dagbladet, 2015

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

ERIC: a new governance tool for Biobanking

Reichel, Jane; Lind, Anna-Sara; Hansson, Mats G.; Litton, Jan-Eric

Ingår i European Journal of Human Genetics, s. 1055-1057, 2014

• DOI för ERIC: a new governance tool for Biobanking

Why participating in (certain) scientific research is a moral duty

Stjernschantz Forsberg, Joanna; Hansson, Mats G.; Eriksson, Stefan

Ingår i Journal of Medical Ethics, s. 325-328, 2014

• DOI för Why participating in (certain) scientific research is a moral duty

Ethical Review Boards are poor advocates for patient perspectives

Masterton, Malin; Renberg, Tobias; Hansson, Mats G; Kälvemark Sporrong, Sofia

Ingår i Research Ethics, s. 169-181, 2014

• DOI för Ethical Review Boards are poor advocates for patient perspectives

Making researchers moral: Why trustworthiness requires more than ethics guidelines and review

Johnsson, Linus; Eriksson, Stefan; Helgesson, Gert; Hansson, Mats G.

Ingår i Research Ethics, s. 29-46, 2014

• DOI för Making researchers moral: Why trustworthiness requires more than ethics guidelines and review
• Ladda ner fulltext (pdf) av Making researchers moral: Why trustworthiness requires more than ethics guidelines and review

Children's Views on Long-Term Screening for Type 1 Diabetes

Swartling, Ulrica; Helgesson, Gert; Ludvigsson, Johnny; Hansson, Mats G. et al.

Ingår i Journal of Empirical Research on Human Research Ethics, s. 1-9, 2014

• DOI för Children's Views on Long-Term Screening for Type 1 Diabetes

Rare diseases and now rare data?

Mascalzoni, Deborah; Knoppers, Bartha Maria; Aymé, Ségolène; Macilotti, Matteo et al.

Ingår i Nature reviews genetics, s. 372, 2013

Phase 1 clinical trials in end-stage cancer: patient understanding of trial premises and motives for participation

Godskesen, Tove; Nygren, Peter; Nordin, Karin; Hansson, Mats et al.

Ingår i Supportive Care in Cancer, s. 3137-3142, 2013

• DOI för Phase 1 clinical trials in end-stage cancer: patient understanding of trial premises and motives for participation

Finding ways to improve the use of biobanks

Paradiso, Angelo; Hansson, Mats

Ingår i Nature Medicine, s. 815-815, 2013

• DOI för Finding ways to improve the use of biobanks

International guidelines on biobank research leave researchers in ambiguity: why is this so?

Stjernschantz Forsberg, Joanna; Hansson, Mats G.; Evers, Kathinka

Ingår i European Journal of Epidemiology, s. 449-451, 2013

• DOI för International guidelines on biobank research leave researchers in ambiguity: why is this so?

Transition to noncurative end-of-life care in paediatric oncology: a nationwide follow-up in Sweden

Jalmsell, Li; Forslund, Martin; Hansson, Mats G.; Henter, Jan-Inge et al.

Ingår i Acta Paediatrica, s. 744-748, 2013

• DOI för Transition to noncurative end-of-life care in paediatric oncology: a nationwide follow-up in Sweden

Rare diseases and now rare data?

Mascalzoni, Deborah; Knoppers, Bartha Maria; Ayme, Segolene; Macilotti, Matteo et al.

Ingår i Nature reviews genetics, s. 372-372, 2013

• DOI för Rare diseases and now rare data?

Patients would benefit from simplified ethical review and consent procedure

Hansson, Mats G.; van Ommen, Gert Jan; Chadwick, Ruth; Dillner, Joakim

Ingår i The Lancet Oncology, s. 451-453, 2013

• DOI för Patients would benefit from simplified ethical review and consent procedure

Adequate trust avails, mistaken trust matters: On the moral responsibility of doctors as proxies for patients' trust in biobank research

Johnsson, Linus; Helgesson, Gert; Hansson, Mats G.; Eriksson, Stefan

Ingår i Bioethics, s. 485-492, 2013

• DOI för Adequate trust avails, mistaken trust matters: On the moral responsibility of doctors as proxies for patients' trust in biobank research

Cheating is the name of the game: Conventional cheating arguments fail to articulate moral responses to doping

Atry, Ashkan; Hansson, Mats G.; Kihlbom, Ulrik

Ingår i Physical Culture and Sport. Studies and Research, s. 21-32, 2013

• DOI för Cheating is the name of the game: Conventional cheating arguments fail to articulate moral responses to doping

Biobanks: Validate gene findings before telling donors

Hansson, Mats G.

Ingår i Nature, s. 455-455, 2012

• DOI för Biobanks: Validate gene findings before telling donors

Commercialization of Biobanks

Evers, Kathinka; Stjernschantz Forsberg, Joanna; Hansson, Mats

Ingår i Biopreservation and Biobanking, s. 45-47, 2012

• DOI för Commercialization of Biobanks

Medical registries represent vital patient interests and should not be dismantled by stricter regulation

Hansson, Mats G; Simonsson, Bengt; Feltelius, Nils; Forsberg, Joanna Stjernschantz et al.

Ingår i Cancer Epidemiology, s. 575-578, 2012

• DOI för Medical registries represent vital patient interests and should not be dismantled by stricter regulation

Where should we draw the line between quality of care and other ethical concerns related to medical registries and biobanks?

Hansson, Mats

Ingår i Theoretical Medicine and Bioethics, s. 313-323, 2012

• DOI för Where should we draw the line between quality of care and other ethical concerns related to medical registries and biobanks?

Ethics bureaucracy: a significant hurdle for collaborative follow-up of drug effectiveness in rare childhood diseases

Hansson, Mats G.; Gattorno, Marco; Stjernschantz Forsberg, Joanna; Feltelius, Nils et al.

Ingår i Archives of Disease in Childhood, s. 561-563, 2012

• DOI för Ethics bureaucracy: a significant hurdle for collaborative follow-up of drug effectiveness in rare childhood diseases

Beyond the Individual: Sources of Attitudes Towards Rule Violation in Sport

Atry, Ashkan; Hansson, Mats G.; Kihlbom, Ulrik

Ingår i Sport, Ethics and Philosophy, s. 467-479, 2012

• DOI för Beyond the Individual: Sources of Attitudes Towards Rule Violation in Sport

Biobank research: who benefits from individual consent?

Stjernschantz Forsberg, Joanna; Hansson, Mats G.; Eriksson, Stefan

Ingår i The BMJ, 2011

• DOI för Biobank research: who benefits from individual consent?

Biobank Research and Consent: Authors' reply to Sheehan

Forsberg, Joanna Stjernschantz; Hansson, Mats G.; Eriksson, Stefan

Ingår i The BMJ, 2011

• DOI för Biobank Research and Consent: Authors' reply to Sheehan

Is medical ethics doing its job?: Introduction

Hansson, Mats G.; Chadwick, R.

Ingår i Journal of Internal Medicine, s. 366-369, 2011

• DOI för Is medical ethics doing its job?: Introduction

Biobanking Within the European Regulatory Framework: Opportunities and Obstacles

Hansson, Mats G.

Ingår i Biopreservation and Biobanking, s. 165-167, 2011

• DOI för Biobanking Within the European Regulatory Framework: Opportunities and Obstacles

The Risks and Benefits of Re-Consent

Stjernschantz Forsberg, Joanna; Hansson, Mats G.; Eriksson, Stefan

Ingår i Science, s. 306-306, 2011

"My parents decide if I can. I decide if I want to.": Children's views on participation in medical research

Swartling, Ulrica; Hansson, Mats G.; Ludvigsson, Johnny; Nordgren, Anders

Ingår i Journal of Empirical Research on Human Research Ethics, s. 68-75, 2011

• DOI för "My parents decide if I can. I decide if I want to.": Children's views on participation in medical research

Gene Doping and the Responsibility of Bioethicists

Atry, Ashkan; Hansson, Mats G.; Kihlbom, Ulrik

Ingår i Sport, Ethics and Philosophy, s. 149-160, 2011

• DOI för Gene Doping and the Responsibility of Bioethicists

In search of the missing subject: narrative identity and posthumous wronging

Masterton, Malin; Hansson, Mats G.; Höglund, Anna T.

Ingår i Studies in History and Philosophy of Science Part C, s. 340-346, 2010

• DOI för In search of the missing subject: narrative identity and posthumous wronging

The use of human tissue in epidemiological research: ethical and legal considerations in two biobanks in Belgium

Truyers, Carla; Kellen, Eliane; Arbyn, Marc; Trommelmans, Leen et al.

Ingår i Medicine, Health care and Philosophy, s. 169-175, 2010

• DOI för The use of human tissue in epidemiological research: ethical and legal considerations in two biobanks in Belgium

Changing defaults in biobank research could save lives too

Stjernschantz Forsberg, Joanna; Eriksson, Stefan; Hansson, Mats G

Ingår i European Journal of Epidemiology, s. 65-68, 2010

• DOI för Changing defaults in biobank research could save lives too

Hypothetical and factual willingness to participate in biobank research

Johnsson, Linus; Helgesson, Gert; Rafnar, Thorunn; Halldorsdottir, Ingibjörg et al.

Ingår i European Journal of Human Genetics, s. 1261-1264, 2010

• DOI för Hypothetical and factual willingness to participate in biobank research
• Ladda ner fulltext (pdf) av Hypothetical and factual willingness to participate in biobank research

Taking the patient's side: the ethics of pharmacogenetics

Hansson, Mats G.

Ingår i Personalized Medicine, s. 75-85, 2010

• DOI för Taking the patient's side: the ethics of pharmacogenetics

Ulysses contracts for the doctor and for the patient

Hansson, Mats G; Hakama, Matti

Ingår i Contemporary Clinical Trials, s. 202-206, 2010

• DOI för Ulysses contracts for the doctor and for the patient

Ethical Issues in Cancer Register Follow-Up of Hormone Treatment in Adolescence

Hultman, Christina M; Lindgren, Ann-Christin; Hansson, Mats G; Carlstedt-Duke, Jan et al.

Ingår i Public Health Ethics, s. 30-36, 2009

• DOI för Ethical Issues in Cancer Register Follow-Up of Hormone Treatment in Adolescence

Concern for privacy in relation to age during physical examination of children: an exploratory study

Hansson, Mats G; Kihlbom, Ulrik; Tuvemo, Torsten; Rodriguez, Alina

Ingår i Acta Paediatrica, s. 1349-1354, 2009

• DOI för Concern for privacy in relation to age during physical examination of children: an exploratory study

Practical matters, rather than lack of trust, motivate non-participation in a long-term cohort trial

Helgesson, Gert; Hansson, Mats G; Ludvigsson, Johnny; Swartling, Ulrica

Ingår i Pediatric Diabetes, s. 408-412, 2009

• DOI för Practical matters, rather than lack of trust, motivate non-participation in a long-term cohort trial

Pregnant women are satisfied with the information they receive about prenatal diagnosis, but are their decisions well informed?

Ferm Widlund, Kjerstin; Gunnarsson, Cecilia; Nordin, Karin; Hansson, Mats G

Ingår i Acta Obstetricia et Gynecologica Scandinavica, s. 1128-1132, 2009

• DOI för Pregnant women are satisfied with the information they receive about prenatal diagnosis, but are their decisions well informed?

Split views among parents regarding children's right to decide about participation in research: a questionnaire survey

Swartling, U.; Helgesson, G.; Hansson, M. G.; Ludvigsson, J.

Ingår i Journal of Medical Ethics, s. 450-455, 2009

• DOI för Split views among parents regarding children's right to decide about participation in research: a questionnaire survey

Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results

Stjernschantz Forsberg, Joanna; Hansson, Mats G; Eriksson, Stefan

Ingår i European Journal of Human Genetics, s. 1544-1549, 2009

• DOI för Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results

Biobanks: questioning distinctions

Hansson, Mats G.; Maschke, Karen J.

Ingår i Science, s. 797-797, 2009

• DOI för Biobanks: questioning distinctions

Parental authority, research interest and children's right to decide in medical research - an uneasy tension?

Swartling, Ulrica; Helgesson, Gert; Hansson, Mats G

Ingår i Clinical Ethics, s. 69-74, 2008

• DOI för Parental authority, research interest and children's right to decide in medical research - an uneasy tension?

Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study

Johnsson, Linus; Hansson, Mats G; Eriksson, Stefan; Helgesson, Gert

Ingår i BMJ. British Medical Journal, 2008

• DOI för Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study

Opt-out from biobanks better respects patients' autonomy

Johnsson, Linus; Hansson, Mats G; Eriksson, Stefan; Helgesson, Gert

Ingår i BMJ. British Medical Journal, 2008

• DOI för Opt-out from biobanks better respects patients' autonomy

Ethics takes time, but not that long

Hansson, Mats G; Kihlbom, Ulrik; Tuvemo, Torsten; Olsen, Leif et al.

Ingår i BMC Medical Ethics, s. 1-7, 2007

• DOI för Ethics takes time, but not that long

Developing ethical competence in health care organizations

Kälvemark Sporrong, Sofia; Arnetz, Bengt; Hansson, Mats G.; Westerholm, Peter et al.

Ingår i Nursing Ethics, s. 825-837, 2007

• DOI för Developing ethical competence in health care organizations

Can the Dead be Brought into Disrepute?

Masterton, Malin; Hansson, Mats; Höglund, Anna; Helgesson, Gert

Ingår i Theoretical Medicine and Bioethics, s. 137-149, 2007

• DOI för Can the Dead be Brought into Disrepute?

Queen Christina's moral claim on the living: Justification of a tenacious moral intuition

Masterton, Malin; Helgesson, Gert; Höglund, Anna; Hansson, Mats

Ingår i Medicine, Health care and Philosophy, s. 321-327, 2007

• DOI för Queen Christina's moral claim on the living: Justification of a tenacious moral intuition

Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: a population-based study

Kettis, Åsa; Ring, Lena; Viberth, Eva; Hansson, Mats G.

Ingår i Scandinavian Journal of Public Health, s. 148-156, 2007

• DOI för Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: a population-based study

For the safety and benefit of current and future patients

Hansson, Mats G.

Ingår i Pathobiology (Basel), s. 198-205, 2007

• DOI för For the safety and benefit of current and future patients

Living with Multiple Endocrine Neoplasia Type 1: Decent Care-Insufficient Medical and Genetic Information A Qualitative Study of MEN 1 Patients in a Swedish Hospital

Stromsvik, N; Nordin, K; Berglund, G; Engebretsen, L et al.

Ingår i Journal of Genetic Counseling, s. 105-117, 2007

• DOI för Living with Multiple Endocrine Neoplasia Type 1: Decent Care-Insufficient Medical and Genetic Information A Qualitative Study of MEN 1 Patients in a Swedish Hospital

Ethical framework for previously collected biobank samples

Helgesson, Gert; Dillner, Joakim; Carlson, Joyce; Bartram, Claus R et al.

Ingår i Nature Biotechnology, s. 973-976, 2007

• DOI för Ethical framework for previously collected biobank samples

Commentary: Isolated Stem Cells - Patentable as Cultural Artifacts?

Hansson, Mats G.; Helgesson, Gert; Wessman, Richard; Jaenisch, Rudolf

Ingår i Stem Cells, s. 1507-1510, 2007

• DOI för Commentary: Isolated Stem Cells - Patentable as Cultural Artifacts?

Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think?

Kettis, Åsa; Ring, Lena; Viberth, Eva; Hansson, Mats G.

Ingår i European Journal of Public Health, s. 433-440, 2006

• DOI för Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think?

Parents' perspectives on research involving children.

Rodriguez, Alina; Tuvemo, Torsten; Hansson, Mats G

Ingår i Ups J Med Sci, s. 73-86, 2006

Combining efficiency and concerns about integrity when using human biobanks.

Hansson, Mats G

Ingår i Stud Hist Philos Biol Biomed Sci, s. 520-32, 2006

Should donors be allowed to give broad consent to future biobank research?

Hansson, Mats G; Dillner, Joakim; Bartram, Claus R; Carlson, Joyce A et al.

Ingår i Lancet Oncol, s. 266-9, 2006

”We are white coats whirling round”: moral distress in Swedish pharmacies

Kälvemark Sporrong, Sofia; Höglund, Anna T.; Hansson, Mats G.; Westerholm, Peter et al.

Ingår i Pharmacy World & Science, s. 223-229, 2005

• DOI för ”We are white coats whirling round”: moral distress in Swedish pharmacies

Science and society: International perspectives on engaging the public in neuroethics.

Illes, Judy; Blakemore, Colin; Hansson, Mats G; Hensch, Takao K et al.

Ingår i Nat Rev Neurosci, s. 977-82, 2005

Building on relationships of trust in biobank research.

Hansson, M G

Ingår i J Med Ethics, s. 415-8, 2005

Quality of life in patients with multiple endocrine neoplasia type 1 (MEN 1).

Berglund, G; Lidén, A; Hansson, M G; Oberg, K et al.

Ingår i Fam Cancer, s. 27-33, 2003

Coping style, psychological distress, risk perception, and satisfaction in subjects attending genetic counselling for hereditary cancer

Nordin, Karin; Lidén, A; Hansson, Mats; Rosenquist, Richard et al.

Ingår i Journal of Medical Genetics, s. 689-694, 2002

• DOI för Coping style, psychological distress, risk perception, and satisfaction in subjects attending genetic counselling for hereditary cancer

Vilket värde har våra värderingar kring genteknik?

Hansson, M G

Ingår i Kungl. Skogs- och Lantbruksakademiens Tidskrift, s. 31-35, 2002

Ethical management of hereditary cancer information.

Hansson, M G

Ingår i Acta Oncol, s. 305-8, 1999

Introduction to discussion on ethical matters

Hansson, M G

Ingår i Acta Agriculture Scandinavica, s. 62-66, 1998

Preferences, attitudes and views regarding genetic newborn screening (gNBS) for rare diseases: a systematic review of the literature and synthesis from 2009 to 2022

Martin, Sylvia; Kyosovska-Peshtenska, Gergana; Audi, Jennifer; Zarakowska, Kaja et al.

Ingår i Orphanet Journal of Rare Diseases, 2026

• DOI för Preferences, attitudes and views regarding genetic newborn screening (gNBS) for rare diseases: a systematic review of the literature and synthesis from 2009 to 2022
• Ladda ner fulltext (pdf) av Preferences, attitudes and views regarding genetic newborn screening (gNBS) for rare diseases: a systematic review of the literature and synthesis from 2009 to 2022

The case for open science: rare diseases

Rubinstein, Yaffa R.; Robinson, Peter N.; Gahl, William A.; Avillach, Paul et al.

Ingår i JAMIA Open, s. 472-486, 2020

• DOI för The case for open science: rare diseases
• Ladda ner fulltext (pdf) av The case for open science: rare diseases

From Epigenetic Associations to Biological and Psychosocial Explanations in Mental Health.

Renzi, Chiara; Provencal, Nadine; Bassil, Katherine C; Evers, Kathinka et al.

Ingår i Progress in Molecular Biology and Translational Science, s. 299-323, 2018

• DOI för From Epigenetic Associations to Biological and Psychosocial Explanations in Mental Health.

RD-Connect: An Integrated Platform Connecting Databases, Registries, Biobanks and Clinical Bioinformatics for Rare Disease Research

Thompson, Rachel; Johnston, Louise; Taruscio, Domenica; Monaco, Lucia et al.

Ingår i Journal of general internal medicine, 2014

• DOI för RD-Connect: An Integrated Platform Connecting Databases, Registries, Biobanks and Clinical Bioinformatics for Rare Disease Research

RD-Connect: An Integrated Platform Connecting Databases, Registries, Biobanks and Clinical Bioinformatics for Rare Disease Research

Thompson, Rachel; Johnston, Louise; Taruscio, Domenica; Monaco, Lucia et al.

Ingår i Journal of general internal medicine, 2014

• DOI för RD-Connect: An Integrated Platform Connecting Databases, Registries, Biobanks and Clinical Bioinformatics for Rare Disease Research

A model of study for human cancer: Spontaneous occurring tumors in dogs. Biological features and translation for new anticancer therapies

Ranieri, G.; Gadaleta, C. D.; Patruno, R.; Zizzo, N. et al.

Ingår i Critical reviews in oncology/hematology, s. 187-197, 2013

• DOI för A model of study for human cancer: Spontaneous occurring tumors in dogs. Biological features and translation for new anticancer therapies

Ethics and biobanks

Hansson, Mats G.

Ingår i British Journal of Cancer, s. 8-12, 2009

• DOI för Ethics and biobanks

MIND THE RISK · DEN GENETISKA RISKINFORMATIONENS ETIK FÖR INDIVID OCH SAMHÄLLE: SLUTRAPPORT FRÅN ETT FORSKNINGSPROGRAM

Hansson, Mats G.; Holm, Anna; Segerdahl, Pär

Makadam Förlag, 2019

The Private Sphere: An Emotional Territory and Its Agent

Hansson, Mats G

Springer Science + Business Media B.V., 2008

The Use of Human Biobanks: Ethical, Social, Economical and Legal Aspects

Hansson, Mats G.

Uppsala University, 2001

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

Access to health data in registries and the cost of privacy concerns: introducing a privacy ombudsman while extending access to data

Hansson, Mats G.

Ingår i Information and Law in Transition, s. 325-338, Liber, 2015

The ethics of PGD-regulation

Hansson, M G

Ingår i PGD and Embryo Selection, s. 82-92, The Nordic Committee on Bioethics, Copenhagen 2006, 2006

Biobanks as Resources for Health

Hansson, Mats G; Levin, Marianne

Ingår i Biobanks as Resources for Health, s. 9-20, Uppsala universitet, 2003

Att respektera människor som moraliskt och politiskt myndiga - Om integritet som etiskt begrepp med tillämpning på medicinsk forskning

Hansson, M G

Ingår i Annales. Acadmiae Regiae Scientiarum Upsaliensis 35, s. 57-65, 2003

In the interests of efficiency and integrity

Hansson, Mats G.

Ingår i The Use of Human Biobanks, s. 35-40, Uppsala University, 2001

They want the Truth while Still Being Allowed to Hope - An Interview Study with Severely Ill Children on Receiving Bad News

Jalmsell, Li; Lovgren, M.; Hansson, Mats G.; Kreicbergs, U. et al.

2015

Doping and The Participatory Responsibility of Sports Physicians

Atry, Ashkan; Hansson, Mats G.; Kihlbom, Ulrik

2013

Biobanks as resources for health

Hansson, Mats G; Levin, Marianne

Uppsala University, 2003

Good Conduct in Research. An extract from the Swedish parliamentary investigation into research ethics 1999

Hansson, M G

Forskningsrådsnämnden, Stockholm, 1999

Idédokument från konferensen genetisk insyn. Genforskningens konsekvenser för individ och samhälle. Probleminventering - Idéer till forskningsinitiativ

Hansson, M G

GENOM-gruppen c/o Medicinska forskningsrådet, Stockholm, 1994

Research Data Inquiry investigating national exceptions under the General Data Protection Regulation

Reichel, Jane; Lind, Anna-Sara; Hansson, Mats G.

2016

Genomics for policy makers and for researchers. Review of: Genomics and society-Ethical, Legal, Cultural and Socioeconomic Implication. Edited by: Dhavendra Kumar and Ruth Chadwick.

Hansson, Mats G.

Ingår i European Journal of Human Genetics, s. 1835-1835, 2016

• DOI för Genomics for policy makers and for researchers. Review of: Genomics and society-Ethical, Legal, Cultural and Socioeconomic Implication. Edited by: Dhavendra Kumar and Ruth Chadwick.

Swedish biotechnology and bioethics go hand in hand

Hansson, M G

2002