Mats G Hansson


Ontology type: schema:Person     


Person Info

NAME

Mats G

SURNAME

Hansson

Publications in SciGraph latest 50 shown

  • 2019-04 “A perfect society”— Swedish policymakers’ ethical and social views on preconception expanded carrier screening in JOURNAL OF COMMUNITY GENETICS
  • 2018-12 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 in BMC RHEUMATOLOGY
  • 2018-11-15 Patient Perspectives on the Value of Patient Preference Information in Regulatory Decision Making: A Qualitative Study in Swedish Patients with Rheumatoid Arthritis in THE PATIENT - PATIENT-CENTERED OUTCOMES RESEARCH
  • 2017-06 Giving Patients’ Preferences a Voice in Medical Treatment Life Cycle: The PREFER Public–Private Project in THE PATIENT - PATIENT-CENTERED OUTCOMES RESEARCH
  • 2016-12 Genomics and society—Ethical, Legal, Cultural and Socioeconomic Implication in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-11 The risk of re-identification versus the need to identify individuals in rare disease research in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-07 International Charter of principles for sharing bio-specimens and data in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016 Incidental Findings and Their Handling in the Swedish CArdioPulmonary bioImage Study (SCAPIS) in INCIDENTAL RADIOLOGICAL FINDINGS
  • 2015-06 International Charter of principles for sharing bio-specimens and data in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015 Incidental Findings: The Time Is not yet Ripe for a Policy for Biobanks in ETHICS, LAW AND GOVERNANCE OF BIOBANKING
  • 2015 Making Researchers Moral in ETHICS, LAW AND GOVERNANCE OF BIOBANKING
  • 2014-09 ERIC: a new governance tool for Biobanking in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2014-08 RD-Connect: An Integrated Platform Connecting Databases, Registries, Biobanks and Clinical Bioinformatics for Rare Disease Research in JOURNAL OF GENERAL INTERNAL MEDICINE
  • 2014-04 Incidental findings: the time is not yet ripe for a policy for biobanks in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-11 Phase 1 clinical trials in end-stage cancer: patient understanding of trial premises and motives for participation in SUPPORTIVE CARE IN CANCER
  • 2013-07 Finding ways to improve the use of biobanks in NATURE MEDICINE
  • 2013-06 International guidelines on biobank research leave researchers in ambiguity: why is this so? in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2013-06 Rare diseases and now rare data? in NATURE REVIEWS GENETICS
  • 2012-08 Where should we draw the line between quality of care and other ethical concerns related to medical registries and biobanks? in THEORETICAL MEDICINE AND BIOETHICS
  • 2012-04-25 Biobanks: Validate gene findings before telling donors in NATURE
  • 2010-11 Hypothetical and factual willingness to participate in biobank research in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-09-23 The Need to Downregulate: A Minimal Ethical Framework for Biobank Research in METHODS IN BIOBANKING
  • 2010-05 The use of human tissue in epidemiological research; ethical and legal considerations in two biobanks in Belgium in MEDICINE, HEALTH CARE AND PHILOSOPHY
  • 2010-02 Changing defaults in biobank research could save lives too in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2009-12 Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-01 Ethics and biobanks in BRITISH JOURNAL OF CANCER
  • 2007-12 Ethics takes time, but not that long in BMC MEDICAL ETHICS
  • 2007-09 Ethical framework for previously collected biobank samples in NATURE BIOTECHNOLOGY
  • 2007-09 Queen Christina’s moral claim on the living: Justification of a tenacious moral intuition in MEDICINE, HEALTH CARE AND PHILOSOPHY
  • 2007-04 Can the Dead be Brought into Disrepute? in THEORETICAL MEDICINE AND BIOETHICS
  • 2007-02 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 in JOURNAL OF GENETIC COUNSELING
  • 2005-12 International perspectives on engaging the public in neuroethics in NATURE REVIEWS NEUROSCIENCE
  • 2005-06 “We are White Coats Whirling Round” – Moral Distress in Swedish Pharmacies in INTERNATIONAL JOURNAL OF CLINICAL PHARMACY
  • 2003-04 Quality of life in patients with multiple endocrine neoplasia type 1 (MEN1) in FAMILIAL CANCER
  • 2002-03 Imaginative ethics – bringing ethical praxis into sharper relief in MEDICINE, HEALTH CARE AND PHILOSOPHY
  • 2000-03 Protecting research integrity in SCIENCE AND ENGINEERING ETHICS
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