Deborah Mascalzoni


Ontology type: schema:Person     


Person Info

NAME

Deborah

SURNAME

Mascalzoni

Publications in SciGraph latest 50 shown

  • 2021-07-09 Return of research results (RoRR) to the healthy CHRIS cohort: designing a policy with the participants in JOURNAL OF COMMUNITY GENETICS
  • 2021-05-25 Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries in GENOME MEDICINE
  • 2021-05-13 Balancing scientific interests and the rights of participants in designing a recall by genotype study in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2019-12-04 Microbiota, type 2 diabetes and non-alcoholic fatty liver disease: protocol of an observational study in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2019-04-17 The GDPR and the research exemption: considerations on the necessary safeguards for research biobanks in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-12-07 The Role of Solidarity(-ies) in Rare Diseases Research in RARE DISEASES EPIDEMIOLOGY: UPDATE AND OVERVIEW
  • 2017-09-26 The challenges of the expanded availability of genomic information: an agenda-setting paper in JOURNAL OF COMMUNITY GENETICS
  • 2017-09-25 How to responsibly acknowledge research work in the era of big data and biobanks: ethical aspects of the Bioresource Research Impact Factor (BRIF) in JOURNAL OF COMMUNITY GENETICS
  • 2017-09-18 Legal issues in governing genetic biobanks: the Italian framework as a case study for the implications for citizen’s health through public-private initiatives in JOURNAL OF COMMUNITY GENETICS
  • 2017-01-25 Dynamic Consent: a potential solution to some of the challenges of modern biomedical research in BMC MEDICAL ETHICS
  • 2016-06-16 Erratum: International Charter of principles for sharing bio-specimens and data in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-04-06 ‘You should at least ask’. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-02-10 Improving the informed consent process in international collaborative rare disease research: effective consent for effective research in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-11-05 The Cooperative Health Research in South Tyrol (CHRIS) study: rationale, objectives, and preliminary results in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2015-01-23 Ethics Law and Governance of Biobanking: A Very Complex Normative Puzzle in ETHICS, LAW AND GOVERNANCE OF BIOBANKING
  • 2014-09-24 International Charter of principles for sharing bio-specimens and data in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-04-23 Rare diseases and now rare data? in NATURE REVIEWS GENETICS
  • 2012-04-03 From patients to partners: participant-centric initiatives in biomedical research in NATURE REVIEWS GENETICS
  • 2009-10-14 Comparison of participant information and informed consent forms of five European studies in genetic isolated populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-06-05 The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives in BMC MEDICAL GENETICS
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