Biomedical researchers collect large amounts of personal data about individuals, which are frequently shared with repositories and an array of users. Typically, research data holders implement measures to protect participants’ identities and unique attributes from unauthorized disclosure. These measures, however, can be less effective if people disclose their participation in a research study, which they may do for many reasons. Even so, the people who provide these data for research often understandably expect that their privacy will be protected. We discuss the particular challenges posed by self-disclosure and identify various steps that researchers should take to protect data in these cases to protect both the individuals and the resear...
While data sharing is becoming increasingly common in quantitative social inquiry, qualitative data ...
From 1970 onwards the handwritten medical cards which the General Practitioner (GP) used were replac...
Deficiencies or unclear statements in consent forms used for research with human participants may le...
When sharing research data for verification and reuse, behavioural researchers should protect partic...
This talk will illustrate a new area of service support for academic research data services: privacy...
Sharing research data is increasingly required by key stakeholders, such as funding agencies and jou...
The protection of identity of participants in medical research has traditionally been guaranteed by ...
Research data often have special security requirements. This presentation will show a framework for ...
Political science research in both qualitative and quantitative traditions frequently uses data that...
Objective: De-identified clinical data in standardized form (eg, diagnosis codes), derived from elec...
Background : Data from individual collections, such as biobanks and cohort studies, are now being sh...
Introduction. The sharing and reuse of research data is gradually becoming best practice in research...
Medical research has a long history in the United Kingdom and has generally enjoyed good public supp...
Respecting the confidentiality of personal data contributed to genomic studies is an important issue...
Centre for Brain Sciences, Brain research Imaging CentreSharing data is beneficial in many ways: it ...
While data sharing is becoming increasingly common in quantitative social inquiry, qualitative data ...
From 1970 onwards the handwritten medical cards which the General Practitioner (GP) used were replac...
Deficiencies or unclear statements in consent forms used for research with human participants may le...
When sharing research data for verification and reuse, behavioural researchers should protect partic...
This talk will illustrate a new area of service support for academic research data services: privacy...
Sharing research data is increasingly required by key stakeholders, such as funding agencies and jou...
The protection of identity of participants in medical research has traditionally been guaranteed by ...
Research data often have special security requirements. This presentation will show a framework for ...
Political science research in both qualitative and quantitative traditions frequently uses data that...
Objective: De-identified clinical data in standardized form (eg, diagnosis codes), derived from elec...
Background : Data from individual collections, such as biobanks and cohort studies, are now being sh...
Introduction. The sharing and reuse of research data is gradually becoming best practice in research...
Medical research has a long history in the United Kingdom and has generally enjoyed good public supp...
Respecting the confidentiality of personal data contributed to genomic studies is an important issue...
Centre for Brain Sciences, Brain research Imaging CentreSharing data is beneficial in many ways: it ...
While data sharing is becoming increasingly common in quantitative social inquiry, qualitative data ...
From 1970 onwards the handwritten medical cards which the General Practitioner (GP) used were replac...
Deficiencies or unclear statements in consent forms used for research with human participants may le...