JAMIA Open is a peer-reviewed, online-only, and Gold Open Access journal, JAMIA Open provides a global forum for the publication of novel research and insights in the major areas of informatics for biomedicine and health (e.g., translational bioinformatics, clinical research informatics, clinical informatics, public health informatics, and consumer health informatics), as well as related areas such as data science, qualitative research, and implementation science.
JAMIA Open articles, which include application notes, database notes, and patient/community perspectives, alongside original research, reflect the broad diversity of the field of informatics community, focusing on the intersection of informatics, health, communication, and technology, and how that intersection can support patient care through research, practice, and education. JAMIA Open authors are encouraged to make data and source code accessible through publicly accessible repositories that can be cited using digital object identifiers. Accepted manuscripts are required to have a patient/community facing abstract that highlights key findings. Author guidelines.
Neil Sarkar, PhD, MLIS, FACMI, is the Editor-in-Chief and leads a team of informatics leaders serving as the JAMIA Open Editorial Board and Associate Editors.
Access
JAMIA Open is an open access journal and does not require a login or AMIA membership to read articles.
Recent JAMIA Open Articles
De-identified data quality assessment approaches by data vendors who license data to healthcare and life sciences researchers.
December 1, 2022
To gain insights into how data vendor companies (DVs), an important source of de-identified/anonymized licensed patient-related data (D/ALD) used in clinical informatics research in life sciences and the pharmaceutical industry, characterize, conduct, and communicate data quality assessments to researcher purchasers of D/ALD.
Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials.
December 1, 2022
The coronavirus disease 2019 (COVID-19) pandemic has disproportionately affected racial/ethnic minorities in the United States, who are underrepresented in clinical trials. We assessed the feasibility of using the University of Pennsylvania Health System electronic health record patient portal to diversify the pool of participants in COVID-19 vaccine clinical trials. The […]
Disparities in mobile phone use among adults with type 2 diabetes participating in clinical trials 2017-2021.
December 1, 2022
Despite smartphone ownership becoming ubiquitous, it is unclear whether and where disparities persist in experience using health apps. In 2 diverse samples of adults with type 2 diabetes collected 2017-2018 and 2020-2021, we examined adjusted disparities in smartphone ownership and health app use by age, gender, race, education, annual household […]
The benefit of augmenting open data with clinical data-warehouse EHR for forecasting SARS-CoV-2 hospitalizations in Bordeaux area, France.
December 1, 2022
The aim of this study was to develop an accurate regional forecast algorithm to predict the number of hospitalized patients and to assess the benefit of the Electronic Health Records (EHR) information to perform those predictions.