Percorrer por data de Publicação, começado por "2025-09-09"
A mostrar 1 - 3 de 3
Resultados por página
Opções de ordenação
- Extrapulmonary manifestations of SARS-CoV-2 infection and COVID-19 vaccine adverse effectsPublication . Botelho, Monica Catarina; Poma, Anello Marcello; Wu, JianNo abstract available
- FAIREHR: A Novel Online Research Registry PlatformPublication . Galea, Karen S.The FAIREHR (Findable, Accessible, Interoperable, Reusable Environmental and Health Registry) is a state-of-the-art online registry platform designed to enhance the transparency, reproducibility, and comparability of environmental health research, focusing on human biomonitoring (HBM) studies as a starting point. This platform is developed in response to the Europe Regional Chapter of the International Society of Exposure Science (ISES Europe) HBM working group strategic objectives to generate high quality HBM by harmonising the data life cycle and implementation of FAIR (findable, accessible, interoperable and reusable) guiding principles. The registry enables preregistration of studies, capturing key metadata on study design, data management, and planned methods before recruitment od the participants. FAIREHR is the first registry tailored for HBM studies and is also first registry promoting FAIR by design studies. Benefits of FAIREHR include increased research visibility, improved data comparability, enhanced collaboration, and better-informed decision-making. We will discuss the unique propositions of FAIREHR, emphasizing its role in enhancing the exchange of information, with its implementation expected to yield significant benefits for researchers, policymakers, and public health through effective utilization of HBM data.
- MIR-HBM: The Minimum Information Requirements Guidance for Human Biomonitoring StudiesPublication . Hopf, Nancy B.Background To fully understand the context, methods, data, and interpretations of a human biomonitoring (HBM) study, access to comprehensive background information is essential. However, the diversity in HBM study designs, coupled with varying levels of detail in the data collected, often makes meaningful comparisons, data reuse, and interpretation across different studies challanging. Materials and methods To address this need, the Minimum Information Requirements for Human Biomonitoring (MIR-HBM) was developed by the European Chapter of the International Society of Exposure Science (ISES Europe) HBM working group and the HBM Global Network. MIR-HBM describes the minimal set of information that must be provided to enable effective communication of the setup of an HBM study to others. It enables the generation of the metadata ('data about the data') that will cover all components of the study, including rationale and objectives, study population characteristics, biological specimen collection, laboratory analysis and method parameters, data analysis plan, data interpretation, and communication and reporting. Results Adherence to these reporting guidelines will result in publications of increased clarity,quality, comparability, and usefulness to the scientific community and other stakeholders. Integrating MIR-HBM as a FAIR metadata schema into the FAIREHR (Findable, Accessible, Interoperable, and Reusable Environmental and Health Registry) platform is the next key step planned to enable its implementation and adoption. Conclusions Overall, the MIR-HBM on HBM study metadata promotes transparency and completeness in reporting and enhances rapid capturing of the contents of the HBM study, thereby stimulating findability and accessibility to HBM data and supporting effective quality assessment.
