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By October 1, 2024, over 450,000 COVID-19 manuscripts were published, with 10% posted as unreviewed preprints. While they accelerate knowledge sharing, their inconsistent quality complicates systematic studies.

Electronic Health Records (EHRs) sampled from different populations can introduce unwanted biases, limit individual-level data sharing, and make the data and fitted model hardly transferable across different population groups. In this context, our main goal is to design an effective method to transfer knowledge between population groups, with computable guarantees for suitability, and that can be applied to quantify treatment disparities.

Immunotherapy has emerged as a promising treatment for advanced non-small cell lung cancer (NSCLC), but accurately predicting which patients will benefit from it remains a major clinical challenge. To address this, we aim to develop a novel multimodal method, DeepAFM, that integrates histopathology, genomic features, and clinical information to predict patient responses to anti-PD-(L)1 immunotherapy.

In real-world data (RWD), defining the observation period-the time during which a patient is considered observable-is critical for estimating incidence rates (IRs) and other outcomes. Yet, in the absence of explicit enrollment information, this period must often be inferred, introducing potential bias.

This paper presents the results from a competition challenging participants to develop entity linking models using a subset of annotated MIMIC-IV-Note data and the SNOMED CT Terminology.

To explore the potential effects of recent restrictions on discussions regarding diversity, equity, and inclusion (DEI) in the field of biomedical informatics.

Clinicians retrieve data from electronic health record (EHR) systems and summarize them into clinical information to accomplish clinical reasoning and decision-making tasks. Visualization, using meaningful summarization methods and intuitive presentation approaches, can enhance this process. This systematic review examines how EHR data are summarized, visualized, and aligned with the 7 clinical reasoning and decision-making tasks shared by clinicians.

Family data are a valuable data source in bioinformatic research. This is because family members often share common genetic and environmental exposures. Collecting this family data is traditionally very labor intensive but advances in electronic health record (EHR) data mining has proven useful when identifying pedigrees linked to longitudinal health histories. These are called e-pedigrees. Unfortunately, e-pedigrees tend to miss the oldest patients who inherently have the longest and richest [...]

Risk prediction models are used in hospitals to identify pediatric patients at risk of clinical deterioration, enabling timely interventions and rescue. The objective of this study was to develop a new explainer algorithm that uses a patient's clinical notes to generate text-based explanations for risk prediction alerts.

Real-world data (RWD) analyses primarily rely on structured clinical documentation collected through routine clinical care or driven by medical billing requirements. Patient-reported outcome measures (PROMs), integrated into electronic health records (EHRs), are an additional data source that could offer valuable insights into a patient's perspective and contribute to a more comprehensive understanding of health outcomes in RWD studies. This study aims to characterize agreement between PROMs symptoms and structured clinical [...]