arXiv subjects

Linshanshan Wang

Publications and source records attributed to Linshanshan Wang.

4 recordsLinked to original sources

arXiv2026

Representation learning to advance multi-institutional studies with electronic health record data from US and France

The widespread adoption of electronic health records has created new opportunities for translational clinical research, yet this promise remains constrained by fragmented data across privacy-siloed institutions and substantial heterogeneity in local coding practices. While privacy-preserving collaborative learning allows institutions to work together without sharing patient-level data, it does not address inconsistencies in how clinical concepts are represented across sites. We introduce a graph-based framework that addresses this gap by treating data harmonization as a scalable representation learning problem. Rather than relying on fixed standards or manual mappings, the framework integrates institution-specific summary statistics from health records, curated biomedical knowledge graphs, and semantic information derived from large language models to learn a shared semantic space. This joint learning approach aligns diverse, site-specific vocabularies while preserving patient privacy. Evaluated across seven institutions and two languages, the framework provides a robust, data-centric foundation for training and deploying clinical models across heterogeneous healthcare systems.

cs.AI↗

arXiv2025

A Common Pipeline for Harmonizing Electronic Health Record Data for Translational Research

Despite the growing availability of Electronic Health Record (EHR) data, researchers often face substantial barriers in effectively using these data for translational research due to their complexity, heterogeneity, and lack of standardized tools and documentation. To address this critical gap, we introduce PEHRT, a common pipeline for harmonizing EHR data for translational research. PEHRT is a comprehensive, ready-to-use resource that includes open-source code, visualization tools, and detailed documentation to streamline the process of preparing EHR data for analysis. The pipeline provides tools to harmonize structured and unstructured EHR data to standardized ontologies to ensure consistency across diverse coding systems. In the presence of unmapped or heterogeneous local codes, PEHRT further leverages representation learning and pre-trained language models to generate robust embeddings that capture semantic relationships across sites to mitigate heterogeneity and enable integrative downstream analyses. PEHRT also supports cross-institutional co-training through shared representations, allowing participating sites to collaboratively refine embeddings and enhance generalizability without sharing individual-level data. The framework is data model-agnostic and can be seamlessly deployed across diverse healthcare systems to produce interoperable, research-ready datasets. By lowering the technical barriers to EHR-based research, PEHRT empowers investigators to transform raw clinical data into reproducible, analysis-ready resources for discovery and innovation.

stat.ML↗

arXiv2025

Semi-supervised Clustering Through Representation Learning of Large-scale EHR Data

Electronic Health Records (EHR) offer rich real-world data for personalized medicine, providing insights into disease progression, treatment responses, and patient outcomes. However, their sparsity, heterogeneity, and high dimensionality make them difficult to model, while the lack of standardized ground truth further complicates predictive modeling. To address these challenges, we propose SCORE, a semi-supervised representation learning framework that captures multi-domain disease profiles through patient embeddings. SCORE employs a Poisson-Adapted Latent factor Mixture (PALM) Model with pre-trained code embeddings to characterize codified features and extract meaningful patient phenotypes and embeddings. To handle the computational challenges of large-scale data, it introduces a hybrid Expectation-Maximization (EM) and Gaussian Variational Approximation (GVA) algorithm, leveraging limited labeled data to refine estimates on a vast pool of unlabeled samples. We theoretically establish the convergence of this hybrid approach, quantify GVA errors, and derive SCORE's error rate under diverging embedding dimensions. Our analysis shows that incorporating unlabeled data enhances accuracy and reduces sensitivity to label scarcity. Extensive simulations confirm SCORE's superior finite-sample performance over existing methods. Finally, we apply SCORE to predict disability status for patients with multiple sclerosis (MS) using partially labeled EHR data, demonstrating that it produces more informative and predictive patient embeddings for multiple MS-related conditions compared to existing approaches.

stat.ME↗

arXiv2022

Semi-supervised Transfer Learning for Evaluation of Model Classification Performance

In modern machine learning applications, frequent encounters of covariate shift and label scarcity have posed challenges to robust model training and evaluation. Numerous transfer learning methods have been developed to robustly adapt the model itself to some unlabeled target populations using existing labeled data in a source population. However, there is a paucity of literature on transferring performance metrics of a trained model. In this paper, we aim to evaluate the performance of a trained binary classifier on unlabeled target population based on receiver operating characteristic (ROC) analysis. We proposed $\bf S$emi-supervised $\bf T$ransfer l$\bf E$arning of $\bf A$ccuracy $\bf M$easures (STEAM), an efficient three-step estimation procedure that employs 1) double-index modeling to construct calibrated density ratio weights and 2) robust imputation to leverage the large amount of unlabeled data to improve estimation efficiency. We establish the consistency and asymptotic normality of the proposed estimators under correct specification of either the density ratio model or the outcome model. We also correct for potential overfitting bias in the estimators in finite samples with cross-validation. We compare our proposed estimators to existing methods and show reductions in bias and gains in efficiency through simulations. We illustrate the practical utility of the proposed method on evaluating prediction performance of a phenotyping model for Rheumatoid Arthritis (RA) on a temporally evolving EHR cohort.

stat.ME↗