activity
20242026
collaborators

8 papers

cs.LG2026

Accelerating Reproducible Research in Synthetic EHR Generation

Jalen Jiang, Chufan Gao, Ethan Rasmussen +2

The generation of high-fidelity synthetic Electronic Health Records (EHR) is crucial for advancing medical research while preserving patient privacy. However, head-to-head comparis…

cs.AI2026

How Well Do Multimodal Models Reason on ECG Signals?

Maxwell A. Xu, Harish Haresamudram, Catherine W. Liu +11

While multimodal large language models offer a promising solution to the "black box" nature of health AI by generating interpretable reasoning traces, verifying the validity of the…

cs.CL2026

: Benchmarking Eligibility Criteria Amendments in Clinical Trials

Trisha Das, Mandis Beigi, Jacob Aptekar +1

Clinical trial amendments frequently introduce delays, increased costs, and administrative burden, with eligibility criteria being the most commonly amended component. We introduce…

cs.CL2025

Process-Supervised Reward Models for Verifying Clinical Note Generation: A Scalable Approach Guided by Domain Expertise

Hanyin Wang, Chufan Gao, Qiping Xu +9

Process-supervised reward models (PRMs) excel at providing step-by-step verification for large language model (LLM) outputs in domains like mathematics and coding. However, their a…

cs.AI2025

SECRET: Semi-supervised Clinical Trial Document Similarity Search

Trisha Das, Afrah Shafquat, Beigi Mandis +2

Clinical trials are vital for evaluation of safety and efficacy of new treatments. However, clinical trials are resource-intensive, time-consuming and expensive to conduct, where e…

cs.AI2025

Automatically Labeling Clinical Trial Outcomes: A Large-Scale Benchmark for Drug Development

Chufan Gao, Jathurshan Pradeepkumar, Trisha Das +2

Background The cost of drug discovery and development is substantial, with clinical trial outcomes playing a critical role in regulatory approval and patient care. However, access…