Biomedical Informatics & Data Science
As a health informatician with a background in medicine, I bring clinical domain expertise to health wearables and biosignal analytics in cardiology (with a focus on cardio-oncology)—anchoring wearable data in physiological rationale and cardiovascular modeling while developing evaluation frameworks for trustworthy clinical AI.
Developing rigorous evaluation frameworks, physiological modeling, and computational infrastructure to ensure clinical AI and wearable technologies are reliable, evidence-grounded, and safely deployable in healthcare workflows.
Anchoring continuous wearable biosignals (PPG, ECG) in cardiovascular modeling for cardio-oncology and digital biomarker discovery.
Learn more →Evaluation frameworks for hallucination detection, reliability, calibration, and clinically meaningful performance metrics in generative models.
Learn more →Methods for determining whether generated clinical claims are explicitly supported by appropriate biomedical evidence and source EHR notes.
Learn more →FHIR-oriented data representation, granular segmentation, and deployment-focused clinical AI infrastructure for privacy-preserving data exchange.
Learn more →Six-month post-discharge follow-up of clinical outcomes and costs for apheresis therapies in COVID-19 survivors, finding limited long-term cost-effectiveness.
Evaluation of SHARES, a FHIR-based data segmentation platform for protecting sensitive substance-use health information, benchmarked on 11,519 synthetic patient records.
An open research framework that tests whether language models change their sensitive-data judgments when patient context is added, and whether those changes match the shifts physicians show.
A port of GEM Cutter III, the Yale Center for Medical Informatics' desktop tool for marking up clinical guidelines in the Guideline Elements Model (GEM III, ASTM E2210), to a static web page that reads and writes the desktop application's files.
An interactive teaching lab, in the browser, for learning how accelerometer signals are processed: record or load a walk, filter it, look at its spectrum, and compare step detectors side by side. A teaching tool, not a validated gait instrument.
An open-source bridge that reads vital signs from standard Bluetooth health services and serves them as US Core FHIR R4 Observations through a local, read-only API. Research and education only; not a medical device.
An auditable, evidence-grounded research pipeline for extracting structured clinical attributes from scientific PDFs with W3C JSON-LD provenance and a 4-stage quality control loop.
Presented early evidence that context-aware LLMs can classify sensitive health data for consent-driven record sharing.
Presented an explainable model for early acute kidney injury prediction from the first 24 hours of physiologic and clinical data.
Following an unprecedented 19-day export control freeze, Anthropic’s Claude Fable 5 and Mythos 5 are back online under strict restrictions. Here is a deep analysis of Project Glasswing, real-time KYC, and how health-tech teams can build resilient AI architectures.
A practical guide to HL7 FHIR Security Labels, 42 CFR Part 2 compliance, and context-aware LLM classifiers for sensitive health data exchange.
Personal reflections on transitioning from practicing family medicine across rural and urban clinics to developing rigorous clinical AI evaluation frameworks at ASU.
Why standard NLP benchmark metrics fail to quantify clinical hallucination risk, and how a domain-specific error taxonomy bridges model evaluation and bedside safety.
Why general LLM benchmarks like MMLU or GSM8K fall short in medicine, and how evidence grounding, hallucination bounds, and FHIR interoperability redefine clinical AI safety.
Anthropic’s Fable 5 suspension shows why health-tech AI needs due process, lifecycle governance, validated fallbacks, and risk-based regulation—not opaque shutdowns over imperfect models.