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Hamed, A. A.

Publications and source records attributed to Hamed, A. A..

2 recordsLinked to original sources

Scaling Network Medicine with LLMs for Combinatorial Drug Repurposing in ER+ Breast Cancer

Drug repurposing can accelerate therapy discovery for ER+ breast cancer, but combination selection remains difficult. We developed an LLM-driven network medicine framework that extracts drug--target relationships from 595,122 PubMed abstracts, builds a cross-model consensus network, overlays it onto the KEGG estrogen signaling pathway, and enumerates complementary drug pairs. Candidate combinations are ranked by ComboRank, which aggregates pathway coverage, LLM consensus, RAG validation, cross-method agreement, and ClinicalTrials.gov precedent. The framework identified 166 significant pairs at FDR <= 0.05, including 31 with clinical-trial precedent, with 393 shared drug--target pairs across extraction strategies and 11 exact pairs additionally supported by the pathway overlay.

bioinformatics↗

MarkerScout: A Disease-Agnostic Machine Learning Framework for Biomarker Prediction from Multi-Scale Mechanistic Models

Identifying robust biomarkers from high-dimensional biomedical data is a central challenge in translational research, but candidate rankings produced by any single feature-selection or classification method depend on algorithmic choices and rarely reproduce across pipelines. We present a disease-agnostic machine-learning framework that addresses this dependence by systematically benchmarking 25 (feature-selection x classifier) pipelines under five-fold stratified cross-validation, aggregating per-feature evidence by two independent methods (a weighted-selection consensus score and Robust Rank Aggregation), and characterizing the direction of each candidate using Cohens d. We demonstrate the framework on immune-response measurements from two clinical phases: SARS-CoV-2 hospitalization and intensive-care admission; obtaining cross-validated mean F1 above 0.99 with balanced classification errors and producing tiered, direction-aware biomarker lists per phase. Interleukin-18 (IL-18) reached the strongest tier in both phases with consistent direction. The framework generalizes to any binary clinical classification problem and supports principled, reproducible biomarker prioritization.

bioinformatics↗