# Causal Inference, Biomarker Discovery, Graph Neural Network, Feature Selection

arXiv: https://arxiv.org/abs/2511.13295 · HTML: https://mlsanity.com/paper/2511.13295/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 6 of its 41 references that are in the map.
- First posted on arXiv 17 Nov 2025.

## Builds on (most cited first, 6 of 6)

- [Semi-Supervised Classification with Graph Convolutional Networks](https://mlsanity.com/paper/1609.02907/) (2016)
- [Convolutional Neural Networks on Graphs with Fast Localized Spectral Filtering](https://mlsanity.com/paper/1606.09375/) (2016)
- [Metrics for Multi-Class Classification: an Overview](https://mlsanity.com/paper/2008.05756/) (2020)
- [On the definition of a confounder](https://mlsanity.com/paper/1304.0564/) (2013)
- [Deep Feature Screening: Feature Selection for Ultra High-Dimensional Data via Deep Neural Networks](https://mlsanity.com/paper/2204.01682/) (2022)
- [Orthogonal Least Squares Based Fast Feature Selection for Linear Classification](https://mlsanity.com/paper/2101.08539/) (2021)

## Abstract (arXiv)

Biomarker discovery from high-throughput transcriptomic data is crucial for advancing precision medicine. However, existing methods often neglect gene-gene regulatory relationships and lack stability across datasets, leading to conflation of spurious correlations with genuine causal effects. To address these issues, we develop a causal graph neural network (Causal-GNN) method that integrates causal inference with multi-layer graph neural networks (GNNs). The key innovation is the incorporation of causal effect estimation for identifying stable biomarkers, coupled with a GNN-based propensity scoring mechanism that leverages cross-gene regulatory networks. Experimental results demonstrate that our method achieves consistently high predictive accuracy across four distinct datasets and four independent classifiers. Moreover, it enables the identification of more stable biomarkers compared to traditional methods. Our work provides a robust, efficient, and biologically interpretable tool for biomarker discovery, demonstrating strong potential for broad application across medical disciplines.
