Evidence map›Paper›PMID 40705488›Full record

ArticleBiometrics2025

Tree-based additive noise directed acyclic graphical models for nonlinear causal discovery with interactions.

Fangting Zhou, Kejun He, Yang Ni

Abstract read
In one paragraph

Article in Biometrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Fangting ZhouDepartment of Biostatistics, Yale University, New Haven, CT 06520, United States.ORCID 0000-0001-7604-4542
Kejun HeCenter for Applied Statistics, Institute of Statistics and Big Data, Renmin University of China, Beijing 100872, China.ORCID 0000-0002-3996-6246
Yang NiDepartment of Statistics, Texas A&M University, College Station, TX 77840, United States.

Funding

Bayesian Differential Causal Network and Clustering Methods for Single-Cell Data (R01GM148974)R01GM148974 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI NI, YANG · 2022 to 2025
$1.2M
National Key Research and Development Program of China 2023YFC3304701NIGMS NIH HHS R01 GM148974NIH HHS 1R01GM148974NSF DMS-2112943
6 · The paper itself

Abstract

Directed acyclic graphical models with additive noises are essential in nonlinear causal discovery and have numerous applications in various domains, such as social science and systems biology. Most such models further assume that structural causal functions are additive to ensure causal identifiability and computational feasibility, which may be too restrictive in the presence of causal interactions. Some methods consider general nonlinear causal functions represented by, for example, Gaussian processes and neural networks, to accommodate interactions. However, they are either computationally intensive or lack interpretability. We propose a highly interpretable and computationally feasible approach using trees to incorporate interactions in nonlinear causal discovery, termed tree-based additive noise models. The nature of the tree construction leads to piecewise constant causal functions, making existing causal identifiability results of additive noise models with continuous and smooth causal functions inapplicable. Therefore, we provide new conditions under which the proposed model is identifiable. We develop a recursive algorithm for source node identification and a score-based ordering search algorithm. Through extensive simulations, we demonstrate the utility of the proposed model and algorithms benchmarking against existing additive noise models, especially when there are strong causal interactions. Our method is applied to infer a protein-protein interaction network for breast cancer, where proteins may form protein complexes to perform their functions.

Indexed as

CausalityModels, StatisticalNonlinear DynamicsAlgorithmsBiometryComputer SimulationHumansAdditive noise modelBayesian networkCausal identifiabilityCausal interactionStructural equation modelTree

Identifiers

PMID40705488
PMCPMC12288665

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.