Demo Data from VLDB 2026 / reviewers in the wild / expert
Xueliang Cui
dblp:415/4917
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2025
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Artificial intelligence and machine learning · 1 · 1 since 2021Graphics, computer vision, multimedia, augmented reality and games · 1 · 1 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Artificial intelligence
1 paper |
Probabilistic and Bayesian machine learning · 67% Knowledge representation and reasoning · 33% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Machine learning › Probabilistic and Bayesian machine learning › causal inference › causal discovery
additive noise model |
0.9 | 1 | 2025 | Identifying Causal Mechanism Shifts Under Additive Models with Arbitrary Noise · IJCAI 2025 |
Machine learning › Probabilistic and Bayesian machine learning
causal inference |
0.9 | 1 | 2025 | Identifying Causal Mechanism Shifts Under Additive Models with Arbitrary Noise · IJCAI 2025 |
Knowledge, reasoning and agents › Knowledge representation and reasoning › causal reasoning
causal mechanism shift identification |
0.9 | 1 | 2025 | Identifying Causal Mechanism Shifts Under Additive Models with Arbitrary Noise · IJCAI 2025 |
Methods — techniques the papers use, named apart from their topics
nonlinear additive noise models · 0.9
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | Identifying Causal Mechanism Shifts Under Additive Models with Arbitrary NoiseabstractIn many real-world scenarios, the goal is to identify variables whose causal mechanisms change across related datasets. For example, detecting abnormal root nodes in manufacturing, and identifying key genes that influence cancer by analyzing differences in gene regulatory mechanisms between healthy individuals and cancer patients. This can be done by recovering the causal structure for each dataset independently and then comparing them to identify differences, but the performance is often suboptimal. Typically, existing methods directly identify causal mechanism shifts based on linear additive noise models (ANMs) or by imposing restrictive assumptions on the noise distribution. In this paper, we introduce CMSI, a novel and more general algorithm based on nonlinear ANMs that identifies variables with shifting causal mechanisms under arbitrary noise distributions. Evaluated on various synthetic datasets, CMSI consistently outperforms existing baselines in terms of F1 score. Additionally, we demonstrate CMSI's applicability on gene expression datasets of ovarian cancer patients at different disease stages. Yewei Xia, Xueliang Cui, Hao Zhang 0079, Yixin Ren, Feng Xie 0002, Jihong Guan, Ruxin Wang 0001, Shuigeng Zhou |
IJCAI | 2 |