Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Loka Li

dblp:371/1096 · DBLP profile ↗
← Back
4ranked-venue papers
2as first author
4since 2021 · last 2025
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 4 · 2 first-author · 4 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
4 papers
Probabilistic and Bayesian machine learning · 36% Representation and self-supervised learning · 31% Language models and text generation · 21%
Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 10 heaviest of 11, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Machine learning › Probabilistic and Bayesian machine learning › causal inference
causal discovery
1.522024
On Causal Discovery in the Presence of Deterministic Relations · NeurIPS 2024
Federated Causal Discovery from Heterogeneous Data · ICLR 2024
Natural language and speech › Language models and text generation › decoding
autoregressive decoding
0.912025
Reflection-Window Decoding: Text Generation with Selective Refinement · ICML 2025
Machine learning › Representation and self-supervised learning
causal representation learning
0.912025
Causal Representation Learning from Multimodal Biomedical Observations · ICLR 2025
Natural language and speech › Language models and text generation › decoding
decoding strategy
0.912025
Reflection-Window Decoding: Text Generation with Selective Refinement · ICML 2025
Machine learning › Representation and self-supervised learning › causal representation learning
identifiability
0.912025
Causal Representation Learning from Multimodal Biomedical Observations · ICLR 2025
Machine learning › Representation and self-supervised learning › causal representation learning › identifiability
latent variable identifiability
0.912025
Causal Representation Learning from Multimodal Biomedical Observations · ICLR 2025
Machine learning › Probabilistic and Bayesian machine learning › causal inference › causal discovery
federated causal discovery
0.812024
Federated Causal Discovery from Heterogeneous Data · ICLR 2024
Machine learning › Probabilistic and Bayesian machine learning › causal inference › causal discovery
score-based causal discovery
0.812024
On Causal Discovery in the Presence of Deterministic Relations · NeurIPS 2024
Bioinformatics and computational biology
biomedical data analysis
0.312025
Causal Representation Learning from Multimodal Biomedical Observations · ICLR 2025
Machine learning › Efficient and distributed learning
federated learning
0.212024
Federated Causal Discovery from Heterogeneous Data · ICLR 2024

Methods — techniques the papers use, named apart from their topics

structural sparsity · 1.7nonparametric latent distribution · 1.7sliding reflection window · 0.9pausing criterion · 0.9surrogate variable · 0.8independent change principle · 0.8greedy equivalent search · 0.8exact search · 0.8conditional independence test · 0.8
YearPublicationVenuePosition
2025 Causal Representation Learning from Multimodal Biomedical Observations
abstract
Prevalent in biomedical applications (e.g., human phenotype research), multimodal datasets can provide valuable insights into the underlying physiological mechanisms. However, current machine learning (ML) models designed to analyze these datasets often lack interpretability and identifiability guarantees, which are essential for biomedical research. Recent advances in causal representation learning have shown promise in identifying interpretable latent causal variables with formal theoretical guarantees. Unfortunately, most current work on multimodal distributions either relies on restrictive parametric assumptions or yields only coarse identification results, limiting their applicability to biomedical research that favors a detailed understanding of the mechanisms. In this work, we aim to develop flexible identification conditions for multimodal data and principled methods to facilitate the understanding of biomedical datasets. Theoretically, we consider a nonparametric latent distribution (c.f., parametric assumptions in previous work) that allows for causal relationships across potentially different modalities. We establish identifiability guarantees for each latent component, extending the subspace identification results from previous work. Our key theoretical contribution is the structural sparsity of causal connections between modalities, which, as we will discuss, is natural for a large collection of biomedical systems. Empirically, we present a practical framework to instantiate our theoretical insights. We demonstrate the effectiveness of our approach through extensive experiments on both numerical and synthetic datasets. Results on a real-world human phenotype dataset are consistent with established biomedical research, validating our theoretical and methodological framework.
Yuewen Sun, Guangyi Chen 0002, Loka Li, Gongxu Luo, Zijian Li 0001, Yixuan Zhang 0001, Yujia Zheng 0001, Mengyue Yang, Petar Stojanov, Eran Segal, Eric P. Xing, Kun Zhang 0001
ICLR4
2025 Reflection-Window Decoding: Text Generation with Selective Refinement
abstract
The autoregressive decoding for text generation in large language models (LLMs), while widely used, is inherently suboptimal due to the lack of a built-in mechanism to perform refinement and/or correction of the generated content. In this paper, we consider optimality in terms of the joint probability over the generated response, when jointly considering all tokens at the same time. We theoretically characterize the potential deviation of the autoregressively generated response from its globally optimal counterpart that is of the same length. Our analysis suggests that we need to be cautious when noticeable uncertainty arises during text generation, which may signal the sub-optimality of the generation history. To address the pitfall of autoregressive decoding for text generation, we propose an approach that incorporates a sliding reflection window and a pausing criterion, such that refinement and generation can be carried out interchangeably as the decoding proceeds. Our selective refinement framework strikes a balance between efficiency and optimality, and our extensive experimental results demonstrate the effectiveness of our approach.
Zeyu Tang 0002, Zhenhao Chen, Xiangchen Song, Loka Li, Yunlong Deng, Yifan Shen 0004, Guangyi Chen 0002, Peter Spirtes, Kun Zhang 0001
ICML4
2024 Federated Causal Discovery from Heterogeneous Data
abstract
Conventional causal discovery methods rely on centralized data, which is inconsistent with the decentralized nature of data in many real-world situations. This discrepancy has motivated the development of federated causal discovery (FCD) approaches. However, existing FCD methods may be limited by their potentially restrictive assumptions of identifiable functional causal models or homogeneous data distributions, narrowing their applicability in diverse scenarios. In this paper, we propose a novel FCD method attempting to accommodate arbitrary causal models and heterogeneous data. We first utilize a surrogate variable corresponding to the client index to account for the data heterogeneity across different clients. We then develop a federated conditional independence test (FCIT) for causal skeleton discovery and establish a federated independent change principle (FICP) to determine causal directions. These approaches involve constructing summary statistics as a proxy of the raw data to protect data privacy. Owing to the nonparametric properties, FCIT and FICP make no assumption about particular functional forms, thereby facilitating the handling of arbitrary causal models. We conduct extensive experiments on synthetic and real datasets to show the efficacy of our method. The code is available at https://github.com/lokali/FedCDH.git.
Loka Li, Ignavier Ng, Gongxu Luo, Biwei Huang, Guangyi Chen 0002, Tongliang Liu, Bin Gu 0001, Kun Zhang 0001
ICLR1
2024 On Causal Discovery in the Presence of Deterministic Relations
abstract
Many causal discovery methods typically rely on the assumption of independent noise, yet real-life situations often involve deterministic relationships. In these cases, observed variables are represented as deterministic functions of their parental variables without noise. When determinism is present, constraint-based methods encounter challenges due to the violation of the faithfulness assumption. In this paper, we find, supported by both theoretical analysis and empirical evidence, that score-based methods with exact search can naturally address the issues of deterministic relations under rather mild assumptions. Nonetheless, exact score-based methods can be computationally expensive. To enhance the efficiency and scalability, we develop a novel framework for causal discovery that can detect and handle deterministic relations, called Determinism-aware Greedy Equivalent Search (DGES). DGES comprises three phases: (1) identify minimal deterministic clusters (i.e., a minimal set of variables with deterministic relationships), (2) run modified Greedy Equivalent Search (GES) to obtain an initial graph, and (3) perform exact search exclusively on the deterministic cluster and its neighbors. The proposed DGES accommodates both linear and nonlinear causal relationships, as well as both continuous and discrete data types. Furthermore, we investigate the identifiability conditions of DGES. We conducted extensive experiments on both simulated and real-world datasets to show the efficacy of our proposed method.
Loka Li, Haoyue Dai, Hanin Al Ghothani, Biwei Huang, Jiji Zhang, Shahar Harel, Isaac Bentwich, Guangyi Chen 0002, Kun Zhang 0001
NeurIPS1