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Alex Markham

Alex Markham contributes to research discovery and scholarly infrastructure.

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Published work

4 published item(s)

preprint2026arXiv

Coarsening Linear Non-Gaussian Causal Models with Cycles

Recent work on causal abstraction, in particular graphical approaches focusing on causal structure between clusters of variables, aims to summarize a high-dimensional causal structure in terms of a low-dimensional one. Existing methods for learning such summaries from data assume that both the high- and low-dimensional structures are acyclic, which is helpful for causal effect identification and reasoning but excludes many high-dimensional models and thus limits applicability. We show that in the linear non-Gaussian (LiNG) setting, the high-dimensional acyclicity assumption can be relaxed while still allowing recovery of a low-dimensional causal directed acyclic graph (DAG). We further connect identifiability of this low-dimensional DAG to existing results: LiNG models with cycles are observationally identifiable only up to an equivalence class whose members differ by reversals of directed cycles; our low-dimensional DAG, which is invariant across all members of a given equivalence class, thus forms a natural representative of the class. While existing approaches for learning this observational equivalence class over high-dimensional variables have exponential time complexity, our low-dimensional summary is learned in worst-case cubic time and comes with explicit bounds on the sample complexity. We provide open source code and experiments on synthetic data to corroborate our theoretical results.

preprint2022arXiv

A Distance Covariance-based Kernel for Nonlinear Causal Clustering in Heterogeneous Populations

We consider the problem of causal structure learning in the setting of heterogeneous populations, i.e., populations in which a single causal structure does not adequately represent all population members, as is common in biological and social sciences. To this end, we introduce a distance covariance-based kernel designed specifically to measure the similarity between the underlying nonlinear causal structures of different samples. Indeed, we prove that the corresponding feature map is a statistically consistent estimator of nonlinear independence structure, rendering the kernel itself a statistical test for the hypothesis that sets of samples come from different generating causal structures. Even stronger, we prove that the kernel space is isometric to the space of causal ancestral graphs, so that distance between samples in the kernel space is guaranteed to correspond to distance between their generating causal structures. This kernel thus enables us to perform clustering to identify the homogeneous subpopulations, for which we can then learn causal structures using existing methods. Though we focus on the theoretical aspects of the kernel, we also evaluate its performance on synthetic data and demonstrate its use on a real gene expression data set.

preprint2022arXiv

A Transformational Characterization of Unconditionally Equivalent Bayesian Networks

We consider the problem of characterizing Bayesian networks up to unconditional equivalence, i.e., when directed acyclic graphs (DAGs) have the same set of unconditional $d$-separation statements. Each unconditional equivalence class (UEC) is uniquely represented with an undirected graph whose clique structure encodes the members of the class. Via this structure, we provide a transformational characterization of unconditional equivalence; i.e., we show that two DAGs are in the same UEC if and only if one can be transformed into the other via a finite sequence of specified moves. We also extend this characterization to the essential graphs representing the Markov equivalence classes (MECs) in the UEC. UECs partition the space of MECs and are easily estimable from marginal independence tests. Thus, a characterization of unconditional equivalence has applications in methods that involve searching the space of MECs of Bayesian networks.

preprint2020arXiv

Measurement Dependence Inducing Latent Causal Models

We consider the task of causal structure learning over measurement dependence inducing latent (MeDIL) causal models. We show that this task can be framed in terms of the graph theoretic problem of finding edge clique covers,resulting in an algorithm for returning minimal MeDIL causal models (minMCMs). This algorithm is non-parametric, requiring no assumptions about linearity or Gaussianity. Furthermore, despite rather weak assumptions aboutthe class of MeDIL causal models, we show that minimality in minMCMs implies some rather specific and interesting properties. By establishing MeDIL causal models as a semantics for edge clique covers, we also provide a starting point for future work further connecting causal structure learning to developments in graph theory and network science.