MOCA: A Transformer-based Modular Causal Inference Framework with One-way Cross-attention and Cutting Feedback

Causal inference, estimating causal effects from observational data, is a fundamental tool in many disciplines. Of particular importance across a variety of domains is the continuous treatment setting, where the variable of intervention has a continuous range. This setting is far less explored and represents a substantial shift from the binary treatment setting, with models needing to represent effects across a continuum of treatment values. In this paper, we present the first causal foundation model for the continuous treatment setting. Our model meta-learns the ability to predict causal effects across a wide variety of unseen tasks without additional training or fine-tuning. First, we design a novel prior over data-generating processes with continuous treatment variables in order to generate a rich causal training corpus. We then train a transformer to reconstruct individual treatment-response curves given only observational data, leveraging in-context learning to amortize expensive Bayesian posterior inference. Our model achieves state-of-the-art performance on individual treatment-response curve reconstruction tasks compared to causal models which are trained specifically for those tasks. Inference code (including trained model weights) can be found at https://github.com/layer6ai-labs/CCPFN-inference .

Causal discovery from observational data remains challenging due to the need to recover directed structure and latent confounding without interventions. We propose FoundCause, an amortized causal discovery model trained entirely on synthetic data that maps datasets directly to causal graphs in a single forward pass. By learning from large collections of simulated structural causal models, FoundCause captures transferable statistical patterns that generalize beyond individual datasets. The architecture incorporates several key inductive biases for causal discovery. It uses a permutation-invariant transformer encoder with alternating attention over samples and variables to jointly model cross-variable dependence and per-variable distributions. Pairwise statistical features derived from classical asymmetry measures are injected through statistics-conditioned attention, guiding the model toward known causal signals. A factorized decoder separates edge existence from direction, while a triangular refinement module enables reasoning over higher-order causal motifs such as chains and colliders. In addition, a dedicated confounder module based on learnable latent tokens explicitly models hidden common causes, and the model explicitly handles missing data via its masked input representation. To our knowledge, FoundCause is the first amortized causal discovery approach to explicitly model latent confounding. FoundCause outperforms 11 classical non-amortized methods (e.g., PC, GES, NOTEARS-style optimization) and 4 amortized causal discovery methods on 15 real-world datasets, achieving +9.6% improvement in $F_1$, +1.2% in AUROC, and an 18.9% reduction in structural Hamming distance relative to the strongest non-amortized methods, while performing inference in a single forward pass.

Causal inference usually concerns a scalar treatment, yet in many problems the treatment is unstructured: a text, an image, or a sequence of clinical decisions. Consider an instructor writing a course description to attract more students: the treatment is the course description, and the outcome is enrollment. The standard target, the average treatment effect of fixing the treatment to one exact value versus another, runs into two problems. It cannot be estimated, because almost no exact description recurs across courses, leaving no comparable group from which to measure its effect; and it would be of little use even if it could, since no one wants every course to carry the same description. What the instructor actually wants to know is which features of a description raise enrollment, and which of those features can be acted on across many courses. To this end, we propose a causal query for unstructured treatments: the maximally influential feature (MIF), the feature of the treatment that most strongly influences the outcome. We formalize the MIF as a binary feature of the treatment, defined by a feature-scoring function, constrained so that both of its values stay well populated, and chosen to maximize the causal effect it induces. Turning the feature on shifts the distribution of treatments toward those that display it, turning it off shifts away, and the MIF effect contrasts the two average potential outcomes. We study identification conditions for the MIF, develop algorithms to estimate it, and make it actionable through a nudging algorithm that revises a treatment along the MIF into an outcome-improving version. We illustrate the MIF algorithm across applications in text, image, and dynamic treatment sequences.