Researcher profile

William Sutcliffe

William Sutcliffe contributes to research discovery and scholarly infrastructure.

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Published work

2 published item(s)

preprint2026arXiv

Joint Treatment Effect Estimation from Incomplete Healthcare Data: Temporal Causal Normalizing Flows with LLM-driven Evolutionary MNAR Imputation

Target trial emulation (TTE) enables causal questions to be studied with observational data when randomized controlled trials (RCTs) are infeasible. Yet treatment-effect methods often address causal estimation, missingness, and temporal structure separately, limiting their robustness in electronic health records (EHRs), where time-varying confounding and missing-not-at-random (MNAR) biomarkers can reach 50%--80%. We propose a two-stage pipeline for treatment effect estimation from incomplete longitudinal EHRs. First, CausalFlow-T, a directed acyclic graph (DAG)-constrained normalizing flow with long short-term memory (LSTM)-encoded patient history, performs exact invertible counterfactual inference, avoiding approximation errors from variational inference and separating confounding through explicit causal structure. Ablations on four synthetic and one semi-synthetic benchmark with known counterfactuals show that DAG constraints and exact inference address distinct failure modes: neither compensates for the other. Second, because CausalFlow-T requires completed inputs, we introduce an LLM-driven evolutionary imputer that proposes executable imputation operators rather than individual entries, and evaluate it with three large language model (LLM) backends, including two open-source models. Across 30%--80% MNAR missingness, this imputer achieves the best pooled rank over biomarker and causal metrics, leading in point-wise accuracy and temporal extrapolation while preserving average treatment effect (ATE) recovery as statistical baselines degrade. On Swiss primary-care EHRs from adults with type 2 diabetes initiating a GLP-1 receptor agonist or SGLT-2 inhibitor, the pipeline estimates a per-protocol weight-loss difference of -0.98 kg [95% CI -1.01, -0.96] favoring GLP-1 receptor agonists, consistent with randomized evidence and obtained from realistically incomplete real-world EHRs.

preprint2026arXiv

Towards replacing detector simulation with heterogeneous GNNs in flavour physics analyses

Driven by the increasing volume of recorded data, the demand for simulation from experiments based at the Large Hadron Collider will rise sharply in the coming years. Addressing this demand solely with existing computationally intensive workflows is not feasible. This paper introduces a new fast simulation tool designed to address this demand at the LHCb experiment. This tool emulates the detector response to arbitrary multibody decay topologies at LHCb. Rather than memorising specific decay channels, the model learns generalisable patterns within the response, allowing it to interpolate to channels not present in the training data. Novel heterogeneous graph neural network architectures are employed that are designed to embed the physical characteristics of the task directly into the network structure. We demonstrate the performance of the tool across a range of decay topologies, showing the networks can correctly model the relationships between complex variables. The architectures and methods presented are generic and could readily be adapted to emulate workflows at other simulation-intensive particle physics experiments.