The proliferation of social network data has unlocked unprecedented opportunities for extensive, data-driven exploration of human behavior. The structural intricacies of social networks offer insights into various computational social science issues, particularly concerning social influence and information diffusion. However, modeling large-scale social network data comes with computational challenges. Though large language models make it easier than ever to model textual content, any advanced network representation methods struggle with scalability and efficient deployment to out-of-sample users. In response, we introduce a novel approach tailored for modeling social network data in user detection tasks. This innovative method integrates localized social network interactions with the capabilities of large language models. Operating under the premise of social network homophily, which posits that socially connected users share similarities, our approach is designed to address these challenges. We conduct a thorough evaluation of our method across seven real-world social network datasets, spanning a diverse range of topics and detection tasks, showcasing its applicability to advance research in computational social science.

Abstract--While developments in machine learning led to impressive performance gains on big data, many human subjects data are, in actuality, small and sparsely labeled. Existing methods applied to such data often do not easily generalize to out-of-sample subjects. Instead, models must make predictions on test data that may be drawn from a different distribution, a problem known as zero-shot learning. To address this challenge, we develop an end-to-end framework using a meta-learning approach, which enables the model to rapidly adapt to a new prediction task with limited training data for out-of-sample test data. We use three real-world small-scale human subjects datasets (two randomized control studies and one observational study), for which we predict treatment outcomes for held-out treatment groups. Our model learns the latent treatment effects of each intervention and, by design, can naturally handle multitask predictions. However, these methods have had limited success in I. Though such studies remain the gold standard large amount of labeled data yet have limited capacity for of scientific discovery [1], [3], many are small and sparsely transferring knowledge [14], [15], hindering their ability to labeled due to regulatory challenges, ethical considerations generalize to complex yet small human subjects datasets and [4], data availability (e.g., investigating rare diseases [3]), tasks [16].