Qing Yao
Author directory2026
The Emergence and Sparsification of a Syntactic Circuit
Qing Yao | Sasha Boguraev | Tiago Pimentel | Kyle Mahowald
Proceedings of the 2026 Conference on Empirical Methods in Natural Language Processing
Qing Yao | Sasha Boguraev | Tiago Pimentel | Kyle Mahowald
Proceedings of the 2026 Conference on Empirical Methods in Natural Language Processing
To understand the emergence of grammatical behavior in language models, we track circuits for subject–verb number agreement in pythia-1b and ten seeds of pythia-410m across training. We find that subject–verb agreement is learned early, and is initially handled by a diffuse collection of neurons. However, after agreement *behavior* has stabilized, the *mechanisms* responsible for it continue to reorganize. The attention heads which mediate agreement often shift during training: in the case of pythia-1b, behavior is controlled by two heads early in training but by a third (different) head later. Furthermore, the circuit shrinks over training, with pythia-1b’s final circuit being strikingly sparse. We take these results to be informative about how linguistic knowledge emerges and is represented in a language model.
What’s in a Name? Morphological Shortcuts by LLMs in Pharmacology
Kaijie Mo | Thomas Yang | Chantal Shaib | Qing Yao | William Rudman | Ramez Kouzy | Kanishka Misra | Byron C Wallace | Junyi Jessy Li
Proceedings of the 2026 Conference on Empirical Methods in Natural Language Processing
Kaijie Mo | Thomas Yang | Chantal Shaib | Qing Yao | William Rudman | Ramez Kouzy | Kanishka Misra | Byron C Wallace | Junyi Jessy Li
Proceedings of the 2026 Conference on Empirical Methods in Natural Language Processing
The morphological form of a word can often give cues to its meaning, but purely relying on these mappings can lead to overgeneralization in high-stakes domains. In the medical domain, for instance, LLMs can confidently reason about fictitious drugs from their affixes alone (e.g., wugcillin) and generate plausible-looking clinical content. We present a behavioral and mechanistic study of LLM ”affix heuristics” in pharmacology. Using fictitious drug names built from real affixes, we show that affix signals alone elicit class-level pharmacological responses. We introduce a framework for identifying whether a model’s drug semantics are driven mainly by the affix, the stem, or the drug name as a whole. Applied across 653 drugs, our framework reveals that models often induce drug meaning primarily through affix cues, yet rarely explicitly indicate this reliance, and sometimes incorrectly conflate properties among affix-sharing drugs. Activation patching across models further localizes this behavior to early-mid layers. These findings show that morphological shortcuts pose a subtle but measurable risk to safety.