Score contribution per author:
α: calibrated so average coauthorship-adjusted count equals average raw count
Multivalued treatment models have typically been studied under restrictive assumptions: ordered choice, and more recently, unordered monotonicity. We show how treatment effects can be identified in a more general class of models that allows for multidimensional unobserved heterogeneity. Our results rely on two main assumptions: treatment assignment must be a measurable function of threshold‐crossing rules, and enough continuous instruments must be available. We illustrate our approach for several classes of models.