Riccardo Cadei
Research Subjects
Research Interests
Riccardo Cadei has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Daniela Maria Garcia
Department of Biostatistics, Harvard School of Public Health, Boston, Massachusetts, United States of America
2 shared publications - Falco Joannes Bargagli Stoffi
Department of Biostatistics University of California Los Angeles California USA
2 shared publications - Kwonsang Lee
Department of Statistics, Seoul National University, Seoul, Republic of Korea
2 shared publications - Naeem Khoshnevis
University Research Computing and Data Services Harvard University Cambridge Massachusetts United States of America
2 shared publications
Latest Publications
- Open Access
- 15 December 2023
- Published by The Open Journal in Journal of Open Source Software
- Vol. 8 (92) , 5587
CRE: An R package for interpretable discovery and inference of heterogeneous treatment effects
In health and social sciences, it is critically important to identify interpretable subgroups of the study population where a treatment has notable heterogeneity in the causal effects with respect to the average treatment effect (ATE). Several approaches have already been proposed for heterogeneous treatment effect (HTE) discovery, either estimating first the conditional average treatment effect (CATE) and identifying heterogeneous subgroups in a second stage (Bargagli-Stoffi et al., 2020, 2022; Foster et al., 2011; Hahn et al., 2020), either estimating directly these subgroups in a direct data-driven procedure (Nagpal et al., 2020; Wang & Rudin, 2022). Many of these methodologies are decision tree-based methodologies. Tree-based approaches are based on efficient and easily implementable recursive mathematical programming (e.g., HTE maximization), they can be easily tweaked and adapted to different scenarios depending on the research question of interest, and they guarantee a high degree of interpretability—i.e., the degree to which a human can understand the cause of a decision (Lakkaraju et al., 2016). Despite these appealing features, single-tree heterogeneity discovery is characterized by two main limitations: instability in the identification of the subgroups and reduced exploration of the potential heterogeneity. To accommodate these shortcomings, Bargagli-Stoffi et al. (2023) proposed Causal Rule Ensemble, a new method for interpretable HTE characterization in terms of decision rules, via an extensive exploration of heterogeneity patterns by an ensemble-of-trees approach. CRE is an R package providing a flexible implementation of Causal Rule Ensemble. The package allows for multiple variants of Causal Rule Ensemble algorithm, also including different internal individual average treatment effect (IATE) estimators—i.e., AIPW (Robins et al., 1994), Causal Forest (Athey et al., 2019), Causal BART (Hill, 2011), S-Learner (Hill, 2011), T-Learner (Hansotia & Rukstales, 2002), X-Learner (Künzel et al., 2019).
- 15 December 2023
- Published by The Open Journal in Journal of Open Source Software
- Vol. 8 (92) , 5587
Open AccessCRE: An R package for interpretable discovery and inference of heterogeneous treatment effects
In health and social sciences, it is critically important to identify interpretable subgroups of the study population where a treatment has notable heterogeneity in the causal effects with respect to the average treatment effect (ATE). Several approaches have already been proposed for heterogeneous treatment effect (HTE) discovery, either estimating first the conditional average treatment effect (CATE) and identifying heterogeneous subgroups in a second stage (Bargagli-Stoffi et al., 2020, 2022; Foster et al., 2011; Hahn et al., 2020), either estimating directly these subgroups in a direct data-driven procedure (Nagpal et al., 2020; Wang & Rudin, 2022). Many of these methodologies are decision tree-based methodologies. Tree-based approaches are based on efficient and easily implementable recursive mathematical programming (e.g., HTE maximization), they can be easily tweaked and adapted to different scenarios depending on the research question of interest, and they guarantee a high degree of interpretability—i.e., the degree to which a human can understand the cause of a decision (Lakkaraju et al., 2016). Despite these appealing features, single-tree heterogeneity discovery is characterized by two main limitations: instability in the identification of the subgroups and reduced exploration of the potential heterogeneity. To accommodate these shortcomings, Bargagli-Stoffi et al. (2023) proposed Causal Rule Ensemble, a new method for interpretable HTE characterization in terms of decision rules, via an extensive exploration of heterogeneity patterns by an ensemble-of-trees approach. CRE is an R package providing a flexible implementation of Causal Rule Ensemble. The package allows for multiple variants of Causal Rule Ensemble algorithm, also including different internal individual average treatment effect (IATE) estimators—i.e., AIPW (Robins et al., 1994), Causal Forest (Athey et al., 2019), Causal BART (Hill, 2011), S-Learner (Hill, 2011), T-Learner (Hansotia & Rukstales, 2002), X-Learner (Künzel et al., 2019).
- 18 October 2022
- Published by The R Foundation
CRE: Interpretable Discovery and Inference of Heterogeneous Treatment Effects
- 18 October 2022
- Published by The R Foundation
CRE: Interpretable Discovery and Inference of Heterogeneous Treatment Effects