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Sriram Somanchi

dblp:41/7118 · DBLP profile ↗
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4ranked-venue papers
2as first author
3since 2021 · last 2025
0000-0002-3153-1248ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 3 · 1 first-author · 2 since 2021Databases, data management, data science and information retrieval · 3 · 2 first-author · 2 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Databases, data mining, and information retrieval
2 papers
Data mining · 81% Information retrieval · 19%
Artificial intelligence
1 paper
Probabilistic and Bayesian machine learning · 100%
Interdisciplinary, comprehensive, and emerging computing
2 papers
Computational social science and digital humanities · 60% Medical and health informatics · 40%
Human-computer interaction and pervasive computing
1 paper
Usability and user experience research · 100%

Topics — the 11 heaviest of 11, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Data mining
causal inference
0.912025
Difference-in-Differences Subset Scan · KDD (2) 2025
Data mining
pattern mining
0.912025
Difference-in-Differences Subset Scan · KDD (2) 2025
Data mining › pattern mining
subgroup discovery
0.912025
Difference-in-Differences Subset Scan · KDD (2) 2025
Machine learning › Probabilistic and Bayesian machine learning
causal inference
0.712023
Exploiting Discovered Regression Discontinuities to Debias Conditioned-on-observable Estimators · J. Mach. Learn. Res. 2023
Machine learning › Probabilistic and Bayesian machine learning › causal inference › causal effect estimation
treatment effect estimation
0.712023
Exploiting Discovered Regression Discontinuities to Debias Conditioned-on-observable Estimators · J. Mach. Learn. Res. 2023
Computational social science and digital humanities
causal inference
0.712023
Exploiting Discovered Regression Discontinuities to Debias Conditioned-on-observable Estimators · J. Mach. Learn. Res. 2023
Information retrieval
retrieval evaluation
0.712023
Examining User Heterogeneity in Digital Experiments · ACM Trans. Inf. Syst. 2023
Usability and user experience research
user modeling
0.712023
Examining User Heterogeneity in Digital Experiments · ACM Trans. Inf. Syst. 2023
Medical and health informatics
clinical prediction
0.212015
Early Prediction of Cardiac Arrest (Code Blue) using Electronic Medical Records · KDD 2015
Medical and health informatics › clinical prediction
early warning
0.212015
Early Prediction of Cardiac Arrest (Code Blue) using Electronic Medical Records · KDD 2015
Data mining › causal inference
online controlled experiments
0.212023
Examining User Heterogeneity in Digital Experiments · ACM Trans. Inf. Syst. 2023

Methods — techniques the papers use, named apart from their topics

regression discontinuity detection · 1.3observational estimator · 1.3extrapolation · 1.3double machine learning · 1.3causal inference · 1.3a/b testing · 1.3subset scan · 0.9generalized likelihood ratio · 0.9difference-in-differences · 0.9
YearPublicationVenuePosition
2025 Difference-in-Differences Subset Scan
abstract
Difference-in-differences (DiD) has been extensively applied in the literature to elicit the average causal effect of an intervention or policy. Though researchers explore heterogeneity in the treatment effect with respect to time or some observed covariate (usually driven by domain knowledge), there is limited work on a principled, algorithmic approach to discovering the subgroups that exhibit heterogeneity in the treatment effect in DiD settings. In this research, we propose the Difference-in-Differences Subset Scan (DiD-Scan), which finds subregions of the observed covariate space corresponding to anomalous patterns in the conditional mean treatment effect. We mold our method to the DiD setting by also enabling a scan for dynamic effects over time and across multiple outcome variables. This supports the discovery of patterns where a subset of outcomes are highly impacted for a limited time window. We develop a generalized likelihood ratio-based scoring function to quantify the treatment effect of a given subgroup and propose a computationally efficient method to discover the subgroups with the largest treatment effect. We extend the method to consider correlations across time, a common condition in difference-in-difference settings that increases the difficulty of subset identification. Lastly, we demonstrate the efficacy and interpretability of the method with both simulations and applications to real datasets, replicating and extending two published studies.
Will Stamey, Sriram Somanchi, Edward McFowland
KDD (2)2
2023 Exploiting Discovered Regression Discontinuities to Debias Conditioned-on-observable Estimators
abstract
Regression discontinuity (RD) designs are widely used to estimate causal effects in the absence of a randomized experiment. However, standard approaches to RD analysis face two significant limitations. First, they require a priori knowledge of discontinuities in treatment. Second, they yield doubly-local treatment effect estimates, and fail to provide more general causal effect estimates away from the discontinuity. To address these limitations, we introduce a novel method for automatically detecting RDs at scale, integrating information from multiple discovered discontinuities with an observational estimator, and extrapolating away from discovered, local RDs. We demonstrate the performance of our method on two synthetic datasets, showing improved performance compared to direct use of an observational estimator, direct extrapolation of RD estimates, and existing methods for combining multiple causal effect estimates. Finally, we apply our novel method to estimate spatially heterogeneous treatment effects in the context of a recent economic development problem.
Benjamin Jakubowski, Sriram Somanchi, Edward McFowland, Daniel B. Neill
J. Mach. Learn. Res.2
2023 Examining User Heterogeneity in Digital Experiments
abstract
Digital experiments are routinely used to test the value of a treatment relative to a status quo control setting — for instance, a new search relevance algorithm for a website or a new results layout for a mobile app. As digital experiments have become increasingly pervasive in organizations and a wide variety of research areas, their growth has prompted a new set of challenges for experimentation platforms. One challenge is that experiments often focus on the average treatment effect (ATE) without explicitly considering differences across major sub-groups — heterogeneous treatment effect (HTE). This is especially problematic because ATEs have decreased in many organizations as the more obvious benefits have already been realized. However, questions abound regarding the pervasiveness of user HTEs and how best to detect them. We propose a framework for detecting and analyzing user HTEs in digital experiments. Our framework combines an array of user characteristics with double machine learning. Analysis of 27 real-world experiments spanning 1.76 billion sessions and simulated data demonstrates the effectiveness of our detection method relative to existing techniques. We also find that transaction, demographic, engagement, satisfaction, and lifecycle characteristics exhibit statistically significant HTEs in 10% to 20% of our real-world experiments, underscoring the importance of considering user heterogeneity when analyzing experiment results, otherwise personalized features and experiences cannot happen, thus reducing effectiveness. In terms of the number of experiments and user sessions, we are not aware of any study that has examined user HTEs at this scale. Our findings have important implications for information retrieval, user modeling, platforms, and digital experience contexts, in which online experiments are often used to evaluate the effectiveness of design artifacts.
Sriram Somanchi, Ahmed Abbasi, Ken Kelley, David G. Dobolyi, Ted Tao Yuan
ACM Trans. Inf. Syst.1
2015 Early Prediction of Cardiac Arrest (Code Blue) using Electronic Medical Records
abstract
Code Blue is an emergency code used in hospitals to indicate when a patient goes into cardiac arrest and needs resuscitation. When Code Blue is called, an on-call medical team staffed by physicians and nurses is paged and rushes in to try to save the patient's life. It is an intense, chaotic, and resource-intensive process, and despite the considerable effort, survival rates are still less than 20% [4]. Research indicates that patients actually start showing clinical signs of deterioration some time before going into cardiac arrest [1][2[][3], making early prediction, and possibly intervention, feasible. In this paper, we describe our work, in partnership with NorthShore University HealthSystem, that preemptively flags patients who are likely to go into cardiac arrest, using signals extracted from demographic information, hospitalization history, vitals and laboratory measurements in patient-level electronic medical records. We find that early prediction of Code Blue is possible and when compared with state of the art existing method used by hospitals (MEWS - Modified Early Warning Score)[4], our methods perform significantly better. Based on these results, this system is now being considered for deployment in hospital settings.
Sriram Somanchi, Samrachana Adhikari, Allen Lin, Elena Eneva, Rayid Ghani
KDD1