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Elias Chaibub Neto

dblp:157/8116 · DBLP profile ↗
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6ranked-venue papers
5as first author
3since 2021 · last 2025
0000-0002-9575-861XORCID · verified

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

Artificial intelligence and machine learning · 5 · 5 first-author · 3 since 2021Databases, data management, data science and information retrieval · 2 · 2 first-authorApplied, interdisciplinary, general and emerging computing · 1

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.

Artificial intelligence
4 papers
Trustworthy machine learning · 68% Generative modeling · 22% Probabilistic and Bayesian machine learning · 10%
Interdisciplinary, comprehensive, and emerging computing
2 papers
Computational social science and digital humanities · 54% Medical and health informatics · 46%

Topics — the 9 heaviest of 10, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Machine learning › Generative modeling › diffusion model
tabular data generation
0.912025
TabSDS: a Lightweight, Fully Non-Parametric, and Model Free Approach for Generating Synthetic Tabular Data · ICML 2025
Machine learning › Trustworthy machine learning › robustness › distribution shift
robustness to distribution shift
0.512021
Causality-aware counterfactual confounding adjustment as an alternative to linear residualization in anticausal prediction tasks based on linear learners · ICML 2021
Machine learning › Trustworthy machine learning
fairness
0.412020
A Causal Look at Statistical Definitions of Discrimination · KDD 2020
Machine learning › Trustworthy machine learning › fairness
fairness criteria
0.412020
A Causal Look at Statistical Definitions of Discrimination · KDD 2020
Machine learning › Trustworthy machine learning › fairness › fairness criteria
predictive parity
0.412020
A Causal Look at Statistical Definitions of Discrimination · KDD 2020
Machine learning › Probabilistic and Bayesian machine learning › causal inference
deconfounding
0.412019
A Permutation Approach to Assess Confounding in Machine Learning Applications for Digital Health · KDD 2019
Machine learning › Trustworthy machine learning
robustness
0.412019
A Permutation Approach to Assess Confounding in Machine Learning Applications for Digital Health · KDD 2019
Computational social science and digital humanities › algorithmic decision-making
algorithmic fairness
0.112020
A Causal Look at Statistical Definitions of Discrimination · KDD 2020
Medical and health informatics
digital health
0.112019
A Permutation Approach to Assess Confounding in Machine Learning Applications for Digital Health · KDD 2019

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

rank transformation · 0.9data shuffling · 0.9faithfulness assumption · 0.9causal inference · 0.9permutation testing · 0.8inverse probability weighting · 0.8linear residualization · 0.5causality-aware predictive modeling · 0.5
YearPublicationVenuePosition
2025 TabSDS: a Lightweight, Fully Non-Parametric, and Model Free Approach for Generating Synthetic Tabular Data
abstract
The development of deep generative models for tabular data is currently a very active research area in machine learning. These models, however, tend to be computationally heavy and require careful tuning of multiple model parameters. In this paper, we propose TabSDS - a lightweight, non-parametric, and model free alternative to tabular deep generative models which leverages rank and data shuffling transformations for generating synthetic data which closely approximates the joint probability distribution of the real data. We evaluate TabSDS against multiple baselines implemented in the Synthcity Python library across several datasets. TabSDS showed very competitive performance against all baselines (including TabDDPM - a strong baseline model for tabular data generation). Importantly, the execution time of TabSDS is orders of magnitude faster than the deep generative baselines, and also considerably faster than other computationally efficient baselines such as adversarial random forests.
Elias Chaibub Neto
ICML1
2024 Causality-Aware Predictions in Static Anticausal Machine Learning Tasks
abstract
We propose a counterfactual approach to train "causality-aware" predictive models that are able to leverage causal information in static anticausal machine learning tasks (i.e., prediction tasks where the outcome influences the inputs). In applications plagued by confounding, the approach can be used to generate predictions that are free from the influence of observed confounders. In applications involving observed mediators, the approach can be used to generate predictions that only capture the direct or the indirect causal influences. Mechanistically, we train supervised learners on (counterfactually) simulated inputs that retain only the associations generated by the causal relations of interest. We focus on linear models, where analytical results connecting covariances, causal effects, and prediction mean square errors are readily available. Quite importantly, we show that our approach does not require knowledge of the full causal graph. It suffices to know which variables represent potential confounders and/or mediators. We investigate the stability of the method with respect to dataset shifts generated by selection biases and also relax the linearity assumption by extending the approach to additive models better able to account for nonlinearities in the data. We validate our approach in a series of synthetic data experiments and illustrate its application to a real dataset.
Elias Chaibub Neto
IEEE Trans. Neural Networks Learn. Syst.1
2021 Causality-aware counterfactual confounding adjustment as an alternative to linear residualization in anticausal prediction tasks based on linear learners
abstract
Linear residualization is a common practice for confounding adjustment in machine learning applications. Recently, causality-aware predictive modeling has been proposed as an alternative causality-inspired approach for adjusting for confounders. In this paper, we compare the linear residualization approach against the causality-aware confounding adjustment in anticausal prediction tasks. Our comparisons include both the settings where the training and test sets come from the same distributions, as well as, when the training and test sets are shifted due to selection biases. In the absence of dataset shifts, we show that the causality-aware approach tends to (asymptotically) outperform the residualization adjustment in terms of predictive performance in linear learners. Importantly, our results still holds even when the true model generating the data is not linear. We illustrate our results in both regression and classification tasks. Furthermore, in the presence of dataset shifts in the joint distribution of the confounders and outcome variables, we show that the causality-aware approach is more stable than linear residualization.
Elias Chaibub Neto
ICML1
2020 A Causal Look at Statistical Definitions of Discrimination
abstract
Predictive parity and error rate balance are both widely accepted and adopted criteria for assessing fairness of classifiers. The realization that these equally reasonable criteria can lead to contradictory results has, nonetheless, generated a lot of debate/controversy, and has motivated the development of mathematical results establishing the impossibility of concomitantly satisfying predictive parity and error rate balance. Here, we investigate these fairness criteria from a causality perspective. By taking into consideration the data generation process giving rise to the observed data, as well as, the data generation process giving rise to the predictions, and assuming faithfulness, we prove that when the base rates differ across the protected groups and there is no perfect separation, then a standard classifier cannot achieve exact predictive parity. (Where, by standard classifier we mean a classifier trained in the usual way, without adopting pre-processing, in-processing, or post-processing fairness techniques.) This result holds in general, irrespective of the data generation process giving rise to the observed data. Furthermore, we show that the amount of disparate mistreatment for the positive predictive value metric is proportional to the difference between the base rates. For the error rate balance, as well as, the closely related equalized odds and equality of opportunity criteria, we show that there are, nonetheless, data generation processes that can still satisfy these criteria when the base rates differ by protected group, and we characterize the conditions under which these criteria hold. We illustrate our results using synthetic data, and with the re-analysis of the COMPAS data.
Elias Chaibub Neto
KDD1
2019 A Permutation Approach to Assess Confounding in Machine Learning Applications for Digital Health
abstract
Machine learning applications are often plagued with confounders that can impact the generalizability of the learners. In clinical settings, demographic characteristics often play the role of confounders. Confounding is especially problematic in remote digital health studies where the participants self-select to enter the study, thereby making it difficult to balance the demographic characteristics of participants. One effective approach to combat confounding is to match samples with respect to the confounding variables in order to improve the balance of the data. This procedure, however, leads to smaller datasets and hence negatively impact the inferences drawn from the learners. Alternatively, confounding adjustment methods that make more efficient use of the data (such as inverse probability weighting) usually rely on modeling assumptions, and it is unclear how robust these methods are to violations of these assumptions. Here, instead of proposing a new method to control for confounding, we develop novel permutation based statistical tools to detect and quantify the influence of observed confounders, and estimate the unconfounded performance of the learner. Our tools can be used to evaluate the effectiveness of existing confounding adjustment methods. We evaluate the statistical properties of our methods in a simulation study, and illustrate their application using real-life data from a Parkinson's disease mobile health study collected in an uncontrolled environment.
Elias Chaibub Neto, Abhishek Pratap, Thanneer Malai Perumal, Meghasyam Tummalacherla, Brian M. Bot, Lara M. Mangravite, Larsson Omberg
KDD1
2017 Mindboggling morphometry of human brains
abstract
Mindboggle (http://mindboggle.info) is an open source brain morphometry platform that takes in preprocessed T1-weighted MRI data and outputs volume, surface, and tabular data containing label, feature, and shape information for further analysis. In this article, we document the software and demonstrate its use in studies of shape variation in healthy and diseased humans. The number of different shape measures and the size of the populations make this the largest and most detailed shape analysis of human brains ever conducted. Brain image morphometry shows great potential for providing much-needed biological markers for diagnosing, tracking, and predicting progression of mental health disorders. Very few software algorithms provide more than measures of volume and cortical thickness, while more subtle shape measures may provide more sensitive and specific biomarkers. Mindboggle computes a variety of (primarily surface-based) shapes: area, volume, thickness, curvature, depth, Laplace-Beltrami spectra, Zernike moments, etc. We evaluate Mindboggle's algorithms using the largest set of manually labeled, publicly available brain images in the world and compare them against state-of-the-art algorithms where they exist. All data, code, and results of these evaluations are publicly available.
Arno Klein, Satrajit S. Ghosh, Forrest Sheng Bao, Joachim Giard, Yrjö Häme, Eliezer Stavsky, Noah Lee, Brian Rossa, Martin Reuter 0001, Elias Chaibub Neto, Anisha Keshavan
PLoS Comput. Biol.10