Evidence map›Paper›PMID 42812347›Full record

ArticleFrontiers in psychiatry2026

An interpretable computational phenotyping pipeline for adult autism using routine electronic health records.

Jordi Rodeiro-Boliart, Maria Nuñez-Jimenez, Beatriz Olaya, Elena Huerta-Ramos, Elisabet Golobardes

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Article in Frontiers in psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jordi Rodeiro-BoliartImpacte i prevenció dels trastorns mentals, Institut de Recerca Sant Joan de Déu, Sant Boi de Llobregat, Spain.
Maria Nuñez-JimenezEtiopathogenesis and Treatment of Severe Mental Disorders, Sant Joan de Déu Research Institute, Sant Joan de Déu Foundation, Barcelona, Spain.
Beatriz OlayaImpacte i prevenció dels trastorns mentals, Institut de Recerca Sant Joan de Déu, Sant Boi de Llobregat, Spain.
Elena Huerta-RamosEtiopathogenesis and Treatment of Severe Mental Disorders, Sant Joan de Déu Research Institute, Sant Joan de Déu Foundation, Barcelona, Spain.
Elisabet GolobardesSmart Society Research Group, Engineering Department, La Salle-Universitat Ramon Llull, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Electronic health records (EHRs) provide new opportunities for computational phenotyping in mental health, but routinely collected diagnostic data are often sparse, heterogeneous, and challenging to interpret. While numerous computational approaches have been applied to identify patient subgroups, clinically useful phenotyping requires workflows capable of transforming routine diagnostic information into interpretable patient profiles. The goal of this work is to develop and evaluate an end-to-end computational phenotyping pipeline for routine ICD-10 diagnostic data and demonstrate its feasibility in adults with autism spectrum disorder (ASD). Methods: A retrospective observational study was conducted using routine EHR data from adults with ASD receiving care at a specialized mental health service. ICD-10 diagnoses were extracted, aggregated into clinically meaningful diagnostic categories, and transformed into binary patient-level representations. A self-organizing map (SOM) was used to organize patients according to diagnostic similarity, followed by hierarchical clustering to identify phenotype groups. Cluster solutions were evaluated using internal validity metrics, cluster size distributions, and interpretability. The resulting phenotypes were identified through diagnostic prevalence profiles and SOM-based visualizations. Results: The study included 927 adults with ASD, of whom 744 presented at least one comorbid diagnostic category and were included in the computational phenotyping analysis. The proposed pipeline identified four phenotypes characterized by distinct patterns of psychiatric and developmental comorbidity. The SOM structure provided an interpretable visualization of the diagnostic landscape, while hierarchical clustering enabled the identification of coherent phenotype groups. Internal validation metrics supported the selected solution while preserving informative subgroup sizes. Discussion: This study presents an end-to-end computational phenotyping pipeline that transforms routinely collected psychiatric EHR data into interpretable patient phenotypes. By integrating diagnostic extraction, clinically informed aggregation, representation learning, clustering, visualization, and characterization, the workflow provides a practical framework for analyzing complex diagnostic data in real-world mental health settings. Future studies should evaluate its applicability across other psychiatric and neurodevelopmental populations.

Indexed as

autism spectrum disorderclusteringcomputational phenotypingelectronic health recordsexplainable AImental healthself-organizing map

Identifiers

PMID42812347
PMCPMC13619622

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.