Evidence map›Paper›PMID 42303230›Full record

ArticleJournal of chemical information and modeling2026

Can Graph Neural Networks Understand Chemical Elements?

Victor Kyllesbech, David A Poole Iii, Dimitrios Alivanistos, Michael Cochez, Halima Mouhib, Daan P Geerke

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Victor KyllesbechDepartment of Computer Science, Vrije Universiteit Amsterdam, 1081 HVAmsterdam, The Netherlands.ORCID 0000-0003-2614-9826
David A Poole IiiDepartment of Chemistry and Pharmaceutical Sciences, Vrije Universiteit Amsterdam, 1081 HZAmsterdam, The Netherlands.ORCID 0000-0002-5065-4112
Dimitrios AlivanistosDepartment of Computer Science, Vrije Universiteit Amsterdam, 1081 HVAmsterdam, The Netherlands.
Michael CochezDepartment of Computer Science, Vrije Universiteit Amsterdam, 1081 HVAmsterdam, The Netherlands.
Halima MouhibDepartment of Computer Science, Vrije Universiteit Amsterdam, 1081 HVAmsterdam, The Netherlands.
Daan P GeerkeDepartment of Chemistry and Pharmaceutical Sciences, Vrije Universiteit Amsterdam, 1081 HZAmsterdam, The Netherlands.

Funding

Accenture NAElsevier Discovery Lab NAEuropean Commission 101093202European Cooperation in Science and Technology CA23147Nederlandse Organisatie voor Wetenschappelijk Onderzoek 1292.19.272Vrije Universiteit Amsterdam NA
6 · The paper itself

Abstract

Classical machine learning (ML) has proven itself successful in a vast range of chemical applications. These successes often only come after substantial effort in feature engineering to obtain an effective data representation for the model input. Graph neural networks (GNNs) limit this feature engineering by learning their own representation directly from molecular graphs. However, the lack of an expert-generated representation may put larger requirements on training data set size compared to classical ML approaches. GNNs often still require vertex and edge features to provide information that cannot be learned from graph connectivity alone, such as chemical elements and bond orders. In this work, we investigate if chemically inspired representations of these features (specifically chemical elements) can combat GNN data requirements and/or improve performance or generalizability of the models. To this end, nine representations of chemical elements were created that encode trends in elemental reactivity and behavior. We tested these representations across GNN model size, data set size and additional degrees of featurization, utilizing the prediction of molecular pKa values as a benchmark. Our results suggest that the models largely classify elements, converting all representations into a largely orthogonal representation used internally. This mechanism explains our findings of minimal differences in model performance and generalizability between elemental representation. However, slight performance benefits are observed with more orthogonal elemental representations, probably because they better match the internal representation of the models. These findings led us to investigate the use of representations with increased orthogonality in the form of (i) atom-typing (effectively including information on atomic neighbors of the graph vertices), which yielded modest performance gains, and (ii) similarity typing as a novel atomic representation (encoding for similarity between atom types), which provided further performance gains but with substantial increase in computational cost for data set preparation.

Indexed as

Graph Neural NetworksMachine Learning

Identifiers

PMID42303230
PMCPMC13471721

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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.