Evidence map›Paper›PMID 42173906›Full record

ArticleNPJ systems biology and applications2026

Molecular maps of diseases from omics data and network embeddings.

Dewei Hu, Anna-Lisa Schaap-Johansen, Julia Villarroel, Clara Ekebjærg, Simon Rasmussen, Daniel Hvidberg Hansen, Rasmus Wernersson, Lars Juhl Jensen

Abstract read
In one paragraph

Article in NPJ systems biology and applications, 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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

8 authors.

Dewei Hu *Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Anna-Lisa Schaap-Johansen *ZS Associates, ZS Discovery, Kgs, Lyngby, Denmark.
Julia VillarroelZS Associates, ZS Discovery, Kgs, Lyngby, Denmark.
Clara EkebjærgZS Associates, ZS Discovery, Kgs, Lyngby, Denmark.
Simon RasmussenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Daniel Hvidberg HansenZS Associates, ZS Discovery, Kgs, Lyngby, Denmark.
Rasmus WernerssonZS Associates, ZS Discovery, Kgs, Lyngby, Denmark.
Lars Juhl JensenZS Associates, ZS Discovery, Kgs, Lyngby, Denmark. larsjuhl.jensen@zs.com.

Funding

Novo Nordisk Fonden NNF14CC0001Novo Nordisk Fonden NNF23SA0084103
6 · The paper itself

Abstract

Identifying disease-relevant proteins and pathways remains a fundamental challenge in understanding disease mechanisms and supporting therapeutic development. While omics analyses can provide valuable insights, they typically consider each gene/protein separately rather than at the level of biological systems. This can be addressed by combining the omics data with protein networks. We integrate disease-specific omics data with a universal functional association network from STRING, which we represent using node2vec embedding. This way, we constructed disease maps for seven diseases spanning inflammatory, oncological, neurological, and vascular diseases based on genetics, transcriptomics, somatic mutation, and proteomics data. Compared to omics analysis alone, the use of a simple linear model on top of network embedding enabled us to identify 2-4 times as many known disease-relevant proteins at the same specificity. Clustering of the resulting disease maps revealed both functional modules shared by many diseases, such as inflammatory pathways and cancer hallmarks, and disease-specific modules, such as keratinization in atopic dermatitis and extracellular matrix remodeling in aortic aneurysm. Together, these results highlight the value of protein network embedding when analyzing omics data to understand diseases.

Indexed as

Computational BiologyGene Expression ProfilingGene Regulatory NetworksGenomicsHumansMultiomicsProtein Interaction MapsProteomics

Identifiers

PMID42173906
PMCPMC13470450

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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.