Evidence map›Paper›PMID 40400525›Full record

ArticleRoyal Society open science2025

Polygenic prediction and gene regulation networks.

Juan F Poyatos

Abstract read
In one paragraph

Article in Royal Society open science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

1 citing paper in PubMed.

  1. Polygenic prediction and gene regulation networks.Royal Society open science · 2025
    Article
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

1 author.

Juan F PoyatosLogic of Genomic Systems Lab, Consejo Superior de Investigaciones Cientificas, Madrid, Spain.ORCID https://orcid.org/0000-0003-4575-8723

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exploring the degree to which phenotypic variation, influenced by intrinsic nonlinear biological mechanisms, can be accurately captured using statistical methods is essential for advancing our comprehension of complex biological systems and predicting their functionality. Here, we examine this issue by combining a computational model of gene regulation networks with a linear additive prediction model, akin to polygenic scores utilized in genetic analyses. Inspired by the variational framework of quantitative genetics, we create a population of individual networks possessing identical topology yet showcasing diversity in regulatory strengths. By discerning which regulatory connections determine the prediction of phenotypes, we contextualize our findings within the framework of core and peripheral causal determinants, as proposed by the omnigenic model of complex traits. We establish connections between our results and concepts such as global sensitivity and local stability in dynamical systems, alongside the notion of sloppy parameters in biological models. Furthermore, we explore the implications of our investigation for the broader discourse surrounding the role of epistatic interactions in the prediction of complex phenotypes.

Indexed as

complex traitgene regulation networkphenotype predictionpolygenic score

Identifiers

PMID40400525
PMCPMC12092097

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.