Evidence map›Paper›PMID 33329721›Full record

ArticleFrontiers in genetics2020

Exploring the Link Between Additive Heritability and Prediction Accuracy From a Ridge Regression Perspective.

Arthur Frouin, Claire Dandine-Roulland, Morgane Pierre-Jean, Jean-François Deleuze, Christophe Ambroise, Edith Le Floch

Abstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Evaluating Genetic Regulators of MicroRNAs Using Machine Learning Models.International journal of molecular sciences · 2025
    Article
  2. 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

6 authors.

Arthur FrouinCNRGH, Institut Jacob, CEA - Université Paris-Saclay, Évry, France.
Claire Dandine-RoullandCNRGH, Institut Jacob, CEA - Université Paris-Saclay, Évry, France.
Morgane Pierre-JeanCNRGH, Institut Jacob, CEA - Université Paris-Saclay, Évry, France.
Jean-François DeleuzeCNRGH, Institut Jacob, CEA - Université Paris-Saclay, Évry, France.
Christophe AmbroiseLaMME, Université Paris-Saclay, CNRS, Université d'Évry val d'Essonne, Évry, France.
Edith Le FlochCNRGH, Institut Jacob, CEA - Université Paris-Saclay, Évry, France.

Funding

Medical Research Council MC_PC_17228Medical Research Council MC_QA137853
6 · The paper itself

Abstract

Genome-Wide Association Studies (GWAS) explain only a small fraction of heritability for most complex human phenotypes. Genomic heritability estimates the variance explained by the SNPs on the whole genome using mixed models and accounts for the many small contributions of SNPs in the explanation of a phenotype. This paper approaches heritability from a machine learning perspective, and examines the close link between mixed models and ridge regression. Our contribution is two-fold. First, we propose estimating genomic heritability using a predictive approach via ridge regression and Generalized Cross Validation (GCV). We show that this is consistent with classical mixed model based estimation. Second, we derive simple formulae that express prediction accuracy as a function of the ratio

Indexed as

best linear unbiased predictorgeneralized cross validationheritabilitymixed modelprediction accuracyridge regression

Identifiers

PMID33329721
PMCPMC7672157

What OpenQuestion holds

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Registered trials

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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.