Evidence map›Paper›PMID 23893343›Full record

ArticleGenetic epidemiology2013

Ridge regression in prediction problems: automatic choice of the ridge parameter.

Erika Cule, Maria De Iorio

Abstract read
In one paragraph

Article in Genetic epidemiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Evaluating Genetic Regulators of MicroRNAs Using Machine Learning Models.International journal of molecular sciences · 2025
    Article
  10. Reduced myelin contributes to cognitive impairment in patients with monogenic small vessel disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors.

Erika CuleDepartment of Epidemiology and Biostatistics, Imperial College London, London, United Kingdom; Statistical Consulting Group, GlaxoSmithKline, Stevenage, United Kingdom.
Maria De Iorio

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To date, numerous genetic variants have been identified as associated with diverse phenotypic traits. However, identified associations generally explain only a small proportion of trait heritability and the predictive power of models incorporating only known-associated variants has been small. Multiple regression is a popular framework in which to consider the joint effect of many genetic variants simultaneously. Ordinary multiple regression is seldom appropriate in the context of genetic data, due to the high dimensionality of the data and the correlation structure among the predictors. There has been a resurgence of interest in the use of penalised regression techniques to circumvent these difficulties. In this paper, we focus on ridge regression, a penalised regression approach that has been shown to offer good performance in multivariate prediction problems. One challenge in the application of ridge regression is the choice of the ridge parameter that controls the amount of shrinkage of the regression coefficients. We present a method to determine the ridge parameter based on the data, with the aim of good performance in high-dimensional prediction problems. We establish a theoretical justification for our approach, and demonstrate its performance on simulated genetic data and on a real data example. Fitting a ridge regression model to hundreds of thousands to millions of genetic variants simultaneously presents computational challenges. We have developed an R package, ridge, which addresses these issues. Ridge implements the automatic choice of ridge parameter presented in this paper, and is freely available from CRAN.

Indexed as

Models, GeneticPhenotypeAlgorithmsBipolar DisorderGenetic Predisposition to DiseaseGenetic VariationGenotypeHumansPolymorphism, Single NucleotideRegression AnalysisROC CurveSoftwareGWASpenalised regressionpredictionshrinkage methodssoftware

Identifiers

PMID23893343
PMCPMC4377081

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.