Evidence map›Paper›PMID 16565924›Full record

ArticleJournal of pharmacokinetics and pharmacodynamics2006

A genetic algorithm-based, hybrid machine learning approach to model selection.

Robert R Bies, Matthew F Muldoon, Bruce G Pollock, Steven Manuck, Gwenn Smith, Mark E Sale

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of pharmacokinetics and pharmacodynamics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
–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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Go beyond the limits of genetic algorithm in daily covariate selection practice.Journal of pharmacokinetics and pharmacodynamics · 2024
    Article
  10. Article
  11. Article
  12. Population pharmacokinetic model selection assisted by machine learning.Journal of pharmacokinetics and pharmacodynamics · 2022
    Article
  13. Article
  14. Article
  15. Machine Learning in Drug Discovery and Development Part 1: A Primer.CPT: pharmacometrics & systems pharmacology · 2020
    Article
  16. MinimaxHealth systems (Basingstoke, England) · 2019
    Article
  17. Article
  18. Article
  19. Covariate selection in pharmacometric analyses: a review of methods.British journal of clinical pharmacology · 2015
    Review
  20. Review
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.

Robert R BiesDepartment of Pharmaceutical Sciences and Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA. rrb47@pitt.edu
Matthew F Muldoon
Bruce G Pollock
Steven Manuck
Gwenn Smith
Mark E Sale

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe a general and robust method for identification of an optimal non-linear mixed effects model. This includes structural, inter-individual random effects, covariate effects and residual error models using machine learning. This method is based on combinatorial optimization using genetic algorithm.

Indexed as

AlgorithmsArtificial IntelligenceModels, BiologicalAntidepressive Agents, Second-GenerationCitalopramComputer SimulationHumansInfusions, IntravenousModels, GeneticSoftwareAntidepressive Agents, Second-GenerationCitalopram

Identifiers

What OpenQuestion holds

Textmetadata
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.