Evidence map›Paper›PMID 19087179›Full record

ArticleEvolution; international journal of organic evolution2009

Connecting QTLS to the g-matrix of evolutionary quantitative genetics.

John K Kelly

Abstract read
In one paragraph

Article in Evolution; international journal of organic evolution, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Bridging developmental and statistical approaches to variation and evolution.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. Antagonistic selection and pleiotropy constrain the evolution of plant chemical defenses.Evolution; international journal of organic evolution · 2019
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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

1 author.

John K KellyDepartment of Ecology and Evolutionary Biology, University of Kansas, Lawrence, Kansas 66045, USA. jkk@ku.edu

Funding

Genomic Analysis of Complex Trait Variation in MimulusR01GM073990 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI KELLY, JOHN K · 2006 to 2015
$2.6M
NIGMS NIH HHS GM073990NIGMS NIH HHS R01 GM073990
6 · The paper itself

Abstract

Evolutionary quantitative genetics has recently advanced in two distinct streams. Many biologists address evolutionary questions by estimating phenotypic selection and genetic (co)variances (G matrices). Simultaneously, an increasing number of studies have applied quantitative trait locus (QTL) mapping methods to dissect variation. Both conceptual and practical difficulties have isolated these two foci of quantitative genetics. A conceptual integration follows from the recognition that QTL allele frequencies are the essential variables relating the G-matrix to marker-based mapping experiments. Breeding designs initiated from randomly selected parental genotypes can be used to estimate QTL-specific genetic (co)variances. These statistics appropriately distill allelic variation and provide an explicit population context for QTL mapping estimates. Within this framework, one can parse the G-matrix into a set of mutually exclusive genomic components and ask whether these parts are similar or dissimilar in their respective features, for example the magnitude of phenotypic effects and the extent and nature of pleiotropy. As these features are critical determinants of sustained response to selection, the integration of QTL mapping methods into G-matrix estimation can provide a concrete, genetically based experimental program to investigate the evolutionary potential of natural populations.

Indexed as

Biological EvolutionGenetics, PopulationQuantitative Trait LociSelection, GeneticData Interpretation, StatisticalGene FrequencyGenetic Variation

Identifiers

PMID19087179
PMCPMC5972393

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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.