Evidence map›Paper›PMID 25764302›Full record

ArticleeLife2015

Nuclear genomic signals of the 'microturbellarian' roots of platyhelminth evolutionary innovation.

Christopher E Laumer, Andreas Hejnol, Gonzalo Giribet

Abstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing 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

79 citing papers in PubMed.

  1. Article
  2. Unusual inheritance of a functionalScience advances · 2025
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  14. Metabolites play an underappreciated role in development.Proceedings of the National Academy of Sciences of the United States of America · 2024
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19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Christopher E LaumerMuseum of Comparative Zoology, Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, United States.ORCID http://orcid.org/0000-0001-8097-8516
Andreas HejnolSars International Centre for Marine Molecular Biology, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0003-2196-8507
Gonzalo GiribetMuseum of Comparative Zoology, Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flatworms number among the most diverse invertebrate phyla and represent the most biomedically significant branch of the major bilaterian clade Spiralia, but to date, deep evolutionary relationships within this group have been studied using only a single locus (the rRNA operon), leaving the origins of many key clades unclear. In this study, using a survey of genomes and transcriptomes representing all free-living flatworm orders, we provide resolution of platyhelminth interrelationships based on hundreds of nuclear protein-coding genes, exploring phylogenetic signal through concatenation as well as recently developed consensus approaches. These analyses robustly support a modern hypothesis of flatworm phylogeny, one which emphasizes the primacy of the often-overlooked 'microturbellarian' groups in understanding the major evolutionary transitions within Platyhelminthes: perhaps most notably, we propose a novel scenario for the interrelationships between free-living and vertebrate-parasitic flatworms, providing new opportunities to shed light on the origins and biological consequences of parasitism in these iconic invertebrates.

Indexed as

Biological EvolutionGenomeAnimalsCell NucleusLikelihood FunctionsParasitesPhylogenyPlatyhelminthsevolutionary biologygenomicsparasitismphylogenyPlatyhelminthesRNA-seq

Identifiers

PMID25764302
PMCPMC4398949

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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.