Evidence map›Paper›PMID 23026724›Full record

ArticleCurrent opinion in genetics & development2012

Phenotypic models of evolution and development: geometry as destiny.

Paul François, Eric D Siggia

Abstract read
In one paragraph

Article in Current opinion in genetics & development, 2012. 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. Generative epigenetic landscapes map the topology and topography of cell fates.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Dynamical systems of fate and form in development.Seminars in cell & developmental biology · 2025
    Review
  3. Article
  4. Time and space in segmentation.Interface focus · 2021
    Article
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  15. Signalling dynamics in vertebrate segmentation.Nature reviews. Molecular cell biology · 2014
    Review
  16. Review
  17. Article
  18. Mechanisms and constraints shaping the evolution of body plan segmentation.The European physical journal. E, Soft matter · 2013
    Article
  19. 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.

Paul FrançoisMcGill University, 3600 rue University, H3A2T8, Montreal, QC, Canada. paulf@physics.mcgill.ca
Eric D Siggia

Funding

Dynamic readout of TGFb signaling and modeling of cell fate specification in humaR01GM101653 · NIGMS · ROCKEFELLER UNIVERSITY · PI BRIVANLOU, ALI H, SIGGIA, ERIC D. · 2012 to 2020
$2.6M
NIGMS NIH HHS R01 GM101653
6 · The paper itself

Abstract

Quantitative models of development that consider all relevant genes typically are difficult to fit to embryonic data alone and have many redundant parameters. Computational evolution supplies models of phenotype with relatively few variables and parameters that allows the patterning dynamics to be reduced to a geometrical picture for how the state of a cell moves. The clock and wavefront model, that defines the phenotype of somitogenesis, can be represented as a sequence of two discrete dynamical transitions (bifurcations). The expression-time to space map for Hox genes and the posterior dominance rule are phenotypes that naturally follow from computational evolution without considering the genetics of Hox regulation.

Indexed as

Biological EvolutionEmbryonic DevelopmentBody PatterningGene Expression Regulation, DevelopmentalGenes, HomeoboxPhenotypeSomites

Identifiers

PMID23026724
PMCPMC3609406

What OpenQuestion holds

Textmetadata
LicenceTDM
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.