Evidence map›Paper›PMID 38315722›Full record

ArticlePLoS biology2024

Relation of connectome topology to brain volume across 103 mammalian species.

Maria Grazia Puxeddu, Joshua Faskowitz, Caio Seguin, Yossi Yovel, Yaniv Assaf, Richard Betzel, Olaf Sporns

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Correspondence of large-scale functional brain network decline across aging mice and humans.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. 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

7 authors at 2 institutions in 2 countries.

Maria Grazia PuxedduDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana, United States of America.ORCID 0000-0001-8725-465X
Joshua FaskowitzDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana, United States of America.
Caio SeguinDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana, United States of America.
Yossi YovelSchool of Neurobiology, Biochemistry and Biophysics, Tel Aviv University, Tel Aviv, Israel.
Yaniv AssafSchool of Neurobiology, Biochemistry and Biophysics, Tel Aviv University, Tel Aviv, Israel.
Richard BetzelDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana, United States of America.
Olaf SpornsDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana, United States of America.
Indiana University Bloomington · USTel Aviv University · IL

Funding

CRCNS: The Evolution of the Mammalian ConnectomeR01MH122957 · NIMH · TRUSTEES OF INDIANA UNIVERSITY · PI SPORNS, OLAF · 2019 to 2021
$485k
NIMH NIH HHS R01 MH122957
6 · The paper itself

Abstract

The brain connectome is an embedded network of anatomically interconnected brain regions, and the study of its topological organization in mammals has become of paramount importance due to its role in scaffolding brain function and behavior. Unlike many other observable networks, brain connections incur material and energetic cost, and their length and density are volumetrically constrained by the skull. Thus, an open question is how differences in brain volume impact connectome topology. We address this issue using the MaMI database, a diverse set of mammalian connectomes reconstructed from 201 animals, covering 103 species and 12 taxonomy orders, whose brain size varies over more than 4 orders of magnitude. Our analyses focus on relationships between volume and modular organization. After having identified modules through a multiresolution approach, we observed how connectivity features relate to the modular structure and how these relations vary across brain volume. We found that as the brain volume increases, modules become more spatially compact and dense, comprising more costly connections. Furthermore, we investigated how spatial embedding shapes network communication, finding that as brain volume increases, nodes' distance progressively impacts communication efficiency. We identified modes of variation in network communication policies, as smaller and bigger brains show higher efficiency in routing- and diffusion-based signaling, respectively. Finally, bridging network modularity and communication, we found that in larger brains, modular structure imposes stronger constraints on network signaling. Altogether, our results show that brain volume is systematically related to mammalian connectome topology and that spatial embedding imposes tighter restrictions on larger brains.

Indexed as

ConnectomeAnimalsBrainCommunicationDatabases, FactualMammalsNerve Net

Identifiers

PMID38315722
PMCPMC10868790
OpenAlexW4391528430

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.