Evidence map›Paper›PMID 41275407›Full record

ArticleThe Journal of physiology2026

Causal disconnectomics of motion perception networks: insights from transcranial magnetic stimulation-induced BOLD responses.

Estelle Raffin, Roberto F Salamanca-Giron, Krystel R Huxlin, Olivier Reynaud, Loan Mattera, Roberto Martuzzi, Friedhelm C Hummel

Abstract read
In one paragraph

Article in The Journal of physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Estelle RaffinNeuro-X Institute (INX), Defitech Chair of Clinical Neuroengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), Geneva, Switzerland.ORCID 0000-0003-3262-5251
Roberto F Salamanca-GironNeuro-X Institute (INX), Defitech Chair of Clinical Neuroengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), Geneva, Switzerland.ORCID 0009-0008-5743-6805
Krystel R HuxlinThe Flaum Eye Institute and Center for Visual Science, University of Rochester, Rochester, New York, USA.ORCID 0000-0001-7138-6156
Olivier ReynaudMRI Platform, Fondation Campus Biotech Geneva (FCBG), Campus Biotech, Geneva, Switzerland.
Loan MatteraMRI Platform, Fondation Campus Biotech Geneva (FCBG), Campus Biotech, Geneva, Switzerland.
Roberto MartuzziMRI Platform, Fondation Campus Biotech Geneva (FCBG), Campus Biotech, Geneva, Switzerland.ORCID 0000-0003-3811-0961
Friedhelm C HummelNeuro-X Institute (INX), Defitech Chair of Clinical Neuroengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), Geneva, Switzerland.ORCID 0000-0002-4746-4633

Funding

Bertarelli Foundation Catalyst BC77O7Defitech FoundationSwiss National Science Foundation PRIMA PR00P3_179867
6 · The paper itself

Abstract

Understanding how focal perturbations trigger large-scale network reorganization is essential for uncovering the neural mechanisms that support perception and behaviour. Here we used a transcranial magnetic stimulation (TMS) perturbational approach by applying brief 10 Hz TMS to early visual areas (EVAs) or the medio-temporal (MT) area in healthy participants while recording concurrent functional magnetic resonance imaging (fMRI). TMS delivered during the early stages of motion processing specifically impaired direction discrimination at both sites, whereas disruption of the later processing phase impaired performances only for the MT condition. Despite a similar local increase in BOLD activity induced by EVA and MT stimulation, the broader network responses diverged significantly. Perturbation of EVA elicited a more robust and efficient pattern of functional reorganization, manifesting as more constrained BOLD changes, consistent with greater resilience to focal disruption. In contrast behavioural impairments induced by MT stimulation were accompanied by a disorganized and less-efficient network configuration, characterized by smaller small-world properties and longer path lengths. The decrease in performances induced by MT stimulation scaled with lower clustering coefficients, implying a more random or decentralized network structure. These findings demonstrate that TMS-fMRI coupling provides a powerful framework for causally mapping the relationships between local neural perturbations, large-scale network dynamics and behavioural performance. KEY POINTS: Transcranial magnetic stimulation (TMS)-induced perturbation of the early visual areas (EVAs) or the medio-temporal (MT) area selectively impairs motion direction discrimination. The TMS perturbation is associated with a context-dependent local upscaling of blood-oxygen-level dependent (BOLD) activity in both areas. The two visual areas exhibit distinct topological networks' adaptation in response to TMS, reflecting different levels of network resilience to a focal lesion. TMS-functional magnetic resonance imaging (fMRI) coupling can be used to assess 'causal disconnectomics' and to precisely map how a local perturbation propagates to large-scale behavioural deficits.

Indexed as

Motion PerceptionTranscranial Magnetic StimulationVisual CortexAdultFemaleHumansMagnetic Resonance ImagingMaleYoung Adultfunctional disconnectomicsmotion direction discriminationnetwork analysesonline TMS–functional magnetic resonance imaging (fMRI)transcranial magnetic stimulation (TMS) perturbation

Identifiers

PMID41275407
PMCPMC12783956

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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.