Evidence map›Paper›PMID 39779374›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Voxel-Based Lesion-Symptom Mapping Localizes Residual Visual Function in Hemianopia.

Hanna E Willis, Junaid Hameed, Lucy Starling, Carina Kaltenbach, Margaret Jane Moore, Amirah Khan, Rachel Maxwell, Marco Tamietto, Sara Ajina, Holly Bridge

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Hanna E WillisWellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, United Kingdom.
Junaid HameedWellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, United Kingdom.
Lucy StarlingWellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, United Kingdom.
Carina KaltenbachWellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, United Kingdom.
Margaret Jane MooreDepartment of Experimental Psychology, University of Oxford, Oxford OX2 6GG, United Kingdom.
Amirah KhanWellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, United Kingdom.
Rachel MaxwellWellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, United Kingdom.
Marco TamiettoDepartment of Psychology, University of Torino, Torino 10124, Italy.
Sara AjinaWellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, United Kingdom s.ajina@ucl.ac.uk.
Holly BridgeWellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford OX3 9DU, United Kingdom.ORCID 0000-0002-8089-6198

Funding

Medical Research Council MR/V034723/1Wellcome Trust
6 · The paper itself

Abstract

Damage to the primary visual cortex (V1) results in visual field deficits on the contralateral side of the world corresponding to the damaged region. Patients with such loss nonetheless show varying residual vision within this apparently blind region, with the neural mechanisms underlying this ability obscured by small study populations. We identified lesions on structural scans from 39 patients (12 female) with hemianopia and occipital lobe damage. We estimated the proportion of damage throughout the visual cortex and correlated this with performance in up to three different tests of residual vision in the blind field. We then performed voxel-based lesion-symptom mapping (VLSM) to determine the precise neural regions associated with residual vision. V1 damage did not show a relationship with residual vision measured with any task, although the extent of damage to V4 and hMT+/V5 both correlated with the ability to detect contrast-modulated stimuli. Indeed, damage to hMT+/V5 severely impacted performance across all three tasks, particularly motion detection. Although hMT+/V5 appeared necessary for residual vision, some patients with intact hMT+/V5 had no residual vision, indicating this area alone was not sufficient. VLSM revealed that damage to the optic radiation laterally was most highly associated with poor residual vision. Thus, VLSM indicates that hMT+/V5 and the optic radiation specifically are critical for residual vision in hemianopia.

Indexed as

Brain MappingHemianopsiaVisual CortexAdultAgedFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedPhotic StimulationVisual FieldsVisual Pathwaysblindsighthemianopiamotionprimary visual cortex (V1)residual visionvoxel-based lesion–symptom mapping (VLSM)

Identifiers

PMID39779374
PMCPMC11866999

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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.