Evidence map›Paper›PMID 41654559›Full record

ArticleNature communications2026

Physiological basis of resolution acuity in vision.

Keaton M Ramsey, Philipp Tellers, Alexander Meadway, Pavan Tiruveedhula, Austin Roorda, Lawrence C Sincich

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Keaton M Ramsey *Neuroengineering PhD Program, School of Engineering and School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0009-0003-2900-6908
Philipp Tellers *Department of Optometry and Vision Science, School of Optometry, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0002-7252-7261
Alexander MeadwayDepartment of Optometry and Vision Science, School of Optometry, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0001-9815-7783
Pavan TiruveedhulaHerbert Wertheim School of Optometry and Vision Science, University of California, Berkeley, CA, USA.ORCID 0009-0001-5672-4046
Austin RoordaHerbert Wertheim School of Optometry and Vision Science, University of California, Berkeley, CA, USA.ORCID 0000-0002-3785-0848
Lawrence C SincichDepartment of Optometry and Vision Science, School of Optometry, University of Alabama at Birmingham, Birmingham, AL, USA. sincich@uab.edu.ORCID 0000-0002-1684-2283

Funding

Visual Phenotyping CoreP30EY003039 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Paul Douglas Gamlin · 1985 to 2026
$16.9M
UC Berkeley Vision Science COREP30EY003176 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI RICHARD H KRAMER · 1985 to 2026
$16.4M
Short Term Adaptations in PhotoreceptorsR01EY023603 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KRAFT, TIMOTHY W, SINCICH, LAWRENCE C · 2014 to 2022
$3.1M
Photoreceptor Signaling in the Early Visual SystemR01EY023581 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SINCICH, LAWRENCE C · 2013 to 2017
$1.7M
Elementary Cone Photoreceptor Representation in Primary Visual CortexR01EY036825 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LAWRENCE C SINCICH · 2025 to 2026
$1.1M
Deutsche Forschungsgemeinschaft (German Research Foundation) TE 1182/1-1NEI NIH HHS P30 EY003039NEI NIH HHS P30 EY003176NEI NIH HHS R01 EY023581NEI NIH HHS R01 EY023603NEI NIH HHS R01 EY036825United States Department of Defense | United States Air Force | AFMC | Air Force Office of Scientific Research (AF Office of Scientific Research) FA9550-21-1-0230U.S. Department of Health & Human Services | NIH | National Eye Institute (NEI) P30-EY003039U.S. Department of Health & Human Services | NIH | National Eye Institute (NEI) R01-EY023581U.S. Department of Health & Human Services | NIH | National Eye Institute (NEI) R01-EY023591U.S. Department of Health & Human Services | NIH | National Eye Institute (NEI) R01-EY023603U.S. Department of Health & Human Services | NIH | National Eye Institute (NEI) R01-EY036825
6 · The paper itself

Abstract

Vision is the primary sensory modality for many animals, especially humans and other primates. A fundamental constraint on visual resolution acuity is set by the size and spacing of cone photoreceptors, notably in the fovea of the retina where cones are the smallest. To optimally utilise this cone array, neurons in the retina and lateral geniculate nucleus (LGN) must have receptive field centres comprised of only one cone, yet such receptive fields have never been observed directly. Here we comprehensively map parafoveal LGN receptive fields in male macaques using an adaptive optics microstimulator and align them to the underlying cone mosaic. The receptive field centres of parvocellular LGN neurons were most often defined by signals originating from a single cone photoreceptor, a finding confirmed by biophysical light capture modelling and spatial frequency tuning data. Our results demonstrate that visual acuity originating at the fovea is mediated by LGN neurons working at the limit of cone photoreceptor spacing. Revealing this physiological basis of spatial resolution reconciles longstanding anatomical and perceptual data over what mechanism limits acuity prior to cortical processing, underscoring the centrality of optical correction for attaining peak visual resolving power.

Indexed as

Geniculate BodiesRetinal Cone Photoreceptor CellsVision, OcularVisual AcuityAnimalsFovea CentralisMacaca mulattaMalePhotic StimulationRetinaVisual Fields

Identifiers

PMID41654559
PMCPMC12992762

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.