Evidence map›Paper›PMID 42379135›Full record

ReviewAnnual review of vision science2026

Diversity and Feature Selectivity of Primate Retinal Ganglion Cells.

Natalie G Bernstein, Teresa Puthussery

Abstract readReview
In one paragraph

Review in Annual review of vision science, 2026. 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. Natural motion statistics unify direction computations.bioRxiv : the preprint server for biology · 2026
    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.

Natalie G BernsteinNeuroscience Graduate Program, University of California, Berkeley, California, USA.
Teresa PuthusseryNeuroscience Graduate Program, University of California, Berkeley, California, USA.

Funding

Structure and Function of Primate Retinal CircuitsR01EY024265 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI PUTHUSSERY, TERESA · 2014 to 2025
$4.4M
NEI NIH HHS R01 EY024265
6 · The paper itself

Abstract

The primate retina transmits visual information to the brain through parallel pathways carried by diverse retinal ganglion cell (RGC) types, each of which encodes specific features in the visual environment. These parallel channels provide input to a variety of brain regions to support both conscious and reflexive visual functions. Although the midget, parasol, and small bistratified pathways have dominated classical models of primate vision, accumulating evidence points to a broader diversity of wide-field RGC types whose functions are less well understood. Recent breakthroughs in single-cell sequencing have provided new insights into the transcriptomic signatures of these wide-field cells, uncovering molecular markers that can be used to link sparse RGC types to their distinct morphologies and physiological functions. This review synthesizes current knowledge about the diversity of wide-field RGCs in the primate retina and highlights recent insights into cells that encode complex visual features, such as direction-selective ganglion cells. We emphasize how integrative methodological approaches are refining our understanding of the roles of different wide-field RGC types in primate vision.

Indexed as

PrimatesRetinal Ganglion CellsAnimalsHumansVisual Pathwayscell classificationdirection-selectivityfoveahumanmacaque

Identifiers

PMID42379135
PMCPMC13657633

What OpenQuestion holds

Textmetadata
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.